Subject: Concrete Technology Sub Code: 10Cv42
Subject: Concrete Technology Sub Code: 10Cv42
Subject: Concrete Technology Sub Code: 10Cv42
Prepared by,
Poornima H.R
Assistant Professor
Dept. of Civil Engg.
ACE, Banglore
Dept. of Civil engg, ACE, Banglore Page 1
CONCRETE TECHNOLOGY
UNIT – 1
INTRODUCTION
Definition:
Cement is defined in many ways as follows,
• Cement, any material that hardens and becomes strongly adhesive after
application.
• Manufactured substance consisting of gypsum plaster, or Portland cement.
• Portland cement hardens and adheres after being mixed with water.
History of Cement:
• The term “Portland cement” was first used in 1824 by Joseph Aspdin, a British
cement-maker, because of the resemblance between concrete made from his
cement and Portland stone, which was commonly used in buildings in Britain.
• At that time cements were usually made in upright kilns where the raw materials
were spread between layers of coke, which was then burnt.
• The first rotary kilns were introduced about 1880. Portland cement is now almost
universally used for structural concrete.
Manufacturing Process:
• Main ingredients used in the manufacture of cement are:
• Limestone
– Calcium
• Clay, shale
– Silica/Alumina
• Quarrying
– local resources necessary: no market
• Limestone (CaCO3) and Clay are two main raw materials used for
manufacturing Portland cement clinker.
• Clays have various amount of SiO2 and Al2O3.
• In the manufacturing process of Portland cement, clinker consist essentially of
grinding the raw materials, mixing them in appropriate proportion, burning the
raw material in a kiln at a temperature of 1400-1500oC until material partially
fuses into balls known as Clinker and grinding cooled clinker together with a
small amount of gypsum rock.
• The mixture of raw material is burned in a rotary kiln.
THE KILN
The heart of the cement plant
• Largest moving part of any machine.
• inclined, rotates.
• up to 50m long and 5m diam.
• Heated by fire jet
• The rotary kiln is along steel cylinder lined with refractory brick (length
/diameter ~30). Modern kilns may reach 6m in diameter and over 180m in
height with a production capacity exceeding 1000 tones a day.
• The kiln is inclined a few degrees from the horizontal ( about 4 cm\m )
and is rotated about its axis at a speed of about 60 to 150 revolution\hour ).
• Pulverized coal or gas is used as the source of heat. The heat is supplied
from the lower end of the kiln. The max. temperature near the lower end
of the kiln is generally about 1400-1500 OC.
• The upper end of the kiln the temperature is around 150 OC.
• The mixture of the raw material is fed from the upper end of the kiln.This
material move toward the lower end by effect of inclanation and rotation
of the kiln. Thus the materials are subjected to high temperature at lower
end of the kiln.
• The materials that are introduced into the rotary kiln are subjected to
several distinct process as they move downward.
• When the raw materials are fed into the kiln, drying of the material takes
place, and any free water in the raw material is evaporated.
• Clay losses its water about 150 to 350 OC.
• Sculptural
• Improbable
CONCRETE
Concrete is a mixture of Cement paste and aggregate
• Compression: up to 120 MPa
– Comparable to Al
• Tension: <10 MPa
• Tension reinforcement
– steel bars
Cement
(Chemical Composition and Hydration)
Oxide Composition of Portlant Cement
• Portland cement is composed of four major oxides: lime ( CaO ), silica ( SiO2 ),
alumina ( Al2O3 ), and iron ( Fe2O3 ).
• Also Portland cement contains small amount of magnesia ( MgO ), alkalies
(Na2O and K2O ), and sulfuric anhydrite ( SO3 ).
Hydration of cement
• When Portland cement is mixed with water its chemical compound constituents
undergo a series of chemical reactions that cause it to harden. This chemical
reaction with water is called "hydration". Each one of these reactions occurs at a
different time and rate. Together, the results of these reactions determine how
Portland cement hardens and gains strength.
OPC hydration
• Hydration starts as soon as the cement and water are mixed.
• The rate of hydration and the heat liberated by the reaction of each compound is
different.
• Each compound produces different products when it hydrates.
• Tricalcium silicate (C3S). Hydrates and hardens rapidly and is largely
responsible for initial set and early strength. Portland cements with higher
percentages of C3S will exhibit higher early strength.
• Tricalcium aluminate (C3A). Hydrates and hardens the quickest. Liberates a
large amount of heat almost immediately and contributes somewhat to early
strength. Gypsum is added to Portland cement to retard C3A hydration. Without
gypsum, C3A hydration would cause Portland cement to set almost immediately
after adding water.
• Dicalcium silicate (C2S). Hydrates and hardens slowly and is largely responsible
for strength increases beyond one week.
• Tetracalcium aluminoferrite (C4AF). Hydrates rapidly but contributes very little
to strength. Its use allows lower kiln temperatures in Portland
cementmanufacturing. Most Portland cement color effects are due to C4AF.
• Reactions of Hydration
• 2C3S + 6H = C3S2H3 + 3Ca(OH)2
(100 + 24 = 75 + 49 )
• 2 C2S + 4H = C3S2H3 + Ca(OH)2
(100 + 21 = 99 + 22 )
• C3A + 6H = C3AH6
[C3A + CaSO4 . 2H2O = 3Cao. Al2O3. 3CaSO4. 31H2O]
Calcium Sulfoaluminate
Heat of Hydration
• The heat of hydration is the heat generated when water and Portland cement
react. Heat of hydration is most influenced by the proportion of C3S and C3A in
the cement, but is also influenced by water-cement ratio, fineness and curing
temperature. As each one of these factors is increased, heat of hydration increases.
• For usual range of Portland cements, about one-half of the total heat is liberated
between 1 and 3 days, about three-quarters in 7 days, and nearly 90 percent in 6
months.
• The heat of hydration depends on the chemical composition of cement
Concrete The Extensively used material after water because of the following
reasons
_ Versatile
_ Pliable when mixed
_ Strong & Durable
_ Does not Rust or Rot
_ Does Not Need a Coating
_ Resists Fire
_ Almost Suitable for any Environmental Exposure Conditions
CONCRETE TECHNOLOGY
CEMENT
• Cement, any material that hardens and becomes strongly adhesive after
application.
• Manufactured substance consisting of gypsum plaster, or Portland cement
• Portland cement hardens and adheres after being mixed with water.
HISTORY OF CEMENT:
• The term “Portland cement” was first used in 1824 by Joseph Aspdin, a British
cement-maker, because of the resemblance between concrete made from his
cement and Portland stone, which was commonly used in building in Britain.
• The first modern Portland cement, made from lime and clay materials heated
until they formed clinkers was produced by Isaac Charles Johnson in Britain in
1845.
• At that time cements were usually made in upright kilns where the raw materials
were spread between layers of coke, which was then burnt.
• The first rotary kilns were introduced about 1880. Portland cement is now almost
universally used for structural concrete.
HOW IS IT MADE?
Limestone for calcium and Clay or shale for Silica/Alumina is used as raw
materials.
The manufacturing process of Portland cement clinker consist essentially of
grinding the raw materials, mixing them in appropriate proportion, burning the
raw material in a kiln at a temperature of 1400-1500 oC until material partially
fuses into balls known as clinker and grinding to cooled clinker together with a
small amount of gypsum rock.
The mixture of raw material is burned in a rotary kiln.
The Kiln:
• The kiln is inclined a few degrees from the horizontal ( about 4 cm\m ) and is
rotated about its axis at a speed of about 60 to 150 revolution \ hour ).
• Pulverized coal or gas is used as the source of heat. The heat is supplied from the
lower end of the kiln. The max. Temperature near the lower end of the kiln is
generally about 1400-1500 OC.
• The upper end of the kiln the temperature is around 150 OC.
• The mixture of the raw material is fed from the upper end of the kiln.This
material move toward the lower end by effect of inclanation and rotation of the
kiln. Thus the material is subjected to high temperature at lower end of the kiln.
• The materials that are introduced into the rotary kiln are subjected to several
distinct process as they move downward.
• When the raw materials are fed into the kiln, drying of the material takes place,
and any free water in the raw material is evaporated.
• Clay losses its water about 150 to 350 OC.
• Clay decompose at a range of 350 to 650 OC.
• Magnesite in raw material loss about 600 OC.
• The limestone losses its CO2 at about 900 OC.
• At 1250 to 1280 OC some liquid formation begins and compound formation
start to takes place.
• Clinkering begins at about 1280 OC. The liquid that forms during the burning
process causes the charge to agglomerate into nodules of various size, usually
1-25 mm in diameter known as Portland cement clinker.
• All exhaust gases produced during the burning process of the materials leave
the kiln through the stack.
CEMENT:
Physical Properties
Fineness
• Fineness or particle size of Portland cement affects Hydration rate and thus the
rate of strength gain. The smaller the particle size, the greater the surface areato-
volume ratio, and thus, the more area available for water-cement interaction
per unit volume. The effects of greater fineness on strength are generally seen
during the first seven days.
• When the cement particles are coarser, hydration starts on the surface of the
particles. So the coarser particles may not be completely hydrated. This causes
low strength and low durability.
• For a rapid development of strength a high fineness is necessary.
Soundness
When referring to Portland cement, "soundness" refers to the ability of a hardened
cement paste to retain its volume after setting without delayed expansion. This
expansion is caused by excessive amounts of free lime (CaO) or magnesia (MgO).
Most Portland cement specifications limit magnesia content and expansion.
Setting Time
• Cement paste setting time is affected by a number of items including: cement
fineness, water-cement ratio, chemical content (especially gypsum content) and
admixtures. Setting tests are used to characterize how a particular cement paste
sets. For construction purposes, the initial set must not be too soon and the final
set must not be too late. Normally, two setting times are defined:
• Initial set. Occurs when the paste begins to stiffen considerably.
• Final set. Occurs when the cement has hardened to the point at which it can
sustain some load.
• Setting is mainly caused by C3A and C3S and results in temperature rise
in the cement paste.
• False set :No heat is evolved in a false set and the concrete can be remixed
without adding water
• Occures due to the conversion of unhydreous/semihydrous gypsum to hydrous
gypsum(CaSO4.2H2O)
• Flash Set: is due to absence of Gypsum. Specifically used for under water repair.
Strength
• Cement paste strength is typically defined in three ways: compressive, tensile
and flexural. These strengths can be affected by a number of items including:
water-cement ratio, cement-fine aggregate ratio, type and grading of fine
aggregate, curing conditions, size and shape of specimen, loading conditions and
age.
Duration of Testing
Typically, Durations of testing are:
• 1 day (for high early strength cement)
• 3 days, 7 days, 28 days and 90 days (for monitoring strength progress)
• 28 days strength is recognised as a basis for control in most codes.
• When considering cement paste strength tests, there are two items to consider:
• Cement mortar strength is not directly related to concrete strength. Cement paste
strength is typically used as a quality control measure.
• Strength tests are done on cement mortars (cement + water + sand) and not on
cement pastes.
CEMENT
Chemical Composition
Oxide composition
Mass Percentage
Mass Percentage
C3A 14 15 7
C4AF 4 10 14
Hydration
When Portland cement is mixed with water its chemical compound constituents
undergo a series of chemical reactions that cause it to harden. This chemical
reaction with water is called "hydration". Each one of these reactions occurs at a
different time and rate. Together, the results of these reactions determine how
Portland cement hardens and gains strength.
OPC hydration
Heat
Compounds Reaction Am ount of Strength Liberation
Rate Liberated
Low
C2S Slow Low initially, Low
high later
Reactions of Hydration
Heat of Hydration
The heat of hydration is the heat generated when water and Portland cement react.
Heat of hydration is most influenced by the proportion of C3S and C3A in the
cement, but is also influenced by water-cement ratio, fineness and curing
temperature. As each one of these factors is increased, heat of hydration increases.
•For usual range of Portland cements, about one-half of the total heat is liberated
between 1 and 3 days, about three-quarters in 7 days, and nearly 90 percent in 6
months.
• The heat of hydration depends on the chemical composition of cement.
This test is conducted on cylindrical concrete core specimens removed from the
hardened concrete by a drilling operation. A core drilling machine is used for
cutting and removing the concrete samples. This machine is equipped with
diamond cutters located on the end of a cylindrical (tube-like) cutting device. As
the machine is operated, the cylinder shaped cutter rotates at a high speed.
The diameter of the concrete core specimen removed from the hardened concrete
depends on the inner diameter of the cylindrical cutting device. Usually concrete
cores having diameters of 10 cm or 15 cm are obtained.
The removed core specimens may have different lengths depending on the
thickness of the hardened concrete that they are cut from.
If the core specimen is too long, it is shortened so that it will have a
length/diameter ratio of 2.0.
Core specimens which have a length/diameter ratio of less than 2.0 can also be
used for compressive strength testing purposes, but a specimen having a
length/diameter ratio of less than 1.0 should not be used.
If the ratio of the length to the diameter of the specimen is less than 2.0, allowance
is made; the compressive strength found by the test should be multiplied with the
correction factors shown in Table.
1.75 0.98
1.50 0.96
1.25 0.93
1.00 0.87
Modulus Elasticity
Defining modulus of elasticity of concrete is difficult;Because concrete is not a
linearly elastic material Since the slope of σ-ε curve of concrete is not constant.
We must first describe modulus of elasticity (Ec). In general; Modulus of elasticity
defined for concrete is the instantaneous Ec. This is not influenced by the time
effect (mean Ec is function of many variables)
Instantaneous Ec can be defined in 3 ways.
– Initial Modulus of Elasticity, E
– Secant modulus
– Tangent modulus
Modulus Elasticity
C) because seperate linear curves exist for the loading and unloading
brunches of stress-strain diagram and permanent deformation exists after
removal of load.
D) described as non linear and non elastic behaviour.
E-aggregate-concrete
The properties of aggregate also influence the modulus of elasticity although they
don‟t affect the compressive Strength. The relation between the modulus of
elasticity of concrete and Strength depends also on age.
Poisson’s ratio
• The design and analysis of some type of structure requıre the knowledge of
poissons ratio.viz. The ratio of the lateral strain.The sign of the strains is
ignored.We are usually interested in applied compression and therefore have axial
conctraction and lateral extension.
• Generally poisson ratio for normal weight and light weight lies in range of 0.15
to 0.20 when determinerd from strain meausurements taken in the static modulus
of elasticity tests
• An alternative method of determinig poissons ratio is by dynamic means.
CREEP
(to). If this applied load is left on concrete producing a constant stress, the
instantaneous elastic strain ε (to) begins to increase.
• The rate of increase is fast during the first 3 months, after which it begins to slow
down.
• Whichever slowing rate, creep continues for years
• Creep of Concrete resulting from the action of a sustained stress is a gradual
increase in strain with time; it can be of the same order of magnitude as drying
shrinkage.
• Creep does not include any immediate elastic strains caused by loading or any
shrinkage or swelling caused by moisture changes.
• When a concrete structural element is dried under load the creep that occurs is
one to two times as large as it would be under constant moisture conditions.
Adding normal drying shrinkage to this and considering the fact that creep can be
several times as large as the elastic strain on loading, it may be seen that these
factors can cause considerable deflection and that they are of great importance in
structural mechanics.
Mix proportions.
• the major portion of creep is due to removal of water from between the sheets of
a calcium silicate crystallite and to a possible rearrangement of bonds between the
surfaces of the individual crystallites.
• When hydrated cement is completely dried, little or no creep occurs
• Water/cement ratio is the main factor influencing the porosity and theStrength of
concrete so that lower water/ cement ratio results in a higher Strength.Now for a
constant cement paste, the effect of a decrease in water/ cement ratio is to decrease
creep.
• İn normal weight of aggragate concrete,the source of creep is hardened cement
paste since the aggregate is not liable to creep at the level of stress existing in
concrete. Because aggragate is stiffer than the cement paste then the main role of
the aggragate is to restrain the creep in the cement paste, the effect dependş on the
elastic modulus of aggragate and its volumetric proportion
• concretes made with different aggregates exhibit creep of varying magnitudes.
Hence, the stiffer aggragate, the lower creep.
• And higher volume of aggragate is the lower creep.
Humidity,temperature
• for a given concrete basicaly, the lower the relative humidity, the higher the
creep;the lower the temperature, the lower the creep.
• Change of humidity and temperature has already negative affect on creep
• Experiments have shown that creep continues for a very long time; detectable
changes have been found after as long as 30 years.
• The rate decreases continuously, however, and it is generally assumed that creep
tends to a limiting value. It has been estimated that 75 per cent of 20-year creep
occurs during the first year.
Effects of Creep
• Creep of plain concrete does not by itself affect strength, although under very
high stresses creep hastens the approach of the limiting strain at which failure
takes place.
• The influence of creep on the ultimate strength of a simply supported, reinforced
concrete beam subjected to a sustained load is insignificant, but deflection
increases considerably and may in many cases be a critical consideration in
design..
• Another instance of the adverse effects of creep is its influence on the stability of
the structure through increase in deformation and consequent transfer of load to
other components.
• Thus, even when creep does not affect the ultimate strength of the component in
which it takes place, its effect may be extremely serious as far as the performance
of the structure as a whole is concerned.
• The loss of prestress due to creep is well known and accounted for the failure of
all early attempts at prestressing. Only with the introduction of high tensile steel
did prestressing become a successful operation.
• The effects of creep may thus be harmful. On the whole, however, creep unlike
shrinkage is beneficial in relieving stress concentrations and has contributed to the
success of concrete as a structural material.
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UNIT-2
CHEMICAL ADMIXTURES
Introduction
The realization that properties of concrete, in both the fresh and gardened states,
can be modified by adding certain materials to concrete mixtures is responsible for
the large growth of the concrete admixtures industry during the last 40 years.
Hundreds of products are being marketed today, and in some countries it is not
uncommon that 70 to 80 percent of all the concrete produced contains one or more
admixtures; therefore, it is quite important that civil engineers be familiar with the
commonly used admixtures, together with their typical applications and
limitations. Admixtures vary in composition from surfactants and soluble salts and
polymers to insoluble minerals. The purposes for which they are generally used in
concrete include improvement of workability, acceleration or retardation of setting
time, control of strength development, and enhancement of resistance to frost
action, thermal cracking, alkali-aggregate expansion, and acidic and sulfate
solutions. Important classes of concrete admixtures, their physical-chemical
characteristics, mechanism of action, applications and side effects are as follows.
DEFINITION
An admixture is defined as a material other than water, aggregate, hydraulic
cements and fiber reinforcement, used as an ingredient of concrete or mortar and
added to the batch immediately before or during mixing.
reinforcement.
2. The workability, compressive strength and the slump loss of concrete with and
without the use of admixtures shall be established during the trial mixes before use
of admixtures.
3. The relative density of liquid admixtures shall be checked for each drum
containing admixtures and compared with the specified value before acceptance.
4. The chloride content of admixtures shall be independently tested for each
batch before acceptance.
5. If two or more admixtures are used simultaneously in the same concrete mix,
data should be obtained to assess their interaction and to ensure their
compatibility.
CLASSIFICATION OF ADMIXTURES:
Admixtures are commonly classified by their function in concrete but often they
exhibit some additional action.
The classification is as follows:
1. Plasticizers
2. Super plasticizers
3. Retarders and retarding plasticizers
4. Accelerators and Accelerating Plasticizers
5. Air-entraining Admixtures
6. Mineral Admixtures
7. New generation super plasticizers
ACTION OF PLASTICIZERS
The action of plasticizers is mainly to fluidify the mix and improve the workability
of concrete, mortar or grout. The mechanisms that are involved could be explained
in the following way:
Dispersion: Portland cement, being in fine state of division, will have a tendency
of flocculate in wet concrete. These flocculation entraps certain amount of water
used in the mix and thereby all the water is not freely available to fluidify the mix.
When plasticizers are used, they get adsorbed on the cement particles. The
adsorption of charged polymer on the particles of cement creates particle-to-
particle repulsive forces which overcome the attractive forces. This repulsive force
is called Zeta Potential, which depends on the base, solid content, quantity of
plasticizer used. The overall result is that the cement particles are deflocculated
and dispersed. When cement particles are deflocculated, the water trapped inside
the flocs gets released and now available to fluidify the mix.
When cement particles get flocculated there will be interparticles friction between
particle to particle and floc to floc. But in the dispersed condition there is water in
between the cement particle and hence the interparticle friction is reduced.
Retarding Effect: The plasticizer will get adsorbed on the surface of cement
particles and form a thin sheath. This thin sheath inhibits the surface hydration
reaction between water and cement as long as sufficient plasticizer molecules are
available at the particle/solution interface. The quantity of available plasticizers
will progressively decrease as the polymers become entrapped in hydration
products.
Compressive strength , percent of control sample , minimum
1 day --
3 days 110
7 days 110
28 days 110
6 months 100
1 year 100
It is the use of superplasticizer which has made it possible to use w/c as low as
0.25 or even lower and yet to make flowing concrete to obtain strength of the
order 120 Mpa or more. It is the use of superplasticizer which has made it possible
to use fly ash, slag and particularly silica fume to make high performance
concrete.
aggregate will make the test more complex and often erratic. Whereas using grout
alone will make the test simple, consistent and indicative of the fluidifying effect
of superplasticizer with cement. The following procedure is adopted in Marsh
cone test.
Marsh cone is a conical brass vessel, which has a smooth aperture at the bottom of
diameter 5 mm. The profile of the apparatus is shown in Fig.
Take 2 kg cement, proposed to be used at the project. Take one liter of water (w/x
=0.5) and say 0.1% of plasticizer. Mix them thoroughly in a mechanical mixer
(Hobart mixer is preferable) for two minutes. Hand mixing does not give
consistent results because of unavoidable lump formation which blocks the
aperture. If hand mixing is done, the slurry should be sieved through 1.18 sieve to
exclude lumps. Take one liter slurry and pour it into Marsh cone duly closing the
aperture with a finger. Start a stop watch and simultaneously remove the finger.
Find out the time taken in seconds, for complete flow out of the slurry. The time in
seconds is called the “Marsh Cone Time”. Repeat the test with different dosages of
plasticizer. A typical graph is shown in Fig.
The dose at which the Marsh cone time is lowest is called the saturation point. The
dose is the optimum dose for that brand of cement and plasticizer or super
plasticizer for that w/c ratio.
FACTORS AFFECTING WORKABILITY
1. Type of super plasticizers
2. dosage
3. mix composition
4. variability in cement composition and properties
5. mixing procedure
6. equipments
The retarders are used in casting and consolidating large number of pours without
the formation of cold joints. They are also used in grouting oil wells. Oil wells are
sometimes taken up to a depth of about 6000 meter deep where the temperature
may be about 2000C. The annular spacing between the steel tube and the wall of
the well will have to be sealed with cement grout. Sometimes at that depth
stratified or porous rock strata may also require to be grouted to prevent the entry
of gas or oil into some other strata... for all these works cement grout is required to
be in mobile condition for about 3 to 4 hours, even at that high temperature
without getting set. Use of retarding agent is often used for such requirements.
Sometimes concrete may have to be placed in difficult conditions and delay may
occur in transporting and placing. In ready mixed concrete practices, concrete is
manufactured in central batching plant and transported over a long distance to the
job sites which may take considerable time. In the above cases the setting of
concrete will have to be retarded, so that concrete when finally placed and
compacted is in perfect plastic state.
Common sugar is one of the most effective retarding agents used as an admixture
for delaying the setting time of concrete without detrimental effect on the ultimate
strength. Addition of excessive amounts will cause indefinite delay in setting. At
normal temperatures addition of sugar 0.05 to 0.10 percent have little effect on the
rate of hydration, but if the quantity is increased to 0.2 percent, hydration can be
retarded to such an extent that final set may not take place for 72 hours or more.
Skimmed milk powder (casein) has a retarding effect mainly due to sugar content.
Other admixtures which have been successfully used as retarding agents are Ligno
sulphonic acids and their salts, hydroxylated carboxylic acids and their salts which
in addition to the retarding effect also reduce the quantity of water requirement for
a given workability.
RETARDING ADMIXTURES
It is mentioned earlier that all the plasticizers and super plasticizers by themselves
show certain extent of retardation. Many a time this extent of retardation of setting
time offered by admixtures will not be sufficient. Instead of adding retarders
separately, retarders are mixed with plasticizers or super plasticizers at the time of
commercial production. Such commercial brand is known as retarding plasticizers
or retarding super plasticizers.
PHYSICAL REQUIREMENTS ACCORDING TO IS 9103: 1999
Compressive strength, percent of control sample, min: 28 days 90
Flexural strength: 90
ACCELERATORS
Accelerating admixtures are added to concrete to increase the rate of early strength
development in concrete to
• permit earlier removal of formwork;
• reduce the required period of curing;
• advance the time that a structure can be placed in service;
• partially compensate for the retarding effect of low temperature during cold
weather concreting;
• in the emergency repair work.
In the past one of the commonly used materials as an accelerator was calcium
chloride. But, now a days it is not used. Instead, some of the soluble carbonates,
silicates fluosilicates and some of the organic compounds such as triethenolamine
are used. Accelerators such as fluosilicates and triethenolamine are comparatively
expensive. The recent studies have shown that calcium chloride is harmful for
reinforced concrete and prestressed concrete.
It may be used or plain cement concrete in comparatively high dose. Some of the
accelerators produced these days are so powerful that it is possible to make the
cement set into stone hard in a matter of five minutes are less. With the availability
of such powerful accelerator, the under water concreting has become easy.
Similarly, the repair work that would be carried out to the waterfront structures in
the region of tidal variations has become easy. The use of such powerful
accelerators have facilitated, the basement waterproofing operations. In the field of
prefabrication also it has become an invaluable material. As these materials could
be used up to -100C, they find an unquestionable use in cold weather concreting.
Some of the modern commercial accelerating materials are Mc-Schnell OC, Mc-
Schnell SDS, Mc-Torkrethilfe BE, manufactured by Mc-Bauchemic (Ind) Pvt.
Ltd. MC-Torkrethilfe BE is a material specially formulated to meet the demand
for efficient and multifold properties desired for sprayed concrete and shotcreting
operations. A field trial is essential to determine the dose for a given job and
temperature conditions when the above materials are used.
ACCELERATING PLASTICIZERS
Certain ingredients are added to accelerate the strength development of concrete to
plasticizers or super plasticizers. Such accelerating super plasticizers, when added
to concrete result in faster development of strength. The accelerating materials
added to plasticizers or super plasticizers are triethenolamine chlorides, calcium
nitrite, nitrates and fluosilicates etc. The accelerating plasticizers or accelerating
super plasticizers manufactured by well known companies are chloride free.
AIR-ENTRAINING ADMIXTURE
Perhaps one of the important advancements made in concrete technology was the
discovery of air entrained concrete. Since 1930 there has been an ever increasing
use of air entrained concrete all over the world especially, in the United States and
Canada. Due to the recognition of the merits of air entrained concrete, about 85
per cent of concrete manufactured in America contains on or the other type of air
entraining agent. So much so that air entraining agents have almost come to be
considered a necessary „fifth ingredient‟ in concrete making. Air entrained
concrete is made by mixing a small quantity of air entraining agent or by using
air entraining cement. These air entraining agents incorporate millions of no-
coalescing air bubbles, which will act as flexible ball bearings and will modify the
properties of plastic concrete regarding workability, segregation, bleeding and
finishing quality of concrete. It also modifies the properties of hardened concrete
regarding its resistance to frost action and permeability.
The air voids present in concrete can be brought under two groups:
(a) Entrained air (b) Entrapped air.
Entrained air is intentionally incorporated, minute spherical bubbles of size
ranging from 5 microns to 80 microns distributed evenly in the entire mass of
concrete. The entrapped air is the void present in the concrete due to insufficient
compaction. These entrapped air voids may be of any shape and size normally
embracing the contour of aggregate surfaces. Their size may range from 10 to
1000 microns or more and they are not uniformly distributed throughout the
concrete mass.
Incidentally air entrainment will also affect the properties of concrete in the
following ways:
(a) Reduces the tendencies of segregation.
(b) Reduces the bleeding and laitance.
(c) Decreases the permeability.
(d) Increases the resistance to chemical attack.
(e) Permits reduction in sand content.
(f) Improves placeability, and early finishing.
(g) Reduces the cement content, cost, and heat of hydration.
(h) Reduces the unit weight.
(i) Permits reduction in water content.
(j) Reduces the alkali-aggregate reaction.
(k) Reduces the modulus of elasticity.
The cumulative effect of this pressure becomes considerable, with the result
that surface scaling and disruption of concrete at the weaker section takes place.
Similarly, surface scaling and disruption also takes place in plain concrete when
subjected to the action of salt used for deicing purpose. Similar pattern of failure
of plain concrete is also noticed in concrete structures at the tidal zone and spray
zone. It has been firmly established that air entrainment in concrete increases the
resistance by about three to seven times in such situations.
EFFECT ON WORKABILITY
The entrainment of air in fresh concrete by means of air entraining agent improves
workability. It was seen that the placeability of air entrained concrete having 7.5
cm slump is superior to that of non-air entrained concrete having 12.5 cm slump.
This easier placeability of a lower slump should be recognized by the people
concerned with concrete construction in difficult situations. Better placeability of
air entrained concrete results in more homogeneous concrete with less segregation,
bleeding and honeycombing. The concrete containing entrained air is more plastic
and „fatty‟ and can be more easily handled than ordinary concrete. The pump
ability of the mix also increases enormously.
EFFECT ON STRENGTH
It can be generally stated that air entrainment in concrete reduces the compressive
strength of concrete. But when the process is applied properly, taking advantage of
the benefits accrued on account of air-entrainment, little or no loss of strength
should take place and it is even possible that under certain circumstances a gain of
strength may be possible. It is true that at a given water/cement ratio, an increase
in air content results in loss of strength, but the air entrainment enables reduction
of water/cement ratio and sand content, for the given workability, thereby
regaining most of not all the lost strength.
EFFECT ON PERMEABILITY
The entrainment of air does appear to have much effect on the permeability of
concrete. Greater uniformity of concrete with entrained air due to its increased
workability, modified pore-structure of the air entrained concrete, reduction of
water channel due to reduction in bleeding, are some of the reasons for improving
the permeability characteristics of air entrained concrete. Cement stored in silos
built of air entrained concrete, has been found to show no caking of cement,
whereas, cement stored in silos made of ordinary concrete revealed caking along
the periphery of the silo. The minute disconnected air bubbles offer a better barrier
to the passage of water. The reduced water/cement ratio also is one of the factors
for reduced permeability.
ALKALI-AGGREGATE REACTION
There are evidences that air entrainment reduces the alkali-aggregate reaction. Use
of air entraining agent has frequently been recommended as a means for
controlling expansion due to alkali-aggregate reaction in mortar and concrete.
MODULUS OF ELASTICITY
Available data indicate that the modulus of elasticity of concrete mix having the
same water/cement ratio and the same aggregate is reduced by 2 to 3 per cent for
each per cent of air entrainment.
ABRASION RESISTANCE
Concrete containing less than 6 per cent air entrainment has about the same
resistance to abrasion as normal concrete, when cement contents of the
comparable concrete are constant. However, there is a progressive decrease in
abrasion resistance with further increase in air content. When the air entrainment
is of the order of about 10 per cent, abrasion resistance is markedly low. Since
concrete used in pavements is generally specified to have not more than 3 to 6 per
cent of entrained air, the abrasion resistance should be satisfactory.
natural cement during the latter part of the 18th century, the Portland cement in the
early 19th century, the practice of using pozzolans declined, but in more recent
times, Pozzolans have been extensively used in Europe, USA and Japan, as an
ingredient of Portland cement concrete particularly for marine and hydraulic
structures. It has been amply demonstrated that the best pozzolans in optimum
proportions mixed with Portland cement improves many qualities of concrete,
such as:
(a) Lower the heat of hydration and thermal shrinkage;
(b) Increase the water tightness;
(c) Reduce the alkali-aggregate reaction;
(d) Improve resistance to attack by sulphonate soils and sea water;
(e) Improve extensibility;
(f) Lower susceptibility to dissolution and leaching;
(g) Improve workability;
(h) Lower costs.
In addition to these advantages, contrary to the general opinion, good pozzolans
will not unduly increase water requirement or drying shrinkage.
FLY ASH:
Fly ash is finely divided residue resulting from the combustion of powdered coal
and transported by the flue gases and collected by electrostatic precipitator. In
U.K. it is referred as pulverized fuel ash (PFA). Fly ash is the most widely used
pozzolanic material all over the world.
Fly ash was first used in large scale in the construction of Hungry Horse dam in
America in the approximate amount of 30 per cent by weight of cement. Later on
it was used in Canyon and Ferry dams etc. In India, Fly ash was used in Rihand
dam construction replacing cement upto about 15 per cent.
In the recent time, the importance and use of fly ash in concrete has grown so
much that it has almost become a common ingredient in concrete, particularly for
making high strength and high performance concrete. Extensive research has been
done all over the world on the benefits that could be accrued in the utilization of
fly ash as a supplementary cementitious material. High volume fly ash concrete is
a subject of current interest all over the world.
The use of fly ash as concrete admixture not only extends technical advantages to
the properties of concrete but also contributes to the environmental pollution
control. In India alone, we produce about 75 million tons of fly ash per year, the
disposal of which has become a serious environmental problem. The effective
utilization of fly ash in concrete making is, therefore, attracting serious
considerations of concrete technologies and government departments.
There are two ways that the fly ash can be used: one way is to intergrind certain
percentage of fly ash with cement clinker at the factory to produce Portland
pozzolana cement (PPC) and the second way is to use the fly ash as an admixture
at the time of making concrete at the site of work. The latter method gives freedom
and flexibility to the user regarding the percentage addition of fly ash.
ASTM broadly classifies fly ash into two classes.
Class F: Fly ash normally produced by burning anthracite or bituminous coal,
usually has less than 5% CaO. Class F fly ash has pozzolanic properties only.
Class C: Fly ash normally produced by burning lignite or sub-bituminous coal.
Some class C fly ash may have CaO content in excess of 10%. In addition to
pozzolanic properties, class C fly ash also possesses cementitious properties.
Fly ash, when tested in accordance with the methods of test specified in IS: 1727-
1967.
DURABILITY OF CONCRETE
Sufficiently curved concrete containing good quality fly ash shows dense structure
which offers high resistivity to the infiltration of deleterious substances.
A point for consideration is that the pozzolanic reactivity reduces the calcium
hydroxide content, which results in reduction of passivity to the steel
reinforcement and at the same time the additional secondary cementitious material
formed makes the paste structure dense, and there by gives more resistance to the
corrosion of reinforcement. Which one will have an overriding effect on the
corrosion of reinforcement will be a point in question. Published data reports that
concrete with fly ash shows similar depth of carbonation as that of concrete
without fly ash, as long as the compressive strength level is same.
It is also recognized that the addition of fly ash contributes to the reduction of the
expansion due to alkali-aggregate reaction. The dilution effect of alkali and
reduction of the water permeability due to dense texture may be one of the factors
for reduction of alkali-aggregate reaction. In conclusion it may be said that
although fly ash is an industrial waste, its use in concrete significantly improve the
long term strength and durability and reduce heat of hydration. In other words
good fly ash will be an indispensable mineral admixture for high performance
concrete.
SILICA FUME
Silica fume, also referred to as micro silica or condensed silica fume, is another
material that is used as an artificial pozzolanic admixture. It is a product resulting
from reduction of high purity quartz with coal in an electric arc furnace in the
manufacture of silicon or ferrosilicon alloy. Silica fume rises as an oxidized vapor.
It cools, condenses and is collected on cloth bags. It is further processed to remove
impurities and to control particle size. Condensed silica fume is essentially silicon
dioxide in noncrystalline form. Since it is an airborne material like fly ash, it has
spherical shape. It is extremely fine with particle size less than 1 micron and
with an average diameter of about 0.1 micron, about 100 times smaller than
average cement particles. Silica fume has specific surface area of about 20000
m2/kg, as against 230 to 300 m2/kg that of cement. Since silica fume or micro
silica is an important new material, let us see this material in some detail.
• Micro silica is initially produced as an ultra fine undensified powder
• At least 85% SiO2 content
• Mean particle size between 0.1 and 0.2 micron
• Minimum specific surface area is 15000 m2/kg
• Spherical particle shape.
Available forms
• Undensified forms with bulk density of 200-300 kg/cum
• Densified forms with bulk density of 500-600 kg/cum
• Micro-palletized forms with bulk density of 600-800 kg/cum
• Slurry forms with density 1400 kg/cum
• Slurry is produced by mixing undensified micro silica powder and water in equal
proportions by weight. Slurry is the easiest and most practical way to introduce
micro silica into the concrete mix
• Surface area 15-20 m2/g
• Standard grade slurry pH value 4.7
POZZOLANIC ACTION
Micro silica is much more reactive than fly ash or any other natural pozzolana.
The reactivity of a pozzolana can be quantified by measuring the amount of
calcium hydroxide in the cement paste at different times.
INFLUENCE ON FRESH CONCRETE
Water demand increases in proportion to the amount of microsilica added. The
increase in water demand of concrete containing microsilica will be about 1% for
every 1% of cement substituted.
UNIT - 3
CONCRETE MIX DESIGN
Introduction
The requirements which form the basis of selection and proportioning of mix
ingredients are :
a ) The minimum compressive strength required from structural consideration
b) The adequate workability necessary for full compaction with the compacting
equipment available.
c) Maximum water-cement ratio and/or maximum cement content to give adequate
durability for the particular site conditions
d) Maximum cement content to avoid shrinkage cracking due to temperature cycle
in mass concrete.
2.1 Types of Mixes
i. Nominal Mixes
In the past the specifications for concrete prescribed the proportions of cement,
fine and coarse aggregates. These mixes of fixed cement-aggregate ratio which
ensures adequate strength are termed nominal mixes. These offer simplicity and
under normal circumstances, have a margin of strength above that specified.
However, due to the variability of mix ingredients the nominal concrete for a
given workability varies widely in strength.
ii. Standard mixes
The nominal mixes of fixed cement-aggregate ratio (by volume) vary widely in
strength and may result in under- or over-rich mixes. For this reason, the minimum
compressive strength has been included in many specifications. These mixes are
termed standard mixes. IS 456-2000 has designated the concrete mixes into a
number of grades as M10, M15, M20, M25, M30, M35 and M40. In this
designation the letter M refers to the mix and the number to the specified 28 day
cube strength of mix in N/mm2. The mixes of grades M10, M15, M20 and M25
correspond approximately to the mix proportions (1:3:6), (1:2:4), (1:1.5:3) and
(1:1:2) respectively.
iii. Designed Mixes
In these mixes the performance of the concrete is specified by the designer but the
mix proportions are determined by the producer of concrete, except that the
minimum cement content can be laid down. This is most rational approach to the
selection of mix proportions with specific materials in mind possessing more or
less unique characteristics. The approach results in the production of concrete with
the appropriate properties most economically. However, the designed mix does not
serve as a guide since this does not guarantee the correct mix proportions for the
prescribed performance. For the concrete with undemanding performance nominal
or standard mixes (prescribed in the codes by quantities of dry ingredients per
cubic meter and by slump) may be used only for very small jobs, when the 28-day
strength of concrete does not exceed 30 N/mm2. No control testing is necessary
reliance being placed on the masses of the ingredients.
3. Factors affecting the choice of mix proportions
The various factors affecting the mix design are:
3.1. Compressive strength
It is one of the most important properties of concrete and influences many other
describable properties of the hardened concrete. The mean compressive strength
required at a specific age, usually 28 days, determines the nominal water-cement
ratio of the mix. The other factor affecting the strength of concrete at a given age
and cured at a prescribed temperature is the degree of compaction. According to
Abraham‟s law the strength of fully compacted concrete is inversely proportional
to the water-cement ratio.
3.2. Workability
The degree of workability required depends on three factors. These are the size of
the section to be concreted, the amount of reinforcement, and the method of
compaction to be used. For the narrow and complicated section with numerous
corners or inaccessible parts, the concrete must have a high workability so that full
compaction can be achieved with a reasonable amount of effort. This also applies
to the embedded steel sections. The desired workability depends on the
Note: In case the coarse aggregate is not angular, then also the volume of CA may
be required to be increased suitably based on experience.
A-10 The slump shall be measured and the water content and dosages of
admixture shall be adjusted for achieving the required slump based on trials, if
required. The mix proportions shall be reworked for the actual water content and
checked for durability requirements.
A-11 Two more trials having variation of ± 10 percent of water cement ratio in
A-10 shall be carried out keeping water content constant, and a graph between
three water cement ratios and their corresponding strengths shall be plotted to
work out the mix proportions for the given target strength for field trials.
However, durability requirements shall be met.
Problem 2
Illustrative examples on concrete mix proportioning [M40 pumpable concrete with
fly ash]
A-1 Design stipulations for proportioning
m) Grade designation : M40
n) Type of cement : OPC 43 grade confirming to IS 8112
o) Type of mineral admixture : Fly ash confirming to IS 3812 (Part-1)
p) Maximum nominal size of aggregates : 20 mm
q) Minimum cement content : 320 kg/m3
r) Maximum water cement ratio : 0.45
s) Workability : 100 mm (slump)
t) Exposure condition : Severe (for reinforced concrete)
u) Method of concrete placing : Pumping
v) Degree of supervision : Good
w) Type of aggregate : Crushed angular aggregate
x) Maximum cement content : 450 kg/m3
y) Chemical admixture type : Superplsticiser
A-2 TEST DATA FOR MATERIALS
h) Cement used : OPC 43 grade confirming to IS 8112
From Table-2, maximum water content = 186 liters (for 25mm – 50mm slump
range and for 20 mm aggregates) Estimated water content for 100 mm slump =
186 + 6/100 x186 = 197 liters As superplsticiser is used, the water content can be
reduced up to 20 percent and above Based on trials with SP water content
reduction of 29 percent has been achieved. Hence the water content arrived = 19 x
0.71 =140 liters
A-6 CALCULATION OF CEMENT CONTENT
Water cement ratio = 0.40
Cement content = 140/0.40 = 350 kg/m3
From Table 5 of IS: 456, minimum cement content for severe exposure condition
= 320 kg/m3
350 kg/m3 > 320 kg/m3, hence OK
For proportioning fly ash concrete, the suggested steps are; Decide the
percentage of fly ash to be used based on [project requirement and quality of
Materials In certain situations increase in cementitious material content may be
warranted. The decision on increase in cementitious material content and its
percentage may be based on experience and trial. The example is with increase of
10% of cementitious material content.
Cementitious material content 1.1 x 350 = 385 kg/m3
Water content = 140 kg/m3
Water cement ratio = 140/385 = 0.364 _0.40
Let us use fly as at 30 percent of cementitious material content in addition to
cement Fly ash = 385 x 0.3 = 115 kg/m3
Cement =385-115=270 kg/m3
(Saving of cement compared to previous design = 350-279 = 80 kg/m3 and
fly ash utilization = 115 kg/m3)
A-7 PROPORTION OF VOLUME OF COARSE AGGREGATE AND FINE
AGGREGATE CONTENT
Problem 3
Design of M20 concrete mix as per IS:10262-2009, Concrete mix proportioning-
guidelines(First revision)
A-1 Design stipulations for proportioning
i. Grade designation : M20
ii. Type of cement : OPC 43 grade confirming to IS 8112
iii. Maximum nominal size of aggregates : 20 mm
iv. Minimum cement content : 320 kg/m3
v. Maximum water cement ratio : 0.55
vi. Workability : 75 mm (slump)
Problem 4
Design of M30 concrete mix as per IS:10262-2009, Concrete mix proportioning-
guidelines(First revision)
A-1 Design stipulations for proportioning
xii. Grade designation : M30
xiii. Type of cement : OPC 43 grade confirming to IS 8112
xiv. Maximum nominal size of aggregates : 20 mm
xv. Minimum cement content : 350 kg/m3
xvi. Maximum water cement ratio : 0.50
xvii. Workability : 25 - 50 mm (slump)
xviii. Exposure condition : Moderate
xix. Degree of supervision : Good
xx. Type of aggregate : Crushed angular aggregate
xxi. Maximum cement content : 450 kg/m3
xxii. Chemical admixture : Not recommended
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UNIT - 4
DURABILITY OF CONCRETE STRUCTURES
Definition:
A long service life is considered synonymous with durability. Since durability
under one set of conditions does not necessarily mean durability under another, it
is customary to include a general reference to the environment when defining
durability. According to ACI Committee 201, durability of Portland cement
concrete is defined as its ability to resist weathering action, chemical attack,
abrasion, or any other process of deterioration; that is, durable concrete will retain
its original form, quality, and serviceability when exposed to its environment. No
material is inherently durable; as a result of environmental interactions the
microstructure and, consequently, the properties of materials change with time. A
material is assumed to reach the end of service life when its properties under given
conditions of use have deteriorated to an extent that the continuing use of the
material is ruled either unsafe or uneconomical.
Materials Related Failures
Concrete Deterioration can be caused by:
- The use of inappropriate materials.
- Poor construction practices.
Environmental Related Causes of Concrete Durability Problems The inferior
durability characteristics of concrete may be caused by the environment that the
concrete is exposed to. The following environmental condition can affect the
concrete durability:
- Temperature.
- Moisture.
- Physical factors.
- Chemical factors.
- Biological factors.
These factors may be due to weathering conditions (temperature, and moisture
changes), or to abrasion, attack by natural or industrial liquids and gases, or
biological agents. Durability problems related to environmental causes include the
following: steel corrosion, delamination, cracking, carbonation, sulfate attack,
chemical attack, scaling, spalling, abrasion and cavitation.
Dimensional Stability
The influence of shrinkage and creep on concrete cracking: under restraining
conditions in concrete, the interplay between the elastic tensile stresses induced by
shrinkage strains and the stress relief due to the viscoelastic behavior is at the heart
of the deformations and cracking in most structures. To understand the reason why
a concrete element may not crack at all or may crack but not soon after exposure
to the environment, we have to consider how concrete would respond to sustained
stress or to sustained strain. The phenomenon of a gradual increase in strain with
time under a given level of sustained stress is called creep.
The phenomenon of gradual decrease in stress with time under a given level of
sustained strain is called stress relaxation. Both manifestations are typical of
viscoelastic materials. When a concrete element is restrained, the viscoelasticity of
concrete will manifest into a progressive decrease of stress with time (Fig. 4-1
curve b from Mehta textbook). Thus under the restraining conditions present is
concrete, the interplay between elastic tensile stresses induced by shrinkage strains
and stress relief due to viscoelastic behavior is at the heart of deformations and
cracking in most structure.
THERMAL SHRINKAGE
In general, solids expand on heating and contract on cooling. The strain associated
with change in temperature will depend on the coefficient of thermal expansion of
the material and the magnitude of temperature drop or rise. Except under extreme
climatic conditions, ordinary concrete structures suffer little or no distress from
changes in ambient temperature. However, in massive structures, the combination
of heat produced by cement hydration and relatively poor heat dissipation
conditions results in a large rise in concrete temperature within a few days after
placement. Subsequently, cooling to the ambient temperature often causes the
concrete to crack.
Since the primary concern in the design and construction of mass concrete
structures is that the completed structure remains a monolith, free of cracks, every
effort to control the temperature rise is made through selection of proper materials,
mix proportions, curing conditions, and construction practices.
With low tensile strength materials, such as concrete, it is the shrinkage strain
from cooling that is more important than the expansion from heat generated by
cement hydration. This is because, depending on the elastic modulus, the degree of
restraint, andstress relaxation due to creep, the resulting tensile stresses can be
large enough to cause cracking. For instance, assuming that the coefficient of
thermal expansion of concrete is 10 × 10−6 per °C, and the temperature rise above
the ambient from heat of hydration is 15 °C, then the thermal shrinkage caused by
the 15 °C temperature drop will be 150×10−6. The elastic modulus (E) of ordinary
concrete may be assumed as 3 × 106 psi. If the concrete member is fully restrained
(Dr = 1), the cooling would produce a tensile stress of 450 psi. Since the elastic
tensile strength of ordinary concrete is usually less than 450 psi, it is likely to
crack if there is no relief due to stress relaxation.
Factors Affecting Thermal Stresses
Degree of restraint (Kr ) . A concrete element, if free to move, would have no
stress development associated with thermal deformation on cooling. However, in
practice, the concrete mass will be restrained either externally by the rock
foundation or internally by differential deformations within different areas of
concrete due to the presence of temperature gradients. For example, assuming a
rigid foundation, there will be full restraint at the concrete-rock interface (Kr =
1.0), however, as the distance form the interface increases, the restraint
will decrease, as shown in the following Figure .
cement/natural silica sand, and for concrete mixtures of different aggregate types
are approximately 18, 12, and 6 to 12 × 10−6 per °C, respectively. The coefficient
of thermal expansion of commonly used rocks and minerals varies from about 5 ×
10−6 per °C for limestones and gabbros to 11 to 12 × 10−6 per °C for sandstones,
natural gravels, and quartzite. Since the coefficient of thermal expansion can be
estimated from the weighted average of the components, assuming 70 to 80
percent aggregate in the concrete mixture, the calculated values of the coefficient
for various rock types (both coarse and fine aggregate from the same rock) are
shown in Fig. 4-24. The data in the figure are fairly close to the experimentally
measured values of thermal coefficients reported in the published literature for
concrete tested in moist condition, which is representative of the condition of
typical mass concrete.
Specific heat is defined as the quantity of heat needed to raise the temperature of a
unit mass of a material by one degree. The specific heat of normal weight concrete
is not very much affected by the type of aggregate, temperature and other
parameters. Typically the values of specific heat are in the range of 0.22 to 0.25
Btu/lb.F.
Thermal conductivity gives the flux transmitted through a unit area of a material
under a unit temperature gradient. The thermal conductivity of concrete is
influenced by the mineralogical characteristics of aggregate, and by the moisture
content, density, and temperature of concrete. Typical values of thermal
conductivity for concretes containing different aggregate types range between 23-
25 25 Btu in/h.ft2.F.
In general, high strength concretes are more prone to cracking because of greater
shrinkage and lower creep; on the other hand, low strength concretes tend to crack
less, probably because of lower shrinkage and higher creep.
Temperatures greater than 95°C (203°F) can have significant effects on concrete.
The total volume change in concrete is the sum of the volume changes of the
cement paste and aggregates. At high temperatures, the cement paste will shrink
due to dehydration of the calcium silicate hydrate (C-S-H), while the aggregate
will expand. For normal aggregate concrete, there is a net expansion. Therefore,
exposure to very high temperatures (i.e. fire) will result in concrete spalling,
particularly when the concrete is exposed to high temperatures for a long time.
Several factors influence the behavior of concrete at high temperatures. These
factors include concrete moisture content, aggregate type and stability, cement
content, duration of concrete exposure, the rate that temperatures rise, the age of
the concrete, and any restraint.
The Environmental-related Problems of Temperature
Environmental problems are ascribable to the daily and seasonal changes in
temperature.
Daily Changes in Temperature
Daily changes in temperature can be up to 20°C (36°F) at the coast and somewhat
higher inland. The limiting tensile strain for concrete is frequently quoted to be
between 10-4 and 2X10-4. If the coefficient of thermal expansion of concrete is
assumed to be 10 millionths per degree Celsius (5.5 millionths per degree
Fahrenheit), a temperature change of 10°C to 20°C (18°F to 36°F) would be
sufficient to cause the restrained concrete to crack. Repeated tensile stresses cause
the cracks to grow and lead to scaling, spalling, and delamination. If the cracks
develop to the level of the reinforcing steel, ingress of salt and moisture will cause
the steel to corrode.
Seasonal Changes in Temperature
Seasonal changes in temperature are considerably greater than the daily
fluctuations. Seasonal changes in temperature range up to 50°C (90°F) between
the summer and winter. Seasonal temperature changes cause higher stresses than
daily temperature changes, and they result in more extensive cracking. In, some
cases, cracks developed at low temperatures may close when the concrete
temperature increases in the summer. If dirt or debris enters the cracks when the
openings are at their maximum, an increase in temperature will cause the
compressive stresses to develop. In slabs on grade and sidewalks, if large
compressive stresses are developed due to the expansion of the
concrete, the slab may buckle upward and crack.
MOISTURE
Changes in the moisture content in concrete will result in either concrete
expansion or contraction. When concrete gains moisture, the concrete will slightly
expand or swell. When concrete loses moisture, the concrete will contract or
shrink. The effects of moisture gains and losses on the volume of concrete are
illustrated in Figure 2.
Concrete will slightly expand if the concrete is kept continuously wet, however,
concrete drying causes the concrete to shrink. Further, wetting and drying of the
concrete can cause the concrete to alternately swell and shrink. As concrete drying
occurs, the portion of concrete near the surface will dry and shrink faster than the
inner portion of the concrete. This drying and shrinking of the concrete surface
will cause the concrete surface to develop tensile stresses and possible cracks. If a
section of the concrete is restrained, and if concrete joints are not provided, major
random cracks may develop.
Shrinkage of reinforced concrete is less than the shrinkage of plain concrete. The
difference depends on the amount of reinforcing steel used. Steel reinforcement
restricts but does not prevent drying shrinkage. The concrete will crack if the
shrinkage strain of the concrete exceeds the limiting tensile strain of the concrete.
Environmental-related Problem of Moisture
The three main problems with moisture and concrete are as follows:
− Carbonation
− The moisture cycle
− Contaminants
Carbonation
In addition to shrinkage upon drying, concrete undergoes shrinkage due to
carbonation. Carbon dioxide (CO2) present in the atmosphere reacts in the
presence of moisture with the hydrated cement minerals (i.e. the agent usually
being the carbonic acid). Carbonation may lead to crazing. The extent of
carbonation depends on the permeability of the concrete and on the concentration
of carbon dioxide in the air. The penetration of carbon dioxide beyond the exposed
surface of concrete is extremely slow. The alkaline conditions of hydrated cement
paste are neutralized by carbonation. This neutralization, by dropping the pH from
over 12 to about 9, affects the protection of reinforcing steel from corrosion. Thus,
if the entire concrete cover to steel were carbonated, corrosion of steel would
occur in the presence of moisture and oxygen.
Moisture Cycles
Stresses caused by changes in moisture content of the concrete may be additive to
stresses caused by temperature changes. Tensile stresses usually increase the
tendency for cracking, scaling, spalling, and delamination. Rapidly fluctuating
humidity (up to 70% in one day) can lead to moisture changes in the concrete.
Condensation on concrete surfaces enters surface cracks and is absorbed into
the concrete. Although the surface of the concrete may dry off rapidly, the water in
the concrete and in the micro-cracks takes longer time to evaporate. If the moisture
level at the reinforcing steel reaches 60% to 90% and sufficient chlorides are
present, the steelwill .corrode. The influence of the relative humidity on steel
corrosion is shown in Table.
Relative
Remarks Corrosion Risk
Humidity
If the relative humidity is maintained at 80% and the temperature surrounding the
reinforced concrete is increased, there will be a resulting increase in the rate of
steel corrosion. Concrete that is subjected to moisture cycles may accumulate salts
in the capillaries near the evaporating surface. This accumulation of salt may
contribute to the chemical attack and/or salt scaling. Moisture movements in
concrete may result in the concentrations of chlorides and sulphates in the
concrete. Concentrations of chlorides in the concrete will cause the reinforcing
steel to corrode and will also cause the concrete to crack and disintegrate.
Contaminants
Contaminants in the water that is absorbed into the concrete may cause staining,
steel corrosion, or sulphate attack. Contaminants include: chloride and sulphate
salts, carbonates, etc. Alternate cycles of wetting and drying allow the
concentration of salts to increase and thereby increase the severity of their attack.
An increase in the size of salt crystals in the capillaries near the evaporating
surface causes cracking and scaling. If the salts are drawn to the surface and
deposited at places where water evaporates, efflorescence will occur. The build-up
of soluble salts depends on many factors, including the permeability of the
concrete and the concentration of salts in the water that is being absorbed.
PHYSICAL FACTORS
Under many circumstances, concrete surfaces are subjected to wear. Concrete
wear may be caused by the sliding, scraping or impact of objects that fall onto the
concrete. In hydraulic structures, the action of the abrasive materials carried by
flowing water generally leads to erosion of the concrete. Another cause of damage
to concrete in flowing water is cavitation . Abrasion damage to concrete may be
caused by the sliding or scraping of equipment across the concrete. Abrasion
damage to concrete may also be caused by subjecting the concrete to abrasive
materials (such as sand) that are carried by wind or water. Test results indicate the
following facts;
Concrete that is affected by cavitation has an irregular, jagged, and pitted surface.
In contrast, concrete that is eroded by water-borne solids has a smooth surface.
Damage to the concrete surface does not progress steadily. After an initial period
of small damage, rapid deterioration will occur. This rapid deterioration is
followed by damage to the concrete at a slower rate.
Fire around concrete structures can weaken the superstructure and decrease the
concrete strength tremendously. Damage by fire may include total or partial
collapse of the structure, distortion, excessive deflection and expansion, buckling
of the steel, spalling and shattering of the concrete, discoloration, and reduction of
the physical properties of the steel and concrete.
Factors that tend to promote spalling include the high moisture content, restraint to
expansion (e.g., panels within a frame), low porosity and low permeability, closely
spaced reinforcement, and rapid temperature rise. Spalling can also result from
differential expansion of the mix constituents. Another common cause of spalling
is the rapid quenching of hot fires by fire hoses. Rapid quenching of fire can cause
serious structural damage. Concrete that is made with various types of siliceous or
limestone aggregate shows a change in color with temperature. These color
changes are due to the presence of iron oxide in the concrete; however, these color
changes are not always apparent.
The effects of the high temperatures caused by fires are shown in Table 2.
Table 2. Impact of Fire Temperature on Concrete
Above 600°C (1112°F) Color changes to black, gray; very little residual
strength
About 900°C (1652°F) Color changes to buff; total loss of strength
A key factor in the amount of damage that is caused to concrete is the duration of
the fire. Because of the low thermal conductivity of concrete, it takes considerable
time for the interior of concrete to reach damaging temperatures. For instance,
damage commonly does not extend to more than about 10 to 30 mm (3/8 to 1 1/4
inches) below the surface of the concrete. Note that the interior of the concrete can
never be more damaged from fire than its surfaces.
BIOLOGICAL FACTORS
Concrete may be damaged by live organisms such as plants, sponges, boring
shells, or marine borers.
Mosses and lichens, which are plants of a higher order, cause insignificant
damage to concrete. These plants produce weak acids in the fine hair roots. The
roots enable mosses and lichens to adhere to the concrete. The acids that are
produced from mosses and lichens will attack the cement paste and cause the
concrete to disintegrate and scale. In some cases, carbonic acids are produced from
plants, such as mosses and lichens, when substances from these plants decompose.
The carbonic acid that is produced will attack the concrete.
Mosses on concrete.
Rotting seaweed has been known to produce sulfur. Sulfur can be easily converted
to sulfuric acid. The presence of sulfuric acid on concrete leads to concrete
disintegration. The growth of seaweed may also create a problem if the seaweed is
exposed at low tide. When the seaweed is exposed at low tide, the seawater that is
retained by the seaweed becomes more concentrated by evaporation. The effect of
seawater on concrete increases as the concentration of seawater increases.
Seaweed on concrete
Rock boring mollusks and sponges, which are common in reefs or areas where the
seabed is composed of limestone, may invade underwater concrete structures and
piles containing limestone aggregate. The pattern of infestation greatly differs
between organisms. When mollusks attack concrete, their pattern of infestation is
widespread and relatively deep. The holes that the mollusks create tend to extend
through both the aggregate and cement paste. Boreholes created by mollusks are
located perpendicular to the outer surface of the concrete and can measure up to 10
mm (3/8 inch) in diameter. Although the depths of boreholes from mollusks vary,
growth measurements indicate a rate of borehole penetration of about 10 mm (3/8
inch) per year. Boreholes serve solely as protective enclosures for the mollusks.
The pattern of infestation created by boring sponges are shallow, closely spaced,
with small diameter holes that average 1 mm (1/25 inch) in diameter. The
Dept. of Civil engg, ACE, Banglore Page 97
CONCRETE TECHNOLOGY
boreholes created by boring sponges are often interconnected. The attack of boring
sponges on concrete is generally concentrated in small areas. As the degree of
honeycomb in the concrete increases, the surface material of the concrete
crumbles. Rock boring mollusks and sponges were discovered in the concrete piles
of the Juaymah NGL Trestle in April 1982. This discovery took place about four
years after the construction of the Juaymah NGL Trestle. The Juaymah NGL
Trestle is approximately 10 kilometer (6.2 miles) long and is supported on 1500
precast, post-tensioned concrete cylinder piles. These concrete cylinder piles have
outside diameters that range from 1.37 to 1.68 meters (4.5 to 5.5 feet). To stop the
penetration of these mollusks and sponges, the concrete piles of the Juaymah NGL
Trestle were encapsulated from about 1.2 meters (4 feet) to about 6 meters (20
feet) below the Indian Spring Low Water datum.
Environmental-related Biological Problems
Marine borers, such as mollusks and sponges, tend to form bore holes into
underwater concrete structures. Marine borers reduce the concrete's load-carrying
capacity as well as expose the concrete's outer reinforcing steel to the corrosive
seawater. Boring sponges produce interconnected bore holes. As the degree of
interconnection increases, the surface material of the concrete crumbles.
Disintegration of the surface layer exposes a new substrate of the concrete to the
boring sponges. Deterioration of concrete due to a boring sponge attack is
relatively slow. Rock boring mollusks and sponges will also chemically bore holes
into concrete containing calcareous substances.
CHEMICAL FACTORS
Chemical Corrosion
The resistance of concrete to deterioration processes triggered by chemical
reactions involves generally, but not necessarily, chemical interactions between
aggressive agents present in the external environment and the constituents of the
cement paste. Among the exceptions are alkali-aggregate reactions which occur
between the alkalies in cement paste and certain reactive materials when present in
Large concentrations of Na+, K+, and OH− ions account for the high pH value,
12.5 to 13.5, of the pore fluid in Portland cement pastes. It is obvious that portland
cement concrete would be in a state of chemical disequilibrium when it comes in
contact with an acidic environment. Again, it needs to be emphasized that
chemical reactions manifest into detrimental physical effects, such as increase in
porosity and permeability, decrease in strength, and cracking and spalling. In
practice, several chemical and physical processes of deterioration act at the same
time and may even reinforce each other. For the purpose of developing a clear
understanding, the chemical processes can be divided into three subgroups shown
in Fig. 5-10, and discussed one at a time.
Chemical corrosion results from the breaking down and dissolution of the cement
paste and/or the chemical action of the aggressive agent. Combined physical and
chemical corrosion may occur in cases where the aggressive agent combines with
the cement or aggregate to form compounds that have a volume greater than the
volume of the original constituents. This expansion may lead to a disruption in the
concrete. The nature, concentration, and rate of replenishment of aggressive agents
affect the rate of concrete deterioration that is caused by exposure to the
aggressive agents. If an aggressive agent is carried by a flowing stream over the
concrete surface of a pipe or canal, the replenishment of this aggressive agent will
be maintained indefinitely. Indefinite replenishment of an aggressive agent will
result in greater damage than would occur if the concrete were in contact with a
limited quantity of the aggressive agent.
When the concrete is in direct contact with aggressive soils, the aggressive
solution may be drawn into the concrete by capillary action. If evaporation at the
surface of the concrete is possible, the concentration of salts in the capillaries may
become dangerously high. A similar situation may occur when one surface of the
concrete is exposed to an aggressive solution under hydrostatic pressure and the
other surface is dry. The solution is forced into the capillaries of the concrete and,
if evaporation at the exposed face is possible, a heavy build up of salts may be
expected in the pores of the concrete surface. Chemical corrosion in Saudi Aramco
is manifested by steel corrosion, alkali aggregate reactivity, sulphate attack, and
acid attack. Salt in the surrounding ground, ground water, or air diffuses into the
concrete. Steel corrosion results in an increase in the volume of the corroded
portion (Le. surficial layer) of the reinforcing steel bar.
This increase in steel volume causes the concrete to crack and to disintegrate. The
first evidence of steel corrosion may be the appearance of a brown stain on the
concrete surface. The appearance of this brown stain is followed by the
development of a fine crack running through the stain and roughly following the
line of the steel. The increase in the volume of the steel corrosion products
eventually bursts the concrete cover. Pieces of concrete are spalled off.
The spalling of concrete leaves the steel exposed. . The pieces of concrete that are
spalled are usually sound and show no evidence of concrete deterioration.
Temperature and relative humidity play an important part in determining the rate
of steel corrosion in concrete, as was explained in Table 1 under the topic of
"Moisture".
Chemical Attack
Solid salts do not attack concrete, but when they are in the form of a solution, they
can directly react with the hardened cement paste. Some soils contain alkali,
magnesium and calcium sulphates. When these sulphates come into contact with
groundwater, they form a sulphate solution. Seawater may also contain significant
sulphate content. Attack of the hardened cement paste can occur when the
sulphates react with the Ca(OH)2 and the calcium aluminate hydrates. This
reaction is called sulphate attack. Due to the increase in volume, these expansive
reactions can produce a sufficient pressure that disrupts the cement paste. This
disruption of the cement paste results in concrete cracking and disintegration. Over
a period of time, excessive amounts of sulphates in soil or water can attack and
destroy concrete that is not properly designed and protected.
The rate of a sulphate attack increases with an increase in the strength of the
sulphate solution. The concentration of the sulphates is expressed as the number of
parts of the weight of S04 per million parts of the solution (ppm). 1000 ppm is
considered to be a moderately severe sulphate content. 2000ppm is considered to
be a very severe sulphate content, especially if MgSO4 is the predominant
constituent. The parallel values of soluble sulphates in the soil itself are 0.2 and
0.5 percent. The movement of the groundwater must be known in order to estimate
the danger of a sulphate attack. A high rate of attack may occur because the
sulphate that is removed by the reaction with the cement hydration products can be
replenished. Likewise, alternating saturation and drying of the concrete can lead to
rapid deterioration by sulphate attack.
Sulphate attack conditions are less severe when the concrete is completely buried
and a channel for the groundwater does not exist. Concrete that is attacked by
sulphates has a characteristically whitish appearance.
Sulphate damage usually starts at the edges and corners of the concrete member
and is followed by a progressive cracking and spalling of the concrete. Cracking
and spalling of the concrete reduces the concrete to a friable or even soft state.
Some concrete structures may be subjected to chemical attack on one or more
surfaces. Concrete can be attacked by water, acids, alkali, salt solutions, or a wide
variety of
organic chemicals. Damage may be limited to only surface discoloration or surface
roughening. Damage could be as catastrophic as acid attack, with the resulting loss
of structural integrity. The affected surfaces are generally covered with barrier
materials. A barrier material separates the concrete surface from the environment.
In damp conditions, SO2 CO2, SO3 and other acid forms that are present in the
atmosphere may attack concrete by dissolving in water and removing parts of the
cement paste. These acids will leave a soft and mushy mass behind. This form of
attack occurs in sewers, chimneys, and in/around sulfur pits. Almost all types of
mineral acids will have a destructive effect on concrete. The rate of an acid attack
is determined by some factors such as the amount and concentration of acid, the
cement content, the type of aggregate used in respect to the aggregate's solubility
in acids, and the permeability of the concrete. When the hydrated cement reacts
with an acid, the lime in the cement tends to neutralize the acid. If the concrete is
made with a siliceous aggregate, neutralization can only be affected by the
breaking down of the cement binder. If a calcareous aggregate, such as
limestone, is used in the concrete, the aggregate is also active in the neutralization
of the acid.
It is also found that, when there are sufficient moisture and alkali, maximum
expansion of concrete due to AAR occurs when the content of reactive minerals in
aggregate is within a sensitive region, some refer to this as "pessimum" content.
Content of reactive minerals below or greater than the pessimum value, AAR
expansion reduces. From the above, it can be seen that, for a damage AAR
expansion to occur, it is necessary to have
• sufficient moisture supply,
• high content of alkali in concrete, and
• pessimum amount of reactive minerals in aggregate.
d. Admixtures
Admixture in the context of AAR in concrete means chemical agents added to
concrete at the mixing stage. These include accelerators, water reducers
(plasticizers), retarders, superplasticizers, air entraining, etc. Some of the
chemicals contain sodium and potassium compounds which may contribute to the
alkali content of concrete.
e. Water
Water may contain certain amount of alkali. PNAP 180 states that acid-soluble
alkali content of water be determined in accordance with American Public Health
Association (APHA) (17ed. 1989) Sections 3500-K and 3500-Na.
f. Alkalis from outside the concrete
In area of cold whether, de-icing salt containing sodium compounds may increase
alkali content on the surface layer of concrete. Soils containing alkali may also
increase alkali content on the surface of concrete.
ALKALI CONTENT AND AAR
Research show that when the total alkali content, in terms of equivalent sodium
oxide, is less than 3 kg/m3, damage expansion due to AAR is unlikely to happen,
provide that known highly alkali-reactive minerals, such as opal and glass, are not
present in the concrete. Because of the above research findings, and also because
no reliable universal testing method have been established for the determination of
reactivity of an aggregate, limiting alkali content in concrete has become the most
widely used approach for the control of AAR. In Hong Kong, PNAP 180 specifies
that, in the absence of alternative approach for AAR control, the alkali content of
concrete expressed as the equivalent sodium oxide shall not exceed 3.0 kg per
cubic meter of concrete.
REACTIVE AGGREGATE
General types of AAR
There are mainly three types of AAR found in concrete. These are
• alkali-silica reaction
• alkali-silicate reaction and
• alkali-carbonate reaction
Alkali-silica reaction is a reaction between alkali hydroxides and free silica in
aggregate form a alkali-silica gel.
SiO2 + 2NaOH + H2O _ Na2SiO3×2H2O
Silica Alkali Water Alkali-silica gel Alkali-silicate reaction is the same as alkali-
silica reaction except that in this case the reactive constituent is not free silica
present in the combined form of phyllosilicates. Alkali-carbonate reaction occurs
in concrete when alkalis react with certain dolomitic lime stones containing clay.
Reaction causes cracks allowing water to enter which causes the clay to swell and
disrupt the aggregate. Majority of the structures affected by AAR is found due to
alkali-silica reaction. Alkalisilicate and alkali-carbonate reaction is relatively rear.
Tests for aggregate reactivity
Many test methods have been proposed by researchers for identifying potential
reactivity of aggregate all over the world. These may be classified into three types.
• Petrographic examinations
• Chemical tests
• Expansion tests
Petrographic examination is the process of identifying the types of minerals in
aggregate or concrete section by observation using microscope or other aids. This
method can identify types of minerals in the aggregate and give suggestions as for
whether the aggregate is potentially reactive or not. Because the uncertainties
involved in the test, the method is generally used as a screening test as a part of an
investigation. Many proposed test methods using chemical analyses to identify
potential reactivity of aggregate. ASTM C389-87 chemical test (ASTM 1987a),
One of such measures is to place the specimens at 38°C or 40°C and 100% relative
humidity. In such a condition the AAR and its expansion complete within a few
months time. In another such test using mortar bar as specimens, the mortar bars
are immersed in a NaOH solution at 80°C. This method is also referred to as
Accelerated Mortar Bar Test.
It should be noted that the methods that have been proposed so far have their
limitations. Some succeeds in identifying reactivity for certain aggregates whereas
fails for others. Therefore it is difficult to ascertain an aggregate is absolutely non-
reactive using the currently available testing methods.
Concrete in Seawater
The following Table shows the concentration of major ions in some of the
world seas.
Concentration (mg/l)
Major Black Marmara Mediterranean North Atlantic Baltic Arabian BRE** Red
Sea
Ions Sea Sea Sea Ocean Sea Gulf Exposure Sea
Sodium 4,900 8,100 12,400 12,200 11,100 2,190 20,700 9,740 11,350
Magnesium 640 1,035 1,500 1,110 1,210 260 2,300 1,200 1,867
Chloride 9,500 14,390 21,270 16,550 20,000 3,960 36,900 18,200 22,660
Sulfate 1,362 2,034 2,596 2,220 2,180 580 5,120 2,600 3,050
TDS 17,085 26,409 38,795 33,060 35,370 7,110 66,650 32,540 40,960
TDS Ratio* 3.90 2.52 1.72 2.02 1.88 9.37 1.00 2.05 1.63
Theoretical Aspects
From the standpoint of chemical attack on hydrated Portland cement in
unreinforced concrete, when alkali reactive aggregates are not present, one might
anticipate that sulfate and magnesium are the harmful constituents in seawater. It
may be recalled that with groundwaters, sulfate attack is classified as severe when
the sulfate ion concentration is higher than 1500 mg/liter; similarly, Portland
cement paste can deteriorate by cation exchange reactions when magnesium ion
concentration exceeds, for instance, 500 mg/liter.
Building Code Commentary that cements with C3A up to 10 percent may be used
if the maximum water/cement ratio is further reduced to 0.40. The fact that the
presence of uncombined calcium hydroxide in concrete can cause deterioration by
an exchange reaction involving magnesium ions was known as early as 1818 from
investigations on disintegration of lime-pozzolan concretes by Vicat, who
undoubtedly is regarded as one of the founders of the technology of modern
cement and concrete.
Since seawater analyses seldom include the dissolved CO2 content, the potential
for loss of concrete mass by leaching away of calcium from hydrated cement paste
due to carbonic acid attack is often overlooked. According to Feld, in 1955, after
21 years of use, the concrete piles and caps of the trestle bends of the James River
Bridge at Newport News, Virginia, required a $ 1.4 million repair and replacement
job which involved 70 percent of the 2500 piles. Similarly, 750 precast concrete
piles driven in 1932 near Ocean City, New Jersey had to be repaired in 1957 after
25 years of service; some of the piles had been reduced from the original 550 mm
diameter to 300 mm. In both cases, the loss of material was associated with higher
than normal concentrations of dissolved CO2 present in the seawater.
It should be noted that in permeable concrete the normal amount of CO2 present
in seawater is sufficient to decompose the cementitious products eventually. The
presence of thaumasite (calcium silicocarbonate), hydrocalumite (calcium
carboaluminate hydrate), and aragonite (calcium carbonate) have been reported in
cement pastes derived from deteriorated concretes exposed to seawater for long
periods.
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Dept. of Civil engg, ACE, Banglore Page 113
CONCRETE TECHNOLOGY
Unit - 5
READY MIX CONCRETE
• RMC industry is about 12 years old in India, while it was introduced in other
countries much earlier
- PATENTED IN GERMANY
• 1913- FIRST DELIVERY OF RMC (BALTIMORE)
• 1926- BIRTH OF TRANSIT MIXER
• 1931- ERECTION OF FIRST COMMERCIAL PLANT IN LONDON
• 1950-1974 REMARKABLE GROWTH OF RMC – 31 MILLION CUBIC
METRE OF CONCRETE PER YEAR
Factors Delaying Entry of RMC in India
• RMC is highly mechanized activity and entails initial high cost. Especially due
to import of basic equipment and machinery.
• Smaller size of construction in unorganized sector highly competitive and cost
conscious.
• Availability of abundant cheap labour for making and transporting concrete.
• Differential taxation between RMC and SMC. Especially before 1997 when
excise duty @16% also existed.
Factors that Prompted Introduction of RMC
• Increasing stakes in the reliability and durability of construction of emerging
users.
• Decreasing share of construction cost in overall cost of the facility.
• Increasing awareness on environmental factors and convenience.
• Globalization – adoption of best practices across the globe.
• Bigger size of projects and Time is recognised as a cost factor.
Concrete Concrete
Cement Total requirement Concrete requirement
SI. Year concrete requirement
demand on major within
No. requirement in rural areas
million tons 3 projects 3 domain of RMC
million m 3 million m 3
million m million m
No. of Plants
Geographical Distribution
2001 – 2002 2004 – 2005
Bangalore – Mysore Belt 12 35
Chennai – Trichannapali 8 25
Hyderabad – Vizag 6 12
Pune 2 10
Kolkatta 1 3
Ahemdabad, Surat - 3
Jaipur - 2
Sundry - 5
Total 47 147
In many cases, information regarding Concrete Mix Design adopted for the type
of material available in the plant may not be available. Properties of the
constituents may not be available due to lack of testing facilities at RMC plant.
Three test specimens shall be made up for each sample for testing at 28 days. The
purchaser shall inform the producer if his requirements for sampling and testing
are higher than one sample every 50 m3 or 50 batches, whichever is the greater
frequency Acceptance criteria as per IS 456-2000: The test results of the sample
shall be average of the strength of the three specimens. The individual variation
should not be more than ±15% of the average.
UNIT -6
SELF COMPACTING CONCRETE
Normal Concrete
Traditionally Concrete is made by mixing:
• CEMENT
• WATER
• COARSE AND FINE AGGREGATES
Problems persist……
• Lack of adequate compaction in normal concrete
• Compaction requires the use of heavy, noisy, expensive, energy-consuming
vibrators – sometimes non available
• More advanced complex RC design - high density of reinforcing bars, complex
shapes - shortage of skilled labour for supervision
There is a quest amongst concrete engineers for a still higher strength/ higher
performance/ higher ductility concrete
• The answer could be …… SCC
Designer / client
• Use in more complex design & heavy reinforcement
• Improved aesthetics & durability
• Quicker construction time
• Less variation in the production of concrete & more homogeneous concrete
• Better surface finish
“The ability of SCC to flow into and fill completely all spaces within the
formwork, under its ownweight.”
Passing ability
“The ability of SCC to flow through tight openings such as spaces between steel
reinforcing bars without segregation or blocking.”
• Segregation resistance
“The ability of SCC to remain homogeneous in composition during transport and
placing.”
CHARACTERSTICS OF SCC
• If SCC should not segregate- it must have mortar rich in fines & is also able to
transport the coarse aggregate & keep them in viscous suspension
• Cement cannot be the only finer/filler material
• Mineral admixtures are used to enhance the deformability & stability of concrete
• Chemical admixtures are a must for achieving excellent flow at low water
content. VMA reduces bleeding & improves the stability of the concrete mixture
Compared to Conventional Concrete, SCC has
• Higher powder content in the order of 450-600 Kg/m3
• Lower water/cement ratio. Typical range of water is 160 to 185 kg/ m3 &
water/binder ratio, by volume in the range of 0.7 to 1.25. Volume of paste 0.36 to
0.43
• Lower coarse/fine aggregate ratio
• Use of superplasticizers & VMA compatible with cement in small percentages.
TEST METHODS FOR DETERMINIG FRESH SCC PROPERTIES
_ FILLING ABILITY
• Slump flow & T
50CM slump flow
• V- Funnel
_ PASSING ABILITY
• L-Box
• U-box
• J-ring
• Fill Box
_ SEGREGATION RESISTANCE
• V-Funnel at T5 Minutes
• GTM Screen stability test
Slump flow (spread)
• Most popular method
• Assess the horizontal free flow of concrete in the absence of obstruction
• Measures the filling ability
• Normal range of flow recommended
o 650 mm to 800 mm
TEST METHODS
Slump flow (spread)
• Secondary measurement of T50 cm can be made
• Represents time taken in seconds to reach horizontal diameter of 500 mm
• Recommended limits are-2sec to 5sec
V-Funnel Test
• To assess the flowability of fresh concrete
• The time taken for concrete to flow through the narrow end is measured
• Measures viscosity of concrete
V-Funnel Test
Dept. of Civil engg, ACE, Banglore Page 129
CONCRETE TECHNOLOGY
TEST METHODS
L-Box Test
• Passing ability of fresh concrete.
• T 20 cm and T 40 cm marks of horizontal section of L – box are the indications
of ease of flow of concrete.
L-Box Test
U-Box Test
• Also called as „Box-shaped‟
• Measures the filling ability of concrete.
• The difference in height of two sections is measured.
• Recommended value:
o difference in the height of the limbs < 30 mm
J-Ring Test
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Unit -7
FIBER REINFORCED CONCRETE-
BEHAVIOUR PROPERTIES AND
APPLICATION
Introduction
The weak matrix in concrete, when reinforced with steel fibres, uniformly
distributed across its entire mass, gets strengthened enormously, thereby rendering
the matrix to behave as a composite material with properties significantly different
from conventional concrete. Because of the vast improvements achieved by the
addition of fibers to concrete, there are several applications where Fibers
Reinforced Concrete (FRC) can be intelligently and beneficially used. These fibers
have already been used in many large projects involving the construction of
industrial floors, pavements, highway-overlays, etc. in India. The principal fibers
in common commercial use for Civil Engineering applications include steel
(SFRC/SFRS), glass, carbon and aramid. These fibers are also used in the
production of continuous fibers and are used as a replacement to reinforcing steel.
High percentages of steel fibers are used extensively in pavements and in
tunnelling. This invention uses Slurry Infiltrated Fiber Concrete (SIFCON).
Fibers in the form of mat are also being used in the development of high
performance structural composite. Continuous fiber-mat high performance fiber
reinforced concrete (HPFRCs) called Slurry Infiltrated Mat Concrete (SIMCON)
is used in the production of High performance concrete. Use of basalt fibers are
picking up in western countries. Steel fibers are also used in the production new
generation concretes such as Reactive Powder Concrete (RPC), Ductal and
Compact Reinforcing Concrete (CRC). Properties and applications of SFRC and
some of these new generation fiber concrete materials are discussed.
The weak matrix in concrete, when reinforced with steel fibres, uniformly
distributed across its entire mass, gets strengthened enormously, thereby rendering
the matrix to behave as a composite material with properties significantly different
from conventional concrete.
In general, SFRC is very ductile and particularly well suited for structures which
are equired to exhibit:
• Resistance to impact, blast and shock loads and high fatigue
• Shrinkage control of concrete (fissuration)
• Very high flexural, shear and tensile strength
• Resistance to splitting/spalling, erosion and abrasion
• High thermal/ temperature resistance
• Resistance to seismic hazards.
The degree of improvement gained in any specific property exhibited by SFRC is
dependent on a number of factors that include:
• Concrete mix and its age
• Steel fibre content
• Fibre shape, its aspect ratio (length to diameter ratio) and bond characteristics.
The efficiency of steel fibres as concrete macro-reinforcement is in proportion to
increasing fibre content, fibre strength, aspect ratio and bonding efficiency of the
fibres in the concrete matrix. The efficiency is further improved by deforming the
fibres and by resorting to advanced production techniques. Any improvement in
the mechanical bond ensures that the failure of a SFRC specimen is due mainly to
fibres reaching their ultimate strength, and not due to their pull-out.
1.1 Mix Design for SFRC
Just as different types of fibres have different characteristics, concrete made with
steel fibres will also have different properties. When developing an SFRC mix
design, the fibre type and the application of the concrete must be considered.
There must be sufficient quantity of mortar fraction in the concrete to adhere to the
fibres and allow them to flow without tangling together, a phenomenon called
„balling of fibres‟. Cement content is, therefore, usually higher for SFRC than
conventional mixes Aggregate shape and content is critical. Coarse aggregates of
sizes ranging from 10 mm to 20 mm are commonly used with SFRC. Larger
aggregate sizes usually require less volume of fibres per cubic meter. SFRC with
The use of steel fibres in concrete generally reduces the slump by about 50 mm.
To overcome this and to improve workability, it is highly recommended that a
super plasticizer be included in the mix. This is especially true for SFRC used for
highperformance applications.Generally, the ACI Committee Report No. ACI 554
„Guide for Specifying, Mixing, Placing and Finishing Steel Fibre Reinforced
Concrete‟ is followed for the design of SFRC mixes appropriate to specific
applications.
1.2 Factors Controlling SFRC
• Aspect ratio, l/d
• Volume fraction, vf
• Fiber reinforcing index, RI=l/d x vf
• Critical length, lmin
• Balling of fibers
• Good mix design: more matrix, small aggregate, workable
• Type of fibers-size, shape, strength, modulus
Workability
• We know that it is usually wrong to add water to concrete for workability.
• The main problem with workability of steel fiber reinforced concrete is in getting
proper distribution of the fibers so that they don't ball up.
• This difficulty is usually overcome by slow, continuous and uniform feeding of
the fibers into the wet or dry mix by means of vibratory feeders.
• Sometimes the fibers are passed through screens as they are introduced. Proper
feeding can virtually eliminate the problem of balling. On the other hand, addition
of water to improve workability can reduce the flexural strength significantly, a
critical matter when one considers that one of the main reasons for using steel
fibers is to improve the flexural strength.
• In such cases use of suitable admixture probably would improve the workability
to certain extent and may not to the extent that you require
Test for workability
• Slump test- subsidence in mm
• Inverted slump test-time in seconds
• Compacting factor test-degree of compaction
• VB test-time in seconds. The relationship among the different workability
parameters are shown in Fig. 3. The effect of volume fraction and aspect ratio on
VB time is shown in Fig.
Fibre Shotcreting
“Shotcreting” using steel fibres is being successfully employed in the construction
of domes, ground level storage tanks, tunnel linings, rock slope stabilization and
repair and retrofitting of deteriorated surfaces and concrete. Steel fibre reinforced
shotcrete is substantially superior in toughness index and impact strength
compared to plain concrete or mesh reinforced shotcrete. In Scandinavian
countries, shotcreting is done by the wet process and as much as 60% of ground
support structures (tanks and domes) in Norway are constructed using steel fibres.
In many countries including India, steel fibre shotcrete has been successfully used
in the construction of several railway and penstock tunnels.
1.4 Applications of SFRC
The applications of SFRC depend on the ingenuity of the designer and builder in
taking advantage of its much enhanced and superior static and dynamic tensile
strength, ductility, energy-absorbing characteristics, abrasion resistance and
fatigue strength. Growing experience and confidence by engineers, designers and
contractors has led to many new areas of use particularly in precast, cast in-situ,
and shotcrete applications. Traditional application where SFRC was initially used
as pavements, has now gained wide acceptance in the construction of a number of
airport runways, heavy-duty and container yard floors in several parts of the world
due to savings in cost and superior performance during service.
The advantages of SFRC have now been recognised and utilised in precast
application where designers are looking for thinner sections and more complex
shapes. Applications include building panels, sea-defence walls and blocks, piles,
blast-resistant storage cabins, coffins, pipes, highway kerbs, prefabricated storage
tanks, composite panels and ducts. Precast fibre reinforced concrete manhole
covers and frames are being widely used in India, Europe and USA. Cast in-situ
application includes bank vaults, bridges, nosing joints and water slides. “Sprayed-
in” ground swimming pools is a new and growing area of shotcrete application
in Australia.
SFRC shotcrete has recently been used for sealing the recesses at the anchorages
of post stressing cables in oil platform concrete structures. Recent developments in
fibre types and their geometry and also in concrete technology and equipment for
mixing, placing and compaction of SFRC and mechanized methods for shotcreting
have placed Scandinavian and German consultants and contractors in a front
position in fibreshotcreting operations world wide.
Laboratory investigations have indicated that steel fibres can be used in lieu of
stirrups in RCC frames, beams, and flat slabs and also as supplementary shear
reinforcement in precast, thin-webbed beams. Steel fibre reinforcement can also be
added to critical end zones of precast prestressed concrete beams and columns and
in cast-in-place concrete to eliminate much of the secondary reinforcement. SFRC
may also be an improved means of providing ductility to blast-resistant and
seismic-resistant structures especially at their joints, owing to the ability of the
fibres to resist deformation and undergo large rotations by permitting the
development of plastic hinges under over-load conditions.
f) Special Structures
Machine Foundations, Currency Vaults and Strong Rooms, Impact and Fiber-
Protective Shells and Lost Forms, Column-Beam Joints in Seismic-Resistant
Structures, End Zones of Prestressed Concrete Elements, High Volume Steel Fiber
Reinforce Concrete structures made out of SIFCON and CRC (Slurry Infiltrated
Fiber Concrete and Compact Reinforced Concrete)
Advantages of using SFRC
• Improved performances under action of any kind of loading
• High seismic-resistance in buildings due to ductile behaviours of joints and
Connections
Technical Approach
Partially cast-in-place HPCFSs are built using stay-in-place formwork elements
made by encasing light steel sections and tubes into advanced cementitious
composites including (1) continuous HPFRCs and (2) discontinuous fiber
HPFRCs. The "core" of the beam and column members is cast-in-place HS-LWS
FRC. The stay-in-place formwork also serves as surface reinforcement, thus
replacing conventional steel reinforcement and simplifying casting of the member
core by eliminating reinforcement congestion. Furthermore, by encasing steel
elements into HPFRC, their fire resistance and durability is improved. The
construction procedure consists of first welding or bolting together of the stay-in-
place formwork, followed by casting in place of HS-LWA FRC in both(1) the
member core and (2) the beam-column joint region.
Since the subsequent floor can be erected as soon as the steel elements are bolted
together, it is anticipated that the speed of construction per story can be
comparable to that of conventional, prefabricated steel frames. If successful, the
proposed concept will result in advanced concrete frame systems exhibiting high
strength and seismic resistance, while being faster and more cost effective to
construct than conventional cast-in-place systems.
While in conventional SFRC, the steel fibre content usually varies from 1 to 3
percent by volume, it varies from 4 to 20 percent in SIFCON depending on the
geometry of the fibres and the type of application. The process of making SIFCON
is also different, because of its high steel fibre content. While in SFRC, the steel
fibres are mixed intimately with the wet or dry mix of concrete, prior to the mix
being poured into the forms, SIFCON is made by infiltrating a low-viscosity
cement slurry into a bed of steel fibres „pre-packed‟ in forms/moulds The matrix
in SIFCON has no coarse aggregates, but a high cementitious content. However, it
may contain fine or coarse sand and additives such as fly ash, micro silica and
latex emulsions.
Proportions of cement and sand generally used for making SIFCON are 1: 1, 1:1.5,
or 1:2. Cement slurry alone can also be used for some applications. Generally, fly
ash or silica fume equal to 10 to 15% by weight of cement is used in the mix. The
water-cement ratio varies between 0.3 and 0.4, while the percentage of the super
plasticizer varies from 2 to 5% by weight of cement. The percentage of fibres by
volume can be any where from 4 to 20%, even though the current practical range
ranges only from 4 to 12%.
The fibre volume can, hence, be substantially less than that required for making of
SIFCON, still achieving identical flexural strength and energy absorbing
toughness. SIMCON is made using a non-woven “steel fibre mats” that are
infiltrated with a concrete slurry. Steel fibres produced directly from molten metal
using a chilled wheel concept are interwoven into a 0.5 to 2 inches thick mat. This
mat is then rolled and coiled into weights and sizes convenient to a customer‟s
application (normally up to 120 cm wide and weighing around 200 kg).
As in conventional SFRC, factors such as aspect ratio and fibre volume have a
direct influence on the performance of SIMCON. Higher aspect ratios are
desirable to obtain increased flexural strength. Generally, because of the use of
mats, SIMCON the aspect ratios of fibres contained in it could well exceed 500.
Since the mat is already in a preformed shape, handling problems are significantly
minimised resulting in savings in labour cost. Besides this, “balling” of fibres does
not become a factor at all in the production of SIMCON.
Indian Scenerio
In India, SIFCON, CRC, SIMCON and RPC are yet to be used in any major
construction projects. For that matter, even the well-proven SFRC has not found
many applications yet, in spite of the fact that its vast potentials for civil
engineering uses are quite well known. The reason for these materials not finding
favour with designers as well as user agencies in the country could be attributed to
the non-availability of steel fibres on a commercial scale till a few years ago. The
situation has now changed. Plain round or flat and corrugated steel fibres are
presently available in the country in different lengths and diameters. It is,
therefore, possible now to use new-age construction materials like SIFCON and
CRC in our country in the construction of several structures that demand high
standards of strength coupled with superior performance and durability.
Leadline Rods/Tendons
Leadline reinforcing elements are circular rods that are pultruded using
unidirectional carbon fibers at 65% fiber volume fraction with an epoxy resin. The
rods have a specific gravity of 1.6, a relaxation ratio of 2-4% at 20°C, and a
coefficient of thermal expansion of 0.68 x 10-6 /°C in the longitudinal direction.
The rods have a tensile modulus of 147 GPa and 1.5 to 1.7% elongations at break.
Rods are available in a number of diameters with four major surface types.
For highway pavement applications, concretes with early strength are attractive for
potential use in repair and rehabilitation with a view towards early opening of
traffic. In this direction lot of work has been done on high early strength fiber
reinforced concrete (HESFRC) and is being used in practice. Technical papers and
reports provide an extensive database and a summary of comprehensive
experimental investigation on the fresh and mechanical properties of HESFRC.
The control high early strength (HES) concrete (used with the fiber addition) were
In 1990, the American Concrete Institute formed the ACI Committee 440 on Non-
Metallic Reinforcement. The Committee has just developed a state-of-the-art
report on Fiber Reinforced Plastic (FRP) for Concrete Structures [ACI Committee
440 1996].
The materials are intermingled. There is an interface between the materials, and
often an inter phase region such as the surface treatment used on fibers to improve
matrix adhesion and other performance parameters via the coupling agent.
Glass has been the predominant fiber for many civil engineering applications
because of an economical balance of cost and specific strength properties. Glass
fibers are commercially available in "E-Glass" formulation (for "Electrical"
grade), the most widely used general-purpose form of composite reinforcement,
high strength S-2 glass and ECR Glass, a modified E-Glass which offers greater
alkali resistance. Although considerably more expensive than glass, other fibers
including carbon and aramid are used for their strength or modulus properties or in
special situations as hybrids with glass.
Field Applications
Composite materials have been used in a variety of civil engineering applications
with both reinforced and prestressed concrete. They are manufactured as
reinforcing elements, as prestressing and post-tensioning tendons and rods, and as
strengthening materials for rehabilitation of existing structures. Several new
structures utilizing FRP reinforcement are currently underway in USA and Japan.
Fast track concrete paving (FTCP) was developed originally by the concrete
paving industry in Iowa. It was pointed out that the benefits of applying FTCP
technology in such applications are (1) a reduced contract period, thus reducing
the contract overhead cost, (2) early opening of the pavement to traffic, (3)
minimizing the use of expensive concrete paving plant and traffic management
systems, and (4) reduced traffic delay costs.
The Technology
Reactive Powder Concrete is an ultra high-strength and high ductility composite
material with advanced mechanical properties. Developed in the 1990s by
Bouygues' laboratory in France, it consists of a special concrete where its
microstructure is optimized by precise gradation of all particles in the mix to yield
maximum density. It uses extensively the pozzolanic properties of highly refined
silica fume and optimization of the Portland cement chemistry to produce the
highest strength hydrates. RPC represents a new class of Portland cement-based
material with compressive strengths in excess of 200 MPa range. By introducing
fine steel fibers, RPC can achieve remarkable flexural strength up to 50 MPa. The
material exhibits high ductility with typical values for energy absorption
approaching those reserved for metals.
The benefits
• RPC is a better alternative to High Performance Concrete and has the potential to
structurally compete with steel.
• Its superior strength combined with higher shear capacity results in significant
dead load reduction and limitless structural member shape.
• With its ductile tension failure mechanism, RPC can be used to resist all but
direct primary tensile stresses. This eliminates the need for supplemental shear and
other auxiliary reinforcing steel.
• RPC provides improve seismic performance by reducing inertia loads with
lighter members, allowing larger deflections with reduced cross sections, and
providing higher energy absorption.
• Its low and non-interconnected porosity diminishes mass transfer making
CRC has structural similarities with reinforced concrete in the sense that it also
incorporates main steel bars, but the main bars in CRC are large in number and are
uniformly reinforced. Owing to this and also because of the large percentage of
fibres used in its making, it exhibits mechanical behavior more like that of
structural steel, having almost the same strength and extremely high ductility.
CRC specimens are produced using 10-20% volume of main reinforcement (in the
form of steel bars of diameter from about 5 mm to perhaps 40 or 50 mm) evenly
distributed across the cross section) and 5-10% by volume of fine steel fibres. The
water-cement ratio is generally very low, about 0.18% and the particle size of sand
in the cement slurry is between 2 and 4mm.The flow characteristics while mixing
and pouring is aided by the use of micro silica and a dispersant. High-frequency
vibration is often resorted to for getting a the mix compacted and to obtain
homogeneity. Prolonged processing time for mixing, about 15-20 minutes, ensures
effective particle wetting and high degree of microhomogeneity.
Applications
• Large plates and shells designed for very large local loads from shocks and
explosives, large pressure tanks
• High strength to density ratio-used where weight and inertia are important as in
ships and vehicles
• To support large machinery parts
• Used in Hybrid structures-High performance structural joints in steel-concrete
structures
• Used as an alternative to steel where corrosion and fire are the main criterion.
*****************************************************************
UNIT - 8
HIGH PERFORMANCE CONCRETE
INTRODUCTION
Concrete is the most widely used construction material in India with annual
consumption exceeding 100 million cubic metres. It is well known that
conventional concrete designed on the basis of compressive strength does not meet
many functional requirements such as impermeability, resistance to frost, thermal
cracking adequately. Conventional
Portland cement concrete is found deficient in respect of:
• Durability in severe environs (Shorter service life and require maintenance)
• Time of construction (longer release time of forms and slower gain of strength)
• Energy absorption capacity (for earthquake-resistant structures)
• Repair and retrofitting jobs
High performance concrete (HPC) successfully meets the above requirement.
HPC is an engineered concrete possessing the most desirable properties during
fresh as well as hardened concrete stages. HPC is far superior to conventional
cement concrete as the ingredients of HPC contribute most optimally and
efficiently to the various properties.
The American Concrete Committee on HPC includes the following six criteria for
material selections, mixing, placing, and curing procedures for concrete.
(1) Ease of placement
(2) Long term mechanical properties
(3) Early-age strength
(4) Toughness
(5) Life in severe environments
(6) Volumetric stability
The above-mentioned performance requirements can be grouped under the
following three general categories.
(a) Attributes that benefit the construction process
(b) Attributes that lead to enhanced mechanical properties
(c) Attributes that enhance durability and long-term performance
Definition of HPC
The performance requirements of concrete cannot be the same for different
applications. Hence the specific definition of HPC required for each industrial
application is likely to vary. The Strategic Highway Research Programme (SHRP)
has defined HPC for highway application on the following strength, durability,
and w/c ratio criteria.
(a) It should satisfy one of the following strength criteria:
A more broad definition of HPC was adopted by the ACI. HPC was defined as
concrete, which meets special performance and uniformity requirements that
cannot be always be achieved routinely by using only conventional materials and
normal mixing, placing and curing practices. The requirements may involve
enhancement of placement and compaction without segregation, long term
mechanical properties, early age strength, volume stability or service life in severe
environments. Concretes possessing many of these characteristics often achieve
higher strength. Therefore, HPC is often of high strength, but high strength
concrete may not necessarily be of high performance.
1) High C3A content in cement generally leads to a rapid loss of flow in fresh
concrete. Therefore, high C3A content should be avoided in cements used for
HPC.
2) The total amount of soluble sulphate present in cement is a fundamental
consideration for the suitability of cement for HPC.
3) The fineness of cement is the critical parameter. Increasing fineness increases
early strength development, but may lead to rheological deficiency.
4) The superplasticizer used in HPC should have long molecular chain in which
the sulphonate group occupies the beta position in the poly condensate of
formaldehyde and melamine sulphonate or that of naphthalene sulphonate.
5) The compatibility of cement with retarders, if used, is an important
requirement. Ronneburg and Sandrik (1990) suggested tailor-made cements with
characteristics suitable for HPC (Table 2). Note that SP30 is ordinary Portland
cement. SP30-4A and SP30- 4A (mod) are two varieties of tailor-made special
cements. It is to be noted that the two special cements recommended to produce
very high strength concrete have low C3A content, sulphate level, and heat of
hydration apart from phase composition.
Coarse aggregate
The important parameters of coarse aggregate that influence the performance of
concrete are its shape, texture and the maximum size. Since the aggregate is
generally stronger than the paste, its strength is not a major factor for normal
strength concrete, or for HES and VES concretes. However, the aggregate strength
becomes important in the case of high performance concrete. Surface texture and
mineralogy affect the bond between the aggregates and the paste as well as the
stress level at which micro cracking begins. The surface texture, therefore, may
also affect the modulus of elasticity, the shape of the stress-strain curve and to a
lesser degree, the compressive strength of concrete. Since bond strength increases
at a slower rate than compressive strength, these effects will be more pronounced
in HES and VES concretes. Tensile strengths may be very sensitive to differences
in aggregate surface texture and surface area per unit volume.
reaction the pozzolanas react with calcium hydroxide, Ca(OH)2, (free lime)
liberated during hydration of cement, which comprises up to 25 per cent of the
hydration product, and the water to fill voids with more calcium-silicate-hydrate
(non-evaporable water) that binds the aggregate particles together.
The pozzolanas may also react with other alkalis such as sodium and potassium
hydroxides present in the cement paste. These reactions reduce permeability,
decrease the amounts of otherwise harmful free lime and other alkalis in the paste,
decrease free water content, thus increase the strength and improve the durability.
Fly ash used as a partial replacement for cement in concrete, provides very good
performance. Concrete is durable with continued increase in compressive strength
beyond 28 days. There is little evidence of carbonation, it has low to average
permeability and good resistance to chloride-ion penetration. Chloride-ion
penetration rating of high volume fly ash (HVFA) concrete is less than 2000
coulombs, which indicate a very low permeability concrete. It continues to
improve because many fly ash particles react very slowly, pushing the coulomb
value lower and lower.
Silica fume not only provides an extremely rapid pozzolanic reaction, but its very
fine size also provides a beneficial contribution to concrete. Silica fume tends to
improve both mechanical properties and durability. Silica fume concretes continue
to gain strength under a variety of curing conditions, including unfavorable ones.
Thus the concretes with silica fume appear to be more robust to early drying than
similar concretes that do not contain silica fume. Silica fume is normally used in
combination with high-range water reducers and increases achievable strength
levels dramatically. Since no interaction between silica fume, ground granulated
blast-furnace slag and fly ash occurs, and each component manifests its own
cementitious properties as hydration proceeds, higher strength and better
flowability can be achieved by adding a combination of SF, FA and GGBFS to
OPC which provides, a system with wider particle-size distribution.
A look at this table reveals that silica and alumina content vary widely. However,
these chemical differences do not significantly influence the properties of
concrete. Fly ashes generally contain less silica and more alumina compared to
natural pozzolanas. Both fly ash and blast furnace slag have high calcium and
magnesium oxide content. Highly active admixtures such as silica fume and rice
husk ash contain high content of silica. Metakaolin contains roughly equal
proportions of silica and alumina.
The ground, granulated blast furnace slag and rice husk ash have to be ground to
the required fineness to assist pozzolanic activity. Typically, particles less than 10
μm in size contribute to early strength; particles between 10 and 45 μm show
strength gain up to 28 days; particles larger than 45 μm contribute little to the
strength. The slag is generally ground to Blaine fineness of 450-550 m2/kg. The
typical BET surface area of silica fume is 12,000 m2/kg.
This is because the particle size of silica fume is in the range of 0.01-0.45 μm.
However, the rice husk ash is ground only to a fineness of 6-10μm because of the
porous structure. The metakaolin is ground to a fineness of about 1-2 μm.
The pozzolanic material with large surface area shows excellent reactivity. It
imparts stability and cohesiveness to the mixture and prevents bleeding as well as
segregation. A summary of the characteristics of different mineral admixtures is
given in Table .
Characteristics of mineral admixtures.
Type ClassificationChemical compositionParticle characteristics
Ground Cementitious Silicate glass containiUnprocessed materials a
granulated blasand pozzolanicng re
calcium magnesium grains like sand. These a
t
silicate re
furnace slag
ground to size < 45 µm (
Calcium-
(GGBS) Cementitious Silicate glass containiPowder consists of parti
rich fly ng
and pozzulanic cles
500
Ash mainly calcium, < 2 µm. However, 10-
m45/kg Blaine) particles a
nd
magnesium, aluminiu15%
have a rough texture.
m are more than 45 µm.
alkides. Also containsParticles are solid sphere
2%
C3A, silica
Condensed siliHighly activePure CaO, ofC3non- 3s of
S, C4AExtremely fine powder
ca pozzolana crystalline form 20 µm. surface
consisting is genera
of solid spher
S
Fume
llyof
traces unburnt carbones
1- smooth.
0.1 µm average diamete
r,
Rice husk ash Highly activeConsists essentially oParticles are <45 mm bu
pozzolana f t 2
about 20 m /kg surface
pure silica in non- areas
have cellular and porous
Low- CementitiousMostly silicate glass Powder
estimatedhaving particles
by nitrogen
calcium fly and pozzolanicrystalline form
containing aluminium
structure.
of
absorption method.
Ash 15-30% > 45 µm. most
c and iron and alkides,
particles are solid spher
small quantities of qu
Natural materiNatural Contains alumino siliParticles
e. are <45 µm an
al artz,
pozzolana cate d
Cenosph-eres and
hematite,
glass, etc. pozzolahave rough texture. con
natural
plerospheres may be pre
Slowly cooledWeak nas
Consists of crystallinsists
Pulverized to fine powd
sent
blast furnace pozzolana containing quartz, er,
e of crystalline silicate
silicate material and ground materials ha
slag, bottom as feldspar, and mica material
ve
h,
rough texture.
field burnt rice
husk ash
Dept. of Civil engg, ACE, Banglore Page 175
CONCRETE TECHNOLOGY
Superplasticizers or HRWR
The superplasticizers are extensively used in HPCs with very low
watercementitious material ratios. In addition to deflocculation of cement grains
and increase in the fluidity, the other phenomena that are likely to be present are
the following.
(a) Induced electrostatic repulsion between particles.
(b) Dispersion of cement grains and consequent release of water trapped within
cement flocks.
(c) Reduction of surface tension of water.
(d) Development of lubrication film between particles.
(e) Inhibition of the surface hydration reaction of the cement particles, leaving
more water to fluidify the mix.
(f) Change in morphology of hydration products.
(g) Induced steric-hindrance preventing particle to particle contact.
The main objectives for using superplasticizers are the following.
(i) To produce highly dense concrete to ensure very low permeability with
adequate resistance to freezing-hawing.
(ii) To minimize the effect of heat of hydration by lowering the cement content.
(iii) To produce concrete with low air content and high workability to ensure high
bond strength.
(iv) To lower the water-cement ratio in order to keep the effect of creep and
shrinkage to a
minimum.
(v) To produce concrete of lowest possible porosity to protect it against external
attacks.
(vi) To keep alkali content low enough for protection against alkali-aggregate
reaction and to keep sulphate and chloride contents as low as possible for
prevention of reinforcement corrosion.
(vii) To produce pumpable yet non-segregating type concrete.
Mix Proportion
The main difference between mix designs of HPC and CC is the emphasis laid on
performance aspect also (in fresh as well as hardened stages of concrete) besides
strength, in case of HPC, whereas in design of CC mixes, strength of concrete is
an important criterion. By imposing the limitations on maximum water–cement
ratio, minimum cement content, workability (slum, flow table, compaction factor,
Vee-Bee consistency), etc., it is sought to assure performance of CC; rarely any
specific tests are conducted to measure the durability aspects of CC, during the
mix design. In HPC, however, besides strength, durability considerations are given
utmost importance. To achieve high durability of HPC, the mix design of HPC
should be based on the following considerations:
i) The water-binder (w/b) ratio should be as less as possible, preferably 0.3 and
below.
ii) The workability of concrete mix should be enough to obtain good compaction
(use suitable chemical admixtures such as superplasticizer (SP)).
iii) The transition zone between aggregate and cement paste should be
strengthened (add fine fillers such as silica fume (SF)).
iv) The microstructure of cement concrete should be made dense and impermeable
(add pozzolanic materials such as fly ash (FA), ground granulated blast furnace
slag powder (GGBFSP), SF, etc.)
v) Proper curing regime of concrete should be established (this is to overcome the
problems associated with usual adoption of very low water content and high
cement content in HPC mixes)
f). The suggestion of sand content at 28% (for MSA of 10mm) and 25% (for MSA
of 25mm) in the BIS method leas to fine aggregates: coarse aggregate ratios of the
order of 1:2 to 1:3 (by weight). From the published literature on HPCs these ratios
seem to be quite high and hence, the cohesiveness of HPCs would be affected if
these ratios are adopted. As the HPCs utilize SPs, it would be necessary to use
more sand in order to avoid segregation of cement paste from aggregate due to the
dispersing/flowing effect of SP on the cement paste.
g). The BIS code allows the use of Zone IV sand which may have particles passing
through 300 micron sieve, to an extent of 50%. As the HPCs have usually very
low water content, this large content of small particles (less than 300 microns) of
sand would reduce the workability of the HPCs. More over, the fine particles of
sand may not be required in HPCs as these concrete usually have high cement
contents and also have often pozzlanic powdery materials such as FA, SF, etc.
ACI Method
This Code covers 28-day compressive strength upto about 60 MPa as seen from
the curve of compressive strength-Vs-w/c ratio, suggested by this Code. The
minimum water cement ratio covered is 0.3. As HPCs have often strengths more
than 60 MPa and w/c ratio 0.3 and below, the ACI method can not give
proportions for HPC.
Road Note No.4
This method covers up to a minimum w/c ratio of 0.35 which is more than the w/c
ratio adopted usually in HPCs and hence, this method cannot be adopted for HPC.
IRC-44 Method
This method refers to a curve of compressive strength-Vs-w/c ratios in which
minimum w /c ratio is 0.4 and maximum compressive strength is about 50 MPa.
The HPCs usually have w/c ratio is 0.3 and less, which is quite less than 0.4 the
value referred in this method. The HPCs usually have the strengths more than 50
MPa. Thus, it can be seen that the IRC-44 method cannot be used for the design of
HPC mixes.
GENERAL COMMENTS ON CONVENTIONAL MIX DESIGN METHODS
It is observed from the study of conventional mix design methods (CMDs) that
they are not generally applicable to HPC because of the following reasons:
i) The compressive strength levels covered by CMDs are far less than those
usually obtained in case of HPCs.
ii) W/C or W/B ratio of CMD, are generally higher or quite close to the highest
level of W/b ratio encountered in HPCs.
iii) The CMDs do not take in to account for changes in properties of fresh as well
as hardened concrete due to incorporation of water reducing admixtures such as
SP and also the permeability reducing mineral additives such as FA, SF, GGBS,
SF, etc.
iv) The CMDs do not consider exclusively the durability aspects affecting
properties of concrete such as porosity, impermeability, electric receptivity, etc.
v) Many a time the type and strength of aggregate limit the strength level of HPCs
that can be achieved with the given aggregate. Such limitations are not usually
encountered in case of CC designated by CMDs.
vi) The CMDs do not account for strength of transition zone. In HPCs,
considerations with regard to the development of suitable transition zone need
special attention.
vii) As the HPCs tend to have usually high cementitious content, use of cement
replacement materials such as FA, SF, GGBS, SP, etc, is almost essential to
reduce the ill effects of high
cement content in a concrete.
viii) The strength developed in case of HPCs after conventional 28-days period is
quantitatively considerable; hence, later age strength (say 90-day) is better
criterion for design of HPC mixes.
ix) The standard deviations of HPCs could be less than those of CCs since the
HPCs are produced under stricter quality control measures. This would help in
making economical mix design of HPCs.
TYPICAL HPC MIX DESIGN METHODS IN PUBLISHED LITERATURE
The properties of HPCs not only depend upon the w/b ratio but also vary
considerably with the richness of mix and the type and strengths of concrete of
aggregates. Workability of HPCs depends upon the type of cement and its
compatibility with chemical admixtures, shape of aggregate, method of mixing of
ingredients of HPCs, etc. Thus, the properties of materials and mix preparation
techniques have very high influence on the HPC mixes, suitable mix proportions
cannot be suggested for HPCs. Therefore, any mix design procedure of HPCs can
strictly be only a guideline and a separate development of HPC mix in the
laboratory for the various ingredients, type of structure and concreting conditions
etc., is very much essential. Hence, the HPC mix design can be only application
specific. It should be noted that the strength increase as the w/c is reduced
(provided the compatibility of concrete is maintained), and that for a given w/c,
the strength is decreased as a mix is made richer (by adding more cement) beyond
a limit. Therefore, the advantage of increase in strength due to lowering of the w/c,
which also reduces consequently the workability. Hence, the HPCs require
approaches other than the increase of cement content in order to achieve the high
strength.
Though the strengths are not always true indicators of durability, the high strength
associated with the HPCs generally tend to impart also high durability to them,
due to reduced w/b and use of pozzolanic admixtures.
4. Estimation of aggregate content: From the total aggregate volume 0.65 m3,
assuming a 2:3 volumetric ratio between fine and coarse aggregate, individual
volume fractions are calculated.
5. Calculation of batch weights: From the typical specific gravity values of
ingredients the batch weights are determined.
6. Superplastizer dosage: If there is no prior experience with the superplasticizer, it
is suggested to start with 1% and continue till the required workability is obtained.
7. Moisture correction: Depending on the moisture condition of batch aggregates,
the appropriate moisture correction for fine and coarse aggregate must be made.
8. Trial batch adjustment: Several laboratory trials using the actual materials may
be required before one arrives at the right combination of materials and mix
proportions, which satisfy the given criteria of workability and strength.
ACI 211.4R Standard Practice
Data needed include- F.M. of sand, dry rodded unit weight of the C.A., Specific
gravity of the aggregates.
1. Slump selection: Selected from the given table
The target strength fcr = (fc + 9.65) / 0.9
fcr = Specified design compressive strength
fc = Required average compressive strength
2. Selection of maximum size of aggregate (MSA): Based on the strength
requirement, select the maximum size of aggregate.
3. Selection of optimum coarse aggregate content:
Weight of C.A. = (%xDRUW)x DRUW
4. Estimation of mixing water and air content: From the table get the estimate of
mixing water and air content percentage.
Mixing Water adjustment, kg/m3 + (V-35)x4.74
5. Selection of W / (C+P) Ratio: Table gives the recommended maximum W /
(C+P) ratio as the function of the maximum size of aggregate to achieve different
age for concretes having compressive strengths ranging from 17 to 79 Mpa. Based
on the available information, Poisson‟s ratio of HPC in the elastic range seems
comparable to the expected range of values for lower strength concretes.
Modulus of Rupture
For usual concrete modulus of rupture and splitting tensile strength are quite low
and don‟t vary much, because they are very much influenced by the tensile
strength of the hydrated cement paste. However, this is no longer the case for high
performance concrete, for which the water binder ratio and the compressive
strength can vary over a wide range. The relationships that have been suggested
between compressive strength and modulus of rupture for usual concrete lose
some of their predictive value when going from usual concrete to highperformance
concrete.
Splitting Tensile Strength
Dewar studied the relationship between the indirect tensile strength and the
compressive strength of concretes having compressive strengths upto 83 MPa at
28 days. He concluded that at low strengths, the indirect tensile strengths may be
as high as 10 percent of the compressive strength but at higher strengths it may
reduce to 5 percent. He observed that the tensile splitting strength was about 8
percent higher for crushed rock aggregate concrete than for gravel aggregate
concrete. He also found that the indirect tesile strength was about 70 percent of the
flexural strength at 28 days.
Shrinkage
Little information is available on the shrinkage behaviour of High-Performance
concrete. A relatively high initial rate of shrinkage has been reported, but after
drying for 180 days there is little difference between the shrinkage of high-
strength and lower strength concrete made with dolomite or limestone. Reducing
the curing period from 28 to 7 days caused a slight increase in the shrinkage.
Shrinkage was unaffected by w/c ratio but is approximately proportional to the
percentage of water by volume in the concrete. Other laboratory and field studies
The creep coefficient decreases while the strength increases, that is to say while
the w/c ratio decreases. For ordinary concretes, the value of the creep coefficient ¢
is generally taken equal to 2.0 when loading is applied at 28 days. It seems that
this coefficient may be as low as 1.0 for some C60 concretes and 0.50 for some C
100 concretes. The creep of high-performance concrete made with high-range
water reducers is reported to be decreased significantly. The maximum specific
creep was less for high-strength concrete than for lower-strength concrete loaded
at the same age.
Ductility
Compression tests show that the stronger the concrete the more brittle it is. This
could be of concern since modern design methods take into account the plasticity
of materials. Flexural tests run on the reinforced HPC beams show that their
ductility is similar to that of beams with ordinary concrete. Care should
nevertheless be exercised concerning HPC elements such as columns submitted to
axial loads. Experiments are being carried out in France in order to set the rules
concerning minimum longitudinal and transverse reinforcements in such pieces.
Fatigue strength
As the static strength of concrete increases, it becomes increasingly more brittle
and its ultimate strain capacity does not increase proportionately with the increase
in strength. Therefore high performance concrete would be vulnerable to fatigue
loading. However in HPC the elastic modulus of the paste and that of aggregate
are more similar, thereby reducing stress concentrations at the aggregate-paste
interface is less susceptible to fatigue loading. Thus due to reduced microcracking
in HPC, the fatigue life built-up damages are smaller when compared with those in
normal strength concrete.
Alkali-Aggregate Reaction
Fly ash, blast furnace slag, and silica fume supplementary cementatious
pozzolanic additions to the concrete mixture (SCM) have shown to be effective
ingredients in resisting alkali-aggregate reaction. The effect of the addition
pozzolanic fly ash (PFA), blast furnace slag (BFS), and condensed silica fume
(CSF) are effective in reducing the expansion in concrete, provided that they are
used correctly and of the appropriate quality and amount. Coating the aggregates
with acrylic or epoxy might be a solution, but effectiveness and cost does not
match the other solution.
Abrasion Resistance
Abrasion resistance of concrete is of major importance in highway pavements and
concrete bridge decks. Work available on the abrasion resistance of high-
performance concretes has shown that increase in strength results in substantially
increased service life, as documented by Gjorv et. al. In this work, an increase in
concrete strength from 50 MPa to 100 MPa can reduce the abrasion deterioration
by almost 50%. While the type of aggregate and its abrasion resistance affects the
performance of the concrete, its effect becomes less significant at the highest
compressive strength to abrasion. Service life of pavements ranged from 7 years
in 40 MPa to 31 years in153 MPa ultrhigh strength concrete.
Carbonation
Carbonation is the chemical reaction caused by the defusion of carbon dioxide
(CO2) in the air into the permeable concrete and its reaction with Ca(OH)2
compound of the hydrated cement such that it carbonates to CaCo3. This
decomposition of the calcium compounds in the hydrated matrix combined with
alternating wetting and drying in air containing CO2 leads to an increase in the
magnitude of irreversible shrinkage, contributing to crazing of the exposed surface
and increase in the weight of the concretes, with progressive scaling of the
concrete protective cover to the reinforcement. Use of pozzolanic cementations
replacements in concrete such as silica fume or fly ash does not seem to have any
significant effect on the carbonation development or rate. However, if scaling is
prevented because of the higher tensile strength of the high-performance concrete,
its dense composition and extremely low pore volume and permeability inhibit the
oxidation process that causes corrosion of the reinforcement.
Porosity and Permeability
The exceptional properties of HPCs proceed essentially from their reduced
porosity and not from their high compressive strength which is only one of their
many facets; it is their reduced porosity which makes them new material with
multiple advantages. It is generally agreed that mixing water is indirectly
responsible for permeability of the hydrated cement paste because its content
determines at the first instance the total space and subsequently the unfilled space
after the water is consumed by either cement hydration reactions or evaporation
to the environment. In other words porosity of concrete resides principally in the
cement paste.
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