Water-Soluble Salts On Substrate - Bresle Method
Water-Soluble Salts On Substrate - Bresle Method
Water-Soluble Salts On Substrate - Bresle Method
The performance of protective coatings applied to steel can be significantly affected by the
condition of the steel surface immediately prior to painting. The key factors influencing the
coatings performance are:
The International Standards ISO 8501, ISO 8502 and ISO 8503 describe the methods of
assessing these factors, while ISO 8504 provides guidance on surface preparation methods
available for cleaning steel substrates. However, they do not provide recommendations for
the protective coating systems to be used, neither, do they contain recommendations
regarding the required surface cleanliness for specific situations. Normally these
requirements are provided by the coating suppliers and / or the users, such as yards /
applicators and owners.
The International Standard ISO 8502 (Part 6 & 9) describe the field method (Bresle method)
of extracting water-soluble contaminants from a substrate and the assessment of the total
surface density of various water-soluble salts (mostly chlorides and sulphates) on steel
surfaces. However, the individual surface density of different type of salts (chlorides,
sulphates, etc.) cannot be determined by this method.
Water-soluble salts are not easy to detect (visually) as they are almost colourless and may
be present even when the steel substrate is dry blast-cleaned to Sa 3 in accordance to ISO
8501-1 / ISO 8501-2. Water-soluble salts beneath a coating may lead to a chemical reaction
resulting in blistering, corrosion and adhesion failure between the substrate and the applied
protective coating.
Typical examples of steel substrates likely to be contaminated with non-visible water-soluble
salts are, but not limited to:
- Structures exposed to or being near by marine environment
- Structures exposed to or being near by industrial environment and / or acid rain
- Tanks internals, e.g. water-ballast tanks, crude-oil, cargo tanks, process or storage
tanks containing aqueous liquids, etc.
- Surface exposed to road de-icing salts
Blasting medium with higher level of water-soluble salts and corrosion products may be a
source of surface contamination as well.
Although the ISO 8502-9 describes a field method for assessment of the total amount of
water-soluble salts, the more aggressive ionic type contaminants (i.e. Cl, SO4 , HCO3,
Na+, Ca+, etc.) causing corrosion and blistering are easily dissolved and determined,
whereas the less aggressive and not easily dissolved minor part of contaminant will remain
un-assessed. Therefore the main attention is given to Chlorides, as they are one of the most
aggressive salts and most abundant in the marine environment.
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WATER-SOLUBLE SALTS
Any salt can be dissolved in water to a certain extent, depending on the type of salt.
Solubility can be defined in three groups:
Water-soluble salt when dissolved will change its form and split in ions. The formed salt
solution is electro-conductive (electrolyte).
CONDUCTIVITY
Conductivity depends on the type of salt, the concentration / volume of water used and the
temperature. Every salt has a different conductivity constant (characteristic conductivityconcentration relationship) and normally surface contamination does not consist of one
single type of salt. Because it is impossible to know / predict the type and concentration of
salts present on the substrate the ISO 8502 describes the method for assessment of the
total surface density of various water-soluble salts (mostly chlorides and sulphates) on steel
substrate and gives interpretation of the amount of salts in mg/m as equivalent to:
-
mixed salts
chloride ( Cl )
Generally conductivity is measured in S/cm (micro-Siemens per centimetre) or mS/m (milliSiemens per meter).
1 mS/m = 10S/cm
and
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The relation between conductivity and salt content depends on a number of factors.
Basically, patch size, volume of water used, type of salt are the main variables. As it is
impossible to know / predict which salts are present on the substrate, an assumption is
made for the analysis of soluble contaminants on the substrate. For example, the term
measured as Sodium Chloride indicates that the mixture of salts is interpreted as Sodium
Chloride only.
The formula for calculating the salt content on a surface is as followed:
SC mg/m = (((( C S/cm / SF ) / 1000 ) x V ) / patch size ) x 10000
Where:
(For further details please refer to ISO 8502-6 and / or PPG PMC Information Sheet 1468)
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The following table can be used to convert the conductivity reading into an equivalent
amount of water-soluble salts measured as:
Chloride ( Cl )
Sodium Chloride ( NaCl )
Mixed Salts
This means that despite the fact that not all salts on the substrate will be in example Sodium
Chloride, it is assumed that Sodium Chloride is the only salt present on the substrate.
mS/m
1
4
5
10
16
20
24
30
40
50
60
70
80
90
100
200
250
300
0.1
0.5
1
1,6
2
2.4
3
4
5
6
7
8
9
10
20
25
30
As Chloride
[ Cl ]
g/cm
mg/m
0.36
1.44
1.8
3.6
5,8
7.2
8.6
10.8
14.4
18
21.6
25.2
28.8
32.4
36
72
90
108
3.6
14.4
18
36
58
72
86
108
144
180
216
252
288
324
360
720
900
1080
As Sodium Chloride
[ NaCl ]
g/cm
mg/m
0.6
2.4
3
6
9.6
12
14.4
18
24
30
36
42
48
54
60
120
150
180
6
24
30
60
96
120
144
180
240
300
360
420
480
540
600
1200
1500
1800
As mixed salts
g/cm
mg/m
0.5
2
2.5
5
8
10
12
15
20
25
30
35
40
45
50
100
125
150
5
20
25
50
80
100
120
150
200
250
300
350
400
450
500
1000
1250
1500
The formula for calculating the salt content on a surface from the conductivity readings is:
S/cm x CF = mg/m
Where:
Note:
A common source of error is coming from the fact that the composition of the contamination being
measured is unknown.
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APPENDIX
The following table gives the PPG PMC requirements regarding the maximum acceptable
level of water soluble salts on substrates prior to coating application. The water-soluble salts
levels were determined in accordance with the Bresle method using standard Bresle
Sampler (patch) A-1250 (12.5 cm).
The stipulated figures are based on extensive analytic and laboratory testing work as well
as practical experience.
PPG PMC Maximum limits of water-soluble salts on steel substrate prior to coating
S/cm
As
Chloride
[ Cl ]
mg/m
As Sodium
Chloride
[ NaCl ]
mg/m
As
mixed
salts
mg/m
14.4
24
20
Distilled water
10
36
60
50
16
58
96
80
20
72
120
100
24
86
144
120
250
900
1500
1250
Conductivity
The IMO MSC.215(82) Resolution for Water Ballast Tanks requires that the water-soluble
salts as equivalent to Sodium Chlorides should not be higher than 50 mg/m (this is equal
to 8.3 S/cm measured by the Bresle method using a standard sampler A-1250).
Notes:
*
These above figures represent the maximum allowable levels of water-soluble salts on
the substrate prior to coating application. Widespread industry testing has shown that
lowering water-soluble salt contamination to the minimum attainable levels will optimize
the performance of the applied coating system.
Some projects / clients might have their own requirements, which might be more severe
than the PPG PMC requirements. In such a case the requirements imposed by the
client and agreed in the contractual specification will prevail.
The ISO 8502-6 requires that the test is done at 23C and Relative Humidity of 50%.
However, some conductivity gauges have automatic temperature compensation
function. Therefore reference should be made to the conductivity gauge manufacturer
instruction manual.
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