Material Balance Problems
Material Balance Problems
Material Balance Problems
4.1. Introduction
Material balances are important first step when designing a new process or analyzing an
existing one. They are almost always prerequisite to all other calculations in the solution of
process engineering problems.
Material balances are nothing more than the application of the law of conservation of mass,
which states that mass can neither be created nor destroyed. Thus, you cannot, for example,
specify an input to a reactor of one ton of naphtha and an output of two tons of gasoline or
gases or anything else. One ton of total material input will only give one ton of total output,
i.e. total mass of input = total mass of output.
A material balance is an accounting for material. Thus, material balances are often compared
to the balancing of current accounts. They are used in industry to calculate mass flow rates of
different streams entering or leaving chemical or physical processes.
Suppose propane is a component of both the input and output streams of a continuous process
unit shown below, these flow rates of the input and output are measured and found to be
different.
Process unit
If there are no leaks and the measurements are correct, then the other possibilities that can
account for this difference are that propane is either being generated, consumed, or
accumulated within the unit.
A balance (or inventory) on a material in a system (a single process unit, a collection of units,
or an entire process) may be written in the following general way:
Input
+
(enters
through
system
boundaries)
generation
(produced
within
system
boundaries)
output
(leaves
through
system
boundaries)
consumption
(consumed
within
system)
accumulation
(buildup
within
system)
This general balance equation may be written for any material that enters or leaves any
process system; it can be applied to the total mass of this material or to any molecular or
atomic species involved in the process.
The general balance equation may be simplified according to the process at hand. For
example, by definition, the accumulation term for steady-state continuous process is zero.
Thus the above equation becomes:
Input + generation = output + consumption
For physical process, since there is no chemical reaction, the generation and consumption
terms will become zero, and the balance equation for steady-state physical process will be
simply reduced to:
Input = Output
3. Write material balance equations. Note in here the maximum number of independent
equations you can write for each system is equal the number of species in the input and
output streams of this system. Also note to first write balances that involve the fewest
unknown variables.
4. Solve the equations derived in step 3 for the unknown quantities to be determined.
Notes
i. Minimize the symbols assigned to unknown quantities by utilizing all the given process
specifications and using laws of physics.
ii. After doing calculations on certain basis, you may scale up or scale down (convert to new
basis) while keeping the process balanced. This is done by multiplying all streams (except
mass or mole fractions) by the scale factor which is equal to the ratio of the new stream
amount or flow rate to the old one. You can only scale between mass amount or flow rates
regardless of units used but not from mass to molar quantity or flow rate.
The examples below will illustrate the procedure of balances on physical processes:
Solution
We could take a basis of 2310 lbm product/min, but for illustrative purposes and to have
neater numbers to work with let us choose a different basis and scale the final results.
Basis: 100 g Feed Solution
Draw and label the flowchart, remembering that the amount of the product stream is now
unknown.
100 g
0.20 g NaOH/g
0.80 g H2O/g
Q2 (g)
0.080 g NaOH/g
0.920 g H2O/g
Q1 (g H2O)
(Since the known stream amount is given in grams, it is convenient to label all unknown
amounts with this unit.)
There are two unknowns - Q1 and Q2 - and since there are two substances - NaOH and H2O in the input and output streams, two balances may be written to solve for them. The total
mass balance and the water balance involve both unknowns, but the NaOH balance involves
only one.
NaOH Balance
(g
NaOH )in
= (g NaOH )out
(0.20)(100 g ) = 0.080 Q2
Q 2 = 250 g
It is a good practice to write calculated variable values on the flowchart as soon as they are
known for ease of use in later calculations; at this point, 250 would therefore be written in
place of Q2 on the chart.
Total Mass Balance
100 g + Q1 = Q 2
= 250 g
Q1 = 150 g H 2 O
Q1 (g H 2 O)
100 g feed solution
Q2 (g H 2 O)
100 g feed solution
Q1 = 150
Q2 = 250
1.5
g H 2O
g feed solution
2.5
g product
g feed solution
The scale factor is obtained as the true flow rate of the product stream divided by the rate
calculated on the assumed basis.
2310 lb m product/min
lb /min
= 9.24 m
250 g product
g
lb feed solution
100 g 9.24 lb m /min
= 924 m
g
min
lb H O
150 g 9.24 lb m /min
= 1386 m 2
min
g
Check:
A 60 - 40 mixture (by moles) of A and B is separated into two fractions. A flowchart of the
process is shown here.
50.0 mol
0.95 mol A/mol
0.05 mol B/mol
100.0 mol
0.60 mol A/mol
0.40 mol B/mol
12.5 mol A
37.5 mol B
It is desired to achieve the same separation with a continuous feed of 1250 lb-moles/h. Scale
the flowchart accordingly.
Solution
The masses of all streams in the batch process are converted to flow rates as follows:
Feed:
(50.0)(12.5)
= 625 lb-moles/h
(12.5)(12.5)
(37.5)(12.5)
The units of the mole fractions in the top product stream may be changed from mol/mol to lbmole/lb-mole, but their values remain the same. The flowchart for the scaled-up process is
shown here.
625 lb-moles/hr
0.95 lb-mole A/b-mole
0.05 lb-mole B/b-mole
1250 lb-moles/hr
0.60 lb-mol A/lb-mole
0.40 lb-mol B/lb-mole
A mixture containing 45% benzene (B) and 55% toluene (T) by mass is fed to a distillation
column. An overhead stream of 95 wt% B is produced, and 8% of the benzene fed to the
column leaves in the bottom stream. The feed rate is 2000 kg/h. Determine the overhead flow
rate and the mass flow rates of benzene and toluene in the bottom stream
Solution
2000 kg/h
0.45 kg B/kg
0.55 kg T/kg
Contains 8% of the B
in the feed
wB kg B/kg
wT kg T/kg
There are three unknowns on the chart - D, wB, and wT - and therefore three equations are
needed. We are entitled to write only two material balances since two species are involved in
the process; the third equation must therefore come from additional given information (the
amount of benzene in the bottom stream.) The latter relation is.
B in bottom stream = 0.080 (B in feed)
wB = 72 kg B/h
Toluene and total mass balances each involve two unknowns, D and wT, but a benzene
balance involves only one, D.
Benzene Balance
(0.45)(2000) kg
= 0.95 D + wB
wB = 72 kg B/h
kg
= D + w B + wT
h
D = 870 kg/h
wB = 72 kg/h
wT = 1060 kg T/h
40 kg/h
0.900 kg A/kg
0.100 kg B/kg
100 kg/h
0.500 kg A/kg
0.500 kg B/kg
30 kg/h
0.300 kg A/kg
0.700 kg B/kg
Solution
The systems about which balances might be taken are shown on the following representation
of the flowchart.
30 kg/h
0.600 kg A/kg
0.400 kg B/kg
40 kg/h
0.900 kg A/kg
0.100 kg B/kg
100 kg/h
0.500 kg A/kg
0.500 kg B/kg
Q2 (kg/h)
Q1 (kg/h)
x1 (kg A/kg)
1- x1 (kg B/kg)
x2 (kg A/kg)
1- x2 (kg B/kg)
30 kg/h
0.300 kg A/kg
0.700 kg B/kg
Q3 (kg/h)
x3 (kg A/kg)
1- x3 (kg B/kg)
The outer boundary encompasses the entire process. Two of the interior boundaries surround
the individual process units, and the fourth boundary encloses a stream junction point.
Basis: Given Flow Rates
There are two unknowns in the streams that enter and leave the total process, Q3 and x3, and
since there are two independent components in these streams (A and B) we may write two
balances.
Overall Mass Balance
(100 + 30) kg
h
= (40 + 30 )
kg
+ Q3
h
Q3 = 60 kg/h
Overall Balance On A
x 3 = 0.0833 kg A/kg
To determine the flow rate and composition of a connecting stream, we must write balances
on a subsystem whose boundary intersects this stream. Of the three such boundaries shown in
the flowchart, the middle one (about the stream junction) would not be a good one to use at
this point since its input and output streams contain four unknown quantities (Q1, x1, Q2, x2),
while the boundaries about the process units each intersect streams that contain two
unknowns.
Let us choose the boundary about unit 1 for the next set of balances. There are two
unknowns, Q1 and x1, in the streams that intersect this boundary, and up to two balances may
be written.
Total Mass Balance on Unit 1
100 kg / h = 40
kg
+ Q1
h
Q1 = 60 kg / h
Balance on A in Unit 1
(0.500)(100) = (0.900)(40) + 60x1
x1 = 0.233 kg A/kg
To find Q2 and x2, we could write balances about either the stream mixing point or Unit 2.
Let us choose the first alternative.
Mass Balance About Mixing Point
Q1 + 30 kg/h = Q2
Q1 = 60 kg/h
Q2 = 90 kg/h
Balance on A About Mixing Point
Q1 x1 + (0.300)(30) kg A/h = Q2 x 2
Q1 = 60 kg/h
x1 = 0.233 kg A/kg
Q2 = 90 kg/h
x2 =
0.255 kg A/kg
10
EXAMPLE:
2SO2+O2 2SO3.
Solution The number that precede SO2 is 2. Therefore, stoichiometric coefficient of SO2 is
2.
In a stoichiometric equation, the number of atoms in both sides of the equation must be
balanced. In this example, the number of atoms of S and O are 2 and 6, respectively, in both
sides of equation.
Ratio of stoichiometric coefficients of two species is known as stoichiometric ratio.
EXAMPLE:
Solution
2SO2+O2 2SO3.
2 mole of SO 2 reacted
2 mole of SO 3 produced
= 1
If proportion of chemical species fed to a reactor is same as the stoichiometric ratio, then
chemical species combine in stoichiometric proportion, otherwise one or more species will
be in excess of the other. The chemical compound which is present less than its
stoichiometric amount, will disappear first. This reactant will be the limiting reactant and all
the others will be excess reactants. Fractional and percentage excess are given by the
following formulas.
n nS
nS
n nS
percentage excess =
100
nS
where
n = number of moles fed
fractional excess =
n nS
100 = 100%
nS
In many cases, chemical reactions do not go to completion and only a fraction will be
converted. Therefore, fractional and percentage conversions are used. They are defined as
follows,
fractional conversion (f) =
mole reacted
mole fed to the reactor
EXAMPLE: 200 moles of SO2 and 100 moles O2 are fed to a reactor. Only 100 moles of
SO2 react according to 2SO2+O22SO3 Find fractional conversion, percentage
conversion and fraction unreacted?
Solution
mole reacted
=100/200=0.5
mole fed to the reactor
When a reaction is not complete, remaining amount in the reactor will be given by
n i = n io + i
12
where,
The same equation is true if quantities (i.e., moles) are replaced by flow rates (mole/hr).
EXAMPLE: 200 moles of SO2 and 100 moles O2 are fed to a reactor. Only 50 moles of O2
react according to 2SO2+O22SO3 Find the moles remaining for all species?
Solution
For O2,
For SO2,
For SO3,
When the chemical reaction proceeds in one direction only, we call it irreversible. If the
reaction proceeds in forward and backward directions then it is reversible. When forward
reaction rate and reverse reaction rate becomes equal, reaction is said to be in equilibrium.
Equilibrium constant (K) for a gas phase reaction, A(gas) + B(gas)<=> C(gas) + D (gas), is
given by
K=
yCyD
,
yA yB
C3 H 6 + NH3 +
3
O 2 C3H 3 N + 3 H 2 O
2
The feed contains 10 mole% propylene, 12% ammonia, and 78% air. A fractional conversion
of 30% of the limiting reactant is achieved. Determine which reactant is limiting, the
percentage by which each of the other reactants is in excess, and the molar flow rates of all
product gas constituents for a 30% conversion of the limiting reactant, taking 100 mol of feed
as a basis.
13
Solution
Basis : 100 mol Feed
100 mol
n C 3 H 6 mol C3 H 6
n NH 3 mol NH3
n o 2 mol O 2
n N 2 mol N 2
n C 3 H 3 N mol C3H 3 N
n H 2 O mol H 2O
(C
(NH 3 )in
= 12.0 mol
(O 2 )in
(NH3 )stoich
(O 2 )stoich
(% excess)NH
(NH 3 )0
(NH 3 ) stoich
(NH 3 ) stoich
100%
(% excess)O
= 3.0.
Then,
n NH 3 = 12.0
n O2
= 16.4 1.5
n C3H 6 N =
n N2
= (N 2 ) 0
n H 2 O = 3
9.0 mol NH 3
= 11.9 mol O 2
=
3.00 mol C 3 H 3 N
= 61.6 mol N 2
=
9.0 mol H 2 O
= K (T)
Solution
The strategy is to express all mole fractions in terms of a single variable (e, the extent of
reaction at equilibrium), substitute in the equilibrium relation, solve for e, and backsubstitute to calculate the mole fractions and any other desired quantity.
15
n CO = 1.00 e
n H 2O = 2.00 e
n CO 2 = e
n H 2 = 1 e
n total = 3.00
from which
y CO
= (1.00 e )/3.00
y H 2O = (2.00 e )/3.00
y CO 2 = e /3.00
y H2
= e /3.00
(1.00 e )(2.00 e )
= 1.00
This may be rewritten as a standard quadratic equation and solve to yield e = 0.667. This
quantity may in turn be substituted back into the expressions for yi(e) to yield
y CO = 0.111,
y H 2O = 0.444,
y CO 2 = 0.222, y H 2 = 0.222
In a chemical process, our objective is to produce a certain product (desired product), but
there may be several unwanted reactions which will produce undesirable by products.
Therefore, we must maximize the production of a desired product in the process. Two
quantities, yield and selectivity, are used for this purpose and they are defined as follows,
16
yield =
selectivity =
When we have multiple reactions, the remaining amount or flow rate will be given by
n i = n io + ij j
j
where
i = compound i
j = reaction j
j = extent of reaction for the jth reaction
ij = +i, stoichiometric coefficient of a product i in the jth reaction
= -i, stoichiometric coefficient of a reactant i in the jth reaction
= 0, inert
A 2B (desired)
A C (undesired)
100 moles of A are fed to a batch reactor and the final product contains 10 mol of A, 160 mol
of B and 10 mol of C. Calculate (1) percentage yield of B, (2) the selectivity of B relative to
C and (3) the extents of the reactions.
Solution
Percentage Yield
17
Extent of Reactions
n i = n io + ij j
j
10 = 0 + 2
160 = 0 + 21 ,
this gives
this gives
1 = 80
2 = 10.
check: for A,
10 = 100 1 2 ,
10 = 100 80 10 = 10
The reactions
C2 H 6 C2 H 4 + H 2
C 2 H 6 + H 2 2 CH 4
take place in a continuous reactor at steady state. The feed contains 85.0 mole% ethane
(C2H6) and the balance inerts (I). The fractional conversion of ethane is 0.501, and the
fractional yield of ethylene is 0.471. Calculate the molar composition of the product gas and
the selectivity of ethylene to methane production.
Solution
Basis: 100 mol Feed
100 mol
n 1 (mol C 2 H 6 )
n 2 (mol C 2 H 4 )
n 3 (mol H 2 )
n 4 (mol CH 4 )
n 5 (mol I)
0.850 C2H6
0.150 I
18
n1 =
) = 40.0 mol
C 2 H 4 = 1
n 3 = 1 2
= 37.4 mol H 2
n 4 = 2 2 = 5.2 mol CH 4
n 5 = 15.0 mol I
n tot = (42.4 + 40.0 + 37.4 + 5.2 + 15.0) = 140.0 mol
30.3% C 2 H 6 , 28.6% C 2 H 4 ,
mol C 2 H 4
mol CH 4
EXAMPLE: In a steady state process, 100 moles ethane (C2H6) react to produce ethylene
(C2H4) and hydrogen (H2) according to C2H6C2H4 + H2. Product gas shows
40 moles of hydrogen remaining. Perform molecular balances for all species.
Solution:
40 mol of H2
q1 mol of C2H6
q2 mol of C2H4
q1 = 60 moles
C2H4 (generated) = q2
q2 = 40 moles
According to conservation principle, atoms can neither be created (produced) nor destroyed
(consumed). Therefore, in atomic balances there is no generation or consumption terms.
Simply, input = output.
Solving these two atomic balance equations, you will get the same answer as above.
Methane is burned with oxygen to yield carbon dioxide and water. The feed contains 20
mole% CH4, 60% O2, and 20% CO2, and a 90% conversion of the limiting reactant is
achieved. Calculate the molar composition of the product stream using (1) balances on
molecular species, (2) atomic balances, (3) the extent of reaction.
Solution
Basis : 100 mol Feed
100 mol
n CH 4 (mol CH 4 )
n O 2 (mol O 2 )
n CO 2 (mol CO 2 )
n H 2 O (mol H 2 O)
0.200 CH4
0.600 O2
0.200 CO2
CH 4 + 2 O 2 CO 2 + 2 H 2 O
Since a 2:1 ratio of O2 to CH4 would be stoichiometric and the actual ratio is 3:1, CH4 is the
limiting reactant and O2 is in excess.
Before the balances are written, the given process information should be used to determine
the unknown variables or relations between them. In this case, the methane conversion of
90% tells us that 10% of the methane fed to the reactor emerges in the product, or
21
CH 4 reacted =
= 38 mol CO 2
= 36 mol H 2 O
In summary, the output quantities are 2 mol CH4, 24 mol O2, 38 mol CO2, and 36 mol
H2O, for a total of 100 mol. (Since 3 moles of products are produced for every 3 moles of
reactants consumed, it should come as no surprise that total moles in = total moles out.)
The mole fractions of the product gas components are thus:
0.02 mol CH4/mol,
0.24 mol O2/mol,
0.38 mol CO2/mol,
0.36 mol H2O/mol
22
2. Atomic Balances
Referring to the flowchart, we see that a balance on atomic carbon involves only one
unknown ( n CO 2 ), and a balance on atomic hydrogen also involves one unknown ( n H 2 O ),
but a balance on atomic oxygen involves three unknowns. We should therefore write the
C and H balances first, and then the O balance to determine the remaining unknown
variable. All atomic balances have the form input = output. (We will just determine the
component amounts; calculation of the mole fractions then follows as in part 1.)
C Balance
20.0 mol CO 2 1 mol C
1 mol C
+
1 mol CO 2
1 mol CH 4
n
mol
CO 2 1 mol C
2.0 mol CH 4 1 mol C
CO 2
=
+
1 mol CO 2
1 mol CH 4
= 38 mol CO 2
20.0 mol CH 4
n CO 2
H Balance
20 mol CH 4
2 mol CH 4 4 mol H
4 mol H
=
1 mol CH 4
1 mol CH 4
n H 2 O mol H 2 O 2 mol H
+
1 mol H 2 O
n H 2 O = 36 mol H 2 O
O Balance
60 mol O 2
n O2
20 mol CO 2 2 mol O
2 mol O
+
1 mol O 2
1 mol O 2
= (n O 2 mol O 2 ) (2) + (38 mol CO 2 ) (2) + (36 mol H 2 O)(1)
= 24 mol O 2
3. Extent of Reaction
As discussed earlier, for all reactive species
n out = n in + i
For the species in this problem, we may write
23
n CH 4
n C2
n C2
n H 2O
n CH 4 = 2 mol CH 4
= 20.0 mol
= 18.0 mol
= 60.0 mol 2 = 60.0 (2)(18.0) = 24.0 mol O 2
= 20.0 mol + = 20.0 + 18.0 = 38.0 mol CO 2
= 0 + 2 = (2)(18.0) = 36.0 mol H 2 O
overall conversion =
Reactor
25 mol A/min
Product
Separator
75 mol B/min
75 mol B/min
overall conversion of A =
24
Solution
Fresh feed
100 mol C3H8
Reactor
P1 mol C3H8
Separation
Unit
P2 mol C3H6
P3 mol H2
Q1 mol C3H8
Q2 mol C3H6
Q2 mol H2
Note: In labeling the feed stream to the reactor, we have implicitly used balances on
propane and propylene about the stream junction.
In terms of the labeled variables, the quantities to be calculated are
Qr1 + Qr 2
100
25
Q1
, ... etc.
Q1 + Q2 + Q3
Single-Pass Conversion:
( 100 + Qr 1 ) P1
( 100 + Qr 1 )
100%
We must therefore calculate the values of Q1, Q2, Q3, Qr1, Qr2 and P1.
Let us first examine the overall process.
Overall conversion = 95%
100 mol C 3 H 8 Q1
= 0.95
100 mol C 3 H 8
Q1 = 5 mol C 3 H 8
Overall Propane Balance:
output = generation
Q2 = 95 mol C3H 6
Similarly, overall H2 balance yields
Q3 = 95 mol H2
The analysis of the product is, therefore,
5 mol C3H8
2.6 % C3H8
95 mol C3H 6
48.7% C3H 6
95 mol H 2
48.7% H 2
26
Q1 = 0.00555 P1
Qr 2 = 0.05 Q2
Q1 = 5 mol C 3 H 8
Q2 = 95 mol C 3 H 6
Next, write balances around the separation unit (which is nonreactive, so that input = output
for all species.)
C3H8 Balance About Separation Unit
P1 = Q1 + Qr1
9.00
(100 + Qr 1 ) P1
100%
(100 + Qr 1 )
Qr 1 = 895 mol C 3 H 8
P1 = 900 mol C 3 H 8
9.55%
27
Solution
Basis : 100 mol Fresh Feed.
N2 + 3H2 2NH3
n8(mol recycled)
0.125 I
x N2
0.875 - x H2
n7(mol purged)
n3 (mol. I)
n4 (mol N2)
n5 (mol H2)
0.125 I
x N2
0.875 - x H2
100 mol
n1 (mol N2)
n2 (mol H2)
n3 (mol I)
0.2475 N2
0.7425 H2
0.0100 I
Strategy:
Reactor
n4 (mol N2)
n5 (mol H2)
n6 (mol NH3)
n3 (mol I)
Condenser
n6 (mol NH3)
Overall I balance:
n 6 = 46.0 mol NH 3
28
n2 = 276 mol H2
moles purge
8
=
= 0.025
moles leaving condenser 8 + 307
100
moles fresh feed
= 0.245
92 + 276 + 39.4
mol fed to reactor
CO 2 + 3 H 2 CH 3OH + H 2O
The fresh feed to the process contains hydrogen and carbon dioxide in stoichiometric
proportion, and 0.5 mole% inerts (I). The reactor effluent passes to a condenser, which
removes essentially all of the methanol and water formed, none of the reactants or inerts. The
latter substances are recycled to the reactor. To avoid build-up of the inerts in the system, a
purge stream is withdrawn from the recycle. The feed to the reactor contains 2% inerts, and
the single-pass conversion is 60%. Calculate the molar flow rates of the fresh feed, the total
feed to the reactor, and the purge stream for methanol production rate of 1000 mol/h.
Solution
As a general rule, the combined feed to the reactor is a convenient stream to use as a basis of
calculation for recycle problems, provided that its composition is known. Since in this
process the reactants are fed in stoichiometric proportion and they are never separated from
each other, they must be present in stoichiometric proportion throughout the process; that is,
(CO2/H2) = 1/3. The feed thus contains 2 mol I (2% of 100 mol), and 98 mol CO2 + H2, of
which 24.5 mol are CO2 (1/4 of 98) and 73.5 mol are H2.
29
n5 mol
n5 mol
n0 mol
100 mol
Condenser
Reactor
n1 mol CO2
3n1 mol H2
n2 mol CH3OH
n3 mol H2O
2 mol I
n2 mol CH3OH
n3 mol H2O
Take a moment to examine the chart labeling. In particular, notice that we have built in
facts that CO2 and H2 are always present in a 1:3 ratio and that the compositions of
gaseous effluent from the condenser, the purge stream, and the recycle stream are
identical. The more of this sort of information you can incorporate in the chart labeling,
easier the subsequent calculations become. Let us outline the solution, referring to
flowchart.
the
the
all
the
the
1. Calculate n1, n2, and n3, from the feed to the reactor, the single-pass conversion and reactor
balances.
2. Calculate n4, from a total mole balance about the condenser, and then x4 from a CO2
balance about the condenser.
3. Calculate n0, and n6, from balances on total moles and I about the recycle-fresh-feed
mixing point. (Two equations, two unknowns.) Then calculate n5, from a mole balance
about the recycle-purge split point.
4. Scale up the calculated flows of fresh feed, combined reactor feed, and purge streams by
the factor (1000/n2). The results will be the flow rates in mol/h corresponding to a
methanol production of 1000/h.
30
2 4 n1 + n2 + n3 = n2 + n3 + n4
substitute for n1
n4 = 41.2 mol
CO2 Balance About Condenser
n1 = n4 x4
0.00500 n0 + n6 (1 4 x4 ) = 2
x4 = 0.2379
0.00500n0 + 0.0484n6 = 2
Solving the above two equations simultaneously yields
no = 65.4 mol fresh feed
n6 = 34.6 mol recycle
Mole balance About Purge Takeoff
n4 = n5 + n6
31
n2 = 14.7
68.03 h 1
Combustion is a rapid reaction of fuel with oxygen. Combustion products are CO2, NO, CO,
H2O, and SO2. In a combustion reaction if CO is formed, then the reaction is incomplete and
referred as incomplete combustion or partial combustion. During a complete combustion of
a fuel, carbon will be oxidized to CO2, hydrogen will be oxidized to H2O, and sulfur will be
oxidized to SO2.
C + O2 CO2
H2+O2 H2O
C + O2 CO,
S+O2 SO2
Complete and incomplete combustion of C3H8 are given by the following chemical reactions,
complete
C3H8 +5O2 3CO2 + 4H2O
incomplete
Product gas that leaves the combustion chamber is called stack or flue gas. Composition of a
flue gas is given on a wet (including water ) or dry basis (excluding water).
EXAMPLE: Suppose a stack gas contains equimolar amounts of CO2, N2 and H2O. Find the
composition on wet and dry basis?
Solution
32
moles of CO 2
100 = (n/3n)100 = 33.33%
total moles on wet basis
moles of CO 2
100 = (n/2n)100 = 50%.
total moles on dry basis
EXAMPLE: A stack gas contains 60 mole% N2, 15% CO2, 10% O2, and the balance H2O.
Calculate the molar composition of the gas on a dry basis.
Solution
60 mol N 2
15 mol CO 2
10 mol O 2
85 mol dry gas
60
mol N 2
= 0.706
85
mol dry gas
mol CO 2
15
= 0.176
mol dry gas
85
mol O 2
10
= 0.118
mol dry gas
85
An Orsat analysis (a technique for stack gas analysis) yields the following dry basis
composition:
N2
65%
CO 2
14%
CO
O2
11%
10%
A humidity measurement shows that the mole fraction of H2O in the stack gas is 0.07.
Calculate the stack gas composition on a wet basis.
33
Solution
0.07
lb mole H 2O
lb mole dry gas
0.93
lb mole wet gas
lb mole wet gas
The mole fractions of each stack gas component may now easily be calculated:
y H 2O =
4.6.3.
7.53 lb moles H 2 O
lb moles H 2 O
= 0.070
,. . . etc.
lb moles wet gas
107.5 lb moles wet gas
Theoretical oxygen is the amount needed for complete combustion of reactants to form CO2
and H2O. Air that contains the theoretical amount of oxygen is called theoretical air.
Theoretical air does not depend on how much of a reactant is converted. The difference
between the amount of air initial fed and the theoretical air is known as excess air. Therefore,
percentage excess air is defined as,
One hundred mol per hour of butane (C4H10) and 5000 mol per hour of air are fed into a
combustion reactor. Calculate the percent excess air.
34
Solution
First, calculate the theoretical air from the feed rate of fuel and the stoichiometric equation
for complete combustion of butane.
13
O 2 4 CO 2 + 5 H 2O
2
100 mol C 4 H10 6.5 mol O 2 required
(O 2 ) theoretical =
h
mol C 4 H10
C 4 H10 +
mol O 2
h
650 mol O 2 4.76 mol air
mol air
=
= 3094
h
mol O 2
h
= 650
(air ) th
Hence
% excess air =
If instead you had been given 61.6% excess air, you could have calculated
(air)fed = 1.616 (air)th = 1.616 (3094) = 5000 mol/h.
When doing material balances for combustion reactions, one should consider balances of the
followings:
a. inert N2 at both inlet and outlet
b. unreacted fuel
c. excess oxygen
d. combustion products CO2, H2), CO etc.
Suppose 15% excess of oxygen is fed,
oxygen fed = 1.15 theoretical oxygen
nitrogen fed = (79/21) oxygen fed
air fed = (100/21) oxygen fed
35
Ethane (C2H6) is burned with 50% excess air. The percentage conversion of the ethane is
90%; of the ethane burned, 25% reacts to form CO and the balance to form CO2. Calculate
the composition of the fuel gas and the ratio of water to dry fuel gas.
Solution
q 2 mol O 2
q 3 mol N 2
q 4 mol CO
q 5 mol CO 2
q 6 mol H 2 O
7
O 2 2 CO 2 + 3 H 2O
2
5
C2H 6 +
O 2 2 CO + 3 H 2O
2
C2H 6 +
Note:
1. Since no product stream mole fractions are known, subsequent calculations are easier if
individual component amounts rather than a total amount and mole fractions are labeled.
2. Known information about the composition of air has been used to label the incoming N2
79
stream 3.76 =
.
21
O2 Fed
N2 Fed
Q = (1.5)(350 ) =
36
C2H6 Reacted
C2H6 Balance
Output = generation
q4 =
2 mol CO formed
1 mol C 2 H 6 reacted
q4 = 45 mol CO
Atomic C Balance
Input = Output
C2H 6
100 mol C 2 H 6
CO
CO 2
678 678
678
2 mol C
= (q1 )(2 ) + (q4 )(1) + (q4 )(1)
1 mol C 2 H 6
q1 = 10
q4 = 45
q5 = 135 mol CO 2
Atomic H Balance
Input = Output
100 mol C 2 H 6
6 mol H
10 mol C 2 H 6
6 mol H
=
1 mol C 2 H 6
1 mol C 2 H 6
+
q 6 (mol H 2O)
q6 = 270 mol H 2O
37
2 mol H
1 mol H 2O
Atomic O Balance
Input = Output
525 mol O 2
2 mol O
45 mol C O 1 mol O
q ( mol O 2 ) 2 mol O
= 2
+
1 mol O 2
1 mol O 2
1 mol CO
+
135 mol CO 2
2 mol O
1 mol CO 2
270 mol H 2O
1 mol O
1 mol H 2O
q2 = 232 mol O 2
y1 =
10 mol C 2 H 6
mol C 2 H 6
= 0.00417
2396 mol dry gas
mol
y2 =
232 mol O 2
mol O 2
= 0.0970
2396 mol dry gas
mol
y3 =
1974 mol N 2
mol N 2
= 0.824
2396 mol dry gas
mol
y4 =
45 mol CO
mol CO
= 0.019
2396 mol dry gas
mol
y5 =
135 mol CO 2
mol CO 2
= 0.0563
2396 mol dry gas
mol
38
1.5% CO
6.0% CO2
8.2% O2
84.3% N2
Calculate the ratio of hydrogen to carbon in the gas, and speculate on what the gas might be.
Solution
Basis: 100 mol Dry Flue Gas
Since the composition of the fuel is unknown, label it as though carbon and hydrogen were
entering separately.
qH mol H
qC mol C
qO2 mol O2
3.76 qO2 mol N2
Qw mol H2O
Qw =
39
Atomic H Balance
qH =
Q w (mol H 2 O) 2 mol H
= 2 14.9 = 29.8 mol H
mol H 2 O
from which
qH
29.8 mol H
mol H
=
= 3.97
qC
7.5 mol C
mol C
The natural gas may therefore be written with the formula (CH3.97)n. Since there is only one
hydrocarbon for which the ratio of H to C is close to 3.97 - that is, CH4 - we may conclude in
this case that the natural gas is essentially pure methane, with perhaps trace amounts of other
hydrocarbons. [If we had obtained, say, qH/qC 2, we could have gone no further than to
write the fuel as (CH2)n: from the information given, there would have been no way to
distinguish between C2H4, C3H6, a mixture of CH4 and C2H2, etc].
40
References
1.
Felder, R. and Rousseau, R. W., Elementary Principles of Chemical Processes, 2nd ed.,
John Wily & Sons, 1986.
2.
Himmelblau, D. M., Basic Principles and Calculations in Chemical Engineering, 4th ed.,
Prentice Hall, New Jersey, 1982.
3.
Perry, R. H. and Green, D., Perrys Chemical Engineering Handbook, 6th ed., McGraw
Hill, New York, 1984.
4.
41