Chapter 4

MATERIAL BALANCES AND APPLICATIONS

 MATERIAL BALANCES AND APPLICATIONS

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.

4.2. The General Balance Equation

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
qin (kg propane/h) qout (kg propane/h)

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:

1
Input + generation  output  consumption = accumulation
(enters (produced (leaves (consumed (buildup
through within through within within
system system system system) system)

boundaries) boundaries) boundaries)

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

4.3. Balances on Single and Multiple Physical Systems

4.3.1. Procedure for Material Balance Calculations

In material balance problems, you will usually be given a description of a process, the
values of several process variables, and a list of quantities to be determined. In order to be
trained on using a systematic procedure to solve material balance problems, you are
advised to follow the steps summarized below:

1. Draw and label the process flow chart (block diagram). When labeling, write the values
of known streams and assign symbols to unknown stream variables. Use the minimum
number possible of symbols.

2. Select a basis of calculation. This is usually the given stream amounts or flow rates, if no
given then assume an amount of a stream with known composition.
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:

EXAMPLE: Balance on a mixing unit

An aqueous solution of sodium hydroxide contains 20% NaOH by mass. It is desired to

produce an 8% NaOH solution by diluting a stream of the 20% solution with a stream of
pure water.

1. Calculate the ratios (g H2O/g feed solution) and (g product solution/g feed solution).

2. Determine the feed rates of 20% solution and diluting water needed to produce
2310 lbm/min of the 8% solution.

Solution

We could take a basis of 2310 lb m 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 Q2 (g)
0.20 g NaOH/g
0.80 g H2O/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 H 2O -
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  Q2  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

 2  250 g
Q


Q1  150 g H 2 O
The desired ratios can now be calculated:

Q1 (g H 2 O) Q1  150
g H 2O
100 g feed solution  1.5
g feed
solution
Q2 (g H 2 O) Q2  250
g product
100 g feed solution  2.5
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 lbm product/min lbm /min

250 g product  9.24 g

Feed Solution Flow Rate

100 g 9.24 lbm /min  924 lbm feed solution

g min

Dilution Water Flow Rate

150 g 9.24 lbm /min  1386 lbm H 2 O

g min

Check: (924 + 1386) lbm/min = 2310 lbm/min

EXAMPLE: Scale up of a separation process flowchart

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 scale factor is

1250 lbmoles / h lbmoles / h
100 mol  12.5 mol

The masses of all streams in the batch process are converted to flow rates as follows:

100 mol 12.5 lb - moles/h  1250 lb - moles (as specified)

Feed:
mol h

Top product stream: (50.0)(12.5) = 625 lb-moles/h

Bottom product stream: (12.5)(12.5) = 156 lb-moles A/h

(37.5)(12.5) = 469 lb-moles B/h

The units of the mole fractions in the top product stream may be changed from mol/mol to
lb- mole/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

1250 lb-moles/hr 0.05 lb-mole B/b-mole

0.60 lb-mol A/lb-mole

0.40 lb-mol B/lb-mole

156 lb-moles A/hr

469 lb-moles B/hr
EXAMPLE: Material balances on a distillation column

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

Basis : Given Feed Rate

The labeled flowchart is as

follows.
D kg/h
0.95 kg B/kg
0.05 kg T/kg
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 (kg B/h)  0.080[(0.45)(2000) kg/h]

(Write 72 in place of w on the chart)
wB  72 kg B/h B

Toluene and total mass balances each involve two unknowns, D and wT, but a benzene
balance involves only one, D.

Benzene
Balance
kg
0.452000  0.95 D  wB
B
h
 wB  72 kg B/h

D  870 kg/h (Write it on the chart)
Total Mass Balance (A toluene balance could be used equally well)

kg
2000
h  D  wB  wT

D  870 kg/h
 w  72 kg/h
B


wT  1060 kg T/h

EXAMPLE: Two Unit Distillation Process

A labeled flowchart of a continuous steady-state two-unit distillation process is shown

below. Each stream contains two components, A and B, in different proportions. Three
streams whose flow rates and/or compositions are not known are labeled 1, 2 and 3.

40 kg/h 30 kg/h
0.900 kg A/kg 0.600 kg A/kg
0.100 kg B/kg 0.400 kg B/kg

100 kg/h 1 2 3
0.500 kg A/kg
0.500 kg B/kg

30 kg/h
0.300 kg A/kg 0.700 kg B/kg

Calculate the unknown flow rates and compositions of streams 1, 2, and 3.

Solution

The systems about which balances might be taken are shown on the following
representation of the flowchart.

40 kg/h 30 kg/h
0.900 kg A/kg 0.600 kg A/kg
0.100 kg B/kg 0.400 kg B/kg

100 kg/h Q1 (kg/h) Q2 (kg/h) Q3 (kg/h)

0.500 kg A/kg x1 (kg A/kg) x2 (kg A/kg) 1- x2 (kg B/kg) x3 (kg A/kg) 1- x3 (kg B/kg)
0.500 kg B/kg 1- x1 (kg B/kg)

30 kg/h
0.300 kg A/kg 0.700 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
kg kg
100  30  40  30  Q3
h h

Q3  60 kg/h

Overall Balance On A

0.500100  0.30030 0.90040  0.60030  60x 3 

 
x3  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
kg
100 kg /  40 Q
h
1
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

Q 1 x1
 (0.300)(30) kg A/h Q2 x2
 Q1  60 kg/h
 x1  0.233 kg A/kg
Q2  90 kg/h

x2  0.255 kg A/kg

4.4. Balances on Reactive Systems

4.4.1. Stoichiometry, Limiting and Excess Reactants

For reactive systems, in addition to input and output of materials, generation and
consumption terms should be considered in the general mole balance equation. Theory of
proportions in which chemical compounds react is called stoichiometry. A statement of the
relative number of moles or molecules reacting to produce products is given by a chemical
equation known as stoichiometric equation. For example, 2 moles of SO 2 and one mole of
O2 react to produce 2 moles of SO 3. Then the stoichiometric equation will be
2SO2+O22SO3. Numbers that precede the formulas are known as stoichiometric coefficients.
EXAMPLE: 2SO2+O2 2SO3. What is the stoichiometric coefficient of SO2?

Solution The number that precede SO2 is 2. Therefore, stoichiometric coefficient of SO 2 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: 2SO2+O2 2SO3. What is the stoichiometric ratio of SO2 to SO3?

2 mole of SO2 reacted
Solution stoichiometric ratio of SO2 to SO3 = =1
2 mole of SO 3 produced

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
fractional excess =
nS
nnS
percentage excess  100
nS
= where
n = number of moles fed
ns = number of moles corresponding to stoichiometric amount

EXAMPLE: 100 moles of SO2 and 100 moles O2 are fed to a reactor and they react
according to 2SO2+O2 2SO3. Find the limiting reactant, excess reactant,
fractional excess and percentage excess?

Solution

ratio of SO2 to O2 fed = 100/100 = 1

stoichiometric ratio of SO2/O2 = 2/1=2

Therefore, SO2 is fed less than the stoichiometric proportion (or stoichiometric ratio). SO 2 is
the limiting reactant. The other reactant (O2) will be the excess reactant.
n = number of moles of excess reactant (O 2) fed = 100

ns = stoichiometric amount of O2 to react with 100 moles of the limiting reactant SO2 = 50
Therefore, fractional excess nn 100  50
= S  50  1.0
nS

percentage excess nnS

=  100  100%
nS

4.4.2. Fractional Conversions, Extent of Reaction, Chemical Equilibrium

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,
mole reacted
fractional conversion (f) =
mole fed to the reactor

percentage conversion = f 100

fraction unreacted = (1-f)

EXAMPLE: 200 moles of SO2 and 100 moles O2 are fed to a reactor. Only 100 moles of
SO2 react according to 2SO 2+O22SO3 Find fractional conversion, percentage
conversion and fraction unreacted?

Solution
mole reacted
fractional conversion of SO2 (f) =
mole fed to the =100/200=0.5
reactor

percentage conversion = f

100=0.5100=50% fraction unreacted = (1-

f)=1-0.5=0.5

When a reaction is not complete, remaining amount in the reactor will be given by

ni  nio  i
where,  = extent of reaction (mole reacted or produced/i)
i = compound i, ni = remaining amount
nio = amount initially put in the reactor
i = +i, stoichiometric coefficient of a product
= -i , stoichiometric coefficient of a reactant
= 0 , inert

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+O22SO3 Find the moles remaining for all species?

Solution

For O2,  = 50, nio = 100, i = -i = -1, n i  nio   i  = 100-150=50 moles

For SO2,  = 50, nio = 200, i = -i = -2, ni = 200-250=100 moles

For SO3,  = 50, nio = 0, i = +i = +2, ni = 0+250=100 moles

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
yC y D
K , where y is the mole fraction of the components in the gas
phase. y A y B

EXAMPLE: Reaction Stoichiometry

Acrylonitrile is produced by the reaction of propylene, ammonia, and oxygen.

3
C H  NH  O  C H N  3 H O
3 6 3 2 3 3 2
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.
Solution

Basis : 100 mol Feed

100 mol
0.100 mol C3H6/mol
0.120 mol NH3/mol nC H mol C3 H6
3 6

0.780 mol air/mol n NH mol NH3

3
(0.21 mol O2/mol air
0.79 mol N2/mol air) no mol O2
2

n N mol N2
2

nC H N mol C3H3N
33

nH O mol H O
2 2

The feed to the reactor contains

CH 
3 6 in  10.0 mol
NH 3 in  12.0 mol

O 2in 78.0 air 0.210 mol O

 16.4 mol
 2
mol mol air


NH 3 /C 3 H 6  12.0/10.0  1.20 is in excess
in  NH

NH 3 /C3 H stoich  1/1 1 


3

O 2 / C 3 H 6  16.4/10.0  1.64 is in excess

in 
O
O 2 / C3 H stoich  1.5/1  1.5  2

Since propylene is fed in less than the stoichiometric proportion relative to the two other
reactants, propylene is the limiting reactant.

To determine the percentages by which ammonia and oxygen are in excess, we must first
determine the stoichiometric amounts of these reactants corresponding to the amount of
propylene in the feed (10 mol).

10.0 mol C3 H6 1 mol NH3

NH   1 mol C3H6  10.0 mol NH3
3 stoich
O2 stoich  10.0 mol C3 H6 1.5 mol O2
 15.0 mol O2
1 mol C3H6

%
excess NH 3  (NH3 )stoich  100%
0
NH3
(NH )stoich3

 12  10/10  100%  20% excess NH 3

% excess  (16.4  15.0)/15.0  100%  9.3% excess O 2

O2

If the fractional conversion of C3H6 is 30%

(C3H6)out = 0.700(C3H6)in = 7.0 mol C3H6

But  10.0  ξ
n The extent of reactions is therefore: ξ  3.0.
. CH
36

Then,
n 3
 12.0  ξ  9.0 mol NH3
NH
 16.4  1.5ξ  11.9 mol O 2
nO
2
3.00 mol C3 H 3 N
nC H Nξ 
36
61.6 mol N 2
n  (N 2 ) 0 
N2 9.0 mol H 2 O
n H2O  3ξ 

EXAMPLE: Calculation of an Equilibrium Composition

If the water-gas shift reaction,

CO(g) + H2O(g)  CO2(g) + H2(g)

proceeds to equilibrium at a temperature T(K), the mole fractions of the four reactive
species satisfy the relation

y CO y H
y CO y H2 O  K (T)
2 2

where K (T) is the reaction equilibrium constant. At T = 1105 K (832C), K = 1.00.

Suppose the feed to a reactor contains 1.00 mol CO, 2.00 mol of H2O, and no CO2 or H2,
and the reaction mixture comes to equilibrium at 1105 K. Calculate the equilibrium
composition and the fractional conversion of the limiting reactant.
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 back-
substitute to calculate the mole fractions and any other desired quantity.
n CO  1.00  (number of mols of CO present at equilibrium)
e
n H2O  2.00  e
n CO2  e
n H2  1e
n total  3.00

from which
y CO  (1.00  ξ e )/3.00
y  (2.00  ξ e )/3.00
H2O  ξ e /3.00
y  ξ e /3.00
CO2

y H2

Substitution of these expressions in the equilibrium relation (with K = 1.00) yields

2 
e
(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 y i(e) to yield

y CO  0.111, y 0.444,
H2O y CO 2  0.222, y 2H 0.222

The limiting reactant in this case is CO (verify). At equilibrium,

n CO
 1.00  0.667  0.333

The fractional conversion of CO at equilibrium is therefore

fCO = (1.00 - 0.333) mol reacted/(1.00 mol fed) = 0.667

4.4.3. Multiple Reactions, Yield and Selectivity

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,
moles of desired product formed
yield =
moles of desired product formed if there were no
side reactions and the limiting reactant reacts
completely

moles of desired product formed

selectivity = moles of undesired product formed

When we have multiple reactions, the remaining amount or flow rate will be given by

n i  n io    
j ij 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 j th reaction
= -i, stoichiometric coefficient of a reactant i in the j th reaction
= 0, inert

EXAMPLE: Consider the following pair of reactions.

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

moles of desired product (B) formed = 160

moles of desired product formed if there were no side reactions and the limiting reactant
reacts completely = 100 moles of A  2 moles of B produced 1
mole of A reacted
= 200 moles

yield (%) = 160/200*100 = 80%

Selectivity

moles of desired product (B) formed = 160

moles of undesired product (C) formed = 10

moles of desired product formed

selectivity = moles of undesired product = 160/10 = 16.
formed

Extent of Reactions

n i  n io    
j ij j

for two reaction system as above, n i  n io  i1 1  i 2  2

applying this equation for

160  0  21 , this gives 1 = 80
B,

for
10  0   this gives 2 = 10.
C, 2

check: for A,

10  100  1   2 , 10  100  80  10  10

EXAMPLE: Yield and Selectivity in a Dehydrogenation Reactor

The reactions
C2H6  C2H4  H2
C2H6  H2  2 CH4

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

0.850 C2H6
0.150 I
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)

The outlet component amounts in terms of extents of reaction are as follows:

 n1 (mol C2H6) = 85.0 - 1 - 2
n2 (mol C2H4) = 1
n3 (mol H2) = 1 - 2
n4 (mol CH4) = 22 n5
(mol I) = 15.0

Ethane Conversion

n1  (1.000  0.501) mol C 2 H 6 unreacted 85.0 mol C 2 H 6 fed

mol C 2 H 6 fed

42.4 mol C 2 H  85.0  1   2
6

Ethylene Yield

Maximum possible ethylene  85.0 mol C 2 H 6 fed 1 mol C 2 H 4

 85.0 mol
1 mol C 2 H 6

n 2  0.471 
85.0 mol C2 H 4   40.0 mol C 2 H  1
4

Substituting 40.0 for 1 in (1) yield 2 = 2.6 mol. Then

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 , 26.7% H 2 , 3.7% CH 4 , 10.7% I

Selectivity = (40.0 mol C2H4)/(5.2 mol CH4)  mol C2H4

7.7 mol CH4

4.4.4. Atomic and Molecular Balances

In a chemical process, molecules are either generated (produced) or consumed. Therefore,
one should take into account the amounts (moles) generated, consumed, fed and remaining
in molecular balances.
EXAMPLE: In a steady state process, 100 moles ethane (C 2H6) react to produce ethylene
(C2H4) and hydrogen (H2) according to C2H6C2H4 + 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

100 mol C2H6

Then, the molecular balance of H 2 is as follows,

input + generated (produced) = output + consumed (reacted)

input = 0.0
output = 40
consumed = 0

0 + generated (produced) = 40+ 0  H2 (generated) = 40 moles.

Molecular balance of C2H6 is as follows,

input + generated (produced) = output + consumed (reacted)

input = 100
generated = 0
output = q1

100 + 0 = q1 + consumed  C2H6 (consumed) = 100-q1

H2 (generated) = 40 moles=C2H6 (consumed) = 100-q1  q1 = 60 moles

Molecular balance of C2H4 is as follows,

input + generated (produced) = output + consumed (reacted)

input = 0
output = q2
consumed = 0

0 + generated = q2 + 0  C2H4 (generated) = q2

C2H4 (generated) = q2 = H2 (generated) = 40 moles  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.

EXAMPLE: For the same problem as above, do atomic balances?

Solution

Atomic carbon balance: 1002 = q12 + q22

Atomic hydrogen balance 1006 = 402 + q16 +

q24

Solving these two atomic balance equations, you will get the same answer as above.

EXAMPLE: Combustion of Methane

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

0.200 CH4 0.600 O2

n CH 4 (mol CH 4 )
0.200 CO2 n O2 (mol O 2 )
n CO 2 (mol CO )
2
n H2O (mol H 2 O)

CH 4
 2 O 2  CO 2  2 H 2O

Since a 2:1 ratio of O 2 to CH4 would be stoichiometric and the actual ratio is 3:1, CH 4 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
n CH  0.100 (20.0 mol CH fed)  2.0 mol CH
4 4
4

Now all that remains are the balances. We will proceed by each of the indicated methods.

1. MolecularBalances

20.0 mol CH 4 fed 0.900 mol react

CH
reacted  mol fed  18 mol CH react
4
4

CO
Balanc (input  generation output)
2
e 

100 mol 0.200 mol CO 2  18 mol CH 4 react 1 mol CO 2 produced 

CO2
mol fed 1 mol CH 4 n


n CO2  38 mol CO 2

H 2 O Balance (generation  output)

18 mol CH 4 react2 mol H 2 O produced

 n H2O
1 mol CH 4 react


n H2O  36 mol H O
2

O2 Balance (input  output  consumption)

100 mol 0.600 mol O 2 18 mol CH 4 react 2 mol O 2 react

 n O2 
mol 1 mol CH 4 react


n O2  (60  36) mol O  24 mol O 2
2

In summary, the output quantities are 2 mol CH 4, 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
2. Atomic Balances

Referring to the flowchart, we see that a balance on atomic carbon involves only one
unknown ( nCO 2 ), and a balance on atomic hydrogen also involves one unknown ( n H 2O
), 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 CH 4 1 mol C  20.0 mol CO 2 1 mol C
1 mol CH 4 1 mol CO 2
n
2.0 mol CH 4 1 mol C  CO 2 mol CO 2 1 mol C

1 mol CH 4 1 mol CO 2

n CO2  38 mol CO 2

H Balance
20 mol CH 44 mol H 2 mol CH 44 mol H

1 mol CH 4 1 mol CH 4
n H 2O mol H2O 2 mol H

1 mol H 2 O

n H2 O  36 mol H 2 O

O
Balance
60 mol O 2 mol O  20 mol CO 2 2 mol O
2
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)

nO  24 mol O 2
2

confirming the results obtained using molecular balances.

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

n CH
4
 20.0 mol  ξ n CH 4  2 mol CH 4
 ξ  18.0 mol
n C2  60.0 mol  2ξ  60.0  (2)(18.0)  24.0 mol O 2
n C2  20.0 mol  ξ  20.0  18.0  38.0 mol CO 2
n HO
2
 0  2ξ  (2)(18.0)  36.0 mol H 2 O

again, the previous solutions are obtained.

4.5. The Case of Recycle and Purge

4.5.1. Overall and Single Pass Conversion

Two definitions of conversion are used in the analysis of chemical reactors with product
separation and recycle of unconsumed reactants:

reactant input to the process - reactant output from the

overall conversion
= process reactant input to the process

reactant input to the reactor - reactant output from the reactor

single pass conversion
= reactant input to the reactor

EXAMPLE : Find the overall and single pass conversion of A ?

75 mol A/min100 mol A/min Product Separator

25 mol A/min 75 mol B/min
Reactor
75 mol B/min

overall conversion of A = (75 mol A/min)in - (0 mol A/min)out  100  100%

(75 mol A/min)in

single pass conversion of A (100 mol A/min)in - (25 mol A/min) out
(100 mol A/min)in  100  75%
=
4.5.2. Recycle and Purge

A material such as an inert gas or impurities which enter with the feed will remain in the
recycle stream. This material will accumulate and the process will never reach steady state.
To prevent this buildup, a portion of the recycle stream must be withdrawn as a purge
stream.

EXAMPLE: Dehydrogenation of Propane

Propane is dehydrogenated to from propylene in a catalytic reactor

C3H8  C3H6  H2

The process is to be designed for a 95% overall conversion of propane. The reaction
products are separated into two streams: the first, which contains H2, C3H6, and 0.555% of
the propane that leaves the reactor, is taken off as product; the second stream, which
contains the balance of the unreacted propane and 5% of the propylene in the product
stream, is recycled to the reactor. Calculate the composition of the product, the ratio (moles
recycled)/(moles fresh feed), and the single-pass conversion.

Solution

Basis : 100 mol Fresh Feed

Reactor
Fresh feed 100 mol C3H8 Separation
100 + Qr1 mol C3H8 P1 mol C3H8Unit Q mol13 C8 H
Qr2 mol C3H6
P mol23 C6 H
Q2 mol C3H6
P3 mol H2 Q2 mol H2

Qr1 mol C3H8

Qr2 mol C3H6

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

Q1
Mole Fractions of Product Stream ,... etc.
Components: Q1  Q2 
Q3

Recycle Qr1  Qr 2
Ratio:
100
Single-Pass
Conversion:
(100  Qr 1 )  P1
 100%
(100  Qr 1 )

We must therefore calculate the values of Q1, Q2, Q3, Qr1, Qr2 and P1.

Let us first examine the overall process.

100 mol C3 H 8  Q1
Overall conversion  95% 
 0.95
100 mol C3 H 8


Q1  5 mol C3 H 8

Overall Propane Balance: input = output + consumption

100 mol C3H8  5 mol C3H8  C (mol C3H8 reacted)


C  95 mol C3H8 reacted

Overall Propylene Balance: output = generation

95 mol C3H8 reacted 1 mol C3H6 formed

Q2 
1 mol C3H8 reacted


Q2  95 mol C3H6

Similarly, overall H2 balance yields

Q3 = 95 mol H2

The analysis of the product is, therefore,

5 mol C3H8 2.6 % C3H8

95 mol C3H6  48.7% C3H6
95 mol H2 48.7% H2
195 mol total

We may now proceed to the analysis of the interior streams including the recycle stream.
First, we summarize the information given in the problem statement.

Q1  0.00555 P1 Q1  5 mol C3H8

 P1  900 mol C3H8
 Qr 2  0.05 Q2 Q2  95 mol C3H6
 Qr 2  4.75 mol C3H6

Next, write balances around the separation unit (which is nonreactive, so that input = output
for all species.)

C3H8 Balance About Separation Unit

P1  Q  Q
1 r1

 P1  900 mol C3H8

Q1  5 mol C3H8
Qr1  895 mol C3H8

We now have all the variable values we need. The desired quantities are

Recycle ratio (Qr1  Qr 2 ) mol recycle

 100 mol fresh feed
Qr1  895 mol
 Q  4.75 mol
r2
mol recycle
9.00
mol fresh feed

Single  pass (100  Qr 1 )  P1  100%

 (100  Qr 1 )
conversion
Qr 1  895 mol C H
 3 8
P1  900 mol C 3 H 8

9.55%

EXAMPLE: Recycle and Purge in the Synthesis of Ammonia

The fresh feed to an ammonia production process contains 24.75 mole % nitrogen, 74.25
mole% hydrogen, and the balance inerts (I). The feed is combined with a recycle stream
containing the same species, and the combined stream is fed to a reactor in which a 25%
single-pass conversion of nitrogen is achieved. The products pass through a condenser in
which essentially all of the ammonia is removed, and the remaining gases are recycled.
However, to prevent buildup of the inerts in the system, a purge stream must be taken off.
The recycle stream contains 12.5 mole% inerts. Calculate the overall conversion of
nitrogen, the ratio (moles purge gas/mole of gas leaving the condenser), and the ratio
(moles fresh feed/mole fed to the reactor).
Solution

Basis : 100 mol Fresh

Feed.
N2 + 3H2  2NH3

n8(mol recycled) n7(mol purged)

0.125 I 0.125 I
n3 (mol. I) n4 (mol N2) n5 (mol H2) x N2
x N2
0.875 - x H2 0.875 - x H2

100 mol
Reactor Condenser
0.2475 N2 n1 (mol N2) n4 (mol N2) n6 (mol NH3)
0.7425 H2 n2 (mol H2) n5 (mol H2)
0.0100 I n3 (mol I) n6 (mol NH3)
n3 (mol I)

Strategy: Overall N, H, I balances  n6, n7, x  overall conversion of N2

n6, 25% single pass conversion  n1, n4
n7, x, n4, n2 balance around purge-recycle split point  n8
H2, I balances around recycle-fresh mixing point  n2, n3

Overall I balance: (0.0100)(100) = 0.125 n7  n7 = 8.00 mol purge gas

Overal  n
N balance (100)(0.2475)(2)  8.00 ( x) (2)  n 
l 6  46.0 mol NH3
: 6 

x  0.219 mol N 2 /mol
Overal H balance (100)(0.7425)(2)  8.00 (0.875  x) (2)  3n 6
l : 
92.9%
Overal 24.75 mol fed  (0.219)(8.00) molin effluent
l N 2 balance  x 100% 
24.75 mol fed

25% Single Pass Conversion: n1 mol N 2 fed 0.25 mol 2 mol NH3  46.0 mol NH
react 1 mol N 2
3
1 mol fed


n1  92.0 mol N 2 feed to reactor
n 4  (0.75)(92.0)  69.0 mol N 2
N2 balance around purge-recycle split point: 69.0 = (0.219)n8 + (0.219)(8.00)

n8 = 307 mol recycled

H2 balance around mixing point: (100)(0.7425) + (307) (0.875 - 0.219) = n2


n2 = 276 mol H2

I balance around mixing point: (100)(0.01) + (307)(0.125) = n3  n3 = 39.4 mol I

moles purge
8
moles leaving condenser  8  307  0.025

100
 0.245 moles fresh feed
92  276  39.4 molfed to reactor

EXAMPLE: Recycle and Purge in the Synthesis of Methanol

Methanol may be produced by the reaction of carbon dioxide and hydrogen.

CO2  3H2  CH3OH  H2O

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

Basis: 100 mol Combined Feed to the Reactor

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 CO 2 + H2,
of which 24.5 mol are CO2 (1/4 of 98) and 73.5 mol are H2.
 n5 mol n5 mol
x4 mol CO2 /mol 3x4 mol H2 /mol (1-4x4) mol I/mol
x4 mol CO2 /mol 3x4 mol H2 /mol (1-4x4) mol I/mol

n4 mol CO2 /mol x4 mol CO2 /mol 3x4 mol H2 /mol (1-4x4) mol I/mol

n0 mol 100 mol Reactor

Condenser
0.249 mol CO2 /mol 24.5 mol CO2 n1 mol CO2
0.746 mol H2 /mol 75.5 mol H2 3n1 mol H2
2 mol I n2 mol CH3OH
0.005 mol I/mol
n3 mol H2O n2 mol CH3OH
2 mol I n3 mol H2O

Take a moment to examine the chart labeling. In particular, notice that we have built in the
facts that CO2 and H2 are always present in a 1:3 ratio and that the compositions of the
gaseous effluent from the condenser, the purge stream, and the recycle stream are all
identical. The more of this sort of information you can incorporate in the chart labeling, the
easier the subsequent calculations become. Let us outline the solution, referring to the
flowchart.

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.

60% Single-Pass Conversion

n1  0.400(24.5)  9.80 mol CO2

3n1  29.4 mol H2
0.60024.5  14.7 mol CO2 react
 Balances on CH3OH, H2O : output  generation
n2  14.7 mol CH3OH
n3  14.7 mol H2O
Mole Balance About Condenser
 2 4n1  n2  n3  n2

 n3  n4
 substitute for n1
n4  41.2 mol

CO2 Balance About Condenser

n1  n x
4 4

x4  (9.80 / 41.2)  0.2379 mol CO2 / mol

Mole Balance About Mixing Point

n0 + n6 =100

I Balance About Mixing Point

0.00500 n0  n6 (1  4 x4 )  2
 x  0.2379
4

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

n5  41.2  34.6  6.6 mol purge

The required scale factor is

1000 mol / h  / mol n2 14.7 68.03 h

1

n2
The desired flow rates are therefore

65.4  68.06 = 4450 mol fresh feed/h

100.0  68.03 = 6803 mol/h fed to reactor
6.6  68.03 = 449 mol/h purge

4.6. Combustion Reactions and Their Material Balances

4.6.1. Complete and Partial Combustion

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+½O2  H2O

C + ½O2  CO, S+O2  SO2

Complete and incomplete combustion of C3H8 are given by the following chemical reactions,
complete C3H8 +5O2  3CO2 + 4H2O
incomplete C3H8 + 7/2O2  3CO + 4H2O

4.6.2. Wet and Dry Basis

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

Suppose we have n moles of each, then

composition of CO2 on wet basis moles of CO 2

=  100 = (n/3n)100 = 33.33%
total moles on wet basis
 moles of CO 2
composition of CO2 on dry basis  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

Basis: 100 mol Wet

Gas
60 mol N2
15 mol CO2
10 mol O2
85 mol dry gas

60
 0.706 mol N2
85 mol dry gas
15
 0.176 mol CO2
85 mol dry gas
10
 0.118 mol O2
85 mol dry gas

EXAMPLE: Dry Basis  Wet Basis

An Orsat analysis (a technique for stack gas analysis) yields the following dry basis
composition:

N2 65%
CO2 14%
CO 11%
O2 10%

A humidity measurement shows that the mole fraction of H 2O in the stack gas is 0.07.
Calculate the stack gas composition on a wet basis.
Solution

Basis: 100 lb-moles Dry Gas

lb  mole H 2O lb  mole dry gas

0.07 0.93
lb  mole wet gas

lb  mole wet gas 

0.07 lb  mole H2 O / lb  mole wet lb  mole H2O

gas  0.0753
lb  mole dry gas
0.93 lb  mole dry gas / lb  mole wet
gas

100 lb  mole dry gas 0.0753lb  mole H 2O

 7.53 lb  moles H2O
lb  mole wet gas

100 lb  mole dry gas 0.650 lb  mole N2  65.0

lb  mole N2
lb  mole dry gas
(100)(0.140)  14.0 lb  mole CO
2
(100)(0.110)  11.0 lb  mole CO

10.00 lb  mole O
(100)(0.100)  107.5lb  mole wet2 gas

The mole fractions of each stack gas component may now easily be calculated:

lb  moles H 2 O
y H 2O  7.53 lb  moles H 2 O  0.070 ,... etc.
107.5 lb  moles wet gas lb  moles wet gas

4.6.3. Theoretical and Excess Air

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,

% excess air = [Air (fed) - Air (theoretical)]/Air (theoretical)100.

EXAMPLE: Theoretical and Excess Air

One hundred mol per hour of butane (C 4H10) and 5000 mol per hour of air are fed into a
combustion reactor. Calculate the percent excess air.
 Solution

First, calculate the theoretical air from the feed rate of fuel and the stoichiometric equation
for complete combustion of butane.
13
C H  O  4 CO  5 H O
4 10 2 2 2
2
(O )  100 mol C4H10 6.5 mol O2 required
2 theoretical hmol C4H10

mol
 2650
O
(air) h 4.76 mol air mol air
 3094
650 mol O2
th 
h mol O2 h

Hence

% excess air  (air)fed  (air) th  

5000  3094
 100%  61.6%
100%
(air) th 3094

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.

4.6.4. Combustion Material Balances

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

EXAMPLE: Combustion of Ethane

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 CO 2. Calculate
the composition of the fuel gas and the ratio of water to dry fuel gas.

Solution

Basis: 100 mol Ethane

Fed q1 mol C 2 H 6
100 mol C H
26
q2 mol O 2
50% excess air q 3 mol N 2
Q mol O2
q 4 mol CO
3.76Q mol N2
q5 mol CO 2
q6 mol H 2 O

7
C2H6  O2  2 CO2  3 H 2O
2
C2H6  5
O2  2 CO  3 H 2O
2
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
stream 3.76  79 
 .
21 

3. If the ethane reacted completely, q1 would be omitted.

4. Since excess air is supplied, O2 must appear in the product stream.

Theoretical O2
100 mol C 2 H 6 3.50 mol O2
 350 mol
1 mol C 2 H 6

O2 Fed
Q  1.5350  525 mol O 2 fed

N2 Fed
 (3.76)(525) = 1974 mol N2 fed
C2H6 Reacted
(0.90)(100) = 90 mol C2H6 reacted

C2H6 Balance

Output = input - consumption ==> q1 = 100 - 90 = 10 mol

N2 Balance
1974 mol N2 = q3
Input = output ==>

CO Balance
Output  generation
q4  0.25 x 90 mol C 2H6 react to form CO2 mol CO formed
1 mol C2H6 reacted

q4  45 mol CO

Atomic C Balance

Input  Output
C2 H6 CO CO2
 678  678  678 
100 mol C2H 62 mol C

1 mol C2H6
q1 2 q4 1 q4 1

q1  10
 q  45
4
q5  135 mol CO2

Atomic H Balance

Input  Output
100 mol C 2H66 mol H 10 mol C 2H66 mol H

1 mol C2H 6 1 mol C2H6

q6 (mol H2O)2 mol H


1 mol H2O


 q6  270 mol H2O
Atomic O
Balance
Input  Output
525 mol O22 mol O q2 ( mol O2 )2 mol O 45 mol CO1 mol O
 
1 mol O2 1 mol O2 1 mol CO

135 mol CO22 mol O


1 mol CO2

270 mol H 2O1 mol O


1 mol H2O


q2  232 mol O 2

The analysis of the stack gas is now complete. Summarizing:

q1  10 mol C2H6
q2  232 mol O2
q3  1974 mol N2
q4  45 mol CO
q5  135 mol CO2
2396 mol dry gas
 q6  270 mol H2 O
2666 mol total

Hence the flue gas composition on a dry basis is

y1  10 mol C2 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 2 135 mol

CO 2  0.824
2396 mol dry gas
2396
y4  45 mol CO mol dry
gas  0.019
2396 mol dry gas
y5 
 0.0563 m
o
l

m
o
l

m
o
l

C
O

m
o
l

m
o
l

C
O

m
o
l
and the mole ratio of water to dry flue gas is

270 mol H2 O mol H 2O mol dry flue gas

 0.113
2396 mol dry flue gas

EXAMPLE: Combustion of a Natural Gas

A natural gas of an unknown composition is burned with air. An analysis of the product gas
yields the following results

0.130 mole H2O/mole wet gas

Orsat analysis of flue gas: 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

100 mol dry gas 

 0.015 mol CO / mol 
qO2 mol O 2  
3.76 qO2 mol N2  0.060 mol CO 2 / mol
 0.082 mol O / mol 
 2 
 0.843 mol N 2 / mol 
Qw mol H2O

From the given mole fraction of water,

100 mol dry gas0.130 mol H 2O

Qw   14.9 mol H2 O
0.870 mol dry gas
Atomic Carbon Balance qc 
  6447448   7.5 mol
C 100 0.06 1
100 mol flue gas 0.015 mol CO 1 mol C
C in CO2 mol flue gas 1 mol CO

Atomic H Balance

q H  Qw (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 (CH 3.97)n. Since there is only one
hydrocarbon for which the ratio of H to C is close to 3.97 - that is, CH 4 - 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].
References

1. Felder, R. and Rousseau, R. W., Elementary Principles of Chemical Processes, 2 nd ed.,

John Wily & Sons, 1986.

2. Himmelblau, D. M., Basic Principles and Calculations in Chemical Engineering, 4 th ed.,

Prentice Hall, New Jersey, 1982.

3. Perry, R. H. and Green, D., Perry’s Chemical Engineering Handbook, 6 th ed., McGraw
Hill, New York, 1984.

4. Al-Amer, M. J., Session 1 of a Short Course on “Introduction to Chemical

Engineering for Non-Chemical Engineers”, KFUPM, Dhahran, 1998.
0.00500n0  0.0484n6  2