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Ebook Elements of Chemical Reaction Engineering 4Th Edition Fogler Solutions Manual Full Chapter PDF
Ebook Elements of Chemical Reaction Engineering 4Th Edition Fogler Solutions Manual Full Chapter PDF
0.35
CA 0.6
0.3
0.5
0.25
0.4
SB/XY
0.2
0.3
0.15
CY
0.2
0.1
CB 0.1
0.05
CX
0 0
0 200 400 600 800 0 200 400 600 800
!
!
See Polymath program P6-2-a.pol.
POLYMATH Results
No Title 02-16-2006, Rev5.1.233
6-1
ODE Report (RKF45)
V C ! CA C AO ! C A 40 ! 0.112
"= = AO = 2
= sec
vO ! rA k1 A + k 2 A C A + k 3 A C A 0.0001 + 0.00168 + 0.0001
! = 21217 sec
6-2
P6-2 (c) Example 6-4
(1) For k1 = k2, we get
2
k 2 k1 (" !) = 1
1
! =
" OPT
k1 k 2
(3) T = 310.52oC
6-3
" !k1C A0
CB =
(" !k 2 + 1)(" !k1 + 1)
POLYMATH Results
No Title 02-14-2006, Rev5.1.233
6-4
P6-2 (d) Example 6-5
KC = Ke = 0.25
& 2 C N CO #
r2 N 2 = k 2 N 2 $C NO ' 2 2!
% KC "
& 2 C N CO #
rNO = 'k1NO C NH 3 C 1NO
.5
' 2k 2 N 2 $C NO ' 2 2!
% KC "
5 ' 2 C N CO $ 1
rN 2 = k1NO C NH 3 C 1NO.5
+ k 2 N 2 %C NO ! 2 2 " ! k 3O2 C N 2 C 022
6 & KC # 2
' 2 C N CO $
rO2 = k 2 N 2 %C NO ! 2 2 " ! k 3O2 C N 2 C 022
& KC #
P6-2 (e) Example 6-6
For liquid phase, F j = vo C j
dFNO dC NO
Equation (E 6-6.3): =vO = !kC NH 3 C 1NO.5 2
! 2k 2 N 2 C NO
dV dV
dC NO
" = !kC NH 3 C 1NO.5 2
! 2k 2 N 2 C NO
d#
dFNO2 dC NO 2
Equation (E6-6.8): =vO = k 3O2 C N 2 C O22
dV dV
dC NO 2
! = k 3O2 C N 2 C O22
d"
P6-2 (f) Example 6-7
For equal molar feed in hydrogen and mesitylene.
CHO = y HOCTO = (0.5)(0.032)lbmol/ft3 =0.016 lbmol/ft3
CMO = 0.016 lbmol/ft3
Using equations from example, solving in Polymath,
we get
! opt = 0.38 hr. At ! = 0.5 hr all of the H2 is reacted and only the decomposition of X takes place..
Ex 6-7 This question
XH 0.50 0.99
CH 0.0105 0.00016
CM 0.0027 0.0042
CX 0.00507 0.0077
! 0.2hr 0.38hr
~ 0.596 1.865
S X /T
See Polymath program P6-2-f.pol.
6-5
POLYMATH Results
Calculated values of the DEQ variables
~
Increasing θH decreases τopt and S X/T.
POLYMATH Results
NLES Solution
Variable Value f(x) Ini Guess
CH 4.783E-05 -4.889E-11 1.0E-04
CM 0.0134353 -1.047E-11 0.013
CX 0.0023222 -9.771E-12 0.002
tau 0.5
K1 55.2
K2 30.2
CHo 0.016
CMo 0.016
6-6
NLES Report (safenewt)
Nonlinear equations
[1] f(CH) = CH-CHo+K1*(CM*CH^.5+K2*CX*CH^.5)*tau = 0
[2] f(CM) = CM-CMo+K1*CM*CH^.5*tau = 0
[3] f(CX) = (K1*CM*CH^.5-K2*CX*CH^0.5)*tau-
CX = 0
Explicit equations
[1] tau = 0.5
[2] K1 = 55.2
[3] K2 = 30.2
[4] CHo = 0.016
[5] CMo = 0.016
(2) The selectivity becomes 6.52 when the first reaction is changed to A+2B D
6-7
P6-2 (i) Example 6-10
Original Case – Example 6-10 P6-2 i
The reaction does not go as far to completion when the changes are made. The exiting concentration of D,
E, and F are lower, and A, B, and C are higher.
See Polymath program P6-2-i.pol.
P6-2 (j)
At the beginning, the reactants that are used to create TF-VIIa and TF-VIIaX are in high concentration. As
the two components are created, the reactant concentration drops and equilibrium forces the production to
slow. At the same time the reactions that consume the two components begin to accelerate and the
concentration of TF-VIIa and TF-VIIaX decrease. As those reactions reach equilibrium, the reactions that
are still producing the two components are still going and the concentration rises again. Finally the
reactions that consume the two components lower the concentration as the products of those reactions are
used up in other reactions.
6-8
P6-2 (k)
Base case Equal-molar feed
Increasing yM0 will increase the production of m-xylene and methane, but will result in a large amount of
un-reacted mesitylene.
P6-3 Solution is in the decoding algorithm given with the modules ( ICM problem )
P6-4 (a)
Assume that all the bites will deliver the standard volume of venom. This means that the initial
concentration increases by 5e-9 M for every bite.
After 11 bites, no amount of antivenom can keep the number of free sites above 66.7% of total sites. This
means that the initial concentration of venom would be 5.5e-8 M. The best result occurs when a dose of
antivenom such that the initial concentration of antivenom in the body is 5.7e-8 M, will result in a
minimum of 66.48% free sites, which is below the allowable minimum.
P6-4 (b)
The victim was bitten by a harmless snake and antivenom was injected. This means that the initial
concentration of venom is 0. From the program below, we see that if an amount of antivenom such that the
initial concentration in the blood is 7e-9 M, the patient will die.
6-9
POLYMATH Results
Calculated values of the DEQ variables
6-10
P6-4 (c)
The latest time after being bitten that antivenom can successfully be administerd is 27.49 minutes. See the
cobra web module on the CDROM/website for a more detailed solution to this problem
P6-5 (a)
Plot of CA, CD and CU as a function of time (t):
POLYMATH Results
Calculated values of the DEQ variables
6-11
Explicit equations as entered by the user
[1] k1 = 1.0
[2] k2 = 100
[3] K1a = 10
[4] K2a = 1.5
[5] Cao = 1
[6] X = 1-Ca/Cao
To maximize CD stop the reaction after a long time. The concentration of D only increases with time
P6-5 (b)
Conc. Of U is maximum at t = 0.31 min.(CA = 0.53)
P6-5 (c)
Equilibrium concentrations:
CAe = 0.08 mol/dm3
CDe = 0.8 mol/dm3
CUe = 0.12 mol/dm3
P6-5 (d)
See Polymath program P6-5-d.pol.
POLYMATH Results
NLES Solution
Variable Value f(x) Ini Guess
Ca 0.0862762 -3.844E-14 1
Cd 0.7843289 -2.631E-14 0
Cu 0.1293949 6.478E-14 0
Ca0 1
k1 1
k2 100
K1a 10
K2a 1.5
t 100
6-12
NLES Report (safenewt)
Nonlinear equations
[1] f(Ca) = Ca0-t*(k1*(Ca-Cd/K1a)+k2*(Ca-Cu/K2a))-Ca = 0
[2] f(Cd) = t*k1*(Ca-Cd/K1a)-Cd = 0
[3] f(Cu) = t*(k2*(Ca-Cu/K2a))-Cu = 0 ! 1 min 10 min 100min
Explicit equations CAexit 0.295 0.133 0.0862
[1] Ca0 = 1 CDexit 0.2684 0.666 0.784
[2] k1 = 1
CUexit 0.436 0.199 0.129
[3] k2 = 100
[4] K1a = 10 X 0.705 0.867 0.914
[5] K2a = 1.5
[6] t = 100
[7] X = 1-Ca/Ca0
P6-6 (a)
1/ 2
1/ 2 & mol #
A! X rX = k1C A k1 = 0.004$ 3 ! min
% dm "
A! B rB = k 2C A k 2 = 0.3 min !1
2 dm 3
A!Y rY = k3C A k3 = 0.25
mol. min
Sketch SBX, SBY and SB/XY as a function of CA
rB k C k
1) SB/X = = 2 1A/ 2 = 2 C A1 / 2
rX k1C A k1
rB k C k
2) SB/Y = = 2 A2 = 2
rY k 3C A k 3C A
6-13
rB k 2C A
3) SB/XY = =
rX + rY k1C A / 2 + k 3C A 2
1
P6-6 (b)
Volume of first reactor can be found as follows
We have to maximize SB/XY
From the graph above, maximum value of SBXY = 10 occurs at CA* = 0.040 mol/dm3
So, a CSTR should be used with exit concentration CA*
Also, CA0 = PA/RT = 0.162 mol/dm3
And ! rA = rX + rB + rY = (k1C A1 / 2 + k 2 C A + k 3C A 2 )
v0 (C A0 ! C A* ) v0 (C A0 ! C A* )
=> V = = * * *
= 92.4dm 3
! rA 1 / 2 2
(k1 (C A ) + k 2 C A + k 3 (C A ) )
P6-6 (c)
Effluent concentrations:
CB CB mol
We know, τ = 9.24 min => "= = ! C B * = 0.11 3
rB k 2C A dm
mol mol
Similarly: CX * = 0.007 3 and CY * = 0.0037 3
dm dm
P6-6 (d)
6-14
Conversion of A in the first reactor:
C A0 " C A = C A0 X ! X = 0.74
P6-6 (e)
A CSTR followed by a PFR should be used.
Required conversion = 0.99
dV FA0
=> For PFR, Mole balance: =
dX ! rA
0.99
dX
" V = 10 ! 0.162 ! # 1/ 2 2
= 92.8dm 3
0.74 ( k1C A + k 2 C A + k 3C A )
P6-6 (f)
If we notice that E2 is the smallest of the activation energies, we get a higher selectivity at lower
temperatures. However, the tradeoff is that the reaction rate of species B, and therefore production of B,
decrease as temperature drops. So we have to compromise between high selectivity and production. To do
this we need expressions for k1, k2, and k3 in terms of temperature. From the given data we know:
" ! Ei #
ki = Ai exp $ %
& 1.98T '
Since we have the constants given at T = 300 K, we can solve for Ai.
.004
A1 = = 1.49e12
! #20000 "
exp $$ %%
& 1.98 (300 ) '
.3
A2 = = 5.79e6
! #10000 "
exp $$ %%
& 1.98 (300 ) '
.25
A3 = = 1.798e21
! #30000 "
exp $$ %%
& 1.98 (300 ) '
Ci = ! ri
6-15
Using these equations we can make a Polymath program and by varying the temperature, we can find a
maximum value for CB at T = 306 K. At this temperature the selectivity is only 5.9. This may result in too
much of X and Y, but we know that the optimal temperature is not above 306 K. The optimal temperature
will depend on the price of B and the cost of removing X and Y, but without actual data, we can only state
for certain that the optimal temperature will be equal to or less than 306 K.
POLYMATH Results
NLE Solution
Variable Value f(x) Ini Guess
Ca 0.0170239 3.663E-10 0.05
T 306
R 1.987
k1 0.0077215
k2 0.4168076
Cao 0.1
Cb 0.070957
k3 0.6707505
tau 10
Cx 0.0100747
Cy 0.0019439
Sbxy 5.9039386
Nonlinear equations
[1] f(Ca) = (Cao-Ca)/(k1*Ca^.5+k2*Ca+k3*Ca^2)-10 = 0
Explicit equations
[1] T = 306
[2] R = 1.987
[3] k1 = 1.49e12*exp(-20000/R/T)
[4] k2 = 5790000*exp(-10000/R/T)
[5] Cao = .1
[6] Cb = 10*k2*Ca
[7] k3 = 1.798e21*exp(-30000/R/T)
[8] tau = 10
[9] Cx = tau*k1*Ca^.5
[10] Cy = tau*k3*Ca^2
[11] Sbxy = Cb/(Cx+Cy)
P6-6 (g)
Concentration is proportional to pressure in a gas-phase system. Therefore:
P
S B / XY which would suggest that a low pressure would be ideal. But as before the
P + P2
tradeoff is lower production of B. A moderate pressure would probably be best.
P6-7
US legal limit: 0.8 g/l
Sweden legal limit: 0.5 g/l
k1 k2
A !! " B !! "C
Where A is alcohol in the gastrointestinal tract and B is alcohol in the blood stream
6-16
dC A
= !k1C A
dt
dCB
= k1C A ! k2
dt
k1 = 10 hr !1
g
k2 = 0.192
L hr
Two tall martinis = 80 g of ethanol
Body fluid = 40 L
80 g g
C A0 = =2
40 L L
Now we can put the equations into Polymath.
See Polymath program P6-7.pol.
POLYMATH Results
Calculated values of the DEQ variables
P6-7 (a)
In the US the legal limit it 0.8 g/L.
This occurs at t = 6.3 hours..
P6-7 (b)
In Sweden CB = 0.5 g/l , t = 7.8 hrs.
P6-7 (d)
For this situation we will use the original Polymath code and change the initial concentration of A to 1 g/L.
Then run the Program for 0.5 hours. This will give us the concentration of A and B at the time the second
martini is ingested. This means that 1 g/l will be added to the final concentration of A after a half an hour.
At a half an hour CA = 0.00674 g/L and CB = 0.897 g/L. The Polymath code for after the second drink is
shown below.
6-17
See Polymath program P6-7-d.pol.
POLYMATH Results
Calculated values of the DEQ variables
P6-7 (e)
The mole balance on A changes if the drinks are consumed at a continuous rate for the first hour. 80 g of
ethanol are consumed in an hour so the mass flow rate in is 80 g/hr. Since volume is not changing the rate
of change in concentration due to the incoming ethanol is 2 g/L/hr.
POLYMATH Results
Calculated values of the DEQ variables
US: CB never rises above 0.8 g/L so the is no time that it would be illegal.
Sweden: t = 2.6 hours
6-18
Russia: t = 5.2 hours
P6-7 (f)
60 g of ethanol immediately CA = 1.5 g/L
So the person has about 4 minutes and 40 seconds to get to their destination.
P6-7 (g)
A heavy person will have more body fluid and so the initial concentration of CA would be lower. This
means a heavier person will reach the legal limit quicker. The opposite is true for a slimmer person. They
will take longer to reach the legal limit, as their initial concentration will be higher.
P6-8 (a)
POLYMATH Results
Calculated values of the DEQ variables
6-19
[3] k4 = 0.2
[4] k3 = if(Cb<0)then (k1*Ca-k4*Cb) else (0.1)
P6-8 (b)
P6-8 (c)
If one takes initially two doses of Tarzlon, it is not recommended to take another dose within the first six
hours. Doing so will result in build up of the drug in the bloodstream that can cause harmful effects.
6-20
P6-8 (d)
If the drug is taken on a full stomach most of it will not reach the wall at all. The processed food can also
drag the drug to the intestines and may limit its effectiveness. This effect can be seen in the adsorption
constant k1 and elimination constant k2 values. If k1 decreases this means that the adsorption process is slow
and if k2 increases means that the rate of elimination of Tarzlon increases. The next graph shows the
concentration profiles for k1 = 0.10 h-1 and k2 = 0.8 h-1. Note that the maximum amount of the drug in the
bloodstream is reduced by two.
Concentration Profiles
Ca (mg/dm3)
8 Cb (mg/dm3) 0.6
CA (mg/dm )
CB (mg/dm3)
6
3
0.4
4
0.2
2
0 0
0 2 4 6 8 10 12
Time (h)
Concentration profile for Tarzlon in the stomach (A) and bloodstream
(B). The maximum amount of Tarzlon in the bloodstream is 0.3 mg/dm3.
P6-9 (a)
Reactor selection
A+ B!D rD = !r1 A r1 A = 10 exp(!8000 K / T )C AC B
A + B !U rU = !r2 A r2 A = 100 exp(!1000 K / T )C A C B
1/ 2 3/ 2
1/ 2
r 10 exp(!8000 K / T )C A C B exp(!8000 K / T )C A
SDU = D = 1/ 2 3/ 2
= 1/ 2
rU 100 exp(!1000 K / T )C A C B 10 exp(!1000 K / T )C B
At T = 300K
1/ 2
7.35 "10 !12 C A
k1 = 2.62 x 10-11 & k2 = 3.57 SD/U = 1/ 2
CB
At T = 1000K
1/ 2
-3 9.2 " 10 !5 C A
k1 = 3.35 x 10 & k2 =36.78 SD/U = 1/ 2
CB
Hence In order to maximize SDU, use higher concentrations of A and lower concentrations of B. This can be
achieved using:
1) A semibatch reactor in which B is fed slowly into a large amount of A
2) A tubular reactor with side streams of B continually fed into the reactor
3) A series of small CSTR’s with A fed only to the first reactor and small amounts of B fed to each reactor.
6-21
Also, since ED > EU, so the specific reaction rate for D increases much more rapidly with temperature.
Consequently, the reaction system should be operated at highest possible temperature to maximize SDU.
1
2
"C #
Note that the selectivity is extremely low, and the only way to increase it is to keep $ B % < 10!6 and
& CA '
add B drop by drop.
P6-9 (b)
A+ B!D and r1 A = 100 exp(!1000 K / T )C AC B
A + B !U and r2 A = 10 6 exp(!8000 K / T )C AC B
rD 100 exp(!1000 K / T )C AC B exp(!1000 K / T )
SDU = = 6 = 4
rU 10 exp(!8000 K / T )C AC B 10 exp(!8000 K / T )
At T = 300K
k1 = 3.57 & k2 = 2.623 SDU = 1.14 x106
At T = 1000K
k1 = 36.78 & k2 = 3354.6 SDU = 0.103
Hence we should keep the temperature low to maximize SDU but not so low that the desired reaction
doesn’t proceed to a significant extent.
P6-9 (c)
A+ B!D and r1 A = 10 exp(!8000 K / T )C ACB
B + D !U and r2 A = 109 exp(!10, 000 K / T )CB CD
r1 A 10 exp (!8000 K / T )C ACB
S DU = = 9
r2 A 10 exp (!10000 K / T )CB CD
exp (!8000 / T )C A
S DU = 8
10 exp (!10000 / T )CD
Therefore the reaction should be run at a low temperature to maximize SDU, but not too low to limit the
production of desired product. The reaction should also take place in high concentration of A and the
concentration of D should be limited by removing through a membrane or reactive distillation.
P6-9 (d)
A! D and r1 A = 4280 exp(!12000 K / T )C A
D ! U1 and r2 D = 10,100 exp(!15000 K / T )C D
A !U2 and r3 A = 26 exp(!10800 K / T )C A
6-22
rD 4280 exp(!12000 K / T )C A ! 10,100 exp(!15000 K / T )C D
S D / U 1U 2 = =
rU 1 + rU 2 10,100 exp(!15000 K / T )C D + 26 exp(!10800 K / T )C A
At T = 300K
k1 = 1.18 x 10-14 & k2 = 1.94 X 10-18 & k3 = 6.03 x 10-15
At T = 1000K
k1 = 0.026 & k2 = 3.1 X 10-3 & k3 = 5.3 x 10-4
P6-9 (e)
A+ B!D and r1 A = 10 9 exp(!10000 K / T )C A C B
D! A+ B and r2 D = 20 exp(!2000 K / T )C D
A + B !U and r3 A = 10 3 exp(!3000 K / T )C AC B
rD 10 9 exp(!10000 K / T )C A C B ! 20 exp(!2000 K / T )C D
S D /U = =
rU 10 3 exp(!3000 K / T )C A C B
At T = 300K
k1 = 3.34 x 10-6 & k2 = 0.025 & k3 = 0.045
The desired reaction lies very far to the left and CD is probably present at very low concentrations so that:
At T = 1000K
k1 = 45399.9 & k2 = 2.7 & k3 = 49.7
6-23
P6-9 (f)
A+ B!D and !r1 A = 10 exp(!8000 K / T )C ACB
A !U and !r2 A = 26 exp(!10,800 K / T )C A
U!A and !r3U = 1000 exp(!15, 000 K / T )CU
r 10 exp(!8000 K / T )C ACB
S D /U = D =
rU 26 exp(!10,800 K / T )C A ! 1000 exp (!15, 000 K / T )CU
We want high concentrations of B and U in the reactor. Also low temperatures will help keep the
selectivity high.
P6-9 (g)
A+ B!D and !r1 A = 800 exp(!8000 K / T )C A0.5CB
A + B ! U1 and !r2 B = 10 exp(!300 K / T )C ACB
D + B ! U2 and !r3 D = 106 exp(!8000 K / T )CD CB
(1)
800 exp (!8000 / T )C A0.5CB 80 exp (!8000 / T )
S D / U1 = =
10 exp (!300 / T )C ACB exp (!300 / T )C A0.5
At T = 300
2.098*10!10
S D / U1 =
0.368C A0.5
At T = 1000
29.43
S D / U1 =
0.7408C A0.5
To keep this selectivity high, low concentrations of A, and high temperatures should be used.
800 exp (!8000 / T )C A0.5CB 800C A0.5
S D /U 2 = = 6
106 exp (!8000 / T )CD CB 10 CD
To keep this selectivity high, high concentrations of A and low concentrations of D should be used. Try to
remove D with a membrane reactor or reactive distillation. The selectivity is not dependant on temperature.
6-24
To keep optimize the reaction, run it at a low temperature to maximized SD/U1 in a membrane reactor that
allows only D to diffuse out.
(2)
800 exp (!8000 / T )C A0.5CB
S D / U 1U 2 =
10 exp (!300 / T )C ACB + 106 exp (!8000 / T )CD CB
800 exp (!8000 / T )C A0.5
S D / U 1U 2 =
10 exp (!300 / T )C A + 106 exp (!8000 / T )CD
At T = 300
2.09*10!9 C A0.5
S D / U 1U 2 = "0
3.67C A + 2.62*10!6 CD
If temperature is the only parameter that can be varied, then the highest temperature possible will result in
the highest selectivity. Also removing D will help keep selectivity high.
P6-9 (i)
rD exp(!7000 K / T )C A1/ 2
=
rU 10CB1/ 2
dFA dFB
= rA = rB + RB
dV dV
dFU dFD
= rU = rD
dV dV
F
RB = A0
VT
A+ B!D rD = !r1 A r1 A = !10 exp(!8000 K / T )C ACB
A + B !U rU = !r2 A r2 A = !100 exp(!1000 K / T )C A1/ 2CB 3/ 2
rA = rB = r1 A + r2 A
F FB
C A = CT 0 A CB = CT 0
FT FT
mol dm3
CT 0 = 0.4 v0 = 10
dm3 s
FA0 = CT 0 v0
These equations are entered into Polymath and the plots below are for the membrane reactor. The code can
be modified to compare with the PFR results.
6-25
POLYMATH Results
Calculated values of the DEQ variables
6-26
P6-9 (j) No solution will be given
P6-9 (k) No solution will be given
P6-9 (l) No solution will be given
P6-10 (a)
6-27
P6-10 (b)
For CSTR, ! = 0.5h
First calculate k1 and k2 :
! E ! 1 1 ""
k = k0 exp $ $ # % %
$R T T %
& & 0 ''
! 10, 000 ! 1 1 ""
k1 = 0.4 exp $ $ # %%
& R & 373 T ' '
! 20, 000 ! 1 1 ""
k2 = 0.01exp $ $ # %%
& R & 373 T ' '
See Polymath program P6-10-b-nle.pol or P6-10-b-DEQ.pol.
6-28
[4] R = 1.987
[5] k1 = 0.4*exp(E1/R*(1/373-1/T))
[6] E2 = 20000
[7] k2 = 0.01*exp(E2/R*(1/373-1/T))
[8] ra = -k1*Ca
[9] rb = k1*Ca-k2*Cb
[10] rc = k2*Cb
6-29
0.8
0.7
0.6
Therefore, CB is
0.5
CB [mol/dm 3]
maximum at T=440K.
0.4
0.3
0.2
0.1
0.0
200 250 300 350 400 450 500 550 600 650 700
T [K]
P6-10 (c)
6-30
P6-10 (d)
P6-10 (e)
6-31
P6-11 (a)
Intermediates (primary K-phthalates) are formed from the dissociation of K-benzoate with a CdCl2 catalyst
reacted with K-terephthalate in an autocatalytic reaction step:
k1 k2
A !! " R !! "S Series
k3
R + S !! " 2S Autocatalytic
P 110kPa
C AO = = 3
= 0.02mol / dm3
RT ! kPa.dm "
# 8.314 $ (683K )
% mol.K &
Maximum in R occurs at t = 880 sec.
See Polymath program P6-11-a.pol.
POLYMATH Results
Variable initial value minimal value maximal value final value
t 0 0 1500 1500
A 0.02 0.003958 0.02 0.003958
R 0 0 0.0069892 0.005868
S 0 0 0.0100382 0.0100382
k1 0.00108 0.00108 0.00108 0.00108
k2 0.00119 0.00119 0.00119 0.00119
k3 0.00159 0.00159 0.00159 0.00159
ODE Report (RKF45)
Differential equations as entered by the user
[1] d(A)/d(t) = -k1*A
[2] d(R)/d(t) = (k1*A)-(k2*R)-(k3*R*S)
[3] d(S)/d(t) = (k2*R)-(k3*R*S)
Explicit equations as entered by the user
[1] k1 = 1.08e-3
[2] k2 = 1.19e-3
[3] k3 = 1.59e-3
P6-11 (b)
1) T = 703 K
CAO = 0.019 mol/dm3
! E ! 1 1 ""
k1' = k1 exp $ 1 $ # ' % %
& R & T T ''
6-32
" (42600cal / mol ) " 1 1 ##
k1' = (1.08 $10!3 s !1 ) exp % % ! !3 !1
& & = 2.64 $10 s
' (1.987cal / mol.K ) ' 683K 703K ( (
Similarly,
k2' = 3.3 "10!3 s !1
And, k3' = 3.1"10!3 dm3 / mol.s
Maxima in R occurs at around t =320 sec.
See Polymath program P6-11-b1.pol.
POLYMATH Results
Calculated values of the DEQ variables
Variable initial value minimal value maximal value final value
t 0 0 1500 1500
A 0.019 3.622E-04 0.019 3.622E-04
R 0 0 0.0062169 8.856E-04
S 0 0 0.0174625 0.0174625
k1 0.00264 0.00264 0.00264 0.00264
k2 0.0033 0.0033 0.0033 0.0033
k3 0.0031 0.0031 0.0031 0.0031
2) T = 663 K
CAO = 0.19 mol/dm3
POLYMATH Results
Calculated values of the DEQ variables
Variable initial value minimal value maximal value final value
t 0 0 10000 10000
A 0.019 2.849E-04 0.019 2.849E-04
R 0 0 0.0071414 0.0012573
S 0 0 0.016889 0.016889
k1 4.2E-04 4.2E-04 4.2E-04 4.2E-04
k2 4.0E-04 4.0E-04 4.0E-04 4.0E-04
k3 7.8E-04 7.8E-04 7.8E-04 7.8E-04
6-33
ODE Report (RKF45)
Differential equations as entered by the user
[1] d(A)/d(t) = -k1*A
[2] d(R)/d(t) = (k1*A)-(k2*R)-(k3*R*S)
[3] d(S)/d(t) = (k2*R)-(k3*R*S)
Explicit equations as entered by the user
[1] k1 = 0.42e-3
[2] k2 = 0.4e-3
[3] k3 = 0.78e-3
Independent variable
variable name : t
initial value : 0
final value : 10000
P6-11 (c)
Use the Polymath program from part (a) and change the limits of integration to 0 to 1200. We get:
CAexit = 0.0055 mol/dm3
CRexit = 0.0066 mol/dm3
CSexit = 0.0078 mol/dm3
P6-12 (e)
6-34
P6-12 (h)
Mole balance: C AO " C A = (" rA )!
C C = (rC )!
C D = (rD )!
& 1 #
Rate law: rA = ' $k1 A C A + k 2 D C A C C2 !
% 3 "
&1 2 #
rC = $ k1 A C A ' k 2 D C A C C2 ' k 3 E C C C D !
%3 3 "
& 4 #
rD = $k 2 D C A C C2 ' k 3 E C C C D !
% 3 "
Solving in polymath: C A = 0.0069 M C B = 0.96 M C C = 0.51M C D = 0.004 M
SB/D = rB/r D = 247 SB/C = 1.88
See Polymath program P6-12-h.pol.
POLYMATH Results
NLES Solution
Variable Value f(x) Ini Guess
Ca 0.0068715 -2.904E-10 3
Cb 0.9620058 -1.332E-15 0
Cc 0.5097027 -1.67E-08 0
Cd 0.0038925 -2.391E-08 0
Ce 0.2380808 1.728E-08 0
kd 3
ka 7
rb 0.0160334
ra -0.0498855
ke 2
rc 0.008495
rd 6.488E-05
re 0.003968
tau 60
Cao 3
Nonlinear equations
[1] f(Ca) = Cao-Ca+ra*tau = 0
[2] f(Cb) = Cb - rb*tau = 0
[3] f(Cc) = Cc-rc*tau = 0
6-35
[4] f(Cd) = Cd-rd*tau = 0
[5] f(Ce) = Ce - re*tau = 0
Explicit equations
[1] kd = 3
[2] ka = 7
[3] rb = ka*Ca/3
[4] ra = -(ka*Ca+kd/3*Ca*Cc^2)
[5] ke = 2
[6] rc = ka*Ca/3 - 2/3*kd*Ca*Cc^2 - ke*Cd*Cc
[7] rd = kd*Ca*Cc^2 - 4/3*ke*Cd*Cc
[8] re = ke*Cd*Cc
[9] tau = 60
[10] Cao = 3
P6-12 (i)
For PFR and gas phase:
dFA dFB dFC dFD dFE
Mole balance: = rA = rB = rC = rD = rE
dV dV dV dV dV
& 1 #
Rate law: rA = ' $k1 A C A + k 2 D C A C C2 !
% 3 "
&1 #
rB = $ k1 A C A !
%3 "
& 1 2 #
rC = $ k1 A C A ' k 2 D C A C C2 ' K 3 E C C C D !
%3 3 "
& 4 #
rD = $k 2 D C A C C2 ' k 3 E C C C D !
% 3 "
rE = [k 3 E C C C D ]
FA F FD
Stoichiometry: C A = CTO y C C = CTO C y C D = CTO y
FT FT FT
FT = FA + FB + FC + FD + FE
dy " ! FT
=
dV 2 y FTO
Plot of CB and CC are overlapping.
See Polymath program P6-12-i.pol.
POLYMATH Results
Calculated values of the DEQ variables
6-36
Cc 0 0 0.0993605 0.0993325
ka 7 7 7 7
kd 3 3 3 3
ke 2 2 2 2
Ca 0.2 1.367E-05 0.2 1.367E-05
rb 0.4666667 3.191E-05 0.4666667 3.191E-05
ra -1.4 -1.4 -9.586E-05 -9.586E-05
Cd 0 0 3.0E-04 2.56E-04
Fto 20 20 20 20
rc 0.4666667 -1.923E-05 0.4666667 -1.923E-05
rd 0 -7.012E-05 8.653E-04 -6.742E-05
re 0 0 5.908E-05 5.087E-05
alfa 1.0E-04 1.0E-04 1.0E-04 1.0E-04
X 0 0 0.9999543 0.9999543
6-37
P6-12 (j) Changes in equation from part (i):
dFC
= rC ! RC RC = k diffuse C C k diffuse = 2 min !1
dV
See Polymath program P6-12-j.pol.
P6-13 (a)
m-xylene → benzene + methane
A → B + M
m-xylene → p-xylene
A → P
See Polymath program P6-13-a.pol.
POLYMATH Results
Calculated values of the DEQ variables
6-38
Cto 0.05 0.05 0.05 0.05
Ca 0.0375 0.0026257 0.0375 0.0026257
r1 -0.00825 -0.00825 -5.777E-04 -5.777E-04
Cb 0 0 0.0070067 0.0070067
r2 -0.026625 -0.026625 -0.0018643 -0.0018643
Cp 0 0 0.0226125 0.0226125
Spb 0 0 3.2272267 3.2272267
tau 0 0 3 3
Y 0 0 0.7634409 0.7634409
X 0 0 0.9185694 0.9185694
P6-13 (b)
CSTR
Mole Balances:
FA = FA0 + rAV FB = rBV FM = rM V FP = rPV
6-39
C A = C A0 + rA! C B = rB! C M = rM ! C P = rP!
Rate Laws:
rA = !(k1 + k 2 )C A rB = rM = k1C A rP = k 2 C A
&E , 1 1 )#
k1 = k1@ 946 K exp $ 1 * - '!
% R + 946 T ("
&E , 1 1 )#
k 2 = k 2 @ 946 K exp $ 2 * - '!
% R + 946 T ("
Combining:
C A = C A0 " (k1 + k 2 )!C A
C A0
CA =
1 + (k1 + k 2 )!
k 2!C A0
C P = k 2!C A =
1 + (k1 + k 2 )!
Using these equations and Polymath we find the optimal temperature is 878.6 K. The maximum
concentration of p-xylene is 0.0264 mol/dm3
See Polymath program P6-13-b.pol.
POLYMATH Results
No Title 03-06-2006, Rev5.1.233
6-40
ODE Report (RKF45)
0.03
0.025
0.02
CP [mol/dm ]
3
0.015
0.01
0.005
0
400 600 800 1000 1200 1400 1600
T [K]
P6-14(a)
6-41
See Polymath program P6-14-a.pol.
6-42
[2] kf3 = 5
[3] ke2 = .1
[4] kd1 = 0.25
[5] rf3 = kf3*Cb*Cc^2
[6] rd1 = kd1*Ca*Cb^2
[7] re2 = ke2*Ca*Cd
[8] rf = rf3
[9] re = re2
[10] rd = rd1-2*re2+rf3
[11] ra = -rd1-3*re2
[12] rb = -2*rd1-rf3
[13] rc = rd1+re2-2*rf3
2.5
Ca
Concentration [mol/dm 3]
2 Cb
Cc
Cd
Ce
1.5 Cf
0.5
0
0 5 10 15 20 25 30 35 40 45 50
3
V [dm ]
P6-14 (b)
6-43
P6-14 (c)
6-44
6-45
Another random document with
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“‘I, Haji Mahomed, of Se Deh, and I, Jaffer Kūli, his son-in-law,
give and let, for the journey to Resht, from Ispahan, viâ Koom,
Hajeeb, Doong, Kasvin, to make twenty stages and halt four days at
our own expense, and at the wish of the sahib; twelve mules, four for
the mule litter, two for the kajawehs (covered mule paniers), and six
for loads; we hereby acknowledge five hundred and fifty kerans, and
two hundred more are to be paid in Resht; our hire is sixty-two and a
half kerans per mule; we will start to-morrow, and have affixed our
seals.’”
Here they all call on the prophet; and both muleteers seal, and the
merchant witnesses the document, which is handed to me. I give
them a cheque for five hundred and fifty kerans, and we all go off to
my house to look at the loads. On seeing these, both men begin to
vociferate. “Ah, loads, such loads, no one ever took such loads; on
no account will we go.”
“All useless, Haji,” we reply, and a pipe is given them.
They then proceed to sing their own praises, and we (the
merchant and I) profess to love them like brothers. They now retire,
and I and my wife and servants begin to pack up our road-kit
seriously; the travelling gear, got ready long ago, is dragged out and
re-examined; tarpaulin is nailed firmly on the roof of the takhtrowan
(horse litter), and the same is done to the kajawehs; then thin red
covers are put on and patched, new straps and buckles are added to
the bedding-bags, and the bedding packed so as to get each side
one weight; movable curtains are hung in the takhtrowan and its
harness is renewed. In the morning the assistant muleteers arrive,
and proceed to cord each box with heavy ropes, leaving the ends
loose; these ends are afterwards tied together; and so each half load
hangs on a side of the pack-saddle; a long broad band with an iron
ring at each end is flung over the mule and his load, and gradually
tightened. Thus loaded, the mule and his burden seldom, or never,
part company.
The muleteer, having had some of his hire, signed his agreement
and roped some of his loads, is by Persian law bound to go, and we
calmly prepared to start on the morning of April 4th.
April 4th.—No sign of muleteer. We use our road kit, and are in the
same plight as when marching.
April 5th.—Muleteer arrives, and requests us to take back our
money. Mutual threats and curses deep. Muleteer refuses to salaam.
Muleteer is threatened with the Governor. Muleteer demands a
present. Muleteer is offered a thrashing. Muleteer is insolent.
Muleteer is pursued. Muleteer flees.
April 6th., eight a.m.—Muleteer arrives at six a.m. Harnesses the
takhtrowan to two beasts, who shy and kick, and can’t be made to
move. Again offers to return money. Is again threatened with the
Governor, and called a Jew. Retires in violent passion.
Four p.m.—Arrival of muleteer with fairish horses (by the way, the
man’s beasts are all yabūs or horses). They are tried and found
satisfactory. Assistant muleteer addressed as “Hadji” (“pilgrim,” a title
very agreeable to the lower class of Persians), and regaled with
pipes. Head muleteer addressed as “That.”
Muleteer declines definitely to start, and offers to refund, but will
go for increased hire. Muleteer publicly threatened with Governor,
and called “That wind-bag.”
Muleteer retires, swearing he will die rather than start.
April 7th., eight a.m.—No muleteer. Nine a.m.—Arrival of muleteer
and nine mules (i. e. ponies), four assistants, and a donkey.
Assistant muleteer is secretly promised twenty kerans if he becomes
the slave of hirer, to be given in Resht. Eleven a.m.—Mules at last
loaded; they start. The wives of the servants come and weep on
them. The takhtrowan is carried to the high-road. Twelve noon.—I
take N⸺ (our English nurse), Frank, and the baby to the starting-
place, and put them into the takhtrowan, placing Charlie, our eldest,
with a nurse-boy, in one kajaweh, the woman-servant Bēbē in the
other. They leave.
Half-past twelve.—I go round my rooms for the last time.
A⸺ (my wife) and I mount, with our table-servant, last of all. We
leisurely walk our horses out. When we have got a quarter of a mile,
our servant swears he has dropped his whip. I refuse to let him go
back, as I don’t want to lose sight of him. Scene with him.
Grumblings, threats.
We pass the Missionary house. We bid them all good-bye at the
door. While this is taking place Ibrahim, the head-man, disappears. I
gallop after him, leaving A⸺ to come on with the bedding and the
groom. After a chase of two miles I catch him. He swears I told him
to get up to the takhtrowan. Threats. Whispered curses. I shout
myself hoarse. We cross the river, pass through the town, four miles
out of which we reach the caravan. On over a sandy and muddy
plain to Gez. Four farsakhs. Time, half-past four p.m. Tea, five p.m.
Rest of caravan arrive. Eight, dinner. Nine, bed.
April 8th.—Leave Gez at nine a.m. Over a sandy plain, six
farsakhs, twenty-three miles, to Mūrchicah. Cold wind, dull day, rain
threatening. Arrive at “chupper-khana” (post-house) at five, having
breakfasted among some ruins on the road, about half-way. The
post-house keeper at this place was the man who behaved so well to
me, and lent me clothes when I was robbed, so I gave him a double
present, as usual, and a bottle of wine.
April 9th.—Left this morning at seven for Soh, six long farsakhs;
left the plain, half-way breakfasted, and at the dam, a long farsakh
from Soh, were met by Sergeant McG⸺. After ten minutes it began
to rain heavily, and though we cantered for two miles, we got pretty
wet ere we got our rugs. On their reaching us it left off raining. Mrs.
McG⸺ gave us a magnificent high tea. Soh is a terribly cold place.
We were hospitably entertained and well fed, but it is impossible to
get warm, even with huge fires.
April 10th.—In the morning at five a.m. the ground was covered
with snow, and the weather was severe; it also rained till seven,
when it cleared a little. Started the caravan at eight, selves at nine.
Rain and drizzle till we got to the Kohrūd Pass, when it suddenly
came on to snow heavily.
The track was through snowdrifts half melted, and before we had
got a dozen yards up the steep ascent, A⸺’s mare was off the
track, trembling with fear, and up to her girths. A⸺, too, fancied, I
think, that it was all over with us. The muleteers began to call on
God, Ali, and the other saints, but we blundered along, one mule
only falling. The snow got very thick, but our goggles protected our
eyes, and we were heavily wrapped up. One side (the windward)
soon got white, and A⸺ appreciated the big, old-fashioned, silk
handkerchief which I gave her, to keep her sun hat on, and protect
her face from the snow. After an hour and a half of this, we cleared
the pass, the takhtrowan having got over in safety, and N⸺ and
the babies not having had to get out, which, if they had been obliged
to do, would, with knee-deep snow and two feet of mud, have been a
serious matter.
The snow melted into drizzle, and in a quarter of an hour we were
in a sheltered valley, in a strong sun, and entering the village of
Kohrūd. We got to the post-house, and there took off our wet wraps
and hung them up. About two hours before sunset. Six farsakhs.
Seven hours in the saddle, all but the last two being severe work for
a lady.
April 11th.—Started early, as we have seven farsakhs (twenty-six
miles and a half) to do. Though we expected to feel the heat, we had
soon to take to our wraps, as a strong Scotch mist, with occasional
cold showers, followed us all through the mountains to the
caravanserai of Guebre-abad (which is supposed to be haunted).
We found it empty, and breakfasted with our horses there, but the
weather was too awful for N⸺ and the children to get out, so we
sent them on.
Half-way to Guebre-abad we had to pass down the causeway cut
in the side of the mountain, which skirts the reservoir fed by the
Kohrūd torrent, where is stored the water for the town of Kashan. It is
simply a valley, closed at one end by a huge wall of masonry. This
retains the waters, the surplus falling over the top, like the Staubach
on a small scale.
Within two farsakhs of Kashan the climate changed; our faces
seemed on fire. We found wheat two feet high, clover the same
height, and the little rain that fell was warm and refreshing. We got to
the telegraph-office at five-thirty, and were immediately regaled with
tea by Mr. S⸺, the clerk there. An hour and a half afterwards the
caravan came in. Here the men went to the bath, Bēbē started
washing clothes, and after dinner we inaugurated the new hot bath,
just built in the Government quarters (a great luxury).
Here at Kashan we determined to halt a day, and enjoy the genial
warmth, doors all open, and the luxury of not having to start in the
morning.
Kashan is celebrated for silk and velvet weaving, but the silk is
generally of very sad colours, and the objects useless to the
European, so we could merely buy a few handkerchiefs and some
velvet curtains.
The water supply from the Kohrūd torrent is collected in the
reservoir we passed, and on reaching Kashan is stored in “ab
umbars,” or water-cellars, and when they are emptied they are
regularly re-filled, thus getting a supply of fresh and clear water.
All about are curious, conical buildings of mud, some ten and
twelve yards high. They have small terraces a few inches wide at
top, others a foot or two wide at bottom. These are the grain stores
of the place, and seem peculiar to Kūm and Kashan.
I tried to pick up some curios in the bazaar, but found it hopeless.
The copper bazaar was particularly good and fine, but all of the work
was useful, not ornamental. Was bothered by visitors the greater part
of the afternoon, most of whom came for advice gratis. Near this
place is Feen, one of the royal palaces, well worth a visit, but as our
horses needed a rest as well as ourselves, and it is a four-mile ride,
and I had seen it, we did not go.
April 13th.—Bid good-bye to Mr. S⸺. He had most hospitably
entertained us. Left Kashan for Sinsin, six farsakhs. Found the
immediate neighbourhood of the town well sprinkled with villages;
they however soon ceased, and we came to a sandy desert, where it
was very hot. Arrived about half-past three. Directly we got in we
poisoned the kanaat (the underground canal for irrigation) in order to
get a dish of fish. In about an hour the fish came to the surface quite
intoxicated, and were caught and gutted at once. They were very
good, and the poison did not affect us. I used six berries only of
cocculus indicus, and we got about six pounds of fish. We got a
good dinner at nine—soup, fish, roast lamb, pâté de foie gras, tinned
peas, apricots and custard, Ispahan wine, port, coffee, cherry-
brandy. This gives some idea of what a good road-cook can do.
Directly we arrive in a place, our “farrash” and table-man (who keep
up with us) drag out our carpets, sweep the little dirty rooms out,
spread the carpets, fill our bags with chaff for beds, make our beds,
prepare tea, and bring me a water-pipe. Then when this is
completed, the “takhtrowan,” loads, children, tables and chairs
arrive; N⸺ and the children go to their room. We get chairs and
have tea and biscuits, or bread and jam (of course we have already
had déjeuner à la fourchette with three or four dishes and tea on the
road). In the early morning we have a slice of bread-and-butter and a
“snack,” with chocolate and milk. After afternoon tea we doze, read,
write, and stretch ourselves, or go for a little walk near the chupper-
khana, or caravanserai, as it may be. The little sketch of the
chupper-khana at Sinsin I made on the spot, and it gives a good idea
of the regulation Persian post-house. In these post-houses the
traveller in Persia passes a good deal of his time: they are all built
upon this plan, and pretty much alike; the wall at the top is seen to
be crumbling; most of them are in varying stages of dilapidation.
They are all built of sun-dried bricks, except in the extreme north,
and plastered with mud and cut straw (kah-gil). In the front is seen a
takhtrowan or horse-litter, in which ladies of rank, or invalids, usually
travel.
A CHUPPA KHANA OR POST-HOUSE. (SINSIN.)