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GATE - 2001 1 of 9

CHEMICAL ENGINEERING
SECTION - A
ONE MARKS QUESTIONS (1-25) c. temperature, pressure, and liquid
composition xi only
This question consists of TWENTY FIVE sub- d. temperature, pressure, liquid
questions (1 - 25) of ONE mark each. For each composition xi, and vapour
of these sub-questions, four possible answers (A, composition yi.
B, C and D) are given, out of which only one is 4. High pressure steam is expanded
correct. Answer each sub-question by darkening adiabatically and reversibly through a well
the appropriate bubble on the OBJECTIVE insulated turbine which produces some
RESPONSE SHEET (ORS) using a soft MB shaft work. If the enthalpy change and
pencil. Do not use the ORS for any rough work. entropy change across the turbine are
You may like to use the Answer Book for any represented by ΔH and ΔS, respectively,
rough work, if needed. for this process:
(Marks: 1 × 25 = 25) a. ΔH = 0 and ΔS = 0
b. ΔH ≠ 0 and ΔS = 0
1. The value of the following determinant c. ΔH ≠ 0 and ΔS ≠ 0
1 0 0 0 0 d. ΔH = 0 and ΔS ≠ 0
−2 2 0 0 0 5. For the case of a fuel gas undergoing
3 5 3 0 0 is combustion with air, if the air/fuel ratio is
increased, the adiabatic flame temperature
−1 4 7 4 0
will
−5 −6 2 1 1
a. increase
a. 24 b. decrease
b. 32 c. increase or decrease depending on the
c. -112 fuel type
d. 0 d. not change
2. The value of (1 + i)8, where i = −1 , is 6. The Power number for a stirred tank
a. 8 + 4i becomes constant at high Reynolds
number. In this limit, the variation of
b. 8 – 4i power input with impeller rotational speed
c. 16 (N) is proportional to
d. 8 a. N0
3. A reasonably general expression for b. N1
vapour-liquid phase equilibrium at low to c. N2
moderate pressures is
d. N3
φi yi P = γ i xi fi 0 7. The operation of a Rota meter is based on
where φi is a vapour fugacity coefficient, γi a. variable flow area
is the liquid activity coefficient, and f i 0 is b. rotation of a turbine
the fugacity of pure component i. The Ki c. pressure drop across a nozzle
value (yi = Kixi) is therefore, in general, a d. pressure at a stagnation point
function of
8. Applying a pressure drop across capillary
a. temperature only results in a volumetric flow rate Q under
b. temperature and pressure only laminar flow conditions. The flow rate, for
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the same pressure drop, in a capillary of transfer coefficient of moisture in air; hG:
the same length but half the radius is heat transfer coefficient; CS: heat capacity
a. Q/2 of vapour- gas mixture)
b. Q/4 hG2
a. =1
c. Q/8 kY CS
d. Q/16 kY CS2
9. The heat transfer by radiation from a mild b. =1
hG
steel surface is to be reduced by reducing
the emissivity of the surface. This can be hG
c. =1
best achieved by kY CS
a. painting the surface black kY2 hG
b. painting the surface white d. =1
CS
c. giving the surface a mirror finish
14. The conversion for a second order,
d. roughening the surface irreversible reaction (constant volume),
10. Heat transfer by natural convection is A ⎯⎯k2
→ B, in batch mode is given by
enhanced in systems with
1
a. high viscosity a.
1 + k 2 C A 0t
b. high coefficient of thermal expansion
c. low temperature gradients k 2 C A 0t
b.
d. low density change with temperature 1 + k 2 C A 0t
11. The surface renewal frequency in ( k2C A 0t )
2

Danckwerts’ model of mass transfer is c.


given by (kL: mass transfer coefficient, 1 + k 2 C A 0t
m/s) k2C A0t
d.
(1 + k2C A0t )
2
a. k L2 DA
b. k L2 DA 15. The reaction rate constants at two different
temperatures T1 and T2 are related by
c. k L2 / DA
⎛k ⎞ E⎛ 1 1 ⎞
a. ln ⎜ 2 ⎟ = ⎜ − ⎟
d. k L / DA2 ⎝ k1 ⎠ R ⎝ T2 T1 ⎠
12. For gas absorption the height of a transfer ⎛k ⎞ E⎛ 1 1 ⎞
unit, based on the gas phase, is given by b. ln ⎜ 2 ⎟ = ⎜ − ⎟
(G: superficial molar gas velocity; L: ⎝ k1 ⎠ R ⎝ T1 T2 ⎠
superficial molar liquid velocity; FG: mass ⎛k ⎞ E⎛ 1 1 ⎞
transfer coefficient, mol/m2s; a: interfacial c. exp ⎜ 2 ⎟ = ⎜ − ⎟
area per unit volume of tower) ⎝ k1 ⎠ R ⎝ T1 T2 ⎠
G ⎛k ⎞ E⎛ 1 1 ⎞
a. d. exp ⎜ 2 ⎟ = ⎜ − ⎟
FG a ⎝ k1 ⎠ R ⎝ T2 T1 ⎠
FG 16. The E-curve for a non-ideal reactor defines
b.
Ga the fraction of fluid having age between t
Ga and t + dt
c.
FG a. at the inlet
b. at the outlet
L
d. c. in the reactor
FG G
d. averaged over the inlet and outlet
13. The Lewis relation for air-water
humidification is given by (kY: mass
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17. The calibration data of a thermocouple ph − dt
with its cold junction at 0°C are given c.
ph
below
ph − d h
d.
ph
The hot junction of the thermocouple is 21. The ends of a cylindrical vessel can be
placed in a bath at 80°C while its cold closed by a head, which can be one of the
junction is at 20°C. What is the emf of the four shapes. For the same thickness,
thermocouple? choose the one which can withstand the
a. 3.26 mV highest pressure.
b. 0.80 mV a. flat plate
c. 2.46 mV b. hemispherical
d. 2.43 mV c. torispherical
18. A process is initially at steady state with d. ellipsoidal
its output y = I for an input u = 1. The 22. An investment of Rs. 100 lakhs is to be
input is suddenly changed to 2 at time r = made for construction of a plant which will
0. The output response is y(t) = 1 + 2r . take two years to start production. The
The transfer function of the process is annual profit from operation of the plant is
2 Rs. 20 lakhs. What will be the payback
a. time?
s
a. 5 years
2
b. 1 + 2 b. 7 years
s
c. 12 years
2
c. 1 + d. 10 years
s
23. One of the steps during refining of cane
1⎛ 2⎞
⎜1 + ⎟
d. sugar consists of addition of hydrated lime
s⎝ s⎠ to the sugar syrup followed by carbonation
19. The inherent characteristics of an equal of the resulting solution. The purpose of
percentage valve relating flow rate q with this step is to
valve stem movement x are described by a. Adjust the pH of the syrup.
the equation b. Remove the coloring matter from the
dq syrup.
a. =k
dx c. Reduce the viscosity of the syrup.
dq d. Improve the rate of crystallization of
b. = kq sugar.
dx
dq k 24. Styrene is produced from ethylbenzene by
c. = the process of
dx q
a. Dehydrogenation
dq
d. = kq 2 b. Oxidation
dx c. Alkylation
20. A perforated plate has holes of diameter dh d. Dehydration
arranged in a pitch, ph. Each hole has a
tube of i.d., dt, passing through it. The 25. In the fluid catalytic cracker (FCC), the
ligament efficiency is given by cracking reaction is ---(a)--- and the
regeneration is ---(b)--
ph − d h
a. a. (a) Exothermic (b) Endothermic.
ph
b. (a) Exothermic (b) Exothermic.
ph − d h dt / 2 c. (a) Endothermic (b) Endothermic.
b.
ph d. (a) Endothermic (b) Exothermic.
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b. ( ∂S / ∂P )T = − ( ∂V / ∂T )P
c. ( ∂V / ∂S )P = ( ∂T / ∂P )S
TWO MARKS QUESTIONS (26-50)
This question consists of TWENTY FIVE sub- d. ( ∂S / ∂V )T = ( ∂P / ∂T )V
questions (26 - 50) of TWO marks each. For 30. At 100°C, water and methylcyclohexane
each of these sub-questions, four possible both have vapour pressures of 1.0 atm.
answers (A, B, C and D) are given, out of which Also at 100°C, the latent heats of
only one is correct. Answer each sub-question by vapourization of these compounds are
darkening the appropriate bubble on the 40.63 kJ/mol for water and 31.55 kJ/mol
OBJECTIVE RESPONSE SHEET (ORS) using for methylcyclohexane. The vapour
a soft HB pencil. Do not use the ORS for any pressure of water at 150°C is 4.69 atm. At
rough work. You may like to use the Answer 150°C, the vapour pressure of
Book for any rough work, if needed. methylcyclohexane would be expected to
(Marks: 2 × 25 = 50) be:
a. significantly less than 4.69 atm
26. The function f ( x, y ) = x 2 + y 2 − xy − x − y + 5 b. nearly equal to 4.69 atm
has the c. significantly more than 4.69 atm
a. Maximum at (1, 1) d. indeterminate due to a lack of data
b. Saddle point at (1, 1) 31. A Bingham fluid of viscosity μ = 10 Pa s,
c. Minimum at (1, 1) and yield stress τ0 = 10 kPa, is sheared
between flat parallel plates separated by a
d. None of the above at (1, 1).
distance 10-3 m. The top plate is moving
27. A fair die is rolled four times. Find the with a velocity of 1 m/s. The shear stress
probability those six shows up twice. on the plate is
1 a. 10 kPa
a.
2 b. 20 kPa
16 c. 30 kPa
b.
325 d. 40 kPa
1 32. Air enters an adiabatic compressor at 300
c.
36 K. The exit temperature for a compression
25 ratio of 3, assuming air to be an ideal gas
d. (γ = Cp /Cv = 7/5) and the process to be
216
reversible, is
28. A butane isomerization process produces
70 kmol/h of pure isobutane. A purge a. 300(32/7)
stream, removed continuously, contains b. 3O0(33/5)
85% n-butane and 15% impurity (mole %). c. 300(33/7)
The feed stream is n-butane containing 1% d. 300(35/7)
impurity (mole %). The flow rate of the
33. The energy required per unit mass to grind
purge stream will be:
limestone particles of very large size to
a. 3 kmol/h 100 μm is 12.7 kWh/ton. An estimate
b. 4 kmol/h (using Bond’s Law) of the energy to grind
c. 5 kmol/h the particles from a very large size to 50
d. 6 kmol/h μm is
29. The Maxwell relation derived from the a. 6.35 kWh/ton
differential expression for the Helmholtz b. 9.0 kWh/ton
free energy (dA) is: c. 18 kWh/ton
a. ( ∂T / ∂V )S = − ( ∂P / ∂S )V d. 25.4 kWh/ton
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34. The Sieder-Tate correlation for heat content at the end of the drying period is
transfer in turbulent flow in a pipe gives (in kg moisture/kg thy solid)
Nu ∞ Re0.8 , where Nit is the Nusselt a. 0.5
number and Re is the Reynolds number for b. 0.05
the flow. Assuming that this relation is c. 0.1
valid, the heat transfer coefficient varies
with pipe diameter (D) as d. 0.15
a. D-1.8 39. In a single stage extraction process, 10 kg
of pure solvent S (containing no solute A)
b. D-0.2 is mixed with 30 kg of feed F containing A
c. D0.2 at a mass fraction xf = 0.2. The mixture
d. D1.8 splits into an extract phase E and a
35. The overall heat transfer coefficient for a raffinate phase R, containing A at xE = 0.5
shell and tube heat exchanger for clean and xR = 0.05, respectively. The total mass
surfaces is U0 = 400 W/m2K. The fouling of the extract phase is (in kg)
factor after one year of operation is found a. 6.89
to be hdo = 2000 W/m2K. The overall heat b. 8.89
transfer coefficient at this time is c. 10
a. 1200 W/m2K d. 8.25
b. 894 W/m2K 40. The mean conversion in the exit stream,
c. 333 W/m2K for a second-order, liquid phase reaction in
d. 287 W/m2K a non-ideal flow reactor is given by
∞ k C t
E ( t ) dt
36. The heat flux (from outside 10 inside)
a. ∫ 2 A0
across an insulating wall with thermal 0 1+ k C t
2 A0
conductivity k = 0.04 W/m K and
∞ 1
thickness 0.16 m is 10W/m2. The b. ∫ E ( t ) dt
temperature of the inside wall is -5°C. The 0 1 + k2C A0t
outside wall temperature is
(1 − E ( t )τ ) dt
∞ 1
a. 25°C c. ∫
0 1 + k2C A0t
b. 30°C
∞ exp ( − k2C A0t )
c. 35°C d. ∫ E ( t ) dt
0 1 + k 2C A 0t
d. 40°C
37. The interfacial area per unit volume of 41. For a vapor phase catalytic reaction (A + B
dispersion, in a gas-liquid contactor, for → F) which follows the Rideal mechanism
fractional hold-up of gas = 0.1 and gas and the reaction step is rate controlling, the
bubble diameter = 0.5 mm is given by (in rate of reaction is given by (reaction step is
m2/m3) irreversible, product also adsorbs)
a. 500 kp A pB
a. − rA =
b. 1200 1 + K A pA + K p p p
c. 900 kp A2 − p p
d. 800 b. − rA =
1 + K A pA + K p p p
38. 200 kg of solid (on dry basis) is subjected
kp A pB
to a drying process for a period of 5000s. c. − rA =
The drying occurs in the constant rate 1 + K A p A + K B pB + K p p p
period with the drying rate as NC = 0.5 × kp A pB
10 kg/m2s. The initial moisture content of d. − rA =
the solid is 0.2 kg moisture/kg dry solid. 1 + K A pA
The interfacial area available for drying is 42. The first-order, gas phase reaction
4 m2/100 kg of dry solid. The moisture A ⎯⎯
k1
→ 2 B is conducted isothermally in
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batch mode. The rate of change of d. = τ2/τ1
conversion with time is given by 46. An investment of Rs. 1000 is carrying an
dX A interest of 10% compounded quarterly.
= k1 (1 − X A ) (1 + 2 X A )
2
a.
dt The value of the investment at the end of
dX A five years will be
b. = k1 (1 − X A )(1 + 0.5 X A ) 20
dt ⎛ 0.1 ⎞
a. 1000 ⎜1 + ⎟
dX A ⎝ 4 ⎠
c. = k1 (1 − X A )
dt b. 1000 (1 + 0.10 )
20

dX A
d. = k1 (1 − X A ) / (1 + X A ) ⎛ 0.1 ⎞
5
dt c. 1000 ⎜1 + ⎟
43. An ideal PID controller has the transfer ⎝ 4 ⎠
function ⎡⎣1 + 1/ ( 0.5s ) + 0.2s ⎤⎦ . The ⎛ 0.1 ⎞
5

d. 1000 ⎜1 + ⎟
frequency at which the Magnitude Ratio of ⎝ 2 ⎠
the controller is 1, is 47. P is the investment made on an equipment,
0.5 S is its salvage value and ii is the life of
a.
0.2 the equipment in years. The depreciation
0.2 for the mth year by the Sum-of-Years-
b. Digits method will be
0.5
P−S
c. 0.2 × 0.5 a.
n
1
d. 1

⎛P⎞
m
0.2 × 0.5 b. 1 − ⎜ ⎟
44. The block diagram of an integrating level ⎝S⎠
process is given below. For unit step m
change in the set point Δhset = 1 with
c. (P − S)
n
Δd = 0 , the offset exhibited by the system 2 ( n − m + 1)
is d. (P − S)
n ( n + 1)
48. In a cylindrical vessel subjected to internal
pressure, the longitudinal stress σL, and the
circumferential stress, σh, are related by
Kc a. σ h = 2σ L
a.
1 + Kc b. σ h = σ L
1 σL
b. c. σ h =
1 + Kc 2
c. 0 d. No relation exists
2Kc 49. In the converter of the contact process for
d.
1 + 2Kc the manufacture of H2SO4, the equilibrium
conversion of SO2 ---(a)--- with increase in
45. A second order system can be obtained by
the temperature and ---(b)--- with increase
connecting two first order systems
in the mole ratio of SO2 to air.
l/(τ1s + 1) and 1/(τ2s + 1) in series. The
damping ratio of the resultant second order a. (a) increases (b) decreases.
system for the case τ1 ≠ τ2 will be b. (a) decreases (b) increases.
a. > 1 c. (a) increases (b) increases.
b. = 1 d. (a) decreases (b) decreases.
c. < 1
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50. For the hydrogenation of oils, ---(a)--- is to propylene). Assume that the amount of
commonly used as catalyst, arid ---(b)--- is carbon formed on the catalyst is negligible.
a catalyst poison. The product flow rate (stream S5) is 50
a. (a) Platinum (b) Sulfur. kmol/h. Calculate the flow rates of all the
b. (a) Palladium (b) Oxygen. other streams. Notice that all streams
except stream S3 are pure.
c. (a) Nickel (b) Sulfur.
d. (a) Nickel (b) Oxygen.

SECTION - B 54. 100 m3 of carbon dioxide initially at 423 K


and 50 bar (50 × 105 Pa) is to be
FIVE MARKS QUESTIONS (51-70)
isothermally compressed in a frictionless
This section consists of TWENTY questions of piston and cylinder device to a final
FIVE marks each. ANY FIFTEEN out of these pressure of 300 bar (300 × 105Pa).
questions have to be answered on the Answer Assuming ideal gas behaviour (R = 8.314
Book provided. × 102 bar m3/kmol K),
(Marks: 5 × 15 = 75) a. Write a general expression for the
energy balance for the gas within the
51. The parametric equation of a curve is: piston and cylinder device as the
2 system, and define all the terms.
r ( t ) = ri + j where t is the parameter. b. Calculate the volume of the
t
compressed carbon dioxide gas at 300
a. What type of conic (parabola, circle,
bar.
ellipse, and hyperbola) does the curve
represent? c. Calculate the work done to compress
the carbon dioxide gas.
b. Find the unit tangent to the curve at t =
1. d. Calculate the heat flow on
compression.
c. Find the unit normal to the curve at r =
1. 55. Normal pentane is isomerized to
isopentane and neopentane at 500 K and
52. Laplace transforms:
atmospheric pressure. Determine the
a. Show that the Laplace transform of eωt equilibrium composition (mole %) of the
is three components. State any assumptions
made. Consider the reactions to be:
a. n − C5 H12 ( g ) ⇔ iso − C5 H12 ( g )
b. Show from (a) that:
b. n − C5 H12 ( g ) ⇔ neo − C5 H12 ( g )
Equilibrium constant for reaction (a) at
c. Show from (b) that: 500K, K1 = 3,519
Equilibrium constant for reaction (b) at
500 K, K2 = 0.682
53. The process schematic of a propane 56. The inlet velocity of water (ρ = 1000
dehydrogenation plant is shown below. It kg/m3) in a right angled bend-reducer is v1
is desired to set up a simplified version of = 1m/s, as shown below. The inlet
the material balance for this plant. Assume diameter is D1 = 0.8 m and the outlet
that the only reaction is the diameter is D2 = 0.4 m. The flow is
dehydrogenation of propane to propylene; turbulent and the velocity profiles at the
there are no side reactions. The yield of inlet and outlet are flat (plug flow).
propylene per pass is 30% (i.e., 30% of the Gravitational forces are negligible.
propane entering the reactor is converted
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m dT
Cp = π DU (Ts − T )
N dz
where T is the temperature of the
liquid, N is the number of tubes in a
pass, z is the distance along the tube, D
is the inner diameter of the tubes and U
is the overall heat transfer coefficient
based on the inside surface area.
a. Find the pressure drop (P1 – P2) across b. Obtain an expression for the
the bend assuming negligible friction temperature of the liquid at the exit of
losses. the heat exchanger, T2. The length of
b. If the actual pressure drop is (P1 – P2) the tubes is L and liquid enters the heat
= 8.25 kPa, find the friction loss factor exchanger at temperature T0.
(Kf ) based on the velocity v1. 60. For a counter-current, multistage contact,
57. The volumetric flow rate during constant show that if the driving force for solute
pressure filtration is transfer is constant for all trays, then the
number of stages is given by
dV 1
= YN − Y1
dt K cV + 1q0 N p = p+1
Y1 − mX 0
where V is the total volume of filtrate
collected in time t, and Kc and q0 are
constants.
a. Integrate the above equation to obtain
a relation between V and t.
b. Make a sketch of t/V versus V from
your results.
c. Given V = 1.0 litre at t = 41.3 sand V = 61. A sugary substance A is added to a pot of
2.0 liter at t = 108.3 s, find Kc. milk (initially containing no A) and stirred
58. A 200 W heater has a spherical casing of vigorously by a spoon so that the
diameter .0.2 m. The heat transfer concentration of A, CA, is uniform
coefficient for conduction and convection everywhere. The mass transfer coefficient
from the casing to the ambient air is for the transfer of A into the liquid is ksl =
obtained from Nu = 2 + 0.6 Re1/2 Pr1/3 with 1 × 10-4 m/s. Solid A is added in great
Re = 104 and Pr = 0.69. The temperature excess compared to the saturation capacity
of the ambient air is 30°C and the thermal of milk to dissolve A. Assume that the
conductivity of air is k = 0.02 W/m K. solid-liquid interfacial area stays constant
throughout the dissolution process and is
a. Find the heat flux from the surface at
given by a = 1000 cm2. Derive the
steady state.
expression for. CA versus time, t. Find the
b. Find the steady state surface
time taken for C A / C A* = 0.95 .
temperature of the casing.
c. Find the temperature of the casing at C A* = 5 × 10−2 kmil/m3; VL = 1000 cm3.
steady state for stagnant air. Why is 62. The concentration versus batch time data
this situation physically infeasible? for a constant volume, isothermal batch
59. A 1-2 shell and tube heat exchanger has reactor is given in the Table below.
liquid (specific heat Cp) flowing at a mass Assuming the reaction to be first order in
flow rate m in the tubes and saturated A. find the best value of k1 by least
steam (temperature Ts) condensing on the squares regression.
shell side.
a. Carry out a differential energy balance
on a single tube to show that 63. A CSTR and a PFR of equal volume V
(each) are given for the conduct of a
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second-order, isothermal, liquid phase = 1.5 kg/m3. The liquid flow rate, L = 30
reaction. The reactors are to be arranged kg/s and liquid density ρL = 1000 kgm3.
sequentially (in series). Find the values of The column is to be designed for a
the conversionr for the two possible pressure drop of 42 mm H2O. Norton’s
reactor arrangements. correlation for this pressure drop is
A ⎯⎯→ B, k2 = 1m /kmol s, C A0 = 0.1
k2 3
⎛μ ⎞
0.1
2
kmol/m3s and τ = 5 s (for volume V). 1331G ⎜ L ⎟
⎝ ρL ⎠
W

64. Find the expression for the effectiveness K=


factor of a catalyst pellet in the form of a
ρG ( ρ L − ρG )
thin slab such that the area of two opposite where K = flow coefficient, μL, liquid
faces is much larger than the area of the viscosity = 10-3 Ns/m2, Gw = gas flow rate
other four faces. Material A can diffuse per unit cross sectional area, kg/(m2s), Fp =
from both the large faces. Assume a first packing factor = 170 m-1. K is given by the
order reaction and isothermal, irreversible equation: K = 0.62 - 0,5(m - 0.5) for 0.5 ≤
conditions. The two large faces are m ≤ 1.0 where
separated by a distance 2w, the effective L ρC
diffusivity of A in the slab is DAe and the m=
G ρL
rate constant is denoted by k1.
65. The hot junction of a thermocouple having Calculate the diameter of the contactor.
time constant r mm. is initially at room 68. A plant designer has to choose between
temperature of 30°C. At time t = 0 min., it equipment 1 and equipment 2. Equipment
is placed in a bath held at 100°C. The 1 is made of special material and requires
thermocouple is connected to a recorder no maintenance, The cost of the equipment
which has fast dynamics. At t = 2 min., the is Rs. 3,00,000. Equipment 2 is of a lower
hot junction is withdrawn from the bath cost material and costs Rs. 1,50,000. For
and held in the air which is at 30°C. From maintenance of equipment 2, a
the recorded data, the value of dT/dt at t = maintenance cost of Rs 10,000 has to be
2+ min. is given to you. dT/dt = - paid at the end of each year. Life of
2.5°C/min. at t = 2+ min. Is this data equipment 2 is four years while that of
sufficient to calculate the time constant of equipment I is 8 years. Interest rate is 15%
the thermocouple? If so, suggest a compounded annually. Calculate the
procedure for calculation of the time present worth of investment to be made for
constant τ. each equipment and choose the option
66. The transfer function of a system which has the lower present worth.
consisting of a thermal process, valve and Equipment 1 has a salvage value of Rs
measuring system is given by 30,000 while equipment 2 has no salvage
ΔT ( s ) 5
value.
= 69. Using appropriate structural formulae,
ΔI ( s ) ( 5s + 1)( 0.5s + 1)( 0.1s + 1) write the equations representing the
Initially a proportional controller with following reactions in the
proportional sensitivity Kc is used. The stoichiometricatly balanced form.
controller equation is a. Dehydrogenation of isopropanol to
ΔI ( s ) = K c ( ΔTset ( s ) − ΔT ( s ) ) where Tset is acetone.
the set point. Find the value of Kc = Kc,max b. Hydroformylation of propylene to
above which the closed loop will be butyraldehyde.
unstable. Can you use the results of the c. Nitration of toluene to o-nitrotoluene.
closed loop response at Kc = Kc,max to tune d. Oxidation of cumene to cumene
a PID controller to be used in place of the hydroperoxide using oxygen.
proportional controller? If so, calculate the e. Isomerisation of n-butane to isobutane.
tuning parameters of the controller. 70. Answer each of the following questions in
67. A packed gas liquid contactor employs one sentence.
ceramic Intalox saddles (38 mm). The gas
flow rate, G = 1.5 kg/s and gas density, ρG
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a. What function does the membrane
perform in the membrane cell for the
manufacture of NaOH?
b. What is the generic chemical name for
the class of polymers which are
commercially known as nylons?
c. Name the commonly used process for
the manufacture of synthesis gas from
the natural gas.
d. What change in the design of the
synthesis gas compressors has
revolutionized the ammonia
manufacture during the recent years?
e. State the major advantage of the Kraft
process over the other processes for the
manufacture of paper pulp?

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