A. ?
C. 70
D. 100
A. Temperature of the system
B. Pressure of the system
D. Composition of the component only
A. Total pressure of the system
C. Initial concentration of N2 and H2
D. Volume of the reactor
A. Decreases
B. Increases
D. Unpredictable
A. High temperature and low pressure
C. High pressure and low temperature
D. Low pressure & temperature
A. Constant proportion
B. Multiple proportion
C. None of these
B. ?T
C. exp (-E/2RT)
D. exp (-E/RT)
B. A N
C. A
D. N
B. Concentration of the product
C. Time
D. Concentration of the reactant
A. Only chemical
B. Only physical
D. Neither A. nor B.
A. 4
B. 3
D. 1
A. Reactor volume
B. Extent of reaction
C. Feed rate
A. Continuously decreases
B. Continuously increases
D. Passes through a minimum
A. Junkers calorimeter
B. Kjeldahl
C. Dumas
A. Olefins
B. Naphthenes
A. Pressure
C. Both A. & B.
A. 1.33
C. 0.8
D. 2.67
A. Stability
B. Selectivity
D. Chemisorbed
A. Elementary
B. None of these
C. Parallel
A. Employs mixing in axial direction only
B. Is same as plug-flow reactor
D. Is most suitable for gas phase reaction
A. CSTRs connected in series
B. A plug-flow reactor
C. A well stirred batch reactor
A. Potential
D. Kinetic
A. Mercaptans
C. Naphthenic acid
D. Paraffins
A. Litre/mole
C. Moles/litre.second
D. Litre/second
A. (E + ED)/2
B. The intrinsic activation energy E
C. (E + ED) where ED is activation due to diffusion
A. Temperature
C. Pressure
D. Composition of reactant
A. 0
C. > 1
D. ?
A. Both forward and backward reactions will be exothermic
B. Neither of the reactions will be endothermic
D. othermic</strong>
E. The combination reaction will be endothermic, while the dissociation reaction will be
F. thermic
B. An active surface of the catalyst
C. Large catalyst particle size
D. Small pore diameter
B. Only
C. To a greater extent than that of the backward reaction
D. And decreases that of the backward reaction
A. For large diameter tubular reactor
C. For narrow diameter tubular reactor
D. For CSTR
A. None of these
C. Equilibrium constant
D. Heat of reaction
C. Inversely proportional to
D. Directly proportional to
A. 50 atm & 750C
C. 30 atm & 200C
D. 10 atm & 500C
B. Desorption
C. Adsorption
D. Surface chemical reaction
A. Tank in series
B. Dispersion
A. More than
B. Less than
D. Either B. or C.
A. 0.3
C. 0.9
D. 0.15
A. Series of CSTR
B. Plug flow reactor
D. PFR in series
A. Lack of intraparticle diffusion resistance
B. Presence of two mobile phases
B. Liquid petroleum gas
C. Liquid petrol gas
D. Liquefied petrol gas
A. HF
B. H2SO4
D. H3PO4
A. Is always equal to the overall order of reaction
B. May not be equal to the order of reaction
C. Cant have a fractional value
A. Discoloration
B. Thermal cracking
C. Gum formation
C. 0
A. Quality & yield cannot be achieved in continuous processes, because of long residence time
B. Sales demand is fluctuating
B. Yellow
C. Black
D. Red
A. A plug flow reactor followed by CSTR
B. A CSTR
C. CSTR in series
A. 22
C. 28
D. 3
A. Use high pressure and eliminate inerts, when a > b
B. Use CSTR with a high conversion, when a > b
C. Use batch reactor or plug flow reactor, when a > b
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