Govt. Exams
Entrance Exams
For high activation energy reactions, the increasing temperature from adiabatic exothermic reactions in PFR increases reaction rate progressively, improving conversion over CSTR where temperature is uniform and lower.
For consecutive reactions, [B]max occurs at t_max = ln(k₁/k₂)/(k₁-k₂) = ln(2)/0.05 = 13.86 minutes
RTD in plug flow reactors is independent of flow rate only for ideal reactors without dispersion. In real reactors, axial dispersion effects vary with flow rate.
For second-order reactions with equal initial concentrations CA0 = CB0, the integrated form simplifies to: CA = CA0/(1+kCA0×t), leading to pseudo-first order kinetics behavior
Chain termination by combination or disproportionation determines when polymer chains stop growing, directly controlling final molecular weight and its distribution
Exothermic reactions generate heat; to achieve higher conversion without temperature runaway, external cooling must be provided to maintain reactor temperature within safe operating limits
Pore size distribution determines which reactants/products can access active sites, while active site specificity ensures desired reaction pathway is favored in parallel reactions
For reversible reactions, K = kf/kr = 0.1/0.02 = 5.0. This represents the ratio of forward to reverse rate constants at equilibrium
Using ln(k2/k1) = (Ea/R)×(1/T1 - 1/T2) = (80000/8.314)×(1/300 - 1/310) ≈ 0.693, so k2/k1 ≈ 2.0
Batch reactors provide excellent temperature control through jacket systems and are ideal for fine chemicals production where reaction conditions are critical and batch processing is economical