论文部分内容阅读
用浸渍法制备CeO_2/SiO_2催化剂.催化剂灼烧温度在300-500℃时2-丁烯异构化活性保持一常数;600℃灼烧时活性下降,活载比在1/32-1/5范围内,随活载比增加催化剂活性呈线性增加.在2-丁烯分压较低时,t-2-丁烯及c-2-丁烯异构成1-丁烯的反应级数接近于一级.1-丁烯分压较大时1-丁烯异构成t-2-丁烯及c-2-丁烯的动力学服从于反应物、反应产物吸附的L-H动力学方程.用正交设计法估计动力学参数.1-丁烯、t-2-丁烯及c-2-丁烯吸附热的估计值与脉冲法测定值一致.
The CeO 2 / SiO 2 catalyst was prepared by impregnation method.The isomerization activity of 2-butene was kept constant at the calcination temperature of 300-500 ℃, the activity decreased when calcined at 600 ℃, and the viability ratio was 1 / 32-1 / 5 Within the range, the catalyst activity increases linearly with the increase of the living load ratio. When the partial pressure of 2-butene is low, the reaction order of the isomerization of t-2-butene and c-2-butene to 1-butene is close to one order. The kinetics of the isomerization of 1-butene to t-2-butene and c-2-butene at 1-butene partial pressure is obeyed by L-H kinetics equation of reactant and reaction product adsorption. Estimating kinetic parameters by orthogonal design. The estimates of 1-butene, t-2-butene and c-2-butene heat of adsorption are consistent with those of the pulsed method.