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Enhancing consecutive reactions during three phase hydrogenation with a semibatch liquid phase

机译:半间歇液相在三相氢化过程中增强连续反应

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摘要

Kinetics for citral hydrogenation was investigated over a Ni/Al2O3 catalyst both in semibatch and in batch mode with respect to the liquid phase. In the former case the liquid phase was pumped out from the reactor continuously, while the amount of catalyst was kept constant during the hydrogenation in the latter case. The idea with liquid phase drainage was to increase the catalyst bulk density with increasing reaction time. The effect of increasing catalyst bulk density on reaction kinetics and selectivity was investigated both qualitatively and quantitatively. The main parameters were hydrogen pressure (5-21 bar) and temperature (50-90 degC). The product selectivity, which should theoretically be independent on the changes in catalyst bulk density, varied with varying catalyst bulk density, especially at higher reaction temperatures due to catalyst deactivation. The simplified kinetic model with lumped kinetic and deactivation parameters was applied to the experimental data being able to explain results obtained under semibatch conditions with continuous liquid phase drainage out of the reactor.
机译:在Ni / Al2O3催化剂上以半间歇和间歇方式对柠檬酸进行了动力学研究。在前一种情况下,将液相连续地从反应器中泵出,而在后一种情况下,在氢化期间催化剂的量保持恒定。液相排水的想法是随着反应时间的增加而增加催化剂的堆积密度。定性和定量地研究了增加催化剂堆积密度对反应动力学和选择性的影响。主要参数是氢气压力(5-21巴)和温度(50-90摄氏度)。理论上应独立于催化剂堆积密度变化的产物选择性随催化剂堆积密度的变化而变化,特别是由于催化剂失活而在较高的反应温度下。将具有集总动力学和失活参数的简化动力学模型应用于实验数据,该实验模型能够解释在半间歇条件下连续液相排出反应器的结果。

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