甲酚的催化加氢裂化

Khalil Ahmed Moghul, Y. Yamazaki, T. Kawai
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引用次数: 1

摘要

脱羟基;在加氢裂化前阶段还检测到歧化和异构化反应。在Al2O3 (cat-A)上负载的CoO-MoO3倾向于去羟基化而非去甲基化,而在MgO(cat-B)上负载的NiO倾向于去甲基化而非去羟基化。猫- a的歧化和异构化反应比猫- b的更明显。检测产物为苯酚、甲苯、2,6-二甲基苯酚、2,4-二甲基苯酚和间、对二甲苯。动力学使用传统的Langmuir-Hinshelwood模型进行关联。甲酚为一级反应模型,并提出了以羰基离子络合物为基础的反应机理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Catalytic Hydrocracking of Cresols
dehydroxylation; disproportionation and isomerization reactions were also detected in the advance stages of hydrocracking. CoO-MoO3 supported on Al2O3 (cat-A) favoured dehydroxylation over demethylation and NiO supported on MgO(cat-B) favoured demethylation over dehydroxylation. Disproportionation and isomerization reactions were more pronounced by cat-A than by cat-B. Products detected were phenol, toluene, 2,6-dimethylphenol, 2,4-dimethylphenol and m-, p-xylenes. Kinetics was correlated using a conventional Langmuir-Hinshelwood model. The model was first order with respect to cresol, and the reaction mechanism based on carbonium ion complex formation was suggested.
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