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The Alkylation of Mononuclear Aromatic Hydrocarbons and Related Reactions over H-ZSM-5 Catalysts Modified with Lanthanum and Cerium Oxides

机译:用镧和氧化铈改性的H-ZSM-5催化剂的单核芳烃和相关反应的烷基化

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The ethylation of ethylbenzene and the disproportionation of toluene were examined over H-ZSM-5 impregnated with lanthanum and cerium oxides. The selectivities for p-diethylbenzene and p-xylene were improved in both reactions by the impregnation of these oxides: lanthanum modification was more effective than cerium modification. The cracking of 1, 3, 5-triisopropylbenzene was effectively deactivated by the impregnation with both oxides, whereas the activity for the cracking of cumene was maintained over modified H-ZSM-5 catalysts. Adsorption of o-xylene was retarded significantly by lanthanum modification, whereas the adsorption to cerium modified H-ZSM-5 was in almost the same level as unmodified H-ZSM-5 although the rate of adsorption decreased by the modification. From these results, the improvement of the selectivities of p-isomers in both the ethylation of ethylbenzene and the disproportionation of toluene is due to the retardation of the isomerization of p-isomers at the external acid sites. The improvement of p-selectivity for H-ZSM-5 modified with lanthanum oxide is also due to the reactant selectivity by preferential diffusion of p-isomers from pores narrowed by the modification.
机译:通过浸渍镧和氧化铈的H-ZSM-5检查乙苯的乙基和甲苯的歧化。通过浸渍这些氧化物的反应在两种反应中改善了对二乙苯和p-二甲苯的选择性:镧改性比铈改性更有效。通过用两种氧化物浸渍有效地失活的裂化为1,3,5-三异丙基苯,而异丙苯裂解的活性在改性的H-ZSM-5催化剂上保持。通过镧改性,对O-二甲苯的吸附显着延迟,而对铈改性的H-ZSM-5的吸附几乎与未改性的H-ZSM-5几乎相同的水平,尽管通过改性吸附速率降低。从这些结果来看,乙苯的乙基乙基和甲苯的歧化中的P-异构体的选择性的改善是由于外酸位点对P-异构体的异构化的延迟。用氧化镧改性的H-ZSM-5的p型选择性的改善也是由于反应物选择性通过优先通过改性而变窄的P孔的优先扩散。

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