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Aromatic transformations over aluminosilicate micro/mesoporous composite materials

机译:铝硅酸盐微/介孔复合材料的芳香转化

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摘要

Catalytic behavior of micro/mesoporous ZSM-5/MCM-41 composites were investigated in the transformation of 1,2,4-trimethylbenzene (TMB), meta-xylene transformation and in the cracking of 1,3,5-triisopropylbenzene (TIPB). The samples were characterized by XRD, TGA, SEM, nitrogen sorption and FTIR of pyridine adsorption. The composite materials exhibited exceptional catalytic performance compared with the microporous ZSM-5 in the transformation of 1,2,4-trimethylbenzene and m-xylene. In the cracking of 1,3,5-triisopropylbenzene, the composite materials showed higher activity as compared with the conventional Y-zeolite. The distinctive catalytic performance of these micro/mesoporous composite materials in the reactions studied was attributed to the excellent accessibility of the active sites provided by the mesopores for both reactant and product molecules. In the transformation of m-xylene, selectivity towards para-xylene over all catalysts under study follows the order: conventional ZSM-5≈ ZM41A1 < ZM41A2 < ZM41A3.
机译:在1,2,4-三甲基苯(TMB),荟萃二甲苯转化和1,3,5-3,5-三甲苯甲苯(TIPB)的破裂中,研究了微/介孔ZSM-5/MCM-41复合材料的催化行为。 。样品的特征是XRD,TGA,SEM,氮吸附和吡啶吸附的FTIR。与微孔ZSM-5相比,复合材料在1,2,4-三甲基苯和M-二甲苯的转化中表现出非凡的催化性能。在1,3,5-三异丙基苯的破裂中,复合材料与常规Y-沸石相比显示出更高的活性。这些反应中这些微/介孔复合材料的独特催化性能归因于中孔为反应物和产物分子提供的活性位点的出色可访问性。在M-二甲苯的转化中,对所有研究的催化剂对二甲苯的选择性遵循:常规ZSM-5≈ZM41A1

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