Chem. J. Chinese Universities

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Conversion of Hydrocarbons over Nano-HZSM-5 Catalysts

ZHANG Pei-Qing1, GUO Hong-Chen2, ZHU Hong-Jie1, WANG Xiang-Sheng2, JIANG Xue-Mei1, WANG Ping1   

    1. Institute of Applied Catalysis, Yantai University, Yantai 264005, China;
    2. State Key Laboratory of Fine Chemicals, Institute of Industrial Catalysts, Dalian University of Technology, Dalian 116012, China
  • Received:2006-01-10 Revised:1900-01-01 Online:2006-12-10 Published:2006-12-10
  • Contact: ZHANG Pei-Qing

Abstract: The nanoscale HZSM-5(20—50nm) catalyst was prepared, and characterized by XRF, TEM, NH3-TPD and so on. The performance of the nanoscale HZSM-5 catalysts for conversion of n-octane, the mixture of n-octane and benzene was evaluated. The transformation behavior of both single and mixing hydrocarbons as the model reactants over the nanoscale HZSM-5 catalyst was investigated, the influences of the reaction conditions on product distribution were investigated, and reaction mechanism was also studied. The results indicate that the nanoscale HZSM-5 catalyst exhibits a higher ability to convert hydrocarbons, and the hydrocarbons were converted mainly into aromatics and iso-paraffins which have a high octane value by isomerization, aromatization, alkylation reactions and so on, as a result, the total amount of the iso-paraffins(C4—C6)and aromatics in products was above 90%(mass fraction). The aromatization from single hydrocarbons mainly produced benzene via dehydrocyclization process, whereas the aromatization from the mixing hydrocarbons formed alkyl-aromatics mostly by alkylation of benzene and small molecule hydrocarbons. The formation of benzene and C+9 could be restrained by regulating the reaction conditions. The analysis of the products shows that the cracking, aromatization and isomerization reaction of hydrocarbons such as octane and benzene-n-octane over the nanoscale HZSM-5 catalyst followed the carbonium ion mechanism.

Key words: Nanoscale HZSM-5 zeolite, n-Octane, Benzene, Isomerization, Aromatization, Alkylation

CLC Number: 

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