期刊
MICROPOROUS AND MESOPOROUS MATERIALS
卷 210, 期 -, 页码 52-59出版社
ELSEVIER SCIENCE BV
DOI: 10.1016/j.micromeso.2015.02.018
关键词
Toluene methylation; Methanol conversion; Xylene isomerization; p-Xylene selectivity; Acid chemistry in zeolites
类别
资金
- Deutsche Forschungsgemeinschaft (DFG) [JE 260-10/1]
- Fonds der Chemischen Industrie
The p-xylene selectivity in toluene methylation was investigated over medium pore-size zeolites (H-ZSM5, H-ZSM11 and H-NU10) as well as after deposition of tetraethyl orthosilicate on the surface, isomorphous substitution of aluminum by iron and variation the crystal size. Higher reaction temperatures consistently resulted in higher p-xylene selectivity in the three reaction pathways for the formation of p-xylene during toluene methylation, i.e., methylation of toluene, isomerization of xylenes, further methylation and subsequent formation of xylenes after dealkylation of light hydrocarbons. The increased selectivity is attributed to the accumulation of slowly diffusing reaction products in the zeolite pores. Thus, the isomerization of m- and o-xylenes, as well as dealkylation of higher alkylated products influenced the xylene selectivity most strongly at high temperatures, while the intrinsic selectivity of the toluene alkylation dominates at lower reaction temperatures due to the absence of transport restrictions. (c) 2015 Elsevier Inc. All rights reserved.
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