详细信息

Petaloid Znalox/Hzsm-5 Catalyst with Metal Modification for Highly Selective Conversion of Syngas to Value-Added Aromatics  ( EI收录)  

文献类型:期刊文献

英文题名:Petaloid Znalox/Hzsm-5 Catalyst with Metal Modification for Highly Selective Conversion of Syngas to Value-Added Aromatics

作者:Wang, Zihao[1]; Li, Minzhe[1]; Nawaz, Muhammad Asif[1]; Liu, Dianhua[1]

机构:[1] Engineering Research Center of Large Scale Reactor Engineering and Technology, Ministry of Education, State Key Laboratory of Chemical Engineering, School of Chemical Engineering, East China University of Science and Technology, Shanghai, 200237, China

年份:2023

外文期刊名:SSRN

收录:EI(收录号:20230169052)

语种:英文

外文关键词:Alkylation - Catalyst selectivity - Manganese compounds - Synthesis gas - Synthesis gas manufacture - Zeolites - Zinc compounds

摘要:Syngas can be efficiently converted to multimethylbenzenes by integrating a methanol synthesis catalyst with HZSM-5 zeolites, where 1,2,4,5-tetramethylbenzene (durene) is a high value-added product used in polyimide synthesis. Here, we synthesized a Mn modified ZnAlOx catalyst with petaloid structure and integrated with HZSM-5 as a bifunctional catalyst for targeting the high selectivity durene. Various characterization approaches including XRD, BET, XPS, SEM, TEM, TPD, TPR, and in-situ FTIR were adopted to illustrate the deeper analysis of highly efficient catalyst. It was demonstrated that the strong synergy of ZnAlOx staggered sheet and nanoclusters MnOx caused higher concentration of H3CO* species and methanol/DME intermediates, which promote the methylation of trimethylbenzene over HZSM-5 zeolites. The combination 7%Mn-ZnAlOx/ HZSM-5 exhibited a high CO conversion of 56.4% and 44.6% tetramethylbenzene selectivity at 360 ℃ and 5.0 MPa, with an excellent stability of 100h. In addition, through trace methanol co-feeding experiment, it was proposed that there is an appropriate amount of methyl intermediates to match with the synthesized zeolite to obtain a maximum selectivity to tetramethylbenzene. ? 2023, The Authors. All rights reserved.

参考文献:

正在载入数据...

版权所有©华东理工大学 重庆维普资讯有限公司 渝B2-20050021-7 
渝公网安备 50019002500408号 违法和不良信息举报中心