Hydrogen transfer versus olefins methylation: On the formation trend of propene in the methanol-to-hydrocarbons reaction over Beta zeolites
文献类型:期刊论文
作者 | Yuan, Yangyang1; Zhang, Jie1,2; Xu, Lanjian1,2; Zhang, Yanfei1,2; Huang, Zhihua1,2; Zhang, Xiaomin1; Zhang, Xinzhi1; Xu, Lei1 |
刊名 | JOURNAL OF CATALYSIS
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出版日期 | 2018-12-01 |
卷号 | 368页码:248-260 |
关键词 | Methanol to hydrocarbons Beta Bronsted acid site density Hydrogen transfer Methylation Cracking |
ISSN号 | 0021-9517 |
DOI | 10.1016/j.jcat.2018.10.015 |
通讯作者 | Yuan, Yangyang(yuanyangyang@dicp.ac.cn) ; Xu, Lei(leixu@dicp.ac.cn) |
英文摘要 | Beta zeolites with similar textural properties but variable Bronsted acid site (BAS) densities in the range of 25.5-203.8 mu mol g(-1) were fabricated and investigated as catalysts in the methanol-to-hydrocarbons reaction. The intrinsic influence of BAS amount, BAS density and methanol conversion on the reaction mechanism was investigated. Interestingly, methanol conversion depends on the BAS amount regardless of the BAS density. The increase of methanol concentration could modulate the product distribution by promoting the methanol -induced hydrogen transfer reaction and enhancing the olefins methylation as well as inhibiting the cracking of higher olefins. As the BAS density decreases from 203.8 to 56.6 mu mol g(-1), hydrogen transfer reaction is gradually restrained while the olefin interconversion is enhanced, leading to gradual replacement of aromatics-based cycle by the olefins-based cycle and thus increasing the propene selectivity. However, as BAS density further decreases from 56.6 mu mol g(-1), the propene selectivity declines because the methylation route in the olefins-based cycle is much more favoured than the cracking route. After detailed investigation of the deactivation behaviours of involved Beta zeolites, it has been found that the accumulation of long-chain alkanes and large polycyclic aromatics is responsible for the catalyst deactivation. These results provide further insights into the effect of BAS density on the reaction mechanism and product selectivity. (C) 2018 Elsevier Inc. All rights reserved. |
WOS关键词 | REACTION-MECHANISM ; CATALYTIC PERFORMANCE ; SHAPE SELECTIVITY ; PROPYLENE PRODUCTION ; PRODUCT SELECTIVITY ; COKE FORMATION ; MTO REACTION ; CONVERSION ; H-ZSM-5 ; DEACTIVATION |
资助项目 | National Natural Science Foundation of China[21576252] ; National Natural Science Foundation of China[21506202] |
WOS研究方向 | Chemistry ; Engineering |
语种 | 英语 |
WOS记录号 | WOS:000452582500024 |
出版者 | ACADEMIC PRESS INC ELSEVIER SCIENCE |
资助机构 | National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China ; National Natural Science Foundation of China |
源URL | [http://cas-ir.dicp.ac.cn/handle/321008/166446] ![]() |
专题 | 大连化学物理研究所_中国科学院大连化学物理研究所 |
通讯作者 | Yuan, Yangyang; Xu, Lei |
作者单位 | 1.Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China 2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China |
推荐引用方式 GB/T 7714 | Yuan, Yangyang,Zhang, Jie,Xu, Lanjian,et al. Hydrogen transfer versus olefins methylation: On the formation trend of propene in the methanol-to-hydrocarbons reaction over Beta zeolites[J]. JOURNAL OF CATALYSIS,2018,368:248-260. |
APA | Yuan, Yangyang.,Zhang, Jie.,Xu, Lanjian.,Zhang, Yanfei.,Huang, Zhihua.,...&Xu, Lei.(2018).Hydrogen transfer versus olefins methylation: On the formation trend of propene in the methanol-to-hydrocarbons reaction over Beta zeolites.JOURNAL OF CATALYSIS,368,248-260. |
MLA | Yuan, Yangyang,et al."Hydrogen transfer versus olefins methylation: On the formation trend of propene in the methanol-to-hydrocarbons reaction over Beta zeolites".JOURNAL OF CATALYSIS 368(2018):248-260. |
入库方式: OAI收割
来源:大连化学物理研究所
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