浆料反应器中二甲醚合成低烯烃的Mg/HZSM-5催化剂失活特性

A. Stashenko, T. Batova, T. Obukhova, N. Kolesnichenko
{"title":"浆料反应器中二甲醚合成低烯烃的Mg/HZSM-5催化剂失活特性","authors":"A. Stashenko, T. Batova, T. Obukhova, N. Kolesnichenko","doi":"10.18412/1816-0387-2023-3-24-31","DOIUrl":null,"url":null,"abstract":"In a slurry reactor, the formation of compaction products on Mg/HZSM-5 catalysts, irrespective of the SiO2 /Al2O3 molar ratio in the zeolite, proceeds predominantly on strong acidic sites. The composition of compaction products (mostly trimethyl- and tetramethylbenzenes) virtually does not change with a growth of the molar ratio; however, their amount decreases, which is related to a growth of the mesopore volume with an increase in the SiO2 /Al2O3 ratio. This leads to a decrease in diffusion limitations and contribution of secondary reactions and enhances the removal of coke precursors from the zeolite surface, thus promoting the catalyst activity (the conversion of DME increases twofold). The composition of reaction products changes only slightly with a growth of the SiO2 /Al2O3 molar ratio, the total selectivity to lower olefins is ca. 70 wt.%. A rapid loss of the Mg/HZSM-5 activity with extending the operation time in a slurry reactor is caused not by coking, but rather by «clogging» of the catalyst with decomposition products of the dispersion medium (polydimethylsiloxane).","PeriodicalId":17783,"journal":{"name":"Kataliz v promyshlennosti","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-06-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Features of the deactivation of Mg/HZSM-5 catalysts for the synthesis of lower olefins from dimethyl ether in a slurry reactor\",\"authors\":\"A. Stashenko, T. Batova, T. Obukhova, N. Kolesnichenko\",\"doi\":\"10.18412/1816-0387-2023-3-24-31\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In a slurry reactor, the formation of compaction products on Mg/HZSM-5 catalysts, irrespective of the SiO2 /Al2O3 molar ratio in the zeolite, proceeds predominantly on strong acidic sites. The composition of compaction products (mostly trimethyl- and tetramethylbenzenes) virtually does not change with a growth of the molar ratio; however, their amount decreases, which is related to a growth of the mesopore volume with an increase in the SiO2 /Al2O3 ratio. This leads to a decrease in diffusion limitations and contribution of secondary reactions and enhances the removal of coke precursors from the zeolite surface, thus promoting the catalyst activity (the conversion of DME increases twofold). The composition of reaction products changes only slightly with a growth of the SiO2 /Al2O3 molar ratio, the total selectivity to lower olefins is ca. 70 wt.%. A rapid loss of the Mg/HZSM-5 activity with extending the operation time in a slurry reactor is caused not by coking, but rather by «clogging» of the catalyst with decomposition products of the dispersion medium (polydimethylsiloxane).\",\"PeriodicalId\":17783,\"journal\":{\"name\":\"Kataliz v promyshlennosti\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-06-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Kataliz v promyshlennosti\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.18412/1816-0387-2023-3-24-31\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Kataliz v promyshlennosti","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18412/1816-0387-2023-3-24-31","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

在泥浆反应器中,无论沸石中SiO2 /Al2O3的摩尔比如何,Mg/HZSM-5催化剂上的压实产物主要在强酸性部位形成。压实产物(主要是三甲基苯和四甲基苯)的组成几乎不随摩尔比的增长而变化;随着SiO2 /Al2O3比的增大,介孔体积增大,其含量逐渐减少。这降低了扩散限制和二次反应的贡献,增强了焦炭前驱体从沸石表面的去除,从而提高了催化剂的活性(二甲醚的转化率提高了两倍)。随着SiO2 /Al2O3摩尔比的增加,反应产物的组成变化不大,对低烯烃的总选择性约为70 wt.%。随着浆料反应器中操作时间的延长,Mg/HZSM-5活性的快速损失不是由焦化引起的,而是由分散介质(聚二甲基硅氧烷)的分解产物“堵塞”催化剂引起的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Features of the deactivation of Mg/HZSM-5 catalysts for the synthesis of lower olefins from dimethyl ether in a slurry reactor
In a slurry reactor, the formation of compaction products on Mg/HZSM-5 catalysts, irrespective of the SiO2 /Al2O3 molar ratio in the zeolite, proceeds predominantly on strong acidic sites. The composition of compaction products (mostly trimethyl- and tetramethylbenzenes) virtually does not change with a growth of the molar ratio; however, their amount decreases, which is related to a growth of the mesopore volume with an increase in the SiO2 /Al2O3 ratio. This leads to a decrease in diffusion limitations and contribution of secondary reactions and enhances the removal of coke precursors from the zeolite surface, thus promoting the catalyst activity (the conversion of DME increases twofold). The composition of reaction products changes only slightly with a growth of the SiO2 /Al2O3 molar ratio, the total selectivity to lower olefins is ca. 70 wt.%. A rapid loss of the Mg/HZSM-5 activity with extending the operation time in a slurry reactor is caused not by coking, but rather by «clogging» of the catalyst with decomposition products of the dispersion medium (polydimethylsiloxane).
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信