有机定向结构剂合成纯二氧化硅分子筛的进一步研究

K. Tsuji, M.E. Davis
{"title":"有机定向结构剂合成纯二氧化硅分子筛的进一步研究","authors":"K. Tsuji,&nbsp;M.E. Davis","doi":"10.1016/S0927-6513(97)00024-2","DOIUrl":null,"url":null,"abstract":"<div><p>Several organic structure-directing agents (SDAs) that are variations of a 4,4′-trimethylenebis(<em>N</em>-methyl, <em>N</em>-R<sub>1</sub>-piperidinium) moiety were synthesized and used for the synthesis of pure-silica molecular sieves. Pure-silica MTW, MFI, BEA and the MCM-41-type mesoporous materials could be prepared by changing only the R<sub>1</sub> group. When R<sub>1</sub> was pentyl or hexyl, MFI was crystallized, suggesting that each SDA molecule spans two channel intersections. For R<sub>1</sub> groups smaller than pentyl, MTW was formed. Pure-silica BEA could easily be prepared when R<sub>1</sub> was benzyl or cyclohexylmethyl. Numerous variations of the organics used to crystallize BEA were explored and the features necessary to structure direct the formation of BEA elucidated. When R<sub>1</sub> was either octyl or nonyl, the MCM-41-type mesoporous materials were formed, indicating that these organics can act as surfactants. The results presented provide further evidence that organic molecules can serve as structure-directing agents for the synthesis of pure-silica molecular sieves.</p></div>","PeriodicalId":100926,"journal":{"name":"Microporous Materials","volume":"11 1","pages":"Pages 53-64"},"PeriodicalIF":0.0000,"publicationDate":"1997-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0927-6513(97)00024-2","citationCount":"24","resultStr":"{\"title\":\"Further investigations on the synthesis of pure-silica molecular sieves via the use of organic structure-directing agents\",\"authors\":\"K. Tsuji,&nbsp;M.E. Davis\",\"doi\":\"10.1016/S0927-6513(97)00024-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Several organic structure-directing agents (SDAs) that are variations of a 4,4′-trimethylenebis(<em>N</em>-methyl, <em>N</em>-R<sub>1</sub>-piperidinium) moiety were synthesized and used for the synthesis of pure-silica molecular sieves. Pure-silica MTW, MFI, BEA and the MCM-41-type mesoporous materials could be prepared by changing only the R<sub>1</sub> group. When R<sub>1</sub> was pentyl or hexyl, MFI was crystallized, suggesting that each SDA molecule spans two channel intersections. For R<sub>1</sub> groups smaller than pentyl, MTW was formed. Pure-silica BEA could easily be prepared when R<sub>1</sub> was benzyl or cyclohexylmethyl. Numerous variations of the organics used to crystallize BEA were explored and the features necessary to structure direct the formation of BEA elucidated. When R<sub>1</sub> was either octyl or nonyl, the MCM-41-type mesoporous materials were formed, indicating that these organics can act as surfactants. The results presented provide further evidence that organic molecules can serve as structure-directing agents for the synthesis of pure-silica molecular sieves.</p></div>\",\"PeriodicalId\":100926,\"journal\":{\"name\":\"Microporous Materials\",\"volume\":\"11 1\",\"pages\":\"Pages 53-64\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1997-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S0927-6513(97)00024-2\",\"citationCount\":\"24\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Microporous Materials\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0927651397000242\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Microporous Materials","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0927651397000242","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 24

摘要

合成了几种由4,4′-三亚甲基二(n -甲基,n - r1 -哌替啶)组成的有机结构导向剂(sda),并将其用于合成纯二氧化硅分子筛。仅改变R1基团即可制备纯二氧化硅MTW、MFI、BEA和mcm -41型介孔材料。当R1为戊基或己基时,MFI结晶,表明每个SDA分子跨越两个通道交叉点。小于戊基的R1基团形成MTW。当R1为苄基或环己基甲基时,可以很容易地制备出纯硅BEA。探索了用于BEA结晶的多种有机物,并阐明了指导BEA形成的结构所必需的特征。当R1为辛基或壬基时,形成mcm -41型介孔材料,表明这些有机物可以作为表面活性剂。这些结果进一步证明了有机分子可以作为结构导向剂用于纯硅分子筛的合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Further investigations on the synthesis of pure-silica molecular sieves via the use of organic structure-directing agents

Several organic structure-directing agents (SDAs) that are variations of a 4,4′-trimethylenebis(N-methyl, N-R1-piperidinium) moiety were synthesized and used for the synthesis of pure-silica molecular sieves. Pure-silica MTW, MFI, BEA and the MCM-41-type mesoporous materials could be prepared by changing only the R1 group. When R1 was pentyl or hexyl, MFI was crystallized, suggesting that each SDA molecule spans two channel intersections. For R1 groups smaller than pentyl, MTW was formed. Pure-silica BEA could easily be prepared when R1 was benzyl or cyclohexylmethyl. Numerous variations of the organics used to crystallize BEA were explored and the features necessary to structure direct the formation of BEA elucidated. When R1 was either octyl or nonyl, the MCM-41-type mesoporous materials were formed, indicating that these organics can act as surfactants. The results presented provide further evidence that organic molecules can serve as structure-directing agents for the synthesis of pure-silica molecular sieves.

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