Experimental verification of double-four-ring-type aluminosilicate molecule as a single-source precursor for zeolite synthesis

IF 3.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Bulletin of the Chemical Society of Japan Pub Date : 2024-06-08 DOI:10.1093/bulcsj/uoae060
Akira Imaizumi, Yurika Ohnishi, Akinobu Nakada, Akinori Honda, Takeshi Matsumoto, Kenji Katayama, Ho-Chol Chang
{"title":"Experimental verification of double-four-ring-type aluminosilicate molecule as a single-source precursor for zeolite synthesis","authors":"Akira Imaizumi, Yurika Ohnishi, Akinobu Nakada, Akinori Honda, Takeshi Matsumoto, Kenji Katayama, Ho-Chol Chang","doi":"10.1093/bulcsj/uoae060","DOIUrl":null,"url":null,"abstract":"\n While a variety of functional zeolites have been synthesized using hydrothermal methods with conventional discrete Al and Si sources, control of the composition, structure, and function of the targeted zeolites often involves costly and time-consuming trial-and-error approaches. Despite ongoing efforts to manipulate zeolite formation by adjusting Al and Si sources and reaction conditions, limited attention has been given to studies on zeolite synthesis using molecular precursors (MPs) with pre-organized Al–O–Si bonds. Here, we demonstrate the synthesis of LTA-type zeolites using [TMA]4[Al4Si4O12(OH)8]·13H2O ([MP]; TMA = tetramethylammonium cation) with a double-four-ring (D4R)-type core structure, which is known to be a secondary building unit (SBU) in the LTA-type zeolite, as a MP. Here, we demonstrate the successful synthesis of LTA-type zeolites using [MP] under hydrothermal conditions at 100–200 °C in the presence of 1 equivalent of NaOH or NaCl. Notably, when discrete Al and Si sources were used instead of [MP] under otherwise identical conditions (the same Si/Al ratio, Na+ content, and temperature), GIS-, SOD-, and FAU-type zeolites lacking the D4R structure were obtained in addition to the LTA-type zeolites.","PeriodicalId":9511,"journal":{"name":"Bulletin of the Chemical Society of Japan","volume":null,"pages":null},"PeriodicalIF":3.3000,"publicationDate":"2024-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Bulletin of the Chemical Society of Japan","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1093/bulcsj/uoae060","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

While a variety of functional zeolites have been synthesized using hydrothermal methods with conventional discrete Al and Si sources, control of the composition, structure, and function of the targeted zeolites often involves costly and time-consuming trial-and-error approaches. Despite ongoing efforts to manipulate zeolite formation by adjusting Al and Si sources and reaction conditions, limited attention has been given to studies on zeolite synthesis using molecular precursors (MPs) with pre-organized Al–O–Si bonds. Here, we demonstrate the synthesis of LTA-type zeolites using [TMA]4[Al4Si4O12(OH)8]·13H2O ([MP]; TMA = tetramethylammonium cation) with a double-four-ring (D4R)-type core structure, which is known to be a secondary building unit (SBU) in the LTA-type zeolite, as a MP. Here, we demonstrate the successful synthesis of LTA-type zeolites using [MP] under hydrothermal conditions at 100–200 °C in the presence of 1 equivalent of NaOH or NaCl. Notably, when discrete Al and Si sources were used instead of [MP] under otherwise identical conditions (the same Si/Al ratio, Na+ content, and temperature), GIS-, SOD-, and FAU-type zeolites lacking the D4R structure were obtained in addition to the LTA-type zeolites.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
双四环型硅酸铝分子作为沸石合成单源前驱体的实验验证
虽然利用传统离散铝源和硅源的水热法合成了多种功能沸石,但要控制目标沸石的组成、结构和功能,往往需要采用成本高、耗时长的试错法。尽管人们一直在努力通过调整铝和硅源及反应条件来操纵沸石的形成,但对使用具有预组织铝-氧-硅键的分子前驱体(MPs)合成沸石的研究却关注有限。在此,我们展示了使用具有双四环(D4R)型核心结构的[TMA]4[Al4Si4O12(OH)8]-13H2O([MP];TMA = 四甲基铵阳离子)作为 MP 合成 LTA 型沸石的过程,双四环(D4R)型核心结构是 LTA 型沸石中已知的二级构建单元(SBU)。在此,我们展示了在 100-200 °C 水热条件下,在 1 个等量的 NaOH 或 NaCl 存在下,利用 [MP] 成功合成 LTA 型沸石的过程。值得注意的是,在其他条件相同(相同的硅/铝比例、Na+含量和温度)的情况下,当使用离散的铝和硅源代替[MP]时,除了获得LTA型沸石外,还获得了缺乏D4R结构的GIS型、SOD型和FAU型沸石。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
6.40
自引率
5.00%
发文量
194
审稿时长
3-8 weeks
期刊介绍: The Bulletin of the Chemical Society of Japan (BCSJ) is devoted to the publication of scientific research papers in the fields of Theoretical and Physical Chemistry, Analytical and Inorganic Chemistry, Organic and Biological Chemistry, and Applied and Materials Chemistry. BCSJ appears as a monthly journal online and in advance with three kinds of papers (Accounts, Articles, and Short Articles) describing original research. The purpose of BCSJ is to select and publish the most important papers with the broadest significance to the chemistry community in general. The Chemical Society of Japan hopes all visitors will notice the usefulness of our journal and the abundance of topics, and welcomes more submissions from scientists all over the world.
期刊最新文献
Catalytic Combustion of Toluene over Co3O4 loaded on ZrSn1−xFexO4−δ The activity of thermostable NiO/CeO2 heterointerface structure toward low-temperature catalytic CO–NO reaction Deoxygenative Functionalizations of Aromatic Dicarbonyls and Aldehydes Black Phosphorus Quantum Dots Functionalized with Photochromic Poly(vinylspiropyran)-Grafted Polydopamine for Transient Digital-Type Memristors Sulfonate-Functionalized Covalent Organic Frameworks for Capacitive Deionization
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1