Characterization of Mo Species Supported on SiO2 Modified with Be2+ and Mg2+

Phryni Aroni
{"title":"Characterization of Mo Species Supported on SiO2 Modified with Be2+ and Mg2+","authors":"Phryni Aroni","doi":"10.1002/bbpc.199700018","DOIUrl":null,"url":null,"abstract":"<p>Two series of modified carriers (m.c.) have been prepared by doping silica with various amounts of Be<sup>2+</sup> and Mg<sup>2+</sup>. The prepared m.c. have been used as supports for the preparation of supported Mo<sup>(VI)</sup> oxide catalysts. The magnitude of interactions between SiO<sub>2</sub> and Be<sup>2+</sup> or Mg<sup>2+</sup> nitrates depends on the kind and content of the cation. After calcination at 600°C a greater fraction of cations remains on the support surface as well dispersed M(NO<sub>2</sub>)<sub>2</sub> in the case of Mg<sup>2+</sup> m.c. Concerning the Mo containing samples it was found that doping by Be<sup>2+</sup> and Mg<sup>2+</sup> causes a solid state transformation of octahedral Mo<sup>(VI)</sup> to tetrahedral Mo<sup>(VI)</sup>. As before, the extent of the effect differs between Be<sup>2+</sup> and Mg<sup>2+</sup> and it varies with the content of cation. This effect has been attributed to the inhibition of the polymerization of monomeric Mo<sup>(VI)</sup> species and/or to the formation of molybdate salts.</p>","PeriodicalId":100156,"journal":{"name":"Berichte der Bunsengesellschaft für physikalische Chemie","volume":"101 10","pages":"1544-1548"},"PeriodicalIF":0.0000,"publicationDate":"2014-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/bbpc.199700018","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Berichte der Bunsengesellschaft für physikalische Chemie","FirstCategoryId":"1085","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/bbpc.199700018","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Two series of modified carriers (m.c.) have been prepared by doping silica with various amounts of Be2+ and Mg2+. The prepared m.c. have been used as supports for the preparation of supported Mo(VI) oxide catalysts. The magnitude of interactions between SiO2 and Be2+ or Mg2+ nitrates depends on the kind and content of the cation. After calcination at 600°C a greater fraction of cations remains on the support surface as well dispersed M(NO2)2 in the case of Mg2+ m.c. Concerning the Mo containing samples it was found that doping by Be2+ and Mg2+ causes a solid state transformation of octahedral Mo(VI) to tetrahedral Mo(VI). As before, the extent of the effect differs between Be2+ and Mg2+ and it varies with the content of cation. This effect has been attributed to the inhibition of the polymerization of monomeric Mo(VI) species and/or to the formation of molybdate salts.

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
Be2+和Mg2+改性SiO2负载Mo物质的表征
通过在二氧化硅中掺杂不同量的Be2+和Mg2+,制备了两种改性载体(m.c)。所制备的金属氧化物用作载体,用于制备负载型Mo(VI)氧化物催化剂。SiO2与Be2+或Mg2+硝酸盐相互作用的大小取决于阳离子的种类和含量。在600℃煅烧后,Mg2+ Mg2的载体表面保留了较大比例的阳离子,并且分散了M(NO2)2。对于含Mo样品,Be2+和Mg2+的掺杂导致八面体Mo(VI)向四面体Mo(VI)的固态转变。和前面一样,Be2+和Mg2+的作用程度不同,且随阳离子含量的变化而变化。这种效应归因于抑制单体Mo(VI)的聚合和/或钼酸盐的形成。
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
自引率
0.00%
发文量
0
期刊最新文献
Shock Tube Study of the Reaction of Si Atoms with SiCl4 Electrochemistry of Steel Electrodes: A Combined Study by Linear Reflectivity Measurements and Second Harmonic Generation G. Lagaly, O. Schulz und R. Zimehl: Dispersionen und Emulsionen, ca. 420 Seiten, 243 Abb., Steinkopff, Darmstadt, ISBN 3-7985-1087-3, DM 78,00 Correlation Times and Quadrupole Coupling Constants in Liquid N-Methylformamide and N-Methylacetamide Investigation of the Pyrolysis and Crystallization of Lead Zirconate Titanate Ceramics Prepared via the Sol Gel Process
×
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