Characterisation of stoichiometric sol–gel mullite by fourier transform infrared spectroscopy

P Padmaja, G.M Anilkumar, P Mukundan, G Aruldhas, K.G.K Warrier
{"title":"Characterisation of stoichiometric sol–gel mullite by fourier transform infrared spectroscopy","authors":"P Padmaja,&nbsp;G.M Anilkumar,&nbsp;P Mukundan,&nbsp;G Aruldhas,&nbsp;K.G.K Warrier","doi":"10.1016/S1466-6049(01)00189-1","DOIUrl":null,"url":null,"abstract":"<div><p><span>Fourier Transform Infrared Spectroscopic investigation has been carried out to study the structural changes and coordination of Al and Si in the mullite system as a function of temperature (60–1400°C). The FTIR spectral patterns of the gel and the gel calcined at 200°C show bands corresponding to Al–O–Al and Si–O–Si vibrations. At higher temperatures hydroxyl groups and organics present have been removed. The absence of fine structure in the region 400–900 cm</span><sup>−1</sup> in the temperature range 400–1000°C is interpreted as due to the existence of nanostructured alumina, silica and alumina–silica agglomeration in the amorphous state. Analysis of the spectra indicates the presence of both octahedral and tetrahedral coordination at 1000°C, the temperature around which spinel is formed. The shifting of the asymmetric stretching frequencies of the Si–O–Si and Al–O–Si networks to higher wave numbers indicate the formation of mullite at 1200°C. Crystalline nature of the product is indicated by the sharpening of spectral peaks. The spectra also indicates the completion of mullite formation at 1250°C.</p></div>","PeriodicalId":100700,"journal":{"name":"International Journal of Inorganic Materials","volume":"3 7","pages":"Pages 693-698"},"PeriodicalIF":0.0000,"publicationDate":"2001-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1466-6049(01)00189-1","citationCount":"150","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International Journal of Inorganic Materials","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1466604901001891","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 150

Abstract

Fourier Transform Infrared Spectroscopic investigation has been carried out to study the structural changes and coordination of Al and Si in the mullite system as a function of temperature (60–1400°C). The FTIR spectral patterns of the gel and the gel calcined at 200°C show bands corresponding to Al–O–Al and Si–O–Si vibrations. At higher temperatures hydroxyl groups and organics present have been removed. The absence of fine structure in the region 400–900 cm−1 in the temperature range 400–1000°C is interpreted as due to the existence of nanostructured alumina, silica and alumina–silica agglomeration in the amorphous state. Analysis of the spectra indicates the presence of both octahedral and tetrahedral coordination at 1000°C, the temperature around which spinel is formed. The shifting of the asymmetric stretching frequencies of the Si–O–Si and Al–O–Si networks to higher wave numbers indicate the formation of mullite at 1200°C. Crystalline nature of the product is indicated by the sharpening of spectral peaks. The spectra also indicates the completion of mullite formation at 1250°C.

化学计量溶胶-凝胶莫来石的傅里叶变换红外光谱表征
利用傅里叶变换红外光谱研究了莫来石体系中Al和Si的结构变化和配位随温度(60-1400℃)的变化。凝胶和200°C煅烧凝胶的FTIR谱图显示对应于Al-O-Al和Si-O-Si的振动带。在较高的温度下,羟基和有机物被去除。在400-1000°C温度范围内,400-900 cm−1区域没有精细结构,这可以解释为由于纳米结构的氧化铝、二氧化硅和氧化铝-二氧化硅在无定形状态下团聚的存在。光谱分析表明,尖晶石在1000℃形成时同时存在八面体和四面体配位。Si-O-Si和Al-O-Si网络的不对称拉伸频率向更高波数的移动表明在1200℃时莫来石的形成。该产品的结晶性质由光谱峰的锐化表示。光谱还表明,在1250℃时莫来石形成完成。
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 求助全文
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:604180095
Book学术官方微信