Infrared spectroscopic study of natural hydrotalcites carrboydite and hydrohonessite

被引:43
作者
Frost, RL
Weier, ML
Clissold, ME
Williams, PA
机构
[1] Queensland Univ Technol, Ctr Instrumental & Dev Chem, Brisbane, Qld 4001, Australia
[2] Univ Western Sydney, Sch Sci Food & Hort, Ctr Ind & Proc Mineral, Penrith, NSW 1797, Australia
基金
澳大利亚研究理事会;
关键词
hydrotalcite; infrared spectroscopy; Raman microscopy; molecular assembly; structured water;
D O I
10.1016/S1386-1425(03)00160-4
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Infrared spectroscopy has proven most useful for the study of anions in the interlayer of natural hydrotalcites. A suite of naturally occurring hydrotalcites including carrboydite, hydrohonessite, reevesite, motukoreaite and takovite were analysed. Variation in the hydroxyl stretching region was observed and the band profile is a continuum of states resulting from the OH stretching of the hydroxyl and water units. Infrared spectroscopy identifies some isomorphic substitution of sulphate for carbonate through an anion exchange mechanism for the minerals carrboydite and hydrohonessite. The infrared spectra of the CO3 and SO4 stretching region of takovite is complex because of band overlap. For this mineral some sulphate has replaced the carbonate in the structure. In the spectra of takovites, a band is observed at 1346 cm(-1) and is attributed to the carbonate anion hydrogen bonded to water in the interlayer. Infrared spectroscopy has proven most useful for the study of the interlayer structure of these natural hydrotalcites. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:3313 / 3319
页数:7
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