Raman study of cation effect on sulfate vibration modes in solid state and in aqueous solutions

被引:169
作者
Ben Mabrouk, Kawther [1 ,2 ,3 ]
Kauffmann, Thomas H. [1 ,2 ]
Aroui, Hassen [3 ]
Fontana, Marc D. [1 ,2 ]
机构
[1] Univ Lorraine, Lab Mat Opt Photon & Syst, EA 4423, F-57070 Metz, France
[2] Supelec Lab Mat Opt Photon & Syst, EA 4423, F-57070 Metz, France
[3] Univ Tunis, Ecole Super Sci & Tech Tunis, Lab Dynam Mol & Mat Photon, Tunis 1008, Tunisia
关键词
sulfates; cation dependence; calibration; Raman study; MINERALS;
D O I
10.1002/jrs.4374
中图分类号
O433 [光谱学];
学科分类号
0703 ; 070302 ;
摘要
Raman spectra of potassium, sodium, and ammonium sulfates (K2SO4, Na2SO4, and (NH4)(2)SO4) are reported and analyzed. These sulfates have been investigated under two states: solid (anhydrous and hydrated) salts and aqueous solutions. The effects of monovalent ions (K+, Na+, and NH4+) and hydration on the position of Raman lines assigned to internal vibrations of sulfate anion SO42- are discussed. In solid salts, the line position of each Raman peak is shown to decrease with increasing radius of the cation. The main (1) mode of sulfate molecule is particularly affected. It is emphasized that this sensitivity in solid sulfates vanishes in aqueous solutions. As a consequence, this mode can be probed by Raman spectroscopy as the main signature of SO42- to determine its concentration within a single calibration. Copyright (c) 2013 John Wiley & Sons, Ltd.
引用
收藏
页码:1603 / 1608
页数:6
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