In Situ Real Time Infrared Spectroscopy of Sorption of (Poly)molybdate Ions into Layered Double Hydroxides

被引:41
作者
Davantes, A. [1 ]
Lefevre, G. [1 ]
机构
[1] CNRS ENSCP, LECIME UMR7575, F-75231 Paris 05, France
关键词
HYDROTALCITE-LIKE COMPOUNDS; ANION-EXCHANGE REACTIONS; ATR-IR SPECTROSCOPY; PILLARED HYDROTALCITE; AQUEOUS-SOLUTIONS; RAMAN-SPECTRA; MOLYBDATE; ADSORPTION; CARBONATE; OXIDE;
D O I
10.1021/jp408885k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The sorption of (poly)molybdate ions into layered double hydroxides (LDHs), with Zn2+ and Al3+ cations, has been followed by in situ infrared spectroscopy using the attenuated total reflection technique. The exchange between solution molybdate species and interlayer anions has been followed in real time, illustrating the different behavior of molybdate ions and polymolybdate species. In a first part, the Mo(VI) speciation in solution was performed by comparison of thermodynamical calculations and infrared spectroscopy of solutions with different pH. Decomposition of bands between 800 to 1000 cm(-1), corresponding to the (Mo-O) stretching vibration, has permitted to identify major (poly)-molybdate species. In the presence of LDH, the measurements have shown a high affinity for heptamolybdate (Mo7O246-) species, and its preferential sorption in comparison with molybdate ions or other protonated polymolybdate species even if it represents very small fractions. From these measurements, the affinity series Mo7O246- > CO32- > MoO42- > SO42- have been directly obtained.
引用
收藏
页码:12922 / 12929
页数:8
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