In-situ FTIR study of dehydration and rehydration mechanisms of natural scolecite

被引:5
|
作者
Prasad, Pinnelli S. R. [1 ]
Prasad, Kanapuram Shiva
Sreedhar, Bojja
Murthy, Sarabu Ramana
机构
[1] Natl Geophys Res Inst, Hyderabad 500007, Andhra Pradesh, India
[2] Osmania Univ, Dept Phys, Hyderabad 500007, Andhra Pradesh, India
[3] Indian Inst Chem Technol, Hyderabad 500007, Andhra Pradesh, India
关键词
scolecite; zeolite; dehydration mechanism; rehydration mechanism; FTIR; NIR;
D O I
10.1127/0935-1221/2006/0018-0265
中图分类号
P57 [矿物学];
学科分类号
070901 ;
摘要
In-situ FTIR spectroscopy was used to investigate the dehydration mechanism of naturally occurring scolecite from the Deccan traps. The dehydration and rehydration processes were studied by monitoring the thermally induced variations of fundamental bending (nu(2)) and stretching (nu(3) and nu(1)) modes of the water molecules in the range 1550-1800 cm(-1) and 3000-3600 cm(-1), as well as the corresponding second-order modes in the wavenumber region 4000-8000 cm(-1). Completely reversible spectral variations of the fundamental modes indicate that the transformation of scolecite to meta-scolecite at 495 K is reversible. Two-step dehydration behaviour is clearly observed in the thermally induced variations of the second-order modes. A combination mode in scolecite, due to Al-OH bonding around 4609 cm(-1), is seen to disappear in the meta-scolecite phase. Growth of a new mode around 4485 cm(-1) is observed in the temperature range 630-675 K, indicating the presence of hydroxyl groups in the amorphous phase, created by the breaking of T-O-T bonds.
引用
收藏
页码:265 / 272
页数:8
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