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Understanding the effects of chlorine ion on water structure from a Raman spectroscopic investigation up to 573 K
被引:21
|作者:
Hu, Qingcheng
[1
]
Zhao, Haiwen
[1
]
机构:
[1] Inner Mongolia Univ Sci & Technol, Key Lab Integrated Exploitat Bayan Obo Multimet R, Baotou 014010, Peoples R China
基金:
中国国家自然科学基金;
关键词:
Chlorine ion;
Hydrogen bonding;
Raman spectroscopy;
Water structure;
Temperature;
X-RAY-DIFFRACTION;
AQUEOUS NACL SOLUTIONS;
TERAHERTZ SPECTROSCOPY;
NEUTRON-DIFFRACTION;
MOLECULAR-DYNAMICS;
SODIUM-CHLORIDE;
LIQUID;
POTASSIUM;
HYDRATION;
ICE;
D O I:
10.1016/j.molstruc.2019.01.053
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 OH stretch band features on Raman spectra of aqueous KCl-H2O solutions have been investigated at temperatures (T) up to 573 K. KCl greatly reduces the relative intensity of the shoulder at similar to 3245 cm(-1) and the band width, but these effects are slightly reversed at temperatures over similar to 513 K. Also, KCl causes a blue shift (T < 433 K) but a red shift (T> 433 K) of the main peak. These spectral features are interpreted that Cl- breaks the tetrahedral hydrogen bonding (HB) structure and bonds to water molecules with the non-tetrahedral HB configurations. The single donor is likely the preferred configuration between the water molecules in the Cl- hydration shells. Cl- tends to promote the HB degree in solutions at T > 433 K. (C) 2019 Elsevier B.V. All rights reserved.
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页码:191 / 196
页数:6
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