Excess Partial Molar Absorptivity of Aqueous Solutions of KCl, KBr, CsCl and CsBr: Are There Three Universal Chromophores in the Excess Molar Absorptivity of the ν 2?+?
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  • 作者:Fumie Sebe ; Keiko Nishikawa ; Yoshikata Koga
  • 关键词:Partial molar absorptivity ; Aqueous electrolytes ; Alkali metal halides ; Three universal chromophores
  • 刊名:Journal of Solution Chemistry
  • 出版年:2015
  • 出版时间:September 2015
  • 年:2015
  • 卷:44
  • 期:9
  • 页码:1833-1843
  • 全文大小:1,164 KB
  • 参考文献:1.Koga, Y., Sebe, F., Minami, T., Otake, K., Saitow, K., Nishikawa, K.: Spectrum of excess partial molar absorptivity. I. Near infrared spectroscopic study of squeous acetonitrile and acetone. J. Phys. Chem. B. 113, 11928-1935 (2009)CrossRef
    2.Sebe, F., Nishikawa, K., Koga, Y.: Spectrum of excess partial molar absorptivity. Part II: a near infrared spectroscopic study of aqueous Na-halides. Phys. Chem. Chem. Phys. 14, 4433-439 (2012)CrossRef
    3.Koga, Y., Sebe, F., Nishikawa, K.: Effects of tetramethyl- and tetraethylammonium chloride on H2O: calorimetric and near-infrared spectroscopic study. J. Phys. Chem. B. 117, 877-83 (2013)CrossRef
    4.Li, Q., Wang, N., Zhou, Q., Sun, S., Yu, Z.: Excess infrared absorption spectroscopy and its applications in the studies of hydrogen bonds in alcohol-containing binary mixtures. Appl. Spectrosc. 62, 166-70 (2008)CrossRef
    5.Ikehata, A.: Concept of differential molar absorptivity. 3rd Symposium of the NIR Division, The Spectroscopy Society of Japan. January 21, Osaka, Japan (2008)
    6.Koga, Y.: Partial molar quantity of an intensive mother function. J. Chem. Phys. 137, 124503 (2012)CrossRef
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    13.Morita, T., Westh, P., Nishikawa, K., Koga, Y.: How much weaker are the effects of cations than those of anions? the effects of K+ and Cs+ on the molecular organization of liquid H2O. J. Phys. Chem. B. 118, 8744-749 (2014)CrossRef
    14.Saitow, K., Kobayashi, K., Nishikawa, K.: How are hydrogen bonds perturbed in aqueous NaClO4 solutions depending on the concentration?: a near infrared study of water. J. Solution Chem. 33, 689-98 (2004)CrossRef
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  • 作者单位:Fumie Sebe (1) (2)
    Keiko Nishikawa (1)
    Yoshikata Koga (3)

    1. Graduate School of Advanced Integration Sciences, Chiba University, Chiba, 263-8522, Japan
    2. Research and Development, Power System Company, Toshiba, Yokohama, Japan
    3. Department of Chemistry, The University of British Columbia, Vancouver, BC, V6T 1Z1, Canada
  • 刊物类别:Chemistry and Materials Science
  • 刊物主题:Chemistry
    Physical Chemistry
    Industrial Chemistry and Chemical Engineering
    Geochemistry
    Oceanography
    Inorganic Chemistry
    Condensed Matter
  • 出版者:Springer Netherlands
  • ISSN:1572-8927
文摘
A new analysis methodology of the ν 2 + ν 3 band of H2O developed by us earlier was applied for aqueous solutions of KCl, KBr, CsCl and CsBr. We isolate the effect of inter-molecular interactions among solute ions and solvent molecules on the near infrared spectra as the excess absorptivity, ε E, and then take its mole fraction derivative, \( \varepsilon_{\text{S}}^{\text{E}} \) (S stands for the solute). \( \varepsilon_{\text{S}}^{\text{E}} \) then signifies the effect of solute S on ε E, the transition moment of the ν 2 + ν 3 combination band due only to the intermolecular interactions. Together with the earlier similar studies on aqueous NaCl, NaBr, NaI, (CH3)4Cl, and (C2H5)4Cl, we found that ε E has apparently three universal bands among all the aqueous salts studied so far; a negative band centered at 4873 cm?, a positive one at 5123 cm?, and a negative band at 5263 cm?. They were attributed to “solid-like- “liquid-like-and “gas-like-H2O chromophores, respectively, depending on the local and instantaneous completeness of hydrogen bonding. Our recent thermodynamic studies indicated that K+, Cs+, and Cl?/sup> ions are “hydration centers-that are hydrated by a number of H2O molecules, but the bulk H2O away from hydration shells is left unperturbed. Br?/sup> is a “hydrophile-ion that forms hydrogen bonds directly to the fleetingly and yet permanently existing hydrogen bond network of H2O, but pins down the fluctuations inherent in pure H2O. The distinction between Cl?/sup> and Br?/sup> are apparent only in the behavior of \( \varepsilon_{\text{S}}^{\text{E}} \) at the 5123 cm? “liquid-like-chromophore band. The quantitative differences in the hydration numbers among Na+, K+, and Cs+ are not conspicuous in either of these three chromophores. We stress, however, that at the ε E level there seem to be three bands at 4873, 5123, and 5263 cm? that could be universal among aqueous solutions of electrolyte solutes. Keywords Partial molar absorptivity Aqueous electrolytes Alkali metal halides Three universal chromophores

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