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Structural Change of Ionic Species in the α-Al2O3 Powder/CoCl2 Aqueous Solution System

✍ Scribed by Shigehito Deki; Minoru Mizuhata; Shin-ya Nakamura; Akihiko Kajinami; Yukio Kanaji


Publisher
Elsevier Science
Year
1993
Tongue
English
Weight
481 KB
Volume
159
Category
Article
ISSN
0021-9797

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✦ Synopsis


Visible (VIS) absorption spectra were measured for the dispersion system consisting of (\alpha-\mathrm{Al}{2} \mathrm{O}{3}) powder and (\mathrm{CoCl}{2}) aqueous solution. The VIS spectra of the paste differed from that of the bulk solution. The absorption bands of the (\mathrm{Co}) (II) octahedral complex were shifted and broadened, whereas the intensity of the (\mathrm{Co}) (II) tetrahedral complex ( (\left[\mathrm{CoCl}{4}\right]^{2-}) ) at ca. (15,000 \mathrm{~cm}^{-1}) increased with the solid content and the specific surface area of (\alpha-\mathrm{Al}{2} \mathrm{O}{3}) powder. The intensity ratio of the absorption bands of the tetrahedral complex to the octahedral complex, (R_{4 / 6}), correlated with the apparent average thickness of the impregnating liquid layer. The relationship between the VIS spectra and electrical conductivity was also examined. The activation energies for the electrical conductivity, (\Delta E_{\mathrm{a}}), and (R_{4 / 6}) were correlated linearly. It is concluded that variation of the VIS spectra of the paste sample was caused by the structural change of the dissolved ionic species in the liquid layer which is ca. (\mathbf{2 0 - 3 0} \mathrm{nm}) thick near the solid surface. 1993 Academic Press. Inc.


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