| Project/Area Number |
61550569
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
無機工業化学
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| Research Institution | Faculty of Engineering, Yamanashi University |
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Principal Investigator |
KINOMURA Nobukazu Yamanashi University Associate Professor, 工学部, 助教授 (50029732)
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| Co-Investigator(Kenkyū-buntansha) |
KUMADA Nobuhiro Yamanashi University Research Associator, 工学部, 助手 (90161702)
武藤 文夫 山梨大学, 工学部, 教授 (10020380)
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| Project Period (FY) |
1986 – 1987
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| Project Status |
Completed (Fiscal Year 1987)
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| Budget Amount *help |
¥1,900,000 (Direct Cost: ¥1,900,000)
Fiscal Year 1987: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1986: ¥1,400,000 (Direct Cost: ¥1,400,000)
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| Keywords | Layered Compoun / Intercalation / Redox Reaction / ディリシェーション / リン酸タングステン / インターカレーション化合物 / リン酸塩 |
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| Research Abstract |
Diphosphato oxotungsten (VI), [WO(P_2O_7)], which has electrically neutral layers was reduced with aqueous solutions of Na_2S_2O_4 and SnCl_2. After the reaction, increase of the basal spacing was observed and the intercalation compound, A_xH_yWOP_2O_7・nH_2O (A=Na, Sn) was prepaed. The most reduced product was found to be Na_1._4WOP_2O_7・nH_iO which was obtained in the Na_2S_2O_4 solution. The least reduced product was found to be Sn_xH_yWOP_2O_7・nH_2O (2x+y=0.5), prepared in the SnCl_2 solution. These facts mean that the area per unit negative charge on the layer can be varied from 8 to 37<ang>^2. The former value is close to the lower limit observed for other layered compounds and the latter is comparable to some clay minerals which are generally known to have the extraordinarily large area. Ion exchange of these compounds with metal and n-alkylammonium ions was also investigated as well as intercalation of n-alkylamines to WOP_2O_7.
Layered oxide composed of reduced transition metal and lithium ions, such as LiNbO_2 and Li_2MoO_3, was oxidized with acetonitril solutions of iodine and bromine. The products had less Li^+ ions in the structure than the starting materials and showed a peculiar dependence of the crystallographic axes on the amount of Li^+ ions in the interlayer spaces.
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