Preparation of High Purity Vanadium Metal for Hydrogen Storage Using the Direct Reduction and Simultaneous Molten Salt Electrolysis
Preparation of High Purity Vanadium Metal for Hydrogen Storage Using the Direct Reduction and Simultaneous Molten Salt Electrolysis
批准号:
18360367
负责人:
SUZUKI Ryosuke
金额:
$7.92万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (B)
财政年份:
2006
资助国家:
日本
项目状态:
已结题
起止时间:
2006 至 2007
中文摘要
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英文摘要
A New process was developed that the metallic vanadium (V) was prepared by the direct reduction from the molten vanadium oxide melt (V_2O_5). Two steps (A) and (B) were combined: (A) The solid oxides was directly reduced by calcium dissolved in the molten salt, and (B) the by-product CaO was electrochemically decomposed into the metallic calcium. This combination is hereafter called as OS process, which is extended to the molten oxide V_2O_5, in addition to the solid lower oxides.By applying OS process in the molten CaCl_2, the optimization of electrodes arrangement was studied in order to react efficiently with the molten oxide V_2O_5 and Ca existing near the cathode. Mo or V was taken for the cathodic material. The current efficiency decreased when the crucible-type electrode was used. The anodic carbon was set more closely to the cathode, such as in a few mm, and we obtained the excellent quality of vanadium metal containing only 2000 ppm oxygen. The phase transformation during the reduction was studied in addition to the analysis of electrochemical behavior and current efficiency at the various electrode arrangements. The reduction rate corresponded well to the supplied current. A high current efficiency could be achieved at the initial stage of reaction. At the later stage of reduction, however, the deoxidation from the obtained vanadium metal was dominant, and both the current and the current efficiency decreased. The decreasing rate of oxygen content could be expressed in an unique formula against the supplied electric charge over the whole experimental time. This implies that the rate-determining step in OS process is the diffusion of Ca or CaO into the molten CaCl_2 bulk.
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溶融塩化カルシウム中でのカルシウム還元
熔融氯化钙中的钙还原
DOI:
--
发表时间:
2006
期刊:
溶融塩および高温化学 No.1(印刷中)
影响因子:
--
作者:
[Kuwamura, H., Tanaka, N., Sugimoto, H., Kohno, A, 鈴木亮輔]
通讯作者:
鈴木亮輔
Reduction of V_20_5 by the Molten Salt Electrolysis of (CaCl_2+CaO)
(CaCl_2 CaO)熔盐电解还原V_20_5
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[H. Sakai, Y. Oka and R.O. Suzuki, 岡佑一, 岡佑一, Y. Oka and R.O.Suzuki]
通讯作者:
Y. Oka and R.O.Suzuki
Preparation of Hydrogen Storage Ti-V-Cr Alloy from the Oxide Mixture in CaCl_2Molten CaCl_2
CaCl_2熔融CaCl_2氧化物混合物制备储氢Ti-V-Cr合金
DOI:
--
发表时间:
2007
期刊:
影响因子:
--
作者:
[岡佑一, 鈴木亮輔, R. O. Suzuki, R. O. Suzuki, R.O.Suzuki]
通讯作者:
R.O.Suzuki
溶融塩化カルシウム浴を用いた酸化バナジウムの直接還元
使用熔融氯化钙浴直接还原氧化钒
DOI:
--
发表时间:
2008
期刊:
日本金属学会誌
影响因子:
--
作者:
[岡佑一, 鈴木亮輔]
通讯作者:
鈴木亮輔
Dissolution of CO_2 into the Molten Salt of (CaCl_2+CaO)
CO_2溶解到(CaCl_2 CaO)熔盐中
DOI:
--
发表时间:
2008
期刊:
影响因子:
--
作者:
[J. Hashidume, Y. Oka and R.O. Suzuki]
通讯作者:
Y. Oka and R.O. Suzuki
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