An ESR study on the working states of a pure V2O5 crystal under the CO-oxidation.
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概要
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The V<SUB>2</SUB>O<SUB>5</SUB> crystal, prepared from the pure V<SUB>2</SUB>O<SUB>5</SUB> powder by a zone-melting method in the air, did not show any ESR signal. When the crystal came into contact with a mixture of CO and O<SUB>2</SUB> ((CO/O<SUB>2</SUB>)≥4), an ESR spectrum with the hfs of 15-lines (<I>g</I><SUB>⁄⁄</SUB>=1.932, <I>g</I><SUB>⊥</SUB>=1.978; 〈<I>g</I>〉=1.963), which has been previously ascribed to an oxygen defect, was found at the beginning, but after prolonged contact a sharp spectrum (〈<I>g</I>〉=1.954) appeared. The intensity of the hf-lines was constant but that of the sharp spectrum increased with the contact time. The <I>g</I>-value and line shape of both spectra did not change with the contact time. The same spectra were also found in the crystal grown under a mixture of CO and O<SUB>2</SUB>. On the thermal decomposition of pure NH<SUB>4</SUB>VO<SUB>3</SUB> <I>in vacuo</I> a similar spectrum with a sharp line was found. The <I>g</I>-value became lower in the sample reduced further by SO<SUB>2</SUB> after the thermal decomposition. With reference to the data of TGA, DTA, magnetic susceptibility (χ<SUB>mol</SUB>), and X-ray analysis of the vanadium oxides, the sharp spectrum was ascribed to a lower oxide or oxide state such as V<SUB>3</SUB>O<SUB>7</SUB>. Based on the ESR results, the working state of pure V<SUB>2</SUB>O<SUB>5</SUB> crystal under CO-oxidation and its catalytic property are discussed.
- 公益社団法人 日本化学会の論文
著者
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Kera Yoshiya
Department Of Applied Chemistry Faculty Of Science And Engineering Kinki University
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Kuwata Keiji
Department Of Chemistry Faculty Of Science Osaka University
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