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首页> 外文期刊>Catalysis Communications >Advance in the study of limonene epoxidation with H2O2 catalyzed by Cu(II) complex heteropolytungstates
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Advance in the study of limonene epoxidation with H2O2 catalyzed by Cu(II) complex heteropolytungstates

机译:Cu(II)配合物杂多钨酸盐催化H2O2对柠檬烯环氧化的研究进展

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摘要

The complex heteropolyoxotungstates of formula K_(10)[M4(H2O)2(PW9O_(34))2]·20H2O (PWM) with M = Co(II), Zn(II), Cu(II) and Mn(II), and their precursor, △-Na8HPW9O34·19H2O (△-PW9), were evaluated as bulk in limonene epoxidation using H2O2 as oxidant, 1,2 dicloroethane as solvent and metiltricaprilamonium chloride (Aliquat 336) as a phase transfer agent at 2 °C. In these biphasic conditions PWCu was the most active phase. Subsequently this phase was supported on γ-Al2O3, the metal load was determined by AAS, 1CP and X-ray fluorescence and the preservation of PWCu structure was confirmed by XPS and Raman microprobe. PWCu/7-Al2O3 was evaluated at 70 °C with acetonitrile as solvent. The pure PWCu showed a higher conversion to epoxide but lower selectivity due to the formation of secondary products.
机译:分子式为K_(10)[M4(H2O)2(PW9O_(34))2]·20H2O(PWM)的复杂杂多氧杂钨酸盐,M = Co(II),Zn(II),Cu(II)和Mn(II)在2°C下,以H2O2作为氧化剂,1,2二氯乙烷作为溶剂,氯化甲il腈(Aliquat 336)作为相转移剂,在柠檬烯环氧化中评估了其前体△-Na8HPW9O34·19H2O(△-PW9)的体积。 。在这些双相条件下,PWCu是最活跃的相。随后将此相负载在γ-Al2O3上,通过AAS,1CP和X射线荧光确定金属负载,并通过XPS和拉曼微探针确认PWCu结构的保留。在70°C下以乙腈为溶剂评估PWCu / 7-Al2O3。纯的PWCu表现出较高的环氧化物转化率,但由于形成副产物而具有较低的选择性。

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