无相转移催化剂条件下AlPMo12O40催化H2O2模型燃料新型氧化脱硫研究

M. J. Silva, L. Santos
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引用次数: 16

摘要

以Keggin杂多酸及其铝盐为催化剂,建立了一种无相转移催化剂氧化脱硫(ODS)新工艺。在异辛烷/乙腈的双相混合物中,以二苯并噻吩(DBT)为模型硫化合物,过氧化氢为氧化剂进行反应。值得注意的是,只有alpmo12o40催化的反应才能使DBT完全氧化为DBT砜,DBT砜被乙腈完全萃取,使异辛烷的硫含量从1000 ppm降至H3PMo12O40 > AlPW12O40 > H3PW12O40。没有PTC、酸性有机过氧化物以及使用过氧化氢(一种环境友好的氧化剂)构成了alpmo12o40催化ODS反应的积极方面。在这些反应中,在较短的时间内(约2小时)和温和的反应条件下,DBT的去除率很高(约100%)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Novel Oxidative Desulfurization of a Model Fuel with H2O2 Catalyzed by AlPMo12O40 under Phase Transfer Catalyst-Free Conditions
A novel process was developed for oxidative desulfurization (ODS) in the absence of a phase transfer catalyst (PTC) using only Keggin heteropolyacids and their aluminum salts as catalysts. Reactions were performed in biphasic mixtures of isooctane/acetonitrile, with dibenzothiophene (DBT) as a model sulfur compound and hydrogen peroxide as the oxidant. Remarkably, only the AlPMo12O40-catalyzed reactions resulted in complete oxidation of DBT into DBT sulfone, which was totally extracted by acetonitrile, reducing the sulfur content of isooctane from the 1000 ppm to  H3PMo12O40 > AlPW12O40 > H3PW12O40. The absence of a PTC, acidic organic peroxides, and the use of hydrogen peroxide, an environmentally benign oxidant, make up the positive aspects of AlPMo12O40-catalyzed ODS reactions. In these reactions, high rates of DBT removal (ca. 100%) were achieved within a short time (ca. 2 hours) and under mild reaction conditions.
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