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钴负载MCM-41分子筛催化臭氧氧化水中氯代苯甲酸 被引量:6

Catalytic ozonation of chlorobenzoic acid over cobalt oxide supported on MCM-41 mesoporous molecular sieves
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摘要 通过水热法合成介孔分子筛MCM-41,采用等体积浸渍法制备了Co负载MCM-41分子筛催化剂(Co/MCM-41).小角X-射线粉末衍射(XRD)、紫外-可见漫反射光谱(UV-vis DRS)、N2吸附-脱附等温线及透射电镜(TEM)等对催化剂的成分、结构的表征结果显示,Co/MCM-41保持了纯硅MCM-41有序的介孔结构,钴元素以钴氧化物形式存在,比表面达到772 m.2g-1.将Co/MCM-41分子筛用于催化臭氧氧化水中对氯苯甲酸(p-CBA)的研究,结果表明,在优化条件下(2%负载量和25℃反应温度),催化剂的加入显著改善了TOC去除率,达到84.6%,是单独臭氧氧化的1.6倍. MCM-41 mesoporous molecular sieve was synthesized by a hydrothermal method and Co/MCM-41 was prepared by an incipient wetness impregnation method.The materials were characterized by a low angle X-ray powder diffraction(XRD),UV-Vis diffuse reflection spectroscopy(UV-DRS),N2 adsorption-desorption and transmission electron microscopy(TEM).The results showed that the material retained a highly ordered mesopore structure of pure silica MCM-41 and had a surface area of 772 m2·g-1,Cobalt ions mainly exist as cobalt oxide clusters distributed on the surface of molecular sieve.In this study,Co/MCM-41 mesoporous molecular sieve was used for catalytic ozonation of p-CBA.The results showed that under the optimal condition(2% cobalt load and 25 ℃),the mineralization of p-CBA increased to 84.6% in the presence of catalyst,which is 1.6 times that of ozone alone at the reaction time of 60 min.
机构地区 华南师范大学
出处 《环境化学》 CAS CSCD 北大核心 2012年第5期663-668,共6页 Environmental Chemistry
基金 国家自然科学基金(20977036)资助
关键词 催化臭氧氧化 MCM-41 catalytic ozonation MCM-41 cobalt.
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