AlZn基Co和Ni催化剂对生物乙醇部分氧化的影响-不同合成工艺的影响

H. Ehrich, E. Kraleva
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引用次数: 5

摘要

Co和Ni催化剂在AlZn混合氧化物载体上的催化性能取决于其制备的合成工艺。本研究采用常规的混合氧化物溶胶-凝胶合成法,然后用过渡金属浸渍载体(SG =溶胶-凝胶法),以及采用柠檬酸作为螯合剂(CM =柠檬酸盐法),用所有组分的盐形成凝胶的单步法制备了CoAlZn和NiAlZn催化剂。通过氮吸附、XRD和TPR测试对催化剂的结构和形貌进行了表征。在600 ~ 750℃条件下,它们对乙醇的部分氧化表现出较高的活性,但其性能与制备方法有关。柠檬酸盐方法制备的催化剂性能更高,在制备过程中过渡金属被纳入载体的晶体结构中,是基于形态和结构的变化,导致更多的活性位点暴露在表面上。与Co催化剂相比,Ni催化剂表现出更高的性能。这可能是由于更高的还原性和更小的Ni颗粒尺寸,这使得在NiAlZn催化剂中与载体有更好的相互作用。
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AlZn based Co and Ni catalysts for the partial oxidation of bioethanol — influence of different synthesis procedures
The catalytic performance of Co and Ni catalysts on AlZn mixed oxide supports depends on the synthesis procedure used for their preparation. For this study CoAlZn and NiAlZn catalysts were prepared by conventional sol-gel synthesis of the mixed oxide and subsequent impregnation of the support with the transition metal (SG = sol gel method) as well as by a single-step method were a gel is formed based on salts of all components using citric acid as chelating agent (CM = citrate method). The structure and morphology of the catalysts were characterized by nitrogen sorption, XRD and TPR measurements. They showed high activity in the partial oxidation of ethanol at 600–750 °C, but their properties depend on the preparation method. The higher performance of the catalysts prepared by the citrate method, where the transition metal is incorporated into the crystal structure of the support during preparation, is based on a change in morphology and structure, resulting in more active sites exposed on the surface. Compared to the Co catalysts, Ni catalysts showed a higher performance. This might be due to the higher reducibility and the smaller Ni particles size, which allows a better interaction with the support in NiAlZn catalysts.
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