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Y修饰CuO/ZrO_2催化剂高效催化水煤气变换反应制氢
引用本文:Y修饰CuO/ZrO催化剂高效催化水煤气变换反应制氢.Y修饰CuO/ZrO_2催化剂高效催化水煤气变换反应制氢[J].燃料化学学报,2017,45(9):1137-1145.
作者姓名:Y修饰CuO/ZrO催化剂高效催化水煤气变换反应制氢
作者单位:1. Department of Chemistry and Chemical Engineering, Minjiang University, Fuzhou 350108, China; 2. National Engineering Research Center of Chemical Fertilizer Catalyst, Fuzhou University, Fuzhou 350002, China; 3. Engineering Research Center of Green Dyeing and Finishing in Fujian Provincial University, Fuzhou 350108, China
基金项目:国家自然科学基金(21503105),福建省自然科学基金(2017J05025,2017J01584),福建省教育厅JK类项目(JK2015038),福建省中青年教师教育科研项目(JA15419)和福建省高校杰出青年科研人才培育计划(2016)资助
摘    要:采用水热法制备了具有不同Y掺杂量的单分散ZrO_2纳米粒子(n(Y)/n(Y+Zr)=0-5%),并以其为载体采用沉积-沉淀法制得CuO/ZrO_2催化剂;考察了富氢气氛下上述催化剂的水煤气变换反应(WGS)催化性能。结果表明,掺杂Y后催化剂的活性明显提高,其中,载体掺杂2%Y的催化剂具有最佳的催化活性,在270℃时的CO转化率高达91.4%,明显高于研究较多的CuO/ZnO和CuO/CeO_2催化剂。X射线粉末衍射、N_2物理吸附-脱附、N_2O滴定、扫描电镜和CO程序升温还原等表征结果表明,Y~(3+)掺入了ZrO_2的晶格并对催化剂的结构和还原性能产生直接影响。Y助剂的引入一方面促进了CuO在ZrO_2表面的分散,提高了催化剂表面活性Cu-O]-Zr物种的含量;另一方面,改善了催化剂的颗粒单分散性和织构性能。载体掺杂2%Y助剂的样品具有较高的Cu-O]-Zr物种含量、较佳的颗粒单分散性和织构性能,且其表面的Cu-O]-Zr物种和活性羟基具有较佳的还原性能,因而表现出较高的催化活性

关 键 词:CuO/ZrO2催化剂  水煤气变换反应  Y助剂  氧空位  表面羟基  
收稿时间:2017-05-18

Highly active Y-promoted CuO/ZrO2 catalysts for the production of hydrogen through water-gas shift reaction
ZHANG Yan-jie,CHEN Chong-qi,ZHAN Ying-ying,LIN Qi,LOU Ben-yong,ZHENG Guo-cai,ZHENG Qi.Highly active Y-promoted CuO/ZrO2 catalysts for the production of hydrogen through water-gas shift reaction[J].Journal of Fuel Chemistry and Technology,2017,45(9):1137-1145.
Authors:ZHANG Yan-jie  CHEN Chong-qi  ZHAN Ying-ying  LIN Qi  LOU Ben-yong  ZHENG Guo-cai  ZHENG Qi
Abstract:ZrO2 doped with various concentrations of yttrium(0-5%) was prepared by a hydrothermal homogeneous co-precipitation method and CuO was then deposited on ZrO2 by a deposition-precipitation method to get the yttrium promoted CuO/ZrO2 catalyst; its performance in the water-gas shift reaction for producing hydrogen was then investigated. The results indicate that the catalytic activity of CuO/ZrO2 can be effectively improved by yttrium modification; over the yttrium promoted CuO/ZrO2 catalyst with an yttrium concentration of 2%, the CO conversion reaches 91.4% at 270℃, much higher than those over the conventional CuO/ZnO and CuO/CeO2 catalysts. The XRD, N2-physisorption, N2O titration, SEM and CO-TPR characterization results reveal that Y3+ is successfully incorporated into the lattice of ZrO2, which has a great influence on the structure and reducibility of the CuO/ZrO2 catalysts. Y3+ doping into ZrO2 introduces oxygen vacancies, improving the dispersion of CuO and increasing the proportion of catalytically active Cu-O]-Zr species. In addition, the introduction of yttrium improves the monodispersity and modifies the texture properties of the CuO/ZrO2 catalysts. As a result, the superior activity of 2% yttrium promoted CuO/ZrO2 catalyst is probably attributed to the abundance of Cu-O]-Zr species, high reducibility of Cu-O]-Zr species and surface hydroxyl groups, high monodispersity and proper textural properties.
Keywords:CuO/ZrO2 catalyst  water-gas shift reaction  yttrium promoter  oxygen vacancy  surface hydroxyl groups  
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