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K促进的纳米片状水滑石衍生CoAlO金属氧化物催化碳烟燃烧
引用本文:任伟,田野,邢令利,杨岳溪,丁彤,李新刚. K促进的纳米片状水滑石衍生CoAlO金属氧化物催化碳烟燃烧[J]. 高等学校化学学报, 2019, 40(8): 1670. DOI: 10.7503/cjcu20190161
作者姓名:任伟  田野  邢令利  杨岳溪  丁彤  李新刚
作者单位:天津化学化工协同创新中心,天津市应用催化科学与工程重点实验室,天津大学化工学院,天津300354;天津化学化工协同创新中心,天津市应用催化科学与工程重点实验室,天津大学化工学院,天津300354;天津化学化工协同创新中心,天津市应用催化科学与工程重点实验室,天津大学化工学院,天津300354;天津化学化工协同创新中心,天津市应用催化科学与工程重点实验室,天津大学化工学院,天津300354;天津化学化工协同创新中心,天津市应用催化科学与工程重点实验室,天津大学化工学院,天津300354;天津化学化工协同创新中心,天津市应用催化科学与工程重点实验室,天津大学化工学院,天津300354
基金项目:国家自然科学基金(批准号:21878213)和高等学校学科创新引智计划(批准号:B06006)资助.
摘    要:采用水热法合成了负载K的纳米片状水滑石衍生CoAlO金属氧化物,其表现出优异的催化碳烟燃烧活性.氢气-程序升温还原(H2-TPR)实验结果表明,K与Co之间的相互作用提高了催化剂的氧化还原性能.X射线光电子能谱(XPS)分析结果表明,K的负载增大了表面Co2+/Co3+的比例,促进了氧空位的产生,提高了催化剂对气相氧的吸附能力.碳烟-程序升温还原(Soot-TPR)实验结果表明,K的负载增加了表面吸附氧数量.动力学实验结果表明,K的负载增加了单位质量催化剂上的活性氧数量、反应速率和转化频率(TOF),从而提高了催化剂的本征活性.另外,碳烟颗粒可以分散在纳米片的层间,与活性位点的接触效率得到提高,也有利于提高催化碳烟燃烧活性.

关 键 词:水滑石衍生金属氧化物  K与Co相互作用  氧空位  碳烟燃烧  纳米片形貌
收稿时间:2019-03-18

K Promoted Nanosheets-like Hydrotalcite-derived CoAlO Metal Oxides for Catalytic Soot Combustion
REN Wei,TIAN Ye,XING Lingli,YANG Yuexi,DING Tong,LI Xingang. K Promoted Nanosheets-like Hydrotalcite-derived CoAlO Metal Oxides for Catalytic Soot Combustion[J]. Chemical Research In Chinese Universities, 2019, 40(8): 1670. DOI: 10.7503/cjcu20190161
Authors:REN Wei  TIAN Ye  XING Lingli  YANG Yuexi  DING Tong  LI Xingang
Affiliation:Collaborative Innovation Center of Chemical Science and Engineering(Tianjin), Tianjin Key Laboratory of Applied Catalysis Science and Engineering, School of Chemical Engineering & Technology, Tianjin University, Tianjin 300354, China
Abstract:We synthesize the K supported nanosheets-like hydrotalcite-derived CoAlO metal oxide by a facile hydrothermal method, which exhibits the superior catalytic performance for soot combustion. The H2-TPR results show that the interaction between K and Co leads to the improved redox ability of 5K/CoAlO. The Co2p XPS results show that the Co2+/Co3+ ratios get increased after loading K on the CoAlO support. It demonstrates that the K loading promotes the transition of cobalt species from Co3+ to Co2+, which leads to the generation of oxygen vacancies. The O1s XPS results show that the Oads/(Oads + Olat) ratio increases after K loading. The soot-TPR results indicate that the interaction between K and Co contributes to the adsorption of gaseous O2 remarkably. During kinetic experiments, 5K/CoAlO exhibits the high reaction rate per unit mass of catalyst, active oxygen(O*) amount per unit mass of catalyst and TOF, which demonstrates that the interaction between K and Co improves the intrinsic activities of 5K/CoAlO. In addition, owing to the nanosheets-like morphology of 5K/CoAlO, the soot particulates could be highly dispersed on the nanosheets-like layers of 5K/CoAlO and get more access to active components, which is favorable to soot combustion. In summary, the improved amount of active oxygen species and the increased soot-catalyst contact efficiency guarantee the high soot combustion activity of our K supported CoAlO catalysts. Our work provides a novel approach to designing a highly efficient Co-based hydrotalcite-derived oxides catalyst for catalytic soot combustion.
Keywords:Hydrotalcite-derived metal oxide  Interaction between K and Co  Oxygen vacancy  Soot combustion  Nanosheets-like morphology  
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