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作 者:张传驹 李明航 谈冠希 苗杰 靳广洲[1] Zhang Chuanju;Li Minghang;Tan Guanxi;Miao Jie;Jin Guangzhou(College of Chemical Engineering,Beijing Key Laboratory of Fuels Cleaning and Advanced Catalytic Emission Reduction Technology,Beijing Institute of Petro-Chemical Technology,Beijing 102617,China)
机构地区:[1]北京石油化工学院化学工程系,燃料清洁化及高效催化减排技术北京市重点实验室,北京102617
出 处:《石油化工》2018年第10期52-58,共7页Petrochemical Technology
基 金:国家重点基础研究发展计划资助项目(2012CB215002)。
摘 要:采用柠檬酸络合法制备了一系列的CuCe-O/γ-Al_2O_3催化剂,利用XRD,H_2-TPR,BET,SEM等手段对不同热解温度、热解气氛下制备的CuCe-O/γ-Al_2O_3催化剂进行表征,并在连续固定床微反装置上评价了CuCe-O/γ-Al_2O_3催化剂的CO氧化性能。实验结果表明,改变热解温度及热解气氛对CuCe-O/γ-Al_2O_3试样的比表面积及形貌特征影响较小,CuCe-O/γ-Al_2O_3试样中CuO在γ-Al_2O_3载体表面呈高度分散状态,弱氧气氛增强了CuO/CeO_2两相间的相互作用,加剧了Ce^(3+)从CuO中获取氧的趋势,提高了氧化铜的氧化还原能力,相应的H_2-TPR还原温度向低温区偏移;在15%(φ)空气+85%(φ)N_2热解气氛及230℃热解温度下制备的CuCe-O/γ-Al_2O_3试样具有优良的CO氧化活性,表明适宜的热解条件可以增强CuO/CeO_2两相的相互作用,进而提高CuCe-O/γ-Al_2O_3试样的氧化还原能力。A series of CuCe-O/γ-Al2O3 catalysts were prepared by using amorphous citric precursor method,and characterized by XRD,H2-TPR,BET and SEM techniques.The CO oxidation performance of each CuCe-O/γ-Al2O3 catalyst was evaluated by a continuous fixed-bed microreactor.The results indicated that changing the pyrolysis temperature and atmosphere had little effect on the BET surface area and morphology of the CuCe-O/γ-Al2O3 catalyst,and CuO in the CuCe-O/γ-Al2O3 sample was highly dispersed on the surface of theγ-Al2O3 carrier.The poor oxygen atmosphere enhanced the interaction between CuO and CeO2,aggravated the tendency of Ce3+to acquire oxygen from CuO and increased the redox ability of the CuO,with the H2-TPR reduction temperature shifting to low temperature region accordingly.The CO oxidation results showed that the CuCe-O/γ-Al2O3 catalyst prepared in 15%(φ)air+85%(φ)N2 atmosphere at 230℃had excellent CO oxidation activity,indicating that the suitable pyrolysis conditions enhanced the interaction of CuO/CeO2,and then increased the redox ability of the CuCe-O/γ-Al2O3 catalyst.
关 键 词:CuCe-O/γ-Al2O3 热解温度 热解气氛 CO氧化
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