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作 者:高仲良[1] 黄伟[1] 阴丽华[1] 吉鹏[1] 赵金珍[1] 刘源[1] 彭芬[1]
机构地区:[1]太原理工大学煤化工研究所,煤科学与技术教育部和山西省重点实验室,太原030024
出 处:《高等学校化学学报》2012年第1期158-165,共8页Chemical Journal of Chinese Universities
基 金:国家“九七三”计划项目(批准号:2005CB221204);国家自然科学基金(批准号:20676085)资助
摘 要:以混合钴源为前驱体,采用等体积浸渍法制备了Co-Pd/TiO2催化剂,考察了其对CH4和CO2梯阶转化直接合成乙酸的催化性能,采用XRD,XPS,NH3-TPD和BET对催化剂进行了表征.结果表明,催化剂具有适宜的表面酸性、高比表面积和孔结构,有利于提高催化剂的活性.在m(CoCl2)∶m[Co(NO3)2]=2∶5,m(Co)∶m(Pd)=2∶1,常压,150℃条件下,乙酸的生成速率达到6.13 mg·g-1Cat·h-1,选择性达到81.6%,分别比以单一Co源制备的催化剂提高了134%和16%.Co-Pd/TiO2 catalysts were prepared from mixed cobalt salts by incipient impregnation method.The catalytic performance of the catalysts for direct synthesis of acetic acid from CH4 and CO2 by a step-wise reaction technology was investigated.These catalysts were also characterized by XRD,XPS,NH3-TPD and BET.The results show that when the precursor is from mixed cobalt salts,a suitable surface acidity,high specific surface area and pore structure are formed,which favors the activity of catalysts.On the condition of m(CoCl2)∶ m[Co(NO3)2]=2∶ 5,m(Co)∶ m(Pd)=2∶ 1 and 150 ℃,the formation rate and selectivity of acetic acid reach 6.13 mg·g-1Cat·h-1and 81.6%,respectively.Compared with the catalysts prepared from single cobalt,the rate and selectivity increase by 134% and 16%.
关 键 词:混合钴源 Co-Pd/TiO2催化剂 CH4-CO2两步梯阶转化法 乙酸
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