检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:徐军科[1,2] 周伟[2,3] 汪吉辉[4] 李兆静[4] 马建新[2,3]
机构地区:[1]同济大学环境科学与工程学院,上海200092 [2]同济大学新能源汽车工程中心,上海201804 [3]同济大学汽车学院,上海201804 [4]华东理工大学资源与环境工程学院,上海200237
出 处:《催化学报》2009年第11期1076-1084,共9页
基 金:Supported by the Canada-China Scientific and Technological Cooperation Project (2007DFC61690) ;Henkel Professorship of Tongji University (081591)
摘 要:用传统的等体积浸渍法或蒸发法制备了Ni/La2O3/γ-Al2O3与Ni/La2O3/α-Al2O3催化剂,在没有稀释气体的条件下进行了甲烷干重整反应.采用H2程序升温还原、N2吸附脱附、X射线衍射、透射电子显微镜、热重-差示扫描热量以及程序升温加氢等手段对新鲜的与反应后的催化剂以及沉积的碳进行了表征.结果表明,催化剂上有四种含碳物种,以三种形态存在,即无定形碳(聚合态)、丝状碳或石墨碳.这些催化剂上积炭的数量与种类各不相同,依赖于催化剂中金属Ni颗粒的大小与载体的织构特性.丝状碳的形成及其形貌与金属Ni颗粒的大小有着密切的联系.Ni颗粒小于15nm时能抑制丝状碳的形成与沉积,减少积炭的数量,同时能产生较多的活性Cα物种,从而在一定程度上导致催化剂具有较好的活性与稳定性.Ni/La2O3/γ-Al2O3 and Ni/La2O3/α-Al2O3 catalysts were prepared by the incipient wetness impregnation and evaporation methods. Their catalytic properties for the dry reforming of methane without a diluting gas were studied. The fresh and used catalysts and deposited carbon were characterized by H2 temperature-programmed reduction, N2 adsorption-desorption, X-ray diffraction, transmission electron microscopy, thermogravimetry coupled to differential scanning calorimetry, and temperature-programmed hydrogenation. The results showed that there were four carbon species that existed as three types, namely, amorphous (polymeric), filamentous, and graphitic carbon. The amount and type of carbon species on the catalysts depended on the size of Ni particles and texture of the support. The formation and morphology of filamentous carbon were clearly related to the size of Ni particles. Ni particles less than 15 nm suppressed the formation and deposition of filamentous carbons, decreased the amount of carbon deposition, and had more active C, species, resulting in a better activity and higher stability of the catalysts.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:216.73.216.249