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
机构地区:[1]中国科学院大连化学物理研究所催化基础国家重点实验室
出 处:《催化学报》1997年第3期216-220,共5页
摘 要:催化剂Mo/HZSM-5在甲烷无氧脱氢芳构化反应中表现出很高的活性.用XRD,BET比表面,NH3-TPD及TPR等手段,对氨水抽提前后催化剂上的活性Mo物种进行了研究.XRD结果表明,Mo物种高度分散于分子筛表面.随着Mo担载量的提高,BET比表面积有所下降;但氨水抽提后,比表面积有很大程度的恢复.NH3-TPD结果表明,Mo物种优先占据分子筛中的强酸位.TPR结果显示出有MoO3晶相存在的催化剂较易被还原;但氨水抽提后,基本上无还原峰存在.据此可以认为,分子筛上担载的Mo物种随担载量的不同,形成了多种不同的结构类型,如单层分散的四配位和六配位结构,MoO3微晶以及Al2(MoO4)3晶体等.其中MoO3微晶与分子筛的结合力较弱,可被氨水抽提,它可能是甲烷无氧脱氢芳构化反应的主要活性物种.Mo/HZSM 5 catalysts show high catalytic activity in the absence of O 2 for dehydroaromatization of CH 4. The active Mo species on Mo/HZSM 5 catalysts before and after NH 4OH extraction were investigated by XRD, BET, NH 3 TPD and TPR analyses. The XRD patterns show that the Mo species are well dispersed on the zeolite surface. The specific surface area decreases with increasing Mo loading but they can be restored by NH 4OH extraction. NH 3 TPD results suggest that the Mo species prefer to deposit on the strong acid sites of HZSM 5 zeolite. TPR profiles show that there is a kind of Mo species which is easily reduced. No TPR peak can be obviously observed after NH 4OH extraction. There are several kinds of Mo species deposited on the surface. By referring to the Mo species of MoO 3 supported on Al 2O 3, it is proposed that the dissoluble Mo species in NH 4OH solution are MoO 3 crystallites and their aggregation in octahedral coordination, while the insoluble Mo species mainly are Al 2(MoO 4) 3 and MoO 2- 4 in tetrahedral coordination. The catalytic performance of Mo/HZSM 5 catalysts before and after NH 4OH extraction illustrates that the Mo species in MoO 3 micro crystallites in octahedral coordination are active for CH 4 activation in the absence of O 2, while the Mo species in tetrahedral coordination is less active for the reaction.
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:216.73.216.203