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作 者:刘振林[1] 孟明[1] 伏义路[1] 姜明[1] 胡天斗[2] 谢亚宁[2] 刘涛[2]
机构地区:[1]中国科学技术大学化学物理系,合肥230026 [2]中国科学院高能物理研究所,北京100039
出 处:《物理化学学报》2001年第7期631-635,共5页Acta Physico-Chimica Sinica
基 金:国家自然科学基金(29873044);BSRF重点课题资助项目
摘 要:采用程序升温氮化的方法制备了分子筛负载的钼氮化物催化剂,并用EXAFS方法研究了氮化前后Mo原子的局域配位情况.氮化前负载MoO_3样品的径向结构函数中有三个峰,其中前两个峰对应着最近的Mo-O配位壳层,但是第一个峰与第二个峰的比例比晶体MoO_3中的比例大很多,表明分子筛负载的MoO_3具有更紧密的结构.氮化以后,Mo_2N样品的径向结构函数中有三个峰,对应于一个Mo-N和两个Mo-Mo配位壳层,与面心立方模型符合得很好.根据XRD和EXAFS谱的计算表明,Mo_2N中的N原子使Mo-Mo键拉长并削弱.分子筛负载的Mo2N样品具有与非负载Mo_2N样品近似相同的径向结构函数,只是对应于Mo-N壳层的峰较弱,表明负载的Mo_2N具有更大的结构无序性.Zeolites supported Mo nitrides were prepared via MoO_3+NH_3 reaction in temperature programmed mannar.The XRD data show that the frame structure of NaY and Na-ZSM-5 zeolites can still be maintained after nitridation at 973K.By analysis of the extended X-ray absorption fine structure(EXAFS) of the Mo K-absorption edge,the structural informations of both oxidic and nitrided Mo catalysts were obtained.The supported MoO_3 samples show three peaks in the radial structure function(RSF).The first two peaks correspond to the nearest Mo-O coordination shell,but the ratio of the first peak to the second one is much larger than that of the MoO_3.This suggests that the MoO_3 supported on zeolites has more compact structure than the unsupported one.There are three peaks in the RSF of Mo_2N,representing one Mo-N and two Mo-Mo shells,which is in good agreement with the face-centered cubic model.Calculation from X-ray diffraction data and EXAFS spectra reveals that the N atoms in Mo_2N lengthen the distance between Mo atoms and weaken the Mo-Mo bond.Supported Mo_2N samples give out nearly the same RSFs as the Mo_2N,only the peak corresponding to Mo-N shell is weak,suggesting that the supported Mo_2N has more structural disorder than the unsupported one.Mo_2N supported on Na-ZSM-5 gives out shorter coordination distance than supported on NaY,suggesting stronger interaction between Mo_2N and Na-ZSM-5.
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