摘要
BaCO_3/La_2O_3中用离了半径更接近La ̄(3+)的Ca ̄(2+)取代部分Ba ̄(2+),制成(Ca_yBa_(8-y))La_2Ow,以增大低价离子在La_2O_3中的溶解度,增加结构缺陷,在620~680℃内,其乙烷氧化脱氢(ODE)的催化活性随C ̄(2+)的增加而持续上升,乙烯的选择性则单调下降。XRD和XPS检测证实,该体系于反应条件下形成的CaBa(CO_3)_2混合碳酸盐在表面上于较低的温度下分解为氧化物或过氧化物,这是它有较高ODE催化活性的又一原因。这些构成了探索高性能乙烷氧化制乙烯催化剂的基础。
In order to increase the solubility of the cation with lower valency in host oxideand provide higher concentration fo anionic vacanciee,the subetitution of Ba ̄(2+) over (Ca_yBa_(8-y))La_2Oweatalyst system with Ca ̄(2+) was carried out, since the ionic radii of Ca ̄(2+) and La ̄(3+) were comparable. Asthe results,between the temperature range of ODE reaction(620~680℃),the conversion of ethanefor oxidative dehydrogenation was enhanced,while the selectivity of ethene was declined monotonous-ly as the concentration of Ca ̄(2+) increased.with XRD and XPS analysis,it had determined that themixed carbonate CaBa(CO_3)_2 which formed under ODE reaction conditions, decomposed into corre-spondent oxides or peroxides,and it was the another reason for the CaO-BaCO_3/La_2O_3 having highercatalytic activity. These conclusions constituted the fundamental basic to search suitable catalyst sys-tem with higher ethene selectivity and /or higher conversion of ethane.
出处
《厦门大学学报(自然科学版)》
CAS
CSCD
北大核心
1994年第S1期184-189,共6页
Journal of Xiamen University:Natural Science
基金
国家自然科学基金和石油化工总公司资助项目