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MgAPO-11分子筛的合成及Pt/MgAPO-11在正十二烷临氢异构化反应中的催化性能

Synthesis of MgAPO-11 Molecular Sieves and the Catalytic Performance of Pt/MgAPO-11 for n-Dodecane Hydroisomerization

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【作者】 杨晓梅徐竹生马怀军徐云鹏田志坚林励吾

【Author】 YANG Xiaomei~ 1,2 , XU Zhusheng~1, MA Huaijun~ 1,2 , XU Yunpeng~1, TIAN Zhijian~ 1* , LIN Liwu~ 1,3 (1 Dalian Institute of Chemical Physics, The Chinese Academy of Sciences, Dalian 116023, Liaoning, China; 2 Graduate University of The Chinese Academy of Sciences, Beijing 100049, China; 3 State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, The Chinese Academy of Sciences, Dalian 116023, Liaoning, China)

【机构】 中国科学院大连化学物理研究所中国科学院大连化学物理研究所 辽宁大连116023中国科学院研究生院北京100049辽宁大连116023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

【摘要】 采用常规水热合成法合成了系列MgAPO-11分子筛,考察了晶化时间、P/Al投料比和Mg源对MgAPO-11分子筛的物相、酸性以及Pt/MgAPO-11催化正十二烷临氢异构化反应性能的影响.分别用X射线衍射、X射线荧光光谱和NH3程序升温脱附测定了样品的晶相、Mg含量和酸性质.结果表明,合成条件影响着合成产物的晶相组成、Mg含量及酸性质,从而影响到Pt/MgAPO-11在正十二烷临氢异构化反应中的催化性能.反应结果显示,Pt/MgAPO-11催化剂的催化活性与MgAPO-11分子筛的强酸位数目密切相关.较短的晶化时间、合成凝胶的P/Al摩尔比为1·0以及使用Mg(NO3)2为Mg源有利于提高MgAPO-11的强酸位数目,从而提高Pt/MgAPO-11的催化活性.

【Abstract】 A series of MgAPO-11 molecular sieves have been synthesized by varying the crystallization time, the P/Al molar ratio, and the Mg source. X-ray diffraction, X-ray fluorescence spectroscopy, and temperature-programmed desorption of NH3 have been employed to characterize the crystalline phase, the Mg content, and the acidity of MgAPO-11, respectively. The results show that the synthesis conditions have an effect on the crystalline phase, the Mg content, the acidity, and thereby the catalytic performance of Pt/MgAPO-11 in the hydroisomerization of n-dodecane. The reaction data reveal that the activity of Pt/MgAPO-11 is dependent on the amount of strong acid sites of MgAPO-11. Short crystallization time, P/Al molar ratio of 1.0, and Mg(NO32 as the Mg source favor the increase in the amount of the strong acid sites of MgAPO-11 and hence promote the catalytic activity of Pt/MgAPO-11 for the hydroisomerization of n-dodecane.

  • 【文献出处】 催化学报 ,Chinese Journal of Catalysis , 编辑部邮箱 ,2006年11期
  • 【分类号】O643.32
  • 【被引频次】12
  • 【下载频次】259
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