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Ni2P/SAPO-41双功能催化剂的制备及其加氢异构化反应性能

Preparation of the Bifunctional Catalysts Ni2P/SAPO-41 and Their Catalytic Performance in the Hydroisomerization

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【作者】 蓝先恩贾国志魏小盟张玉琪吴骐杨心悦白雪峰吴伟

【Author】 LAN Xian-en;JIA Guo-zhi;WEI Xiao-meng;ZHANG Yu-qi;WU Qi;YANG Xin-yue;BAI Xue-feng;WU Wei;National Center for International Research on Catalytic technology, College of Chemistry and Material Sciences, Heilongjiang University;Institute of Petrochemistry, Heilongjiang Academy of Sciences;

【通讯作者】 吴伟;

【机构】 黑龙江大学化学化工与材料学院国家级催化技术国际联合研究中心黑龙江省科学院石油化学研究院

【摘要】 以二正丁胺为模板剂合成的SAPO-41分子筛为酸性载体,用程序升温还原法制备不同担载量的x Ni2P/SAPO-41(x为Ni2P的质量百分含量)系列双功能催化剂,并作为对比制备了3Ni/SAPO-41催化剂。分别采用X射线衍射(XRD)、N2物理吸附、透射电镜(TEM)、吡啶吸附的红外光谱(Py-IR)和H2-化学吸附等方法对催化剂的物理化学性能进行了表征,并采用固定床反应器对其催化正十六烷加氢异构化反应性能进行了评价。结果表明,与3Ni/SAPO-41催化剂相比,x Ni2P/SAPO-41系列双功能催化剂表现出更高的催化活性和异十六烷的选择性,其中3Ni2P/SAPO-41的催化性能最佳,在正十六烷转化率为80.7%时,异十六烷的选择性和收率分别高达82.5%和66.6%。

【Abstract】 The SAPO-41 molecular sieve as acidic supports is synthesized with the di-n-butylamine(DBA)as template,and a series of bifunctional catalysts xNi2P/SAPO-41(x is the mass percentage of Ni2P)with different Ni2P loadings are prepared by temperature programmed reduction method.A 3Ni/SAPO-41 catalyst is prepared as a comparison.The physicochemical properties of the catalysts are characterized by X-ray diffraction(XRD),N2physical adsorption,transmission electron microscopy(TEM),IR spectroscopy of adsorbed pyridine(Py-IR)and H2-chemical adsorption methods.The catalytic performance in the hydroisomerization of n-hexadecane is evaluated in a fixed bed reactor.The results show that the xNi2P/SAPO-41 series of bifunctional catalysts exhibits a higher catalytic activity and selectivity for iso-hexadecane than the 3Ni/SAPO-41 catalyst,among which the 3Ni2P/SAPO-41 displays the best catalytic performance,when the conversion of n-hexadecane is 80.7%,the selectivity and the yield of iso-hexadecane can reach 82.5%and 66.6%respectively.

【基金】 国家自然科学基金项目(编号:21676074);国家级大学生创新训练计划项目(编号:201810212001)
  • 【文献出处】 化学与黏合 ,Chemistry and Adhesion , 编辑部邮箱 ,2019年03期
  • 【分类号】TQ426;TE667
  • 【下载频次】293
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