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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:《高等学校化学学报》1998年第10期1645-1649,共5页Chemical Journal of Chinese Universities
基 金:国家自然科学基金
摘 要:以钼磷酸+硝酸钴、仲钼酸铵+硝酸钴、仲钼酸铵为前体活性相组元及γ-Al2O3为载体,制备了负载型双(单)组元过渡金属氮化物[CoMoN-(Ⅰ,Ⅱ,Ⅲ),MoN-Ⅳ],并利用BET、XPS、H2-TPD及Raman等手段进行了表征;以正己烷+环己烷+吡啶为模型底物考察了上述催化剂的吡啶加氢脱氮活性.与CoMoN-Ⅱ、CoMoN-Ⅲ和MoN-Ⅳ相比,CoMoN-I具有较高的吡啶加氢脱氮活性.γ Alumina supported bi(mono)metallic transition metal nitrides were prepared respectively with 12 phosphomolybdic acid plus cobalt nitrate(denoted as CoMoN Ⅰ and CoMoN Ⅱ related with the precursor of the nitride, CoMoN Ⅰ, calcined at 773 K for 6 h before nitriding), ammonium heptamolybdate plus cobalt nitrate(denoted as CoMoN Ⅲ), and only ammonium heptamolybdate(denoted as MoN Ⅳ) as the precursor active phases, using temperature programmed reduction with NH 3, and characterized with BET, XRD, XPS, H 2 TPD and Raman. Pyridine was selected as a model substrate in order to evaluate the HDN catalytic activity of nitrides synthesized above. It was found that CoMoN Ⅰ possesses conspicuously high pyridine HDN activity as compared to that of CoMoN Ⅱ, CoMoN Ⅲ and MoN Ⅳ.
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