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TiO_2的加入对非负载的Ni_2P催化剂加氢脱氮性能的促进作用 被引量:6

PROMOTING EFFECT OF TiO_2 ADDITION ON HYDRODENITROGENATION PERFORMANCE OF NICKEL PHOSPHIDE
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摘要 分别采用共沉淀法和浸渍法将TiO2引入到非负载的磷化镍(Ni2P)催化剂中,并以喹啉(Q)作为模型化合物,考察了2种方法制备的Ti-Ni2P催化剂对喹啉加氢脱氮(HDN)反应性能的影响。同时,采用XRD、N2吸附和XPS手段表征了所制备的催化剂。结果表明,采用共沉淀法和浸渍法引入的TiO2均对Ni2P催化剂HDN反应活性有很大的促进作用,用浸渍法制备的Ni2P催化剂活性更高。存在于Ni2P表面的TiO2与Ni2P之间存在相互作用是促进Ni2P HDN活性的主要原因。浸渍法制备的Ni2P催化剂表面的TiO2含量更高,因此对HDN反应活性的促进效果更加显著。 The bulk Ti-Ni2 P catalysts were prepared by co-precipitation and impregnation of TiO2 on Ni2P, then characterized by XRD, XPS and TPR. Their hydrodenitrogenation (HDN) activities were evaluated by means of 1% quinoline in decalin. HDN activity of Ni2P was improved by TiO2 introduced by the two methods. However, the Ti-Ni2P catalyst prepared by impregnation showed higher activity in quinoline HDN reaction than Ti-Ni2P catalyst prepared by co-precipitation. The TiO2 species were mainly located on the surface of Ti-Ni2P catalysts and had strong interactions with surface Ni and P species, which was the main reason of HDN activity enhancement. More TiO2 species on the surface of the Ti-Ni2P catalyst prepared by impregnation may be responsible for higher HDN activity of the catalyst.
出处 《石油学报(石油加工)》 EI CAS CSCD 北大核心 2009年第4期522-526,共5页 Acta Petrolei Sinica(Petroleum Processing Section)
基金 国家自然科学基金(20503003 20333030) 教育部博士点专项基金(20030141026) 江苏高校自然科学重大基础研究项目(05KJA43004)资助
关键词 磷化镍(Ni2P) TiO2 加氢脱氮(HDN) 喹啉 nickel phosphide (Ni2P) TiO2 hydrodenitrogenation (HDN) quinoline
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参考文献15

  • 1KNUDSEN K G, COOPER B H, TOPSOE H. Catalyst and process technologies for ultra low sulfur diesel[J]. Appl Catal A: Gen, 1999, 189(2): 205-215.
  • 2SONG C S. An overview of new approaches to deep desulfurization for ultra-clean gasoline, diesel fuel and jet fuel[J]. Catal Today, 2003, 86(1-4): 211-263.
  • 3PHILIPS D C, SAWHILL S J, SELF R, et al. Synthesis, characterization, and hydrodesulfurization properties of silica-supported molybdenum phosphide catalysts[J]. J Catal, 2002, 207(2): 266-273.
  • 4OYAMA S T. Novel catalysts for advanced hydroprocessing: Transition metal phosphides [J]. J Catal, 2003, 216(1-2): 343-352.
  • 5STINNER C, PRINS R, WEBER T. Formation, structure, and HDN activity of unsupported molybdenum phosphide[J]. J Catal, 2000, 191 (2):438- 444.
  • 6ZUZANIUK V, PRINS R. Synthesis and characterization of silica-supported transition-metal phosphides as HDN catalysts[J]. J Catal, 2003, 219 (1) : 85-96.
  • 7STINNER C, PRINS R, WEBER T. Binary and ternary transition-metal phosphides as HDN[J].J Catal, 2001,202(1): 187-194.
  • 8RODRIGUEZ J A, KIM J Y, HANSON J C, et al. Physical and chemical properties of MoP, Ni2P, and MoNiP hydrodesulfurization catalysts: Time-resolved X-ray diffraction, density functional, and hydrodesulfurization activity studies[J].J Phys Chem B, 2003, 107(26): 6276-6285.
  • 9SUN F, WU W, WU Z, et al. Dibenzothiophene hydrodesulfurization activity and surface sites of silica- supported MoP, Ni2P, and NiMoP catalysts [J]. J Catal, 2004, 228(2): 298-310.
  • 10ABU I I, SMITH K J. The effect of cobalt addition to bulk MoP and Ni2 P catalysts for the hydrodesulfurization of 4, 6-dimethyldibenzothiophene [J]. J Catal, 2006, 241(2): 356-366.

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