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还原温度对磷化NiW催化剂噻吩HDS反应活性的影响 被引量:2

EFFECT OF REDUCTION TEMPERATURE ON THE THIOPHENE HDS ACTIVITY OF PHOSPHATE TREATED NiW CATALYST
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摘要 采用磷酸氢二铵溶液对工业NiW催化剂进行了磷化处理,用TG,XRD,BET方法对所得的磷化催化剂进行表征,考察还原温度对磷化催化剂噻吩HDS(加氢脱硫)反应活性的影响。实验结果表明,随着焙烧温度提高,磷化催化剂前体的起始磷化还原温度升高,而磷化还原过程的失重率减小。还原温度对磷化催化剂的体相结构影响很小;随着还原温度的升高,磷化催化剂的比表面积增加。磷化催化剂有利于高温时的噻吩HDS反应,其噻吩HDS转化率随还原温度的增加而降低,适宜的NiW催化剂的磷化还原温度为550℃,此时该催化剂在反应温度为300℃和360℃时的噻吩HDS反应转化率分别为61.15%和99.45%。 A commercial NiW catalyst was treated with diammonium phosphate solution followed by calcination,and was characterized by TG/DTA, XRD and BET method. The hydrodesulfurization(HDS) activity of the treated catalyst reduced at various temperatures was investigated using thiophene as reactant. Results showed that the initial reduction temperature of the treated NiW catalyst increased with the increase of calcination temperature,and the weight loss during reduction decreased with the increase of calcination temperature. The reduction temperature had minor effect on the catalyst bulk structure, whereas surface area increased with the reduction temperature. The phosphate treated NiW catalyst exhibited good HDS activity at high reaction temperature(e, g. 360 ℃),and its HDS activity decreased with the increase of reduction temperature. Under the optimum catalyst reduction temperature of 550 ℃, at reaction temperatures of 300 ℃ and 360 ℃ ,the thiophene HDS conversion was 61.15% and 99. 45%, respectively.
出处 《石油炼制与化工》 CAS CSCD 北大核心 2007年第7期26-29,共4页 Petroleum Processing and Petrochemicals
基金 北京市自然科学基金项目(2052009) 北京市教委资助项目(KM200510017003) 中国石油化工股份有限公司资助项目(X04009)
关键词 磷酸氢二铵 催化剂 噻吩 加氢脱硫 diammonium phosphate catalyst thiophene hydrodesulfurization
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  • 1Do-Woan Kim, Dong-Keun Lee, Son-Ki Ihm, et al . CoMo bimetallic nitride catalysts for thiophene HDS[J]. Catal Lett A, 1997,43(1,2) :91-95.
  • 2Dhandapani B, St Clair T, Oyama S T, et al . Simultaneous hydrodesulfurization , hydrodeoxygenation, and hydrogenation with molybdenum carbide[J]. Appl Catal A, 1998, 168(2) :219-228.
  • 3Cruz Reyes J, Lopez-Agudo A, Lopez-Cordero R, et a] . Influence of phosphorus on the structure and the hydrodesulphurization and hydrodesulphurization activity of W/Al2O3 catalysts[J]. Catal Lett A, 1996,42(3,4) :119-126.
  • 4Paul Clark, Wei Li, Ted Oyama S. Synthsis and activity of a new catalyst for hydroprocessing tungsten phosphide[ J]. J Catal,2000, 200(1):140-147.
  • 5Stinner C, Prins R, Weber Th. Binary and ternary transition-metal phosphides as HDN catalysts[J]. J Catal, 2001, 202(1):187-194.
  • 6Furimsky E. Carbides and nitrides as potential catalysts for hydroprocessing[J]. Applied Catalysis A:General, 2003,240(1): 1-28.
  • 7Oyama S T. Novel catalysts for advanced hydroprocessing: transition metal phosphides[J]. J Catal, 2003, 216 (2):343-352.
  • 8Stinner C, Prins R, Weber T. Binary and ternary transition-metal phosphides as HDN catalysts[J]. J Catal, 2001, 202(1) : 187-194.
  • 9Clark P, Wang X, Oyama S T. Characterization of silica-supported molybdenum and tungsten phosphide hydroprocessing catalysts by 31p nuclear magnetic resonance spectroscopy[J]. J Catal, 2002, 207(2): 256-265.
  • 10Clark P, Li W, Oyama S T. Synthesis and activity of a new catalyst for hydroprocessing: tungsten phosphide[J]. J Catal, 2001, 200(1): 140-147.

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