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镁-铝氟化物催化剂的制备及其催化1,1,1,3,3-五氟丙烷气相脱氟化氢反应性能的研究 被引量:1

Preparation of magnesium-aluminum fluoride catalyst and its catalytic performance in gas-phase dehydrofluorination of 1,1,1,3,3-pentafluoropropane
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摘要 利用多元醇氟化法制备了氟化铝、氟化镁及镁铝复合型氟化物等催化剂,并对所制催化剂在1,1,1,3,3-五氟丙烷(HFC-245fa)气相脱氟化氢制备1,3,3,3-四氟丙烯(HFO-1234ze)反应中的催化性能进行了研究。结果表明,单一氟化镁催化剂活性较低,HFC-245fa转化率仅为7.8%;以摩尔分数为9%Al/MgF_2作为催化HFC-245fa脱氟化氢反应催化剂,在反应温度为280℃,接触时间为25 s,催化剂用量为5 m L时,HFC-245fa的转化率、HFO-1234ze的选择性分别达到53%和100%,与单一组分氟化铝催化性能相当,且运行200 h后保持96%的初始活性。 Gas-phase catalytic dehydrofluorination of 1,1,1,3,3-pentafluoropropane( HFC-245 fa) to prepare 1,3,3,3-tetrafluoropropylene( HFO-1234 ze) is investigated over a series of magnesium fluoride,aluminum fluoride and magnesium-aluminum fluoride catalysts that are prepared by polyols mediated fluorination method. The results show that the conversion of HFC-245 fa is only 7. 9% over single magnesium fluoride catalyst. Higher conversion of HFC-245 fa( 53%) and higher selectivity of HFO-1234 ze( 100%) are achieved over 9 mol. % Al/MgF2 catalyst when the dosage of catalyst is 5 m L,the reaction temperature is 280℃ and the contact time is 25 s. The catalytic performance is same as single aluminum fluoride catalyst.The catalyst can still retain 96% of initial activity after it has been used for 200 hours.
作者 贾兆华 毛伟 白彦波 李晨 吕剑 JIA Zhao-hua;MAO Wei;BAI Yan-bo;LI Chen;LV Jian(Xi'an Modem Chemistry Research Institute, Xi'an 710065, China;State Key Laboratory for Efficient Development and Utilization of Fluorine & Nitrogen Chemicals, Xi'an 710065, China)
出处 《现代化工》 CAS CSCD 北大核心 2018年第4期87-90,共4页 Modern Chemical Industry
基金 国家自然科学基金项目(21327011 21503610)
关键词 镁-铝氟化物催化剂 1 1 1 3 3-五氟丙烷 1 3 3 3-四氟丙烯 脱氟化氢 magnesium-aluminum fluoride catalyst 1, 1, 1, 3, 3-pentafluoropropane 1, 3, 3, 3- tetrafluoropropylene dehydrofluorination
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  • 1张伟,吕剑.第三代发泡剂HFC-245fa[J].化工新型材料,2004,32(8):17-19. 被引量:8
  • 2吕剑,李惠黎,彭少逸.氟化物催化剂合成1,1,1,2-四氟乙烷的进展[J].工业催化,1996,4(2):11-16. 被引量:10
  • 3佐久冬彦,日比野泰雄.用于生产1,3,3,3-四氟丙烯的方法:中国.1014666656A[P].2007-06-11.
  • 4郜谷买.平流层臭氧的破坏及CFC消减问题.含氟材料,1987,61(4):22-28.
  • 5Molina M J, Rowland F S. Stratospheric sink for chlorofluoromethanes: chlorine atom-catalyzed destruction of ozone [ J]. Nature, 1974,249(5640 ) :810 - 812.
  • 6Winfield J M. From complex fluorides to CFC alternative-an account of fluorine chemistry at Glasgow [ J ]. J Fluorine Chem, 1999,100:235 - 246.
  • 7蒙特利尔协议书[Z].1987.
  • 8Lu Jü, Yang H E, Chen S K, et al. Systhesis of HFC-134a over CrF3/AlF3 catalysts [ J ]. Catal Lett, 1996,41 ( 3/4 ) : 221 - 224.
  • 9Rajiv R S, Hang T P, David P W, et al. Azeotrope-like compositions of tetrafluoropropene and trifluoroiodomethane: US,6969701 [ P]. 2005 - 11 -29.
  • 10Haszeldine R N. Reactions of fluorocarbon radicals part Ⅶ. Addition to trifluoromethyl-substituted acetylenes [ J ]. J Chem Soc, 1953,3490 - 3497.

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