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CuCl对Et_3NHCl/AlCl_3离子液体催化性能的影响 被引量:22

Effect of CuCl Additive on Catalytic Performance of Et_3NHCl/AlCl_3 Ionic Liquid in C_4 Alkylation
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摘要 用CuCl对Et3 NHCl/AlCl3 离子液体进行改性 ,并考察了其对异丁烷 丁烯烷基化反应的催化性能 .结果表明 ,烷基化油的收率达到 178% ,C8组分的含量达到 85 % ,辛烷值 (RON)达到 94 8.通过结构组成及电荷分布分析可知 ,在CuCl改性的Et3 NHCl/AlCl3 离子液体中形成了新的配位结构AlCl4CuCl-,它作为更好的碳正离子受体 ,在反应过程中可降低碳正离子的浓度 ,进而降低烯烃的聚合程度 ,抑制较长碳链烷烃的生成 ,改善烷基化油的组成 . In order to solve the highly corrosive and environmentally detrimental problem caused by the use of sulfuric acid and hydrofluoric acid as catalysts in alkylation of isobutane and butene, the environmentally benign acidic ionic liquid with CuCl additive was investigated as the catalyst for alkylation of isobutane and butene. The results showed that the modified ionic liquid was an excellent catalyst for the reaction, the yield of alkylate reached 178% to the butene volume, the total C 8 content in product alkylate was up to 85% and the RON of product alkylate was 94 8. The ratio of trimethylpentanes (TMP) to dimethylhexanes (DMH) in the product alkylate, which is considered as an important criterion for examining the alkylate quality (higher TMP/DMH ratio implies higher RON), increased sharply from 1 1 to 6 5 with the CuCl additive. The large change in catalytic activity of the modified ionic liquid was due to the formation of AlCl 4CuCl - species, which acted as a good acceptor for carbonium ions so as to hold back the formation of longer carbon chains.
出处 《催化学报》 SCIE CAS CSCD 北大核心 2004年第9期693-696,共4页
基金 国家青年自然科学基金资助项目 ( 2 0 2 0 60 18) 中国石油天然气集团公司科技中青年创新基金资助项目 ( 0 3E70 16)
关键词 氯化亚铜 三乙基氯化铵 氯化铝 离子液体 异丁烷 丁烯 烷基化 cuprous chloride, triethyl ammonium chloride, aluminum chloride, ionic liquid, isobutane, butene, alkylation
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  • 1[1]Kazarian S G,Briscoe B J,Welton T.Chem Commun,2000,(20):2047
  • 2[2]Blanchard L A,Hancu D,Beckman E J,Brennecke J F.Nature,1999,399(6731):28
  • 3[3]Nanjundiah C,McDevitt S F,Koch V R.J Electrochem Soc,1997,144(10):3392
  • 4[4]Gordon C M,McLean A J.Chem Commun,2000,(15):1395
  • 5[5]Boulaire V L,Gree R.Chem Commun,2000,(21):2195
  • 6[6]Gu Y L,Shi F,Deng Y Q.J Org Chem,2004,69(2):391
  • 7[7]Huddleston J G,Willauer H D,Swatloski R P,Visser A E,Rogers R D.Chem Commun,1998,(16):1765
  • 8[8]Carmichael A J,Haddleton D M,Bon S A F,Seddon K R.Chem Commun,2000,(14):1237
  • 9[11]Zhang Y H,Liu Zh Ch,Huang Ch P,Gao J S.催化学报(Chin J Catal),2003,24(10):729
  • 10[15]Ipatieff V N,Grosse A V.J Am Chem Soc,1935,57(9):1616

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