期刊文献+

离子液体催化合成高黏度指数基础油工艺研究 被引量:4

Study of Synthetic Process of High Viscosity Index Base Oil with Ionic Liquid as Catalyst
下载PDF
导出
摘要 为制备高黏度指数合成基础油,以1-癸烯为齐聚原料、[Emim]Cl/Al Cl3离子液体为催化剂合成聚a-烯烃基础油,考察[Emim]Cl/Al Cl3摩尔比、催化剂用量、反应温度、反应时间和原料含水量对反应产物性能及收率的影响。结果表明,提高催化剂Al Cl3:[Emim]Cl摩尔比或降低反应温度,合成润滑油的黏度增加;增加催化剂用量可提高产物黏度,但会增加异构化等副反应,降低产物黏度指数;反应原料中含水量变化对聚合度有重要影响,但黏度指数保持稳定。在Al Cl3/[Emim]Cl摩尔比为2∶1,催化剂质量分数为10%,反应温度为60℃,反应时间4 h的条件下,合成油的100℃运动黏度在10.34 mm2/s以上,黏度指数高于143,适合作为柴油机多级润滑油基础油。 For the production of high viscosity index lubricating base stock, 1-decene was used to synthesize poly α-olefin with [ Emim ] Cl/AlCl3 ionic liquid as catalyst.The influences of AlCl3 and [ Emim ] Cl molar ratio, catalyst dosage, reaction temperature, reaction time and reactant water content on the product property and yield were studied.The experimental results indicate that increasing the molar ratio of AlCl3 and [ Emim] Cl or lowering reaction temperature will increase the viscosity of base oil.Excessive catalyst will leadto isomerization of product while increasing the viscosity.Water plays an important role in the degree of polymerization without significant effect on viscosity index of product.When molar ratio of AlCl3 and [ Emim] Cl is 2 : 1 ,catalyst weight is 10% ,reaction temperature is 60 ℃ ,reaction time is 4 h, the synthesized PAO,with viscosity above 10. 34 mm^2/s at 100 % and viscosity index higher than 143, is ideal to be the base stock of muhigrade lube oil for diesel engine.
出处 《润滑与密封》 CAS CSCD 北大核心 2015年第11期19-22,共4页 Lubrication Engineering
基金 中央高校基本科研业务费专项资金项目(3132014323)
关键词 离子液体 聚a-烯烃 合成基础油 ionic liquid poly-a-olefins synthetic base stock
  • 相关文献

参考文献6

  • 1贾宝军,韩宁,张克铮.汽车的节能要求与润滑剂技术的发展[J].润滑与密封,2006,31(3):175-180. 被引量:9
  • 2王东升,赵增辉,郎笑梅,赵成才,吴伟,扎哈洛夫A.V..Ziegler-Natta催化剂及其在聚乙烯生产中的应用研究进展[J].现代化工,2011,31(8):27-30. 被引量:7
  • 3Liu Z, Zhang X, Huang H, et al. Synthesis of ( co- ) polyethy- lene with broad molecular weight distribution by the heteroge-nous Ziegler-Natta catalysts via one-pot strategy [ J].Journal of Industrial and Engineering Chemistry, 2012, 18 ( 6 ) : 2217 - 2224.
  • 4Janiak C. Metallocene and related catalysts for olefin, alkyne and silane dimerization and oligomerization [ J ]. Coordination Chemistry Reviews, 2006,250 ( 1 ) : 66- 94.
  • 5Quijada R, Guevara J L, Galland G B,et al.Synthesis and prop- erties coming from the copolymerization of propene with o-ole- fins using different metallocene catalysts [ J ]. Polymer, 2005, 46(5) :1567-1574.
  • 6张普玉,娄帅,金邻豫,李文斌.离子液体应用研究进展[J].精细化工,2005,22(5):324-327. 被引量:46

二级参考文献101

  • 1郭子方,张敬梅,陈伟,周俊领,杨红旭.新型高效淤浆工艺聚乙烯催化剂的制备及其催化性能[J].石油化工,2005,34(9):840-843. 被引量:39
  • 2Zhu Z, Chang M, Aarons C J. High activity and good hydrogen response Ziegler-Natta polyethylene catalyst: US, 7153803 [ P ]. 2006 - 12 - 26.
  • 3Yashiki T, Minami S. Solid titanium catalyst component, ethylene polymerization catalyst containing the same, and ethylene polymerization process : US,6806222 [P]. 2004 - 10 - 19.
  • 4Wolf C R, Maria M C, Joao H Z, et al. Characterization of the nature of chemical species of heterogeneous Ziegler-Natta catalysts for the production of HDPE [ J ]. Catalysis Today, 2005,107/108 : 451 - 457.
  • 5Padmanabhan S,Sarma K R,Rupak K,et al. Synthesis of uhra high molecular weight polyethylene:A differentiate material for specialty applications [ J ]. Materials Science and Engineering B, 2010,168 ( 1/2/3 ) : 132 - 135.
  • 6Czaja K. Polymerization of ethylene by oxide-supported titanium halide catalyst:kinetic model with a deactivation of active species [J]. Polymer,2000,41 ( 11 ) :3937 - 3943.
  • 7Ferraro A, Dall' Occo T, Cecchin G. Process for the preparation of ethylene copolymers : US,7371806 [ P ]. 2008 - 05 - 13.
  • 8Yang C B, Kim S Y, Kim H Y,et al. Method of producing a catalyst for ethylene homo-and co-polymerization: US, 7045478 [ P ]. 2006 - 05 - 16.
  • 9肖明威,余世炯,叶晓峰.一种聚乙烯催化剂及其制备方法:中国,1624011A[P].2005-06-08.
  • 10Chen Y P, Fan Z Q. Ethylene/1-hexene copolymerization with TiCl4/MgCl2/AlCl3 catalyst in the presence of hydrogen[J]. European Polymer Journal, 2006,42 ( 10 ) : 2441 - 2449.

共引文献59

同被引文献45

引证文献4

二级引证文献8

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部