期刊文献+

甲醇多相羰化制甲酸甲酯新催化体系的研究 被引量:1

Studies on A New Catalytic System for Heterogeneous Carbonylation of Methanol to Methyl Formate
下载PDF
导出
摘要 By using zeolite-supported alkali methoxide liquid-film catalysts, such as KOCH3-PEG/NaZSM-5(or NaY), the heterogeneous catalytic carbonylation of methanol to methyl formate was realized in a fixed-bed continuous flow reactor. Under the reaction conditions of 353 K,1.0 MPa, feedgas composition of CO/CH3OH=6.48(molar ratio) and GHSV=11160h-1, the STY of MF reached up to 1900mg/(h·gcat.), with selectivity to MF at 100%.The experimental results indicated that methoxide anion CH3O- was crucial catalyti-cally active species. The role of the additive polyethylene glycol(PEG) in generating a liquid-film environment, in which the carbonylation reaction would take place, is important,espe-cially in the case of supports with large pore-diameter as SiO2. However, in the case of some support materials with abundant micropore structure such as ZSM-5 or Y-type zeolite, it is probable to design and select appropriate reaction conditions(mainly, temperature and partial pressure of methanol in feedstream) to generate directly liquid-film of methanol by means of the "capillary condensation effect", as a consequence, addition of PEG may be cut down, or even, avoided. By using zeolite-supported alkali methoxide liquid-film catalysts, such as KOCH3-PEG/NaZSM-5(or NaY), the heterogeneous catalytic carbonylation of methanol to methyl formate was realized in a fixed-bed continuous flow reactor. Under the reaction conditions of 353 K,1.0 MPa, feedgas composition of CO/CH3OH=6.48(molar ratio) and GHSV=11160h-1, the STY of MF reached up to 1900mg/(h·gcat.), with selectivity to MF at 100%.The experimental results indicated that methoxide anion CH3O- was crucial catalyti-cally active species. The role of the additive polyethylene glycol(PEG) in generating a liquid-film environment, in which the carbonylation reaction would take place, is important,espe-cially in the case of supports with large pore-diameter as SiO2. However, in the case of some support materials with abundant micropore structure such as ZSM-5 or Y-type zeolite, it is probable to design and select appropriate reaction conditions(mainly, temperature and partial pressure of methanol in feedstream) to generate directly liquid-film of methanol by means of the 'capillary condensation effect', as a consequence, addition of PEG may be cut down, or even, avoided.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 1997年第8期1364-1366,共3页 Chemical Journal of Chinese Universities
基金 国家教育委员会博士点基金
关键词 甲醇 甲酸甲酯 多相催化 羰化 MF 催化剂 Methanol, Methyl formate, Heterogeneous carbonylation, Supported liquid-film catalyst
  • 相关文献

同被引文献21

  • 1张一平.均相催化剂的固载化研究[J].浙江教育学院学报,2004(5):13-18. 被引量:6
  • 2Cornils B,Herrmann W A.Applied homogeneous catalysis with organometallic compounds[M].Weinheim:John Wiley & Sons,2000.
  • 3Cornils B,Herrmann W A,Eckl R W.Industrial aspects of aqueous catalysis[J].J Mol Catal A:Chem,1997,116:27 -33.
  • 4Arhancet J P,Davis M E,Merola J S,et al.Hydroformylation by supported aqueous-phase catalysis:A new class of heterogeneous catalysts[J].Nature,1989,339:454.
  • 5Reilly C R,Lerou J J.Supported liquid phase catalysis in selective oxidation[J].Catalysis Today,1998,41:433-441.
  • 6Arhancet J P,Davis M E,Merola J S,et al.Supported aqueous-phase catalysts[J].J Catal,1990,121:327-339.
  • 7Bhanage B M,Shirai M,Arai M.Heterogeneous catalyst system for Heck reaction using supported ethylene glycol phase Pd-TPPTS catalyst with inorganic base[J].J Mol Catal A:Chem,1999,145:69 -74.
  • 8Fujita S,Yoshida T,Bhanage B M,et al.Palladiumbased supported liquid phase catalysts[J].J Mol Catal A:Chem,2002,180:277-284.
  • 9Fujita S,Yoshida T,Bhanage B M,et al.Heaction reaction with a silica supported Pd-TPPTS liquid phase catalyst[J].J Mol Catal A:Chem,2002,188:37 -43.
  • 10Diza E,Adrio G,Ordonez S,et al.Cyclohexene reactivity over palladium acetate supported in liquid phase[J].Catal lett,2004,96 (3-4):169-175.

引证文献1

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