期刊文献+

CO_2 capture from binary mixture via forming hydrate with the help of tetra-n-butyl ammonium bromide 被引量:22

CO_2 capture from binary mixture via forming hydrate with the help of tetra-n-butyl ammonium bromide
下载PDF
导出
摘要 Hydrate formation rate and separation effect on the capture of CO2 from binary mixture via forming hydrate with 5 wt% tetra-n-butyl ammonium bromide (TBAB) solution were studied. The results showed that the induction time was 5 min, and the hydrate formation process finished in 1 h at 4.5 ℃ and 4.01 MPa. The hydrate formation rate constant reached the maximum of 1.84× 10^-7 molZ/(s.J) with the feed pressure of 7.30 MPa. The CO2 recovery was about 45 % in the feed pressure range from 4.30 to 7.30 MPa. Under the feed pressure of 4.30 MPa, the maximum separation factor and CO2 concentration in hydrate phase were 7.3 and 38.2 mol%, respectively. The results demonstrated that TBAB accelerated hydrate formation and enriched CO2 in hydrate phase under the gentle condition. Hydrate formation rate and separation effect on the capture of CO2 from binary mixture via forming hydrate with 5 wt% tetra-n-butyl ammonium bromide (TBAB) solution were studied. The results showed that the induction time was 5 min, and the hydrate formation process finished in 1 h at 4.5 ℃ and 4.01 MPa. The hydrate formation rate constant reached the maximum of 1.84× 10^-7 molZ/(s.J) with the feed pressure of 7.30 MPa. The CO2 recovery was about 45 % in the feed pressure range from 4.30 to 7.30 MPa. Under the feed pressure of 4.30 MPa, the maximum separation factor and CO2 concentration in hydrate phase were 7.3 and 38.2 mol%, respectively. The results demonstrated that TBAB accelerated hydrate formation and enriched CO2 in hydrate phase under the gentle condition.
出处 《Journal of Natural Gas Chemistry》 EI CAS CSCD 2009年第1期15-20,共6页 天然气化学杂志(英文版)
关键词 CO2 CAPTURE HYDRATE tetra-n-butyl ammonium bromide CO2 capture hydrate tetra-n-butyl ammonium bromide
  • 相关文献

参考文献29

  • 1Aaron D,Tsouris C.Sep Sci Technol,2005,40(1-3):321 被引量:1
  • 2Yang H Q,Xu Z,Fan M,Fan M,Gupta R,Slimane R B,Bland A E,Wright I.J Environ Sci,2008,20:14 被引量:1
  • 3Figueroa J D,Fout T,Pi S,Plasynski S,McIlvried H,Srivastava R D.Int J Greenhouse Gas Contr,2008,2:9 被引量:1
  • 4Seo Y T,Moudrakovski I L,Ripmeester J A,Lee J W,Lee H.Environ Sci Technol,2005,39:2315 被引量:1
  • 5Linga P,Adeyemo A,Englezos P,Environ Sci Technol,2008,42:315 被引量:1
  • 6Guillemette G.US 3085832,1962 被引量:1
  • 7Fan S S,Cheng H Y,Chen G J,Guo T M.Xiandai Huagong (Modern Chem Ind),1999,19(2):11 被引量:1
  • 8Wang X L,Chen G J,Yang L Y,Zhang L W.Science in China Series B-Chemistry,2008,51(2):171 被引量:1
  • 9Max M D.US 6767471B2,2004 被引量:1
  • 10Purwanto Y A,Oshita S,Seo Y,Kawagoe Y.J Food Eng,2001,47(2):133 被引量:1

同被引文献100

引证文献22

二级引证文献114

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