首页 | 本学科首页   官方微博 | 高级检索  
     


Hydrate-based pre-combustion carbon dioxide capture process in the system with tetra-n-butyl ammonium bromide solution in the presence of cyclopentane
Authors:Xiao-Sen Li  Chun-Gang Xu  Zhao-Yang Chen  Hui-Jie Wu
Affiliation:a Key Laboratory of Renewable Energy and Gas Hydrate, Guangzhou Institute of Energy Conversion, Chinese Academy of Sciences, Guangzhou 510640, PR China
b Guangzhou Center for Gas Hydrate Research, Chinese Academy of Sciences, Guangzhou 510640, PR China
c Graduate University of Chinese Academy of Sciences, Beijing 100083, PR China
Abstract:Effects of 0.29 mol% tetra-n-butyl ammonium bromide (TBAB) solution in conjunction with cyclopentane (CP) on the hydrate-based pre-combustion CO2 capture are investigated by the measurements of the gas uptakes, CO2 separation efficiencies and induction time of the hydrate formation at the different temperature-pressure conditions. The results show that the volume of the TBAB has an effect on the CO2 separation and the induction time, and the addition of the CP into the TBAB solution remarkably enhances the CO2 separation and shortens the induction time. The system with the CP/TBAB solution volume ratio of 5 vol% and TBAB solution/reactor effective volume ratio of 0.54 is optimum to obtain the largest gas uptake and the highest CO2 separation efficiency at 274.65 K and 4.0 MPa. Compared to the results with tetrahydrofuran (THF) as an additive [1], the gas uptake is enhanced by at least 2 times and the induction time is shortened at least 10 times at the similar temperature-pressure condition. In addition, the CO2 concentration in the decomposed gas from the hydrate slurry phase reaches approximately 93 mol% after the first-stage separation at 274.65 K and 2.5 MPa. The gas uptakes of more than 80 mol% are obtained after 400 s at the temperature range of 274.65-277.65 K and the pressure range of 2.5-4.5 MPa.
Keywords:Tetra-n-butyl ammonium bromide   Cyclopentane   Hydrate   IGCC   CO2 capture   Gas uptake   Induction time
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号