CO2 Adsorption-Based Separation by Metal Organic Framework (Cu-BTC) versus Zeolite (13X)

被引:390
作者
Liang, Zhijian [1 ,2 ]
Marshall, Marc [2 ]
Chaffee, Alan L. [1 ,2 ]
机构
[1] Monash Univ, Cooperat Res Ctr Greenhouse Gas Technol CO2CRC, Clayton, Vic 3800, Australia
[2] Monash Univ, Sch Chem, Clayton, Vic 3800, Australia
关键词
CARBON-DIOXIDE; HYDROGEN STORAGE; HIGH-CAPACITY; METHANE; ISOTHERMS; ADSORBENT; WATER;
D O I
10.1021/ef800938e
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
The potential for the metal organic framework (MOF) Cu-BTC to selectively adsorb and separate CO2 is considered. Isotherms for CO2, CH4, and N-2 were measured from 0 to 15 bar and at temperatures between 25 and 105 degrees C. The isotherms suggest a much higher working capacity (x4) for CO2 adsorption on Cu-BTC relative to the benchmark zeolite 13X over the same pressure range. Higher CO2/N-2 and CO2/CH4 selectivities in the higher pressure range (1 similar to 15 bar) and with lower heats of adsorption were also demonstrated. Cu-BTC was observed to be stable in O-2 at 25 degrees C, but its crystallinity was reduced in humid environments. The CO2 adsorption capacity was progressively reduced upon cyclic exposure to water vapor at low relative humidity (<30%), but leveled out at 75% of its original value after several water adsorption/desorption cycles.
引用
收藏
页码:2785 / 2789
页数:5
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