吸附
复合数
材料科学
化学工程
结晶
石墨烯
溶剂
氧化物
多孔性
成核
复合材料
化学
有机化学
纳米技术
工程类
冶金
作者
Shanshan Shang,Zeyu Tao,Chao Yang,Aamir Hanif,Liangchun Li,Daniel C.W. Tsang,Qinfen Gu,Jin Shang
标识
DOI:10.1016/j.cej.2020.124666
摘要
Easily regenerable adsorbents are highly desirable for CO2 capture. In this regard, a modified synthesis method for preparing CuBTC and its graphene oxide ([email protected]) composites as adsorbents is developed using a mixed solvent strategy at 323 K for the first time. The addition of N, N-Dimethylformamide was vital for the crystallization of CuBTC at low temperature by accelerating the nucleation. The newly synthesized CuBTC showed much higher surface area and total pore volume, compared with CuBTC synthesized by conventional method. As a result, the as-synthesized CuBTC showed a CO2 adsorption capacity of 8.02 mmol/g at 273 K, 1 bar, which was 17–90% higher than the reported CO2 capacity of CuBTC prepared by conventional method. The fabrication of [email protected] composites enhanced the CO2 adsorption capacity mainly through the improved porosity and dispersion force. Compared with CuBTC, an improved CO2/N2 selectivity for [email protected]%GO was obtained from the binary breakthrough experiments, which is beneficial to practical gas separations. The partition coefficient of CuBTC and [email protected] composite were evaluated at different breakthrough levels, e.g., 5%, 10% and 100%, with an inlet CO2 partial pressure of 0.15 bar. [email protected]%GO displayed higher partition coefficient values than CuBTC at all three breakthrough levels. The cyclic adsorption experiments for regenerability evaluation showed that the CO2 adsorption reversibility for [email protected]%GO composite could maintain above 90%, while that of CuBTC dropped to less than 74% after five adsorption-desorption cycles. The [email protected] composite would be a promising CO2 capture adsorbent with both high CO2 adsorption capacity and remarkable regeneration performance.
科研通智能强力驱动
Strongly Powered by AbleSci AI