Excitation generated preferential binding sites for ethane on porous carbon-copper porphyrin sorbents: ethane/ethylene adsorptive separation improved by light

激发在多孔碳-铜卟啉吸附剂上产生了乙烷的优先结合位点:光照改善了乙烷/乙烯的吸附分离。

阅读:1

Abstract

Energy-efficient separation of C(2)H(6)/C(2)H(4) is a great challenge, for which adsorptive separation is very promising. C(2)H(6)-selective adsorption has big implications, while the design of C(2)H(6)-sorbents with ideal adsorption capability, particularly with the C(2)H(6)/C(2)H(4)-selectivity exceeded 2.0, is still challenging. Instead of the current strategies such as chemical modification or pore space modulation, we propose a new methodology for the design of C(2)H(6)-sorbents. With a Cu-TCPP [TCPP = 5,10,15,20-tetrakis(4-carboxyphenyl)porphyrin] framework dispersed onto a microporous carbon and a hierarchical-pore carbon, two composite sorbents are fabricated. The composite sorbents exhibit enhanced C(2)H(6)-selective adsorption capabilities with visible light, particularly the composite sorbent based on the hierarchical-pore carbon, whose C(2)H(6) and C(2)H(4) adsorption capacities (0 °C, 1 bar) are targetedly increased by 27% and only 1.8% with visible light, and therefore, an C(2)H(6)-selectivity (C(2)H(6)/C(2)H(4) = 10/90, v/v) of 4.8 can be realized. With visible light, the adsorption force of the C(2)H(6) molecule can be asymmetrically enhanced by the excitation enriched electron density over the adsorption sites formed via the close interaction between the Cu-TCPP and the carbon layer, whereas that of the C(2)H(4) molecule is symmetrically altered and the forces cancelled each other out. This strategy may open up a new route for energy-efficient adsorptive separation of C(2)H(6)/C(2)H(4) with light.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。