LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

A charge-decorated porous framework with polar pores and open O donor sites for CO2/CH4 and C2H2/C2H4 separations.

Photo from wikipedia

Developing efficient adsorbent materials towards energy gas purification, e.g. CO2 removal from natural gas or hydrocarbon separation, is an important but extremely challenging task. Herein, taking advantage of a cationic… Click to show full abstract

Developing efficient adsorbent materials towards energy gas purification, e.g. CO2 removal from natural gas or hydrocarbon separation, is an important but extremely challenging task. Herein, taking advantage of a cationic bipyridinium ligand in competition with a multicarboxylate ligand for binding with metal ions, a porous material with open carboxylate oxygen atoms exposed on the pore surface has been demonstrated as an efficient adsorbent for gas separation. The polar environment arising from the cationic pyridinium moiety and the negative carboxylate group endows the title compound with selective affinity to CO2 over CH4. Moreover, the rich open O donor sites on the channel surface enable the resultant coordination polymer to selectively adsorb C2H2 over C2H4 through H-bonding interactions. The separation mechanism has been revealed by theoretical studies. This work provides a specific guidance for the design of applicable porous materials toward energy resource purification.

Keywords: donor sites; co2 ch4; c2h2 c2h4; open donor

Journal Title: Dalton transactions
Year Published: 2022

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.