Novel Covalent Triazine Framework for High-Performance CO2 Capture and Alkyne Carboxylation Reaction
Source abstract
Abstract
Carbon dioxide capture and conversion have attracted extreme enthusiasm from the scientific community owing to global warming and environmental problems. However, conversion of CO2 under atmospheric pressure is of great challenge because of the inertness of CO2. Herein, we present a novel covalent triazine framework (CTF-DCE) prepared via ZnCl2-catalyzed ionothermal trimerization reaction of di(4-cyanophenyl)ethyne, which displays a high Brunauer–Emmett–Teller surface area of 1355 m2 g–1 and an excellent CO2 capture capacity of 191 mg/g at 273 K/1 bar. More importantly, silver species can be successfully fixed on the CTF matrix to produce a stable CTF-DCE-Ag heterogeneous catalyst for outstanding catalysis in the terminal alkyne carboxylation reactions under atmospheric pressure. CTF-DCE-Ag exhibited over sixfold higher turnover numbers than Ag@MIL-101. The recyclability test of the CTF-DCE-Ag catalyst demonstrated a great potential application in various environmental and energy-related applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Carbon dioxide utilization in catalysis · Covalent Organic Framework Applications · CO2 Reduction Techniques and Catalysts
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemistry & Material Science, Shanxi Normal University, Linfen, Shanxi 041004, China
The Inspection and Quarantine Technology Center of Inner Mongolia Entry−Exit Inspection and Quarantine Bureau, Hohhot 010020, China
Funding
National Natural Science Foundation of China · Shanxi University · Central Committee of the Communist Party of China · Science Foundation for Youths, Shanxi Province
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