Heteroatom-N,S co-doped porous carbons derived from waste biomass as bifunctional materials for enhanced CO2 adsorption and conversion

被引:26
|
作者
Luo, Lan [1 ]
Yang, Chunliang [1 ]
Liu, Fei [1 ]
Zhao, Tianxiang [1 ]
机构
[1] Guizhou Univ, Sch Chem & Chem Engn, Key Lab Green Chem & Clean Energy Technol, Guiyang 550025, Peoples R China
关键词
CO2; Adsorption; N; S co-doped; conversion; Cyclic carbonate; CYCLIC CARBONATES; ACTIVATED CARBON; EFFICIENT ADSORBENTS; POLYMER PRECURSOR; RECENT PROGRESS; IONIC LIQUID; N CONTENT; CAPTURE; SEPARATION; NITROGEN;
D O I
10.1016/j.seppur.2023.124090
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Biochar, a sustainable porous material, can be modified by doping heteroatomic active sites into the skeleton to make it equip specific properties. In this work, a series of N,S co-doped porous carbons were prepared by two-step carbonization method, using waste distiller's grains as raw material and thiourea as N and S source. The effects of activation temperature, activator dosage, and thiourea dosage on the structure and CO2 uptake of porous carbons were investigated, respectively. The results showed that the prepared N,S co-doped porous carbon with the high CO2 adsorption capacity was due to abundant micropores and the high specific surface area. Notably, NSAC-(1:1)550(1) exhibited the highest CO2 uptake of 7.02 mmol center dot g(-1) at 273.15 K and 1 bar, which was higher than that of the same type of biochar adsorbent reported in the literature. More importantly, these N,S codoped porous carbons can also be used as a recyclable promoter for the cycloaddition of CO2 with epoxide, affording the cyclic carbonates with up to 99 % yield under solvent-free conditions. This study provides a sustainable scheme for the development of low-cost bifunctional carbon materials to achieve efficient CO2 capture and conversion.
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页数:15
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