Graphitic Carbon Nitride Functionalized with Polyethylenimine for Highly Effective Capture of Carbon Dioxide

被引:28
作者
Peng, Hai-Long [1 ]
Zhong, Fu-Yu [1 ]
Zhang, Jian-Bo [1 ]
Zhang, Jia-Yin [1 ]
Wu, Ping-Keng [3 ]
Huang, Kuan [1 ]
Fan, Jie-Ping [1 ]
Jiang, Li-Long [2 ]
机构
[1] Nanchang Univ, Sch Resources Environm & Chem Engn, Key Lab Poyang Lake Environm & Resource Utilizat, Minist Educ, Nanchang 330031, Jiangxi, Peoples R China
[2] Fuzhou Univ, Sch Chem Engn, Natl Engn Res Ctr Chem Fertilizer Catalyst NERC C, Fuzhou 350002, Fujian, Peoples R China
[3] IIT, Dept Chem Engn, Chicago, IL 60616 USA
基金
中国国家自然科学基金;
关键词
CO2; CAPTURE; ORGANIC POLYMER; ELECTROCATALYST; PERFORMANCE; COMPOSITES; CONVERSION; ADSORBENTS; NANOSHEETS; EVOLUTION; SORPTION;
D O I
10.1021/acs.iecr.8b02275
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Graphitic carbon nitride (g-C3N4) is a kind of two-dimensional material with unique properties, and can be facilely prepared from low-cost precursors. It has promising application in CO2 capture. However, the low alkalinity of nitrogen species in g-C3N4 makes its interaction with CO2 very weak. Aiming to promote the use of g-C3N4 for CO2 capture, a class of amine-functionalized g-C3N4 adsorbents were designed in the present work. The amine-functionalized g-C3N4 adsorbents were prepared by physical impregnation of polyethylenimine (PEI), which contains many amine groups and exhibits extremely low volatility, into the stacked pores of g-C3N4. It is found that, after the amine functionalization, the performance of g-C3N4 for CO, capture (including capacities and selectivities) are significantly improved. The highest CO2 capacity of PEI-g-C3N4 composites is 3.77 mmol/g when determined at 100 degrees C and ambient pressure, being superior to most of those of other g-C3N4 materials and solid amines reported in the literature. Furthermore, the CO2 adsorbed by PEI-g-C3N4 composites can be facilely stripped out by concentration swing, and the loss in CO2 capacity is negligible after 10 cycles of adsorption and desorption.
引用
收藏
页码:11031 / 11038
页数:8
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