TY - JOUR
T1 - A new choice of polymer precursor for solvent-free method
T2 - Preparation of N-enriched porous carbons for highly selective CO2 capture
AU - Zhang, Peixin
AU - Zhong, Yao
AU - Ding, Jian
AU - Wang, Jun
AU - Xu, Mai
AU - Deng, Qiang
AU - Zeng, Zheling
AU - Deng, Shuguang
N1 - Funding Information:
This research was partially supported by the “Thousand Talent Program” of China, National Nature Science Foundation of China (No. 51672186 ), Nanchang University (China) and Arizona State University .
Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2019/1/1
Y1 - 2019/1/1
N2 - A facile one-pot melting-assisted and solvent-free method was successfully developed for the first time for preparing nitrogen-containing polymers. Followed by activation at temperatures ranging from 600 to 800 °C led to the formation of N-rich microporous carbons possessing narrow pore size distribution (ca. 0.5–3 nm), high specific surface area (ca. 1021.4–3657.0 m2 g−1), large pore volume (ca. 0.43–2.00 cm3 g−1) and high nitrogen content (ca. up to 5.11 wt%). Particularly, the porous carbons exhibited outstanding CO2 adsorption capacity of 2.65 and 7.38 mmol g−1 at 273 K and 0.15 and 1 bar, respectively; meanwhile, it also exhibited extremely large CO2 storage capacity of 22.06 mmol g−1 at 298 K and 20 bar. Moreover, the outstanding CO2/N2, CO2/CH4 and CH4/N2 selectivity up to 36.5, 6.9 and 5.1 at 298 K and 1 bar were achieved. The determinant factors on CO2 capture at 0.15, 1 and 20 bar were carefully investigated. Furthermore, this method could be 10-fold scaled up to produce almost identical high-performance carbons. For real-world applications, pressure/vacuum swing adsorption (P/VSA) working capacity, gas-mixture transit breakthrough experiment, and recycle feasibility are evaluated. Thus, these novel materials are promising candidates for CO2 capture from dilute gas mixtures.
AB - A facile one-pot melting-assisted and solvent-free method was successfully developed for the first time for preparing nitrogen-containing polymers. Followed by activation at temperatures ranging from 600 to 800 °C led to the formation of N-rich microporous carbons possessing narrow pore size distribution (ca. 0.5–3 nm), high specific surface area (ca. 1021.4–3657.0 m2 g−1), large pore volume (ca. 0.43–2.00 cm3 g−1) and high nitrogen content (ca. up to 5.11 wt%). Particularly, the porous carbons exhibited outstanding CO2 adsorption capacity of 2.65 and 7.38 mmol g−1 at 273 K and 0.15 and 1 bar, respectively; meanwhile, it also exhibited extremely large CO2 storage capacity of 22.06 mmol g−1 at 298 K and 20 bar. Moreover, the outstanding CO2/N2, CO2/CH4 and CH4/N2 selectivity up to 36.5, 6.9 and 5.1 at 298 K and 1 bar were achieved. The determinant factors on CO2 capture at 0.15, 1 and 20 bar were carefully investigated. Furthermore, this method could be 10-fold scaled up to produce almost identical high-performance carbons. For real-world applications, pressure/vacuum swing adsorption (P/VSA) working capacity, gas-mixture transit breakthrough experiment, and recycle feasibility are evaluated. Thus, these novel materials are promising candidates for CO2 capture from dilute gas mixtures.
KW - Biogas upgrading
KW - CO capture
KW - IAST selectivity
KW - N-doped porous carbon
KW - Solvent-free method
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U2 - 10.1016/j.cej.2018.08.219
DO - 10.1016/j.cej.2018.08.219
M3 - Article
AN - SCOPUS:85052911833
SN - 1385-8947
VL - 355
SP - 963
EP - 973
JO - Chemical Engineering Journal
JF - Chemical Engineering Journal
ER -