Sustainable synthesis of alkaline metal oxide-mesoporous carbons via mechanochemical coordination self-assembly

被引:24
|
作者
Shan, Weida [1 ,2 ]
Zhang, Pengfei [3 ,4 ]
Yang, Shize [3 ]
Zhu, Huiyuan [3 ]
Wu, Peiwen [3 ]
Xing, Huabin [1 ]
Dai, Sheng [2 ,3 ]
机构
[1] Zhejiang Univ, Coll Chem & Biol Engn, Key Lab Biomass Chem Engn, Minist Educ, Hangzhou 310027, Zhejiang, Peoples R China
[2] Univ Tennessee, Dept Chem, Knoxville, TN 37996 USA
[3] Oak Ridge Natl Lab, Chem Sci Div, Oak Ridge, TN 37830 USA
[4] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Shanghai 200240, Peoples R China
基金
中国国家自然科学基金;
关键词
ELECTROCHEMICAL ENERGY-STORAGE; NANOPOROUS CARBON; ACIDIC CONDITIONS; BLOCK-COPOLYMERS; METHYL-ORANGE; CO2; CAPTURE; NITROGEN; ADSORPTION; POLYMER; FORMALDEHYDE;
D O I
10.1039/c7ta08994e
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A simple, solvent-free, solid-state self-assembly strategy for the synthesis of alkaline-metal-oxide-doped mesoporous carbons (MCs) with tunable mesopores (similar to 5-9 nm), high surface areas (up to 571 m(2) g(-1)) and large pore volumes (up to 0.65 cm(3) g(-1)) is developed via mechanochemical assembly between polyphenol-Ca2+/Mg2+ composites and F127 copolymers. Interestingly, the as-made MgO-MCs not only offer good CO2 capacities (up to 1.6 mmol g(-1) at 0.15 bar and 273 K) and competitive CO2/N-2 selectivities (up to 41) but also exhibit high dye adsorption capacities (541 mg g(-1) for methylene blue and 435 mg g(-1) for methyl orange).
引用
收藏
页码:23446 / 23452
页数:7
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