Enhancement of CO2 adsorption on phenolic resin-based mesoporous carbons by KOH activation

被引:131
作者
de Souza, Luiz K. C. [1 ,2 ]
Wickramaratne, Nilantha P. [1 ]
Ello, Aime Serge [1 ,3 ]
Costa, Maria J. F. [1 ,4 ]
da Costa, Carlos E. F. [2 ]
Jaroniec, Mietek [1 ]
机构
[1] Kent State Univ, Dept Chem & Biochem, Kent, OH 44242 USA
[2] Fed Univ Para UFPA, ICEN, Dept Chem, Lab Catalysis & Oilchem, BR-66075110 Belem, Para, Brazil
[3] Univ Felix Houphouet Boigny Cocody, Lab Chim Phys, Abidjan, Cote Ivoire
[4] Univ Fed Rio Grande do Norte, Inst Chem, BR-59078970 Natal, RN, Brazil
关键词
MOLECULAR-SIEVES; SMALL MICROPORES; DIOXIDE; CAPTURE; TEMPERATURE;
D O I
10.1016/j.carbon.2013.08.034
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
Carbons with high surface area and large volume of ultramicropores were synthesized for CO2 adsorption. First, mesoporous carbons were produced by soft-templating method using triblock copolymer Pluronic F127 as a structure directing agent and formaldehyde and either phloroglucinol or resorcinol as carbon precursors. The resulting carbons were mainly mesoporous with well-developed surface area, large total pore volume, and only moderate CO2 uptake. To improve CO2 adsorption, these carbons were subjected to KOH activation to enhance their microporosity. Activated carbons showed 2-3-fold increase in the specific surface area, resulting from substantial development of microporosity (3-5-fold increase in the micropore volume). KOH activation resulted in enhanced CO2 adsorption at 760 mmHg pressure: 4.4 mrnol g(-1) at 25 degrees C, and 7 mmol g(-1) at 0 degrees C. This substantial increase in the CO2 uptake was achieved due to the development of ultramicroporosity, which was shown to be beneficial for CO2 physisorption at low pressures. The resulting materials were investigated using low-temperature nitrogen physisorption, CO2 sorption, and small-angle powder X-ray diffraction. High CO2 uptake and good cyclability (without noticeable loss in CO2 uptake after five runs) render ultramicroporous carbons as efficient CO2 adsorbents at ambient conditions. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:334 / 340
页数:7
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