Scanning curves of water adsorption on graphitized thermal carbon black and ordered mesoporous carbon

被引:39
作者
Horikawa, Toshihide [1 ]
Muguruma, Takahiro [1 ]
Do, D. D. [2 ]
Sotowa, Ken-Ichiro [1 ]
Alcantara-Avila, J. Rafael [1 ]
机构
[1] Univ Tokushima, Inst Sci & Technol, Dept Adv Mat, Tokushima 7708506, Japan
[2] Univ Queensland, Sch Chem Engn, St Lucia, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
BPL ACTIVATED CARBON; CAPILLARY CONDENSATION; ORGANIC-COMPOUNDS; ISOSTERIC HEAT; VAPOR; COADSORPTION; CAPTURE; CO2;
D O I
10.1016/j.carbon.2015.08.034
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
Adsorption isotherms of water on porous carbons generally show large hysteresis loops whose origin is believed to be different from simple gases adsorption in mesoporous solids. In this paper, we discussed in details the behavior of water adsorption isotherms and their descending scanning curves for two carbons of different topologies, a highly graphitized thermal carbon black, Carbopack F, and a highly ordered mesoporous carbon, Hex. For both solids, very large hysteresis loops are observed, but their behaviors are different. For Carbopack F, the loop extends over a very wide range of pressure and the loop is larger when the descending is started from a higher loading; while for Hex, the hysteresis loop shows distinct steps, the number of which depends on the loading where the descending starts. By carefully analyzing the scanning curves from different loadings, we established the mechanism of water adsorption in Hex as a sequence of three steps: (1) water molecules adsorb on functional groups located at the junctions between adjacent basal planes of graphene layers, (2) growth of water clusters around the functional groups, and (3) bridging of adjacent clusters to form larger clusters, followed by a complete filling of mesopores. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:137 / 143
页数:7
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