Preparation of nitrogen-doped porous carlbon by ammonia gas treatment and the effects of N-doping on water adsorption

被引:228
作者
Horikawa, Toshihide [1 ]
Sakao, Noriyuki [1 ]
Sekida, Tomoki [1 ]
Hayashi, Jun'ichi [2 ]
Do, D. D. [3 ]
Katoh, Masahiro [1 ]
机构
[1] Univ Tokushima, Inst Sci & Technol, Dept Adv Mat, Tokushima 7708506, Japan
[2] Kansai Univ, Dept Chem Energy & Environm Engn, Suita, Osaka 5648680, Japan
[3] Univ Queensland, Sch Chem Engn, St Lucia, Qld 4072, Australia
基金
澳大利亚研究理事会;
关键词
OXIDIZED CARBON-FIBERS; BPL ACTIVATED CARBON; COAL-TAR PITCH; SURFACE-CHEMISTRY; CATALYTIC-ACTIVITY; PYROLYSIS; MECHANISM; COADSORPTION; FORMALDEHYDE; PRECURSORS;
D O I
10.1016/j.carbon.2011.12.033
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
Nitrogen-doped porous carbons (N-RFCC) were prepared by NH3-N-2 mixture gas treatment at high temperature during the carbonization process on resorcinol-formaldehyde cryogels. To show the role of N-doping on the adsorption behavior we carried out water adsorption, and it was found that the amount of water adsorbed is directly related to the nitrogen content over the low pressure region (P/P-o < 0.3). Applying the theoretical water adsorption model, Horikawa-Do (HD) model, to the adsorption isotherms of N-RFCCs, we could analyze the effects of nitrogen-doping on the adsorption mechanism. Although the concentration of functional groups of N-RFCC is almost equal to that of the non-doped RFCC, which was measured by Boehm titration method, the water adsorbed amounts of N-RFCCs over the low pressure region were larger. This is due to part of the doped nitrogen atoms act as functional groups, contributing to the total concentration of functional groups. The saturated concentrations depend on the packing fraction of water molecules, which in turn depends on the pore size. The packing fractions of N-RFCCs are larger than those of RFCCs, and this could be attributed to the high affinity between water clusters and N-doped surfaces, resulting in a reduced hydrophobicity of the surface. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1833 / 1842
页数:10
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