Tailoring the surface chemistry and porosity of activated carbons: Evidence of reorganization and mobility of oxygenated surface groups

被引:72
|
作者
Vivo-Vilches, Jose F. [1 ]
Bailon-Garcia, Esther [1 ]
Perez-Cadenas, Agustin F. [1 ]
Carrasco-Marin, Francisco [1 ]
Maldonado-Hodar, Francisco J. [1 ]
机构
[1] Univ Granada, Fac Ciencias, Dept Quim Inorgan, E-18071 Granada, Spain
关键词
NITRIC-ACID; ADSORPTION; SITES; CO2; SIZE; DESORPTION; COMPLEXES; OXIDATION; MERCURY; XPS;
D O I
10.1016/j.carbon.2013.11.030
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
An activated carbon with developed porosity and surface area (S-BET = 2387 m(2) g(-2)) was prepared by chemical activation and then oxidized with ammonium peroxydisulfate. The oxidation treatment destroyed mesopore walls leading to a severe surface area reduction. Specific thermal treatments were carried out in different portions of the oxidized sample to selectively remove the oxygenated surface complexes. The combination of different techniques revealed that thermal treatment between 300 and 500 degrees C produces a strong reorganization of oxygenated groups on the chemical structure of carbons. CO2-evolving groups (around 75 wt.%) are selectively transformed into CO-evolving groups. These processes only occur inside the pores, and involve CO2 desorption and re-adsorption in this temperature range. At a higher treatment temperature (700 degrees C), re-oxidation is prevented and the surface chemistry becomes quite similar to the original activated carbon. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:520 / 530
页数:11
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