New insights into the influence of activated carbon surface oxygen groups on H2O2 decomposition and oxidation of pre-adsorbed volatile organic compounds

被引:49
作者
Anfruns, Alba [1 ]
Garcia-Suarez, Eduardo J. [2 ]
Montes-Moran, Miguel A. [2 ]
Gonzalez-Olmos, Rafael [1 ]
Martin, Maria J. [1 ]
机构
[1] Univ Girona, Inst Environm, LEQUIA, E-17071 Girona, Catalonia, Spain
[2] CSIC, Inst Nacl Carbon, E-33080 Oviedo, Spain
关键词
HYDROGEN-PEROXIDE; CATALYTIC DECOMPOSITION; AQUEOUS-SOLUTION; PART I; CHEMISTRY; WATER; 4-CHLOROPHENOL; CONTAMINANTS; ADSORPTION; OZONATION;
D O I
10.1016/j.carbon.2014.05.009
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
In this study, the influence of the surface oxygen groups of activated carbons (ACs) on the decomposition of H2O2 and the consequent (OH)-O-center dot radicals generation is investigated. The oxidation of pre-adsorbed volatile organic compounds by H2O2 is also studied. Four ACs, with low percentage of inorganic matter (<0.2%), similar textural properties but differing in their surface oxygen content were evaluated. The surface oxygen groups of the ACs were characterised by using appropriate characterisation techniques (temperature programmed desorption and X-ray photoelectron spectroscopy). The kinetic curves of H2O2 decomposition were very similar for all the ACs. However, different profiles in the production of (OH)-O-center dot radicals were observed. (OH)-O-center dot radicals generation seemed to be promoted by low surface oxygen contents. Oxidation of two volatile organic compounds (VOCs) of different polarity, methyl ethyl ketone (MEK) and toluene, pre-adsorbed onto the ACs was finally investigated. H2O2 was used as oxidising agent. Both VOCs presented similar maximum oxidation rates, around 70%, in spite of their different hydrophobicity. Some evidences are provided supporting that oxidation of pre-adsorbed VOCs can take place in the inner pore structure of the ACs. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:89 / 98
页数:10
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