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
相关论文
共 32 条
[1]   H2O2-based oxidation processes for the regeneration of activated carbons saturated with volatile organic compounds of different polarity [J].
Anfruns, Alba ;
Montes-Moran, Miguel A. ;
Gonzalez-Olmos, Rafael ;
Martin, Maria J. .
CHEMOSPHERE, 2013, 91 (01) :48-54
[2]  
[Anonymous], CARBON MAT CATALYSIS
[3]  
Bansal R.C., 1988, ACTIVE CARBON
[4]   The use of cyclic voltammetry to assess the activity of carbon materials for hydrogen peroxide decomposition [J].
Dominguez, C. M. ;
Quintanilla, A. ;
Ocon, P. ;
Casas, J. A. ;
Rodriguez, J. J. .
CARBON, 2013, 60 :76-83
[5]   Hydroxyl radical/ozone ratios during ozonation processes. II. The effect of temperature, pH, alkalinity, and DOM properties [J].
Elovitz, MS ;
von Gunten, U ;
Kaiser, HP .
OZONE-SCIENCE & ENGINEERING, 2000, 22 (02) :123-150
[6]   Modification of the surface chemistry of activated carbons [J].
Figueiredo, JL ;
Pereira, MFR ;
Freitas, MMA ;
Orfao, JJM .
CARBON, 1999, 37 (09) :1379-1389
[7]   Characterization of active sites on carbon catalysts [J].
Figueiredo, Jose L. ;
Pereira, Manuel F. R. ;
Freitas, Maria M. A. ;
Orfao, Jose J. M. .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2007, 46 (12) :4110-4115
[8]   Basic surface oxides on carbon materials:: A global view [J].
Fuente, E ;
Menéndez, JA ;
Suárez, D ;
Montes-Morán, MA .
LANGMUIR, 2003, 19 (08) :3505-3511
[9]   SURFACE CHARACTERIZATION OF CARBON-FIBERS USING ANGLE-RESOLVED XPS AND ISS [J].
GARDNER, SD ;
SINGAMSETTY, CSK ;
BOOTH, GL ;
HE, GR ;
PITTMAN, CU .
CARBON, 1995, 33 (05) :587-595
[10]   Interaction of adsorption and catalytic reactions in water decontamination processes Part I. Oxidation of organic contaminants with hydrogen peroxide catalyzed by activated carbon [J].
Georgi, A ;
Kopinke, FD .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2005, 58 (1-2) :9-18