The influence of structure and surface chemistry of carbon materials on the decomposition of hydrogen peroxide

被引:109
|
作者
Ribeiro, Rui S. [1 ]
Silva, Adrian M. T. [2 ]
Figueiredo, Jose L. [2 ]
Faria, Joaquim L. [2 ]
Gomes, Helder T. [1 ,2 ]
机构
[1] Polytech Inst Braganca, Sch Technol & Management, Dept Chem & Biol Technol, P-5300857 Braganca, Portugal
[2] Univ Porto, Fac Engn, LCM Lab Catalysis & Mat, Associate Lab LSRE LCM, P-4200465 Oporto, Portugal
关键词
ACTIVATED-CARBON; HYDROXYL RADICALS; CATALYTIC DECOMPOSITION; OXIDATION; ADSORPTION; DEGRADATION; KINETICS; OXIDE; ACID; H2O2;
D O I
10.1016/j.carbon.2013.06.001
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
Carbon materials with different structural and chemical properties, namely activated carbons, carbon xerogels, carbon nanotubes, graphene oxide, graphite and glycerol-based carbon materials, were tested under different operating conditions for their ability to catalyse hydrogen peroxide (H2O2) decomposition in aqueous solutions. Activated carbons treated with concentrated sulphuric acid (ACS) are the most active catalytic materials for H2O2 decomposition in most of the conditions studied, due to the presence of sulphur containing functional groups at their surface. In addition, ACS proved to be a stable catalyst in reutilization tests for H2O2 decomposition. Methanol was used as selective scavenger of hydroxyl radicals (HO center dot), to show that activated carbons with a markedly basic character lead to the highest yield of HO center dot formed during the H2O2 decomposition process (14%, after 150 min of reaction). Overall, from the mechanistic interpretation of H2O2 decomposition, it is concluded that the presence of sulphur containing functional groups at the surface of the activated carbons improves the removal of H2O2 in aqueous solutions, but, on the other hand, the selective decomposition of H2O2 via HO center dot formation is enhanced by the presence of basic active sites on the Carbon surface. (c) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:97 / 108
页数:12
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