The role of activated carbons functionalized with thiol and sulfonic acid groups in catalytic wet peroxide oxidation

被引:78
作者
Gomes, Helder T. [1 ,2 ]
Miranda, Sandra M. [1 ]
Sampaio, Maria J. [1 ]
Figueiredo, Jose L. [2 ]
Silva, Adrian M. T. [2 ]
Faria, Joaquim L. [2 ]
机构
[1] Polytech Inst Braganca, Dept Chem & Biol Technol, Sch Technol & Management, P-5301857 Braganca, Portugal
[2] Univ Porto, Dept Chem Engn, Fac Engn, Lab Catalysis & Mat LCM,Associate Lab LSRE LCM, P-4200465 Oporto, Portugal
关键词
Activated carbon; Surface chemistry; Sulfur containing functional groups; Thiols; Sulfonic acids; Catalytic wet peroxide oxidation; ORGANIC CONTAMINANTS; HYDROGEN-PEROXIDE; AQUEOUS-SOLUTION; SURFACE; PHENOL; ADSORPTION; WATER; H2O2; IRON; DECOMPOSITION;
D O I
10.1016/j.apcatb.2011.05.044
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
Norit ROX 0.8 commercial activated carbon was subjected to liquid phase treatments with sulfuric acid at different concentrations (5-18 M) and temperatures (353 and 423 K), to generate different amounts (760-1000 mu mol g(-1)) of sulfur groups (thiol and sulfonic acid), with varying surface acidity. The prepared materials were chemically characterized by the determination of the point of zero charge (2.0-5.8) and by mass titration, temperature programmed desorption and X-ray photoelectron spectroscopy, to evaluate the nature and concentration of acidic surface functionalities. The materials were tested as catalysts in the catalytic wet peroxide oxidation of aqueous solutions of the acid dye Chromotrope 2R. A correlation between the surface acidic strength and the efficiency for dye removal from solution was found, which was ascribed both to adsorption and to reaction. In general, dye removal by adsorption is increased when using adsorbents with lower acidic character, due to enhanced electrostatic attraction between the acid dye and the catalyst surface. In addition, the introduction of sulfur containing groups promotes the decomposition of hydrogen peroxide, leading to increased production of hydroxyl radicals close to the pollutant and subsequent improved dye degradation. (C) 2011 Elsevier B.V. All rights reserved,
引用
收藏
页码:390 / 397
页数:8
相关论文
共 33 条
[21]   Catalytic wet peroxide oxidation of phenol over Fe/AC catalysts: Influence of iron precursor and activated carbon surface [J].
Rey, A. ;
Faraldos, M. ;
Casas, J. A. ;
Zazo, J. A. ;
Bahamonde, A. ;
Rodriguez, J. J. .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2009, 86 (1-2) :69-77
[22]   Role of the Activated Carbon Surface on Catalytic Wet Peroxide Oxidation [J].
Rey, Ana ;
Faraldos, Marisol ;
Bahamonde, Ana ;
Casas, Jose A. ;
Zazo, Juan A. ;
Rodriguez, Juan J. .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 2008, 47 (21) :8166-8174
[23]   Activated carbon surface modifications by adsorption of bacteria and their effect on aqueous lead adsorption [J].
Rivera-Utrilla, J ;
Bautista-Toledo, I ;
Ferro-García, MA ;
Moreno-Castilla, C .
JOURNAL OF CHEMICAL TECHNOLOGY AND BIOTECHNOLOGY, 2001, 76 (12) :1209-1215
[24]   The role of carbon materials in heterogeneous catalysis [J].
Rodriguez-Reinoso, F .
CARBON, 1998, 36 (03) :159-175
[25]   Decolourisation of dye solutions by oxidation with H2O2 in the presence of modified activated carbons [J].
Santos, V. P. ;
Pereira, M. F. R. ;
Faria, P. C. C. ;
Orfao, J. J. M. .
JOURNAL OF HAZARDOUS MATERIALS, 2009, 162 (2-3) :736-742
[26]  
Smith R.M., 2004, Understanding mass spectra: A basic approach
[27]  
Stasinakis AS, 2008, GLOBAL NEST J, V10, P376
[28]   Further insights into the role of carbon surface functionalities in the mechanism of phenol adsorption [J].
Terzyk, AP .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 2003, 268 (02) :301-329
[29]   Advanced oxidation processes: mechanistic aspects [J].
von Sonntag, C. .
WATER SCIENCE AND TECHNOLOGY, 2008, 58 (05) :1015-1021
[30]   XPS demonstration of π-π interaction between benzyl mercaptan and multiwalled carbon nanotubes and their use in the adhesion of Pt nanoparticles [J].
Yang, D. -Q. ;
Hennequin, B. ;
Sacher, E. .
CHEMISTRY OF MATERIALS, 2006, 18 (21) :5033-5038