Dye-effect in TiO2 catalyzed contaminant photo-degradation:: Sensitization vs. charge-transfer formalism

被引:69
作者
Hilal, H. S.
Majjad, L. Z.
Zaatar, N.
El-Hamouz, A.
机构
[1] An Najah N Univ, Dept Chem, Nablus, W Bank, Israel
[2] An Najah N Univ, Dept Chem Engn, Nablus, W Bank, Israel
关键词
TiO2; 2,4,6-triphenylpyrilium hydrogen sulfate; photo-degradation; phenol; benzoic acid; sensitization;
D O I
10.1016/j.solidstatesciences.2006.10.001
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Anatase TiO2 surfaces have been treated with 2,4,6-triphenylpyrilium hydrogen sulfate (TPPHS) dye to yield the modified TiO2/TPPHS surface. The modified TiO2/TPPHS surface was then supported onto activated carbon (AC) surfaces to yield a new class of catalytic system AC/TiO2/TPPHS. The catalytic activities of naked TiO2, TPPHS solution, TiO2/TPPHS and AC/TiO2/TPPHS systems were examined in photo-degradation of phenol and benzoic acid in water, using both UV and visible regions. All studied systems showed low catalytic activity when used in the visible region. In UV, the AC/TiO2/TPPHS showed highest activity, whereas the naked TiO2 and TPPHS solutions were the least active systems. The dye role, in enhancing activity of modified surfaces in UV degradation of contaminants, is understandable by a charge-transfer catalytic effect rather than a sensitizing effect. AC role is explainable by its ability to adsorb contaminant molecules and bringing them closer to catalytic sites. (c) 2006 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:9 / 15
页数:7
相关论文
共 51 条
[1]   A study of the influence of hydrophobicity of activated carbon on the adsorption equilibrium of aromatics in non-aqueous media [J].
Ahnert, F ;
Arafat, HA ;
Pinto, NG .
ADSORPTION-JOURNAL OF THE INTERNATIONAL ADSORPTION SOCIETY, 2003, 9 (04) :311-319
[2]  
Ajmera AA, 2002, CHEM ENG TECHNOL, V25, P173, DOI 10.1002/1521-4125(200202)25:2<173::AID-CEAT173>3.0.CO
[3]  
2-C
[4]   Combination effect of activated carbon with TiO2 for the photodegradation of binary pollutants at typical indoor air level [J].
Ao, CH ;
Lee, SC .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 2004, 161 (2-3) :131-140
[5]  
*AOAC INT, 1998, 97913 AOAC
[6]   FTIR study of gas-phase alcohols photocatalytic degradation with TiO2 and AC-TiO2 [J].
Araña, J ;
Doña-Rodríguez, JM ;
Cabo, CGI ;
González-Díaz, O ;
Herrera-Melián, JA ;
Pérez-Peña, J .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2004, 53 (04) :221-232
[7]   TiO2 activation by using activated carbon as a support -: Part I.: Surface characterisation and decantability study [J].
Araña, J ;
Doña-Rodríguez, JM ;
Rendón, ET ;
Cabo, CGI ;
González-Díaz, O ;
Herrera-Melián, JA ;
Pérez-Peña, J ;
Colón, G ;
Navío, JA .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2003, 44 (02) :161-172
[8]   Suppression of band edge migration at the p-GaInP2/H2O interface under illumination via catalysis [J].
Bansal, A ;
Turner, JA .
JOURNAL OF PHYSICAL CHEMISTRY B, 2000, 104 (28) :6591-6598
[9]   PHOTOCATALYTIC HYDROXYLATION OF BENZOIC-ACID IN AQUEOUS TITANIUM-DIOXIDE SUSPENSION [J].
BREZOVA, V ;
CEPPAN, M ;
BRANDSTETEROVA, E ;
BREZA, M ;
LAPCIK, L .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1991, 59 (03) :385-391
[10]   Photoelectrochemical cell for the combined photocatalytic oxidation of organic pollutants and the recovery of metals from waste waters [J].
Byrne, JA ;
Eggins, BR ;
Byers, W ;
Brown, NMD .
APPLIED CATALYSIS B-ENVIRONMENTAL, 1999, 20 (02) :L85-L89