Early stages in the TiO2-photocatalyzed degradation of simple phenolic and non-phenolic lignin model compounds

被引:46
作者
Antunes, CSA [1 ]
Bietti, M [1 ]
Salamone, M [1 ]
Scione, N [1 ]
机构
[1] Univ Roma Tor Vergata, Dipartimento Sci & Tecnol Chim, I-00133 Rome, Italy
关键词
lignin model compounds; semiconductor photocatalysis; photochemical degradation; electron scavenger; radical cations; hydroxyl/superoxide radicals;
D O I
10.1016/j.jphotochem.2004.01.018
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
The TiO2-photocatalyzed degradation of phenolic and non-phenolic benzyl alcohols, which can be considered simple lignin model compounds has been studied in aqueous solution under a variety of conditions, with the aim of acquiring fundamental information on the early stages of the degradation process. The role of the electron scavengers O-2, K2S2O8 and N2O on the degradation process as well as the influence of pH have been investigated. A major role in the degradation process is played by (OH)-O-. and O-2(.-), while SO4.- plays a minor role. (OH)-O-. plays a fundamental role in the conversion of non-phenolic substrates into phenolic ones, while O-2(.-) exerts its role mainly by reacting with phenoxyl radicals to give aromatic ring-opening products. Addition of K2S2O8 as electron scavenger allows substantial substrate degradation also in the absence of O-2, while N2O which is an excellent scavenger for the hydrated electron seems to be a very poor electron scavenger under the heterogeneous conditions employed. A general mechanistic scheme which proceeds through the formation of aromatic radical cations via one-electron oxidation of the neutral substrates by TiO2 (h(+)), accounting for all the experimental observations has been proposed. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:453 / 462
页数:10
相关论文
共 37 条
[1]   USE OF CATALASE AND SUPEROXIDE-DISMUTASE TO ASSESS THE ROLES OF HYDROGEN-PEROXIDE AND SUPEROXIDE IN THE TIO2 OR ZNO PHOTOCATALYTIC DESTRUCTION OF 1,2-DIMETHOXYBENZENE IN WATER [J].
AMALRIC, L ;
GUILLARD, C ;
PICHAT, P .
RESEARCH ON CHEMICAL INTERMEDIATES, 1994, 20 (06) :579-594
[2]   THE GC-MS IDENTIFICATION OF SOME ALIPHATIC INTERMEDIATES FROM THE TIO2 PHOTOCATALYTIC DEGRADATION OF DIMETHOXYBENZENES IN WATER [J].
AMALRIC, L ;
GUILLARD, C ;
PICHAT, P .
RESEARCH ON CHEMICAL INTERMEDIATES, 1995, 21 (01) :33-46
[3]  
Argyropoulos D. S., 1997, BIOTECHNOLOGY PULP P, P127
[4]   Photo-oxidative fragmentation of some α-alkyl substituted 4-methoxybenzyl alcohols and methyl ethers sensitized by TiO2 [J].
Baciocchi, E ;
Bietti, M ;
Ferrero, MI ;
Rol, C ;
Sebastiani, GV .
ACTA CHEMICA SCANDINAVICA, 1998, 52 (02) :160-164
[5]  
Baciocchi E, 1998, EUR J ORG CHEM, V1998, P299, DOI 10.1002/(SICI)1099-0690(199802)1998:2<299::AID-EJOC299>3.0.CO
[6]  
2-B
[7]  
Baciocchi E, 2001, CHEM-EUR J, V7, P1408, DOI 10.1002/1521-3765(20010401)7:7<1408::AID-CHEM1408>3.0.CO
[8]  
2-M
[9]   Mechanistic aspects of β-bond-cleavage reactions of aromatic radical cations [J].
Baciocchi, E ;
Bietti, M ;
Lanzalunga, O .
ACCOUNTS OF CHEMICAL RESEARCH, 2000, 33 (04) :243-251
[10]   Lifetime, reduction potential and base-induced fragmentation of the veratryl alcohol radical cation in aqueous solution. Pulse radiolysis studies on a ligninase "mediator" [J].
Bietti, M ;
Baciocchi, E ;
Steenken, S .
JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (38) :7337-7342