Copper-aided photo sterilization of microbial cells on TiO2 film under irradiation from a white light fluorescent lamp

被引:40
作者
Sato, Takashi [1 ]
Taya, Masahito [1 ]
机构
[1] Osaka Univ, Grad Sch Engn Sci, Dept Mat Engn, Div Chem Engn, Toyonaka, Osaka 5608531, Japan
关键词
titanium dioxide; photocatalytic sterilization; Escherichia coli; copper-aided reaction; reactive oxygen species;
D O I
10.1016/j.bej.2006.04.002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The copper-aided photosterilization of Escherichia coli was examined on TiO2 thin films under a lighting condition with less UV rays from a white light fluorescent lamp. It was found that the coexistence of Cu2+ and H2O2 in liquid phase exerted the synergistic effect on killing E. coli cells though these chemical species were individually at nontoxic levels to the cells (less than 10 mmol/m(3)). At an incident light intensity of I-0 = 28 W/m(2), the addition of Cu2+, (10 mmol/m(3)) to liquid phase on TiO2 film gave the apparent deactivation rate constant of k' = 12 x 10(-2) min(-1), the value of which was about 5 times as large as that on TiO2 film in the absence of Cu2+. This result suggested that in the liquid phase, CU2+ was reduced to Cu+ by receiving electron from photo-excited TiO2, and then Cu+ reacted with photocatalysis-derived H2O2 to produce (OH)-O-center dot via Fenton-type reaction. The deactivation tests were also examined using a modified film preparation made from copper-incorporated TiO2. On this film, the k' value was 23 x 10(-2) min(-1) at 10 = 28 W/m(2), which was respectively about two and nine times as large as those on the original TiO2 film with and without Cu2+ addition (10 mmol/m(3)). The enhancement of biocidal activity on the modified TiO2 film was considered to arise from promoted (OH)-O-center dot formation by the aid of copper component anchored in TiO2 solid phase. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:199 / 204
页数:6
相关论文
共 24 条
[1]   Visible-light photocatalysis in nitrogen-doped titanium oxides [J].
Asahi, R ;
Morikawa, T ;
Ohwaki, T ;
Aoki, K ;
Taga, Y .
SCIENCE, 2001, 293 (5528) :269-271
[2]   Highly enhanced photoreductive degradation of perchlorinated compounds on dye-sensitized metal/TiO2 under visible light [J].
Bae, E ;
Choi, W .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2003, 37 (01) :147-152
[3]  
Blair D., 1961, Talanta, V7, P163, DOI [10.1016/0039-9140, DOI 10.1016/0039-9140]
[4]   PHOTOREDOX BEHAVIOR OF CHLOROCOPPER(II) COMPLEXES IN ACETONITRILE - MECHANISM AND QUANTUM YIELDS [J].
CERVONE, E ;
CAMASSEI, FD ;
GIANNINI, I ;
SYKORA, J .
JOURNAL OF PHOTOCHEMISTRY, 1979, 11 (05) :321-332
[5]   HYDROXYL-RADICAL-INDUCED IRON-CATALYSED DEGRADATION OF 2-DEOXYRIBOSE - QUANTITATIVE-DETERMINATION OF MALONDIALDEHYDE [J].
CHEESEMAN, KH ;
BEAVIS, A ;
ESTERBAUER, H .
BIOCHEMICAL JOURNAL, 1988, 252 (03) :649-653
[6]   Homogeneous photocatalysis by transition metal complexes in the environment [J].
Ciesla, P ;
Kocot, P ;
Mytych, P ;
Stasicka, Z .
JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL, 2004, 224 (1-2) :17-33
[7]   Photo-irradiated titanium dioxide catalyzes site specific DNA damage via generation of hydrogen peroxide [J].
Hirakawa, K ;
Mori, M ;
Yoshida, M ;
Oikawa, S ;
Kawanishi, S .
FREE RADICAL RESEARCH, 2004, 38 (05) :439-447
[8]   Ag/AgBr/TiO2 visible light photocatalyst for destruction of azodyes and bacteria [J].
Hu, C ;
Lan, YQ ;
Qu, JH ;
Hu, XX ;
Wang, AM .
JOURNAL OF PHYSICAL CHEMISTRY B, 2006, 110 (09) :4066-4072
[9]   Mineralization of bacterial cell mass on a photocatalytic surface in air [J].
Jacoby, WA ;
Maness, PC ;
Wolfrum, EJ ;
Blake, DM ;
Fennell, JA .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1998, 32 (17) :2650-2653
[10]   Photocatalytic bactericidal effect of TiO2 thin films: Dynamic view of the active oxygen species responsible for the effect [J].
Kikuchi, Y ;
Sunada, K ;
Iyoda, T ;
Hashimoto, K ;
Fujishima, A .
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1997, 106 (1-3) :51-56