Self-cleaning cotton textiles surfaces modified by photoactive SiO2/TiO2 coating

被引:245
|
作者
Yuranova, T
Mosteo, R
Bandara, J
Laub, D
Kiwi, J [1 ]
机构
[1] Inst Chem Sci & Engn, Lab Photon & Interfaces, CH-1015 Lausanne, Switzerland
[2] Swiss Fed Inst Technol, CIME, CH-1015 Lausanne, Switzerland
[3] Inst Fundamental Studies, Kandy 20000, Sri Lanka
关键词
self-cleaning; cotton textiles; wine stains; TiO2-SiO2; coating; photocatalysis;
D O I
10.1016/j.molcata.2005.08.059
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 photocatalytic activity of TiO2-SiO2 -coated cotton textiles was investigated through the self-cleaning of red wine stains. It was shown that a TiO2-SiO2 species could be produced at temperatures of 100 degrees C with acceptable photo-activity on non-heat resistant materials. The most suitable Ti-content of the coating was found to be 5.8% and for SiO2, the content was 3.9% (w/w). The discoloration of red wine led to CO2 evolution that was more efficient for TiO2-SiO2-coated cotton for samples than of TiO2-coated ones. The reasons for these results are discussed. The textile surface did not show any change after several consecutive light-induced discoloration cycles of a red wine stain. By high-resolution transmission electron microscopy (HRTEM), the TiO2-SiO2 layer thickness on the cotton fibers was detected to 20-30 nm. The TiO2 and SiO2 were both observed to have particle sizes between 4 and 8 nm. Further electron microscopy work coupled with energy dispersive spectroscopy (EDS) showed that the Ti-particles were always surrounded by amorphous SiO2 and never alone by themselves. Infrared spectroscopy revealed that no modification of the cotton could be detected after photo-discoloration processes with TiO2-SiO2 taking a wine stain as model compound. The mixed TiO2 and SiO2 colloids lead during the dip-coating and subsequent thermal treatment on cotton to an organized structure of highly dispersed TiO2 particles always surrounded by amorphous silica. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:160 / 167
页数:8
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