PHOTODEGRADATION OF CHLOROFORM AND UREA USING AG-LOADED TITANIUM DIODE AS CATALYST

被引:73
作者
KONDO, MM [1 ]
JARDIM, WF [1 ]
机构
[1] INST QUIM, UNICAMP CP 6154, BR-13081 CAMPINAS, SP, BRAZIL
基金
巴西圣保罗研究基金会;
关键词
PHOTODEGRADATION; CHLOROFORM; UREA; AG-LOADED TIO2; PHOTOCATALYST; SEMICONDUCTORS;
D O I
10.1016/0043-1354(91)90162-J
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The photodegradation of chloroform and of urea in aqueous solutions was investigated under near-u.v. and visible radiation using the anatase form of TiO2 as catalyst. It has been shown that the catalytic activity of the TiO2 can be increased by loading silver, in a proportion of 1% (w/w), onto the oxide surface. In a solution containing 200 mg l-1 of chloroform, the photodegradation achieved using the Ag-loaded oxide was 44% compared to the 35% obtained using the pure (unloaded) oxide. This photoactivity was further enhanced in a solution containing 25 mg l-1 of chloroform. Upon reuse, a decrease in the photocatalytic activity was observed in both oxides, but to a lesser extent in the Ag-loaded TiO2. An increase in the photocatalytic activity of the silver-loaded oxide was also noted in the degradation of a 100 mg l-1 aqueous solution of urea. After 12 min of irradiation, the Ag-loaded oxide destroyed 83% of this compound, compared to a 16% efficiency obtained for the pure form of anatase. After 6 h of irradiation, 0.5 mg l-1 of silver ions were detected in the Ag-loaded TiO2 suspension.
引用
收藏
页码:823 / 827
页数:5
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