二氧化钛
光催化
化学
二氧化碳
磷钨酸
催化作用
无机化学
磺酸
三氟乙酸
矿化(土壤科学)
水溶液
有机化学
材料科学
氮气
冶金
作者
Ralf Dillert,Detlef W. Bahnemann,Hisao Hidaka
出处
期刊:Chemosphere
[Elsevier]
日期:2007-03-01
卷期号:67 (4): 785-792
被引量:121
标识
DOI:10.1016/j.chemosphere.2006.10.023
摘要
The UV-photon-induced degradation of heptafluorobutanoic acid was investigated in acidic aqueous solutions in the presence of titanium dioxide. Heptafluorobutanoic acid could be degraded with this photocatalyst in a light-induced reaction generating carbon dioxide and fluoride anions. Carbon dioxide evolution in a significant amount occurred only in the presence of molecular oxygen and the photocatalyst. The light-induced degradation of trifluoroacetic acid, pentafluoropropanoic acid, nonafluorobutanoic acid, pentadecafluorooctanoic acid, nonafluorobutanesulfonic acid, and heptadecafluorooctanesulfonic acid in the presence of titanium dioxide was also studied. The perfluorocarboxylic acids under investigation are degraded to generate CO2 and fluoride anions while both perfluorinated sulfonic acids are persistent under the experimental conditions employed in this study. For all compounds photonic efficiencies of the mineralization reaction were estimated to be smaller than 1 × 10−5. To increase the photocatalytic activity mixed systems containing homogeneous phosphotungstic acid and heterogeneous titanium dioxide catalysts were also investigated. In the mixtures of these two photocatalysts, the formation rate of CO2 increased with illumination time.
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