首页> 外文期刊>Journal of the Chinese Institute of Environmental Engineering >ITERFERENCE OF Mn~(2+), Co~(2+), Ni~(2+) AND Cu~(2+) IONS IN THE HETEROGENEOUS UV-CATALYSIS USING A TiO_2 SUSPENSION SYSTEM
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ITERFERENCE OF Mn~(2+), Co~(2+), Ni~(2+) AND Cu~(2+) IONS IN THE HETEROGENEOUS UV-CATALYSIS USING A TiO_2 SUSPENSION SYSTEM

机译:TiO2悬浮体系在非均相紫外光催化中Mn〜(2 +),Co〜(2 +),Ni〜(2+)和Cu〜(2+)离子的干扰

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摘要

The influence of transition metal ions, Mn~(2+), Co~(2+) , Ni~(2+) and Cu~(2+) , on the rate of pho-tocatalytic oxidation of 2-chlorophenol was studied at pH 3. The results shown that the photo-catalytic oxidation of 2-chlorophenol presenting in metal ions follows the Langmuir-Hinshelwood type behavior and the reaction byproducts display an inhibiting effect on degradation rate. Results of the theoretical analysis can be used to explain the inverse initial concentration effect of 2-chlorophenol in the apparent degradation rate constant. The surface oxidation rate of 2-chlorophenol was related with the oxidation and reduction potential of metal's standard potential. The higher electron voltage of metal ion the higher reaction rate of the surface oxida-tive was observed. From the analysis of mineralization of 2-chlorophenol, the transition metals ions generate a complex with the 2-chlorophenol oxidizing intermediate was proposed. The surface property was related with complex formation of metal ions and organic. The selectivity formation was relate with the organic-metal-complex competitive with 2-chlorophenol induces the reaction rate when increases the initial 2-chlorophenol concentration.
机译:研究了过渡金属离子Mn〜(2 +),Co〜(2 +),Ni〜(2+)和Cu〜(2+)对2-氯苯酚的光催化氧化速率的影响。 pH 3.结果表明,金属离子中存在的2-氯苯酚的光催化氧化遵循Langmuir-Hinshelwood型行为,反应副产物对降解速率显示出抑制作用。理论分析的结果可用于解释表观降解速率常数中2-氯苯酚的初始浓度反作用。 2-氯苯酚的表面氧化速率与金属标准电位的氧化还原电位有关。金属离子的电子电压越高,观察到的表面氧化反应速率越高。通过对2-氯苯酚矿化的分析,提出了过渡金属离子与2-氯苯酚氧化中间体生成配合物的方法。表面性质与金属离子和有机物的复杂形成有关。选择性的形成与有机金属配合物的竞争有关,当增加初始的2-氯苯酚浓度时,与2-氯苯酚的竞争性引起反应速率。

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