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Deming ZHAO Jie CHENG Michael R. HOFFMANN 《Frontiers of Environmental Science & Engineering》2011,5(1):57-64
Aqueous solutions of phenol were oxidized by hydrogen peroxide assisted by microwave (MW) irradiation. A simple kinetic model for the overall degradation of phenol in the presence of excess H2O2 is proposed in which the degradation rate of phenol is expressed as a linear function of the concentrations of phenol and H2O2. A detailed parametric study showed that the degradation rate of phenol increased with increasing [H2O2] until saturation was observed. Phenol degradation followed apparent zero-order kinetics under MW radiation or H2O2 oxidation. However, after 90 min of irradiation, the observed kinetics shifted to pseudo first order. The overall reaction rates were significantly enhanced in the combined MW/H2O2 system, mainly because microwave could accelerate H2O2 to generate hydroxyl radical (·OH) and other reactive oxygen intermediates. The observed synergetic effects of the MW/H2O2 process resulted in an increased in the net reaction rate by a factor of 5.75. When hydrogen peroxide is present in a large stoichiometric excess, the time required to achieve complete mineralization is reduced significantly. 相似文献
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以化工园区废水厂二级出水作为实验废水,采用臭氧氧化工艺对其进行处理,采用分子量分级、亲疏水性分离和傅里叶红外等手段对臭氧氧化前后水质进行了系统分析。结果表明,在进水COD为126 mg/L,臭氧氧化60 min的条件下,COD和UV254的去除率分别为37.9%和55%;臭氧氧化对水中疏水性物质去除效率高于亲水性物质,部分疏水性物质氧化成亲水性小分子有机物。臭氧氧化可以改变废水中有机物的分子结构,使水中分子量小于1×103 kDa的有机物比例从56.3%提高至71.2%,分子量大于1×105 kDa的有机物比例由原来的24.2%下降至9.6%。红外光谱分析表明,臭氧氧化具有一定的选择性,可显著去除水中含不饱和键、酚类、醇类等有机物,但对饱和烷烃基本无降解效果。 相似文献