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Adsorbable organic halogens formed during treatment of Cl--containing wastewater by sulfate and hydroxyl radical-based advanced oxidation processes

机译:通过硫酸盐和羟基自由基的高级氧化方法处理在处理Cl型废水期间形成的可吸附的有机卤素

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The formation of adsorbable organic halogens (AOX) in two typical advanced oxidation processes (AOPs), (OH)-O-center dot-based (UV/H2O2) and SO4 center dot--based (UV/potassium persulfate (PDS)) processes, was investigated during the treatment of Cl--containing wastewater. Compared with the original AOX concentration (0.08 mg/L), a significant increase in the AOX concentration was observed in both AOPs under the condition that TOC concentration was minimized. Higher concentration of AOX was formed in the UV/PDS process than that in the UV/H2O2 process under all experimental conditions, although the former showed a better performance on TOC removal. An increase of effluent AOX concentration from 0.4 mg/L to 1.1 mg/L in the UV/H2O2 process and from 1.9 mg/L to 3.4 mg/L in the UV/PDS process was observed, respectively, when the Cl- concentration increased from 1800 mg/L to 10000 mg/L. This enhancement of high Cl- concentration on the AOX formation was attributed to the reactive halogen species generated in the AOP treatment. The term AOX(MFP) was created to determine the AOX formation potential of wastewater and AOPs system. The results showed that organic matters with a molecular weight (MW) between 1 k similar to 100 k Da tend to form AOX more easily than those with a MW lower than 1 k Da and higher than 100 k Da. In addition, eight and fourteen kinds of formed organic halogens were identified in UV/H2O2 and UV/PDS treated wastewater, respectively. Five kinds of them have been proved to be toxic, which partially contributed to the increase of acute toxicity of effluent. The results of this work provides a new perspective to evaluate, in terms of eco-safety and efficiency, the application of AOPs to wastewater containing high concentration of Cl-.
机译:在两个典型的晚期氧化过程(AOX)中形成可吸附有机卤素(AOX),(OH)-O中心点基(UV / H2O2)和SO4中心基于SO4基于SO4(UV / PETULFATE(PDS))在治疗含Cl含硫废水期间研究了方法。与原始AOX浓度(0.08mg / L)相比,在TOC浓度最小化的条件下,在两个AOP中观察到AOX浓度的显着增加。在UV / PDS过程中形成较高浓度的AOx,而不是在所有实验条件下的UV / H2O2过程中的浓度,尽管前者在TOC去除时表现出更好的性能。在CL-浓度增加时,分别观察到在UV / H 2 O 2工艺中的0.4mg / L至1.1mg / L的污水氧氧氧浓度从0.4mg / L至1.1mg / L的增加,并且在UV / PDS过程中的1.9mg / L至3.4mg / L.从1800 mg / l到10000 mg / L.在AOX形成上的这种高Cl浓度的增强归因于AOP处理中产生的反应性卤素物质。术语AOX(MFP)创建以确定废水和AOX系统的AOX形成电位。结果表明,在1 k之间的分子量(MW)的有机物倾向于比具有低于1kDa的MW和高于100kda的MW更容易形成氧化氧肟。此外,分别在UV / H 2 O 2和UV / PDS处理的废水中鉴定出八种和十四种形成的有机卤素。已经证明了五种它们是有毒的,这有助于增加急性毒性的流出物。这项工作的结果提供了一种新的视角,以评估AOP施加AOP与含有高浓度CL-的废水的施用。

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