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811.
Fenton及电-Fenton处理难降解有机废水技术 总被引:1,自引:0,他引:1
Fenton法与电-Fenton法属于高级氧化技术(Advanced Oxidation Technologjes,AOTs),是由H2O2与催化剂Fe2 所构成的氧化体系.在Fenton体系中,H2O2在Fe2 的催化剂作用下,能产生两种活泼的氢氧自由基(HO2·和·OH),从而引发和传播自由基链反应,加快有机物和还原性物质的氧化.本文简要介绍了Fenton法与电-Fenton反应的机理和应用在催化氧化难降解废水领域中的处理技术及研究进展. 相似文献
812.
Impact of chemical oxidation on soil quality 总被引:2,自引:0,他引:2
Oxidation treatment helps to reduce the polycyclic aromatic hydrocarbon (PAH) load in contaminated soils but it may also have an effect on the soil quality. The impact of permanganate and Fenton oxidation on soil quality is investigated. Soil quality is restricted here to the potential for plant growth. Soil samples were collected from an agricultural field (S1) and a former coking plant (S4). Agricultural soil was spiked with phenanthrene (PHE) and pyrene (PYR) at two concentrations (S2: 700 mg PHE kg−1, S3: 700 mg PHE kg−1 and 2100 mg PYR kg−1). Soils were treated with both oxidation processes, and analyzed for PAHs and a set of agronomic parameters. A plant germination and growth test was run with rye-grass on treated soils. Results showed that both treatments produced the expected reduction of PAH concentration (from 64% to 97%). Besides, a significant loss of organic C and N, and strong changes in available nutrients were observed. Permanganate treatment increased the specific surface area and the cation exchange capacity in relation to manganese dioxide precipitation, and produced a rise in pH. Fenton oxidation decreased soil pH and increased the water retention capacity. Plant growth was negatively affected by permanganate, related to lower soil permeability and aeration. Both treatments had an effect on soil properties but Fenton oxidation appeared to be more compatible with revegetation. 相似文献
813.
814.
光助Fenton氧化法降解水中六氯苯的研究 总被引:7,自引:2,他引:5
采用光助Fenton氧化法处理六氯苯模拟废水,考察了反应时间、Fe3 与H2O2摩尔比、Fenton试剂用量、初始pH、六氯苯初始浓度、光强对六氯苯降解效果的影响,并初步探讨了六氯苯的降解动力学规律.结果表明.光助Fenton法降解六氯苯的最佳工艺条件为:紫外灯功率为300 W、Fe3 投加量为1.0 mmol/L、H2O2投加量为5.0 mmol/L、反应时间为60 min、初始pH为3,在此条件下,浓度为500μg/L的HCB的去除率可达91.3%.UV辐射与Fenton氧化对HCB的降解具有协同效应.光助Fenton法对HCB的降解符合一级反应动力学方程,表观速率常数为0.04 min-1,与Fenton法相比,提高了近9倍. 相似文献
815.
Costs of the electrochemical oxidation of wastewaters: a comparison with ozonation and Fenton oxidation processes 总被引:2,自引:0,他引:2
In the work described here the technical and economic feasibilities of three Advanced Oxidation Processes (AOPs) have been studied: Conductive-Diamond Electrochemical Oxidation (CDEO), Ozonation and Fenton oxidation. The comparison was made by assessing the three technologies with synthetic wastewaters polluted with different types of organic compounds and also with actual wastes (from olive oil mills and from a fine-chemical manufacturing plant). All three technologies were able to treat the wastes, but very different results were obtained in terms of efficiency and mineralization. Only CDEO could achieve complete mineralization of the pollutants for all the wastes. However, the efficiencies were found to depend on the concentration of pollutant (mass transfer control of the oxidation rate). Results obtained in the oxidation with ozone (at pH 12) or by Fenton's reagent were found to depend on the nature of the pollutants, and significant concentrations of oxidation-refractory compounds were usually accumulated during the treatment. Within the discharge limits that all of the technologies can reach, the economic analysis shows that the operating cost of Fenton oxidation is lower than either CDEO or ozonation, although CD\EO can compete satisfactorily with the Fenton process in the treatment of several kinds of wastes. Likewise, the investment cost for the ozonation process seems to be higher than either CDEO or Fenton oxidation, regardless of the pollutant treated. 相似文献
816.
Fenton试剂预处理H酸废水的影响因素及其可生化性 总被引:10,自引:0,他引:10
采用Fenton度剂预处理低浓度难降解的H酸废水,探讨了pH,Fe^2 ,H2O2,反应时间和H酸浓度对废水CODcr去除效果的影响,结果表明,各因素对废水CODcr去除效果影响较大,对CODcr为810mg.l^-1的H酸废水,Fenton试剂预处理的最佳条件;pH为5.5,3%H2O2的观加量为5%,10g.l^-1FeSO4的投加量为7%,反应时间为90min,此条件下CODcr去除率为55.3%-58.7%,可生化值CODB/CODcr从6.3%-6.7%上升到62.2%-68.4%。 相似文献
817.
Lihui Gao Yijun Cao Lizhang Wang Shulei Li 《Frontiers of Environmental Science & Engineering》2022,16(6):77