共查询到19条相似文献,搜索用时 147 毫秒
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目前,在水源受到污染并且污染物经常超过标准,而水厂常规处理工艺又无法满足饮用水水质标准的情况下,臭氧-生物活性炭工艺是微污染水源深度处理的有效方法。文章介绍了该工艺对嗅味、有机物、新兴污染物等特定污染物的去除机理,总结了工艺运行过程中温度、臭氧投加方案、生物活性炭性能等因素对处理效果的影响,以及工艺当前存在的微生物泄漏、溴酸盐生成及其他问题的控制措施,并分析了多种组合工艺的优缺点及具体的工程案例,以对水厂的工艺运行提供参考及技术支持。最后,结合最新的研究成果及当前研究存在的不足对工艺进行了展望,可以为研究者提供新的研究方向。 相似文献
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近年来,我国经济发展势头强劲的珠江流域的水质不断受到污染,珠海市给水厂的水源也受到污染.建议通过臭氧生物活性炭深度处理工艺进一步提高污染物的去除率.研究采用小试试验对臭氧生物活性炭深度处理工艺进行研究.重点考察了臭氧质量浓度为1.0 mg/L、活性炭柱空床时间为15 min和臭氧质量浓度为1.5 mg/L、活性炭空床时间为30 min这两个工况下,2-甲基异莰醇、土臭素、TOC、UV254、浑浊度的去除效果,以及对消毒副产物前体物的控制效果,并通过分子量分布和三维荧光对水中的溶解性有机物进行分析,发现臭氧-生物活性炭工艺可以很好地去除2-甲基异莰醇和土臭素.臭氧-生物活性炭工艺可以有效地去除水中的溶解性有机物,对三卤甲烷和含氮类消毒副产物的前体物也有一定的去除作用,但是对于HAAs卤乙酸类的DBPs消毒副产物前体物的去除效果不佳.同时,文中也给出了臭氧生物活性炭深度处理工艺运行工况的建议. 相似文献
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随着水源污染的不断加剧以及饮用水标准的日益提高,臭氧-生物活性炭深度处理工艺在国内外得到广泛应用。本研究选取江苏省以长江、太湖、淮河和沂沭泗水系为水源的地表水厂,分析其采用臭氧生物活性炭工艺前后长达一年的水质数据,发现原水受水厂在进行深度处理改造后,出厂水浑浊度月平均值均有明显的降低,仅为0.1-0.4 NTU,对浑浊度的最大去除率可达98.7%;出厂水COD_(Mn)月平均值也有明显的降低,为1.0~2.7 mg/L,对COD去除率最大提升27.2%;不同水系水源出厂水中三卤甲烷含量降低了19.4%~78.7%。运行结果分析表明:采用臭氧-生物活性炭处理工艺较常规水处理工艺能够有效改善出厂水水质,具有较大的推广应用价值。 相似文献
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淮河流域某水源水面临微量有机污染物种类增多、藻类季节性暴发而导致消毒副产物前体物增多的问题。试验在淮河流域某水厂建立的深度处理中试装置进行,重点探讨不同臭氧投加量条件下各处理单元对三卤甲烷前体物(THMFP)与卤乙酸前体物(HAAFP)的去除规律。结果表明,预臭氧-强化常规处理(生物强化滤柱)工艺主要去除三氯甲烷前体物(TCMFP),去除率为70.2%;臭氧-生物活性炭(O_3-BAC)深度处理单元以去除二溴一氯甲烷前体物(CDBMFP)为主,去除率为56.8%。针对卤乙酸前体物(HAAFP),预臭氧-强化常规单元和O_3-BAC深度处理单元都以去除二氯乙酸前体物(DCAAFP)为主,去除率分别为67.9%和45.5%。当预臭氧投加量为1.1 mg/L,主臭氧投加量为2 mg/L时,整个工艺对TTHMFP及THAAFP的去除率分别可达78.1%和52.4%,说明采用预氧化-强化常规处理-深度处理组合工艺可以有效去除水中的消毒副产物前体物,保障出厂水水质安全。 相似文献
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臭氧活性炭联合工艺去除微污染水中有机物 总被引:5,自引:2,他引:5
采用臭氧活性炭联合工艺(O3+BAC)对以长江为水源的某水厂砂滤水进行深度处理。试验结果表明,该工艺对水中有机物有稳定的去除效果,在臭氧投加量为1mg/L,活性炭空床接触时间为8.6min时,对CODMn,UV254,DOC,THMEP(三氯甲烷生成势)和AOC(可同化有机碳)的平均去除率分别为32%,40%,22%,19%,7%。在DOC较低的情况下,三氯甲烷生成势与UV254有较好的正相关性。 相似文献
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臭氧生物活性炭工艺处理饮用水时各阶段的特点 总被引:4,自引:1,他引:4
论述了臭氧生物活性炭工艺中的臭氧发生系统、臭氧尾气处理系统、臭氧预氧化及后氧化、生物活性炭滤池各阶段的应用现状及特点。指出:臭氧发生系统采用氧气为原料来提高臭氧浓度,臭氧质量分数可达6%左右;由于电加热分解臭氧尾气反应速度快,可在1.5~2s内完全分解,应是今后自来水厂臭氧尾气处理技术应用的重点;臭氧预氧化一般采用静态混合器或水射器单点投加,投加量为1~2mg/L,接触时间为1~4min;臭氧后氧化一般采用微孔曝气盘以微气泡的形式多点投加,水中臭氧余量控制在0.2~0.4mg/L,接触时间大于10min;生物活性炭滤池对苯类化合物和相对分子质量在500~1000范围内的腐殖质去除率达70%~86.7%。 相似文献
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Pilot study of the removal of THMs, HAAs and DOC from drinking water by GAC adsorption 总被引:2,自引:0,他引:2
K.G. Babi K.M. Koumenides A.D. Nikolaou C.A. Makri F.K. Tzoumerkas T.D. Lekkas 《Desalination》2007,210(1-3):215-224
The objective of this pilot study was to evaluate the performance of a GAC postfilter-adsorber for the removal from the drinking water of Athens, Greece, of the two main groups of chlorination by-products, trihalomethanes (THMs) and haloacetic acids (HAAs), as well as of dissolved organic carbon (DOC). The analyses performed during the whole operation period (638 days) showed that the GAC breakthrough capacity for DOC was much higher than the capacity for total HAAs, which was higher than that for total THMs. The removal of THMs and the most part of the removal of HAAs and DOC should be attributed to adsorption by GAC, while that of a smaller part of HAAs and DOC may be attributed to biodegradation in the adsorber bed, where dechlorination, caused catalytically by the carbon surface, favoured microbial growth. Additionally, the GAC postfilter-adsorber showed a much higher adsorption efficiency than a GAC filter-adsorber, due to the smaller size of the carbon and the lower hydraulic loading rate. Also, observed desorption incidents of THMs (mainly) and HAAs, especially during the postfilteradsorber operation, were favoured by the same factors. Formation of THMs within the GAC bed was also indicated by the mass balance of total THMs during the whole cycle. 相似文献
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超滤与粉末活性炭组合工艺处理饮用水 总被引:9,自引:0,他引:9
采用超滤与粉末活性炭组合工艺,研究了粉末活性炭的投加对超滤膜运行性能的影响。结果表明:随粉末活性炭投量的增加,膜稳定运行时间延长,膜通量下降率降低。粉末活性炭的投加对膜过滤阻力影响不大。采用粉末活性炭和超滤组合工艺处理饮用水,在CODMn和TOC的质量浓度分别为5.5~9.5和1.8~3.5 mg/L,UV254为0.069~0.093 cm-1,浊度为1.29~1.98 NTU时,其平均去除率分别为68.5%、75%、55%和96%以上,粉末活性炭超滤膜组合工艺可用于制备优质饮用水。 相似文献
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Juan F. García‐Araya Fernando J. Beltrán Almudena Aguinaco 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2010,85(6):798-804
BACKGROUND: The aim of this work was to establish the efficiency of single ozonation at different pH levels (5, 7 and 9) and with different TiO2 photolytic oxidizing systems (O2/UV‐A/TiO2, O3/UV‐A/TiO2 or UV‐A/TiO2) for diclofenac removal from water, with especial emphasis on mineralization of the organic matter. RESULTS: In the case of single ozonation processes, results show fast and practically complete elimination of diclofenac, with little differences in removal rates that depend on pH and buffering conditions. In contrast, total organic carbon (TOC) removal rates are slow and mineralization degree reaches 50% at best. As far as photocatalytic processes are concerned, diclofenac is completely removed from the aqueous solutions at high rates. However, unlike single ozonation processes, TOC removal can reach 80%. CONCLUSION: In single ozonation processes, direct ozone reaction is mainly responsible for diclofenac elimination. Once diclofenac has disappeared, its by‐products are removed by reaction with hydroxyl radicals formed in the ozone decomposition and also from the reaction of diclofenac with ozone. In the photocatalytic processes hydroxyl radicals are responsible oxidant species of diclofenac removal as well as by‐products. Copyright © 2010 Society of Chemical Industry 相似文献