共查询到20条相似文献,搜索用时 78 毫秒
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针对黄浦江源水砂滤出水,进行了紫外线单独作用的研究,同时对于紫外线与消毒剂联合消毒时消毒剂的投加方式对灭菌作用和消毒副产物的影响进行了研究。实验结果表明:当紫外线剂量达到42 mJ/cm2时出水水质已达到了生活饮用水卫生标准中对细菌总数和大肠杆菌数的要求,且在相同紫外剂量下,高强度时对细菌的灭活效果要好于低强度时的效果;先紫外消毒后消毒剂消毒对于微生物具有很好的杀灭作用,但是不能减少消毒副产物的产生;紫外线和消毒剂同时作用对于微生物的杀灭作用不佳,但是出水的消毒剂余量高,消毒副产物量少,这样有利于出水的安全稳定性;先消毒剂消毒再紫外消毒,发现对于消毒副产物没有多大的降解作用,更浪费了高的紫外剂量。 相似文献
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对环境友好消毒技术需求的增长,推动了过氧化物消毒技术的快速发展,并已被广泛应用于反化学和生物恐怖袭击、化生灾害处置、环境污染治理等领域.在综述了过氧化物消毒剂α亲核取代/氧化消毒反应机制研究进展的基础上,介绍了以过氧化物为活性组分的水基消毒溶液、消毒泡沫、消毒乳液、消毒凝胶、消毒气雾、自消毒材料、纳米材料催化消毒技术等典型消毒体系.针对现有过氧化物消毒技术消毒效率偏低、对个别毒剂消毒效果不理想的缺点,建议在过氧化物消毒技术研究中,加强消毒反应机制、多相体系界面相互作用研究,开发新型催化剂、多功能表面活性剂、自消毒材料和消毒剂缓蚀技术,以实现真正的绿色消毒. 相似文献
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二氧化氯消毒无机消毒副产物控制技术进展研究 总被引:1,自引:0,他引:1
日常生活、生产中,饮用水消毒剂受到广泛关注.中国《生活饮用水卫生标准》(GB 5749-2006)规定二氧化氯可作为饮用水消毒剂,但其在消毒过程中所产生的无机消毒副产物,对人类健康存在潜在的危害.随着检测和控制技术水平的发展,对饮用水中无机消毒副产物的研究已成为热点.文章参考大量文献,对饮用水中无机消毒副产物的控制技术进行了详细讨论. 相似文献
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新型二氧化氯协同消毒剂发生器及其应用 总被引:1,自引:0,他引:1
从保护饮用水的安全与卫生出发,介绍了替代液氯和其它氯制品消毒剂设备的新一代消毒设备--二氧化氯协同消毒剂发生器的基本大批量和主要特点。这种新型专利设备不仅可应用于饮用水消毒灭菌,而且也适用于生活污水和工业废水的处理。 相似文献
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环境友好消毒剂二氧化氯的灭活效果和消毒副产物 总被引:1,自引:0,他引:1
消毒是一个非常重要水处理单元过程,但常规消毒剂氯气会产生具有"三致"作用的消毒副产物.二氧化氯(ClO2)灭活效率高,消毒副产物的危害小,是一种环境友好消毒剂.总结了ClO2对水中细菌、病毒、乙肝表面抗原(HBsAg)、原生动物、浮游动物、藻类等的灭活效果,分析了温度、pH、CT(ClO2浓度×灭活时间)等对ClO2灭活水中微生物效果的影响,探讨了ClO2消毒过程中产生的副产物的性质,提出了相应的控制方法,展望了ClO2在水处理中的应用前景. 相似文献
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茶多酚具有消毒能力,可作为一种饮用水辅助消毒剂,但消毒后水中细菌再生长规律尚不清晰。对茶多酚投入水中后的水质进行监测分析,发现可能是茶多酚和菌体蛋白质结合生成了生物可降解有机物(BDOC),成为管网水中异养菌增长的动力,从而使管网水的生物稳定性随着消毒接触时间的延长而降低。试验结果表明,茶多酚在水中的衰减速率和BDOC生成速率有较好相关性。辅助消毒剂投入水中6 h内茶多酚浓度衰减很快,消毒效率指数较低,随着时间的延长,茶多酚浓度降低,消毒效率指数随之提高。因此,茶多酚作为辅助消毒剂时,建议其投加方式不宜采用一次投加,而应连续投加。采用连续投加的方式可以降低茶多酚的衰减速率,提高出水的生物稳定性。 相似文献
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亚氯酸钠-苯磺酸制备二氧化氯的方法进行了系统研究,通过正交试验确定了最佳反应条件,并考察了反应时间和反应温度对二氧化氯浓度和纯度的影响。该法反应迅速,可以制备出高纯二氧化氯,反应易于控制,苯磺酸可作为快速释放型二氧化氯固体制剂的活化剂。 相似文献
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融雪剂是一把双刃剑,在快速除雪保障交通畅通的同时,也给城市带来了一系列的环境问题。对融雪剂对城市环境的影响进行了探讨分析,并提出了今后使用融雪剂的建议和策略。 相似文献
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Daekyun Kim Nuray Ates Sehnaz Sule Kaplan Bekaroglu Meric Selbes Tanju Karanfil 《环境科学学报(英文版)》2017,29(8):155-162
The main objective of this study was to assess the combined use of chlorine dioxide (ClO2) and chlorine (Cl2) on the speciation and kinetics of disinfection by-product (DBP) formation in swimming pools using synthetic pool waters prepared with a body fluid analog (BFA) and/or fresh natural water. At 1:25 (mass ratio) of ClO2 to Cl2, there was no significant reduction in the formation of trihalomethanes (THMs) and haloacetic acids (HAAs) for both BFA solution and natural water compared to the application of Cl2 alone. When the mass ratio of ClO2 to Cl2 increased to 1:1, substantial decreases in both THMs and HAAs were observed in the natural water, while there was almost no change of DBP formations in the BFA solution. Haloacetonitriles and halonitromethanes levels in both water matrices remained similar. In the presence of bromide, the overall DBP formation increased in both BFA solution and natural water. For the DBP formation kinetics, after 72 hr of contact time, very low formation of THMs and HAAs was observed for the use of ClO2 only. Compared to Cl2 control, however, applying the 1:1 mixture of ClO2/Cl2 reduced THMs by > 60% and HAAs by > 50%. Chlorite was maintained below 1.0 mg/L, while the formation of chlorate significantly increased over the reaction time. Finally, in a bench-scale indoor pool experiment, applying ClO2 and Cl2 simultaneously produced less THMs compared to Cl2 control and kept chlorite at < 0.4 mg/L, while HAAs and chlorate accumulated over 4-week operation period. 相似文献
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Chao Liu 《环境科学学报(英文版)》2021,33(12):140-149
Maintaining a residual disinfectant/oxidant (e.g., chlorine and chlorine dioxide), is a generally used strategy to control microbial contaminants and bacterial regrowth in distribution systems. Secondarily oxidant, such as hypobromous acid (HOBr), can be formed during chlorination of bromide-containing waters. The decay of oxidants and formation of disinfection byproducts (DBPs) due to the interaction between oxidants and selected metal oxides were studied. Selected metal oxides generally enhanced the decay of these halogen-containing oxidants via three pathways: (1) catalytic disproportionation to yield an oxidized form of halogen (i.e., halate) and reduced form (halide for chlorine and bromine or chlorite for chlorine dioxide), (2) oxygen formation, and (3) oxidation of a metal in a reduced form (e.g., cuprous oxide) to a higher oxidation state. Cupric oxide (CuO) and nickel oxide (NiO) showed significantly strong abilities for the first pathway, and oxygen formation was a side reaction. Cuprous oxide can react with oxidants via the third pathway, while goethite was not involved in these reactions. The ability of CuO on catalytic disproportionation of HOBr remained stable up to four cycles. In chlorination process, bromate formation tends to be important (exceeding 10 µg/L) when initial bromide concentration is above 400 µg/L in the presence of dissolved organic matter. Increasing initial bromide concentrations increased the formation of DBPs and calculated cytotoxicity, and the maximum was observed at pH 8.6 during chlorination process. Therefore, the possible disinfectant loss and DBP formation should be carefully considered in drinking water distribution systems. 相似文献