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首页> 外文期刊>Chemical engineering journal >Identification and quantification of ineffective chlorine by NaAsO2 selective quenching method during drinking Water disinfection
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Identification and quantification of ineffective chlorine by NaAsO2 selective quenching method during drinking Water disinfection

机译:NaAsO2选择性猝灭法在饮用水消毒中无效氯的鉴定与定量。

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摘要

To ensure the safety of drinking water with enough residual chlorine, a part of residual chlorine named "ineffective chlorine" was uniquely identified and quantified by NaAsO2 selective quenching method. NaAsO2 showed a weak reducibility and was easier to be controlled compared to other common quenchers including NaHSO3, ascorbic acid, Na2SO3.and Na2S2O3. Due to the different oxidizing abilities among the species in total residual chlorine, NaAsO2 can selectively and completely quench the strong oxidizing residual chlorine parts (free chlorine, NH2Cl, NHCl2 and some organic chloramines) but leave the weak or no oxidizing parts for the quantification as ineffective chlorine. During the chlorination of Suwannee River humic acid, ineffective chlorine formation increased from <0.02 to 0.08 mg/L (as Cl-2) as the dissolved organic carbon of humic acid increased from 0 to 15 mg-C/L. Finished water samples from three drinking water treatment plants (DWTPs) and one tap water sample were collected to examine the presence of ineffective chlorine. The quantified ineffective chlorine ranged from 3.3% to 27.8% of the total residual chlorine. Formation of ineffective chlorine was positively correlated with the dissolved organic nitrogen concentration in drinking water. As the reaction time increased from 4 to 48 h, the ineffective chlorine in the finished water from DWTP1 (water source: Yangtze River) was fairly stable at 0.15 mg/L as Cl-2, and its proportion in total residual chlorine increased from 27.8% to 78.9%. The ineffective chlorine was verified to be much weaker than free chlorine, NH2Cl and NHCl2 in Escherichia coli inactivation. (C) 2015 Elsevier B.V. All rights reserved.
机译:为了确保具有足够残留氯的饮用水的安全性,通过NaAsO2选择性猝灭法对残留氯中的一部分称为“无效氯”进行了唯一鉴定和定量。与其他常见的淬灭剂(包括NaHSO3,抗坏血酸,Na2SO3和Na2S2O3)相比,NaAsO2的还原性较弱并且更易于控制。由于物种之间在总残留氯中的氧化能力不同,因此NaAsO2可以有选择地完全淬灭强氧化性残留氯部分(游离氯,NH2Cl,NHCl2和某些有机氯胺),但留下弱或无氧化部分进行定量氯无效。在Suwannee River腐殖酸的氯化过程中,无效的氯形成从<0.02增至0.08 mg / L(以Cl-2计),因为腐殖酸的溶解有机碳从0增至15 mg-C / L。收集了来自三个饮用水处理厂(DWTP)的成品水样品和一个自来水样品,以检查无效氯的存在。定量的无效氯占残留氯总量的3.3%至27.8%。无效氯的形成与饮用水中溶解的有机氮浓度呈正相关。随着反应时间从4小时增加到48小时,来自DWTP1(水源:长江)的最终水中的无效氯以Cl-2计为0.15 mg / L时相当稳定,其在总余氯中的比例从27.8增加%至78.9%。在大肠杆菌灭活中,无效氯被证明比游离氯,NH2Cl和NHCl2弱得多。 (C)2015 Elsevier B.V.保留所有权利。

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