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ACS ES T Water. 2022 Oct 28;2(12):2431-2440. doi: 10.1021/acsestwater.2c00292.
2
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本文引用的文献

1
Characterizing Ohio River NOM Variability and Reconstituted-Lyophilized NOM as a Source Surrogate.表征俄亥俄河天然有机物的变异性以及重构冻干天然有机物作为源替代物的特性。
J Am Water Works Assoc. 2017;109(1):E1-E9. doi: 10.5942/jawwa.2017.109.0008.
2
Comparison of the yields of mono-, Di- and tri-chlorinated HAAs and THMs in chlorination and chloramination based on experimental and quantum-chemical data.基于实验和量子化学数据比较氯化和氯胺化过程中单、二、三氯代卤乙酸和三卤甲烷的产率。
Water Res. 2020 Feb 1;169:115100. doi: 10.1016/j.watres.2019.115100. Epub 2019 Oct 18.
3
Modeling the formation of TOCl, TOBr and TOI during chlor(am)ination of drinking water.建立饮用水氯化(氨)过程中生成三氯氧碳(TOCl)、三溴氧碳(TOBr)和三碘氧碳(TOI)的模型。
Water Res. 2016 Jun 1;96:166-76. doi: 10.1016/j.watres.2016.03.051. Epub 2016 Mar 25.
4
Kinetics of bromochloramine formation and decomposition.溴氯胺的形成与分解动力学。
Environ Sci Technol. 2014;48(5):2843-52. doi: 10.1021/es4036754. Epub 2014 Feb 11.
5
Modeling bromide effects on yields and speciation of dihaloacetonitriles formed in chlorinated drinking water.建立溴化物对氯化饮用水中形成的二卤乙腈产量和形态的影响模型。
Water Res. 2013 Oct 15;47(16):5995-6006. doi: 10.1016/j.watres.2013.07.018. Epub 2013 Jul 31.
6
Disinfection byproduct formation in reverse-osmosis concentrated and lyophilized natural organic matter from a drinking water source.反渗透浓缩和冻干饮用水源天然有机物中的消毒副产物形成。
Water Res. 2012 Oct 15;46(16):5343-54. doi: 10.1016/j.watres.2012.07.020. Epub 2012 Jul 20.
7
Iodate and iodo-trihalomethane formation during chlorination of iodide-containing waters: role of bromide.含碘水氯化过程中碘酸盐和碘三卤甲烷的形成:溴化物的作用。
Environ Sci Technol. 2012 Jul 3;46(13):7350-7. doi: 10.1021/es301301g. Epub 2012 Jun 21.
8
I-THM formation and speciation: preformed monochloramine versus prechlorination followed by ammonia addition.I-THM 的形成与形态:预形成的一氯胺与预氯化后再加氨。
Environ Sci Technol. 2011 Dec 15;45(24):10429-37. doi: 10.1021/es202745t. Epub 2011 Nov 29.
9
Concentration, chlorination, and chemical analysis of drinking water for disinfection byproduct mixtures health effects research: U.S. EPA's Four Lab Study.饮用水消毒副产物混合物健康影响研究的浓度、氯化和化学分析:美国环保署的四实验室研究。
Environ Sci Technol. 2010 Oct 1;44(19):7184-92. doi: 10.1021/es9039314.
10
Innovative method for prioritizing emerging disinfection by-products (DBPs) in drinking water on the basis of their potential impact on public health.创新方法,根据新兴消毒副产物(DBPs)对公众健康的潜在影响对其进行优先排序。
Water Res. 2010 May;44(10):3147-65. doi: 10.1016/j.watres.2010.02.004. Epub 2010 Mar 11.

预制一氯胺与处理后的天然有机物反应性评估及浓水结垢方法学开发

Evaluation of Preformed Monochloramine Reactivity with Processed Natural Organic Matter and Scaling Methodology Development for Concentrated Waters.

作者信息

Kennicutt Alison R, Rossman Paul D, Bollman Jacob D, Aho Taylor, Abulikemu Gulizhaer, Pressman Jonathan G, Wahman David G

机构信息

York College of Pennsylvania, York, Pennsylvania 17403, United States.

National Research Council Research Associateship Programs, Postdoctoral Research Associate, Cincinnati, Ohio 45268, United States.

出版信息

ACS ES T Water. 2022 Oct 28;2(12):2431-2440. doi: 10.1021/acsestwater.2c00292.

DOI:10.1021/acsestwater.2c00292
PMID:36968336
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10031650/
Abstract

To evaluate natural organic matter (NOM) processing impacts on preformed monochloramine (PM) reactivity and as a first step in creating concentrated disinfection byproduct (DBP) mixtures from PM, a rational methodology was developed to proportionally scale PM NOM-related demand in unconcentrated source waters to waters with concentrated NOM. Multiple NOM preparations were evaluated, including a liquid concentrate and reconstituted lyophilized solid material. Published kinetic models were evaluated and used to develop a focused reaction scheme (FRS) that was relatively simple to implement and focused on monochloramine loss, including considerations for inorganic chloramine stability (i.e., autodecomposition) and bromide and iodide impacts. The FRS included critical reaction pathways and accurately simulated (without modification) monochloramine experimental data with and without bromide and iodide present over a range of PM-dosed NOM-free waters. For NOM-containing waters, addition of two NOM reactions in the FRS allowed (i) apportioning monochloramine loss to either inorganic or NOM-related reactions and (ii) selecting experiment conditions to provide an equivalent monochloramine NOM-related demand in unconcentrated and concentrated waters. The methodology provides a framework for future experimentation to evaluate DBP scaling and their speciation in concentrated water matrices when providing an equivalent NOM-related monochloramine demand in unconcentrated and concentrated matrices.

摘要

为评估天然有机物(NOM)处理对预形成一氯胺(PM)反应活性的影响,并作为从PM制备浓缩消毒副产物(DBP)混合物的第一步,开发了一种合理的方法,将未浓缩源水中与NOM相关的PM需求量按比例放大至含有浓缩NOM的水体中。对多种NOM制剂进行了评估,包括液体浓缩物和重构的冻干固体材料。对已发表的动力学模型进行了评估,并用于开发一种聚焦反应方案(FRS),该方案相对易于实施,且专注于一氯胺损失,包括对无机氯胺稳定性(即自分解)以及溴化物和碘化物影响的考虑。FRS包括关键反应途径,并准确模拟(无需修改)了在一系列添加PM的无NOM水体中存在和不存在溴化物及碘化物情况下的一氯胺实验数据。对于含NOM的水体,在FRS中添加两个NOM反应能够(i)将一氯胺损失分配到无机或与NOM相关的反应中,以及(ii)选择实验条件,以在未浓缩和浓缩水体中提供等效的与NOM相关的一氯胺需求量。该方法为未来的实验提供了一个框架,以便在未浓缩和浓缩基质中提供等效的与NOM相关的一氯胺需求量时,评估DBP的放大情况及其在浓缩水基质中的形态。