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The spatial variability of disinfection by-products relative to regional chemical gradients

机译:消毒副产物相对于区域化学梯度的空间变异性

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Background and Problem Statement- A spatial analysis of disinfection by-products(DBPs) in public water supplies in Maine showed a progressive prevalence oftrihalomethanes (THM) over haloacetic acids (HAA) with increasing distance from theocean, as well as a parallel increase in total DBPs. Since proximity to the ocean controlsthe deposition of salt from marine aerosols, background chloride was suspected as animportant factor in DBP formation. The character of dissolved organic carbon (DOC) isknown to be related to landscape factors that also vary from coastal to inland areas.Project Description and Setup- The experimental approach involved an analysis of theinfluences of chloride and DOC on the formation of different types of DBPs using rawand finished water samples (lakes or rivers) collected from 21 public water supplies inMaine. Sample locations ranged along a 300 km transect from coastal to inland areas.Water samples were analyzed for general water chemistry, specific UV absorbance(SUVA), and DBPs. Additional raw water samples were collected for salt (NaCl)addition experiments while monitoring DBP formation. The character of the DBPsformed was analyzed using chromatography coupled to a novel ultra-high resolutionFourier transform ion cyclotron resonance mass spectrometer (GC/FT-ICR MS).Results- Field data exhibited an inverse relationship between dissolved organic carbon(DOC) and chloride concentrations. There was also a positive relationship betweenSUVA, DOC, and DBPs that probably relates to DOC precursors of DBPs. However,paired samples of raw and finished water showed no correlation between the type of DBPformed and chloride concentrations.Significance to the Industry and Recommendations- The types and quantities of DBPsformed are controlled in part by the raw water chemistry. Chloride has been considered tobe relatively inert but its presence is correlated with different types of DBPs. Thepotential exists for DBP precursors to be formed in source watersheds under naturalbiogeochemical conditions. Water utilities may be able to gain additional DBP reductionthrough understanding and managing these conditions in source watersheds.
机译:背景和问题陈述-缅因州公共供水中消毒副产物(DBPs)的空间分析表明,三卤甲烷(THM)在卤代乙酸(HAA)上的发病率呈逐步上升趋势,且与海洋的距离越来越远,并且总海洋生物平行增加DBP。由于靠近海洋可控制海洋气溶胶中盐的沉积,因此怀疑背景氯化物是DBP形成的重要因素。已知溶解性有机碳(DOC)的特性与沿海至内陆地区的景观因素有关。项目描述和设置-实验方法涉及分析氯化物和DOC对不同类型DBP形成的影响使用从缅因州的21个公共供水中收集的原水和成品水样本(湖泊或河流)。从沿海地区到内陆地区,样品位置沿300 km的横断面范围进行了分析,分析了水样品的一般水化学,比吸收率(SUVA)和DBP。收集其他原水样品进行盐(NaCl)添加实验,同时监控DBP的形成。通过色谱法结合新型超高分辨率傅里叶变换离子回旋共振质谱仪(GC / FT-ICR MS)分析了DBP的特征。结果-现场数据显示溶解有机碳(DOC)与氯化物浓度呈反比关系。 SUVA,DOC和DBP之间也存在正相关关系,这可能与DBP的DOC前体有关。然而,成对的原水和最终水样品显示DBP形成的类型与氯化物浓度之间没有相关性。对行业的意义和建议-形成的DBP的类型和数量部分受原水化学性质的控制。氯化物被认为是相对惰性的,但其存在与不同类型的DBP相关。在自然生物地球化学条件下,在源流域形成DBP前体的潜力。自来水公司可以通过了解和管理源流域中的这些条件来获得额外的DBP降低。

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