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Nanofiltration of pretreated Lake Houston water:Disinfection by-product speciation,relationships,and control

机译:预处理的休斯敦湖水的纳滤:消毒副产物的形态,关系和控制

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Water quality results related to disinfection by products(DBPs)from a bench-scale study designed to evaluate surface water nanofiltration(NF)for the City of Houston are analyzed to provide insights into mechanisms of DBP formation and control.One contribution of this manuscript is that we report on DBP speciation following NF of Lake Houston water containing very low concentrations of the bromide ion(<~50 mu g/L or 0.6 mu M).Rejection of natural organic matter(NOM)and DBP precursors decreased with increasing recovery indicating diffusion-limited transport of these macromolecular contaminants under conditions typical of drinking water NF.Additional evidence of diffusivity effects on transport was provided by decreasing permeation coefficients of polyethylene glycols with molecular weight.Haloacetic acid(HAA)molar concentrations were higher than corresponding trihalomethane(THM)concentrations in NF permeates contrary to expectations from the DBP rule where lower mass-based maximum contaminant levels are enforced for HAAs.Similar to conventional treatment,ultraviolet absorbance at 254 nm(UV254),dissolved organic carbon(DOC),and chlorine consumption were found to be excellent surrogates for aqueous DBP concentrations even in chlorinated nanoflltered waters.Mole fractions of mono-,di-,and trihalogenated HAA species were invariant with respect to changes in Br~-/DOC molar ratio suggesting that the brominated HAAs are formed through the same mechanisms as the chlorinated ones in NF permeate waters.Additionally,bromine incorporation into both THMs and HAAs increased with increasing Br/DOC ratio suggesting that the brominated THM and HAA species form first consuming the reactive precursor sites and in the process restricting formation of the chlorinated species.Bromide utilization was observed to decrease with Br"/DOC molar ratio demonstrating that nanofilter permeate waters were substantially limited with respect to NOM and DBP precursors.
机译:通过对旨在评估休斯敦市地表水纳滤(NF)的台式研究进行的与副产品消毒(DBPs)相关的水质结果进行分析,以提供对DBP形成和控制机理的见解。我们报告了休斯顿湖水中NF含量极低(<〜50μg / L或0.6μM)的DBP形态。天然有机物(NOM)和DBP前体的排斥随着回收率的增加而降低,表明在饮用水NF的典型条件下,这些大分子污染物的扩散限制迁移。通过降低分子量的聚乙二醇的渗透系数,提供了扩散扩散对迁移的影响的证据。卤乙酸(HAA)的摩尔浓度高于相应的三卤甲烷(THM) )NF浓度的渗透与DBP规则的预期相反,在DBP规则中,基于质量的最大污染物含量较低与常规处理相似,即使在氯化纳米过滤水中,DBA水溶液的254 nm(UV254)紫外线吸收,溶解的有机碳(DOC)和氯消耗量也是DBP浓度的优良替代物。单,二和三卤代HAA的Br〜-/ DOC摩尔比的变化是不变的,这表明溴化HAA的形成机理与NF渗透水中的氯代形成的机理相同。 THMs和HAA随着Br / DOC比的增加而增加,这表明溴化THM和HAA物种首先消耗了反应性前体位点,并在此过程中限制了氯化物的形成。观察到溴化物的利用随着Br“ / DOC摩尔比的降低而降低。关于NOM和DBP前驱物,纳滤器渗透水受到很大限制。

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