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Formation of brominated trihalomethanes during chlorination or ozonation of natural organic matter extracts and model compounds in saline water

机译:在盐水中天然有机物质提取物和模型化合物的氯化或臭氧化过程中形成溴化三卤甲烷

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Oxidation experiments (chlorine, ozone and bromine) were carried out with synthetic saline waters containing natural organic matter (NOM) extracts and model compounds to evaluate the potential of these surrogates to mimic the formation of brominated trihalomethanes (Br-THMs) in natural saline waters. Synthetic saline water with Pony Lake fulvic acid (PLFA) showed comparable results to natural brackish and sea water for Br-THMs formation during chlorination and ozonation for typical ballast water treatment conditions ([Cl-2](0) = 5 mg/L or [O-3](0) = 3 mg/L). The molar CHBr3 yield in synthetic saline waters is higher for chlorination than for ozonation, since ozone reacts slower with bromide and faster with THM precursors. For bromination, the molar yields of CHBr3 for the NOM model compounds phenol, resorcinol, 3-oxopentanedioic acid and hydroquinone are 28, 62, 91 and 11%, respectively. CHBr3 formation is low during chlorination or ozonation of resorcinol-containing synthetic saline waters due to the faster reaction of resorcinol with these oxidants compared to the bromine formation from bromide. Oxidation experiments with mixtures of hydroquinone and phenol (or resorcinol) were conducted to mimic various functional groups of NOM reacting with Cl-2 (or O-3) in saline water. With increasing hydroquinone concentrations, the CHBr3 formation increases during both chlorination and ozonation of the mixtures, except for chlorination of the mixture of hydroquinone and resorcinol. The formation of THMs during chlorination of the mixture of hydroquinone and resorcinol is similar to that of resorcinol alone due to the much faster reaction of HOX with resorcinol compared to hydroquinone. In general, PLFA seems to be a reasonable DOM surrogate to simulate CHBr3 formation for realistic ballast water treatment. During chlorination, CHBr3 formations from phenol- and PLFA-containing synthetic brackish waters are comparable, for similar phenol contents. (C) 2018 Elsevier Ltd. All rights reserved.
机译:用含有天然有机物(NOM)提取物和模型化合物的合成盐水进行氧化实验(氯,臭氧和溴),以评估这些替代物模仿天然盐水中溴化三卤甲烷(Br-THMs)形成的潜力。 。在典型压舱水处理条件下,氯化和臭氧化过程中,用小马湖黄腐酸(PLFA)合成的咸水显示出与天然咸水和海水相当的结果,从而形成溴化THMs([Cl-2](0)> = 5 mg / L或[O-3](0)> = 3 mg / L)。在合成盐水中,氯化氢的摩尔CHBr3产率要高于臭氧氧化的摩尔产率,因为臭氧与溴化物的反应速度较慢,与THM前体的反应速度更快。对于溴化,NOM模型化合物苯酚,间苯二酚,3-氧戊二烯二酸和对苯二酚的CHBr3摩尔产率分别为28%,62%,91%和11%。在含间苯二酚的合成盐水进行氯化或臭氧化过程中,由于与由溴化物形成的溴相比,间苯二酚与这些氧化剂的反应更快,CHBr3的形成较低。进行了氢醌和苯酚(或间苯二酚)混合物的氧化实验,以模拟在盐水中与Cl-2(或O-3)反应的NOM的各种官能团。随着对苯二酚浓度的增加,在混合物的氯化和臭氧化过程中,除了对苯二酚和间苯二酚的混合物进行氯化外,CHBr3的形成均增加。对苯二酚和间苯二酚混合物氯化过程中THM的形成与单独的间苯二酚相似,这是因为HOX与间苯二酚的反应比对苯二酚快得多。通常,PLFA似乎是模拟CHBr3形成以进行压载水处理的合理DOM替代品。在氯化过程中,对于苯酚含量相似的情况,从含苯酚和PLFA的合成微咸水中形成的CHBr3是可比的。 (C)2018 Elsevier Ltd.保留所有权利。

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