G'/> Ferrate(VI) decomposition in water in the absence and presence of natural organic matter (NOM)
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Ferrate(VI) decomposition in water in the absence and presence of natural organic matter (NOM)

机译:在缺乏和存在天然有机物(NOM)的水中脱气(VI)分解

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Graphical abstractDisplay OmittedHighlights?Fe(VI) decomposition in the absence and presence of NOM exhibits biphasic and three-stage kinetic patterns, respectively.?NOM can cause an instant Fe(VI) loss, which is in direct proportion to initial DOC.?Fe(VI) instantaneously reacts with UV-absorbing moieties of NOM.?Humic acid and fulvic acid isolates cause a greater initial Fe(VI) consumption than hydrophilic fraction.AbstractThe kinetics of ferrate(VI) decomposition in natural water were assessed in the absence and presence of natural organic matter (NOM) (pH?=?7.50, [Fe(VI)]?=?54??M, DOC?=?0.00–10.00 and 1.00–8.57?mg/L for a simulated natural water and six real natural waters, respectively). Without NOM, Fe(VI) decomposition in simulated natural water exhibited a biphasic kinetics pattern, i.e. a 2nd-order reaction with respect to Fe(VI) concentration followed by a 1st-order reaction. However, an additional instant Fe(VI) loss was observed at the onset in the presence of NOM for both simulated and real natural waters, thereby rendering Fe(VI) decay with NOM a unique three-stage kinetics pattern. The initial instant Fe(VI) loss was caused due to the homogenous Fe(VI) self-decay and the rapid reactions between Fe(VI) and NOM. The latter accounted for a major fraction of the initial Fe(VI) loss and was in direct proportion with the initial DOC (DOC0) (Δ[Fe(VI)]0DOC?=?αNOMDOC0; αNOM?=?1.45??M Fe(VI)·L/mg DOC for the simulated natural water, and 0.66–1.35??M Fe(VI)·L/mg DOC for the six natural waters). Fe(VI) decomposition experiments with different Suwannee River NOM isolates revealed that hydrophobic NOM fractions (i.e. fulvic acid (FA) and humic acid (HA)) caused a more significant initial Fe(VI) loss than the hydrophilic group (HPI), suggesting that Fe(VI) preferentially reacted with hydrophobic NOM molecules rather than hydrophilic compounds. Furthermore, an approach developed for the estimation of αNOMrevealed a linear correlation between αNOMand specific UV absorbance (SUVA) (αNOM?=?0.27SUVA?+?0.18, R2?=?0.71). This study provides essential information regarding Fe(VI) decomposition for the determination of Fe(VI) dose and exposure for effective water treatment.]]>
机译:<![cdata [ 图形摘要 显示省略 突出显示 < CE:简单段ID =“SP0010”View =“全部”> fe(vi)分解在缺席和存在的NOM中分别表现出双相和三级动力学模式。 nom可能导致ins Tant Fe(VI)损失,它与初始文档直接比例。 Fe(vi)瞬间与Nom吸收部分的uV吸收部分反应。 腐殖酸和富乙酸分离物导致更大的初始Fe(VI)消耗量而不是亲水性分数。 抽象 在缺乏和存在的天然有机物(NOM)(pHα= 7.50 ,[fe(vi)]?=?54 ?? m,doc?= 0.00-10.00和1.0 0-8.57?MG / L分别用于模拟天然水和六个真正的天然水域)。没有NOM,模拟天然水中的Fe(VI)分解表现出双相动力学模式,即2 Nd - 相对于Fe(vi)浓度的反应遵循通过A 1 ST -Order反应。然而,在模拟和真正的天然水域的NOM存在下,在发病中观察到另外的即时Fe(VI)损失,从而用NOM A独特的三级动力学模式衰减Fe(VI)衰减。由于均匀的Fe(vi)自我衰减和Fe(vi)和Nom之间的快速反应引起了初始的即时Fe(vi)损失。后者占初始Fe(VI)损失的主要部分,并与初始DOC直接比例(DOC 0 )(Δ[FE(VI) )] 0 doc ?=?α NOM DOC 0 NOM ?=?1.45 ?? M FE(VI)·L / MG DOC用于模拟天然水,六个天然水域的0.66-1.35··L / MG DOC)。 Fe(VI)与不同Suwannee河NOM分离株的FE(VI)分解实验揭示了疏水性NOM分数(即富含酸(FA)和腐殖酸(HA))引起比亲水基团(HPI)更明显的初始Fe(VI)损失,提示该Fe(VI)优先与疏水性NOM分子而不是亲水化合物反应。此外,为估计α nom 在α和特定的紫外线吸光度(SUVA)(α NOM ?=?0.27SUVA?+?0.18,R 2 ?=?0.71)。本研究提供了关于Fe(VI)分解的基本信息,用于测定Fe(VI)剂量和有效水处理的暴露。 ] ]

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