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反渗透卤水中碘造影剂的高级氧化:猝灭的影响。

Advanced oxidation of iodinated X-ray contrast media in reverse osmosis brines: the influence of quenching.

机构信息

Faculty of Civil & Environmental Engineering and Grand Water Research Institute, Technion-Israel Institute of Technology, Haifa 32000, Israel.

Faculty of Civil & Environmental Engineering and Grand Water Research Institute, Technion-Israel Institute of Technology, Haifa 32000, Israel.

出版信息

Water Res. 2014 Oct 1;62:107-16. doi: 10.1016/j.watres.2014.05.041. Epub 2014 Jun 6.

Abstract

Among the main restrictions for the implementation of advanced oxidation processes (AOPs) for removal of micropollutants present in reverse osmosis (RO) brines of secondary effluents account the quenching performed by background organic and inorganic constituents. Natural organic matter (NOM) and soluble microbial products (SMP) are the main effluent organic matter constituents. The inorganic fraction is largely constituted by chlorides and bicarbonate alkalinity with sodium and calcium as main counterions. The quenching influence of these components, separately and their mixture, in the transformation of model compounds by UVA/TiO2 was studied applying synthetic brines solutions mimicking 2-fold concentrated RO secondary effluents brines. The results were validated using fresh RO brines. Diatrizoate (DTZ) and iopromide (IOPr) were used as model compound. They have been found to exhibit relative high resistance to oxidation process and therefore represent good markers for AOPs techniques. Under the conditions applied, oxidization of DTZ in the background of RO brines was strongly affected by quenching effects. The major contribution to quenching resulted from organic matter (≈70%) followed by bicarbonate alkalinity (≈30%). NOM displayed higher quenching than SMP in spite of its relative lower concentration. Multivalent cations, i.e., Ca(+2), were found to decrease effectiveness of the technique due to agglomeration of the catalyst. However this influence was lowered in presence of NOM. Different patterns of transformation were found for each model compound in which a delayed deiodination was observed for iopromide whereas diatrizoate oxidation paralleled deiodination.

摘要

在反渗透(RO)二级出水的浓盐水实施高级氧化工艺(AOPs)去除痕量污染物时,主要的限制因素之一是背景有机和无机成分的猝灭作用。天然有机物(NOM)和可溶解性微生物产物(SMP)是主要的出水有机物质成分。无机部分主要由氯化物和碳酸氢盐碱度组成,其中钠和钙是主要的抗衡离子。本研究应用模拟 2 倍浓缩 RO 二级出水浓盐水的合成盐水溶液,分别研究了这些成分及其混合物对 UVA/TiO2 转化模型化合物的猝灭影响,并使用新鲜 RO 浓盐水对结果进行了验证。二噁嗪(DTZ)和碘普罗胺(IOPr)被用作模型化合物。研究发现它们对氧化过程具有相对较高的抗性,因此是 AOPs 技术的良好标志物。在应用的条件下,RO 浓盐水中 DTZ 的氧化受到猝灭效应的强烈影响。猝灭的主要贡献来自有机物(≈70%),其次是碳酸氢盐碱度(≈30%)。尽管 NOM 的浓度相对较低,但它的猝灭作用仍高于 SMP。多价阳离子,如 Ca(+2),由于催化剂的团聚作用,被发现会降低该技术的有效性。然而,在存在 NOM 的情况下,这种影响会降低。对于每种模型化合物,都发现了不同的转化模式,其中碘普罗胺的碘化延迟,而二噁嗪的氧化与碘化平行。

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