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反渗透膜浓水中痕量有机物降解的 UV/H2O2 和 UV/S2O8(2-) 高级氧化过程中基质成分的影响。

Effect of matrix components on UV/H2O2 and UV/S2O8(2-) advanced oxidation processes for trace organic degradation in reverse osmosis brines from municipal wastewater reuse facilities.

机构信息

State Key Laboratory of Urban Water Resource and Environment, Harbin Institute of Technology, Harbin, 150090, China.

Department of Environmental Sciences, The Connecticut Agricultural Experiment Station, 123 Huntington St., P.O. Box 1106, New Haven, 06504-1106, CT, USA.

出版信息

Water Res. 2016 Feb 1;89:192-200. doi: 10.1016/j.watres.2015.11.049. Epub 2015 Dec 2.

Abstract

When reverse osmosis brines from potable wastewater reuse plants are discharged to poorly-flushed estuaries, the concentrated organic contaminants are a concern for receiving water ecosystems. UV/hydrogen peroxide (UV/H2O2) and UV/persulfate (UV/S2O8(2-)) advanced oxidation processes (AOPs) may reduce contaminant burdens prior to discharge, but the effects of the high levels of halide, carbonate and effluent organic matter (EfOM) normally present in these brines are unclear. On the one hand, these substances may reduce process efficiency by scavenging reactive oxygen species (ROS), hydroxyl (OH) and sulfate (SO4(-) radicals. On the other, the daughter radicals generated by halide and carbonate scavenging may themselves degrade organics, offsetting the effect of ROS scavenging. UV/H2O2 and UV/S2O8(2-) AOPs were compared for degradation of five pharmaceuticals spiked into brines obtained from two reuse facilities and the RO influent from one of them. For UV/H2O2, EfOM scavenged ∼75% of the OH, reducing the degradation efficiency of the target contaminants to a similar extent; halide and carbonate scavenging and the reactivities of associated daughter radicals were less important. For UV/S2O8(2-), anions (mostly Cl(-)) scavenged ∼93% of the SO4(-). Because daughter radicals of Cl(-) contributed to contaminant degradation, the reduction in contaminant degradation efficiency was only ∼75-80%, with the reduction driven by daughter radical scavenging by EfOM. Conversion of SO4(-) to more selective halogen and carbonate radicals resulted in a wider range of degradation efficiencies among the contaminants. For both AOPs, 250 mJ/cm(2) average fluence achieved significant removal of four pharmaceuticals, with significantly better performance by UV/S2O8(2-) treatment for some constituents. Accounting for the lower brine flowrates, the energy output to achieve this fluence in brines is comparable to that often applied to RO permeates. However, much higher fluence was required for the least reactive pharmaceutical. Comparing AOP application to the RO influent or brine, equal or greater removal was achieved for brine treatment for comparable energy input. AOP treatment of brines could be applied to reduce, but not eliminate, contaminant burdens prior to discharge.

摘要

当饮用水再利用厂的反渗透海水浓盐水被排放到冲洗不良的河口时,浓缩的有机污染物是受纳水生态系统关注的问题。紫外线/过氧化氢 (UV/H2O2) 和紫外线/过硫酸盐 (UV/S2O8(2-)) 高级氧化工艺 (AOPs) 可以在排放前减少污染物负荷,但这些海水中通常存在的高浓度卤化物、碳酸盐和出水中的有机物 (EfOM) 的影响尚不清楚。一方面,这些物质可能通过清除活性氧 (ROS)、羟基 (OH) 和硫酸盐 (SO4(-) 自由基来降低过程效率。另一方面,卤化物和碳酸盐清除产生的女儿自由基本身可能会降解有机物,从而抵消 ROS 清除的影响。比较了 UV/H2O2 和 UV/S2O8(2-) AOP 对从两个再利用设施获得的海水浓盐水和其中一个设施的 RO 进水添加的五种药物的降解情况。对于 UV/H2O2,EfOM 清除了约 75%的 OH,将目标污染物的降解效率降低到相似的程度;卤化物和碳酸盐的清除以及相关的女儿自由基的反应性不太重要。对于 UV/S2O8(2-),阴离子(主要是 Cl(-))清除了约 93%的 SO4(-)。由于 Cl(-)的女儿自由基有助于污染物的降解,污染物降解效率的降低仅约为 75-80%,降低驱动力是 EfOM 对女儿自由基的清除。SO4(-) 转化为更具选择性的卤素和碳酸盐自由基,导致污染物降解效率的范围更广。对于两种 AOP,平均 250 mJ/cm(2) 的辐照通量实现了四种药物的显著去除,对于一些成分,UV/S2O8(2-) 处理的性能明显更好。考虑到海水浓盐水的低流量,在海水中达到该辐照通量的能量输出与通常应用于 RO 渗透物的能量输出相当。然而,对于反应性最低的药物,需要更高的辐照通量。将 AOP 应用于 RO 进水或海水浓盐水的比较表明,对于可比的能量输入,海水浓盐水处理可以实现相同或更大的去除率。AOP 处理海水浓盐水可以在排放前减少,但不能消除污染物负荷。

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