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首页> 外文期刊>Journal of Photochemistry and Photobiology, A. Chemistry >Assessment of advanced oxidation processes for the degradation of three UV filters from swimming pool water
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Assessment of advanced oxidation processes for the degradation of three UV filters from swimming pool water

机译:评估水池水中三种UV过滤器降解的先进氧化过程

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This work assesses different advanced oxidation processes (AOPs) for the elimination of 3 UV filters, ensulizole (PBSA), benzophenone-4 (BP-4) and benzophenone-3 (BP-3), in concentrations of few micrograms per liter, from synthetic and real swimming pool waters. AOPs experiments were performed in a lab-scale tubular photoreactor irradiated by UVA (lambda = 360 nm) or UVC (lambda = 254 nm) light. First, UVA heterogeneous photocatalysis using cellulose acetate monolithic structures coated with thin films of commercial Fe2O3 and TiO2 (P25, PC105, and PC500) nanoparticles were employed. The highest removal efficiencies values for PBSA (44%), BP-4 (90%) and BP-3 (91%) using synthetic swimming pool waters, after 30 min of irradiation, were achieved using TiO2-P25 (3 dips). The addition of H2O2 to the TiO2-P25/UVA and Fe2O3/UVA systems improved substantially the reaction rate, especially for the TiO2-P25/UVA system. The second approach consisted in the photochemical oxidation of the UV filters using a UVC/H2O2 system. The optimal H2O2 concentration obtained was 0.59 mM, resulting in removal efficiencies of 77%, 98% and 95% for PBSA, BP-4, and BP-3, respectively, after 6 min of irradiation, with photolysis half-lifes lower than 3 min. UVC (lambda = 254 nm) and UVA (lambda = 360 nm) photolysis showed lower degradation rates for the three target compounds when compared with the AOPs tested. Finally, heterogeneous TiO2-P25/UVA photocatalysis and photochemical UVC/H2O2 oxidation systems, under their optimal conditions, were applied to the treatment of real swimming pool waters containing simultaneously the three UV filters, reaching a complete degradation (LOD) for BP-4 and BP-3 and 50% for the recalcitrant PBSA in less than 6 min. Although several by-products, including chlorinated compounds, were identified during the oxidation process, its abundance was substantially decreased for extended period of reaction time. (C) 2017 Elsevier B.V. All rights reserved.
机译:该作品评估了不同的晚期氧化方法(AOP),用于消除3个UV过滤器,算子(PBSA),二苯甲酮-4(BP-4)和二苯甲酮-3(BP-3),以少量微克每升,来自合成和真正的游泳池水域。在由UVA(Lambda = 360nm)或UVC(Lambda = 254nm)光照射的实验室鳞片管状光反应器中进行AOP实验。首先,采用使用涂覆有商业Fe2O3和TiO2(P25,PC105和PC500)纳米颗粒的薄膜的纤维素乙酸盐单铁结构的UVA异质光催化。使用TiO2-P25(3次浸渍)实现了使用合成游泳池水的PBSA(44%),BP-4(90%)和BP-3(91%)的最高去除效率值。将H 2 O 2加入TiO2-P25 / UVA和Fe2O3 / UVA系统的基本上改善了反应速率,特别是对于TiO2-P25 / UVA系统。使用UVC / H2O2系统,第二种方法包括UV滤光器的光化学氧化。获得的最佳H 2 O 2浓度为0.59mm,在6分钟照射后,PBSA,BP-4和BP-3分别去除77%,98%和95%,光解半寿命低于3闵。与测试的AOP相比,UVC(Lambda = 254nm)和UVA(Lambda = 360nm)光解显示三个靶化合物的降低降解速率。最后,在其最佳条件下,非均相TiO2-P25 / UVA光催化和光化学UVC / H2O2氧化系统应用于同时含有三个UV过滤器的真实游泳池水处理,达到BP的完全降解(& lod) -4和BP-3和&顽抗PBSA在不到6分钟的50%。虽然在氧化过程中鉴定了几种副产物,包括氯化化合物,但在延长的反应时间内,其丰度显着降低。 (c)2017 Elsevier B.v.保留所有权利。

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