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亚铁/过一硫酸盐氧化预处理陶瓷超滤膜:控制天然有机物污染和莠去津降解。

Ferrous iron/peroxymonosulfate oxidation as a pretreatment for ceramic ultrafiltration membrane: Control of natural organic matter fouling and degradation of atrazine.

机构信息

State Key Laboratory of Urban Water Resource and Environment (SKLUWRE), Harbin Institute of Technology, 73 Huanghe Road, Nangang District, Harbin, 150090, PR China.

School of Municipal and Environmental Engineering, Shandong Jianzhu University, 1000 Fengming Road, Licheng District, Jinan, 250101, PR China.

出版信息

Water Res. 2017 Apr 15;113:32-41. doi: 10.1016/j.watres.2017.01.055. Epub 2017 Feb 1.

Abstract

Ferrous iron/peroxymonosulfate (Fe(II)/PMS) oxidation was employed as a pretreatment method for ultrafiltration process to control membrane fouling caused by natural organic matter, including humic acid (HA), sodium alginate (SA), bovine serum albumin (BSA), and their mixture (HA-SA-BSA). To evaluate the mechanism of fouling mitigation, the effects of Fe(II)/PMS pretreatment on the characteristics of feed water were examined. The degradation of atrazine (ATZ) was also investigated and the species of generated radicals were preliminarily determined. Under the test exposure (15 and 50 μM), Fe(II)/PMS pretreatment effectively mitigated membrane fouling caused by HA, SA and HA-SA-BSA mixture, and the performance improved with the increase of Fe(II) or PMS dose; whereas aggravated BSA fouling at lower doses and fouling alleviation was observed only at a higher dose (50/50 μΜ). The fouling mitigation was mainly attributed to the effective reduction of organic loadings by coagulation with in-situ formed Fe(III). Its performance was comparable or even slightly higher than single coagulation with Fe(III), most likely due to the oxidation by Fe(II)/PMS process. Fe(II)/PMS oxidation showed better performance in reducing DOC and UV, fluorescence intensities of fluorescent components and UV-absorbing compounds than single coagulation. In addition, Fe(II)/PMS pretreatment was efficient in ATZ degradation due to the generation of sulfate and hydroxyl radicals, whereas coagulation was ineffective to remove it.

摘要

亚铁/过一硫酸盐(Fe(II)/PMS)氧化被用作超滤过程的预处理方法,以控制由天然有机物引起的膜污染,包括腐殖酸(HA)、海藻酸钠(SA)、牛血清白蛋白(BSA)及其混合物(HA-SA-BSA)。为了评估减轻污染的机制,考察了 Fe(II)/PMS 预处理对进水特性的影响。还研究了莠去津(ATZ)的降解情况,并初步确定了生成的自由基种类。在测试暴露(15 和 50 μM)下,Fe(II)/PMS 预处理有效减轻了 HA、SA 和 HA-SA-BSA 混合物引起的膜污染,且性能随 Fe(II)或 PMS 剂量的增加而提高;而在较低剂量下加剧了 BSA 污染,仅在较高剂量(50/50 μΜ)下观察到污染缓解。污染缓解主要归因于原位形成的 Fe(III)的混凝作用有效降低了有机负荷。其性能与单独使用 Fe(III)的混凝作用相当,甚至略高,这很可能是由于 Fe(II)/PMS 过程的氧化作用。与单独的混凝作用相比,Fe(II)/PMS 氧化在降低 DOC 和 UV、荧光物质的荧光强度和紫外吸收化合物方面表现出更好的性能。此外,Fe(II)/PMS 预处理由于硫酸根和羟基自由基的生成,对 ATZ 的降解效率很高,而混凝作用则无法有效去除它。

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