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溶解有机物对臭氧微纳米气泡水选择性氧化甲苯的影响。

Effect of dissolved organic matter on selective oxidation of toluene by ozone micro-nano bubble water.

机构信息

Zhejiang Provincial Key Laboratory of Solid Waste Treatment and Recycling, Zhejiang Engineering Research Center of Non-ferrous Metal Waste Recycling, School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou 310012, PR China.

Zhejiang Provincial Key Laboratory of Solid Waste Treatment and Recycling, Zhejiang Engineering Research Center of Non-ferrous Metal Waste Recycling, School of Environmental Science and Engineering, Zhejiang Gongshang University, Hangzhou 310012, PR China; Instrumental Analysis Center of Zhejiang Gongshang University, Hangzhou 310012, PR China.

出版信息

Chemosphere. 2023 Jun;325:138400. doi: 10.1016/j.chemosphere.2023.138400. Epub 2023 Mar 14.

Abstract

The oxidation capacity of ozone micro-nano bubble water (OMBW) was always higher than ozonated water due to enhanced contact by bubble interface, while the effect of coexisted dissolved organic matter (DOM) on the oxidation efficiency was still unclear. In this paper, batch experiments were carried out to investigate the selective oxidation of toluene by both OMBW and ozonated water (OW) with coexisted DOM in water. Five types of background solutions were applied in this study, including humic acid solution, fulvic acid solution and three types of diluted landfill leachates at the same content of total organic carbon. Results showed that coexisted DOM had a greater inhibition effect on toluene oxidation rate by OMBW, and the oxidation rate of toluene by OMBW and OW became close. It was mainly caused by the decreased reaction rate between toluene and hydroxyl radical (k) in OMBW after the introduction of DOM, which competed for the adsorption sites on micro-nano bubble interface. The fraction of ozone to oxidize toluene as well as k was in positive correlations with SUVA and the content of humic acid-like substances, but negatively correlated with E/E, content of tryptophan-like proteins and content of fulvic acid-like substances. In addition, increasing the ozone dose was not effective in increasing the utilization rate of ozone in OMBW due to limited adsorption sites on micro-nano bubble interface. The paper was conductive to the application of ozone micro-nano bubble water in groundwater remediation with complex water matrices.

摘要

臭氧微纳米气泡水(OMBW)的氧化能力由于气泡界面的增强接触始终高于臭氧水,而共存溶解有机物(DOM)对氧化效率的影响仍不清楚。本文通过批实验研究了共存 DOM 对 OMBW 和臭氧水(OW)氧化甲苯的选择性影响。本研究应用了 5 种背景溶液,包括腐殖酸溶液、富里酸溶液和三种相同总有机碳含量的稀释垃圾渗滤液。结果表明,共存 DOM 对 OMBW 氧化甲苯速率有更大的抑制作用,OMBW 和 OW 氧化甲苯的速率变得相近。这主要是由于 DOM 的引入降低了 OMBW 中甲苯与羟基自由基(k)之间的反应速率,而 DOM 竞争了微纳米气泡界面上的吸附位点。氧化甲苯的臭氧分数和 k 与 SUVA 和腐殖酸类物质含量呈正相关,与 E/E、色氨酸类蛋白含量和富里酸类物质含量呈负相关。此外,由于微纳米气泡界面上的吸附位点有限,增加臭氧剂量并不能有效提高 OMBW 中臭氧的利用率。本文有助于臭氧微纳米气泡水在复杂水质地下水修复中的应用。

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