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生物膜定殖的黑色微塑料与原始黑色微塑料对加速水环境中四环素光降解的作用:潜在机制分析

Biofilm-Colonized versus Virgin Black Microplastics to Accelerate the Photodegradation of Tetracycline in Aquatic Environments: Analysis of Underneath Mechanisms.

作者信息

Ding Rui, Ouyang Zhuozhi, Zhang Xue, Dong Yankai, Guo Xuetao, Zhu Lingyan

机构信息

College of Natural Resources and Environment, Northwest A&F University, Yangling, Shaanxi 712100, China.

Key Laboratory of Plant Nutrition and the Agro-Environment in Northwest China, Ministry of Agriculture, Yangling, Shaanxi 712100, China.

出版信息

Environ Sci Technol. 2023 Apr 11;57(14):5714-5725. doi: 10.1021/acs.est.3c00019. Epub 2023 Mar 30.

DOI:10.1021/acs.est.3c00019
PMID:36995247
Abstract

Tire wear particles (TWPs) exposed to the aquatic environment are rapidly colonized by microorganisms and provide unique substrates for biofilm formation, which potentially serve as vectors for tetracycline (TC) to influence their behaviors and potential risks. To date, the photodegradation capacity of TWPs on contaminants due to biofilm formation has not been quantified. To accomplish this, we examined the ability of virgin TWPs (V-TWPs) and biofilm-developed TWPs (Bio-TWPs) to photodegrade TC when exposed to simulated sunlight irradiation. V-TWPs and Bio-TWPs accelerated the photodegradation of TC, with rates () of 0.0232 ± 0.0014 and 0.0152 ± 0.0010 h, respectively ( increased by 2.5-3.7 times compared to that for only TC solution). An important factor of increased TC photodegradation behavior was identified and linked to the changed reactive oxygen species (ROS) of different TWPs. The V-TWPs were exposed to light for 48 h, resulting in more ROS for attacking TC, with hydroxyl radicals (OH) and superoxide anions (O) playing a dominant role in TC photodegradation measured using scavenger/probe chemicals. This was primarily due to the greater photosensitization effects and higher electron-transfer capacity of V-TWPs in comparison to Bio-TWPs. In addition, this study first sheds light on the unique effect and intrinsic mechanism of the crucial role of Bio-TWPs in TC photodegradation, enhancing our holistic understanding of the environmental behavior of TWPs and the associated contaminants.

摘要

暴露于水生环境中的轮胎磨损颗粒(TWPs)会迅速被微生物定殖,并为生物膜形成提供独特的基质,这可能作为四环素(TC)的载体,影响其行为和潜在风险。迄今为止,由于生物膜形成,TWPs对污染物的光降解能力尚未得到量化。为了实现这一目标,我们研究了原始TWPs(V-TWPs)和生物膜形成的TWPs(Bio-TWPs)在模拟阳光照射下光降解TC的能力。V-TWPs和Bio-TWPs加速了TC的光降解,速率分别为0.0232±0.0014和0.0152±0.0010 h(与仅TC溶液相比,增加了2.5-3.7倍)。确定了TC光降解行为增加的一个重要因素,并将其与不同TWPs中活性氧(ROS)的变化联系起来。V-TWPs光照48小时,产生更多用于攻击TC的ROS,使用清除剂/探针化学物质测量,羟基自由基(OH)和超氧阴离子(O)在TC光降解中起主导作用。这主要是由于与Bio-TWPs相比,V-TWPs具有更大的光敏化效应和更高的电子转移能力。此外,本研究首次揭示了Bio-TWPs在TC光降解中关键作用的独特效应和内在机制,增强了我们对TWPs及其相关污染物环境行为的整体理解。

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