Exploring electrochemical mechanisms for clindamycin degradation targeted at the efficient treatment of contaminated water.

Chemosphere Pub Date : 2024-10-01 Epub Date: 2024-10-18 DOI:10.1016/j.chemosphere.2024.143563
Julia Faria, William Santacruz, Rodrigo De Mello, Maria Valnice Boldrin, Artur J Motheo
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Abstract

Numerous studies reveal pollutants like clindamycin (CLD) in the environment, posing environmental and health risks. Conventional water treatment methods are ineffective at removing these contaminants, typically found in low concentrations. An innovative treatment approach is introduced through pre-concentration via adsorption, which is highly efficient, energy-saving, and reusable. The innovation uses solvents like methanol or ethanol to desorb pollutants, creating concentrated CLD solutions for more effective electrochemical degradation than conventional methods. Thus, this study explores, for the first time, the behavior of CLD electro-oxidation in different media-water, methanol, and ethanol-using a Dimensionally Stable Anode (DSA®-Cl₂). The study reveals distinct degradation mechanisms and offers new insights into solvent-assisted electrochemical treatments. After 30 min of electrolysis, all the current densities evaluated promoted significant degradation, ranging from 90 to 92%. The energy consumption was 2.9 Wh m⁻³ per percentage point at current densities of 2 and 3.5 mA cm⁻2. This demonstrates that using higher current densities over shorter electrolysis times is feasible, achieving removal rates of approximately 90%.The performance of chloride-based electrolytes was superior to that of sulfate-based electrolytes due to the ability of DSA®-Cl2 electrodes to generate reactive chlorine species more efficiently. A higher concentration of supporting electrolytes initially improved CLD removal, but no significant changes were observed after 1 h. Neutral pH conditions optimized CLD degradation, achieving up to 91% removal. Higher pollutant concentrations were associated with lower kinetic constants and decreased removal percentages. Methanol and ethanol enhanced removal rates to 98.3% and 92.3%, respectively, by generating oxidizing species such as methoxy, hydroxymethyl, and ethoxy radicals. The degradation by-products differed across the three media, with each solvent exhibiting distinct oxidation mechanisms. These findings highlight the potential of using methanol or ethanol as an electrolytic medium with efficiency comparable to water.

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探索克林霉素降解的电化学机制,以高效处理受污染的水。
大量研究显示,环境中存在克林霉素(CLD)等污染物,对环境和健康造成危害。传统的水处理方法无法有效去除这些通常浓度较低的污染物。通过高效、节能和可重复使用的吸附预浓缩技术,引入了一种创新的处理方法。这种创新方法使用甲醇或乙醇等溶剂来解吸污染物,形成浓缩的 CLD 溶液,从而实现比传统方法更有效的电化学降解。因此,本研究首次利用尺寸稳定阳极(DSA®-Cl₂)探讨了 CLD 在不同介质(水、甲醇和乙醇)中的电氧化行为。这项研究揭示了不同的降解机制,并为溶剂辅助电化学处理提供了新的见解。电解 30 分钟后,所有评估的电流密度都促进了显著降解,降解率从 90% 到 92% 不等。在电流密度为 2 和 3.5 mA cm-2 时,每个百分点的能耗为 2.9 Wh m-³。这表明,在较短的电解时间内使用较高的电流密度是可行的,可实现约 90% 的去除率。由于 DSA®-Cl2 电极能够更有效地生成活性氯物种,因此氯基电解质的性能优于硫酸基电解质。中性 pH 值条件优化了 CLD 降解,去除率高达 91%。污染物浓度越高,动力学常数越低,去除率也越低。甲醇和乙醇通过产生甲氧基、羟甲基和乙氧基自由基等氧化物种,将去除率分别提高到 98.3% 和 92.3%。三种介质的降解副产物各不相同,每种溶剂都表现出不同的氧化机制。这些发现凸显了使用甲醇或乙醇作为电解介质的潜力,其效率可与水媲美。
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