Role of oxygen-containing functional surface groups of activated carbons on the elimination of 2-hydroxybenzothiazole from waters in A hybrid heterogeneous ozonation system

H. Valdés, M. Sánchez-Polo, C. Zaror
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引用次数: 1

Abstract

Abstract The influence of the variation of chemical surface properties of activated carbons on the sorption capacity of activated carbons used in hybrid heterogeneous ozonation systems is still under discussion. In this study, the effect of long exposure of activated carbon to ozone and its implication on the removal of emerging organic pollutants from waters is evaluated. A commercial activated carbon (Filtrasorb-400) is used here as a raw material. It is chemically modified by continuous ozone exposure. 2-hydroxybenzothiazole (OHBT) is chosen as a target organic contaminant, representative of emerging micro-pollutants. Results obtained here reveal that extensive exposition of activated carbon surface to ozone weakens adsorbate–adsorbent interactions. Highly exposed activated carbon to ozone increases the concentration of oxygen-containing acidic functional groups, leading to a higher concentration of surface electron-withdrawing groups such as carboxylic acid anhydrides and carboxylic acids and reducing the sorption capacity toward OHBT in the hybrid heterogeneous ozonation system. At pH conditions around the point of zero charge (pHPZC), such sorption reduction could be due to a decrease on dispersive interactions among π-electrons of aromatic ring of OHBT molecules and the π-electron system of carbon graphene layers, coming after extensive exposition of activated carbon surface to ozone. However, at pH >pHPZC low removal of OHBT is obtained because of the appearing of repulsive electrostatic interactions among the ionised form of OHBT molecules and the de-protonated form of oxygen-containing functional groups that appears after long contact with ozone. In addition, a new concept to predict activated carbon performances in a hybrid heterogeneous ozonation process is proposed.
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杂化非均相臭氧化体系中活性炭含氧官能团对水中2-羟基苯并噻唑的去除作用
摘要活性炭表面化学性质的变化对杂化非均相臭氧化系统中活性炭吸附性能的影响仍在研究中。在本研究中,评估了活性炭长期暴露于臭氧的影响及其对去除水中新出现的有机污染物的影响。这里使用一种商用活性炭(Filtrasorb-400)作为原料。它通过持续接触臭氧而发生化学修饰。选择2-羟基苯并噻唑(OHBT)作为目标有机污染物,是新兴微污染物的代表。结果表明,大量暴露于臭氧的活性炭表面会削弱吸附剂-吸附剂的相互作用。高暴露于臭氧的活性炭增加了含氧酸性官能团的浓度,导致羧酸酸酐和羧酸等表面吸电子基团浓度升高,降低了杂化非均相臭氧化体系对OHBT的吸附能力。在零电荷点(pHPZC)附近的pH条件下,这种吸附减少可能是由于活性炭表面大量暴露于臭氧后,OHBT分子芳环π-电子与碳石墨烯层π-电子系统之间的色散相互作用减少。然而,在pH >pHPZC时,OHBT的去除率较低,因为OHBT分子的离子化形式和与臭氧长时间接触后出现的含氧官能团的去质子化形式之间出现了排斥静电相互作用。此外,还提出了一种预测混合非均相臭氧化过程中活性炭性能的新概念。
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来源期刊
CiteScore
0.88
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0.00%
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0
审稿时长
1 months
期刊介绍: The Journal of advanced oxidation technologies (AOTs) has been providing an international forum that accepts papers describing basic research and practical applications of these technologies. The Journal has been publishing articles in the form of critical reviews and research papers focused on the science and engineering of AOTs for water, air and soil treatment. Due to the enormous progress in the applications of various chemical and bio-oxidation and reduction processes, the scope of the Journal is now expanded to include submission in these areas so that high quality submission from industry would also be considered for publication. Specifically, the Journal is soliciting submission in the following areas (alphabetical order): -Advanced Oxidation Nanotechnologies -Bio-Oxidation and Reduction Processes -Catalytic Oxidation -Chemical Oxidation and Reduction Processes -Electrochemical Oxidation -Electrohydraulic Discharge, Cavitation & Sonolysis -Electron Beam & Gamma Irradiation -New Photocatalytic Materials and processes -Non-Thermal Plasma -Ozone-based AOTs -Photochemical Degradation Processes -Sub- and Supercritical Water Oxidation -TiO2 Photocatalytic Redox Processes -UV- and Solar Light-based AOTs -Water-Energy (and Food) Nexus of AOTs
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