Photoelectrocatalytic degradation of organophosphate esters using tio2 electrodes produced from 3d-printed ti substrates.

IF 5.8 3区 环境科学与生态学 0 ENVIRONMENTAL SCIENCES
Gustavo C Tedesco, Belisa L Soares, Enelton Fagnani, Joyce Cristale, Cynthia A Joll, David J Henry
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引用次数: 0

Abstract

3D printed electrode substrates with novel geometries may significantly improve the efficacy of photoelectrocatalysis for degradation of recalcitrant pollutants such as organophosphate flame retardants (OPFRs). However, the 3D printed substrates often have an irregular topology that can lead to a less uniform arrangement of nanotubes following anodisation. This study investigated the effect of polishing 3D-printed Ti substrates prior to anodisation to form TiO2 nanotube array electrodes, and their subsequent applicability for photoelectrocatalytic treatment of OPFRs in water matrices. Polished and non-polished electrodes exhibited differences in morphology in terms of average roughness, (0.38 and 3.10 µm, respectively), leading to more uniform TiO2 nanotubes of the former. Water contact angle measurements revealed the non-polished electrode was super-hydrophilic and the polished electrode hydrophilic (water contact angles of 6.4˚ and 16.1˚, respectively). Despite these differences, the polished and non-polished electrodes exhibited very similar electrochemical responses. In fact, the purity and electrical conductivity of water matrices affected the photoelectrocatalytic performance more than the electrode morphology. The purified water (PW) matrix facilitated the highest degradation/removal of OPFRs, compared to tap water matrices. In particular, individual OPFR degradation levels in PW were 74% ± 9, 37% ± 10, 33% ± 9, 31% ± 11 and 3% ± 5 for triphenyl phosphate, tris(butyl) phosphate, tris(isobutyl) phosphate, tris(2-butoxyethyl) phosphate and tris(2-chloroisopropyl) phosphate, respectively. The removal of OPFRs was relative to their reactivity to hydroxyl radicals, which was higher for the aryl then alkyl straight-chain and then chlorinated compounds. This study reveals that polishing of electrode substrates is not required for the preparation of effective photoelectrocatalytic reactors to treat recalcitrant pollutants (e.g. OPFRs), Importantly, future development of novel high-profile 3D printed electrode will not be hindered by the requirement to polish the substrates prior to anodisation.

使用由 3d 印刷 ti 基底制成的 tio2 电极光电催化降解有机磷酸酯。
具有新颖几何形状的三维打印电极基底可显著提高光电催化降解有机磷阻燃剂(OPFR)等难降解污染物的功效。然而,3D 打印基底通常具有不规则的拓扑结构,这可能导致阳极氧化后纳米管的排列不够均匀。本研究调查了在阳极氧化形成 TiO2 纳米管阵列电极之前对 3D 打印钛基底进行抛光的效果,以及这些电极随后在光电催化处理水基质中的 OPFR 方面的适用性。抛光和非抛光电极在平均粗糙度(分别为 0.38 和 3.10 µm)方面表现出不同的形态,前者的二氧化钛纳米管更为均匀。水接触角测量显示,未抛光电极具有超亲水性,而抛光电极具有亲水性(水接触角分别为 6.4˚ 和 16.1˚)。尽管存在这些差异,但抛光和非抛光电极表现出非常相似的电化学反应。事实上,水基质的纯度和导电性对光电催化性能的影响大于电极形态。与自来水基质相比,纯净水(PW)基质对 OPFR 的降解/去除率最高。其中,磷酸三苯酯、磷酸三(丁基)酯、磷酸三(异丁基)酯、磷酸三(2-丁氧基乙基)酯和磷酸三(2-氯异丙基)酯在 PW 中的单个 OPFR 降解水平分别为 74% ± 9、37% ± 10、33% ± 9、31% ± 11 和 3% ± 5。OPFR 的去除率与它们对羟基自由基的反应活性有关,先是芳基化合物,然后是直链烷基化合物,最后是氯化化合物。这项研究表明,在制备有效的光电催化反应器以处理难降解污染物(如 OPFRs)时,无需对电极基底进行抛光。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.70
自引率
17.20%
发文量
6549
审稿时长
3.8 months
期刊介绍: Environmental Science and Pollution Research (ESPR) serves the international community in all areas of Environmental Science and related subjects with emphasis on chemical compounds. This includes: - Terrestrial Biology and Ecology - Aquatic Biology and Ecology - Atmospheric Chemistry - Environmental Microbiology/Biobased Energy Sources - Phytoremediation and Ecosystem Restoration - Environmental Analyses and Monitoring - Assessment of Risks and Interactions of Pollutants in the Environment - Conservation Biology and Sustainable Agriculture - Impact of Chemicals/Pollutants on Human and Animal Health It reports from a broad interdisciplinary outlook.
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