CIEPQPF - Chemical Engineering Processes and Forest Products Research Center, Department of Chemical Engineering, Faculty of Sciences and Technology, University of Coimbra, Rua Sílvio Lima, 3030-790, Coimbra, Portugal.
CNC - Center for Neuroscience and Cell Biology and Department of Physics, Faculty of Sciences and Technology, University of Coimbra, Rua Larga, 3004-516, Coimbra, Portugal.
Environ Sci Pollut Res Int. 2018 Mar;25(8):7346-7357. doi: 10.1007/s11356-017-1025-8. Epub 2017 Dec 23.
Parabens are widely used as antimicrobial and preservatives in pharmaceutical and personal care products and are continuously reaching the water streams. Conventional wastewater treatments are proven inefficient on the removal of this kind of contaminants from wastewater. Therefore, catalytic ozonation appears as a suitable option, due to the oxidant power of ozone and its high capacity of hydroxyl radical generation in the presence of a suitable catalyst. The main drawback of catalytic ozonation is related with the choice of stable and active catalysts at low cost. On this way, two volcanic rocks were tested to enhance the removal of a mixture of parabens by ozonation, improving their degradation. Indeed, catalytic ozonation with volcanic rock allowed total paraben degradation using a transferred ozone dose (TOD) of 55 mg/L which corresponds to a reduction of about threefold the amount of TOD comparatively with single ozonation (170 mg/L of TOD). Due to the presence of semiconductors on volcanic rock composition, the effect of UVA irradiation on paraben degradation was analyzed. The neutral and basic conditions enhanced catalytic ozonation comparatively to acid conditions. Higher pH values allowed a total methylparaben degradation with 35 mg O/L, whereas for low pH values, 55 mg O/L was required. The use of a radical scavenger proven that hydroxyl radicals are the main responsible for paraben degradation with catalytic ozonation. This was confirmed through the analysis of the by-products, where 4-hydroxybenzoic acid, 3,4-dihydroxybenzoic acid (3,4-diHBA), 2,4-dihydroxybenzoic acid, and hydroquinone were quantified.
对羟基苯甲酸酯被广泛用作医药和个人护理产品中的抗菌和防腐剂,并且不断进入水流中。传统的废水处理方法已被证明无法有效去除废水中的此类污染物。因此,催化臭氧化作为一种合适的选择,由于臭氧的氧化剂能力及其在合适催化剂存在下生成高浓度羟基自由基的能力。催化臭氧化的主要缺点与选择稳定且廉价的催化剂有关。在这种情况下,测试了两种火山岩以增强臭氧化去除对羟基苯甲酸酯混合物的效果,从而提高其降解能力。事实上,使用火山岩进行催化臭氧化可在 55 mg/L 的转移臭氧剂量(TOD)下实现对羟基苯甲酸酯的完全降解,与单独臭氧化(TOD 为 170 mg/L)相比,TOD 的用量减少了约三倍。由于火山岩组成中存在半导体,因此分析了 UVA 辐射对对羟基苯甲酸酯降解的影响。中性和碱性条件比酸性条件更能增强催化臭氧化作用。较高的 pH 值允许 35 mg O/L 完全降解甲基对羟基苯甲酸酯,而对于低 pH 值,需要 55 mg O/L。自由基清除剂的使用证明了羟基自由基是催化臭氧化降解对羟基苯甲酸酯的主要原因。这通过对副产物的分析得到了证实,其中定量分析了 4-羟基苯甲酸、3,4-二羟基苯甲酸(3,4-二 HBA)、2,4-二羟基苯甲酸和对苯二酚。