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Ozonation for the removal of bisphenol A

机译:去除双酚A的臭氧化物

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The mechanism of byproduct formation and oxidation pathway of bisphenol A (BPA) during ozonation process have been compared under acidic, neutral and alkaline conditions at an applied ozone dose of 5.3 mg.L-1 min(-1). Alkaline conditions promoted the fastest removal and the pseudo first-order reaction rate constant was calculated as 0.15 min(-1). Complete removal under alkaline conditions (after 30 minutes of reaction time) was achieved with 1.59 mg ozone per mg BPA and 52% mineralization was achieved at 6.04 mg ozone application per mg total organic carbon (after 90 minutes of reaction time). Hydroxyl radical dominated degradation pathway (pH 10) resulted with opening of ring-structured products into Heptanoic acid, methyl ester. Sixty per cent BPA removal occurred under acidic conditions where the ozone was dominant and formation of Cyclohexene-1-carboxylic acid, ethyl ester, Benzaldehyde, 4-hydroxy-3,5-dimethyl- and 2-Phenylbenzoquinone were evidenced. Despite the fact that complete removal was achieved under neutral conditions, mineralization was not remarkable and both hydroxyl radical and ozone-based degradation pattern was evidenced after the treatment.
机译:在酸性的臭氧剂量为5.3mg.L-1min(-1)的酸性,中性和碱性条件下,在臭氧处理过程中进行了副产物A(BPA)的副产物A(BPA)的机制。碱性条件促进了最快的去除率,并且伪一阶反应速率常数计算为0.15分钟(-1)。在碱性条件下完全除去(在反应时间后30分钟),通过每Mg BPA的1.59mg臭氧获得,每Mg总有机碳(反应时间90分钟后,在6.04mg臭氧施用下达到52%的矿化。羟基自由基主导的降解途径(pH10)导致环结构产物的开口进入庚酸,甲酯。在酸性条件下发生六十百分之的BPA去除,其中臭氧占优势,形成环己烯-1-羧酸,乙酯,苯甲醛,4-羟基-3,5-二甲基和2-苯基苯并醌的形成。尽管在中性条件下实现了完全去除,但矿化不是显着的,并且治疗后,羟基自由基和臭氧的降解模式都显着。

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