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Degradation of Ozone-Refractory Organic Phosphates in Wastewater by Ozone and Ozone/Hydrogen Peroxide (Peroxone): The Role of Ozone Consumption by Dissolved Organic Matter

机译:臭氧和臭氧/过氧化氢(Peroxone)对废水中难降解的有机磷酸盐的降解:溶解性有机物消耗臭氧的作用

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摘要

Ozonation is very effective in eliminating micropollutants that react fast with ozone (k > 10~3 M~(-1)M~(-1)s~(-1)), but there are also ozone-refractory(k< 10 M~(-1)s~(-1)) micropollutants such as X-ray contrast media, organic phosphates, and others. Yet, they are degraded upon ozonation to some extent and this is due to 'OH radicals generated in the reaction of ozone with organic matter in wastewater (DOM, determined as DOC). The elimination of tri-n-butyl phosphate (TnBP) and tris-2-chloroisopropyl phosphate (TCPP), added to wastewater in trace amounts, was studied as a function of the ozone dose and found to follow first-order kinetics. TnBP and TCPP concentrations are halved at ozone to DOC ratios of -0.25 and ~1.0, respectively. The ·OH rate constant of TCPP was estimated at (7 ± 2) x 10~8 M~(-1) s~(-1) by pulse radiohlysis. Addition of 1 mg H_2O_2/L for increasing the ·OH yield had very little effect This is due to the low rate of reaction of H_2O_2 with ozone at wastewater conditions (pH 8) that competes unfavorably with the reaction of ozone with wastewater DOC. Simulations based on the reported (Nothe et al., ES&T 2009,43, 5990-5995) ·OH yield |13%) and ·OH scavenger capacity ofwastewater(3.2 x 10~4(mgC/ L)~(-1)s~(-1)) confirm the experimental data. Based on a typically applied molar ratio of ozone and H_2O_2 of 2, the contribution of H_2O_2 addition on the 'OH yield is shown to become important only at high ozone doses.
机译:臭氧化对于消除与臭氧快速反应的微污染物非常有效(k> 10〜3 M〜(-1)M〜(-1)s〜(-1)),但也有难降解的臭氧(k <10 M 〜(-1)s〜(-1))微污染物,例如X射线造影剂,有机磷酸盐等。但是,它们在臭氧化后会在一定程度上降解,这是由于臭氧与废水中的有机物(DOM,确定为DOC)反应生成的'OH自由基。根据臭氧剂量的函数研究了消除痕量添加到废水中的磷酸三正丁酯(TnBP)和磷酸三-2-氯异丙基酯(TCPP)的方法,发现其遵循一级动力学。在臭氧与DOC的比率分别为-0.25和〜1.0时,TnBP和TCPP浓度减半。 TCPP的·OH速率常数通过脉冲放射水解估计为(7±2)x 10〜8 M〜(-1)s〜(-1)。添加1 mg H_2O_2 / L来提高·OH收率几乎没有效果,这是由于在废水条件(pH 8)下H_2O_2与臭氧的反应速率低,不利于臭氧与废水DOC的反应。根据已报道的数据进行模拟(Nothe等人,ES&T 2009,43,5990-5995)·OH收率| 13%)和·OH清除剂容量(3.2 x 10〜4(mgC / L)〜(-1)s 〜(-1))确认实验数据。基于典型的臭氧与H_2O_2的摩尔比为2,仅在高臭氧剂量下,H_2O_2添加量对'OH收率的贡献就显示为重要。

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  • 来源
    《Environmental Science & Technology》 |2010年第21期|p.8248-8253|共6页
  • 作者单位

    Instrumental Analytical Chemistry, University Duisburg-Essen, Universitaetsstr. 5, 45141 Essen, Germany,Departamento de Ingenieria Qulmica y Qutmica-Flsica, Universidad de Extremadura, Avenida de Elvas S/N, 06071 Badajoz Spain;

    rnInstrumental Analytical Chemistry, University Duisburg-Essen, Universitaetsstr. 5, 45141 Essen, Germany;

    rnLeibniz-Institut fuer Oberflaechenmodifizierung (IOM),Permoserstrasse 15, 04303 Leipzig Germany;

    rnInstrumental Analytical Chemistry, University Duisburg-Essen, Universitaetsstr. 5, 45141 Essen, Germany,Max-Planck-lnstitut fur Bioanoganbche Chemie, Stiftstrasse 34-36, 45413 Muelheim an der Ruhr, Germany ,Universita't Dortmund, Fachbereich Bio- und Ingenieurwesen,Lehrstuhl Umwelttechnik, Emil-Figgestrasse 70,44227 Dortmund, Germany;

    rnInstrumental Analytical Chemistry, University Duisburg-Essen, Universitaetsstr. 5, 45141 Essen, Germany;

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