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一种去除化学需氧量分析中过氧化氢干扰的新方法。

A new method for removal of hydrogen peroxide interference in the analysis of chemical oxygen demand.

机构信息

Department of Civil, Architectural and Environmental Engineering, University of Miami, 1251 Memorial Drive, MEB 314, Coral Gables, Florida 33146, United States.

出版信息

Environ Sci Technol. 2012 Feb 21;46(4):2291-8. doi: 10.1021/es204250k. Epub 2012 Feb 9.

Abstract

Many advanced oxidation processes involve addition of hydrogen peroxide (H(2)O(2)) with the aim of generating hydroxyl radicals to oxidize organic contaminants in water. However, chemical oxygen demand, a common measure of gross residual organic contamination, is subject to interference from residual H(2)O(2) in the treated water. A new method, involving catalytic decomposition of H(2)O(2) with addition of heat and sodium carbonate (Na(2)CO(3)), is proposed in this work to address this problem. The method is demonstrated experimentally, and modeled kinetically. Results for 5 mM H(2)O(2) in deionized (DI) water included reduction to below the COD detection limit after 60 min heating (90(◦)C) with addition of 20 g/L Na(2)CO(3) concentrated solution, whereas 900 min were required in treated municipal wastewater. An approximate second order rate constant of 11.331 M(-1)·min(-1) at Na(2)CO(3) dosage of 20 g/L was found for the tested wastewater. However, kinetic modeling indicated a two-step reaction mechanism, with formation of peroxocarbonate (CO(4)(2-)) and ultimate decomposition to H(2)O and O(2) in pure H(2)O(2) solution. A similar mechanism is apparent in wastewater at high catalyst concentrations, whereas at low Na(2)CO(3) addition rates, the catalytic effects of other constituents appear important.

摘要

许多高级氧化工艺涉及添加过氧化氢(H₂O₂)的目的是生成羟基自由基以氧化水中的有机污染物。然而,化学需氧量(COD)是衡量总残留有机污染物的常用指标,它会受到处理水中残留 H₂O₂的干扰。本工作提出了一种新的方法,涉及在添加热和碳酸钠(Na₂CO₃)的情况下催化分解 H₂O₂,以解决此问题。该方法已通过实验证明,并进行了动力学模拟。在去离子(DI)水中 5mM H₂O₂的实验结果包括,在添加 20g/L 碳酸钠浓缩溶液并加热 60 分钟(90°C)后,将其还原至低于 COD 检测限以下,而在处理后的城市废水中则需要 900 分钟。在 20g/L 的 Na₂CO₃用量下,对于测试废水,发现近似的二级速率常数为 11.331M⁻¹·min⁻¹。然而,动力学模拟表明存在两步反应机制,在纯 H₂O₂溶液中形成过碳酸盐(CO₄²⁻),并最终分解为 H₂O 和 O₂。在高催化剂浓度下,废水呈现出类似的机制,而在低 Na₂CO₃添加速率下,其他成分的催化作用似乎更为重要。

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