过氧乙酸
化学
过氧化氢
吸附
氧化剂
流出物
水溶液
弗伦德利希方程
吸附
朗缪尔
离子交换
反应速率常数
核化学
无机化学
动力学
离子
有机化学
环境工程
物理
工程类
量子力学
作者
Monika Wawrzkiewicz,Urszula Kotowska,Aneta Sokół
出处
期刊:Processes
[Multidisciplinary Digital Publishing Institute]
日期:2021-10-26
卷期号:9 (11): 1911-1911
被引量:12
摘要
Textile effluent containing azo dyes such as C.I. Acid Violet 1 (AV1) can be degraded to toxic aromatic amines in the environment. Thus, there is a legitimate need to treat such effluents before they are discharged to surface waters. Two methods were proposed to remove AV1 from aqueous solutions: adsorption and advanced oxidation processes (AOPs). The sorption capacity of the strongly basic anion exchanger Purolite A520E of the polystyrene matrix determined from the Langmuir isotherm model was found to be 835 mg/g, while that of Lewatit S5428 of the polyacrylamide matrix Freundlich model seems to be more appropriate for describing the experimental data. The pseudo-second-order kinetic model and external diffusion are the rate limiting steps of adsorption. The removal efficiency of AV1 by the anion exchangers was higher than 99% after 40 min of phase contact time. AOPs involved the usage of hydrogen peroxide and peracetic acid (PAA) as oxidizing agents, while Fe2+ and simulated sunlight were used as oxidizing activators. AV1 oxidation followed the pseudo-first-order kinetics, and the systems with the highest values of the rate constants turned out to be those in which Fe2+ was present. The efficiency of oxidation measured by the degree of decolorization in the systems with Fe2+ was higher than 99% after 10–60 min. AV1 mineralization was slower, but after 120 min of oxidation it was higher than 98% in the H2O2/Fe2+, PAA/Fe2+ and PAA/Fe2+/sunlight systems.
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