Ferrioxalate-mediated photodegradation and mineralization of 4-Chlorophenol

INTENTION, GOAL, SCOPE, BACKGROUND: Advanced oxidation processes are powerful methods which are capable of transforming refractory, nonbiodegradable and/or toxic organic compounds into harmless end products such as carbon dioxide and water. However, one commen problem of all advanced oxidation processes is the high demand of electrical energy for ultraviolet lamps, which causes high operational costs. Minimization of the required irradiation time, and therefore the energy consumption, by optimization of other reaction conditions such as catalyst-oxidant type and concentration, pH, temperature, pollutant/oxidant ratio etc., therefore continues to gain importance. OBJECTIVE: The main objective of this study was the minimization of the required irradiation time through optimization of the use of a newly patented catalyst, ferrioxalate, and also to compare the performance of this catalyst with the performance of other AOPs. METHODS: Oxidation of 4-chlorophenol by photo-Fenton process using potassium ferrioxalate as a mediator was studied in a lab scale photoreactor. The influence of parameters such as hydrogen peroxide and ferrioxalate concentrations, initial pH, power-output, oxalate/iron ratio and different iron sources was evaluated. An upflow photoreactor equipped with a 1000 Watt high-pressure mercury vapour lamp and operating in a recirculation mode was used during photodegradation experiments. The extent of the reduction of 4-chlorophenol, Total Organic Carbon and Chemical Oxygen Demand was used to evaluate the photodegradation reaction. RESULTS AND DISCUSSION: The optimum pH range observed was found to be 2.7-3. The efficiency of 4-chlorophenol oxidation increased with increasing concentrations of hydrogen peroxide and ferrioxalate, reaching a plateau after the addition of 10 and 0.072 mM of those reagents, respectively. Using an Oxalate/iron ratio of 12 was 18% less efficient than using a ratio of 3:1. The efficiency increased with increasing radiation power. However, this increase was not linear. The UV/ferrioxalate/H2O2 process, by which complete mineralization of 100 mg l(-1) 4-chlorophenol was achieved in 20 min of total reaction time, was the most efficient process among the alternatives applied. CONCLUSIONS: The use of ferrioxalate as the catalyst was found to be more efficient than the use of Fe(II) and Fe(III) iron species. It was possible to completely mineralize 4-chlorophenol. RECOMMENDATION AND OUTLOOK: The results of this study demonstrate that the ferrioxalate-mediated degradation of 4-chlorophenol requires less irradiation times than other advanced oxidation processes. There are mainly 19 phenol isomers and other toxic and nonbiodegradable organic compounds. We recommend that similar studies should be performed on many such compounds in order to attain a clear understanding of the performance of this catalyst. Because of its light sensitivity, this catalyst should be used immediately after its preparation. The use of low pressure mercury vapour lamps in this process should also be considered, since low power outputs may be enough for the process.     

非均相Fenton反应技术研究进展

Fenton氧化法是较为常用的一种高级氧化技术。非均相Fenton反应适用的pH值范围较宽，能避免均相Fenton反应产生铁泥沉淀的缺点，成为近年来Fenton反应的重要研究方向。本文对非均相Fenton氧化技术的研究现状及发展动态进行较为详尽的评述。     

气溶胶中多环芳烃光降解的初步研究

本文以大容量空气脱悬浮微粒采样器采集了大气中的气溶胶样品,以石英滤膜为载体,研究了气溶胶中的多环芳烃在紫外光照下的光降解规律。     

水体表面微层中酞酸酯的光降解研究

研究了水体表面微层中酞酸酯化合物光降解的动力学,指出光催化降解符合一级动力学过程,实验证明：催化剂ＴｉＯ２为２ｇ．ｌ＾－１,ｐＨ为６,并有Ｈ２Ｏ２存在时,是ＤＢＰ,ＤＥＨＰ光降解的最佳条件,溶解氧增加有利于光降解,实际表面微层水样的光催化降解速率比模拟水样快。     

几种草酸铁络合物体系光降解酞酸酯比较研究

文章在比较研究了几种草酸铁络合物体系对两种酞酸酯DBP和DEHP的光催化降解情况.结果表明:草酸铁络合物和草酸铁络合物/H2O2体系在遮光条件下对DBP和DEHP没有降解作用.在中性pH值条件下,DBP和DEHP在几种反应体系中的降解速率依次为:UV/草酸铁络合物/H2O2＞UV/H2O2＞UV/草酸铁络合物＞UV＞太阳光/草酸铁络合物.UV与草酸铁络合物对DBP和DEHP光降解的协同作用不强,增强因子f分别为1.20和1.07.UV、草酸铁络合物与H2O2的对DBP光降解协同作用也不明显,增强因子f=1.18. UV与H2O2对DBP光降解存在明显的协同作用,增强因子f=8.78.     

藻引发水中染料的光降解

通过分光光度法研究了鱼腥藻和小球藻对两种不同结构染料的光降解 ,以及降解效果的影响因素 ,为利用可再生的水体生物资源来治理染料废水提供了新的思路     

2,4,4'-三溴联苯醚的光降解研究

以固相微萃取(SPME)结合气相色谱(GC)、气相色谱-质谱联用(GC/MS)技术作为分析检测手段,研究光源、有机溶剂、无机盐与腐殖酸对BDE-28光降解的影响,实验结果表明,光源是影响其降解的主要因素,其次,丙酮、铜离子和腐殖酸对其降解的影响较显著.光源对BDE-28光降解速率的影响为300 W汞灯500 W金卤灯100 W汞灯500 W氙灯;有机溶剂对BDE-28降解速率的影响为甲醇/水(1∶1)甲醇己烷甲苯乙腈丙酮;无机离子的影响各有差别:K+、Na+、SO2-4、NO-3、Cl-对BDE-28降解影响不明显,而Fe3+、NH+4促进BDE-28的降解,Fe2+、Cu2+、Br-抑制BDE-28的降解;腐殖酸抑制BDE-28的降解.     

纳米TiO_2光催化降解水溶性染料溶液的研究

研究了纳米ＴｉＯ２光催化剂对活性黄Ｘ６Ｇ、活性红Ｘ３Ｂ、活性蓝ＸＢＲ、碱性绿、碱性紫５ＢＮ、碱性品红等６种染料溶液的光解脱色效果。结果表明，在ｐＨ２的酸性溶液中，对浓度为６０ｍｇ／Ｌ的６种染料溶液的脱色率均超过９３．３％；即使对浓度达２００ｍｇ／Ｌ的活性蓝溶液，其脱色率仍可达７８．８％。染料溶液的ｐＨ值对纳米ＴｉＯ２光催化脱色效果影响较大     

Photodegradation of Benthiocarb

The photodegradation of ¹⁴C-benthiocarb in water, on a glass surface, on soil and silica gel TLC plates was studied. the study was designed to obtain some information of its dissipation and photodegradation under various laboratory conditions. Benthiocarb degrades readily when exposed to either sunlight or UV light (254 nm). However, it is degraded much faster by UV light than by sunlight. Also, benthiocarb decomposes faster in water or on a glass surface or silica gel surface than on a soil surface. the half-life of benthiocarb exposed to UV light was: 1 hr on glass surface; 1.5 hrs in water; 2 hrs on silica gel TLC plate; 20 hrs on soil TLC plate. Benthiocarb in water, and exposed to sunlight, had a half-life of approximately 3 days. the following major photodegradation products were identified: 4-chlorobenzyl alcohol; 4-chlorobenzaldehyde; 4-chlorobenzoic acid.     

高碑店湖表层水中雌激素的分布及其光降解影响因素

雌激素等内分泌干扰物在水体中普遍存在,其在再生水中的存在以及在水体中的迁移转化会产生潜在的健康和生态风险。光降解是水体中雌激素消除的主要途径之一,水体中共存的无机离子及有机质等对雌激素的光解存在不同的影响。对高碑店湖再生水体中雌激素的污染状况进行了调查,结果显示表层水中天然雌激素雌酮(E1)和人工合成雌激素17α-乙炔基雌二醇(EE2)的浓度最高。在模拟太阳光照射条件下对E1在水溶液中的降解规律及影响因素进行了研究,发现在模拟1 SUN的光密度条件下,15 min时E1降解率可达85%(C0=5μg·L-1),而氨氮对E1的光降解存在一定的抑制作用,并且抑制作用随着氨氮的升高而变大。与纯水系统相比,高碑店湖表层水基质中E1的光降解速率较低,说明整体上氨氮、HCO-3、浊度等因素对E1光降解产生的抑制作用占主导。对雌酮及其降解产物进行了红外光谱分析,结果显示1 720 cm-1对应的C=O键特征峰在光照时间为0、10和20 min样品中的强度逐渐减弱,而2 854 cm-1和2 925 cm-1对应的脂肪碳的C-H键特征峰先增强后减弱,可能是因为E1结构中的C-C=O发生了反应生成了C=C-OH,而随着反应的继续,C=C也被进一步氧化,但降解产物的结构需要进一步研究推断。随着E1的光降解,E1水溶液的内分泌干扰活性逐渐下降,氨氮虽然对E1的光降解有一定的抑制作用,但随着降解反应的进行E1水溶液的内分泌干扰活性依然呈下降趋势。