含铬固体废渣中Cr~(3+) 的氧化

研究了ｐＨ、温度对铬渣中Ｃｒ３＋的氧化速率的影响．结果表明，在碱性条件下，空气中的氧气具有相当强的氧化性，足以将Ｃｒ３＋氧化为Ｃｒ６＋，且随ｐＨ、温度的升高而加快．     

UNITANK+接触氧化工艺处理制皂废水

采用 U NITANK系统和生物接触氧化工艺处理主要污染物为油脂、甘油等的制皂工业废水。经过试验研究 ,工艺参数选择和运行处理效果分析 ,结果证明 ,采用该工艺处理制皂工业废水 ,三格池好氧 U NITANK系统的容积负荷为1.5 kg CODCr/m3· d时 ,COD去除率可达 80 % ,接触氧化池的 COD去除率亦在 80 %左右 ,处理效果稳定     

改良A2/O型氧化沟处理城市污水工程实例

介绍了重庆市童家溪区污水处理厂的工艺流程,及其各构筑物和主要设备的参数.该工艺采用改良A2/O型氧化沟处理城市污水,该工艺将A2/O与氧化沟相结合,具有两者的优点,且能耗省、脱N除P的特点,出水水质达到<城镇污水处理厂污染物排放标准>(GB18918-2002)中的一级标准的B标准.     

印染废水处理工艺改造的实践与探讨

根据某印染废水的特点 ,在原有传统处理工艺的基础上进行了工艺改造 ,将调节池改为水解酸化池 ,将活性污泥曝气池改为接触氧化池 ,在池内形成了合理的微生物分布 ,大大地改善了出水水质 ,使 COD、SS、硫化物、色度的去除率分别提高了 2 2 %、10 %、36 .4%、2 5 %。既满足废水排放标准 ,又节约了土建资金。     

水解-酸化-好氧工艺处理染料废水的应用

介绍了水解-酸化-好氧工艺处理染料生产废水。长期运行结果表明，当染料生产废水的COD质量浓度〈2000mg．L^-1时，在水解反应器、酸化反应器和曝气池的水力停留时间（HRD分别为7．0，7．0和6．0h的条件下，出水可以达到国家二级排放标准。水解-酸化过程提高了染料生产废水的可生化性，为后续好氧处理创造了条件。     

含氰废水的氧化处理

介绍了处理含氰废水碱氯氧化法、双氧水氧化法、臭氧氧化法等几种氧化法的基本原理，并进行了对比分析。     

氧化沟污水处理技术在炼油厂的实际应用

本文简明地阐述了氧化沟污水处理技术的工艺原理及特点，着重指出了该工艺中溶解氧实时控制的重要性，使沧州炼油厂污水处理效果有了明显提高     

Cyclohexane oxidation and carbon deposition over metal oxide catalysts

Catalytic activity of V, Mn, Ni, Cu, Zn, Mo, Zr and Ce oxides over an -alumina support was evaluated for cyclohexane oxidation under oxygen deficient conditions in order to understand the relation between carbon deposition and catalytic activity/selectivity. Carbon formation over the catalysts during the oxidation reaction was measured by means of Fourier transformed infrared spectroscopy (FTIR). Catalysts Mn/Al₂O₃ and Ce/Al₂O₃, which are selective for deep oxidation of cyclohexane, possessed relatively carbon free surfaces. The catalysts with relatively high carbon deposition (V, Ni, Cu, Zn, Mo and Zr) produced CO in addition to CO₂. Traces of formaldehyde were produced over the catalysts Mo and V.     

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.     

Experimental determination of the kinetic rate law for the oxidation of perchloroethylene by potassium permanganate

Flushing soils contaminated with trichloroethylene (TCE) and perchloroethylene (PCE) with a permanganate (MnO₄⁻) solution has been shown to reduce the solvent content of the soil. Experiments were performed to quantify the rate at which KMnO₄ oxidizes aqueous solutions of PCE over a range of concentrations. In a series of homogeneous reactors, aqueous phase PCE concentrations were monitored over time in nine experimental trials with excess oxidant concentrations ranging from 5 to 30 g/l. Analysis of the data was performed to quantify the oxidation reaction order with respect to PCE and KMnO₄ and the reaction rate constant. The reaction between PCE and KMnO₄ was determined to be first-order with respect to both PCE and KMnO₄ with an overall specific reaction rate coefficient of 2.45±0.65 M⁻¹ min⁻¹.