Catalytic oxidation effect of MnSO4 on As(III) by air in alkaline solution

The catalytic oxidation effect of MnSO₄ on As(III) by air in an alkaline solution was investigated. According to the X-ray diffraction (XRD), scanning electron microscope-energy dispersive spectrometer (SEM-EDS) and X-ray photoelectron spectroscopy (XPS) analysis results of the product, it was shown that the introduction of MnSO₄ in the form of solution would generate Na_0.55Mn₂O₄·1.5H₂O with strong catalytic oxidation ability in the aerobic alkaline solution, whereas the catalytic effect of the other product MnOOH is not satisfactory. Under the optimal reaction conditions of temperature 90°C, As/Mn molar ratio 12.74:1, air flow rate 1.0 L/min, and stirring speed 300 r/min, As(III) can be completely oxidized after 2 hr reaction. The excellent catalytic oxidation ability of MnSO₄ on As(III) was mainly attributed to the indirect oxidation of As(III) by the product Na_0.55Mn₂O₄·1.5H₂O. This study shows a convenient and efficient process for the oxidation of As(III) in alkali solutions, which has potential application value for the pre-oxidation of arsenic-containing solution or the detoxification of As(III).     

Treatment of 2-phenylamino-3-methyl-6-di-n-butylaminofluoran production effluent by combination of biological treatments and Fenton＇s oxidation

High strength refractory organic stream is produced during the production of 2-phenylamino-3-methyl-6-di-n-butylaminofluoran （One Dye Black 2, abbr. ODB 2）, a novel heat-sensitive material with a promising market. In this study, a combination of acidificationprecipitation, primary biological treatment, Fenton＇s oxidation and another biological treatment was successfully used for the removal of COD from 18000-25000 mg/L to below 200 mg/L from the ODB 2 production wastewater in a pilot experiment. A COD removal of 70%-80% was achieved by acidification-precipitation under a pH of 2.5-3.0. The first step biodegradafion permitted an average COD removal of 70% under an hydraulic residence time （HRT） of 30 h. By batch tests, the optimum conditions of Fenton＇s oxidation were acquired as： Fe^2＋ dose 6.0 mmol/L; H2O2 dose 3000 mg/L; and reaction time 6 h. The second step biological treatment could ensure an effluent COD below 200 mg/L under an HRT of 10 h following the Fenton＇s treatment.     

皮革和毛皮加工废水处理技术

采用混凝沉淀-酸化水解-悬挂链曝气-生物接触氧化组合工艺处理皮革和毛皮加工生产废水。实验结果表明;进水COD为2400mg/L,处理后出水COD≤100mg/L,去除率≥95.8%。各项水质指标均稳定地达到了GB8978-96污水综合排放一级标准。     

Promotional effect of cobalt doping on catalytic performance of cryptomelane-type manganese oxide in toluene oxidation

The cryptomelane-type manganese oxide (OMS-2)-supported Co (xCo/OMS-2; x = 5, 10, and 15 wt.%) catalysts were prepared via a pre-incorporation route. The as-prepared materials were used as catalysts for catalytic oxidation of toluene (2000 ppmV). Physical and chemical properties of the catalysts were measured using the X-ray diffraction (XRD), Fourier transform infrared spectroscopic (FT-IR), scanning electron microscopic (SEM), X-ray photoelectron spectroscopy (XPS), and hydrogen temperature-programmed reduction (H₂-TPR) techniques. Among all of the catalysts, 10Co/OMS-2 performed the best, with the T_90%, specific reaction rate at 245°C, and turnover frequency at 245°C (TOF_Co) being 245°C, 1.23 × 10⁻³ mol_toluene/(g_cat·sec), and 11.58 × 10⁻³ sec⁻¹ for toluene oxidation at a space velocity of 60,000 mL/(g·hr), respectively. The excellent catalytic performance of 10Co/OMS-2 were due to more oxygen vacancies, enhanced redox ability and oxygen mobility, and strong synergistic effect between Co species and OMS-2 support. Moreover, in the presence of poisoning gases CO₂, SO₂ or NH₃, the activity of 10Co/OMS-2 decreased for the carbonate, sulfate and ammonia species covered the active sites and oxygen vacancies, respectively. After the activation treatment, the catalytic activity was partly recovered. The good low-temperature reducibility of 10Co/OMS-2 could also facilitate the redox process accompanied by the consecutive electron transfer between the adsorbed O₂ and the cobalt or manganese ions. In the oxidation process of toluene, the benzoic and aldehydic intermediates were first generated, which were further oxidized to the benzoate intermediate that were eventually converted into H₂O and CO₂.     

接触氧化-电解工艺处理印染废水

主要介绍了采用生物接触氧化 电解工艺处理印染废水的设计及运行情况。处理系统运行结果表明 :当进水CODCr、BOD5和色度分别为 764 5mg L、2 63 7mg L和 42 0倍时 ,系统出水CODCr、BOD5和色度分别为 160 5mg L、48 9mg L和 12倍 ,去除率分别为 79%、81 5 %和 97 1%。该工艺运行稳定 ,操作控制方便     

全程自养脱氮工艺的研究

以悬浮填料床作为全程自养脱氮反应器，用不含有机碳的合成氨氮废水进行反应器的启动。系统的氨氮和总氮去除率分别达80％和60％左右。通过批式实验对全程自脱氮做进一步的研究。结果表明，通过控制反应器中DO的浓度，可以控制氨氧化和反硝化的比率；当DO为0.8mg/L时，氨氮几乎完全转化为氮气，氨氧化和反硝化在此时达到了动态平衡；在低DO情况下，氨氮和亚硝氮同时存在，氨氮和总氮的转化率都大幅度的提高，说明氨氮可以亚硝氮为电子受体，在无外加有机碳源的情况下进行反硝化。     

氧化铝载体下二氧化氯催化氧化处理印染废水

研究了二氧化氯化学氧化体系和二氧化氯催化氧化体系。实验结果表明:单用二氧化氯化学氧化处理COD为2700mg/L的活性艳红染料配制废水时,最佳反应pH值为10,氧化剂经济用量为800mgClO2/L废水,反应时间为30min,COD去除率可达63%左右,氧化指数(COD削减量∶ClO2投加量)=2.18。当二氧化氯与自制催化剂所组成的催化氧化体系用于对活性艳红染料配制废水的处理时,最佳反应pH值为10左右,氧化剂经济用量为1000mgClO2/L废水,反应时间为90min,COD去除率可达83.4%,氧化指数=2.25。结果表明,二氧化氯催化氧化法是一种新型高效的处理难降解废水的技术,有着广阔的应用前景。     

氧化塘处理高速公路服务区污水技术初探

提出并试验研究了氧化塘处理高速公路服务区污水的方法，所得结果可用于高等级公路服务区及管理区污水处理。     

长炼第二污水处理场氧化沟工艺运行小结

臭伯尔氧化沟池容大，停留时间长，运行稳定，对氧化沟污泥培养及开工运行进行了小结，并结合运行过程中的几个问题进行了分析和探讨。     

太阳热反射涂料的研制

根据涂料反射太阳热的原理,以丙烯酸树脂为基料,以金红石型钛白粉、云母粉及空心玻璃微珠为原料,制备了隔热性能和耐候性能均良好的太阳热反射隔热涂料,并研究了颜料、填料种类、粒径、涂层厚度对涂料隔热性能的影响。