微曝气Fenton氧化法处理模拟双酚A废水的效果及其生物验证

研究了微曝气Fenton氧化法关键工艺参数对模拟双酚A（BPA）废水处理效果的影响,并从活性污泥性质和污染物去除率两方面,采用膜生物反应器(membrane bioreactor, MBR)对微曝气Fenton氧化法的处理效果进行了实验验证,为实现BPA废水的生物处理奠定基础。结果表明,初始pH值、反应时间、H₂O₂/COD(质量浓度比)、H₂O₂/Fe²⁺ (摩尔浓度比)、反应温度及曝气量均对预处理效果有较大影响,在最佳条件下,COD去除率可达70%,BOD/COD值则由原废水的0.02提高到0.50以上。MBR处理上述出水的结果表明,经微曝气Fenton氧化处理BPA的废水,可较好地适应后续的生化处理。     

对苯二甲酸生产废水回用实验研究

采用高级氧化工艺对对苯二甲酸生产废水进行处理,系统考察了氧化剂投加量、废水pH等对处理效果的影响,得出了最佳工艺条件。经过处理的PTA废水,水质达到了车间用水的要求。本方法具有处理效果好、操作简单和环境友好等优点。     

含中间层的DSA电极电催化氧化硝基苯废水的研究

为了提高难降解有机废水的可生化性,以及更高效地去除废水中的特征污染物,同时避免二次污染,利用自制的含锡锑中间层的钌钯氧化物涂层电极对有机废水中的硝基苯进行处理,并利用SEM、XRD等方法对电极中间层、表层进行微观表征。微观测试表明,基体、中间层、表层之间结合力较强,有利于增强电极寿命;水处理实验表明,电催化氧化反应体系适合高浓度有机废水的处理,由于该反应体系需要外加电解质加强传质,这在实际运用中为废水中盐度的处理提供了一种新的途径,当电流密度为20 mA/cm²、电解质浓度为10 g/L、pH=5、极板间距=2 cm时,电催化氧化体系对硝基苯具有较高的去除效率。     

基于超临界水氧化过程的能源环境系统设计

阐述了超临界水氧化过程的工艺路线,介绍了超临界水氧化过程的特点,提出了基于超临界水氧化过程的能源环境系统,设计了几种热量与能量回收系统程的耦合工艺,为提高超临界水氧化过程的经济性奠定了基础。     

厌氧序批式反应器内挥发性脂肪酸积累特性研究

小试规模的厌氧序批式反应器（ASBR）,通过人工配水,研究了启动3个月时间以及一个运行周期内反应器内挥发性脂肪酸（VFA）的积累情况,并通过分析期间产甲烷活性的变化说明了控制VFA积累的重要性。经过近120 d的运行,乙酸和丙酸的最大比产甲烷活性分别提高了1.8和2.2倍,说明反应器的启动过程即是微生物群落的优化和选择的过程,ASBR的抗冲击的能力较强说明随启动的进行和种群的优化,活性污泥凝聚性能增强,对VFA的降解能力增强。     

阳离子染料废水治理技术

介绍了阳离子染料废水的特点,以及近年来阳离子染料废水的各种处理技术,并对阳离子染料废水处理技术的发展进行了展望,指出阳离子废水处理技术正朝着各种工艺优化组合的方向发展。     

Ru/γ-Al_2O_3和Ru/AC催化剂的制备及其对氨氧化反应的催化性能

分别以γ-Al_2O_3和活性炭(AC)为载体,采用浸渍法制备了Ru质量分数均为2.0%的Ru/γ-Al_2O_3和Ru/AC催化剂,并用X射线衍射仪和透射电子显微镜等方法对催化剂结构进行了表征.实验结果表明:Ru/AC中Ru沉积在AC表面,分散度较低;而Ru/γ-Al_2O_3中Ru进入到γ-Al_2O_3内部,形成了一种高度分散体系.Ru/γ-Al_2O_3对氨的催化活性高于Ru/AC,氨在Ru/γ-Al_2O_3和Ru/AC上的起活温度分别为200 ℃和266 ℃,T_(90)(氨去除率达90%时的反应温度)分别为267℃和320 ℃.随混合气体空速增大,Ru/γ-Al_2O_3催化剂的T_(90)逐渐升高,气体空速分别为3 600,4 800,5 400 h~(-1)时,T_(90)分别为235,266,303 ℃.随反应前混合气体中氨质量分数增加,氨的去除率降低.     

Dechlorination of polyvinyl chloride in NaOH/ethylene glycol solution by microwave heating

This study investigated the dehydrochlorination of flexible polyvinyl chloride (PVC) containing 59.2% PVC, 29.7% dioctyl phthalate (DOP), and approximately 12% stabilizers. Flexible PVC was treated with NaOH/ethylene glycol (NaOH/EG) solutions at NaOH concentrations in the range 0.5–4 mol/l and was heated in a microwave heater at a temperature between 100° and 160°C for 0–30 min. All chlorides were completely eliminated by internal heating at 160°C using microwaves for 10 min in a 1 mol/l NaOH/EG solution, and the residue was made up of hydrocarbons. The weight loss rate reached a maximum of 74.7% at a temperature of 160°C. It was discovered that the use of microwaves significantly shortened the reaction time compared to using conventional electric heaters or other external heating systems and also allowed the use of lower concentrations of NaOH. Chemical Feedstock Recycling & Other Innovative Recycling Techniques 6     

The Effect of Masterbatch Addition on the Mechanical, Thermal, Optical and Surface Properties of Poly(lactic acid)

There has been considerable interest in the use of the biodegradable polymer poly(lactic acid) (PLA) as a replacement for petroleum derived polymers due to ease of processability and its high mechanical strength. Other material properties have however limited its wider application. These include its brittle properties, low impact strength and yellow tint. In an attempt to overcome these drawbacks, PLA was blended with four commercially available additives, commonly known as masterbatches. The effect of the addition of 1.5 wt% of the four masterbatches on the mechanical, thermal, optical and surface properties of the polymer was evaluated. All four masterbatches had a slight negative effect on the tensile strength of PLA (3–5% reduction). There was a four fold increase in impact resistance however with the addition of one of the masterbatches. Differential scanning calorimetry demonstrated that this increase corresponded to a decrease in the polymer crystallinity. However there was an associated increase in polymer haze with the addition of this masterbatch. The clarity of PLA was improved through the addition of an optical brightener masterbatch, but the impact resistance remained low. The glass transition and melting temperatures of PLA were not affected by the addition of the masterbatches, and no change was observed in surface energy. Some delay in PLA degradation, in a PBS degradation medium at 50 °C, was observed due to blending with these masterbatches.     

过氯乙烯滤膜采样-酸消解-钼蓝光度法测定磷酸雾

建立了过氯乙烯滤膜采样 -酸消解 -钼蓝分光光度法测定磷化车间磷酸雾的监测方法。实验室模拟采样的捕集效率为 95 7%～ 99 1 %。单个实验室对含 5μg和 1 5μg样品进行多次测定 ,其相对标准差小于 5% ,样品加标回收率为 98 2 %～ 1 0 0 5% ,方法检测限为 0 0 0 7mg/m3。对标样测定 ,结果均在给定值范围内。用该法与等离子发射光谱法(ICP)对 5个样品进行比对测定 ,结果均令人满意。