水中本底成分对催化臭氧化分解微量硝基苯的影响

考察了水中本底成分对催化臭氧化分解水中微量硝基苯的影响规律.对比试验结果表明,单独臭氧氧化、臭氧/蜂窝陶瓷催化氧化和臭氧/改性蜂窝陶瓷催化氧化工艺在自来水中比蒸馏水中对硝基苯的去除率分别增加了4.90%、2.47%和5.12%.单独臭氧氧化对硝基苯的分解效率随着镁离子浓度的升高(0～8 mg.L^-1)而增加了6.25%,在相同实验条件下,臭氧/蜂窝陶瓷催化氧化和臭氧/改性蜂窝陶瓷催化氧化对硝基苯的降解效率随着镁离子浓度的升高却降低了11.41%和17.64%;单独臭氧氧化、臭氧/蜂窝陶瓷催化氧化和臭氧/改性蜂窝陶瓷催化氧化在氯离子浓度增加(0～40 mg.L^-1)的情况下对硝基苯的去除率分别下降了4.42%、9.38%和12.24%;低浓度的腐殖酸促进了硝基苯的降解,高浓度的腐殖酸抑制了硝基苯的降解.实验还研究了臭氧投加量和硝基苯初始浓度对硝基苯降解效率的影响.     

Degradation of atrazine by catalytic ozonation in the presence of iron scraps: performance,transformation pathway,and acute toxicity

Degradation of atrazine by catalytic ozonation in the presence of iron scraps (ZVI/O₃) was carried out. The key operational parameters (i.e., initial pH, ZVI dosage, and ozone dosage) were optimized by the batch experiments, respectively. This ZVI/O₃ system exhibited much higher degradation efficiency of atrazine than the single ozonation, ZVI, and traditional ZVI/O₂ systems. The result shows that the pseudo-first-order constant (0.0927?min^?1) and TOC removal rate (86.6%) obtained by the ZVI/O₃ process were much higher than those of the three control experiments. In addition, X-ray diffraction (XRD) analysis indicates that slight of γ-FeOOH and Fe₂O₃ were formed on the surface of iron scrap after ZVI/O₃ treatment. These corrosion products exhibit high catalytic ability for ozone decomposition, which could generate more hydroxyl radical (HO^?) to degrade atrazine. Six transformation intermediates were identified by liquid chromatography-mass spectrometry (LC-MS) analysis in ZVI/O₃ system, and the degradation pathway of atrazine was proposed. Toxicity tests based on the inhibition of the luminescence emitted by Photobacterium phosphoreum and Vibrio fischeri indicate the detoxification of atrazine by ZVI/O₃ system. Finally, reused experiments indicate the approving recyclability of iron scraps. Consequently, the ZVI/O₃ system could be as an effective and promising technology for pesticide wastewater treatment.     

皮带输煤暗道通风排尘改造方案优化研究

为了解决皮带输煤暗道运输过程中粉尘污染严重及冬季供暖不足问题，对暗道通风供热系统进行了优化改造研究。以中煤平朔安家岭264输煤暗道为例，基于气固两相流理论，利用CFD模拟方法，对暗道内由风速对悬浮粉尘浓度分布的影响规律进行数值仿真。模拟结果显示:当输煤暗道排尘风速由0.25 m/s升至0.35 m/s时，粉尘浓度降为3.2 mg/m3，暗道最大通风阻力为245.94 Pa，最低换热量747.68 kW。基于数值模拟结果，从3种优化方案中选定一压一抽联合式通风除尘方案进行改造，现场实测除尘效果良好，表明所提出的输煤暗道通风除尘方案具有实践指导意义。     

A novel approach to treat combined domestic wastewater and excess sludge in MBR

Domestic wastewater was treated by combined anaerobic biofilm-aerobic membrane bioreactor(MBR) process, and part biomass in MBR was withdrawn, to treat with ozone, then the ozonated sludge was returned to anaerobic inlet. In aerobic MBR, MLSS and DO were controlled at 3000—3500 mg/L and 0.8 mg/L respectively. Comparing the experimental results of two stages, it was noticed that ozonation did not affect the removal efficiency for organics but had a significant influence on the removals of NHs-N and TN. During the ozonation period of two months, no excess sludge was wasted, and a zero sludge yield was obtained.     

催化臭氧化去除水中氯乙酸的研究

运用催化臭氧化技术去除水中消毒副产物氯乙酸。结果表明：（1）Ni/Al2O3是一种高效催化臭氧化氯乙酸的催化剂；（2）催化臭氧化分解氯乙酸的效率，明显高于单独臭氧化和单独吸附去队氯乙酸效率之和；（3）低pH对氧化氯乙酸较为有利。     

炼油厂污水回用处理研究

研究表明，炼油厂外排污水采用悬浮载体生物接触氧化、砂滤和臭氧生物活性炭工艺深度处理，主要污染物都有良好的去除效果，总出水清澈、无色，可以满足多种回用要求。分析表明，大部分还原性污染物通过生物深度处理而去除，而微量有机物主要由臭氧生物活性炭去除。工艺系统具有除污染效率高、运行稳定、抗冲击能力强等优点。     

负载型TiO_2催化臭氧化去除腐殖酸的实验研究

以实验室自制的负载型TiO2为催化剂,研究了其对水中溶解性腐殖酸的催化臭氧化效能。结果表明负载型TiO2对臭氧化去除溶解性腐殖酸有明显的催化作用,反应25min,对腐殖酸的去除率可达到86.8%,较单独臭氧化提高了28.8%;通过Na2CO3对催化反应的影响间接推断TiO2催化臭氧化反应遵循自由基反应的原理;实验最佳条件为:催化剂涂膜层数6层、焙烧温度700℃、溶液pH=10、放电电流0.4A、反应溶液初始浓度10mg/L;催化剂重复使用8次后,其催化活性变化较小,溶液中无钛离子溶出。     

金属离子对有机垃圾两相厌氧系统中UASB处理效果的促进作用

在"水解溶出 UASB反应器"处理城镇有机垃圾的两相厌氧系统中,向UASB反应器进水中添加K、Mg、Fe、Co、Ni 5种金属离子的组合促进剂,通过对UASB反应器容积负荷、产气量、产甲烷量在添加组合促进剂前后的比较,研究了组合促进剂(K、Mg、Fe、Co、Ni)对有机垃圾浸出液厌氧消化过程的促进作用.试验结果表明,添加组合促进剂后,反应器的平均容积负荷从12.89 kg COD/m3·d提高到17.79 kg COD/m3·d;平均污泥负荷从0.82 kg COD/kg VSS·d提高到1.07 kg COD/kg VSS·d.此外,平均每千克COD产气量为392.5 L,比添加组合促进剂之前增大了6.4%;而平均每千克COD产甲烷量为297.5 L,比添加组合促进剂之前增大了10.5%.对于氨氮、挥发性脂肪酸(VFA)、pH及碱度来说,在添加组合促进剂之后则无大的变化.     

Characteristics of MnO2 catalytic ozonation of sulfosalicylic acid and propionic acid in water

The characteristics of different types of MnO₂ catalytic ozonation of sulfosalicylic acid (SSal) and propionic acid (PPA) have been investigated in this paper. The experimental results show the dependence of catalytic activity of MnO₂ on organic compounds and the pH of solutions, but it is independent on the type of MnO₂. For example, three types of MnO₂ have not any catalytic activity when ozonation of PPA under the condition of this experiment. All MnO₂ catalytic ozonation of SSal at pH=1.0 have a greater total organic carbon removal than ozonation alone has, however, at pH=6.8 and 8.5, catalytic efficiency is not observed. Furthermore, the batch experimental results indicate that there are no direct relationship between the activity of metal oxide catalytic decomposition of ozone and that of its catalytic degradation of organic compounds.     

臭氧氧化降解水溶液中1—萘酚的动力学研究

本文研究了水溶液中１－萘酚在鼓泡反应釜内臭氧氧化的消失动力学,考察了ｐＨ值、温度、自由基清除剂和１－萘酚的起始反应浓度等因素对反应的影响。结果表明,ｐＨ值、反应温度的提高有利于１－萘酚的降解。１－萘酚初始浓度低时其消失速率较高。该反应是有自由基反应贡献的分子臭氧氧化反应。在重碳酸盐存在下,１－萘酚的臭氧氧化降解符合一级反应动力学。