氧化沟中微孔曝气器的技术特性分析

曝气设备是氧化沟污水处理系统中最主要的设备,本文分析了微孔曝气的技术性能,及其在氧化沟中的特性分析和工程应用。     

氧化-微絮凝-高速过滤应用于再生水生产的研究

以中国北方缺水地区污水再生利用为目标,采用常规滤料双层过滤探讨高速微絮凝、氧化过滤再生水处理技术,试验通过不同的滤料级配、滤层厚度的对比试验;采用3种混凝剂和3种助凝剂做筛选试验,发现采用1#混凝剂,HFO助凝剂做絮凝氧化剂效果较理想,得出高速微絮凝氧化过滤工艺处理城市污水厂二级出水的工艺是可行的。试验装置的滤池单位面积周期产水量为50m3/(m2.h),最佳工艺条件下出水浊度去除率为92.21%,平均浊度为0.889NTU;COD去除率为55.58%,平均为22.33mg/L;PO34--P去除率为84%,平均为0.135mg/L;色度去除率为80.7%,平均为1.45度,完全符合GB/T18920-2002《城市污水再生利用城市杂用水质》要求。     

高度有序的TiO2纳米管阵列光催化性能研究

采用恒压阳极氧化法在纯钛箔表面制备TiO2纳米管阵列,利用SEM和XRD对其进行了形貌和晶型的分析和表征,并通过TiO2纳米管阵列膜对甲基橙光催化降解,探讨光照时间、甲基橙溶液的初始浓度、溶液的初始pH值和H2O2加入浓度等因素对甲基橙的脱色率影响.结果表明,H2O2加入浓度为50mg·L-1,紫外光照射2h,溶液为中性时,在30 mg·L-1的甲基橙溶液(50mL)中,甲基橙溶液的脱色率达到100%.当H2O2加入浓度进一步增大到100 mg·L-1时,光催化的效率进一步提高,紫外光照射1h,甲基橙溶液的脱色率就已经达到了100%,并未出现抑制光催化的现象.同时还研究了TiO2纳米管阵列电极的稳定性.实验结果表明,随着TiO2纳米管阵列使用次数的增加,其光催化效果略有所下降.     

混凝沉淀-水解酸化-生物吸附-UBF-接触氧化一氧化沟-吸附工艺处理聚醚多元醇废水

对聚醚多元醇废水采用混凝沉淀-水解酸化-生物吸附-UBF-接触氧化一氧化沟-吸附等进行连续处理。结果表明，该处理工艺具有废水处理效果好、出水水质稳定（出水水质达GB8978—1996中的一级标准）、操作管理方便等优点，是处理该类化工废水的有效方法之一。     

Water quality characteristics along the course of the Huangpu River （China）

Huangpu River is about 114.5 km from upriver Dianfeng to downriver Wusong,near the estuary of the Yangtze River.It plays a key role in supplying water for production,life,shipment and irrigation.With the industrial development,the pollution of the Huangpu River has become serious recently.The biological oxygen demand (BOD),total nitrogen (TN),total phosphorus (TP),oil,phenol and suspended solids (SS) were lower in the upstream sites than in the downstream sites,indicating pollutants being input along its course. Water quality was the worst in the Yangpu site,near the center of Shanghai City.Dissolved oxygen (DO) content was less than 2 mg/L in the site of Yangpu in July.Among relations between thirteen characteristics,relations between BOD,DO,TN,TP,NH_4~ -N, NO_3~--N and the count of total bacteria or Escherichia coli were significant and interdependent.Inner relationships between these main characteristics in the Huangpu River were studied.High nutrient concentration led to growth of microorganisms,including E.coli. Degradation of organic matters and respiration of bacteria made oxygen concentration decreased in the water body,and DO was a key factor for nitrification-denitrification process of nitrogen.In the Yangpu site,DO was decreased to less than 3.0 mg/L with BOD higher than 7.5 mg/L in May and July.Low DO concentration will decrease nitrification rate.Nitrification need at higher DO value than other organic substrate oxidation.Consequently,river water contains low NO_3~--N values with high amounts of TN and NH_4~ -N there.This will block the self-purification of surface water,by decreasing the rate of nitrification-denitrification transformation process in the water body.     

超大城市SO2排放对硫酸盐区域分布影响的观测与模拟

2002年8月14—24日在临安采集气溶胶样品,对气溶胶质往往w量和离子成分的尺度分布进行分析.结果表明:SO₄2-主要集中在粒径<2.1 μm的细粒子中,约占所有尺度段上SO42-质量总和的94%;细粒子(PM_2.1)中,ρ(SO₄2-)和ρ(NH₄+)最高,二者之和占所分析离子质量浓度总和的89%. 利用公共多尺度空气质量模式(CMAQ)的过程分析对影响硫酸盐气溶胶分布特征的主要因子进行定量评估,结果表明:经过云内液相氧化和湿清除形成硫酸盐气溶胶的速率为0.19 μg/(m3·h),其对硫酸盐气溶胶的贡献最大;SO₂液相氧化反应中速率最大的是H₂O₂〔5.26 μg/(m3·h)〕,其次是O₂〔4.14 μg/(m3·h)〕和O₃〔1.56 μg/(m3·h)〕. 模拟分析证明,采样期间研究区域SO₄2-主要是由上海及其以南的浙江沿海一带通过SO₂云内与H₂O₂和O₂的液相氧化反应生成. 通过模式敏感性试验发现,在个例的风场配置下,上海排放的SO₂对临安地区的SO₂和硫酸盐的贡献率分别达15%和22%.      

Photodegradation of amoxicillin by catalyzed Fe3+/H2O2 process

Three oxidation processes of UV-Fe³⁺(EDTA)/H₂O₂ (UV: ultraviolet light; EDTA: ethylenediaminetetraacetic acid), UV-Fe³⁺/H₂O₂ and Fe³⁺/H₂O₂ were simultaneously investigated for the degradation of amoxicillin at pH 7.0. The results indicated that, 100% amoxicillin degradation and 81.9% chemical oxygen demand (COD_Cr) removal could be achieved in the UV-Fe³⁺ (EDTA)/H₂O₂ process. The treatment efficiency of amoxicillin and COD_Cr removal were found to decrease to 59.0% and 43.0% in the UV-Fe³⁺/H₂O₂ process; 39.6% and 31.3% in the Fe³⁺/H₂O₂ process. Moreover, the results of biodegradability (biological oxygen demand (BOD₅)/COD_Cr ratio) revealed that the UV-Fe³⁺ (EDTA)/H₂O₂ process was a promising strategy to degrade amoxicillin as the biodegradability of the effluent was improved to 0.45, compared with the cases of UV-Fe³⁺/H₂O₂ (0.25) and Fe³⁺/H₂O₂ (0.10) processes. Therefore, it could be deduced that EDTA and UV light performed synergetic catalytic effect on the Fe³⁺/H₂O₂ process, enhancing the treatment efficiency. The degradation mechanisms were also investigated via UV-Vis spectra, and high performance liquid chromatography-mass spectra. The degradation pathway of amoxicillin was further proposed.     

pH值对纳米零价铁吸附降解2,4-二氯苯酚的影响

在不同pH条件下,对纳米铁(颗粒粒径为30～40 nm)及其降解2,4-二氯苯酚反应体系进行取样,并进行透射电子显微镜(TEM)、扫描电子显微镜-能谱联用(SEM-EDX)以及电感耦合等离子体发射光谱(ICP-OES)等形貌观测与分析表征,以考察pH值在纳米零价铁降解氯酚反应过程中的影响和作用.结果表明,在降解2,4-二氯苯酚的过程中纳米铁由分散的颗粒逐渐团聚,其表面逐渐氧化,并最终被呈针状结晶的碱式氧化亚铁(FeOOH)覆盖,从而阻碍了降解反应的进一步进行.在酸性体系中,纳米零价铁的氧化和团聚现象有所缓解,尽管会造成一部分铁量的损失,但反应产生大量的亚铁离子参与并促进了脱氯降解反应的进行,反应过程中溶液pH值有逐渐升高的趋势.不同pH条件下,纳米铁对氯酚的去除率随pH值的降低而升高,酸性条件有利于提高氯酚的还原降解速率,当pH=3时,24 h内氯酚的去除率可达到90%以上.     

超临界水处理有机废物研究新进展

超临界水处理废物以通过添加氧化剂的超临界水氧化和不加氧化剂的超临界水萃取两种方式实现，超临界水氧化应用较多，与其它废物处理技术相比有显著优点。本文总结了超临界水氧化流程和反应机理，评述了添加剂，温度，压力及停留时间，催化剂等对超临界水氧化反应的影响，同时介绍了超临界水氧化和超临界水萃取的最新应用研究状况及尚需解决问题。     

钴氨溶液脱除NO研究

利用Co(NH₃)₆²⁺离子作主催化剂(由可溶性钴盐溶于氨水中形成),烟道气中的O₂作氧化剂,碘阴离子作助催化剂,在液相中实现NO的催化氧化和回收、SO₂的吸收和氧化.与过氧化氢和Fe-EDTA法相比该法具有持续时间长、效率高等优点,NO的脱除率可达80%以上;SO₂的脱除率可达100%,能实现高效率地同时脱硫脱硝.