西安市重污染与清洁天PM2.5组分及其活性氧物质对比

针对重霾污染,在西安市冬季重污染日(2015-11-30~2015-12-09)和清洁日(2016-01-13~2016-01-22)各进行了为期10d的PM_(2.5)采集,测量其中的有机碳、元素碳,及NH_4~+、NO_3~-、SO_4~(2-)等无机水溶性离子,探讨两种污染条件下的组分特征及其成因.结果表明:观测期,重霾日和清洁日PM_(2.5)质量浓度分别为(170±47.5)μg·m~(-3)和(48.6±17.9)μg·m~(-3),且重霾日伴随低能见度、高湿静风等多种不利气象条件;重霾日二次无机离子(NH_4~+、NO_3~-、SO_4~(2-))组分占PM_(2.5)质量浓度的49.8%±13.1%,而清洁日为19.4%±5.95%,并且重霾日硫氧化速率(sulfur oxidation ratio,SOR)和氮氧化速率(nitrogen oxidation ratio,NOR)分别为0.282±0.157和0.269±0.124,远高于清洁日(SOR和NOR分别为0.189±0.057和0.077±0.046),重霾日二次有机组分浓度[(6.22±3.87)μg·m~(-3)]是清洁日[(1.44±1.63)μg·m~(-3)]的5倍,表明二次污染及不利气象条件是造成重霾期间相关组分浓度升高的重要原因.最后,通过二氯荧光黄双乙酸盐(2',7'-DCFH)化学荧光分析法测定了其中活性氧物质(reactive oxygen species,ROS)的浓度,探讨其对于二次无机组分形成的影响,结果表明观测期ROS平均浓度(以H_2O_2计)分别为(4.99±1.54)nmol·m~(-3)(重霾期),(0.492±0.356)nmol·m~(-3)(清洁期),二次反应及积累效应可能是西安重霾条件下ROS浓度升高的主要原因.NO_3~-、SO_4~(2-)与ROS均呈现正相关(P0.05),表明ROS可能通过二次氧化过程参与到二次无机组分形成过程中.     

Research on the degradation mechanism of pyridine in drinking water by dielectric barrier discharge

Pyridine, an important chemical raw material, is widely used in industry, for example in textiles,leather, printing, dyeing, etc. In this research, a dielectric barrier discharge(DBD) system was developed to remove pyridine, as a representative type of nitrogen heterocyclic compound in drinking water. First, the influence of the active species inhibitors tertiary butanol alcohol(TBA),HCO_3~-, and CO_3~(2-)on the degradation rate of pyridine was investigated to verify the existence of active species produced by the strong ionization discharge in the system. The intermediate and final products generated in the degradation process of pyridine were confirmed and analyzed through a series of analytical techniques, including liquid chromatography–mass spectrometry(LC–MS), high performance liquid chromatography(HPLC), ion chromatography(IC), total organic carbon(TOC) analysis, ultraviolet(UV) spectroscopy, etc. The results showed that the degradation of pyridine was mainly due to the strong oxidizing power of ozone and hydroxyl radical produced by the DBD system. Several intermediate products including 3-hydroxyl pyridine, fumaric acid, 2, 3-dihydroxypyridine, and oxalic acid were detected. Nitrogen was removed from the pyridine molecule to form nitrate. Through analysis of the degradation mechanism of pyridine, the oxidation pathway was deduced. The study provided a theoretical and experimental basis for the application of DBD strong ionization discharge in treatment of nitrogen heterocyclic compounds in drinking water.     

Control of aliphatic halogenated DBP precursors with multiple drinking water treatment processes: Formation potential and integrated toxicity

The comprehensive control efficiency for the formation potentials(FPs) of a range of regulated and unregulated halogenated disinfection by-products(DBPs)(including carbonaceous DBPs(C-DBPs), nitrogenous DBPs(N-DBPs), and iodinated DBPs(I-DBPs)) with the multiple drinking water treatment processes, including pre-ozonation, conventional treatment(coagulation–sedimentation, pre-sand filtration), ozone-biological activated carbon(O_3-BAC) advanced treatment, and post-sand filtration, was investigated. The potential toxic risks of DBPs by combing their FPs and toxicity values were also evaluated.The results showed that the multiple drinking water treatment processes had superior performance in removing organic/inorganic precursors and reducing the formation of a range of halogenated DBPs. Therein, ozonation significantly removed bromide and iodide,and thus reduced the formation of brominated and iodinated DBPs. The removal of organic carbon and nitrogen precursors by the conventional treatment processes was substantially improved by O_3-BAC advanced treatment, and thus prevented the formation of chlorinated C-DBPs and N-DBPs. However, BAC filtration leads to the increased formation of brominated C-DBPs and N-DBPs due to the increase of bromide/DOC and bromide/DON.After the whole multiple treatment processes, the rank order for integrated toxic risk values caused by these halogenated DBPs was haloacetonitriles(HANs)》haloacetamides(HAMs) haloacetic acids(HAAs) trihalomethanes(THMs) halonitromethanes(HNMs) 》I-DBPs(I-HAMs and I-THMs). I-DBPs failed to cause high integrated toxic risk because of their very low FPs. The significant higher integrated toxic risk value caused by HANs than other halogenated DBPs cannot be ignored.     

人工湿地植物水体净化效能研究进展

通过检索近20年来人工湿地植物在净化水质方面代表性文献,筛选出50种常见人工湿地植物,包括水生植物(挺水植物、浮水植物及浮叶植物、沉水植物)、湿生植物、旱生植物,对该50种常见植物的净化效能进行分析比较;指出湿地植物在净化水体时可能受物种、环境因子、种类配置模式三方面的影响;提出未来人工湿地植物选择应用方面发展方向为:应进一步扩大其种类的选择范围,加强探究维持其生长代谢的机理,加强与微生物的耦合作用完成水体污染物净化的效能研究,根据不同人工湿地和水体污染物类型进行配置等4个方面。     

广西壮族自治区污水处理厂运行状况及特征分析

基于广西壮族自治区126座污水处理厂2015年运行状况的调查数据,分析广西污水处理厂的工艺特点、污泥处置、出水水质达标情况、运行负荷率和运行费用,评估污水处理厂运行的效率和效果,分析存在的问题,并就污水处理厂的运行和管理提出建议。     

变电站污水处理现状与展望

变电站一般位于城市郊区或乡村环境等市政设施尚不完善的区域,无法接入市政污水管网,许多变电站粗放式的污水处理方式无法满足环保要求.随着变电站智能化水平的提高,站内工作人员越来越少,传统的污水处理方式无法适应新形势下变电站内污水处理要求.因此,针对变电站粗放式的污水管理方式及新条件下传统污水处理方式等不满足环保要求的问题,根据站址外环境创新变电站污水处理方式成为关键.通过对变电站既有污水处理方式的研究,结合变电站智能化的发展进程,进行总结,可为变电站污水处理设计或水环境管理提供参考.     

污水处理厂消毒技术对抗生素抗性菌的强化去除

基于消毒技术对污水处理厂出水中总异养菌(total heterotrophic bacteria,HPC)及5种抗生素抗性菌(antibiotic resistant bacteria,ARB):氨苄霉素抗性菌(AMP)、红霉素抗性菌(ERY)、四环素抗性菌(TET)、卡那霉素抗性菌(KAN)、环丙沙星抗性菌(CIP)的去除情况研究,分析消毒技术对ARB的强化去除效果.结果表明,实际污水处理厂的紫外消毒对ARB去除率仅为18.2%~40.9%,且AMP含量最高;另外,消毒技术对ERY有选择性去除效果,对其他4种ARB无明显选择性去除效果(P0.05);最后结合次氯酸钠、臭氧、紫外消毒处理对COD、NH_4~+-N的去除效果,确定强化去除ARB的消毒方式中臭氧,次氯酸钠和紫外的最佳浓度和剂量依次为5.0 mg·L~(-1)、25.0 mg·L~(-1)和45.0 m J·cm~(-2),ARB去除率依次为45.5%~74.5%、66.1%~85.5%、68.6%~85.5%,另外次氯酸钠耦合紫外消毒强化去除ARB的效果更佳.     

废弃尾矿库15种植物对重金属Pb、Zn的积累和养分吸收

在废弃的铅锌尾矿库进行人工植被恢复试验.对3年生15种植物重金属积累和养分吸收特性的研究表明,植物对土壤重金属和养分的吸收积累因植物种类、部位、金属种类和种植时间的不同而有显著差异.树木不同器官Pb质量浓度高低的总趋势为根〉叶〉茎,部分树种Zn质量浓度表现为叶〉根和茎;在15种参试植物中,加拿大紫荆根系Pb和Zn质量浓度均处于最高水平（分别为1 803 mg.kg-1和2 120 mg.kg-1）,盐肤木具有最高的茎枝Pb、叶片Pb和Zn质量浓度（分别为280、546和1 507 mg.kg-1）,旱柳具有最高的茎枝Zn质量浓度（729 mg.kg-1）和较高的叶片Zn质量浓度（1 153 mg.kg-1）.枫香、紫花苜蓿对Pb,旱柳、盐肤木、紫花苜蓿对Zn的转移系数TF值均〉1.植物Pb的富集系数BCF值均小于0.17,旱柳、盐肤木、紫花苜蓿Zn的BCF值达0.37～0.43.固氮植物体内N含量显著高于其它植物,火炬树、臭椿对P和夹竹桃对K的吸收积累能力强.随着种植时间的增加,植株体内有重金属质量浓度增加、营养元素含量下降的趋势.盐肤木、旱柳等重金属积累树种及紫穗槐、紫花苜蓿、截叶胡枝子、桤木等固氮植物在铅锌尾矿治理中具有应用前景.     

黄土丘陵区坡面水蚀对降雨和下垫面微观格局的响应

黄土高原严重的土壤侵蚀是降雨和复杂脆弱的下垫面共同作用的结果.以微型小区尺度上(1.2 m×1.2 m;2 m×1.2m)模拟降雨技术为基本研究手段,定量刻画了降雨量和降雨强度等基本降雨特征值对定西安家沟自然坡面上荒草、沙棘中位、沙棘下位、沙棘上位、结皮裸地和裸地等不同植株微观格局及其处理下的水蚀过程的影响.主要取得以下结果:①雨强和雨量对水蚀的发生均能产生显著影响,但以雨强的影响力更大;②前期土壤含水量与产流时间显著负相关,而与径流量和侵蚀量显著正相关.前期含水量相同时,不同植株微景观格局对产流时间发挥了关键作用;③不同植株及其微观格局遏制地表径流的能力迥异.在50～60 mm.h-1的大雨强作用下,有沙棘覆盖的小区径流系数仅为5%～8%,荒草地为25%,结皮裸地为45%,而裸地则高达63%;④有沙棘覆盖的小区中,沙棘在小区中所处的具体位置对于水土流失效应又极为重要,以沙棘下位的水土保持效果最好.     

植物对纳米颗粒的吸收、转运及毒性效应

随着工程纳米颗粒的广泛使用,这些纳米材料不可避免地进入环境,对环境造成未知影响.植物是高等生物暴露于纳米颗粒的一条主要途径,工程纳米颗粒可能通过食物链使其在高营养水平生物中积累.植物与纳米颗粒间的相互作用应该受到关注和重视.已有的文献表明纳米颗粒能被植物选择性地吸收并引起植物毒性,但纳米颗粒进入植物体内的机制仍不明确.多数关于植物吸收纳米颗粒的研究是在理想条件如水培实验下开展,并且集中在植物的种子发芽或是幼苗生长阶段.描述纳米颗粒在植物体内的生物转化和在植物体内分配的报道较少,而且这方面的机制没有阐述清楚.目前有许多研究者关注纳米颗粒的植物毒性效应,但这方面的研究需要进一步深入.