灰霾的健康效应

灰霾是颗粒物和气体污染物导致的可察觉到的能见度降低的污染天气现象.近年来,随着城市化进程的快速发展,城市大气污染加剧,灰霾天气也随之增多.总结了灰霾这一污染型天气的特征,介绍了灰霾的化学成分、污染机制等,并从影响机制和流行病学角度出发,对国内外灰霾对人体的健康效应研究成果进行了综合评述,提出目前急需解决的科学问题和今后的研究方向.     

Cytotoxicity and DNA damage of five organophosphorus pesticides mediated by oxidative stress in PC12 cells and protection by vitamin E

Previous studies have demonstrated that pesticides could induce cytotoxicity and genotoxicity in vivo and in vitro, and that oxidative stress may be an important factor involved. However, investigations comparing the capability of different organophosphorous (OP) compounds to induce cytotoxicity, genotoxicity and oxidative stress are limited. Hence, the aim of this paper was to access the cytotoxic and genotoxic effects of five OPs or metabolites, Acephate (ACE), Methamidophos (MET), Chloramidophos (CHL), Malathion (MAT) and Malaoxon (MAO), and to clarify the role of oxidative stress, using PC12 cells. The results demonstrated that MET, MAT and MAO caused significant inhibition of cell viability and increased DNA damage in PC12 cells at 40 mg L^?1. MAO was more toxic than the other OPs. ACE, MET, MAT and MAO increased the levels of intracellular reactive oxygen species (ROS) and malondialdehyde (MDA), and decreased the activity of superoxide dismutase (SOD), catalase (CAT) and glutathione (GSH) at 20 mg L^?1 and 40 mg L^?1 to different degrees. Pre-treatment with vitamin E(600 μM)caused a significant attenuation in the cytotoxic and genotoxic effect; pre-treatment reversed subsequent OP-induced elevation of peroxidation products and the decline of anti-oxidant enzyme activities. These results indicate that oxidative damage is likely to be an initiating event that contributes to the OP-induced cytotoxicity.     

温度及外加碳源对生物脱氮除磷过程的影响

针对污水处理厂普遍面临的进水碳源不足及冬季低温时出水氮磷不能稳定达标的问题,研究了温度(21、15和10℃)和外加碳源(乙酸)对活性污泥缺氧条件下反硝化及释磷过程的影响。结果表明,在缺氧条件下投加乙酸,释磷与反硝化反应可同时进行,且乙酸投量的增加仅延长快速碳源反硝化阶段及缺氧释磷阶段的反应时间;温度降低为15℃和10℃时,快速碳源反硝化阶段反硝化速率及缺氧释磷速率较21℃分别降低了约29.2%、42.2%和26.1%、32.3%。当硝态氮目标去除量与磷酸盐目标释放量之比超过5时,乙酸的最优投量以满足反硝化要求为准,计算得出21、15和10℃时常州某城镇污水处理厂乙酸最优投加量计算值约为30、39和46 mg/L。     

氧活性粒子氧化NO生成HNO_3

采用强电离介质阻挡放电方法制取高浓度氧活性粒子(O+2、O3)并注入气体外排烟道中,实现O+2、O3氧化NO转化成资源酸(HNO3)的等离子化学反应。描述强电离放电的氧活性粒子产生器,讨论烟道中O+2、O3氧化NO成HNO3等离子体反应机制,分析回收酸液的NO-2、NO-3离子种类及浓度。考察强电离放电等离子体源的输入功率、水体积百分比、气体温度、气体流速对NOx氧化率的影响。氧化率为97.2%的最佳实验条件是:O+2浓度为1.38×1010个/cm3,O3浓度为210 mg/L,烟气温度为65℃,H2O体积浓度为5.6%,停留时间为0.94 s。     

Assessing heavy metal pollution in the surface soils of a region that had undergone three decades of intense industrialization and urbanization

Heavy metals in the surface soils from lands of six different use types in one of the world’s most densely populated regions, which is also a major global manufacturing base, were analyzed to assess the impact of urbanization and industrialization on soil pollution. A total of 227 surface soil samples were collected and analyzed for major heavy metals (As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, and Zn) by using microwave-assisted acid digestion and inductively coupled plasma–mass spectrometry (ICP-MS). Multivariate analysis combined with enrichment factors showed that surface soils from the region (>7.2?×?10⁴ km²) had mean Cd, Cu, Zn, and As concentrations that were over two times higher than the background values, with Cd, Cu, and Zn clearly contributed by anthropogenic sources. Soil pollution by Pb was more widespread than the other heavy metals, which was contributed mostly by anthropogenic sources. The results also indicate that Mn, Co, Fe, Cr, and Ni in the surface soils were primarily derived from lithogenic sources, while Hg and As contents in the surface soils were controlled by both natural and anthropogenic sources. The pollution level and potential ecological risk of the surface soils both decreased in the order of: urban areas?>?waste disposal/treatment sites?～?industrial areas?>?agricultural lands?～?forest lands?>?water source protection areas. These results indicate the significant need for the development of pollution prevention and reduction strategies to reduce heavy metal pollution for regions undergoing fast industrialization and urbanization.     

基于修正的化学品评分排序模式识别油田废弃物中的主要污染物

油田废弃物中污染物数量众多,对环境危害较大,需要对其中的主要污染物进行识别,以便有重点的监管油田废弃物.采用化学品评分排序模式(SCRAM)对油田废弃物中的污染物进行筛选,针对SCRAM在应用过程中存在的问题,对SCRAM进行了修正:在总分计算时增加了检出率和检出浓度2个因子,并且使用几何级数法定义检出浓度的5级赋分标准.在确定油田废弃物中污染物的初选名单后,应用修正SCRAM对液态废弃物、固态废弃物中直接检测以及使用浸出毒性法检测的污染物进行排序.通过对比SCRAM修正前后污染物排名的变化,论证了模型修正的必要性.最终得出54种油田废弃物中的主要污染物.     

Fe^0-厌氧微生物体系处理活性艳红X-3B的试验研究

采用间歇式摇床试验,研究了葡萄糖共基质条件下Fe^0-厌氧微生物体系中Fe^0投加量、pH值、染料初始浓度对活性艳红X-3B模拟废水脱色率的影响,比较了Fe^0-厌氧微生物、纯厌氧微生物及纯Fe^0 3种体系中废水的脱色效果。结果表明：Fe^0-厌氧微生物体系中初始浓度（50～500mg／L）对活性艳红X-3B的脱色率影响不大;而Fe^0投加量、pH值存在一个最佳范围;当Fe^0投加量为260mg／L,pH值为6．0,污泥浓度为0．35gVSS／L,停留时间约为30h时,体系中活性艳红X-3B的脱色率可达90％左右,比相同试验条件下纯Fe^0、纯厌氧微生物体系达到此脱色率所需时间分别缩短了约1／2、7／10。在Fe^0-厌氧微生物体系中,由紫外可见分光光度分析可推测活性艳红X-3B的脱色机理主要是其偶氮键发生断裂,生成苯胺和萘类物质,而且苯胺和萘类物质能得到进一步降解。     

污水处理中的人工湿地强化技术研究

人工湿地作为一种新型污水生态处理工艺受到越来越广泛的重视,在生活污水、特种工业废水、采矿污水、农业和畜牧业污水以及水产养殖废水等处理中得到了广泛的应用.但是其本身的局限却限制了它在高浓度废水、某些工业废水处理等方面的应用,在寒冷地区的应用也受到限制.本研究分析了一些强化技术(如湿地内部要素强化、工艺强化和工程强化等)在提高人工湿地的净化效能以及扩大其应用范围的可能性.     

污染当量数在区域现状污染源评价中的应用

阐述了污染当量数评价法中的污染当量含义和污染当量的应用、污染当量值、污染当量数以及计算等,介绍r污染当量评价方法和特点。通过对等标污染负荷法和污染当量数评价法的两种评价方法比较,表明污染当量数评价法的评价结果可靠、直观,具有可比性和合理性,是评价污染源区域现状简便、实用的方法。     

望虞河西岸九里河中四种除草剂的污染现状

基于气相色谱-质谱联用(GC-MS)法结合固相萃取(SPE)前处理技术,建立了水中4种除草剂氯草定、阿特拉津、乙草胺和异丙甲草胺残留的分析方法,于2018年春(4、5月)、秋(9、10月)和冬(1、3月)季对太湖流域望虞河西岸九里河水体中4种除草剂的污染现状进行调查分析。结果表明,4种除草剂的加标回收率为71. 2%～108%,RSD均10%,方法检出限为3. 5～6. 0 ng/L。九里河水体中氯草定、阿特拉津、乙草胺和异丙甲草胺4种除草剂质量浓度分别为未检出～0. 025 7,0. 019 1～1. 19,未检出～0. 026 0和未检出～0. 094 3μg/L。4种除草剂中阿特拉津最高值接近《地表水环境质量标准》(GB 3838—2002)限值,其他3种其值较低,氯草定首次在太湖流域水体中检出。