乌鲁木齐市近年来大气降尘变化规律及空间分布特征

基于乌鲁木齐市多年监测的降尘数据,对乌鲁木齐市城区的降尘量进行了统计分析,得出了乌鲁木齐市近10年来降尘的总体变化规律;利用方差分析方法检验了不同季节降尘的显著性差异,发现采暖期的降尘量明显大于非采暖期;按行政区分析降尘量的分布变化,结果为不同行政区存在差别;利用秩相关系数法对其进行了趋势分析。结果表明,乌鲁木齐市的降尘呈下降趋势。利用Arc GIS9.3中的普通克里格插值方法绘制了乌鲁木齐市城市自然降尘的空间分布图。     

磁性分散固相萃取气相色谱法测定地表水中有机磷化合物

应用磁性分散固相萃取技术对环境水体中有机磷化合物进行萃取测定,并对萃取剂的用量、萃取时间、解吸溶剂、盐度等实验影响因素进行了优化。在优化条件下,有机磷的回收率为80.1%~93.1%,相对标准偏差为4.6%~5.9%,检出限为0.000 2~0.000 4 mg/L。与传统的液液萃取及固相萃取相比,该磁性分散固相萃取方法操作更为简单、迅速,有机溶剂消耗量很少,方法环保。能很好的满足环境水体中有机磷化合物的测定。     

泰州市冬季空气质量变化特征

为了解泰州市冬季空气质量变化特征,于2013年12月27日—2014年1月7日对NO2,SO2,O3,CO,PM10和PM2.5进行了监测,结合地面气象资料和HYSPLIT轨迹模式分析了污染物的来源与传输过程。结果表明,观测期间AQI优良率仅为25%,PM10和PM2.5日均值超标率分别为58.3%,75.0%;有机碳是泰州市ρ(PM2.5)中最高的化学组分,其次是富钾和元素碳。PM2.5主要来源为汽车尾气、工业源、燃煤,分别占来源比例21.76%,16.52%,15.54%。局地污染源和不利气象条件是造成大气污染的主要原因。     

杭州夏季一次降雨过程雨水中全氟化合物及主要化学组分的变化特征

采用分段采样的方式收集杭州市2018年8月2日—3日一场降水样品,测定其中16种全氟化合物（PFCs）及主要化学组分浓度。结果发现,此次降雨过程水样的pH值范围为5.04～5.32,均为弱酸性降水,酸雨类型为复合型,检出的主要阳离子为NH+4,主要阴离子为SO2-4和NO-3;样品中检出7种中短链PFCs,包括2种全氟烷基磺酸（PFSAs）和5种全氟烷基羧酸（PFCAs）,ΣPFCs质量浓度范围为4.41 ng/L～25.2 ng/L,主要污染因子全氟辛酸（PFOA）质量浓度范围为096 ng/L～13.1 ng/L;降雨过程对大气污染清除作用的统计结果表明,区域大气环境中的主要化学组分及除全氟丁酸（PFBA）之外的PFCs污染主要吸附在云下大气颗粒物上;雨水中各污染因子浓度变化特征及相关性统计结果提示,杭州市大气中PFCAs和PFSAs两类PFCs可能来自不同的污染源。     

江苏省12大湖泊水环境现状与污染控制建议

江苏面积大于50km^2的12个湖泊的水质恶化、面积减少、富营养化、湖泊生态系统退化与湖泊受TP、TN的污染和围湖造田等有关。经济快速发展,第二产业结构偏重,排放污染的总量超过湖泊承载力,湖泊底泥释放N、P及入糊河流携带污染物为造成湖泊环境问题的根本原因。建议调整产业结构,执行严格的排放标准,围绕重点区域、重点行业、重点企业和重点污染源治理,由控制COD为主转为控制COD和N、P并重,引水调控水质,建立湖泊资源数据库和生态系统信息网络,开展湖泊污染物来源分析和富营养化机理研究,开展跨界区域统筹对湖泊综合治理。     

Seasonal variation of polycyclic aromatic hydrocarbons in soil and air of Dalian areas, China: an assessment of soil-air exchange

The seasonal variations of concentrations of PAHs in the soil and the air were measured in urban and rural region of Dalian, China in 2007. In soil, mean concentrations of all PAHs in summer were larger than those in winter, whereas the concentrations of heavier weight PAHs in winter were larger than those in summer. Winter/summer concentration ratios for individual PAHs (R(W/S)) increased with the increase of molecular weight of PAHs in soil, indicating that PAHs with high molecular weight were more easily deposited to soil in winter than summer. In air, mean concentrations of all PAHs in winter were larger than those in summer. In comparison with the R(W/S) in soil, all the values of R(W/S) in air were larger than one indicating that the entire individual PAH concentrations in winter were larger than those in summer. The average concentration composition for each PAH compound in soil and air samples was determined and the seasonal change of PAH profile was very small. It was suggested that PAHs in soils and air had the same or similar sources both in winter and summer. The approach to the soil-air equilibrium was assessed by calculating fugacity quotients between soil and air using the soil and air concentrations. The calculated soil-air fugacity quotients indicated that soil acted as a secondary source to the atmosphere for all lighter weight PAHs (two-three rings) and it will continue to be a sink for heavier weight PAHs (five-six rings) in the Dalian environment, both in winter and summer. Medium weight PAHs (four-five rings) were close to the soil-air equilibrium and the tendency shifted between soil and air when season or function region changed. The fugacity quotients of PAHs in summer (mean temperature 298 K) were larger than those in winter (mean temperature 273 K), indicating a higher tendency in summer than winter for PAHs to move from soil to air. The variation of ambient conditions such as temperature, rainfall, etc. can influence the movement of PAHs between soil and air. Most of the fugacity quotients of PAHs for the urban sites were larger than that for the rural site both in winter and summer. This phenomenon may be related with that the temperatures in urban sites were higher than those in the rural site because of the urban heat island effect.     

液相色谱-质谱法测定土壤中四溴双酚A和六溴环十二烷

文章建立了液相色谱-串联四级杆质谱仪同时测定土壤中四溴双酚A及3种六溴环十二烷同分异构体的分析方法。土壤样品经快速溶剂仪萃取,全自动凝胶净化系统净化后,使用液相色谱-串联四级杆质谱仪,负离子电喷雾多反应监测模式监测,内标法定量分析。结果表明,土壤中四溴双酚A、α-六溴环十二烷、β-六溴环十二烷和γ-六溴环十二烷的检出限为0.1~1.2 pg/g,加标回收率为81.8%~113%,相对标准偏差小于10%。该方法分析时间短,灵敏度高,操作简单,对电子固废拆解场地中的179个土壤样品进行分析,取得满意结果。     

工业类建设项目验收技术规范编制内容探讨

简述了我国建设项目环保验收技术规范颁布实施,以及国外对建设项目实行全过程监管方式现状,指出现行环保验收技术规范在行业性内容、验收监测频次、质量控制措施、总量核算方面存在的问题,提出,应出台总工业类环保验收技术规范,对出台行业类验收技术规范严格把关,并加大验收技术科研力度的建议.     

南京市冬季大气颗粒态汞的分布特征

采集了南京市2012年冬季4个功能区的PM2．5、PM10、TSP样品,对不同粒径大气颗粒物中的颗粒态汞测试。结果表明,南京冬季大气颗粒物TSP中汞的质量浓度为49．26 pg/m3～257．14 pg/m3,平均质量浓度为161．27 pg/m3;PM10中汞的质量浓度为44．82 pg/m3～228．29 pg/m3,平均质量浓度为147．38 pg/m3;PM2．5中汞的质量浓度为35．98 pg/m3～178．58 pg/m3,平均质量浓度为104．10 pg/m3。不同功能区大气颗粒态汞质量浓度的分布趋势为：交通综合区＞旅游区＞住宿综合区＞商业区。大气颗粒态汞60％以上存在于可吸入肺的PM2．5中,细颗粒物富集汞的能力比粗颗粒物强。     

室内空气中的气态多环芳烃的被动采样监测

利用自制被动采样装置,在2011年秋冬季对南京市部分地区室内空气中5种气态多环芳烃(PAHs)(萘、苊烯、苊、芴、菲)进行了为期100d的连续采样检测,被动采样器的采样速率为0.012m3/d,5种PAHs的回收率在63%～105%之间,方法检出限在1.1～2.4ng范围内。结果表明,南京市5处不同室内环境空气中萘的浓度最高,占总量的90%以上。室内环境空气中5种PAHs的总浓度为230～1564ng/m3。住宅内人体对5种PAHs的暴露速率为479～560ng/h。