聊城市春季交通源大气污染特征分析

为研究交通源空气污染状况，通过采用自动监测系统，于2009年春季期间，对在聊城市主干道附近布设的6个监测点的空气质量进行监测，获得了其空气污染物浓度特征：（1）所有监测点SO2、NOx日均值与O3小时均值均未超标，且O3污染指数很低，表明二次污染甚微；（2）CO是首要污染物，PM10次之，两者日均值超标率均为100％。分析了超标污染物与交通流量的关系，结果表明，PM10浓度与交通量有较高的线性相关性，而CO浓度与交通流量无显著相关性。     

上海市典型综合型地下空间空气污染特征分析

对上海市某综合型城市地下空间空气进行采样、监测,得到CO 2、TVOC、甲醛、微生物、PM 10、PM 2.5等6类污染物的特征分布,基于国内外不同的空气质量标准作分析比较。结果表明,该典型综合型地下空间的空气污染情况较普遍,其中甲醛、TVOC污染较为突出,平均浓度超标倍数分别为1.056倍、3.755倍;共发现9种潜在致病菌属,占总数的0.893%。地下空间污染物的累积与内部建筑的设计、装修、功能属性、空调系统等众多因素有关。     

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。     

杭州市大气污染物排放清单及特征

以杭州市区为研究区域,通过调查整合多套污染源数据库及其他统计资料,研究文献报道及模型计算的各种污染源排放因子,获得杭州市区各行业PM10、PM2.5、SO2、NOx、CO、VOCs、NH3等污染物的排放量,建立了杭州市区2010年1 km×1 km大气污染物排放清单。结果表明,2010年杭州市区PM10、PM2.5、SO2、NOx、CO、VOCs和NH3的排放总量分别为7.96×104、4.02×104、7.23×104、8.98×104、73.90×104、39.56×104、3.32×104t。从排放源的行业分布来看,机动车尾气排放是杭州市区大气污染物最重要排放源之一,对PM10、PM2.5、NOx、CO和VOCs的贡献分别达到14.4%、27.1%、40.3%、21.4%、31.1%。道路扬尘、电厂锅炉、工业炉窑、植被、畜禽养殖对不同污染物分别有着重要贡献,道路扬尘对PM10和PM2.5的贡献分别为44.6%和20.0%、电厂锅炉对SO2和NOx的贡献分别为37.0%和25.7%、工业炉窑对CO的贡献为41.5%、植被排放对VOCs的贡献为27.1%、畜禽养殖对NH3的贡献为76.5%。从空间分布来看,萧山区和余杭区对SO2、NH3和植被排放BVOC的贡献要显著高于主城区;而主城区机动车对PM2.5、NOx和VOCs的贡献分别达到36.3%、56.0%和47.4%,较市区范围内显著增加,表明机动车尾气排放已成为杭州主城区大气污染最重要的来源之一。     

新的污染物环境危害评价指标——超标强度

污染物的危害程度不仅与超标率和超标倍数有关,而且与污染物超标持续时间有关。同样高的污染物浓度,如果其持续时间长短不同,其对环境的生态效应是不同的。为此,在充分分析超标率、超标倍数所存在缺陷的基础上,通过实例分析对比,以直观图解的方式提出了一套新的污染物环境危害评价指标体系——超标强度指标体系。超标强度指标体系中涉及的主要概念和指标有标准面积、超标面积、超标持续时间、超标强度和综合超标强度。在阐述了各指标的概念含义和计算方法后,以同一组监测数据为例,用超标率和超标倍数与超标强度指标进行了对比评价。结果表明,用超标强度及其指标体系可以科学、准确区分和评判超标率、超标倍数指标体系所不能区分和评判的真实存在的客观事实,而且非常精确地给出了污染物超标持续时间。超标强度指标所涵盖的内容比超标率和超标倍数更丰富,评价的结果更准确,所反映的生态环境质量状况更客观准确、科学真实。超标持续时间表明了污染物超标状态的持续时间。     

环境空气质量综合指数计算方法比选研究

环境空气质量综合指数是进行逐月城市环境空气质量比较和排序的重要方法,提出了4种涵盖SO2、NO2、PM10、PM2.5、CO、O3等6项污染物的综合指数计算方法,基于2013年74个城市逐月污染物浓度数据使用主成分分析方法进行了对比分析。结果表明,综合指数计算方法中污染物统计指标和标准化方法不同对于主要污染物的判定有重要影响,各种计算方法中PM2.5、PM10、O3是出现频率最多的主要污染物;除O3外其他5项污染物逐月统计指标间均有极显著的正相关性,冬季O3统计指标与SO2、NO2、PM10、PM2.5呈显著负相关,夏季则呈显著正相关;主成分分析结果表明,在去除冗余信息后,PM2.5、PM10的权重被相对削弱,SO2、NO2、CO的权重得到相对强化,O3的权重夏季得到强化、冬季被削弱;综合考虑不同方案下主要污染物频率分布情况和PM2.5、PM10、O3权重变化特征,建议计算逐月环境空气质量综合指数时,SO2、NO2、PM10、PM2.5宜以月均值除以年均值标准进行标准化,CO、O3宜以特定百分位数浓度除以日均值标准(或8 h均值标准)进行标准化;该方法可延伸到季、半年和年度的环境空气质量综合指数计算。     

绍兴市新装修住房空气质量调查与分析

为了解室内装修对室内空气质量的影响,文章随机抽取浙江省绍兴市60户新装修居室进行室内空气主要污染物监测,结果表明,以甲醛和总挥发性有机物(TVOC)超标最为严重,超标率分别为32.2%和65.6%。不同功能房间中,卧室、书房甲醛和总挥发性有机物浓度明显高于客厅。另外,总挥发性有机物与装修后时间长短有很大关系,装修后3个月时,超标率为98.3%,6个月超标率为75.0%,12个月超标率降低到23.3%。     

室内甲醛污染及对人体健康的影响

通过对三种不同类型居室内甲醛监测表明,甲醛浓度与室内装饰、吸烟和燃料的不完全燃烧有关.兰州地区夏季室内甲醛超标率高,为41.0％～51.3％.室内主要污染物除TSP以外,甲醛居第2位,且一天中浓度最高值在中午.新建居室比普通居室甲醛浓度高,在所有情况下,室内浓度高于室外.     

太原市2013年环境空气质量变化特征分析

为全面了解太原市的环境空气质量状况及污染物的时间变化规律,本文选取太原市8个站点2013年1月至12月六种主要污染物(SO2、NO2、PM10、CO、O3、PM2.5)为期一年的监测数据,评价该市2013年环境空气质量的总体情况,研究各污染物在不同时间尺度的变化特征及相互之间的关系。结果表明,2013年太原市环境空气质量以良和轻度污染为主,首要污染物主要为PM2.5和PM10;SO2、NO2、PM10、CO和PM2.5的小时变化规律较为一致,都呈现"双峰型"的变化特征,O3则呈显著的"单峰型"变化规律;上述六种污染物具有明显的季节变化特征,SO2的浓度峰值主要集中在供暖期,NO2和O3—8h浓度在夏季要高于其他季节,PM10的浓度峰值出现在春季(3月)和秋季(10月),CO的浓度峰值集中在11月和12月,PM2.5的浓度峰值主要集中在冬季;相关性分析结果表明,SO2、NO2、PM10、CO、PM2.5浓度日均值在全年各时段均具有很好的正相关性,化石燃料的燃烧可能是上述污染物质的共同来源。     

室内环境空气污染调查

论述了室内空气污染的主要原因。主要污染物及其危害。并对室内空气污染现状进行了调查。结果显示住宅中甲醛超标率在33.3%-100%之间，甲醛最高超标10.9倍；总挥发性有机物（TVOC）超标率在55.6%-75.0%之间，最高超标24.0倍；氨超标率在33.3%-41.7%之间，最高超标5.1倍；氡未见超标，同时，对室内空气污染提出了具体防治措施。     

兰州市冬季和春季PM2.5金属元素浓度水平与分布

为了解兰州市大气PM2.5中金属元素的污染水平和分布,于2013年冬季和春季在兰州市区4个在线监测点进行PM2.5样品采集,利用ICP-MS分析金属元素浓度。结果表明,Pb、B元素含量高于200 ng/m3,V、Fe元素含量在100~200 ng/m3,其余元素含量低于100 ng/m3,其中Pb含量最高,平均含量达到373.8 ng/m3.各监测点元素含量在冬季和春季各有不同,整体上是冬季高于春季。金属元素在兰州市区的空间分布与兰州市工业排放和气象因素有关,工业排放为主导因素。     

Long-term changes in acidity and DOC in throughfall and soil water in Finnish forests

The main objective of this study was to examine if any detectable trends in dissolved organic carbon (DOC), sulphate (SO₄-S) concentrations and acid neutralizing capacity (ANC) in throughfall (TF) and soil water (SW) could be found during 1990–2010 and to relate them to recent changes in decreased acid deposition. The study was conducted in seven boreal coniferous forest sites: four of which are managed and three unmanaged forests sites. Generally, temporal trend showed a significant decrease in SO₄-S concentrations in bulk precipitation (BP), TF and SW. At some of the sites, there was an increasing tendency in BP and TF in the DOC concentrations. This feature coincides with decreasing SO₄-S concentration, indicating that SO₄-S may be an important driver of DOC release from the canopy. However, a slightly increased temperature, larger senescing needle mass and consequently increased decaying activity in the canopy may partly explain the increasing trend in DOC. In SW, no consistent DOC trend was seen. At some sites, the decreased base cation concentrations mostly account for the decrease in the ANC values in SW and TF.     

太原市冬、夏季醛酮化合物污染特征及来源分析

针对太原市空气臭氧污染较为严重的问题,开展臭氧主要前体物醛酮化合物质量浓度及其变化规律研究.利用2,4-二硝基苯肼固相吸附/高效液相色谱方法,通过对太原市2019年冬季和夏季大气的醛酮化合物进行分析,发现太原市冬季总醛酮化合物的平均质量浓度为13μg/m3,低于夏季的27μg/m3.其中甲醛、乙醛和丙酮质量浓度最高,且...     

Pesticides and Nitrate in Groundwater and Rainwater in the Province of Limburg in The Netherlands

The purpose of this study was to investigate the occurrence ofhigh levels of pesticides in groundwater and rainwater in TheProvince of Limburg in The Netherlands. In groundwater samplesin particular the presence of triazines – atrazine, simazine and propazine – was observed; besides these pesticides, dieldrin has also been observed. Atrazine and simazine were found to exceed the groundwater standard of 100 ng L^-1. In the rainwater samples, the presence of 13 of 23 different analyzed pesticides was observed. A number of pesticides werefound in high concentrations; e.g. atrazine (>200 ng L^-1). Two pesticides detected in rainwater (+-HCH and atrazine) were found to exceed the groundwater standard. Seven pesticides in rainwater were found to exceed the target value and three pesticides the maximum tolerable risk value (DDT, heptachlor and heptachlorepoxide A), which are used as ecotoxicological standards in The Netherlands.Nitrate in 15 of 16 analyzed natural springs was found toexceed the guideline value for nitrate in drinking waterof 50 mg L^-1, up to levels of about 200 mg L^-1. Nitrate concentrations in rainwater samples were observed up to 4.5 mg L^-1. A risk analysis of exposure to high pesticide levels in groundwater or rainwater has been performed using the model HESP. For atrazine levels due todeposition of rainwater in two different locations, exceedance of the T.D.I. level of 0.5 g kg^-1 day^-1 based on WHO criteria was observed for children using both an urban and a rural scenario and use of groundwater as drinking water.     

Organochlorine insecticide residues in drinking and ground water in and around Delhi

A multiresidue method was developed for the estimation of 15organochlorine pesticides in water. 50 samples of drinking watersupplied by the Municipal Corporation to the residential areasof Delhi and 20 ground water samples from nearby villages usedfor irrigation were monitored for the presence of organochlorineinsecticides by the method developed. Although, organochlorinepesticides were detected in the ground water and irrigationwater samples, the levels of pesticides were below the MaximumContaminant Level as prescribed by WHO. No organochlorineinsecticides were detected in any of the drinking water samples.     

郑州大气及颗粒物中多环芳烃的分布特征与来源解析

对2012年郑州市大气中气态和颗粒态多环芳烃(PAHs)的分布特征与来源进行了分析。结果表明,ρ(∑PAHs)(包括气相与颗粒相)为23.27~194.61 ng/m3,气相中∑PAHs高于颗粒相,四环以下的PAHs大都存在于气态中;在夏、春2季,较小分子质量(≤178)的PAHs占比较高,冬季,较大分子质量(≥252)的PAHs占比明显较高;各功能区ρ(PAHs)排序为工业区交通密集区医疗、文化、行政混合区。郑州大气和颗粒物中PAHs可能主要来自煤和液体燃料(汽油柴油)的燃烧。     

宽甸土壤及部分农作物中硼的分布及污染分析

用ICP-MS测定了辽宁宽甸23个土壤样品中的硼。背景地区和污染地区的土壤硼含量分别在 39.2～82.4mg/kg和133～1195mg/kg之间。其中硼矿开采区的土壤硼含量高达1195mg/kg。还用同样的方法分析了背景地区和污染地区几种农作物中硼的含量,结果表明,背景地区的大豆、土豆、玉米和豆角的硼含量(干基)分别为:37.4～47.9、5.8～6.3、24.4～25.5和1.24～2.74mg/kg,而污染地区相应农作物的硼含量分别为:34.0、12.0～12.8、40.7和2.48～2.64mg/kg。     

DDT residue in soil and water in and around abandoned DDT manufacturing factory

Dichlorodiphenyltrichloroethane (DDT) belongs to one of the most hazardous groups of chemicals called persistent organic pollutants. Many organochlorine pesticides including p,p(')-DDT are long lasting due to their non-degradability can travel to distant places and being fat soluble can accumulate in animals and human bodies. Due to the persistent nature of p,p(')-DDT, its adverse environmental and health impacts, the present study was undertaken to examine the residual p,p(')-DDT in and around abandoned p,p(')-DDT manufacturing factory in Amman Gharh, Nowshera, NWFP. Samples of soil, sediments and water were collected in and around the factory area, nearby p,p(')-DDT stores, main factory drain leading to river Kabul and nearby villages. Standard procedures were used for the collection, transportation and storage of samples for analyses. Extraction of each sample for p,p(')-DDT analyses was carried out in triplicates using Soxhelt extraction. p,p(')-DDT contents in the samples were analyzed by capillary GC with electron capture detector. Most of the samples collected up to half kilometer distance from the site of the DDT factory were found contaminated. Further the level of p,p(')-DDT decreased with increasing depth from top to bottom and with distance from the site. The results indicate that there is no immediate threat to underground water reservoirs.     

大同市地表水及工业废水中氯苯和酚类化合物的监测

对流经大同市的主要河流和重点工业污染源所排放废水中的氯苯和酚类化合物做了分析测定.对酚类化合物的测定方法进行了改进.研究表明,大同市污染源对御河氯苯类污染物贡献较小,焦化厂酚类化合物排放量较高.