齐齐哈尔市春季PM2.5中水溶性离子特征分析

2014年4—6月,在齐齐哈尔大学设立采样点,采集PM2.5样品。采用离子色谱法测定其中的主要水溶性无机离子,分析主要组成及污染来源。结果表明,齐齐哈尔市春季PM2.5平均质量浓度为46μg/m3,水溶性无机离子平均质量浓度为20.67μg/m3,占PM2.5质量浓度的42.82%。齐齐哈尔市PM2.5中二次组分主要以酸式硫酸盐形式存在。来源分析发现,PM2.5主要来源于移动源(如汽车尾气)、生物质燃烧及垃圾焚烧、固定源(化石燃料燃烧)、土壤及建筑尘。     

沈阳市城区采暖期PM2.5中水溶性离子的化学特征

2013年11月—2014年3月采暖期在沈阳市沈河区设置采样点采集环境空气中的PM2.5。利用离子色谱法测定PM2.5中水溶性无机离子,分析PM2.5中水溶性无机离子的组成和污染特征等。结果表明,沈阳市冬季采暖期PM2.5平均质量浓度为106μg/m3,PM2.5中总水溶性离子占PM2.5的比例为41.7%,含量较高的二次离子依次为SO2-4、NO-3、NH+4,三者均有较好的相关性,SO2-4以(NH4)2SO4形式存在,采暖期PM2.5偏酸性。     

上海浦东新区城区大气PM2.5中水溶性离子污染特征研究

为研究大气中细颗粒物(PM2.5)在中低浓度水平下的污染特征及来源,于2018-2020年在上海市浦东新区采用在线气体组分及气溶胶监测系统对大气ρ(PM2.5)及其水溶性离子的质量浓度进行了在线连续观测.结果表明,2018-2020年ρ(PM2 5)变化总体均呈现冬季较高,春、秋季其次,夏季较低的特征.PM2.5中水溶...     

南通市冬季PM2.5中水溶性离子污染特征

根据南通市2016和2017年冬季大气多参数站自动监测PM2.5数据和在线离子色谱分析仪Marga监测的PM2.5中水溶性离子数据,分析了南通市冬季PM2.5中水溶性离子污染特征。结果表明,南通市2016和2017年冬季,ρ(PM2.5)分别为58和54μg/m 3,均高出其年均值(14μg/m^3);ρ(水溶性离子)总占ρ(PM2.5)百分比分别为74.5%和74.3%;二次离子ρ(NO3^-、SO4^2-和NH4^+)占ρ(PM2.5)百分比分别为66.8%和66.6%;各水溶性离子占比大小依次为:NO3^-、SO4^2-、NH4^+、Cl^-、K^+、Na^+、Ca^2+、Mg^2+。对ρ(NO3^-)/ρ(SO 4^2-)分析表明,移动源已经成为南通市冬季的主要污染源,且呈逐年增强趋势。对氯氧化率和硫氧化率的分析表明,南通市冬季存在较明显的二次污染,SO2的转化程度大于NO2。除Na^+和Mg^2+外,其他离子与PM2.5均呈显著相关性,NO3^-、SO4^2-与NH4^+之间的相关系数最高,Cl^-与除Na^+外的所有阳离子均呈显著相关性。     

沈阳市大气中PM2.5来源解析研究

通过2015年在沈阳市采集PM2.5样品及源类样品,分析样品的质量浓度和化学组成,用化学质量平衡(CMB)模型对该市PM2.5来源进行解析。结果表明:沈阳市大气中PM2.5浓度时空变化特征明显;各主要源类对沈阳市PM2.5的分担率依次为煤烟尘(28.03%)、二次无机离子(22.63%)、机动车尾气尘(17.27%)、城市扬尘(13.28%)、建筑尘(5.94%)、土壤风沙尘(5.82%)、道路尘(3.04%)、生物质燃烧尘(2.74%)和冶金尘(1.25%)。燃煤和机动车的有效控制既能降低本类源的贡献,也能降低二次无机离子,体现了多源类综合治理原则。     

燃煤工业城市大气细颗粒物中水溶性无机离子的季节变化特征及来源解析——以邯郸市为例

为探究典型燃煤工业城市邯郸市的大气细颗粒物(PM2.5)污染水平及水溶性无机离子特征,于2016年1—12月采集了当地大气PM2.5样品,然后利用离子色谱法测得水溶性无机离子的组分,分析了不同季节水溶性无机离子随PM2.5的浓度变化特征。通过对PM2.5中的阴离子、阳离子进行分析发现,SO4^2-、NO3^-和NH4^+在春夏秋冬四季均为PM2.5中的主要离子成分,SO4^2-、NO3^-和NH4^+的浓度之和在春夏秋冬四季占各季节总的水溶性无机离子浓度的百分比分别为84.6%、77.4%、89.9%、62.5%。其中,在春季和冬季含量最高的3种离子分别是NO3^-、SO4^2-和NH4^+,夏季含量最高的3种离子分别是SO4^2-、NH4^+和NO3^-,而秋季含量最高的3种离子分别是NH4^+、SO4^2-和NO3^-。相关性分析发现,2016年春季、夏季和秋季PM2.5为酸性,冬季为碱性。SO4^2-、NO3^-、NH4^+浓度分析表明,冬季PM2.5中的一次建筑扬尘排放较多。通过主成分分析法得出,PM2.5中水溶性无机离子主要来源于二次转化和生物质燃烧。     

大同市大气颗粒物浓度与水溶性离子季度分布特征

为研究大同市大气颗粒物质量浓度与水溶性离子组成特征,于2013年2、7、9、12月,分别对大同市及其对照点庞泉沟国家大气背景点进行了PM2.5及PM10的采样,通过超声萃取-IC法测定了样品中的9种水溶性离子,结果表明,大同市大气颗粒物污染1、4季度重于2、3季度,PM2.5季度均值全年均未超标,PM10仅第1季度超标1.4倍,污染状况总体良好,PM2.5与PM10相关系数R为0.75,说明大同市颗粒物污染有较为相近的来源,且不同季节均以粗颗粒物为主;大同市PM2.5中水溶性离子浓度分布为SO2-4、NO-3、NH+4Cl-、Ca2+K+、Na+F-、Mg2+,PM10中Ca2+浓度仅次于SO2-4、NO-3,控制扬尘将有效降低PM10的浓度;PM2.5及PM10中的9种水溶性离子在不同季度的浓度与颗粒物浓度分布规律类似,1、4季度较高,2、3季度较低;由阴阳离子平衡计算结果可知,相关性方程的斜率K为1.045,表明大同市大气颗粒物中阳离子相对亏损,大气细粒子组分偏酸性。NO-3与SO2-4浓度比值均小于1,大同市以硫酸型污染为主,大气中的SO2-4主要来源于人类活动排放。     

宁波市PM10、PM2.5中水溶性无机阴离子浓度水平及分布特征

研究了宁波市PM10、PM2.5中无机阴离子浓度水平及分布特征。结果表明,PM10中Cl-为1.00μg/m3,具有较明显的海洋特征,SO24-、NO3-离子浓度为9.90、3.70μg/m3;Cl-主要存在于粒径为2.5-10μm的颗粒物中,而NO3-、SO42-主要存在于PM2.5中,成为PM2.5的重要组成部分。PM10中水溶性无机阴离子季节变化明显,呈冬天高,夏天低的趋势。     

春节期间烟花爆竹燃放对乌鲁木齐市区PM2.5及其组分影响分析

为了解春节期间烟花爆竹燃放对乌鲁木齐市区PM2.5及其组分的影响,利用超级站在线监测仪器(包括颗粒物分析仪、在线离子色谱、激光雷达和重金属分析仪)对环境空气中的PM2.5浓度、颗粒物水溶性离子和重金属浓度进行连续监测.结果表明,大量烟花爆竹的集中燃放造成了PM2.5短时严重污染,最高质量浓度达到了423μg/m3.烟花...     

南通市PM2.5中水溶性离子季节分布特征

对南通市2016年12月-2018年10月大气污染季节分布特征进行了分析。结果表明,南通市ρ(PM2.5)和ρ(水溶性离子)为冬、春季高,夏、秋季低。春夏秋冬四季ρ(水溶性离子)占ρ(PM2.5)百分比分别为68.2%,70.6%,64.5%和74.5%,其中二次离子SNA(NO3-、SO42-和NH4+)占ρ(PM2.5)的百分比分别为63.1%,67.0%,59.3%和66.8%;ρ(NO3-)/ρ(SO42-)表明,移动源已成为南通市春、秋、冬季的主要污染源,四季均存在不同程度的二次转化,且SO2的转化率均大于NO2,NO2冬季转化率最大、夏季最小,SO2夏季转化率最大、秋季最小。南通市NO2转化为硝酸盐的主要形式是气相均相反应,非均相反应和均相反应对SO2转化为硫酸盐的贡献差异不大。     

化工废水中邻苯二甲酸酯的研究

对北京市五个化工厂的废水中8种邻苯二甲酸酯类环境激素进行分析和调查研究.在化工废水中普遍检出的邻苯二甲酸酯有邻苯二甲酸二丁酯(DBP)、邻苯二甲酸二(2-乙基己基)酯(DEHP)、邻苯二甲酸丁基苄基酯(BBP)、邻苯二甲酸二环己酯(DCHP),其中邻苯二甲酸二乙酯(DEP)、邻苯二甲酸二正丙酯(DPrP)、邻苯二甲酸二戊酯(DAP)和邻苯二甲酸二正己酯(DHP)4种物质未检出.废水中DEHP和DBP的浓度均低于排放标准.     

Flame ionization gas chromatographic determination of phthalate esters in water, surface sediments and fish species in the Ogun river catchments, Ketu, Lagos, Nigeria

The detection and quantification of four phthalate esters??dimethyl phthalate (DMP), diethyl phthalate (DEP), dibutyl phthalate (DBP), and diethylhexyl phthalate (DEHP)??in water, sediment, and some fish species were carried out using flame ionization gas chromatography. The samples were collected from the Ogun river catchments, Ketu, Lagos. The DMP was not detected in the water and fish samples but was detected in sediments collected from four of the six sampling sites. The concentration of DEP, DBP, and DEHP in the fish species ranged from 320.0?C810.0, 380.0?C1,080.0, and 40.0?C150.0 ??g/kg in Tilapia sp.; 310.0?C860.0, 400.0?C1,170.0, and 40.0?C110.0 ??g/kg in Chrysichthys sp.; and 320.0?C810.0, 400.0?C3,970.0, and 30.0?C300.0 ??g/kg (DEHP) in Synodontis sp., respectively. The differences in fish phthalate levels are not statistically significant at p?<?0.05, an indication that phthalate esters accumulation is not fish species dependent. The DEP, DBP, and DEHP values recorded are considerably higher than the maximum allowed concentrations for drinking water prescribed by the US Environmental Protection Agency. The phthalate pollution index and biosediment accumulation factor values were also calculated.     

Phthalate levels in Norwegian indoor air related to particle size fraction

Phthalates are found in numerous consumer products, including interior materials like polyvinyl chloride (PVC). Several studies have identified phthalates in indoor air. A recent case-control study demonstrated associations between allergic symptoms in children and the concentration of phthalates in dust collected from their homes. Here we have analyzed the content of selected phthalates in particulate matter (PM): PM(10) and PM(2.5) filter samples collected in 14 different indoor environments. The results showed the presence of the phthalates di-n-butyl phthalate (DBP), butyl benzyl phthalate (BBP), dicyclohexyl phthalate (DCHP) and diethyl hexyl phthalate (DEHP) in the samples. The dominating phthalate in both PM(10) and PM(2.5) samples from all locations was DBP. More than a 10-fold variation in the mean concentration of total phthalates between sampling sites was observed. The highest levels of total phthalates were detected in one children's room, one kindergarten, in two primary schools, and in a computer room. The relative contribution of total phthalates in PM(10) and PM(2.5) was 1.1 +/- 0.3% for both size fractions. The contribution of total phthalates in PM(2.5) to total phthalates in PM(10) ranged from 23-81%, suggesting different sources. Of the phthalates that were analyzed in the PM material, DBP was found to be the major phthalate in rubber from car tyres. However, our analyses indicate that tyre wear was of minor importance for indoor levels of both DBP as well as total phthalates. Overall, these results support the notion that inhalation of indoor PM contributes to the total phthalate exposure.     

大中型商场PM10、PM2.5污染水平与来源分析

利用便携式气溶胶监测仪,对平顶山市区的中原商场、商业大楼、食品城总店三家大型商场不同楼层空气PM10和PM2.5进行了现场测定。结果显示,平顶山市大中型商场可吸入颗粒物污染严重,PM10、PM2.5污染平均超标率分别为13.7%和48.0%;PM10、PM2.5的质量浓度在时间和空间分布上存在很大差异;PM10中PM2.5所占比例为83%。     

重庆典型岩溶区地下河水体PAEs分布特征研究

分别采集了重庆典型岩溶区5条地下河水体10个样品,用气相色谱法对样品中的邻苯二甲酸酯类(PAEs)含量进行测定,分析其在重庆典型岩溶区地下河水体中的分布特征。结果表明,常见的19种邻苯二甲酸酯类(PAEs)在重庆典型岩溶区地下河水体中均有检出,其浓度范围为103.29~2268.78μg/L;5种被美国环保局列为优先控制的PAEs类污染物中,邻苯二甲酸二丁酯(DBP)和邻苯二甲酸双(2-乙基己基)酯是主要的污染物;与国内外其他地区水体进行比较,重庆典型岩溶区地下河水体PAEs含量处于较高污染水平。     

以长春为例研究环境空气中TSP、PM_(10)和PM_(2.5)的相关性

选取长春市解放大路与人民大街的交叉口为研究地点,分别进行TSP、PM10和PM2.5的采样和分析.然后利用相关系敷法和t检验对测定结果进行相关性分析,得到备元素的含量在三种污染物中的相关系敖:在TSP与PM10中为0.9349;在PM2.5与PM10中为0.8797;在TSP与PM2.5中为0.7824.得到各元素含量在三种污染物中的T检验统计值,在TSP与PM10中为0.90103;在PM2.5与PM10中为0.04745;在TSP与PM2.5中为0.047986.从分析结果可以看出,各元素含量在TSP与PM10中的相关性最好,在PM2.5与PM10中次之,研究结果为相关环境管理提供科学依据.     

Distributions of phthalic esters carried by total suspended particulates in Nanjing, China

Atmospheric trace phthalic esters (PAEs) carried by total suspended particulates were systematically investigated. A total of 450 air samples were collected at six typical locations and three specific micro-environmental sites (a stadium with a new plastic track, new cars, and a farming greenhouse with plastic film) in Nanjing metropolitan area of China from April 2009 to January 2010. The samples were analyzed by high-performance liquid chromatography and ultraviolet detection. The results are summarized as follows: (1) The dominant PAEs are dimethyl phthalate (DMP), dibutyl phthalate (DBP), and diethylhexyl phthalate (DEHP), which were found in the atmosphere of Nanjing. The average concentrations of DMP, DBP, and DEHP were 10.5?±?1.2, 62.3?±?4.5, and 33.3?±?2.5?ng?m(-3), respectively, constituting 9.9%, 58.7%, and 31.4% of total PAEs (106?±?8.2?ng?m(-3)). (2) The dynamic variations of atmospheric PAEs in the three specific micro-environmental sites showed that the PAE concentrations in the stadium with a new plastic track reduced to normal after 1?month remediation, while new cars need 6?months to remove their effect. The levels of PAEs in a farming greenhouse with plastic film were relatively high, but little PAEs accumulated in vegetables. (3) The vertical profiles from 1.5 to 40?m above ground display some fluctuations in PAE concentration, but no significant height dependence. This information will make a valuable contribution to the examination of the influence of atmospheric PAEs on the environment and human health.     

Phthalates removal efficiency in different wastewater treatment technology in the Eastern Cape,South Africa

The removal capacity of different wastewater treatment plant (WWTP) technologies adopted in rural areas for phthalate was investigated in the Eastern Cape, South Africa. Wastewater samples collected from three selected WWTPs which use activated sludge (AS), trickling filter (TF), and oxidation pond (OP) technology were extracted using the solid-phase extraction method followed by gas chromatography-mass spectrometry (GC-MS) analysis. The six selected phthalate esters (PAEs) dimethyl phthalate (DMP), diethyl phthalate (DEP), di-n-butyl phthalate (DBP), benzyl butyl phthalate (BBP), di(2-ethyl hexyl) phthalate (DEHP), and di-n-octyl phthalate (DOP) were detected in all the samples collected from the WWTPs. DBP was the most abundant compound in the influent, effluent, and sludge samples with a maximum detection of 2497 μgL^?1, 24.2 μgL^?1, and 1249 μg/g dW, respectively, followed by DEHP and BBP. There was a relatively high removal capacity achieved by AS in Alice, TF in Berlin, and OP in Bedford with a removal efficiency that varied between 77 and 99%, 76 and 98%, and 61 and 98%, respectively. A high significant correlation of PAE removal with total suspended solids (TSS) and turbidity suggests that the removal performance proceeded more through adsorption on settling particles and sludge than on biodegradation. However, the concentrations of PAEs detected in the final effluent and sludge samples exceeded acceptable levels allowed internationally for a safe aquatic environment. AS may have exhibited a more stable and better performance across the different seasons; however, pollution source control still deserves a special attention to prevent the risk posed by these micropollutants.     

Survey of Levels of Phthalate Ester Plasticizers in a Sewage Lagoon Effluent and a Receiving Stream

In this study, samples from a sewage treatment lagoon and those from a receiving stream were analyzed for their phthalate esters content. Knowledge of the distribution of ubiquitous phthalate esters in the sewage lagoon and the receiving stream was necessary because of the reports of their subtle toxicity to aquatic biota and humans. Liquid–liquid extraction, Clean-up experiment and High Performance Liquid Chromatography (HPLC) were the methods employed for the quantitative determination of the Phthalates. A study of uncontaminated water was done to establish blank levels. The sewage lagoon and the receiving stream were grossly polluted as several phthalate ester plasticizers: DMP, DEP, DPhP, DBP, DEHP, DOP and DINP were found present at monthly mean levels of between 24.02 mg/L and 139.25 mg/L in the sewage treatment lagoon and 10.41 mg/L and 80.53 mg/L in the receiving stream. The results showed higher levels of phthalate esters in the sewage lagoon compared to the receiving stream. The sewage lagoon was identified as a pollution point source into the receiving stream. Levels of phthalates obtained from the receiving stream are much higher than the water criteria of 3 μg/L phthalates recommended by the United States Environmental Protection Agency (USEPA) for the protection of fish and other aquatic life in water and the Suggested No-Adverse Effect Levels (SNAEL) of 7.5–38.5 μg/L for drinking water. This should give cause for great environmental concern. Peoples’ health downstream is at stake and so is the ‘health’ of the ecosystem.     

垃圾渗滤液中DEHP与DBP的迁移演化规律研究

采用一维土柱下渗实验和垂向入渗模型相结合的方式，研究垃圾渗滤液中邻苯二甲酸二乙基己基酯（DEHP）和邻苯二甲酸二正丁酯（DBP）在土壤中的垂向迁移演化规律。结果表明：原状土和混有石英砂土的土柱对DBP的吸附能力均强于DEHP，而混有石英砂的土柱中DEHP、DBP均出现不同程度的穿透现象，且DEHP的穿透速度比DBP要快2倍；做或不做防渗处理，DEHP和DBP渗出量均呈前期快速增长而后期归于稳定的趋势，防渗对DBP效果较DEHP好；垂向入渗模型与一维土柱实验结果一致，该模型可用于其他区域有机污染物在土壤中垂向迁移的研究。