焦作市大气污染物特征和相关性分析

为研究焦作市大气污染特征及其相关性,对2015—2017年焦作市4个国控空气监测点位的监测数据进行统计分析。结果表明:2015—2017年城区环境空气污染SO_2、NO_2、CO、PM_(10)、PM_(2.5)浓度均呈逐年下降趋势;大气污染浓度季节变化特征明显,PM_(10)、PM_(2.5)、SO_2、NO_2、CO的浓度均为冬季最高、夏季最低,空气质量指数也在冬季达到最高值; O_3浓度则为夏季最高、冬季最低。2017年焦作市沙尘天气共计36 d,严重影响了环境空气中颗粒物的浓度。由PM_(2.5)与PM_(10)的比值说明大气颗粒物污染以PM_(2.5)为主。通过SPSS软件分析,SO_2、NO_2、CO、PM_(10)、PM_(2.5)浓度间呈两两正相关,O_3浓度与NO_2、CO呈负相关。     

无锡市区大气污染物状况及变化趋势分析

使用2012—2015年无锡市区的6种大气污染物监测数据,对无锡市区各污染物的年度变化、空间分布、影响因素进行了分析。结果表明:(1)2012—2015年无锡市区SO_2、O_3质量浓度呈下降趋势,且趋势显著;NO_2质量浓度呈下降趋势,但不明显;CO、PM_(10)、PM_(2.5)的质量浓度年际变化比较平稳。(2)无锡市区SO_2、NO_2、PM_(10)、PM_(2.5)、CO的空气质量分指数(IAQI)均为冬季最高、夏季最低;O_3的IAQI则为夏季最高、冬季最低。(3)SO_2、NO_2、PM_(10)、PM_(2.5)、CO浓度间呈两两正相关,且相关性极显著;O_3浓度与NO_2、CO呈显著负相关,与SO_2、PM_(10)、PM_(2.5)浓度之间没有明显的关联。(4)分析了无锡市区各项大气污染物浓度的空间分布特征。(5)SO_2、NO_2、PM_(10)浓度周内变化具有"周末效应"的特征,而O_3、CO和PM_(2.5)浓度周内变化出现"反周末效应"。     

不同季节常州市气团来源差异性研究

利用NCEP全球再分析资料和HYSPLIT4模式,计算了2014年常州市不同季节的气流后向轨迹。结合聚类分析方法和常州市PM_(2.5)、PM_(10)、SO_2、NO_2和O_3监测数据,分析了各季节不同类型气团来源对各污染物浓度的影响。结果表明,常州市的气团来源具有明显的季节性特征,春季以东北偏东方向的气团为主,西南气流对应的PM_(2.5)和PM_(10)平均值较高,分别为93和157μg/m3;夏季受海洋型气团影响为主,东南气团对应的O_3平均值较高,为90μg/m3。秋季西北气流增多,其对应的PM_(2.5)和PM_(10)平均值较高,分别为71和107μg/m3,东南气团对应的SO_2和NO_2平均值较高,分别为40和43μg/m3;冬季受大陆型气团影响更显著,京津冀等北方气团和杭州湾方向的南面气团对应的PM_(2.5)和PM_(10)值较高,分别在100和150μg/m3以上。冬季随着空气污染加重,本地和本区域的气团逐渐占主导地位,说明加强长三角区域内的污染物协同管控,对于改善空气质量会具有明显的效果。     

北京地区不同季节PM2.5和PM10浓度对地面气象因素的响应

利用2013年1月—2014年12月北京地区PM_(2.5)和PM_(10)监测数据和同期近地面气象观测数据,采用非参数分析法(Spearman秩相关系数)研究了北京地区PM_(2.5)和PM_(10)的浓度对不同季节地面气象因素的响应。结果表明:北京地区大气颗粒物浓度水平具有明显的季节特征,冬季大气颗粒物污染最严重,夏季最轻。不同季节影响颗粒物浓度水平的气象因素各不相同,其中风速和日照时数为主要影响因素。PM_(2.5)和PM_(10)质量浓度对气象因素变化的响应程度也有较大区别,PM_(2.5)/PM_(10)比值冬季最高,PM_(2.5)影响最大,春季最低,PM_(10)影响最大。这些结论可对制订科学有效的大气污染控制策略提供参考。     

衡阳城区冬季PM2.5中水溶性离子污染特征

为探究衡阳冬季PM_(2.5)和水溶性离子污染特征及其来源,于2019年1月在衡阳市城区采集大气PM_(2.5)样品,使用重量法和离子色谱法测得PM_(2.5)和水溶性离子组分质量浓度,并分析其浓度特征、酸碱度和来源等问题。结果表明:采样期间衡阳大气PM_(2.5)平均质量浓度为94.25μg/m~3,总水溶性离子质量浓度为52.94μg/m~3,占PM_(2.5)总质量浓度的56.43%;阴阳离子当量之比为1.12,PM_(2.5)呈酸性,其中SNA(SO_4~(2-)、NO_3~-和NH_4~+)占总水溶性离子质量浓度的95.06%。污染期间二次转化明显,SNA主要以(NH_4)_2SO_4和NH_4NO_3形式存在。源解析发现大气PM_(2.5)受化石燃料和生物质燃烧、垃圾焚烧、建筑扬尘、气态前体物二次转化、外来输送等多重因素影响,其中机动车尾气排放的NO_x在大气中二次转化形成的硝酸盐是衡阳重污染的最主要原因。     

传感技术在环境空气监测中的方法适用性研究

采用某品牌3台传感器,对环境空气中气态污染物(NO_2、SO_2、O_3、CO)和颗粒物(PM_(10)、PM_(2.5))进行为期1个月的连续监测,探讨传感技术在环境空气监测中的方法适用性。研究表明,3台传感器监测的各污染物质量浓度均显著相关,Pearson相关系数0.9(p0.01);监测的颗粒物与国控点数据显著相关且质量浓度水平接近,Pearson相关系数0.9(p0.01);PM_(2.5)传感器测定值相对于国控点数据的平均相对误差仅为-7.3%,均值绝对误差2μg/m~3;传感器在高湿度下的PM_(2.5)测定值与国控点数据相吻合,当相对湿度为80%～90%时,平均相对误差仅为-0.9%;传感器气态污染物测定值与国控点数据之间存在差异,电化学原理气态污染物传感器性能仍有待提升。     

崇明岛PM2.5中硫酸根、硝酸根及其前体物变化特征及来源

2016年8月1日—2017年7月31日在上海市崇明岛森林公园空气质量观测站进行了为期1年的大气气体污染物、PM_(2.5)水溶性成分在线监测。各项常规大气污染物在该站浓度均较低,但污染物极值较高,说明崇明地区仍有显著的区域污染现象。PM_(2.5)中硝酸根平均浓度(10. 0μg/m~3)高于硫酸根(6. 8μg/m~3),2种成分均在冬季出现最高值。崇明地区PM_(2.5)污染中污染物区域传输是主要贡献因子,但夏季硫酸根二次生成较为明显。风速风向及后向气流轨迹分析表明,南通工业区及城区是崇明地区PM_(2.5)二次无机成分气态前体物的重要贡献来源,而来自山东中部、江苏北部及长三角苏锡常地区的污染传输过程亦对硫酸根、硝酸根浓度有显著贡献。     

重庆市主城区二次有机碳气溶胶污染特征研究

为研究重庆市大气PM_(2.5)中二次有机气溶胶污染特征,于2013年1—12月运用URG-3000ABC型中流量颗粒物采样仪连续同步采集重庆市主城区大气PM_(2.5)样品,选取OC/EC比值对PM_(2.5)中的SOC污染进行估算,结果表明,该市主城区PM_(2.5)中SOC年平均质量浓度为12.5μg/m3,占OC质量浓度的50.0%,占PM_(2.5)质量浓度的10.1%,SOC质量浓度为冬季秋季夏季春季。机动车排放是SOC前体物的主要来源。     

沿海城市PM10和PM2.5自动监测过程中质量浓度“倒挂”现象分析与成因探讨

2020年2—3月,位于福建沿海地区中部的莆田市在环境空气质量自动监测过程中出现了严重的PM_(10)和PM_(2.5)质量浓度"倒挂"现象,小时值"倒挂"率为19.86%,日均值"倒挂"率为16.67%。在高相对湿度和低风速气象条件下,颗粒物会出现严重的"倒挂"现象,"倒挂"过程中常伴随着颗粒物和气态污染物(SO_2、NO_2和CO)质量浓度的增加。因此,于2020年2月16日—3月26日开展了颗粒物自动监测和手工监测比对,并结合气象参数、气态污染物质量浓度,以及PM_(10)和PM_(2.5)中水溶性离子和液态水的含量特征,进一步探讨了莆田市颗粒物质量浓度"倒挂"的主要成因。研究表明,PM_(10)和PM_(2.5)自动监测仪器检测原理的差异是导致颗粒物质量浓度"倒挂"的重要原因之一,而气象条件(相对湿度、气温和风速等)、颗粒物质量浓度、颗粒物中主要吸湿组分(NO_3~-、SO_4~(2-)和NH_4~+)和液态水的含量也是颗粒物质量浓度"倒挂"的主要影响因素。莆田市2020年2—3月出现高频率"倒挂"现象是多重因素共同作用的结果,解决该问题需要同时考虑监测仪器检测原理、气象参数、颗粒物质量浓度和吸湿组分等的影响。     

兰州城市大气中PM_(1.0)污染特征研究

运用不同类型的PM_(1.0)自动监测仪,于2017年11月至2018年11月对兰州城市大气PM_(1.0)开展了为期一年的观测,分析了兰州PM_(1.0)污染特征及来源,以及气象条件和SO_2、NO_2等污染物对PM_(1.0)浓度特征的影响,重点分析了重污染天气过程PM_(1.0)的演变情况。结果表明:研究期内,兰州城市PM_(1.0)日均最大浓度为117.5μg/m~3,最小浓度为8.3μg/m~3,平均浓度为33.7μg/m~3;4个季节的PM_(1.0)平均浓度排序为冬季秋季春季夏季,冬季PM_(2.5)中PM_(1.0)的占比超过70%。从全年来看,PM_(1.0)主要来源于内蒙古西北部地区污染气团输入。PM_(2.5)与PM_(1.0)的来源区域具有一致性,但PM_(1.0)的来源范围更广泛,而PM_(2.5)的来源更集中。重污染阶段,PM_(1.0)与PM_(2.5)、PM_(10)污染演变趋势呈现负相关,PM_(2.5)与PM_(10)呈现正相关,且秋冬季PM_(1.0)和PM_(2.5)的潜在污染来源距离兰州较近,范围更集中。     

北京市大气气态汞变化特征

采用Tekran 2537X大气汞分析仪在线测量北京市城区大气中气态元素汞(GEM,简称大气汞) 浓度,研究大气汞浓度随不同气象条件的变化特征。通过分析2016年10月—2017年9月大气汞监测数据发现,该监测点全年大气汞浓度为0.48～16.25 ng/m³,均值为(3.41±1.79)ng/m³。春季、夏季、秋季和冬季大气汞浓度均值依次为2.93 、2.95、4.27、3.37 ng/m³,其中,秋季大气汞浓度明显高于其他季节 。秋季大气汞浓度显著偏高可能由不利的大气扩散条件导致。大气汞夜间浓度显著高于白天浓度。同时,将大气汞与SO₂、CO及PM_2.5进行相关性分析,发现大气汞浓度变化趋势与SO₂、CO和PM_2.5呈显著正相关。结合风向和风速进行污染来源分析,得到该点位大气汞在西南和东北方向上受人为排放源影响较大。污染源类型分析表明,冬季大气汞与CO同源性强,主要来自本地供暖用煤。     

不同模式版本对长三角区域大气污染物模拟结果对比评估

选取2015年1、4、7、10月(分别代表冬、春、夏、秋4季),应用CMAQv4.7.1和CMAQv5.1模式模拟长三角区域的空气质量,对比了NO2、SO2、O3、PM2.54个常规污染物的模拟结果,表明CMAQv5.1对NO2、SO2和PM2.5的模拟效果优于CMAQv4.7.1,而CMAQv4.7.1的O3模拟效果优于CMAQv5.1;CMAQv5.1的NO2模拟值更接近地面观测值,比起不同版本的化学机制对NO2模拟效果的影响,NO2的模拟偏差受排放高估的影响更大;2个版本SO2的模拟值差距较小,且都与地面观测值之间差异较小;CMAQv5.1 PM2.5的模拟值比CMAQv4.7.1更接近观测值,气溶胶模块机制的更新(例如新增细分的PM2.5模式物种和部分二次有机气溶胶生成机制的改进等)对PM2.5模拟效果的改善显著;CMAQv5.1的O3模拟值比CMAQv4.7.1高,CMAQv5.1的O3模拟值在O3观测值的高值时段更接近观测值,而CMAQv4.7.1的O3模拟值在低值时段更接近观测值,CMAQv5.1在日最大8小时平均(MDA8)O3观测浓度超标日的O3模拟效果相比CMAQv4.7.1有一定程度的改善,但在非超标日模拟效果变差,CMAQv5.1的O3模拟效果总体相比CMAQv4.7.1并未得到有效提升。提出,未来针对低值时段和低值区域的O3模拟机制的改进将进一步提升O3模拟效果。     

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。     

Characterisation of gaseous and particulate atmospheric pollutants in the East Mediterranean by diffusion denuder sampling lines

A field study aimed to characterize atmospheric pollutants in the gaseous and the particulate phases was conducted during the fall-winter of 2004 and the summer of 2005 in the Ashdod area, Israel. The site is influenced by both anthropogenic sources (power plants, refineries, chemical and metal industries, a cargo port, road traffic) and natural sources (sea-spray and desert dust). The use of diffusion lines--a series of annular diffusion denuders for sampling gaseous compounds followed by a cyclone and a filter pack for determining PM(2.5) composition--allowed a good daily characterization of the main inorganic compounds in both the gaseous (HCl, HNO(3), SO(2), NH(3)) and the particulate phase (Cl(-), NO(3)(-), SO(4)(=), NH(4)(+), and base cations). During the summer campaign two other activities were added: an intensive 3-h sampling period and the determination of PM(2.5) bulk composition. The results were interpreted on the basis of meteorological condition, especially the mixing properties of the lower atmosphere as determined by monitoring the natural radioactivity due to Radon progeny, a good proxy of the atmospheric ability to dilute pollutants. Several pollution episodes were identified and the predominance of different sources was highlighted (sea-spray, desert dust, secondary photochemical pollutants). During the summer period a considerable increase of nitric acid and particulate sulphate was observed. Secondary inorganic pollutants (nitrate, sulphate and ammonium) constituted, on the average, 57% of the fine particle fraction, organic compounds 20%, primary anthropogenic compounds 14%, natural components (sea-spray and crustal elements) 9%. The advantages of the diffusion lines in determining gaseous and particulate N- and S- inorganic compounds are discussed.     

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。     

Mathematical models for accurate prediction of atmospheric visibility with particular reference to the seasonal and environmental patterns in Hong Kong

Atmospheric visibility impairment has gained increasing concern as it is associated with the existence of a number of aerosols as well as common air pollutants and produces unfavorable conditions for observation, dispersion, and transportation. This study analyzed the atmospheric visibility data measured in urban and suburban Hong Kong (two selected stations) with respect to time-matched mass concentrations of common air pollutants including nitrogen dioxide (NO(2)), nitrogen monoxide (NO), respirable suspended particulates (PM(10)), sulfur dioxide (SO(2)), carbon monoxide (CO), and meteorological parameters including air temperature, relative humidity, and wind speed. No significant difference in atmospheric visibility was reported between the two measurement locations (p > or = 0.6, t test); and good atmospheric visibility was observed more frequently in summer and autumn than in winter and spring (p < 0.01, t test). It was also found that atmospheric visibility increased with temperature but decreased with the concentrations of SO(2), CO, PM(10), NO, and NO(2). The results showed that atmospheric visibility was season dependent and would have significant correlations with temperature, the mass concentrations of PM(10) and NO(2), and the air pollution index API (correlation coefficients mid R: R mid R: > or = 0.7, p < or = 0.0001, t test). Mathematical expressions catering to the seasonal variations of atmospheric visibility were thus proposed. By comparison, the proposed visibility prediction models were more accurate than some existing regional models. In addition to improving visibility prediction accuracy, this study would be useful for understanding the context of low atmospheric visibility, exploring possible remedial measures, and evaluating the impact of air pollution and atmospheric visibility impairment in this region.     

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。     

Temporal and spatial variations of the quality of ambient air in the Kingdom of Bahrain during 2007

The main objective of the present investigation is to study the temporal and spatial variations of the quality of ambient air in the Kingdom of Bahrain. The non-parametric Kruskal-Wallis (KW) test showed significant spatial variations and interactions of spatial-temporal among five mobile monitoring stations for 11 air pollutants. The Mann Whitney (MW) test demonstrated the seasonality of spring over winter for the PM(10), PM(2.5), NO(2), CO and p-xylene, the seasonality of winter over spring for O(3), and no significant seasonal variation for NH(3), benzene, SO(2), toluene and H(2)S. It is concluded that emissions from automobile exhaust, industrial and developmental projects are responsible for the spatial air pollution, and that air temperature is the controlling factor for the seasonal variations.     

Inventory of emissions of primary air pollutants in the city of Kocaeli, Turkey

This study aims to obtain a reliable inventory of the emission rates of the principal air pollutants including PM, SO2, NOx) and CO in Kocaeli, Turkey. In the first stage, the pollutant sources classified as point, area and line sources are determined in the area. Then the annual emission rates of the pollutants released from these sources are estimated by the emission factors given by USEPA and CORINAIR. Results show that the annual emission rates for PM, SO2, NOx) and CO are 2195 tons, 5342 tons, 14632 tons and 23095 tons, respectively. On the other hand, the pollutant group with the highest contribution to total emission rate is determined as the point sources for NOx, which is responsible for 73% of total NOx emission, while it is the area sources for PM, SO2 and CO with the contribution percentages of 75, 76 and 69, respectively.     

Analysis of the air pollution climate at a background site in the Po valley

The Po valley in northern Italy is renowned for its high air pollutant concentrations. Measurements of air pollutants from a background site in Modena, a town of 200 thousand inhabitants within the Po valley, are analysed. These comprise hourly data for CO, NO, NO(2), NO(x), and O(3), and daily gravimetric equivalent data for PM(10) from 1998-2010. The data are analysed in terms of long-term trends, annual, weekly and diurnal cycles, and auto-correlation and cross-correlation functions. CO, NO and NO(2) exhibit a strongly traffic-related pattern, with daily peaks at morning and evening rush hour and lower concentrations over the weekend. Ozone shows an annual cycle with a peak in July due to local production; notwithstanding the diurnal cycle dominated by titration by nitrogen oxide, the decreasing long term trend in NO concentration did not affect the long term trend in O(3), whose mean concentration remained steady over the sampling period. PM(10) shows a strong seasonality with higher concentration in winter and lower concentration in summer and spring. Both PM(10) and ozone show a marked weekly cycle in summer and winter respectively. Regressions of PM(10) upon NO(x) show a consistently greater intercept in winter, representing higher secondary PM(10) in the cooler months of the year. There is a seasonal pattern in primary PM(10) to NO(x) ratios, with lower values in winter and higher values in summer, but the reasons are unclear.