成都典型秸秆燃烧季节PM2.5中化学成分研究

采集2012年春季和秋季成都城区的PM2.5(空气动力学当量直径小于等于2.5μm的颗粒物,即细颗粒物)样品,分析得到水溶性离子、有机碳(OC)和元素碳(EC)等化学成分。结果表明,春季和秋季PM2.5的浓度分别为101±64μg m~(-3)和88±30μg m~(-3),是环境空气质量标准(GB3095-2012)日均值的1.3倍和1.2倍。基于K~+、OC/EC(OC浓度/EC浓度)和K~+/EC(K~+浓度/EC浓度)指标判别生物质燃烧事件,结果发现春、秋季生物质燃烧期间PM2.5中OC、EC和K~+、Cl~-等成分明显高于非生物质燃烧期;SO_4~(2-)、NH_4~+、Ca~(2+)、Mg~(2+)、NO_3~-、Na~+等其它水溶性离子浓度在生物质燃烧期均有不同程度升高。春、秋季生物质燃烧期间OC浓度分别是非生物质燃烧期的4.2倍和1.8倍,EC为非生物质燃烧期的2.3倍和2.3倍。K~+和Cl~-浓度在春季生物质燃烧期超过平均值的3倍,在秋季生物质燃烧期超过平均浓度的0.8倍和0.9倍。     

乌鲁木齐降水化学成分及来源分析

降水是大气中主要和次要污染物的重要收集器,是清除大气中颗粒物和气态污染物最好的清除剂。为了了解乌鲁木齐降水特征,本文利用离子色谱分析了2010年降水样品,研究表明,该区降水pH值在5.6~7.77之间,年均值为6.19,电导率变化范围为18.7~172.5μs·cm~(-1),年均值为57.73μs·cm~(-1)。降水中主要离子浓度排序为Ca~(2+)SO_4~(2-)NH_4~+Na~+Mg~(2+)Cl~-NO_3~-K~+F~-,Ca~(2+)是最主要的阳离子,SO2-4是最主要的阴离子,表明乌鲁木齐降水中的致酸物质主要是硫酸盐。总离子浓度季节变化特征表现为秋季高,冬季低。FA平均值为0.001,表明99.9%的降水酸度被碱性成分中和,NF计算结果表明Ca~(2+)具有很强的中和能力。从相关分析、富集因子来看,SO_4~(2-)和NO_3~-主要受人为源的控制,K+主要存在于土壤扬尘或生物质燃烧产生的细颗粒物中;Mg~(2+)主要来自陆源的土壤扬尘等;Cl~-主要来自海相输入,生物质燃烧、人类生活污水排放以及化工厂排放对Cl-也有很大贡献。     

中国和日本降水化学特性的分析比较

本文对中国33个站、日本29个站及美国9个站的降水化学资料进行了分析比较.结果表明,中、日、美三国的降水化学特性有很大不同.三国都有酸雨,但以美国的pH平均值最低.雨水中离子总浓度以中国为最高,其中SO_4~=,NH_4~+和Ca~(++)的浓度特别高.日本雨水中Cl~-和Na~+的浓度很高.NO_3~-在美国雨水中最高.从雨水中离子结构组成和几种重要参量的比值分析表明,中国雨水中的离子浓度受陆地源影响很大,而影响日本雨水中离子浓度最大因素是海洋.在美国以工业交通污染的影响相对最大.文中还对中、日两国不同地区的降水化学特性进行了分析和讨论.     

MEASUREMENT OF pH AND CHEMICAL ANALYSIS OF RAIN WATER IN RURAL AREA OF INDIA

Large number of rain water samples, at 7 rural locations in the semi-arid region of the DeccanPlateau were collected during 4 consecutive monsoon seasons (1979-1982).pH, conductivityand the major ionic components (C1~-, SO_4~= , NO_3~- , NH_4~+ , Na~+, K~+, Ca~(++), Mg~(++) of the abovesamples were determined. The pH of rain water was found to be highly alkaline and the valuesvaried from 6.4 to 7.8. Soil-oriented elements showed good correltioan (r~0.6) with pH valuesof rain water. The high concentration of soil-oriented elements, specially Ca~(++), is found to play animportant role in neutralizing the acidity of rain water and maintaining high alkaline pH. The studysuggested that the contribution of atmospheric aerosol of natural sources (sea and soil) to thechemical composition of rain water is more than that of anthropogenic origin.     

庐山云雾水化学组分的某些特征

在庐山电视台采集的云雾水与同时段、同一地点采集的雨水相比,除Cl~-外各种离子浓度前者明显高些,pH值也较高。云雾水和地面同时段雨水相比较,云雾水中NO~-_3,SO~-_4,NH~+_4,Ca~(++),F~-及Mg~(++)等离子浓度也较高,但云雾水和雨水二者比值较小,云雾水的pH值也较高。云雾水中离子浓度和上风向污染源关系密切,其主要通过气溶胶的输送从而影响云雾水成份。有雨情况下云雾水中的离子浓度随时间推移而逐渐减少。     

伊宁市降水化学成分及来源分析

降水是大气中主要和次要污染物的重要收集器,是大气中颗粒物和气态污染物最好的清除剂。本文利用离子色谱分析了2011年伊宁市90个降水样品,结果表明,该区降水pH月均值在5.27—7.1之间,年均值为6.26,电导率变化范围为34.64~63μs·cm~(-1),年均值为45.7μs·cm~(-1)。降水中主要离子浓度排序为Ca~(2+)SO_4~(2-)NH_4~+Mg~(2+)Cl~-NO_3~-Na~+F~-K~+,Ca~(2+)是最主要的阳离子,年均值为421.76μeq·L~(-1),SO_4~(2-)是最主要的阴离子,年均值为149.09μeq·L~(-1),表明伊宁降水中的致酸物质主要是硫酸盐。总离子浓度季节变化特征表现为春夏季高,秋冬季低,总离子浓度明显低于乌鲁木齐和沈阳,与北京类似,远高于杭州、广州,表明伊宁降水污染比北方城市轻,但是陆源贡献远大于南方城市。FA平均值为0.003,表明99.7%的降水酸度被碱性成分中和,NF计算结果表明Ca~(2+)的中和能力最强,其次是NH_4~+。从相关分析和因子分析来看,F~-、SO_4~(2-)、NO_3~-、Cl~-、NH_4~+主要受人为源的控制,Ca~(2+)、K~+主要来源于土壤和浮尘,Na~+、Mg~(2+)主要来源为土壤盐碱化、风化、干旱浮尘等自然源。     

苏州市大气PM_(2.5)中水溶性无机离子的源解析及其气象因子分析

为了探明PM_(2.5)中水溶性无机离子的来源和气象因子对其浓度变化的影响,利用2012年2、5、8和11月苏州市PM_(2.5)中水溶性无机离子浓度和本站气象观测数据,分析了苏州市水溶性无机离子的时间变化特征,解析了当地PM_(2.5)中水溶性无机离子的主要来源,探讨了气象因素对离子组分的影响。结果表明:(1)苏州市PM_(2.5)中水溶性无机离子年均浓度大小依次为:SO_4~(2-)NO_3~-NH_4~+Na~+Cl~-K~+Ca~(2+)Mg~(2+)F~-;SO_4~(2-)、NH_4~+和NO_3~-为PM_(2.5)中最重要的3种水溶性无机离子物种,其总和占PM_(2.5)总质量浓度的50.9%。各离子的季节浓度特征均为冬季最高、夏季最低。(2)通过运用主成分分析法对苏州市PM_(2.5)中水溶性无机离子进行来源分类解析,发现第一类为二次污染源和生物质燃烧,其贡献率为32.84;第二类为道路扬尘及工业排放,其贡献率为19.99%;第三类为海盐污染,其贡献率为18.43%。(3)通过水溶性无机离子与气象条件的相关性分析发现,风向、风速和温度与水溶性无机离子浓度的相关性较显著,这三者是颗粒物浓度变化的主要影响因子。(4)利用HYSPLIT后向轨迹模式对外来污染物进入苏州市的轨迹进行聚类分析后发现:因受季风气候影响,苏州市外来污染物的输入路径存在明显的季节性变化特征,其中夏半年输送主径源自海上,冬半年主径源自内陆。     

潮州沿海大气气溶胶无机离子浓度分布与气象要素的相关分析

根据2004年广东潮州沿海地区的气溶胶浓度观测资料,分析潮州沿海大气气溶胶无机离子浓度分布特征及气象要素对其的影响。结果表明:离子浓度季节性差异明显,总离子浓度呈现春夏季低、秋冬季高的特征,系由当地不同季节降雨量和风向分布不同造成的;气溶胶无机成分与海水近似,表明海盐是当地气溶胶的重要来源之一,但Cl-与Na+不一致,表明可能存在除海盐颗粒以外的异地气溶胶长距离输送;总离子浓度随采样点高度增加而降低,随采样时海陆风变化而变化;阳离子浓度日际变化不明显,阴离子浓度易受天气条件影响。     

城市降水酸度分布与气溶胶水冲刷

在湖南省邵阳市工业区测量表明,该区颗粒物含量处于相当高的水平,颗粒物的主要水溶性成分为Ca~(2 )、SO_4~(-)、NO_3~-、NH_4~ 和Na~ 。Ca~(2 )在大颗粒(dp>9.0um)富集度最高,而SO_4~(2-)在小颗粒(dp<2.0um)中最丰富。所有尺度的颗粒都具有中和酸的能力,随粒径增大而提高。讨论表明,颗粒物水冲刷对雨滴化学成分和酸度的影响对直径小于2000um的雨滴是相当灵敏的,这种影响主要由大颗粒提供。讨论结果与降水成分的监测资料相一致。气溶胶水冲刷机制有效地解释了城市酸雨频率的规律分布。     

海盐气溶胶影响酸碱气体及无机盐气溶胶的敏感性试验

利用热力学平衡模式ISORROPIA及与之耦合的气相化学模式,通过两类敏感性试验,探讨了海盐气溶胶、相对湿度、温度对3种无机盐（硫酸盐、硝酸盐、铵盐,包括液态和固态）和3种酸碱气体（氨气、气态硝酸、氯化氢）浓度的影响,以及不同海盐气溶胶浓度对热力学平衡的影响。试验结果表明,海盐浓度相对较低、相对湿度达到0．4～0．5以上、温度在-10～15℃之间时对各物种的平衡浓度影响比较显著。温度升高抑制硝酸盐、铵盐的生成,同时引起气态硝酸、氨气和氯化氢浓度的增加。而湿度升高时对硝酸盐、铵盐的生成有促进作用,反而造成气态硝酸、氨气和氯化氢浓度的降低。海盐气溶胶、相对湿度及温度的变化对硫酸盐气溶胶没有影响。在热力学平衡中如果考虑海盐气溶胶（主要成分NaGl）的作用会使得硝酸盐气溶胶、氨气浓度增加,而硝酸气体、铵盐气溶胶浓度减小,其中硝酸盐和气态硝酸的改变最为明显。由于海盐气溶胶和硫酸、硝酸的反应,产生了氯化氢气体,造成海盐气溶胶的氯亏损现象。     

Particle-size distribution of inorganic water soluble ions in the venezuelan savannah atmosphere during burning and nonburning periods

The results presented are the first complete analysis of inorganic soluble ions in a tropical savannah region. Atmospheric particles were collected in six rural Venezuelan savannah sites. Concentrations and size distribution of NO₃ ^–, SO₄ ^2-, CI^–, PO₄ ^3-, NH₄ ⁺, Na⁺, K⁺, Ca²⁺ and Mg²⁺ were determined in samples collected with Hi Vol samplers equipped with five-stage cascade impactors. Concentrations were higher in the dry season, with a maximum during the burning periods. Using Na⁺ as a reference, the results show a deficit of Cl^– and, with the exception of Mg²⁺, an enrichment of all other ions with respect to marine aerosols. Significant variations were observed in particle-size distribution between different periods. Various pairs of ions present similar size distributions: SO₄ ^2- and NH₄ ⁺; Cl^– and Na⁺; PO₄ ^3- and K⁺; Ca²⁺, Mg²⁺ and NO₃ ^–; indicating that the ions were produced by the same source and/or were involved in similar atmospheric processes. Possible primary sources, the gas-to-particle atmospheric process, environmental implication of long-range transport of nutrients during dry seasons, etc., are discussed.     

武汉市冬季灰霾期PM2.5中水溶性无机离子的特征

2018年1月,利用颗粒物采样器采集武汉市大气PM_2.5样品并进行水溶性无机离子（F^-、Cl^-、NO₃^-、SO₄^2-、Na⁺、NH₄⁺、K⁺、Mg²⁺、Ca²⁺）的分析.结果表明,NO₃^-、SO₄^2-、NH₄⁺是PM_2.5中最主要的3种水溶性无机离子,除Mg²⁺与Ca²⁺外,PM_2.5与WSⅡs （水溶性无机离子）之间的相关性显著,且移动源贡献占主导地位.阴阳离子平衡表明武汉市冬季灰霾期PM_2.5呈中性或弱酸性.通过混合单粒子拉格朗日综合轨迹模式模拟并采用分层聚类得出了4种主要的后向气流轨迹及相应的PM_2.5和水溶性离子浓度,结果表明区域传输对此次灰霾期影响较大.     

Chemical compositions of wet precipitation and anthropogenic influences at a developing urban site in southeastern China

A comprehensive study on the chemical compositions of wet precipitation was carried out from January 2004 to December 2004 in Jinhua, southeastern China's Zhejiang Province. All samples were analyzed for pH, electrical conductivity and major ions (F⁻, Cl⁻, NO₃⁻, SO₄²⁻, K⁺, Na⁺, Ca²⁺, Mg²⁺ and NH₄⁺). The rainwater was typically acidic with a volume-weighted mean pH of 4.54, which ranged from 3.64 to 6.76. SO₄²⁻ and NO₃⁻ were the main anions, while NH₄⁺ and Ca²⁺ were the main cations. The concentrations of these major ions were generally higher compared to those reported in other parts of the world, but much lower than those in northern China.Wet deposition fluxes of major ions showed pronounced seasonal variations with maximum in spring and minimum in autumn. Significant correlations were found in soil-derived species among Ca²⁺, Mg²⁺ and K⁺ and sea-salt species between Na⁺ and Cl⁻. Other relatively good correlations were also observed between Ca²⁺ and SO₄^2-, Mg²⁺ and SO₄^2-, Mg²⁺ and NO₃⁻, Mg²⁺ and Cl⁻. Principal component analysis was also performed on individual precipitation to find possible sources of the major ionic species. Varimax rotated four components accounting for 85.9% of the total variance, and were interpreted as acid and alkaline pollutants, sea spray and mixed source, soil and acid/neutralization. Calculation of enrichment factors for rainwater components relative to soil and seawater indicated that Ca²⁺ and K⁺ mainly originated from the terrestrial source, and SO₄^2- and NO₃⁻ were mostly attributed for the anthropogenic activities in the study area. In general, the results suggested that precipitation chemistry is strongly influenced by anthropogenic sources rather than natural and marine sources. The pollutants in rainwater were mainly derived from long distance transport, local industry and traffic sources.     

Chemical composition of rainwater at Lijiang on the Southeast Tibetan Plateau: influences from various air mass sources

Daily rainwater samples collected at Lijiang in 2009 were analyzed for pH, electrical conductivity, major ion (SO₄ ^2?, Cl^?, NO₃ ^?, Na⁺, Ca²⁺, Mg²⁺, and NH₄ ⁺) concentrations, and δ¹⁸O. The rainwater was alkaline with the volume-weighted mean pH of 6.34 (range: 5.71 to 7.11). Ion concentrations and δ¹⁸O during the pre-monsoon period were higher than in the monsoon. Air mass trajectories indicated that water vapor from South Asia was polluted with biomass burning emissions during the pre-monsoon. Precipitation during the monsoon was mainly transported by flow from the Bay of Bengal, and it showed high sea salt ion concentrations. Some precipitation brought by southwest monsoon originated from Burma; it was characterized by low δ¹⁸O and low sea salt, indicating that the water vapor from the region was mainly recycled monsoon precipitation. Water vapor from South China contained large quantities of SO₄ ^2?, NO₃ ^?, and NH₄ ⁺. Throughout the study, Ca²⁺ was the main neutralizing agent. Positive matrix factorization analysis indicated that crustal dust sources contributed the following percentages of the ions Ca²⁺ 85 %, Mg²⁺ 75 %, K⁺ 61 %, NO₃ ^? 32 % and SO₄ ^2? 21 %. Anthropogenic sources accounted for 79 %, 68 %, and 76 % of the SO₄ ^2?, NO₃ ^? and NH₄ ⁺, respectively; and approximately 93 %, 99 %, and 37 % of the Cl^?, Na⁺, and K⁺ were from a sea salt source.     

Chemical Composition of Wet Precipitation in Irbid, Jordan

Rainwater samples were collected in Irbid city using 24 hour sampling periods from December 1996 to April 1998. All samples were analyzed for major cations (Na⁺, K⁺, Ca²⁺ and Mg²⁺), major anions (Cl^–, NO₃ ^– and SO₄ ^2–) and pH. High levels of Ca²⁺ and SO₄ ^2– were observed. Together, Ca²⁺ and SO₄ ^2– made up more than 52.4% of the total ion mass, while Ca²⁺ alone contributed over 39.0% of the total cation. The majority of the rain samples collected had pH values higher than 5.6. The average pH was 6.4±0.9. High values of pH are attributed to the neutralization by natural alkaline local dusts which contain large fractions of calcite. Correlation and mineralogical analyses indicated that Ca²⁺, K⁺ and fractions of Na⁺, SO₄ ^2– and Mg²⁺ are of crustal origin. Results of the present study suggested that the atmospheric composition in the city is strongly influenced by natural sources rather than anthropogenic.     

Episodes of extreme rainwater pollution and its relationship with synoptic situation (Wielkopolski National Park,Poland)

Synoptic conditions of extreme rainwater pollution episodes, evidenced by maximum values of parameters measured in the protected area of Wielkopolski National Park (western-central Poland), were analysed in this study. Precipitation samples were tested for the following parameters: pH, electrical conductivity and the concentration of the following elements: F^-, Cl^-, NO₂^-, NO₃^-, PO₄^3-, SO₄^2- and Na⁺, NH₄⁺, K⁺, Mg²⁺, Ca²⁺. It was assumed, that in winter, western advection of Atlantic air masses was the most frequent aerosol and pollution transport scenario for the investigated area. In summer the most heavily pollution occur at the intensified meridional flow over the central Europe, indicating advection of cooler air from northern Europe and the North Sea. In most of cases, the weather conditions causing extreme concentration of examined pollutants, were determined by the movement of weather fronts over considerable parts of Poland and by precipitation caused by those fronts.     

STUDY ON THE CHEMICAL CHARACTERISTICS OF POLLUTING FOG IN GUANGZHOU AREA IN SPRING

Samples of fog water collected in the area of Guangzhou during February, March and April of 2005 are used in this work to study the chemical composition of fog water in polluting fog there. Three typical episodes of polluting fog are analyzed in terms of ionic concentration and their possible sources. It is found that the concentration of various ions in fog water is much higher than those in rainwater. Fog not only blocks visual range but contains liquid particles that result in high degree of pollution and are very harmful to human health. SO₄⁼ is the anion with the highest concentration in fog water, followed by NO₃^-.For the cation, Ca⁺⁺ and NH₄⁺ are the highest in concentration. It is then known that rainwater is more acidic than fog water, indicating that ionic concentration of fog water is much higher than that of rainwater, but there are much more buffering materials in fog water, like NH₄⁺ and Ca⁺⁺. There is significant enrichment of Ca⁺⁺, SO₄⁼, and Mg⁺⁺ in fog water. In the Guangzhou area, fog water from polluting fog is mainly influenced continental environment and human activity. The episodes of serious fog pollution during the time have immediate relationships with the presence of abundant water vapor and large amount of polluting aerosol particles.     

Ambient air dry deposition and ionic species analysis by using various deposition collectors in Shalu, central Taiwan

This study describes the chemical composition of dry deposition collected at a highway traffic site in central Taiwan during daytime and nighttime periods by using a dry deposition plate (DDP) and water surface sampler (WSS). In addition, the characterization for mass and water-soluble species of total suspended particulate (TSP), both PM_2.5 and PM₁₀, was studied at the study site from August 22 to November 30, 2006. Dry deposition fluxes of ambient air particulates and inorganic species (Na⁺, NH₄⁺, K⁺, Mg²⁺, Ca²⁺, Cl⁻, NO₃⁻ and SO₄²⁻) were analyzed by Ion Chromatography (DIONEX-100).Results of the particulate dry deposition fluxes and mass concentrations are higher in the water surface sampler with respect to the dry deposition plate used in this study. Statistical results also showed the average dry deposition flux of the ionic species (Na⁺, NH₄⁺, K⁺, Cl⁻, NO₃⁻ and SO₄²⁻) obtained by the DDP and WSS displayed significant differences. Also, the average concentrations of Mg²⁺ and, Ca²⁺ were statistically the same at this study site.