南京市环境空气中挥发性有机物的组成与特点

参照美国EPATO17的方法研究南京市不同功能区(交通区、商业旅游区、居住区、工业区和清洁对照点)环境空气中挥发性有机物(VOCs)在一年四季中的组成及浓度水平。共检出189种挥发性有机物,并随气温下降而减少;苯系物稳定存在于各功能区,浓度秋季最高。交通区污染最严重。     

郑州市环境空气中挥发性有机物的组成及分布特点

初步探查研究了郑州市不同功能区环境空气中挥发性有机物(VOCs)的种类组成及TVOC和苯系物浓度分布特点,共检测出221种VOCs.交通密集区VOCs污染较重,汽车尾气是目前VOCs主要来源.     

天津市大气中挥发性有机物的组成及分布特点

参照美国EPA TO17的方法研究天津市不同功能区大气中挥发性有机物(VOCs)冬夏季中的组成及浓度水平,共检出62种挥发性有机物,冬季VOCs浓度水平低于夏季;苯系物稳定存在于各功能区且所占比例最高;VOCs的主要来源是机动车尾气。     

常州某农药生产场地土壤中挥发性有机物污染状况调查

对常州某农药生产场地土壤中挥发性有机物污染状况进行了调查。数据表明,该场地土壤中挥发性有机物污染以苯系物和卤代烃为主。苯系物浓度为0～56.7mg/kg,卤代烃浓度为0～1.14mg/kg,有潜在风险。     

南京市玄武湖隧道挥发性有机物特征谱研究

2014年12月采集南京市玄武湖隧道内不同点位、不同行驶工况及加油站环境中VOCs样品,比较隧道内不同测点、拥堵与非拥堵、隧道环境与燃油挥发样品VOCs浓度、组分及特征污染物的变化情况。结果表明,隧道样品中106种目标化合物全部检出;拥堵情况下VOCs体积分数较非拥堵情况下升高了7.4倍;加油站环境和隧道环境的VOCs组分中烷烃、烯烃和芳烃存在显著差异。     

便携式傅里叶红外分析仪测定水中挥发性有机污染物

发明了一种利用GASMET FTIR Dx4020便携式傅里叶红外分析仪测定水中挥发性有机物的实用方法,该方法可以定性定量25个水中挥发性有机物.该方法具有简便快捷、灵敏度高等特点,以苯系物中各单组分物质为例,方法检测限为11 ～45μg/L,相对标准偏差为3.4％ ～ 6.6％,加标回收率为98％ ～ 109％,在浓度范围内具有良好的线性.但对苯系物混合物定量准确性还需进一步研究提高.     

宜兴市臭氧和挥发性有机物的浓度特征研究

于2016年对宜兴市大气挥发性有机物(VOCs)和臭氧(O_3)的变化特征进行了分析。结果表明,宜兴市O3年均值为62.92μg/m~3,其中冬季值最低(31.19μg/m~3),夏季值最高(94.96μg/m~3)。φ(VOCs)为(11.00~42.45)×10~(-9),其中丙酮(12.7%)、乙酸乙酯(8.8%)和丙烯(3.3%)等在VOCs中占比位于前3位。各站点φ(甲苯)/φ(苯)2,全年的φ(甲苯)/φ(苯)φ(乙苯)/φ(苯)φ(间、对二甲苯)/φ(苯)。指出VOCs主要来源为有机溶剂和道路交通,并受到一定的外来输送影响。各站点φ(VOCs)/φ(NOx)为0.94~2.44,O3处于VOCs敏感区。     

泰州市环境空气中挥发性有机物分布特征

于2018年4—9月对泰州市环境空气中挥发性有机物(VOCs)组分开展现场观测,结合观测数据分析该市大气中VOCs的时空分布特征.结果表明:观测期间泰州市环境空气中VOCs平均摩尔比为45.1 nmol/mol,其中含氧挥发性有机物占比为57.8％;受周边排放源和地理位置影响,下风向点位的VOCs测定值高于其他点位;V...     

室内空气污染现状与特征研究

对几种典型室内空气质量进行监测，并就室内装修对空气质量的影响进行了研究，结果表明，室内空气质量状况不容乐观，PM10是不同类型室内空气的共同特征污染因子，PM10和细菌总数是公共场所的特征污染因子，室内装修是造成甲醛和苯系物等挥发性有机物污染的主要原因。     

杭州市交通干线空气中挥发性有机物研究

研究了杭州市四季交通干线空气中挥发性有机物分布和浓度特征,得出汽车尾气是市区交通干线空气中挥发性有机物的主要污染来源,且有机物浓度与交通干线繁忙程度成正比,杭州市交通干线空气中挥发性有机物污染以春季最为严重,秋季最轻。     

Distribution Of Volatile Organic Compounds In Ambient Air Of Kaohsiung, Taiwan

Automobile emissions have created a major hydrocarbon pollution problem in the ambient air of Taiwan. The aim of this study was to determine the volatile organic compounds (VOCs) in the ambient air of Kaohsiung, Taiwan. The spatial distribution, temporal variation, and correlations of VOCs at three study sites, selected based on traffic densities and distances from a freeway, were discussed. Sixty-four hydrocarbons were identified in the ambient air. Among all of the VOC species, acetone, aromatic and aliphatic compounds constituted the major constituents. Higher concentrations of VOCs existed further away from major arteries as compared to those found near the freeway. Therefore, the distance from the freeway may not be a sufficient index for reflecting actual air quality in the study area. Weather conditions, wind speed and direction did not affect the distribution of VOC concentrations in the three study sites. Other factors, such as the height and density of buildings, traffic conditions or commercial activities, might affect the distribution of VOCs.     

Soil-Water Partitioning and Desorption Hysteresis of Volatile Organic Compounds from a Louisiana Superfund Site Soil

The adsorption and desorption of three volatile organic compounds (1,2- dichloroethane, 1,1,2- trichloroethane and 1,1,2,2-tetrachloroethane) from a previously uncontaminated clayey soil sample from a Superfund site in North Baton Rouge,Louisiana was studied. In the linear range of the adsorption isotherm, the partition constants were not affected by the presence of the co-solutes. The adsorption isotherms over a wide concentration range on the soil followed the nonlinearFreundlich isotherm. The desorption of the compounds showedsignificant hysteresis at all concentrations studied. Approximately 20 to 70% of the adsorbed mass of organic compounds resisted the desorption even after five months ofsuccessive desorption steps. The desorption of four compounds(1,2-dichloroethane, 1,1,2-trichloroethane, 1,4-dichlorobenzeneand hexachlorobutadiene) from a contaminated soil sample fromthe same site was also studied. The aqueous concentration declined as the successive desorption steps progressed. For hexachlorobutediene the desorption can be visualized as occurring in two stages. The first stage involved a loosely bound or reversible fraction and the second stage involveda tightly bound or resistant fraction.     

人体接触挥发性有机化合物的生物标志物

生物标志物是阐明接触与健康损害之间关系的工具。综述了３７ 篇文献,简单论述了挥发性有机化合物的各种生物标志物,这些生物标志物包括暴露生物标志物,效应生物标志物和易感性生物标志物。还简述了各种生物标志物之间的相互关系,并介绍了各种生物标志物的研究现状和发展前景,以及应用它们来评价ＶＯＣｓ对人体健康的影响。     

滨州市大气VOCs污染现状及防控措施分析

利用挥发性有机物(VOCs)手工监测和走航监测技术,分析了滨州市城区、各县(市、区)涉VOCs工业园区的VOCs排放情况.结果表明,城区大气VOCs各组分的体积分数差异较为明显,烷烃类占比最高,其次是挥发性含氧有机物和芳香烃.排名前3的组分为异戊烷、正丁烷、丙烷,主要来自以液化石油气为燃料的车辆排放.各县(市、区)不同...     

水质中多种挥发性有机物的同时测定

在采用双柱双检测器的基础上,对水中24种挥发性有机物进行了同时测定。当进样体积为5ml时,最低检测限为0．5俐L,线性范围及测定范围为0．5～50倒L,1μg/L和20μg/L浓度水平的加标回收率在80．0％-110％之间,变异系数为0．6％～9．2％,实验结果令人满意。     

城市大气中挥发性有机化合物监测技术进展

挥发性有机物(VOCs)是臭氧及二次有机颗粒物(SOA)的主要前体物。近年来,我国逐步将VOCs纳入大气污染物控制体系。准确可靠的监测技术是大气VOCs研究及控制的重要前提保障。按照采样方法、分析方法 2个方面介绍并讨论了城市大气中VOCs的现有监测方法,较为详细地介绍了几类广泛采用的离线及在线监测技术,简要讨论了目前VOCs监测中存在的一些问题,展望了今后的发展趋势。     

南京市臭氧、VOCs和PANs污染特征及变化趋势

对2013—2016年基于国家环境空气质量监测站以及省建大气多参数站所获取的南京市O_3、NO_2、CO、VOCs、PANs观测结果进行综合评价,结果表明:2016年南京市O_3第90百分位日最大8 h平均质量浓度比2013年上升33.3%,超标天数中O_3引起的超标占比增至32.0%。南京市区大气中非甲烷总烃冬季浓度高于夏季,含氧挥发性有机物则与之相反;在5—9月,含氧挥发性有机物组分在日变化过程中出现峰值的时间先后顺序依次为醚、醛、酮类,且O_3和过氧乙酰硝酸酯(PANs)生成存在有一定的线性关系。VOCs/NOx比值表明南京市处于VOCs控制区,因此对NO_2浓度下降不敏感,植物源挥发性有机物连续3年上升,夏季大气光化学反应活性未显著下降,这些现象是城市O_3浓度维持在较高水平的重要因素。     

空气中挥发性有机物污染状况及健康风险评价

为了了解南京某县空气中挥发性有机污染物(VOCs)的污染状况,采用苏码罐采样-气相色谱-质谱法分析了该县不同功能区空气中的VOCs,探讨了其可能来源并采用国际公认的评价模型,对空气中的VOCs进行了健康风险评价。     

Ambient Air Quality at the Site of a Former Manufactured Gas Plant

Prior to the 1950's, manufactured gas was commerciallyproduced from the pyrolysis of coal, coke, and oil atfacilities that are termed manufactured gas plants (MGPs). The constituents of residual coal tar present on many MGPsites are an environmental health concern because of theirtoxicity and the possibility for their off-site migration viawater and air. Atmospheric concentrations of five volatileorganic compounds (VOCs, e.g., benzene), sixteen polycyclicaromatic hydrocarbons (PAHs, e.g., naphthalene), and particulate matter less than 10 microns in aerodynamicdiameter (PM₁₀) were measured at the site of a former MGP. Air samples were obtained before, during, and after excavationof subterranean coal tar at the site. The results of thisinvestigation indicate that subterranean coal tar was not aprimary source of VOCs and PAHs in the local atmosphere beforeor after remediation of the site. However, excavation,treatment, blending, and transfer of the coal tar duringremediation generated concentrations of selected aromatic andsemi-volatile organic compounds that were substantiallygreater than typical ambient levels. In addition, these datasuggest that blending and mixing of coal tars could lead toexceedance of the U.S. National Ambient Air Quality Standardfor PM₁₀, although additional research is required to fullyevaluate this possibility. Nuisance odors associated with thesite remediation were likely the result of naphthalene andpossibly isomers of xylene. Air pollutant concentrationsmeasured adjacent to the excavation area and at the siteperimeter during remediation activities were less than therelevant occupational and environmental exposure limits.