改进气相色谱法测定总烃与非甲烷总烃

采用十通阀、双定量环进样(进样量0.5 m L),专用的甲烷柱和总烃柱分别分离两路气样,单FID检测器检测的方法测定环境空气和固定污染源废气中的总烃和非甲烷总烃(NMHC)。实验结果表明:总烃与甲烷工作曲线的相关系数分别为0.997 7和0.999 0;总烃与甲烷测定结果的相对标准偏差均未超过1.5%;总烃与NMHC的检出限均为0.04 mg/m~3;总烃的加标回收率为90.3%~113.0%,NMHC的加标回收率为91.1%~110.0%。上述指标均满足HJ 604—2011和HJ/T 38—1999中对总烃及NMHC的测定要求。用注射器采样后的气样应尽量避光保存,放置时间宜在8 h之内。该方法无需制备除烃空气,大幅提升了检测效率。     

气相色谱法测定大气和废气中非甲烷总烃

介绍了用双柱双氢焰离子化检测器气相色谱法分析气体样品中非甲烷烃。方法的检出限为０．０３５ｍｇ／ｍ＾３,测定范围为０．１２－８．０ｍｇ／ｍ＾３。     

油田储油罐非甲烷总挥发实验及仿真模拟

针对油田单井拉油罐非密封生产带来的油气泄漏问题,建立小型原油储油罐挥发损耗实验模拟平台,通过气相色谱法探究各因素对其损耗的影响,利用Fluent仿真软件模拟储油罐的泄漏扩散。结果表明:储液温度和有无风环境对储油罐非甲烷总烃(NMHC)挥发影响较大,储液高度和环境温度对其影响较小;仿真模拟无风环境下,储油罐泄漏口短时间内存在油气积聚现象;有风环境下,当风速为1 m/s,油气积聚不明显;随风速增大,扩散浓度场面积不断增大,油品损耗量增大,在风速为5 m/s的环境下,扩散300 s时的浓度场面积相比扩散200 s时较小,但泄漏口处的油气积聚面积增大。     

定量构效关系应用于水中有机污染物降解过程的研究进展

基于化合物分子结构与反应活性之间的定量构效关系(QSAR)研究在化工、环境、医药等领域受到广泛关注,对于模拟预测未知化合物的反应活性和作用机制具有重要意义.本文介绍了QSAR的原理及常用的建模方法,综述了QSAR在水中有机污染物光降解、高级氧化降解、生物降解过程中反应活性模拟预测以及机理解释研究领域的应用,最后对QSA...     

Risk Analysis of Volatile Organic Compounds Through Daily Life Cycle in the Industrial City in Korea

This study analyzed the risk of exposure to volatile organic compounds (VOCs) through a study of activity patterns in the Korean industrial city, Ulsan. The daily life cycle patterns(LCPs) of 331 people in Ulsan were surveyed and the average LCPs in Ulsan were obtained by statistical analysis. Nine to twelve personal air samples of VOC exposure at the breathing zones were collected at each LCP. This included hours for sleeping,cooking and eating, going to and from work, working, participating in field or outdoor activities, reading, watchingTV, and shopping. The components and concentrations of the collected VOCs were identified by a Gas Chromatography-MassDetector (GC-MS). The overall reproducibility of all GC analytical procedures of the simultaneously collected duplicatesample pairs represented a mean of percent differences rangingfrom about 9 to 13%. For the general population of Ulsan, thecarcinogenic and non-carcinogenic risk of exposure to theVOCs during the LCPs was evaluated. The carcinogenic riskwas analyzed using both the chronic daily exposure orlifetime average daily exposure (CDI) and the cancerpotency factor. The non-carcinogenic risk was analyzedusing both the CDI and the chronic reference dose.The major chemical forms of the identified VOCs were oxidized forms (43%), aliphatic alkanes (29%) and aromatics (15%). Even though the highest total exposure strength per unit time of each activity was observed during shopping, the highest totalamount of exposure to VOCs was identified as the exposure duringwork. The total carcinogenic risk of exposure to the carcinogenicVOCs through daily life cycle in Ulsan was 2.0 × 10^-4which is substantially exceeding the permissible carcinogenicrisk level, 10^-5 10^-6. The carcinogenic riskduring most of the life cycle activities, except forreading, mainly performed indoors, was higher than that ofthe activities performed outdoors. The carcinogenic risk bybenzene exposure was about 56% (time weighted average) ofthe total carcinogenic risk by the exposure to thecarcinogenic VOCs. During cooking and eating, shopping andout door activities, however, the carcinogenic risk by theexposure to chlorinated compounds like chloroform exceededthe exposure to benzene. The overall hazard index (non-carcinogenic risk) by a chronic exposure to carcinogenicand non-carcinogenic VOCs through daily life cycle in Ulsanwas evaluated as 3.91 × 10^-1, which is much less than1.0 considered as a hazard level to human health, and thusit seems likely not to produce a severe health hazard.     

Electrical Resistance Heating of Volatile Organic Compounds in Sedimentary Rock

Electrical resistance heating (ERH) is a common method of remediation for volatile organic compounds in unconsolidated soils, both above and below the water table. In the past eight years, ERH has been used to successfully treat 10 or more contaminated sedimentary bedrock sites. Sedimentary bedrock treatment has recently expanded to greater depths and into karst limestone environments. This article describes the implementation issues for rock remediation and provides case studies of three sites remediated by ERH in Pennsylvania and Alabama. With proper design, the remediation of sedimentary bedrock can be completed as effectively as the remediation of overburden materials. © 2014 Wiley Periodicals, Inc.     

GC/MS法测定大气中挥发性有机污染物

介绍了用ＧＣ／ＭＳ法分析大气中挥发性有机污染物。以８种苯系物为试剂进行试验,结果表明：相对标准偏差小于９％,回收率大于９５％;当采样量为１０Ｌ时,８种苯系物的最低检出质量浓度均低于２μｇ／ｍ＾３。     

绿色有机电合成与可持续发展

综述了有机电合成的发展状况、基本原理及优点,阐述了有机电合成技术在实施“绿色化工”战略过程中的重要作用及主要应用领域,论述了有机电合成与可持续发展的关系。     

油品储运行业挥发性有机物排放控制技术评估

分析了我国油品储运行业的VOCs排放环节和特点。选取燃烧法、吸收法、吸附法、冷凝法、膜分离法等VOCs排放末端控制技术作为研究对象,介绍了各方法的原理和适用条件。建立了包括环境性能、技术性能、经济性能3方面共10项指标的综合评价指标体系。采用模糊评价方法分析了油品储运行业VOCs排放末端控制备选技术的综合性能。结果表明,冷凝法和膜分离法具有良好的综合性能,是油品储运行业VOCs排放的最佳末端控制技术。     

挥发性有机物废气的膜法处理工艺研究进展

简要介绍了挥发性有机物废气的来源，分类及其对人体和环境的危害，以及国内外近年来的排放状况。较详细地论述了蒸汽渗透，气体膜分离，膜基吸收3种膜技术用于废气中挥发性有机化合物去除和回收的研究进展和工业应用现状。     

挥发性有机物的物化性质与活性炭饱和吸附量的相关性研究

采用kc-4．0型颗粒活性炭对甲苯、对二甲苯、乙酸甲酯、乙酸乙酯、乙醇、正丙醇进行吸附实验,研究挥发性有机物的物化性质与活性炭饱和吸附量之间的相关性。实验结果表明,活性炭对乙酸甲酯、乙醇和正丙醇的吸附性能较差,对乙酸乙酯、甲苯和对二甲苯的的吸附性能较好,饱和吸附量最大的是甲苯（达312．92mg／g）,饱和吸附量最小的是乙酸甲酯（为224．93mg／g）。6种挥发性有机物的吸附等温线用Langmuir方程进行拟合,效果良好。挥发性有机物的比蒸发速度、饱和蒸气压和电离势能与活性炭饱和吸附量具有显著的相关性。比蒸发速度越快、饱和蒸气压越高或电离势能越大,活性炭饱和吸附量越小。     

等离子体联合技术处理挥发性有机化合物废气的研究进展

挥发性有机化合物（VOCs）废气污染面广、气量大、浓度低,含VOCs废气的排放将会受到越来越严格的控制,需要不断研究开发新的VOCs废气处理技术。等离子体联合技术具有多功能作用的效果,对污染物的降解率、能量利用率及对污染物的选择性均高于单一的等离子体技术。综述了等离子体与吸附剂、催化剂、铁电性物质联合处理VOCs废气技术的研究进展,展望了该技术的发展方向。     

Volatile Organic Compounds Selection for Incorporation in Photochemical Mechanisms and the Development of Secondary Pollution Reduction Strategies

In the present work a method for the evaluation of the importance of the VOCs species is presented, aiming to provide criteria for the incorporation of these species into atmospheric photochemical mechanisms and for the successful application of secondary pollution reduction strategies. According to the method presented here, the species can be divided into more important and less important ones, taking into account their mixing ratios and emission values in combination with their reactivity. For this classification three quantitative and one qualitative criteria were introduced. Overall, it is concluded that alkenes with more than a few carbon atoms in their chain appear to be more important in urban and suburban areas, while in background conditions the alkanes, having the smaller chain (ethane, propane), become more important. In the case of alkenes there is no clear species classification, except for the biogenically emitted compounds, isoprene and limonene. In general, more important alkenes appear to be those with the smaller chain (ethene, propene, butene). Most abundant aromatics are benzene, toluene, and xylene. In background conditions higher aromatics are also important, especially 1,2,3-, 1,3,5-, and 1,2,4-trimethylbenzene. The most important carbonylic compounds are formaldehyde, acetaldehyde, and acetone. Finally, taking into account the results mentioned above, a new photochemical mechanism was developed. The species and species groups used in the proposed mechanism are: ethane, higher alkanes, ethene, propene, 2- butene, 1-alkenes, 2-alkenes, higher alkenes, benzene, toluene, m-, o-, p-xylene, 1,3,5-, 1,2,3-, 1,2,4-trimethylbenzene, higher aromatics, formaldehyde, acetaldehyde, higher aldehydes, isoprene, limonene, and other biogenic VOCs.