基于SOA和O3生成潜势的杭州市PM2.5和O3协同控制

2019年3月1日～2019年5月31日期间采用Syntech Spectras GC955在线气相色谱仪对杭州市大气环境中挥发性有机物（VOCs）进行了在线连续监测,分析了VOCs体积分数的组成特征、 PM_2.5和O₃协同控制的优控VOCs物种和VOCs特征污染物比值.结果表明,烷烃是VOCs体积分数中最重要的组分,贡献了62.40%. C2～C6的烷烃、苯系物、乙烯和乙炔是VOCs关键物种.烯烃和芳香烃是OFP的主要贡献组分,贡献率分别为41.35%和37.50%.芳香烃是SOA的主要贡献者,贡献率超过90%.低碳的烷烃、低碳烯烃和苯系物是OFP的关键贡献物种,控制好甲苯、间/对-二甲苯和邻-二甲苯这3种苯系物,是O₃和PM_2.5协同控制的关键.采样点大气中VOCs除了受机动车尾气的影响外,溶剂使用等工业排放的影响也较为显著.     

结合外场观测分析珠三角二次有机气溶胶的数值模拟

结合2008年11月18~25日期间珠三角地区的二次有机气溶胶(SOA)外场观测数据,验证区域空气质量模式WRF/Chem(weather research and forecasting model with chemistry)中两种SOA化学机制——VBS(volatile basis set)和SORGAM(secondary organic aerosol model)对珠三角SOA的模拟效果.VBS机制考虑了更为广泛的SOA前体物和化学老化过程,SOA模拟值更接近观测值,能合理反映SOA观测值的逐天变化趋势,与观测值的平均绝对偏差和相关性分别是-4.88μg·m-3和0.91,而SORGAM机制的分别为-5.32μg·m-3和0.18.利用VBS机制模拟区域内SOA的时空分布,结果显示SOA浓度具有显著的昼夜变化特征,浓度峰值出现在中午时段.受到输送和臭氧区域分布的影响,各城市SOA浓度差异显著,下风向的城市(如中山、珠海、江门)SOA浓度较高.     

乘用车内空气质量开发与管控研究

本文主要介绍了乘用车内(文中简称车内)空气质量污染源、管控项目及对应检测方法,整车制造商车内空气质量性能开发模式与管控机制。     

南通市夏季VOCs污染特征与来源研究

运用大气挥发性有机物(VOCs)快速在线连续自动监测系统,于2018年7月对南通市区环境空气中VOCs进行观测,分析VOCs的浓度状况、组成特征、对臭氧生成潜势的贡献及主要来源。结果表明:观测期间共检出100种VOCs,总挥发性有机物(TVOCs)的平均体积分数为(38. 18±23. 63)×10^-9,各物种体积分数从大到小顺序依次为烷烃>含氧有机物>芳香烃>卤代烃>烯、炔烃;芳烃和烯烃是最主要的活性物种,间/对二甲苯、甲苯、邻二甲苯等是VOCs的关键活性组分;利用PMF模型解析得到VOCs的主要污染来源是工业排放与溶剂使用、机动车尾气排放、燃料挥发排放和生物源排放。     

典型三床RTO设备燃爆危险性数值模拟研究*

为研究苯、甲苯、二甲苯混合废气在三床蓄热式废气焚烧炉内部的燃烧过程,基于FLUENT软件建立典型的三床蓄热式废气焚烧炉的物理模型和数值模型,重点分析进气风量和混合可燃气体-空气摩尔占比对其内部压力变化规律的影响,以期可为其安全设计提供借鉴。研究结果表明:燃烧室内的温度变化与燃烧速度变化保持一致,可通过监测RTO燃烧室内的温度来定性评估气体燃烧速度,随着进气风量的增加,混合废气燃烧速度先升高后下降后再升高;从能源损耗和安全生产2个方面综合考虑,得出RTO运行的最佳进气风量为15 000 m3/h到30 000 m3/h,最佳的混合可燃气体-空气摩尔占比为0.15~0.2,这与RTO实际工况相符合,解释RTO装置内废气积聚导致爆炸事故的原因,燃烧过程中压力出现2次峰值超压,实际生产中需在2个时间节点多加防范。     

紫外光降解高浓度氯苯气体的研究

为评价紫外光降解作为高浓度挥发性有机物生物预处理的可行性,系统考察了其对高浓度氯苯气体的去除性能及其影响因素.所考察的影响因素包括紫外光波长、进口ρ(氯苯)、空塔停留时间和气体相对湿度等.结果表明:复合254和185 nm波长紫外光照射对氯苯的去除效果优于单一254 nm波长;紫外光降解反应器的进口ρ(氯苯)在2 300～2600 mg/m3,空塔停留时间为27 s时,对氯苯气体的去除率可达40%,继续延长空塔停留时间对氯苯去除率的提高作用有限;进口ρ(氯苯)在150～3 000 mg/m3时,氯苯去除速率随进口浓度单调增加,当高于3 000 mg/m3时,氯苯去除速率基本保持不变;增加气体相对湿度可以提高紫外光降解反应器对氯苯的去除效果.      

吸附-电氧化法降解气态乙二醇乙醚乙酸酯(EGEA)的研究

采用吸附-电氧化两步联动降解VOCs,结果表明,相同电压下以铁作为阳极时的CODCr脱除率达到80%以上,比用不锈钢阳极时高40%左右.电解质溶液的pH值和CODCr值随时间有规律地变化,也验证了反应器中所发生的反应.     

我国部分商品瓶装饮用水中挥发性有机物的研究

应用Tekmar3000吹扫捕集-气相色谱质谱组合分析仪,参照USEPA的标准分析方法,对我国某些商品瓶装饮用水中挥发性有机物进行了定量分析,结果表明,其含量一般在1～8μg/L,其中普遍含有具三致潜力的卤代烃与苯系物。虽然这些毒理性指标均可达到我国瓶装饮用纯净水卫生标准,但与国外优质瓶装饮用水相比,存在明显的差距。瓶装饮用水中挥发性有机物主要与深度处理技术和组合工艺有关,可通过改进这些技术而得以有效控制。      

小东江底泥中挥发酚的垂向分布研究

将沿小东江流域布点采集到的底泥样,根据其理化性质,从上到下分为A(0～10cm)、B(10～20cm)、C(20～35cm)、D(35～65cm)层,分析发现:挥发酚含量B>A>C>D层;A～D层挥发酚含量最高点分别对应的是细砂土、面砂土、砂粘土和面砂土.      

ENHANCEMENTS OF NONPOINT SOURCE MONITORING OF VOLATILE ORGANIC COMPOUNDS IN GROUND WATER1

ABSTRACT: The U.S. Geological Survey (USGS) has compiled a national retrospective data set of analyses of volatile organic compounds (VOCs) in ground water of the United States. The data are from Federal, State, and local nonpoint‐source monitoring programs, collected between 1985–95. This data set is being used to augment data collected by the USGS National Water‐Quality Assessment (NAWQA) Program to ascertain the occurrence of VOCs in ground water nationwide. Eleven attributes of the retrospective data set were evaluated to determine the suitability of the data to augment NAWQA data in answering occurrence questions of varying complexity. These 11 attributes are the VOC analyte list and the associated reporting levels for each VOC, well type, well‐casing material, type of openings in the interval (screened interval or open hole), well depth, depth to the top and bottom of the open interval(s), depth to water level in the well, aquifer type (confined or unconfined), and aquifer lithology. VOCs frequently analyzed included solvents, industrial reagents, and refrigerants, but other VOCs of current interest were not frequently analyzed. About 70 percent of the sampled wells have the type of well documented in the data set, and about 74 percent have well depth documented. However, the data set generally lacks documentation of other characteristics, such as well‐casing material, information about the screened or open interval(s), depth to water level in the well, and aquifer type and lithology. For example, only about 20 percent of the wells include information on depth to water level in the well and only about 14 percent of the wells include information about aquifer type. The three most important enhancements to VOC data collected in nonpoint‐source monitoring programs for use in a national assessment of VOC occurrence in ground water would be an expanded VOC analyte list, recording the reporting level for each analyte for every analysis, and recording key ancillary information about each well. These enhancements would greatly increase the usefulness of VOC data in addressing complex occurrence questions, such as those that seek to explain the reasons for VOC occurrence and nonoccurrence in ground water of the United States.