绍兴市柯桥区工业园区挥发性有机物污染特征研究

为更好地管控和治理绍兴市柯桥区工业园区的挥发性有机物(VOCs),利用柯桥区现有的两工业园区VOCs监测站点(园区1站、园区2站)2019年3月至2020年2月的监测数据分析柯桥区工业园区VOCs污染特征并进行溯源.结果表明:园区1站每月VOCs质量浓度平均值为125μg/m3,园区2站为137μg/m3,都呈现出3月...     

春节与疫情管控期间珠三角VOCs的组成和来源变化

挥发性有机物(VOCs)是对流层中臭氧(O3)生成过程的关键前体物,是O3与PM2.5协同治理的重要管控对象.基于2020年1月1日～2月29日珠江三角洲(珠三角)4个站点的在线VOCs观测数据,分析了春节与疫情管控期间珠三角地区VOCs组分、活性、臭氧生成潜势和来源的变化.结果表明,春节与疫情管控期间珠三角地区φ(V...     

微生物共代谢在氯代有机物生物降解中的作用

概述了微生物共代谢的生化机制,研究进展以及在氯化有机物生物降解中的作用,提出了微生物共代谢这种尚未被人们透彻了解的生物过程在氯代有机物等难解化合物生物处理中的应用前景。     

有机膨润土吸附苯酚的性能及其在水处理中的应用初探

分别用氯化十六烷基吡啶（CPC）和溴化十六烷基三甲铵（CTMAB）改性膨润土,试验了制备有机膨润土的适宜条件及其对吸附苯酚性能的影响。上述两种有机膨润土吸附水中苯酚很快能达到平衡。pH值为3─9时,有机膨润土处理苯酚的效果基本一致;pH>11时,有较高的去除率。CPC－膨润土或CTMAB－膨润土对苯酚的饱和吸附容量分别为103.5mg/g和75.0mg/g。有机膨润土处理苯酚的效果比原土提高8倍以上。     

微生物降解硝基芳香烃及其在环境保护中的应用

综述降解硝基芳烃的微生物类群,代谢途径,遗传操作及其在环境保护中的应用等方面的研究概况。     

VOCs源强不确定性对臭氧生成及污染防治影响的模拟分析

本文基于三维区域空气质量模式WRF-Chem,通过修改模式化学模块,量化输出过程量和诊断量,提供了一种定量分析挥发性有机化合物(VOCs)源强不确定性对O3生成影响的方法.为无法定量计算VOCs源强导致的臭氧生成率[P(O3)]偏差,以及由此对O3体积分数分布和污染控制相关联的VOCs敏感区和NOx 敏感区分布的误判提供了方法参考.采用标准统计参数对WRF-Chem模式的气象场与污染场模拟性能进行了评估,相关指标均优于前人结果.以INTEX-B(intercontinental chemical transport experiment-phase B)人为源、FINNv1(fire inventory from NCAR version 1)生物质燃烧源和 MEGAN(model of emissions of gases and aerosols from nature)生物源作为基准源,并以卫星观测数据作为约束,对排放源进行改进,评估了源改进前后臭氧生成率[P(O3)]、O3体积分数和O3控制敏感区指标(Ln/Q)的变化情况.仅人为VOCs(AVOCs)源增加68％后,P(O3)模拟峰值增升比例达13％～82％,以北京观测站点为例,P(O3)模拟月均峰值增加42％(22.5×10-9 h-1).对P(03)形成贡献比例最大的主要化学反应是HO2+NO(占比约68％),AVOCs源增加68％后,该反应贡献比例下降至65％.在改进源下,P(O3)普遍增加达到2×10-9～4×10-9h-O3各季节增幅较大的区域均主要集中在京津冀、长三角和珠三角中心城市及周边区域,与我国大型城市区基本都是VOCs敏感区的结论一致.整体而言,VOCs源强改进后,Nox敏感区O3体积分数增加幅度不大,不超过4×10-9,而部分VOCs敏感区增幅超过20 x10-9.VOCs源强的不确定性会影响O3形成过程中Nox和VOCs敏感区的判断,特别是VOCs源强明显低估会夸大VOCs敏感区的范围,从而降低O3调控对策的有效性.     

珠三角某石化园区VOCs排放特征及影响评价

石化行业是挥发性有机物(VOCs)的重要来源之一,然而,当前石化行业VOCs研究多集中于炼油厂VOCs排放特征分析,针对有机化工和合成材料等子行业的研究较为缺乏.选取珠三角地区某石化园区中石油炼制、合成材料和有机化工3个主要行业的8家代表性企业和园区周围敏感点为研究对象,采集分析了包含22种含氧VOCs(OVOCs)在...     

Quantitative analysis of pyrrolizidine alkaloids sequestered from diverse host plants in Longitarsus flea beetles (Coleoptera, Chrysomelidae)

Summary. Several species of the flea beetles genus Longitarsus are able to sequester pyrrolizidine alkaloids (PAs) from their host plants. In five Longitarsus species we compare the concentration of PAs present in their host plants belonging to the Asteraceae or Boraginaceae with those found in the beetles. To get an estimate of the intrapopulation variability, three samples of five beetles each and five individual plants were analyzed for each comparison. A strong intrapopulation variability could be detected both among plant and beetle samples. The total concentration found in the beetles varied strongly between species. The local host plant and its phenology influence the concentrations present in the beetles as evidenced in comparisons of a single beetle species from two different hosts and of one beetle species collected at the same site at different times of the year. In addition, different beetle species apparently vary in their capacity to sequester the alkaloids, at the lowest extreme the mean PA concentration in the beetles (0.034 μg PA/mg dry weight) was 1/30 of the mean concentration found in the plant leaves (L. aeruginosus from Eupatorium cannabinum), at the highest extreme (2.098 μg PA/mg dw) the concentration in the beetles was a 1000 fold higher than in the plant leaves (L. nasturtii from Symphytum officinale). The highest mean concentration found in the beetles was 3.446 μg/mg dw (L. exoletus from Cynoglossum officinale). The absolute concentrations found in the beetles are comparable to other insects which have been shown to be effectively defended against their potential predators. Received 22 June 1999; accepted 25 August 1999     

A review of biomarker compounds as source indicators and tracers for air pollution

An overview of the application of organic geochemistry to the analysis of organic matter on aerosol particles is presented here. This organic matter is analyzed as solvent extractable bitumen/ lipids by gas chromatography-mass spectrometry. The organic geochemical approach assesses the origin, the environmental history and the nature of secondary products of organic matter by using the data derived from specific molecular analyses. Evaluations of production and fluxes, with cross-correlations can thus be made by the application of the same separation and analytical procedures to samples from point source emissions and the ambient atmosphere. This will be illustrated here with typical examples from the ambient atmosphere (aerosol particles) and from emissions of biomass burning (smoke). Organic matter in aerosols is derived from two major sources and is admixed depending on the geographic relief of the air shed. These sources are biogenic detritus (e.g., plant wax, microbes, etc.) and anthropogenic particle emissions (e.g., oils, soot, synthetics, etc.). Both biogenic detritus and some of the anthropogenic particle emissions contain organic materials which have unique and distinguishable compound distribution patterns (C₁₄-C₄₀). Microbial and vascular plant lipids are the dominant biogenic residues and petroleum hydrocarbons, with lesser amounts of the pyrogenic polynuclear aromatic hydrocarbons (PAH) and synthetics (e.g., chlorinated compounds), are the major anthropogenic residues. Biomass combustion is another important primary source of particles injected into the global atmosphere. It contributes many trace substances which are reactants in atmospheric chemistry and soot paniculate matter with adsorbed biomarker compounds, most of which are unknown chemical structures. The injection of natural product organic compounds into smoke occurs primarily by direct volatilization/steam stripping and by thermal alteration based on combustion temperature. Although the molecular composition of organic matter in smoke particles is highly variable, the molecular tracers are generally still source specific. Retene has been utilized as a tracer for conifer smoke in urban aerosols, but is not always detectable. Dehydroabietic acid is generally more concentrated in the atmosphere from the same emission sources. Degradation products from biopolymers (e.g., levoglucosan from cellulose) are also excellent tracers. An overview of the biomarker compositions of biomass smoke types is presented here. Defining additional tracers of thermally-altered and directly-emitted natural products in smoke aids the assessment of the organic matter type and input from biomass combustion to aerosols. The precursor to product approach of compound characterization by organic geochemistry can be applied successfully to provide tracers for studying the chemistry and dispersion of ambient aerosols and smoke plumes. Presented at the 6th FECS Conference on Chemistry and the Environment, Atmospheric Chemistry and Air Pollution, August 26–28, 1998, Copenhagen.     

基因重组细胞在环境样品多氯联苯检测中的应用

为发展快速、简便和廉价的检测环境和生物样品中的多氯联苯技术,本研究利用重组有绿色荧光蛋白(GFP)和荧光素酶(Luc)报告基因的2个细胞系,检测从野外环境中所采集的水、底泥和生物样品中的多氯联苯的含量.研究结果表明,GFP和Luc荧光强度与多氯联苯标样浓度的相关性很好,相关系数分别达到0.99188和0.98239;具有很好的剂量-效应关系.与气相色谱-电子捕获器法(GC-ECD)的仪器分析比较,GFP和Luc的荧光强度与环境样品中的多氯联苯化合物含量也具有很好的相关性.因此可用于受多氯联苯污染的环境样品筛选和半定量快速、简便、廉价检测.