罐采样-正压进样-气相色谱法测定环境空气中温室气体

建立了罐采样-正压进样-气相色谱法测定环境空气中温室气体的分析方法。用正压采样器采集环境空气样品至罐中呈正压状态,用气相色谱仪进行分析,并对氮气空白、除烃空气、不同湿度、不同环境温度、不同罐压及精确控制进样压力等因素进行研究。在最佳实验条件下,N₂O、CO₂、CH₄、SF₆和CO的方法检出限分别为7 nmol/mol、1.5μmol/mol、0.1μmol/mol、9 pmol/mol、0.2μmol/mol,标准曲线相关系数均大于0.995,低、中、高浓度水平测定结果相对标准偏差均小于2.0%。利用该法对环境空气样品进行了检测分析,与该站点现有的高精度在线监测仪器同时测定结果进行比对,比对结果较好,该方法适用于城市环境空气和无组织废气中温室气体的准确测定。     

2019—2021年徐州市大气细颗粒物化学组成特征及来源解析

徐州市地处四省交界,大气污染物来源复杂,颗粒物污染在气象条件不利时较为显著。通过地面观测数据、颗粒物组分连续观测、源解析及轨迹溯源等方法,对徐州市2019—2021年颗粒物变化特征进行了全面分析,以定量解析各类污染源的贡献,识别对颗粒物贡献显著的化学成分。结果表明：PM_2.5各组分质量占比中二次无机盐和有机碳相对较高,其中二次无机盐SNA(SO■、NO^-₃、NH⁺₄)占比达到59.1%～62.7%;水溶性离子总浓度逐年降低,但Mg²⁺和Ca²⁺浓度2021年分别同比增加2%和12.5%,说明扬尘污染存在反弹。秋冬季水溶性离子明显较高,Cl^-浓度明显高于其他季节,表明徐州市秋冬季受移动源、燃煤源和二次有机气溶胶共同影响。PM_2.5中OC与EC质量浓度比为4.88～8.40,说明徐州市颗粒物受多源影响,柴油、汽油机动车尾气排放以及燃煤排放对颗粒物贡献较大。后向轨迹分析表明,污染严重的1月污染物主...     

2017年厦门金砖会晤期间PM2.5的化学特征及来源

为了探讨厦门金砖会晤期间的排放控制措施以及天气形势对大气颗粒物污染特征的影响,于2017年8月10日至9月10日对厦门气态污染物、细颗粒物(PM2.5)中的水溶性离子以及有机碳(OC)、元素碳(EC)等主要化学成分开展了高时间分辨率的在线监测。根据空气质量管控措施和天气形势将研究期分为6个阶段。管控前、管控期Ⅰ(非台风)和管控期Ⅱ(非台风) PM2.5质量浓度分别为(33. 12±9. 48)、(30. 30±17. 00)、(16. 01±4. 71)μg/m^3。管控期Ⅰ(台风)和管控期Ⅱ(台风) PM2.5质量浓度分别为(12. 40±3. 73)、(12. 45±3. 28)μg/m^3。结果表明:管控期Ⅰ(非台风)阶段受静稳天气的影响,管控效果削弱,PM2.5质量浓度下降幅度小;台风对颗粒物质量浓度下降的影响比管控更显著。管控初期,PM2.5中二次无机离子的质量浓度下降明显;台风对碳质组分质量浓度的影响不如无机组分显著。PMF源解析结果表明,二次无机源是PM2.5主要来源,随着管控措施的实行,扬尘源的贡献从21%降低到6%,而机动车源的贡献降幅不明显。台风期间SO4^2-、NO3^-、SO2、NO2以及硫酸盐氧化比值(SOR)均明显低于非台风期间,氮氧化比值(NOR)反而升高。台风和非台风期间NOR的日变化特征一致,NOR与阳离子的相关性分析结果表明,台风或高风速海风期间NOR与Na^+呈现很强的正相关性,说明海盐粒子可促进NO2非均相反应生成NO3-。     

“十四运”期间西安PM2.5中水溶性无机离子污染特征

为探究中国第十四届运动会(简称“十四运”)期间西安大气PM_2.5中水溶性无机离子浓度水平及来源,利用高分辨率MARGA ADI 2080离子在线分析仪对西安“十四运”前、“十四运”期间和“十四运”后水溶性无机离子进行实时观测,分析了不同时段水溶性无机离子组分污染特征、pH变化及污染来源。结果表明,“十四运”前、“十四运”期间和“十四运”后PM_2.5质量浓度分别为13.4、11.9、32.6μg/m³,SNA(NO^-₃、SO₄^2-和NH⁺₄三者统称)质量浓度分别为5.8、5.4、13.3μg/m³,占总水溶性无机离子的91.6%～93.6%。“十四运”前和“十四运”期间NO^-₃与SO₄^2-质量浓度比分别为0.7和0.9,表明移动源的比例增加,主要受交通管控的影响。“十四运”后NO     

台州市区PM2.5和O3污染特征及相互作用关系

基于2016—2020年台州市区大气污染物监测数据及气象观测资料,分析了台州市区PM_2.5和O₃的污染特征及受气象因素影响情况,并探究了不同季节下的PM_2.5浓度和O₃浓度的相关性及相互作用关系。2016—2020年,台州市区PM_2.5年均浓度和超标天数呈显著下降趋势,O₃-8 h年均浓度和超标天数总体呈上升趋势。PM_2.5浓度在冬季最高,且易发生超标;O₃浓度在春、夏、秋季均较高,且均会发生超标。通过相关性分析可知：PM_2.5浓度与气温、相对湿度、风速、降水量呈负相关,与大气压呈正相关;O₃浓度与气温、风速呈正相关,与相对湿度、降水量呈负相关。不同季节下的PM_2.5浓度与O₃浓度均呈正相关,两者存在协同增长。在春、夏、秋季,二次PM_2.5在总PM_2.5中的占比随着O₃     

北京市大气气态汞变化特征

采用Tekran 2537X大气汞分析仪在线测量北京市城区大气中气态元素汞(GEM,简称大气汞) 浓度,研究大气汞浓度随不同气象条件的变化特征。通过分析2016年10月—2017年9月大气汞监测数据发现,该监测点全年大气汞浓度为0.48～16.25 ng/m³,均值为(3.41±1.79)ng/m³。春季、夏季、秋季和冬季大气汞浓度均值依次为2.93 、2.95、4.27、3.37 ng/m³,其中,秋季大气汞浓度明显高于其他季节 。秋季大气汞浓度显著偏高可能由不利的大气扩散条件导致。大气汞夜间浓度显著高于白天浓度。同时,将大气汞与SO₂、CO及PM_2.5进行相关性分析,发现大气汞浓度变化趋势与SO₂、CO和PM_2.5呈显著正相关。结合风向和风速进行污染来源分析,得到该点位大气汞在西南和东北方向上受人为排放源影响较大。污染源类型分析表明,冬季大气汞与CO同源性强,主要来自本地供暖用煤。     

七虎林河流域上游溶解性有机质光谱特性分析

七虎林河源头区地表腐殖质随着径流的冲刷进入水体,形成了天然有机质(NOM),其中,溶解性有机质(DOM)易对河流水质造成影响。为了研究七虎林河中DOM的时空分布特征及其对水质的影响,开展了6次采样,分析了水体及土壤吸收光谱和荧光光谱特征参数,利用平行因子(PARAFAC)算法解析了水体DOM的特性及来源。结果表明：七虎林河上游水体五日生化需氧量(BOD₅)、高锰酸盐指数(COD_Mn)、化学需氧量(COD)、可溶性有机碳(DOC)的浓度分别为1.4 mg/L±0.2 mg/L、6.1 mg/L±3.0 mg/L、21 mg/L±8 mg/L、7.0 mg/L±3.2 mg/L,BOD₅/COD平均值为0.08,说明流域内水体DOM的可生化性差,对水质影响较小。光谱特征参数紫外吸收系数(SUVA₂₅₄)、荧光指数(FI)、腐殖化指数(HIX)、生物源指数(BIX)分析结果表明,七虎林河上游云山水库库上林区河段DOM的物质组成与水库及库下河段差异显著。库上河段DOM的芳香碳含量更高、分子量更大、自生源组分...     

苏州工业园区春季一次典型臭氧污染过程分析

基于臭氧(O₃)及前体物监测数据,综合运用正定矩阵因子分解模型(PMF)、O₃生成敏感性(EKMA)曲线、O₃来源解析工具(OSAT)等方法,对苏州工业园区2022年春季一次典型O₃污染过程成因开展研究。结果表明,高温及前体物的累积是导致园区O₃超标的主要成因,个别污染时段O₃及前体物受浙江、上海传输影响;污染期间园区处于典型VOCs控制区,VOCs主要来源为油气储运(35.6%)、区域背景(28.8%)、塑料制品生产(16.0%)、移动源(13.6%)、溶剂使用(6.0%)。为有效削减不利气象条件下O₃峰值浓度,应重点加强本地溶剂使用、油品挥发、有机合成等污染环节VOCs的管控。     

基于复合LSTM模型的PM2.5浓度预测

在对淄博市19个空气质量监测站点监测数据进行分析后,提出了一种基于机器学习的复合模型——灰色关联度分析(GRA)-改进的完备总体经验模态分解(ICEEMD)-长短期记忆网络(LSTM)模型。通过分析淄博市2019年大气污染物和气象数据,选用LSTM模型预测PM_2.5浓度。由于传统单一模块机器学习模型具有训练时间较长和预测精度较低的问题,提出了复合LSTM模型。该模型由3部分组成：GRA,用于PM_2.5浓度影响因素变量筛选;ICEEMD,用于PM_2.5分解、分量筛选和原始大气污染物及气象数据处理;LSTM,用于PM_2.5浓度预测。预测结果表明：淄博市中部丘陵地带PM_2.5浓度高于南部山区和北部平原,东部高于西部;淄博市逐月PM_2.5浓度呈“U”形分布,1月最高,8月最低;淄博市PM_2.5浓度受PM₁₀和CO影响较大,受湿度和温度影响较小。对比单一LSTM模型和GRA-LSTM模型,GRA-ICEEMD-LSTM模型...     

2017年江苏省PM2.5数值模拟及内外源解析

根据江苏省72个国控点监测数据,采用了区域大气模式和多尺度空气质量模式系统(RAMS-CMAQ)模拟了2017年江苏省ρ(PM_2.5)的时空分布,耦合综合源追踪算法(ISAM)分析了不同地区排放源对ρ(PM_2.5)的贡献特征。结果表明,PM_2.5模拟与观测值的相关系数(r)=0.76,标准平均偏差(NMB)=5.2%,均方根误差(RMSE)=23.4μg/m₃,模拟结果落于观测结果0.5~2倍的比例(FAC2)=84.2%。源追踪模块结果显示,夏季主要受东南风控制,本地排放的贡献更大(省内贡献为52.34%),其他季节受偏北风输送影响,外源输送的影响较大(省外贡献为53.48%~56.84%);冬季苏北5市的排放贡献比沿江8市的更大,而春、夏季沿江8市排放贡献较大。     

我国沙尘暴灾害及其治理对策初步研究

分析研究了沙尘暴的成因、时空分布、发展趋势及造成的灾害，结合国外经验提出了我国治理的对策建议。     

新疆室内环境污染监测和治理工作现状与建议

针对目前室内环境监测工作出现的种种问题，就如何规范的开展室内环境监测工作，更好地为社会提供真实、准确、有效的监测数据，本文提出相关的探讨。     

太原市冬、夏季醛酮化合物污染特征及来源分析

针对太原市空气臭氧污染较为严重的问题,开展臭氧主要前体物醛酮化合物质量浓度及其变化规律研究.利用2,4-二硝基苯肼固相吸附/高效液相色谱方法,通过对太原市2019年冬季和夏季大气的醛酮化合物进行分析,发现太原市冬季总醛酮化合物的平均质量浓度为13μg/m3,低于夏季的27μg/m3.其中甲醛、乙醛和丙酮质量浓度最高,且...     

Dissipation and residue of metalaxyl and cymoxanil in pepper and soil

A simple and accurate method of determining metalaxyl and cymoxanil in pepper and soil was developed by ultra-performance liquid chromatography–photodiode array detection. The limits of detection were 0.015 mg/kg for metalaxyl and 0.003 mg/kg for cymoxanil. The limits of quantification were 0.05 mg/kg for metalaxyl in pepper and soil as well as 0.01 mg/kg for cymoxanil in pepper and soil. Recoveries of pepper and soil were investigated at three spiking levels and ranged within 77.52 to 102.05 % for metalaxyl and 87.15 to 103.21 % for cymoxanil, with relative standard deviations below 9.30 %. For field experiments, the half-lives of metalaxyl were 3.2 to 3.9 days in pepper and 4.4 to 9.5 days in soil at the three experimental locations in China. At harvest, pepper samples were found to contain metalaxyl and cymoxanil well below the maximum residue limit MRLs of the European Union (EU) following the recommended dosage and the interval of 21 days after last application.     

Disembodied and Disembedded? The Social and Economic Implications of Atmospheric Change and Biodiversity

The social and economic implications of atmospheric change on biodiversity need to be seen in a global context of major shifts in the conceptualization and management of our relationship with nature. Traditionally, we have conceptualized the atmosphere and the other creatures of the biosphere as separate from the human, but their quasi-autonomy is now becoming subject to more and more human management. This raises not only economic issues, but social, political, and ethical concerns that will have substantial influence on public policy. Among these are the commodification of genetic material; the privatization of traditional knowledge; and the management of information. In this broader context, the paper examines an array of current and proposed strategies of response to changes in biodiversity as a result of climatic and other stresses.     

Atmospheric Change and Biodiversity: Co-Networks and Networking

Canada responded to the Global Biodiversity Convention by completing the Canadian Biodiversity Strategy in 1995. At the same time, Environment Canada also completed a national Science Assessment on Biodiversity. During this period, the Smithsonian Institution, in partnership with Parks and Environment Canada, initiated the implementation of a global biodiversity monitoring program in Canada. Under the auspices of the United Nations Man and the Biosphere Program, the SI/MAB monitoring protocols and plots have spread across Canada at an unprecedented rate. National champions in the science and educational sectors, working within an inter-disciplinary ecological framework, have guided the development, education, quality control and sharing of atmosphere-biodiversity observations electronically.Atmospheric-Biodiversity Networks and Networking have traditionally operated within separate mandates with little degree of integration. Air-Bio Networks were designed within an integrated framework to better understand the atmospheric stress on biodiversity and the adaptation actions, nationally and regionally. Detailed examples of the cumulative effects of climate change, stratospheric ozone depletion, acid deposition, ground-level ozone, suspended particulate matter and hazardous air pollutants on biodiversity will be discussed using a Southern Ontario case study. In addition, recommendations will be presented for future paired SI/MAB plots, linked networks and networking for adaptation within the context of climate, chemical and ecological gradients.     

Determination and study on dissipation and residue of bismerthiazol and its metabolite in Chinese cabbage and soil

A simple and accurate method for the determination of bismerthiazol and its metabolite 2-amino-5-mercapto-1,3,4-thiadiazole was developed in Chinese cabbage and soil by high-performance liquid chromatography-diode array detection in this study. The limits of detection were 0.06 mg/kg for bismerthiazol and 0.03 mg/kg for 2-amino-5-mercapto-1,3,4-thiadiazole, respectively. Recoveries of cabbage and soil were investigated at three spiking levels and were in the range of 84.0–96.0 % for bismerthiazol and 71.0–74.6 % for 2-amino-5-mercapto-1,3,4-thiadiazole, with relative standard deviations below 7.0 %. For field experiments, the half-life of bismerthiazol was 2.4–2.5 days in Chinese cabbage and 2.5–4.8 days in soil at the two experimental locations in China. Dissipation residues of 2-amino-5-mercapto-1,3,4-thiadiazole were lower than 0.72 mg/kg. Terminal residues of bismerthiazol and its metabolite were less than 3.0 and 0.3 mg/kg in Chinese cabbage, respectively. No bismerthiazol or metabolite residues were detected in soil on days 5, 7, 10, and 14 after the last spraying at the two dosage levels.     

环境监理与环境管理的区别与联系

阐述了环境监理与环境管理的关系，指出了以制度和程序规范两者的分工与合作可充分发挥环境监理在环境管理中的作用     

废旧干电池的环境污染防治及回收利用

介绍了各种干电池的基本化学组成，分析了废旧干电池污染环境的主要途径及对人类的危害，并就回收利用问题提出建议。     

Residues and dissipation of trifloxystrobin and its metabolite in tomatoes and soil

A simple residue analytical method using the quick, easy, cheap, effective, rugged, and safe (QuEChERS) procedure for the determination of trifloxystrobin and its metabolite trifloxystrobin acid (CGA321113) in tomato and soil was developed using high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS). The limits of detection were 0.0005 mg/kg for trifloxystrobin and 0.001 mg/kg for trifloxystrobin acid, respectively. The average recoveries in tomato and soil ranged from 73–99 % for trifloxystrobin and 75–109 % for trifloxystrobin acid, with relative standard deviations below 15 %. The method was then used to study the dissipation and residues in tomato and soil. The dissipation half-lives of trifloxystrobin in tomato were 2.9 days (Beijing) and 5.4 days (Shandong), while in soil were 1.9 days (Beijing) and 3.0 days (Shandong), respectively. The final results showed that the major residue compound was trifloxystrobin in tomato whereas it was its metabolite, trifloxystrobin acid, in soil. The final residues of total trifloxystrobin (including trifloxystrobin acid) were below the EU maximum residue limit of 0.5 mg kg^?1 in tomato 3 days after the treatment.