空气质量AQI实时发布的改进探讨

针对《环境空气质量指数(AQI)技术规定(试行)》(HJ 633-2012)中对空气质量AQI实时发布存在的欠缺,从增加颗粒物1 h浓度的AQI分级浓度限值及颗粒物24 h滑动平均值计算方法改进着手,解决PM2.5和PM10的24 h滑动平均值实时延迟、1 h平均值代替24 h滑动平均值偏高等问题。     

济南市空气污染现状及控制对策

利用2013年1—12月济南市大气监测数据,分析该市空气质量现状及时空分布特征,结果表明:2013年济南市空气主要污染物质量浓度均超过《环境空气质量标准》(GB 3095—2012)二级标准限值,空气污染严重时段为冬季采暖期,颗粒物污染严重区域为该市西部和西北部地区,SO2、NO2污染严重区为中心城区,并从点源、面源和移动源3个方面提出相应的污染防治对策。在SO2、NOx和工业烟粉尘分别减排22.5%、18.2%和31.4%的条件下,运用Models-3/CMAQ模型模拟计算得出:2015年1月和7月,济南市空气中SO2、NO2、PM10和PM2.5的质量浓度与2010年同期相比将分别降低23.9%和29.7%、11.4%和15.9%、21.9%和32.6%、13.5%和26.9%,空气质量得到明显改善。     

泰州市冬季空气质量变化特征

为了解泰州市冬季空气质量变化特征,于2013年12月27日—2014年1月7日对NO2,SO2,O3,CO,PM10和PM2.5进行了监测,结合地面气象资料和HYSPLIT轨迹模式分析了污染物的来源与传输过程。结果表明,观测期间AQI优良率仅为25%,PM10和PM2.5日均值超标率分别为58.3%,75.0%;有机碳是泰州市ρ(PM2.5)中最高的化学组分,其次是富钾和元素碳。PM2.5主要来源为汽车尾气、工业源、燃煤,分别占来源比例21.76%,16.52%,15.54%。局地污染源和不利气象条件是造成大气污染的主要原因。     

长三角城市群污染输送相互影响的敏感性试验

利用WRF-Chem模式,对2013年11月29日至12月11日长江三角洲地区的严重空气污染事件进行数值模拟,研究长三角核心区不同污染物本地源和外来输送所占比重。分析长三角核心区排放源对本地不同污染物浓度的污染贡献。结果表明,在2013年12月的这一次污染事件中,颗粒物平均本地贡献与外来输送基本比重相当;而SO_2、CO、NH_3、NO_x这4种气体污染物则以本地贡献为主,本地贡献的差异与气体的化学反应活性有关,活性越强本地贡献比重越大。污染过程中12月7日至12月9日00:00为污染最严重的时段,污染物的本地贡献有明显上升。区域间输送的方向和强度与地面风向、风速有紧密的联系。在边界层高度范围内,大部分污染物越往高空本地排放源的贡献越弱,外来输送主导作用增强,而硝酸盐在地面、1 km和1.5 km的本地贡献差异远小于其他污染物。     

天津市基于新标准的空气质量预报模型效果评估

利用2015年环境空气质量监测数据,对天津市OPAQ空气质量统计预报模型预测效果进行验证评估。结果表明,模型对天津市AQI和PM_(2.5)、PM_(10)、O_3、NO——2的预测结果与实测结果具有较好的趋势一致性,且预测时间越临近,拟合度越好,24 h预报的相关系数r全部达到0.8以上。对PM_(2.5)的预报性能明显优于PM_(10)、O_3和NO_2,PM_(2.5)平均值预测略呈正偏差,但重污染预测值偏低约15%;O_3和NO_2预测值呈明显负偏差,O_3峰值预测不足,NO_2预测值整体偏低,均以24 h预报趋势性最好,但负偏差最为突出。     

低温浓缩-气相色谱/质谱法分析固定污染源废气中的丙烯腈

建立了固定污染源废气中丙烯腈的气袋采样-低温浓缩-气相色谱/质谱分析方法。结果表明,该法在丙烯腈质量浓度16.1~4 050μg/m~3范围内具有良好的线性,相关系数R~20.999,检出限为9.54μg/m~3,回收率、日内与日间精密度均符合质控要求,能够满足废气中丙烯腈分析的要求。     

2016年武汉市大气污染物时空分布特征及影响因素

利用统计学和GIS方法对2016年武汉市各区不同污染物的时空分布特征及相关性进行分析。结果表明：武汉市大气污染季节性特征明显,春季和冬季颗粒物（PM2.5、PM10）及NO2污染突出,夏季O3污染严重。污染物空间差异显著,主城区和东西湖区颗粒物及NO2污染严重,郊区O3污染严重。平均气温、平均水汽压与SO2、NO2、CO、PM2.5和PM10均呈显著负相关,而与O3呈显著正相关;降水量与SO2、NO2和CO呈显著负相关。     

Modelling Tracer Dispersion from Landfills

Several wind tunnel experiments of tracer dispersion from reduced-scale landfill models are presented in this paper. Different experimental set-ups, hot-wire anemometry, particle image velocimetry and tracer concentration measurements were used for the characterisation of flow and dispersion phenomena nearby the models. The main aim of these experiments is to build an extensive experimental data set useful for model validation purposes. To demonstrate the potentiality of the experimental data set, a validation exercise on several mathematical models was performed by means of a statistical technique. The experiments highlighted an increase in pollutant ground level concentrations immediately downwind from the landfill because of induced turbulence and mean flow deflection. This phenomenon turns out to be predominant for the dispersion process. Tests with a different set-up showed an important dependence of the dispersion phenomena from the landfill height and highlighted how complex orographic conditions downwind of the landfill do not affect significantly the dispersion behaviour. Validation exercises were useful for model calibration, improving code reliability, as well as evaluating performances. The Van Ulden model proved to give the most encouraging results.     

Extension of the EUROS Integrated Air Quality Model to Fine Particulate Matter by Coupling to CACM/MADRID 2

The European Operational Smog (EUROS) integrated air quality modelling system has been extended to model fine particulate matter (PM). From an extended literature study, the Caltech Atmospheric Chemistry Mechanism and the Model of Aerosol Dynamics, Reaction, Ionisation and Dissolution were selected and recently coupled to EUROS. Currently, modelling of mass and chemical composition of aerosols in two size fractions (PM_2.5 and PM_10–2.5) is possible. The chemical composition is expressed in terms of seven components: ammonium, nitrate, sulphate, elementary carbon, primary inorganic compounds, primary organic compounds and secondary organic compounds. Calculated PM₁₀ concentrations and chemical composition are presented for two summer months of the year 2003 (1 July to 31 August).     

Flotability and flotation separation of polymer materials modulated by wetting agents

The surface free energy, surface tension and contact angles were performed to investigate the properties of wetting agents. Adsorption of wetting agents changes wetting behavior of polymer resins. Flotability of polymer materials modulated by wetting agents was studied, and wetting agents change significantly flotability of polymer materials. The flotability decreases with increasing the concentration of wetting agents, and the wetting ability is lignin sulfonate (LS) > tannic acid (TA) > methylcellulose (MC) > triton X-100 (TX-100) (from strong to weak). There is significant difference in the flotability between polymer resins and plastics due to the presence of additives in the plastics. Flotation separation of two-component and multicomponent plastics was conducted based on the flotability modulated by wetting agents. The two-component mixtures can be efficiently separated using proper wetting agent through simple flotation flowsheet. The multicomponent plastic mixtures can be separated efficiently through multi-stage flotation using TA and LS as wetting agents, and the purity of separated component was above 94%, and the recovery was more than 93%.