空气中PAHs的优化采样及分析方法研究

改装了HVS-1000型大流量采样器,实际工作中用滤膜"XAD-2加PUF"同时采集空气颗粒物和气相中的PAHs,有效地提高了采样效率,并初步定量评价了PAHs在颗粒物和气相中的分配;用添加替代物的方法评价了预处理过程的回收率;用乙腈和水梯度洗脱、PAHs专用色谱柱分离、紫外检测的方法对USEPA规定的16种PAHs类优先污染物进行了定性和定量分析.      

室内空气采样及几种重要污染物的监测分析方法探讨

随着人们对室内空气质量重视程度的提高,室内空气监测技术近年来也不断得到发展。采样是监测中最重要的环节,采样时间、位置选择的正确与否直接影响测定的成功与否。采样目的是确定采样方案过程中的指导原则,一个成功的采样应用具备明确的目的性。氡、气溶胶、VOCs、甲醛是重要的室内污染物,其采样和测定技术逐步走向成熟。     

基于蒙特卡洛方法的着陆擦机尾风险预测

为解决对航班和机队着陆时擦机尾风险客观预测问题，基于飞行QAR数据和蒙特卡洛模拟方法，建立擦机尾风险预测模型，将某航空公司Boeing737-800机队的380套QAR数据作为样本数据，运用MATLAB编程进行5 000次模拟抽样试验，得到不同机队着陆时俯仰角的分布和擦机尾风险预测曲线。研究结果表明:当着陆俯仰角大于4.5°时，机队2擦机尾风险较大；运用蒙特卡洛模拟预测的飞机着陆俯仰角更为稳定和准确。该模型可进一步软件化，为航空公司的擦机尾超限事件管理提供可靠性指标参考，实现对飞行员操作风险的动态管理。     

Continuous Safety Sampling Methodology

This research introduces a proactive methodology for accident prevention, called Continuous Safety Sampling Methodology, by utilizing the principles of work sampling and control charting. Sampling is performed to observe the occurrence of conditions that may become hazardous in a given system. These conditions, known as dendritics, may become hazards and could result in an accident or occupational disease. Continuous Safety Sampling Methodology performs a random sampling for the occurrence of these dendritics. The collected data are then used to generate a control chart. Based on the pattern of the control chart, a system “under control” is not disturbed whereas a system “out of control” is investigated for potential conditions becoming hazardous. Appropriate steps are then taken to eliminate or control these conditions to maintain a desired safe system.     

气相动态顶空法分析水源水中61种挥发性有机物

建立了用于饮用水源水中61种挥发性有机物（VOCs）同时进行分析的气相-动态顶空进样-气相色谱-质谱法（D-HS-GC-MS）,VOCs包括集中式生活饮用水地表水源地特定项目中的31种VOCs。用D-HS-GC-MS法对水样中VOCs进行分析,获得良好的标准曲线线性关系（均大于0.995,溴二氯甲烷除外）,除乙醛、丙烯醛、丙烯腈和环氧氯丙烷的方法检出限分别为15 g/L、13 g/L、11 g/L和11 g/L外,其余VOCs的方法检出限均介于0.10～0.58 g/L,饮用水源水实际样品加标回收率和RSD分别为75.8%～116%和1.16%～21.6%（n=3）。气相-动态顶空进样法相对于常见的吹脱捕集法具有不直接接触样品的优势,避免了仪器被样品污染,用于饮用水源水中几十种VOCs的同时分析,在常规监测中可节省大量的人力物力投入。     

Spatial variability of arsenic and chromium in the soil water at a former wood preserving site

Contamination of industrial sites by wood preservatives such as chromated copper arsenate (CCA) may pose a serious threat to groundwater quality. The objective of this study was to characterise the spatial variability of As and Cr concentrations in the solid phase and in the soil water at a former wood impregnation plant and to reveal the fundamental transport processes. The soil was sampled down to a depth of 2m. The soil water was extracted in situ from the vadose zone over a period of 10 months at depths of 1 and 1.5m, using large horizontally installed suction tubes. Groundwater was sampled from a depth of 4.5m. Results showed that arsenic and chromium had accumulated in the upper region of the profile and exhibited a high spatial variability (As: 21-621 mg kg(-1); Cr: 74-2872 mg kg(-1)). Concentrations in the soil water were high (mean As 167 microg L(-1); Cr: 62 microg L(-1)) and also showed a distinct spatial variability, covering concentration ranges up to three orders of magnitude. The variability was caused by the severe water-repellency of the surface soil, induced by the concurrent application of creosote wood preservatives, which leads to strong preferential flow as evident from a dye experiment. In contrast to soil water concentrations, only low As concentrations (<12 microg L(-1)) were detected in the groundwater. High Cr concentrations in the groundwater (approx. 300 microg L(-1)), however, illustrated the pronounced mobility of chromium. Our study shows that at sites with a heterogeneous flow system in the vadose zone a disparity between flux-averaged and volume-averaged concentrations may occur, and sampling of soil water might not be adequate for assessing groundwater concentrations. In these cases long-term monitoring of the groundwater appears to be the best strategy for a groundwater risk assessment.     

Assessment of ambient air quality in Eskişehir, Turkey

This paper presents an assessment of air quality of the city Eskişehir, located 230 km southwest to the capital of Turkey. Only five of the major air pollutants, most studied worldwide and available for the region, were considered for the assessment. Available sulphur dioxide (SO₂), particulate matter (PM), nitrogen dioxide (NO₂), ozone (O₃), and non-methane volatile organic carbons (NMVOCs) data from local emission inventory studies provided relative source contributions of the selected pollutants to the region.The contributions of these typical pollution parameters, selected for characterizing such an urban atmosphere, were compared with the data established for other cities in the nation and world countries. Additionally, regional ambient SO₂ and PM concentrations, determined by semi-automatic monitoring at two sites, were gathered from the National Ambient Air Monitoring Network (NAAMN). Regional data for ambient NO₂ (as a precursor of ozone as VOCs) and ozone concentrations, through the application of the passive sampling method, were provided by the still ongoing local air quality monitoring studies conducted at six different sites, as representatives of either the traffic-dense-, or coal/natural gas burning residential-, or industrial/rural-localities of the city. Passively sampled ozone data at a single rural site were also verified with the data from a continuous automatic ozone monitoring system located at that site. Effects of variations in seasonal-activities, newly established railway system, and switching to natural gas usage on the temporal changes of air quality were all considered for the assessment. Based on the comparisons with the national [AQCR (Air Quality Control Regulation). Ministry of Environment (MOE), Ankara. Official Newspaper 19269; 1986.] and a number of international [WHO (World Health Organization). Guidelines for Air Quality. Geneva; 2000. Downloaded in January 2006, website: http://www.who.int/peh/; EU (European Union). Council Directive 1999/30/EC relating to limit values for sulfur dioxide, nitrogen dioxide and lead in ambient air. Of J Eur Communities L 163: 14–30; 29.6.1999; EU (European Union). Council Directive 2002/3/EC relating to ozone in ambient air. Of J Eur Communities. L 67: 14–30; 9.3.2002.; USEPA (U.S. Environmental Protection Agency). National Ambient Air Quality Standards (NAAQS). Downloaded in January 2006, website: http://www.epa.gov/ttn/naaqs/] ambient air standards, among all the pollutants studied, only the annual average SO₂ concentration was found to exceed one specific limit value (EU limit for protection of the ecosystem). A part of the data (VOC/NO_x ratio), for determining the effects of photochemical interactions, indicated that VOC-limited regime was prevailing throughout the city.