Determination of Trace Organochlorinated Pesticides and Polychlorinated Biphenyls in Water

A modified steam distillation liquid-liquid extraction (SDE) device is developed for the enrichment of trace organochlorinated pesticides (OCPs) and polychlorinated biphenyls (PCBs) in up to one litre of water samples. One ml of n-hexane is sufficient to extract the analytes. The extract can be analysed directly by a capillary gas chromatography-electron capture detector. The recoveries range from 84.6 to 102.3% for OCPs and 80.5 to 106.2% for PCBs, respectively. Matrice materials such as lipids and humic substances were removed by the SDE method from the extract and no further cleanup and concentration steps were needed.     

采样系统中金属氧化物对SO2测定值影响分析

通过实验与实际工程相结合，定量描述了大气采样系统中金属氧化物的存在对ＳＯ２测定值的影响，并阐述了其反应机理，提出了相应措施。     

Preliminary studies of a fast screening method for polycyclic aromatic hydrocarbons in soil by using solvent microextraction-gas chromatography

Solvent microextraction (SME) was applied to the extraction of polycyclic aromatic hydrocarbons (PAHs) from spiked and real environmental soil samples with different matrices. Soil sample was mixed with 7 mL of acetone and 14 mL of water to allow partitioning of the PAHs from the soil to the liquid phase. A 2 microL octane drop suspended from a microsyringe needle tip was then immersed into the stirred solution-soil mixture for extraction. After an 11 min extraction, the octane drop was withdrawn into the syringe and injected directly into the GC for identification and quantification. The whole analysis procedure took 27 min, with an extraction time of 11 min, and a GC separation time of 16 min. A second extraction could be undertaken whilst the GC is running, hence the GC run time currently limits the sample throughput. In this method, a small amount of organic solvent was used for the extraction process, which produced little waste. The limits of detection for lower molecular weight (< 230) PAHs range from 0.13 to 0.36 mg kg-1, and for higher molecular weight (> 250) PAHs are estimated to be between 0.5 and 1.0 mg kg-1, with RSD values generally under 20%. Due to the small volumes of organic solvent used, the consumable cost per extraction is only US$ 0.12. This is the first report of the application of SME to solid samples, and the first report of the use of SME for the analysis of PAHs.     

用密切值法评价沙湾荒漠区生态环境质量

利用多目标决策中的密切值法进行沙湾荒漠区生态环境综合评价。该方法简便、适用、且分辨率较高，对各监测点群的定量描述符合实际状况。     

塔里木油田环境空气质量状况及评价

根据塔里木油田１９９３－１９９６年环境空气监测数据，对其环境空气质量状况进行了分析和评价。     

2017年上半年北京市及周边地区空气质量特征分析

依托北京市、廊坊市和保定市高密度的地面空气质量监测、气象要素监测以及PM_2.5化学组分监测和后向轨迹分析等手段，对2017年上半年三地的空气质量进行分析。研究发现：三地中北京市空气质量较好，保定市较差。分污染物来看，保定市SO₂浓度水平明显高于廊坊市和北京市，颗粒物PM₁₀和PM_2.5也呈现保定市最高、北京市最低的规律。从污染物日变化来看，CO、SO₂、NO₂、PM₁₀和PM_2.5呈双峰型分布，O₃呈单峰型分布。从区域整体分布规律来看，PM_2.5和SO₂呈现明显的"南高北低"特征。PM_2.5化学组分分析结果表明：1—4月燃煤对该区域空气质量的影响较大，5—6月机动车排放的影响更为凸显。后向轨迹分析结果表明：在2017年上半年到达北京市的气流中有24%来自于北京市南部，且这些气流多为低空传输，表明区域传输对于北京市空气质量具有一定的影响。     

某铀矿工人头发中总α,总β,铀,钍放射性水平的调查

本文对某铀矿职业工人和非职业工人头发中的总β、总α放射性水平和铀、钍含量进行了分析测定.结果表明,该矿工人体内铀和钍的蓄积量均在正常放射性本底水平范围内,从头发中检验未观察到工人体内铀、钍放射性水平有明显的升高.     

我国海洋环境污染监测质量保证的回顾与展望

我国海洋环境污染监测质量保证的发展历史可大致分为三个阶段：孕育阶段（１９７２～１９７７年）起步阶段（１９７８～１９８３年）和发展阶段（１９８４～）。各个阶段有不同的特色和侧重点，１９７８年前主要探索与污染物质的分析方法，１９８４年后是监测质量保证工作进入管理时期。     

分光光度法测定染色废水的色度

为消除测定染色废水色度的主观误差，采用分光光度法测定染色废水的色度，与稀释倍数法相比，具有精确，重现性好，适用范围广等特点，ＰＨ值对色度的测定有明显影响，控制ＰＨ值为７．６０，测定色度具有可比性。     

唐山市空气中SO2与TSP污染状况分析

分析了唐山市从1988年至1992年大气中SO2和TSP的污染状况和变化规律，取得对该市环境管理的科学依据。