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101.
T. E. Lewis A. B. Crockett R. L. Siegrist 《Environmental monitoring and assessment》1994,30(3):213-246
Concerns over data quality have raised many questions related to sampling soils for volatile organic compounds (VOCs). This paper was prepared in response to some of these questions and concerns expressed by Remedial Project Managers (RPMs) and On-Scene Coordinators (OSCs). The following questions are frequently asked:
- Is there a specific device suggested for sampling soils for VOCs?
- Are there significant losses of VOCs when transferring a soil sample from a sampling device (e.g., split spoon) into the sample container?
- What is the best method for getting the sample from the split spoon (or other device) into the sample container?
- Are there smaller devices such as subcore samplers available for collecting aliquots from the larger core and efficiently transferring the sample into the sample container?
- Are certain containers better than others for shipping and storing soil samples for VOC analysis?
- Are there any reliable preservation procedures for reducing VOC losses from soil samples and for extending holding times?
- Open test pit or trench.
- Surface soils (<5 ft in depth).
- Subsurface soils (>5 ft in depth).
102.
On February 26, 1988, the U.S. Environmental Protection Agency promulgated Standards of Performance for residential wood heaters, or woodstoves. Over the past several years, a number of field studies have been undertaken to determine the actual level of emission reduction achieved by new technology woodstoves in everyday use. These studies have required the development and use of particulate and gaseous emission sampling equipment compatible with operation in private houses. Since woodstoves are tested for certification in the laboratory using EPA Methods 5G and 5H, it is of substantial interest to determine the correlation between these regulatory methods and the in-house equipment. Two in-house sampling systems have been used most widely. One is an intermittent, pump-driven particulate sampler which collects particulate and condensable organics on a filter and organic adsorbent resin. Oxygen concentration is measured by a sensor in the sample line. The sampler is controlled by a data logger which also records other parameters of interest. The second system uses an evacuated cylinder as the motive force. Particulate and condensable organics are collected in a condenser and dual filter. The sampler operates continuously whenever the stack temperature is above the set point. Average stack gas concentrations are measured from the evacuated cylinder at the conclusion of the sampling period. Both samplers were designed to operate unattended for 1-week periods. A large number of tests have been run comparing Methods 5G and 5H to both of the field samplers. This paper presents these comparison data and determines the relationships between laboratory certification sampling methods and field samplers. 相似文献
103.
以国家标准分析方法为依据 ,结合企业实际 ,具体阐述了六价铬、铜、镍的半定量分析方法 ,该方法具有测试准、投入少、易掌握、速度快等特点 ,对电镀废水处理设施的调试测定以及企业日常监测管理具有实际指导意义 相似文献
104.
大气环境质量综合评价加权灰色关联模型的建立与应用 总被引:1,自引:2,他引:1
利用灰色理论建立大气环境质量综合评价加权灰色关联模型 ,运用污染贡献率确定权重系数。与其它评价模型相比 ,加权灰色关联模型还具有排序功能 ,实例表明该模型是简便有效的 相似文献
105.
Stoichev T Rodriguez Martin-Doimeadios RC Amouroux D Molenat N Donard OF 《Journal of environmental monitoring : JEM》2002,4(4):517-521
The concentration levels of mercury (Hg) species in natural water samples are usually low. Consequently, accurate analysis with low detection limits is still a major problem. In this work, a method was applied for the simultaneous direct determination of dissolved mercury species in water samples by on-line hydride generation (HG), cryogenic trapping (CT), gas chromatography (GC) and detection by atomic fluorescence spectrometry (AFS). The suitability of the method for real samples with different organic matter and chloride contents was evaluated by recovery experiments in synthetic and natural spiked water samples. The HG method was compared with other current available methods for mercury analysis with respect to the different fraction of mercury analysed, i.e. 'reactive', 'reducible' or total. HG derivatization and SnCl2 reduction (with and without previous oxidation with BrCl) were applied to synthetic and natural (spiked and non-spiked) water samples. The influence of chloride and dissolved organic matter concentrations was studied. The results suggest that the HG procedure is suitable for the simultaneous determination of Hg2+ and MeHg+ in surface water samples. Inorganic mercury analysed by HG (i.e. reducible) is close to the total inorganic mercury. 相似文献
106.
本文从发展我国环境监测技术产业的角度论述了环境监测技术产业的主要内容,分析了我国环境监测技术产业的发展和存在的问题,对发展我国环境监测技术产业提出了建议。 相似文献
107.
石墨炉原子吸收光谱法测定海河下游水中痕量镉 总被引:2,自引:0,他引:2
原子吸收光谱法直接测定高盐水中痕量镉时,有很大背景吸收和误差。本文采用络合—萃取技术使共存元素与待测元素分离,既消除了基体干扰,又达到了富集作用,使测定结果准确可靠。 相似文献
108.
超临界二氧化碳萃取-GC/MS测定土壤中的多环芳烃 总被引:10,自引:2,他引:10
本文开发了一种采用超临界二氧化碳萃取土壤中多环芳烃、不须经过纯化步骤,直接可用于GC/MS分析的简便、高效的方法。本实验中超临界革取的流体是二氧化碳,改善剂是5%的二氯甲烷/甲醇,萃取温度为120℃、压力为34MPa。GC/MS分析时除了采用外标外,还加入了6种同位素PAHs内标以校正各段PAHs的响应因子。采用本方法成功地测定了我国未开垦森林土壤中的PAHs。 相似文献
109.
J. Christian Franson William L. Hohman Joseph L. Moore Milton R. Smith 《Environmental monitoring and assessment》1996,43(2):181-188
We used 363 blood samples collected from wild canvasback dueks (Aythya valisineria) at Catahoula Lake, Louisiana, U.S.A. to evaluate the effect of sample storage time on the efficacy of erythrocytic protoporphyrin as an indicator of lead exposure. The protoporphyrin concentration of each sample was determined by hematofluorometry within 5 min of blood collection and after refrigeration at 4 °C for 24 and 48 h. All samples were analyzed for lead by atomic absorption spectrophotometry. Based on a blood lead concentration of 0.2 ppm wet weight as positive evidence for lead exposure, the protoporphyrin technique resulted in overall error rates of 29%, 20%, and 19% and false negative error rates of 47%, 29% and 25% when hematofluorometric determinations were made on blood at 5 min, 24 h, and 48 h, respectively. False positive error rates were less than 10% for all three measurement times. The accuracy of the 24-h erythrocytic protoporphyrin classification of blood samples as positive or negative for lead exposure was significantly greater than the 5-min classification, but no improvement in accuracy was gained when samples were tested at 48 h. The false negative errors were probably due, at least in part, to the lag time between lead exposure and the increase of blood protoporphyrin concentrations. False negatives resulted in an underestimation of the true number of canvasbacks exposed to lead, indicating that hematofluorometry provides a conservative estimate of lead exposure.The U.S. Government's right to retain a non-exclusive, royalty-free licence in and to any copyright is acknowledgedDeceased 相似文献
110.