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非甲烷总烃测定中若干问题的研究 总被引:4,自引:3,他引:1
结合环境监测工作的实际情况,应用双柱双检测器气相色谱法,比较了非甲烷总烃不同的测定方法,探讨了在实际环境监测分析中非甲烷总烃测定过程的一些关键性技术问题,对色谱条件提出了几点优化建议,发现非甲烷总烃测定结果以甲烷计更接近实际监测情况,并验证了HJ/T 38—1999和HJ 604—2011方法中2种总烃标准曲线绘制方法的等效性,但在实际环境监测中HJ 604—2011方法操作更加简捷。双柱双检测器气相色谱法测定非甲烷总烃也存在严重的不足,基于FID响应值的非甲烷总烃不能准确全面反映空气有机污染程度,可能会掩盖空气中某些有机污染。 相似文献
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目前,总烃的测定通常是采用氮气作载气空气作助燃气的气相色谱法。我们认为,此法的不足是空气中的氧对测定总烃产生正干扰,实际总烃含量需从测定值减去干扰值。 采用除烃空气作载气和助燃气,直接进样气相色谱法测定大气中总烃,可以消除空气中氧的干扰,简便快速,最低检出限为0.1mg/m~3(以甲烷计,仪器噪声的两倍,进样1.5ml)。 相似文献
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建立了罐采样-气相色谱法测定环境空气中非甲烷总烃的分析方法。用罐采集环境空气样品至微负压状态,经除烃空气加压后,用气相色谱仪进行分析。并对氮气空白、除烃空气、样品保存期限、不同压力进样、不同正压压力进样、不同湿度、不同种类物质对总烃的贡献等进行了研究,在最佳实验条件下,非甲烷总烃的方法检出限为0.04μmol/mol,标准曲线相关系数均大于0.999 5,低、中、高浓度水平测定结果相对标准偏差均小于2.0%,低、中、高浓度的质控样品相对误差均小于2.0%。利用该方法对环境空气样品进行了检测分析,该法完全满足国家标准质控的要求,适用于环境空气和污染源无组织废气中非甲烷总烃的准确测定。 相似文献
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采用正压、负压、大气平衡3种进样方式,研究了VOCs在线监测系统对非甲烷总烃测定的影响。探讨在大气平衡进样方式下定量环内压力、平衡时间、进样流量对非甲烷总烃测定的影响,研究结果表明:采用正压进样方式,定量环内正压增大,非甲烷总烃质量浓度偏高;采用负压进样方式,定量环内负压增大,非甲烷总烃质量浓度降低;采用大气平衡进样方式,定量环内压力、平衡时间、进样流量的增大或减小对非甲烷总烃测定没有明显影响。比较3种进样方式,大气平衡进样方式的VOCs在线监测系统能够提高非甲烷总烃在线监测结果的准确性和可靠性,更适用于污染源废气在线监测。 相似文献
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对便携式催化氧化-FID法测定非甲烷总烃的检出限、精密度、准确度、催化效率等性能指标开展研究,考察该方法测定固定污染源废气中非甲烷总烃的适用性。结果表明:催化氧化装置的转化效率为98.1%~99.7%,方法检出限为0.05 mg/m3(以碳计);2个质量浓度水平的甲烷和丙烷混合标准气体测定结果的相对误差分别为-6.4%~6.1%、-4.7%~-0.5%,实验室内、实验室间测定结果的RSD分别为2.9%~5.9%和1.6%~2.5%、1.5%和0.6%。用该方法和国标法同时测定实际样品,两种方法测定结果的相对误差为6.4%~21.4%。 相似文献
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夏季受东南季风、湖流等因素影响,太湖蓝藻向西北部水域集聚,该区域平均藻密度可高达1×109个/L以上,其中蓝藻集中堆积的近湖岸区域藻类密度更高,蓝藻在不同生命阶段释放的藻源性VOCs的成分谱和产生量有较大差异,其中烯烃和有机胺反应活性较强。蓝藻水华高发期太湖西岸非甲烷总烃的浓度约为常州市区的3.3倍,日变化趋势符合蓝藻代谢规律。太湖西部蓝藻水华、湖西区的非甲烷总烃浓度和臭氧污染程度时空变化规律表明:太湖西部(宜兴)是整个流域臭氧污染最严重的区域,其臭氧污染的形成与太湖蓝藻水华暴发有关联性。 相似文献
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The concentrations of 56 volatile organic hydrocarbons (VOCs) were measured simultaneously in the southbound bore, the northbound bore and the exhaust air shafts of the Hsuehshan tunnel near Yilan, Taiwan during 2007 and 2008. A total of 60 integrated air samples were collected using stainless steel canisters and analyzed using GC/FID and GC/MS. The highest temperature and lowest relative humidity were observed at the exit of the tunnel owing to the accumulation in the tunnel of waste heat that was exhausted from vehicles. The five most abundant species in all samples were ethylene, acetylene, isopentane, propylene, and toluene. The exit/entrance ratios of total non-methane hydrocarbon (NMHC) concentration were 7.8 and 4.8 for the southbound and northbound bores, respectively. Furthermore, the most abundant species of emission rate (ER) is toluene (21.93-42.89 mg s(-1)), followed by isopentane, ethylene, propylene and 1-butene, with ER ranging from 2.50 to 9.31 mg s(-1) for the three shafts. The ozone formation potential (OFP)/total NMHC ratios in three exhaust air shafts show that the reactivities of these emissions are similar to those of vehicle emissions. 相似文献
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用100mL玻璃注射器采集气样,直接进入气相色谱仪,卤代烃经HP—101毛细管柱分离、ECD测定。方法检出限为0.007mg/m^3-0.05mg/m^3,相对标准偏差为3.4%-7.6%,加标回收率为94%-106%。 相似文献
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热脱附-气相色谱法测定环境空气中芳烃和卤代烃 总被引:17,自引:3,他引:14
建立了热脱附-气相色谱法测定环境空气中9种芳烃和卤代烃方法。阐述了样品管制备、采样袋预处理、现场采样和实验富集等过程。采用保留时间定性、外标法定量。进行了自动热脱附仪的吸附和解吸效率的试验,各组分的吸附效率均在97%以上,解吸效率达98 9%。最低检出质量浓度氯乙烯为0 0003mg/m3、1,2-二氯乙烷和1,2-二氯丙烷为0 0002mg/m3、苯、甲苯、乙苯、对二甲苯、苯乙烯和邻二甲苯均为0 0001mg/m3。试图以不更换TenaxTA吸附剂标准冷阱来测定齐鲁石化环境空气中特征污染物乙烯,由于冷阱对乙烯的二级吸附未能很好地解决,试验效果不理想,有待进一步研究。 相似文献
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E. Tsani-Bazaca A. E. McIntyre J. N. Lester R. Perry 《Environmental monitoring and assessment》1984,4(4):361-377
Air quality in the vicinity of airports is examined with particular reference to a detailed study of Gatwick Airport (UK). Ambient air concentrations of carbon monoxide, hydrocarbons (total and non-methane), oxides of nitrogen, smoke and airborne particulate lead have been measured at seven locations around the airport. The results obtained have been compared with ambient air quality guidelines, where available, and with results from other monitoring sites in the UK. It is concluded that the airport cannot be considered to be a significantly more important contributor to average pollutant ground-level concentrations than other sources in the area. 相似文献
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Sommar J Feng X Gårdfeldt K Lindqvist O 《Journal of environmental monitoring : JEM》1999,1(5):435-439
Although it makes up only a few per cent. of total gaseous mercury (TGM) in the atmosphere, the fraction of oxidised (divalent) mercury plays a major role in the biogeochemical cycle of mercury due to its high affinity for water and surfaces. Quantitative knowledge of this fraction present in mixing ratios in the parts-per-10(15) (ppq) range is currently very scarce. This work is based on approximately 220 data for divalent gaseous mercury (DGM) collected during 1995-99 in ambient air. Over the course of the measurements, the sampling and analytical methods were modified and improved. This is described here in detail and includes transition from wet leaching and reduction procedures to thermo-reductive desorption, the use of annular as well as tubular denuders and adoption of an automated sampling system. The concentration of DGM exhibited a strong seasonal behaviour in contrast to atomic gaseous mercury, with low values in winter and maximum values in summer. The DGM/TGM ratios were frequently found to be below the detection limit (< or = 1%) and in the range 1-5%. A trend of diurnal DGM patterns was observed and implies photolytically induced sources. Scavenging of DGM during rain events was also noticed. 相似文献
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Odraska P Dolezalova L Piler P Oravec M Blaha L 《Journal of environmental monitoring : JEM》2011,13(5):1480-1487
The main objective of the study was to evaluate the applicability of two solid sorbent media (Anasorb 708 and Strata X), the impinger filled with distilled water and PTFE filters for determination of airborne cyclophosphamide (CP) in the hospital working environment. For this purpose, air contamination of Masaryk Memorial Cancer Institute (Czech Republic) was monitored using the sampling apparatus containing the samplers described above. In addition, the surface contamination was also determined using the wipe sampling technique. During the monitoring, contamination of three different workplaces (storage room, preparation room and outpatient clinic) was studied. Using Strata X solid sorbent tubes, airborne CP was determined in all (n = 5) samples collected at the outpatient clinic over a 5 day monitoring period (concentration range: 0.3-4.3 ng m(-3)). Other samplers (including PTFE filters) did not collect any detectable amount of CP (the limit of detection, LOD ≤ 0.1 ng m(-3)). Negative results detected at filter samples indicate that CP determined at Strata X samples was most probably of gaseous origin. Surface contamination ranged from <2 to 19, <8 to 418 and 133-15,500 pg cm(-2) at the storage room, preparation room and outpatient clinic, respectively. The study showed that evaporation of antineoplastic drugs should not be neglected, albeit the concentrations determined in our study are relatively low. Therefore, proper monitoring of airborne contamination should involve simultaneous sampling of both particle-bonded and gaseous phases. In this way, Strata X sorbent tubes seem to be an effective tool for the sampling of gaseous CP in the indoor air. 相似文献