GC—MS方法测定垃圾焚烧炉飞灰中的二恶英

采用索氏抽提，多级硅胶／氧化铝柱层析等预处理方法，提纯分离出垃圾焚烧炉飞灰中的恶英并进行ＧＣ－ＭＳ分析，检出所测样品中存在的６￣８个氯取代的二恶英。     

GC/MS在监测甲胺磷工业废水中的应用

就甲胺磷工业废水监测中甲胺磷及其干扰组分进行了色谱分离及质谱定性分析,并以火焰光度检定量,用甲胺磷工业原油作为标准,圆满完成了甲胺磷工业废水的监测任务。     

GC/MS法测定润滑油基础油中多环芳烃

对润滑油基础油中多环芳烃的气相色谱/质谱(GC/MS)测定方法进行了研究,探讨了样品的提取,固相萃取柱净化等前处理方法,同时也对仪器测定条件进行了优化.结果表明,在检测润滑油基础油中多环芳烃时,经优化的GC/MS法的加标回收率和精密度均达到较满意的水平.     

土壤中半挥发性有机物的GC／MS分析

介绍了萧山下沙经济技术开妪土壤中半挥发性有机物的提取及利用ＧＣ／ＭＳ技术对所提取化合物进行定性定量分析。     

超声波萃取-GC/MS法测定橡胶轮胎中的多环芳烃

建立了超声波萃取-气相色谱/质谱(GC/MS)联用测定轮胎制品中多环芳(PAHs)的分析方法.优化了超声波萃取条件,采用MS的选择离子检测方式对PAHs进行定性定量分析.结果表明,16种PAHs的平均加标回收率为75.4%～88.0%,相对标准偏差(n=5)为0.66%～11.90%,方法检出限在1.0～4.0 ng/mL.     

饮用水源水、出厂水有机污染物GC/MS分析

于1998年对成都市饮用水源水、出厂水的有机污染物进行了GC／MS分析,该市饮用水和出厂水均存在有机物污染,且含有优先控制污染物;污染来源主要为生活污水。枯水期有机物检出率高于丰水期。     

超声波辅助萃取GC／MS法测定垃圾渗滤液中的有机污染物

垃圾渗滤液中有机污染物众多,成分复杂.以二氯甲烷为萃取剂,超声波辅助萃取后用GC/MS法测定垃圾渗滤液中的有机污染物.与传统振荡萃取相比,超声波辅助萃取明显提高了萃取效率.在GC/MS分析部分,研究了不同极性色谱柱对有机污染物分析结果的影响.实验结果表明,极性柱比较适于测定垃圾渗滤液中极性大的有机酸、醇类等物质.非极性柱能大大提高难生化降解的烷烃类、酯类等物质的检出率.     

SPE和LC-MS／MS联用同时检测水体中的15种抗生素

采用（SPE）固相萃取柱进行分离富集，使用LC—MS／MS联用仪进行检测，建立了一种高效、低成本的可同时检测水体中多种抗生素的方法，并在河北省子牙河流域汪洋沟水体抗生素污染现状调查中得到应用。实验结果表明，（1）最优实验条件的选择为：水样体积为1L，洗脱剂用量为10mL，pH为3．0；（2）回收率达到69．2％～86．3％，相对标准偏差在1．8％～8．4％之间，表明检测结果准确度和灵敏度均较高；（3）在所检测的15种抗生素中，头孢西丁、土霉素、氯唑西林和布洛芬4种抗生素是该河流的主要抗生素污染物，其含量比重（中位数）高达73．5％，检测浓度最高（中位数）的是磺胺类抗生素，浓度为100．4ng／L；（4）各抗生素的含量从上游到下游大体呈逐渐衰减的趋势，这主要归因于下游支流的稀释作用，但水体中抗生素浓度仍远高于已有报道的地区；（5）污染源解析表明，水体中抗生素主要来源于制药企业的废水，部分来源于附近居民的生活污水。     

加速溶剂萃取-GC/MS法研究济南市环境空气颗粒物中的多环芳烃

以济南市为研究区域,利用TH-150C型智能中流量总悬浮颗粒物采样器采集了7个点位环境空气颗粒物样品,采用加速溶剂萃取、旋转蒸发、硅胶柱层析、氮吹仪氮吹后用GC/MS测定的实验研究方法,获得了济南市7个点位环境空气颗粒物中16种PAHs的质量浓度和ΣPAHs值.结果表明,7个点位环境空气颗粒物中ΣPAHs的含量在103...     

运用GC—MS联用技术对垃圾渗滤液中有机污染物成分的分析

通过测定垃圾填埋场渗滤液的色度、BOD5、CODCr、TOC、NH3—N、NO2^-—N、NO3^-—N、TKN、TP、总硬度等指标来分析渗滤液的水质特性。利用GC—MS联用技术对渗滤液中有机污染物的组分进行了鉴定，共检测出主要有机污染物63种。     

Interpretation of air pollution mortality: number of deaths or years of life lost?

This paper examines the relation between the results of epidemiologic studies of air pollution mortality and impact indicators that can be informative for environmental policy decisions. Using models that are simple and transparent, yet contain the essential features, it is shown that (1) number of deaths is not meaningful for air pollution, whereas loss of life expectancy (LLE) is an appropriate impact indicator; (2) the usual short-term (time series) studies yield a change in daily number of deaths attributable to acute effects of pollution, without any information on the associated LLE (although some information on this has recently become available by extending the observation window of time series); and (3) long-term studies yield a change in age-specific mortality, which makes it possible to calculate the total population averaged LLE (acute and chronic effects) but not the total number of premature deaths attributable to air pollution. The latter is unobservable because one cannot distinguish whether few individuals suffer a large or many suffer a small LLE. The paper calculates the LLE from exposure to PM10, as implied by the long-term mortality studies of adults and infants; population LLE for infants turns out to be an order of magnitude smaller than for adults. The LLE implied by short-term studies is a small fraction of the total loss implied by long-term studies, even if one assumes a very high loss per death. Applied to environmental policy, taking a permanent 50-70% reduction of PM10 as a reasonable goal, one finds a corresponding increase of average life expectancy in urban areas of the European Union (EU) and the United States of approximately four months.     

GC-ECD和LC-MS/MS测定垃圾焚烧飞灰中氯苯和氯酚的方法

氯苯和氯酚是生活垃圾焚烧过程产生的重要污染物,目前对垃圾焚烧炉飞灰中氯苯和氯酚的研究较少。本文采用超声萃取法结合GC-ECD、LC-MS/MS,建立了飞灰等固体介质中的氯苯氯酚的定量检测方法,通过实验确定出较优的前处理条件,飞灰样品中滴加少量浓硫酸,以正己烷/丙酮(1∶1)为萃取溶剂,40℃超声萃取20 min,萃取3次,然后液相萃取分离氯酚氯苯,分别净化,浓缩,最后进机检测,对三、四、五、六氯代苯和所有的氯酚均获得较好的回收率。应用建立的检测方法测试了3座正常运行过程中的生活垃圾焚烧炉飞灰的氯苯和氯酚含量,样品中一到四氯代氯酚的含量都在定量限以下,五氯酚含量范围为5~11 ng·g-1,三氯苯、四氯苯、五氯苯和六氯苯的含量在3~70 ng·g-1的范围。     

Effects of anthropogenic activities on hydrochemical characteristics of ground water of Da’an irrigation area in Western of Jilin Province

Environmental Science and Pollution Research - The groundwater environment changes under the influence of anthropogenic activities. Because of the construction of the Da’an irrigation area,...     

环境水体中四溴双酚A的HPLC-MS/MS分析方法的建立与应用

四溴双酚A(tetrabromobisphenol A,TBBPA)是目前使用量最大的溴代阻燃剂.随着它的广泛应用,已经引起了大气、水体、沉积物和土壤等环境介质及相关生态系统的严重污染.建立了环境水体中TBBPA的高效液相色谱-串联质谱(HPLC-MS/MS)分析方法.该方法采用电喷雾电离(ESI)负离子模式进行扫描,...     

Measurements of air–surface exchange rates of volatile organic compounds

Vertical gradients of volatile organic compounds (VOCs) were measured over a maize field and a soybean field in 1995 and 1996, respectively, in the Lower Coastal Plains of North Carolina. The measurements over the maize field were conducted in its early growth period, during May 1995, and the measurements over the soybean field were conducted in its middle and later growth periods during July through August 1996 at the same location. These measurements were combined with micrometeorological flux measurements to determine emission flux measurements for various VOCs. This measurement programme was part of project NOVA (Natural emissions of Oxidant precursors: Validation of techniques and Assessment) to estimate the flux of VOCs. Methanol was identified as the major biogenic compound for both years with the average flux of 3450 ± 1456 µg/m²/hr over maize and 3079 ± 2766 µg/m²/hr over soybean. Acetone is another compound that was identified as a biogenic compound for both years with the average flux of 425 ± 223 µg/m²/hr over maize and 2701 ± 1710 µg/m²/hr over soybean. In addition to biogenic compounds, a large number of aromatic compounds, including styrene and 1,2,4-trimethylbenzene, were also identified as emissions from the ground over the soybean field.     

Release of uranium from rock matrix--a record of glacial meltwater intrusions?

Uranium release observed in a rock matrix around water-carrying fractures was studied using U-series disequilibrium (USD) modelling and mass balance calculations. Several release scenarios were tested, with specific attention to the glacial aspects. The release appears to have occurred in two or three violent episodes during the last 300 ky. A release after the last glaciation can be excluded on mass flow grounds. Continuous release for more than 300 ky can be excluded on radioactive disequilibrium grounds. Repeated inflows of oxic glacial meltwater seem to have triggered the release episodes.     

Comparison of line– and point–source releases of tracer gases

Field measurements were made of greenhouse gas emissions from a wastewater treatment system using open path monitoring with detection by FTIR spectroscopy. Emission rates were determined by the ratio technique using a sulfur hexafluoride tracer gas released from a line source. As a quality control check, a second tracer gas – ethylene – was released from various single point locations. This paper presents a comparison of the line-source and point-source tracer releases for approximating emissions from the area source. The two types of tracer release showed excellent agreement when both release points were two hundred meters from the FTIR beam path. Data for other release points also were comparable, once differences in vertical dispersion as a function of distance are taken into account.     

吹扫捕集-GC/MS法测定南宁市竹排冲黑臭河道水体嗅味物质

利用吹扫捕集-GC/MS法对引起南宁市竹排冲河道水体黑臭的嗅味物质进行检测分析。结果表明,导致竹排冲水体黑臭的嗅味物质主要为苯系物、硫类化合物和氯苯类化合物,其中甲硫醚(相对含量1.70%)、二甲基二硫醚(相对含量3.19%)、甲基丙基二硫醚(相对含量6.11%)等挥发性有机物为竹排冲水体中的主要致嗅物质,是竹排冲水体嗅味产生的主要原因。     

Dating of marine sediments and time evolution of heavy metal concentrations in the Bay of Cádiz, Spain

In this paper the time evolution of heavy metal concentration of Pb, Zn, Cd and Hg, in the sediments of the Bay of Cádiz (southwest of Spain) is studied during the past century, as a result of the industrial influence in the zone. The study has been performed using sedimentary profiles that have been extracted from the seabed. The measurement of 210Pb and 137Cs radionuclides has provided the dating of the sediment layers, up to a depth corresponding to the age of 115 years. The relative sedimentation rates obtained are around 0.2 cm/year. The 137Cs activity profile reflects the concentration of this radionuclide in the atmosphere and into aquatic systems during the second half of the twentieth century. This profile has been used to ratify the results provided by the 210Pb dating method.     

COVID-19: unbalanced management of occupational risks—case of the analysis of the chemical risk related to the use of disinfectants in the dairy industry in Morocco

Environmental Science and Pollution Research - Moroccan employers have a strong responsibility for the safety and health of their employees in the workplace and for protecting them from the risk of...