便携式质谱仪应用于交通干线苯系物污染特征分析

介绍了EcoSys-P便携式质谱仪在无车日前后对交通干线环境空气中苯系物现场监测中的情况,同时该方法与经典的气相-质谱联机进行了对比试验,相对偏差≤25%,能够满足交通干线环境空气苯系物的现场监测要求.     

便携式GC-MS选择离子快速测定水中丙烯醛和丙烯腈

便携式气相色谱-质谱仪(GC-MS)能同时对多组分复杂有机物进行定性、定量分析,在环境监测尤其是事故现场应急监测中发挥越来越重要的作用。文章建立了便携式顶空-GC-MS选择离子测定水中丙烯醛、丙烯腈的分析方法,其相关性大于0.997,检测限为5～10μg/L,回收率为93.3%～99.5%,该方法适用于水中丙烯腈、丙烯醛的应急现场及日常实验室分析工作。     

两种环境应急监测仪器在突发性环境污染事故中的作用

突发性环境污染事故虽然出现频率小,但危害极大,是威胁人类健康、破坏生态环境的重要因素。对于突发性污染事故的应急监测和处置,必须做到及时、快速、简便、准确。在某次苯泄漏事故的应急监测中,采用先进的傅里叶红外便携式气体分析仪监测环境空气质量,采用便携式气相色谱仪监测水质,结果表明,便捷、高效的监测仪器为此次污染事故的成功处置提供了技术支持,为以后类似突发污染事故的应急监测提供了参考。     

便携式质谱仪测定某化工园某企业大气中特征有机物

采用便携式质谱仪,通过对某化工园区某企业有机污染物调查,分析确定了该企业的特征污染物。为企业排污治理、安装有机物在线监测设备和加强环境监督管理提供科学依据。     

浦东新区环境空气质量监测对比研究及发展对策探讨

以浦东新区为例,介绍了上海区域环境空气质量变化历程,对比研究了中、美环境空气监测发展历程及成效,提出了区域尤其是浦东新区环境空气监测发展方向、环境空气污染控制及监测相结合进行阶段评估并不断调整的发展战略。     

南京市国控环境空气监测网络优化

对南京市现有的国控环境空气监测网络现状进行了分析,指出了其存在的问题,提出了环境空气监测网络优化方案.     

典型医化园区废气和环境空气中挥发性有机物污染特征

对典型医化园区中的挥发性有机物(VOCs)污染特征进行研究,采用便携式气相色谱质谱法监测园区及周边14个点位的环境空气,大气预浓缩气相色谱质谱法监测10个点位排气筒中废气。结果表明,废气中非甲烷总烃为1. 77～218 mg/m3,环境空气中甲苯、二氯甲烷、丙酮、乙酸乙酯、四氢呋喃的质量浓度分别为0. 048～0. 833,0. 022～3. 07,0. 011～0. 312,0. 004～0. 754和0. 004～0. 529 mg/m3;废气和环境空气中均检出含量较高的芳香烃、卤代烃、酯类、酮类等化合物,以及园区特征的氟苯类和噻吩类化合物。园区环境空气明显受到工业源VOCs污染,分布趋势为生产越密集区域VOCs值越高,经过园区后沿着风向逐渐降低,园区下风向11 km处可测到园区特征氟苯类物质。     

环境空气中汞的直接测定方法研究与应用

研究了环境空气中汞浓度的直接测定方法。利用金汞齐富集－便携式测汞仪对环境空气中的汞进行直接测定，具有简便、快捷、不使用化学试剂的优点。经测试，该方法在0～180 ng／m^3范围内具有良好的线性关系，最低检出浓度为5 ng／m^3。     

环境空气质量自动监测系统质量保证工作的探索

根据全国多个省市的环境空气自动监测质量保证工作的经验和做法,结合乌鲁木齐市环境空气自动监测质量保证工作实际情况,对点位设置要求、制度体系建立、仪器质量控制难点、数据审核与研判等环境空气自动监测质量保证工作的关键环节进行探索,为加强环境空气自动监测质量保证体系提供参考依据.     

广州市天地空一体化环境空气质量监测网络的建设

简述了原有广州市环境空气自动监测网络情况,通过对环境空气自动监测网络的集成优化,增设站点、扩展监测项目和引入新技术,建立了一个"金字塔形"的集天地空一体化的环境空气监测网络,弥补了原有监测网络在反映环境空气质量总体水平、污染来源解析、预报预警所需的环境质量信息、对环境空气质量的评估等方面的不足,该网络已成功应用于广州亚运会的空气质量保障。     

食品企业周边空气中异味挥发性有机物测定方法比较

以1个典型食品生产企业(酱菜厂)周边的异味挥发性有机物监测为例,介绍了罐采样-GC/MS、便携式GC/MS、SPME-GC/MS以及SPME-异味分析系统等4种监测方法的实际应用,从定性、定量监测结果等方面,比较了4种监测方法的特点。罐采样-GC/MS、便携式GC-MS 2种方法适用于定性、定量检测,在有标准样品的前提下,定量结果总体可比;SPME-GC/MS以及SPME-异味分析系统2种方法更适用于定性检测。     

超声提取-气相色谱质谱法测定大气PM2.5中正构烷烃

建立了超声提取-气相色谱质谱法测定大气PM2.5中32种正构烷烃方法,经离子温度优化、前处理比较、空白滤膜考察等获得了最佳的实验条件。研究发现,高、中、低3种浓度标准曲线的相关系数均在0.995以上,3种浓度的空白样品加标回收率分别为72.2%~117.8%、73.5%~104.4%、73.8%~109.5%,精密度均小于10%,实际样品加标回收率为75.7%~108.9%。当采样体积为24 m3时,各目标化合物的方法检出限为0.046~2.6 ng/m~3;经正构烷烃浓度范围为0.17~64.3 ng/m~3的1月及浓度范围为0.53~7.67 ng/m~3的6月的实际样品验证,该方法的检出限和测量范围也可较好的满足实际样品的测定。     

便携式烟气预处理器技术在比对监测中的应用

对2种便携式烟气预处理器在比对监测中的实际应用进行探讨,通过对2种烟气预处理器工作原理及在实际应用中的监测数据进行分析比较,显示在"高湿低硫"条件下,电子冷凝预处理器析出的冷凝液会造成二氧化硫的损失,在应用中应加快除水,减少烟气与冷凝水接触的时间,并防止冷凝液出现在伴热管线与预处理器烟气入口之间。而便携式Nafion预处理器由于具有独特的干燥性能,抗干扰能力,在"高湿低硫"的比对监测中具有较好的可比性和适用性。     

三重串联四极杆气相质谱联用仪测定饮用水源地水体中的多氯联苯

建立了以液-液萃取、三重串联四极杆气相质谱多反应监测法同时测定饮用水源地水体中18种多氯联苯的方法,给出了测量线性范围,线性关系良好,相关系数大于0.998。水中加标浓度为1.00、5.00、10.0ng/L时,平均加标回收率分别为75.6%～96.0%、90.6%～105%和92.4%～102%,相对标准偏差分别为19.8%～11.8%、4.2%～12.9%和4.3%～9.9%,检出限为0.29～0.57ng/L。结果表明,在测定水体中痕量多氯联苯方面,三重串联四极杆气相质谱相对于气相色谱-电子捕获检测和气相色谱质谱-选择离子检测具有更高的灵敏度和准确度,具有更广泛的应用。     

PM10 Concentration Measurements in Dublin City

Mass Concentration of ambient particulate matter with an aerodynamic diameter less than 10µm (PM10) are reported for the first time for a range of sites in Dublin City over a 6 month period from January 1st 1996 to June 30th 1996. PM10 gravimetric mass concentration measurements are made with low flow Partisol 2000 air samplers using an impaction type PM10 inlet and 47mm diameter glass fibre filters. In addition, much finer time resolution measurements (minimum sampling frequency of 30 minutes) are made using a tapered element oscillating microbalance (TEOM) PM10 mass monitor. These PM10 mass concentrations methods are also compared with mass concentration inferred using the standard black smoke method. Analysis of the ambient mass concentration data with reference to traffic density and meteorological influences are presented. Results for the first six months of 1996 show that the average PM10 values range from a high of 49 µg m-3 at the Dublin city centre site to 14 µg m-3 at one of the suburban sites. Intercomparison between PM10 and black smoke mass concentrations show that the relationship is site specific. Statistical analysis between PM10 levels and car traffic number show a positive correlation while a weak negative correlation is found between PM10 levels and rainfall amount, wind speed and air temperature.     

A comparison of X-ray fluorescence and wet chemical analysis for lead on air filters from different personal samplers used in a bronze foundry

Portable X-ray fluorescence (XRF) technology may provide faster turn-around without compromising accuracy when assessing personal exposures to metals such as lead, but it has only been tested in limited field environments. This study is part of a series, where different sampler types are used to collect airborne lead in different environments for presentation to a portable XRF analyzer. In this case personal samples were taken at a bronze foundry where lead is added to an alloy of copper, zinc and iron to improve casting, using the closed-face 37 mm cassette, the 37 mm GSP or "cone" sampler, the 25 mm Institute of Occupational Medicine (IOM) inhalable sampler, the 25 mm Button sampler, and the open-face 25 mm cassette. Mixed cellulose-ester filters were used in all samplers. Following XRF analysis the samples were extracted with acid and analyzed by inductively coupled plasma optical emission spectroscopy (ICP). For lead, all five samplers gave correlations (r(2)) greater than 0.9 between the two analytical methods over the entire range of found lead mass, which encompassed both the action level and the permissible exposure limit enforced in the USA by the Occupational Safety and Health Administration (OSHA). However, a correction was required to adjust linear regression trendlines to give a 1 : 1 correlation for the average of three readings across the GSP sampler, and a similar correction was required for the single readings from the IOM sampler and the 25 mm filter cassette. The bias possibly is due to interference from other metals, possibly copper which can absorb the fluorescent radiation of lead. In the case of the Button sampler, the bias is larger, indicating a further source of error, perhaps due to the thickness of the deposit. However, in all cases, correction of the lead results did not greatly affect the overall percentage of samples where the XRF result was within 25% of the ICP result, although it did improve the overall accuracy of the results. The GSP, IOM and Button samplers are suitable candidates for further evaluation as compatible with on-site XRF analysis for lead and other metals. It is important to check carefully factory pre-set instrument calibrations, as a bias in the calibration for copper was observed.     

Polychlorinated biphenyls (PCBs) analysis using a miniaturized high-resolution time-of-flight mass spectrometer "MULTUM-S II"

In this study, we conducted polychlorinated biphenyls (PCBs) analysis using fast gas chromatography (GC)/high-resolution mass spectrometry (HRMS). Mass spectrometry (MS) was performed with a miniature multi-turn time-of-flight (TOF) analyzer called "MULTUM-S II". MULTUM-S II is truly a portable high resolution mass spectrometer. The mass spectrometer's high resolution capability is due to its theoretical infinite flight path utilizing perfect space and time focusing within a closed flight orbit. Mass resolution above 10?000 was easily achievable employing this portable system. This mass resolution is comparable to magnetic sector mass spectrometers, which have traditionally performed PCB analyses in the past. At a resolution of 10?000, a limit-of-detection of 1 ppb was determined using a heptachlorinated biphenyl standard sample. Using this fast GC/HRMS, 66 PCB congeners were analyzed within 5 min. In addition experiments aimed at confirming interference of PCB signal peaks and matrix peaks in diluted dielectric coolant fluids were performed. We found that the PCB signal peaks were detected without matrix interference via high mass resolution.     

气相色谱／质量选择检测器测定死鱼水体中有机污染物

为查明有机污染物的种类,取死鱼水经GDX-501树脂富集后,用气相色谱/质量选择检测器分析。检出水中82种污染物。     

电感耦合等离子体质谱法同时测定地下水中钴和钼

建立了一种用电感耦合等离子体质谱法同时测定水源地地下水中微量元素钴和钼的方法。与常规的元素测试方法相比,该方法可以同时快速有效地完成钴和钼测试,测试方法简单,结果准确可靠。