Daughtrey E H, Oliver K D, Adams J R, Kronmiller K G, Lonneman W A, McClenny W A
ManTech Environmental Technology Inc, Research Triangle Park, NC 27709, USA.
J Environ Monit. 2001 Feb;3(1):166-74. doi: 10.1039/b007158g.
A carefully designed study was conducted during the summer of 1998 to collect samples of ambient air by canisters and compare the analysis results to direct sorbent preconcentration results taken at the time of sample collection. Thirty-two 1 h sample sets were taken, each composed of a "near-real-time" sample analyzed by an autoGC-MS XonTech 930/Varian Saturn 2000 system, and Summa and Silco canisters. Hourly total non-methane organic carbon (TNMOC), ozone, and meteorological measurements were also made. Each canister was analyzed on the autoGC-MS system for a target list of 108 volatile organic compounds (VOCs) and on a manual cryosampling GC-FID system. Comparisons were made between the collection and analysis methods. Because of the low sample loading (150-250 ppbC TNMOC), these comparisons were a stringent test of sample collection and analysis capabilities. The following specific conclusions may be drawn from this study. Reasonable precision (within 15% mean difference of duplicate analyses from the same canister) can be obtained for analyses of target VOCs at low-ppbC concentrations. Relative accuracy between the GC-MS and GC-FID analysis methods is excellent, as demonstrated by comparisons of analyses of the same canisters, if measurements are sufficiently above the detection limits. This is especially significant as the GC-MS and GC-FID were independently calibrated. While statistically significant differences may be observed between the results from canister and near-real-time samples, the differences were generally small and there were clear correlations between the canister results and the near-real-time results. Canister cleanliness limits detection below the EPA Method TO-14 acceptance standard of 0.2 ppbv (0.2-2 ppbC for target analytes).
1998年夏天开展了一项精心设计的研究,通过罐采样收集环境空气样本,并将分析结果与采样时直接进行的吸附剂预浓缩结果进行比较。共采集了32组1小时的样本,每组样本都包括一个通过自动气相色谱 - 质谱联用仪(XonTech 930/Varian Saturn 2000系统)分析的“近实时”样本,以及Summa罐和Silco罐样本。同时还进行了每小时的总非甲烷有机碳(TNMOC)、臭氧和气象测量。每个罐样本在自动气相色谱 - 质谱联用仪系统上针对108种挥发性有机化合物(VOCs)的目标清单进行分析,并在手动低温采样气相色谱 - 火焰离子化检测器(GC - FID)系统上进行分析。对采集和分析方法进行了比较。由于样本负载量较低(TNMOC为150 - 250 ppbC),这些比较是对样本采集和分析能力的严格测试。从这项研究中可以得出以下具体结论。对于低ppbC浓度的目标VOCs分析,可获得合理的精密度(同一罐重复分析的平均差异在15%以内)。如果测量值足够高于检测限,通过对同一罐样本的分析比较表明,气相色谱 - 质谱联用仪(GC - MS)和气相色谱 - 火焰离子化检测器(GC - FID)分析方法之间的相对准确度非常好。这一点尤为重要,因为GC - MS和GC - FID是独立校准的。虽然罐样本和近实时样本的结果之间可能会观察到统计学上的显著差异,但差异通常较小,并且罐样本结果与近实时结果之间存在明显的相关性。罐的清洁程度限制了检测低于美国环境保护局(EPA)方法TO - 14的验收标准0.2 ppbv(目标分析物为0.2 - 2 ppbC)。