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采用预浓缩和抑制电导检测,离子色谱法分离和定量大气气体和颗粒物中的烷基甲胺和乙胺。

Ion chromatographic separation and quantitation of alkyl methylamines and ethylamines in atmospheric gas and particulate matter using preconcentration and suppressed conductivity detection.

机构信息

Department of Chemistry, University of Toronto, 80 St. George St., Toronto, Ontario M5S 3H6, Canada.

出版信息

J Chromatogr A. 2012 Aug 24;1252:74-83. doi: 10.1016/j.chroma.2012.06.062. Epub 2012 Jun 26.

DOI:10.1016/j.chroma.2012.06.062
PMID:22784696
Abstract

Two methods based on ion chromatography (IC) were developed for the detection of methyl and ethyl alkyl amines (methylamine (MA), ethylamine (EA), dimethylamine (DMA), diethylamine (DEA), trimethylamine (TMA) and triethylamine (TEA)) and NH(3)/NH(4)(+) in online atmospheric gas-particle and size-resolved particulate samples. The two IC methods were developed to analyze samples collected with an ambient ion monitor (AIM), an online gas-particle collection system, or with a Micro Orifice Uniform Deposit Impactor (MOUDI) for size-resolved particle samples. These methods enable selective and (semi-) quantitative detection of alkyl amines at ambient atmospheric concentrations (pptv and pgm(-3)) in samples where significant interferences can be expected from Na(+) and NH(4)(+), for example marine and rural air masses. Sample pre-concentration using a trace cation column enabled instrumental detection limits on the order of pmol (sub-ng) levels per sample, an improvement of up to 10(2) over current IC methods. Separation was achieved using a methanesulfonic acid gradient elution on Dionex CS12A and CS17 columns. The relative standard deviations in retention times during 3 weeks continuous (hourly) sampling campaigns ranged from 0.1 to 0.5% and 0.2 to 5% for the CS12A and CS17 across a wide dynamic range of atmospheric concentrations. Resolution of inorganic and organic cations is limited to 25min for online samples. Mass-dependent coelution of NH(4)(+)/MA/EA occurred on the CS12A column and DEA/TMA coeluted on both columns. Calibrations of ammonium show a non-linear response across the entire calibration range while all other analytes exhibit high linearity (R(2)=0.984-0.999), except for EA and TEA on the CS12A (R(2)=0.960 and 0.941, respectively). Both methods have high analytical accuracy for the nitrogenous bases ranging from 9.5 to 20% for NH(3) and <5-15% for the amines. Hourly observations of amines at Egbert, ON in October 2010 showed gaseous DMA and TMA+DEA at 1-10pptv in air, while particulate DMA and TMA+DEA were present at 0.5-4ng m(-3). A size-resolved particulate sample collected over 23h was found to contain DMA, TMA+DEA and MEA at 1.78, 8.15 and 0.03ngm(-3) mass loadings, with the amine mass enhanced in particle sizes between 100 and 1000nm. These results highlight a need for very sensitive and selective detection of methyl and ethyl amines in addition to NH(3) in continuous online monitoring strategies.

摘要

两种基于离子色谱(IC)的方法被开发用于检测甲基和乙基烷基胺(甲胺(MA)、乙胺(EA)、二甲胺(DMA)、二乙胺(DEA)、三甲胺(TMA)和三乙胺(TEA))和 NH(3)/NH(4)(+)在在线大气气-粒和粒径分辨颗粒物样品中。这两种 IC 方法是为了分析用环境离子监测仪(AIM)、在线气-粒采集系统或微射流均匀沉积撞击器(MOUDI)采集的粒径分辨颗粒物样品而开发的。这些方法能够在存在显著的 Na(+)和 NH(4)(+)干扰的情况下,选择性地(半定量地)检测环境大气浓度(pptv 和 pgm(-3))下的烷基胺,例如海洋和农村空气团。使用痕量阳离子柱进行样品预浓缩,可使仪器检测限达到 pmol(亚纳克)级水平,比当前的 IC 方法提高了 10(2)倍。使用 Dionex CS12A 和 CS17 柱通过甲烷磺酸梯度洗脱实现分离。在 3 周连续(每小时)采样过程中,CS12A 和 CS17 的保留时间的相对标准偏差在 0.1%到 0.5%和 0.2%到 5%之间,在广泛的大气浓度动态范围内。在线样品中,无机和有机阳离子的分辨率限于 25 分钟。在 CS12A 柱上,NH(4)(+)/MA/EA 发生质量依赖性共洗脱,而 DEA/TMA 在两个柱上都共洗脱。铵的校准显示整个校准范围内的非线性响应,而所有其他分析物均表现出高线性(R(2)=0.984-0.999),除了 CS12A 上的 EA 和 TEA(R(2)=0.960 和 0.941)。两种方法对氮碱基的分析准确性都很高,NH(3)的准确度为 9.5%至 20%,胺的准确度为<5-15%。2010 年 10 月在安大略省 Egbert 的 hourly 观测显示,空气中 DMA 和 TMA+DEA 的浓度为 1-10pptv,而颗粒状 DMA 和 TMA+DEA 的浓度为 0.5-4ng m(-3)。在 23 小时内采集的粒径分辨颗粒物样品中,发现 DMA、TMA+DEA 和 MEA 的质量负荷分别为 1.78、8.15 和 0.03ngm(-3),在 100 到 1000nm 的粒径范围内,胺的质量增加。这些结果突出表明,在连续在线监测策略中,除了 NH(3)之外,还需要对甲基和乙基胺进行非常敏感和选择性的检测。

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