Department of Civil and Environmental Engineering, Texas A&M University, College Station, TX, USA.
Department of Geology and Geophysics, Texas A&M University, College Station, TX, USA.
Talanta. 2022 May 1;241:123236. doi: 10.1016/j.talanta.2022.123236. Epub 2022 Jan 19.
We present novel chemical separation protocols for isotopic analysis of low mass aliquots (0.3 mg and 25 mg) of several reference materials and real-world samples of relevance to urban airborne particulate matter (PM) investigations. A high-yielding gravity flow column chromatography scheme was developed for facile and quantitative separation of Sr, Nd, and Hf prior to multi collector - inductively coupled plasma - mass spectrometry (MC-ICP-MS). Because we are interested in isolating and accurately quantitating individual anthropogenic and natural aerosol sources in complex industrial/metropolitan atmospheric environments, laboratory protocols were optimized using National Institute of Standards and Technology Standard Reference Material (SRM) 1648a (urban atmospheric PM), SRM 1633b (coal fly ash), and European Commission standards BCR-723 (vehicular road dust), and BCR-2 (basalt rock standard). Sr, Nd, and Hf procedural blanks from column chromatography were low (averaging only 37 pg, 17 pg, 11 pg, respectively) and recoveries were high (averaging 95%, 82%, and 92%, respectively). A volume-adjustment protocol was established using isotope reference solutions SRM 987 (SrCO), JNdi (NdO), and in-house Hf standards to dilute the dried samples prior to MC-ICP-MS based on projected uncertainties for low sample masses. Sr/Sr, Nd/Nd, and Hf/Hf isotopic ratios in SRM 1648a, BCR-723, and SRM 1633b are reported for the first time that can serve as provisional reference values. The novel method was used to characterize isotopic ratios and elemental abundances in two anthropogenic urban aerosol sources, namely motor vehicles and petroleum refining using airborne fine PM collected in a vehicular tunnel and fluidized-bed catalytic cracking catalysts, respectively. Two other important mineral-rich urban PM sources, namely soil (i.e., resuspended crustal material) and concrete/cement dust (i.e., construction activity) were also characterized. These are the first isotopic measurements in these environmental compartments and were compared with literature data for long-range transported North African dust, which is a prominent summertime PM source in urban regions in southeastern United States. We demonstrate the capability of coupled Sr-Nd-Hf isotopes to uniquely trace different mineral dust sources with overlapping elemental composition (Sahara-Sahel region, local soil, and concrete/cement) and accurately isolate various urban PM sources demonstrating the superiority of isotopic markers over elemental tracers.
我们提出了新的化学分离方案,用于对低质量的几种参考物质和与城市空气颗粒物(PM)研究相关的实际样品进行同位素分析。开发了一种高产率的重力流柱层析方案,用于在多收集器 - 电感耦合等离子体质谱(MC-ICP-MS)之前轻松、定量地分离 Sr、Nd 和 Hf。由于我们有兴趣在复杂的工业/都会大气环境中分离和准确定量单个人为和天然气溶胶源,因此使用美国国家标准与技术研究院标准参考物质(SRM)1648a(城市大气 PM)、SRM 1633b(煤飞灰)和欧洲委员会标准 BCR-723(车辆道路尘)和 BCR-2(玄武岩岩石标准)优化了实验室方案。来自柱层析的 Sr、Nd 和 Hf 程序空白值很低(平均仅为 37 pg、17 pg 和 11 pg),回收率很高(平均为 95%、82%和 92%)。使用同位素参考溶液 SRM 987(SrCO)、JNdi(NdO)和内部 Hf 标准建立了体积调整方案,以便根据低样品质量的预测不确定性,在 MC-ICP-MS 之前稀释干燥样品。首次报告了 SRM 1648a、BCR-723 和 SRM 1633b 中 Sr/Sr、Nd/Nd 和 Hf/Hf 同位素比值,可作为暂定参考值。该新方法用于表征在车辆隧道中收集的空气中细颗粒物和流化催化裂化催化剂中两种人为城市气溶胶源(即汽车和石油精炼)的同位素比值和元素丰度。还对另外两个重要的富含矿物质的城市 PM 源,即土壤(即再悬浮的地壳物质)和混凝土/水泥粉尘(即建筑活动)进行了表征。这些是这些环境成分中的第一批同位素测量值,并与文献中关于长距离传输的北非尘埃的数据进行了比较,北非尘埃是美国东南部城市地区夏季 PM 的主要来源。我们证明了 Sr-Nd-Hf 同位素的结合能够独特地追踪具有重叠元素组成的不同矿物质尘埃源(撒哈拉-萨赫勒地区、当地土壤和混凝土/水泥),并准确分离各种城市 PM 源,证明同位素标记物优于元素示踪剂的优越性。