Dial Angela R, Misra Sambuddha, Landing William M
Department of Earth, Ocean, and Atmospheric Science, Florida State University; National High Magnetic Field Laboratory, Geochemistry, 1800 East Paul Dirac Drive, Tallahassee, FL, 32310, USA.
Department of Earth Sciences, University of Cambridge, Downing Street, Cambridge, CB2 3EQ, UK.
Rapid Commun Mass Spectrom. 2015 Apr 30;29(8):707-18. doi: 10.1002/rcm.7152.
Accurate determination of trace metals has many applications in environmental and life sciences, such as constraining the cycling of essential micronutrients in biological production and employing trace metals as tracers for anthropogenic pollution. Analysis of elements such as Fe, As, Se, and Cd is challenged by the formation of polyatomic mass spectrometric interferences, which are overcome in this study.
We utilized an Octopole Collision/Reaction Cell (CRC)-equipped Quadrupole-Inductively Coupled Plasma Mass Spectrometer for the rapid analysis of small volume samples (~250 μL) in a variety of matrices containing HNO3 and/or HCl. Efficient elimination of polyatomic interferences was demonstrated by the use of the CRC in Reaction Mode (RM; H2 gas) and in Collision-Reaction Mode (CRM; H2 and He gas), in addition to hot plasma (RF power 1500 W) and cool plasma (600 W) conditions.
It was found that cool plasma conditions with RM achieved the greatest signal sensitivity while maintaining low detection limits (i.e. (56) Fe in 0.44 M HNO3 has a sensitivity of 160,000 counts per second (cps)-per-1 µg L(-1) and a limit of detection (LoD) of 0.86 ng L(-1) ). The average external precision was ≤ ~10% for minor (≤10 µg L(-1) ) elements measured in a 1:100 dilution of NIST 1643e and for iron in rainwater samples under all instrumental operating conditions.
An improved method has been demonstrated for the rapid multi-element analysis of trace metals that are challenged by polyatomic mass spectrometric interferences, with a focus on (56) Fe, (75) As, (78) Se and (111) Cd. This method can contribute to aqueous environmental geochemistry and chemical oceanography, as well as other fields such as forensic chemistry, agriculture, food chemistry, and pharmaceutical sciences.
痕量金属的准确测定在环境科学和生命科学中有许多应用,例如限制生物生产中必需微量营养素的循环以及使用痕量金属作为人为污染的示踪剂。铁、砷、硒和镉等元素的分析受到多原子质谱干扰形成的挑战,本研究克服了这一问题。
我们使用配备八极杆碰撞/反应池(CRC)的四极杆电感耦合等离子体质谱仪,对含有硝酸和/或盐酸的各种基质中的小体积样品(约250微升)进行快速分析。除了热等离子体(射频功率1500瓦)和冷等离子体(600瓦)条件外,通过在反应模式(RM;氢气)和碰撞-反应模式(CRM;氢气和氦气)下使用CRC,证明了多原子干扰的有效消除。
发现冷等离子体条件下的RM在保持低检测限的同时实现了最大的信号灵敏度(即0.44 M硝酸中的(56)Fe灵敏度为每秒160,000计数(cps)/每1微克/升,检测限(LoD)为0.86纳克/升)。在所有仪器操作条件下,对NIST 1643e的1:100稀释液中测量的痕量(≤10微克/升)元素以及雨水样品中的铁,平均外部精密度≤约10%。
已证明一种改进的方法可用于快速多元素分析受多原子质谱干扰影响的痕量金属,重点是(56)Fe、(75)As、(78)Se和(111)Cd。该方法可应用于水环境地球化学和化学海洋学,以及法医学、农业、食品化学和制药科学等其他领域。