双语化学辞典Chem Lexicon
技术 · 分析化学 · 原子光谱 Analytical chemistry · Atomic spectrometry

电感耦合等离子体质谱Inductively coupled plasma mass spectrometry

拼音Pinyin diàn gǎn ǒu hé děng lí zǐ tǐ zhì pǔ 别名Also ICP-MS;ICP-MS

定义Definition

电感耦合等离子体质谱是以高温氩等离子体作为离子源,把样品中的元素原子化并电离为单电荷正离子,再用质谱按质荷比分离检测的元素和同位素分析技术。它是目前灵敏度最高的多元素分析方法之一,检出限可达 ng/L 甚至 pg/L 级。

ICP-MS uses a hot argon plasma as an ion source to atomise the elements in a sample and ionise them to singly charged positive ions, which a mass spectrometer separates and counts by m/z. It is one of the most sensitive multi-element and isotopic techniques, with detection limits of ng/L or even pg/L.

原理Principle

液体样品经雾化器雾化后进入约 6000–10000 K 的氩等离子体,在毫秒内去溶剂、原子化、电离,绝大多数金属元素电离效率超过 90%。离子通过采样锥和截取锥进入高真空,经离子透镜聚焦后由四极杆(或扇形磁场、飞行时间)质量分析器分离,电子倍增器计数。主要干扰包括多原子离子干扰(如 ⁴⁰Ar³⁵Cl⁺ 干扰 ⁷⁵As⁺、⁴⁰Ar¹⁶O⁺ 干扰 ⁵⁶Fe⁺)和同量异位素干扰,常用碰撞/反应池(He、H₂、NH₃)或高分辨质谱消除。

Liquid samples are nebulised into an argon plasma at about 6000–10,000 K, where within milliseconds they are desolvated, atomised and ionised, with ionisation efficiencies above 90% for most metals. Ions pass through sampler and skimmer cones into high vacuum, are focused by ion lenses, separated by a quadrupole (or magnetic sector or time-of-flight) analyser and counted by an electron multiplier. The main interferences are polyatomic ions, such as ⁴⁰Ar³⁵Cl⁺ on ⁷⁵As⁺ and ⁴⁰Ar¹⁶O⁺ on ⁵⁶Fe⁺, and isobaric overlaps, removed with collision/reaction cells (He, H₂, NH₃) or high-resolution MS.

由来Origin

1980 年英国萨里大学的格雷与美国艾姆斯实验室的霍克等人合作,首次报道了 ICP 与四极杆质谱联用。1983 年第一台商品化 ICP-MS 问世。此后多接收器 ICP-MS(MC-ICP-MS)、激光剥蚀进样(LA-ICP-MS)和单颗粒、单细胞 ICP-MS 相继发展。

In 1980 Gray at the University of Surrey and Houk and colleagues at the Ames Laboratory in the United States first reported coupling an ICP to a quadrupole mass spectrometer. The first commercial ICP-MS appeared in 1983, followed by multicollector ICP-MS (MC-ICP-MS), laser-ablation sampling (LA-ICP-MS) and single-particle and single-cell ICP-MS.

应用Applications

ICP-MS 用于饮用水和食品中的超痕量重金属检测、半导体超纯试剂和晶圆杂质分析、稀土元素和铂族元素测定、地质年代学(锆石 U-Pb 定年,LA-ICP-MS)、同位素示踪和核法证、临床血液和尿液微量元素、药品元素杂质(ICH Q3D)、纳米颗粒表征,以及与色谱联用进行元素形态分析(如区分无机砷和有机砷)。

ICP-MS measures ultra-trace heavy metals in drinking water and food, impurities in ultrapure semiconductor reagents and wafers, rare-earth and platinum-group elements, geochronology (zircon U–Pb dating by LA-ICP-MS), isotopic tracing and nuclear forensics, trace elements in blood and urine, elemental impurities in drugs (ICH Q3D), nanoparticles, and, coupled with chromatography, elemental speciation such as inorganic versus organic arsenic.

反应Reactions

M(样品) Ar 等离子体, ~8000 K⟶ M+ + e−M Ar Plasma (physics), ~8000 K⟶ M+ + e−

大多数金属形成单电荷正离子。

Most metals form singly charged positive ions.

年表Timeline

  • 1980

    首次报道 ICP-MS

    ICP-MS is first reported

  • 1983

    首台商品化 ICP-MS

    The first commercial ICP-MS

  • 1985

    激光剥蚀 ICP-MS

    Laser-ablation ICP-MS

  • 1992

    多接收器 ICP-MS

    Multicollector ICP-MS