Haas K, Feldmann J, Wennrich R, Stärk H J
University of Aberdeen, Department of Chemistry, Scotland, UK.
Fresenius J Anal Chem. 2001 Jul;370(5):587-96. doi: 10.1007/s002160100797.
The analytical performance of an axial inductively-coupled-plasma time-of-flight mass spectrometer (ICP-TOFMS) as a detector for fast transient chromatographic signals resulting from the coupling to capillary gas chromatography (CGC) was investigated. A cryotrapping GC-ICP-TOFMS method for the determination of volatile metal(loid) compounds (VOMs) in gases was used and the suitability of the TOF mass analyzer for multielemental speciation analysis and multi-isotope ratio determinations was studied in terms of accuracy and precision. Isotope ratios 118Sn/120Sn and 121Sb/123Sb have been determined in in-house gas standard atmospheres in Tedlar bags at two different levels (100 pg and 1 ng) for different elemental species (SnH4, MeSnH3, Me2SnH2, Me3SnH, BuSnH3, SbH3, and MeSbH2). A limitation arising from counting statistics in both detection modes could be shown. A solution containing rhodium (10 ng mL(-1)) and cadmium (40 ng mL(-1)) was introduced simultaneously to the GC outlet. Rhodium acts as a continuous internal standard and Cd is used for mass-bias correction (by measuring the 111Cd/113Cd ratio). The detection system in both pulse counting and analog mode was examined. The best attainable precision was established for Me2SnH2 (analog mode, 12 replicates, 1 ng, RSD 0.34%, accuracy 0.31%) whereas most other species ranged between 0.4 and 0.5% RSD if higher concentrations were used. The limitations of the pulse counting system are clearly seen, with peak heights of more than 2000 counts reaching saturation (for an integration time of 100 ms), which reduces the accuracy of isotope ratio determinations. A dozen VOM could be detected in an aged landfill gas sample; several unidentified Sn compounds were present. Although their isotope ratios are within the confidence value of the standards, it is not yet clear if the acquired precision is good enough to identify isotopic fractionation of metal(loid)s through biovolatilization processes. With the precision achieved, the combination of cryotrapping GC and ICP-TOFMS is a powerful tool for monitoring volatile multi-element species in multi-tracer experiments and isotope dilution methodology.
研究了轴向电感耦合等离子体飞行时间质谱仪(ICP - TOFMS)作为与毛细管气相色谱(CGC)联用产生的快速瞬态色谱信号的检测器的分析性能。采用了一种低温捕集GC - ICP - TOFMS方法测定气体中的挥发性金属(类金属)化合物(VOMs),并从准确度和精密度方面研究了TOF质量分析器用于多元素形态分析和多同位素比测定的适用性。在Tedlar袋中的室内气体标准气氛中,针对不同元素种类(SnH4、MeSnH3、Me2SnH2、Me3SnH、BuSnH3、SbH3和MeSbH2)在两个不同水平(100 pg和1 ng)下测定了同位素比118Sn/120Sn和121Sb/123Sb。可以看出两种检测模式下计数统计产生的一个局限性。将含有铑(10 ng mL(-1))和镉(40 ng mL(-1))的溶液同时引入GC出口。铑用作连续内标,镉用于质量偏差校正(通过测量111Cd/113Cd比)。对脉冲计数和模拟模式下的检测系统进行了检查。对于Me2SnH2确定了可达到的最佳精密度(模拟模式,12次重复,1 ng,相对标准偏差0.34%,准确度0.31%),而如果使用更高浓度,大多数其他种类的相对标准偏差在0.4%至0.5%之间。脉冲计数系统的局限性很明显,计数超过2000的峰高达到饱和(积分时间为100 ms),这降低了同位素比测定的准确度。在一个老化的垃圾填埋气样品中可以检测到十几种VOM;存在几种未鉴定的Sn化合物。尽管它们的同位素比在标准的置信值范围内,但获得的精密度是否足以识别通过生物挥发过程的金属(类金属)同位素分馏尚不清楚。凭借所达到的精密度,低温捕集GC和ICP - TOFMS的组合是多示踪剂实验和同位素稀释方法中监测挥发性多元素种类的有力工具。