Sessions Alex L
Division of Geological and Planetary Sciences, California Institute of Technology, Pasadena, CA 91125, USA.
J Sep Sci. 2006 Aug;29(12):1946-61. doi: 10.1002/jssc.200600002.
Instrumentation and methods exist for highly precise analyses of the stable-isotopic composition of organic compounds separated by GC. The general approach combines a conventional GC, a chemical reaction interface, and a specialized isotope-ratio mass spectrometer (IRMS). Most existing GC hardware and methods are amenable to isotope-ratio detection. The interface continuously and quantitatively converts all organic matter, including column bleed, to a common molecular form for isotopic measurement. C and N are analyzed as CO2 and N2, respectively, derived from combustion of analytes. H and O are analyzed as H2 and CO produced by pyrolysis/reduction. IRMS instruments are optimized to provide intense, highly stable ion beams, with extremely high precision realized via a system of differential measurements in which ion currents for all major isotopologs are simultaneously monitored. Calibration to an internationally recognized scale is achieved through comparison of closely spaced sample and standard peaks. Such systems are capable of measuring 13C/12C ratios with a precision approaching 0.1 per thousand (for values reported in the standard delta notation), four orders of magnitude better than that typically achieved by conventional "organic" mass spectrometers. Detection limits to achieve this level of precision are typically < 1 nmol C (roughly 10 ng of a typical hydrocarbon) injected on-column. Achievable precision and detection limits are correspondingly higher for N, O, and H, in that order.
存在用于对通过气相色谱法分离的有机化合物的稳定同位素组成进行高精度分析的仪器和方法。一般方法是将传统的气相色谱仪、化学反应接口和专门的同位素比率质谱仪(IRMS)结合起来。现有的大多数气相色谱硬件和方法都适用于同位素比率检测。该接口将包括柱流失在内的所有有机物连续定量地转化为用于同位素测量的共同分子形式。碳和氮分别作为分析物燃烧产生的二氧化碳和氮气进行分析。氢和氧作为热解/还原产生的氢气和一氧化碳进行分析。IRMS仪器经过优化,可提供高强度、高度稳定的离子束,通过同时监测所有主要同位素异构体离子电流的差分测量系统实现极高的精度。通过比较间隔很近的样品峰和标准峰,实现与国际认可标准的校准。这样的系统能够以接近千分之一的精度测量13C/12C比率(以标准δ符号表示的值),比传统“有机”质谱仪通常达到的精度高四个数量级。达到这种精度水平的检测限通常是柱上进样量<1 nmol C(约10 ng典型烃类)。对于氮、氧和氢,可达到的精度和检测限依次相应更高。