Alonso Sobrado Laura, Robledo Fernández Mario, Cueto Díaz Sergio, Ruiz Encinar Jorge, García Alonso J Ignacio
Department of Physical and Analytical Chemistry, University of Oviedo, Julián Clavería 8, 33006 Oviedo, Spain.
Department of Physical and Analytical Chemistry, University of Oviedo, Julián Clavería 8, 33006 Oviedo, Spain.
J Chromatogr A. 2015 Nov 6;1419:99-108. doi: 10.1016/j.chroma.2015.09.071. Epub 2015 Sep 26.
We describe the instrumental modification of a commercial gas chromatography isotope ratio mass spectrometer (GC-IRMS) and its application for on-line carbon isotope dilution. The main modification consisted in the addition of a constant flow of enriched (13)CO2 diluted in helium after the chromatographic column through the splitter holder located inside the chromatographic oven of the instrument. In addition, and in contrast to the conventional mode of operation of GC-IRMS instruments where the signal at m/z 45 is amplified 100-fold with respect to the signal at m/z 44, the same signal amplification was used in both Faraday cups at m/z 44 and 45. Under these conditions isotope ratio precision for the ratio 44/45 was around 0.05% RSD (n=50). The evaluation of the instrument was performed with mixtures of organic compounds including 11 n-alkanes, 16 PAHs, 12 PCBs and 3 benzothiophenes. It was observed that compounds of very different boiling points could be analysed without discrimination in the injector when a Programmable Temperature Vaporizer (PTV) injector was employed. Moreover, the presence of heteroatoms (Cl or S) in the structure of the organic compounds did not affect their combustion efficiency and therefore the trueness of the results. Quantitative results obtained for all the analytes assayed were excellent in terms of precision (<3% RSD) and accuracy (average relative error≤4%) and what is more important using a single and simple generic internal standard for quantification.
我们描述了对商用气相色谱同位素比率质谱仪(GC - IRMS)的仪器改装及其在线碳同位素稀释的应用。主要改装在于通过位于仪器色谱炉内的分流器支架,在色谱柱后添加恒定流量的氦气稀释的富集(^{13}CO_2)。此外,与传统的GC - IRMS仪器操作模式不同,传统模式下(m/z 45)处的信号相对于(m/z 44)处的信号放大100倍,而在本研究中,(m/z 44)和(m/z 45)处的法拉第杯均采用相同的信号放大。在这些条件下,(44/45)比率的同位素比率精密度约为(0.05%)相对标准偏差((n = 50))。使用包括11种正构烷烃、16种多环芳烃、12种多氯联苯和3种苯并噻吩的有机化合物混合物对该仪器进行了评估。结果表明,当采用可编程温度汽化器(PTV)进样器时,沸点差异很大的化合物在进样器中均可无差别地进行分析。此外,有机化合物结构中杂原子(Cl或S)的存在并不影响其燃烧效率,因此不影响结果的准确性。所测定的所有分析物的定量结果在精密度((<3%)相对标准偏差)和准确度(平均相对误差(\leq4%))方面都非常出色,更重要的是,使用单一且简单的通用内标进行定量。