Rüger Christopher P, Schwemer Theo, Sklorz Martin, O'Connor Peter B, Barrow Mark P, Zimmermann Ralf
1 Joint Mass Spectrometry Centre/Chair of Analytical Chemistry, University of Rostock, Rostock, Germany.
2 Department of Chemistry, University of Warwick, Coventry, UK.
Eur J Mass Spectrom (Chichester). 2017 Feb;23(1):28-39. doi: 10.1177/1469066717694286. Epub 2017 Jan 1.
The analysis of petrochemical materials and particulate matter originating from combustion sources remains a challenging task for instrumental analytical techniques. A detailed chemical characterisation is essential for addressing health and environmental effects. Sophisticated instrumentation, such as mass spectrometry coupled with chromatographic separation, is capable of a comprehensive characterisation, but needs advanced data processing methods. In this study, we present an improved data processing routine for the mass chromatogram obtained from gas chromatography hyphenated to atmospheric pressure chemical ionisation and ultra high resolution mass spectrometry. The focus of the investigation was the primary combustion aerosol samples, i.e. particulate matter extracts, as well as the corresponding fossil fuels fed to the engine. We demonstrate that utilisation of the entire transient and chromatographic information results in advantages including minimisation of ionisation artefacts and a reliable peak assignment. A comprehensive comparison of the aerosol and the feed fuel was performed by applying intensity weighted average values, compound class distribution and principle component analysis. Certain differences between the aerosol generated with the two feed fuels, diesel fuel and heavy fuel oil, as well as between the aerosol and the feed were revealed. For the aerosol from heavy fuel oil, oxidised species from the CHN and CHS class precursors of the feed were predominant, whereas the CHO class is predominant in the combustion aerosol from light fuel oil. Furthermore, the complexity of the aerosol increases significantly compared to the feed and incorporating a higher chemical space. Coupling of atmospheric pressure chemical ionisation to gas chromatography was found to be a useful additional approach for characterisation of a combustion aerosol, especially with an automated utilisation of the information from the ultra-high resolution mass spectrometer and the chromatographic separation.
对源自燃烧源的石化材料和颗粒物进行分析,对于仪器分析技术而言仍是一项具有挑战性的任务。详细的化学表征对于解决健康和环境影响至关重要。诸如与色谱分离联用的质谱等精密仪器能够进行全面表征,但需要先进的数据处理方法。在本研究中,我们针对从与大气压化学电离和超高分辨率质谱联用的气相色谱获得的质量色谱图,提出了一种改进的数据处理程序。研究重点是一次燃烧气溶胶样品,即颗粒物提取物,以及供给发动机的相应化石燃料。我们证明,利用整个瞬态和色谱信息会带来诸多优势,包括将电离假象降至最低以及可靠的峰归属。通过应用强度加权平均值、化合物类别分布和主成分分析,对气溶胶和进料燃料进行了全面比较。揭示了使用两种进料燃料(柴油和重质燃料油)产生的气溶胶之间以及气溶胶与进料之间的某些差异。对于来自重质燃料油的气溶胶,进料中CHN和CHS类前体的氧化物种占主导,而CHO类在轻质燃料油燃烧气溶胶中占主导。此外,与进料相比,气溶胶的复杂性显著增加,且占据更高的化学空间。发现将大气压化学电离与气相色谱联用是表征燃烧气溶胶的一种有用的附加方法,尤其是在自动利用来自超高分辨率质谱仪的信息和色谱分离方面。