Abstract

Coal tar is a complex mixture of organic compounds obtained from the thermal treatment of coal; it contains several different chemical classes of compounds, such as polycyclic aromatic hydrocarbons, phenols and different heterocyclic compounds including sulphur derivatives. In the present research, a target analysis was carried out for the characterisation of fourteen different classes of organic sulphur compounds in coal tar by using cryogenically-modulated (CM) comprehensive two-dimensional gas chromatography-high resolution time-of-flight mass spectrometry (GC×GC-HR ToFMS) with the support of target analyte finding, a specific software function. Furthermore, absolute quantification data were obtained by using eight pure standard sulphur compounds, and 1-fluoronaphthalene as internal standard. Several figures-of-merit of the proposed method were measured (linearity, intra-day precision, limits of detection and quantification). Finally, the overall analytical performance of CM GC×GC-HR ToFMS was evaluated, in relation to MS similarities, mass accuracies, second-dimension peak widths, peak capacity and tailing factors. The approach proved itself as being a powerful analytical platform, benefiting from the high sensitivity, selectivity and resolving power, of both the GC and MS sides.

Highlights

  • The concept of comprehensive two-dimensional gas chromatography (GC×GC) was introduced in the early 1990s by Liu and Phillips [1], bringing a great evolution to the GC field

  • One of the main objectives of the work was to make a direct comparison between gas chromatography-single quadrupole mass spectrometry (GC-QMS) and GC×GC coupled with low resolution time-of-flight mass spectrometry (LR ToFMS)

  • The overall analytical performance related to the method, in its various aspects, can be considered as satisfactory

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Summary

Introduction

The concept of comprehensive two-dimensional gas chromatography (GC×GC) was introduced in the early 1990s by Liu and Phillips [1], bringing a great evolution to the GC field.

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