Molecular Characterization of Thiols in Fossil Fuels by Michael Addition Reaction Derivatization and Electrospray Ionization Fourier Transform Ion Cyclotron Resonance Mass Spectrometry

• Published in: Analytical chemistry (Washington) Vol. 88; no. 19; pp. 9837 - 9842
• Main Authors: Wang, Meng, Zhao, Suoqi, Liu, Xuxia, Shi, Quan
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 04-10-2016
• Subjects: Crude oil; Cyclotron resonance; Fossil fuels; Fourier transforms; Ionization; Ions; Mass spectrometry; Michael reaction; Molecules; Organic chemicals; Thiols
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/acs.analchem.6b02997

Thiols widely occur in sediments and fossil fuels. However, the molecular composition of these compounds is unclear due to the lack of appropriate analytical methods. In this work, a characterization method for thiols in fossil fuels was developed on the basis of Michael addition reaction derivatization followed by electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI FT-ICR MS). Model thiol compound studies showed that thiols were selectively reacted with phenylvinylsulfone and transformed to sulfones with greater than 98% conversions. This method was applied to a coker naphtha, light and heavy gas oils, and crude oils from various geological sources. The results showed that long alkyl chain thiols are readily present in petroleum, which have up to 30 carbon atoms. Large DBE dispersity of thiols indicates that naphthenic and aromatic thiols are also present in the petroleum. This method is capable of detecting thiol compounds in the part per million range by weight. This method allows characterization of thiols in a complex hydrocarbon matrix, which is complementary to the comprehensive analysis of sulfur compounds in fossil fuels.