Literature DB >> 23239384

Abundant naphthenic acids in oil sands process-affected water: studies by synthesis, derivatisation and two-dimensional gas chromatography/high-resolution mass spectrometry.

Charles E West1, Alan G Scarlett, Jos Pureveen, Erik W Tegelaar, Steven J Rowland.   

Abstract

RATIONALE: The large volumes of 'supercomplex' mixtures of reputedly toxic organic compounds in acidic extracts of oil sands process-affected waters (OSPW) represent a challenging goal for complete characterisation. To date, comprehensive two-dimensional gas chromatography/time-of-flight mass spectrometry (GCxGC/TOFMS) has allowed the acquisition and interpretation of numerous electron ionisation mass spectra including many of those confirmed to be tricyclic and pentacyclic carboxylic acids by reference to the spectra and retention positions of authentic or synthetic compounds. This has allowed the toxicities of some of the identified acids to be determined and their environmental significance to be better assessed.
METHODS: Synthesis, derivatisation (methyl, trideuteriomethyl and trimethylsilyl esters) and GCxGC/TOFMS with nominal mass and higher mass accuracy (ca. 5 ppm) were used to study three abundant unknown acids present in OSPW samples from two different industrial suppliers.
RESULTS: GCxGC/TOFMS with nominal mass accuracy, of methyl, trideuteriomethyl and trimethylsilyl esters of three abundant acids in two OSPW samples, produced mass spectra consistent with their assignment as either C(16) tetracyclic acids or as isobaric pentacyclic C(15) hydroxy acids ('O(3)') or sulfur-containing ('SO(2)') species. The synthesis of several isomeric pentacyclic C(15) hydroxy acids and examination of the GCxGC retention times and mass spectra (nominal mass) of their derivatives suggested that the unknown OSPW acids were not hydroxy acids, and GCxGC/TOFMS with higher mass accuracy ruled out the possibility. The possibility that they were isobaric 'SO(2)' species could also be dismissed as this was inconsistent with accurate masses, the derivatisation reactions observed, the fragmentation patterns and the isotope distributions, which excluded the presence of sulphur.
CONCLUSIONS: The data support the contention that the three abundant unknowns were indeed C(16) tetracyclic acids. An equally rigorous approach will be necessary to characterise further acids in such mixtures. This is important so that chemistry can be used to guide the search for toxic modes of action.
Copyright © 2012 John Wiley & Sons, Ltd.

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Year:  2013        PMID: 23239384     DOI: 10.1002/rcm.6452

Source DB:  PubMed          Journal:  Rapid Commun Mass Spectrom        ISSN: 0951-4198            Impact factor:   2.419


  4 in total

1.  Differential protein expression during growth on model and commercial mixtures of naphthenic acids in Pseudomonas fluorescens Pf-5.

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Journal:  Microbiologyopen       Date:  2021-08       Impact factor: 3.139

2.  Diamondoid naphthenic acids cause in vivo genetic damage in gills and haemocytes of marine mussels.

Authors:  Awantha Dissanayake; Alan G Scarlett; Awadhesh N Jha
Journal:  Environ Sci Pollut Res Int       Date:  2016-02-16       Impact factor: 4.223

3.  Advances in Distinguishing Groundwater Influenced by Oil Sands Process-Affected Water (OSPW) from Natural Bitumen-Influenced Groundwaters.

Authors:  L Mark Hewitt; James W Roy; Steve J Rowland; Greg Bickerton; Amila DeSilva; John V Headley; Craig B Milestone; Alan G Scarlett; Susan Brown; Christine Spencer; Charles E West; Kerry M Peru; Lee Grapentine; Jason M E Ahad; Hooshang Pakdel; Richard A Frank
Journal:  Environ Sci Technol       Date:  2020-01-17       Impact factor: 9.028

4.  Diamondoids are not forever: microbial biotransformation of diamondoid carboxylic acids.

Authors:  Benjamin D Folwell; Terry J McGenity; Corinne Whitby
Journal:  Microb Biotechnol       Date:  2019-11-12       Impact factor: 5.813

  4 in total

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