Porous graphite as stationary phase for the chromatographic separation of polymer additives - determination of adsorption capability by Raman spectroscopy and physisorption

•Porous graphitic carbon (HypercarbTM) enables LC separation of polymer stabilizers.•Raman spectroscopy exhibits shifts of the graphite-band caused by adsorption.•Argon physisorption provides proof for adsorption of polymer additives.•Adsorption reduces the specific surface area of HypercarbTM. Addi...

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Veröffentlicht in:Journal of Chromatography A 2020-08, Vol.1625, p.461302, Article 461302
Hauptverfasser: Kot, David, Zou, Mingyi, Brunnengräber, Kai, Arndt, Jan-Hendrik, Macko, Tibor, Etzold, Bastian J.M., Brüll, Robert
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Sprache:eng
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Zusammenfassung:•Porous graphitic carbon (HypercarbTM) enables LC separation of polymer stabilizers.•Raman spectroscopy exhibits shifts of the graphite-band caused by adsorption.•Argon physisorption provides proof for adsorption of polymer additives.•Adsorption reduces the specific surface area of HypercarbTM. Additives are added to polymers in small concentration to achieve desired application properties widely used to tailor the properties. The rapid diversification of their molecular structures, with often only minute differences, necessitates the development of adequate chromatographic techniques. While modified silica so far is the workhorse as stationary phase we have probed the potential of porous graphitic carbon (HypercarbTM) for this purpose. The results show that the multitude of physicochemical interactions between analyte molecules and the graphitic surface enables separations of polyolefin stabilizers with unprecedented selectivity. To support the chromatographic results the adsorption capability of HypercarbTM for selected antioxidants and UV absorbers has been determined by Raman spectroscopy and argon physisorption measurements. The shift of the Graphite-band in the Raman spectra of HypercarbTM upon infusion with additives correlates with the changes in the Adsorption Potential Distributions. The results of argon physisorption measurements go hand in hand with the chronology of desorption of the additives in liquid chromatography experiments. The elution sequence can be explained by van der Waals or London forces, π-π-interactions and electron lone pair donor-acceptor interactions between the graphite surface and analyte functional groups.
ISSN:0021-9673
DOI:10.1016/j.chroma.2020.461302