4.6 Article

Deformation and degradation of polymers in ultra-high-pressure liquid chromatography

Journal

JOURNAL OF CHROMATOGRAPHY A
Volume 1218, Issue 39, Pages 6930-6942

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.chroma.2011.08.014

Keywords

Deborah number; Slalom chromatography; Degradation of polymers in liquid chromatography; Hydrodynamic chromatography; Polystyrene standards

Funding

  1. Dutch Polymer Institute [597]

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Ultra-high-pressure liquid chromatography (UHPLC) using columns packed with sub-2 mu m particles has great potential for separations of many types of complex samples, including polymers. However, the application of UHPLC for the analysis of polymers meets some fundamental obstacles. Small particles and narrow bore tubing in combination with high pressures generate significant shear and extensional forces in UHPLC systems, which may affect polymer chains. At high stress conditions flexible macromolecules may become extended and eventually the chemical bonds in the molecules can break. Deformation and degradation of macromolecules will affect the peak retention and the peak shape in the chromatogram, which may cause errors in the obtained results (e.g. the calculated molecular-weight distributions). In the present work we explored the limitations of UHPLC for the analysis of polymers. Degradation and deformation of macromolecules were studied by collecting and re-injecting polymer peaks and by off-line two-dimensional liquid chromatography. Polystyrene standards with molecular weight of 4 MDa and larger were found to degrade at UHPLC conditions. However, for most polymers degradation could be avoided by using low linear velocities. No degradation of 3-MDa PS (and smaller) was observed at linear velocities up to 7 mm/s. The column frits were implicated as the main sources of polymer degradation. The extent of degradation was found to depend on the type of the column and on the column history. At high flow rates degradation was observed without a column being installed. We demonstrated that polymer deformation preceded degradation. Stretched polymers eluted from the column in slalom chromatography mode (elution order opposite to that in SEC or HDC). Under certain conditions we observed co-elution of large and small PS molecules though a convolution of slalom chromatography and hydrodynamic chromatography. (C) 2011 Elsevier B.V. All rights reserved.

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