Determination of physical emulsion stabilization mechanisms of wood hemicelluloses: Via rheological and interfacial characterization

K. S. Mikkonen*, D. Merger, P. Kilpeläinen, L. Murtomäki, U. S. Schmidt, M. Wilhelm

*Corresponding author for this work

    Research output: Contribution to journalArticleScientificpeer-review

    53 Citations (Scopus)
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    Abstract

    Materials manufacturing industries seek efficient, economic, and sustainable compounds for stabilizing dispersed systems such as emulsions. In this study, novel, abundant biobased hydrocolloids spruce galactoglucomannans (GGM) and birch glucuronoxylans (GX) were obtained from a forestry biorefining process and characterized as versatile stabilizers of rapeseed oil-in-water emulsions. For the first time, GGM and GX isolated by pressurized hot water extraction (PHWE) of spruce and birch saw meal, respectively, were studied in emulsions. The PHWE wood hemicelluloses - polysaccharides with relatively low molar mass - facilitated the formation of emulsions with small average droplet size and efficiently prevented droplet coalescence. GGM and GX lowered the surface tension of emulsions' oil-water interface and increased the viscosity of the continuous phase. However, viscosity of the wood hemicellulose-based systems was low compared to that of commercial polymeric stabilizers. GGM-stabilized emulsions with varying oil volume fractions were characterized in terms of their rheological properties, including large amplitude oscillation shear (Laos) measurements, and compared to emulsions prepared with a classical small-molecular surfactant, Tween20. The physical emulsion stabilization mechanisms of GGM and GX are suggested as steric repulsion assisted by Pickering-type stabilization. Wood hemicelluloses have potential as highly promising future bioproducts for versatile industrial applications involving colloidal systems and soft materials.

    Original languageEnglish
    Pages (from-to)8690-8700
    Number of pages11
    JournalSoft Matter
    Volume12
    Issue number42
    DOIs
    Publication statusPublished - 2016
    MoE publication typeA1 Journal article-refereed

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