4.7 Article

The impact of model rigid fillers in acid-induced sodium caseinate/xanthan gum cooperative protein gels

Journal

FOOD HYDROCOLLOIDS
Volume 113, Issue -, Pages -

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.foodhyd.2020.106439

Keywords

Particle reinforcement; Particle filled gel; Elastic modulus; Fracture mechanics; Composite gel; Sodium caseinate

Funding

  1. Ontario Ministry of Agriculture, Food and Rural Affairs (OMAFRA)
  2. National Science and Engineering Research Council of Canada (NSERC)
  3. Canadian Dairy Commission

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This study evaluates the impact of model rigid fillers on the deformation and fracture behavior of biopolymer gels and finds that filler size and surface chemistry have a significant effect on their mechanical properties, influencing the elastic modulus and fracture strain of the gels.
This work evaluates the impact of model rigid fillers on the deformation and fracture behavior of acid-set sodium caseinate/xanthan gum (NaCas/XG) mixed biopolymer gels. Glass microspheres of varying size ranges were used as idealized filler particles. The large deformation elastic modulus showed a power law scaling behavior with increasing filler volume fraction ((phi(f)) for all fillers. The magnitude of this response was strongly dependent on filler size, as decreasing filler diameter produced a higher scaling exponent. For the smallest fillers tested (8 mu m), the presence of amino functional groups on the filler surface produced a further increase in the scaling behavior. The stark increase in elastic modulus indicates the microspheres behaved as active fillers which bound to the electrostatically-induced cooperative gel network. The fracture strain (epsilon(r)*) of both the neat and amino-coated 8 mu m microspheres showed an abrupt decrease at low phi(f), which roughly followed the theoretically expected response proposed by Nielsen. In contrast, the larger fillers (90 mu m and 180 mu m) produced a roughly linear decrease in epsilon(r)* with increasing filler loading. Above a threshold values of (phi(f) similar to 0.15, the fracture stress ((sigma(r)*) displayed a power law scaling behavior, with the effect of filler size and surface chemistry analogous to that seen for the elastic modulus. Water loss results correlated well with the increase in mechanical strength, and T-2 relaxometry suggested the hydrophilic fillers reduce water mobility within the gel network. These results indicate that the effect of filler size and surface chemistry can be used to modulate the large deformation and fracture mechanics of particle-filled food gels. This work adds to the growing body of literature on developing a more fundamental understanding of foods as composite soft materials.

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