Abstract
The structure of sodium caseinate particles, as affected by the presence of calcium ions (Ca2+), in aqueous solution and in oil (toluene)-in-water emulsions, was investigated by small-angle X-ray and neutron scattering (SAXS and SANS). SAXS analyses indicated that the sodium caseinate dispersed in water as small particles with electrostatic interactions, which has a radius of gyration (Rg) of ~5 nm and an effective radius (Reff) of ~ 10 nm with an assuming spherical shape. In the presence of Ca2+, the caseinate particles aggregated as large particles with a hydrodynamic diameter > 100 nm as determined by dynamic light scattering. The networks within the large particles were self-assembled from the small Ca2+-cross-linked particles (Rg ~ 6.5–8.0 nm), as probed by SAXS. The fractal-like dimension increased from 2.5 to 3.4 with increasing protein and CaCl2 concentrations, suggesting a denser structure. The integrity of the caseinate particles at the oil-water interface was enhanced by Ca2+ cross-linking, as observed by transmission electron microscopy. The oilwater interface stabilised by Ca2+-cross-linked caseinate particles was ~ 30 nm thick, six times thicker than that stabilised by sodium caseinate (~ 5 nm) as analysed by SANS with contrast variation technique. Quantifying the structure of sodium caseinate in an aqueous solution and at the oil-water interface provides valuable insights for designing new casein-based functional materials.
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