José Miguel AguileraEvelin Aquino Rojas2026-03-222026-03-22199610.1111/j.1365-2621.1996.tb10911.xhttps://doi.org/10.1111/j.1365-2621.1996.tb10911.xhttps://andeanlibrary.org/handle/123456789/46864Citaciones: 91ABSTRACT Mixed gels of cassava starch (CS) and a whey protein isolate (WPI), obtained by heating solutions of 10% total solids, pH 5.75 to 85°C, were characterized as a function of the starch fraction, θ s , by axial compression, small‐amplitude oscillatory rheometry, differential scanning calorimetry (DSC) and scanning electron microscopy (SEM). Gelation did not occur for θ s > 0.7. In the range 0<θ s < 0.4 mixed gels showed higher mechanical (E, elastic modulus) and rheological (G′, storage modulus) properties than pure gels, with maximum values for θ s = 0.2–0.3. Viscoelastic measurements as a function of time showed that gels containing higher levels of WPI developed a larger G. Blends of both biopolymers showed independent thermal transitions in DSC measurements, related to gelatinization and denaturation. Microstructure of a mixed gel formed at θ s = 0.2 showed a continuous matrix formed by strands of WPI particle aggregates and an independent CS phase.enDifferential scanning calorimetryRheometryWhey protein isolateRheologyWhey proteinStarchDynamic mechanical analysisMicrostructureMaterials scienceScanning electron microscopearticle