Laboratory of Food Proteins and Colloids, School of Food Science and Engineering, Guangdong Province Key Laboratory for Green Processing of Natural Products and Product Safety, South China University of Technology, Guangzhou 510640, China.
Laboratory of Food Proteins and Colloids, School of Food Science and Engineering, Guangdong Province Key Laboratory for Green Processing of Natural Products and Product Safety, South China University of Technology, Guangzhou 510640, China; Food Processing Teaching and Research Section, Guangdong Polytechnic of Science and Trade, Guangzhou 510430, China.
Food Res Int. 2021 Feb;140:110076. doi: 10.1016/j.foodres.2020.110076. Epub 2020 Dec 29.
The linear and nonlinear rheological behaviors of heterogeneous emulsions gels made from natural glycyrrhizic acid (GA) nanofibrils and sitosterol-oryzanol mixtures (sterols) were investigated using small amplitude oscillatory shear (SAOS) and large amplitude oscillatory shear (LAOS). The nonlinear rheological response was qualitatively analyzed using normalized Lissajous-Bowditch curves. The microstructure of the emulsion gels strongly depended on the concentration of sterols in the oil phase, and showed a percolated segregated network at 10-20 wt% sterols due to the partial coalescence of droplets, and a jamming transition without coalescence at higher sterols concentration of 30 wt%. The microstructure differences led to different linear and nonlinear viscoelastic behaviors of these emulsion gels. SAOS tests showed that the oil phase structuring by the sterols significantly enhance the viscoelasticity of GA nanofibril emulsion gels, and the percolating emulsion gels exhibited higher elasticity than the jammed emulsion gel, as evidenced by a lower damping factor and frequency power-law exponent. The data of crossover strain, phase angle, and the normalized Lissajous-Bowditch curves from LAOS tests further revealed that compared to the samples in a jammed state or without oil phase structuring, the emulsion gels with a percolating segregated network showed higher structural elasticity and thus were more resistant to large deformations, probably due to the slow relaxation of rigid, hydrodynamically interacting clusters of partially coalesced droplets. These findings could potentially aid in the design of novel emulsion gels, based on all-natural and sustainable building blocks, with specific textural and functional properties for foods, cosmetics, and pharmaceutical applications.
利用小振幅振荡剪切(SAOS)和大振幅振荡剪切(LAOS)研究了由天然甘草次酸(GA)纳米原纤维和甾醇-谷维素混合物(甾醇)制成的不均匀乳液凝胶的线性和非线性流变行为。使用归一化 Lissajous-Bowditch 曲线对非线性流变响应进行定性分析。乳液凝胶的微观结构强烈依赖于油相中的甾醇浓度,由于液滴部分聚结,在 10-20wt%甾醇下表现出渗透分离的网络结构,而在较高甾醇浓度 30wt%下则表现出无聚结的堵塞转变。微观结构的差异导致这些乳液凝胶具有不同的线性和非线性黏弹性行为。SAOS 测试表明,甾醇对油相的结构化显著增强了 GA 纳米原纤维乳液凝胶的黏弹性,并且渗透乳液凝胶表现出比堵塞乳液凝胶更高的弹性,这表现为更低的阻尼因子和频率幂律指数。LAOS 测试中的交叉应变、相位角和归一化 Lissajous-Bowditch 曲线的数据进一步表明,与处于堵塞状态或没有油相结构化的样品相比,具有渗透分离网络的乳液凝胶表现出更高的结构弹性,因此更能抵抗大变形,这可能是由于部分聚结液滴的刚性、流体力学相互作用的簇的缓慢松弛。这些发现可能有助于设计基于全天然和可持续构建块的新型乳液凝胶,这些乳液凝胶具有特定的质地和功能特性,适用于食品、化妆品和制药应用。