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表面活性生物聚合物的界面流变学:阿拉伯树胶与疏水改性淀粉的比较。

Interfacial rheology of surface-active biopolymers: Acacia senegal gum versus hydrophobically modified starch.

作者信息

Erni Philipp, Windhab Erich J, Gunde Rok, Graber Muriel, Pfister Bruno, Parker Alan, Fischer Peter

机构信息

Institute of Food Science and Nutrition and Materials Research Center, ETH Zürich, 7 Rue de la Bergère, Zürich, Switzerland.

出版信息

Biomacromolecules. 2007 Nov;8(11):3458-66. doi: 10.1021/bm700578z. Epub 2007 Oct 20.

Abstract

Acacia gum is a hybrid polyelectrolyte containing both protein and polysaccharide subunits. We study the interfacial rheology of its adsorption layers at the oil/water interface and compare it with adsorbed layers of hydrophobically modified starch, which for economic and political reasons is often used as a substitute for Acacia gum in technological applications. Both the shear and the dilatational rheological responses of the interfaces are considered. In dilatational experiments, the viscoelastic response of the starch derivative is just slightly weaker than that for Acacia gum, whereas we found pronounced differences in shear flow: The interfaces covered with the plant gum flow like a rigid, solidlike material with large storage moduli and a linear viscoelastic regime limited to small shear deformations, above which we observe apparent yielding behavior. In contrast, the films formed by hydrophobically modified starch are predominantly viscous, and the shear moduli are only weakly dependent on the deformation. Concerning their most important technological use as emulsion stabilizers, the dynamic interfacial responses imply not only distinct interfacial dynamics but also different stabilizing mechanisms for these two biopolymers.

摘要

阿拉伯胶是一种含有蛋白质和多糖亚基的混合聚电解质。我们研究了其在油/水界面吸附层的界面流变学,并将其与疏水改性淀粉的吸附层进行比较,由于经济和政治原因,疏水改性淀粉在技术应用中常被用作阿拉伯胶的替代品。我们考虑了界面的剪切流变响应和拉伸流变响应。在拉伸实验中,淀粉衍生物的粘弹性响应仅比阿拉伯胶略弱,而我们发现剪切流存在明显差异:覆盖有植物胶的界面像刚性、类固体材料一样流动,具有较大的储能模量,线性粘弹性区域仅限于小剪切变形,超过此范围我们观察到明显的屈服行为。相比之下,由疏水改性淀粉形成的薄膜主要是粘性的,剪切模量仅微弱地依赖于变形。关于它们作为乳液稳定剂最重要的技术用途,动态界面响应不仅意味着这两种生物聚合物有不同的界面动力学,而且意味着不同的稳定机制。

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