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自修复鱼明胶/钠蒙脱石生物杂化凝聚物:结构和流变学特性。

Self-healing fish gelatin/sodium montmorillonite biohybrid coacervates: structural and rheological characterization.

机构信息

Polymer Division, School of Chemistry, College of Science, University of Tehran, Tehran, Iran.

出版信息

Biomacromolecules. 2012 Jul 9;13(7):2136-47. doi: 10.1021/bm3005319. Epub 2012 Jun 15.

DOI:10.1021/bm3005319
PMID:22642874
Abstract

Complex coacervation driven by associative electrostatic interactions was studied in mixtures of exfoliated sodium-montmorillonite (Na(+)-MMT) nanoplatelets and fish gelatin, at a specific mixing ratio and room temperature. Structural and viscoelastic properties of the coacervate phase were investigated as a function of pH by means of different complementary techniques. Independent of the technique used, the results consistently showed that there is an optimum pH value at which the coacervate phase shows the tightest structure with highest elasticity. The solid-like coacervates showed an obvious shear-thinning behavior and network fracture but immediately recovered back into their original elastic character upon removal of the shear strain. The nonlinear mechanical response characterized by single step stress relaxation experiments revealed the same trend for the yield stress and isochronal shear modulus of the coacervates as a function of pH with a maximum at pH 3.0 and lower values at 2.5 and 3.5 pHs, followed by a very sharp drop at pH 4.0. Finally, small-angle X-ray scattering (SAXS) data confirmed that at pHs lower than 4.0 the coacervate phases were dense and structured with a characteristic length scale (ξ(SAXS)) of ~7-9 nm. Comparing the ξ(SAXS) with rheological characteristic length (ξ(rheol)) estimated from low-frequency linear viscoelastic data and network theory, it was concluded that both the strength of the electrostatic interactions and the conformation of the gelatin chains before and during of the coacervation process are responsible for the structure and rigidity of the coacervates.

摘要

在特定的混合比例和室温下,研究了由关联静电相互作用驱动的剥离钠蒙脱石 (Na(+)-MMT) 纳米片和鱼明胶的混合物中的复杂凝聚。通过不同的互补技术,研究了凝聚相的结构和粘弹性能随 pH 值的变化。无论使用哪种技术,结果都一致表明,在凝聚相具有最紧密结构和最高弹性的最佳 pH 值下,存在一个最佳 pH 值。固态凝聚物表现出明显的剪切稀化行为和网络断裂,但在剪切应变消除后,立即恢复到其原始弹性状态。由单步应力松弛实验表征的非线性力学响应表明,凝聚物的屈服应力和等时剪切模量随 pH 值的变化趋势相同,在 pH 3.0 处达到最大值,在 2.5 和 3.5 pH 值处较低,然后在 pH 4.0 处急剧下降。最后,小角 X 射线散射 (SAXS) 数据证实,在 pH 值低于 4.0 时,凝聚相致密且具有特征长度尺度 (ξ(SAXS))为~7-9nm。将 ξ(SAXS)与从低频线性粘弹性数据和网络理论估计的流变学特征长度 (ξ(rheol))进行比较,可以得出结论,静电相互作用的强度和凝聚过程前后明胶链的构象都对凝聚物的结构和刚性负责。

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