Rheological study of the chitosan/glutaraldehyde chemical gel system

Polymer Gels and Networks Pub Date : 1998-12-01 Epub Date: 1999-05-25 DOI:10.1016/S0966-7822(98)00032-X
W. Argüelles-Monal , F.M. Goycoolea , C. Peniche , I. Higuera-Ciapara
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引用次数: 91

Abstract

Chitosan dissolved in 0.1 mol l-1 acetic acid shows an apparent yield stress at very low frequencies, probably due to a structuring process yielding gel-like response. It reflects complex relaxation mechanisms once chains disentangle and relax, presumably due to incipient hydrophobic contacts reinforced by the relative stiffness of the chitosan chains, which tend to slow down reptation. When chemical cross-linkages are introduced, the weak self-associated network of chitosan is gradually replaced by a permanent covalent network as the molar ratio of aldehyde/amine groups, R, is increased. At R=0.4 a glass-to-rubber-type transition is observed, while at R=0.5 the form of the mechanical spectrum suggests the co-existence of a chemically cross-linked gel ‘dissolved’ in a second entangled network formed by chitosan chains of restricted mobility. At higher cross-linking levels (R>1) a strong permanent gel is formed. The observed frequency dependence near the rheological gel point suggests several modes of relaxation processes.

壳聚糖/戊二醛化学凝胶体系流变学研究
壳聚糖溶解于0.1 mol l-1的乙酸中,在极低频率下表现出明显的屈服应力,这可能是由于结构过程产生了凝胶样响应。它反映了复杂的弛豫机制,一旦链解开和放松,可能是由于壳聚糖链的相对刚度加强了初期的疏水接触,这往往会减缓重复。当引入化学交联时,壳聚糖的弱自缔合网络随着醛胺摩尔比R的增加而逐渐被永久共价网络所取代。在R=0.4时,观察到玻璃到橡胶型的转变,而在R=0.5时,力学谱的形式表明,化学交联凝胶“溶解”在由限制迁移率的壳聚糖链形成的第二纠缠网络中。在较高的交联水平(R>1)下,形成牢固的永久凝胶。在流变凝胶点附近观察到的频率依赖性表明了几种松弛过程模式。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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