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pH-Dependent Gelation of a Stiff Anionic Polysaccharide in the Presence of Metal Ions

机译:在金属离子存在下硬阴离子多糖的pH依赖性胶凝

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摘要

Cross-linking of polysaccharides by metal ions provides polymer gels highly required by industrial applications. In this article, we study the rheological properties and microstructure of solutions of a stiff anionic polysaccharide xanthan cross-linked by chromium (III) ions, and we demonstrate that their properties are highly sensitive to the preparation pH. Stable gels are obtained in a wide range of pH from 2.4 to 7.8. The maximum elastic modulus is observed for the gels made at pH 6.3, and by freeze-fracture transmission electron microscopy it is shown that they are characterized by the most dense network structure. However, out of this pH interval, no gelation is observed. At low pH (< 2.4) it is due to high protonation of carboxylic groups of xanthan preventing their interaction with chromium ions, and to the disappearance of oligomeric ions, which are effective in cross-linking. At high pH (> 7.8) the absence of gelation is caused by the transformation of reactive chromium ions into insoluble chromium hydroxide. At the same time, for the gels initially formed at pH 6.3, subsequent change of pH to strongly acidic (1.4) or basic (8.9) medium does not affect appreciably their properties, meaning that chromium cross-links are stable once they are formed. These observations open a reliable route to produce polysaccharide gels with required mechanical properties in a wide pH range where they initially cannot be prepared. It is also shown that the increase of pH to 6.3 of the initially ungelled solution prepared at pH 1.5 results in gelation. This effect offers a facile way for delayed gelation of polysaccharides, which is especially required by oil industry.
机译:多糖通过金属离子的交联提供了工业应用高度需要的聚合物凝胶。在本文中,我们研究了通过铬(III)离子交联的硬质阴离子多糖黄原胶溶液的流变性质和微观结构,我们证明了它们的性质对制备pH值高度敏感。在2.4至7.8的广泛pH范围内均可获得稳定的凝胶。对于在pH 6.3下制得的凝胶,观察到最大弹性模量,并且通过冷冻断裂透射电子显微镜显示,它们的特征在于最致密的网络结构。但是,在此pH间隔之外,未观察到凝胶化。在低pH值(<2.4)下,这是由于黄原胶的羧基高度质子化,阻止了它们与铬离子的相互作用,以及低聚离子的消失,它们对交联有效。在高pH(> 7.8)下,由于反应性铬离子转变为不溶性氢氧化铬而导致没有凝胶化。同时,对于最初在pH 6.3时形成的凝胶,随后将pH改变为强酸性(1.4)或碱性(8.9)介质不会明显影响其性能,这意味着一旦形成铬交联,它们就会保持稳定。这些发现为在最初无法制备的宽pH范围内生产具有所需机械性能的多糖凝胶开辟了一条可靠的途径。还显示出在pH 1.5下制备的初始去胶溶液的pH增加至6.3导致凝胶化。这种作用为多糖的延迟胶凝提供了一种简便的方法,这是石油工业特别需要的。

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