Gravanis G, Milas M, Rinaudo M, Clarke-Sturman A J
Centre de Recherches sur les Macromolécules Végétales, Laboratoire Propre du CNRS, Associé à l'Université Joseph Fourier, Grenoble, France.
Int J Biol Macromol. 1990 Jun;12(3):201-6. doi: 10.1016/0141-8130(90)90033-7.
We report the rheological behaviour of a succinoglycan polysaccharide in dilute and semi-dilute solutions as a function of temperature, ionic strength and the nature of counterion. We have examined the viscosity dependence as a function of molecular weight using samples obtained by ultrasonication. We have also prepared samples lacking succinate substitutes and compared their behaviour with that of the native polymer. In both cases, we observed that, after heating a polymer solution for the first time above the conformational transition temperature, a different ordered state was obtained on cooling. This state had a lower molecular weight and intrinsic viscosity but identical chemical structure and local properties. A role for the side chain in the stabilization of breaks in the backbone is suggested. Nevertheless, a unique curve is obtained for the specific viscosity as a function of the overlap parameter c[eta] for different polymer concentrations of both the native and heated forms. However, different curves are obtained for normal and succinate-free polymers, and the succinate-free polymer is characterized by a lower Huggins constant.
我们报告了琥珀酰聚糖多糖在稀溶液和半稀溶液中的流变行为,该行为是温度、离子强度和抗衡离子性质的函数。我们使用通过超声处理获得的样品研究了粘度随分子量的变化。我们还制备了不含琥珀酸酯替代物的样品,并将它们的行为与天然聚合物的行为进行了比较。在这两种情况下,我们观察到,在首次将聚合物溶液加热到构象转变温度以上后,冷却时会得到不同的有序状态。这种状态具有较低的分子量和特性粘度,但化学结构和局部性质相同。有人提出侧链在主链断裂的稳定中起作用。然而,对于天然和加热形式的不同聚合物浓度,比浓粘度作为重叠参数c[eta]的函数可得到一条独特的曲线。然而,对于正常聚合物和无琥珀酸酯聚合物可得到不同的曲线,且无琥珀酸酯聚合物的哈金斯常数较低。