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Rheology of concentrated isotropic and anisotropic rigid polysaccharide solutions: Xanthan and scleroglucan.

机译:浓各向同性和各向异性硬质多糖溶液的流变学:黄原胶和硬葡聚糖。

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The rheology of concentrated isotropic and anisotropic solutions of rigid polysaccharides xanthan and scleroglucan has been studied with a Rheometrics RFS II Fluids Spectrometer in both steady shear and oscillatory modes. Two xanthan samples, one of low molecular weight and is rigid rodlike, the other of intermediate molecular weight and is serniflexible wormlike, have been prepared and their rheological behaviors are found to be quite different from each other. The rigid rodlike sample behaves mostly like Newtonian fluid, and obeys the Cox-Merz rule for all the solutions studied. No cross over of storage and loss modulus is observed because the rigid xanthan sample is too short and rigid to form network. But the semiflexible xanthan sample possesses gel-like properties when it is in the concentrated isotropic regime and the strength of network formed increases with salt concentration. It does not obey the Cox-Merz rule in any salt concentration, and crossover of storage and loss moduli is observed. Although the two xanthan samples behave differently, they do have common points: both have viscosity peaks corresponding to the phase boundary concentration for isotropic and biphasic regimes, and the rheological parameters do not increase further with concentration in fully anisotropic regime, unlike flexible high molecular weight xanthan samples. The scleroglucan sample studied has very interesting properties: In isotropic regime, it is like Newtonian fluid and obeys the Cox-Merz rule like rigid rodlike xanthan, but it follows Matheson's theory in terms of the viscosity increase with concentration from isotropic to fully anisotropic regimes, similar to flexible xanthan. And yet the scleroglucan sample is not flexible enough to form networks as observed for intermediate molecular weight xanthan. So, the scleroglucan sample studied has something in common with every xanthan conformation, either rigid rodlike, or semiflexible, or flexible, but they are also different.
机译:使用Rheometrics RFS II流体光谱仪在稳态剪切和振荡模式下研究了硬多糖黄原胶和硬葡聚糖的浓各向同性和各向异性溶液的流变学。制备了两种黄原胶样品,一种低分子量,呈刚性杆状,另一种中等分子量,与可弯曲的蠕虫状,其流变行为差异很大。刚性棒状样品的行为主要类似于牛顿流体,并且对于所有研究的溶液都遵循Cox-Merz规则。由于刚性黄原胶样品太短且刚性不足以形成网状结构,因此未观察到存储和损耗模量的交叉。但是半柔性黄原胶样品在浓的各向同性状态下具有凝胶状性质,并且形成的网络的强度随盐浓度的增加而增加。它在任何盐浓度下均不遵守Cox-Merz规则,并且观察到存储的交叉和损耗模量。尽管这两种黄原胶样品的行为不同,但它们确实有共同点:它们都具有与各向同性和双相体系相边界浓度相对应的粘度峰,并且在完全各向异性体系中,流变学参数不会随着浓度的增加而进一步增加,这与柔性高分子量不同黄原胶样品。所研究的硬葡聚糖样品具有非常有趣的特性:在各向同性状态下,它像牛顿流体一样,服从Cox-Merz规则,就像刚性棒状黄原胶一样,但是它遵循了Matheson的理论,即粘度从各向同性到完全各向异性,随着浓度的增加而增加,类似于柔性黄原胶。然而,正如中等分子量的黄原胶所观察到的那样,硬葡聚糖样品的柔性不足以形成网络。因此,所研究的硬葡聚糖样品在每种黄原胶构象上都有一些共同点,无论是刚性棒状,半柔性还是柔性,但它们也有所不同。

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