Department of Chemical Engineering, Engineering and Technology Institute Groningen, University of Groningen, Nijenborgh 3, 9747 AG Groningen, The Netherlands.
Biomacromolecules. 2024 Oct 14;25(10):6883-6898. doi: 10.1021/acs.biomac.4c01125. Epub 2024 Sep 16.
This study investigates the rheological behavior of two plant-based polysaccharides, with different degrees of hydrophilicity, agar (highly hydrophilic) and guar gum (hydrophilic), in water and 1-ethyl-3-methylimidazolium acetate (EMImAc). The rheological response of these polymers is highly dependent on the solvent's ability to disrupt intermolecular associations. In water, agar forms hydrogels, while guar gum behaves as a viscoelastic liquid with slow modes. The plateau modulus () scales with polymer concentration () as ∼ , consistent with other natural polymers. In EMImAc, both polysaccharides form viscoelastic liquids, exhibiting ∼ , as expected for semiflexible polymer solutions. However, the terminal relaxation time, τ, and the specific viscosity, η, scale as τ ∼ and η ∼ , indicative of intermolecular chain-chain associations. Despite the solvent or polysaccharide, the fractional viscosity overshoot and the shear strain at the maximum stress show a terminal Weissenberg number dependence similar to other synthetic polymers.
本研究考察了两种植物来源多糖的流变性,它们具有不同的亲水性程度,琼脂(高度亲水)和瓜尔胶(亲水),在水中和 1-乙基-3-甲基咪唑醋酸盐(EMImAc)中。这些聚合物的流变响应高度依赖于溶剂破坏分子间相互作用的能力。在水中,琼脂形成水凝胶,而瓜尔胶表现为具有慢模式的粘弹性液体。平台模量(G')与聚合物浓度(c)的关系为 G' ∼ c^2 ,与其他天然聚合物一致。在 EMImAc 中,两种多糖都形成粘弹性液体,表现出 G' ∼ c,这是半刚性聚合物溶液的预期结果。然而,末端松弛时间 τ 和比浓粘度 η 遵循 τ ∼ 和 η ∼ ,表明存在分子间链链相互作用。尽管溶剂或多糖不同,但分数粘度过冲和最大应力下的剪切应变表现出与其他合成聚合物相似的末端 Weissenberg 数依赖性。