Hatsopoulos Microfluids Laboratory, Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts 02139, United States.
Applied Physics Department, Experimental Science Building,Universidade de Vigo, 36310 Vigo, Spain.
Biomacromolecules. 2022 May 9;23(5):1958-1969. doi: 10.1021/acs.biomac.1c01623. Epub 2022 Apr 20.
Ionic liquids (ILs) hold great potential as solvents to dissolve, recycle, and regenerate cellulosic fabrics, but the dissolved cellulose material system requires greater study in conditions relevant to fiber spinning processes, especially characterization of nonlinear shear and extensional flows. To address this gap, we aimed to disentangle the effects of the temperature, cellulose concentration, and degree of polymerization (DOP) on the shear and extensional flows of cellulose dissolved in an IL. We have studied the behavior of cellulose from two sources, fabric and filter paper, dissolved in 1-ethyl-3-methylimidazolium acetate ([CCIm][OAc]) over a range of temperatures (25 to 80 °C) and concentrations (up to 4%) that cover both semidilute and entangled regimes. The linear viscoelastic (LVE) response was measured using small-amplitude oscillatory shear techniques, and the results were unified by reducing the temperature, concentration, and DOP onto a single master curve using time superposition techniques. The shear rheological data were further fitted to a fractional Maxwell liquid (FML) model and were found to satisfy the Cox-Merz rule within the measurement range. Meanwhile, the material response in the non-LVE (NLVE) regime at large strains and strain rates has special relevance for spinning processes. We quantified the NLVE behavior using steady shear flow tests alongside uniaxial extension using a customized capillary breakup extensional rheometer. The results for both shear and extensional NLVE responses were described by the Rolie-Poly model to account for flow-dependent relaxation times and nonmonotonic viscosity evolution with strain rates in an extensional flow, which primarily arise from complex polymer interactions at high concentrations. The physically interpretable model fitting parameters were further compared to describe differences in material response to different flow types at varying temperatures, concentrations, and DOP. Finally, the fitting parameters from the FML and Rolie-Poly models were connected under the same superposition framework to provide a comprehensive description within the wide measured parameter window for the flow and handling of cellulose in [CCIm][OAc] in both linear and nonlinear regimes.
离子液体 (ILs) 在溶解、回收和再生纤维素织物方面具有巨大的潜力,但溶解纤维素的材料体系需要在与纤维纺丝过程相关的条件下进行更深入的研究,特别是对非线性剪切和拉伸流动的特性进行研究。为了解决这一差距,我们旨在分离温度、纤维素浓度和聚合度 (DOP) 对溶解在离子液体中的纤维素的剪切和拉伸流动的影响。我们研究了两种来源的纤维素(织物和滤纸)在 1-乙基-3-甲基咪唑乙酸盐 ([CCIm][OAc]) 中的溶解行为,温度范围为 25 至 80°C,浓度范围为 0.04%至 4%,涵盖了半浓和缠结两种体系。通过使用时间叠加技术将温度、浓度和 DOP 简化为单个主曲线,使用小振幅振荡剪切技术测量线性粘弹性 (LVE) 响应。剪切流变数据进一步拟合到分数马克斯韦尔液体 (FML) 模型中,并在测量范围内满足 Cox-Merz 规则。同时,在大应变和应变率下的非 LVE (NLVE) 区域的材料响应对于纺丝过程具有特殊意义。我们使用稳态剪切流测试和定制的毛细管断裂拉伸流变仪进行的单轴拉伸来量化 NLVE 行为。剪切和拉伸 NLVE 响应的结果均由 Rolie-Poly 模型描述,以解释在拉伸流动中与应变率相关的松弛时间和非单调粘度演变,这主要是由于高浓度下复杂的聚合物相互作用。进一步将可物理解释的模型拟合参数进行比较,以描述不同温度、浓度和 DOP 下不同流动类型对材料响应的差异。最后,在相同的叠加框架下连接 FML 和 Rolie-Poly 模型的拟合参数,以在宽测量参数窗口内提供在 [CCIm][OAc] 中纤维素的线性和非线性流动和处理的综合描述。