Extensional Rheological Properties of Poly-γ-benzyl-l-glutamate Solutions across the Isotropic-Cholesteric Liquid Crystalline Phase Transition

IF 5.2 1区 化学 Q1 POLYMER SCIENCE Macromolecules Pub Date : 2025-03-07 DOI:10.1021/acs.macromol.4c03188
Adam Linscott, Nadia N. Nikolova, Brooke Husar, Vivek Sharma, Svetlana Morozova
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Abstract

Connecting macromolecular properties and microstructure to macroscopic flow behavior and rheological response is of fundamental interest to scientists and formulators interested in the interplay of structure, properties, processability, and application. Here, we characterize the macromolecular properties and flow behavior of poly(γ-benzyl-l-glutamate) (PBLG) solutions that appear to form cholesteric liquid crystalline phases above certain polymer concentrations. Solutions of PBLG with two molecular weights of 90,000 and 150,000 g/mol were characterized with light scattering and optical microscopy. PBLG is rodlike in 1,2-dicholoroethane (DCE) solutions and forms cholesteric liquid crystalline (LC) phases at higher concentrations with the transition depending on the overall contour length of the molecule. Using dripping-onto-substrate (DoS) rheometry, we characterize the pinching dynamics and extensional rheology response of PBLG solutions, including concentrations that appear liquid crystalline. The radius evolution data for all solutions display a power law (PL) response characteristic of shear-thinning fluids. However, after the onset of the LC phase within solutions, the PL response is followed by an elastocapillary response with an exponential decay in the filament radius that provides measurement of extensional relaxation time. Increasing the polymer concentration deeper into the liquid crystalline phase leads to a significant increase in extensional relaxation time. Imaging pinching necks in polarized light enables the visualization of the changes in neck shape, size, and birefringence as markers of underlying macromolecular stretching, alignment, liquid crystallinity, and dynamics. This work presents a novel chapter in the rheology of ordered, liquid crystalline solutions and provides new insights into the extensional flows of PBLG and polymeric rigid rods.

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聚γ-苄基-谷氨酸溶液在各向同性胆甾型液晶相变中的拉伸流变特性
将大分子性质和微观结构与宏观流动行为和流变响应联系起来,是对结构、性质、可加工性和应用的相互作用感兴趣的科学家和配方师的基本兴趣。在这里,我们表征了聚(γ-苄基-谷氨酸)(PBLG)溶液的大分子性质和流动行为,这些溶液在一定的聚合物浓度以上似乎形成胆甾液晶相。用光散射和光学显微镜对分子量为90000和150000 g/mol的PBLG溶液进行了表征。PBLG在1,2-二氯乙烷(DCE)溶液中呈棒状,在较高浓度下形成胆甾型液晶(LC)相,其转变取决于分子的总轮廓长度。利用滴入基质(DoS)流变学,我们表征了PBLG溶液的挤压动力学和拉伸流变响应,包括出现液晶的浓度。所有溶液的半径演化数据都显示出剪切变薄流体的幂律响应特征。然而,在溶液中LC相开始后,PL响应之后是弹性毛细管响应,其灯丝半径呈指数衰减,可测量拉伸弛豫时间。当聚合物浓度增加到液晶相深处时,拉伸弛豫时间显著增加。在偏振光下成像挤压颈,可以可视化颈形状、大小和双折射的变化,作为潜在大分子拉伸、排列、液体结晶度和动力学的标记。这项工作提出了一个新的章节,在有序的流变性,液晶溶液,并提供了新的见解延伸流动的PBLG和聚合物刚性棒。
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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