Properties of Zone-Annealed Miscible Polymer Blends

IF 5.1 1区 化学 Q1 POLYMER SCIENCE
Nicholas F. Mendez, Mason Martell, Monika Król, Vighnesh Pai, Isabella C. Huang, Janne Ruokolainen, Frederic Sansoz, Alejandro J. Müller, Linda Schadler, Sanat K. Kumar
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Abstract

We examine the morphology and properties of zone-annealed (ZA) poly(ethylene oxide) (PEO) and its miscible blends with poly(methyl methacrylate) (PMMA) over a range of compositions where PEO is semicrystalline. Small angle X-ray scattering, and transmission electron microscopy show that the ZA results in layered structures with alternating crystal–amorphous layers oriented parallel to the ZA direction (i.e., the crystal–amorphous interphases are normal to the ZA direction). Instead of concentrating impurities at the end of the sample as has been found for metal and semiconductor materials, the noncrystalline polymer (PMMA) is concentrated into the amorphous regions between the lamellae. Differential scanning calorimetry shows that the ZA samples have higher crystallinity, as expected. The mechanical properties of both neat PEO and its blends, processed by quenching and ZA, were examined using tensile testing. The most striking result is that ZA leads to increased blend toughness (despite toughness decreasing in the quenched samples), with these differences particularly manifesting for PMMA weight fractions larger than 0.2. There is no directionality associated with this property, i.e., we get the same toughness parallel vs perpendicular to the ZA direction. Similarly, ZA had no (directional) effect on the blends’ Young’s modulus, even though the modulus itself increased with the addition of the glassy PMMA. In contrast, the modulus of neat PEO is significantly increased in the direction parallel to the ZA relative to the perpendicular direction and the quenched sample. We propose that the anisotropic properties that arise from ZA of neat PEO results from the contrast in mechanical properties of the crystalline lamella and rubbery amorphous region, while in the blends, both the crystal and the amorphous phases are hard solids with little contrast–this effect being caused by the interlamellar PMMA being a glassy polymer at room temperature–evidently yielding no directionality to properties.

Abstract Image

区域退火共混聚合物的性能
我们研究了区域退火(ZA)聚环氧乙烷(PEO)及其与聚甲基丙烯酸甲酯(PMMA)的混相共混物的形貌和性能,其中PEO是半结晶的。小角度x射线散射和透射电镜显示,ZA形成了平行于ZA方向的晶体-非晶交替层状结构(即晶体-非晶界面相垂直于ZA方向)。不像金属和半导体材料那样将杂质集中在样品的末端,非晶体聚合物(PMMA)被集中在片层之间的无定形区域。差示扫描量热法表明,ZA样品具有较高的结晶度。采用拉伸试验研究了经淬火和ZA处理的纯PEO及其共混物的力学性能。最显著的结果是,ZA导致共混韧性增加(尽管淬火样品的韧性降低),这些差异在PMMA重量分数大于0.2时尤其明显。这个性质没有方向性,也就是说,我们得到平行于ZA方向和垂直于ZA方向的相同韧性。同样,ZA对共混物的杨氏模量没有(方向)影响,尽管模量本身随着玻璃状PMMA的加入而增加。相对于垂直方向和淬火试样,纯PEO在平行于ZA方向上的模量显著增加。我们认为,整齐PEO的ZA产生的各向异性是由于晶体片层和橡胶无定形区力学性能的对比,而在共混物中,晶体和无定形相都是硬固体,几乎没有对比——这种影响是由于层间PMMA在室温下是玻璃状聚合物造成的——显然对性能没有方向性。
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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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