Preparation of Oriented β-Form Poly(l-lactic acid) by Solid-State Coextrusion:  Effect of Extrusion Variables

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Macromolecules Pub Date : 2003-04-18 DOI:10.1021/ma030050z
Daisuke Sawai, Kazuyo Takahashi, Aki Sasashige, Tetsuo Kanamoto, Suong-Hyu Hyon
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引用次数: 174

Abstract

A film of melt-crystallized poly(l-lactic acid) (PLLA) consisting of α-form crystals was uniaxially drawn by solid-state coextrusion at 110?170 °C using split billets of different polymers. The effects of extrusion variables, including the extrusion draw ratio (EDR), temperature (Text), and pressure (Pext), on the crystal transformation from the initial α-form to the oriented β-form crystals were studied. The crystal transformation proceeded rapidly with EDR. It was found that when coextrusion was made at a constant Pext and EDR but at different Text's, there was a Text (130 °C) where the crystal transformation proceeded most efficiently. Furtheremore, when coextrusion was made at a constant Text and EDR but at different Pext's, the transformation proceeded more efficiently at a higher Pext. These results show that crystal transformation proceeds with the EDR most efficiently for the coextrusion at a Text of 130 °C and a higher Pext. As a result of the specific effect for each of the extrusion variables on the crystal transformation and ductility, a highly oriented film consisting of β crystals alone was obtained by coextrusion to the highest EDR of ~14 achieved at a high Text of 170 °C, near the Tm, and a high Pext of ~50 MPa.

固态共挤出法制备定向β-型聚乳酸:挤出变量的影响
采用固态共挤压法在110℃下单轴拉伸出由α-型晶体组成的熔融结晶聚乳酸(PLLA)薄膜。170°C,使用不同聚合物的分离坯料。研究了挤压拉伸比(EDR)、温度(Text)、压力(Text)等挤压变量对晶体由初始α-型向定向β型转变的影响。EDR使晶体转变迅速进行。结果发现,当在恒定的ext和EDR下,但在不同的Text下共挤压时,有一个Text(130°C)的晶体转变进行得最有效。在相同的文本和EDR下,在不同的像素点进行共挤压时,在更高的像素点上进行转化的效率更高。结果表明,在温度为130℃及更高的温度下,共挤压过程中EDR的晶体转变效率最高。由于每种挤压变量对晶体转变和延展性的特定影响,通过共挤压获得了由β晶体组成的高取向薄膜,在170°C的高温度下,在Tm附近获得了最高的EDR ~14,高温度为~50 MPa。
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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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