聚结乳胶共混物的成膜能力和机械性能

3区 工程技术 Q1 Materials Science
S. Lepizzera, C. Lhommeau, G. Dilger, T. Pith, M. Lambla
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引用次数: 43

摘要

研究了胶乳共混物(硬胶乳+软胶乳)的成膜能力和胶乳共混物(含硬性夹杂物的软基体)在有限应变下的力学行为。形成透明无裂纹薄膜的硬胶乳颗粒的最大重量分数(ϕmax)作为成膜能力的判据。结果表明,当软胶乳的Tg较低(Tg < 0℃)时,由于硬颗粒之间的接触控制成膜能力,故ϕmax为常数,其值为0.55。然而,当Tg(软)高于0℃时,观察到Tg(软)对成膜能力的预期影响(即,当Tg(软)增加时,ϕmax减小)。从力学行为的角度来看,控制乳胶共混膜力学行为的两个主要参数是:软聚合物的力学性能,因为它代表了连续的基体;硬乳胶颗粒的重量分数,因为它们增强了基体在载荷下的局部变形。然而,也证明了在单轴应变实验中,Tg乳胶颗粒和低Tg基体之间的脱脱发生得很快(延伸率≈30%),为了彻底了解这些双相薄膜的力学行为,必须考虑到这一点。©1997 John Wiley & Sons, Inc[J] .高分子材料科学与工程学报,2003,19 (5):559 - 561
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Film‐forming ability and mechanical properties of coalesced latex blends
The film-forming ability of latex blends (hard latex + soft latex) and the mechanical behavior at finite strain of latex blend films (soft matrix with tough inclusions) has been investigated. The maximum weight fraction of hard latex particles (ϕmax) which still gives rise to transparent and crack-free films has been used as film-forming ability criterion. It was shown that when the Tg of the soft latex is low (Tg(soft) < 0°C), ϕmax is constant and equal to 0.55 because the film-forming ability is controlled by contacts between hard particles. Nevertheless, the expected effect of Tg(soft) on film-forming ability is observed (i.e., ϕmax decreases when Tg(soft) increases) when Tg(soft) is above 0°C. From the mechanical behavior point of view, it was shown that the two main parameters controlling the mechanical behavior of latex blend films are: the mechanical properties of the soft polymer because it represents the continuous matrix and the weight fraction of hard latex particles since they enhance the local deformation of matrix under load. However, it was also proven that debounding between the Tg latex particles and low Tg matrix occurs rapidly (at an elongation ratio ≈ 30%) during uniaxial strain experiments and has to be taken into account in order to gain a thorough understanding of the mechanical behavior of these biphasic films. © 1997 John Wiley & Sons, Inc. J Polym Sci B: Polym Phys 35: 2093–2101, 1997
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来源期刊
CiteScore
5.90
自引率
0.00%
发文量
0
审稿时长
2.1 months
期刊介绍: Since its launch in 1946 by P. M. Doty, H. Mark, and C.C. Price, the Journal of Polymer Science has provided a continuous forum for the dissemination of thoroughly peer-reviewed, fundamental, international research into the preparation and properties of macromolecules. From January 2020, the Journal of Polymer Science, Part A: Polymer Chemistry and Journal of Polymer Science, Part B: Polymer Physics will be published as one journal, the Journal of Polymer Science. The merged journal will reflect the nature of today''s polymer science research, with physics and chemistry of polymer systems at the heart of the scope. You can continue looking forward to an exciting mix of comprehensive reviews, visionary insights, high-impact communications, and full papers that represent the rapid multidisciplinary developments in polymer science. Our editorial team consists of a mix of well-known academic editors and full-time professional editors who ensure fast, professional peer review of your contribution. After publication, our team will work to ensure that your paper receives the recognition it deserves by your peers and the broader scientific community.
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