调整功能化聚烯烃基热熔胶的粘接强度:意想不到的结果带来新的机遇

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Jakub Kruszynski, Weronika Nowicka, Farhan Ahmad Pasha, Lanti Yang, Artur Rozanski, Miloud Bouyahyi, Ralf Kleppinger, Lidia Jasinska-Walc, Rob Duchateau
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引用次数: 0

摘要

轻量化、多组件产品的开发需要适应性强且坚固的粘接解决方案。热熔胶由于结合了良好的粘合强度、易于加工和成本效益而日益引起工业的兴趣。最近,我们的小组报道了羟基功能化丙基共聚物在极性和非极性表面上的显著粘合性能。所获得的粘接强度被证明是太高的应用,如一次性包装,这需要低到中等粘结力易于打开。从工业规模生产的角度来看,通过制造具有不同羟基官能团含量的众多功能化聚烯烃牌号来调整粘接强度是具有挑战性的。在此,我们阐明了一种通过将功能化的丙烯共聚物与非功能化的同系物共混来调整粘合性能的替代方法。为了了解所研究的稀释共混物的结构-性能关系,对形貌、物理性能、结晶和粘弹性行为进行了全面的表征。结果表明,非官能化聚烯烃的结晶度及其与官能化聚烯烃的混相对共混物的粘接强度起着至关重要的作用。要么发现黏附强度随稀释而逐渐降低,要么─令人惊讶的是─根本没有观察到黏附强度的损失,甚至在稀释100倍后也没有!分子动力学模拟揭示了羟基功能化聚烯烃向氧化铝表面迁移并与之相互作用的内在趋势。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Tuning the Adhesive Strength of Functionalized Polyolefin-Based Hot Melt Adhesives: Unexpected Results Leading to New Opportunities

Tuning the Adhesive Strength of Functionalized Polyolefin-Based Hot Melt Adhesives: Unexpected Results Leading to New Opportunities
The development of lightweight, often multicomponent products requires adaptable and robust bonding solutions. Hot melt adhesives increasingly attract industrial interest as they combine good adhesive strength, facile processability, and cost-efficiency. Recently, our group has reported on the remarkable adhesive performance of hydroxyl-functionalized propylene-based copolymers in bonding both polar and nonpolar surfaces. The obtained adhesive strength proved to be too high for applications such as single-use packaging, which requires low to moderate adhesion for easy opening. Tuning the adhesive strength by manufacturing numerous functionalized polyolefin grades with varying contents of hydroxyl-functional groups is challenging in view of industrial-scale production. Herein, we elucidate an alternative approach to tune the adhesive performance by blending the functionalized propylene copolymers with nonfunctionalized congeners. To understand the structure–property relationship of the investigated diluted blends, a thorough characterization of morphology, physical properties, crystallization, and viscoelastic behavior was performed. It appeared that the crystallinity of the nonfunctionalized polyolefin and its miscibility with the functionalized polyolefin play a crucial role on the adhesive strength of the blends. Either a gradual decrease in adhesive strength with dilution was noticed or─surprisingly─no loss of adhesive strength was observed at all, not even after diluting 100 times! Molecular dynamics simulations revealed an intrinsic tendency of the hydroxyl-functionalized polyolefin to migrate to and interact with the aluminum oxide surface.
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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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