矛盾粘附及聚乙烯基塑料/塑料层合复合材料的改进多酚改性聚丙烯酸酯胶乳压敏胶粘剂

IF 5.1 3区 工程技术 Q1 CHEMISTRY, APPLIED Reactive & Functional Polymers Pub Date : 2025-03-01 Epub Date: 2025-01-12 DOI:10.1016/j.reactfunctpolym.2025.106158
Chunyuan Jiang , Xinrui Zhang , Xinyue Zhang , Yudong Wang , Zhizhong Ma , Xingjian Li , Yinwen Li
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引用次数: 0

摘要

保护膜以其柔韧性好、可折叠性好、使用方便等特点受到广泛欢迎。然而,它们往往伴随着较低的粘接性能,而且,聚丙烯酸酯胶乳型压敏胶(psa)的层合复合效率差,特别是在低表面能聚乙烯(PE)基塑料/塑料保护膜层合复合工艺中,也存在着一个紧迫的关键问题。以甲基丙烯酸缩水甘油酯(GMA)为官能团制备聚丙烯酸酯乳液型聚丙烯酸酯(pssa),然后在聚丙烯酸酯结构上接枝环氧基多巴胺(DOPA),得到新型多酚改性聚丙烯酸酯乳液型聚丙烯酸酯(PPSAs)。考察了功能单体(GMA和DOPA)用量对ppsa的粘度、粒径和分布、附着力和耐水性的影响。结果表明,与传统的聚丙烯酸酯乳液型聚丙烯酸酯相比,功能性GMA单体提高了聚丙烯酸酯的交联密度和内聚力,但对聚丙烯酸酯的初粘结力有负面影响;然而,通过进一步引入具有显著粘附性能的功能性DOPA组分,也改善了ppsa的初始粘性和保持粘性。正是由于GMA和DOPA的引入有效地实现了ppsa的附着力和内聚力的统一,因此当GMA和DOPA的添加量分别为5.0 wt%和0.5 wt%时,PPSA5表现出良好的稳定性,平均粒径(196.4 nm)和分布(PDI, 0.12),最佳的粘接性能为初粘性(5.17 N/25 mm), 180°剥离强度(6.62 N/25 mm)和保持力(>72 h/25 mm)。当ppsa进一步用作层压复合胶粘剂用于塑料/塑料层压复合的PE基保护膜。模拟的PE基保护膜和改进的180°剥离强度测试结果表明,与传统的聚丙烯酸酯胶乳型psa相比,ppsa具有非常高的防撕裂复合效率,并且仅仅是利用多酚和环氧基在PE基塑料/塑料层合界面上与电晕处理引入的官能团形成有效的化学键桥。协同提高ppsa的层合复合效率。因此,本研究为ppsa作为层压复合胶粘剂在低表面能塑料/塑料层压领域的应用提供了一个非常有前途和广泛的策略。
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Paradoxical adhesion and polyethylene based plastic/plastic laminated composite improvement of polyphenols modified polyacrylate latex pressure-sensitive adhesives
Protective films are widely welcomed for its excellent flexibility, good foldability, and ease of use, etc. However, they are often accompanied with low adhesive performance, moreover, there are also a pressing critical issue about poor laminated composite efficiency for polyacrylate latex type pressure-sensitive adhesives (PSAs) especially in low surface energy polyethylene (PE) based plastic/plastic laminated composite process of protective films. Polyacrylate latex type PSAs were prepared by using glycidyl methacrylate (GMA) as functional comonomer, and then novel polyphenols modified polyacrylate latex PSAs (PPSAs) were further obtained by grafting dopamine (DOPA) with epoxy groups in PSAs structures. The effects of functional monomer dosages (GMA and DOPA) on the viscosity, particle size and distribution, adhesion, and water resistance of PPSAs were investigated. The results showed that, compared with traditional polyacrylate latex type PSAs, functional GMA monomer improved the crosslinking density and cohesion of PPSAs but also accompanied with negative impact on initial adhesion; Nevertheless, while by the further introduction of functional DOPA component with significant adhesive property also improved the initial and holding tack for PPSAs. Precisely because of the introduction of GMA and DOPA effectively realized the unity of the adhesive force and cohesive force of PPSAs, and thus when the amount of GMA and DOPA were 5.0 wt% and 0.5 wt%, PPSA5 behaved with good stability, average particle size (196.4 nm) and distribution (PDI, 0.12), and best adhesive properties with initial tack (5.17 N/25 mm), 180° peel strength (6.62 N/25 mm) and holding power (>72 h/25 mm). When PPSAs further used as laminated composite adhesives for plastic/plastic laminated composite of PE based protective films. The simulated PE based protective films and improved 180° peel strength measurement results showed PPSAs behaved with tremendously tearproof laminated composite efficiency which differed from traditional polyacrylate latex type PSAs, and just by utilizing the polyphenols and epoxy groups to form effective chemical bonding bridges with functional groups introduced by corona treatment at PE based plastic/plastic lamination interface, and synergistically improving the laminated composite efficiency of PPSAs. Thus, this work presents a highly promising and broad strategy for utilization of PPSAs as laminated composite adhesives in low surface energy plastic/plastic lamination field.
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来源期刊
Reactive & Functional Polymers
Reactive & Functional Polymers 工程技术-高分子科学
CiteScore
8.90
自引率
5.90%
发文量
259
审稿时长
27 days
期刊介绍: Reactive & Functional Polymers provides a forum to disseminate original ideas, concepts and developments in the science and technology of polymers with functional groups, which impart specific chemical reactivity or physical, chemical, structural, biological, and pharmacological functionality. The scope covers organic polymers, acting for instance as reagents, catalysts, templates, ion-exchangers, selective sorbents, chelating or antimicrobial agents, drug carriers, sensors, membranes, and hydrogels. This also includes reactive cross-linkable prepolymers and high-performance thermosetting polymers, natural or degradable polymers, conducting polymers, and porous polymers. Original research articles must contain thorough molecular and material characterization data on synthesis of the above polymers in combination with their applications. Applications include but are not limited to catalysis, water or effluent treatment, separations and recovery, electronics and information storage, energy conversion, encapsulation, or adhesion.
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