材料科学
胶粘剂
热塑性弹性体
复合材料
热塑性塑料
粘弹性
弹性体
造型(装饰)
共聚物
聚合物
粘附
图层(电子)
作者
Mitchell Maw,Alexander K. Tanas,Erfan Dashtimoghadam,Evgeniia A. Nikitina,Dimitri A. Ivanov,Andrey V. Dobrynin,Mohammad Vatankhah‐Varnosfaderani,Sergei S. Sheiko
标识
DOI:10.1021/acsami.3c07821
摘要
Hot-melt pressure-sensitive adhesives (HMPSAs) are used in applications from office supplies to biomedical adhesives. The major component in HMPSA formulations is thermoplastic elastomers, such as styrene-based block copolymers, that provide both mechanical integrity and moldability. Since neat polymer networks are unable to establish an adhesive bond, large quantities of plasticizers and tackifiers are added. These additives enhance the adhesive performance but complicate the phase behavior and property stability of the pressure-sensitive adhesive. Herein, we introduce an alternative additive-free approach to HMPSA design based on self-assembly of bottlebrush graft-copolymers, where side chains behave as softness, strength, and viscoelasticity mediators. These systems maintain moldability of conventional thermoplastic elastomers, while architecturally disentangled bottlebrush network strands empower several benefits such as extreme softness for substrate wetting, low melt viscosity for molding and 3D-printing, and a broad frequency range of viscoelastic responses for adhesion regulation within almost four orders of magnitude. The brush graft-copolymers implement five independently controlled architectural parameters to regulate the Rouse time, work of adhesion, and debonding mechanisms.
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