Institute for Polymer Materials (POLYMAT) and Grupo de Ingeniería Química, Departamento de Química Aplicada, University of the Basque Country, Joxe Mari Korta Zentroa, Tolosa Etorbidea 72, 20018 Donostia-San Sebastián, Spain.
Langmuir. 2011 Apr 5;27(7):3878-88. doi: 10.1021/la104830u. Epub 2011 Mar 11.
Waterborne polyurethane-acrylic hybrid nanoparticles for application as pressure-sensitive adhesives (PSAs) were prepared by one-step miniemulsion polymerization. The addition of polyurethane to a standard waterborne acrylic formulation results in a large increase in the cohesive strength and hence a much higher shear holding time (greater than seven weeks at room temperature), which is a very desirable characteristic for PSAs. However, with the increase in cohesion, there is a decrease in the relative viscous component, and hence there is a decrease in the tack energy. The presence of a small concentration of methyl methacrylate (MMA) in the acrylic copolymer led to phase separation within the particles and created a hemispherical morphology. The tack energy was particularly low in the hybrid containing MMA because of the effects of lower energy dissipation and greater cross-linking. These results highlight the great sensitivity of the viscoelastic and adhesive properties to the details of the polymer network architecture and hence to the precise composition and synthesis conditions.
由一步细乳液聚合制备了用作压敏胶 (PSA) 的水基聚氨酯-丙烯酸混合纳米粒子。在标准水性丙烯酸配方中添加聚氨酯会导致内聚强度大大增加,因此剪切保持时间更长(在室温下大于七周),这是 PSA 的一个非常理想的特性。然而,随着内聚强度的增加,相对粘性成分减少,因此粘性能量减少。丙烯酸共聚物中少量甲基丙烯酸甲酯 (MMA) 的存在导致颗粒内相分离,并形成半球形形态。由于耗散能量较低和交联程度较大,含 MMA 的混合物的粘性能量特别低。这些结果突出表明,粘弹性和粘附性能对聚合物网络结构的细节非常敏感,因此对精确的组成和合成条件也非常敏感。