ACS Appl Mater Interfaces. 2011 Apr;3(4):941-4. doi: 10.1021/am200082v. Epub 2011 Mar 16.
Water-borne, underwater adhesives were created by complex coacervation of synthetic copolyelectrolytes that mimic the proteins of the natural underwater adhesive of the sandcastle worm. To increase bond strengths, we created a second polymer network within cross-linked coacervate network by entrapping polyethylene glycol diacrylate (PEG-dA) monomers in the coacervate phase. Simultaneous polymerization of PEG-dA and cross-linking of the coacervate network resulted in maximum shear bond strengths of ∼1.2 MPa. Approximately 40% of the entrapped PEG-dA polymerized based on attenuated total reflectance-Fourier transform infrared spectroscopy. The monomer-filled coacervate had complex flow behavior, thickening at low shear rates and then thinning suddenly with a 16-fold drop in viscosity at shear rates near 6 s(-1). The microscale structure of the complex coacervates resembled a three-dimensional porous network of interconnected tubules. The sharp shear thinning behavior is conceptualized as a structural reorganization between the interspersed phases of the complex coacervate. The bond strength and complex fluid behavior of the monomer-filled coacervates have important implications for medical applications of the adhesives.
水基水下胶粘剂是通过模拟沙堡蠕虫天然水下胶粘剂的合成共聚电解质的复杂凝聚而制成的。为了提高粘结强度,我们通过将聚乙二醇二丙烯酸酯 (PEG-dA) 单体包埋在凝聚相中,在交联凝聚体网络内创建了第二个聚合物网络。PEG-dA 的同时聚合和凝聚体网络的交联导致最大剪切粘结强度约为 1.2 MPa。基于衰减全反射傅里叶变换红外光谱,约有 40%的包埋 PEG-dA 发生聚合。单体填充的凝聚体具有复杂的流动行为,在低剪切速率下变厚,然后在剪切速率接近 6 s(-1)时突然变稀,粘度降低 16 倍。复杂凝聚体的微尺度结构类似于相互连接的小管的三维多孔网络。急剧的剪切变稀行为被概念化为复杂凝聚体的分散相之间的结构重排。单体填充凝聚体的粘结强度和复杂流体行为对胶粘剂在医学中的应用具有重要意义。