Swiss Federal Laboratories for Materials Science and Technology, Empa, Duebendorf, Switzerland.
Langmuir. 2013 Apr 16;29(15):4760-71. doi: 10.1021/la400263r. Epub 2013 Apr 5.
The ability of amphiphilic polymers to self-assemble and form a gel or gel-like layer has been investigated by means of both experimental and theoretical studies on alkylated derivatives of poly(acrylic acid). Experiments were performed to determine the relationship between amphiphilic polymer chemistry, structure, water retention, and friction in the presence of hydrophobic substrates. The results indicate that the amphiphilic polymer forms a water-enriched, friction-reducing adsorbed layer on hydrophobic surfaces. The shear moduli and viscosities of the adsorbed layers, as determined by fitting the Voigt model to QCM-D data, were consistent with the presence of a gel. Computational studies on HPAA-12 were performed and are consistent with the presence of adsorbed conformations, in which the lowest free energy in the model corresponded to a partially adsorbed molecule, with a small fraction of hydrophobic side chains being compelled, for configurational reasons, to point into the bulk water. This would support the possibility of the formation of either a gel-like layer or surface aggregation. However, because the adsorption experiments showed no evidence of aggregation, this strongly suggests the formation of a gel.
通过对聚(丙烯酸)的烷基化衍生物的实验和理论研究,研究了两亲聚合物自组装并形成凝胶或凝胶状层的能力。实验旨在确定两亲聚合物化学、结构、水保持和存在疏水基底时的摩擦之间的关系。结果表明,两亲聚合物在疏水表面上形成富含水、减少摩擦的吸附层。通过将 Voigt 模型拟合到 QCM-D 数据来确定吸附层的剪切模量和粘度,与凝胶的存在一致。对 HPAA-12 进行了计算研究,与吸附构象一致,在该模型中,能量最低的自由能对应于部分吸附的分子,一小部分疏水性侧链由于构象原因被迫指向本体水。这将支持形成凝胶状层或表面聚集的可能性。然而,由于吸附实验没有显示聚集的证据,这强烈表明形成了凝胶。