Laurer JH, Smith SD, Samseth J, Mortensen K, Spontak RJ
Departments of Materials Science & Engineering and Chemical Engineering, North Carolina State University, Raleigh, North Carolina 27695, Corporate Research Division, The Procter & Gamble Company, Cincinnati, Ohio 45239, Department of Physics, Institute for Energy Technology, N-2007 Kjeller, Norway, and Department of Condensed Matter Physics & Chemistry, Risø National Laboratory, DK-4000 Roskilde, Denmark.
Macromolecules. 1998 Jul 28;31(15):4975-85. doi: 10.1021/ma980200j.
Addition of a relatively low-molecular-weight parent homopolymer to a lamellar AB diblock copolymer constitutes a reliable means by which to induce, in controllable fashion, transitions to other morphologies. In this study, we examine the effect of interfacial modification on such transitions in "extended" A(A/B)B copolymer/homopolymer blends in which (i) the A/B midblock fraction (relative to the copolymer molecular weight) is varied from 0.0 to 0.4 in 0.1 increments and (ii) the overall concentration of A ranges from 0.50 to 0.95. As this A/B fraction is increased at constant blend composition, the extent of homopolymer-induced lamellar swelling becomes measurably less pronounced, indicating that the A/B midblock serves to delocalize repulsion along the interphase separating adjacent lamellae. At higher homopolymer concentrations, an increase in the A/B fraction results in the formation of either unilamellar vesicles or a randomly connected bilayered membrane, rather than micelles. These membranes become unstable and transform to micelles at high copolymer dilution. The results presented here are discussed in terms of the complex morphologies observed in, and predicted for, low-molar-mass (co)surfactant systems.
向层状AB二嵌段共聚物中添加相对低分子量的母体均聚物,是一种以可控方式诱导向其他形态转变的可靠方法。在本研究中,我们研究了界面改性对“扩展”A(A/B)B共聚物/均聚物共混物中此类转变的影响,其中:(i) A/B中间嵌段分数(相对于共聚物分子量)以0.1的增量从0.0变化到0.4,(ii) A的总浓度范围为0.50至0.95。在共混物组成恒定的情况下,随着该A/B分数的增加,均聚物诱导的层状溶胀程度明显减弱,这表明A/B中间嵌段有助于使沿相邻层片间界面的排斥作用离域化。在较高的均聚物浓度下,A/B分数的增加会导致形成单层囊泡或随机连接的双层膜,而不是胶束。在高共聚物稀释度下,这些膜会变得不稳定并转变为胶束。本文给出的结果是根据在低摩尔质量(共)表面活性剂体系中观察到的和预测的复杂形态来讨论的。