Meng Zhiyong, Cho Jae Kyu, Debord Stella, Breedveld Victor, Lyon L Andrew
J Phys Chem B. 2007 Jun 28;111(25):6992-7. doi: 10.1021/jp073122n. Epub 2007 May 31.
The equilibrium phase behavior and the dynamics of colloidal assemblies composed of soft, spherical, colloidal particles with attractive pair potentials have been studied by digital video microscopy. The particles were synthesized by precipitation copolymerization of N-isopropylacrylamide (NIPAm), acrylic acid (AAc), and N,N'-methylene bis(acrylamide) (BIS), yielding highly water swollen hydrogel microparticles (microgels) with temperature- and pH-tunable swelling properties. It is observed that in a pH = 3.0 buffer with an ionic strength of 10 mM, assemblies of pNIPAm-AAc microgels crystallize due to a delicate balance between weak attractive and soft repulsive forces. The attractive interactions are further confirmed by measurements of the crystal melting temperatures. As the temperature of colloidal crystals is increased, the crystalline phase does not melt until the temperature is far above the lower critical solution temperature (LCST) of the microgels, in stark contrast to what is typically observed for phases formed due to purely repulsive interactions. The unusual thermal stability of pNIPAm-AAc colloidal crystals demonstrates an enthalpic origin of crystallization for these microgels.
通过数字视频显微镜研究了由具有吸引性对势的软质球形胶体颗粒组成的胶体聚集体的平衡相行为和动力学。这些颗粒是通过N-异丙基丙烯酰胺(NIPAm)、丙烯酸(AAc)和N,N'-亚甲基双丙烯酰胺(BIS)的沉淀共聚合成的,得到了具有温度和pH可调溶胀特性的高度水溶胀水凝胶微粒(微凝胶)。观察到在离子强度为10 mM的pH = 3.0缓冲液中,pNIPAm-AAc微凝胶的聚集体由于弱吸引力和软排斥力之间的微妙平衡而结晶。通过测量晶体熔化温度进一步证实了吸引力相互作用。随着胶体晶体温度的升高,直到温度远高于微凝胶的低临界溶液温度(LCST),晶相才会熔化,这与通常观察到的由于纯粹排斥相互作用形成的相形成了鲜明对比。pNIPAm-AAc胶体晶体不寻常的热稳定性证明了这些微凝胶结晶的焓起源。