Thees Michael F, McGuire Jennifer A, Roth Connie B
Department of Physics, Emory University, Atlanta, Georgia 30322, USA.
Soft Matter. 2020 Jun 21;16(23):5366-5387. doi: 10.1039/d0sm00565g. Epub 2020 May 4.
Recent studies suggest chain adsorption in the melt may be responsible for a number of property changes in thin films by making correlations between the residual adsorbed layer thickness h(t) measured after a given solvent washing procedure as a function of annealing time t of the film at an elevated temperature prior to this solvent rinse. This procedure, frequently called "Guiselin's experiment", refers to the thought experiment proposed in a 1992 theoretical treatment by Guiselin that assumed chain segments in contact with the surface are irreversibly adsorbed whereby unadsorbed chains could be washed away by solvent without disturbing the adsorbed substrate contact points in the melt. In the present work, we review this recent literature, identifying and experimentally testing a common protocol for forming adsorbed layers h(t) from solvent washing melt films. We find h(t) curves to be far less reproducible and reliable than implied in the literature, strongly dependent on solvent washing and substrate cleaning conditions, and annealing at elevated temperatures is unnecessary as densification of films sitting at room temperature makes the glassy film harder to wash off, leaving behind h of comparable thickness. This review also summarizes literature understanding developed over several decades of study on polymer adsorption in solution, which experimentally demonstrated that polymer chains in solution are highly mobile, diffusing and exchanging on the surface even in the limit of strong adsorption, contradicting Guiselin's assumption. Preformed adsorbed layers of different thicknesses h are shown to not affect the average glass transition temperature or physical aging of 30 nm thick films. In summary, a number of open questions and implications are discussed related to thin films and polymer nanocomposites.
最近的研究表明,熔体中的链吸附可能是薄膜中许多性质变化的原因,这是通过将给定溶剂洗涤程序后测量的残余吸附层厚度h(t)与该溶剂冲洗之前薄膜在高温下的退火时间t建立关联来实现的。这个过程,通常被称为“吉塞林实验”,指的是1992年吉塞林在理论处理中提出的思想实验,该实验假设与表面接触的链段被不可逆地吸附,从而未吸附的链可以被溶剂冲走,而不会干扰熔体中吸附的底物接触点。在本工作中,我们回顾了这一最新文献,确定并通过实验测试了一种从溶剂洗涤熔体薄膜形成吸附层h(t)的通用方案。我们发现h(t)曲线远不如文献中所暗示的那样可重复和可靠,强烈依赖于溶剂洗涤和底物清洁条件,并且在高温下退火是不必要的,因为室温下薄膜的致密化使得玻璃态薄膜更难洗掉,留下厚度相当的h。这篇综述还总结了几十年来关于聚合物在溶液中吸附的研究所形成的文献理解,实验表明溶液中的聚合物链具有高度的流动性,即使在强吸附极限下也能在表面扩散和交换,这与吉塞林的假设相矛盾。不同厚度h的预形成吸附层被证明不会影响30纳米厚薄膜的平均玻璃化转变温度或物理老化。总之,讨论了一些与薄膜和聚合物纳米复合材料相关的未解决问题和影响。