Saleh Omar A
Materials Department and BMSE Program, University of California, Santa Barbara, California 93106, USA.
J Chem Phys. 2015 May 21;142(19):194902. doi: 10.1063/1.4921348.
I review theoretical and experimental results on the force-extension response of single polymers, with a focus on scaling pictures of low-force elastic regimes, and recent measurements of synthetic and biological chains that explore those regimes. The mechanical response of single polymers is an old theoretical problem whose exploration was instigated by the curious thermomechanical behavior of rubber. Up until the 1990s, the main utility of those calculations was to explain bulk material mechanics. However, in that decade, it became possible to directly test the calculations through high-precision single-chain stretching experiments (i.e., force spectroscopy). I present five major single-chain elasticity models, including scaling results based on blob-chain models, along with analytic results based on linear response theory, and those based on freely jointed chain or worm-like chain structure. Each model is discussed in terms of the regime of force for which it holds, along with the status of its rigorous assessment with experiment. Finally, I show how the experiments can provide new insight into polymer structure itself, with particular emphasis on polyelectrolytes.
我回顾了关于单链聚合物力-伸长响应的理论和实验结果,重点关注低力弹性区域的标度图像,以及对探索这些区域的合成链和生物链的最新测量。单链聚合物的力学响应是一个古老的理论问题,对它的探索是由橡胶奇特的热机械行为引发的。直到20世纪90年代,这些计算的主要用途是解释块状材料的力学性能。然而,在那个十年里,通过高精度的单链拉伸实验(即力谱学)直接检验这些计算成为可能。我介绍了五个主要的单链弹性模型,包括基于链段链模型的标度结果,以及基于线性响应理论的解析结果,还有基于自由连接链或蠕虫状链结构的结果。每个模型都根据其适用的力的范围进行了讨论,并介绍了其与实验进行严格评估的情况。最后,我展示了实验如何能为聚合物结构本身提供新的见解,特别强调了聚电解质。