4.5 Article

Theoretical rheo-physics of silk: Intermolecular associations reduce the critical specific work for flow-induced crystallization

期刊

JOURNAL OF RHEOLOGY
卷 66, 期 3, 页码 515-534

出版社

SOC RHEOLOGY
DOI: 10.1122/8.0000411

关键词

Silk protein; Associating polymers; Non-linear rheology; Flow-induced cyrstallisation; Molecular dynamics

资金

  1. Engineering and Physical Sciences Research Council
  2. University of York high-performance computing service
  3. [EP/N031431/1]

向作者/读者索取更多资源

Silk, a semidilute solution of associating polypeptide chains, crystallizes under stretch-induced disruption in strong extensional flow. Simulations and calculations show that the associations hinder chain alignment but facilitate stretching at low specific work. The chemical tunability of associations in silkworms optimizes chain alignment and stretching in different locations along the spinning duct, highlighting the potential advantages of chemically tunable processing of synthetic association polymers for biomimetic industrial purposes.
Silk is a semidilute solution of randomly coiled associating polypeptide chains that crystallize following the stretch-induced disruption, in the strong extensional flow of extrusion, of the solvation shell around their amino acids. We propose that natural silk spinning exploits both the exponentially broad stretch distribution generated by associating polymers in extensional flow and the criterion of a critical concentration of sufficiently stretched chains to nucleate flow-induced crystallization. To investigate the specific-energy input needed to reach this criterion in start-up flow, we have coupled a model for the Brownian dynamics of a bead-spring-type chain, whose beads represent coarse-grained Gaussian chain segments, to the stochastic, strain-dependent binding and unbinding of their associations. We have interpreted the simulations with the aid of analytic calculations on simpler, tractable models with the same essential physical features. Our simulations indicate that the associations hamper chain alignment in the initial slow flow, but, on the other hand, facilitate chain stretching at low specific work at later, high rates. We identify a minimum in the critical specific work at a strain rate just above the stretch transition (i.e., where the mean stretch diverges), which we explain in terms of analytical solutions of a two-state master equation. We further discuss how the silkworm appears to exploit the chemical tunability of the associations to optimize chain alignment and stretching in different locations along the spinning duct: this delicate mechanism also highlights the potential biomimetic industrial benefits of chemically tunable processing of synthetic association polymers.

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