The elastic properties of Polystyrene (PS) and High Impact Polystyrene (HIPS) have been investigated using one-dimensional and two-dimensional damage mechanics models. The damage mechanism of these polymers is crazing. However, their mechanical properties are different. The PS specimens behave in a
Blendable Peptide-Polymer Nanofibers to Modulate Mechanical Properties of Polymers
✍ Scribed by Jens Hentschel; Hans G. Börner
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 449 KB
- Volume
- 9
- Category
- Article
- ISSN
- 1616-5187
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✦ Synopsis
Abstract
The self‐assembly kinetics of a peptide__‐block‐__poly(n‐butyl acrylate) copolymer (p__n__BA‐$(TV)_{\rm 5}^{{\rm switch}} n{\rm FG}$ conjugate) in solution and the blend behavior of the resulting fibrillar nanoobjects are investigated. By using a switch peptide segment with temporarily suppressed aggregation behavior, the solution self‐assembly of the peptide‐polymer conjugate can be triggered via a small change in the pH~app.~. This results in a controlled assembly of the peptide segments and thus the organization of the bioconjugate. The process was followed by time dependent determination of the dynamic viscosity of the aggregation solution and by AFM that allows visualization of the corresponding structures. The obtained anisotropic nanofibers are characterized in solution and in bulk by SAXS, showing a worm‐like characteristic. Blend behavior is investigated, proving the homogeneous dispersibility of the nanofibers in poly(acrylate)s. It could be demonstrated that the nanofibers are modulating the mechanical properties of p__n__BA by mechanisms of molecular reinforcement, having a distinct stiffening effect.
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