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• W2030569660 abstract "We study the concentration dependence of the conformational and viscometric behaviour of short-chain polymer solutions in shear flow by conducting a series of non-equilibrium molecular dynamics simulations, covering the entire concentration range. Our model explicitly incorporates all of the important generic features of real polymer solutions—excluded volume, hydrodynamic interactions and finite chain extensibility. Hydrodynamic interactions are included exactly by treating the solvent explicitly as an atomic fluid. The polymer molecules studied consist of 20-site bead-rod model molecules, which correspond approximately to 12 Kuhn steps in the melt. For polyethylene, this represents a molar mass of 1800 g mol−1. In some respects, our results are consistent with experimental and theoretical results obtained for long-chain polymer solutions. We calculate the Flory–Fox constant and find a value that agrees reasonably well with results for long chain polymer solutions. Due to the short chain length of the molecules investigated, no semidilute region exists for these solutions. However, the radius of gyration and viscosity still exhibit strong concentration dependence, which is well described by power series, rather than power law expressions, in contrast to the behaviour usually observed in long-chain polymer solutions." @default.
• W2030569660 created "2016-06-24" @default.
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• W2030569660 date "2004-03-01" @default.
• W2030569660 modified "2023-09-27" @default.
• W2030569660 title "Concentration dependence of viscometric properties of model short chain polymer solutions" @default.
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• W2030569660 doi "https://doi.org/10.1016/j.polymer.2003.12.034" @default.
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