Flexible Polymer Chains in Elongational Flow 1999
DOI: 10.1007/978-3-642-58252-3_8
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Birefringence of Dilute PS Solutions in Abrupt Contraction Flow

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Cited by 22 publications
(41 citation statements)
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“…This is a consequence of the increasing molecular elongation of the flexible polymer chains as the external strain is increased and is referred to as strain-hardening or sometimes 'strainstiffening' (Nguyen and Kausch, 1999). This increase in the extensional viscosity is only to be expected if the rate of deformation imposed on the fluid is sufficiently rapid to exceed local relaxation of the chain back towards equilibrium; this criterion is parameterized by the Deborah number of the flow.…”
Section: Strain-hardeningmentioning
confidence: 99%
“…This is a consequence of the increasing molecular elongation of the flexible polymer chains as the external strain is increased and is referred to as strain-hardening or sometimes 'strainstiffening' (Nguyen and Kausch, 1999). This increase in the extensional viscosity is only to be expected if the rate of deformation imposed on the fluid is sufficiently rapid to exceed local relaxation of the chain back towards equilibrium; this criterion is parameterized by the Deborah number of the flow.…”
Section: Strain-hardeningmentioning
confidence: 99%
“…According to the theory [1][2][3], this phenomenon is effective when shear strain occurring on the macromolecule becomes larger than critical value . The latter is inversely proportional to the maximum relaxation time of the polymer chain τ:…”
Section: Conformational Transitions Of Macromolecules In the Free Flowmentioning
confidence: 99%
“…Here A is a constant close to 1. So the critical conditions for CS-transition apply when ߝሶ τ ≈ mass of the polymer, temperature, and polymer chain flexibility, and can be calculated using one of the equations presented in literature [10][11][12]: (2) Here is the solvent's viscosity, M is the molar mass of the polymer, T is the absolute temperature, k is the Boltzmann constant, α is the constant depending on the polymer nature and solvent quality that varies from 1.5 to 1.8, R go is the radius of the gyration of the macromolecule in the static state, and the Fox-Flory parameter Φ 0 . From combining eq.…”
Section: Conformational Transitions Of Macromolecules In the Free Flowmentioning
confidence: 99%
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