1996
DOI: 10.1002/(sici)1099-0488(199610)34:14<2393::aid-polb9>3.3.co;2-h
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A continuum model for the dynamics of flow‐induced crystallization

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Cited by 20 publications
(24 citation statements)
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“…Since the direct experimental observations in 1960s of flowinduced crystalline (FIC) phases occurring in many polymeric materials under certain conditions [3,4], numerous theoretical and experimental research efforts [5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20] have been directed over the past several decades to understand the crystallization process and the resulting structure. It is generally known that the kinetics of nucleation and crystal-growth, the FIC morphology, and its stability, are extremely sensitive to experimental conditions (e.g.…”
Section: Introductionmentioning
confidence: 99%
“…Since the direct experimental observations in 1960s of flowinduced crystalline (FIC) phases occurring in many polymeric materials under certain conditions [3,4], numerous theoretical and experimental research efforts [5][6][7][8][9][10][11][12][13][14][15][16][17][18][19][20] have been directed over the past several decades to understand the crystallization process and the resulting structure. It is generally known that the kinetics of nucleation and crystal-growth, the FIC morphology, and its stability, are extremely sensitive to experimental conditions (e.g.…”
Section: Introductionmentioning
confidence: 99%
“…Examples of the structure determining parameters include the macroscopic strain, [3] the Cauchy stress, [4] the conformation of molecules, [5,6] or a phenomenological molecular deformation factor that influences the induction time. [7,8] A first shortcoming of these models is that they generally only result in the overall degree of crystallinity and do not provide information on the final crystalline structure.…”
Section: Introductionmentioning
confidence: 99%
“…The final thermodynamic driving force is similar to that originally derived by Flory [43], but guarantees that the influence of the chain configuration reduces to zero provided the chain configuration is identical to the equilibrium configuration. Compared to previous thermodynamic analyses of FIC [43,44], it is convenient to consider a configuration tensor of the amorphous part of the chain rather than to consider a configuration tensor for the entire polymer chain, i.e., amorphous plus crystalline parts [44]. For this reason a term describing the change in chain configuration due to crystallization is incorporated into the evolution equation of the chain configuration of the amorphous part of the chain, see Eq.…”
Section: Consistency With Non-equilibrium Thermodynamic Principlesmentioning
confidence: 99%