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Theoretical aspects of polymer crystallization with chain folds: Bulk polymers
Author(s) -
Hoffman J. D.
Publication year - 1964
Publication title -
polymer engineering and science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.503
H-Index - 111
eISSN - 1548-2634
pISSN - 0032-3888
DOI - 10.1002/pen.760040413
Subject(s) - crystallization , materials science , crystallinity , nucleation , crystallization of polymers , polymer , surface energy , thermodynamics , annealing (glass) , isothermal process , micelle , composite material , chemistry , physics , aqueous solution
The Theory of Crystallization of bulk linear polymers with chain folding is discussed in terms of recent developments. Specific topics covered are: (a) Rate of crystal growth and size of folded nuclei, (b) theoretical and experimental estimates of the fold surface free energy, and estimates of the surface free energy of “friged micelle” and “switchbord” type crystals, (c) basic causes of essentially regular folding in bulk, (d) rejection of short chain species during crystallization, (e) melting behavior of thin chain‐folded lamellae, (f) gradual thickening of lamellae on isothermal storage, (g) homogeneous, pseudohomogeneous, and heterogeneous nucleation, (h) voids and included point defects as a paret of the concept of the degree of crystallinity, and (i) phenomena occurring in stage 1 and stage 2 of bulk crystallization isotherms (annealing). A comparison of theory and experiment is carried out using data, some previously unpublished, on polyethylene and polychlorotrifluoroethylene. The theory with essentially regular golding is found to be satisfactory.