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Deformation‐induced bonding of polymer films below the glass transition temperature
Author(s) -
Padhye Nikhil,
Vallabh Ajay
Publication year - 2021
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.50934
Subject(s) - materials science , glass transition , polymer , composite material , amorphous solid , deformation (meteorology) , adhesion , crystallinity , ductility (earth science) , deformation mechanism , crystallography , microstructure , chemistry , creep
Bonding between polymers through interdiffusion of macromolecules is a well‐known mechanism of polymer adhesion. A new polymer bonding mechanism in the solid state, taking place at ambient temperatures well below the glass transition value (T g ), has been recently reported; in this mechanism, bulk plastic compression of polymer films held in contact led to adhesion over timescales of the order of a fraction of a second. In this study, we prepared various blends of plasticized polymer films with desirable ductility from amorphous and semicrystalline powders of hydroxypropyl methylcellulose and polyvinyl alcohol derivatives; then, we observed the bonding of these polymers at ambient temperatures, up to 80 K below T g , purely through mechanical deformation. The deformation‐induced bonding of the polymer films studied in this work led to interfacial fracture toughnesses in the range of 1.0–21.0 J/m 2 when bulk plastic strains between 3% and 30% were imposed across the films. Scanning electron microscopy observation of the debonded interfaces also confirmed that bonding was caused by deformation‐induced macromolecular mobilization and interpenetration. These results expand the range of applicability of sub‐T g , solid‐state, deformation‐induced bonding processes.