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Adhesion at polypropylene‐cellophane interfaces
Author(s) -
Bialski A.,
Manley R. St. J.,
Schreiber H. P.
Publication year - 1977
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.760170707
Subject(s) - cellophane , materials science , polypropylene , adhesion , composite material , polymer science
The shear strength of bonds between isotactic polypropylene and cellophane, formed under standard conditions, has beer studied as a function of cooling rates, following bond formation, and after ageing at temperatures up to 90°C. Rapid cooling produced cohesively failing bonds with shear strengths above 20 kg/em 2 . Weak, adhesively failing joints were produced under slow‐cooling conditions. Strong bonds deteriorated when joints were aged at temperatures above 50°C, but further improvement in bond strength was observed upon ageing at lower temperatures. Experimental observations were consistent with the development of smectic structure in the polypropylene upon rapid cooling; a tendency for transcrystallization in slow‐cooled joints was offset by the presence of weak boundary layers in the interface. Ageing produced further development of weak boundary layers and a transition from smectic to monoclinic crystallization in polypropylene. At higher ageing temperatures, the former effect seemed dominant; at lower temperatures, the structural change was assumed responsible for the observed improvement in bond strength.