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The sorption of poly(vinyl acetate) on cellulose. I. The nature and extent of the sorbed layer
Author(s) -
Alince B.,
Kuniak L.,
Robertson A. A.
Publication year - 1970
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.1970.070140615
Subject(s) - sorption , polymer , cellulose , polymer chemistry , swelling , chemical engineering , cellulose acetate , monolayer , vinyl acetate , chemistry , solvent , materials science , organic chemistry , adsorption , composite material , biochemistry , engineering , copolymer
The sorption of poly(vinyl acetate) from benzene solution onto cellulose fibers has been investigated with particular attention to the nature and extent of the sorbed layer of polymer. The cellulose substrate has been varied by swelling pretreatments with water, ethylenediamine, and 18% sodium hydroxide. The density of the sorbed polymer after drying was found to be similar to that of the bulk polymer (1.19–1.20 g/cm 3 ). Water vapor sorption isotherms were used to evaluate the internal surface of cellulose and the decrease in the surface area accessible to water after sorption of the polymer. This decrease was considered equivalent to the area covered by sorbed polymer. The amount of polymer sorbed per unit area (5.0–5.5 mg PVAc sorbed from benzene per 1 m 2 of cellulose surface) was found to be substantially independent of the amount of sorbed polymer and of the swelling pretreatment, indicating that the thickness of the sorbed layer was quite uniform (40–50 Å). A comparison of the thickness of the sorbed layer in the dry state with the thickness of a monolayer with polymer molecules lying flat on the solid surface indicated that the fraction of the polymer segments attached directly to the surface was about 0.10. The amount of polymer sorbed per unit area of cellulose and consequently the thickness of the sorbed layer and the fraction of attachment can be affected by the nature of the solvent from which the polymer is sorbed.