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Highly branched and tartaric acid‐based water‐borne resins
Author(s) -
Gündüz Güngör,
Gafaroğullari̇ Murat
Publication year - 2001
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 - 10.1002/1097-4628(20010425)80:4<604::aid-app1135>3.0.co;2-o
Subject(s) - monomer , adipic acid , tartaric acid , polymer chemistry , isocyanate , copolymer , chemistry , polyol , polyurethane , prepolymer , polyester , materials science , organic chemistry , polymer , citric acid
In this study, water‐borne polyurethane resins were produced using poly(propylene‐ethylene) copolymer triol, toluene diisocyanate, and hydrophilic monomers, dimethylol propionic acid and tartaric acid. The hydrophilic monomers were used separately. In either case, the ratio of isocyanate functional groups to the sum of hydroxyl groups of polyol and hydrophilic monomer was kept constant. The increase in the amount of hydrophilic monomer increased the hardness of resins when used as varnish. Tartaric acid resulted in higher hardness than dimethylol propionic acid. The dispersions made by using tartaric acid had much larger particle sizes than those of dimethylol propionic acid. In another set of experiments, the samples carrying the optimum properties from the two sets were mixed with methylol urea that served as crosslinker in the baking step. The physical and mechanical properties were determined by changing the weight percentages of the two types of samples in the mixture, and by changing the methylol urea percentage of the mixture which exhibited the maximum hardness. All samples showed superior impact resistance, adhesion, and flexibility. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 604–612, 2001