Journal of Adhesion Science and Technology · 2008 · 78 citations · 25 references
Natural SciencesMaterials EngineeringMaterials SciencePolymer ChemistryPolymer EngineeringPolymer MaterialsAdhesive BondingCross-linking DensityPolymer AdditivesPolymer AdhesionPolymer CharacterizationThermosetsAdhesion PropertiesAdhesive MaterialsAdhesive StrengthAdhesivesPolymer AdhesivesPolyurethane AdhesivesPolyurethane MaterialsX-ray Diffraction Analysis
A series of waterborne polyurethane (WBPU) adhesives were prepared with various ratios of polyol, poly(tetramethylene oxide glycol) (PTMG), and chain extender, ethylene diamine (EDA), at a fixed content of diisocyanate, 4,4-dicyclohexylmethane diisocyanate (H12MDI) and hydrophilic agent, 2,2-dimethylol propionic acid (DMPA). WBPU adhesives were characterized by IR and 1H-NMR spectroscopies, X-ray diffraction (XRD) and gel permeation chromatography (GPC). It was found that the extent of hydrogen bonds between hard–hard segment (i.e., hydrogen bonds between the NH and carbonyl groups) increased with increasing chain extender content (decreasing polyol content). Moreover, the disordered hydrogen bond of carbonyl group (hydrogen bond of urethane groups in the interfacial region) increased with increasing chain extender content (decreasing polyol content). The cyclic urea and allophanate group, which are attributed to the side reaction and cross-linking reaction, respectively, were found above a molar ratio 0.17 of chain extender to diisocyanate. The adhesive strength was maximum with 0.95 wt% and 63.10 wt% chain extender and soft segment (PTMG), respectively (H2 sample) at room temperature for the WBPU adhesive. However, with increasing application temperature the adhesive strength decreased for all samples.
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Hydrogen bonding in polymer blends. 1. FTIR studies of urethane-ether blends
Michael M. Coleman, Daniel J. Skrovanek, Jiangbin Hu et al. · Macromolecules · 1988 · 551 citations