4.2 Article

Structural investigations of polypropylene glycol (PPG) and isophorone diisocyanate (IPDI)-based polyurethane prepolyrner by 1D and 2D NMR spectroscopy

Journal

JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
Volume 43, Issue 6, Pages 1196-1209

Publisher

WILEY
DOI: 10.1002/pola.20583

Keywords

polyurethane; NMR; coatings; poly(propylene)-glycol; isophoron diisocyanate; PPG-IPDI; H-1, C-13, and 2D NMR

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Polyurethane prepolymers are widely used in reactive hot melt adhesives and moisture cured coatings. NCO-terminated polyurethane of polypropylene glycol (PPG)-1000 and isophoron diisocyanate (IPDI) with an NCO/OH ratio of 1.2:1 were prepared without any catalyst or solvent. 1D and 2D NMR spectroscopy was used for the structural investigation of the synthesized prepolymer. H-1 NMR spectra and dibutylamine back-titration were used to monitor the reaction of isocyanate groups with the hydroxyl function of PPG and to allow a good description of the evaluation of the urethane groups. The data on percentage conversion were crosschecked with C-13 NMR spectroscopy in the urethane zone for the methanol endcapped prepolymer. The observations show a higher reactivity of the secondary NCO group than of the primary group. (C) 2005 Wiley Periodicals, Inc.

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