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1.
Biomacromolecules ; 11(4): 911-8, 2010 Apr 12.
Article in English | MEDLINE | ID: mdl-20232886

ABSTRACT

An unsaturated terminal diol, 1,18-octadec-9-endiol (ODEDO), and a saturated terminal diol, 1,9-nonanediol (NDO), were synthesized from oleic acid. The feasibility of utilizing these new diols for the production of thermoplastic polyurethanes (TPUs) was demonstrated by reacting them with a fatty acid-derived diisocyanate, 1,7-heptamethylene diisocyanate (HPMDI), and a commercially available petroleum-derived diisocyanate, 1,6-hexamethylene diisocyanate (HDI). One type of phase structure was obtained for both TPUs in this study, owing to the similarity between the ODEDO and NDO molecular structure. In addition, double yielding behavior (observed for the first time in polyurethanes) was observed in the stress-strain curves for both TPU systems. Compared to the TPUs prepared from HDI, the totally biobased TPUs (ODEDO-NDO-HPDMI) demonstrated comparable properties within acceptable tolerances, considering the impacts on physical properties due to the odd-even effect introduced by the HPDMI. This work is the first that establishes the production of linear thermoplastic polyurethanes entirely from lipid feedstock.


Subject(s)
Biocompatible Materials/chemistry , Cyanates/chemistry , Glycols/chemistry , Oleic Acids/chemistry , Polyurethanes/chemistry , Biocompatible Materials/chemical synthesis , Isocyanates , Magnetic Resonance Spectroscopy , Molecular Structure , Polyurethanes/chemical synthesis , Spectroscopy, Fourier Transform Infrared , Temperature , X-Ray Diffraction
2.
Biomacromolecules ; 10(4): 884-91, 2009 Apr 13.
Article in English | MEDLINE | ID: mdl-19281152

ABSTRACT

A new linear saturated terminal diisocyanate was synthesized from oleic acid via Curtius rearrangement, and its chemical structure was identified by FTIR, (1)H and (13)C NMR, and MS. The feasibility of utilizing this new diisocyanate for the production of polyurethanes (PUs) was demonstrated by reacting it with commercial petroleum-derived polyols and canola oil-derived polyols, respectively. The physical properties of the PUs prepared from fatty acid-derived diisocyanate were compared to those prepared from the same polyols with a similar but petroleum-derived commercially available diisocyanate: 1,6-hexamethylene diisocyanate. It was found that the fatty acid-derived diisocyanate was capable of producing PUs with comparable properties within acceptable tolerances. This work is the first that establishes the production of linear saturated terminal diisocyanate derived from fatty acids and corresponding PUs mostly from lipid feedstock.


Subject(s)
Isocyanates/chemistry , Isocyanates/chemical synthesis , Oleic Acids/chemistry , Plant Oils/chemistry , Polyurethanes/chemistry , Polyurethanes/chemical synthesis , Chromatography, Gas , Cyanates/chemistry , Cyanates/metabolism , Isocyanates/pharmacology , Magnetic Resonance Spectroscopy , Mass Spectrometry , Materials Testing , Polymers/chemistry , Polyurethanes/pharmacology , Spectroscopy, Fourier Transform Infrared , Stress, Mechanical , X-Ray Diffraction
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