FTIR STUDIES ON THE MODEL POLYURETHANE HARD SEGMENTS BASED ON A NEW WATERBORNE CHAIN EXTENDER DIMETHYLOL BUTANOIC ACID (DMBA)*
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FTIR STUDIES ON THE MODEL POLYURETHANE HARD SEGMENTS BASED ON A NEW WATERBORNE CHAIN EXTENDER DIMETHYLOL BUTANOIC ACID (DMBA)*
Vol. 22, Issue 3, Pages: 225-230(2004)
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Published:20 June 2004
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FTIR STUDIES ON THE MODEL POLYURETHANE HARD SEGMENTS BASED ON A NEW WATERBORNE CHAIN EXTENDER DIMETHYLOL BUTANOIC ACID (DMBA)*[J]. 2004, 22(3): 225-230.
DOI:
FTIR STUDIES ON THE MODEL POLYURETHANE HARD SEGMENTS BASED ON A NEW WATERBORNE CHAIN EXTENDER DIMETHYLOL BUTANOIC ACID (DMBA)*[J]. 2004, 22(3): 225-230.DOI:
FTIR STUDIES ON THE MODEL POLYURETHANE HARD SEGMENTS BASED ON A NEW WATERBORNE CHAIN EXTENDER DIMETHYLOL BUTANOIC ACID (DMBA)*
Three model polyurethane hard segments based on dimethylol butanoic acid (DMBA) and 1
6-hexane diisocyanate(HDI)
toluene diisocyanate (TDI) and 4
4'-diphenylmethane diisocyanate (MDI) were prepared by the solution method.Fourier Infrared (FTIR) spectroscopy was employed to study the H-bonds in these model polyurethanes. The model polyurethane hard segment prepared from HDI and 1
4-butanodiol (BDO) was used for comparison. It was found that the incorporation of the pendent carboxyl through DMBA into the model hard segments weakens the original NH…O = C H-bond but gives more H-bond patterns based on the two H-bond donors
urethane NH and carboxylic OH. The carboxylic dimer is one of the main H-bond types and is stronger than another main H-bond type NH…O=C. In addition
the H-bond in aromatic model hard segments is stronger than that of aliphatic hard segments. The appearance of the free C=O and the fact that almost all N—H is H-bonded suggest that there possibly exist either the third H-bond acceptor or the H-bond formed by one acceptor with two donors.
Abstract
Three model polyurethane hard segments based on dimethylol butanoic acid (DMBA) and 1
6-hexane diisocyanate(HDI)
toluene diisocyanate (TDI) and 4
4'-diphenylmethane diisocyanate (MDI) were prepared by the solution method.Fourier Infrared (FTIR) spectroscopy was employed to study the H-bonds in these model polyurethanes. The model polyurethane hard segment prepared from HDI and 1
4-butanodiol (BDO) was used for comparison. It was found that the incorporation of the pendent carboxyl through DMBA into the model hard segments weakens the original NH…O = C H-bond but gives more H-bond patterns based on the two H-bond donors
urethane NH and carboxylic OH. The carboxylic dimer is one of the main H-bond types and is stronger than another main H-bond type NH…O=C. In addition
the H-bond in aromatic model hard segments is stronger than that of aliphatic hard segments. The appearance of the free C=O and the fact that almost all N—H is H-bonded suggest that there possibly exist either the third H-bond acceptor or the H-bond formed by one acceptor with two donors.
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