No abstract

No abstract

A new method for the synthesis of hyperbranched polymers involving the use of ABx macromonomers containing linear units have been investigated. Two types of novel hyperbranched polyurethanes have been synthesized by a one‐pot approach. The structures of monomers and polymers were characterized by elemental analysis, 1H NMR, 13C NMR, Fourier transform infrared spectroscopy, gel permeation chromatography, and thermogravimetric analysis. The hyperbranched polymers have been proven to be extremely soluble in a wide range of solvents. Polymer electrolytes were prepared with hyperbranched polymer, linear polymer as the host, and lithium perchlorate (LiClO4) as the ion source. Analysis of the isotherm conductivity dependence of the ion concentration indicated that these hyperbranched polymers could function as a “solvent” for the lithium salt. The conductivity increased with the increasing concentration of hyperbranched polymers in the host polymer. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 40: 344–350, 2002

No abstract

Sequential interpenetrating polymer networks (IPNs), based on polyurethane and polybenzoxazine, were synthesized. Fourier Transform infrared spectrometry was employed to monitor the formation kinetics, which indicated that only physical bonding existed in the resulting IPNs. Morphological investigations revealed a lightly phase separation behaviour in all of the IPNs studied.

No abstract

ABSTRACT:The matrix polymer of reactive hot-melt adhesive (RHMA) is an isocyanate-terminated urethane prepolymer based on oligoester or oligoether diols and diisocyanates. In this study, we explored wet cure kinetics with both isothermal and nonisothermal differential scanning calorimetry methods. Second-order autocatalytic models were successfully used to evaluate the cure process of both oligoester-and oligoether-based RHMAs. The autocatalyzation effect did not to depend on the structure of diols but on the reaction nature of the end isocyanates. The apparent energy of the overall cure reaction was 86.54 and 84.46 kJ/mol, respectively, which was based on nonisothermal DSC results.

No abstract