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首页> 外文期刊>Journal of Applied Polymer Science >Synthesis and characteristics of nonisocyanate polyurethane composed of bio-based dimer diamine for supercritical CO2 foaming applications
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Synthesis and characteristics of nonisocyanate polyurethane composed of bio-based dimer diamine for supercritical CO2 foaming applications

机译:Synthesis and characteristics of nonisocyanate polyurethane composed of bio-based dimer diamine for supercritical CO2 foaming applications

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摘要

Nonisocyanate polyurethane (NIPU) was synthesized using different concentrations of C-36-alkylenediamine (C(36)DDA), hexamethylene diamine, and a cyclic carbonate monomer synthesized from bisphenol A epoxy resin and carbon dioxide. The structures, molecular weights, thermal behaviors, and stabilities of the NIPU copolymers were evaluated using H-1 nuclear magnetic resonance, Fourier transform infrared spectroscopy, gel permeation chromatography, thermogravimetric analysis, and differential scanning calorimetry measurements. All synthesized NIPUs were amorphous and exhibited good Td-5 thermal stabilities above 250 degrees C; T-g decreased from 73 to 51 degrees C as C(36)DDA content increased from 0 to 10 based on dynamic mechanical analysis tests. Furthermore, ethylenediamine (EDA) as a chain extender incorporating a small amount of crosslinker 1,2,4,5-benzenetetracarboxylic acid (PMA) can enhance the melt strength of a partially three-dimensional network, and the attained NIPU showed elastic properties. Thus, the NIPU synthesized with 7.5 and 10 C(36)DDA containing small amounts of EDA and PMA were suitable choices for supercritical CO2 foaming; their morphologies and mechanical behaviors were examined by scanning electron microscopy and DMA, and the densities of foamed NIPU with 7.5 and 10 C(36)DDA were calculated as 432 and 215 kg m(-3) with pore sizes of 10-20 mu m, respectively. The maximum stresses were attained at 149.5 and 123.4 kPa, and the foamed NIPU displayed rigid foam behaviors owing to the compression behaviors of the stress-strain curves.
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