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  • Macroscopic thermal and mechanical properties of complex aliphatic polycarbonate-based polyurethane (PU) films containing degradable ester units in PU backbone were studied by a combination of several experimental techniques. Differential scanning calorimetry (DSC) revealed that the synthesized oligomeric diol (DL-L) contributes (in addition to polycarbonate diol) to the formation of soft-segment domains, while the hard-segment domains are formed from 1,6-diisocyanatohexane (HDI) and butane-1,4-diol (BD). Three main phase transitions were detected by DSC and by dynamic mechanical thermal analysis. Thermogravimetric analysis (TGA) of two-component PUs showed that the PU made from DL-L and HDI is the least thermostable product, while the PU made from polycarbonate diol and HDI is the most stable one. The differences in the thermal stability of different four-component PUs are not important. Tensile properties very sensitively reflect the changes in composition and in microstructure of PU samples; the best tensile properties exhibits the degradable sample containing the equimolar ratio of hydroxyl groups of macrodiol, oligomeric diol DL-L and butane-1,4-diol.
  • Macroscopic thermal and mechanical properties of complex aliphatic polycarbonate-based polyurethane (PU) films containing degradable ester units in PU backbone were studied by a combination of several experimental techniques. Differential scanning calorimetry (DSC) revealed that the synthesized oligomeric diol (DL-L) contributes (in addition to polycarbonate diol) to the formation of soft-segment domains, while the hard-segment domains are formed from 1,6-diisocyanatohexane (HDI) and butane-1,4-diol (BD). Three main phase transitions were detected by DSC and by dynamic mechanical thermal analysis. Thermogravimetric analysis (TGA) of two-component PUs showed that the PU made from DL-L and HDI is the least thermostable product, while the PU made from polycarbonate diol and HDI is the most stable one. The differences in the thermal stability of different four-component PUs are not important. Tensile properties very sensitively reflect the changes in composition and in microstructure of PU samples; the best tensile properties exhibits the degradable sample containing the equimolar ratio of hydroxyl groups of macrodiol, oligomeric diol DL-L and butane-1,4-diol. (en)
Title
  • Thermal and mechanical properties of multiple-component aliphatic degradable polyurethanes
  • Thermal and mechanical properties of multiple-component aliphatic degradable polyurethanes (en)
skos:prefLabel
  • Thermal and mechanical properties of multiple-component aliphatic degradable polyurethanes
  • Thermal and mechanical properties of multiple-component aliphatic degradable polyurethanes (en)
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  • RIV/61389013:_____/15:00440982!RIV15-GA0-61389013
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  • I, P(GA13-06700S)
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  • 16
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  • 463
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  • RIV/61389013:_____/15:00440982
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  • differential scanning calorimetry; mechanical properties; polyurethanes (en)
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  • US - Spojené státy americké
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  • [48B3F4004C0C]
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  • Journal of Applied Polymer Science
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  • 132
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  • Špírková, Milena
  • Poreba, Rafal
  • Kredatusová, Jana
  • Hodan, Jiří
  • Serkis, Magdalena
http://linked.open...ain/vavai/riv/wos
  • 000348313800028
issn
  • 0021-8995
number of pages
http://bibframe.org/vocab/doi
  • 10.1002/app.41872
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