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Description
| - 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)
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Title
| - 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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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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skos:notation
| - RIV/61389013:_____/15:00440982!RIV15-GA0-61389013
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http://linked.open...avai/riv/aktivita
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http://linked.open...avai/riv/aktivity
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http://linked.open...iv/cisloPeriodika
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http://linked.open...vai/riv/dodaniDat
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http://linked.open...aciTvurceVysledku
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http://linked.open.../riv/druhVysledku
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http://linked.open...iv/duvernostUdaju
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http://linked.open...titaPredkladatele
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http://linked.open...dnocenehoVysledku
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http://linked.open...ai/riv/idVysledku
| - RIV/61389013:_____/15:00440982
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http://linked.open...riv/jazykVysledku
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http://linked.open.../riv/klicovaSlova
| - differential scanning calorimetry; mechanical properties; polyurethanes (en)
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http://linked.open.../riv/klicoveSlovo
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http://linked.open...odStatuVydavatele
| - US - Spojené státy americké
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http://linked.open...ontrolniKodProRIV
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http://linked.open...i/riv/nazevZdroje
| - Journal of Applied Polymer Science
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http://linked.open...in/vavai/riv/obor
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http://linked.open...ichTvurcuVysledku
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http://linked.open...cetTvurcuVysledku
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http://linked.open...vavai/riv/projekt
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http://linked.open...UplatneniVysledku
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http://linked.open...v/svazekPeriodika
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http://linked.open...iv/tvurceVysledku
| - Špírková, Milena
- Poreba, Rafal
- Kredatusová, Jana
- Hodan, Jiří
- Serkis, Magdalena
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http://linked.open...ain/vavai/riv/wos
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issn
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number of pages
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http://bibframe.org/vocab/doi
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