Thermal and mechanical properties of multiple-component aliphatic degradable polyurethanes

被引:10
|
作者
Porerba, Rafal [1 ]
Kredatusova, Jana [1 ]
Hodan, Jiri [1 ]
Serkis, Magdalena [1 ]
Spirkova, Milena [1 ]
机构
[1] Inst Macromol Chem AS CR, Vvi, Prague 16206 6, Czech Republic
关键词
differential scanning calorimetry; mechanical properties; polyurethanes; structure-property relations; thermogravimetric analysis; THERMOPLASTIC POLYURETHANES; MOLECULAR-WEIGHT; ELASTOMERS; BLOCK; NANOCOMPOSITES; HDI; COMPOSITES; RESISTANCE; MORPHOLOGY; STABILITY;
D O I
10.1002/app.41872
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
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 HUT 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. (C) 2015 Wiley Periodicals, Inc.
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页数:12
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