Blends of thermoplastic polyurethane and polyether-polyimide: preparation and properties

Citation
Jn. Chen et al., Blends of thermoplastic polyurethane and polyether-polyimide: preparation and properties, POLYMER, 42(4), 2001, pp. 1493-1500
Citations number
18
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
POLYMER
ISSN journal
00323861 → ACNP
Volume
42
Issue
4
Year of publication
2001
Pages
1493 - 1500
Database
ISI
SICI code
0032-3861(200102)42:4<1493:BOTPAP>2.0.ZU;2-9
Abstract
A series of blends of thermoplastic polyurethane(PU) and polyether-polyimid e (PI) were prepared in two steps. The first step was the preparation of po lyether-amic acid by the reaction of an oligmer based on polytetramethylene oxide glycol di-p-aminobenzoate (APTMO) of different molecular weight (650 , 1000, and 2000) with benzenetetracarboxylic acid dianhydride (PMDA). The second step was mixing polyether-polyurethane and polyether-polyamic acid s olution at room temperature in various weight ratios, and the blend films w ere obtained by casting and then heat imidization. Infrared spectroscopy (I R), dynamic mechanical analysis (DMA), differential scanning calorimetry (D SC), small-angle X-ray scattering (SACS) and wide-angle X-ray diffraction(W AXD) were used to study this family of blends. DSC analysis of the films sh owed that glass transition temperature (T-g) of PU-PI 650 and PU-PI 1000 se ries shifted depending on the ratio of PU and PI components. The shift of T -g, along with the transparency of the films, gave the evidence that soft s egments of PU and PI were miscible to some extent in the PU-PI 650 and PU-P I 1000 series. DMA results indicated that the blends exhibited a well phase -separated structure and had a broad rubbery plateau from about -30 to 200 degreesC, which varied with the PU content. Thermal stability of PU was fou nd to increase by the incorporation of PI. The excellent tensile properties of the blends suggested that they could be potentially used as heat resist ant thermoplastic elastomers. (C) 2000 Elsevier Science Ltd. All rights res erved.