Enhancing glass transition temperature and mechanical properties of poly (propylene carbonate) by intermacromolecular complexation with poly (vinyl alcohol)
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作者:
Cui, Shaoying
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Sichuan Univ, Polymer Res Inst, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R ChinaSichuan Univ, Polymer Res Inst, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
Cui, Shaoying
[1
]
Li, Li
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机构:
Sichuan Univ, Polymer Res Inst, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R ChinaSichuan Univ, Polymer Res Inst, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
Li, Li
[1
]
Wang, Qi
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Sichuan Univ, Polymer Res Inst, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R ChinaSichuan Univ, Polymer Res Inst, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
Wang, Qi
[1
]
机构:
[1] Sichuan Univ, Polymer Res Inst, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
Poly (propylene carbonate) (PPC), a promising biodegradable polymer used in medical materials and packaging, is amorphous with low glass transition temperature (T-g), which limits its application. In order to restrain the segment motion of PPC and improve its T-g, based on the supramolecular science theory, polyvinyl alcohol (PVA) with multi-hydroxyl groups was selected to melt blend with PPC to build a unique physical cross-linked network structure by hydrogen bonding between hydroxyl groups of PVA and carbonyl groups or/and terminal hydroxyl groups of PPC. The interactions between PPC and PVA, and the effects of PVA on T-g, thermal behavior, morphology as well as mechanical properties of PPC/PVA composites were investigated. The shift of nu(O-H) and nu(C=O) in MIR confirmed the formation of intermacromolecular hydrogen bonding between PPC and PVA, which guaranteed the good compatibility between PPC and PVA, and significantly improved T-g from 34.1 degrees C of neat PPC to 44.0 degrees C of 70PPC/30PVA. This interaction also improved low-temperature thermal stability of the composite, which did favor to the thermal stability during processing and the final performance of the composites, e.g. the tensile strength increased from 10.5 MPa to a maximum value of 39.7 MPa at room temperature. (C) 2016 Elsevier Ltd. All rights reserved.
机构:
Euskal Herriko Unibertsitatea, Kimika Fak, Donostia San Sebastian 20080, Euskadi, Spain
DIPC, Donostia San Sebastian 20080, Euskadi, Spain
Basque Fdn Sci, IKERBASQUE, Bilbao 48011, SpainEuskal Herriko Unibertsitatea, Kimika Fak, Donostia San Sebastian 20080, Euskadi, Spain
机构:
Euskal Herriko Unibertsitatea, Kimika Fak, Donostia San Sebastian 20080, Euskadi, Spain
DIPC, Donostia San Sebastian 20080, Euskadi, Spain
Basque Fdn Sci, IKERBASQUE, Bilbao 48011, SpainEuskal Herriko Unibertsitatea, Kimika Fak, Donostia San Sebastian 20080, Euskadi, Spain