MICROSTRUCTURE OF POLYURETHANE IONOMERS DERIVATIZED WITH DODECYLAMINE AND POLYETHYLENE OXIDE IN THE HARD SEGMENT

被引:13
作者
SANTERRE, JP
BRASH, JL
机构
[1] MCMASTER UNIV,DEPT CHEM ENGN,HAMILTON L8S 4L7,ONTARIO,CANADA
[2] MCMASTER UNIV,DEPT PATHOL,HAMILTON L8S 4L7,ONTARIO,CANADA
关键词
D O I
10.1002/app.1994.070520406
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Segmented polyether-polyurethanes containing sulfonate groups in the hard segment were modified by the grafting of polyethylene oxide and C-12 hydrocarbon chains. The grafts were attached via the sulfonate groups. The physical properties of the materials, including stress-strain behavior, thermal behavior, and water uptake were studied. Grafting was found to alter material behavior significantly. Both the alkyl and polyethylene oxide grafts appear to alter the packing of the hard segments in microdomains because the grafted materials, in contrast to their sulfonated precursor, do not exhibit a melting transition. However, the polyethylene oxide chains appear to interact with the hard segments, probably through hydrogen bonding. For the C-12 grafted materials, differential scanning calorimetry showed that a third microphase, consisting largely of C-12 chains, may be formed by annealing. Stress-strain and water uptake data support these interpretations. The grafted materials were found to absorb more water than the sulfonated precursor. Most of the water taken up by the C-12 material appears to be bulk water whereas for the PEO material the absorbed water behaves as if it is bound. (C) 1994 John Wiley & Sons, Inc.
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页码:515 / 523
页数:9
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