Investigations on "near perfect" poly(2-oxazoline) based amphiphilic polymer conetworks with a crystallizable block

被引:15
作者
Schmidt, Martin [1 ]
Raidt, Thomas [1 ]
Ring, Sabine [1 ]
Gielke, Stefan [1 ]
Gramse, Christian [1 ]
Wilhelm, Sascha [1 ]
Katzenberg, Frank [1 ]
Krumm, Christian [1 ]
Tiller, Joerg C. [1 ]
机构
[1] TU Dortmund, Dept Bio & Chem Engn, Biomat & Polymer Sci, Emil Figge Str 66, D-44227 Dortmund, Germany
关键词
RING-OPENING POLYMERIZATION; HYPERBRANCHED FLUOROPOLYMER; POLY(ETHYLENE OXIDE); TRIBLOCK COPOLYMERS; CONTROLLED DRUG; END-GROUPS; NETWORKS; HYDROGELS; COATINGS; MATRICES;
D O I
10.1016/j.eurpolymj.2016.09.046
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Amphiphilic polymer conetworks (APCNs) of "near perfect" structure were prepared by cross-linking defined poly(2-oxazoline)-based block copolymers. To this end, ABA triblock copolymers with poly(2-methyloxazoline) (PMOx) as A block and poly(2-heptyloxazoline) (PHepOx) as B block in different compositions and with different cross-linkable end groups were prepared and crosslinked. The resulting amphiphilic polymer conetworks were characterized with atomic force microscopy (AFM) and small as well as wide angle X-ray scattering (SAXS/WAXS). The results show that the PHepOx block crystallizes in the APCNs if the content is larger than 19 vol.%, but shows no thermal signature in the differential scanning calorimetry if the polymer content is below 68 vol.%. Further, the size of the polymer phase is the same in a composition range of 38-58 vol.% PHepOx. The phase size was confirmed by AFM. The found very regular interconnected structure over a wide range of compositions seems to be the generic structural motive in APCNs and is also formed when inserting a crystallizable polymer block. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:562 / 574
页数:13
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