Supramolecular Multiblock Polystyrene-Polyisobutylene Copolymers via Ionic Interactions

被引:62
|
作者
Zhang, Longhe [1 ]
Kucera, Lauren R. [2 ]
Ummadisetty, Subramanyam [2 ]
Nykaza, Jacob R. [3 ]
Elabd, Yossef A. [3 ]
Storey, Robson F. [2 ]
Cavicchi, Kevin A. [1 ]
Weiss, R. A. [1 ]
机构
[1] Univ Akron, Dept Polymer Engn, Akron, OH 44325 USA
[2] Univ So Mississippi, Sch Polymers & High Performance Mat, Hattiesburg, MS 39406 USA
[3] Drexel Univ, Dept Chem & Biol Engn, Philadelphia, PA 19104 USA
基金
美国国家科学基金会;
关键词
HALATO-TELECHELIC POLYMERS; NANOPOROUS THIN-FILMS; BLOCK-COPOLYMERS; SULFONATED POLYSTYRENE; MOLECULAR-RECOGNITION; SURFACTANT COMPLEXES; TRIBLOCK COPOLYMER; ACID; POLYMERIZATION; BLENDS;
D O I
10.1021/ma500934e
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A supramolecular multiblock copolymer was synthesized by mixing two telechelic oligomers, alpha,omega-sulfonated polystyrene, HO3S-PS-SO3H, derived from a polymer prepared by RAFT polymerization, and alpha,omega-amino-polyisobutylene, H2N-PIB-NH2, prepared by cationic polymerization. During solvent casting, proton transfer from the sulfonic acid to the amine formed ionic bonds that produced a multiblock copolymer that formed freestanding flexible films with a modulus of 90 MPa, a yield point at 4% strain and a strain energy density of 15 MJ/m(3). Small angle X-ray scattering characterization showed a lamellar morphology, whose domain spacing was consistent with the formation of a multiblock copolymer based on comparison to the chain dimensions. A reversible order-disorder transition occurred between 190 and 210 degrees C, but the sulfonic acid and amine functional groups were observed to decompose at those elevated temperatures based on companion optical microscopy and spectroscopy measurements. For high nonlinear strains, the dynamic modulus, G', decreased by nearly an order of magnitude and the loss modulus, G '', decreased by a factor of 1.4, but both recovered to their original values once the strain was reduced to within the linear response region.
引用
收藏
页码:4387 / 4396
页数:10
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