Misichronis Konstantinos, Wang Weiyu, Cheng Shiwang, Wang Yangyang, Shrestha Umesh, Dadmun Mark, Mays Jimmy W, Saito Tomonori
Department of Chemistry, University of Tennessee Knoxville TN 37996 USA.
Chemical Sciences Division, Oak Ridge National Laboratory Oak Ridge TN 37831 USA
RSC Adv. 2018 Jan 29;8(10):5090-5098. doi: 10.1039/c7ra08641e.
Multigraft copolymer superelastomers consisting of a poly(-butyl acrylate) backbone and polystyrene side chains were synthesized and the viscoelastic properties of the non-sulfonated and sulfonated final materials were investigated using extensional rheology (SER3). The non-linear viscoelastic experiments revealed significantly increased true stresses (up to 10 times higher) after sulfonating only 2-3% of the copolymer while the materials maintained high elongation (<700%). The linear viscoelastic experiments showed that the storage and loss modulus are increased by sulfonation and that the copolymers can be readily tuned and further improved by increasing the number of branching points and the molecular weight of the backbone. In this way, we show that by tuning not only the molecular characteristics of the multigraft copolymers but also their architecture and chemical interaction, we can acquire thermoplastic superelastomer materials with desired viscoelastic properties.
合成了由聚丙烯酸丁酯主链和聚苯乙烯侧链组成的多接枝共聚物超弹性体,并使用拉伸流变仪(SER3)研究了未磺化和磺化最终材料的粘弹性。非线性粘弹性实验表明,仅对2%-3%的共聚物进行磺化后,真实应力显著增加(高达10倍),而材料仍保持高伸长率(<700%)。线性粘弹性实验表明,磺化会提高储能模量和损耗模量,并且通过增加支化点数量和主链分子量,可以轻松调节并进一步改善共聚物。通过这种方式,我们表明,不仅可以调节多接枝共聚物的分子特性,还可以调节其结构和化学相互作用,从而获得具有所需粘弹性的热塑性超弹性体材料。