首页> 外文OA文献 >Solvato-morphologically controlled, reversible NIPAAm hydrogel photoactuators \ud
【2h】

Solvato-morphologically controlled, reversible NIPAAm hydrogel photoactuators \ud

机译:溶剂形态可控的NIPAAm水凝胶光致动器\ ud

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。
获取外文期刊封面目录资料

摘要

Photo-actuator hydrogels were generated using a N-isopropylacrylamide-co-acrylated spiropyran-coacrylic\udacid (p(NIPAAm-co-SP-co-AA)) copolymer, in 100-1-5 mole ratio. Different ratios of deionised\udwater: organic solvent (tetrahydrofuran, dioxane and acetone) were used as the polymerisation solvent. By\udchanging the polymerisation solvent, the pore size and density of the hydrogels were altered, which in turn\udhad an impact on the diffusion path-length of water molecules, thus influencing the swelling and photoinduced\udshrinking kinetics of the hydrogel. We successfully demonstrated that the polymerisation solvent\udhas a significant effect on the curing time, the elasticity and morphology of the resulting hydrogel. The\udhighest shrinking ratio was obtained for hydrogels produced using 4:1 acetone: deionised water (CI) as the\udpolymerisation solvent, with the hydrogel reaching 39.56% (±2.37% (n=3)) of its hydrated area after 4\udmin of white light irradiation followed by reswelling in the dark to 61.95% (±5.76% (n=3)) after 11 min.\udConversely, the best reswelling capabilities were obtained for the hydrogels produced using 1:1\udtetrahydrofuran: deionised water (AIII), when the shrunk hydrogel (61.78±0.26% (n=3)) regained 91.31%\ud(±0.22% (n=3)) of its original size after 11 min in the dark. To our knowledge, this is the largest reported\udphoto-induced area change for self-protonated spiropyran containing hydrogels. The shrinking/reswelling\udprocess was completely reversible in DI water with no detectable hysteresis over three repeat irradiation\udcycles.
机译:使用N-异丙基丙烯酰胺-丙烯酸酯化的吡喃吡喃-丙烯酸/二丙烯酸(p(NIPAAm-co-SP-co-AA))共聚物以100-1-5的摩尔比产生光致动器水凝胶。使用不同比例的去离子/水:有机溶剂(四氢呋喃,二恶烷和丙酮)作为聚合溶剂。通过交换聚合溶剂,改变了水凝胶的孔径和密度,这反过来又影响了水分子的扩散路径长度,从而影响了水凝胶的溶胀和光致收缩动力学。我们成功地证明了聚合溶剂对固化时间,所得水凝胶的弹性和形态具有显着影响。对于使用4:1丙酮:去离子水(CI)作为\ udpolymerization溶剂生产的水凝胶,\\最高的收缩率,水凝胶在4 \\后达到其水合面积的39.56%(±2.37%(n = 3))。 udmin的白光照射,然后在11分钟后在暗处重新膨胀至61.95%(±5.76%(n = 3))。\ ud相反,使用1:1 \ udtetrahydrofuran:去离子水制得的水凝胶获得了最佳的溶胀能力(AIII),当收缩的水凝胶(61.78±0.26%(n = 3))在黑暗中11分钟后恢复到其原始大小的91.31%\ ud(±0.22%(n = 3))时。据我们所知,这是报道的自质子化吡喃吡喃水凝胶最大的\ udphoto诱导的面积变化。在去离子水中,收缩/膨胀/扩散过程是完全可逆的,并且在三个重复的照射/循环中没有可检测到的滞后。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号