{"title":"Thermal-responsive poly(N-isopropyl acrylamide)/sodium alginate hydrogels: preparation, swelling behaviors, and mechanical properties","authors":"Huijuan Zhang, Yanan Zhang, Lifen He, Biao Yang, Shujie Zhu, Meihuan Yao","doi":"10.1007/s00396-016-3951-2","DOIUrl":null,"url":null,"abstract":"<p>Temperature-responsive hydrogels with enhanced mechanical properties are desirable in areas such as intelligent device. In this contribution, a poly(N-isopropyl acrylamide)/sodium alginate (PNIPAM/Ca-alginate) hydrogel was prepared by a two-step strategy, obtaining a hydrogel with two kinds of cross-linking: chemical cross-linking and ionic cross-linking. The hydrogels exhibited improved mechanical properties compared with that of the PNIPAM/Na-alginate hydrogel and the compressive strength of PNIPAM/Ca-alginate hydrogels depended significantly on the cross-linking density. In particular, PNIPAM/Ca-alginate hydrogels with the cross-linking agent content of 0.036?g displayed the optimal compressive strength of 308.9?kPa among the hydrogel samples with varied amounts of cross-linking agents. The swelling tests at varying temperatures indicated that PNIPAM/Ca-alginate hydrogels exhibited negative temperature-sensitive swelling behaviors and the lower critical solution temperature (LCST) was determined to be in the temperature range of 30~34?°C. The swelling kinetics study revealed that the mechanism of water uptake of the PNIPAM/Ca-alginate hydrogels followed a less-Fickian mode, while the entire swelling behaviors of hydrogels followed the pseudo-second-order dynamic equation.</p>","PeriodicalId":520,"journal":{"name":"Colloid and Polymer Science","volume":"294 12","pages":"1959 - 1967"},"PeriodicalIF":2.3000,"publicationDate":"2016-10-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1007/s00396-016-3951-2","citationCount":"17","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Colloid and Polymer Science","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s00396-016-3951-2","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 17
Abstract
Temperature-responsive hydrogels with enhanced mechanical properties are desirable in areas such as intelligent device. In this contribution, a poly(N-isopropyl acrylamide)/sodium alginate (PNIPAM/Ca-alginate) hydrogel was prepared by a two-step strategy, obtaining a hydrogel with two kinds of cross-linking: chemical cross-linking and ionic cross-linking. The hydrogels exhibited improved mechanical properties compared with that of the PNIPAM/Na-alginate hydrogel and the compressive strength of PNIPAM/Ca-alginate hydrogels depended significantly on the cross-linking density. In particular, PNIPAM/Ca-alginate hydrogels with the cross-linking agent content of 0.036?g displayed the optimal compressive strength of 308.9?kPa among the hydrogel samples with varied amounts of cross-linking agents. The swelling tests at varying temperatures indicated that PNIPAM/Ca-alginate hydrogels exhibited negative temperature-sensitive swelling behaviors and the lower critical solution temperature (LCST) was determined to be in the temperature range of 30~34?°C. The swelling kinetics study revealed that the mechanism of water uptake of the PNIPAM/Ca-alginate hydrogels followed a less-Fickian mode, while the entire swelling behaviors of hydrogels followed the pseudo-second-order dynamic equation.
具有增强机械性能的温度响应水凝胶在智能设备等领域是理想的。本文采用两步法制备了聚n -异丙基丙烯酰胺/海藻酸钠(PNIPAM/海藻酸钙)水凝胶,得到了具有化学交联和离子交联两种交联方式的水凝胶。与PNIPAM/ na -海藻酸盐水凝胶相比,PNIPAM/ ca -海藻酸盐水凝胶的力学性能得到了改善,而PNIPAM/ ca -海藻酸盐水凝胶的抗压强度主要取决于交联密度。特别是交联剂含量为0.036?G的最优抗压强度为308.9?不同交联剂用量的水凝胶样品的kPa。不同温度下的溶胀实验表明,PNIPAM/海藻酸钙水凝胶表现出负温度敏感溶胀行为,最低临界溶胀温度(LCST)在30~34°C之间。溶胀动力学研究表明,PNIPAM/海藻酸钙水凝胶的吸水机理遵循少菲克模式,而整个水凝胶的溶胀行为遵循伪二阶动力学方程。
期刊介绍:
Colloid and Polymer Science - a leading international journal of longstanding tradition - is devoted to colloid and polymer science and its interdisciplinary interactions. As such, it responds to a demand which has lost none of its actuality as revealed in the trends of contemporary materials science.