Hongcai Wang, Xiuqiong Chen, Yanan Bu, Ting Wu, Huiqiong Yan, Qiang Lin
{"title":"超快速热响应,形状记忆和溶剂驱动的Fe3+-海藻酸盐/聚(n -异丙基丙烯酰胺)为基础的水凝胶驱动器","authors":"Hongcai Wang, Xiuqiong Chen, Yanan Bu, Ting Wu, Huiqiong Yan, Qiang Lin","doi":"10.1039/d4py01047g","DOIUrl":null,"url":null,"abstract":"In recent years, Stimulus-responsive hydrogels have been extensively researched in the field of actuators due to their capacity to undergo significant deformation in response to various external stimuli. However, it is difficult for the existing hydrogel actuators to meet the requirements of simple preparation, fast response speed and shape memory function, which greatly limits their further application. In the present study, a multi-functional Fe3+-sodium alginate/poly (N-isopropyl acrylamide) interpenetrating network (IPN) hydrogel with ultrafast thermal response, shape memory function and solvent drive was prepared via a simple method. The creation of Fe3+-carboxylate coordination within the hydrogel network, coupled with ultraviolet (UV) photodissociation, was employed to achieve shape memory properties. Moreover, the local gradient of the hydrogel could be precisely programmed by manipulating the UV irradiation time and position. As a result, the obtained gradient hydrogels possessed excellent temperature driving and solvent driving properties, which could not only carry out 4 s fast grasp of objects in 70 ℃ water, but also achieve 2D to 3D complex deformation in methanol aqueous solution. This work provided a new manufacturing method and application prospect for the development of novel intelligent hydrogel actuators","PeriodicalId":100,"journal":{"name":"Polymer Chemistry","volume":"116 1","pages":""},"PeriodicalIF":4.1000,"publicationDate":"2025-01-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ultrafast thermal responsive, shape memory and solvent-driven Fe3+-alginate/poly (N-isopropyl acrylamide) based hydrogel actuator\",\"authors\":\"Hongcai Wang, Xiuqiong Chen, Yanan Bu, Ting Wu, Huiqiong Yan, Qiang Lin\",\"doi\":\"10.1039/d4py01047g\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In recent years, Stimulus-responsive hydrogels have been extensively researched in the field of actuators due to their capacity to undergo significant deformation in response to various external stimuli. However, it is difficult for the existing hydrogel actuators to meet the requirements of simple preparation, fast response speed and shape memory function, which greatly limits their further application. In the present study, a multi-functional Fe3+-sodium alginate/poly (N-isopropyl acrylamide) interpenetrating network (IPN) hydrogel with ultrafast thermal response, shape memory function and solvent drive was prepared via a simple method. The creation of Fe3+-carboxylate coordination within the hydrogel network, coupled with ultraviolet (UV) photodissociation, was employed to achieve shape memory properties. Moreover, the local gradient of the hydrogel could be precisely programmed by manipulating the UV irradiation time and position. As a result, the obtained gradient hydrogels possessed excellent temperature driving and solvent driving properties, which could not only carry out 4 s fast grasp of objects in 70 ℃ water, but also achieve 2D to 3D complex deformation in methanol aqueous solution. This work provided a new manufacturing method and application prospect for the development of novel intelligent hydrogel actuators\",\"PeriodicalId\":100,\"journal\":{\"name\":\"Polymer Chemistry\",\"volume\":\"116 1\",\"pages\":\"\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-01-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polymer Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d4py01047g\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d4py01047g","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Ultrafast thermal responsive, shape memory and solvent-driven Fe3+-alginate/poly (N-isopropyl acrylamide) based hydrogel actuator
In recent years, Stimulus-responsive hydrogels have been extensively researched in the field of actuators due to their capacity to undergo significant deformation in response to various external stimuli. However, it is difficult for the existing hydrogel actuators to meet the requirements of simple preparation, fast response speed and shape memory function, which greatly limits their further application. In the present study, a multi-functional Fe3+-sodium alginate/poly (N-isopropyl acrylamide) interpenetrating network (IPN) hydrogel with ultrafast thermal response, shape memory function and solvent drive was prepared via a simple method. The creation of Fe3+-carboxylate coordination within the hydrogel network, coupled with ultraviolet (UV) photodissociation, was employed to achieve shape memory properties. Moreover, the local gradient of the hydrogel could be precisely programmed by manipulating the UV irradiation time and position. As a result, the obtained gradient hydrogels possessed excellent temperature driving and solvent driving properties, which could not only carry out 4 s fast grasp of objects in 70 ℃ water, but also achieve 2D to 3D complex deformation in methanol aqueous solution. This work provided a new manufacturing method and application prospect for the development of novel intelligent hydrogel actuators
期刊介绍:
Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.