Yu Zhao, Bing Hu Xia, Lei Wang, Yang Liu, Lei Zu, Hui Qin Lian, Xiu Guo Cui, Hao Wang
{"title":"硬度高、强度大、抗撕裂的物理水凝胶,其韧性可通过后处理进行广泛调整","authors":"Yu Zhao, Bing Hu Xia, Lei Wang, Yang Liu, Lei Zu, Hui Qin Lian, Xiu Guo Cui, Hao Wang","doi":"10.1515/polyeng-2023-0134","DOIUrl":null,"url":null,"abstract":"Synthetic polymeric hydrogel is a potential substitute for soft biological tissues. However, the poor mechanical properties of traditional synthetic hydrogels limit their applications in biological fields. Herein, a series of tough physical hydrogels have been prepared by micellar polymerization, in the existence of sodium bromide (NaBr), using methacrylic acid (MA) and stearyl acrylate (SA) as monomers, cetyltrimethyl ammonium bromide (CTAB) as cationic surfactant. The hydrogels exhibit excellent mechanical properties: modulus, toughness, and tearing fracture energy up to 7.8 MPa, 34 MJ m<jats:sup>−3</jats:sup>, and 16,600 J m<jats:sup>−2</jats:sup>, respectively. Moreover, it was found that the toughness of the hydrogels can be modulated in a very wide range by different post-treatments, e.g., dried/reswelling, freezing/thawing, or heated treatments. After post-treatments, the elastic physical hydrogels even turn into brittle plastics: modulus and toughness vary by 3 and 4 orders of magnitude, respectively. The mechanism for this wide tunability is attributed to the change of electrostatic attraction, crystallization, and phase separation during post-treatments.","PeriodicalId":16881,"journal":{"name":"Journal of Polymer Engineering","volume":null,"pages":null},"PeriodicalIF":1.7000,"publicationDate":"2024-01-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Stiff, strong, and tear-resistant physical hydrogels with widely tunable toughness by post-treatments\",\"authors\":\"Yu Zhao, Bing Hu Xia, Lei Wang, Yang Liu, Lei Zu, Hui Qin Lian, Xiu Guo Cui, Hao Wang\",\"doi\":\"10.1515/polyeng-2023-0134\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Synthetic polymeric hydrogel is a potential substitute for soft biological tissues. However, the poor mechanical properties of traditional synthetic hydrogels limit their applications in biological fields. Herein, a series of tough physical hydrogels have been prepared by micellar polymerization, in the existence of sodium bromide (NaBr), using methacrylic acid (MA) and stearyl acrylate (SA) as monomers, cetyltrimethyl ammonium bromide (CTAB) as cationic surfactant. The hydrogels exhibit excellent mechanical properties: modulus, toughness, and tearing fracture energy up to 7.8 MPa, 34 MJ m<jats:sup>−3</jats:sup>, and 16,600 J m<jats:sup>−2</jats:sup>, respectively. Moreover, it was found that the toughness of the hydrogels can be modulated in a very wide range by different post-treatments, e.g., dried/reswelling, freezing/thawing, or heated treatments. After post-treatments, the elastic physical hydrogels even turn into brittle plastics: modulus and toughness vary by 3 and 4 orders of magnitude, respectively. The mechanism for this wide tunability is attributed to the change of electrostatic attraction, crystallization, and phase separation during post-treatments.\",\"PeriodicalId\":16881,\"journal\":{\"name\":\"Journal of Polymer Engineering\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2024-01-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Polymer Engineering\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1515/polyeng-2023-0134\",\"RegionNum\":4,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Polymer Engineering","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1515/polyeng-2023-0134","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Stiff, strong, and tear-resistant physical hydrogels with widely tunable toughness by post-treatments
Synthetic polymeric hydrogel is a potential substitute for soft biological tissues. However, the poor mechanical properties of traditional synthetic hydrogels limit their applications in biological fields. Herein, a series of tough physical hydrogels have been prepared by micellar polymerization, in the existence of sodium bromide (NaBr), using methacrylic acid (MA) and stearyl acrylate (SA) as monomers, cetyltrimethyl ammonium bromide (CTAB) as cationic surfactant. The hydrogels exhibit excellent mechanical properties: modulus, toughness, and tearing fracture energy up to 7.8 MPa, 34 MJ m−3, and 16,600 J m−2, respectively. Moreover, it was found that the toughness of the hydrogels can be modulated in a very wide range by different post-treatments, e.g., dried/reswelling, freezing/thawing, or heated treatments. After post-treatments, the elastic physical hydrogels even turn into brittle plastics: modulus and toughness vary by 3 and 4 orders of magnitude, respectively. The mechanism for this wide tunability is attributed to the change of electrostatic attraction, crystallization, and phase separation during post-treatments.
期刊介绍:
Journal of Polymer Engineering publishes reviews, original basic and applied research contributions as well as recent technological developments in polymer engineering. Polymer engineering is a strongly interdisciplinary field and papers published by the journal may span areas such as polymer physics, polymer processing and engineering of polymer-based materials and their applications. The editors and the publisher are committed to high quality standards and rapid handling of the peer review and publication processes.