Facile Fabrication of Tough Super Macroporous Hydrogel via Enhanced Phase Separation

IF 18.5 1区 材料科学 Q1 CHEMISTRY, MULTIDISCIPLINARY Advanced Functional Materials Pub Date : 2024-09-27 DOI:10.1002/adfm.202412412
Yunzhou Guo, Yang Han, Yangyang Cao, Yuping Chen, Jingwen Xie, Hanchen Ding, Shifu Liang, Xin Liu, Wenjing Sun, Jianbin Tang, Shiqun Shao, Jiajia Xiang, Youqing Shen
{"title":"Facile Fabrication of Tough Super Macroporous Hydrogel via Enhanced Phase Separation","authors":"Yunzhou Guo, Yang Han, Yangyang Cao, Yuping Chen, Jingwen Xie, Hanchen Ding, Shifu Liang, Xin Liu, Wenjing Sun, Jianbin Tang, Shiqun Shao, Jiajia Xiang, Youqing Shen","doi":"10.1002/adfm.202412412","DOIUrl":null,"url":null,"abstract":"Super macroporous (SMP) hydrogels have garnered significant attention in biomedical applications due to their high permeability and biomimetic pore structure. However, maintaining toughness in highly porous materials remains a formidable challenge. This study introduces a facile one-step preparation method for fabricating tough alginate hydrogels with an SMP structure by blending polyvinyl alcohol (PVA) and sodium alginate cross-linked with calcium chloride. By capitalizing on the phase separation effect, this method bypasses traditional requirements such as cryogelation and templating that necessitate low temperatures or solvent etching. The presence of PVA molecules promotes the regional aggregation of alginates, leading to enhanced toughness, and also occupies larger interstitial spaces between the densely packed alginate phases, facilitating pore formation. The resulting SMP structure, featuring pore sizes ranging from 50 µm to 700 µm, forms during the polymer cross-linking process and achieves a porosity exceeding 85%. These hydrogels exhibit superior toughness compare to their non-macroporous counterparts. Additionally, this method allows for flexible adjustments in the porous structure and overall gel shape, making it adaptable to various applications. This simple yet effective approach holds great potential for developing novel SMP materials with enhanced toughness.","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":null,"pages":null},"PeriodicalIF":18.5000,"publicationDate":"2024-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1002/adfm.202412412","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Super macroporous (SMP) hydrogels have garnered significant attention in biomedical applications due to their high permeability and biomimetic pore structure. However, maintaining toughness in highly porous materials remains a formidable challenge. This study introduces a facile one-step preparation method for fabricating tough alginate hydrogels with an SMP structure by blending polyvinyl alcohol (PVA) and sodium alginate cross-linked with calcium chloride. By capitalizing on the phase separation effect, this method bypasses traditional requirements such as cryogelation and templating that necessitate low temperatures or solvent etching. The presence of PVA molecules promotes the regional aggregation of alginates, leading to enhanced toughness, and also occupies larger interstitial spaces between the densely packed alginate phases, facilitating pore formation. The resulting SMP structure, featuring pore sizes ranging from 50 µm to 700 µm, forms during the polymer cross-linking process and achieves a porosity exceeding 85%. These hydrogels exhibit superior toughness compare to their non-macroporous counterparts. Additionally, this method allows for flexible adjustments in the porous structure and overall gel shape, making it adaptable to various applications. This simple yet effective approach holds great potential for developing novel SMP materials with enhanced toughness.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
通过增强相分离轻松制造坚韧的超大孔水凝胶
超大孔(SMP)水凝胶具有高渗透性和仿生物孔结构,因此在生物医学应用中备受关注。然而,在高多孔材料中保持韧性仍然是一项艰巨的挑战。本研究通过混合聚乙烯醇(PVA)和氯化钙交联的海藻酸钠,介绍了一种一步制备具有 SMP 结构的韧性海藻酸钠水凝胶的简便方法。通过利用相分离效应,这种方法绕过了传统的低温凝胶化和模板化等需要低温或溶剂蚀刻的要求。PVA 分子的存在促进了海藻酸盐的区域聚集,从而提高了韧性,同时也占据了密集排列的海藻酸盐相之间更大的间隙,有利于孔隙的形成。在聚合物交联过程中形成的 SMP 结构具有 50 微米到 700 微米不等的孔径,孔隙率超过 85%。与无孔的水凝胶相比,这些水凝胶具有更高的韧性。此外,这种方法还能灵活调整多孔结构和凝胶的整体形状,使其适用于各种应用。这种简单而有效的方法在开发具有更高韧性的新型 SMP 材料方面具有巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Advanced Functional Materials
Advanced Functional Materials 工程技术-材料科学:综合
CiteScore
29.50
自引率
4.20%
发文量
2086
审稿时长
2.1 months
期刊介绍: Firmly established as a top-tier materials science journal, Advanced Functional Materials reports breakthrough research in all aspects of materials science, including nanotechnology, chemistry, physics, and biology every week. Advanced Functional Materials is known for its rapid and fair peer review, quality content, and high impact, making it the first choice of the international materials science community.
期刊最新文献
Ambient Sunlight Driven Photothermal Green Syngas Production at 100 m3 Scale by the Dynamic Structural Reconstruction of Iron Oxides with 38.7% Efficiency Strong Ion-Dipole Interactions for Stable Zinc-Ion Batteries with Wide Temperature Range Bagworm Silk-Mimetic Protein Fibers with Extraordinary Stiffness via In Vivo Polymerization and Hierarchical Self-Assembly Metalloid Phosphorus Induces Tunable Defect Engineering in High Entropy Oxide Toward Advanced Lithium-Ion Batteries Bio-Realistic Synaptic-Replicated “V” Type Oxygen Vacancy Memristor
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1