{"title":"Self-Assembly Construction of Biomass Aerogel with Tip-To-Based Gradient Porous Structure to Break Trade-Off Effect for Efficient Water/Oil Separation","authors":"Zirong Liang, Chen Liang, Wanhe Li, Zuqiang Huang, Huayu Hu, Tao Gan, Yanjuan Zhang","doi":"10.1002/adfm.202424873","DOIUrl":null,"url":null,"abstract":"<p>Self-driven water/oil separation is an effective and sustainable strategy for oil dehydration, and regulating the pore structure of separation materials to break the trade-off effect between flux and retention remains a challenge. Inspired by the tip-to-base conduit widening structure of vascular bundle, an enthalpy‒entropy co-driven strategy based on tannin/amylose non-covalent self-assembly and borate ester dynamic crosslinking is innovatively proposed for constructing a gradient porous biomass aerogel (termed as Si@TAP-B), realizing synchronous improvement of separation flux and retention rate. The permeation fluxes of water/oil mixture and water-in-oil emulsion by Si@TAP-B achieve 17914.7 and 10285.6 L m<sup>−2</sup> h<sup>−1</sup>, respectively, and the retention rates remain above 99%. The asymmetric solvent transport induced by gradient porous structure optimizes the hydraulic resistance and breaks the trade-off effect of separation flux and retention. Therefore, the emulsion separation flux under forward osmosis (from large pores to small pores) is twice that under reverse osmosis. Additionally, similar to the self-healing ability of plants, Si@TAP-B can restore the original structure and function after severe damage through reversible crosslinking of borate ester bonds and the flow of low surface energy materials. Overall, this novel strategy is desirable for developing biodegradable, efficient, and durable separation materials with unique structures and functions.</p>","PeriodicalId":112,"journal":{"name":"Advanced Functional Materials","volume":"35 24","pages":""},"PeriodicalIF":19.0000,"publicationDate":"2025-01-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Advanced Functional Materials","FirstCategoryId":"88","ListUrlMain":"https://advanced.onlinelibrary.wiley.com/doi/10.1002/adfm.202424873","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
Self-driven water/oil separation is an effective and sustainable strategy for oil dehydration, and regulating the pore structure of separation materials to break the trade-off effect between flux and retention remains a challenge. Inspired by the tip-to-base conduit widening structure of vascular bundle, an enthalpy‒entropy co-driven strategy based on tannin/amylose non-covalent self-assembly and borate ester dynamic crosslinking is innovatively proposed for constructing a gradient porous biomass aerogel (termed as Si@TAP-B), realizing synchronous improvement of separation flux and retention rate. The permeation fluxes of water/oil mixture and water-in-oil emulsion by Si@TAP-B achieve 17914.7 and 10285.6 L m−2 h−1, respectively, and the retention rates remain above 99%. The asymmetric solvent transport induced by gradient porous structure optimizes the hydraulic resistance and breaks the trade-off effect of separation flux and retention. Therefore, the emulsion separation flux under forward osmosis (from large pores to small pores) is twice that under reverse osmosis. Additionally, similar to the self-healing ability of plants, Si@TAP-B can restore the original structure and function after severe damage through reversible crosslinking of borate ester bonds and the flow of low surface energy materials. Overall, this novel strategy is desirable for developing biodegradable, efficient, and durable separation materials with unique structures and functions.
自驱动水/油分离是一种有效且可持续的油脱水策略,调节分离材料的孔隙结构以打破通量与保留之间的权衡效应仍然是一个挑战。受维管束末端到基部导管加宽结构的启发,创新性地提出了一种基于单宁/直链淀粉非共价自组装和硼酸酯动态交联的焓熵共驱动策略,用于构建梯度多孔生物质气凝胶(称为Si@TAP-B),实现分离通量和保留率的同步提高。Si@TAP-B对油水混合物和油包水乳液的渗透通量分别达到17914.7和10285.6 L m−2 h−1,保留率保持在99%以上。梯度多孔结构引起的不对称溶剂输运优化了水力阻力,打破了分离通量和保留的权衡效应。因此,正渗透(从大孔隙到小孔隙)下的乳液分离通量是反渗透的2倍。此外,与植物的自愈能力类似,Si@TAP-B可以通过硼酸酯键的可逆交联和低表面能材料的流动,在严重损伤后恢复原有的结构和功能。总的来说,这种新策略是开发具有独特结构和功能的可生物降解,高效和耐用的分离材料的理想选择。
期刊介绍:
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