{"title":"Tensile Stress Enhances Moisture Sorption by Increasing Cellulose Hydroxyl Accessibility in Wood Cell Walls","authors":"Fengze Sun, Wenjuan Zhao, Yujing Tan, Kaiwen Chen, Yi Kong, Hui Peng, Zhu Li, Jiali Jiang, Tianyi Zhan, Chi Zhang, Jianxiong Lyu","doi":"10.1021/acs.biomac.6c01305","DOIUrl":null,"url":null,"abstract":"<div><div>Mechanical loading coupled with moisture sorption causes mechano-sorptive creep in wood, but its molecular origin remains unclear. Here, DMA, in situ tensile FTIR, SAXS/WAXS, and MD/GCMC simulations were combined to examine molecular and nanostructural changes in wood cell walls during sorption under tensile stress. Adsorption under stress produced a higher moisture content than stress-free adsorption, whereas viscoelastic creep at constant relative humidity caused no additional uptake. The enhancement was most evident when the loading was approximately parallel to cellulose microfibrils. FTIR revealed changes in cellulose hydroxyl environments consistent with increased accessibility, while SAXS/WAXS showed enlarged interfibrillar distances with nearly unchanged crystalline lattice spacings. Simulations further indicated reduced polymer–polymer hydrogen bonding, greater solvent-accessible surface area, and pore opening during simultaneous adsorption and loading. Together, these findings link tensile-stress-induced cellulose hydroxyl accessibility to enhanced moisture sorption in the wood cell walls.</div></div><div>Mechanical loading coupled with moisture sorption causes mechano-sorptive creep in wood, but its molecular origin remains unclear. Here, DMA, in situ tensile FTIR, SAXS/WAXS, and MD/GCMC simulations were combined to examine molecular and nanostructural changes in wood cell walls during sorption under tensile stress. Adsorption under stress produced a higher moisture content than stress-free adsorption, whereas viscoelastic creep at constant relative humidity caused no additional uptake. The enhancement was most evident when the loading was approximately parallel to cellulose microfibrils. FTIR revealed changes in cellulose hydroxyl environments consistent with increased accessibility, while SAXS/WAXS showed enlarged interfibrillar distances with nearly unchanged crystalline lattice spacings. Simulations further indicated reduced polymer–polymer hydrogen bonding, greater solvent-accessible surface area, and pore opening during simultaneous adsorption and loading. Together, these findings link tensile-stress-induced cellulose hydroxyl accessibility to enhanced moisture sorption in the wood cell walls.</div><div><div><span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (207KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div></div><div><span><figure><span><img><ol><li><span><span>Download: <span>Download high-res image (207KB)</span></span></span></li><li><span><span>Download: <span>Download full-size image</span></span></span></li></ol></span></figure></span></div>","PeriodicalId":30,"journal":{"name":"Biomacromolecules","volume":"27 9","pages":"Pages 6199-6213"},"PeriodicalIF":5.9000,"publicationDate":"2026-09-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Biomacromolecules","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1525779726003922","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/8/28 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Mechanical loading coupled with moisture sorption causes mechano-sorptive creep in wood, but its molecular origin remains unclear. Here, DMA, in situ tensile FTIR, SAXS/WAXS, and MD/GCMC simulations were combined to examine molecular and nanostructural changes in wood cell walls during sorption under tensile stress. Adsorption under stress produced a higher moisture content than stress-free adsorption, whereas viscoelastic creep at constant relative humidity caused no additional uptake. The enhancement was most evident when the loading was approximately parallel to cellulose microfibrils. FTIR revealed changes in cellulose hydroxyl environments consistent with increased accessibility, while SAXS/WAXS showed enlarged interfibrillar distances with nearly unchanged crystalline lattice spacings. Simulations further indicated reduced polymer–polymer hydrogen bonding, greater solvent-accessible surface area, and pore opening during simultaneous adsorption and loading. Together, these findings link tensile-stress-induced cellulose hydroxyl accessibility to enhanced moisture sorption in the wood cell walls.
Mechanical loading coupled with moisture sorption causes mechano-sorptive creep in wood, but its molecular origin remains unclear. Here, DMA, in situ tensile FTIR, SAXS/WAXS, and MD/GCMC simulations were combined to examine molecular and nanostructural changes in wood cell walls during sorption under tensile stress. Adsorption under stress produced a higher moisture content than stress-free adsorption, whereas viscoelastic creep at constant relative humidity caused no additional uptake. The enhancement was most evident when the loading was approximately parallel to cellulose microfibrils. FTIR revealed changes in cellulose hydroxyl environments consistent with increased accessibility, while SAXS/WAXS showed enlarged interfibrillar distances with nearly unchanged crystalline lattice spacings. Simulations further indicated reduced polymer–polymer hydrogen bonding, greater solvent-accessible surface area, and pore opening during simultaneous adsorption and loading. Together, these findings link tensile-stress-induced cellulose hydroxyl accessibility to enhanced moisture sorption in the wood cell walls.
期刊介绍:
Biomacromolecules is a leading forum for the dissemination of cutting-edge research at the interface of polymer science and biology. Submissions to Biomacromolecules should contain strong elements of innovation in terms of macromolecular design, synthesis and characterization, or in the application of polymer materials to biology and medicine.
Topics covered by Biomacromolecules include, but are not exclusively limited to: sustainable polymers, polymers based on natural and renewable resources, degradable polymers, polymer conjugates, polymeric drugs, polymers in biocatalysis, biomacromolecular assembly, biomimetic polymers, polymer-biomineral hybrids, biomimetic-polymer processing, polymer recycling, bioactive polymer surfaces, original polymer design for biomedical applications such as immunotherapy, drug delivery, gene delivery, antimicrobial applications, diagnostic imaging and biosensing, polymers in tissue engineering and regenerative medicine, polymeric scaffolds and hydrogels for cell culture and delivery.