Effect of Dissolution Time on the Development of All-Cellulose Composites Using the NaOH/Urea Solvent System

J. F. Delgado, A. G. Salvay, S. Arroyo, C. Bernal, M. Foresti
{"title":"Effect of Dissolution Time on the Development of All-Cellulose Composites Using the NaOH/Urea Solvent System","authors":"J. F. Delgado, A. G. Salvay, S. Arroyo, C. Bernal, M. Foresti","doi":"10.3390/polysaccharides4010005","DOIUrl":null,"url":null,"abstract":"Innovative and sustainable all-cellulose composites (ACCs) can be obtained by partial dissolution of cellulosic fibers and regeneration of the dissolved fraction. Among cellulose solvents, sodium hydroxide/urea solutions are recognized as promising low-environmental impact systems. In this work, filter paper (FP) was dissolved with a 7 wt% NaOH/12 wt% urea aqueous solution, kept at −18 °C for different time intervals, regenerated with distilled water and finally dried under different conditions. The developed films were characterized in terms of morphology, porosity, optical properties, crystalline structure, hydration and mechanical properties. The porosity of the composites decreased with dissolution time due to the progressive filling of voids as the cellulosic fibers’ surface skin layer was dissolved and regenerated. Samples treated for 4 h showed the minimum values of porosity and opacity, high hydration and a substantial change from cellulose I to cellulose II. Hot pressing during drying led to relevant improvements in ACCs stiffness and strength values.","PeriodicalId":18775,"journal":{"name":"Natural Polysaccharides in Drug Delivery and Biomedical Applications","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2023-02-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Natural Polysaccharides in Drug Delivery and Biomedical Applications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3390/polysaccharides4010005","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1

Abstract

Innovative and sustainable all-cellulose composites (ACCs) can be obtained by partial dissolution of cellulosic fibers and regeneration of the dissolved fraction. Among cellulose solvents, sodium hydroxide/urea solutions are recognized as promising low-environmental impact systems. In this work, filter paper (FP) was dissolved with a 7 wt% NaOH/12 wt% urea aqueous solution, kept at −18 °C for different time intervals, regenerated with distilled water and finally dried under different conditions. The developed films were characterized in terms of morphology, porosity, optical properties, crystalline structure, hydration and mechanical properties. The porosity of the composites decreased with dissolution time due to the progressive filling of voids as the cellulosic fibers’ surface skin layer was dissolved and regenerated. Samples treated for 4 h showed the minimum values of porosity and opacity, high hydration and a substantial change from cellulose I to cellulose II. Hot pressing during drying led to relevant improvements in ACCs stiffness and strength values.
溶解时间对氢氧化钠/尿素溶剂体系制备全纤维素复合材料的影响
创新和可持续的全纤维素复合材料(ACCs)可以通过部分溶解纤维素纤维和再生的溶解部分获得。在纤维素溶剂中,氢氧化钠/尿素溶液被认为是有前途的低环境影响体系。在这项工作中,滤纸(FP)用7 wt% NaOH/12 wt%尿素水溶液溶解,在- 18°C保存不同时间间隔,用蒸馏水再生,最后在不同条件下干燥。从形貌、孔隙度、光学性能、晶体结构、水化性能和力学性能等方面对所制备的膜进行了表征。复合材料的孔隙率随着溶解时间的延长而降低,这是由于纤维素纤维表层的溶解和再生导致空隙的不断填充。处理4 h的样品孔隙度和不透明度最小,水化程度高,从纤维素I到纤维素II变化很大。干燥过程中的热压导致了ACCs刚度和强度值的相应改善。
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 求助全文
来源期刊
自引率
0.00%
发文量
0
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信