Aleksandar Y. Mehandzhiyski , Maria-Ximena Ruiz-Caldas , Patrick Heasman , Varvara Apostolopoulou-Kalkavoura , Lennart Bergström , Igor Zozoulenko
{"title":"有可能使纤维素完全干燥吗?","authors":"Aleksandar Y. Mehandzhiyski , Maria-Ximena Ruiz-Caldas , Patrick Heasman , Varvara Apostolopoulou-Kalkavoura , Lennart Bergström , Igor Zozoulenko","doi":"10.1016/j.carbpol.2025.123803","DOIUrl":null,"url":null,"abstract":"<div><div>Cellulose nanocrystals (CNCs) are widely used in advanced materials due to their unique mechanical and physicochemical properties. However, their interactions with water, particularly in the context of drying, remain poorly understood. The presence of bound water in CNC poses challenges for processing, storage, and applications sensitive to moisture. In this study, we combine molecular simulations and experimental drying investigations to assess the extent of water retention in both native and TEMPO-CNC under different thermodynamic conditions. Our results demonstrate that while native CNCs can be fully dried under low pressure (≤1 mbar) and elevated temperature (110 °C), TEMPO-CNC retain a significant amount of water (1–7 wt%) due to electrostatic interactions between water molecules and the charged surface carboxylic groups and the sodium counter-ions. These findings provide fundamental insights into the drying behavior of functionalized nanocellulose and highlight the importance of considering residual bound water in applications requiring moisture-sensitive performance.</div></div>","PeriodicalId":261,"journal":{"name":"Carbohydrate Polymers","volume":"365 ","pages":"Article 123803"},"PeriodicalIF":10.7000,"publicationDate":"2025-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Is it possible to completely dry cellulose?\",\"authors\":\"Aleksandar Y. Mehandzhiyski , Maria-Ximena Ruiz-Caldas , Patrick Heasman , Varvara Apostolopoulou-Kalkavoura , Lennart Bergström , Igor Zozoulenko\",\"doi\":\"10.1016/j.carbpol.2025.123803\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Cellulose nanocrystals (CNCs) are widely used in advanced materials due to their unique mechanical and physicochemical properties. However, their interactions with water, particularly in the context of drying, remain poorly understood. The presence of bound water in CNC poses challenges for processing, storage, and applications sensitive to moisture. In this study, we combine molecular simulations and experimental drying investigations to assess the extent of water retention in both native and TEMPO-CNC under different thermodynamic conditions. Our results demonstrate that while native CNCs can be fully dried under low pressure (≤1 mbar) and elevated temperature (110 °C), TEMPO-CNC retain a significant amount of water (1–7 wt%) due to electrostatic interactions between water molecules and the charged surface carboxylic groups and the sodium counter-ions. These findings provide fundamental insights into the drying behavior of functionalized nanocellulose and highlight the importance of considering residual bound water in applications requiring moisture-sensitive performance.</div></div>\",\"PeriodicalId\":261,\"journal\":{\"name\":\"Carbohydrate Polymers\",\"volume\":\"365 \",\"pages\":\"Article 123803\"},\"PeriodicalIF\":10.7000,\"publicationDate\":\"2025-05-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Carbohydrate Polymers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0144861725005867\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Carbohydrate Polymers","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0144861725005867","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Cellulose nanocrystals (CNCs) are widely used in advanced materials due to their unique mechanical and physicochemical properties. However, their interactions with water, particularly in the context of drying, remain poorly understood. The presence of bound water in CNC poses challenges for processing, storage, and applications sensitive to moisture. In this study, we combine molecular simulations and experimental drying investigations to assess the extent of water retention in both native and TEMPO-CNC under different thermodynamic conditions. Our results demonstrate that while native CNCs can be fully dried under low pressure (≤1 mbar) and elevated temperature (110 °C), TEMPO-CNC retain a significant amount of water (1–7 wt%) due to electrostatic interactions between water molecules and the charged surface carboxylic groups and the sodium counter-ions. These findings provide fundamental insights into the drying behavior of functionalized nanocellulose and highlight the importance of considering residual bound water in applications requiring moisture-sensitive performance.
期刊介绍:
Carbohydrate Polymers stands as a prominent journal in the glycoscience field, dedicated to exploring and harnessing the potential of polysaccharides with applications spanning bioenergy, bioplastics, biomaterials, biorefining, chemistry, drug delivery, food, health, nanotechnology, packaging, paper, pharmaceuticals, medicine, oil recovery, textiles, tissue engineering, wood, and various aspects of glycoscience.
The journal emphasizes the central role of well-characterized carbohydrate polymers, highlighting their significance as the primary focus rather than a peripheral topic. Each paper must prominently feature at least one named carbohydrate polymer, evident in both citation and title, with a commitment to innovative research that advances scientific knowledge.