Neutral cellulose nanocrystals dispersed in water were shown in a previous work to stabilize oil/water interfaces and produce Pickering emulsions with outstanding stability, whereas sulfated nanocrystals obtained from cotton did not show interfacial properties. To develop a better understanding of the stabilization mechanism, amphiphilic properties of the nanocrystals were modulated by tuning the surface charge density to investigate emulsifying capability on two sources of cellulose: cotton linters (CCN) and bacterial cellulose (BCN). This charge adjustment made it possible to determine the conditions where a low surface charge density, below 0.03 e/nm(2), remains compatible with emulsification, as well as when assisted by charge screening regardless of the source. This study discusses this ability to stabilize oil-in-water emulsions for cellulose nanocrystals varying in crystalline allomorph, morphology, and hydrolysis processes related to the amphiphilic character of nonhydrophobized cellulose nanocrystal.
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Int J Biol Macromol
January 2025
School of Chemical Engineering, Changchun University of Technology, Changchun 130012, China.
In this study, the dispersion behavior of MoS₂ in ionic liquids (ILs) with varying alkyl chain lengths was the primary focus of investigation, followed by the design of a novel PAM/SMA/CMC/PDA@MoS hydrogel. By optimizing the concentrations of CMC and PDA@MoS, a bifunctional hydrogel with both sensing and catalytic functions was successfully developed. Mechanical tests revealed that the PAM/SMA/CMC/0.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
Department of Chemical Engineering, Arak University, Arak, Iran. Electronic address:
Polysaccharides such as chitosan, alginate, cellulose, and carrageenan have emerged as promising adsorbents due to their biodegradability, abundant availability, and diverse chemical functionality. These biopolymers exhibit promising performance for adsorption of a wide range of pollutants including heavy metals (e.g.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Colour Science and Textile Chemistry Research Center, College of Textiles and Clothing, Qingdao University, Qingdao, Shandong 266071, China.
Superhydrophobic fabrics suffer from being commonly penetrated by moisture after laundering, seriously deteriorating their water repellency after air drying. Numerous researchers have successfully recovered superhydrophobicity by drying in fluid ovens; however, high energy consumption and equipment dependence limit practical applications. Herein, the superhydrophobic photothermal self-healing cotton fabric (SPS cotton fabric) was fabricated by depositing a composite layer of cellulose nanocrystal-MXene (C-MXene) and polyacrylate (PA) coatings on the cotton cloth.
View Article and Find Full Text PDFRSC Adv
January 2025
State Key Laboratory of High-performance Precision Manufacturing, Dalian University of Technology Dalian 116024 P. R. China
The ability to convert moisture signals into electrical signals through contactless control underpins a wide range of applications, including health monitoring, disaster warning, and energy harvesting. Despite its potential, the effective utilization of low-grade energy remains challenging, as it often requires complex device architectures that limit scalability and integration, particularly in wearable technologies. Here, we present a soft, flexible moisture-electric converter made from cellulose nanocrystals and polyvinyl alcohol composite films, designed for a novel touchless interactive platform.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
School of Agriculture and Food Science, University College Dublin, Belfield, Dublin 4, Ireland. Electronic address:
Lignocellulosic biomass represents one of the most abundant renewable biological resources on earth. Despite its current underutilization as a source of high-value chemicals, it has promising applications in biomedical and other fields. Presently, lignocellulose is predominantly transformed into high-value-added products, e.
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