Suppr超能文献

在水相环境中,乙酰化纤维素纳米晶体、海藻酸钠和壳聚糖的多糖基生物复合材料的生物降解。

Biodegradation of polysaccharide-based biocomposites with acetylated cellulose nanocrystals, alginate and chitosan in aqueous environment.

机构信息

National Institute of Chemistry, Department of Catalysis and Chemical Reaction Engineering, Hajdrihova 19, SI-1000 Ljubljana, Slovenia.

National Institute of Chemistry, Department of Catalysis and Chemical Reaction Engineering, Hajdrihova 19, SI-1000 Ljubljana, Slovenia; Jožef Stefan International Postgraduate School, Jamova cesta 39, SI-1000 Ljubljana, Slovenia.

出版信息

Int J Biol Macromol. 2023 Dec 1;252:126433. doi: 10.1016/j.ijbiomac.2023.126433. Epub 2023 Aug 19.

Abstract

Biocomposite films from renewable sources are seen to be viable candidates as sustainable, zero-waste packaging materials. In this study, biocomposites films using chitosan and alginate as matrices, and pristine or acetylated cellulose nanocrystals (CNCs) as reinforcement agents, were fabricated, thoroughly characterized in terms of structure (with ATR-FTIR and XRD), morphology (SEM), thermal stability (TGA coupled with FTIR), water content and solubility and mechanical properties and subjected to controlled biological degradation in aqueous environment with added activated sludge. Biodegradation activity was followed through respirometry by measurement of change in partial O pressure using OxiTop® system. While the initial rate of biodegradation is higher in chitosan-based films with incorporated CNCs (both pristine and modified) compared to any other tested biocomposites, it was observed that chitosan-based films are not completely degradable in activated sludge medium, whereas alginate-based films reached complete biodegradation in 107 h to 112 h. Additional study of the aqueous medium with in situ FTIR during biodegradation offered an insight into biodegradation mechanisms. Use of advanced statistical methods indicated that selection of material (ALG vs CH) has the highest influence on biodegradability, followed by solubility of the material and its thermal stability.

摘要

从可再生资源中提取的生物复合材料被视为可持续、零浪费的包装材料的可行候选材料。在这项研究中,以壳聚糖和海藻酸钠为基质,以原纤化或乙酰化纤维素纳米晶体(CNC)为增强剂,制备了生物复合材料薄膜,并从结构(ATR-FTIR 和 XRD)、形态(SEM)、热稳定性(TGA 与 FTIR 联用)、水分含量和溶解度、力学性能等方面进行了全面的特性研究,并在添加活性污泥的水相环境中进行了受控的生物降解。通过使用 OxiTop®系统测量分压的变化,通过呼吸计来跟踪生物降解活性。虽然与任何其他测试的生物复合材料相比,含有 CNC(原纤化和改性)的壳聚糖基薄膜的初始生物降解率更高,但观察到壳聚糖基薄膜在活性污泥介质中不能完全降解,而海藻酸钠基薄膜在 107-112 h 内达到完全降解。在生物降解过程中使用原位 FTIR 对水相介质进行了进一步研究,深入了解了生物降解机制。使用先进的统计方法表明,材料的选择(ALG 与 CH)对生物降解性的影响最大,其次是材料的溶解度及其热稳定性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验