结晶度
纤维素
纳米材料
微晶
化学
羧化
表面改性
滴定法
氧化纤维素
纳米复合材料
高分子化学
化学工程
核化学
有机化学
材料科学
纳米技术
结晶学
物理化学
催化作用
工程类
作者
John P. Moore,Soma Shekar Dachavaram,Shobanbabu Bommagani,Narsimha Reddy Penthala,Priya Venkatraman,E. Johan Foster,Peter A. Crooks,Jamie Hestekin
出处
期刊:Molecules
[Multidisciplinary Digital Publishing Institute]
日期:2020-04-17
卷期号:25 (8): 1847-1847
被引量:3
标识
DOI:10.3390/molecules25081847
摘要
The 2,2,6,6-tetramethylpiperidin-1-oxyl (TEMPO) oxidation of cellulose, when mediated with Oxone® (KHSO5), can be performed simply and under mild conditions. Furthermore, the products of the reaction can be isolated into two major components: Oxone®-mediated TEMPO-oxidized cellulose nanomaterials Form I and Form II (OTO-CNM Form I and Form II). This study focuses on the characterization of the properties of OTO-CNMs. Nanoparticle-sized cellulose fibers of 5 and 16 nm, respectively, were confirmed through electron microscopy. Infrared spectroscopy showed that the most carboxylation presented in Form II. Conductometric titration showed a two-fold increase in carboxylation from Form I (800 mmol/kg) to Form II (1600 mmol/kg). OTO-CNMs showed cellulose crystallinity in the range of 64–68% and crystallite sizes of 1.4–3.3 nm, as shown through XRD. OTO-CNMs show controlled variability in hydrophilicity with contact angles ranging from 16 to 32°, within or below the 26–47° reported in the literature for TEMPO-oxidized CNMs. Newly discovered OTO-CNM Form II shows enhanced hydrophilic properties as well as unique crystallinity and chemical functionalization in the field of bio-sourced material and nanocomposites.
科研通智能强力驱动
Strongly Powered by AbleSci AI