Preparation By Grafting Onto, Characterization, and Properties of Thermally Responsive Polymer-Decorated Cellulose Nanocrystals

被引:210
作者
Azzam, Firas [1 ]
Heux, Laurent [1 ]
Putaux, Jean-Luc [1 ]
Jean, Bruno [1 ]
机构
[1] Univ Grenoble 1, CERMAV CNRS, Ctr Rech Macromol Vegetales, F-38041 Grenoble 9, France
关键词
TEMPO-MEDIATED OXIDATION; NATIVE CELLULOSE; C-13; NMR; RADICAL POLYMERIZATION; SURFACE OXIDATION; ORGANIC-SOLVENTS; PHASE-TRANSITION; MICROFIBRILS; WHISKERS; NANOCOMPOSITES;
D O I
10.1021/bm101106c
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
The grafting of thermosensitive amine-terminated statistical polymers onto the surface of cellulose nanocrystals (CNCs) was achieved by a peptidic coupling reaction, leading to unusual properties like colloidal stability at high ionic strength, surface activity, and thermoreversible aggregation. We have used a large variety of experimental techniques to investigate the properties of the polymer-decorated CNCs at different length-scales and as a function of the different reaction parameters. A high grafting density could be obtained when the reaction was performed in DMF rather than water. Infrared and solid-state NMR spectroscopy data unambiguously demonstrated the covalent character of the bonding between the CNCs and the macromolecules, whereas TEM images showed a preserved individualized character of the modified objects. Dynamic light scattering and zeta potential measurements were also consistent with individual nanocrystals decorated by a shell of polymer chains. Surface tension. measurements revealed that CNCs became surface-active after the grafting of thermosensitive amines. Decorated CNCs were also stable against high electrolyte concentrations. A thermoreversible aggregation was also observed, which paves the way for the design of stimuli-responsive biobased nanocomposite materials.
引用
收藏
页码:3652 / 3659
页数:8
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