Green Process for Chemical Functionalization of Nanocellulose with Carboxylic Acids

被引:148
作者
Espino-Perez, Etzael [1 ,2 ]
Domenek, Sandra [2 ,4 ]
Belgacem, Naceur [1 ,3 ]
Sillard, Cecile [1 ]
Bras, Julien [1 ,3 ]
机构
[1] Univ Grenoble Alpes, LGP2, F-38000 Grenoble, France
[2] AgroParisTech, UMR Ingn Proc Aliments 1145, F-91300 Massy, France
[3] CNRS, LGP2, F-38000 Grenoble, France
[4] INRA, UMR Ingn Proc Aliments 1145, F-91300 Massy, France
关键词
CELLULOSE NANOCRYSTALS; SURFACE MODIFICATION; NANOWHISKERS; POLYMERIZATION; WHISKERS; CHEMISTRY; FIBERS; WOOD;
D O I
10.1021/bm5013458
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
An environmentally friendly and simple method, named SolReact, has been developed for a solvent-free esterification of cellulose nanocrystals (CNC) surface by using two nontoxic carboxylic acids (CA), phenylacetic acid and hydrocinnamic acid. In this process, the carboxylic acids do not only act as grafting agent, but also as solvent media above their melting point. Key is the in situ solvent exchange by water evaporation driving the esterification reaction without drying the CNC. Atomic force microscopy and X-ray diffraction analyses showed no significant change in the CNC dimensions and crystallinity index after this green process. The presence of the grafted carboxylic was characterized by analysis of the bulk CNC with elemental analysis, infrared spectroscopy, and C-13 NMR. The ability to tune the surface properties of grafted nanocrystals (CNC-g-CA) was evaluated by X-ray photoelectron spectroscopy analysis. The hydrophobicity behavior of the functionalized CNC was studied through the water contact-angle measurements and vapor adsorption. The functionalization of these bionanoparticles may offer applications in composite manufacturing, where these nanoparticles have limited dispersibility in hydrophobic polymer matrices and as nanoadsorbers due to the presence of phenolic groups attached on the surface.
引用
收藏
页码:4551 / 4560
页数:10
相关论文
共 52 条
[21]   Stable suspensions of partially silylated cellulose whiskers dispersed in organic solvents [J].
Goussé, C ;
Chanzy, H ;
Excoffier, G ;
Soubeyrand, L ;
Fleury, E .
POLYMER, 2002, 43 (09) :2645-2651
[22]   Quantification of cellulose nanowhiskers sulfate esterification levels [J].
Gu, Jin ;
Catchmark, Jeffrey M. ;
Kaiser, Edward Q. ;
Archibald, Douglas D. .
CARBOHYDRATE POLYMERS, 2013, 92 (02) :1809-1816
[23]   Key advances in the chemical modification of nanocelluloses [J].
Habibi, Youssef .
CHEMICAL SOCIETY REVIEWS, 2014, 43 (05) :1519-1542
[24]   Cellulose Nanocrystals: Chemistry, Self-Assembly, and Applications [J].
Habibi, Youssef ;
Lucia, Lucian A. ;
Rojas, Orlando J. .
CHEMICAL REVIEWS, 2010, 110 (06) :3479-3500
[25]   Cationic surface functionalization of cellulose nanocrystals [J].
Hasani, Merima ;
Cranston, Emily D. ;
Westman, Gunnar ;
Gray, Derek G. .
SOFT MATTER, 2008, 4 (11) :2238-2244
[26]  
Ioelovich M., 2012, ISRN Chemical Engineering, V2012, P7, DOI [10.5402/2012/428974, DOI 10.5402/2012/428974]
[27]   Polymer-Grafted Cellulose Nanocrystals as pH-Responsive Reversible Flocculants [J].
Kan, Kevin H. M. ;
Li, Jian ;
Wijesekera, Kushlani ;
Cranston, Emily D. .
BIOMACROMOLECULES, 2013, 14 (09) :3130-3139
[28]   Nanocelluloses: A New Family of Nature-Based Materials [J].
Klemm, Dieter ;
Kramer, Friederike ;
Moritz, Sebastian ;
Lindstrom, Tom ;
Ankerfors, Mikael ;
Gray, Derek ;
Dorris, Annie .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2011, 50 (24) :5438-5466
[29]   Surface Grafting of Cellulose Nanocrystals with Poly(ethylene oxide) in Aqueous Media [J].
Kloser, Elisabeth ;
Gray, Derek G. .
LANGMUIR, 2010, 26 (16) :13450-13456
[30]   Improving the reproducibility of chemical reactions on the surface of cellulose nanocrystals: ROP of ε-caprolactone as a case study [J].
Labet, Marianne ;
Thielemans, Wim .
CELLULOSE, 2011, 18 (03) :607-617