Surface esterification of cellulose nanofibers by a simple organocatalytic methodology

被引:83
作者
Avila Ramirez, Jhon Alejandro [1 ,2 ]
Juan Suriano, Camila [1 ]
Cerrutti, Patricia [1 ,3 ]
Laura Foresti, Maria [1 ,2 ]
机构
[1] Univ Buenos Aires, Fac Ingn, Inst Tecnol Polimeros & Nanotecnol, Grp Biotecnol & Biosintesis, Buenos Aires, DF, Argentina
[2] Consejo Nacl Invest Cient & Tecn, RA-1033 Buenos Aires, DF, Argentina
[3] Univ Buenos Aires, Fac Ingn, Dept Ingn Quim, Buenos Aires, DF, Argentina
关键词
Bacterial cellulose; Surface esterification; Organocatalysis; Characterization; SOLVENT-FREE ACETYLATION; BACTERIAL CELLULOSE; C-13; NMR; CRYSTALLINITY; SPECTROSCOPY; BEHAVIOR; MEDIA;
D O I
10.1016/j.carbpol.2014.08.020
中图分类号
O69 [应用化学];
学科分类号
070301 [无机化学];
摘要
Bacterial cellulose nanofibers were esterified with two short carboxylic acids by means of a simple and novel organic acid-catalyzed route. The methodology proposed relayed on the use of a non-toxic biobased alpha-hydroxycarboxylic acid as catalyst, and proceeded under moderate reaction conditions in solventless medium. By varying the esterification interval, acetylated and propionized bacterial cellulose nanofibers with degree of substitution (DS) in the 0.02-0.45 range could be obtained. Esterified bacterial cellulose samples were characterized by means of Solid-State CP/MAS C-13 Nuclear Magnetic Resonance spectroscopy (CP/MAS C-13 NMR), Fourier Transform Infrared spectroscopy (FTIR), X-ray Diffraction (XRD), Thermogravimetric Analysis (TGA) and chosen hydrophobicity test assays. TGA results showed that the esterified nanofibers had increased thermal stability, whereas XRD data evidenced that the organocatalytic esterification protocol did not alter their crystallinity. The analysis of the ensuing modified nanofibers by NMR, FTIR, XRD and TGA demonstrated that esterification occurred essentially at the surface of bacterial cellulose microfibrils, something highly desirable for changing their surface hydrophilicity while not affecting their ultrastructure. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:416 / 423
页数:8
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