1H NMR and 1H-13C HSQC surface characterization of chitosan-chitin sheath-core nanowhiskers

被引:74
作者
Pereira, Antonio G. B. [1 ,2 ]
Muniz, Edvani C. [1 ]
Hsieh, You-Lo [2 ]
机构
[1] Univ Estadual Maringa, Dept Chem, Grp Mat Polimer & Compositos, BR-87020900 Maringa, Parana, Brazil
[2] Univ Calif Davis, Fiber & Polymer Sci, Davis, CA 95616 USA
关键词
NMR spectroscopy; Nanowhiskers; Chitin; Chitosan; Surface deacetylation; SPECTROSCOPY;
D O I
10.1016/j.carbpol.2015.01.017
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Surface deacetylation of chitin nanowhiskers (CtNWs) to chitosan-sheath/chitin-core nanowhiskers (CsNWs) was successfully monitored by liquid-state high-resolution NMR of colloidal suspensions of these never-dried nanowhiskers. CtNWs were derived from acid hydrolysis (3 N HCl, 30 mL/g, 90 mm, 104 degrees C) of chitin at 65% yield and 86% Crl. Deacetylation (50% NaOH, 48 h, 50 degrees C) of CtNWs generated CsNWs with unchanged nanowhisker morphology and overall length and width dimensions, but a reduced Crl of 54%. Successful step-wise exchanging the aqueous media with acetone, then D2O prevented agglomeration of nanowhiskers and enabled NMR detection of individual nanowhiskers. The crystalline structure of CtNWs and CsNWs provided different chemical environments for the glucosamine hydrogen atom H2, splitting the NMR signals into 2 peaks (delta 3.0 and delta 3.35 ppm) which differed from that reported for soluble chitosan (delta 3.2 ppm). Besides, H-1-C-13 HSQC was only possible for CsNWs indicating the NMR phenomenon observed to represent that of the surfaces where the outer layers were highly mobile and less crystalline. The degree of acetylation at the surfaces was determined from H-1 NMR data to be 56% and 9% for CtNWs and CsNWs, respectively. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:46 / 52
页数:7
相关论文
共 29 条
[1]  
[Anonymous], 2012, POLYM SCI COMPREHENS, DOI DOI 10.1016/B978-0-444-53349-4.00257-0
[2]   Why do we have so many definitions for nanoscience and nanotechnology? [J].
Balogh, Lajos P. .
NANOMEDICINE-NANOTECHNOLOGY BIOLOGY AND MEDICINE, 2010, 6 (03) :397-398
[3]   Biological properties of "naked" metal nanoparticles [J].
Bhattacharya, Resham ;
Mukherjee, Priyabrata .
ADVANCED DRUG DELIVERY REVIEWS, 2008, 60 (11) :1289-1306
[4]   Chitin characterization by SEM, FTIR, XRD, and 13C cross polarization/mass angle spinning NMR [J].
Cárdenas, G ;
Cabrera, G ;
Taboada, E ;
Miranda, SP .
JOURNAL OF APPLIED POLYMER SCIENCE, 2004, 93 (04) :1876-1885
[5]   Preparation and solubility in acid and water of partially deacetylated chitins [J].
Cho, YW ;
Jang, J ;
Park, CR ;
Ko, SW .
BIOMACROMOLECULES, 2000, 1 (04) :609-614
[6]   An approach to understanding the deacetylation degree of chitosan [J].
de Alvarenga, Elson Santiago ;
de Oliveira, Cristiane Pereira ;
Bellato, Carlos Roberto .
CARBOHYDRATE POLYMERS, 2010, 80 (04) :1155-1160
[7]   Individual chitin nano-whiskers prepared from partially deacetylated α-chitin by fibril surface cationization [J].
Fan, Yimin ;
Saito, Tsuguyuki ;
Isogai, Akira .
CARBOHYDRATE POLYMERS, 2010, 79 (04) :1046-1051
[8]   TEMPO-mediated oxidation of β-chitin to prepare individual nanofibrils [J].
Fan, Yimin ;
Saito, Tsuguyuki ;
Isogai, Akira .
CARBOHYDRATE POLYMERS, 2009, 77 (04) :832-838
[9]   Chitin nanocrystals prepared by TEMPO-mediated oxidation of α-chitin [J].
Fan, Yirnin ;
Saito, Tsuguyuki ;
Isogai, Akira .
BIOMACROMOLECULES, 2008, 9 (01) :192-198
[10]   Insights into biogenic and chemical production of inorganic nanomaterials and nanostructures [J].
Faramarzi, Mohammad Ali ;
Sadighi, Armin .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 2013, 189 :1-20