Molecular Mass and Molecular-Mass Distribution of TEMPO-Oxidized Celluloses and TEMPO-Oxidized Cellulose Nanofibrils

被引:83
作者
Hiraoki, Ryoya [1 ]
Ono, Yuko [1 ]
Saito, Tsuguyuki [1 ]
Isogai, Akira [1 ]
机构
[1] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Biomat Sci, Tokyo 1138657, Japan
基金
日本科学技术振兴机构;
关键词
SIZE-EXCLUSION CHROMATOGRAPHY; MEDIATED OXIDATION; MICROFIBRILLATED CELLULOSE; NATIVE CELLULOSE; LIGHT-SCATTERING; STRENGTH; FIBRILS; NANOCELLULOSES; FIBERS; LENGTH;
D O I
10.1021/bm501857c
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
Native wood cellulose was oxidized by 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO)-mediated oxidation, and the fibrous TEMPO-oxidized celluloses (TOCs) thus obtained were disintegrated in water to prepare TOC nanofibrils (TOCNs). The carboxyl groups of TOCs and TOCNs were methyl-esterified, and the methylated samples were dissolved in 8% LiCl/N,N-dimethylacetamide for size-exclusion chromatography/multiangle laser-light scattering (SEC-MALLS) analysis to obtain their molecular-mass (MM) values and MM distributions (MMDs). The results showed that remarkable depolymerization occurred in TOCs and TOCNs and depended on the oxidation and sonication conditions. Because single peaks without bimodal patterns were observed in the MMDs for all of the TOC and TOCN samples, depolymerization may have randomly occurred on whole cellulose molecules and oxidized cellulose molecules in the microfibrils during these treatments. Compared with the MM values obtained by SEC-MALLS, the intrinsic viscosities of TOCs dissolved in 0.5 M copper ethylenediamine solution provided lower MM values owing to depolymerization during the dissolution and postreduction processes.
引用
收藏
页码:675 / 681
页数:7
相关论文
共 49 条
[1]   Cellulose biosynthesis: A model for understanding the assembly of biopolymers [J].
Brown, RM ;
Saxena, IM .
PLANT PHYSIOLOGY AND BIOCHEMISTRY, 2000, 38 (1-2) :57-67
[2]  
Chen RH, 1997, CARBOHYD RES, V299, P287
[3]   Individualization of cellulose nanofibers from wood using high-intensity ultrasonication combined with chemical pretreatments [J].
Chen, Wenshuai ;
Yu, Haipeng ;
Liu, Yixing ;
Chen, Peng ;
Zhang, Mingxin ;
Hai, Yunfei .
CARBOHYDRATE POLYMERS, 2011, 83 (04) :1804-1811
[4]   HIGHLY SELECTIVE NITROXYL RADICAL-MEDIATED OXIDATION OF PRIMARY ALCOHOL GROUPS IN WATER-SOLUBLE GLUCANS [J].
DENOOY, AEJ ;
BESEMER, AC ;
VANBEKKUM, H .
CARBOHYDRATE RESEARCH, 1995, 269 (01) :89-98
[5]   TEMPO-mediated oxidation of pullulan and influence of ionic strength and linear charge density on the dimensions of the obtained polyelectrolyte chains [J].
deNooy, AEJ ;
Besemer, AC ;
vanBekkum, H ;
vanDijk, JAPP ;
Smit, JAM .
MACROMOLECULES, 1996, 29 (20) :6541-6547
[6]   Nanostructural Reorganization of Bacterial Cellulose by Ultrasonic Treatment [J].
Faria Tischer, Paula C. S. ;
Sierakowski, Maria Rita ;
Westfahl, Harry, Jr. ;
Tischer, Cesar Augusto .
BIOMACROMOLECULES, 2010, 11 (05) :1217-1224
[7]   Temperature and pH stability of cellouronic acid [J].
Fujisawa, Shuji ;
Isogai, Takuya ;
Isogai, Akira .
CELLULOSE, 2010, 17 (03) :607-615
[8]  
HASHIMOTO N, 1981, CHEM PHARM BULL, V29, P1475
[9]   SEC-MALLS analysis of TEMPO-oxidized celluloses using methylation of carboxyl groups [J].
Hiraoki, Ryoya ;
Fukuzumi, Hayaka ;
Ono, Yuko ;
Saito, Tsuguyuki ;
Isogai, Akira .
CELLULOSE, 2014, 21 (01) :167-176
[10]   Glucose/Glucuronic Acid Alternating Co-polysaccharides Prepared from TEMPO-Oxidized Native Celluloses by Surface Peeling [J].
Hirota, Masayuki ;
Furihata, Kazuo ;
Saito, Tsuguyuki ;
Kawada, Toshinari ;
Isogai, Akira .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2010, 49 (42) :7670-7672