Effect of degree of deacetylation of chitosan on the kinetics of ultrasonic degradation of chitosan

被引:53
作者
Tsaih, ML
Chen, RH
机构
[1] Natl Taiwan Ocean Univ, Dept Food Sci, Chilung 202, Taiwan
[2] Ching Kuo Inst Management & Hlth, Dept Food Sci & Technol, Chilung, Taiwan
关键词
chitosan; ultrasonic degradation; degree of deacetylation;
D O I
10.1002/app.13027
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The objective of the study was to explore the effect of the degree of deacetylation (DD) of the chitosan used on the degradation rate and rate constant during ultrasonic degradation. Chitin was extracted from red shrimp process waste. Four different DD chitosans were prepared from chitin by alkali deacetylation. Those chitosans were degraded by ultrasonic radiation to different molecular weights. Changes of the molecular weight were determined by light scattering, and data of molecular weight changes were used to calculate the degradation rate and rate constant. The results were as follows: The molecular weight of chitosans decreased with an increasing ultrasonication time. The curves of the molecular weight versus the ultrasonication time were broken at 1-h treatment. The degradation rate and rate constant of sonolysis decreased with an increasing ultrasonication time. This may be because the chances of being attacked by the cavitation energy increased with an increasing molecular weight species and may be because smaller molecular weight species have shorter relaxation times and, thus, can alleviate the sonication stress easier. However, the degradation rate and rate constant of sonolysis increased with an increasing DD of the chitosan used. This may be because the flexibilitier molecules of higher DD chitosans are more susceptible to the shear force of elongation flow generated by the cavitation field or due to the bond energy difference of acetamido and beta-1,4-glucoside linkage or hydrogen bonds. Breakage of the beta-1,4-glucoside linkage will result in lower molecular weight and an increasing reaction rate and rate constant. (C) 2003 Wiley Periodicals, Inc.
引用
收藏
页码:3526 / 3531
页数:6
相关论文
共 31 条
[1]   IMPROVED METHOD FOR IR DETERMINATION OF THE DEGREE OF N-ACETYLATION OF CHITOSAN [J].
BAXTER, A ;
DILLON, M ;
TAYLOR, KDA ;
ROBERTS, GAF .
INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES, 1992, 14 (03) :166-169
[2]  
CHANG JR, 1996, THESIS NATL TAIWAN O
[3]   Kinetics and products of the degradation of chitosan by hydrogen peroxide [J].
Chang, KLB ;
Tai, MC ;
Cheng, FH .
JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2001, 49 (10) :4845-4851
[4]  
Chen RH, 1997, CARBOHYD RES, V299, P287
[5]   Effects of chain flexibility of chitosan molecules on the preparation, physical, and release characteristics of the prepared capsule [J].
Chen, RH ;
Tsaih, ML ;
Lin, WC .
CARBOHYDRATE POLYMERS, 1996, 31 (03) :141-148
[6]   Ultrasonic depolymerization of aqueous polyvinyl alcohol [J].
Grönroos, A ;
Pirkonen, P ;
Heikkinen, J ;
Ihalainen, J ;
Mursunen, H ;
Sekki, H .
ULTRASONICS SONOCHEMISTRY, 2001, 8 (03) :259-264
[7]   Ultrasonic degradation of polystyrene solutions [J].
Kanwal, F ;
Liggat, JJ ;
Pethrick, RA .
POLYMER DEGRADATION AND STABILITY, 2000, 68 (03) :445-449
[8]  
KASSAI MR, 2001, LIFE SCI, P28
[9]   ULTRASONIC DEGRADATION OF WATER-SOLUBLE POLYMERS [J].
KODA, S ;
MORI, H ;
MATSUMOTO, K ;
NOMURA, H .
POLYMER, 1994, 35 (01) :30-33
[10]  
KULICKE WM, 1993, MAKROMOL CHEM, V194, P751