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European Polymer Journal | 2001

Influence of degree of molar etherification on critical liquid crystal behavior of hydroxypropyl chitosan

Yanming Dong; Yusong Wu; Jianwei Wang; Mian Wang

Abstract Hydroxypropyl chitosan (HPCS) with different degree of molar etherification (DME, from 0.6 to 6.0) were synthesized and characterized by FTIR, 1H-NMR and elemental analysis. The effect of DME on critical concentration forming lyotropic liquid crystal (C*) was investigated in three solvents (formic acid, dichloroacetic acid and water). C* increased as DME raised but presented a platform at low DME (less than about 2.6), which was explained based on both the amount and the size of flexible substituents. HPCS with DME ⩾3.2 were water soluble. C* of HPCS aqueous solutions were evidently lower than those of formic acid or dichloroacetic acid solutions. Typical cholesteric texture appeared in HPCS solutions of all three solvents at proper concentrations.


Carbohydrate Research | 2003

Change of handedness in cholesteric liquid crystalline phase for N-phthaloylchitosan solutions in organic solvents.

Yanming Dong; Yusong Wu; Yaqing Zhao; Huiwu Wang; Yonghong Ruan; Hui Zhang; Xueming Fang

The influence of concentration on the helicoidal change of N-phthaloylchitosan (PhCh) solutions in Me2SO, DMAc and DMF was investigated by means of circular dichroism (CD). The critical concentrations to form liquid crystal phase in these three solvents were 43, 45 and 48 wt.%, respectively as measured with polarized optical microscope. There were two kinds of CD peaks, sharp peaks with absorption maximum at about 330 nm induced by the helical conformation of molecular chain, and very broad peaks covering almost whole visible region induced by the cholesteric helix of mesophase. The later only appeared in concentrated solutions with the concentration higher than the critical concentration. The handedness of both levels of helicoidal structures changed from left- to right-handed with the increase of concentration for PhCh/Me2SO solutions. The chirality transfer occurred between these two chiral levels. For PhCh/DMAc and PhCh/DMF systems, only the handedness of helical conformation reversed, but the cholesteric helix did not change. As a method to measure critical concentration, CD is more sensitive than polarized optical microscopy (POM).


Journal of Applied Polymer Science | 2002

Influence of degree of deacetylation on critical concentration of chitosan/dichloroacetic acid liquid-crystalline solution

Yanming Dong; Congyi Xu; Jianwei Wang; Yusong Wu; Mian Wang; Yonghong Ruan


Polymer Journal | 2001

Influence of molecular weight on critical concentration of chitosan/formic acid liquid crystalline solution

Yanming Dong; Weibi Qiu; Yonghong Ruan; Yusong Wu; Mian Wang; Chongyi Xu


Journal of Applied Polymer Science | 2000

Studies on the effect of substitution degree on the liquid crystalline behavior of cyanoethyl chitosan

Yanming Dong; Qing Yuan; Yusong Wu; Mian Wang


Journal of Polymer Science Part B | 2003

Spherulite morphology studies of N‐alkyl chitosan films cast from formic acid solutions

Yanming Dong; Kensuke Sakurai; Yusong Wu; Yukie Kondo


Polymer Bulletin | 2001

Influence of degree of N-butyrylation on critical concentration of N-butyrylated chitosan/dichloroacetic acid liquid crystalline solution

Yanming Dong; Congyi Xu; Jianwei Wang; Yusong Wu; Yonghong Ruan; Mian Wang


Polymer Journal | 2000

Crystalline morphology developing from cholesteric mesophase in cyanoethyl chitosan solutions

Yanming Dong; Qing Yuan; Yusong Wu; Jianwei Wang; Mian Wang


Polymer Bulletin | 2000

Fine structure in cholesteric fingerprint texture observed by scanning electron microscopy

Yanming Dong; Qing Yuan; Yusong Wu; Mian Wang


Journal of Applied Polymer Science | 2003

Studies on the critical phase-transition behavior of cholesteric N-phthaloyl chitosan/dimethyl sulfoxide solutions by five techniques

Yusong Wu; Yanming Dong; Hua Zhou; Yonghong Ruan; Huiwu Wang; Yaqing Zhao

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