Preparation of regenerated cellulose fiber via carbonation. I. Carbonation and dissolution in an aqueous NaOH solution

被引:18
作者
Oh, SY
Yoo, DI [1 ]
Shin, Y
Lee, WS
Jo, SM
机构
[1] Chonnam Natl Univ, Dept Text Engn, Kwangju 500757, South Korea
[2] Chonnam Natl Univ, Dept Clothing & Text, Kwangju 500757, South Korea
[3] Korea Inst Sci & Technol, Polymer Hybrid Res Ctr, Seoul 130650, South Korea
关键词
cellulose carbonate; CO(2); sodium hydroxide solution; solubility; phase diagram;
D O I
10.1007/BF02875361
中图分类号
TB3 [工程材料学]; TS1 [纺织工业、染整工业];
学科分类号
0805 ; 080502 ; 0821 ;
摘要
Cellulose carbonate was prepared by the reaction of cellulose pulp and CO(2) with treatment reagents, such as aqueous. ZnCl(2) (20-40 wt%) solution, acetone or ethyl acetate, at -5-0degreesC and 30-40 bar (CO(2)) for 2 hr. Among the treatment reagents, ethyl acetate was the most effective. Cellulose carbonate was dissolved in 10% sodium hydroxide solution containing zinc oxide up to 3 wt% at -5-0degreesC. Intrinsic viscosities of raw cellulose and cellulose carbonate were measured with an Ubbelohde viscometer using 0.5 M cupriethylenediamine hydroxide (cuen) as a solvent at 20degreesC according to ASTM D1795 method. The molecular weight of cellulose was rarely changed by carbonation. Solubility of cellulose carbonate was tested by optical microscopic observation, UV absorbance and viscosity measurement. Phase diagram of cellulose carbonate was obtained by combining the results of solubility evaluation. Maximum concentration of cellulose carbonate for soluble zone was increased with increasing zinc oxide content. Cellulose carbonate solution in good soluble zone was transparent and showed the lowest absorbance and the highest viscosity. The cellulose carbonate and its solution were stable in refrigerator (-5degreesC and atmospheric pressure).
引用
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页码:1 / 7
页数:7
相关论文
共 17 条
[1]  
BELLAMY WD, 1974, BIOTECHNOL BIOENG, V26, P869
[2]  
BERGNER C, 1986, CELL CHEM TECHNOL, V20, P591
[3]  
BRANDRUP J, 1999, POLYM HDB, P144
[4]  
Davidson GF, 1937, J TEXT I, V28, P27
[5]  
Fengel D., 1989, WOOD CHEM ULTRASTRUC, P66
[6]  
Franks N.E., 1979, US Patents, Patent No. 4145532
[7]  
HONGU T, 1997, NEW FIBERS, P196
[8]  
HUMPHERY AE, 1975, CELLULOSE CHEM ENERG, P49
[9]  
JINPING Z, 2000, POLYM J, V32, P866
[10]  
Johnson DL, 1969, Brit, Patent No. 1144048