By Albin F. Turbak (Eds.)
content material: Colloidal microcrystalline celluloses / O.A. Battista --
non-stop thiocarbonate-redox grafting on cellulosic substrates / W. James Brickman --
Cellulose derivatives : polymers with a destiny / Clayton D. Callihan --
Silyl cellulose / Robert E. Harmon and Kalyan ok. De --
usage of the radical response of cellulose with amic acids to provide cellulose derivatives containing carboxylic acid teams / Thomas C. Allen and John A. Cuculo --
wooden and wood-based residues in animal feeds / Andrew J. Baker, Meriill A. Millett, and Larry D. Satter --
Enzymes : particular instruments coming of age / Donald F. Durso and Anita Villarreal --
response of alkylene oxides with wooden / Roger M. Rowell --
Alkaline degradation of a nonreducing cellulose, version : 1,5-anhydro-cellobiitol / Ralph E. Brandon, Leland R. Schroeder, and Donald C. Johnson --
Nascent polyethylene-cellulose composite / R.H. Marchessault, B. Fisa, and J.F. Revol --
Formation and homes of combined nonwovens produced via cellulose-cellulose bonding / Raymond A. younger and Bernard Miller --
Marine polymers. five, amendment of paper with partly deacetylated chitin / G.G. Allan, J.F. Friedhoff, M. Korpela, J.E. Laine, and J.C. Powell --
software of GPC to experiences of the viscose procedure. half five, influence of warmth on rayon houses / John Dyer.
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Extra resources for Cellulose Technology Research
No n o t i c e a b l e amount d i s s o l v e d i n the f o l l o w i n g s o l v e n t s : acetone, benzene, carbon t e t r a c h l o r i d e , chloroform, d i e t h y l f o r m amide, e t h y l acetate, e t h y l a l c o h o l , ethylene d i c h l o r i d e , ether (sw), methylene c h l o r i d e , methyl e t h y l ketone (sw), nitromethane, nitropropane, p y r i d i n e (sw), s-tetrachloroethane and xylene. The m a t e r i a l was not s o l u b l e i n the f o l l o w i n g mixtures: acetone (80%), ethanol (15%), e t h y l acetate (5%) (sw) ; toluene (80%), ethanol (20%) (sw); ethylene d i c h l o r i d e (90%), methyl a l c o h o l (10%); and benzene (66%), ethylene d i c h l o r i d e (34%) (sw).
Izv. Vysshikh Uchebn. Zavendenii, Khim. i Khim. , (1965), 8(1), 124-6. ; Vysokomol. , Ser. , (1967), 9 ( 8 ) , 611-12. S. S. S. 3,432,488 (March 1, 1969). ; J. Polym. S c i . , Part A-1, (1969), 7 ( 7 ) , 1947-58. ; J . Amer. Chem. , (1966), 88(14), 3390. ; Carbohyd. , (1973), 31, 407. ; Starke, (1973), 25(12), 429. Nagy, J . ; Makromol. , (1973), 165, 335-8. ; Makromol. , (1969), 126, 139-46. ; ACS Symposium Series; American Chemical Society: Washington, DC, 1975. 5 Utilization of the Novel Reaction of Cellulose with Amic Acids to Produce Cellulose Derivatives Containing Carboxylic Acid Groups THOMAS C.
C U C U L O Department of Textile Chemistry Introduction One of the main reasons f o r the widespread use of c e l l u l o s e has been the abundance of h y d r o x y l groups and t h e i r ability t o r e a c t with a v a r i e t y of compounds t o form c e l l u l o s e d e r i v a t i v e s . These d e r i v a t i v e s e x h i b i t s e l e c t e d d e s i r e d p r o p e r t i e s , depending on the new f u n c t i o n a l group added. Although the m o d i f i c a t i o n of c e l l u l o s e has been s t u d i e d and p r a c t i c e d commercially f o r s e v e r a l years, new r e a c t i o n s and new d e r i v a t i v e s with new p r o p e r t i e s are still being i n v e s t i g a t e d and much of the chemistry i n v o l v e d i s not completely understood.