Cellulose and Cellulose Derivatives (Polymer Science by Kenji Kamide

By Kenji Kamide

Many hugely acclaimed and authoritative books on polymer technology are inclined to concentrate on man made polymers. Cellulose and Cellulose Derivatives is the 1st authoritative booklet at the topic. It examines contemporary advancements, with specific connection with cellulose (in aqueous alkali) and cellulose acetate. jam-packed with examples, the writer takes an in-depth examine the subject, utilizing the main trustworthy experimental info to be had. A entire method of the elemental rules of cellulose and its derivatives in resolution makes Cellulose and Cellulose Derivatives perfect examining for newbies in addition to skilled cellulose scientists. * Outlines the theoretical basics of cellulose and cellulose derivatives* offers entire and trustworthy experimental ends up in figures and tables * hugely illustrated and simple to learn

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ScL, 1963, C-12, 117. 14. K Kamide and WR Moore, /. Polym. Sci. B, 1964, 2, 1029. 15. W Banks and CT Greewood, Makromol. , 1968, 114, 245. 16. W Brown, in Cellulose and Cellulose Derivatives, Part IV, G. Molecular Coformation and Dimensions, p. 557. 17. M Kurata, Chemistry of Polymer Industry, Modem Industrial Chemistry 18, Asakawa, Tokyo, 1975, p. 296. 1 DEFINITIONS OF MOLECULAR STRUCTURE PARAMETERS^ A large number of the industrially useful cellulose derivatives are those in which the hydroxyl groups of the anhydroglucose units are not completely substituted.

WG Harland, /. , 1955, 46, T483. WR Moore and GD Edge, J. Polym. ScL, 1960, 47, 469. G Jayme and W Verburg, Rayon Zellwolle Chemifasem, 1954, 32, 193, 275. PJ Flory, Principles of Polymer Chemistry. Cornell Univ. Press, Ithaca, 1953. PJ Flory, Principles of Polymer Chemistry, p. 613, Fig. 141. and L Mandelkem and PJ Flory, J. Am. Chem. Soc, 1952, 74, 2517. PJ Flory, Principles ofPolymer Chemistry, p. 618, Table XXXIX. and S Newman (unpublished results). PJ Flory, Principles of Polymer Chemistry, p.

At 167-171 ppm; 73, the integrated peak intensity of the O-acetyl methyl carbon (ca. 20 ppm). 49) sample in DMSO-J6 over a wide range of magnetic field. A combination of ratio of peak areas of the 0-acetyl carbons at three different positions (C2, C3, and C6) and <(F)) enables us to evaluate ((/^)). 03 - Ce C3 C2 Ce C3 C2 ""Estimated from the peak area ratios calculated from a triangle approximation. ^Estimated from integrated peak intensity ratios. ^ 42 2. ^ with that determined by the titration method.

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