Interaction and Scale of Mixing in Cellulose Acetate/Poly(N-vinyl Pyrrolidone-co-vinyl Acetate) Blends

Authors: Ohno, Takahiro1; Yoshizawa, Sachiko2; Miyashita, Yoshiharu2; Nishio, Yoshiyuki3

Source: Cellulose, Volume 12, Number 3, June 2005 , pp. 281-291(11)

Publisher: Springer

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Abstract:

Binary blends and pseudo complexes of cellulose acetate (CA) with vinyl polymers containing N-vinyl pyrrolidone (VP) units, poly(N-vinyl pyrrolidone) (PVP) and poly(N-vinyl pyrrolidone-co-vinyl acetate) [P(VP-co-VAc)], were prepared, respectively, by casting from mixed polymer solutions in N,N-dimethylformamide as good solvent and by spontaneous co-precipitation from solutions in tetrahydrofuran as comparatively poor solvent. The scale of miscibility and intermolecular interaction were examined for the blends and complexes by solid-state 13C-NMR spectroscopy. It was revealed that the formation of complexes was due to a higher frequency of hydrogen-bonding interactions between the residual hydroxyl groups of CA and the carbonyl groups of VP residues in the vinyl polymer component. From measurements of CP/MAS spectra and proton spin-lattice relaxation times (T1rhoH) in the NMR study, the existence of the hydrogen-bonding interaction was also confirmed for the miscible blends and the homogeneity of the mixing was estimated to be substantially on a scale within a few nanometers.

Keywords: Blend; Cellulose acetate; 13C NMR; Complex; Interaction; Poly(N-vinyl pyrrolidone); Poly(N-vinyl pyrrolidone-co-vinyl acetate)

Document Type: Research article

DOI: http://dx.doi.org/10.1007/s10570-004-5836-7

Affiliations: 1: Division of Forest and Biomaterials Science, Graduate School of Agriculture, Kyoto University, 606-8502, Kyoto, Japan, 2: Department of Organic and Polymer Materials Chemistry, Tokyo University of Agriculture and Technology, Tokyo, Koganei, Japan, 3: Division of Forest and Biomaterials Science, Graduate School of Agriculture, Kyoto University, 606-8502, Kyoto, Japan, Email: ynishio@kais.kyoto-u.ac.jp

Publication date: 2005-06-01

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