Molecular composite of lignin: Miscibility and complex formation of organosolv lignin and its acetates with synthetic polymers containing vinyl pyrrolidone and/or vinyl acetate units

被引:24
作者
Teramoto, Yoshikuni [1 ]
Lee, Seung-Hwan [2 ]
Endo, Takashi [2 ]
机构
[1] Kyoto Univ, Grad Sch Agr, Div Forest & Biomat Sci, Sakyo Ku, Kyoto 6068502, Japan
[2] Natl Inst Adv Ind Sci & Technol, Biomass Technol Res Ctr BTRC, Higashihiroshima, Hiroshima 7390046, Japan
关键词
organosolv lignin; poly(N-vinyl pyrrolidone); blends; complex; miscibility; FREE ETHANOL COOKING; KRAFT LIGNIN; ENZYMATIC SACCHARIFICATION; LIGNOCELLULOSIC BIOMASS; INTERPOLYMER COMPLEXES; POLY(ETHYLENE OXIDE); BLENDS; PRETREATMENT; ESTERS; POLYVINYLPYRROLIDONE;
D O I
10.1002/app.36294
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Binary blends and pseudo-complexes of organosolv lignin (OSL) or its acetate (OSL-Ac) with synthetic polymers including poly(vinyl acetate) (PVAc), poly(N-vinyl pyrrolidone) (PVP), and poly(N-vinyl pyrrolidone-co-vinyl acetate) (P(VP-co-VAc)) were prepared by casting from mixed polymer solutions in N,N-dimethylformamide as good solvent and by spontaneous coprecipitation from solutions in tetrahydrofuran (THF) as comparatively poor solvent. Thermal analysis by differential scanning calorimetry showed that OSL was not miscible with PVAc; however, OSL(-Ac) was miscible with PVP to form homogeneous blends irrespective of the degree of acetylation of OSL. OSL formed homogeneous blends with P(VP-co-VAc) with =30 mol % of VP contents. Fourier transform infrared spectra measurements for the miscible blends of OSL/PVP revealed the presence of hydrogen bonding interactions between hydroxyls of OSL and carbonyls of VP units. However, there was no evidence for the development of the hydrogen bonding in miscible blends of fully acetylated OSL with PVP. For complexes via THF solutions, its formation was found to be primarily due to a higher frequency of hydrogen bonding interactions. (c) 2012 Wiley Periodicals, Inc. J Appl Polym Sci, 2012
引用
收藏
页码:2063 / 2070
页数:8
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