Structure, properties and biodegradability of water resistant regenerated cellulose films coated with polyurethane/benzyl konjac glucomannan semi-IPN coating

被引:29
作者
Lu, YS [1 ]
Zhang, LN [1 ]
Pu, X [1 ]
机构
[1] Wuhan Univ, Dept Chem, Wuhan 430072, Peoples R China
基金
中国国家自然科学基金;
关键词
regenerated cellulose; polyurethane; benzyl konjac glucomannan; IPN; interfacial structure; biodegradability;
D O I
10.1016/j.polymdegradstab.2003.12.009
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
We prepared a series of novel water-resistant cellulose films by coating castor oil-based polyurethane (PU)/benzyl konjac glucomannan (B-KGM) semi-interpenetrating polymer networks (semi-IPN) on regenerated cellulose (RC) films, which was obtained from cotton linter in 6 wt% NaOH/5 wt% thiourea aqueous solution by coagulating with 5 wt% H2SO4 aqueous solution. The effect of B-KGM content on interfacial structure, thermal stability, mechanical properties in dry and wet states and biodegradability of the coated films were investigated by Fourier transform infrared spectra, ultraviolet spectroscopy, transmission electron microscopy, dynamic mechanical thermal analysis, tensile test and biodegradation test. The results indicate that PU prepolymer molecules in the semi-IPN coating penetrate simultaneously into the RC film, and give rise to a shared PU network between B-KGM and cellulose. B-KGM in the semi-IPN coating layer plays an important role in enhancement of the mechanical properties, water resistivity, thermal stability, light transmittance of the coated films. The tensile strength of the coated films increases from 86.3 to 114.9 MPa in dry state and from 33.8 to 56.4 MPa in wet state, as well as the light transmittance at 800 nm from 79% to 90% when B-KGM content increases from 0 wt% to 80 wt%. The biodegradation rates of the coated films increase with an increase of B-KGM content and the their biodegradation half-time is less than 80 days. (C) 2004 Published by Elsevier Ltd.
引用
收藏
页码:51 / 57
页数:7
相关论文
共 30 条
[1]   Biodegradation of octanoated starch and its blends with LDPE [J].
Bikiaris, D ;
Pavlidou, E ;
Prinos, J ;
Aburto, J ;
Alric, I ;
Borredon, E ;
Panayiotou, C .
POLYMER DEGRADATION AND STABILITY, 1998, 60 (2-3) :437-447
[2]  
Brown W., 1965, EUR POLYM J, V1, P1, DOI [DOI 10.1016/0014-3057(65)90041-8, 10.1016/0014-3057(65)90041-8]
[3]  
Darwis D., 1999, POLYM DEGRAD STABIL, V65, P161
[4]   Detection of toxicity released by biodegradable plastics after composting in activated vermiculite [J].
Degli-Innocenti, F ;
Bellia, G ;
Tosin, M ;
Kapanen, A ;
Itävaara, M .
POLYMER DEGRADATION AND STABILITY, 2001, 73 (01) :101-106
[5]   SIMULTANEOUS INTERPENETRATING NETWORKS BASED ON CASTOR-OIL ELASTOMERS AND POLYSTYRENE .2. SYNTHESIS AND SYSTEMS CHARACTERISTICS [J].
DEVIA, N ;
MANSON, JA ;
SPERLING, LH ;
CONDE, A .
MACROMOLECULES, 1979, 12 (03) :360-369
[6]  
DONATELLI AA, 1974, RECENT ADV POLYM BLE
[7]   Preparation and properties of polyurethane/elaeosterin interpenetrating polymer networks coating to regenerated cellulose films [J].
Gong, P ;
Zhang, LN .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1998, 37 (07) :2681-2686
[8]  
Gong P, 1998, J APPL POLYM SCI, V68, P1313, DOI 10.1002/(SICI)1097-4628(19980523)68:8<1313::AID-APP13>3.0.CO
[9]  
2-#
[10]   Modified polyacrylonitrile blends with cellulose acetate: blend properties [J].
Kim, BK ;
Oh, YS ;
Lee, YM ;
Yoon, LK ;
Lee, S .
POLYMER, 2000, 41 (01) :385-390