Thermogravimetric and FTIR studies of chitosan blends

被引:806
作者
Pawlak, A [1 ]
Mucha, A [1 ]
机构
[1] Tech Univ Lodz, Fac Proc & Environm Engn, PL-93005 Lodz, Poland
关键词
chitosan; blends; starch; PAV; HPC; thermodegradation; thermogravimetric analysis; FTIR analysis;
D O I
10.1016/S0040-6031(02)00523-3
中图分类号
O414.1 [热力学];
学科分类号
摘要
Results of spectrophotometric and thermogravimetric studies of chitosan (CH) blends with polyvinyl alcohol (PVAL), starch (S) and hydroxypropylcellulose (HPC) obtained by casting from solutions in the form of transparent films containing 0-1.0 weight fraction of CH were discussed. Blends containing S are homogeneous only in the case of low-weight fraction of S (to 0.3). On the basis of results of thermodegradation in dynamic and isothermal conditions, thermal stability of the tested systems was estimated. Thermogravimetric measurements in dynamic conditions were carried out in the temperature range of 100-450 degreesC at constant heating rate 15 degreesC/min. From thermogravimetry (TG) and DTG curves the activation energy and characteristic parameters of degradation of the tested blends were determined. The observed growth of activation energy and T-p-temperature of initial weight loss, T-max-temperature of maximal rate and C-e-degree of conversion at the end of the measurement (at temperature 450degreesC) along with the increase of polymer fraction (HPC and S) in the CH blend provides an evidence of improved thermal stability of the systems tested. Investigations in isothermal conditions in air at temperature from 100 to 200 degreesC confirmed appreciable improvement of CH thermal stability in the blends being tested. Infrared spectroscopic analysis of the blends showed a distinct stabilization of the process of chain scission. In the band at 1080 cm(-1) associated with absorption in -C-O-C- group during degradation of the blends at temperature 200 degreesC much smaller decrease due to molecular scission were observed than in the case of pure CH. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:153 / 166
页数:14
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