Abstract

In this study two cellulose fibers, Eucalyptus grandis (CEG) and Pinus taeda (CPT), obtained through the kraft and sulfite pulping processes, respectively, were characterized. Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) and thermogravimetric analysis (TGA) were carried out. From the XRD analysis the interplanar distance, crystallite size and crystallinity index were calculated and the degradation kinetics parameters were determined by TGA at heating rates of 5, 10, 20 and 40 °C min−1 using the Avrami, Flynn-Wall-Ozawa (FWO) and Criado methods. The results obtained by FTIR showed that the composition of the fibers is similar, while from the XRD analysis slight differences in the crystallinity were observed. The thermogravimetric analysis showed higher thermal stability for CPT than CEG while the values for the activation energy (Ea) were higher for CEG than CPT. The results obtained by Avrami and Criado methods showed that the degradation mechanism in the CEG samples involves a diffusion process while in the case of CPT the degradation process is a phase boundary controlled reaction. The degradation mechanisms demonstrated that the difference between thermal stability and Ea may be due to differences in the type of crystalline structure of the samples obtained through the two pulping processes.

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