کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5511710 1540214 2017 32 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Thermal degradation kinetics of polylactic acid/acid fabricated cellulose nanocrystal based bionanocomposites
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی زیست شیمی
پیش نمایش صفحه اول مقاله
Thermal degradation kinetics of polylactic acid/acid fabricated cellulose nanocrystal based bionanocomposites
چکیده انگلیسی
Cellulose nanocrystals (CNC) are fabricated from filter paper (as cellulosic source) by acid hydrolysis using different acids such as sulphuric (H2SO4), phosphoric (H3PO4), hydrochloric (HCl) and nitric (HNO3) acid. The resulting acid derived CNC are melt mixed with Polylactic acid (PLA) using extruder at 180 °C. Thermogravimetric (TGA) result shows that increase in 10% and 50% weight loss (T10, T50) temperature for PLA-CNC film fabricated with HNO3, H3PO4 and HCl derived CNC have improved thermal stability in comparison to H2SO4-CNC. Nonisothermal kinetic studies are carried out with modified-Coats-Redfern (C-R), Ozawa-Flynn-Wall (OFW) and Kissinger method to predict the kinetic and thermodynamic parameters. Subsequently prediction of these parameter leads to the proposal of thermal induced degradation mechanism of nanocomposites using Criado method. The distribution of Ea calculated from OFW model are (PLA-H3PO4-CNC: 125-139 kJmol−1), (PLA-HNO3-CNC: 126-145 kJmol−1), (PLA-H2SO4-CNC: 102-123 kJmol−1) and (PLA-HCl-CNC: 140-182 kJmol−1). This difference among Ea for the decomposition of PLA-CNC bionanocomposite is probably due to various acids used in this study. The Ea calculated by these two methods are found in consonance with that observed from Kissinger method. Further, hyphenated TG-Fourier transform infrared spectroscopy (FTIR) result shows that gaseous products such as CO2, CO, lactide, aldehydes and other compounds are given off during the thermal degradation of PLA-CNC nanocomposite.
ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: International Journal of Biological Macromolecules - Volume 104, Part A, November 2017, Pages 827-836
نویسندگان
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