Volume 108, Issue 4 pp. 2280-2289

New biodegradable blends prepared from polylactide, titanium tetraisopropylate, and starch

Hsin-Tzu Liao

Corresponding Author

Hsin-Tzu Liao

Department of Chemical and Biochemical Engineering, Kao Yuan University, Kaohsiung County, Taiwan 82151, Republic of China

Department of Chemical and Biochemical Engineering, Kao Yuan University, Kaohsiung County, Taiwan 82151, Republic of China===Search for more papers by this author
Chin-San Wu

Chin-San Wu

Department of Chemical and Biochemical Engineering, Kao Yuan University, Kaohsiung County, Taiwan 82151, Republic of China

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First published: 08 February 2008
Citations: 38

Abstract

In this study, new biodegradable nanocomposites were prepared from poly(lactic acid) (PLA) or acrylic acid grafted poly(lactic acid) (PLA-g-AA), titanium tetraisopropylate, and starch by means of an in situ sol–gel process and the melt-blending method. The samples were characterized with X-ray diffractometry, Fourier transform infrared spectroscopy, differential scanning calorimetry, thermogravimetric analysis, scanning electron microscopy, and an Instron mechanical tester. According to the results, a PLA-g-AA/TiO2 hybrid could improve the properties of a PLA/TiO2 hybrid because the carboxylic acid groups of acrylic acid should act as coordination sites for the titania phase to form the TiOC chemical bond. It was also found that both the tensile strength and glass-transition temperature increased to a maximum value and then decreased with increasing TiO2 because excess particles (e.g., greater than 10 wt % TiO2) could cause separation or segregation between the organic and inorganic phases. A PLA-g-AA/TiO2/starch hybrid could obviously enhance the mechanical properties of a PLA-g-AA/starch hybrid because the former could provide a smaller starch phase size and nanoscale dispersion of TiO2 in the polymer matrix. The biodegradable nanocomposites produced in our laboratory could provide a plateau tensile strength at break when the starch content was up to 50 wt %. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci 2008

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