Functional properties of biodegradable corn starch nanocomposites for food packaging applications

•Effects of Na–MMT and glycerol studied on some properties of starch films.•Glycerol decreased tensile strength sharply, while Na–MMT increased it gently.•Transparencies of the samples were investigated using image processing technique.•Na–MMT absorbed UV light from 216 to 266nm.•Hydrophilicity of t...

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Bibliographic Details
Published inMaterials in engineering Vol. 50; pp. 954 - 961
Main Authors Heydari, Amir, Alemzadeh, Iran, Vossoughi, Manouchehr
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 01.09.2013
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Summary:•Effects of Na–MMT and glycerol studied on some properties of starch films.•Glycerol decreased tensile strength sharply, while Na–MMT increased it gently.•Transparencies of the samples were investigated using image processing technique.•Na–MMT absorbed UV light from 216 to 266nm.•Hydrophilicity of the films decreased utilizing Na–MMT and increased with glycerol.•The effects of formulation on the thickness were considered. In this research, response surface methodology (RSM) was applied to study the effects of Na-Montmorillonite (Na–MMT) and glycerol on some functional properties of corn starch films. Films were prepared by casting method according to central composite design (CCD). Originally image processing technique was used in order to estimate transparency of the films. It was found that Na–MMT absorbed UV light from 216 to 266nm. No antimicrobial activities were observed against Escherichia coli and Staphylococcus aureus. Contact angle analysis revealed hydrophilicity of starch films decreased utilizing nanoparticles and increased with plasticizer content. Increase in glycerol content decreased tensile strength sharply, while presence of Na–MMT increased it gently. The minimum of hydrophilicity and the maximum of tensile strength was obtained by maximization of clay and minimization of plasticizer in the considered range, which resulted in minimum transparency.
ISSN:0261-3069
DOI:10.1016/j.matdes.2013.03.084