Comparison of oxygen plasma and cutinase effect on polyethylene terephthalate surface

The aim of the study is to activate inert PET surface in order to introduce the carboxyl groups and to obtain its hydrophilic character. Two advanced and environmentally friendly techniques were used for these purposes: i) oxygen plasma activation; ii) enzymatic treatment by cutinase. Differently tr...

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Published inJournal of applied polymer science Vol. 128; no. 6; pp. 3570 - 3575
Main Authors Tkavc, Tina, Vesel, Alenka, Acero, Enrique Herrero, Fras Zemljič, Lidija
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 15.06.2013
Wiley
Wiley Subscription Services, Inc
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Summary:The aim of the study is to activate inert PET surface in order to introduce the carboxyl groups and to obtain its hydrophilic character. Two advanced and environmentally friendly techniques were used for these purposes: i) oxygen plasma activation; ii) enzymatic treatment by cutinase. Differently treated PET foils were studied in terms of carboxylic group content (non‐aqueous potentiometric titrations, XPS) and hydrophobic/hydrophilic character (goniometry). Moreover, the influence of both activation procedures onto chitosan adsorption was examined by XPS, zeta potential measurements and ATR‐FTIR spectroscopy. Obtained results show that plasma activation gives for around 19% higher amount of carboxylic groups than cutinase treatment and is during the storage less stable. Results clearly show that the use of both surfaces activation processes increases the ability of PET foils for chitosan adsorption. Due to the fact that chitosan is an antimicrobial agent, obtained materials may be applied as an active packaging system. © 2012 Wiley Periodicals, Inc. J. Appl. Polym. Sci., 2013
Bibliography:istex:58D881A338DDFF4A744B258780BC144DCDE1B658
ArticleID:APP38526
ark:/67375/WNG-0RMRKQV1-J
European Cohesion Fund
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0021-8995
1097-4628
DOI:10.1002/app.38526