Water sorption isotherms of molecularly imprinted polymers. Relation between water binding and iprodione binding capacity

Manal Bitar; Gaëlle Roudaut; Jacqueline Maalouly; Stéphane Brandès; Régis D Gougeon; Philippe Cayot; Elias Bou-Maroun

doi:10.1016/j.reactfunctpolym.2017.02.012

Water sorption isotherms of molecularly imprinted polymers. Relation between water binding and iprodione binding capacity

Manal Bitar ^{1, 2, 3} Gaëlle Roudaut ¹ Jacqueline Maalouly ² Stéphane Brandès ⁴ Régis D Gougeon ¹ Philippe Cayot ¹ Elias Bou-Maroun ^{1, *}

* Auteur correspondant

1 PAM - Procédés Alimentaires et Microbiologiques [Dijon]

2 ER004 - Lebanese Food Packaging [Université libanaise]

3 EREN - Laboratoire Energétique et Réactivité à l'Echelle Nanométrique [Université libanaise]

4 ICMUB - Institut de Chimie Moléculaire de l'Université de Bourgogne [Dijon]

Abstract : Molecularly imprinted polymers are often used in aqueous medium in order to recognize specifically a target molecule. The molecular recognition is usually based on hydrogen bonding. In this case, water molecule presents a serious competition towards the target molecule. In this study, the water sorption by molecularly imprinted polymers was studied in aqueous medium. The molecularly imprinted polymers were specific for iprodione fungicide and were prepared using a 24 full factorial experimental design. They were synthesized using EGDMA or TRIM as crosslinker, methacrylamide or styrene as functional monomer and using bulk or precipitation polymerization. The water sorption isotherms were established in a range of water activities 0.05–0.90 at 25 °C. The kinetics of water sorption by the polymers were modeled using Peleg's equation. This model shows that polymers having the highest water sorption capacities have high values of imprinting factor. The Guggenheim–Anderson–de Boer isotherm equations were used to fit the equilibrium data and the corresponding parameters were calculated. This model shows that polymers synthesized with EGDMA have higher water sorption capacities than those synthesized with TRIM due to the higher hydrophobicity of the latter. Peleg and Guggenheim–Anderson–de Boer equations satisfactorily modeled the water sorption on the imprinted and non-imprinted polymers. The results obtained from both equations were practically coincident. Principal component analysis was used as a chemometric tool in order to demonstrate that a polymer having a low adsorption energy and a high capacity of water retention could be applied to extract a target molecule from aqueous media.

Keywords : Peleg's model GAB model Molecularly imprinted polymers Water sorption Iprodione

Type de document :

Article dans une revue

Reactive and Functional Polymers, Elsevier, 2017, 114, pp.1 - 7. 〈10.1016/j.reactfunctpolym.2017.02.012〉

Domaine :

Sciences du Vivant [q-bio] / Ingénierie des aliments

Liste complète des métadonnées

https://hal-univ-bourgogne.archives-ouvertes.fr/hal-01509912
Contributeur : Pam - Université de Bourgogne <>
Soumis le : mardi 18 avril 2017 - 16:53:21
Dernière modification le : jeudi 11 octobre 2018 - 12:03:27

Water sorption isotherms of molecularly imprinted polymers. Relation between water binding and iprodione binding capacity

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Water sorption isotherms of molecularly imprinted polymers. Relation between water binding and iprodione binding capacity

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