Estimation of Ionic Impurities in Poly(propylene Glycol) Diacrylate Monomers/Liquid Crystal E7 Mixtures Using Dielectric Spectroscopy

Author:

Benkouider Tayeb1,Derouiche Yazid12ORCID,Souli Lahcene3,Dubois Frédéric4ORCID,Barrera Ana2ORCID,Bouberka Zohra5,Maschke Ulrich2ORCID

Affiliation:

1. Laboratoire Physico-Chimie des Matériaux et Environnement (LPCME), Faculté des Sciences Exactes et Informatique, University of Djelfa, P.O. Box 3117, Djelfa 17000, Algeria

2. Unité Matériaux et Transformations (UMET), UMR 8207, CNRS, INRAE, Centrale Lille, University Lille, 59000 Lille, France

3. Laboratoire de Chimie Organique et Substances Naturelles (COSNA), Faculté des Sciences Exactes et Informatique, University of Djelfa, P.O. Box 3117, Djelfa 17000, Algeria

4. Unité de Dynamique et Structure des Matériaux Moléculaires (UDSMM), UR 4476, Université du Littoral—Côte d’Opale, CS 80699, 62228 Calais, France

5. Laboratoire Physico-Chimique des Matériaux, Catalyse et Environnement (LPCMCE), Université des Sciences et de la Technologie Mohammed Boudiaf d’Oran (USTO-MB), Oran 31000, Algeria

Abstract

The study investigated the effect of the molecular weight of three difunctional poly(propylene glycol) diacrylates on the temperature-dependent ionic conductivity of these monomers and their blends with an eutectic nematic liquid crystal mixture (E7). The results revealed two distinct regions. At low temperatures, ionic conduction can be described by the Vogel–Tamman–Fulcher (VTF) equation, while at high temperatures, the conductivity data follow the prediction of the Arrhenius model. The Arrhenius and VTF parameters and their corresponding activation energies were determined using the least squares method. In addition, a conductivity analysis based on an ionic hopping model is proposed. Estimates of ion concentrations and diffusion constants were calculated. It was found that both the ionic concentration and the diffusion constant decrease with the increase in the molecular weight of the monomers. The static dielectric permittivity decreases in the following order: TPGDA, PPGDA540, and PPGDA900. This can be explained by the higher dipole moment of TPGDA, which is caused by an enhanced volume density of carbonyl groups.

Publisher

MDPI AG

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