Effects on the properties after addition of lithium salt in poly(Ethylene oxide)/poly(methyl acrylate) blends

• Main Authors: Chan, C.H (Author), Halim, S.I.A (Author), Kressler, J. (Author)
• Format: Article
• Language: English
• Published: MDPI AG, 2020
• Subjects: Aliphatic compounds; Binary mixtures; Blend composition; Chlorine compounds; Dielectric relaxation; Electrochemical impedance spectroscopy; Ethylene; Frequency dependent impedance; Glass transition; Inorganic compounds; Lithium compounds; Lithium perchlorate; Methyl acrylates; Morphology; Other properties; Phase morphology; Polarization and relaxations; Poly (ethylene oxide) (PEO); Poly(ethylene oxide); Poly(methyl acrylate); Polyethylene oxides; Solution-casting technique
• Online Access: View Fulltext in Publisher; View in Scopus

 The studies of phase behavior, dielectric relaxation, and other properties of poly(ethylene oxide) (PEO)/poly(methyl acrylate) (PMA) blends with the addition of lithium perchlorate (LiClO4) were done for different blend compositions. Samples were prepared by a solution casting technique. The binary PEO/PMA blends exhibit a single and compositional-dependent glass transition temperature (Tg), which is also true for ternary mixtures of PEO/PMA/LiClO4 when PEO was in excess with low content of salt. These may indicate miscibility of the constituents for the molten systems and amorphous domains of the systems at room temperature from the macroscopic point of view. Subsequently, the morphology of PEO/PMA blends with or without salt are correlated to the phase behavior of the systems. Phase morphology and molecular interaction of polymer chains by salt ions of the systems may rule the dielectric or electric relaxation at room temperature, which was estimated using electrochemical impedance spectroscopy (EIS). The frequency-dependent impedance spectra are of interest for the elucidation of polarization and relaxation of the charged entities for the systems. Relaxation can be noted only when a sufficient amount of salt is added into the systems. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.