Verification of the changes in the structural and physical properties of PU/PEO embedded with graphene oxide

Blend of polyurethane (PU) and polyethylene oxide (PEO) doped graphene oxide (GO) was prepared and investigated. The main bands of GO were increased with increasing of graphene contents due to oxidant induced chemical attachment of PU/PEO chains to the surface of GO. IR bands were increased attribut...

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Main Authors: Kholoud A. Hamam, L.H. Gaabour
Format: Article
Language:English
Published: Elsevier 2017-01-01
Series:Results in Physics
Online Access:http://www.sciencedirect.com/science/article/pii/S2211379717312159
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spelling doaj-a2705be7659644e18924739d1d7db32e2020-11-24T21:19:13ZengElsevierResults in Physics2211-37972017-01-01724272431Verification of the changes in the structural and physical properties of PU/PEO embedded with graphene oxideKholoud A. Hamam0L.H. Gaabour1Corresponding author.; Department of Physics, Faculty of Science, King Abdulaziz University, Jeddah, Saudi ArabiaDepartment of Physics, Faculty of Science, King Abdulaziz University, Jeddah, Saudi ArabiaBlend of polyurethane (PU) and polyethylene oxide (PEO) doped graphene oxide (GO) was prepared and investigated. The main bands of GO were increased with increasing of graphene contents due to oxidant induced chemical attachment of PU/PEO chains to the surface of GO. IR bands were increased attributed to oxidant-induced chemical attachment between GO and PU/PEO chains. The shift in TGA curves toward higher temperatures than that of PU/PEO which indicate the thermal stability of the samples. The activation energy was increased implying a variation of reactivity as a result of the extent reaction. Moreover, the kinetic parameters ΔS, ΔH and ΔG indicate that the addition of GO cause increase of thermal motion and decrease of the thermal stability. On the other hand, the behavior of ε′ and ε″ curves was decreased at low frequency and become nearly constant at the higher frequency due to the relaxation time. At low frequencies, the electric dipoles have enough time to align with field however at high frequencies attributed to shorter time available for dipoles to align after a rise of the field. A rise for M′ and M″ at the range of higher frequencies due to bulk effect suggesting polarity of relaxation mechanism. Keywords: Nanocomposite, Graphene oxide, Raman shift, FT-IR, TGA, Kinetic parametershttp://www.sciencedirect.com/science/article/pii/S2211379717312159
collection DOAJ
language English
format Article
sources DOAJ
author Kholoud A. Hamam
L.H. Gaabour
spellingShingle Kholoud A. Hamam
L.H. Gaabour
Verification of the changes in the structural and physical properties of PU/PEO embedded with graphene oxide
Results in Physics
author_facet Kholoud A. Hamam
L.H. Gaabour
author_sort Kholoud A. Hamam
title Verification of the changes in the structural and physical properties of PU/PEO embedded with graphene oxide
title_short Verification of the changes in the structural and physical properties of PU/PEO embedded with graphene oxide
title_full Verification of the changes in the structural and physical properties of PU/PEO embedded with graphene oxide
title_fullStr Verification of the changes in the structural and physical properties of PU/PEO embedded with graphene oxide
title_full_unstemmed Verification of the changes in the structural and physical properties of PU/PEO embedded with graphene oxide
title_sort verification of the changes in the structural and physical properties of pu/peo embedded with graphene oxide
publisher Elsevier
series Results in Physics
issn 2211-3797
publishDate 2017-01-01
description Blend of polyurethane (PU) and polyethylene oxide (PEO) doped graphene oxide (GO) was prepared and investigated. The main bands of GO were increased with increasing of graphene contents due to oxidant induced chemical attachment of PU/PEO chains to the surface of GO. IR bands were increased attributed to oxidant-induced chemical attachment between GO and PU/PEO chains. The shift in TGA curves toward higher temperatures than that of PU/PEO which indicate the thermal stability of the samples. The activation energy was increased implying a variation of reactivity as a result of the extent reaction. Moreover, the kinetic parameters ΔS, ΔH and ΔG indicate that the addition of GO cause increase of thermal motion and decrease of the thermal stability. On the other hand, the behavior of ε′ and ε″ curves was decreased at low frequency and become nearly constant at the higher frequency due to the relaxation time. At low frequencies, the electric dipoles have enough time to align with field however at high frequencies attributed to shorter time available for dipoles to align after a rise of the field. A rise for M′ and M″ at the range of higher frequencies due to bulk effect suggesting polarity of relaxation mechanism. Keywords: Nanocomposite, Graphene oxide, Raman shift, FT-IR, TGA, Kinetic parameters
url http://www.sciencedirect.com/science/article/pii/S2211379717312159
work_keys_str_mv AT kholoudahamam verificationofthechangesinthestructuralandphysicalpropertiesofpupeoembeddedwithgrapheneoxide
AT lhgaabour verificationofthechangesinthestructuralandphysicalpropertiesofpupeoembeddedwithgrapheneoxide
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