Synthesis and characterization of poly(vinyl phosphonic acid) (PVPA)–Fe3O4 nanocomposite

Poly(vinyl phosphonic acid) (PVPA)–Fe3O4 nanocomposite is synthesized by the precipitation of Fe3O4 in the presence of PVPA. Structural, surface, morphological, thermal properties and conductivity characterization/evaluation of the nanocomposite were performed by XRD, FT-IR, TEM, TGA and conductivit...

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Published inPolyhedron Vol. 30; no. 2; pp. 419 - 426
Main Authors Durmus, Z., Erdemi, H., Aslan, A., Toprak, M.S., Sozeri, H., Baykal, A.
Format Journal Article
LanguageEnglish
Published Elsevier Ltd 01.02.2011
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Abstract Poly(vinyl phosphonic acid) (PVPA)–Fe3O4 nanocomposite is synthesized by the precipitation of Fe3O4 in the presence of PVPA. Structural, surface, morphological, thermal properties and conductivity characterization/evaluation of the nanocomposite were performed by XRD, FT-IR, TEM, TGA and conductivity measurements, respectively. The capping of PVPA around the Fe3O4 nanoparticles was confirmed by FT-IR spectroscopy, the interaction being via bridging oxygens of the phosphate and the nanoparticle surface. The crystallite and particle size were obtained as 6±2 and 8.7±0.1nm from XRD line profile fitting and TEM image analysis respectively, which reveal nearly single crystalline nature of the Fe3O4 nanoparticles. Magnetic characterization of the bulk magnetite and (PVPA)–Fe3O4 nanocomposite reveals that both are in the superparamagnetic state at room temperature. The average magnetic domain size of the nanoparticles has been calculated using the Langevin function, which was fitted to the measured M–H hysteresis curves as 7.6nm for the nanocomposite. In the nanocomposite, the reduction is due to the adsorption of PVPA onto the magnetite surface, which cancels some of the free spins at the surface causing a magnetically dead layer. Analysis of the conductivity and permittivity measurements revealed the coupling of ionic and polymer segmental motions and strong temperature dependency in the nanocomposite. [Display omitted] ► PVPA coated Fe3O4 nanoparticles have been prepared by the in situ polymerization of PVPA for the first time. ► As a nanocomposite, its dielectric, magnetic, structural and morphological properties were investigated in detail for the first time. ► Organic/inorganic nanocomposite membranes consisting of Fe3O4/PVPA (polyvinyphosphonic acid) hybrids showed a maximum ionic conductivity of 1.0×10−7S/cm at 120°C. ► Although this low conductivity precludes its use, it still has wide technological applications, particularly in biotechnology. Poly(vinyl phosphonic acid) (PVPA)–Fe3O4 nanocomposite is synthesized by the precipitation of Fe3O4 in the presence of PVPA. Structural, surface, morphological, thermal properties and conductivity characterization/evaluation of the nanocomposite were performed by XRD, FT-IR, TEM, TGA and conductivity measurements respectively. The capping of PVPA around the Fe3O4 nanoparticles was confirmed by FT-IR spectroscopy, the interaction being via bridging oxygens of the phosphate and the nanoparticle surface. The crystallite and particle size were obtained as 6±2 and 8.7±0.1nm from XRD line profile fitting and TEM image analysis respectively, which reveal nearly single crystalline nature of the Fe3O4 nanoparticles. Magnetic characterization of the bulk magnetite and (PVPA)–Fe3O4 nanocomposite reveals that both are in the superparamagnetic state at room temperature. The average magnetic domain size of the nanoparticles has been calculated using the Langevin function, which was fitted to the measured M–H hysteresis curves as 7.6nm for the nanocomposite. In the nanocomposite, the reduction is due to the adsorption of PVPA onto the magnetite surface, which cancels some of the free spins at the surface causing a magnetically dead layer. Analysis of the conductivity and permittivity measurements revealed the coupling of ionic and polymer segmental motions and strong temperature dependency in the nanocomposite.
AbstractList Poly(vinyl phosphonic acid) (PVPA)–Fe3O4 nanocomposite is synthesized by the precipitation of Fe3O4 in the presence of PVPA. Structural, surface, morphological, thermal properties and conductivity characterization/evaluation of the nanocomposite were performed by XRD, FT-IR, TEM, TGA and conductivity measurements, respectively. The capping of PVPA around the Fe3O4 nanoparticles was confirmed by FT-IR spectroscopy, the interaction being via bridging oxygens of the phosphate and the nanoparticle surface. The crystallite and particle size were obtained as 6±2 and 8.7±0.1nm from XRD line profile fitting and TEM image analysis respectively, which reveal nearly single crystalline nature of the Fe3O4 nanoparticles. Magnetic characterization of the bulk magnetite and (PVPA)–Fe3O4 nanocomposite reveals that both are in the superparamagnetic state at room temperature. The average magnetic domain size of the nanoparticles has been calculated using the Langevin function, which was fitted to the measured M–H hysteresis curves as 7.6nm for the nanocomposite. In the nanocomposite, the reduction is due to the adsorption of PVPA onto the magnetite surface, which cancels some of the free spins at the surface causing a magnetically dead layer. Analysis of the conductivity and permittivity measurements revealed the coupling of ionic and polymer segmental motions and strong temperature dependency in the nanocomposite. [Display omitted] ► PVPA coated Fe3O4 nanoparticles have been prepared by the in situ polymerization of PVPA for the first time. ► As a nanocomposite, its dielectric, magnetic, structural and morphological properties were investigated in detail for the first time. ► Organic/inorganic nanocomposite membranes consisting of Fe3O4/PVPA (polyvinyphosphonic acid) hybrids showed a maximum ionic conductivity of 1.0×10−7S/cm at 120°C. ► Although this low conductivity precludes its use, it still has wide technological applications, particularly in biotechnology. Poly(vinyl phosphonic acid) (PVPA)–Fe3O4 nanocomposite is synthesized by the precipitation of Fe3O4 in the presence of PVPA. Structural, surface, morphological, thermal properties and conductivity characterization/evaluation of the nanocomposite were performed by XRD, FT-IR, TEM, TGA and conductivity measurements respectively. The capping of PVPA around the Fe3O4 nanoparticles was confirmed by FT-IR spectroscopy, the interaction being via bridging oxygens of the phosphate and the nanoparticle surface. The crystallite and particle size were obtained as 6±2 and 8.7±0.1nm from XRD line profile fitting and TEM image analysis respectively, which reveal nearly single crystalline nature of the Fe3O4 nanoparticles. Magnetic characterization of the bulk magnetite and (PVPA)–Fe3O4 nanocomposite reveals that both are in the superparamagnetic state at room temperature. The average magnetic domain size of the nanoparticles has been calculated using the Langevin function, which was fitted to the measured M–H hysteresis curves as 7.6nm for the nanocomposite. In the nanocomposite, the reduction is due to the adsorption of PVPA onto the magnetite surface, which cancels some of the free spins at the surface causing a magnetically dead layer. Analysis of the conductivity and permittivity measurements revealed the coupling of ionic and polymer segmental motions and strong temperature dependency in the nanocomposite.
Poly(vinyl phosphonic acid) (PVPA)-Fe3O4 nanocomposite is synthesized by the precipitation of Fe3O4 in the presence of PVPA. Structural, surface, morphological, thermal properties and conductivity characterization/evaluation of the nanocomposite were performed by XRD, FT-IR, TEM, TGA and conductivity measurements respectively. The capping of PVPA around the Fe3O4 nanoparticles was confirmed by FT-IR spectroscopy, the interaction being via bridging oxygens of the phosphate and the nanoparticle surface. The crystallite and particle size were obtained as 6 +/- 2 and 8.7 +/- 0.1 nm from XRD line profile fitting and TEM image analysis respectively, which reveal nearly single crystalline nature of the Fe3O4 nanoparticles. Magnetic characterization of the bulk magnetite and (PVPA)-Fe3O4 nanocomposite reveals that both are in the superparamagnetic state at room temperature. The average magnetic domain size of the nanoparticles has been calculated using the Langevin function, which was fitted to the measured M-H hysteresis curves as 7.6 nm for the nanocomposite. In the nanocomposite, the reduction is due to the adsorption of PVPA onto the magnetite surface, which cancels some of the free spins at the surface causing a magnetically dead layer. Analysis of the conductivity and permittivity measurements revealed the coupling of ionic and polymer segmental motions and strong temperature dependency in the nanocomposite.
Author Toprak, M.S.
Erdemi, H.
Aslan, A.
Durmus, Z.
Sozeri, H.
Baykal, A.
Author_xml – sequence: 1
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  surname: Durmus
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– sequence: 2
  givenname: H.
  surname: Erdemi
  fullname: Erdemi, H.
  organization: Department of Polymer Engineering, Yalova University, 77100 Yalova, Turkey
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  givenname: A.
  surname: Aslan
  fullname: Aslan, A.
  organization: Department of Chemistry, Fatih University, B. Cekmece, 34500 Istanbul, Turkey
– sequence: 4
  givenname: M.S.
  surname: Toprak
  fullname: Toprak, M.S.
  organization: TUBITAK-UME, National Metrology Institute, P.O. Box 54, 41470 Gebze-Kocaeli, Turkey
– sequence: 5
  givenname: H.
  surname: Sozeri
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  givenname: A.
  surname: Baykal
  fullname: Baykal, A.
  organization: Department of Chemistry, Fatih University, B. Cekmece, 34500 Istanbul, Turkey
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Snippet Poly(vinyl phosphonic acid) (PVPA)–Fe3O4 nanocomposite is synthesized by the precipitation of Fe3O4 in the presence of PVPA. Structural, surface,...
Poly(vinyl phosphonic acid) (PVPA)-Fe3O4 nanocomposite is synthesized by the precipitation of Fe3O4 in the presence of PVPA. Structural, surface,...
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SourceType Open Access Repository
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StartPage 419
SubjectTerms Chemistry
Conducting polymer
Electrical properties
Kemi
Magnetite
Magnetization
Nanocomposite
NATURAL SCIENCES
NATURVETENSKAP
Title Synthesis and characterization of poly(vinyl phosphonic acid) (PVPA)–Fe3O4 nanocomposite
URI https://dx.doi.org/10.1016/j.poly.2010.11.011
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