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Sökning: WFRF:(Sozeri H.)

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1.
  • Aydin, M., et al. (författare)
  • Synthesis and characterization of poly(3-thiophene acetic acid)/Fe3O4 nanocomposite
  • 2011
  • Ingår i: Polyhedron. - : Elsevier BV. - 0277-5387 .- 1873-3719. ; 30:6, s. 1120-1126
  • Tidskriftsartikel (refereegranskat)abstract
    • Poly(3-thiophene acetic acid)/Fe3O4 nanocomposite is synthesized by the precipitation of Fe3O4 in the presence of poly(3-thiophene acetic acid) (P3TAA). 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 P3TAA around Fe3O4 nanoparticles was confirmed by FT-IR spectroscopy, the interaction being via bridging oxygens of the carboxylate and the nanoparticle surface through bidentate binding. The crystallite and particle size were obtained as 9 +/- 2 nm and 11 +/- 1 nm from XRD line profile fitting and TEM image analysis, respectively, which reveal nearly single crystalline nature of Fe3O4 nanoparticles. Magnetization measurements reveal that P3TAA coated magnetite particles do not saturate at higher fields. There is no coercivity and remanence revealing superparamagnetic character. Magnetic particle size calculated from the theoretical fitting as 9.1 nm which coincides the values determined from TEM micrographs and XRD line profile fitting. The comparison to the TEM particle size reveals slightly modified magnetically dead nanoparticle surface.
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3.
  • Baykal, A., et al. (författare)
  • Triethylene Glycol Stabilized CoFe2O4 Nanoparticles
  • 2012
  • Ingår i: Journal of Superconductivity and Novel Magnetism. - : Springer Science and Business Media LLC. - 1557-1939 .- 1557-1947. ; 25:6, s. 1879-1892
  • Tidskriftsartikel (refereegranskat)abstract
    • We report on the synthesis and detailed composition, thermal, micro-structural, ac-dc conductivity performance and dielectric permittivity characterization of triethylene glycol (TREG) stabilized CoFe 2O 4 nanoparticles synthesized by polyol method. XRD analysis confirmed the inorganic phase as CoFe 2O 4 with high phase purity. Microstructure analysis with TEM revealed well separated, spherical nanoparticles in the order of 6 nm, which is also confirmed by X-ray line profile fitting. FT-IR analysis confirms that TREG is successfully coated on the surface of nanoparticles. Overall conductivity of nanocomposite is approximately two magnitudes lower than that of TREG with increase in temperature. The ac conductivity showed a temperature dependent behavior at low frequencies and temperature independent behavior at high frequencies which is an indication of ionic conductivity. The dc conductivity of the nanocomposites and pure TREG are found to obey the Ar- rhenius plot with dc activation energies of 0.258 eV and 0.132 eV, respectively. Analysis of dielectric permittivity functions suggests that ionic and polymer segmental motions are strongly coupled in the nanocomposite. TREG stabilized CoFe 2O 4 nanoparticles has lower ε and ε than that of pure TREG due to the doping of cobalt. As the temperature increases, the frequency at which (ε ) reaches a maximum shifted towards higher frequencies. On the other hand, the activation energy of TREG for relaxation process was found to be 0.952 eV which indicates the predominance of electronic conduction due to the chemical nature of TREG. Contrarily, no maximum peak of tan ÎŽ was observed for the nanocomposite due to the being out of temperature and frequency range applied in the study.
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4.
  • Deligoz, H., et al. (författare)
  • Synthesis and characterization of poly(1-vinyltriazole)-grafted superparamagnetic iron oxide nanoparticles
  • 2012
  • Ingår i: Synthetic metals. - : Elsevier BV. - 0379-6779 .- 1879-3290. ; 162:7-8, s. 590-597
  • Tidskriftsartikel (refereegranskat)abstract
    • We reported on the synthesis and detailed physicochemical characterization of poly(1-vinyltriazole)-grafted iron oxide nanoparticles. Superparamagnetic iron oxide nanoparticles (SPION) were fabricated by gel-to-crystalline conversion method. Telomerization of poly(1-vinyltriazole) on iron oxide nanoparticles was achieved via silanization process. XRD analysis confirmed the crystalline phase as magnetite, and FT-IR analysis confirmed the presence of PVTri on nanoparticles. Particle morphology was observed to be polygonic, due to the synthesis process, while average size estimated from TEM micrographs is 7 nm. Agreement between crystallite size estimated from XRD and particle size from TEM affirms single crystalline character of these nanoparticles. Dependence of conductivity on temperature showed a strong evidence for thermally activated polarization mechanism. Temperature and frequency dependence of dielectric permittivity revealed interfacial polarization and temperature-assisted-reorganization effects. Magnetic evaluation showed non-saturation and superparamagnetic characteristics of nanoparticles as well as magnetic particles being single domains.
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5.
  • Durmus, Z., et al. (författare)
  • Poly(vinyl phosphonic acid) (PVPA)-BaFe12O19 Nanocomposite
  • 2012
  • Ingår i: Journal of Superconductivity and Novel Magnetism. - : Springer Science and Business Media LLC. - 1557-1939 .- 1557-1947. ; 25:4, s. 1185-1193
  • Tidskriftsartikel (refereegranskat)abstract
    • We present a method for the fabrication of PVPA/BaFe12O19 nanocomposite by in-situ polymerization of vinyl phosphonic acid, VPA in the presence of synthesized BaFe12O19 NPs. Nanoparticles and the nanocomposite were analyzed by XRD, FTIR, TGA, SEM, TEM, VSM, and conductivity techniques for structural and physicochemical characteristics. Nanoparticles, identified as BaFe12O19 from XRD analysis, were successfully coated with PVPA and the linkage was assessed to be via P-O bonds. Electron microscopy analysis revealed aggregation of BaFe12O19 particles and dominantly platelet morphology upon composite formation. TGA analysis revealed the composition of the nanocomposite as 65% BaFe12O19 and 35% polymer. Magnetic evaluation revealed that adsorption of PVPA anions during the preparation of the nanocomposite strongly influenced the magnetic properties resulting in much lower saturation magnetization values. DC conductivity measurements were used to calculate activation energy of PVPA/BaFe12O19 nanocomposite and it was obtained as 0.37 eV.
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6.
  • Durmus, Z., et al. (författare)
  • Synthesis and characterization of L-carnosine coated iron oxide nanoparticles
  • 2011
  • Ingår i: Journal of Alloys and Compounds. - : Elsevier BV. - 0925-8388 .- 1873-4669. ; 509:5, s. 2555-2561
  • Tidskriftsartikel (refereegranskat)abstract
    • L-Carnosine coated iron oxide nanoparticles (CCIO NPs) have been prepared via co-precipitation of iron oxide in the presence of L-carnosine. Crystalline phase was identified as magnetite with an average crystallite size of 8 nm as estimated from X-ray line profile fitting. Particle size estimated from TEM by log-normal fitting was similar to 11 nm. FTIR analysis showed that the binding of carnosine onto the surface of iron oxide is through unidentate linkage of carboxyl group. CCIO NPs showed superparamagnetic charactersitic at room temperature. The magnetic core size of superparamagnetic CCIO NPs was found slightly smaller than the size obtained from TEM, due to the presence of magnetically dead layer. Magnetization measurements revealed that L-carnosine iron oxide composite has immeasurable coercivity and remanence with absence of hysteritic behavior, which implies superparamagnetic behavior at room temperature. The low value of saturation magnetization compared to the bulk magnetite has been explained by spin canting. LDH activity tests showed slight cytotoxicity of high dose of CCIO NPs. The ac conductivity of CCIO NPs was found to be greater than that of carnosine and the effective conduction mechanism was found as correlated barrier hopping (CBH). dc activation energy of the product at around room temperature was measured as 0.312 eV which was in good agreement with the earlier reports.
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7.
  • Durmus, Z., et al. (författare)
  • Synthesis and characterization of poly(vinyl phosphonic acid) (PVPA)-Fe3O4 nanocomposite
  • 2011
  • Ingår i: Polyhedron. - : Elsevier BV. - 0277-5387 .- 1873-3719. ; 30:2, s. 419-426
  • Tidskriftsartikel (refereegranskat)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 +/- 0.1 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.
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8.
  • Karaoglu, E., et al. (författare)
  • Effect of Hydrolyzing Agents on the Properties of Poly (Ethylene Glycol)-Fe3O4 Nanocomposie
  • 2011
  • Ingår i: Nano-Micro Letters. - 2150-5551. ; 3:2, s. 79-85
  • Tidskriftsartikel (refereegranskat)abstract
    • Poly (ethylene glycol) (PEG) assisted hydrothermal route has been used to study the influence of the hydrolyzing agent on the properties of PEG-iron oxide (Fe3O4) nanocomposites. Iron oxide nanoparticles (NPs), as confirmed by X-ray diffraction analysis, have been synthesized by a hydrothermal method in which NaOH and NH3 were used as hydrolyzing agents. Formation of PEG-Fe3O4 nanocomposite was confirmed by Fourier transform infrared spectroscopy (FTIR). Samples exhibit different crystallite sizes, which estimated based on line profile fitting as 10 nm for NH3 and 8 nm for NaOH hydrolyzed samples. The average particle sizes obtained from transmission electron microscopy was respectively 174 +/- 3 nm for NaOH and 165 +/- 4 nm for NH3 gas hydrolyzed samples. Magnetic characterization results reveal superparamagnetic characteristics despite a large particle size, which indicate the absence of coupling between the nanocrystals due to the presence of polymer in the nanocomposites. The conductivity curve demonstrates that sigma(DC) is strongly temperature dependent.
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9.
  • Karaoglu, E., et al. (författare)
  • Hydrothermal Synthesis and Characterization of PEG-Mn3O4 Nanocomposite
  • 2011
  • Ingår i: Nano-Micro Letters. - 2150-5551. ; 3:1, s. 25-33
  • Tidskriftsartikel (refereegranskat)abstract
    • Here, we report on the synthesis of PEG-5/Mn3O4 nanocomposite (NP's) via a hydrothermal route by using Mn(acac)(2), ethanol, NH3 and PEG-400. The crystalline phase was identified as Mn3O4. The crystallite size of the PEG-Mn3O4 nanocomposite was calculated as 12 +/- 5 urn from X-ray line profile fitting and the average particle size from TEM was obtained as 200 nm. This reveals polycrystalline character of Mn3O4 NP's. The interaction between PEG-400 and the Mn3O4 NP's was investigated by FTIR. Temperature independent AC conductivity of PEG-Mn3O4 nanocomposite beyond 20 kHz provides a strong evidence of ionic conduction through the structure. The conductivity and permittivity measurements strongly depend on the secondary thermal transition of nanocomposite beyond 100 degrees C. Above that temperature, Mn3O4 particles may interact with each other yielding a percolated path that will facilitate the conduction. On the other hand, the relatively lower activation energy (E-a=0.172 eV) for relaxation process suggests that polymer segmental motions of PEG and electrons hopping between Mn2+ and Mn3+ may be coupled in the sample below 100 degrees C. Room temperature magnetization curve of the sample does not reach to a saturation, which indicates the superparamagnetic character of the particles. As the temperature increases, the frequency at which (epsilon '') reaches a maximum shifted towards higher frequencies. The maximum peak was observed at 1.4 kHz for 20 degrees C while the maximum was detected at 23.2 kHz for 90 degrees C.
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10.
  • Karaoglu, E., et al. (författare)
  • Synthesis and characteristics of poly(3-pyrrol-1-ylpropanoic acid) (PPyAA)-Fe(3)O(4) nanocomposite
  • 2011
  • Ingår i: Journal of Alloys and Compounds. - : Elsevier BV. - 0925-8388 .- 1873-4669. ; 509:33, s. 8460-8468
  • Tidskriftsartikel (refereegranskat)abstract
    • Poly(3-pyrrol-1-ylpropanoic acid) (PPyAA)-Fe(3)O(4) nanocomposite was successfully synthesized by an in situ polymerization of 1-(2-carboxyethyl) pyrrole in the presence of synthesized Fe(3)O(4) nanoparticles. Evaluation of structural, morphological, electrical and magnetic properties of the nanocomposite was performed by XRD, FT-IR, TEM, TGA, magnetization and conductivity measurements, respectively. XRD analysis reveals the inorganic phase as Fe(3)O(4) and TGA shows about 90 wt% loading of Fe(3)O(4) in the nanocomposite. FT-IR analysis indicates a successful conjugation of Fe(3)O(4) particles with polypyrrole acetic acid. Magnetization measurements show that polypyrrole acetic acid coating decreases the saturation magnetization of Fe(3)O(4) significantly. This reduction has been explained by the pinning of the surface spins by the possible adsorption of non-magnetic ions during the polymerization process. The conductivity and dielectric permittivity measurements strongly depend on the thermally activated polarization mechanism and thermal transition of PPyAA in the nanocomposite structure. Large value of dielectric permittivity (epsilon') of the nanocomposite at lower frequency is attributed to the predominance of species like Fe(2+) ions and grain boundary defects (interfacial polarization).
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  • Resultat 1-10 av 36

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