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Sökning: L773:1574 1443 OR L773:1574 1451

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1.
  • Amer, Wael A., et al. (författare)
  • Synthesis and Properties of a Ferrocene-based Metallomesogenic Polymer Containing Bis(4-hydroxyoctoxyphenyl)sulfone
  • 2012
  • Ingår i: Journal of Inorganic and Organometallic Polymers and Materials. - : Springer Nature. - 1574-1443 .- 1574-1451. ; 22:6, s. 1229-1239
  • Tidskriftsartikel (refereegranskat)abstract
    • Poly[bis(4-hydroxyoctoxyphenyl)sulfone 1,1'-ferrocene dicarboxylate] (PHOSFD) was synthesized by solution polycondensation reaction of bis(4-hydroxyoctoxyphenyl)sulfone with 1,1'-ferrocenyl chloride. The synthesized polymer was characterized via the measurement of its H-1 NMR spectrum, UV-Vis spectrum and FTIR spectrum. X-ray diffraction pattern was measured to investigate the crystallinity of the synthesized polymer and it was found that the polymer is mostly amorphous. The molecular weight of the polymer was determined by gel permeation chromatography. In addition, the electrochemical, the thermal, and the liquid crystalline properties of the synthesized polymer were examined and compared with the properties of poly(diethyleneglycol 1,1'-ferrocene dicarboxylate) (PDEFD) that was synthesized in our earlier study. The electrochemical processes of PHOSFD in CH2Cl2 were confirmed neither to be totally reversible nor completely irreversible. Generally, the electrochemical properties of PHOSFD and PDEFD were found to be similar to each other. PHOSFD was found to be thermally stable but its thermal stability is lower than that of PDEFD. Both of PHOSFD and PDEFD showed liquid crystalline properties and they possessed nematic phase textures with schlieren disclinations during heating and cooling.
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2.
  • Amir, M., et al. (författare)
  • Synthesis and Characterization of CoxZn1−xAlFeO4 Nanoparticles
  • 2015
  • Ingår i: Journal of Inorganic and Organometallic Polymers and Materials. - : Springer Science and Business Media LLC. - 1574-1443 .- 1574-1451. ; 25:4, s. 747-754
  • Tidskriftsartikel (refereegranskat)abstract
    • Nanocrystalline powders of cobalt and aluminum co-substituted zinc ferrites with general formula CoxZn1−xAlFeO4 (x = 0.0–1.0) have been synthesized for the first time. Using the citrate-microwave technique and the citric acid as combustion–complexion agent (fuel), materials with spinel mono-phase cubic spinel structure were successfully prepared. The characterization of products was done by XRD, SEM and VSM. The crystallite size estimated by Scherrer formula has been found in the range of 7.7–9.6 nm. The magnetic properties were studied by room temperature (RT) VSM magnetization measurements. The small remanent magnetization (Mr) and coercivity (Hc) values reveal the superparamagnetic nature of nanoparticles (NPs) at RT. The extrapolated saturation magnetization (Ms) is maximum for Co0.8Zn0.2AlFeO4 (17.15 emu/g) and minimum for ZnAlFeO4 particles (4.22 emu/g). This case is attributed to high or low amount of cation distribution change from normal to mixed spinel structure. The average magnetic diameters (Dmag) were calculated from magnetic fit studies of M–H spectra. Dmag values are between 8.17 and 8.46 nm and this range is in great accordance with the obtained diameters from XRD measurements. The small Mr/Ms ratios (maximum, 0.219) specify the uniaxial anisotropy according to Stoner–Wohlfarth model for CoxZn1−xAlFeO4 NPs. RT effective anisotropy constants (Keff) were calculated by using Ms and Hc values. Keff constants increased with increasing Co content in the spinel NPs.
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3.
  • Baykal, A., et al. (författare)
  • Acid Functionalized Multiwall Carbon Nanotube/Magnetite (MWCNT)-COOH/Fe3O4 Hybrid : Synthesis, Characterization and Conductivity Evaluation
  • 2013
  • Ingår i: Journal of Inorganic and Organometallic Polymers and Materials. - : Springer Science and Business Media LLC. - 1574-1443 .- 1574-1451. ; 23:3, s. 726-735
  • Tidskriftsartikel (refereegranskat)abstract
    • A functionalized multiwall carbon nanotube (MWCNT)-COOH/Fe3O4 hybrid was fabricated by co-precipitation method. Fe3O4 nanoparticles were stably attached to the surface of carboxyl groups (COOH). The presence of Fe3O4 nanoparticles and their surface conjugation to MWCNT have been confirmed by XRD, TEM and FT-IR techniques. Magnetic evaluation revealed a superparamagnetic character of the hybrid and therefore the attached Fe3O4 nanoparticles. The crystallite size (9 +/- A 3 nm), particle size (9 +/- A 2 nm) and magnetic domain size estimated for Fe3O4 are consistent with each other, which reveal the single crystalline character of the nanoparticles. Electrical conductivity and dielectric behavior have also been characterized by utilizing impedance spectroscopy up to 3 MHz for an isotherm line varying from 293 to 393 K by 10 K steps. Electrical characteristics and its complex dielectric approaches might be elucidated with the existence of a conventional tunneling conduction mechanism of temperature-independency. The AC conductivity of MWCNT-COOH/Fe3O4 hybrid could also be a consequence of the estimations of the universal dynamic response.
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4.
  • Bo, Qi-Bing, et al. (författare)
  • Simple directed material design through in situ substitution of proton with Cu+ ions
  • 2009
  • Ingår i: Journal of Inorganic and Organometallic Polymers and Materials. - : Springer Science and Business Media LLC. - 1574-1443 .- 1574-1451. ; 19:4, s. 485-493
  • Tidskriftsartikel (refereegranskat)abstract
    • A new inorganic-organic hybrid material (C10H8N2H)2(Mo8O26) · 2NH4 (1) was prepared under solvothermal conditions (H2O/ethanol), which was then used as a starting material in the synthesis of another material, (C10H8N2Cu)2(Mo8O26) · 2NH4 (2). Each compound has been characterized by single-crystal X-ray diffraction, X-ray powder diffraction, elemental analysis, thermogravimetric analysis, fluorescence, FT-IR, and bond valence sum calculations. The comparative study focuses on the transformation and structural change between 1 and 2, which arises from the simple substitution of the proton in 1 with the Cu+ ions. The other surprising feature is that Cu+ ions can not only directly be used to substitute the proton of 1 but also ameliorate its photoluminescence property. It means that 1 appears to have recognizable functional protons in the solid-state structure and, hence, can very well be considered as an ideal precursor agent to design the functional materials with special architectures and photoactive properties.
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5.
  • Ebin, Burcak, 1983 (författare)
  • Simple Preparation of Ni and NiO Nanoparticles Using Raffinate Solution Originated from Spent NiMH Battery Recycling
  • 2018
  • Ingår i: Journal of Inorganic and Organometallic Polymers and Materials. - : Springer Science and Business Media LLC. - 1574-1451 .- 1574-1443. ; 28:6, s. 2554-2563
  • Tidskriftsartikel (refereegranskat)abstract
    • Nickel (Ni) and nickel oxide (NiO) nanoparticles were produced by a combination of precipitation and reduction/calcination methods using the raffinate solution originated from laboratory scale spent NiMH recovery process. Ni recovery from the solution reached 99.8% by a simple precipitation step using baking soda. X-ray diffraction, FTIR spectroscopy, carbon analyzer and thermal gravimetric analysis techniques were used to characterize the precipitate. Metallic and oxide nanoparticles were obtained by hydrogen reduction and calcination under air atmosphere of the precipitate at 400 °C, respectively for 30–90 min residence times. The crystal structure, crystallite size, morphology, particle size and surface area of the samples, as well as carbon residue content in the particles were detected by particle characterization methods. The results indicate that spherical Ni nanoparticles have a crystallite size about 37 nm, and particle sizes of around 100 nm. The agglomeration of the nanoparticles reduces by increasing residence time. NiO nanoparticles have finer crystallite and particle sizes than the metallic samples produced at the same temperature and residence times. The results show that the combination of the simple methods presented can be an alternative process for producing advanced particles from spent NiMH batteries.
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6.
  • El Hachmi, A., et al. (författare)
  • Structural, Magnetic and Optical Properties Study of Tellurium-Based Perovskites : Sr3-xPbxFe2TeO9 (0 <= x <= 2.25)
  • 2020
  • Ingår i: JOURNAL OF INORGANIC AND ORGANOMETALLIC POLYMERS AND MATERIALS. - : Springer Science and Business Media LLC. - 1574-1443 .- 1574-1451. ; 30:6, s. 1990-2006
  • Tidskriftsartikel (refereegranskat)abstract
    • Polycrystalline samples of the series of triple perovskites Sr3-xPbxFe2TeO9 (0 <= x <= 2.25) (SPFTO) were synthesized using solid state reaction. These materials have been studied by a combination of X-ray powder diffraction (XRPD), Mossbauer spectrometry, Raman and UV-Vis spectroscopies. The crystal structures were resolved by the Rietveld refinement method, and revealed that this Sr3-xPbxFe2TeO9 (0 <= x <= 2.25) system shows one space group change from tetragonal I4/m (0 <= x <= 1) to another tetragonal form I4/mmm (1.25 <= x <= 1.88) and a second transition to hexagonal R3 over bar m (2.08 <= x <= 2.25). An anti-site disordering of Fe and Te on the B sites has been detected indicating the presence of a partial amount of Te at Fe positions and vice versa. The valence state of iron in the Fe site was determined to be Fe(III) by Mossbauer spectrometry, which also revealed two sites in a concordance with the XRPD measurements. Fe-57 Mossbauer spectra measurements show paramagnetic and magnetic ordering behaviors. The observed Raman spectra as a function of composition show obvious changes on the positions (wavenumbers), the FWHM and the intensities of the modes confirming the phase transformations observed by the XRPD results. These structural transitions led to a distinct change in the optical band gap energy, varying from 2.14 to 1.85 eV.
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7.
  • Esir, S., et al. (författare)
  • Magnetic Properties of Annealed CoFe2O4 Nanoparticles Synthesized by the PEG-Assisted Route
  • 2014
  • Ingår i: Journal of Inorganic and Organometallic Polymers and Materials. - : Springer Science and Business Media LLC. - 1574-1443 .- 1574-1451. ; 24:2, s. 424-430
  • Tidskriftsartikel (refereegranskat)abstract
    • Annealed cobalt inverse spinel-type ferrite nanoparticles were synthesized using polyethylene glycol assisted co-precipitation. The structure, magnetic properties and effect of annealing temperature was investigated in detail. Saturation magnetization, coercivity and remanence magnetization were observed to decrease with increasing temperature. The magnetic hysteresis curves supported the proposition that the CoFe2O4 nanoparticles showed ferromagnetic character from 10 to 400 K. Magnetization measurements showed the blocking temperature to be higher than 400 K. Unsaturated magnetization behavior suggested the existence of disordered spins in the surface layer of the CoFe2O4 nanoparticles.
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8.
  • Esir, S., et al. (författare)
  • SrFe12O19/Zn0.65Ni0.25Cu0.1Fe2O4 Core-Shell Nanocomposite : Synthesis, Chracterization and Catalytic Activity in Aqueous Solution
  • 2014
  • Ingår i: Journal of inorganic and organometallic polymers and materials. - : Springer Science and Business Media LLC. - 1574-1443 .- 1574-1451. ; 24:4, s. 722-728
  • Tidskriftsartikel (refereegranskat)abstract
    • SrFe12O19/Zn0.65Ni0.25Cu0.1Fe2O4 core-shell nanocomposite has been successfully synthesized by sol-gel autocombustion (for SrFe12O19, core) and hydrothermal methods (for Zn0.65Ni0.25Cu0.1Fe2O4, shell). The products were characterized by X-ray powder diffractometer, transmission electron microscopy, fourier transform infrared spectrsocopy, vibrating sample magnetometer, Ultraviolet-visible specroscopy and inductively coupled plasma. Both X-ray powder diffraction, transmission electron microscopy results showed that Zn0.65Ni0.25Cu0.1Fe2O4 shell is on the surface of the SrFe12O19 core. The variations between the magnetic properties of the precursors and nanocomposite may be explained by interphase interactions at the surface of two ferrites. The properties of the SrFe12O19/Zn0.65Ni0.25Cu0.1Fe2O4 core-shell nanocomposite were favourable in its separation, recycling and reuse after reaction. The catalytic activity of SrFe12O19/Zn0.65Ni0.25Cu0.1Fe2O4 core-shell nanocomposite in the presence of NaBH4 were tested against methyl violet.
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9.
  • Hassan, Mohammad L., et al. (författare)
  • Metallo-Terpyridine-Modified Cellulose Nanofiber Membranes for Papermaking Wastewater Purification
  • 2018
  • Ingår i: Journal of Inorganic and Organometallic Polymers and Materials. - : Springer. - 1574-1443 .- 1574-1451. ; 28:2, s. 439-447
  • Tidskriftsartikel (refereegranskat)abstract
    • Metallo-terpyridine compounds and polymers exhibit unique optical, electrical, magnetic and antimicrobial properties. Recently, metallo-terpyridine-modified cellulosic films with interesting porous structure, that exhibit these properties, have been prepared. Herein we report the use of Cu-terpyridine-modified oxidized cellulose nanofibers (OXCNF-Cu-Tpy) as membranes for treatment of effluents of paper mills to produce re-usable water. The OXCNF-Cu-Tpy was prepared by modification of TEMPO-oxidized CNF (OXCNF) using copper(II) complex of 4′-Chloro [2,2′:6′,2″] terpyridine. The modification was proven by elemental analysis and Fourier transform infrared spectroscopy. The prepared OXCNF-Cu-Tpy was also characterized using X-ray diffraction and transmission electron microscopy. The prepared membranes were evaluated regarding their microscopic structure using scanning electron microscopy, atomic force microscopy, contact angle measurement, water flux and rejection of sub-micron size suspended particles in papermaking wastewater effluent. Chemical modification of OXCNF with the Cu-Tpy groups significantly increased pure water flux of the membranes by about 52 and 194% depending on pressure used during filtration (0.5 and 1 MPa, respectively). Although both OXCNF and OXCNF-Cu-Tpy exhibited high efficiency in removing the sub-micron size suspended particles from wastewater effluent, OXCNF-Cu-Tpy membranes showed about 30% higher flux rate than OXCNF membranes.
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10.
  • Jerroudi, M., et al. (författare)
  • Investigation of Novel Low Melting Phosphate Glasses Inside the Na2O-K2O-ZnO-P2O5 System
  • 2020
  • Ingår i: JOURNAL OF INORGANIC AND ORGANOMETALLIC POLYMERS AND MATERIALS. - : SPRINGER. - 1574-1443 .- 1574-1451. ; 30:2, s. 532-542
  • Tidskriftsartikel (refereegranskat)abstract
    • Phosphate glasses containing different concentrations of zinc oxide inside the (1 - x)(NaPO3-KPO3)-xZnO system (0 <= x <= 50 mol%) have been prepared using the conventional melt quenching technique. The prepared glasses were transparent, bubble-free and colourless. Their density, molar volume, glass transition temperature, and structural properties using infrared and Raman spectroscopies are investigated. As the content of ZnO increases, the density increases while the molar volume decreases. The composition dependence of T-g shows a minimum for the glass (x = 20 mol%). Structural approach realized by IR and Raman spectroscopies reveals that zinc ions occupy different sites in the glassy-network, mainly modifier sites and middle phosphate network in low-zinc and high-zinc glasses, respectively. The introduction of ZnO in the network induces some structural rearrangements through the conversion of metaphosphate structural units to pyrophosphate ones. It is also highlighted that the presence of ZnO in the glassy matrix allows the transformation of some P-O-P and P=O bonds to P-O-Zn linkages. From the UV-Visible absorption studies, the values of the optical band gap, E-g, and Urbach energy, Delta E, were evaluated. The optical band gap is found to depend on the glasses composition. E-g and Delta E show a minimum and a maximum respectively, for the glass (x = 20 mol%).
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