5 research outputs found

    Synthesis of lithium ferrites from polymetallic carboxylates

    Get PDF
    Lithium ferrite was prepared by the thermal decomposition of three polynuclear complex compounds containing as ligands the anions of malic, tartaric and gluconic acid: (NH4)2[Fe2.5Li0.5(C4H4O5)3(OH)4(H2O)2]×4H2O (I), (NH4)6[Fe2.5Li0.5(C4H4O6)3(OH)8]×2H2O (II) and (NH4)2[Fe2.5Li0.5(C6H11O7)3(OH)7] (III). The polynuclear complex precursors were characterized by chemical analysis, IR and UV–Vis spectra, magnetic measurements and thermal analysis. The obtained lithium ferrites were characterized by XRD, scanning electron microscopy, IR spectra and magnetic measurements. The single α-Li0.5Fe2.5O4 phase was obtained by thermal decomposition of the tartarate complex annealed at 700 °C for 1 h. The magnetization value ≈ 50 emu g-1 is lower than that obtained for the bulk lithium ferrite due to the nanostructural character of the ferrite. The particle size was smaller than 100 nm

    Synthesis of High-Performance CSA Cements as Low Carbon OPC Alternative

    No full text
    Starting from natural raw materials, cements based calcium sulphoaluminate (CSA) clinkers have been successfully obtained as an eco-friendly alternative to ordinary Portland cement. CSA-based cements with ye’elimite as the main phase have been produced over the years and are widely used today. In this regard, the present paper considers the study of hydration processes for CSA pastes prepared with a water/cement ratio of 0.5 according to the EN-197 standard and their characterization by thermal analysis (DTA-TG), X-ray diffraction analysis (XRD), and scanning electron microscopy coupled with energy dispersive X-ray spectroscopy (SEM-EDX). A mechanical strength of 60.9 MPa was the greatest achieved for mortars hardened for 28 days

    JSCS–3779 Original scientific paper Synthesis of lithium ferrites from polymetallic carboxylates

    No full text
    Abstract: Lithium ferrite was prepared by the thermal decomposition of three polynuclear complex compounds containing as ligands the anions of malic, tartaric and gluconic acid: (NH4) 2[Fe2.5Li0.5(C4H4O5) 3(OH) 4(H2O) 2]�4H2O (I), (NH4) 6[Fe2.5Li0.5(C4H4O6) 3(OH) 8]�2H2O (II) and (NH4) 2[Fe2.5Li0.5(C6H11O7) 3(OH) 7] (III). The polynuclear complex precursors were characterized by chemical analysis, IR and UV–Vis spectra, magnetic measurements and thermal analysis. The obtained lithium ferrites were characterized by XRD, scanning electron microscopy, IR spectra and magnetic measurements. The single �-Li0.5Fe2.5O4 phase was obtained by thermal decomposition of the tartarate complex annealed at 700 °C for 1 h. The magnetization value ≈ 50 emu g-1 is lower than that obtained for the bulk lithium ferrite due to the nanostructural character of the ferrite. The particle size was smaller than 100 nm

    Nanocomposite Hydrogels Based on Poly(<i>N</i>-vinyl pyrrolidone)

    No full text
    Poly(N-vinyl pyrrolidone) (PNVP) is one of the most studied and recognized polymer for use in the pharmaceutical industry and medicine purposes due to its unique combination of highly essential properties such as nontoxicity, biocompatibility with human tissue, chemical stability, and good solubility in water and other solvents. Most of the PNVP-based hydrogels are characterized by low mechanical properties when handled in a swollen state. For this purpose, several methods have been reported to increase the mechanical properties of these gels by introducing an inorganic clay as a reinforcing agent. The present work deals with the preparation and detailed structural characterization of nanocomposite hydrogels based on amidic N-vinyl pyrrolidone (NVP) monomers with or without N,N-methylenbis(acrylamide) (MBA) as chemical crosslinker and different concentrations of Laponite XLG as reinforcing agent. The hydrogels were synthesized by the radical polymerization of the monomers using 2,2-azobisisobutyronitrile (AIBN) as the initiator. In this study, we evaluated the structure of PNVP-based nanocomposites by using FT-IR, their morphology through SEM–EDX, and the influence of different amounts of Laponite XLG on the final properties, by performing rheological measurements and swelling studies. The Laponite XLG, used as reinforcing agent, significantly contributed to the improvement in the mechanical properties of the nanocomposite hydrogels
    corecore