Papers by Author: M. Mitrić

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Abstract: Pulsed laser deposition was used to obtain functionally graded bioactive glass coatings on titanium substrates. An UV KrF* (λ=248 nm, τ>7 ns) excimer laser was used for the multi-pulse irradiation of the targets. The depositions were performed in oxygen while keeping substrate temperature at 400°C. We used sintered glass targets in the system SiO2-Na2O-K2O-CaO-MgOP2O5 that differed in SiO2 content, which was either 57 wt.% (6P57) or 61 wt.% (6P61). A glass 6P61 was used as the first layer in direct contact with the metallic substrate, while the outer bioactive layer was made of glass 6P57. Both the bioactive coatings and the bulk glasses were analyzed by Fourier transform infrared spectrometry (FTIR), grazing incidence X-ray diffraction (GIXRD), and scanning electron microscopy (SEM). The FTIR spectra of the glass powders and glass coatings showed the main vibration modes of the Si-O-Si groups. GIXRD analysis confirmed that the glass coatings had an amorphous structure. The SEM micrographs of the glass coatings showed the films to consist of droplets with diameters ranging from 0.2 to 5 μm. SEM was used to determine the rate of apatite formation on the coating when exposed to simulated body fluid (SBF) solution for 7 days. We demonstrated that pulsed laser deposition leads to good glass-metal adhesion on the substrate and well attached bioactive particles on the surface. We consider therefore this method appropriate for forming implants that can develop an apatite layer after immersion in SBF.
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Abstract: Multilayered BaTi1-xSnxO3 (BTS) ceramics with different Ti/Sn ratios were produced by pressing and sintering at 1420 oC for 2 hours. X-ray diffractometry, scanning electron microscopy and energy dispersive spectroscopy were used for structural, microstructural and elemental analysis, respectively. The dielectric and ferroelectric behavior of sintered samples was studied, too. It is found that in ingredient materials, with increasing Sn content, the tetragonality decreases; Curie temperature moves towards room temperature, while the maximum of the dielectric constant increases, and also, they becomes less hysteretic. It is noticed that multilayered BTS ceramics with different Ti/Sn contents have a broad transition temperature and show a relatively high dielectric constant in a wide temperature range. It is shown that dielectric properties of these materials may be modified by a combination of different BTS powders as well as layers number.
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Abstract: Olivine-type lithium iron phosphate (LiFePO4) powders were synthesized applying three different methods: solid state reaction at high temperature, ultrasonic spray pyrolysis, and sonochemical treatment. The samples were characterized by X-ray powder diffraction (XRPD). Particle morphologies of the obtained powders were determined by scanning electron microscopy (SEM). It was found that structural and microstructural parameters of this material were strongly dependent on the synthesis conditions. We present here the results obtained upon optimization of each procedure for designing this cathode material.
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Abstract: BaTi1-xSnxO3 (BTS) powders, with x ranging from 0 to 1, were synthesized by solid-state reaction technique. The powders were pressed into pellets and sintered at 1370 and 1420 oC. The structural characterization of sintered BTS samples was made at room temperature using X-ray diffraction and Raman spectroscopy measurements. The BTS samples were found to be singlephase solid solutions. Dielectric properties of sintered BTS samples were studied as a function of sintering temperatures and tin contents, too. For samples with x ranging from 0 up to 0.15, it has been found that the Curie temperature decreases while the maximum of the dielectric constant increases with increasing tin content. These samples have relatively high dielectric constants, contrary to x > 0.2 samples with very low dielectric constants. It is noticed that BTS ceramics sintered at 1420 oC exhibit better dielectric properties than those sintered at 1370 oC.
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Abstract: Composite biomaterials based on calcium phosphate ceramic due to their high bioactivity are of interest for biological application and bone tissue repair. Structural and microstructural parameters of inorganic constituent of these materials are very important for the synthesis and characterization of composites. Quantitative and qualitative content, crystallite size of phases, as well as the degree of crystallinity have a great influence on the quality of composites, their application and bone tissue repair. X-ray diffractometry was employed to investigate the components of biocomposite materials, calcium phosphate (CaP) ceramic and poly-DL-lactide-coglycolide (DLPLG) polymer, as well as the biocomposite obtained from the mentioned components. Composite biomaterial was obtained by modified emulsion process. Using the Rietveld refinement, we analyzed CaP as an inorganic component of the composite, whence we have determined structural and microstructural properties of ceramic component of the investigated composite. The results obtained by structure refinement show that calcium phosphate ceramic materials synthesized at room temperature contain hydroxyapatite HAp as a predominant phase. The calculated Ca/P ratio is 1.667. The Rietveld analysis revealed lattice parameters a(Å)=9.4324(7) and c(Å)=6.8785(6) that are in agreement with the theoretical values.
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Abstract: In this paper we report the results on synthesis of a composite biomaterial based on biphasic calcium phosphate (BCP) and poly-(DL-lactide-co-glycolide) (DLPLG). Besides, we have investigated the influence of new synthesis method on the structure and characteristics of the composite. The synthesis of biphasic calcium phosphate from Ca(NO3)2 x 4H2O and (NH4)3 PO4 in alkali environment was performed by means of precipitation technique. Composite material BCP/DLPLG was first prepared from commercial granules using chemical methods. Powdered polymer DLPLG was then homogenized at appropriate ratio with addition of biphasic calcium phosphate into the suspension. All samples were characterized by DSC, IR, X-Ray and SEM techniques.
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