National Institute Of Materials Physics - Romania

Calcium phosphate ceramic powders were synthesized via sol-gel method. The powders were sintered at 600 and 1000 degrees C and characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), electron microscopy (SEM and TEM), elemental microanalysis (EDS), infrared spectroscopy (FTIR), and thermal analysis (TGA and DTA). The XRD analysis revealed a well crystallized hydroxyapatite (HAp) structure at all temperatures. At 1000 degrees C a small amount of CaO (about 1.2 %) was detected. The average crystallite size increased from 19 nm at 80 degrees C to about 125 nm at 1000 degrees C. FTIR spectra showed the presence of various PO43- and OH- groups present in the powders. In order to verify the biocompatibility of HAP powders with hFOB 1.19 osteoblasts cells, an 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) test was applied. It was noticed that the ceramics obtained at 1000 degrees C, increased the cell viability with 10%, 40% and 55% after 6, 12 respectively 24 h, whereas that obtained at 600 degrees C was less effective. Our results proved the high biocompatibility of calcium phosphate ceramic powders obtained by sol-gel and sintered at 1000 degrees C.

LiF:Pb doped crystals were successfully grown by Kyropoulos method, starting with drying powders. The presence of Pb2+ ions in the LiF crystals were evidenced by the absorption band at 278 nm and by 375 nm photoluminescence. The presence of some other Pb structures with oxygen compounds in the as made samples was evidenced, decreasing after some annealing procedures. The local environment and valence state of Pb in LiF were studied by X-ray Absorption Spectroscopy at the Pb L-III and L-I edges. XANES data reveal that Pb is present as Pb2+ whereas EXAFS data show that it is incorporated in the crystal and not forming PbF2 precipitates. Identical spectra are obtained for samples as prepared and after thermal annealing up to 650 degrees C demonstrating the stability of the incorporation site. Also the concentration of Pb in the crystal has no effect on the location site of the metal as the same spectrum is obtained for specimens with different dopant concentrations.

Electrodeposition of manganese doped ZnO wires into polycarbonate membranes from an aqueous solution containing Zn(NO3)(2), Mn(NO3)(2) and lactic acid was investigated using linear sweep voltammetry and electrochemical impedance spectroscopy (EIS). The equivalent electrical circuits used for fitting experimental results were similar to those for characterization of metal/polymer coating systems. The precipitation of metal oxides in the pores of membrane used as template was observed at potentials between -0.9 and -1.15V/SCE. Morphology of the ZnO: Mn submicron wires arrays was observed by scanning electron microscopy and the Mn content of the obtained samples was measured by X-ray analysis. The submicron wires prepared at a potential of -1.1V/SCE have a composition expressed by the formula Zn0.97Mn0.03.

The bio-compatible magnetic nanoparticles of maghemite were prepared by a chemical co-precipitation method and dextran was selected as the surfactant to suspend them. By transmission electron microscopy (TEM), the iron oxide nanoparticles appeared nearly spherical with an average diameter of about 8.0 +/- 1 nm. SAED pattern of iron oxide nanoparticles is indexed by a cubic gamma-Fe(2)O(3), the diffraction rings are attributed to the (220), (311), (400), (422), (511) and (440) planes, respectively. Regular fringes are clearly observed in the nanoparticle with a spacing of 0.24 nm, whigh is the (311) interplanar distance of the cubic maghemite. This is in perfect agreement with the X-Ray Diffraction (XRD) results, indicating that the nanoparticles are well crystallyzed in spite of their ultrafine sized. The attachment of the dextran on the particle surface was confirmed by Fourier Transform Infrared (FTIR) Spectroscopy. The biocompatibility of maghemite nanoparticles covered by dextran with HepG2 cells was checked by MTT test. Cell viability was > 98% when the iron concentration was 12.0 mu g iron/ml and 24.0 mu g iron/ml respectively. In conclusion, these nanoparticles presented a good biocompatibility with HepG2 cells, which was proportionally with the dilution level.

This paper presents a study of two copolymers, maleic anhydride and methylmethacrilate/maleic anhydride and vinyl benzyl chloride, functionalised with polar chromophoric groups such as 2,4 dinitroaniline. Thin films have been prepared by vacuum evaporation and spin coating methods on silicon and glass substrates. UV-VIS, FTIR, XRD and Photoluminescence Spectroscopy have been used to comparatively investigate the effect of the preparation method on the properties of the thin films obtained with functionalized copolymer. SEM has evidenced differences in the morphologies of the layers suggesting a degradation of the polymeric chain during the evaporation process to fragments that conserve unchanged the chromophoric group. This explains the presence of two types of non-linear phenomena, the second harmonic emission and two-photon luminescence emissions for both vacuum evaporated and spin coated films.

Tl+-doped lithium fluoride crystals exhibit very interesting properties concerning the formation of colour centres after X-rays irradiation. The presence of Tl+ ions, even in small concentrations, increases the number of traps which stabilize the H-centre aggregates. These H-centre aggregates become smaller and their number increases, inducing two sets of trapping levels. Photoluminescence measurements after subsequent thermal bleaching of the thermoluminescence peaks show a faster decreasing of the F-3(+) centres, in three steps, compared with the F-2 ones. The F-H recombination processes may induce the excitation-emission transitions of Tl+-ions.

Sucrose is a natural osmolyte accumulated in cells of organisms as they adapt to environmental stress. In vitro sucrose increases protein stability and forces partially unfolded structures to refold. Thin films of sucrose (C12H22O11) were deposited on thin cut glass substrates by thermal evaporation technique (p similar to 10(-5) torr). Characteristics of thin films were putted into evidence by Fourier Transform Infrared Spectroscopy (FTIR), scanning electron microscopy (SEM) and differential thermal analysis and thermal gravimetric analysis (TG/DTA). The experimental results confirm a uniform deposition of an adherent layer.

Single-crystals of potassium hydrogen phthalate (KAP) doped with coumarin 6 (C6) were grown by solution evaporation technique. Powder X-ray diffraction. optical transmission and luminescence measurements were performed. The structure and morphology of the KAP crystals are not changed with the incorporation of the dye. Transparency of the dye-doped crystals is suited for non-linear optical (NLO) applications and UV cut-off is not changed when compared with the pure KAP crystals. The dye-doped crystals present an absorption band at 350 nm while the growth solution exhibits a peak at 400 nm. The doped crystals have a strong emission band at 450 nm that is excited at 350 nm and the second harmonic generating (SHG) properties are demonstrated using luminescence measurements. (C) 2009 Elsevier B.V. All rights reserved.

Crystals of potassium acid phthalate (KAP) doped with rhodamine 6G (Rh 6G) were grown by slow evaporation method from aqueous solutions. Crystals of good optical quality suitable for optical applications were obtained. Different concentrations of rhodamine 6G (10(-5) M, 2x10(-5) M, 5x10(-5) M and 10(-4) M in the growth solutions) were used in order to tune the optical properties of the crystals. Depending of the dye concentration, the absorption spectra of the dye-doped crystals show several bands in the range between 360 nm and 526 nm. The photoluminescence of the KAP crystals induced by the dye-doping reveals two emission bands peaking at 540 nm and 560 nm.

Glass-ceramics of the compositions Bi(4)Ge(3)O(12) (BGO) and Bi(2)O(3)-GeO(2) have been obtained by pouring molten materials onto graphite plates heated below and above the glass transition temperatures. Glass transitions temperatures have been measured by DSC. T(g) is lower in the case of BGO than with the Bi(2)O(3)-GeO(2) glass ceramics material. Crystallization is evaluated by X-ray diffraction and microscopic observations. The XRD measurements confirm the amorphous structure of the samples cast below T(g). The Hruby factor, which measures the stability of the glass-ceramics, is about 0.21 in the case of BGO glass ceramics suggesting a rather stable glass. The fluorescence under U.V. excitation is larger by one order of magnitude in the case of BGO glass-ceramics by comparison to the Bi(2)O(3)-GeO(2) glasses, suggesting it is a good candidate for scintillation materials. The images obtained under U.V. excitation shows structured luminescent centers in the case of BGO glass-ceramics. (C) 2009 Elsevier B.V. All rights reserved.