National Institute Of Materials Physics - Romania

Macroporous polyacrylonitrile/hydroxyapatite (PAN/HAp) composite bead was studied for cadmium removal in a fixed-bed column. The morphology of PAN/HAp composite bead was measured. The adsorption performance of PAN/HAp composite bead in the column was examined by varying bed height and HAp amount in PAN bead. The maximum adsorption capacity and the exhaustion time were determined from the breakthrough curves. Experimental data was described using the Adams-Bohart model. Bed height did not exert large influence on the maximum adsorption capacity and the exhaustion time. The kinetic rate constant and the adsorption capacity of the bed were found to be affected by the total HAp amount.

Due to their physical and chemical properties (such as suitable band gaps, large absorption coefficients and good chemical stability) CdTe thin films are interesting for electronic and optoelectronic devices, including particularly photovoltaic cells for space technology. For that specific application, it is of prime importance to study in this type of materials the influence of ionizing radiations on their physical (structural, electrical and optical) properties. In this paper, the photovoltaic cells based on CdS/CdTe thin films, produced by thermal vacuum sublimation, were irradiated with 3 MeV protons at room temperature. The effects of irradiation were studied by investigating the changes in the electrical and optical properties of the cells. It was found that proton irradiation in the above mentioned conditions results mainly in the introduction of defects at the CdS/CdTe interface. A discussion about the possible origin of those defects is given.

In the first part of this study it has shown that the interaction between collagenous polypeptides (collagen type I with native structure of triple helix and collagen hydrolyzates with no significant secondary structure) and ionic surfactants (sodium dodecyl sulfate and hexadecyl trimethylammonium bromide) involves the formation of micelle-like clusters of ionic surfactant adsorbed onto polypeptide backbone (polypeptide-surfactant complexes) at surfactant concentrations much lower than its cmc. The present investigation is focused on the influence of polypeptide-ionic surfactant complexation on thermal denaturation of the collagen type I extracted from calfskin and young horse tendons. On the basis of capillary viscometry, a good correlation between denaturation temperatures and activation energies of viscous flow for the dilute aqueous collagen-ionic surfactant solutions at pH 2.5 and 8.0 has been found. Beginning from that, it has established that the presence of ionic surfactant reduces thermal stability of the two collagens, with a more pronounced effect in the case of sodium dodecyl sulfate. Accordingly, it has been proposed a thermal denaturation mechanism of the collagen triple helix in the presence of ionic surfactants.

Langmuir films and Langmuir-Blodgett multilayers based on fatty acid (stearic acid, barium stearate) mixed with carbon nanotubes have been prepared and investigated by isothermal compression (for Langmuir films) and X-ray diffraction (for Langmuir-Blodgett multilayers). An irreversible modification has been observed in the case of Langmuir films doped by carbon nanotubes, due to reordering of the nanotubes in the film matrix.

We have studied the growth of ZnSe crystals by chemical transport in a closed system in nonstoichiometric conditions, and we have deduced that the interface kinetics is the phenomenon limiting the growth process. The effect on the growth process of the deviation from stoichiometry of the II-VI compound was investigated using a mathematical model that involves indirect data computed from directly obtained experimental values. The experimental crystallization rate was compared with the maximum value of the transport flux calculated using the Arizumi-Nishinaga model. The influence of the stoichiometry of the source material and of the variations in the growth parameters (supercooling, geometrical dimension, specific loading of the ampoule and iodine concentration) on the ZnSe crystal growth process has also been studied. (C) 2010 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

The synthesis of a new hybrid composite based on PUS nanoparticles and poly( methyl methacrylate-2acrylamido-2-methylpropane sulfonic acid) [P(MMA-AMPSA)] copolymer is reported. The chemical synthesis consists in two steps: (i) a surfactant-free emulsion copolymerization between methyl methacrylate and 2-acrylamido-2-methylpropane sulfonic acid and (ii) the generation of PbS particles in the presence of the P( MMA-AMPSA) latex, from the reaction between lead nitrate and thiourea. The composite was studied by scanning electron microscopy (SEM), X-ray diffraction, FTIR spectroscopy, thermogravimetric analysis and differential scanning calorimetry. The microstructure observed using SEM proves that the PbS nanoparticles are well dispersed in the copolymer matrix. The X-ray diffraction measurements demonstrate that the PbS nanoparticles have a cubic rock salt structure. It was also found that the inorganic semiconductor nanoparticles improve the thermal stability of the copolymer matrix. (C) 2010 Elsevier Ltd. All rights reserved.

Oxyfluoride glass samples in the system SiO2-Al2O3-CaF2-SmF3 were produced by using the melt-quenched technique and the kinetics of non-isothermal crystallization of CaF2 nano-crystals has been investigated. Differential thermal analysis (DTA) has shown an exothermic peak at about 700 degrees C which was assigned to the CaF2 nano-crystals precipitation within the glass matrix as was identified by X-ray diffraction (XRD) analysis of the annealed glass samples. It was shown the Ozawa model is most suitable for describing the behaviour of non-isothermal crystallization of CaF2 nano-crystals within the glass matrix. The mean value of the Avrami exponent was found 1.16 which indicates the diffusion-controlled growth process of nano-particles in the glass system with zero nucleation rate as the single operative mechanism; the activation energy of the crystallization is E-d = 379 +/- 25 kJ/mol (3.93 +/- 0.26 eV). The activation energy of the nano-crystals growth was computed within the same model and agrees very well with the activation energy of the crystallization. (C) 2010 Elsevier B.V. All rights reserved.

A special mechanism of thermoelectric transport is described, consisting of pulses of charge carriers which "fly" periodically through the external circuit from the hot end of the sample to the cold end, with a determined duration of the "on" and "off" times of the electric contacts, while maintaining continuously the thermal contacts. It is shown that such a "resonant" ideal thermogenerator may work cyclically, with the same efficiency quotient as the ideal efficiency quotient of the thermoelectric devices operated in the usual stationary transport regime but the electric flow and power are increased, as a consequence of the concentration of the charge carriers on pulses of small spatial extent. The process is reversible, in the sense that it can be operated either as a thermoelectric generator or as an electrothermal cooler. (C) 2010 American Institute of Physics. [doi: 10.1063/1.3456037]

Electron states at the SiO2/4H-SiC interface have been investigated using capacitor structures and especially, the influence of excess nitrogen, introduced by ion implantation, at the interface is studied in detail. Implanted and nonimplanted n-type samples with an interfacial concentration of nitrogen of similar to 10(19) cm(-3) and 10(16) cm(-3), respectively, were analyzed by capacitance-voltage (C-V) measurements, performed at different temperatures and probe frequencies, and thermal dielectric relaxation current (TDRC) measurements performed in the temperature range of 35-295 K. Three main categories of electron states are disclosed, true interface states (D-it), fast near interface states (NIToxfast) and slow near interface states (NIToxslow). The density versus energy distributions of D-it and NIToxfast have been deduced from the TDRC data and they are shown to give a close quantitative agreement with the shape and frequency dependence of the C-V curves. Further, the amount of NIToxslow extracted from TDRC is demonstrated to be responsible for the parallel shifts and hysterezis effects occurring in the C-V characteristics. All three categories of electron states are reduced in concentration in the implanted samples. This holds particularly for NIToxfast with a peak at similar to 0.1 eV below the conduction band edge of 4H-SiC that is suppressed by at least two orders of magnitude relative to the nonimplanted samples. The decrease for D-it is also substantial (a factor of similar to 10) while the loss for NIToxslow is considerably smaller (only similar to 30%). The results provide firm evidence that NIToxfast and NIToxslow do not originate from the same kind of defect center. (C) 2010 American Institute of Physics. [doi:10.1063/1.3457906]