The aim of this study has been the preparation of dental implants with potential antibacterial properties. Bioactive\ud glasses containing different percentages of silver have been synthesized via the sol–gel method and used to\ud coat titaniumimplants by means of a dip coating technique. The glasses obtained have the following general formula,\ud 70S30CxA,which is related to its composition (inmol%): 70% of SiO2 (S), 30% of CaO (C) and x% of Ag2O(A),\ud with 0.08 ≤ x ≤ 0.27. Fourier Transform Infrared (FTIR) spectroscopy and simultaneous thermogravimetry/differential\ud thermal analysis (TG/DTA) were used to characterize the materials. Scanning electron microscopy\ud (SEM) has been used to investigate the coating morphology. Moreover, the films obtained have been characterized\ud in order to verify their antibacterial activities aswell as their bioactivity and biocompatibility as a function of\ud Ag content. SEM/EDX analysis has shown that the films are bioactive because they are able to stimulate the hydroxyapatite\ud nucleation on their surface when soaked in a simulated body fluid (SBF).WST-8 assay on 3T3 cells\ud seeded on coated titaniumsubstrates has proved that the coatings don't induce cytotoxicity. However, the results\ud have shown that both the bioactivity and biocompatibility of coatings decrease slightly at high Ag contents. In\ud contrast, antibacterial activity of the films against the Staphylococcus aureus increases with an increase of the silver\ud amoun
Titanium biomaterials’ response has been recognized to be affected by particles size, crystal structure, and surface properties. Chemical and structural properties of these nanoparticle materials are important, but their size is the key aspect. The aim of this study is the synthesis of TiO2 nanoparticles by the sol-gel method, which is an ideal technique to prepare nanomaterials at low temperature. The heat treatment can affect the structure of the final product and consequently its biological properties. For this reason, the chemical structure of the TiO2 nanoparticles synthesized was investigated after each heat treatment, in order to evaluate the presence of different phases formed among the nanoparticles. FTIR spectroscopy and XRD have been used to evaluate the different structures. The results of these analyses suggest that an increase of the calcination temperature induces the formation of mixed-crystalline-phases with different content of anatase and rutile phases. The results obtained by SEM measurements suggest that an increase in the particles size accompanied by a noticeable aggregation of TiO2 nanoparticles is due to high temperatures achieved during the thermal treatments and confirmed the presence of different content of the two crystalline phases of titanium dioxide.
The vaporization behaviour and thermodynamics of the ionic liquid 1-butyl-3-methylimidazolium bis(trifluoromethyl)sulfonylimide (BMImNTf2) were studied by combining the Knudsen Effusion Mass Loss (KEML) and Knudsen Effusion Mass Spectrometry (KEMS) techniques. KEML studies were carried out in a large temperature range (398-567) K by using effusion orifices with 0.3, 1, and 3 mm diameters. The vapor pressures so measured revealed no kinetically hindered vaporization effects and provided second-law vaporization enthalpies at the mean experimental temperatures in close agreement with literature. By exploiting the large temperature range covered, the heat capacity change associated with vaporization was estimated, resulting in a value of -66.8 J K(-1) mol(-1), much lower than that predicted from calorimetric measurements on the liquid phase and theoretical calculations on the gas phase. The conversion of the high temperature vaporization enthalpy to 298 K was discussed and the value Δ(l)(g)H(m)(298 K) = (128.6 ± 1.3) kJ mol(-1) assessed on the basis of data from literature and present work. Vapor pressure data were also processed by the third-law procedure using different estimations for the auxiliary thermal functions, and a Δ(l)(g)H(m)(298 K) consistent with the assessed value was obtained, although the overall agreement is sensitive to the accuracy of heat capacity data. KEMS measurements were carried out in the lower temperature range (393-467) K and showed that the largely prevailing ion species is BMIm(+), supporting the common view of BMImNTf2 vaporizing as individual, neutral ion pairs also under equilibrium conditions. By monitoring the mass spectrometric signal of this ion as a function of temperature, a second-law Δ(l)(g)H(m)(298 K) of 129.4 ± 7.3 kJ mol(-1) was obtained, well consistent with KEML and literature results. Finally, by combining KEML and KEMS measurements, the electron impact ionization cross section of BMIm(+) was estimated.
In the present work bioactive powders of the ternary SiO 2 •CaO•P 2 O 5 systems, which differ in the Ca/P molar ratio, were synthesized by means of a sol-gel route, using tetraethyl orthosilicate (TEOS, Si(OC 2 H 5) 4), calcium nitrate tetrahydrate (Ca(NO 3) 2 •4H 2 O) and triethyl phosphate (TEP, OP(OC 2 H 5) 3) as precursors of SiO 2 , CaO and P 2 O 5 , respectively. In order to investigate the influence of the relative amount of each phase (in this study: SiO 2 , CaO and P 2 O 5) the thermal properties of the synthesized gel-glass materials were studied as a function of the Ca/P molar ratio using thermogravimetric and differential thermal analysis (TG/DTA). After dehydration (in a single step), described from a kinetic point of view as a simple water evaporation without rupture of chemical bonds, all gels undergo a complex multi-step decomposition with endo and exothermic effects, followed by crystallization of calcium silicate phases at about 950°C. Furthermore, Fourier Transform Infrared Spectroscopy (FTIR), X-ray diffraction (XRD) and Scanning Electron Microscopy, coupled with energy dispersive spectroscopy (SEM/EDS), allowed us to detect the chemical modifications induced by modifying the Ca/P molar ratio and the sintering. This process is obtained by thermal treatment of the gel-glass precursors after analyzing their thermal behavior in the temperature range 600-1000 °C, with the aim to convert them into ceramic powders, suitable for their applications. The results revealed that when temperature is up to 900 °C, crystallization occurs and pseudowollastonite and wollastonite were formed. Finally, the amount of pseudowollastonite decreased with increasing the sintering temperature, while that of wollastonite increased.
Pyrolysis seems a promising route for recycling of heterogeneous, contaminated and additives containing plastics from waste electrical and electronic equipment (WEEE). This study deals with the thermal and catalytic pyrolysis of a synthetic mixture containing real waste plastics, representative of polymers contained in small WEEE. Two zeolite-based catalysts were used at 400°C: HUSY and HZSM-5 with a high silica content, while three different temperatures were adopted for the thermal cracking: 400, 600 and 800°C. The mass balance showed that the oil produced by pyrolysis is always the main product regardless the process conditions selected, with yields ranging from 83% to 93%. A higher yield was obtained when pyrolysis was carried out with HZSM-5 at 400°C and without catalysts, but at 600 and 800°C. Formation of a significant amount of solid residue (about 13%) is observed using HUSY. The oily liquid product of pyrolysis, analysed by GC-MS and GC-FID, as well as by elemental analysis and for energy content, appeared lighter, less viscous and with a higher concentration of monoaromatics under catalytic condition, if compared to the liquid product derived from thermal degradation at the same temperature. HZSM-5 led to the production of a high yield of styrene (17.5%), while HUSY favoured the formation of ethylbenzene (15%). Energy released by combustion of the oil was around 39MJ/kg, thus suggesting the possibility to exploit it as a fuel, if the recovery of chemical compounds could not be realised. Elemental and proximate analysis of char and GC-TCD analysis of the gas were also performed. Finally, it was estimated to what extent these two products, showing a relevant ability to release energy, could fulfil the energy demand requested in pyrolysis.
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