Preparation and characterization of novel bioactive α-Tricalcium Phosphate doped with Dicalcium Silicate ceramics

This work describes the evaluation of pure α-Tricalcium Phosphate (TCP) and silica containing TCP ceramics in the system Dicalcium Silicate–Tricalcium Phosphate (C₂S–TCP) as a potential substrate for bone tissue engineering. The ceramics were soaked in dynamic simulated body fluid (SBF) for 2 weeks and characterized by SEM-WDS, XRD, and TEM analysis, and the results indicated that a carbonated hydroxyapatite (CHA) was formed on the surface of the ceramics. In addition, cell attachment assay showed that the ceramics supported the adult mesenchymal stem cells of human origin (hMSCs-A) adhesion and spreading, and the cells established close contacts with the ceramics after 24 h of culture. Also, cellular assays have shown a greater ability of hMSCs-A to express markers of the osteoblast phenotype (ALP, Col I, OC) in the C₂S doped α-TCP ceramics, indicating osteoblastic differentiation as a result of the increased concentration of silicon in solid solution in α-TCP. These findings indicate that the C₂S doped α-TCP ceramics possess good bioactivity, and biocompatibility, and might be promising for bone implant material.     

Flexible diamond-like carbon films on rubber: Friction and the effect of viscoelastic deformation of rubber substrates

This paper focuses on the frictional behavior of flexible diamond-like carbon (DLC) film-coated hydrogenated nitrile butadiene rubber. By making use of the substantial thermal mismatch between DLC film and rubber substrate, a dense network of cracks forms in the DLC films and contributes to flexibility. The influence of the size of DLC film microsegments on the frictional performance is studied. The effect of viscoelasticity of the rubber substrate on the frictional behavior of the DLC film-coated system is scrutinized by tribo-tests and theoretical analysis. The importance of adhesive and hysteresis contributions to friction is revealed, and an overarching model is presented.     

Preparation and characterization of conductive polypyrrole/kaolinite composites

Conductive polypyrrole (PPy)/kaolinite clay composites were prepared by in situ chemical polymerization of pyrrole in the presence of kaolinite using FeCl₃ as oxidant. The PPy content and conductivity of the composites reached 32.8% and 8.3×10^?2 S/cm at HCl concentrations of 1.5 M and 0.5 M, respectively. The microhardness of the composites containing different amounts of PPy was higher than that of the PPy and kaolinite components. The highest microhardness observed was 30.17 kg/mm² for the composite containing 9.6% PPy. The electrical resistance of the composites was monitored during heating–cooling cycles over the range 5–120 °C. The change in resistance with temperature was more repeatable for the composite than for PPy. The composites were characterized by Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA) and scanning electron microscopy (SEM). The humidity-sensing properties were also examined.     

Kalman filtering with constrained output injection

In applications involving large scale systems such as discretized partial differential equations, it is often of interest to use data to estimate state variables associated with a subregion of the spatial domain. In this paper we derive an extension of the classical Kalman filter in which data injection is confined to a subspace of the system states.     

Synthesis of Nickel Phosphide Nanorods as Catalyst for the Hydrotreating of Methyl Oleate

Arrays of nickel phosphide nanorods were successfully synthesized by nanocasting using mesostructured silica SBA-15 as a hard template (HT-Ni₂P). After temperature-programmed reduction of the phosphate precursor infiltrated within the pore walls of SBA-15, the unsupported material was obtained by removing the silica matrix with diluted HF. The pore channel of the SBA-15 template stabilizes the Ni₂P particles, preventing sintering after the high reduction temperature and shaping their elongated morphology. Moreover, HT-Ni₂P catalyst shows an improvement in the textural properties with a significantly higher surface area than the reference sample synthesized in the absence of template. X-ray diffraction revealed that the only crystalline phase present in this material was Ni₂P. On the other hand, transmission electron microscopy shows that the catalyst is mainly constituted by agglomerates of nanorods. Through EDX microanalysis the efficient removal of silicon was confirmed. Under hydrotreating conditions, nanorods of Ni₂P show a fourfold enhancement in the conversion of methyl oleate with respect to conventional Ni₂P synthesized in absence of hard template. Nevertheless, when these data are normalized to surface area, the specific activity of HT-Ni₂P nanorods is significantly lower than that of the conventionally prepared sample. Differences in selectivity were also observed as Ni₂P nanorods favored the decarboxylation reaction leading to a higher yield of n-heptadecane.     

Comparative study between large-scale and small-scale electrochemical potentiokinetic reactivation performed on AISI 316L austenitic stainless steel

This work optimizes the application of electrochemical potentiokinetic reactivation (EPR) to assess the degree of sensitization (DOS) of AISI 316L and compares the large-scale and small-scale EPR with the aim of improving the study of the different zones of AISI 316L welded joints by using an electrochemical minicell. The optimized EPR allows to discriminate better than the standardized EPR among different DOS. Small-scale EPR shows greater sensitivity to assess the DOS than large-scale EPR: (i) at lower deformation levels; (ii) for shorter sensitization times; (iii) when localized microstructural regeneration is caused by the combined effect of deformation and subsequent sensitization.     

Stability Studies of Ozonized Sunflower Oil and Enriched Cosmetics with a Dedicated Peroxide Value Determination

Ozonized oils have interesting applications in the cosmetic industry and several patents on enriched products were developed in the last years. Ozonides are known for their high reactivity and stability data are required for enriched cosmetic products during storage. In this paper a dedicated determination of Peroxide Value (PV) was performed on ozonized sunflower oil (Neozone 4000) and on some enriched cosmetics, in order to control their stability during storage. The optimal conditions of the PV method were determined, following the decomposition reaction of ozonides with KI utilizing ¹H-NMR and GC/MS techniques.