The SiO2 thin films were deposited on the surfaces of stainless steel/ NiTi tapes and their activity was particularly investigated from the aspect of the number density of hydroxyl groups on their surfaces. The calculation procedure of density of active OH groups includes determination of average length of silica chains that constitute silica sol particles with almost uniform size, on the base of TGA analysis. The size of SiO2 particles is analyzed by TEM microscopy and dynamic light scattering method. Fibroblast (L929) cell densities on the surfaces of these films were investigated using phase contrast microcopy. It was shown that there is a relationship between OH group densities and density of attached cells. Besides, the cytotoxicity effect was studied and compared for various thermally treated SiO2 thin films.
COBISS.SI-ID: 16965910
Practically all metals and alloys survive high-temperature exposure by growing oxide scales and/or by precipitation of the oxide particles in the matrix. Formed products can grow in shape of external oxide layers on surfaces, or as discrete oxide particles precipitated in a metal matrix. The first case represents external oxidation, and the other case is called internal oxidation. These processes are very important, because they determine the properties and applicability of metallic materials. Generally, they are undesired, because they cause deterioration of the mechanical properties and decomposition of metallic material. On the other side, the controlled process of external oxidation could be used for formation of protective coatings and the internal oxidation for dispersion strengthening of materials. In this paper we present monitoring of hightemperature oxidation of X12Cr13 stainless steel by in-situ electrical resistance measurements at different annealing temperatures in the air atmosphere. We determined the kinetics of oxide scale formation and its morphology with additional metallographic examination made by optical and scanning electron microscopy. The results of this research work show that in-situ monitoring and characterization of high-temperature oxidation present a strong tool that will contribute to a better fundamental understanding of the phenomena that occur during high-temperature oxidation of metallic materials.
COBISS.SI-ID: 17032214
In this paper we focus on the preparation and mechanical properties of the nanosilica-reinforced, epoxy resin Epikote 828LVEL. Epoxy composites containing two sizes of spherical silica nanoparticles, 130 nm and 30 nm, were prepared at a fixed volume fraction (VP = 0.5%). To prevent agglomeration, the silica fillers were initially pre-treated with diglycidyl ether of bisphenol A (BADGE). Due to the low content of silica fillers, their inclusion in the matrix was confirmed by the increased roughness of a fracture surface compared to the smooth surface of the neat epoxy. Raman spectroscopy was employed to obtain additional information about the crack-propagation path. The mechanical properties, characterized by a three-point bending test, revealed a 10-20% increase in the composite's modulus of elasticity with 30-nm and 130-nm silica-filler inclusions. Elongation at break, on the other hand, decreased for 5-10% in both composites compared to neat epoxy, suggesting brittle fracture behavior in silica/epoxy composites. The fracture toughness results showed a 25-30% improved toughening for both composites compared to the pure epoxy. The composite's resistance to failure in terms of the impact energy was, however, strongly dependent on the size of the silica: we observed a 30% increase for the 130-nm, and a 60% increase for the 30-nm, silica/epoxy composites, compared to the pure epoxy.
COBISS.SI-ID: 5124634