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Native and acetylated B-starch was used in biodegradable films after blending with either poly-(ε-caprolactone) (PCL) or ethylene vinyl acetate copolymer (EVA). The following mechanical characteristics of prepared films were derived from the stress-strain curves: Young modulus, yield stress, stress-at-break and strain-at-break. Acetylation of starch molecules in the composites reduced the degradation rate in compost. Optical microscopy, combined with the image analysis system NIS-Elements completed with extended depth of focus (EDF) module, was used to study the PCL/starch and EVA/starch films surface morphology during composting. Parameters of the compost used for film exposition were measured.

Three mechanically alloyed (MA) and spark plasma sintered (SPS) CoCrFeNiNbX (X = 5, 20, and 35 at.%) alloys with an addition of 5 at.% of SiC were investigated. The face-centered cubic (FCC) high-entropy solid solution, NbC carbides, and hexagonal Laves phase already developed during MA. In addition, the SPS compacting led to the formation of oxide particles in all alloys, and the Cr 7 C 3 carbides in the Nb5 alloy. The fraction of the FCC solid solution decreased with increasing Nb concentration at the expense of the NbC carbide and the Laves phase. Long-term annealing at 800 °C led to the disappearance of the Cr 7 C 3 carbide in the Nb5 alloy, and new oxides-Ni 6 Nb 6 O, Cr 2 O 3 , and CrNbO 4 -were formed. At laboratory temperature, the Nb5 alloy, containing only the FCC matrix and carbide particles, was relatively strong and very ductile. At a higher Nb content (Nb20 and Nb35), the alloys became brittle. After annealing for 100 h at 800 °C, the Nb5 alloy conserved its plasticity and the Nb20 and Nb35 alloys maintained or even increased their brittleness. When tested at 800 °C, the Nb5 and Nb20 alloys deformed almost identically (CYS ~450 MPa, UTS ~500 MPa, plasticity ~18%), whereas the Nb35 alloy was much stronger (CYS of 1695 MPa, UCS of 1817 MPa) and preserved comparable plasticity.

A new severe plastic deformation technique, known as the complex shearing of extruded tube (CSET), was applied to a 3003 based model aluminium alloy. This technique, consisting of a combination of extrusion and two consecutive Equal Chanel Angular Pressing (ECAP) passes accompanied with concurrent torsional straining, is capable to produce a fine-grained tubular sample directly from a bulk metallic cylinder in one forming operation. In the present paper, the microstructural development of the alloy during partial processes of CSET was studied in detail using light microscopy, electron backscatter diffraction, and transmission electron microscopy. It was found that CSET technique refines the grain size down to 0.4 µm and, consequently, increases the microhardness from the initial value of 40 HV to the final value of 120 HV. The contributions of partial processes of CSET to the total strain were estimated.

The main aim of this study was to determine the susceptibility of the additively manufactured high strength X3NiCoMoTi 18-9-5 maraging steel to hydrogen embrittlement. For this purpose, samples produced by selective laser melting technology, before and after heat treatment, were used. The examined samples were electrochemically charged with hydrogen in NaCl + NH 4 SCN solution at a current density of 50 mA/cm 2 for 24 h. The H content increased from about 1 to 15 ppm. Heat treatment did not affect the amount of H trapped in the maraging steel. Tensile testing revealed that the tensile strength of the H-charged samples was much lower than that of the uncharged samples. Moreover, the material became brittle after charging compared to the ductile as-printed and heat-treated samples with elongation values of 7% and 2%, respectively. The loss of plasticity was confirmed by fractography, which revealed transformation of the fracture surface morphology from dimple-like in the as-produced state to a brittle one with smooth facets in the H-charged state.