The optimal process conditions concerning the hydrothermal carbonization of digested sewage sludge are crucial to the economically effective technology needed to produce a solid product, hydrochar, for energy purposes. Accordingly, different residence times, 0.5 h, 1 h and 2 h, were investigated in order to understand the effect of residence time on the process. Furthermore, the physical and chemical properties of hydrochar were investigated and compared to the raw material. For these reasons, analyses describing fuel properties were performed, including ultimate and proximate analyses, HHV, and TGA analysis. The latter method was employed to study the combustion process of solid samples. In addition, the oxide content of different elements within the ash of solid samples was determined using the XRF method to calculate indices related to operational problems during the combustion process. The results confirmed that time did not matter significantly and the physical and chemical properties of hydrochar were very similar to each other. However, the contact angle for 2 h of residence time confirmed that a longer processing time resulted in a more hydrophobic character of hydrochar and enabled more effective dewaterability of hydrothermal slurry. It was also noted that the hydrothermal carbonization process affected the sewage sludge in a positive way. In brief, the results confirmed that the hydrochar was a brittle, moderately hydrophilic, solid carbon-containing product that provided a different combustion performance than the raw sewage sludge.

One of the most popular polymeric materials in the building and construction industry is rigid polyurethane foam (RPUF). In order to reduce the number of expensive chemical components, various fillers are used in the RPUF industry. The aim of this work was to investigate the influence of the biomass originated filler soybean-husk-derived ash on the structure and properties of composite RPUF. Firstly, polyurethane foams were obtained using hand mixing and casting techniques. Composite foams contained 5, 10, 15, and 20 wt. % of the filler. Secondly, the obtained composite materials were analyzed considering their cellular structure using optical microscopy and image processing software. All samples were composed of mostly pentagonal, regular-in-shape cells. Their diameters ranged between 100 and 70 µm. The chemical structure of the foams was investigated using infrared spectroscopy. No chemical interactions between matrix and filler were detected. Mechanical testing was performed in order to evaluate the mechanical performance of the materials. Both compressive strength and Young’s modulus were comparable and equaled approx. 130 kPa and 2.5 MPa, respectively. Wettability analysis indicated a hydrophobic nature of the materials. The obtained results suggested that the cellular and chemical structure of the polyurethane matrix was not affected by the filler incorporation.

The purpose of the study was to investigate the electrophoretic deposition (EPD) route, microstructure and surface properties of composite curcumin/chitosan coatings on commercially pure titanium substrates for biomedical applications. Multiple routes of preparation of the dispersed systems for the EPD process and their electrokinetic properties have been investigated to obtain homogeneous coatings. The zeta potential of solutions with various curcumin content in ethanol or isopropanol proved their relatively low electrophoretic mobility. Thus, curcumin was co-deposited with chitosan molecules on the cathode. The surface morphology of the coatings consisted of submicrometric curcumin particles embedded in the chitosan matrix. The increase in the curcumin content in the ethanol caused large agglomerates and undissolved curcumin particles to appear on the coating surface. The coatings were characterized by high adhesion to the substrate and a water contact angle in the range of 85° to 95°. The coatings changed the zeta potential of the titanium surface from significantly negative (−46.7 ± 2.3 mV) to less negative values (−20.6 ± 2.6 mV). The developed coatings are promising for mitigating biofilm formation on the surface of titanium bone implants.

In this study, an Inconel 625–tungsten carbide (WC) composite system was investigated by means of microstructure changes affected by both heating rate and WC content. In order to investigate how the system behaves while exposed to fast thermal processing, controlled melting using a differential thermal analysis (DTA) apparatus was performed on the powders. Two WC powders with different average grain size were used to obtain six compositions of Inconel 625–WC powder mixtures (10, 20, and 30 wt.% WC). They were analyzed under 10 and 30 °C/min heating rate in order to obtain composite samples. Results from DTA together with SEM/energy-dispersive X-ray spectroscopy (EDS) microstructural observations allowed observing material changes during solidification. Because of the extensive microsegregation of alloying elements to liquid and their reactions with C, which derived from dissolved WC, the formation of secondary phases with improved microhardness was possible. The collected results provide a better understanding of material behavior during intensive thermal processing which can be useful when designing materials for the laser additive manufacturing technique.