Asbestos is a widely used name for natural silicate minerals with fibrous properties. Asbestos minerals were one of the most popular and cheapest raw materials used in the construction industry in the past when they was used in the form of cement–asbestos composite material. Nowadays, we know that asbestos possesses carcinogenic properties. Due to this fact, asbestos was banned in many countries including Lithuania. All asbestos-containing materials are considered waste and stored in special landfills, which causes significant environmental pollution. One of the methods proposed to solve the asbestos problem may be thermal treatment. In the present study, asbestos-containing wastes in the form of cement–asbestos materials were examined. These asbestos-containing materials were characterised via chemical analysis (XRF) connected with mineralogical phase analysis with powder X-ray diffraction (XRD) as well as scanning electron microscopy (SEM). The thermal decomposition of samples was studied via differential thermal analysis (DTA) and thermogravimetric measurements with evolved gas analysis (TG–EGA). It was found that thermal treatment is a possible way to destroy asbestos contained in cement–asbestos wastes and convert it into new mineral phases. The work also compared the obtained characteristics of asbestos waste with the characteristics of waste produced in other countries.

The objective of this research was to develop a surface modification for the NiTi shape memory alloy, thereby enabling its long-term application in implant medicine. This was achieved through the creation of innovative multifunctional hybrid layers comprising a nanometric molecular system of silver-rutile (Ag-TiO₂), known for its antibacterial properties, in conjunction with bioactive submicro- and nanosized hydroxyapatite (HAp). The multifunctional, continuous, crack-free coatings were produced using the electrophoretic deposition method (EPD) at 20 V/1 min. Structural and morphological analyses through Raman spectrometry and scanning electron microscopy (SEM) provided comprehensive insights into the obtained coating. The silver within the layer existed in the form of nanometric silver carbonates (Ag₂CO₃) and metallic nanosilver. Based on DTA/TG results, dilatometric measurements, and high-temperature microscopy, the heat treatment temperature for the deposited layers was set at 800 °C for 2 h. The procedures applied resulted in the creation of a new generation of materials with a distinct structure compared with the initial nanopowders. The resulting composite layer, measuring 2 μm in thickness, comprised hydroxyapatite (HAp), apatite carbonate (CHAp), metallic silver, silver oxides, Ag@C, and rutile exhibiting a defective structure. This structural characteristic contributes significantly to its heightened activity, influencing both bioactivity and biocompatibility properties.

Growing requirements in the field of environmental protection and waste management result in the need to search for new and effective methods of recycling various types of waste. From the perspective of technical and natural sciences, the disposal of hazardous waste, which can lead to environmental degradation, is of utmost importance. A particularly hazardous waste is asbestos, used until recently in many branches of the economy and industry. Despite the ban on the production and use of asbestos introduced in many countries, products containing it are still present in the environment and pose a real threat. This paper presents the results of research related to the process of asbestos neutralization, especially the chrysotile variety, by the thermal decomposition method. Changes in the mineralogical characteristics of asbestos waste were studied using the following methods: TG-DTA-EGA, XRD, SEM-EDS and XRF. The characteristics of the chrysotile asbestos sample were determined before and after thermal treatment at selected temperatures. The second part of the study focuses on the kinetic aspect of this process, where the chrysotile thermal decomposition process was measured by two techniques: ex situ and in situ. This study showed that the chrysotile structure collapsed at approximately 600–800 °C through dehydroxylation, and then the fibrous chrysotile asbestos was transformed into new mineral phases, such as forsterite and enstatite. The formation of forsterite was observed at temperatures below 1000 °C, while enstatite was created above this temperature. From the kinetic point of view, the chrysotile thermal decomposition process could be described by the Avrami–Erofeev model, and the calculated activation energy values were ~180 kJ mol⁻¹ and ~220 kJ mol⁻¹ for ex situ and in situ processes, respectively. The obtained results indicate that the thermal method can be successfully used to detoxify hazardous chrysotile asbestos fibers.

Calcium sulphoaluminate cement (CSA) is characterized by a different chemical and mineralogical composition than common cements based mainly on Portland clinker. Its main component is ye’elimite—Ca₄(AlO₂)₆SO₄. This cement is characterized by a shorter setting time and a dynamic increase in strength in the early aging process. Currently, CSA cements are gaining more and more popularity due to their favorable ecological aspects, including a reduction in carbon dioxide emissions and negative impacts on the environment. The aim of the study was to determine the possibility of obtaining ye’elimite from waste materials of anthropogenic origin, which in this case were by-products from the aluminum anodizing process and cement–asbestos waste. The results of this preliminary research indicated the possibility of obtaining ye’elimite from secondary raw materials of anthropogenic origin. In each material, the phase of ye’elimite was identified to be the main mineral component, and the obtained materials displayed binding properties after mixing with water.

The present paper investigates high-temperature sulphate corrosion of basic refractory ceramics containing magnesium spinels (MgAl2O4, MgFe2O4, MgCr2O4 and their solid solutions) widely used in metallurgy, chemical, ceramic and glass industry. This group of refractories are exposed to a number of destructive factors during a working campaign. One of such factors is gas corrosion caused by sulphur oxides. However, gas sulphate corrosion of basic refractory materials containing magnesium spinels, which has a great practical meaning for the corrosion resistance of the material main components, is not sufficiently examined. This work presents a thermodynamic analysis of (MgCr2O4, MgAl2O4, MgFe2O4)−SO2−O2−SO3 system aimed to calculate: i) the standard free enthalpy of chemical reactions, ii) the equilibrium composition of the gas mixture initially containing SO2 and O2 and iii) sulphates equilibrium dissociation pressure and equilibrium partial pressure for the reaction of SO3 with the spinels to predict the temperature range of corrosion products’ stability. A thermochemical calculation provides information about equilibrium state in the analysed system. In real conditions the state of equilibrium does not have to be achieved. For this reason, the results of calculations were compared with experimental data. The experiment results were consistent with the theoretical predictions.

To functionalize the surface of the NiTi alloy, hybrid layers comprising nanometric silica and titanium oxides were synthesized. The TiO₂–SiO₂ nanosystem was chemically prepared and utilized for electrophoretic deposition (EPD) to create multifunctional layers on the alloy surface. The impact of pH on Zeta potential and ceramic particle size was explored to ensure a stable colloidal suspension for EPD, with optimal parameters established at a pH of approximately 6. A uniform layer was formed by applying a voltage of 40 V for 3 min, appearing as a thin film interspersed with regularly spaced larger agglomerates. The thin film primarily consisted of a minor fraction of defective rutile nanoparticles, accompanied by silica and carbon agglomerates from the nanosystem synthesis process. Heat treatment at 800 °C for 2 h induced significant structural changes, developing a novel-generation material with a different structure. An interlayer with strong Si–O–Ti connections was formed. Moreover, the mechanism of layer formation was extensively discussed.