This study investigates the pyrolysis behavior and reaction kinetics of two different types of solid digestates from: (i) sewage sludge and (ii) a mixture of sewage sludge and lignocellulosic biomass—Typha latifolia plant. Thermogravimetric data in the temperature range 25–800 °C were analyzed using Flynn–Wall–Ozawa and Kissinger–Akahira–Sunose kinetic methods, and the thermodynamic parameters ($\mathsf{\Delta }H$, $\mathsf{\Delta }G$, and $\mathsf{\Delta }S$) were also determined. Biochars were characterized using different chemical methods (FTIR, SEM–EDS, XRD, heavy metal, and nutrient analysis) and tested as soil enhancers using a germination test. Finally, their potential for biosorption of NH₄⁺, PO₄³⁻, Cu²⁺, and Cd²⁺ ions was studied. Kinetic and thermodynamic parameters revealed a complex degradation mechanism of digestates, as they showed higher activation energies than undigested materials. Values for sewage sludge digestate were between 57 and 351 kJ/mol, and for digestate composed of sewage sludge and T. latifolia between 62 and 401 kJ/mol. Characterizations of biochars revealed high nutrient content and promising potential for further use. The advantage of biochar obtained from a digestate mixture of sewage sludge and lignocellulosic biomass is the lower content of heavy metals. Biosorption tests showed low biosorption capacity of digestate-derived biochars and their modifications for NH₄⁺ and PO₄³⁻ ions, but high biosorption capacity for Cu²⁺ and Cd²⁺ ions. Modification with KOH was more efficient than modification with HCl. The digestate-derived biochars exhibited excellent performance in germination tests, especially at concentrations between 6 and 10 wt.%.

The main objective of this review is to present the latest research results regarding the importance of the torrefaction process for different biomass materials in the last 12-year period. Despite the fact that the potential of renewable energy sources has been analyzed, research regarding that of energy derived from waste biomass still remains in the infancy state. Torrefaction is known to be one of the most effective methods for enhancing the energy efficiency of biomass. Among different types of torrefactions, the focus in this study is mostly on dry torrefaction. The influential factors, like temperature and residence time, and physico-chemical properties of torrefied products, and the prospective of torrefaction due to its reduced impact on environment, are discussed in-depth. This review provides valuable insights into the torrefaction process, which is conducive to upgrading biomass for achieving net zero carbon emissions, as it has been stated in several works that torrefied biomass can be used instead of coal.

The aim of this work was to purify mixed wastewater from three different production processes in such a manner that they could be reused as process water. The maximum allowed concentrations (MAC) from the Environmental Standards for emissions of substances released into surface water were set as target concentrations. Wastewaters contained solid particles, sodium, aluminium, chloride, and nitrogen in high amounts. Quantitatively, most wastewaters were generated in the production line of alumina washing. The second type of wastewater was generated from the production line of boehmite. The third type of wastewater was from regeneration of ion exchangers, which are applied for feed boiler water treatment. The initial treatment step of wastewater mixture was neutralisation, using 35% HCl. The precoat filtration followed, and the level of suspended solids was reduced from 320 mg/L to only 9 mg/L. The concentrations of ions, such as aluminium, sodium and chlorides remained above the MAC. Therefore, laboratory reverse osmosis was applied to remove the listed pollutants from the water. We succeeded in removal of all the pollutants. The concentration of aluminium decreased below 3 mg/L, the sodium to 145 mg/L and chlorides to 193 mg/L. The concentration of nitrate nitrogen decreased below 20 mg/L.

In this study, three locally available biomasses, namely miscanthus, hops, sewage sludge, and additionally, their mixtures, were subjected to the torrefaction process to improve their fuel properties. The torrefaction process was conducted at 250–350 °C and 10–60 min in a nitrogen (N₂) environment. The torrefaction temperature and time were studied to evaluate the selected biomass materials; furthermore, heating values, mass and energy yields, enhancement factors, torrefaction severity indexes (TSI), and energy-mass co-benefit indexes (EMCI) were calculated. In addition, thermogravimetric (TGA) and Fourier transform infrared analyses (FTIR) were performed to characterize raw and torrefied biomass under the most stringent conditions (350 °C and 60 min). The results showed that with increasing torrefaction temperature and duration, mass and energy yields decreased, and heating values (HHVs) increased for all studied biomasses. The results of the TSI and EMCI indexes showed that the optimum torrefaction conditions were as follows: 260 °C and 10 min for pure miscanthus and hops, whilst this could not be confirmed for the sewage sludge. Furthermore, the combination of sewage sludge and the above-mentioned types of lignocellulosic biomass exhibited better fuel properties than sewage sludge alone.

In this paper, the aim of the research was to obtain a highly efficient wool-based sorbent for the removal of zinc Zn(II) from wastewater. To increase the functional groups for metal binding, the wool was functionalized with chitosan. Chitosan has amino groups through which metals can be complexed easily to chelates. The physical and chemical modification of chitosan on wool was performed to analyze the influence of the coating bond on the final ability of the wool to remove metals. The presence of functional chitosan groups onto wool after adsorption was verified by attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FT-IR) spectra. The effective binding of chitosan to wool was also determined by potentiometric and polyelectrolyte titration methods. The latter titration was used to analyze the chitosan desorption. The main part of the study was the sorption of Zn(II) on natural and functionalized wool. The influence was investigated as a function of contact time, pH, metal ion concentration and temperature on the sorption process. The absorbent with the highest concentration of protonated amino groups (607.7 mmol/kg) and responding sorption capacity of 1.52 mg/g was obtained with wool physically modified by a macromolecular chitosan solution (1%) at pH = 7. Adsorption of Zn(II) onto pristine and modified wool corresponded to pseudo-second order kinetics (R² > 0.9884). The Langmuir model was found to be more suitable (R² > 0.9866) in comparison to the Freundlich model. The Zn(II) sorption process was spontaneous (∆G < 0) and exothermic (∆H < 0). The results found in this study are significant for escalating the possible use of wool modified with polysaccharide coatings as a sustainable source to improve or increase the metal sorption activity of wool.