Jan Hajzler

This study investigated carbonaceous materials prepared from Paulownia tomentosa leaves by hydrothermal carbonization, slow pyrolysis, and HCl post-treatment for the adsorption of metribuzin and tebuconazole from water. Hydrochars were prepared at 180–220 °C, pyrochars at 400–600 °C, and the pyrochar produced at 600 °C was further treated with HCl. The materials were characterized by yield, ash content, active and exchangeable pH, oxidizable organic carbon content, FTIR, SEM, and CO₂-derived surface and pore properties. Increasing processing temperature reduced the yield in both conversion routes. Hydrochars retained more oxygen-containing and oxidizable organic structures, whereas pyrochars showed stronger carbonization, higher ash content, and higher CO₂-derived surface area. HCl treatment decreased the ash residue, thereby resulting in improved CO₂-accessible surface and pore properties and more fragmented morphology. Metribuzin adsorption was better described by the pseudo-second-order kinetic model across all sorbents, with the highest fitted equilibrium adsorbed amount observed following HCl treatment. Tebuconazole showed higher initial uptake toward most untreated materials, but its kinetic profiles were non-monotonic, with a decrease in the adsorbed amount at longer contact times. Consequently, the conventional PFO and PSO models did not adequately describe its complete kinetic behavior. Nonlinear isotherm modeling showed predominantly Freundlich-type fitting for metribuzin, suggesting heterogeneous adsorption sites, whereas tebuconazole was formally better described by Langmuir-type fitting, although with poorer fit quality for several materials. The results show that Paulownia tomentosa leaves are a suitable precursor for carbonaceous sorbents and that HCl-treated pyrochar is the most promising material for metribuzin adsorption.

Carbonaceous sorbents were prepared from Chlorella vulgaris via hydrothermal carbonization (200 °C and 250 °C) and slow pyrolysis (300–500 °C) to assess their effectiveness in removing the herbicide metribuzin from water. The biomass was cultivated under controlled laboratory conditions, allowing for consistent feedstock quality and traceability throughout processing. Using a single microalgal feedstock for both thermal methods enabled a direct comparison of hydrochar and pyrochar properties and performance, eliminating variability associated with different feedstocks and allowing for a clearer assessment of the influence of thermal conversion pathways. While previous studies have examined algae-derived biochars for heavy metal adsorption, comprehensive comparisons targeting organic micropollutants, such as metribuzin, remain scarce. Moreover, few works have combined kinetic and isotherm modeling to evaluate the underlying adsorption mechanisms of both hydrochars and pyrochars produced from the same algal biomass. Therefore, the materials investigated in the present work were characterized using a combination of standard physicochemical and structural techniques (FTIR, SEM, BET, pH, ash content, and TOC). The kinetics of sorption were also studied. The results show better agreement with the pseudo-second-order model, consistent with chemisorption, except for the hydrochar produced at 250 °C, where physisorption provided a more accurate fit. Freundlich isotherms better described the equilibrium data, indicating heterogeneous adsorption. The hydrochar obtained at 200 °C reached the highest adsorption capacity, attributed to its intact cell structure and abundance of surface functional groups. The pyrochar produced at 500 °C exhibited the highest surface area (44.3 m²/g) but a lower affinity for metribuzin due to the loss of polar functionalities during pyrolysis. This study presents a novel use of Chlorella vulgaris-derived carbon materials for metribuzin removal without chemical activation, which offers practical benefits, including simplified production, lower costs, and reduced chemical waste. The findings contribute to expanding the applicability of algae-based sorbents in water treatments, particularly where low-cost, energy-efficient materials are needed. This approach also supports the integration of carbon sequestration and wastewater remediation within a circular resource framework.

This work aims to study whether it would be possible to use alkali metal formates and calcium formate in order to increase the workability of reactive powder concrete (RPC) and how these additives affect hydration, mechanical properties and mineralogical composition of RPC. These substances were added together with superplasticizer. Therefore, paper deals with possibility of increase in workability which would be higher when compared to the sole addition of only the superplasticizer themself. The effect of alkali metal formates and their replacement with calcium formate on slump flow, mechanical properties and pH of RPC was studied. Furthermore, the influence of potassium formate and its replacement with calcium formate and with calcium oxide on the hydration of RPC was observed with the help of isothermal calorimetry and thermal analysis. The results showed that the addition of studied compounds allows to achieve an increase in RPC slump flow. However, it is necessary to add these substances in an optimal ratio of alkali metal formate/calcium formate because a higher content of calcium formate leads to a decrease in slump flow. For ideal ratios, the compressive strength after 90 days is still above 218 MPa and the flexural strength is still above 23 MPa. In calorimetric measurements, it was observed that the addition of potassium formate leads to a decrease in the total amount of heat developed in the induction period. According to thermal analysis, additions of the studied additives to RPC caused changes in the content of portlandite and calcite.

The critical step for any subsequent instrumental analysis of cementitious binders is to stop their hydration reactions, i.e., to remove free water. One of the most available techniques is a solvent exchange method. However, the solvents are known to be strongly bound in ordinary Portland cement (OPC) paste and alter the results of thermogravimetric analysis (TGA) and sensitive hydrates, while their effect on TGA response of alkali-activated slag (AAS) has not been comprehensively investigated. Therefore, the objective of this paper is to track the effects of fundamental aspects of the solvent exchange on the TGA response of AAS with different sodium activators (hydroxide, carbonate, waterglass) and to support these results by X-ray diffraction and effluent gas analysis. All solvents used (acetone, diethyl ether, isopropyl alcohol, ethanol, and methanol) affected the TGA response of all tested pastes, and their effect was enhanced by prolonged immersion time. All solvents induced an additional mass loss at around 800 °C and, especially for OPC paste, increased in situ carbonation, even in an inert atmosphere. Methanol and ethanol had a detrimental effect on ettringite and decreased the basal distance of the C–(A)–S–H gel, while they only marginally affected gaylussite. For AAS, hydration stoppage by washing out the alkali-rich pore solution with water was also investigated and can usually be recommended (except for its detrimental effect on gaylussite), as it is more efficient than organic solvents, which lack solubility for activators. Methanol and ethanol are the most suitable alternatives, particularly for NaOH.

Biochar is a versatile carbon-rich organic material originating from pyrolyzed biomass residues that possess the potential to stabilize organic carbon in the soil, improve soil fertility and water retention, and enhance plant growth. For the utilization of biochar as a soil conditioner, the mutual interconnection of the physicochemical properties of biochar with the production conditions used during the pyrolysis (temperature, heating rate, residence time) and the role of the origin of used biomass seem to be crucial. The aim of the research was focused on a comparison of the properties of biochar samples (originated from oat brans, mixed woodcut, corn residues and commercial compost) produced at different temperatures (400–700 °C) and different residence times (10 and 60 min). The results indicated similar structural features of produced biochar samples; nevertheless, the original biomass showed differences in physicochemical properties. The morphological and structural analysis showed well-developed aromatic porous structures for biochar samples originated from oat brans, mixed woodcut and corn residues. The higher pyrolysis temperature resulted in lower yields; however, it provided products with higher content of organic carbon and a more developed surface area. The lignocellulose biomass with higher contents of lignin is an attractive feedstock material for the production of biochar with potential agricultural applications.

In this study, biochar (BC) derived from slow pyrolysis of spruce sawdust and activated BC with HNO3 were used as sorbents to remove methylene blue (MB) dye from the aqueous solution. BC was prepared by pyrolysis at temperatures of 200, 300, 400, and 500 ?. Based on the screening results, the two BCs (BC prepared at 400 ? and BC prepared at 500 ?) exhibiting a higher percentage of dye removal were selected to investigate further the effect of factors, including contact times 15, 30, and 60 minutes and the amount of dosage - BC 0.01, 0.03, 0.05 g / 8 mL. The sorption efficiency of MB was determined by measuring the absorbance of the solutions after sorption in a UV / VIS area of 665 nm. BC prepared at 500 ? was found to perform better than BC prepared at 400 ? and activated BC by HNO3 and has more than 95 % rate of methylene dye adsorption.

Alkali-activated systems belong to the group of alternative inorganic binders in which the binder properties are dictated by both the aluminosilicate precursor and alkaline activator. In this work, blast furnace slag and three different alkaline activators, namely sodium hydroxide, sodium water glass, and sodium carbonate, were selected. An innovative mixture design based on the same concentration of alkali (Na⁺) of 4 mol/dm³ for all activators and different volume fractions of slag in pastes, ranging from 0.44 to 0.54, was investigated by the flow table test, compressive and flexural strength test, and by a shrinkage test under autogenous conditions. Great differences for various activators for all investigated parameters were obtained. The highest fluidity, regardless of volume fraction of the slag, was observed for the water glass, originating from a greatly decreased yield stress compared to the two other activators. The type of activator and the volume fraction of the slag also played a crucial role in the development of shrinkage and strength.