This study used widely available waste biomass, corn cob (CC), to remove Pb ions from aqueous solutions. A two-step conversion of this material was carried out to improve its adsorption characteristics. Firstly, CC was prepared by hydrothermal carbonization; afterward, the obtained hydrochar was doped by MgCl₂ and pyrolyzed. The synthesized hydro-pyrochar (HCC-Mg) was used for adsorption experiments in a batch system. The surface and structural properties of HCC-Mg were characterized by SEM-EDX and FTIR analysis before and after Pb adsorption. Kinetic and isotherm models were applied to the experimental results. It was confirmed that Pb adsorption on HCC-Mg occurred rapidly, with a maximum adsorption capacity of 87.08 mg/g. The pseudo-second-order model best described the adsorption process, while the best fit of the experimental data was observed with the Sips isotherm model. The results of this study showed that the capacity of the synthesized HCC-Mg material had increased more than 14 times compared with raw CC. In addition, the synthesized material had the potential to be reused for at least five cycles with minimal loss of adsorption capacity and efficiency. Moreover, the results confirmed that HCC-Mg can be used as an efficient, sustainable adsorbent of Pb from polluted water.

Organobentonites have been applied for the removal of two common non-steroidal anti-inflammatory drugs, ibuprofen (IBU) and diclofenac sodium (DS), from aqueous solutions. Two surfactants, one with and the other without benzyl group (octadecyldimethylbenzylammonium chloride, ODMBA, and hexadecyltrimethylammonium bromide, HDTMA), in amounts equivalent to 50, 75, and 100% of the cation exchange capacity of bentonite were used for the preparation of organobentonites. Successful modification of bentonite was confirmed by several methods: X-ray powder diffraction (XRPD), point of the zero charge (pH_PZC), determination of exchanged inorganic cations in bentonite, determination of textural properties, and scanning electron microscopy (SEM). Kinetic and thermodynamic data on the adsorption of IBU and DS showed that drug adsorption was controlled by the type and the amount of surfactant incorporated into the bentonite and by their arrangement in the interlayer space and at the surface of organobentonites. The adsorption of both drugs increased with an increase in the amount of both surfactants in organobentonites. The presence of the benzyl group in organobentonites enhanced the adsorption of IBU and DS and was more pronounced for IBU. Drug adsorption fits the pseudo-second-order kinetic model the best. The thermodynamic data revealed that the adsorption process was endothermic in nature and with increase of the amount of both surfactants drug adsorption processes were more spontaneous. The results obtained from this study revealed that adsorbents based on surfactants modified bentonite are promising candidates for IBU and DS removal from contaminated water.

Three-dimensional hierarchical porous carbons (HPCs) created through hydrothermal carbonization and the subsequent chemical activation of miscanthus were tested as adsorbents of Pb²⁺ and methylene blue from the aqueous solution. The HPC pore structure was customized using various hydrochar precursors obtained through a longer reaction time and by adding acetic acid. HPC obtained from hydrochar derived from acetic acid’s addition exhibited the highest specific surface area due to a larger micropore volume. This adsorbent proved to be the most efficient in removing lead from aqueous solutions. The Langmuir isotherm best described the lead adsorption process onto HPC with q_m = 155.6 mg g⁻¹ and the pseudo-second-order kinetic model. HPC obtained from hydrochar produced with a longer reaction time exhibited improved methylene blue adsorption properties. The pseudo-second-order kinetic model and the Freundlich isotherm best described the experimental data. The theoretical maximum adsorption capacity for methylene blue was 316.0 mg g⁻¹. The type of hydrochar significantly impacted the yield and physical structure of HPCs, while having a lesser effect on the composition of surface functional groups. The results revealed the binding mechanism of each pollutant, highlighting the importance of biomass pretreatment on the structure of the resulting HPC and its effectiveness in water purification.

The correlation between the morphology and crystal structure of zinc dendritic particles produced by electrolysis from the alkaline electrolyte has been established. Morphology and crystal structure of Zn particles electrodeposited by the potentiostatic regime of electrolysis at overpotentials inside (−100 and −160 mV) and outside (−220, −280, and −340 mV) the plateau of the limiting diffusion current density were characterized by scanning electron microscope (SEM) and by X-ray diffraction (XRD), respectively. The particle size distribution (PSD) was performed in order to determine the dependency of the size of dendritic particles on applied electrolysis overpotential. With increasing the overpotential of electrolysis, the shape of particles changed from irregular forms denoted as precursors of dendrites to various forms of dendrites, while the size of the particles simultaneously decreased. All types of Zn dendrites exhibited the strong (002) preferred orientation, while the precursors of dendrites exhibited (101)(002) preferred orientation. The development of strong (002) preferred orientation was explained and discussed by making an analogy with the electrolytic production of lead dendrites from the concentrated nitrate electrolyte. Although zinc and lead belong to different types of crystal lattice (Pb-face-centered cubic type and Zn-hexagonal close-packed type), they have a common characteristic that is manifested by the strong preferred orientation in the crystal plane with the lowest surface energy.

Enormous usage of synthetic dyes in several industrial branches could pose detrimental effects on aquatic and terrestrial organisms. The aim of this work was to examine photocatalytic properties of novely obtained biobased TiO2 (Ac-bTiO2) particles. Namely, photocatalyst was synthesized by cross-linking between aqueous extract of mandarin peels (eMP) and titanium alkoxide, under controlled reaction conditions. Preliminary structural properties of nanooxide particles were investigated by Scanning electron microscopy (SEM), Energy dispersive X-ray spectroscopy (EDS), X Ray Diffraction (XRD) and UV-Visible diffuse reflectance spectroscopy (UV-DRS). Photocatalytic activity was determined under imitated sunlight conditions, measured by UV-Vis spectroscopy. As a model pollutant, aqueous solution of methyl orange (MeOr) was used. Complete decolorization was observed after 60 min, while the degradation kinetics follows pseudo-first order (R2 > 0.98). Photodegradation studies performed in batch system proved that obtained photocatalyst could represent an improved choice for purifying water contaminated by different organics. Satisfying degradation rate of utilized photocatalyst demonstrated possibility for consecutive, multicycle usage under operative conditions.