Degradation of azo dye Reactive Orange 16, a widely used textile dye, was carried out with UV light in the presence of H2O2. The experiments were conducted in the batch mode using low-pressure mercury lamps, emitting at 253.7 nm. Liquid-chromatography tandem mass spectrometry (LC/MS/MS) and high resolution mass spectrometry (FT-ICR) were employed in order to identify some of degradation products as well as to suggest possible degradation pathways. According to the mass spectrum characterization of RO16 dye and MS(n) fragmentation (up to MS(4)), its possible fragmentation pattern was proposed. The results revealed that degradation occurred mainly via hydroxylation, cleavage of the C‒S bond between the aromatic ring and the sulfonate group, cleavage of the azo bond, cleavage of the C‒N bond between azo group and naphthalene ring and aromatic ring opening. Toxicity test with marine photobacterium Vibrio Fisheri was performed to consider whether or not the UV/H2O2 treatment of RO16 dye results in the products with enhanced toxicity for aquatic life.

Bismuth basic nitrates (BBNs) were synthesized via an electrochemical method, i.e., by electrodeposition from an acidic solution of bismuth nitrate, followed by thermal treatment in an air environment. For the first time, the influence of various electrochemical parameters on the morphology, crystal structure, and chemical structure of BBNs was examined. The following synthesis parameters were investigated: electrodeposition current density, thermal treatment temperature of the obtained deposit, and working electrode material (cathode). The obtained materials were characterized by SEM-EDX, XRD, FTIR, TG, and N₂ adsorption/desorption methods and were applied for the sorption of the textile dye RB19. The results showed that the electrodeposition current density and thermal treatment temperature affect the surface morphology, chemical composition, and crystal structure of the obtained materials, as well as the RB19 sorption efficiency. On the other hand, the working electrode material does not affect the properties of the synthesized materials mentioned. Kinetic, isotherm, and thermodynamic analysis of the sorption process were also examined.

A new woodchips-ZrO₂ biosorbent (W-ZrO₂) was synthesized using wood residue material generated from the oak tree (Quercus robur) during furniture manufacturing. Biosorbent was tested for the simultaneous removal of both chromium (Cr) ions: Cr(III) and Cr(VI), in the binary component solution. Biosorbent characterization was performed by scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX), Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction analysis (XRD). To define optimal process parameters for simultaneous removal of both Cr species, effects of pH, temperature, sorbent dosage and Cr ions concentration on the sorption process were investigated. Sorption of Cr ions onto W-ZrO₂ was highly pH-dependent. Optimal pH for simultaneous removal of both Cr(III) and Cr(VI) ions is 4.0 with removal efficiency over 99.5 % in both cases. Equilibrium experimental results are the best fitted by the Langmuir sorption isotherm model. The maximal sorption capacities of the biosorbent for simultaneous removal of Cr(III) and Cr(VI) ions in binary-component system are 16.18 and 83.52 mg g⁻¹, respectively. The present study shows that using wood residue material to produce a low-cost sorbent can effectively decrease the water pollution simultaneously removing both chromium species from water and also reduce wood waste and increase reuse/recycling options.

Extensive utilization of the herbicide 2,4-dichlorophenoxyacetic acid (2,4-D) has resulted in contamination of the aquatic environment; this situation requires effective treatment technology. Ultraviolet-based advanced oxidation processes (UV-AOPs) are widely employed for the removal of organic contaminants from water. This study’s aim was to compare the degradation of the pesticide 2,4-D in UV-C-activated peroxide and peroxydisulfate systems. UV-C irradiation alone exhibited a negligible effect on pesticide degradation, whereas the addition of oxidants significantly enhanced the degradation efficiency relative to 2,4-D. Complete pesticide removal was achieved after 15 min of UV/H₂O₂ treatment, while twice as much time was required with the UV/S₂O₈²⁻ process. COD decreased by 74% and 28% for UV-C-activated peroxide and peroxydisulfate, respectively. Both investigated systems demonstrated good performance for 2,4-D dechlorination. Pesticide degradation rates increased with increasing dosages of the applied oxidants. Acidic conditions were more favorable for degradation of 2,4-D, compared to neutral and basic conditions, for both systems studied. The degradation efficiency relative to 2,4-D decreased in the presence of HA, Cl⁻ and HCO₃⁻ in water matrices. The predominant radical for the UV-C-activated peroxydisulfate was determined to be a sulfate radical. These findings are of fundamental and practical significance in understanding UV-C-activated 2,4-D degradation, paving the way for the selection of preferred processes for the optimal removal of pesticides from various aqueous matrices.

In this study, raw and chemically activated natural zeolite from Zlatokop deposit (Serbia) were investigated by FTIR, XRD, SEM-EDX, TGA and BET in order to define their properties as further potential sorption materials. Obtained results indicate porous (meso-pore range) and defined crystal alumino-silicate structure of these materials, with Na+, K+, such as Ca2+ and Mg2+ as dominating exchangeable cations. Content of clinoptilolite (ca. 90%) indicates the high quality of the zeolite samples. Preliminary sorption analyses of these materials toward copper(II) ion from aqueous solution showed good removal efficiency for base activated zeolite (zVBB) compared to raw natural (zVBN) and acid activated (zVBA) zeolite. Since these were preliminary sorption tests, the investigated zeolites will be further examined under different experimental conditions.

The increased interest in natural, renewable, biodegradable, easily available, low-cost materials makes agricultural residues, such as lignocellulosic biomass, attractive raw materials for the preparation of effective biosorbents for various pollutants (metal ions, anions, dyes, pharmaceutical degradation products, metabolites, organic macromolecules) for the wastewater treatment. Various covalent and non-covalent modification approaches significantly improve the sorption properties of these lignocellulosic functional particles, even improving their dispersion in hydrophobic polymer matrices, associative properties in water, rheological properties, surface-active properties, which can control the sorption of various ionic pollutants both in batch and in flow mode. Advantages over commercial sorbents (techno-economic aspect, no secondary pollution, usability as fertilizers), easy separation from the sorption medium, microstructural properties (strength, porosity, interactivity, stability), as a promising and sustainable biosorbent highlight the environmentally friendly bottle gourd shell. On the example of this biosorbent, the conventional approach to the pollutant sorption process (comparative kinetic, thermodynamic and equilibrium tests) was improved, as well as its shortcomings in predicting optimal process parameters. To fill the gaps of the already unnecessary numerous experiments, a design study involving OVAT experimental approaches integrated with DoE methodology was conducted. This integrated experimental design was implemented in the optimization of the pollutant sorption process.