Publications by authors named "Ana Loncaric Bozic"

The widespread presence of microplastics (MP) in water represents an environmental problem, not only because of the harmful effects of their size and potential to vector other pollutants, but also because of the release of additives, degradation products and residues contained in the polymer matrix. The latter includes metallic catalysts, which are often overlooked. This study focuses on the photo-aging of polypropylene (PP) and the resulting structural changes that promote its fragmentation microplastics (PP-MPs) and release of metals, as well as the resulting toxicity of leachates and their potential to inhibit biodegradation of organics in water.

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Microplastics (MPs) have recently attracted a lot of attention worldwide due to their abundance and potentially harmful effects on the environment and on human health. One of the factors of concern is their ability to adsorb and disperse other harmful organic pollutants in the environment. To properly assess the adsorption capacity of MP for organic pollutants in different environments, it is pivotal to understand the mechanisms of their interactions in detail at the atomic level.

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Graphene, a two-dimensional carbon allotrope with a honeycomb structure, has emerged as a material of immense interest in diverse scientific and technical domains. It is mainly produced from graphite by mechanical, chemical and electrochemical exfoliation. As renewable energy and source utilization increase, including bioenergy from forest and woody residues, processed, among other methods, by pyrolysis treatment, it can be expected that biochar production will increase too.

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Microplastics (MPs) are detected in the water, sediments, as well as biota, mainly as a consequence of the degradation of plastic products/waste under environmental conditions. Due to their potentially harmful effects on ecosystems and organisms, MPs are regarded as emerging pollutants. The highly problematic aspect of MPs is their interaction with organic and inorganic pollutants; MPs can act as vectors for their further transport in the environment.

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Although heterogeneous photocatalysis has shown promising results in degradation of contaminants of emerging concern (CECs), the mechanistic implications related to structural diversity of chemicals, affecting oxidative (by HO•) or reductive (by O•) degradation pathways are still scarce. In this study, the degradation extents and rates of selected organics in the absence and presence of common scavengers for reactive oxygen species (ROS) generated during photocatalytic treatment were determined. The obtained values were then brought into correlation as coefficients (MHO•/MO2•-), denoting the ratio of organics degraded by two occurring mechanisms: oxidation and reduction via HO• and O•.

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FeO/TiO nanocomposites were fabricated via a facile impregnation/calcination technique employing different amounts iron (III) nitrate onto commercial TiO (P25 Aeroxide). The as-prepared FeO/TiO nanocomposites were characterized by X-ray diffraction (XRD), Raman spectroscopy (RS), scanning electron microscopy/energy-dispersive spectroscopy (SEM/EDXS), X-ray photoelectron spectroscopy (XPS), Brunauer-Emmett-Teller analysis (BET), electron impedance spectroscopy (EIS), photoluminescence spectroscopy (PL), and diffuse reflectance spectroscopy (DRS). As a result, 5% () FeO/TiO achieved the highest photocatalytic activity in the slurry system and was successfully immobilized on glass support.

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Sustainable hydrogen production is one of the main challenges today in the transition to a green and sustainable economy. Photocatalytic hydrogen production is one of the most promising technologies, amongst which BiVO-based processes are highly attractive due to their suitable band gap for solar-driven processes. However, the performance of BiVO alone in this role is often unsatisfactory.

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The study of the structural features affecting the adsorption of organics, especially contaminants of emerging concern (CECs), onto TiO P25 in aqueous medium has far-reaching implications for the understanding and modification of TiO P25 in the roles such as an adsorbent and photocatalyst. The effect of pH and γ(TiO P25) as variables on the extent of removal of organics by adsorption on TiO P25 was investigated by response surface methodology (RSM) and quantitative structure-property relationship (QSPR) modeling. Experimentally determined coefficients of adsorption were used as responses in RSM, yielding a quadratic polynomial equation (QPE) for each of the studied organics.

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This study is focused on oxytetracycline (OTC) degradation by direct photolysis (UV-C) and photobased advanced oxidation processes (AOPs) (UV-C/HO and UV-C/SO). OTC degradation pathways were revealed by LC-MS/MS and GC-MS/MS analyses. The evolution/degradation profiles of 12 detected byproducts were correlated with changes in biodegradability and toxicity toward Vibrio fischeri recorded during the treatment.

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Clean water and the increased use of renewable energy are considered to be two of the main goals in the effort to achieve a sustainable living environment. The fulfillment of these goals may include the use of solar-driven photocatalytic processes that are found to be quite effective in water purification, as well as hydrogen generation. H production by water splitting and photocatalytic degradation of organic pollutants in water both rely on the formation of electron/hole (e/h) pairs at a semiconducting material upon its excitation by light with sufficient photon energy.

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Diverse contaminants of emerging concern (CECs) can be found in nowadays aquatic environment, possessing high potential to cause adverse ecological and human health effects. Due to their recalcitrance, conventional water treatment methods are shown to be inadequately effective. Thus, their upgrade by advanced oxidation processes, involving the generation of highly reactive species (HO and SO), is highly demanded.

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Extensive commercial use of aromatic hydrocarbons results with significant amounts of these chemicals and related by-products in waters, causing a severe ecological and health threat, thus requiring an increased attention. This study was aimed at developing models for prediction of the initial toxicity of the aromatic water-pollutants (expressed as EC and TU) as well as the toxicity of their intermediates at half-life of the parent pollutant (TU). For that purpose, toxicity toward Vibrio fischery was determined for 36 single-benzene ring compounds (S-BRCs), diversified by the type, number and position of substituents.

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TiO₂-SnS₂ composite semiconducting photocatalysts with different building component ratios were prepared by hydrothermal synthesis (TiO₂-SnS₂-HT) and by immobilization of commercial TiO₂ and SnS₂ particles (TiO₂-SnS₂-COMM). The band gap values, which determine the catalysts’ photoactivity, were examined by diffuse reflectance spectroscopy and Kubelka⁻Munk transformations. The catalysts’ surface properties: specific surface area, charge and adsorption capacitance at the solid⁻solution interface were characterized using BET analysis, potentiometric titration and electrochemical impedance spectroscopy, respectively.

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In this study, UV-C/HO and UV-C/[Formula: see text] processes as photooxidative Advanced oxidation processes were applied for the treatment of seven pharmaceuticals, either already included in the Directive 2013/39/EU "watch list" (17α- ethynylestradiol, 17β-estradiol) or with potential to be added in the near future due to environmental properties and increasing consumption (azithromycin, carbamazepine, dexamethasone, erythromycin and oxytetracycline). The influence of process parameters (pH, oxidant concentration and type) on the pharmaceuticals degradation was studied through employed response surface modelling approach. It was established that degradation obeys first-order kinetic regime regardless structural differences and over entire range of studied process parameters.

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One of the most important features of photocatalytic materials intended to be used for water treatment is their long-term stability. The study is focused on the application of thermal and chemical treatments for the reactivation of TiO-SnS composite photocatalyst, prepared by hydrothermal synthesis and immobilized on the glass support using titania/silica binder. Such a catalytic system was applied in solar-driven treatment, solar/TiO-SnS/HO, for the purification of water contaminated with diclofenac (DCF).

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The study is aimed at evaluating TiO-SnS composites as effective solar-active photocatalysts for water treatment. Two strategies for the preparation of TiO-SnS composites were examined: (i) in-situ chemical synthesis followed by immobilization on glass plates and (ii) binding of two components (TiO and SnS) within the immobilization step. The as-prepared TiO-SnS composites and their sole components (TiO or SnS) were inspected for composition, crystallinity, and morphology using Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), X-ray diffraction (XRD), and scanning electron microscopy/energy-dispersive X-ray spectroscopy (SEM/EDX) analyses.

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The study was aimed at developing models for predicting the biodegradability of aromatic water pollutants. For that purpose, 36 single-benzene ring compounds, with different type, number and position of substituents, were used. The biodegradability was estimated according to the ratio of the biochemical (BOD) and chemical (COD) oxygen demand values determined for parent compounds ((BOD/COD)), as well as for their reaction mixtures in half-life achieved by UV-C/HO process ((BOD/COD)).

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The study is aimed at evaluating the potential of immobilized TiO2-based zeolite composite for solar-driven photocatalytic water treatment. In that purpose, TiO2-iron-exchanged zeolite (FeZ) composite was prepared using commercial Aeroxide TiO2 P25 and iron-exchanged zeolite of ZSM5 type, FeZ. The activity of TiO2-FeZ, immobilized on glass support, was evaluated under solar irradiation for removal of diclofenac (DCF) in water.

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In this study, the photolysis behavior of commonly used anti-inflammatory drug diclofenac (DCF) was investigated using UV-C and UV-A irradiation. In that purpose, DCF conversion kinetics, mineralization of organic content, biodegradability, and toxicity were monitored and compared. The results showed different kinetics of DCF conversion regarding the type of UV source applied.

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The study was aimed at evaluation of environmental aspects on photooxidative treatment of phenolic compounds by UV/H2O2 process. Hydroxy-, chloro-, nitro- and methyl-phenols substituted in ortho and para positions were used as model pollutants. The influence of pollutant chemical structure on variations of water quality during the photooxidative treatment was investigated.

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The combined influence of substituent type and UV/H(2)O(2) process parameters on the degradation of four aromatic water pollutants was investigated using modified 3(3) full factorial design and response surface methodology. Degradation kinetics was described by the quadratic polynomial model. According to the applied ANOVA, besides pH and [H(2)O(2)], model terms related with the pollutant structure are found to be significant.

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Three photooxidation processes, UV/H(2)O(2), UV/S(2)O(8)(2-) and UV/O(3) were applied to the treatment of model wastewater containing non-biodegradable organic pollutant, azo dye Acid Orange 7 (AO7). Dye degradation was monitored using UV/VIS and total organic carbon (TOC) analysis, determining decolorization, the degradation/formation of naphthalene and benzene structured AO7 by-products, and the mineralization of model wastewater. The water quality during the treatment was evaluated on the bases of ecological parameters: chemical (COD) and biochemical (BOD(5)) oxygen demand and toxicity on Vibrio fischeri determining the EC(50) value.

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In this study the application of advanced oxidation processes (AOPs), dark Fenton and photo-assisted Fenton type processes; Fe(2+)/H(2)O(2), Fe(3+)/H(2)O(2), Fe(0)/H(2)O(2), UV/Fe(2+)/H(2)O(2), UV/Fe(3+)/H(2)O(2) and UV/Fe(0)/H(2)O(2), for degradation of phenol as a model organic pollutant in the wastewater was investigated. A detail kinetic modeling which describes the degradation of phenol was performed. Mathematical models which predict phenol decomposition and formation of primary oxidation by-products: catechol, hydroquinone and benzoquinone, by applied processes were developed.

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