Milan Momčilović

Underground vegetables are important sources of nutrients, but may accumulate potentially toxic elements (PTEs) from contaminated soils. This study determined twelve PTEs (Hg, Pb, Mn, Cr, Ni, Cu, Zn, Co, Fe, Al, Cd, and As) by ICP-MS in 32 composite samples of onion, garlic, leek, celery root, parsley root, beetroot, potato, and carrot from Serbian markets. Non-carcinogenic and carcinogenic risks were assessed using deterministic and Monte Carlo approaches. Iron, Mn, and Zn were predominant, whereas Cd, Pb, and As generally occurred at lower concentrations, with the highest Cd concentration observed in celery root. Hazard index (HI) values ranged from 7.96 × 10⁻⁴ to 2.16 × 10⁻¹ for adults and from 9.68 × 10⁻⁴ to 3.84 × 10⁻¹ for children. Total cancer risk (TCR) ranged from 5.69 × 10⁻⁸ to 5.14 × 10⁻⁵ for adults and from 1.61 × 10⁻⁸ to 2.14 × 10⁻⁵ for children. Monte Carlo simulation showed that P90 HI remained below 1 in both age groups, whereas P90 TCR exceeded 10⁻⁴ only in adults under the aggregate exposure scenario. Integrated lifetime TCR exceeded 10⁻⁴ in one market scenario. Sensitivity analysis identified ingestion rate as the dominant driver of aggregate risk variability, followed by Cd, with As additionally contributing to TCR variability. Overall, the findings support targeted Cd and As monitoring, while cancer risk estimates remain conditional on the assumed Cd slope factor.

Synthetic dyes from textile effluents represent a major environmental concern due to their persistence and toxicity. Reactive Black 5 (RB5) is widely used in the textile industry and is commonly applied as a model azo compound in sorption studies. This study comparatively evaluates the sorption performance of raw and carbonized sorbents derived from industrial hemp (Cannabis sativa L.) biowaste using an integrated experimental and theoretical approach. The sorbents were prepared through washing, drying, and phosphoric acid-assisted carbonization followed by pyrolysis. Structural and physicochemical properties were characterized using elemental analysis, FTIR spectroscopy, and SEM microscopy. Sorption performance toward RB5 was investigated through batch kinetic and equilibrium experiments, supported by kinetic (pseudo-first-order, pseudo-second-order, Elovich, and intraparticle diffusion models) and isotherm (Langmuir, Freundlich, and Temkin) modeling. Molecular docking simulations were performed to provide mechanistic insight into dye–sorbent interactions. Both materials exhibited rapid sorption kinetics, reaching equilibrium within approximately 45 min, with the pseudo-second-order model suggesting that surface-controlled interactions dominate the sorption rate. Molecular modeling, based on extensive conformational sampling, indicated a strong binding affinity between RB5 and cellulose-based structures, primarily associated with hydrogen bonding and other favorable noncovalent interactions. In contrast, graphene-based models revealed sorption governed by π–π interactions and confinement effects, supporting the experimentally observed differences between raw and carbonized sorbents.

This study investigated the application of apricot stone, an agro-industrial by-product, as a sustainable biosorbent for the removal of Zn ions from aqueous solutions and industrial galvanic wastewater. The equilibrium data conformed well to the Sips isotherm model, indicating heterogeneous sorption behavior, and revealed a maximum sorption capacity of 58.2 mg/g. The biosorbent exhibited a high initial removal efficiency of 95% in aqueous Zn solutions, while its performance in real industrial wastewater was reduced to 55%, due to matrix interference. Ecotoxicological test using seed germination assays revealed no phytotoxic effects from the Zn-loaded sorbent. These findings demonstrate that apricot stone is an effective, low-cost, and environmentally friendly sorbent with significant potential for application in Zn-contaminated water treatment systems, contributing to circular economy and waste valorization initiatives.

Background/Objectives: This study investigates the antimicrobial properties of pomegranate peel extract (PoPEx) and its major polyphenolic constituents against Gram-positive and Gram-negative bacteria, employing six clinical isolates of Staphylococcus aureus and five isolates of Escherichia coli. The study further aims to elucidate mechanisms of action through molecular docking and transport studies. Methods: Chemical composition was analyzed using liquid chromatography–mass spectrometry (LC–MS). Antimicrobial activity was determined by the broth microdilution method. Molecular docking was performed with the AutoDock Vina algorithm, and transport studies through porin channels were carried out using Caver software. Results: PoPEx showed stronger activity against Gram-positive (MICs 15.62–500.00 μg/mL) than Gram-negative bacteria (MICs 125.00–500.00 μg/mL). Punicalagin was most active against S. aureus, while gallic acid was most effective against E. coli. Docking revealed high affinities of punicalagin and punicalin, whereas transport studies highlighted the advantage of smaller phenolics like gallic acid in crossing porins. Conclusions: Larger tannins exhibited strong target binding but limited porin permeability, reducing efficacy in Gram-negative bacteria. These findings provide insights into structure–activity relationships of pomegranate polyphenols and support their potential as natural antimicrobial agents.

This study reports the synthesis of activated carbon from dwarf elder, a lignocellulosic precursor, yielding a material with a high specific surface area (500.43 m²/g) and mesoporous structure (median pore radius: 3.88 nm). The physicochemical properties of the obtained carbon were characterized using field-emission scanning electron microscopy (FE-SEM), Brunauer–Emmett–Teller (BET) analysis, and Fourier-transform infrared spectroscopy (FTIR), confirming its suitability for aqueous-phase sorption applications. Batch experiments demonstrated carbon’s efficacy in adsorbing amlodipine besylate (AMB), a model pharmaceutical pollutant, with a maximum capacity of 325.9 mg/g under optimized conditions (pH 10.0, room temperature). Systematic evaluation of key parameters, such as initial AMB concentration, sorbent dosage, pH, and agitation speed revealed that sorption kinetics adhered to pseudo-second-order and Elovich model. The high efficiency of the synthesized carbon material, coupled with its low-cost and eco-friendly synthesis, positions it as a promising candidate for the scalable remediation of AMB and structurally related pharmaceuticals from contaminated water sources.

Industrial hemp (Cannabis sativa L.) was investigated as a sustainable biosorbent for removing Congo Red (CR) and Remazol Brilliant Blue R (RBBR) from wastewater. The unmodified hemp biosorbent exhibited moderate but practically relevant sorption capacities (4.47 mg/g for CR; 2.44 mg/g for RBBR), outperforming several agricultural waste materials. Kinetic studies revealed rapid uptake, with CR following pseudo-first-order kinetics (t₁/₂ < 15 min) and RBBR fitting the Elovich model, indicating heterogeneous surface interactions. Equilibrium data showed CR adsorption was best described by the Temkin isotherm (R² = 0.983), while RBBR followed the Langmuir model (R² = 0.998), reflecting their distinct binding mechanisms. Thermodynamic analysis confirmed spontaneous (ΔG° < 0), exothermic (ΔH° ≈ −2 kJ/mol), and entropy-driven processes for both dyes. Molecular docking elucidated the structural basis for performance differences: CR’s stronger binding (−7.5 kcal/mol) involved weak noncovalent interaction arising from partial overlap between the π-electron cloud of an aromatic ring and σ-bonds C-C or C-H (π-σ stacking) and hydrogen bonds with cellulose, whereas RBBR’s weaker affinity (−5.4 kcal/mol) relied on weak intermolecular interaction between a hydrogen atom (from a C-H bond) and the π-electron system of an aromatic ring (C-H∙∙∙π interactions). This work establishes industrial hemp as an eco-friendly alternative for dye removal, combining renewable sourcing with multi-mechanism adsorption capabilities suitable for small-scale water treatment applications.

Two new surfactant sensors were developed by synthesizing Pt-doped acid-activated multi-walled carbon nanotubes (Pt@MWCNTs). Two different ionophores using Pt@MWCNTs, a new plasticizer, and (a) cationic surfactant 1,3-dihexadecyl-1H-benzo[d]imidazol-3-ium-DHBI (Pt@MWCNT-DHBI ionophore) and (b) anionic surfactant dodecylbenzenesulfonate-DBS (Pt@MWCNT-DBS ionophore) composites were successfully synthesized and characterized. Both surfactant sensors showed a response to anionic surfactants (dodecylsulfate (SDS) and DBS) and cationic surfactants (cetylpyridinium chloride (CPC) and hexadecyltrimethylammonium bromide (CTAB)). The Pt@MWCNT-DBS sensor showed lower sensitivity than expected with the sub-Nernstian response of ≈23 mV/decade of activity for CPC and CTAB and ≈33 mV/decade of activity for SDS and DBS. The Pt@MWCNT-DHBI surfactant sensor had superior response properties, including a Nernstian response to SDS (59.1 mV/decade) and a near-Nernstian response to DBS (57.5 mV/decade), with linear response regions for both anionic surfactants down to ≈2 × 10⁻⁶ M. The Pt@MWCNT-DHBI was also useful in critical micellar concentration (CMC) detection. Common anions showed very low interferences with the sensor. The sensor was successfully employed for the potentiometric titration of a technical grade cationic surfactant with good recoveries. The content of cationic surfactants was measured in six samples of complex commercial detergents. The Pt@MWCNT-DHBI surfactant sensor showed good agreement with the ISE surfactant sensor and classical two-phase titration and could be used as an analytical tool in quality control.