Presented research aimed to develop an alternative approach for the estimation of biosorption capability of sunflower husk. The acid-pretreated sunflower biomass was characterized by scanning electron microscopy combined with energy dispersive X-Ray spectroscopy (SEM-EDX) analysis and Fourier transform infrared (FTIR) spectroscopy. Biosorption efficiency has been evaluated using inductively coupled plasma optical emission spectroscopy (ICP-OES) and laser-induced breakdown spectroscopy (LIBS). The adsorption capacity of the adsorbent was determined as the function of the pH of the solution, the initial concentration of heavy metal solutions, and contact time. The optimal conditions were achieved after 15 min of contact at pH 6, while the percentage of the removal was from 80.0?98.7 %, depending on the element. The results obtained from the kinetic and isotherm studies show that maximum adsorption of ions was quickly reached and followed the pseudo-second-order kinetic model. Real samples were tested and obtained Ni values by LIBS method were 3100?200 and 1240?100 mg kg-1, while estimated values by the ICP-OES were 2995?20 and 1130?10 mg kg-1, respectively. The obtained results prove that LIBS method can be used as a ?green alternative? for the evaluation of biosorption efficiency.

Corn (Zea mays L.) ranks among the most important cereal crops globally, extensively cultivated for food, animal feed, and industrial applications. Its large-scale production generates substantial amounts of agricultural residues such as cobs, husks, stalks, leaves and other, which are often underutilized, leading to environmental concerns. Due to their high carbon content, lignocellulosic structure, and abundant availability, these residues represent a sustainable and low-cost raw material for the synthesis of activated carbon. Corn waste-derived activated carbon has emerged as a promising material for the efficient removal of heavy metals from aqueous solutions. Its high surface area, well-developed porosity, and adjustable surface chemistry, referring to the functional groups on the adsorbent surface that can be modified to enhance affinity toward metal ions, facilitate effective adsorption. This review provides a comprehensive overview of (1) the potential of corn waste biomass as a precursor for activated carbon production, (2) methods of carbonization and activation that influence the textural and chemical properties of the resulting adsorbents, (3) adsorption performance for heavy metal removal under varying experimental parameters such as pH, initial concentration, contact time, and adsorbent dosage, (4) adsorption mechanisms responsible for heavy metal uptake. Reported maximum adsorption capacities vary for different metals, ranging from 2.814–206 mg/g for lead, 0.21–87.72 mg/g for cadmium, 9.6246–175.44 mg/g for chromium, and 0.724–643.92 mg/g for copper. Utilizing corn waste not only provides an eco-friendly approach for managing agricultural residues but also supports the development of efficient adsorbents. Nevertheless, challenges such as scaling up production and evaluating adsorbent performance in real wastewater samples remain and require further investigation. Finally, the review highlights key challenges and knowledge gaps in current research and offers recommendations for future studies aimed at advancing the practical application of corn waste–based activated carbons in water treatment.

This work used activated carbon material obtained by chemical activation of abundantly available agricultural sunflower waste residues to remove metol (4-(methylamino) phenol sulfate, MTL) from aqueous solutions. The adsorbent structure was characterized using SEM-EDS and FT-IR spectroscopy. A modified screen-printed carbon electrode (SPCE) with gold nanoparticles synthesized using the Laser Ablation Synthesis in Solution (LASIS) method was used to detect MTL. The successful LASIS formation of gold nanoparticles was confirmed by the specific dark burgundy–red color. TEM measurements showed uniform pseudo-spherical particles with an average diameter of 7.9 ± 0.2 nm. The modified electrode showed improved electrochemical activity, which was confirmed by comparing it with an unmodified electrode using cyclic voltammetry and electrochemical impedance spectroscopy. The modified electrode was subsequently used to optimize the MTL detection conditions. UV–Vis spectroscopy was used to optimize the adsorption conditions, with the optimal values for pH and contact time found to be 8 and 120 min, respectively. The electrochemical detection of MTL was performed using differential pulse voltammetry, and the linear calibration range was established for concentrations ranging from 0.73–49.35 µM. The obtained limits of detection (LOD) and quantification (LOQ) were 0.06 µM and 0.2 µM, respectively. The efficiency of MTL removal was 100% after a contact time of 1 min and remained at 100% after 120 min.

Various metal-modified titanium dioxide (TiO₂) nanotubes have been widely investigated for water purification due to their large surface area, stability, and photocatalytic activity. In this context, this study investigates the deposition of vanadium-based nanoparticles (V NPs) on TiO₂ nanotubes via immersion in aqueous dispersions of V NPs synthesized by picosecond and nanosecond pulsed laser ablation in liquid at four different output energies (picosecond: 15 and 30 mJ; nanosecond: 120 and 250 mJ), with the aim of improving their photocatalytic performance. By optimizing the concentration of V NPs in the dispersions and the immersion time, the degradation efficiency of Acid Yellow 23 under photocatalytic conditions was enhanced for TiO₂ modified with V NPs synthesized at output energies of 30 and 250 mJ, whereas no improvement was observed for TiO₂ modified with V NPs synthesized at 15 and 120 mJ. A series of V-TiO₂ photocatalysts was fabricated by depositing laser-synthesized V NPs of various sizes on TiO₂ nanotubes prepared by electrochemical anodization of a titanium mesh.

Soil contamination with heavy metal(loid)s derived from anthropogenic activities adversely affects soil quality and agricultural productivity. This study aimed to assess the variations in As, Cd, Cr, Cu, Hg, Ni, Pb, and Zn concentrations in soils from 23 sites, located at varying distances from the Kostolac thermal power plants in northeastern Serbia, and evaluated associated ecological and human health risks. The average concentrations of elements were below average values in the continental crust, with the exception of As and Hg, which were 8.44 and 1.75 times higher, respectively. The maximum allowable concentration was exceeded for Cu and Hg at the same sampling location, with Hg exceeding the limit at an additional location. The ecological risk assessment showed high As enrichment, and elevated enrichment of Hg, Pb. The highest values of pollution load index and potential ecological risk index were obtained at a single site. The total hazard index values for children were above the recommended threshold at three locations, suggesting potential health concerns for children due to cumulative exposure. Total carcinogenic risk values across all sites were within acceptable risk limits, with values slightly higher for children compared to adult.