Magdalena Bosomoiu

The removal of recalcitrant industrial dyes from wastewater has emerged as a critical environmental challenge, particularly in the context of the accelerating decline of global freshwater reserves. Given that these contaminants originate predominantly from the effluents of textile, chemical, and related manufacturing sectors, the deployment of advanced treatment technologies prior to discharge is imperative to mitigate their ecological impact. This study investigates the photocatalytic degradation of indigo carmine using a synthesized MgAl–LDH material. LDH is shown to act as an active photocatalytic component rather than a support, with its remarkably simple synthesis offering a practical alternative to the complex catalysts dominating the current literature. The catalyst’s structural, morphological, and surface characteristics were comprehensively validated through XRD, SEM, EDX, and BET analyses. The catalyst was evaluated under varying hydrogen peroxide doses and across an initial dye concentration range of 5 × 10⁻⁵ to 5 × 10⁻⁴ M. Increasing the H₂O₂ volume (3.5–20 mL, corresponding to H₂O₂ excess ratios of 17.5–100) significantly enhanced the oxidation rate, whereas higher dye concentrations reduced efficiency due to photon competition and partial saturation of catalytic sites. These experiments provided the basis for extracting kinetic parameters and assessing the mechanistic pathways governing the photocatalytic process. The kinetic behavior of indigo carmine degradation was evaluated by fitting the experimental data to zero-order, first-order, and second-order empirical models to identify the rate law that best describes the reaction. Reusability tests showed that MgAl–LDH maintains high activity over multiple cycles, with only a moderate decline, demonstrating its stability and suitability for practical wastewater treatment applications.

Phosphates pollution, primarily from agricultural runoff and wastewater discharge, is a major contributor to water eutrophication, adversely affecting aquatic ecosystems. This study reports the synthesis, characterization, and phosphates adsorption performance of a MgAlFe-layered double hydroxide (MgAlFe-LDH) with a 2:1:1 cationic ratio. The material was prepared via co-precipitation and characterized using digital microscopy, XRD, BET, XPS, and FTIR. Adsorption experiments were conducted at pH 3 and 9 to investigate equilibrium, kinetics, and reusability. The MgAlFe-LDH exhibited a high maximum adsorption capacity (q_max ≈ 215 mg/g) largely independent of pH, with adsorption well described by the Langmuir model. Kinetic studies revealed a pseudo-first-order mechanism, indicating that adsorption is dominated by surface diffusion and electrostatic interactions. Phosphate removal occurs through a dual mechanism involving rapid electrostatic attraction at protonated surface sites and slower ion exchange in the LDH interlayers. The material retained over 75% of its adsorption capacity after five consecutive adsorption–desorption cycles, highlighting its potential for sustainable phosphate recovery. Overall, the MgAlFe-LDH represents a promising, reusable adsorbent for phosphorus removal from wastewater, supporting circular economy strategies.

Soil contamination with heavy metals often resulting from industrial activities and wastewater discharge is a major ecological problem. Bone meal, a by-product of the agri-food industry, is a promising material for remediating soils affected by heavy metal pollution. Bone meal, rich in phosphorus, calcium, and other essential minerals, provides advantages both in immobilizing inorganic pollutants and in improving soil fertility. This study explores the potential of bone meal as an ecological and sustainable solution for the retention of zinc from soils polluted with wastewater. This study analyzes the physicochemical properties of bone meal, the mechanisms of its interaction with metal ions through adsorption processes as revealed by equilibrium and kinetic studies, and its effects on plant germination. The results indicate a maximum adsorption capacity of 2375.33 mg/kg at pH = 6, according to the Langmuir model, while the pseudo-second-order kinetic model showed a coefficient of R² > 0.99, confirming the chemical nature of the adsorption. At pH 12, the retention capacity increased to 2937.53 mg/kg; however, parameter instability suggests interference from precipitation phenomena. At pH 12, zinc retention is dominated by precipitation (Zn(OH)₂ and Zn–phosphates), which invalidates the Langmuir assumptions; accordingly, the Freundlich isotherm provides a more adequate description. Germination tests revealed species-specific responses to Zn contamination and bone meal amendment. In untreated contaminated soil, germination rates were 84% for cress, 42% for wheat, and 50% for mustard. Relative to the soil + bone meal treatment (100% performance), the extent of inhibition reached 19–21% in cress, 24–29% in wheat, and 12% in mustard. Bone meal mitigated Zn-induced inhibition most effectively in wheat (+31% vs. soil; +40% vs. control), followed by cress (+23–27%) and mustard (+14%), highlighting its species-dependent ameliorative potential. Thus, the experimental results confirm bone meal’s capacity to reduce the mobility of zinc ions and improve the quality of the agricultural substrate. By transforming an animal waste product into a material with agronomic value, this study supports the integration of bone meal into modern soil remediation strategies, aligned with the principles of bioeconomy and sustainable development.

In the context of circular economy, waste generated by fruit processing can be used to produce new materials with a wide range of uses. This study presents a method to synthesize biochar from peach kernel or grape pit waste. The adsorbents were tested in the removal of hexavalent chromium from synthetic wastewater with Cr⁶⁺ concentrations specific to plating processes. Characterization by BET, SEM, FTIR, and TG-DTG confirmed the formation of porous structures, and a well-functionalized surface. The effects of contact time, initial Cr⁶⁺ concentration, and adsorbent dose were investigated in static conditions. Both materials are efficient in hexavalent chromium removal, with sorption equilibrium achieved within 180 min. Kinetic studies indicated that the removal process follows a pseudo-second-order model. Equilibrium studies showed that optimal sorption occurred at pH = 6, with sorption capacities of 78.54 mg/g for biochar from peach kernels and 67.57 mg/g for biochar from grape pits. Hexavalent chromium followed a Sips adsorption isotherm for both biochars. Following the reusability study, it can be concluded that biochar from peach kernels maintains removal efficiency higher than 75% after four cycles.

Phosphates are key pollutants involved in the eutrophication of water bodies, creating the need for efficient and low-cost strategies for their removal in order to meet environmental quality standards. This study presents a comparative thermodynamic evaluation of phosphate ion adsorption from aqueous solutions using two sustainable and readily available materials: autoclaved aerated concrete (AAC) and pumice stone (PS). Batch experiments were conducted under acidic (pH 3) and alkaline (pH 9) conditions to determine equilibrium adsorption capacities, and kinetic experiments were carried out for the best-performing adsorbent. Adsorption data were fitted to the Langmuir and the Freundlich isotherm models, while kinetic data were evaluated using pseudo-first-order and pseudo-second-order models. The Freundlich model showed the best correlation (R² = 0.90 − 0.97), indicating the heterogeneous nature of the adsorbent surfaces, whereas the Langmuir parameters suggested monolayer adsorption, with maximum capacities of 1006.69 mg/kg for PS and 859.20 mg/kg for AAC at pH 3. Kinetic results confirmed a pseudo-second-order behavior, indicating chemisorption as the main mechanism and the rate-limiting step in the adsorption process. To the best of our knowledge, this is the first study to compare the thermodynamic performance of AAC and PS for phosphate removal under identical experimental conditions. The findings demonstrate the potential of both materials as efficient, low-cost, and thermodynamically favorable adsorbents. Furthermore, the use of AAC, an industrial by-product, and PS, a naturally abundant volcanic material, supports resource recovery and waste valorization, aligning with the principles of the circular economy and sustainable water management.

Trihalomethanes (THMs) are a class of disinfectant by-products present in chlorinated tap water. Mainly due to their carcinogenic potential, their concentration in drinking water is now limited by regulations. In Romania, little is known about their distribution in urban drinking water supply systems, their magnitude, or their seasonal variation. Drinking water suppliers periodically adapt and optimise their water treatment methods for economic reasons and in response to regulatory changes and technological developments. The formation of THMs is influenced by the physicochemical parameters of water (pH, temperature, total organic carbon—TOC) and by environmental factors (geographical, climatological). Most of these factors have significant seasonal variations that lead to the formation of THMs in variable concentrations. In this study, we analysed the seasonal trends in surface water quality (considering variations in temperature, pH, and TOC) and correlated them with the concentration of THMs in drinking water over two calendar years. Water samples were collected from the Arges River, in a geographical area comprised of plains. The results show that the formation of THMs is enhanced by increasing temperature over the course of a year, with the highest concentrations being obtained in July 2022 (98.7 µg/L THMs at 30.5 °C) and in August 2023 (81.9 µg/L THMs at 30.4 °C). The main parameters that trigger the formation of THMs are the organic matter content and the disinfectant dose; the pH has a moderate effect, and its effect is correlated with the concentration of organic matter. There were noted strong seasonal changes in the concentration of THMs, with the maximum peak being in the middle and late summer and the minimum peak being in winter. This indicates the possibility that the quality of drinking water may change as a result of climate change. In addition, monitoring and chlorination experiments have established that the concentration of THMs is directly proportional with the TOC.

This study explores the bioaccumulation behavior of heavy metals (cadmium (Cd), lead (Pb), and zinc (Zn)) in lavender (Lavandula spp.) cultivated under controlled greenhouse conditions to assess its potential in sustainable phytoremediation. The plants were grown in pots filled with either unpolluted soil or soil artificially enriched with cadmium, lead, or zinc at concentrations exceeding the normal (Cd 1 mg/kg d.w.; Pb 20 mg/kg d.w.; Zn 100 mg/kg d.w.), alert (Cd 3 mg/kg d.w.; Pb 50 mg/kg d.w.; Zn 300 mg/kg d.w.), and intervention (Cd 5 mg/kg d.w.; Pb 100 mg/kg d.w.; Zn 600 mg/kg d.w.) thresholds set for sensitive land use. A comparative analysis of two lavender varieties (lavender and lavandin) over a four-month period revealed an accumulation trend of Pb > Cd > Zn. Empirical modeling indicated that cadmium uptake followed a linear pattern, lead accumulation conformed closely to the Mitscherlich model, while zinc uptake did not align well with any of the tested models. Overall, the results emphasize the potential of lavender species in developing biomimetic approaches for heavy metal remediation and contribute valuable insights into sustainable soil decontamination practices.

Non-degradable plastic bags are a major contributor to marine and soil pollution. They represent a significant percentage of the generated solid waste and can last for hundreds of years in the environment. The aim of the present study was to find alternatives to conventional non-degradable plastic bags by obtaining biodegradable and compostable bags starting from simple materials like starch, poly(lactic acid) (PLA), and glycerol. Increasing the strength and hardness of the polymer was achieved by adding a mineral (talcum). The preliminary studies indicated that two compositions are suitable for advanced testing to produce the initial granular material. These materials were tested for the determination of melt flow index (MFI), Fourier Transform Infrared Spectroscopy (FTIR), and the polymers response to heating (thermogravimetric analysis, TGA and differential scanning calorimetry, DSC). The polymer biodegradability was evaluated by burial in two types of soil. The obtained results were compared with the same set of experiments performed on conventional polyethylene bags. After three months in the soil, only the materials synthesized in this study show signs of accentuated degradation while polyethylene bags are still intact. The surface morphology was explored by scanning electron microscopy (SEM). The results indicated that the biodegradable thermoplastic material meets the requirements of the European standard EN13432/2002 regarding compostable and biodegradable packaging.

The objective of this study is to develop a calcium carbonate-based adsorbent derived from Cellana Tramoscrica seashells, incorporated into a sodium alginate matrix (Na-Alg@CTs) to form hydrogel beads, for the efficient removal of Cu (II) and Zn (II) heavy metals from aqueous solutions. XRD, SEM/EDS, and FTIR analysis confirm the successful synthesis and characterization of the fabricated adsorbent. The adsorption study of Cu (II) and Zn (II) onto Na-Alg@CTs hydrogel beads revealed that the Langmuir model was the most suitable for characterizing the adsorption isotherms, suggesting monolayer coverage. Na-Alg@CTs exhibited a maximum Langmuir adsorption capacity of 368.58 mg/g and 1075.67 mg/g for Cu (II) and Zn (II), respectively. Additionally, the kinetics followed the pseudo-second-order model, indicating that the adsorption process is primarily governed by chemisorption. The thermodynamic study suggests that the uptake of metal ions on Na-Alg@CTs hydrogel beads is spontaneous and endothermic. The exceptional adsorption capacity, eco-friendly nature, and low-cost characteristics of Na-Alg@CTs hydrogel beads make them an ideal adsorbent for the removal of Cu (II) and Zn (II) from wastewater.

Collagen is a non-toxic polymer that is generated as a residual product by several industries (e.g., leather manufacturing, meat and fish processing). It has been reported to be resistant to bacteria and have excellent retention capacity. However, the recovered collagen does not meet the requirements to be used for pharmaceutical and medical purposes. Due to the scarcity of water resources now affecting all continents, water pollution is a major concern. Another major field that could integrate the collagen generated as a by-product is wastewater treatment. Applications of collagen-based materials in wastewater treatment have been discussed in detail, and comparisons with already frequently used materials have been made. Over the last years, collagen-based materials have been tested for removal of both organic (e.g., pharmaceutical substances, dyes) and inorganic compounds (e.g., heavy metals, noble metals, uranium). They have also been tested for the manufacture of oil-water separation materials; therefore, they could be used for the separation of emulsified oily wastewater. Because they have been analysed for a wide range of substances, collagen-based materials could be good candidates for removing contaminants from wastewater streams that have seasonal variations in composition and concentration. The use of recovered collagen in wastewater treatment makes the method eco-friendly and cost efficient. This paper also discusses some of the challenges related to wastewater treatment: material stability, reuse and disposal. The results showed that collagen-based materials are renewable and reusable without significant loss of initial properties. In the sorption processes, the incorporation of experiments with real wastewater has demonstrated that there is a significant competition among the substances present in the sample.