(1) Background: A comparative research study to remove Congo Red (CR) and Methyl Orange (MO) from single and binary solutions by adsorption onto cobalt ferrite (CoFe₂O₄) and cobalt ferrite–chitosan composite (CoFe₂O₄-Chit) prepared by a simple coprecipitation method has been performed. (2) Methods: Structural, textural, morphology, and magnetic properties of the obtained magnetic materials were examined by X-ray diffraction (XRD), Fourier-transform infrared (FTIR) spectroscopy, N₂ adsorption–desorption analysis, Scanning Electron Microscopy (SEM), Transmission Electron Microscopy (TEM), and magnetic measurements. The optimal operating conditions of the CR and MO removal processes were established in batch experiments. The mathematical models used to describe the processes at equilibrium were Freundlich and Langmuir adsorption isotherms. (3) Results: Cobalt ferrite–chitosan composite has a lower specific surface area (S_BET) and consequently a lower adsorption capacity than cobalt ferrite. CoFe₂O₄ and CoFe₂O₄–Chit particles exhibited a superparamagnetic behavior which enabled their efficient magnetic separation after the adsorption process. The research indicates that CR and MO adsorption onto prepared magnetic materials takes place as monolayer onto a homogeneous surface. According to Langmuir isotherm model that best fits the experimental data, the maximum CR/MO adsorption capacity is 162.68/94.46 mg/g for CoFe₂O₄ and 15.60/66.18 mg/g for CoFe₂O₄–Chit in single solutions. The results of the kinetics study revealed that in single-component solutions, both pseudo-first-order and pseudo-second-order kinetics models represent well the adsorption process of CR/MO on both magnetic adsorbents. In binary solutions, adsorption of CR/MO on CoFe₂O₄ better follows the pseudo-second-order kinetics model, while the kinetic of CR/MO adsorption on CoFe₂O₄–Chit is similar to that of the dyes in single-component solutions. Acetone and ethanol were successfully used as desorbing agents. (4) Conclusions: Our study revealed that CoFe₂O₄ and CoFe₂O₄–Chit particles are good candidates for dye-contaminated wastewater remediation.

This research investigates commercial activated carbon (AC) potential to remove methyl orange (MO) dye removal from aqueous solution using a batch process. The AC material was characterized using FTIR spectroscopy and SEM analysis. The effect of the main operating parameters, such as the pH, adsorbent dosage, contact time, and initial dye concentration, was studied. MO removal could be accomplished within 30 min at a pH value of 3. The calculated maximum MO adsorption capacity onto activated carbon was 129.3 mg/g, while the removal efficiency was 97.8%. Adsorption results were analyzed by studying the Langmuir and Freundlich isotherm models. The MO adsorption data on activated carbon were better explained by the Langmuir isotherm than by the Freundlich isotherm. The pseudo-second-order kinetic model may have had an effect on the MO dye adsorption on AC material. This research showed that the commercial activated carbon can be used as an effective sorbent for MO removal from wastewater sample. Moreover, the AC material has good reusability and practical utilization capacities.

The removal of metal ions by biosorption on inexpensive materials is still a challenge for environmental engineering research. In this study, marine green algae biomass (Ulva lactuca sp.) and the biochars obtained from this biomass, at 320 °C (BC-320) and 550 °C (BC-550), were used as biosorbents for the removal of Cu(II) ions from aqueous solution. In addition to comparing the biosorption capacities, the determination of the thermodynamic parameters allows the choice of the most suitable material for the biosorption processes. The experimental results, obtained for Cu(II) ions biosorption on each biosorbent (algae biomass (AB), BC-320 and BC-550), at three different temperatures (10, 30 and 50 °C) were analyzed using Langmuir and Freundlich isotherm models, while pseudo-first order, pseudo-second order and intra-particle diffusions models were used to model the kinetic data. The biosorption of Cu(II) ions is best described by the Langmuir model and the pseudo-second kinetic model, regardless of the type of biosorbent. Such behavior is characteristic for the retention of metal ions on low-cost materials, and is explained in the literature using the concepts of molecular symmetry. The maximum biosorption capacity (q_max, mg/g) depends on the temperature, but also on the type of biosorbent, and follow the order: BC-320 < AB < BC-550. Using the experimental isotherms, the thermodynamic parameters (ΔG⁰, ΔH⁰ and ΔS⁰) for the biosorption of Cu(II) ions on each biosorbent were calculated. The analysis of the obtained values constitutes the main arguments in choosing BC-550 as the most effective biosorbent for the removal of Cu(II) ions from aqueous media.

Microplastics (MPs) pollution has become a persisting problem over the last decades and is a critical issue for environmental protection and human health. In this context, scientific data able to reveal MPs presence and improve the characterization and identification of this pollution via different systems are valuable. The aim of this paper is to assess available techniques for determining MPs in real freshwater samples and subsequently to highlight the occurrence and type of MPs in the study case area (Somesul Mic River). The MPs sampling was performed from fresh water and sediment using planktonic nets and sieves with different mesh sizes (from 20 to 500 µm). Using both classical microscopic techniques as well as scanning electron microscopy (SEM), large (1–5 mm) and small (1 µm to 1 mm) MPs were observed in the shape of fibers, fragments, foam, foils and spheres in various colors (red, green, blue, purple, pink, white, black, transparent, and opaque). Raman and FT-IR spectroscopic methods were used for MPs identification. The presence of polyethylene (PE), polypropylene (PP), and polystyrene (PS) was registered for all sampling points. The MPs laboratory investigations have raised some issues regarding the identification of MPs particles smaller than 500 µm, these being characterized especially under microscope. Some small MPs particles were identified using micro-Raman spectroscopy that highlighted the same type of polymers. No differences were registered between the sampling points due to the widespread presence of MPs. The sediment samples presented a greater abundance as compared to the water samples. Overall, it is necessary to continue the optimization of MPs separation protocol and identification according to the complexity of samples, mainly due to the limitation and lack of spectral databases.

The increasing demand for efficient wastewater treatment technologies, driven by global population growth and industrialisation, highlights the necessity for advanced, reliable solutions. This study investigated the efficacy of a slurry photocatalytic membrane reactor (PMR) for the advanced removal of organic pollutants, quantified via chemical oxygen demand (COD), under natural and simulated solar light irradiation. Employing two variants of iron-doped titania as photocatalysts and a polysulfone-based polymeric membrane for the separation process, the investigation showcased COD removal efficiencies ranging from 66–85% under simulated solar light to 52–81% under natural sunlight over a 7 h irradiation period. The overall PMR system demonstrated COD removal efficiencies of 84–95%. The results confirmed the enhanced photocatalytic activity afforded by iron doping and establish solar-powered slurry PMRs as an effective, low-energy, and environmentally friendly alternative for the advanced treatment of municipal wastewater, with the research providing valuable insights into sustainable water management practices.

New research applications involving the use of cellulosic material derived from maize stalk for on-site treatment of leachate were evaluated for specific removal of Cu(II) and Fe(III) from real, highly polluted tailing pond and mine wastewater samples. Two major issues generated by anthropic mining activities were also tackled: wastewater metal content decrease to improve water quality and subsequently metal specific recovery, increasing the economic efficiency of metal production by using a green technology for residual management. Rapid saturation of the maize stalk mass determined in batch studies and the mine pilot experiment led to diminished metal concentrations in the second pilot experiment, where Cu(II) and Pb(II) from synthetic solutions were monitored in order to test biomaterial performances. In addition, in the second pilot experiment, maize stalk removed Pb(II) in the first 36 h, below the determination limit of the analytical method. The biomaterial bed in the column was saturated after 252 h of inflow solution. FTIR-ATR, TG and SEM techniques probed the interaction between maize stalk polar groups C=O, –OH, C–O and tailing water metallic ions by large FTIR band displacements, intensity decrease and shape changes, modification of thermal stability and by changes in the appearance of adsorbent microstructure images owing mainly to ion exchange mechanism.