The development of efficient antibiotic-releasing materials derived from sustainable and recyclable compounds represents a key area within biomedical materials science, particularly in the treatment of antibacterial infections. Herein, a Fe³⁺/terephthalate-based metal–organic framework (MIL-53) and a novel advanced material made of MIL-53 with biogenic hydroxyapatite (1) were prepared by solvothermal reactions, and these were studied in detail as a Penicillin-G-releasing material. After loading Penicillin G on 1 and MIL-53, the antibiotic percentage release was studied, and the antimicrobial effectiveness of each material was evaluated against two bacterial ATCC strains (E. coli and S. aureus) and various Penicillin-G-resistant uropathogenic strains such as E. coli isolates (HHM 25, ERV 6, and FGI 4). Functional, structural, and morphological characteristics of these materials were thoroughly studied by analytical tools (FTIR, XRD, BET, SEM-EDS, and XPS). The Penicillin G load did not exceed 50% in both materials. The Penicillin G adsorption mechanism involves several types of interactions with the materials. The release of the antibiotic was more efficient from MIL-53, where the load did not exceed 20%. The release was analyzed using mathematical models. They indicated that when Penicillin G is released from MIL-53, the process follows diffusion through a uniform matrix; however, 1 is more porous, which helps with the release by diffusion of Penicillin G, and 1 exhibits more than a 90% inhibition of the growth of bacteria and strains like MIL-53. This suggests a valuable approach to antibiotic activity against resistant pathogens. The use of composite materials derived from the Fe-MOF with a sustainable matrix of hydroxyapatite as antibiotic-releasing materials has been unexplored until now.

CuS nanoparticles (Np) were synthesized and deposited on synthetic sphalerite (S_P) using two different methods. Two nanoparticle products were obtained on the surface of S_P, Np1 and Np2, resulting in two active materials (Np1-S_P and Np2-S_P) with specific characteristics. Nanoparticles and active materials were characterized by TEM, XRD, SEM, and XPS. The collectors PAX and SIPX were adsorbed on Np1-S_P and Np2-S_P to determine the adsorption capacity. Method 1 provides a higher quantity of nanoparticles on S_P, which allows for the adsorption of a higher amount of SIPX. Method 1 was used to deposit nanoparticles on two natural sphalerites (S_N) with different iron contents. S_N, unlike S_P, can be used to test nanoparticle activation results in microflotation experiments. S_N was activated with nanoparticles (Np1-S_N) and using the traditional method (Cu-S_N). The recovery of 75% of zinc using the microflotation process suggests that the hydrophobicity of Np1-S_N is higher than that of Cu-S_N. Nanoparticles improve the hydrophobicity of S_N compared to the traditional activation used in the mining industry. These results suggest that using nanoparticles is an excellent option to activate minerals in flotation processes, decreasing the consumption of reagents and helping to mitigate negative impacts on the environment.

Semicrystalline polystyrene spheroidal nanoparticles (50–100 nm) were obtained via microemulsion polymerization. They were evaluated as coal collectors in a low-rank carbonaceous mineral containing 2% organic carbon. The recovery of coal using nanoparticles as collectors was 88.2%, in contrast to 53.2%, 46.4%, and 44.8% achieved using an amine-type compound, kerosene, and diesel, respectively. X-ray photoelectron spectroscopy (XPS) and zeta potential measurements confirmed the polystyrene–mineral surface chemical interaction. A Box–Behnken experimental design for flotation optimization was applied, and the results showed that the coal recovery increased up to 99.5% when the dosage of the collector was increased. A contact angle study and density functional theory calculations, together with XPS results, allowed us to postulate an interaction mechanism in which polystyrene nanoparticles adsorb onto the coal surface through hydrophobic interactions, rendering the oxidized surface hydrophobic and the coal buoyant by adhering to the gas bubbles.

This work presents a sustainable strategy for the fabrication of multifunctional silver nanoparticles (Ag-NPs) and Ag/jute nanocomposites using Erythroxylum coca tea waste extract as a bioreducing and stabilizing agent, combined with picosecond pulsed laser irradiation. UV–Vis spectroscopy and transmission electron microscopy revealed the formation of Ag-NPs with diverse morphologies and broad size distributions, which became significantly more uniform after laser post-treatment without the need for additional chemical reagents. Following laser irradiation, the initially broad Ag surface plasmon resonance (SPR) peak transformed into a symmetric Gaussian-shaped band, centered at 407 ± 3 nm for all the Ag-NPs systems. The catalytic performance of unsupported Ag-NPs and Ag-NPs supported on jute fibers was comparatively evaluated by degrading Congo red (CR) dye, revealing that the supported nanocomposites exhibited enhanced catalytic stability, higher pollutant removal efficiency, and improved catalyst recovery. Furthermore, multicomponent catalytic reduction experiments involving CR and 4-nitrophenol (4-NP) in the presence of NaBH₄ revealed simultaneous degradation and reduction pathways mediated by the Ag/jute nanocomposites, as evidenced by the emergence of new absorption bands during the reaction. In parallel, the synthesized Ag-NPs demonstrated pronounced antimicrobial activity against Escherichia coli, generating well-defined inhibition zones. Beyond conventional approaches centered on nanoparticle synthesis and morphology optimization, this study establishes a platform that combines agricultural waste valorization, laser-assisted nanoparticle engineering, and natural-fiber-supported nanocomposite fabrication, enabling efficient remediation of both single- and multicomponent pollutant systems while promoting catalyst reusability and environmental sustainability. These findings demonstrate the Ag/jute nanocomposites as sustainable and scalable catalytic materials for wastewater remediation and antimicrobial applications.

Methyl parathion (MP) is an organic pesticide used on crops to control pest populations. However, its indiscriminate use contaminates soil and water, necessitating the development of cost-effective solutions for its removal and detection. In this work, a novel luminescent composite (Pi@Tb-MOF) was successfully synthesized via the in situ growth of a terbium-based metal–organic framework on pistachio shell biomass. The successful formation of the Pi@Tb-MOF composite was confirmed by XRD, SEM-EDS, FTIR, and TGA analyses. The composite was evaluated for the removal and detection of MP in aqueous media. Kinetic data were best described by the second-order and Avrami models, which indicate heterogeneous surface reactions and progressive activation of adsorption sites. Isotherm analysis revealed that the Hill model provided the best fit (K_H = 0.6644), suggesting cooperative adsorption and strong adsorbate–adsorbate interactions on the composite surface. Although the maximum adsorption capacity predicted by the Langmuir model was 1.47 mg/g, the material exhibited a remarkable luminescence response to MP. The Tb-MOF characteristic emission bands decreased progressively upon pesticide adsorption, enabling fluorescence-based detection with a limit of detection of 0.1 µM. The quenching process followed a linear Stern–Volmer relationship at low concentrations (R² = 0.99), demonstrating the composite’s potential as a sensing platform. The fluorescence quenching is attributed to electron transfer interactions between the MOF ligand and the nitroaromatic group of MP combined with adsorption on the pistachio matrix. These results demonstrate that Pi@Tb-MOF is a sustainable composite capable of simultaneously removing and detecting methyl parathion, highlighting its potential as an environmentally friendly material for monitoring pesticide contamination in water. This work reports, for the first time, a novel Pi@Tb-MOF composite based on pistachio shell biomass and a luminescent Tb-MOF, which has not been previously described in the literature and enables the simultaneous adsorption and optical sensing of methyl parathion.