Herein, the prospective applications of green fabricated silver nanoparticles (Ag-NPs) within the biomedical field were investigated. The leaf aqueous extract of Portulaca oleracea L., a safe, cheap, and green method, was used to fabricate Ag-NPs. The maximum plasmon resonance of synthesized NPs has appeared at 420 nm. The various biomolecules present in the plant extract to assemble spherical Ag-NPs with sizes of 5–40 nm were analyzed using Fourier transform infrared and transmission electron microscopy. The Ag was the major content of the formed Ag-NPs with an atomic percent of 54.95% and weight percent of 65.86%, as indicated by EDX. The crystallographic structure of synthesized NPs was confirmed by the diffraction of the X-ray. The dynamic light scattering exhibits the homogeneity and mono-dispersity nature with a polydispersity index of 0.37 in the colloidal fluid and a zeta potential value of –36 mV. The synthesized Ag-NPs exhibited promising antimicrobial efficacy toward various prokaryotic and eukaryotic pathogenic microorganisms with low MIC values of 12.5 µg mL⁻¹ and 6.25 µg mL⁻¹, respectively. Additionally, the P. oleracea-formed Ag-NPs showed optimistic antioxidant activity assessed by DPPH and H₂O₂ assay methods with the highest scavenging percentages of 88.5 ± 2.3% and 76.5 ± 1.7%, respectively, at a concentration of 200 µg mL⁻¹. Finally, the biosynthesized Ag-NPs showed high antiviral properties toward the hepatitis A virus and Cox-B4 with inhibition percentages of 79.16 ± 0.5% and 73.59 ± 0.8%, respectively. Overall, additional research is essential to explore the Ag-NP-based aqueous extract of P. oleracea for human health. In the current investigation the use of synthesized Ag-NPs as antimicrobial, antioxidant, and antiviral agents to protect against pathogenic microbes, degenerative diseases caused by various oxidative stresses, and deadly viruses is recommended.

The spread of organic pollutants in water spoils the environment, and among the best-known sorbents for removing organic compounds are carbonaceous materials. Sunflower seed waste (SFSW) was employed as a green and low-cost precursor to prepare carbon nanoparticles (CNPs) via pyrolysis, followed by a ball-milling process. The CNPs were treated with a nitric–sulfuric acid mixture (1:1) at 100 °C. The scanning electron microscopy (SEM) showed a particle size range of 38 to 45 nm, and the Brunauer–Emmett–Teller (BET) surface area was 162.9 m² g⁻¹. The elemental analysis was performed using energy-dispersive X-ray spectroscopy, and the functional groups on the CNPs were examined with Fourier transform infrared spectroscopy. Additionally, an X-ray diffractometer was employed to test the phase crystallinity of the prepared CNPs. The fabricated CNPs were used to adsorb ciprofloxacin (CFXN) and malachite green (MLG) from water. The experimentally obtained adsorption capacities for CFXN and MLG were 103.6 and 182.4 mg g⁻¹, respectively. The kinetic investigation implied that the adsorption of both pollutants fitted the pseudo-first-order model, and the intraparticle diffusion step controlled the process. The equilibrium findings for CFXN and MLG sorption on the CNPs followed the Langmuir and the Fredulich isotherm models, respectively. It was concluded that both pollutants spontaneously adsorbed on the CNPs, with physisorption being the likely mechanism. Additionally, the FTIR analysis of the adsorbed CFXN showed the disappearance of some functional groups, suggesting a chemisorption contribution. The CNPs showed an excellent performance in removing CFXN and MLG from groundwater and seawater samples and possessed consistent efficiency during the recycle–reuse study. The application of CNPs to treat synthetically contaminated natural water samples indicated the complete remediation of polluted water using the ball-mill-fabricated CNPs.

Pharmaceutical pollution has pervaded many water resources all over the globe. The propagation of this health threat drew the researchers’ concern in seeking an efficient solution. This study introduced toilet paper waste as a precursor for carbon nanoparticles (CRNPs). The TEM results showed a particle size range of 30.2 nm to 48.1 nm, the BET surface area was 283 m² g⁻¹, and the XRD pattern indicated cubical-graphite crystals. The synthesized CRNPs were tested for removing tigecycline (TGCN), chlortetracycline (CTCN), oxytetracycline (OTCN), and doxycycline (DXCN) via the batch process. The adsorption equilibrium time for TGCN, DXCN, CTCN, and OTCN was 60 min, and the concentration influence revealed an adsorption capacity of 172.5, 200.1, 202.4, and 200.0 mg g^−1, respectively. The sorption of the four drugs followed the PSFO, and the LFDM models indicated their high sorption affinity to the CRNPs. The adsorption of the four drugs fitted the multilayer FIM that supported the high-affinity claim. The removals of the four drugs were exothermic and spontaneous physisorption. The fabricated CRNPs possessed an excellent remediation efficiency for contaminated SW and GW; therefore, CRNPs are suggested for water remediation as low-cost sorbent.

Herein, nanoscale MgAl₂O₄ (MOA), 10%CuO@MgAl₂O₄ (10Cu@MOA), 10%NiO@MgAl₂O₄ (10Ni@MOA), and 10%CoO@MgAl₂O₄ (10Co@MOA) were synthesized employing butylated hydroxytoluene (the food additive BHT) as a capping agent. The SEM images illustrated average sizes of 38.8, 30.0, 40.8, and 32.7 nm for MOA, 10Cu@MOA, 10Ni@MOA, and 10Co@MOA, respectively, and their BET surface area were 84.4, 141.8, 126.7, and 105.3, respectively. Doxycycline DXC removal was studied employing the MOA, 10Cu@MOA, 10Ni@MOA, and 10Co@MOA, which resulted in q_t values of 57.3, 106.1, 97.7, and 73.9 mg g⁻¹, respectively. The pseudo-second order model best described the DXC sorption onto MOA, 10Cu@MOA, 10Ni@MOA, and 10Co@MOA, and both film diffusion models influenced the DXC sorptions onto the sorbents. The DXC sorption onto the 10Cu@MOA fitted the Freundlich model. The thermodynamics implied endothermic-spontaneous DXC sorption onto the10Cu@MOA. The pH study exposed that the DXC removal by 10Cu@MOA was more effective in a mildly acidic medium (pH = 6.0). Furthermore, the 10Cu@MOA effectiveness in treating surface water contaminated by 5.0 and 10.0 mg L⁻¹ DXC was 99.9% and 98.1%, respectively, while it was 94.7% and 92.5% in treating the concentrations above in seawater, respectively. The reusability study showed a 10% reduction in the 10Cu@MOA’s removal efficiency at the fourth cycle, which is encouraging for real-life applications.

Coffee skins, a cheap, agricultural waste, were carbonized in a tubular furnace under a nitrogen stream and then ball milled to fabricate coffee skin-carbon-nanoparticles (CCNPs). SEM showed 35.6–41.6 nm particle size. The 26.64 and 43.16 peaks in the XRD indicated a cubic graphite lattice. The FT-IR broadband revealed a 2500–3500 cm⁻¹ peak, suggesting an acidic O-H group. CCNPs possessed a type-H3-loop in the N₂-adsorption-desorption analysis, with a surface of 105.638 m² g⁻¹. Thereafter, CCNPs were tested for ciprofloxacin (CPXN) adsorption, which reached equilibrium in 90 min. CCNPs captured 142.6 mg g⁻¹ from 100 mg L⁻¹ CPXN, and the 5:12 sorbent mass-to-solution volume ratio was suitable for treating up to 75 mg L⁻¹ contamination. The q_t dropped from 142.6 to 114.3 and 79.2 mg g⁻¹ as the temperature rose from 20 °C to 35 °C and 50 °C, respectively, indicating exothermic adsorption. CPXN removal efficiency decreased below pH 5.0 and above pH 8.0. Kinetically, CPXN adsorption fits the second-order model and is controlled by the liquid-film mechanism, indicating its preference for the CCNPs’ surface. The adsorption agreement with the liquid-film and Freundlich models implied the ease of CPXN penetration into the CCNP inner shells and the multilayered accumulation of CPXN on the CCNPs’ surface. The negative ∆H° and ∆G° revealed the exothermic nature and spontaneity of CPXN adsorption onto the CCNP. The CCNPs showed an efficiency of 95.8% during four consecutive regeneration-reuse cycles with a relative standard deviation (RSD) of 3.1%, and the lowest efficiency in the fourth cycle was 92.8%.

This study has successfully developed a practical and straightforward approach for synthesizing nanocomposites with excellent dye removal potential. The SEM inspection of γ-Al₂O₃ (γ-Al) and MgO/MgAl₂O₄ (Mg/MgAl) nanocomposite showed a mean size of 59.0 and 46.4 nm, respectively, while the TEM results show particles with an average size of 26.63 and 13.4 nm, respectively. The surface area of γ-Al and Mg/MgAl was 50.0 and 69.5 m² g⁻¹, respectively. The study of adsorbing indigo carmine (IC) sorption onto γ-Al and Mg/MgAl presented sorption capacities of 41.6 and 55.9 mg g⁻¹, respectively, and both adsorbents attained equilibrium at 90 min. The highest IC sorption onto Mg/MgAl took place at pH 6.0. It is worth mentioning that raising the IC solution’s temperature from 20 °C to 50 °C increased the q_t to 268 mg g⁻¹. The IC sorption onto γ-Al and Mg/MgAl agreed with the pseudo-second-order model, and the liquid-film diffusion controlled the IC sorption. The Mg/MgAl showed an average removal of 98.2% when tested for removing six dyes at 10 mg L⁻¹, particularly malachite green, methylene blue, fast green, methyl orange, rhodamine B, and basic fuchsin, and the removal efficiency was 93.3% when their concentration increased to 20 mg L⁻¹. The Mg/MgAl nanocomposite performed exceptionally well in natural water samples (seawater and groundwater), indicating its potential applicability in managing water contamination.