Search Results (21)

In this work, we focused on the bioactivity and antibacterial behavior of PLA-based electrospun fibers, efibers, reinforced with both MgO and Mg(OH)₂ nanoparticles, NPs. The evolution of PLA-based efibers was followed in terms of morphology, FTIR, XRD, and visual appearance. The bioactivity was discussed in terms of hydroxyapatite growth after 28 days, considered as T28, of immersion in simulated body fluid, SBF. In particular, the biomineralization process evidenced after immersion in SBF started at T14 in both systems. The number of precipitated crystals increased by increasing the amount of both NPs. The chemical composition of the precipitated crystals was also characterized in terms of the Ca/P molar ratio after T28 of immersion in SBF, indicating the presence of hydroxyapatite on the surface of both reinforced efibers. Moreover, a reduction in the average diameter of the PLA-based efibers was observed, reaching a maximum reduction of 46 and 60% in the average diameter of neat PLA and PLA:OLA efibers, respectively, after 28 days of immersion in SBF. The antibacterial behavior of the MgO and Mg(OH)₂ NPs in the PLA-based electrospun fibers was tested against Escherichia coli, E. coli, as the Gram-negative bacteria, and Staphylococcus aureus, S. aureus, as the Gram-positive bacteria, obtaining the best antibacterial activity against the Gram-negative bacteria E. coli of 21 ± 2% and 34 ± 6% for the highest concentration of MgO and Mg(OH)₂ NPs, respectively. Full article

Utilizing MgO as the precursor and deionized water as the solvent, this study synthesized nanoparticles of Mg(OH)₂ via hydrothermal methods, aiming to control its purity, particle size, and morphology by understanding its growth under non-uniform nucleation. Characterization of crystal morphology and structure was conducted through scanning electron microscopy and X-ray diffraction, while laser particle size detection assessed the secondary particle size distribution. The study focused on how MgO’s hydrothermal process conditions influence Mg(OH)₂ crystal growth, particularly through ion concentration and release rate adjustments to direct crystal growth facets. These adjustments shifted the dominant growth plane, enhancing the peak intensity ratio I001/I101 from 1.03 to 2.14, thereby reducing surface polarity and secondary aggregation of crystals. The study of the physicochemical properties of the same sample at different times revealed the pattern of crystal dissolution and recrystallization. A 2 h hydrothermal reaction notably altered the particle size distribution, with a decrease in particles sized 0.2~0.4 μm and an increase in those sized 0.4~0.6 μm, alongside new particles over 1 μm, indicating a shift toward uniformity through dissolution and recrystallization. Optimal conditions (6% magnesium oxide concentration, 160 °C, 2 h) led to the synthesis of highly dispersed, uniformly sized magnesium hydroxide, showcasing a simple, eco-friendly, and high-yield process. Full article

A rapid, eco-friendly, and simple method for the synthesis of long-lasting (2 years) silver nanoparticles (AgNPs) is reported using aqueous leaf and petal extracts of Tagetes erecta L. The particles were characterized using UV-Visible spectrophotometry and the analytical and crystallographic techniques of transmission electron microscopy (TEM). The longevity of the AgNPs was studied using UV-Vis and high-resolution TEM. The antibacterial activity of the particles against Erwinia amylovora was evaluated using the Kirby–Bauer disk diffusion method. The results were analyzed using ANOVA and Tukey’s test (p ≤ 0.05). Both the leaf and petal extracts produced AgNPs, but the leaf extract (1 mL) was long-lasting and quasi-spherical (17.64 ± 8.87 nm), with an absorbance of UV-Vis λ_max 433 and a crystalline structure (fcc, 111). Phenols, flavonoids, tannins, and terpenoids which are associated with -OH, C=O, and C=C were identified in the extracts and could act as reducing and stabilizing agents. The best antibacterial activity was obtained with a nanoparticle concentration of 50 mg AgNPs L⁻¹. The main contribution of the present research is to present a sustainable method for producing nanoparticles which are stable for 2 years and with antibacterial activity against E. amylovora, one of most threatening pathogens to pear and apple productions. Full article

The green synthesis of zinc oxide nanoparticles (ZnO NPs) using plants has grown in significance in recent years. ZnO NPs were synthesized in this work via a chemical precipitation method with Jasminum sambac (JS) leaf extract serving as a capping agent. These NPs were characterized using UV-vis spectroscopy, FT-IR, XRD, SEM, TEM, TGA, and DTA. The results from UV-vis and FT-IR confirmed the band gap energies (3.37 eV and 3.50 eV) and the presence of the following functional groups: CN, OH, C=O, and NH. A spherical structure and an average grain size of 26 nm were confirmed via XRD. The size and surface morphology of the ZnO NPs were confirmed through the use of SEM analysis. According to the TEM images, the ZnO NPs had an average mean size of 26 nm and were spherical in shape. The TGA curve indicated that the weight loss starts at 100 °C, rising to 900 °C, as a result of the evaporation of water molecules. An exothermic peak was seen during the DTA analysis at 480 °C. Effective antibacterial activity was found at 7.32 ± 0.44 mm in Gram-positive bacteria (S. aureus) and at 15.54 ± 0.031 mm in Gram-negative (E. coli) bacteria against the ZnO NPs. Antispasmodic activity: the 0.3 mL/mL sample solution demonstrated significant reductions in stimulant effects induced by histamine (at a concentration of 1 µg/mL) by (78.19%), acetylcholine (at a concentration of 1 µM) by (67.57%), and nicotine (at a concentration of 2 µg/mL) by (84.35%). The antipyretic activity was identified using the specific Shodhan vidhi method, and their anti-inflammatory properties were effectively evaluated with a denaturation test. A 0.3 mL/mL sample solution demonstrated significant reductions in stimulant effects induced by histamine (at a concentration of 1 µg/mL) by 78.19%, acetylcholine (at a concentration of 1 µM) by 67.57%, and nicotine (at a concentration of 2 µg/mL) by 84.35%. These results underscore the sample solution’s potential as an effective therapeutic agent, showcasing its notable antispasmodic activity. Among the administered doses, the 150 mg/kg sample dose exhibited the most potent antipyretic effects. The anti-inflammatory activity of the synthesized NPs showed a remarkable inhibition percentage of (97.14 ± 0.005) at higher concentrations (250 µg/mL). Furthermore, a cytotoxic effect was noted when the biologically synthesized ZnO NPs were introduced to treated cells. Full article

The demand for lithium is constantly increasing due to its wide range of uses in an excessive number of industrial applications. Typically, expensive lithium-based chemicals (LiOH, LiCl, LiNO₃, etc.) have been used to fabricate adsorbents (i.e., lithium manganese oxide) for lithium ion (Li⁺) adsorption from aqueous sources. This type of lithium-based adsorbent does not seem to be very effective in recovering Li⁺ from water from an economic point of view. In this study, an innovative nanocomposite for Li⁺ adsorption was investigated for the first time, which eliminates the use of lithium-based chemicals for preparation. Here, calcium oxide nanoparticles (CaO-NPs), silver-doped CaO nanoparticles (Ag-CaO-NPs), and surfactant (polyvinylpyrrolidone (PVP) and sodium dodecyl sulfate (SDS))-modified Ag-CaO (PVP@Ag-CaO and SDS@Ag-CaO) nanocomposites were designed by the chemical co-precipitation method. The PVP and SDS surfactants acted as stabilizing and capping agents to enhance the Li⁺ adsorption and recovery performance. The physicochemical properties of the designed samples (morphology, size, surface functionality, and crystallinity) were also investigated. Under optimized pH (10), contact time (8 h), and initial Li⁺ concentration (2 mg L⁻¹), the highest Li⁺ adsorption efficiencies recorded by SDS@Ag-CaO and PVP@Ag-CaO were 3.28 mg/g and 2.99 mg/g, respectively. The nature of the Li⁺ adsorption process was examined by non-linear kinetic and isothermal studies, which revealed that the experimental data were best fit by the pseudo-first-order and Langmuir models. Furthermore, it was observed that the SDS@Ag-CaO nanocomposite exhibited the highest Li⁺ recovery potential (91%) compared to PVP@Ag-CaO (85%), Ag-CaO NPs (61%), and CaO NPs (43%), which demonstrates their regeneration potential. Therefore, this type of innovative adsorbents can provide new insights for the development of surfactant-capped nanocomposites for enhanced Li⁺ metal recovery from wastewater. Full article

There exists a multitude of pathogens that pose a threat to human and public healthcare, collectively referred to as ESKAPE pathogens. These pathogens are capable of producing biofilm, which proves to be quite resistant to elimination. Strains of A. baumannii, identified by the “A” in the acronym ESKAPE, exhibit significant resistance to amoxicillin in vivo due to their ability to form biofilm. This study aims to inhibit bacterial biofilm formation, evaluate novel silica nanoparticles’ effectiveness in inhibiting biofilm, and compare their effectiveness. Amoxicillin was utilized as a positive control, with a concentration exceeding twice that when combined with silica NPs. Treatments included pure silica NPs, silica NPs modified with copper oxide (CuO.SiO₂), sodium hydroxide (NaOH.SiO₂), and phosphoric acid (H₃PO₄.SiO₂). The characterization of NPs was conducted using scanning electron microscopy (SEM), while safety testing against normal fibroblast cells was employed by MTT assay. The microtiter plate biofilm formation assay was utilized to construct biofilm, with evaluations conducted using three broth media types: brain heart infusion (BHI) with 2% glucose and 2% sucrose, Loria broth (LB) with and without glucose and sucrose, and Dulbecco’s modified eagle medium/nutrient (DMEN/M). Concentrations ranging from 1.0 mg/mL to 0.06 µg/mL were tested using a microdilution assay. Results from SEM showed that pure silica NPs were mesoporous, but in the amorphous shape of the CuO and NaOH treatments, these pores were disrupted, while H₃PO₄ was composed of sheets. Silica NPs were able to target Acinetobacter biofilms without harming normal cells, with viability rates ranging from 61–73%. The best biofilm formation was achieved using a BHI medium with sugar supplementation, with an absorbance value of 0.35. Biofilms treated with 5.0 mg/mL of amoxicillin as a positive control alongside 1.0 mg/mL of each of the four silica treatments in isolation, resulting in the inhibition of absorbance values of 0.04, 0.13, 0.07, 0.09, and 0.08, for SiO₂, CuO.SiO₂, NaOH.SiO₂ and H₃PO₄.SiO₂, respectively. When amoxicillin was combined, inhibition increased from 0.3 to 0.04; NaOH with amoxicillin resulted in the lowest minimum biofilm inhibitory concentration (MBIC), 0.25 µg/mL, compared to all treatments and amoxicillin, whereas pure silica and composite had the highest MBIC, even when combined with amoxicillin, compared to all treatments, but performed better than that of the amoxicillin alone which gave the MBIC at 625 µg/mL. The absorbance values of MBIC of each treatment showed no significant differences in relation to amoxicillin absorbance value and relation to each other. Our study showed that smaller amoxicillin doses combined with the novel silica nanoparticles may reduce toxic side effects and inhibit biofilm formation, making them viable alternatives to high-concentration dosages. Further investigation is needed to evaluate in vivo activity. Full article

The increasing utilization of nanoparticles (NPs) in agricultural practices has led to a surge in demand for nano-based products. Herein, we investigate the dose-dependent impacts of nickel hydroxide (Ni(OH)₂)/nickel (Ni) NPs, synthesized using Asparagus racemosus Linn. leaf extract, on the seed germination and growth of Vigna radiata (Linn.) Wilczek. In all seed samples, 100% germination was observed in Treatment 1 (2.74 mg mL⁻¹) and Treatment 2 (5.48 mg mL⁻¹) of Ni/Ni(OH)₂ NPs. However, in Treatment 3 (8.22 mg mL⁻¹) and Treatment 4 (10.96 mg mL⁻¹), the germination percentage was lower, reaching 80%. Further, Treatment 5 (13.70 mg mL⁻¹) of Ni/Ni(OH)₂ NPs showed a reduced germination rate of 60%, indicating a prolonged germination process at higher concentrations. Remarkably, the length of seedlings showed a significant increase in all experimental treatments compared to the control group, which received 5 mL of distilled water. Among the investigated parameters, Treatment 2 demonstrated the most promising outcomes, exhibiting the highest chlorophyll stability index (23.73%) and membrane stability index (67.89%) values, as well as the lowest root ion leakage (24.75%). These findings indicate that Ni/Ni(OH)₂ has the capacity to enhance seed germination and foster seedling growth. Full article

Polyurethane (PU) is one of the most well-known polymer coatings because of its favorable characteristics, which include its low density, nontoxicity, nonflammability, longevity, adhesion, simple manufacture, flexibility, and hardness. However, PU does come with several major drawbacks, among which are poor mechanical properties as well as low thermal and chemical stability, particularly in the high-temperature mode, where becomes gets flammable and loses adhesion ability. The limitations have inspired researchers to develop a PU composite to improve the weaknesses by adding different reinforcements. Magnesium hydroxide, having the ability to be produced with exceptional properties such as flammability, has consistently attracted the interest of researchers. Additionally, silica nanoparticles with high strength and hardness are one of the excellent reinforcements of polymers these days. The hydrophobic, physical, and mechanical properties of pure polyurethane and the composite type (nano, micro, and hybrid) fabricated with the drop casting method were examined in this study. 3-Aminopropyl triethoxysilane was applied as a functionalized agent. To confirm that hydrophilic particles turned into hydrophobic, FTIR analysis was carried out. The impact of size, percentage, and kind of fillers on different properties of PU/Mg(OH)${}_2$-SiO${}_2$ was then investigated using different analyses including spectroscopy and mechanical and hydrophobicity tests. The resultant observations demonstrated that different surface topographies can be obtained from the presence of particles of different sizes and percentages on the hybrid composite’s surface. Surface roughness allowed for exceptionally high water contact angles, which confirmed the hybrid polymer coatings’ superhydrophobic properties. According to the particle size and content, the distribution of fillers in the matrix also improved the mechanical properties. Full article

Zero-valent iron nanoparticles (ZVI-NPs) are utilized for the indemnification of a wide range of environmental pollutants. Among the pollutants, heavy metal contamination is the major environmental concern due to their increasing prevalence and durability. In this study, heavy metal remediation capabilities are determined by the green synthesis of ZVI-NPs using aqueous seed extract of Nigella sativa which is a convenient, environmentally friendly, efficient, and cost-effective technique. The seed extract of Nigella sativa was utilized as a capping and reducing agent for the generation of ZVI-NPs. UV-visible spectrophotometry (UV-vis), scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM-EDX), and Fourier transform infrared spectroscopy (FTIR) was used to investigate the ZVI-NP composition, shape, elemental constitution, and perspective functional groups, respectively. The biosynthesized ZVI-NPs displayed a peak of plasmon resonance spectra at 340 nm. The synthesized NPs were cylindrical in shape, with a size of 2 nm and (-OH) hydroxyl, (C-H) alkanes and alkynes N-C, N=C, C-O, =CH functional groups attached to the surface of ZVI-NPs. Heavy metals were successfully remediated from industrial wastewater collected from the various tanneries of Kasur. During the reaction duration of 24 h, different concentrations of ZVI-NPs (10 μg, 20 μg and 30 μg) per 100 mL were utilized for the removal of heavy metals from industrial wastewater. The 30 μg/100 mL of ZVI-NPs proved the pre-eminent concentration of NPs as it removed >90% of heavy metals. The synthesized ZVI-NPs were analyzed for compatibility with the biological system resulting in 87.7% free radical scavenging, 96.16% inhibition of protein denaturation, 60.29% and 46.13% anti-cancerism against U87-MG and HEK 293 cell lines, respectively. The physiochemical and exposure mathematical models of ZVI-NPs represented them as stable and ecofriendly NPs. It proved that biologically synthesized NPs from a seed tincture of Nigella sativa have a strong potential to indemnify heavy metals found in industrial effluent samples. Full article

The initial stages of AM60-AlN nanocomposite and AM60 corrosion behaviors were compared over 30 days of exposure to solution ($\mathrm{NaCl}$, ${\mathrm{Na}}_2{\mathrm{SO}}_4$ and ${\mathrm{NaHCO}}_3$), simulating the marine-coastal environment (SME). The incorporation of AlN nanoparticles (1.0 wt.%) in the AM60 alloy matrix favored the lower roughness of the AM60-AlN, associated with the grain refinement in the matrix. During the immersion of the alloys, pH of the SME solution shifted to alkaline values >9, and therefore, the solubility of AlN aluminum hydroxide phases were raised, followed by a slightly higher release of Mg-ions and corrosion rate increase. The chloride ions attributed to the unstability of the Al-Mn phase and $\mathrm{Al}{\left(\mathrm{OH}\right)}_3$ corrosion product was formed in a low content. The composite AM60-AlN presented lower value of the electrochemical noise resistance $\left({\mathrm{R}}_{\mathrm{n}}\right)$, suggesting that the corrosion process occurs with less difficulty. The localized corrosion near the Al-Mn cathodes seems to be stronger on the composite surface, in area and depth of penetration. The corrosion current fluctuations suggested that the corrosion is a weakly persistent process, dominated by the fractional Gaussian noise (fGn). Full article

In this study, using the Box–Behnken model, we optimized the ethanolic extraction of phytochemicals from Enantia chloranta bark for the first time, assessed the composition with HPLC-MS/MS, performed the green synthesis of silver nanoparticles (AgNPs) and characterized them with UV-Vis spectrophotometry, photon cross-correlation spectroscopy, energy-dispersive X-ray fluorescence spectrometry, and Fourier transform infrared spectroscopy. The antibacterial and antibiotic-resistance reversal properties of optimized extract (O-ECB) and AgNPs were assessed on various microorganisms (15 Gram−, 7 Gram+, and 2 fungi) using the well diffusion method and microbroth dilution assay. The mechanism of action was investigated on growth kinetic and proton pumps of Escherichia coli. The in vivo antimicrobial activity and toxicity were assessed on Galleria mellonella larvae. The optimal mass yield (14.3%) related to the highest antibacterial activity (31 mm vs. S. aureus ATCC 6538) was obtained with the following operating conditions: % EtOH—100%; ratio m/v—20 g/mL; and extraction time—6 h. All the compounds identified in O-ECB were alkaloids and the major constituents were palmatine (51.63%), columbamine +7,8-dihydro-8-hydroxypalmatine (19.21%), jatrorrhizine (11.02%), and pseudocolumbamine (6.33%). Among the minerals found in O-ECB (S, Si, Cl, K, Ca, Mn, Fe, Zn, and Br), Br, Fe, and Cl were the most abundant with mean fluorescence intensities of 4.6529, 3.485,4, and 2.5942 cps/uA, respectively. The synthesized AgNPs revealed a strong absorption plasmon band between 430 and 450 nm and an average hydrodynamic diameter ×50 of 59.74 nm, and the presence of Ag was confirmed by a characteristic peak in the spectrum at the silver Kα line of 22.105 keV. Both O-ECB and AgNPs displayed noteworthy and broad-spectrum antimicrobial activities against 20/24 and 24/24 studied microorganisms, respectively, with recorded minimal inhibitory concentrations (MICs) ranging from 8 to ≥1024 µg/mL and 2 to 64 µg/mL. O-ECB and AgNPs showed antibiofilm properties and significantly enhanced the efficacy of conventional antibiotics against selected multidrug-resistant bacteria, and the mechanistic investigations revealed their interference with bacterial growth kinetic and the inhibition of H+-ATPase proton pumps. LD50s were 40 mg/mL and 0.6 mg/mL for O-ECB and AgNPs, respectively. In conclusion, the current study provides a strong experimental baseline to consider Enantia chlorantha bark and their green synthetized AgNPs as potent antimicrobial compounds in this era of antimicrobial resistance. Full article

The aim of this work is the reduction and decoration of graphene oxide (GO) with magnesium oxide (MgO). In this work, GO was synthesized using modified Hummers’ protocol with (1:2), (1:3) and (1:4) graphite:potassium permanganate mass ratios. Subsequently, all GO samples (GO1:2, GO1:3, GO1:4) were reduced and decorated with magnesium oxide nanoparticles using a reflux technique at 100 °C for 2 h. Sample characterization using X-ray diffraction (XRD) reveals the presence of peaks relative to two different magnesium (Mg) phases: magnesium oxide (MgO) and magnesium hydroxide (Mg(OH)₂). The presence of these spectral features, although characterized by a remarkable broadening, confirms the successful synthesis of Mg(OH)₂-rGO-MgO nanocomposites. X-ray photoelectron spectroscopy (XPS) spectra indicate the presence of peaks assigned to C, O and Mg. The analysis of the high-resolution XPS spectra of these elements confirms once again the presence of Mg(OH)₂-rGO-MgO compounds. The low temperature synthesis of Mg(OH)₂-rGO-MgO nanocomposite exhibiting superior catalytic properties compared to MgO–rGO nanoparticles is an important step forward with respect to the current state of the art. The antioxidant activity of six nanocomposites, namely GO1:2, GO1:3, GO1:4, MgO–rGO1:2, MgO–rGO1:3 and MgO–rGO1:4, was determined using standard protocols based on a DPPH radicals scavenging assay, an H₂O₂ scavenging assay, and a phosphomolybdate assay. All our samples exhibited dose-dependent antioxidant activity. Interestingly, among the different synthesized nanoparticles, GO1:4 and MgO–rGO1:4 showed the best performances. Full article

The photocatalytic reduction of hexavalent chromium, Cr(VI), to the trivalent species, Cr(III), has continued to inspire the synthesis of novel photocatalysts that are capable of achieving the task of converting Cr(VI) to the less toxic and more useful species. In this study, a novel functionalized graphitic carbon nitride (Cu_3.21Bi_4.79S₉/gC₃N₄) was synthesized and characterized by using X-ray diffraction (XRD), thermogravimetry analysis (TGA), energy-dispersive X-ray spectroscopy (EDS), Fourier transform infrared spectroscopy (FTIR), transmission electron microscope (TEM), and scanning electron microscope (SEM). The composite was used for the photocatalytic reduction of hexavalent chromium, Cr(VI), under visible light irradiation. A 92.77% efficiency of the reduction was achieved at pH 2, using about 10 mg of the photocatalyst and 10 mg/L of the Cr(VI) solution. A pseudo-first-order kinetic study indicated 0.0076 min⁻¹, 0.0286 min⁻¹, and 0.0393 min⁻¹ rate constants for the nanoparticles, pristine gC₃N₄, and the nanocomposite, respectively. This indicated an enhancement in the rate of reduction by the functionalized gC₃N₄ by 1.37- and 5.17-fold compared to the pristine gC₃N₄ and Cu_3.21Bi_4.79S₉, respectively. A study of how the presence of other contaminants including dye (bisphenol A) and heavy-metal ions (Ag(I) and Pb(II)) in the system affects the photocatalytic process showed a reduction in the rate from 0.0393 min⁻¹ to 0.0019 min⁻¹ and 0.0039 min⁻¹, respectively. Finally, the radical scavenging experiments showed that the main active species for the photocatalytic reduction of Cr(VI) are electrons (e⁻), hydroxyl radicals (·OH⁻), and superoxide (·O₂⁻). This study shows the potential of functionalized gC₃N₄ as sustainable materials in the removal of hexavalent Cr from an aqueous solution. Full article

Herein, we report the synthesis of magnetic nanoparticle (MNP)-reduced graphene oxide (rGO) and polymethylmethacrylate (PMMA) composite (MNPs/rGO/PMMA) as adsorbent via an in situ fabrication strategy and, in turn, the application for adsorptive removal and recovery of Cr(VI) from tannery wastewater. The composite material was characterized via XRD, FTIR and SEM analyses. Under batch mode experiments, the composite achieved maximum adsorption of the Cr(VI) ion (99.53 ± 1.4%, i.e., 1636.49 mg of Cr(VI)/150 mg of adsorbent) at pH 2, adsorbent dose of 150 mg/10 mL of solution and 30 min of contact time. The adsorption process was endothermic, feasible and spontaneous and followed a pseudo-2nd order kinetic model. The Cr ions were completely desorbed (99.32 ± 2%) from the composite using 30 mL of NaOH solution (2M); hence, the composite exhibited high efficiency for five consecutive cycles without prominent loss in activity. The adsorbent was washed with distilled water and diluted HCl (0.1M), then dried under vacuum at 60 °C for reuse. The XRD analysis confirmed the synthesis and incorporation of magnetic iron oxide at 2θ of 30.38°, 35.5°, 43.22° and 57.36°, respectively, and graphene oxide (GO) at 25.5°. The FTIR analysids revealed that the composite retained the configurations of the individual components, whereas the SEM analysis indicated that the magnetic Fe₃O₄–NPs (MNPs) dispersed on the surface of the PMMA/rGO sheets. To anticipate the behavior of breakthrough, the Thomas and Yoon–Nelson models were applied to fixed-bed column data, which indicated good agreement with the experimental data. This study evaluates useful reference information for designing a cost-effective and easy-to-use adsorbent for the efficient removal of Cr(VI) from wastewater. Therefore, it can be envisioned as an alternative approach for a variety of unexplored industrial-level operations. Full article

In this study, La₂O₃/g-C₃N₄ heterojunction photocatalysts doped with different dosages of La₂O₃ were constructed by a facile ultrasound-assisted calcination approach. The as-prepared photocatalysts were characterized by XRD, FTIR, FESEM, TEM, XPS, PL and DRS to verify the composite photocatalysts’ purity and to investigate their structural, morphological and elemental composition, and their energy band. According to the results, a type of pure rod–sheet-shaped, heterostructured nanoparticle was successfully obtained. Decorated with 10% La₂O₃, 2 g/L of the composite sample had a 93% degradation rate for 20 mg/L tetracycline hydrochloride within 2 h under visible light at a pH of 7. After four successive photocatalytic runs, satisfactory stability and reusability was exhibited, with 70% of the tetracycline hydrochloride being removed in the final experiment. Electrons (e⁻), photogenerated holes (h⁺), superoxide radical anions (·O₂⁻) and hydroxyl radicals (·OH) were the fundamental active species during the photocatalytic process and were investigated via quenching experiments. Furthermore, possible photocatalytic mechanisms were analyzed in this work. Full article