Search Results (8)

In this work, two novel nanoscale zero-valent iron (nZVI) composites (nanoscale zero-valent iron and copper-intercalated montmorillonite (MMT-nFe⁰/Cu⁰) and carbon microsphere-supported sulfurized nanoscale zero-valent iron (CMS@S-nFe⁰)) were used to treat soil contaminated with both Cr(VI) and p-nitrophenol (PNP), and added persulfate (PMS). Experiments found that the pollutant removal effect has a great relationship with the ratio of water to soil, the amount of catalyst, the amount of PMS, and the pH value. When the conditions are adjusted to the best (water–soil = 2:1, catalyst 30 g/kg, PMS 15 g/kg, pH 7–9), both materials fix Cr(VI) well and decompose PNP. The removal rates of Cr(VI) and PNP by the MMT-nFe⁰/Cu⁰ system are 90.4% and 72.6%, respectively, while the CMS@ S-nFe⁰ system is even more severe, reaching 94.8% and 81.3%. Soil column leaching experiments also proved that the fixation effect of Cr can last for a long time and PNP can be effectively decomposed. Through detection methods such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS), we found that Cr(VI) was effectively reduced to Cr(III) by Fe⁰ and Fe²⁺ ions and subsequently transformed into stable FeCr₂O₄ spinel oxides, and the groups produced after the decomposition of PNP could also help fix the metal. This work provides a way to simultaneously treat Cr(VI) and PNP pollution, and also allows the use of multifunctional nZVI composites in complex soil environments. Full article

Soil contamination by polycyclic aromatic hydrocarbons (PAHs) has been an environmental issue worldwide, which aggravates the ecological risks faced by animals, plants, and humans. In this work, the composites of nanoscale zero-valent iron supported on carbonylated activated carbon (nZVI-CAC) were prepared and applied to activate persulfate (PS) for the degradation of PAHs in contaminated soil. The prepared nZVI-CAC catalyst was characterized by scanning electron microscopy (SEM), X-ray diffractometer (XRD), Fourier transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS). It was found that the PS/nZVI-CAC system was superior for phenanthrene (PHE) oxidation than other processes using different oxidants (PS/nZVI-CAC > PMS/nZVI-CAC > H₂O₂/nZVI-CAC) and it was also efficient for the degradation of other six PAHs with different structures and molar weights. Under optimal conditions, the lowest and highest degradation efficiencies for the selected PAHs were 60.8% and 90.7%, respectively. Active SO₄^−• and HO^• were found to be generated on the surface of the catalysts, and SO₄^−• was dominant for PHE oxidation through quenching experiments. The results demonstrated that the heterogeneous process using activated PS with nZVI-CAC was effective for PAH degradation, which could provide a theoretical basis for the remediation of PAH-polluted soil. Full article

In the framework of wastewater treatment plants, sewage sludge can be directed to biochar production, which when coupled with an external iron source has the potential to be used as a carbon–iron composite material for treating various organic pollutants in advanced oxidation processes. In this research, “green” synthesized nano zero-valent iron (nZVI) supported on sewage sludge-based biochar (BC)–nZVI-BC was used in the Fenton process for the degradation of the recalcitrant organic molecule. In this way, the circular economy principles were supported within wastewater treatment with immediate loop closing; unlike previous papers, where only the water treatment was assessed, the authors proposed a new approach to wastewater treatment, combining solutions for both water and sludge. The following phases were implemented: synthesis and characterization of nano zero-valent iron supported on sewage sludge-based biochar (nZVI-BC); optimization of organic pollutant removal (Reactive Blue 4 as the model pollutant) by nZVI-BC in the Fenton process, using a Definitive Screening Design (DSD) model; reuse of the obtained Fenton sludge, as an additional catalytic material, under previously optimized conditions; and assessment of the exhausted Fenton sludge’s ability to be used as a source of nutrients. nZVI-BC was used in the Fenton treatment for the degradation of Reactive Blue 4—a model substance containing a complex and stable anthraquinone structure. The DSD model proposes a high dye-removal efficiency of 95.02% under the following optimal conditions: [RB4] = 50 mg/L, [nZVI] = 200 mg/L, [H₂O₂] = 10 mM. pH correction was not performed (pH = 3.2). Afterwards, the remaining Fenton sludge, which was thermally treated (named FS_treated), was applied as a heterogeneous catalyst under the same optimal conditions with a near-complete organic molecule degradation (99.56% ± 0.15). It could be clearly noticed that the cumulative amount of released nutrients significantly increased with the number of leaching experiments. The highest cumulative amounts of released K, Ca, Mg, Na, and P were therefore observed at the fifth leaching cycle (6.40, 1.66, 1.12, 0.62, 0.48 and 58.2 mg/g, respectively). According to the nutrient release and toxic metal content, FS_treated proved to be viable for agricultural applications; these findings illustrated that the “green” synthesis of nZVI-BC not only provides innovative and efficient Fenton catalysts, but also constitutes a novel approach for the utilization of sewage sludge, supporting overall process sustainability. Full article

Resolving three environmental challenges simultaneously—recycling bone waste, aggregation, oxidation of bare nZVI and benzene, toluene, ethylbenzene, and p-xylene (BTEX) contamination—was conducted by fabricating a highly stable and efficient activator of peroxymonosulfate. In this work, a novel heterogeneous catalyst, ostrich bone ash-supported nanoscale zero-valent iron (Fe⁰-OBA) prepared by pyrolysis of animal bones and reduced Fe²⁺ on the surface of it, was used for the activation of peroxymonosulfate (PMS). Advantageous properties such as extensive availability, low production cost, and high thermal stability make OBA an appealing carbonaceous material for heterogeneous catalysis. The TEM and SEM results revealed that the black ball-shaped nZVI particles were uniformly dispersed on the surface of OBA. The Fe⁰-OBA composite had a porous structure with a specific surface area of 109 m² g⁻¹ according to BET analysis. With BTEX as the refractory pollutant, the PMS-based Fe⁰-OBA system shows great degradation performance as compared to the homogeneous Fe²⁺/PMS system. The effects of various parameters, such as initial pH (2–9), temperature (25–45 °C), initial BTEX concentration (50–200 mg L⁻¹), PMS dosage (0.5–1.25 mM), time of reaction (0–60 min), and Fe⁰-OBA dosage (0.5–5 g L⁻¹) on the BTEX degradation, have been discussed in detail. The pseudo-first-order kinetic model can describe the BTEX degradation by the PMS-based Fe⁰-OBA system. The excellent stability of Fe⁰-OBA even after 10 years, while maintaining the degradation efficiency, shows the high potential of it in a wide range of practical applications. This study illustrated that Fe⁰-OBA could be an effective activator of PMS for the degradation of stubborn organic contaminants in water and wastewater. Full article

P-nitrophenol (PNP), a highly toxic carcinogen, is very stable due to its benzene structure. Advanced oxidation technology is becoming the main means for degrading it. A nano iron-cobalt (Co-nZVI) catalyst, supported by granular activated carbon (GAC), was prepared using liquid-phase reduction, and sodium persulfate’s (PS’s) potential to degrade PNP was studied. The Co-nZVI/GAC nanocomposites were classified, and effects of PS dosage, Co-nZVI/GAC dosage, material system type, PNP concentration, initial pH, and material reuse rate on the reaction were investigated. Activated carbon successfully supported iron and cobalt. At 1 mmol/L of PS, the maximum PNP degradation rate was 99.19%, which was unachievable at other dosages. With only Co-nZVI/GAC present, the rate was 69.8%; with activated persulfate present, it increased to 99.19%. The activated PS system was relatively stable under acidic conditions. Catalysis was induced by adding Co-nZVI/GAC (1.5 g/L). When added four times, the catalytic rate was 57%. Liquid chromatography–mass spectrometry (LC-MS) showed that PNP degradation involves the transfer of PNP to p-benzoquinone (PBQ), the main activators being iron(II) and iron(III) and the key active substances being sulfate (SO₄²⁻) and hydroxide (·OH). In conclusion, Co-nZVI/GAC-activated PS effectively removes PNP. Full article

Fe⁰@Fe₃O₄ nanoparticles with dispersibility and stability better than single nano zero-valent iron (nZVI) were synthesized and combined with hydrogen peroxide to constitute a heterogeneous Fenton-like system, which was creatively applied in the degradation of 2,4-dichlorophenoxyacetic acid (2,4-D). The effects of different reaction conditions like pH, hydrogen peroxide concentration, temperature, and catalyst dosage on the removal of 2,4-D were evaluated. The target pollutant was completely removed in 90min; nearly 66% of them could be mineralized, and the main intermediate product was 2,4-dichlorophenol. Synergistic effects between nZVI and Fe₃O₄ made the 2,4-D degradation efficiency in the Fe⁰@Fe₃O₄/H₂O₂ system greater than in either of them alone. More than a supporter, Fe₃O₄ could facilitate the degradation process by releasing ferrous and ferric ions from the inner structure. The reduction of 2,4-D was mainly attributed to hydroxyl radicals including surface-bound ∙OH and free ∙OH in solution and was dominated by the former. The possible mechanism of this Fe⁰@Fe₃O₄ activated Fenton-like system was proposed. Full article

The biochar treated through several processes can be modified and utilized as catalyst or catalyst support due to specific properties with various available functional groups on the surface. The functional groups attached to the biochar surface can initiate active radical species to play an important role, which lead to the destruction of contaminants as a catalyst and the removal of adsorbent by involving electron transfer or redox processes. Centering on the high potential to be developed in field applications, this paper reviews more feasible and sustainable biochar-based materials resulting in efficient removals of environmental pollutants as catalyst or support rather than describing them according to the technology category. This review addresses biochar-based materials for utilization as catalysts, metal catalyst supports of iron/iron oxides, and titanium dioxide because the advanced oxidation process using iron/iron oxides or titanium dioxides is more effective for the removal of contaminants. Biochar-based materials can be used for the removal of inorganic contaminants such as heavy meals and nitrate or phosphate to cause eutrophication of water. The biochar-based materials available for the remediation of eutrophic water by the release of N- or P-containing compounds is also reviewed. Full article

An emerging pollutant, diatrizoate (DTZ) has been frequently detected in aqueous solution. Unique reticular peanut shell biochar (BC)-supported nano zero-valent iron (nZVI) composite (nZVI/BC) was successfully synthesized and used as a catalyst for activating persulfate (PS) to promote the removal of DTZ. The structure and morphology of the nanocomposite materials were characterized by scanning electron microscopy, X-ray diffraction, Brunauer-Emmett-Teller measurements, and Fourier transform infrared spectroscopy. The degradation of DTZ (20 mg L⁻¹) was achieved by activating PS with the nanocomposite material. The removal of DTZ reached nearly 100% using 25 mM PS and 0.45 g L⁻¹ nZVI/2BC (mass ratio of nZVI and BC at 1:2) nanocomposite material at pH 3.0 and 25 °C. Influencing factors, such as dosages of nZVI/2BC and PS, temperature, and pH were also investigated. The mechanisms of PS activation with nZVI/2BC were discussed, including BC property, electron transfer, and the identification of free radicals in the reaction. The findings demonstrated that nZVI/BC-PS (peanut shell BC-supported nZVI activating PS) is a promising material for the treatment of refractory organic pollutants. Full article