Novel ferromagnetic CuFe2O4/Cu as a highly active catalyst for microwave-Fenton-like reaction | npj Clean Water

Jul 01, 2025

npj Clean Water volume 8, Article number: 56 (2025) Cite this article

To overcome the short retention time in small-scale wastewater treatment plants, it is necessary to develop processes with fast reaction rates. The microwave-Fenton-like reaction (MW-Fenton-like reaction), which combines external energy and catalysts, provides a solution with rapid reaction rate and high degradation efficiency. In this reaction, catalysts significantly influence decomposition efficiency. Developing magnetic catalysts can simplify the separation process. In this study, the superiority of copper-based metal oxides for the MW-Fenton-like reaction was confirmed through comparative experiments of various metal oxides. Based on these findings, highly active CuFe2O4/Cu particles were developed. The synthesized particles, with rough-surfaced solid-sphere morphology, exhibited ferromagnetic properties and were completely separated using a laboratory-scale magnet. CuFe2O4/Cu also showed high degradation over a wide pH range and achieved the highest degradation rate at pH 7. Furthermore, comparison of 4-nitrophenol (4-NP) degradation using MW and conventional heating demonstrated MW was superior in reaction rate, efficiency, and reusability.

According to the effluent discharge regulations enforced globally, it is essential for wastewater generated by various industries such as pharmaceuticals, cosmetics, and textiles to be treated at wastewater treatment facilities, which are predominantly small in scale1,2,3,4,5. However, these small-scale facilities often face issues with treatment efficiency due to short hydraulic retention times6. To meet the increasingly strict effluent standards, there is a direct need to address the constraints of limited hydraulic retention time and improve treatment efficiency.

In industrial wastewater treatment, one of the most widely used reactions is the Fenton reaction, which is particularly effective in degradation of refractory organic pollutants7. This reaction is classified as an advanced oxidation process (AOP), a group of chemical treatment methods that generate highly reactive radicals—such as hydroxyl (∙OH) or sulfate (∙SO4⁻) radicals—to non-selectively oxidize and mineralize a broad range of organic contaminants8. In the Fenton reaction, contaminants are degraded by radicals generated by the reaction between Fe2+/Fe3+ and H2O29. However, since a strongly acidic environment (pH<3) is needed for the efficient degradation of pollutants, pH adjustment processes and a large quantity of chemicals are required to match both the optimal process pH and the effluent discharge regulations pH10,11. Moreover, the Fenton reaction produces iron sludge, necessitating additional processes and treatment costs for removal12. To address the issues of pH dependence and sludge generation in the Fenton reaction, the Fenton-like reaction has been studied by replacing Fe2+/Fe3+ with an insoluble solid catalyst13. Furthermore, recent research has been conducted on the introducing external energy sources into the Fenton-like reaction, not only to overcome the limitations of the Fenton reaction but also to enhance the reaction kinetics14,15. External energies, such as microwaves (MW), light, and vibrations, play a role in increasing the number of reactant particles able to overcome the activation energy barrier16,17. MW, which refers to electromagnetic fields with frequencies ranging from 300 MHz to 300 GHz, is gaining attention for its rapid heating, non-contact heating, and the formation of hotspots with temperatures higher than their surroundings18,19. Moreover, MW reduces the amount of energy required per unit mass (W/g) for processing as the total mass being treated increases, regardless of the process type, equipment used, or operating conditions20. This indicates that the efficiency of MW increases with scale, highlighting its practical feasibility for large-scale processing operations. The combination of MW with an appropriate catalyst enables rapid heating rates and lowers the activation energy, leading to accelerated treatment speeds and high degradation efficiency21,22.

To achieve high activity in MW-Fenton-like reactions, the catalyst must have a high MW absorption capacity and strong intrinsic reactivity of Fenton-like reaction. Various studies over the past decade have confirmed the high reactivity of Cu-based catalysts in MW-Fenton-like reactions23,24,25,26,27,28,29,30,31,32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53,54. A table summarizing these studies is attached in Supplementary information (Supplementary Table 1). Wang et al. and Iboukhoulef et al. used Cu2+ ions as catalysts for the MW-Fenton-like reaction23,24. Additionally, solid-phase Cu-based oxides such as CuO, Cu2O, CuFeO2, CuCo2O4, and Cu-Ni bimetallic oxide have also been studied as catalysts for the MW-Fenton-like reactions25,26,27,28,29,30,31,32,34,36. Cu-based catalysts integrated with carbon-based materials like graphene oxide, activated carbon, and biochar to enhance MW absorption capacity have also gained attention for MW-assisted processes41,42,43,45,46,47,48,49,50,51,52,53,54,55. While these Cu-based catalysts exhibit excellent degradation efficiency and fast reaction rates, they present challenges in separating the catalysts after the degradation process56. Developing magnetic particles such as MFe2O4 (where M = Fe, Cu, or Co) addresses these challenges by allowing for easy separation under a magnetic field27,33,37,40,45,52. Magnetic separation can simplify the process, reduce separation time, and promote the reuse of catalysts57,58.

CuFe2O4 is gaining attention as a catalyst for MW-Fenton-like reactions due to its intrinsic magnetic properties and the presence of catalytically active copper species. CuFe2O4, a spinel ferrite nanoparticle (SFNP) with the general formula AB₂O₄, exhibits excellent magnetic and structural stability, and its properties can be tailored by adjusting synthesis and calcination conditions59,60. Bose et al. synthesized a nanoflower-shaped catalyst by loading CuFe2O4 onto MoS2 to enhance MW absorption capacity33. Xiao et al. loaded CuFe2O4 onto powdered activated carbon (PAC) to improve the catalyst’s stability40. Yao et al. developed CuFe2O4/reduced graphene oxide (CuFe2O4/rGO), taking advantage of the high electronic conductivity of rGO to enhance the redox cycle in MW-Fenton-like reactions44. These CuFe2O4-based catalysts can be used under various pH conditions, but they exhibit optimal efficiency in strongly acidic environments and tend to show decreased efficiency after several repeated reactions.

In this study, to enhance the efficiency of CuFe2O4, a spherical CuFe2O4/Cu composite incorporating a zero-valent copper (Cu0) phase, recognized for its strong reactivity toward organic pollutant removal, was synthesized61. 4-NP, a phenolic compound commonly found in pesticides, dyes, and pharmaceuticals, was used as a model pollutant to assess the degradation performance of the synthesized catalyst62. Control experiments were conducted to evaluate the degradation performance under various experimental conditions and to determine the 4-NP degradation pathway. The synthesized CuFe2O4/Cu showed optimal efficiency at neutral pH, eliminating the need for pH adjustment. Additionally, when comparing the activation of the catalyst using MW and conventional heating, only the MW-activated catalyst demonstrated complete reusability.

MW energy absorbed by the catalyst can be converted into other forms of energy and used in the Fenton-like reaction. Therefore, MW absorption capacity of the catalyst is a key factor in selecting an appropriate catalyst for the MW-Fenton-like reaction. MW absorption is achieved through mechanisms such as magnetic loss and dielectric loss, among others63. Metal oxides, which primarily rely on magnetic loss, are notable materials for MW absorption64. Previous research has shown that MW absorption capacity improves as the number of metal components and the structural complexity of metal oxides65. While many studies has focused on the influence of metal component number and morphology, more investigation is required to understand the impact of different metal types55,66. To investigate the degradation rates based on metal types, an experiment was conducted using 21 different commercial metal oxides to degrade 4-NP (Fig. 1). A variety of metals were used, including an alkaline earth metal (Mg), transition metals (Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Y, Zr, Nb, and Hf), lanthanides (La, Ce, and Gd), and post-transition metals (Al, Sn, and Bi). To account for surface area differences due to size, the hydrodynamic diameter was measured at pH 7 (Supplementary Fig. 1). The particle sizes ranged from 406 nm to 4.947 μm, contributing to variability in surface area among the samples. Among the 21 different metal oxides, copper oxide was the only material to exhibit significant efficiency by degrading the majority of 4-NP within 10 min, despite variations in surface area. Despite not having the largest surface area or the highest MW absorption capacity, copper oxide exhibited high efficiency, likely due to its strong reactivity in the Fenton-like reaction55,65. These results indicate that the reactivity of the catalyst in the Fenton-like reaction is as equally important as MW absorption capability. While magnesium oxide demonstrated a relatively high degradation rate, it failed to achieve complete degradation of 4-NP. Additionally, a significant loss of catalyst was observed in the reactor following the reaction. This observation indicates that catalyst dissolution occurs during the reaction, confirming the extremely low stability and reusability of magnesium oxide. Considering the stability and degradation efficiency of the catalysts, copper oxide appears to be the most suitable choice for MW-Fenton-like reactions.

Degradation of 4-NP by MW-Fenton-like reaction with various monometallic oxide (Initial experimental condition: Cat. 200 ppm, H2O2 300 ppm, 4-NP 10 ppm, 20 °C, pH 7, and 200 W).

A dual-phase CuFe2O4 was synthesized by modifying the magnetic compound CuFe2O4. By adding CTAB and adjusting the heating temperature (300 °C or 350 °C) and gas conditions (Ar or O2), CuFe2O4, CuFe2O4/Fe2O3, and CuFe2O4/Cu were synthesized. In contrast, CuFe2O4/CuO was synthesized under similar condition without using CTAB. All four synthesized CuFe2O4 samples exhibited a spherical shape. The surfactant CTAB acted as a template, resulting in CuFe2O4, CuFe2O4/Fe2O3, and CuFe2O4/Cu being approximately 40% smaller in size compared to CuFe2O4/CuO (Supplementary Fig. 2). XRD measurements revealed that all samples displayed peaks corresponding to CuFe2O4 (Fig. 2). In addition, CuFe2O4/Fe2O3, CuFe2O4/Cu, and CuFe2O4/CuO showed additional peaks corresponding to Fe2O3, Cu, and CuO, respectively. When O2 or air was used as the synthesis atmosphere, additional metal oxide phases such as Fe2O3 or CuO were present. However, when Ar was used, only single-phase CuFe2O4 or additional metallic Cu phases were observed. This phenomenon is likely due to the lack of oxygen in the gas atmosphere.

The peaks of Fe2O3, Cu, and CuO were represented by yellow stars, brown circles, and pink diamond symbols, respectively.

Since catalysis occurs on the surface of the catalyst, the hydrodynamic diameter serves as a critical parameter influencing the accessible surface area. CuFe2O4, CuFe2O4/Fe2O3, and CuFe2O4/CuO have comparable hydrodynamic diameters, while CuFe2O4/Cu has a larger hydrodynamic diameter, leading to a relatively smaller surface area (Supplementary Fig. 3a). Despite the smaller surface area, CuFe2O4/Cu exhibited a faster degradation rate of 4-NP compared to CuFe2O4, CuFe2O4/Fe2O3, and CuFe2O4/CuO (Supplementary Fig. 3b). The elevated degradation rate of CuFe2O4/Cu is attributed to efficient electron transfer driven by the presence of copper in multiple oxidation states67. Based on these experimental results, subsequent experiments focused on CuFe2O4/Cu as the primary catalyst. TEM images revealed that CuFe2O4/Cu has a solid spherical structure with a rough surface (Fig. 3a, b). The rough surface could be one of the factors increasing the surface area, thus enhancing the reactivity with H2O268. The crystallinity of CuFe2O4 in CuFe2O4/Cu was also confirmed by high-magnification TEM images showing a 0.252 nm interplanar spacing, corresponding to the (311) plane of CuFe2O4 (Fig. 3c). Additionally, the uniform distribution of all elements confirmed that the Cu peak observed in the XRD pattern did not originate from copper clusters (Fig. 3d–g).

a–c TEM images of CuFe2O4/Cu and EDS mapping images of d C, e O, f Fe, and g Cu in CuFe2O4/Cu. EDS mapping images share the same scale bar.

An experiment was conducted to compare the efficiency of the synthesized CuFe2O4/Cu with commercial products (Fig. 4a). As commercial CuFe2O4/Cu was not available, an indirect comparison was conducted using commercial CuO, Fe3O4, and CuFe2O4. The commercial Fe3O4 showed a degradation rate of less than 50% even after 10 min of reaction, whereas the copper-containing commercial CuO and CuFe2O4 degraded most of the 4-NP. Additionally, the synthesized CuFe2O4/Cu demonstrated the highest efficiency, despite having a particle size more than four times greater than the commercial CuFe2O4. This suggests that the synthesized CuFe2O4/Cu exhibits high efficiency due to the synergistic effect between Cu0 and CuFe2O4, despite its simple structure and large size. Furthermore, the synthesized CuFe2O4/Cu based on magnetic CuFe2O4 was expected to possess magnetism, which was confirmed through experimentation (Fig. 4b). The magnetic property was easily observed by separating the catalyst in DI water using a magnet, and also confirmed by the SQUID measurement at 295 K. The saturation magnetization value of the synthesized particles was found to be 37.018 emu/g, and the irreversible narrow hysteresis loop indicated that the CuFe2O4/Cu is a soft magnetic material.

a Degradation of 4-NP by MW-Fenton-like reaction with commercial metal oxides and synthesized CuFe2O4/Cu (Initial experimental condition: Cat. 200 ppm, H2O2 200 ppm, 4-NP 10 ppm, 20 °C, pH 7, and 200 W) and b Hysteresis loop of CuFe2O4/Cu at 295 K. The inserted picture shows the separation of CuFe2O4/Cu dispersed in distilled water using a magnet.

The removal of 4-NP can occur through various pathways, including the self-decomposition of H2O2, adsorption by CuFe2O4/Cu, and Fenton-like reaction. Experiments were performed to evaluate the impact of MW irradiation on 4-NP removal in each reaction pathway (Fig. 5). The self-decomposition of H2O2, adsorption by CuFe2O4/Cu, and the Fenton-like reaction achieved degradation rates of 0, 10, and 26%, respectively. While MW alone was unable to degrade the contaminant, its incorporation enhanced the degradation rates in all cases. In particular, the addition of MW to the Fenton-like reaction resulted in the greatest enhancement in both degradation efficiency and reaction rate. The majority of 4-NP was degraded within 5 min under MW irradiation. These results indicate that the majority of 4-NP degradation during the MW-Fenton-like reaction is driven by the Fenton-like reaction itself, rather than by the self-decomposition of H2O2 or adsorption by CuFe2O4/Cu.

Degradation of 4-NP with respect to the combination of MW and Fenton-like reaction (Initial experimental condition: Cat. 200 ppm, H2O2 200 ppm, 4-NP 10 ppm, 20 °C, pH 7, and 200 W).

The concentration of 4-NP, MW power, CuFe2O4/Cu concentration, H2O2 concentration, initial solution temperature, and pH are factors that influence the efficiency of the MW-Fenton-like reaction. To determine the optimal reaction conditions, experiments were conducted to assess the effects of these variables. The impact of pollutant concentration was investigated by measuring degradation rates across a range of 5–80 ppm (Fig. 6a). Complete degradation was observed within 5 min for 5 ppm and 10 ppm, while concentrations of 20 ppm or higher required 6 min. The degradation rate decreased as the pollutant concentration increased, likely because the amount of generated ∙OH was limited. The amount of energy applied influences the number of reactant particles that can overcome the activation barrier, as shown in Fig. 6b. Degradation of 4-NP took 5, 3, 3, 2, and 2 min at 200, 400, 600, 800, and 1000 W, respectively. Although the reaction time decreased with increasing MW power, 200 W provided the best efficiency considering the total energy input required for complete degradation. The concentration of CuFe2O4/Cu affects the number of active sites available, so degradation performance was evaluated over the range of 20–400 ppm (Fig. 6c). To account for potential catalyst aggregation at high concentrations, hydrodynamic diameter measurements were also taken (Supplementary Fig. 4). The hydrodynamic diameter significantly increased from 20 ppm to 200 ppm and remained relatively constant above 200 ppm. The time required for 4-NP degradation at different catalyst concentrations was 9 min for 20 ppm and 40 ppm, 7 min for 100 ppm, and 5 min for 200 ppm and higher. The increase in reaction rate with catalyst concentration was likely due to the increase in active sites outweighing the decrease in surface area caused by aggregations.

a Effect of 4-NP concentration, b Effect of MW power, c Effect of CuFe2O4/Cu concentration, d Effect of H2O2 concentration, e Effect of initial solution temperature, and f Effect of pH. Except for the control factor, others were maintained under the following conditions: Cat. 200 ppm, H2O2 200 ppm, 4-NP 10 ppm, 20 °C, pH 7, and 200 W.

A controlled experiment was carried out to investigate the impact of H2O2 concentration on the decomposition rate (Fig. 6d). Before the main experiment, an experiment was conducted to account for the impact of H2O2 self-decomposition, as shown in Supplementary Fig. 5. The highest degradation rate due to self-decomposition was observed at 100 ppm, reaching 47%, indicating that H2O2 alone cannot completely degrade 4-NP. However, the combination of CuFe2O4/Cu with H2O2 resulted in substantial degradation. The reaction rate increased when the H2O2 concentration was raised from 100 ppm to 200 ppm. However, concentrations of 300 ppm or higher resulted in longer degradation times and a slight decrease in 4-NP removal efficiency. The decreased degradation rate, despite higher H2O2 concentrations, is likely due to the occurrence of side reactions where H2O2 acts as a scavenger of ∙OH (Eqs. 1 and 2)69. These side reactions not only consume two ∙OH per H2O2 molecule but also reduce the amount of H2O2 available for generating ∙OH, effectively consuming four ∙OH per side reaction.

As the MW-Fenton-like reaction proceeds, the heating effect causes the solution temperature to reach the boiling point of water (100 °C) (Supplementary Fig. 6). Since the solution temperature can affect the degradation rate by modifying the activation energy, experiments were carried out to examine its influence. It was impossible to maintain a constant temperature throughout the reaction time due to the structure of the batch experimental system. Therefore, experiments were conducted by varying the initial solution temperature from 20 °C to 100 °C (Fig. 6e). The increase in the initial solution temperature from 20 °C to 100 °C resulted in a reduction in activation energy, thereby enhanced the degradation rate of 4-NP. Furthermore, kinetic analysis based on the initial solution temperatures revealed that the reaction follows pseudo first-order kinetics, and the rate constant increases with rising initial solution temperature (Supplementary Table 2). To isolate the effect of increased temperature and examine the impact of MW-specific characteristics, such as hotspot generation, 4-NP degradation experiments were conducted using conventional heating (Supplementary Fig. 7). When the energy source was changed from MW to conventional heating, the trend of increased decomposition rate and speed with increasing initial solution temperature remained consistent. At an initial solution temperature of 100 °C, where the effect of increasing solution temperature is negligible, the time required for complete degradation of 4-NP was 3 min for MW and 6 min for conventional heating, respectively. These results suggest that hotspot generation positively impacts the degradation process and that MW serves as a more efficient external energy source for catalyst activation compared to conventional heating.

The solution pH is a factor that affects the interaction between 4-NP and CuFe2O4/Cu. The pKa value of 4-NP is 7.15, indicating that the 4-NP form is predominant below this value, while the 4-nitrophenolate form becomes dominant above it70. The point of zero charge (PZC) for CuFe2O4/Cu is at pH 9, which means the surface is positively charged below this value, neutral at pH 9, and negatively charged above it (Supplementary Fig. 8). Additionally, the zeta potential decreases with increasing pH, leading to a sharp increase in the hydrodynamic diameter of CuFe2O4/Cu above pH 8. The interaction between 4-NP and CuFe2O4/Cu was quantitatively confirmed through adsorption experiments of 4-NP at different pH values (Supplementary Fig. 9). At pH 4–7, the attractive forces between the positive charge on CuFe2O4/Cu and the electron-donating groups of 4-NP result in high adsorption. However, from pH 8 onwards, the decreasing surface area leads to a reduction in adsorption. At pH 10, adsorption is negligible due to electrostatic repulsion between CuFe2O4/Cu and 4-NP, as well as a further reduction in surface area. When the decomposition rate was examined at different pH values, rapid decomposition was observed at pH 4, but 4-NP could not be completely decomposed (Fig. 6f). The decomposition rate increased at pH levels between 5 and 7, with the most efficient performance observed at pH 7. Above pH 8, the decomposition rate decreased due to a reduction in surface area caused by catalyst aggregation. The MW-Fenton-like reaction cycle, which regenerates inactive forms into active forms, is a key factor in the generation of reactive oxygen species (ROS) and is influenced by both H+ and OH− (Eqs. 3–6)71. Under neutral and near-neutral conditions (pH 7 and 8), the high degradation rates are likely due to the similar concentrations of H+ and OH−, which promote efficient operation of the cycle.

Under optimal conditions (CuFe2O4/Cu 200 ppm, H2O2 200 ppm, 4-NP 10 ppm, 90 °C, pH 7, and 200 W) identified from previous experiments, the reusability of CuFe2O4/Cu was examined. It was observed that the decomposition rate remained consistent even after five cycles of the MW-Fenton-like reaction (Fig. 7a). Additionally, TEM images confirmed that the structure of the catalyst was maintained after five reactions (Supplementary Fig. 10). However, when conventional heating was used as an external energy source, the decomposition rate significantly decreased over the five cycles (Fig. 7b). TEM images revealed a reduction in catalyst density after repeated heat-Fenton-like reactions. This density reduction is believed to be due to metal leaching, which likely caused the decrease in the decomposition rate. ICP-OES measurements confirmed that the Cu leaching in the 1st cycle of the MW-Fenton-like reaction was 1.27 mg/L, which meets the US EPA effluent standard (1.3 mg/L) (Supplementary Table 3)72. In contrast, the Cu leaching in the 1st cycle of the heat-Fenton-like reaction was 4.13 mg/L, exceeding the standard. Both MW and heat conditions resulted in the highest Cu leaching in the 1st cycle, with decreasing amounts in subsequent cycles. Notably, in MW system, Cu leaching from the 2nd cycle onward was approximately 10% of the 1st cycle value and was considered negligible. For Fe, the leaching was 0 mg/L under all conditions, likely because the leached Fe formed precipitates that were filtered out during the solid separation process73.

a Consecutive degradation runs of MW-Fenton-like reaction (Initial experimental condition: Cat. 200 ppm, H2O2 200 ppm, 4-NP 10 ppm, 90 °C, pH 7, and 200 W) and b Consecutive degradation runs of heat-Fenton-like reaction (Initial experimental condition: Cat. 200 ppm, H2O2 200 ppm, 4-NP 10 ppm, 90 °C, and pH 7).

The catalyst’s surface composition before and after the MW-Fenton-like reaction was analyzed using XPS. It was confirmed that there were no significant changes in the peaks of the XPS spectra despite the repeated reactions, as shown in Fig. 8a. In the Cu 2p spectra, peaks for Cu+, Cu2+, and the satellite were observed at 933.3, 934.9, and 943.0 eV, respectively. As the reaction progressed, Cu+ increased from 25.0% to 59.7%, while Cu2+ decreased from 48.8% to 23.1% (Fig. 8b). In addition, the Raman spectra showed the intensity changes of Cu2O and CuO, which corresponded to the XPS results (Supplementary Fig. 11)74. Despite the change in the Cu+/Cu2+ ratio, the degradation efficiency was not significantly affected. These results indicate that the reduction of Cu2+ to Cu+ (Eq. 4) is more prevalent than the oxidation of Cu+ to Cu2+ (Eq. 3) and confirm that Cu+ acts as the active species in the reaction. The Fe 2p spectra exhibited peaks at 710.8, 712.6, and 716.9 eV for Fe2+, Fe3+, and the satellite, respectively (Fig. 8c). During the reaction, Fe2+ increased from 32.2% to 35.2%, and Fe3+ decreased from 53.9% to 50.5%, with the peak shifting towards the lower binding energy. Based on the pattern of changes observed in the Cu spectra, this suggests that the reduction reaction of Fe ions (Eq. 6) is more dominant than the oxidation reaction (Eq. 5). In contrast to Cu, which exhibited a change of over 20%, Fe showed only about a 5% change, demonstrating that Cu has a more significant impact on 4-NP degradation than Fe. Peaks for lattice oxygen, surface oxygen, and absorbed water oxygen were identified in the O 1s spectra at 530.0, 531.3, and 532.2 eV, respectively (Fig. 8d). During the repetition of reactions, the oxygen in the lattice decreased from 50.7% to 43.8%, while the oxygen on the surface increased from 28.6% to 33.8%. In response to the peak shifts to lower binding energies observed in the Cu 2p and Fe 2p spectra, it appears that oxygen in the lattice is released to maintain the neutrality of the catalyst. The detailed XPS parameters for the MW-Fenton-like reaction samples can be found in Supplementary Table 4. Unlike the MW-Fenton-like reaction, samples subjected to the heat-Fenton-like reaction showed the disappearance of the Cu peak after five cycles in the Cu 2p spectra (Supplementary Fig. 12). The Raman spectra also showed a huge intensity decrease of Cu2O and CuO compared to the MW-Fenton-like reaction sample (Supplementary Fig. 11). The results from XPS, Raman, and ICP-OES consistently reveal significant Cu leaching during the heat-Fenton-like reaction. The results indicate that the synthesized CuFe2O4/Cu catalyst demonstrates high stability and efficiency even after repeated reactions. Additionally, MW is demonstrated to be a more suitable external energy source than conventional heating for maintaining the catalyst’s stability.

a Survey spectra and fine-scanned spectra of b Cu 2p, c Fe 2p, and d O 1s.

In the process of removing 4-NP through the MW-Fenton-like reaction, ROS generated by CuFe2O4/Cu include ∙OH, ∙O2−, and h+. To investigate the impact of each ROS on 4-NP degradation, trapping experiments were conducted using DMSO, EDTA, and BQ (Fig. 9a). DMSO, EDTA, and BQ were used as scavengers for ∙OH, h+, and ∙O2−, respectively. Experimental results indicated that the contributions to 4-NP degradation were in the following order: ∙OH > h+ > ∙O2−. In particular, trapping ∙OH resulted in a decrease of approximately 80% in the degradation rate, suggesting that ∙OH is primarily responsible for most of the degradation.

a ROS trapping experiment of MW-Fenton-like reaction with CuFe2O4/Cu (Initial experimental condition: Cat. 200 ppm, H2O2 200 ppm, 4-NP 10 ppm, 20 °C, pH 7, and 200 W). DMSO, EDTA, and BQ are used as ∙OH, h+, and ∙O2− trapping reagents. b Scheme of mechanism that can generate ∙OH, h+, and ∙O2− during MW-Fenton-like reaction with CuFe2O4/Cu.

The mechanism by which CuFe2O4/Cu generates ROS through the MW-Fenton-like reaction is illustrated in Fig. 9b. CuFe2O4/Cu generates ∙OH and ∙O2− through a Fenton-like reaction, where H2O2 acts as either an oxidizing or reducing agent (Eqs. 3–6). In the control experiment investigating the effects of pH, the pH values after the reaction showed a decreasing trend at all pH levels except pH 4 (Supplementary Table 5). And, higher degradation rates were observed under neutral and mildly basic conditions (pH 7 and 8) (Fig. 6f). This suggests that the reactions in Eqs. 4 and 6, which generate H+, play a more dominant role than those in Eqs. 3 and 5. Furthermore, the decrease in the ratio of high-valent Cu and Fe (Cu2+/Fe3+) and the increase in the ratio of low-valent Cu and Fe (Cu+/Fe2+) after the MW-Fenton-like reaction also support this prediction (Fig. 8b, c). The ∙O2H generated in Eqs. 4 and 6 is converted into H2O2, O2, and OH− through Eqs. 7 and 8, with ∙O2− acting as an intermediate29,75. MW has low energy, making it insufficient to break chemical bonds or excite electrons from the valence band (VB) to the conduction band (CB)76. However, with the increase in temperature and the formation of hotspots due to MW irradiation, the possibility of electron excitation also increases (Eq. 9)77. The generated h⁺ and e− react with OH− and O2 to produce ∙OH and ∙O2− (Eqs. 10 and 11)78.

The ROS generated through the MW-Fenton-like reaction degraded the majority of 4-NP within 5 min and removed 43% of TOC within 10 min (Supplementary Fig. 13). The reduction in TOC indicates that 4-NP was degraded and ultimately mineralized to CO2(g). To investigate the degradation pathway of 4-NP, LC-qTOF-MS analysis was performed at different reaction times (Fig. 10). Significant peaks were observed at m/z = 87, 108, and 138. The peak at m/z = 138 corresponds to the pollutant 4-NP, with its intensity decreasing over time and disappearing after 5 min. The peak at m/z = 108 is likely due to benzoquinone (BQ) (m/z = 107) and hydroquinone (HQ) (m/z = 109). When ∙OH attacks the C-4 position of 4-NP, NO₂ is removed, producing HQ. HQ can be converted to BQ through a reversible redox reaction79, and the peak at m/z = 108 may arise from hydrogen bonding between HQ and BQ80. ∙OH preferentially attack the electrophilic sites of HQ and BQ, leading to aromatic ring cleavage. This process generates pyruvic acid, a three-carbon compound, which is subsequently detected as a peak at m/z = 87 in the mass spectrum. Furthermore, pyruvic acid undergoes further degradation by ∙OH, ultimately being mineralized into CO2. After 10 min of reaction, although 57% of the TOC remained in the solution, no peaks were observed in the mass spectra. The small molecules formed from the degradation of 4-NP, which are expected to contain 2 to 6 carbon atoms, were not observed via LC-MS due to their rapid degradation and low concentration. However, the mineralization process, in which these small molecules are ultimately converted to CO2(g), is expected to occur at a slower rate in comparison.

Mass spectrum of 4-NP with respect to the reaction time (Initial experimental condition: Cat. 200 ppm, H2O2 200 ppm, 4-NP 10 ppm, 20 °C, pH 7, and 200 W).

In this study, magnetic CuFe2O4 was developed and synthesized into a spherical form of CuFe2O4/Cu, which was used as a catalyst in MW-Fenton-like reactions. Unlike Fe2+/Fe3+ typically used in highly acidic environments, the synthesized CuFe2O4/Cu functioned effectively across a wide pH range (4–10) and demonstrated the highest efficiency at neutral pH. Under the optimal conditions as determined from control experiments (CuFe2O4/Cu 200 ppm, H2O2 200 ppm, 4-NP 10 ppm, 90 °C, pH 7, and 200 W), 4-NP was completely degraded. In repeated MW-Fenton-like reaction experiments with magnetic separation, CuFe2O4/Cu maintained its degradation efficiency. This contrasts with the significant decline observed in heat-Fenton-like reaction experiments, demonstrating the superior catalyst stability under MW conditions. These results suggest that CuFe2O4/Cu is a suitable catalyst for MW-Fenton-like reactions and holds promise for effective removal of various organic pollutants.

The cobalt(II, III) oxide nanopowder (<50 nm, 99.5%), copper(II) oxide (<10 μm, 98%), iron(II, III) oxide (50–100 nm, 97%), copper iron oxide (<100 nm, 98.5%), zirconium(IV) oxide, iron(III) oxide (<5 μm, ≥96%), hafnium oxide (98%), niobium(V) oxide (99.9%), vanadium(V) oxide, 4-nitrophenol (ReagentPlus®, ≥99%), sodium hydroxide (ACS reagent, ≥97.0%), sodium bicarbonate (ACS reagent, ≥99.7%), hexadecyltrimethylammonium bromide (CTAB), ethylenediaminetetraacetic acid (EDTA, ACS reagent), p-benzoquinone (BQ, reagent grade), and dimethyl sulfoxide (DMSO, analytical standard) were purchased from Sigma-Aldrich. Bismuth(III) oxide (99.0%), magnesium oxide, glycerol, H2O2 (34.5%), copper(II) nitrate trihydrate, iron(III) nitrate nonahydrate, and HNO3 (68.0–70.0%) were obtained from Samchun. From Kojundo Chemical Laboratory, yttrium(III) oxide (7 μm, 99.9%), cerium(IV) oxide (0.2 μm, 99.99%), chromium(III) oxide (3 μm, 99.9%), lanthanum(III) oxide (99.99%), gallium(III) oxide (99.99%), and manganese(III) oxide (99.9%) were purchased. Manganese(IV) oxide and nickel(II) oxide (99.0%) were gained from Junsei Chemical. Aluminum oxide (135 nm, 99.9%) was purchased from Any One Co., Ltd. TiO2 (99.9%) and Sn2O3 (99.9%) were obtained from Grand Chemical & Material Co., Ltd. 2-Propanol was gained from JT Baker. The deionized (DI) water used in the experiment was ultrapure, with a resistance of 18.2 MΩ, sourced from Milli-Q water (C9209, Millipore Sigma, USA).

CuFe2O4 spheres are synthesized using a solvothermal method81. 1 mmol of CTAB, 0.25 mmol of Cu(NO3)2·3H2O, and 0.5 mmol of Fe(NO3)3·9H2O are dissolved in a solution containing 80 mL of isopropanol and 16 mL of glycerol. After stirring for 1 h, the solution was transferred to a 180 mL Teflon-lined stainless-steel autoclave and subjected to solvothermal treatment at 180 °C for 6 h. The synthesized CuFe glycerate was washed three times with ethanol and dried at 40 °C for 24 h. The dried CuFe glycerate was heat-treated in an Ar atmosphere, with a ramp-up rate of 12 °C/min to 350 °C and held for 2 h to obtain CuFe2O4/Cu. By adjusting parameters such as the volume ratio of isopropanol to glycerol (110:14), the presence of CTAB, the solvothermal synthesis time (12 h), gas conditions (O2 or Air), and the heating temperature (300 °C), different forms including spherical CuFe2O4, CuFe2O4/Fe2O3, and CuFe2O4/CuO were obtained.

The morphology and size of the synthesized CuFe2O4 were analyzed using a Field Emission Scanning Electron Microscope (FESEM, SU5000, HITACHI, Japan) and a Transmission Electron Microscope (TEM, Tecnai G2 F30 S-Twin, FEI, USA). X-ray Diffraction (XRD, MiniFlex600, Rigaku, Japan) was used to confirm the crystallinity of CuFe2O4. The magnetic properties of the particles were verified through measurements with a Superconducting Quantum Interference Device (SQUID, MPMS XL, Quantum Design Inc., USA) at 295 K. X-ray Photoelectron Spectroscopy (XPS, Sigmaprobe, Thermo Fisher Scientific, UK) with a photon energy of 1486.6 eV (Al Kα) was employed for both quantitative and qualitative surface analysis before and after the experiment. Raman Spectroscopy (inVia Raman Microscope, Renishaw, UK) with a 633 nm laser was used to identify the chemical bonds features. A Dynamic Light Scattering instrument (DLS, Zetasizer Ultra Red Label, Malvern Panalytical Ltd., UK) with a 10 mW He-Ne laser measured the particle diameter and zeta potential in water. The amount of metal leached after the reaction was determined using Inductively Coupled Plasma Optical Emission Spectrometry (ICP-OES, ICPE-9000, Shimadzu, Japan). The concentration of 4-NP were monitored at 400 nm using UV-Vis Spectrophotometry (Cary 60 UV-Vis Spectrophotometer, Agilent, USA)70. The residual carbon content in the solution after the reaction was determined using Total Organic Carbon analysis (TOC, TNM-L, Shimadzu, Japan). The intermediates formed during the decomposition of 4-NP were analyzed using a Liquid Chromatography Quadrupole Time-of-Flight Mass Spectrometer (LC-QTOF-MS, impact II, Bruker, USA) with a C18 column (100 mm × 2.1 mm, Intensity Sole2, Bruker, USA). The system operated in negative electrospray ionization mode, with a 30:70 methanol:water mixture flowing at 0.2 mL/min.

To investigate the effects of pH, CuFe2O4/Cu concentration, H2O2 concentration, pollutant concentration, initial solution temperature, and MW power, a series of experiments were designed. All variables were kept at baseline conditions (CuFe2O4/Cu 200 ppm, H2O2 200 ppm, 4-NP 10 ppm, 20 °C, pH 7, and 200 W) except for the one being tested. A total solution volume of 50 mL was prepared in an Erlenmeyer flask, containing CuFe2O4/Cu (20–400 ppm), H2O2 (100–1000 ppm), and 4-NP (5–80 ppm) in DI water. The initial solution temperature (20–100 °C) was set using an electric kettle (FLE-03C, Fellow, USA). An ultrasonic bath (CPX2800H-E, EMERSON, USA) was used to disperse the CuFe2O4/Cu particles in the solution. The pH of the solution (pH 4–10) was adjusted using NaOH and HNO3 solutions prepared in three concentrations (0.01, 0.1, and 1 M), with pH maintained at an accuracy of ± 0.1. The flask was placed in a microwave (MW23GD, LG Electronics Tianjin Applications Co., Ltd., Korea) connected to a condenser. To prevent loss of DI water due to temperature rise during the reaction, cooling water was circulated through the condenser using a pump (75211-15, Cole-Parmer Instrument Company, USA). The MW power (200–1000 W) was adjusted, and samples of 1.2 mL were taken at 1-min intervals for a total reaction time of 10 min. The collected samples were centrifuged at 13,500 rpm for 2 min using a centrifuge (MaXpin C-12mt, DAIHAN Scientific Co., Ltd., Korea) to separate the CuFe2O4/Cu particles. A clean supernatant of 0.6 mL was mixed with 0.6 mL of NaOH to prepare samples for UV-Vis analysis. The concentration of 4-NP was determined by measuring the absorbance at 400 nm70.

To compare the efficiency of MW and conventional heating as external energy sources, the MW reactor was replaced with a heating mantle (100A-0406, Glas-Col, USA). All other experimental conditions were kept constant, including CuFe2O4/Cu at 200 ppm, H2O2 at 200 ppm, 4-NP at 10 ppm, and pH 7. The initial solution temperature (20–100 °C) was set using an electric kettle. During the 10 min of reaction time, the heating mantle and a temperature controller (TXN-700, AS ONE, Japan) maintained the solution temperature within ± 3 °C. The experimental procedures and measurements followed the same protocols as the 4-NP degradation experiments using MW.

Under the optimal conditions determined from the 4-NP degradation experiment (CuFe2O4/Cu 200 ppm, H2O2 200 ppm, 4-NP 10 ppm, 90 °C, pH 7, and 200 W), a catalyst recycling experiment was conducted. The experimental procedure followed the same steps as the degradation experiment, with an additional washing process between each of the five reaction cycles to remove residual H2O2 and 4-NP. The washing process was designed to minimize catalyst loss using a magnet. The catalyst remaining in the microtubes was collected in an Erlenmeyer flask. The catalyst was allowed to settle by gravity and magnetic attraction, and then immobilized using a magnet. Subsequently, 35 mL of the supernatant was removed and replaced with an equal volume of DI water. This washing cycle was repeated 4 times. After the washing process, the sample was prepared with a solution matching the optimal conditions for the next cycle of the experiment.

Further information on research design is available in the Nature Research Reporting Summary linked to this article.

Data will be made available on request.

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This work was supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (MSIT) (No. RS-2022-NR071792), and the Gwangju Institute of Science and Technology (GIST) research fund (Future-leading Specialized Research Project, 2025).

Department of Environmental and Energy Engineering, Gwangju Institute of Science and Technology, Gwangju, Republic of Korea

Yejin Nam, Jong Hoon Joo & Changwoo Kim

Dongnam Regional Division, Korea Institute of Industrial Technology, Busan, Republic of Korea

Deukhyeon Nam & Yoon Myung

Department of Materials Science and Engineering, Korea University, Anam-Dong, Seongbuk-Gu, Seoul, Republic of Korea

Deukhyeon Nam

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Y.N.: Conceptualization, Data curation, Formal analysis, Investigation, Methodology, Visualization, Writing – original draft. D.N.: Data curation, Formal analysis, Investigation, Writing – review and editing. Y.M.: Data curation, Formal analysis, Supervision, Writing – review and editing. J.J.: Resources, Writing – review and editing. C.K.: Funding acquisition, Project administration, Supervision, Writing – review and editing. All authors contributed to this study as described above.

Correspondence to Changwoo Kim.

The authors declare no competing interests.

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Nam, Y., Nam, D., Myung, Y. et al. Novel ferromagnetic CuFe2O4/Cu as a highly active catalyst for microwave-Fenton-like reaction. npj Clean Water 8, 56 (2025). https://doi.org/10.1038/s41545-025-00477-z

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Received: 05 February 2025

Accepted: 09 May 2025

Published: 01 July 2025

DOI: https://doi.org/10.1038/s41545-025-00477-z

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