Organic Wastewater Treatment Research Articles

Ferrocene crosslinked and functionalized chitosan microspheres towards bio-based Fenton-like system for the removal of organic pollutants

Dye-containing wastewater treatment has been a major long-term global challenge. For this purpose, a novel bio-based microspheres (CS-FC) with high specific surface area (63.24 m2·g−1) and nano-channels (17.95 nm) was prepared using chitosan as the framework and ferrocene as a crosslinking active group. CS-FC not only has the ability to rapidly enrich methyl orange (MO) through hydrogen-bonding and electrostatic attraction, but also almost completely degrades it in the presence of H2O2/K2S2O8 through a synergistic radical/non-radical mechanism under the activating effect of ferrocene. Without H2O2/K2S2O8, the maximum MO adsorption capacity of CS-FC is in the range 871–1050 mg·g−1, and conforms to a Langmuir isothermal model with pseudo-second-order kinetics. In the presence of H2O2/K2S2O8, the removal of MO dramatically increased from 32 % to nearly 100 % after incubation for 60 min, due to the simultaneous formation of highly reactive 1O2 and ·OH. The significant contribution from 1O2 endowed CS-FC/H2O2/K2S2O8 with high universality for degrading various organic pollutants (including azo dyes and antibiotics), a wide pH window (2–8), and low sensitivity to co-existing ions. Such cost-effective, recyclable porous bio-based microspheres are suitable for heterogeneous Fenton-like catalysis in organic wastewater treatment that rely on synergistic radical/non-radical reaction pathways.

Microwave synthesis of amino-functionalized MCM-41 from coal gasification fine slag for efficient bidirectional adsorption of anionic and cationic dyes

Coal based solid waste has been recognized as a sustainable raw material for the preparation of high added value materials for wastewater treatment. In this paper, a preparation route was designed for the rapid, efficient, and low-cost preparation of MCM-41 zeolite using coal gasification fine slag as raw material. Functionalization modification of MCM-41 was carried out by grafting amino groups on its surface to improve its application performance. Moreover, the prepared functionalized material is used for bidirectional adsorption of anionic and cationic dyes. The experimental results indicate that MCM-41 zeolite with highly ordered pore structure was rapidly prepared using the advantages of fast heating and strong permeability of microwave synthesis method, with a specific surface area of up to 862.03 m2/g. Amine functionalized MCM-41 exhibits strong adsorption capacity for both cationic and anionic dyes, with maximum adsorption capacities for methylene blue and Congo red being 292.40 mg/g and 354.61 mg/g, respectively. The study of adsorption kinetics and adsorption mechanism indicate that the adsorption process is mainly controlled through chemical adsorption, including electrostatic attraction, hydrogen bonding, and π-π interactions. The results of this study will provide useful references for the use of coal based solid waste to prepare functional materials for the treatment of organic wastewater.

Augmented degradation performance of dielectric barrier discharge plasma via optimized hydroxyl radical generation

Dielectric barrier discharge (DBD) plasma demonstrates significant potential for eliminating chlorinated aromatic compounds (CACs), while its commercial application has been hampered by inadequate generation and diffusion of active species. In response, this work introduced iron-biochar composites (Fe/BC) into DBD system to enhance the generation of highly oxidative hydroxyl radicals (OH) from underutilized O3 and H2O2, thereby reducing the diffusion of OH and accelerating the degradation of CACs. The results indicated that, in just 15 min, the combined system achieved remarkable degradation rates exceeding 95% for six diverse CACs, with the degradation rate constant increasing up to 4.27 times when compared to DBD alone. Moreover, the varied response of pollutants implied that the enhanced degradation efficiency was primarily facilitated by the reduced mass transfer distance between pollutants and formed OH. The activation of O3 on Lewis acidic sites not only directly promoted the generation of OH through free radical chain reactions but also indirectly induced more conversion of H2O2 into OH by facilitating the Fe3+/Fe2+ cycle. The identification of intermediates and toxicity analysis substantiated its environmental sustainability. This study offers a viable technical pathway and theoretical foundation for enhancing the efficiency of plasma-based treatment of organic wastewater.

Roles of entrapped bubbles in methanogenic granules under oscillating pressure: Respiration and embolization for intra-granular transport

Anaerobic granular sludge plays a pivotal role in the treatment of concentrated organic wastewater. However, previous studies on intra- granular transport have generally overlooked lung-like respiration that expedites transport in response to fluctuating pressure. This study explored the activities of calcified and normal granules under simulated hydrostatic pressure oscillations. The results revealed a significant enhancement in the bioactivity of calcified granules under oscillating pressure, contrasting with the comparatively lower bioactivity observed in normal granules. The hypothesis posited that the gas pockets in calcified granules facilitated respiration as the functional structure. The presence of tiny bubbles exhibited a propensity for inducing clogging, thereby diminishing the capillary connectivity essential for substrate diffusion. The proposed respiration and embolization concepts decipher the distinct roles of entrapped bubbles in the granular bioactivity across diverse fluid states. This study offers valuable insights into the impact of fluidization on microscopic transport within granule-based bed reactors.

Mechanism insights into salt tolerance strengthened by CoCe encapsulated N-doped CNTs cathode in microbial fuel cell

To address the challenges of bioanode deactivation and instability of cathode catalysts in the treatment of high-salt organic wastewater using microbial fuel cells (MFCs), a series of CoCe catalysts encapsulated within nitrogen-doped carbon nanotubes (CoCe@NCNTs) was synthesized using a one-pot calcination method. Among the synthesized catalysts, CoCe0.5@NCNTs demonstrated outstanding and stable electrochemical performance in a high-salt environment with 600 mM NaCl, achieving a power density of 144.29 mW m−2, which was 2.7 times higher than that of Co@NCNTs. Notably, the characterization of the catalyst revealed that the addition of Ce element enhanced the stability of the Co crystal structure, mitigated Co leaching, and facilitated the retention of a higher valence state of the Co species after the reaction under high salt conditions. Specifically, the Co3+/(Co2+ + Co3+) ratio in CoCe0.5@NCNTs was 2.82 times larger than that of Co@NCNTs, signifying the favorable influence of the mutual electron conversion between the bimetallic Ce and Co on the performance and stability of catalyst in a high-salt environment. Furthermore, the study assessed the removal efficiency of norfloxacin (NOR), NAD+/NADH ratios, and microbial diversity in conjunction with the stability of cathode electrochemical performance, demonstrating the interconnection between cathode and anode. By considering the practical challenges in treating high-salinity wastewater and the principles of bioelectrochemistry, this paper proposes a mechanism for enhancing anode performance through cathode linkage, thereby providing a novel strategy for MFCs to treat high-salinity organic wastewater treatment.

Efficient osmotic energy recovery from organic wastewater using a two-dimensional porphyrin-based metal-organic frameworks membrane

Harvesting osmotic energy plays a crucial role in addressing the global depletion crisis of fossil energy and achieving a structural transformation in energy. However, current research predominantly focuses on osmotic energy stored in natural seawater, with relatively little attention given to other saline sources such as industrial wastewater. In this study, a two-dimensional Cu-TCPP metal-organic framework (MOFs) nanosheet was prepared, and a nanofluidic membrane with high osmotic energy recovery efficiency from industrial organic saline wastewater was constructed. In a LiCl methanol solution system with a 100-fold salinity gradient, the Cu-TCPP membrane achieved a stable power density of 4.87 W/m2. Simulation analysis suggests that the membrane's efficient ion-selective transport in the organic system can be primarily attributed to abundant diffusion pathways, including intrinsic pores in the nanosheet and two-dimensional nanochannels between adjacent nanosheets. Furthermore, the physicochemical properties of the nanochannel membrane and the type of solvent and ions significantly impact osmotic energy recovery efficiency in organic solvents. This work provides a novel approach to the treatment and resource utilization of industrial organic wastewater in the chemical and pharmaceutical industries.

Efficient utilization of photoelectron-hole at semiconductor-microbe interface for pyridine degradation with assistance of external electric field

In this study, enhanced pyridine bio-photodegradation with assistance of electricity was achieved. Meanwhile, photoelectron-hole played a vital role in accelerating pyridine biomineralization. The significant separation of photoelectron-hole was achieved with an external electric field, which provided sufficient electron donors and acceptors for pyridine biodegradation. The enhanced electron transport system activity also revealed the full utilization of photoelectron-hole by microbes at semiconductor-microbe interface with assistance of electricity. Microbial community analysis confirmed the enrichment of functional species related to pyridine biodegradation and electron transfer. Microbial function analysis and microbial co-occurrence networks analysis indicated that upregulated functional genes and positive interactions of different species were the important reasons for enhanced pyridine bio-photodegradation with external electric field. A possible mechanism of enhanced pyridine biodegradation was proposed, i.e., more photoelectrons and holes of semiconductors were utilized by microbes to accelerate reduction and oxidation of pyridine with the assistance of electrical stimulation. The excellent performance of the photoelectrical biodegradation system showed a potential alternative for recalcitrant organic wastewater treatment.

Recent developments in synthesis of attapulgite composite materials for refractory organic wastewater treatment: a review.

Attapulgite clay, due to its unique crystalline hydrated magnesium-aluminium silicate composition and layer-chain structure, possesses exceptional adsorption and catalytic properties, which enable it or its composites to be utilized as adsorbents and catalysts for wastewater treatment. But the drawbacks of attapulgite are also very obvious, such as relatively low specific surface area (compared to traditional adsorbents such as activated carbon and activated alumina), easy aggregation, and difficulty in dispersion. In order to fully utilize and improve the performance of attapulgite, researchers have conducted extensive research on its modification, but few specialized works have comprehensively evaluated the synthesis, applications and challenges for attapulgite-based composite materials in refractory organic wastewater treatments. This paper provides a comprehensive review of controllable preparation strategies, characterization methods and mechanisms of attapulgite-based composite materials, as well as the research progress of these materials in refractory organic wastewater treatment. Based on this review, constructive recommendations, such as deep mechanism analysis from molecular level multi-functional attapulgite-based material developments, and using biodegradable materials in attapulgite-based composites, were proposed.

Anaerobic MBR for High Organic Wastewater Treatment

Anaerobic MBR for High Organic Wastewater Treatment

Enhanced detection of acrylamide using a versatile solid-state upconversion sensor through spectral and visual analysis

Acrylamide (AM) generally forms in high-temperature processes and has been classified as a potential carcinogen. In this study, we put forward a maneuverable solid-state luminescence sensor using polydimethylsiloxane (PDMS) as the matrix coupled with upconversion nanoparticles as the indicator. The core-shell upconversion nanoparticles emitting cyan light were uniformly encapsulated in PDMS. Then it was further modified with complementary DNA of AM aptamer. The nanocrystalline fluorescein isothiocyanate isomer (FITC), coupled with AM aptamer, was attached to the surface of PDMS. FITC effectively quenched the upconversion luminescence through fluorescence resonance energy transfer (FRET). The introduction of AM resulted in preferentially bound to aptamer caused the separation of the quencher and the donor, and led to luminescence recovery. The developed sensor was applied for both spectral and visual monitoring, demonstrating a detection limit (LOD) of 1.00 nM and 1.07 nM, respectively. Importantly, in the actual foodstuffs detection, there is no obvious difference between the results of this study and the standard method, which indicates the developed method has good accuracy. Therefore, this solid-state sensor has the potential for on-site detection using a smartphone device and an Android application.

Novel process for organic wastewater treatment using aerobic composting technology: Shifting from pollutant removal towards resource recovery

In this study, an organic wastewater treatment process based on aerobic composting technology was developed in order to explore the transition of wastewater treatment from pollutants removal to resource recovery. The novelty of the process focuses towards the microbial metabolic heat that is often ignored during the composting, and taking advantage of this heat for wastewater evaporation to achieve zero-discharge treatment. Meanwhile, this process can retain the wastewater's nutrients in the composting substrate to realize the recovery of resources. This study determined the optimum condition for the process (initial water content of 50 %, C/N ratio of 25:1, ventilation rate of 3 m3/h), and 69.9 % of the total heat generated by composting was used for wastewater treatment under the condition. The HA/FA ratio of composting substrate increased from 0.07 to 0.53 after wastewater treatment, and the retention ratio of TOC and TN was 52.3 % and 61.7 %, respectively, which proved the high recycling value of the composting products. Thermoduric and thermophilic bacteria accounted for 44.3 % of the community structure at the maturation stage, which played a pivotal role in both pollutant removal and resource recovery.

Silver‐anchored dendrimer efficiently Light‐drive conversion of p‐nitrophenol

AbstractEfficient use of solar energy for photocatalytic organic synthesis and degradation of organic matter is one of the most promising ways to solve energy shortage and environmental pollution. Silver/sulfur‐doped polyimide (Ag/SPI) was successfully prepared by anchoring silver nanoparticles on sulfur doped polyimide with dendriform structure by an open‐loop and closed‐loop method. Through the analysis of the structure, morphology and photoelectric properties by different characteristics, it is found that the anchoring of silver nanoparticles greatly reduces the electron‐hole recombination rate of SPI, and the cyclic stability is relatively good, and the electrons generated by photoexcitation can participate in the reduction of p‐nitrophenol more. Therefore, the activity of degradation of organic pollutants was greatly improved under the irradiation of visible light. At 5 minutes, the degradation rate of p‐nitrophenol reached 100 %, and the only product p‐nitrophenol was generated. The reaction time was 12 times that of SPI without anchored metal particles. The Ag/SPI dual‐function catalyst provides a new idea for the application of p‐nitrophenol wastewater treatment and the conversion of p‐aminophenol and provides a new reference direction for the field of organic wastewater treatment and organic synthesis.

Synergistic removal of organics from semi-coke wastewater by persulfate and cyanide tailings

In this study, the persulfate and cyanide tailings (PS-CTs) were used for the synergistic treatment of semi-coke wastewater to achieve advanced oxidation and in-situ coagulation removal of organics in semi-coke wastewater. The effects of persulfate concentration, reaction temperature, cyanide tailing concentration and initial pH on chemical oxygen demand (COD) removal efficiency were investigated, and the synergistic mechanism in the treatment process was further explored. The results showed that the removal efficiency of COD in semi-coke wastewater was 94.49 % under the conditions of persulfate concentration 0.025 mol/L, reaction temperature 60 °C, cyanide tailings concentration 5 g/L, the initial pH value of 3. The results of the mechanistic analysis showed that in PS-CTs system, pyrite was oxidized by persulfate. The dissolved Fe2+ activated the persulfate to produce SO4− and OH and generated Fe3+ in situ. The hydrolysis of Fe3+ produced a series of complex ions and amorphous iron hydroxides, which could remove some organics by adsorption and sweeping netting. The organics in semi-coke wastewater were effectively removed by the combined effect of oxidation and coagulation. In addition, the PS-CTs system also achieved the oxidative de-cyanidation of cyanide tailings simultaneously, and the total cyanide concentration of treated cyanide tailings was 8.21 mg/kg, and the leaching cyanide concentration was 0.12 mg/L, which was in line with the emission standards. This process implemented the concept of “treating waste with waste”, and provided theoretical support for the treatment of semi-coke wastewater and other organic wastewater.

Process-specific volatile organic compounds emission characteristics, environmental impact and health risk assessments of the petrochemical industry in the Beijing-Tianjin-Hebei region.

Volatile organic compounds (VOCs) concentration, source profiles, O3 and SOA formation, and health risks were investigated in the petrochemical industry in Beijing-Tianjin-Hebei. The results showed that total VOCs concentrations were 547.1-1956.5μg·m-3, and alkanes were the most abundant group in all processes (31.4%-54.6%), followed by alkenes (20.6%-29.2%) and aromatics (10.1%-25.1%). Moreover, ethylene (11.3%), iso-pentane (7.1%), n-hexane (5.1%), benzene (4.9%) and 2,2-dimethylbutae (4.8%) were identified as the top five species released for the whole petrochemical industry. The coefficient of divergence between the source profiles from different processes was 0.49-0.73, indicating that most source profiles must not be similar. Moreover, because of the different raw materials and technologies used, the source profiles in this study are significantly different from those of other regions. The ozone and secondary organic aerosol formation potentials (OFPs and SOAPs) were evaluated, suggesting that ethylene, propylene, 1-butene, m,p-xylene, and 1,3-butadiene should be preferentially controlled to reduce OFPs. That benzene, toluene, ethylbenzene, m,p-xylene, isopropylbenzene, o-ethyltoluene, and 1,3,5-trimethylbenzene should be priority control compounds for SOAPs. Additionally, the total hazard ratio for non-cancer risk ranged from 0.9 to 7.7, and only living area was unlikely to be related to adverse health effects. Cancer risks associated with organic chemicals, rubber synthesis, oil refining, and wastewater collection and treatment have definite risks, whereas other processes have probable risks. This study provides a scientific basis for VOCs emission control and management and guides human health in the petrochemical industry.

Mutualistic symbiosis of fungi and nitrogen-fixing bacteria in halophilic aerobic granular sludge treating nitrogen-deficient hypersaline organic wastewater

Hypersaline organic wastewater is characterized as being nitrogen-deficient, and is easily prone to sludge bulking. In this study, the stability of halophilic aerobic granular sludge (HAGS) for the treatment of hypersaline organic wastewater is explored. Along with the decrease of influent ammonium, the bacterial population substantially reduced, whereas the fungal population continuously increased in HAGS. Saccharomycetales in fungi become the dominant sequence (99.78%) in HAGS bulking. Additionally, Halanaerobium (77.47%) remained prevalent in HAGS despite bacterial washout. Halanaerobium, a nitrogen-fixing genus of bacteria, provided nitrogen for ammonium-assimilating fungi. Saccharomycetales encapsulating HAGS reduced the transfer efficiency of dissolved oxygen, thereby creating favorable growth conditions for Halanaerobium. This paper for the first time highlights the mutualistic symbiosis of fungi and bacteria in HAGS treating the hypersaline organic wastewater. The study lays the foundation for the control and recovery of HAGS bulking.

Enhanced oxidative capacity of red mud-lignin composite/peroxydisulfate to degrade sulfamethazine through electron transfer mechanism

Advanced oxidation processes based on peroxydisulfate (PDS-AOPs) have been used for the remediation of organic wastewater. However, the mechanism for the generation of electron transfer sub-stable complexes in the metal–carbon/PDS system has not been fully elucidated. Herein, two environmental solid wastes were selected to synthesize a novel Fe-carbon catalyst (RM@KC1:2–800) using alkali lignin as the carrier and red mud (RM) as the iron source, and applied for peroxydisulfate (PDS) activation in sulfamethazine (SMZ) removal. The complexation of alkali lignin with RM favored the exposure of Fe active sites and adsorption of PDS. 97% of SMZ could be removed efficiently in the RM@KC1:2–800/PDS system, and the degradation efficiency remained at 80.81% after 5 cycles without metal leaching, which was suitable for a variety of natural water bodies. Combined with density functional theory (DFT) and other analyses confirmed that the electron transfer pathway is the main pathway for PDS activation and SMZ degradation. And the reactive Fe species were the active sites that contributed to the adsorption of PDS on the RM@KC1:2–800 surface to form sub-stable complexes (RM@KC-PDS*), whereby the electron transfer occurred. Surprisingly, the prediction of environmental toxicity of the degradation intermediates based on T.E.S.T software and biological experiments proved their environmental friendliness. Overall, this study follows the concept of “waste-to-waste” and proposes a strategy for a suitable and cost-effective Fe-carbon catalyst for large-scale production, while demonstrating its potential application in the treatment of organic wastewater.

Research Progress in the Development and Application of Photocatalysis Technology and Materials

In recent years, photocatalytic technology has become a research hotspot for the treatment of organic wastewater, uranium containing wastewater, and Cr (VI) containing wastewater due to its advantages of environmental friendliness, simple reaction process, and high degradation efficiency. Uranium, as the main component of nuclear fuel, is an important strategic resource. The separation and enrichment technology of uranium is of great significance for the sustainable development of nuclear energy. Previously, a series of solid adsorption materials for uranium extraction have been developed, such as inorganic minerals, mesoporous silica, magnetic nanomaterials, carbon based materials, and advanced porous materials. However, due to the comprehensive performance of stability, removal kinetics, adsorption capacity, selectivity, and reusability, the practical application of these materials is still inevitably limited. And photocatalytic technology can reduce easily soluble and easily flowing U (VI) to more difficult to dissolve and relatively non flowing U (IV), thus overcoming the above problems and achieving the reduction and fixation of uranium. Moreover, this technology only relies on inexhaustible solar energy as energy source, and has the advantage of green and clean. Therefore, the use of photocatalytic technology to separate and enrich uranium is of great significance for the sustainable development of nuclear energy. However, most semiconductor photocatalysts have shortcomings in terms of light absorption capacity and charge separation ability, which limits their practical application in wastewater treatment. In addition, there are many difficulties in photocatalytic treatment of wastewater, such as the fast recombination speed of photo generated electron hole pairs generated by the catalyst, the weak visible light response of most single semiconductor materials, the need to introduce additional sacrificial agents to capture holes in the reaction, and the introduction of inert gases to eliminate the interference of oxygen. This article provides a certain scientific basis for expanding the application of various photocatalytic technologies in wastewater treatment.

Performance and mechanism of enhanced phenolic compounds treatment via mycelial pellets

AbstractBACKGROUNDBiological enhancement in organic wastewater treatment is currently considered an effective and economical method. As a biomass carrier, mycelial pellets are attracting increasing attention, with substantial progress recently being made. To investigate their bioaugmentation effect as a biomass carrier, mycelial pellets with immobilized phenol‐degrading bacteria were applied in a sequencing batch reactor. The phenolic compound removal efficiency of the mycelial pellet‐enhanced system was then studied and compared to the control aerobic activated sludge‐enhanced system. Finally, the settling velocity, internal structure, and surface properties were studied to explore the main bioaugmentation mechanisms of the mycelial pellets.RESULTSThe stable degradation effects of phenolic compounds and total organic carbon (TOC) were observed in both systems. In the mycelial pellet system, the biological removal efficiency was approximately 0.5 mg phenolic compounds L−1 d−1MLSS−1 and 0.4 mg TOC L−1 d−1MLSS−1, which was higher than the aerobic activated sludge system. Bioaugmentation by the pellets was mainly attributed to the structure of the connected macropores, the electrostatic attraction of positive charges, the adsorption of functional groups on the hypha surface, and flocculation due to the extracellular polymeric substances secreted on the pellet.CONCLUSIONThe excellent phenolic compound removal efficiency and bioaugmentation effect of the mycelial pellets suggest their potential to enhance organic wastewater treatment as a biomass carrier. © 2023 Society of Chemical Industry.

A novel bimetallic Fe-Cu-CNT catalyst for effective catalytic wet peroxide oxidation: reaction optimization and mechanism investigation

Treatment of organic wastewater is of great importance and can be carried out by catalysis technologies such as catalytic wet peroxide oxidation (CWPO). A novel bimetallic Fe-Cu-CNT catalyst was first developed by a facile hydrothermal method; Fe species (Fe (Ⅱ) and Fe (Ⅲ)) and Cu species (Cu (Ⅰ) and Cu (Ⅱ)) were used to fabricate the catalyst with the CNTs, which was stable during testing. Methylene blue (MB) was chosen as model compound for the study; the optimization for treatment by the Box-Behnken design indicated that a combination of low pH, high MB concentration and intermediate temperature led to better treatment performance. The CWPO reaction obeyed the 2nd-order kinetic equation and the catalyst activity increased with an increase in the Cu content. The reaction induction period was shortened with decreasing Fe:Cu ratio. The cycling reaction between Fe3+/Fe2+ and Cu2+/Cu+ pairs generated a large number of oxidative radicals and improved the pollutant degradation efficiency. Finally, the reaction rate equation of CWPO over Fe-Cu-CNT was derived, and it was experimentally illustrated that hydroxyl radicals played a crucial role in the treatment. This study demonstrates that the optimized Fe-Cu-CNT has great potentials for treatment of organic wastewater with higher efficiency and lower cost.

Thermally activated natural chalcopyrite for Fenton-like degradation of Rhodamine B: Catalyst characterization, performance evaluation, and catalytic mechanism

In this work, catalytic activity of natural chalcopyrite (CuFeS2) was improved by thermal activation. The modified chalcopyrite was used as efficient catalyst for degradation of organic dye Rhodamine B (RhB) through advanced oxidation process (AOP). Effects of catalyst dosage, H2O2 concentration, reaction temperature, solution pH, anions, and natural organic matter on the degradation efficiency of RhB were investigated. This study revealed that thermal activation at 300 °C changed the chemical valency of surface elements rather than transforming the major chemical phase of natural chalcopyrite. The Fenton-like degradation of RhB was significantly improved by thermally activated chalcopyrite. RhB degradation could be obtained under broad pH and showed high resistance to natural organic matter and anions. Under optimal conditions of H2O2 43.0 mM, catalyst 0.75 g/L, initial pH 5.1, and reaction temperature 25 °C, the degradation of RhB reached 96.7% at 50 min. Based on the rate constant of reaction kinetics, the activation energy for RhB degradation was calculated to be 9 kJ/mol. Radical scavenging experiments and electron paramagnetic resonance (EPR) technique demonstrated that RhB degradation was dominated by the generated hydroxyl radicals in activated chalcopyrite/H2O2 system. The formation of surface sulfates resulted from thermal activation induced the dissolved copper or iron ions, and promoted H2O2 activation and facilitated RhB degradation by reactive hydroxyl radicals. This work provides an in-depth understanding of the mechanism behind thermal activation to enhance the activity of natural chalcopyrite, offering a theoretical basis for utilizing natural minerals for Fenton-like treatment of organic wastewater towards cleaner production.