Mechanism of directed activation of peroxymonosulfate by Fe-N/O unsymmetrical coordination-modulated polarized electric field.

Iron-nitrogen co-doped carbon materials as heterogeneous catalysts have attracted much attention in advanced oxidation processes involving peroxymonosulfate (PMS) due to their unique structure and enormous catalytic potential. However, there is limited research on the influence of different coordination structures on the central iron atoms. Through simple pyrolysis, we introduced oxygen atoms into the Fe-N coordination structure, constructing Fe-N/O@C catalysts with Fe-N2O2 coordination structure, and achieved efficient degradation of bisphenol A (BPA). Quenching experiments, electron paramagnetic resonance, and electrochemical analysis indicate that compared to the free radical activation pathway of Fe-N@C, high-valent iron-oxo species (≡Fe(Ⅳ) = O) are the main reactive oxygen species (ROS) in the Fe-N/O@C/PMS system. Meanwhile, we compared the differences in the oxidation states of Fe atoms and electron density in different coordination structures, revealing the formation of high-valent iron-oxo species and the mechanism of interfacial electron transfer. Therefore, this study provides new insights into the design and development of Fe-N co-doped catalysts for resource-efficient and environmentally friendly catalytic oxidation systems.

Comparative study of Fe2+/H2O2 and Fe2+/persulfate systems on the pre-treatment process of real pharmaceutical wastewater.

Advanced oxidation technologies based on hydroxyl radical (•OH) and sulfate radical (SO4-•) are two common types of advanced oxidation technologies, but there are not many reports on the application of advanced oxidation methods in actual wastewater pretreatment. This article compares the pre-treatment performance of Fe2+/H2O2 and Fe2+/Persulfate systems in actual pharmaceutical wastewater, and combines EEM, GC-MS, and toxicity testing results to explore the differences in TOC, COD, and NH3-N removal rates, optimal catalyst dosage, applicable pH range, toxicity of effluent after reaction, and pollutant structure between the two systems. The results indicate that the Fe2+/H2O2 system has a higher pollutant removal rate (TOC: 71.9%, COD: 66.9%, NH3-N: 34.1%), but also requires a higher catalyst (Fe2+) concentration (6.0 g/L), and its effluent exhibits characteristic peaks of aromatic proteins. The Fe2+/Persulfate system has a wider pH range (pH ≈ 3-7) and is more advantageous in treating wastewater containing more cyclic organic compounds, but the effluent contains some sulfur-containing compounds. In addition, toxicity tests have shown that the toxicity reduction effect of the Fe2+/Persulfate system is stronger than that of the Fe2+/H2O2 system.

Prediction of effluent total nitrogen and energy consumption in wastewater treatment plants: Bayesian optimization machine learning methods.

The control of effluent total nitrogen (TN) and total energy consumption (TEC) is a key issue in managing wastewater treatment plants. In this study, effluent TN and TEC predictive models were established by selecting influent water quality and process control indicators as input features. The prediction performance of machine learning methods under different random seeds was explored, the moving average method was used for data amplification, and the Bayesian algorithm was used for hyperparameter optimization. The results showed that compared with the traditional hyperparameter optimization method for effluent TN prediction, the coefficient of determination (R2) increased by 0.092 and 0.067, reaching 0.725, and the root mean square error (RMSE) decreased by 0.262 and 0.215 mg/L, reaching 1.673 mg/L, respectively, after Bayesian optimization and data amplification. During TEC prediction, R2 increased by 0.068 and 0.042, reaching 0.884, and the RMSE decreased by 232.444 and 197.065 kWh, reaching 1305.829 kWh, respectively.

New insights into toxicity reduction and pollutants removal during typical treatment of papermaking wastewater.

Papermaking wastewater contained various of toxic and hazardous pollutants that pose significant threats to both the ecosystem and human health. Despite these risks, limited research has addressed the detoxification efficiency and mechanism involved in the typical process treatment of papermaking wastewater. In this study, the acute toxicity of papermaking wastewater after different treatment processes was assessed using luminousbacteria, zebrafish and Daphnia magna (D. magna). Meanwhile, the pollution parament of the corresponding wastewater were measured, and the transformation of organic pollutant in the wastewater was identified by three-dimensional fluorescence and other techniques. Finally, the possible mechanism of toxicity variation in different treatment processes were explored in combination with correlation analyses. The results showed that raw papermaking wastewater displayed high acute toxicity to luminousbacteria, and exhibited slight acute toxicity and acute toxicity effect to zebrafish and D. magna, respectively. After physical and biochemical processes, not only the toxicity of the wastewater to zebrafish and D. magna was completely eliminated, but also the inhibitory effect on luminousbacteria was significantly reduced (TU value decreased from 11.07 to 1.66). Among them, the order of detoxification efficiency on luminousbacteria was air flotation > hydrolysis acidification > IC > aerobic process. Correlation analyses revealed a direct link between the reduced of Total Organic Carbon (TOC) and Chemical Oxygen Demand (COD) and the detoxification efficiency of the different processes on the wastewater. In particular, the removal of benzene-containing aromatic pollutant correlated positively with decreased toxicity. However, the Fenton process, despite lowering TOC and COD, increased of the acute toxicity of the luminousbacteria (TU value increased from 1.66 to 2.33). This may result from the transformation generation of organic pollutant and oxidant residues during the Fenton process. Hence, oxidation technologies such as the Fenton process, as a deep treatment process, should be more concerned about the ecological risks that may be caused while focusing on their effectiveness in removing pollutant.

Overlooked role of void-nanoconfined effect in emerging pollutant degradation: Modulating the electronic structure of active sites to accelerate catalytic oxidation.

The efficient removal of emerging pollutant from water is the ultimate frontiers of advanced oxidation processes (AOPs), yet it is challenging to obtain higher catalytic activity and oxidation rate. Herein, a sustainable solution was proposed by optimizing the curvature of confined structure to modulate the electronic state of the active sites in nanochannels for improving the catalytic activity. In addition, the confined effect can enhance the oxidation rate by shorting the mass transfer of active species and pollutants. A void-nanoconfined nanoreactor was prepared by loading Fe2O3 into the nanochannels (<5 nm) of the hollow carbon sphere. An enhancement of 3 orders of magnitude was obtained in the degradation rate constant of void-nanoconfined catalytic system toward sulfamethoxazole (SMX) (6.25 min-1) compared with the non-confined system. The kinetics enhancement was attributed to the larger electron potential difference between the outer and inner nanochannel caused by the curvature increase of carbon sphere, accelerating the electron transfer, so that the energy barrier of SMX degradation reaction was reduced by 31 kcal/mol with the assistance of confinement energy. Importantly, the NC-IN/PDS system exhibited outstanding removal efficiency for the actual river water using a continuous flow reactor. This work provides a new insight into designing an efficient and stable catalytic nanoreactor, enriching the domain of advanced wastewater treatment strategies.

Facilitating Proton Coupled Electron Transfer Reaction through the Interfacial Micro Electric Field with Fe─N4 ─C in FeMOFs Glass.

The proton-coupled electron transfer(PCET) reaction plays a crucial role in the chemical transformation process andhas become one of the most concerned elementary reactions. However, the complex kinetics of PCET reaction, which requires the simultaneous transfer of protons and electrons, leads to the dilemma that thermodynamics and kinetics cannot bebalanced and restricts its further development. In this, an interface micro-electric field (IMEF) basedon Fe─N4 in FeMOFs (Fe-Based Metal-Organic Frameworks) glass is designed tosynchronize proton/electron interface behavior for the first time to realizeefficient PCET reaction and optimize reaction thermodynamics and kinetics. The IMEF facilitates the separation of photogenerated electrons and holes, and accelerates Fe(III)/Fe(II) cycle. Driven by near-surface electric field force, the protons near surfacemigrate to Fe sites and participate in Fe(IV)═O formation and reaction, lowering the reaction energy barrier. Based on the interface regulation ofIMEF, a high-efficiency PCET reaction is realized, and kinetic reactionrate constant of photocatalytic oxidation of emerging contaminants is increasedby 3.7 times. This study highlights a strategy for IMEFs to modulate PEC Treactions for a wide range of potential applications, including environmental and ecological applications.

Unraveling the single-atom Fe-N4 catalytic site selectivity generate singlet oxygen via activation of persulfate: Polarizing electric fields changes the electron transfer pathway.

Single-atom catalysts have been proved to be an effective material for the removal of organic pollutants from water and wastewater, and yet, the relationship between their internal structures and their roles still remains elusive. In this work, a catalyst Fe (MIL)-SAC with single-atom Fe-N4 active site was prepared. Fe (MIL)-SAC/Peroxydisulfate (PDS) system was able to achieve complete degrade of the Sulfamethoxazole (SMX) with kobs at 0.466 min-1, which was faster than the Fenton system under the same conditions (kobs = 0.422 min-1) and 16 times faster than Fe (MIL) (kobs = 0.029 min-1). Density functional calculations reveal that the Fe-N4 structure will affect the electron transport path and lead to selective generation of 1O2 by triggering S-O breakage and O-O polarization in PDS. Furthermore, Fe (MIL)-SAC/PDS system exhibits strong resistance to common influencing factors and has good application prospects. This work provides a new approach for the selectively generation of 1O2 for the efficient treatment of organic pollutants in aqueous environment.

Stability performance analysis of Fe based MOFs for peroxydisulfates activation to effectively degrade ciprofloxacin.

Fe-based metal-organic frameworks (MOFs) show high activity toward the activation of peroxodisulfate (PDS) for the removal of organic micropollutants (OMPs) in wastewater treatment. However, there is a phenomenon of Fe ion dissolution in the Fe-based MOFs' active PDS system, and the reasons and influencing factors that cause Fe ion dissolution are poorly understood. In this study, we synthesized four types of Fe-based MOFs and confirmed their crystal structure through characterization. All types of Fe-based MOFs were found to activate PDS and form sulfate radicals (SO4 -), which effectively remove OMPs in wastewater. During the process of Fe-based MOFs activating PDS for CIP removal, activated species, oxidant reagent, and pH negatively impact the stability performance of the MOFs' structure. The coordination bond between Fe atom and O atom can be attacked by water molecules, free radicals, and H+, causing damage to the crystal structure of MOFs. Additionally, Fe (II)-MOFs exhibit the best stability performance, due to the enhanced bond energy of the coordination bond in MOFs by the F ligands. This study summarizes the influencing factors of Fe-based MOFs' damage during PDS activation processes, providing new insights for the future development of Fe-based MOFs.

Regulating the reaction pathway of nZVI to improve the decontamination performance through magnetic spatial confinement effect.

Nanoscale zero-valent iron (nZVI) shows high effectiveness in the catalyzed removal of contaminants in wastewater treatment. However, the uncontrolled interfacial electron transfer behavior and formation of surface iron oxide (FeOx) layer led to severe electron wasting and occasionally form highly toxic intermediates. Here, we constructed magnetic mesoporous SiO2 shell on surface of nZVI to stimulate a magnetic spatial confinement effect and regulate the electron transfer pattern. Therein, Fe atom facilely spread out from the nZVI core, orderly release electron to surface adsorbed H2O molecule, which is efficiently transformed into active hydrogen (H*). Meanwhile, in-situ Raman revealed that Fe atoms were involved in the formation of penetrable γ-FeOOH rather than FeOx layer, enabling the continuous inward diffusion of H2O and outward diffusion of H* . Employing the catalyzed removal of halogenated phenols as demo reaction, the presence of magnetic mesoporous SiO2 shell utilized the reaction between electrons and H2O to switch the reaction pathway from the reduction/oxidation hybrid process to hydrodehalogantion, and increased the conversion of halogenated phenols-to-phenols by 5.53 times. This study shows the forehand of improving the decontamination performance of nZVI through sophisticated designed surface coating, as well as fine regulating the environmental behavior of magnetic material via micro-magnetic field.

Denitrification efficiency, microbial communities and metabolic mechanisms of corn cob hydrolysate as denitrifying carbon source.

In this study, the denitrification efficacy of corn cob hydrolysate (CCH) was compared and analyzed with that of glucose and acetate to determine its feasibility as an additional carbon source, and its metabolic mechanism as a denitrification carbon source was investigated in depth. By constructing a denitrification reactor, it was found that the TN removal rate exceeded 97% and the effluent COD remained below 70 mg/L during the stable operation with CCH as the carbon source, and the denitrification effect was comparable to that of the glucose stage (GS) and the acetate stage (AS). The analysis of the microbial community showed that the dominant phylum was Proteobacteria and Bacteroidota, where the abundance of Bacteroidota in the hydrolysate stage (HS) (24.37%) was significantly higher than that of GS (4.89%) and AS (11.93%). And the analysis at the genus level showed the presence of a large number of genera of organic matter hydrolysis and acid production in HS that were almost absent in other stages, such as Paludibacter (12.83%), Gracilibacteria (4.27%), f__Prolixibacteraceae_Unclassified (2.94%). In addition, the higher fatty acid metabolism and lower sugar metabolism of HS during carbon metabolism were similar to the ratio of AS, suggesting that CCH was mainly fermented to acids and then involved in the tricarboxylic acid (TCA) cycle. During nitrogen metabolism, the high relative abundance of narG, nirS, and nosZ ensured the denitrification process. The results of this study were expected to provide a theoretical basis and data support for promoting denitrification from novel carbon sources.

Exploring degradation properties and mechanisms of emerging contaminants via enhanced directional electron transfer by polarized electric fields regulation in Fe-N4-Cx.

Heterogeneous catalysis offers an opportunity to overcome the low efficiency and secondary pollution limitations of emerging contaminants (ECs) purification technologies, but it is still challenging to regulate electron directed transport for achieving high catalysis efficiency and selectivity due to insufficient understanding of the electron transfer pathways and behavioral mechanisms during its catalysis. Here, by tuning the defects of the C-N coordination of the support, the polarized electric field (PEF) characteristics are changed, which in turn affects the electron transport behavior. The results show that the charge offset on Fe-N4-Cx forms a PEF, which will induce directional electron transport. After the quantitative structure-activity relationship (QSAR) fitting analysis, the greater the degree of C-N defects, the higher the intensity of the PEF, which in turn enhances the electron transport and promotes the catalytic behavior. In addition, the surface pyrrole N site can adsorb enrofloxacin (ENR) and enrich it on the surface. This can reduce the transport distance of reactive oxygen species (ROS) to synergize catalysis and adsorption, resulting in rapid degradation of ECs. Combined with liquid chromatograph mass spectrometer (LC-MS) results and theoretical calculations, five degradation pathways of ENR were speculated, mainly including the oxidation of piperazine and the cleavage of the quinolone ring. This work proposes a novel PEF regulation strategy and explores its mechanism for safe treatment of ECs.

A novel polydopamine-modified metal organic frameworks catalyst with enhanced catalytic performance for efficient degradation of sulfamethoxazole in wastewater.

In this study, a novel polydopamine (PDA)-modified metal organic frameworks (MOFs) catalyst (MIL/PDA) was successfully fabricated to activate persulfate (PS) for the degradation of sulfamethoxazole (SMX) in wastewater. The experimental results indicated that PDA-modified catalyst exhibited superior catalytic performance and enhanced the degradation of SMX (91.5%) compared to pure MOFs. The physical-chemical properties of the MIL/PDA catalyst were comprehensively characterized, and the applications in the catalytic degradation of SMX were evaluated. It was found that the modification of PDA enhanced the electron transfer, while promoting the redox cycle of Fe(III)/Fe(II), which in turn boosted the production of active oxygen species. Furthermore, MIL/PDA showed high stability and reusable performance over multiple cycles. Both radical and non-radical pathways were jointly involved in the activation process of PS were confirmed by quenching experiments combined with electron paramagnetic resonance (EPR). Based on this, the possible mechanism of the catalytic reaction was investigated. Finally, five degradation pathways of SMX degradation were proposed according to the results of liquid chromatography-mass spectrometry (LC-MS). This work provided a new insight into the design of novel and efficient heterogeneous catalysts for advanced wastewater treatment.

Modulated construction of Fe-based MOF via formic acid modulator for enhanced degradation of sulfamethoxazole：Design, degradation pathways, and mechanism.

Metal-organic frameworks (MOFs) have attracted more attention because of their excellent environmental catalytic capabilities. Modulation approach as an advanced assistant strategy is vital essential to enhancing the performance of MOFs. In this study, the modulated method was used to successfully synthesize a group of Fe-based MOFs, with formic acid as the modulator on the synthesis mixture. The most modulated sample Fe-MOFs-2 exhibit high specific surface areas and higher catalytic activity, which could effectively degrade SMX via PS activation, with almost 95% removal efficiency within 120 min. The results revealed that the % RSE of modulated Fe-MOFs-2 increased from 2.31 to 3.27 when compared with the origin Fe-MOFs. This may be due to the addition of formic acid induces the formation of more coordinatively unsaturated metal sites in the catalyst, resulting in structural defects. In addition, the quenching experiment and EPR analysis verified SO4-·and·OH as the major active free radicals in the degradation process. Modulated Fe-MOFs-2 demonstrated good reusability and stability under fifth cycles. Finally, four possible degradation pathways and catalytic mechanism of Fe-MOFs-2 was tentatively proposed. Our work provides insights into the rational design of modulated Fe-MOFs as promising heterogeneous catalysts for advanced wastewater treatment.

Efficient Shaping of Cellulose Nanocrystals Based on Allomorphic Modification: Understanding the Correlation between Morphology and Allomorphs.

Cellulose nanocrystals (CNC) are green, safe, and renewable nanomaterials with a variety of excellent performances but their morphologies are notoriously difficult to control as this is unfavorable to the diversification of the end products. Allomorphic conversion plays an important role in diversifying the morphology of CNC. However, this further complicates the prediction, design, and control of the geometric dimensions of CNC. Herein, allomorphically modified cellulose (mercerized cellulose, ethylenediamine (EDA)-treated cellulose, and ball-milled cellulose) is designed and used as the starting material for CNC isolation. Subsequently, the morphological evolution of cellulose particles during acid hydrolysis is traced by scanning electron microscopy observations. A mechanism that facilitates further understanding of CNC shaping during sulfuric acid hydrolysis is proposed. According to the CNC shaping mechanism, precise prediction, design, and efficient control of the morphology of CNC (needle-like, ribbon-like, ellipsoid, and spherical) can be realized. CNC with various morphologies are favorable for their applications, such as templating synthesis of porous materials and Pickering emulsion dispersion.

Targeted degradation of TBBPA using novel molecularly imprinted polymer encapsulated C-Fe-Nx nanocomposite driven from MOFs.

To improve the efficacy of organic pollutant removal using sulfate radicals, we designed MIP@C-Fe-Nx, a molecularly imprinted material capable of targeting the degradation of tetrabromobisphenol A (TBBPA), which can be used as both adsorbent and catalyst to recognize and degrade Tetrabromobisphenol A (TBBPA) accurately, and the final removal rate of TBBPA can reach 104.6 mg·g-1. Based on the synergistic effects of MIP@C-Fe-Nx on the excellent organic pollutant recognition and catalytic performance, low concentrations of TBBPA can be pre-targeted, concentrated, and fixed on the surface of MIP, and degraded simultaneously in-situ by·OH and SO4•- which are produced by activating PS with C-Fe-Nx. Recognition experiments demonstrated that MIPs had perfect performance in recognizing and adsorbing TBBPA and debromination intermediates. The DFT calculations and HPLC-MS analysis indicated that MIP@C-Fe-Nx had a targeted recognition and accumulation for TBBPA and debromination intermediates, for example, dibromobisphenol A, monobromobisphenol A, and bisphenol A, thus avoid the formation of toxic intermediates causing secondary contamination.

Fe-N-C catalyst with Fe-NX sites anchored nano carboncubes derived from Fe-Zn-MOFs activate peroxymonosulfate for high-effective degradation of ciprofloxacin: Thermal activation and catalytic mechanism.

Developing high-efficient catalysts is crucial for activating peroxymonosulfate (PMS). Fe-N-C catalysts exhibit excellent performance for PMS activation because of the contribution of doped N, Fe-Nx and Fe3C sites. In our work, a series of Fe-N-C catalysts with high-performance was obtained by pyrolyzing Fe-Zn-MOFs precursors. During pyrolysis process, the change of chemical bonds and formation of active sites in the precursor were elucidated by characterization analysis and related catalytic experiments. Graphitic N, Fe-Nx and Fe3C were confirmed to activate PMS synergistically for ciprofloxacin (CIP) degradation. Besides, the catalytic performance was proportional to the amount of doped iron and calcination temperature. Moreover, the Fe-N-C-3-800/PMS system not only displayed good recycling performance, but also had high anti-interference ability. Integrated with quenching and electron paramagnetic resonance (EPR) experiments, a non-radical pathway dominated by 1O2 was proposed. Furthermore, PMS could bond to Fe-N-C-3-800 to form intermediate for charge transfer, thus accelerate electron transfer between CIP and PMS to realize degradation of CIP. Six main pathways of CIP degradation were proposed, which include bond fission of N-C on piperazine ring and direct oxidation of CIP. This study provided a new idea for the design of heterogeneous carbon catalysts in advanced oxidation field.

Tailored d-Band Facilitating in Fe Gradient Doping CuO Boosts Peroxymonosulfate Activation for High Efficiency Generation and Release of Singlet Oxygen.

In the field of heterogeneous catalysis, limitations of the surface reaction process inevitably make improving the catalytic efficiency to remove pollutants in water a major challenge. Here, we report a unique structure of Fe surface-gradient-doped CuO that improves the overall catalytic processes of adsorption, electron transfer, and desorption. Interestingly, gradient doping leads to an imbalanced charge distribution in the crystal structure, thereby promoting the adsorption and electron transport efficiency of peroxymonosulfate (PMS). The orbital hybridization of Fe also improves the electronic activity. More importantly, the occupied d-orbital distribution is closer to the lower energy level, which improves the desorption of the reaction intermediate (1O2). As a result, the production and desorption of 1O2 have been improved, resulting in excellent BPA degradation ability (kinetic rate increased by 67.3 times). Two-dimensional infrared correlation spectroscopy is used to better understand the doping process and catalytic mechanism of Fe-CuO. Fe-O changes before Cu-O and is more active. The Fe-required active sites, active species intensity, and kinetic reaction rates show a good correlation. This research provides a scientific basis for expanding the purification of toxic organic pollutants in complex water environments by heterogeneous catalytic oxidation.

Modeling the Performance of Full-Scale Anaerobic Biochemical System Treating Deinking Pulp Wastewater Based on Modified Anaerobic Digestion Model No. 1.

The deinking pulp (DIP) is a main resource for paper making, and the wastewater from DIP process needs to be treated. Anaerobic biochemical technique has been widely applied in DIP wastewater treatment, due to the remarkable capability in reducing high chemical oxygen demand (COD). In this study, a mathematical simulation model was established to investigate the performance of a full-scale anaerobic biochemical system for treating DIP wastewater. The model was based on Anaerobic Digestion Model No. 1 (ADM1), which was modified according to the specific anaerobic digestion process for DIP wastewater treatment. The hydrodynamic behavior of a full-scale anaerobic biochemical system was considered in this model. The characteristics of the influent DIP wastewater were assessed, and then, the substrate COD proportion was divided successfully for the necessity of ADM1 applying. The Monte Carlo technique was implemented to distinguish the most sensitive parameters that influenced the model output indicators comprising effluent COD and biogas production. The sensitive parameters were estimated and optimized. The optimized value of k _m_pro is 12.02, K _S_pro is 0.35, k _m_ac is 4.26, K _S_ac is 0.26, k _m_h2 is 16.62, and K _S_h2 is 3.21 × 10-5. The model was calibrated with 150 days operation values measured in the field. The subsequent 100 days on-site values were used to validate the model, and the results obtained by the simulations were in good agreement. This study provides a meaningful and theoretical model guidance for full-scale wastewater anaerobic biochemical treatment simulation.

Targeted degradation of refractory organic compounds in wastewaters based on molecular imprinting catalysts.

Efficient removal of low-concentration refractory pollutants is a crucial problem to ensuring water safety. The use of heterogeneous catalysis of molecular imprinting technology combined with traditional catalysts is a promising method to improve removal efficiency. Presently, the research into molecular imprinting targeting catalysts focuses mainly on material preparation and performance optimization. However, more researchers are investigating other applications of imprinting materials. This review provides recent progress in photocatalyst preparation, electrocatalyst, and Fenton-like catalysts synthesized by molecular imprinting. The principle and control points of target catalysts prepared by precipitation polymerization (PP) and surface molecular imprinting (S-MIP) are introduced. Also, the application of imprinted catalysts in targeted degradation of drugs, pesticides, environmental hormones, and other refractory pollutants is summarized. In addition, the reusability and stability of imprinted catalyst in water treatment are discussed, and the possible ecotoxicity risk is analyzed. Finally, we appraised the prospects, challenges, and opportunities of imprinted catalysts in the advanced oxidation process. This paper provides a reference for the targeted degradation of refractory pollutants and the preparation of targeted catalysts.

Fe@C activated peroxymonosulfate system for effectively degrading emerging contaminants: Analysis of the formation and activation mechanism of Fe coordinately unsaturated metal sites.

Carbon-encapsulated Fe nanocomposites (Fe@C), obtained by pyrolysis of metal-organic frameworks (MOFs), can activate peroxymonosulfate (PMS) to remove emerging contaminants (ECs). Unfortunately, the current MOFs-derived catalysts always inevitably produce more iron-oxide compounds that unfavorable for PMS activation. In this work, according to the thermogravimetric curve of Fe(II)-MOF-74, to discuss the role of pyrolysis temperature on the structural characteristics of Fe@C. The results demonstrated that Fe@C-4 could obtain abundant coordinately unsaturated metal sites and exhibited the best activation performance. Radical-quenching experiments and EPR measurements confirm that the generated sulfate radical (SO4-˙) and singlet oxygen (1O2) only degraded approximately 35% of TBBPA. Meanwhile, negatively charged complex intermediates formed by the weak interaction between Fe@C-4 and PMS was proposed as the dominant reactive species, and approximately 65% of TBBPA was degraded. This work optimizes the synthesis strategy and mechanism of Fe@C and provides a methodological reference for the design of Fe-based catalysts.