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CHEMICAL ENGINEERING JOURNAL · 2025 · IF 13.2

Preparation of MoS2 and Fe3O4/Fe2O3 composites and their photo-Fenton degradation roxarsone efficacy study

Zhenzhong Hu,Hongwei Gao,Guoqing Yang,Jingxia Ning,Honghong Lyu,Sheng-qi Guo,Mengmeng Zhen,Jiawei Zhang,Boxiong Shen

Fenton technology is effective in removing high-risk roxarsone (ROX) from the environment. In this study, MoS 2 -modified magnetic iron oxides were successfully synthesized to serve as catalysts for the photo-Fenton system to efficiently degrade ROX. Under light illumination, these catalysts demonstrated strong arsenic adsorption characteristics and photocatalytic activity. The catalyst 6Mo-Fe achieved a 96.15% removal of 20 mg/L ROX and an 88.95% removal of total arsenic within 120 minutes. The study evaluated the effects of catalyst dosage, H 2 O 2 dosage, initial pH, and common anions on the degradation efficiency. The integration of MoS 2 significantly improved the forbidden band width, light absorption capacity, and electrochemical impedance of iron oxides, facilitating the separation and transfer of charge carriers. MoS 2 provided abundant Mo 4+ reduction sites for Fe 3+ , which, in conjunction with the photocatalytic reaction, promoted the cyclic conversion between Fe 3+ and Fe 2+ , thereby markedly increasing the reaction rate. This study presents an innovative approach using MoS 2 -modified iron oxides for the sustainable and eco-friendly degradation of organoarsenic compounds.

研究领域: 环境科学 · 材料科学
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JOURNAL OF MATERIALS SCIENCE · 2019 ·Vol. 54 ·期 11 ·8236-8246 · IF 3.442

Synergetic effect of Fe2O3 and BiVO4 as photocatalyst nanocomposites for improved photo-Fenton catalytic activity

Wen Yun,Zhao Yue,Guo Mingzhen,Xu Yan

Photo-Fenton reactions and the related functional nanomaterials have been widely studied for applications in wastewater treatment industry. Herein, visible-light-responsive Fe 2 O 3 nanoparticle-decorated BiVO 4 nanoplates were designed and successfully prepared through a one-pot hydrothermal route. The as-prepared Fe 2 O 3 /BiVO 4 nanocomposites exhibit excellent photo-Fenton catalytic activity toward the discoloration of methylene blue (MB) and Rhodamine B (RhB) dye molecules in the presence of H 2 O 2 . The experimental results indicate that nearly 100% of MB (100 mL, 10 mg L −1 ) and RhB (100 mL, 5 mg L −1 ) dye molecules are degraded in the presence of 1 g L −1 Fe 2 O 3 /BiVO 4 -1 (FB-1) photo-Fenton catalyst and 0.5 mL of H 2 O 2 within 20 min. The Fe 2 O 3 /BiVO 4 Fenton photocatalyst also demonstrates high reusability under visible light irradiation with λ ≥ 420 nm. The photoinduced electrons on the conduction band of BiVO 4 nanoplates can move toward the surface of Fe 2 O 3 /BiVO 4 to accelerate the reduction of Fe 3+ ; then, the as-formed Fe 2+ ions on the surface of the catalyst greatly enhance the decomposition of H 2 O 2 to form reactive · OH species for the use in photodegradation of MB and RhB dye molecules. The synergetic effect of Fe 2 O 3 and BiVO 4 reported in this work might provide more opportunity to fabricate other novel semiconductor-based Fenton nanocomposites for contamination treatments in wastewater.

CAS / MDL: 7803-55-6
研究领域: 材料科学 · 环境科学 · 化学工程
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Nanomaterials · 2022 ·Vol. 12 ·期 18 ·3089 · IF 5.719

WSe2/g-C3N4 for an In Situ Photocatalytic Fenton-like System in Phenol Degradation

Li Tan,Yiming Chen,Didi Li,Shaobin Wang,Zhimin Ao

An in situ photo-Fenton system can continuously generate H2O2by photocatalysis, activating H2O2in situ to form strong oxidizing ·OH radicals and degrading organic pollutants. A WSe2/g-C3N4composite catalyst with WSe2as a co-catalyst was successfully synthesized in this work and used for in situ photo-Fenton oxidation. The WSe2/g-C3N4composite with 7% loading of WSe2(CNW2) has H2O2production of 35.04 μmol/L, which is fourteen times higher than pure g-C3N4. The degradation efficiency of CNW2 for phenol reached 67%. By constructing an in situ Fenton-system, the phenol degradation rate could be further enhanced to 90%. WSe2can enhance the catalytic activity of CNW2 by increasing electron mobility and inhibiting the recombination of photogenerated electron–hole pairs. Moreover, the addition of Fe2+activates the generated H2O2, thus increasing the amount of strong oxidative ·OH radicals for the degradation of phenol. Overall, CNW2 is a promising novel material with a high H2O2yield and can directly degrade organic pollutants using an in situ photo-Fenton reaction.Keywords:WSe2/g-C3N4;visible light;in situ photo-Fenton;phenol degradation

研究领域: 环境科学 · 材料科学 · 催化
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JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY · 2019 · IF 3.261

Quantitative investigation into the enhancing utilization efficiency of H2O2 catalyzed by FeOCl under visible light

Binyang Zhang,Mengdie Chen,Dongya Li,Haiming Xu,Dongsheng Xia

FeOCl was prepared by a partial thermal decomposition method to effectively catalyze hydrogen peroxide under the visible light for the degradation of toxic organic wastewater. The combination of DRS and VB-XPS indicated that FeOCl is a narrow band gap catalyst with visible light absorption capacity (Eg =1.63 eV). The degradation rate constant of RhB in FeOCl/H 2 O 2 /Vis system is about 13.4 times that of FeOCl/H 2 O 2 system. Compared to other heterogeneous Photo-Fenton systems, the oxidant utilization efficiency in FeOCl/H 2 O 2 /Vis system is higher. In addition, FeOCl has stable Photo-Fenton activity in a wide pH range (3.0–9.0). The content of Fe(II) increased after 5 cycles reaction through the ESR and XPS characterization, which proves that the electron transfer of Fe(III)/Fe(II) was improved during the reaction. After quantitative analysis of the ·OH generated in the reaction, the formation rate of ·OH in FeOCl/H 2 O 2 /Vis system is increased about 30% compared with FeOCl/H 2 O 2 /dark system. These results indicate that visible light excites FeOCl to generate produces photogenerated electron-hole pairs, accelerating the cycle of Fe(III)/Fe(II), promoting the production rate of ·OH, and enhancing the catalytic efficiency of FeOCl.

研究领域: 环境科学 · 催化化学
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MOLECULES · 2023 ·Vol. 28 ·期 2 ·607 · IF 4.6

Molecular Oxygen Activation by Citric Acid Boosted Pyrite–Photo–Fenton Process for Degradation of PPCPs in Water

Juntao Guo,Yihui Zhang,Jinjun Li,Feng Wu,Liting Luo

Pyrite has been used in photo-Fenton reactions for the degradation of pollutants, but the application of photo-Fenton processes with extra H2O2in real water/wastewater treatment has still been limited by the economic cost of H2O2and artificial light sources. Herein, citric acid (CA) and simulated/natural sunlight are used to develop a pyrite-based photo-Fenton system (pyrite–CA–light) in situ generating H2O2through the enhanced activation of molecular oxygen. The degradation of pharmaceuticals and personal care products (PPCPs), especially acetaminophen (APAP) as the main target pollutant, in the pyrite–CA–light system was investigated. The effects of influencing factors such as various organic acids, APAP concentration, pH, pyrite dosage, CA concentration and co-existing anions (HCO3−, Cl−, NO3−, SO42−and H2PO4−) were examined. At a pyrite dosage of 0.1 g L−1, CA concentration of 0.6 mM and an initial pH of 6.0, the degradation efficiency of APAP (30 μM) was 99.1% within 30 min under the irradiation of xenon lamp (70 W, λ ≥ 350 nm). Almost the same high efficiency of APAP degradation (93.9%) in the system was achieved under natural sunlight irradiation (ca. 650 W m−2). The scavenging experiments revealed that the dominant active species for degrading APAP was hydroxyl radical (HO•). Moreover, a quantitative structural–activity relationship (QSAR) model for pseudo-first-order rate constants (kobs) was established with a high significance (R2= 0.932,p= 0.001) by using three descriptors: octanol–water partition coefficient (logKow), dissociation constant (pKa) and highest occupied molecular orbital (HOMO). This work provides an innovative strategy of the photo-Fenton process for the degradation of PPCPs using natural minerals and ordinary carboxylic acid under sunlight.Keywords:pyrite;citric acid;sunlight;photo-Fenton;PPCPs;QSAR

CAS / MDL: 12068-85-8 1309-36-0
研究领域: 环境科学 · 化学工程
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2018 · IF 11.698

Visible-light Ag/AgBr/ferrihydrite catalyst with enhanced heterogeneous photo-Fenton reactivity via electron transfer from Ag/AgBr to ferrihydrite

Yanping Zhu,Runliang Zhu,Lixia Yan,Haoyang Fu,Yunfei Xi,Huijun Zhou,Gangqiang Zhu,Jianxi Zhu,Hongping He

Herein, we have reported an effective strategy to solve the rate-limiting step in a heterogeneous Fenton reaction, i.e., the generation of Fe(II) from Fe(III), which also inevitably consumes a large amount of H 2 O 2 . For the first time, a novel heterogeneous photo-Fenton catalyst - Ag/AgBr/ferrihydrite (Ag/AgBr/Fh) was successfully developed by combing AgBr with ferrihydrite (Fh) and then in-situ generating Ag nanoparticles on the surface of AgBr/Fh. This strategy can introduce photo-generated electrons from semiconductor-based plasmonic photocatalysts to heterogeneous Fenton catalysts and significantly increase the efficiency to degrade contaminants. The presence of both AgBr and Ag nanoparticles was proved by a combination of structural characterization studies (i.e., XRD, SEM, TEM, and XPS). Under visible light irradiation, the generated Fe(II) on the samples and the degradation rate constants of bisphenol A (BPA) followed the same order: Ag/AgBr/Fh > AgBr/Fh > Fh, which could be attributed to the accelerated reduction of Fe(III) to Fe(II) by the photo-generated electrons from AgBr and Ag nanoparticles, and also profit from the strong electron trapping ability of Ag nanoparticles in separating the electron-hole pairs of AgBr. The Ag/AgBr/Fh system could produce more hydroxyl radicals (•OH), and its catalytic performance was less affected by decreasing H 2 O 2 concentration, which suggested a more efficient utilization of H 2 O 2 . The Ag/AgBr/Fh system exhibits relatively high photo-Fenton reactivity even at neutral pH. In addition, a much lower Fe 3+ dissolution indicates that a large portion of the contribution is from the direct heterogeneous Fenton reaction in this system.

CAS / MDL: 65-85-0 99-96-7
研究领域: 环境科学 · 催化 · 光化学 · 水处理
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ENVIRONMENTAL SCIENCE & TECHNOLOGY · 2020 · IF 7.864

Isomerization and Degradation of Levoglucosan via the Photo-Fenton Process: Insights from Aqueous-Phase Experiments and Atmospheric Particulate Matter

Chi Yang,Chunyan Zhang,Xiaosan Luo,Xiaoyan Liu,Fang Cao,Yan-lin Zhang

So far, studies on the conversion of stereochemistry under photo-Fenton conditions and their atmospheric implication are still rare. Here, we found that the biomass burning marker, the chiral compound levoglucosan (L), undergoes oxidative degradation under photo-Fenton conditions and can be isomerized into mannosan (M) and galactosan (G) simultaneously. Among the formic acid, acetic acid, and oxalic acid in the degradation products of levoglucosan, it was found that the yield of formation of formic acid in the photo-Fenton pathway can be as high as 86%. It is worth noting that both levoglucosan and its isomers are present in the atmosphere and their concentrations are strongly correlated. At the same time, the range of their concentration ratios, L/(G + M), measured in the photo-Fenton experiments in the laboratory was found to agree well with that measured in atmospheric PM2.5 samples. However, the sources of L, G, and M in the atmosphere are complex, and the photo-Fenton reaction may be an essential pathway for the distribution of L, G, and M in the atmosphere.

研究领域: 环境科学 · 大气化学
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2017 · IF 9.446

Mechanisms for the enhanced photo-Fenton activity of ferrihydrite modified with BiVO4 at neutral pH

Tianyuan Xu,Runliang Zhu,Gangqiang Zhu,Jianxi Zhu,Xiaoliang Liang,Yanping Zhu,Hongping He

Heterogeneous photo-Fenton catalysts generally show very weak photo-Fenton activity at near-neutral pH because of the relatively low rate of Fe 2+ regeneration. The aim of this work is to develop novel heterogeneous photo-Fenton catalysts, which can accelerate the regeneration of Fe 2+ and thus have superior photo-Fenton activity at near-neutral pH. In this study, ferrihydrite (Fh) was modified with BiVO 4 to synthesize BiVO 4 /Fh composites, and we expected that the photogenerated electrons from BiVO 4 would accelerate the regeneration of Fe 2+ on Fh. Mechanistic investigation of H 2 O 2 consumption showed that the introduction of BiVO 4 promoted the decomposition of H 2 O 2 into reactive oxygen species (ROS). In addition, the presence of BiVO 4 deterred O 2 − production and accelerated the formation of OH, according to the results of ROS formation, as shown with EPR spectroscopy and fluorescent probes tools. Furthermore, the Fe 2+ concentration on the surface of BiVO 4 /Fh was higher than that on Fh based on the results of XPS characterization and quantitative measurement with a 1,10-phenanthroline spectrophotometric method. These results demonstrated that the introduction of BiVO 4 can accelerate the reduction of Fe 3+ to Fe 2+ by transferring photogenerated electrons from BiVO 4 to Fe 3+ on the surface of Fh. Meanwhile, a higher decolorization efficiency of acid red 18 by BiVO 4 /Fh than by Fh and pure BiVO 4 verified that the introduction of BiVO 4 can significantly enhance the photo-Fenton catalytic activity of Fh even at near-neutral pH. Overall, our work has important implications for understanding the photo-Fenton mechanisms on semiconductor modified heterogeneous photo-Fenton catalysts and confirms that the introduction of a semiconductor can enhance the photo-Fenton catalytic activity of heterogeneous photo-Fenton catalysts in acidic and neutral pH.

研究领域: 环境科学 · 材料科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Multifunctional ferrocene-based photo-Fenton membrane: An efficient integration of rejection and catalytic process

Yan Wang,Tao Yang,Jing Chen,Shaobin Wen,Die Li,Bingyu Wang,Qiang Zhang

A novel ferrocene-based nanofiltration membrane is prepared to combine filtration and photo-Fenton reaction for water treatment. Membranes containing ferrocene groups are successfully fabricated via an integration of layer-by-layer interfacial polymerization and ion exchange reaction. Rejection performance towards bisphenol S (BPS) increases with the growth of the interfacial polymerization layer, and the optimal membrane shows the highest rejection rate of 98.1%. For the optimal photo-Fenton system with H 2 O 2 , UV and ferrocene-based membrane (PS/HTCC-3/FcSO 3 ), the degradation rate of k is 0.092 min −1 , which is 1.8 times higher than that of the system with only H 2 O 2 and UV. Meanwhile, the salinity of BPS in the optimal system is 2 times higher than that of the system with H 2 O 2 and UV. After the heterogeneous photo-Fenton process, PS/HTCC-3/FcSO 3 can reject 65.6% of the BPS degradation by-products based on the variation of total organic carbon (TOC). In addition, quenching experiments prove that ·OH is the primary active radical, and the yield of ·OH in the optimal system is the highest compared with the system with H 2 O 2 and UV. The outstanding performance of ferrocene-based membrane demonstrates its potential for micropollutants treatment.

研究领域: 环境科学 · 材料科学
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ENVIRONMENTAL TECHNOLOGY · 2022 · IF 3.475

Magnetic recyclable heterogeneous catalyst Fe3O4/g-C3N4 for tetracycline hydrochloride degradation via photo-Fenton process under visible light

Kang-Ping Cui,Ting-Ting Yang,Yi-Han Chen,Rohan Weerasooriya,Guang-Hong Li,Kai Zhou,Xing Chen

Antibiotic pollution of water resources is a global problem, and the development of new treatments for destroying antibiotics in water is a priority research. We successfully manufactured recyclable magnetic Fe3O4/g-C3N4 through the electrostatic self-assembly method. Selecting tetracycline (TC) as the target pollutant, using Fe3O4/g-C3N4 and H2O2 developed a heterogeneous optical Fenton system to remove TC under visible light. Fe3O4/g-C3N4 was systematically characterized by SEM, TEM, XRD, FTIR, XPS, DRS, and electrochemical methods. The removal efficiency of 7% Fe3O4/g-C3N4 at pH = 3, H2O2 = 5 mM, and catalyst dosage of 1.0 g/L can reach 99.8%. After magnetic separation, the Fe3O4/g-C3N4 photocatalyst can be recycled five times with minimal efficiency loss. The excellent degradation performance of the prepared catalyst may be attributed to the proper coupling interface between Fe3O4 and g-C3N4 which promotes the separation and transfer of photogenerated electrons. Photogenerated electrons can also accelerate the conversion of Fe3+ to Fe2+, thereby producing more ˙OH. The new Fe3O4/g-C3N4 can be used as a raw material for advanced oxidation of water contaminated by refractory antibiotics.

CAS / MDL: 7722-84-1
研究领域: 环境科学 · 材料科学
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MATERIALS SCIENCE IN SEMICONDUCTOR PROCESSING · 2023 · IF 4.1

Step scheme Fe2O3/S doped g-C3N4 heterojunction photocatalysts for photo-fenton norfloxacin and tetracycline degradation

Zhengqiaoruo Zhu,Nan Zhou,Yakun Li,Xiaoli Zhang,Linlin Zhang

Due to their unique persistence in the environmental cycle, pharmaceuticals and personal care products (PPCPs) are increasing concern in the scientific community. Therefore, the development of new energy-saving and environmentally compatible technologies to remove these pollutants is highly requested. In this work, an S-scheme photocatalytic nanoreactor was synthesized by Fe 2 O 3 nanoparticles to S doped carbon nitride nanosheets . The unique structure of S-scheme Fe 2 O 3 /SCN heterojunction enhances its optical absorption and has a large number of active sites and photogenerated carrier separation. Consequently, the Fe 2 O 3 /SCN demonstrated excellent photo-Fenton degradation activities under visible light irradiation. Remarkedly, 5 mg/L of norfloxacin is completely photo-Fenton degraded following 25 min under visible light irradiation. It further shows that ·OH and ·O 2− play an important role in the photo-Fenton catalytic reaction , leading to the decomposition of norfloxacin. The degradation of tetracycline further demonstrates that this photo-Fenton catalytic system can be effectively used to remediate pharmaceutical and personal care product contamination in environmental waterways.

研究领域: 环境科学 · 材料科学
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Journal of Environmental Chemical Engineering · 2020 · IF 4.3

Synthesis of novel CdSe QDs/BiFeO3 composite catalysts and its application for the photo-Fenton catalytic degradation of phenol

Tao Huang,Jundong Zhu,Shengzhuo Ge,Tianyu Guo,Chongwen Jiang,Le Xie

Heterogeneous photo-Fenton reaction using BiFeO 3 as catalyst was considered as an efficient environmental remediation technique. However, its low catalytic performance limited its application. In this work, CdSe QDs with high electron mobility, small size effect and rich surface properties were loaded on BFO surface by stirring impregnation method. The photo-Fenton catalytic performance of catalysts under visible light irradiation was evaluated by the degradation of phenol. The results showed that the BFO with CdSe QDs uniformly distributed on the surface shows much better photo-Fenton degradation of phenol performance than that of pure BFO. Moreover, when the load content of CdSe QDs comes to 0.5 wt%, the degradation efficiency of phenol increased from 41.5% to 98.5% within 60 min. The results of photochemical experiments confirmed that composite catalyst had a good ability to separate photo-induced carriers and the experiments of free radicals trapping showed that the holes and OH radicals were important active substances. Based on the above research, the possible mechanism of photo-Fenton reaction of catalyst was expounded. Excellent photo-Fenton catalytic performance and superior stability make this material showing a good application prospect for the degradation of organic pollutants in wastewater.

研究领域: 环境科学 · 材料科学
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