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学者姓名：许俊鸽
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Abstract ：
Pyrite-driven autotrophic denitrification (PAD) has been recognized as a promising treatment technology for nitrate removal. Although the occurrence of PAD has been found in recent years, there is a knowledge gap about effects of crystal plane of pyrite on the performance and mechanism of PAD system. Here, this study investigated the effects of crystal planes ({100}, {111} and {210}) of single-crystal pyrite on denitrification performance, electron transfer, and microbial mechanism in PAD system. The removal efficiency of nitrate in B-{210} reached 100%, which was 1.67-fold and 2.86-fold higher than that of B-{100} and B-{111}, respectively. X-ray photoelectron spectroscopy and electrochemical results indicated that Fe-S bonds of pyrite with {210} crystal plane were more susceptible to breakage by Fe3+ oxidation assault, and leaching microbially available Fe2+ and sulfur intermediates to drive autotrophic denitrification. Metagenomic results suggested that community of functional pyrite-driven denitrifiers varied in response to crystal plane, and abundances of N-S transformation and EETrelated microbes and genes in B-{210} notably up-regulated compared to B-{100} and B-{111}. In addition, this work proposed a dual-mode for electron transfer pathway during pyrite oxidation and nitrogen transformation in PAD system. In B-{210}, Fe(II)- and sulfur-driven denitrifiers obtained electron after pyrite oxidation-dissolution, and the enrichment of pyrite-oxidizing bacteria in B-{210} could enhance the electron transfer from pyrite through electron shuttles. This work highlighted that stronger surface reactivity and electron shuttle effect in B-{210} enhanced electron transfer, leading to favorable PAD performance in B-{210}. Overall, this study provides novel insights into the structure-activity relationship between the crystal plane structure of pyrite and denitrification activity in PAD system.
Keyword ：
Autotrophic denitrification Autotrophic denitrification Crystal plane Crystal plane Electron transfer Electron transfer Metagenome analysis Metagenome analysis Pyrite Pyrite
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| GB/T 7714 | Wang, Yingmu , Chen, Shi , Chen, Yuanjing et al. Structure-activity relationship between crystal plane and pyrite-driven autotrophic denitrification efficacy: Electron transfer and metagenome-based microbial mechanism [J]. | WATER RESEARCH , 2025 , 268 . |
| MLA | Wang, Yingmu et al. "Structure-activity relationship between crystal plane and pyrite-driven autotrophic denitrification efficacy: Electron transfer and metagenome-based microbial mechanism" . | WATER RESEARCH 268 (2025) . |
| APA | Wang, Yingmu , Chen, Shi , Chen, Yuanjing , Xu, Junge , Zhou, Jian , He, Qiang et al. Structure-activity relationship between crystal plane and pyrite-driven autotrophic denitrification efficacy: Electron transfer and metagenome-based microbial mechanism . | WATER RESEARCH , 2025 , 268 . |
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The widespread use of plastics has led to significant environmental pollution, but microplastics (MPs) have had a noteworthy impact in this regard and serve as carriers for various toxic pharmaceuticals. Therefore, there is a need to design a water treatment process capable of simultaneously removing MPs and pharmaceuticals. In this study, a novel photocatalytic membrane, composed of a binary C3N4/Bi12O17Cl2 (CN/BOC) heterojunction immobilized on a polyacrylonitrile (PAN) membrane via electrospinning, is developed to address this issue. Comprehensive characterizations confirm the formation of a heterojunction structure that optimizes charge separation and prolongs electron lifetime. The CN/BOC/PAN photocatalytic membrane demonstrates 100 % removal efficiency for 19 out of 20 types of mixed pharmaceuticals within 180 min. Additionally, the membrane converts polylactic acid (PLA) into value-added organic acids, thereby offering a sustainable approach to plastic upcycling. The highest occupied molecular orbital (HOMO), lowest unoccupied molecular orbital (LUMO), and Fukui index are employed to identify the active sites for carbamazepine (CBZ) and PLA degradation. This study provides new insights into the photocatalytic removal of pharmaceuticals and MPs, highlighting the potential for remediating water-borne contaminants.
Keyword ：
Electrospinning Electrospinning Heterojunction structure Heterojunction structure Microplastics conversion Microplastics conversion Pharmaceuticals removal Pharmaceuticals removal Photocatalytic membrane Photocatalytic membrane
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| GB/T 7714 | Wu, Feiyan , Yu, Haixiang , Chang, Fei et al. Fabrication of a C3N4/Bi12O17Cl2 heterojunction photocatalytic membrane applied for pharmaceutical and microplastic treatment [J]. | SEPARATION AND PURIFICATION TECHNOLOGY , 2025 , 364 . |
| MLA | Wu, Feiyan et al. "Fabrication of a C3N4/Bi12O17Cl2 heterojunction photocatalytic membrane applied for pharmaceutical and microplastic treatment" . | SEPARATION AND PURIFICATION TECHNOLOGY 364 (2025) . |
| APA | Wu, Feiyan , Yu, Haixiang , Chang, Fei , Tang, Kai , Xu, Junge , Dou, Yibo et al. Fabrication of a C3N4/Bi12O17Cl2 heterojunction photocatalytic membrane applied for pharmaceutical and microplastic treatment . | SEPARATION AND PURIFICATION TECHNOLOGY , 2025 , 364 . |
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Volatile fatty acids (VFAs) extraction from waste activated sludge (WAS) during anaerobic digestion has gained prominence for its economic advantages over biogas production. Critical strategies include enhancing WAS solubilization and selectively suppressing methanogens to promote VFA accumulation. The efficacy of peracetic acid (PAA) in dissolving WAS has been demonstrated. However, its selective inhibitory effects remain largely unexplored. This work illustrated that PAA-enhanced anaerobic digestion (PAA-AD) utilising a modest dose of PAA (9 mg PAA/g TSS) within the range of 0-18 mg PAA/g TSS resulted in a 330 % increase in VFA accumulation, with VFA concentration and acetate proportion attaining 3235.5 +/- 60.7 mg COD/L and 74.6 %, respectively. The generation of CH3C(O)OO center dot, center dot OH, center dot O2-, and 1O2 impaired the integrity of cell membranes and induced lipid peroxidation. 9 mg PAA/g TSS treatment significantly reduced microbial cell attraction in WAS, overcoming WAS dispersion's energy barrier via the extended XDLVO theory. This study showed that its biological inactivation effect on VFA consumers is much stronger than VFA producers. 16S rDNA and metagenomic analyses demonstrated that PAA treatment facilitated the selective enrichment of hydrolytic acidogenic bacteria (51.2 %), including Paraclostridium, Macelliibacteroides and Clostridium_sensu_stricto_13, while significantly upregulating genes linked to VFA synthesis and downregulating genes associated with methane production. The modulation of Quorum Sensing (QS) and Two-Component Systems (TCS) gene clusters synergistically improved the chemotaxis of aerobic digesting bacteria, facilitating their adaptation to PAA stress. This study introduces a sustainable and economical approach for sludge treatment and resource recovery, designed to meet the carbon neutrality objectives of wastewater treatment plants.
Keyword ：
Anaerobic digestion Anaerobic digestion Metagenome analysis Metagenome analysis Peracetic acid Peracetic acid Volatile fatty acids Volatile fatty acids Waste activated sludge Waste activated sludge
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| GB/T 7714 | Wang, Yingmu , Yang, Jun , Huang, Yanjie et al. Unveiling the oxidative stress and adaptation mechanisms of hydrolytic-acidogenic bacteria in response to peroxyacetic acid during sludge anaerobic fermentation to enhance fatty acid production [J]. | CHEMICAL ENGINEERING JOURNAL , 2025 , 518 . |
| MLA | Wang, Yingmu et al. "Unveiling the oxidative stress and adaptation mechanisms of hydrolytic-acidogenic bacteria in response to peroxyacetic acid during sludge anaerobic fermentation to enhance fatty acid production" . | CHEMICAL ENGINEERING JOURNAL 518 (2025) . |
| APA | Wang, Yingmu , Yang, Jun , Huang, Yanjie , Xie, Shikang , Zhou, Jian , He, Qiang et al. Unveiling the oxidative stress and adaptation mechanisms of hydrolytic-acidogenic bacteria in response to peroxyacetic acid during sludge anaerobic fermentation to enhance fatty acid production . | CHEMICAL ENGINEERING JOURNAL , 2025 , 518 . |
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Pyrite autotrophic denitrification (PAD) is a cost-effective and promising method for nitrogen removal from low C/N wastewater. Recent work has primarily focused on experimental schemes to investigate PAD performance, while overlooking the impact of pyrite's origin on its mineral properties and chemical reactivity. Thus, the optimal strategy for selecting pyrite based on the structure-activity relationship between its mineral characteristics and PAD performance remains unclear. In this work, a series of PAD systems were established using natural pyrite from different origins as electron donors. The results showed that the pyrite from Yunfu (B-YPy38 and BYPy48) exhibited the optimal performance, with nitrate (NO3--N) removal rates of 88.56 +/- 0.60% and 72.26 +/- 3.10% after long-term operation, respectively. The distinct nutrient removal efficiency could be attributed to variations in the mineral crystallization habits and electrochemical properties of pyrites from different origins. XPS analysis revealed that the pyrite from Yunfu contained more Fe(III)-S bonds associated with the breakage of pyrite crystal structure, thereby accelerating the "oxidation-dissolution" process of pyrite to produce Fe(II) and S0, thus providing more electron donors for autotrophic denitrifying bacteria (e.g., Rhodanobacter and Thermomonas). Electrochemical analysis further indicated that the stronger Fe(II)/Fe(III) cycling capacity in pyrite from Yunfu might enhance electron shuttling between pyrite and NO3--N. Microbial community analysis revealed that the higher chemical reactivity and electron transfer in YPy38 and YPy48 promote the enrichment of autotrophic denitrifying bacteria. These findings shed new light on understanding microbial processes in PAD systems, offering a theoretical basis for the optimal selection of pyrite to enhance PAD efficiency for further application.
Keyword ：
Autotrophic denitrification Autotrophic denitrification Electrochemical properties Electrochemical properties Microbial community Microbial community Mineral properties Mineral properties Nutrients removal Nutrients removal Pyrite's origin Pyrite's origin
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| GB/T 7714 | Wang, Yingmu , Su, Mubai , He, Lei et al. Insights into the impact of pyrite mineral properties on nutrient removal and microbial communities: Influence of pyrite origins [J]. | CHEMICAL ENGINEERING JOURNAL , 2025 , 519 . |
| MLA | Wang, Yingmu et al. "Insights into the impact of pyrite mineral properties on nutrient removal and microbial communities: Influence of pyrite origins" . | CHEMICAL ENGINEERING JOURNAL 519 (2025) . |
| APA | Wang, Yingmu , Su, Mubai , He, Lei , Chen, Shi , Peng, Cuiyan , Zhou, Jian et al. Insights into the impact of pyrite mineral properties on nutrient removal and microbial communities: Influence of pyrite origins . | CHEMICAL ENGINEERING JOURNAL , 2025 , 519 . |
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Membrane distillation technology, utilized for treating hypersaline wastewater from seawater desalination, often encounters challenges related to inorganic scaling, adversely affecting membrane performance. Herein, we introduce a innovative approach employing a sacrificial layer on the surface of Thin Film Composite (TFC) membranes to concurrently enhance inorganic scaling resistance and facilitate membrane reusability. The sacrificial layer (Fe3+-TA) 3 +-TA) consisted of tannic acid (TA) complexed with iron ions (Fe3+) 3 + ) and could be removed and regenerated in situ. The results demonstrated that the Fe3+-TA 3 +-TA layer significantly improved the membrane's surface smoothness and densification, maintaining superior anti-scaling performance. The modified membrane exhibited remarkable durability, sustaining six reuse cycles with a flux recovery exceeding 97 % in gypsum scaling tests. Furthermore, the formation of new complexes during gypsum scaling tests confirmed the membrane's augmented scaling retardation capabilities. Thus, integrating of a sacrificial layer into TFC membranes presents a promising strategy for advancing membrane distillation processes in hypersaline wastewater treatment.
Keyword ：
Anti-scaling Anti-scaling Inorganic scaling Inorganic scaling Membrane distillation Membrane distillation Reuse Reuse Sacrificial protective layer Sacrificial protective layer
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| GB/T 7714 | Yan, Zhongsen , Lin, Sufen , Chang, Haiqing et al. Functional of thin-film composite Janus membrane with sacrificial layer for inorganic scaling control in membrane distillation [J]. | JOURNAL OF MEMBRANE SCIENCE , 2024 , 710 . |
| MLA | Yan, Zhongsen et al. "Functional of thin-film composite Janus membrane with sacrificial layer for inorganic scaling control in membrane distillation" . | JOURNAL OF MEMBRANE SCIENCE 710 (2024) . |
| APA | Yan, Zhongsen , Lin, Sufen , Chang, Haiqing , Xu, Junge , Dai, Wenxin , Qu, Dan et al. Functional of thin-film composite Janus membrane with sacrificial layer for inorganic scaling control in membrane distillation . | JOURNAL OF MEMBRANE SCIENCE , 2024 , 710 . |
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Iron-based catalysts have been widely used to treat refractory organic pollutants in wastewater. In this paper, magnetic Co-gamma-Fe(2)O(3 )was synthesized by a facile tartaric acid-assisted hydrothermal method, and Co-gamma-Fe2O3/MoS2 nanocomposite catalyst was obtained via in situ growth of MoS2 nanosheets on Co-gamma-Fe2O3 nanoparticles. The nanocomposite catalysts were used to decompose bisphenol A (BPA) by activating peroxymonosulfate (PMS). It was shown that only 0.15 g/L catalyst and 0.5 mmol/L PMS degraded 10 mg/L of BPA (99.3% within 10 min) in the pH range of 3-9. PMS was activated due to redox cycling among the pairs Co(III)/Co(II), Fe(III)/Fe(II), and Mo(VI)/Mo(IV). Quenching experiments and electron paramagnetic resonance spectroscopy demonstrated that both radical and non-radical pathways were involved in BPA degradation, in which active radical sulfate radical and non-radical singlet oxygen were the main reactive oxygen species. Ten intermediates were identified by liquid chromatography-coupled mass spectrometry, and three possible BPA degradation pathways were proposed. The toxicity of several degradation intermediates was lower, and Co-gamma-Fe2O3/MoS2 exhibited excellent reusability and could be magnetically recovered.
Keyword ：
Bisphenol A Bisphenol A Degradation pathways Degradation pathways Hydrothermal method Hydrothermal method Magnetic Co-gamma-Fe2O3/MoS2 Magnetic Co-gamma-Fe2O3/MoS2 Toxicity analysis Toxicity analysis
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| GB/T 7714 | Xu, Junge , Wang, Dong , Hu, Die et al. Magnetic Co-doped 1D/2D structured γ-Fe2O3/MoS2 effectively activated peroxymonosulfate for efficient abatement of bisphenol A via both radical and non-radical pathways [J]. | FRONTIERS OF ENVIRONMENTAL SCIENCE & ENGINEERING , 2024 , 18 (3) . |
| MLA | Xu, Junge et al. "Magnetic Co-doped 1D/2D structured γ-Fe2O3/MoS2 effectively activated peroxymonosulfate for efficient abatement of bisphenol A via both radical and non-radical pathways" . | FRONTIERS OF ENVIRONMENTAL SCIENCE & ENGINEERING 18 . 3 (2024) . |
| APA | Xu, Junge , Wang, Dong , Hu, Die , Zhang, Ziwei , Chen, Junhong , Wang, Yingmu et al. Magnetic Co-doped 1D/2D structured γ-Fe2O3/MoS2 effectively activated peroxymonosulfate for efficient abatement of bisphenol A via both radical and non-radical pathways . | FRONTIERS OF ENVIRONMENTAL SCIENCE & ENGINEERING , 2024 , 18 (3) . |
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Membrane distillation (MD), boasting high interception efficiency and low operational pressures, emerges as an innovative membrane technology. However, the occurrence of membrane fouling due to interaction between natural organic matter (NOM) and inorganic ions during the MD process curtails water purification efficiency, thereby constraining its potential applications. To address this quandary, this study integrates sulfate radicalbased advanced oxidation processes (SR-AOPs) into MD technology to bolster membrane fouling control. A straightforward hydrothermal method coupled with vacuum filtration was employed to synthesize a Co3O4/ Nitrogen-modified carbon quantum dots (NCDs)/PVDF (CN-PVDF) membrane for the first time, which was utilized in the MD treatment of simulated humic acid (HA) wastewater. Under visible light irradiation (1.9 kW/ m2), CN-PVDF membrane activation of peroxymonosulfate (PMS) effectively altered the chemical attributes of the MD feed solution and reduced organic matter concentration. Moreover, it dismantled the carboxyl sites on HA that interact with Ca2+, consequently attenuating the formation of organic-inorganic complex pollutants. The XDLVO analysis showcased that photo-Fenton oxidation led to a diminishment in pollutant hydrophobicity, correlating with a 17.59 kT reduction in pollutant-membrane adsorption and a 7.47 kT amplification in adhesion barriers. This strategy transformed the initial two-stage fouling mode into a singular one, which significantly decreased the flux decline and the fouling layer thickness. Furthermore, the CN-PVDF membrane demonstrated self-cleaning capabilities via photo-Fenton. This study advances an innovative approach to bolster the fouling resistance of MD membranes and provides substantial theoretical support for the integration of SR-AOPs and MD technologies.
Keyword ：
control control Membrane distillation Membrane distillation Membrane fouling Membrane fouling Self-cleaning Self-cleaning
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| GB/T 7714 | Lu, Zhenyu , Yan, Zhongsen , Chang, Haiqing et al. New insights into antifouling property and interfacial mechanism in photo-Fenton membrane distillation [J]. | CHEMICAL ENGINEERING JOURNAL , 2024 , 492 . |
| MLA | Lu, Zhenyu et al. "New insights into antifouling property and interfacial mechanism in photo-Fenton membrane distillation" . | CHEMICAL ENGINEERING JOURNAL 492 (2024) . |
| APA | Lu, Zhenyu , Yan, Zhongsen , Chang, Haiqing , Wang, Qiankun , Liu, Fujian , Ni, Qichang et al. New insights into antifouling property and interfacial mechanism in photo-Fenton membrane distillation . | CHEMICAL ENGINEERING JOURNAL , 2024 , 492 . |
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Iron-based catalysts have been widely used to treat refractory organic pollutants in wastewater.In this paper,magnetic Co-γ-Fe2O3 was synthesized by a facile tartaric acid-assisted hydrothermal method,and Co-γ-Fe2O3/MoS2 nanocomposite catalyst was obtained via in situ growth of MoS2 nanosheets on Co-γ-Fe2O3 nanoparticles.The nanocomposite catalysts were used to decompose bisphenol A(BPA)by activating peroxymonosulfate(PMS).It was shown that only 0.15 g/L catalyst and 0.5 mmol/L PMS degraded 10 mg/L of BPA(99.3％within 10 min)in the pH range of 3-9.PMS was activated due to redox cycling among the pairs Co(Ⅲ)/Co(Ⅱ),Fe(Ⅲ)/Fe(Ⅱ),and Mo(Ⅵ)/Mo(Ⅳ).Quenching experiments and electron paramagnetic resonance spectroscopy demonstrated that both radical and non-radical pathways were involved in BPA degradation,in which active radical sulfate radical and non-radical singlet oxygen were the main reactive oxygen species.Ten intermediates were identified by liquid chromatography-coupled mass spectrometry,and three possible BPA degradation pathways were proposed.The toxicity of several degradation intermediates was lower,and Co-γ-Fe2O3/MoS2 exhibited excellent reusability and could be magnetically recovered.
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| GB/T 7714 | Junge Xu , Dong Wang , Die Hu et al. Magnetic Co-doped 1D/2D structured γ-Fe2O3/MoS2 effectively activated peroxymonosulfate for efficient abatement of bisphenol A via both radical and non-radical pathways [J]. | 环境科学与工程前沿 , 2024 , 18 (3) : 143-159 . |
| MLA | Junge Xu et al. "Magnetic Co-doped 1D/2D structured γ-Fe2O3/MoS2 effectively activated peroxymonosulfate for efficient abatement of bisphenol A via both radical and non-radical pathways" . | 环境科学与工程前沿 18 . 3 (2024) : 143-159 . |
| APA | Junge Xu , Dong Wang , Die Hu , Ziwei Zhang , Junhong Chen , Yingmu Wang et al. Magnetic Co-doped 1D/2D structured γ-Fe2O3/MoS2 effectively activated peroxymonosulfate for efficient abatement of bisphenol A via both radical and non-radical pathways . | 环境科学与工程前沿 , 2024 , 18 (3) , 143-159 . |
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Pollution from extensive sulfonamide antibiotic use is a critical research focus, particularly in the remediation of these antibiotics using composite materials. This study employed a CuFe2O4/ZIF-8 composite to activate sodium percarbonate (SPC) for the photo-Fenton-like degradation of the sulfonamide antibiotic sulfamethoxazole (SMX). The optimal conditions for SMX degradation were determined using the CuFe2O4/ZIF-8/SPC/Vis system: a ZIF-8 composite ratio of 40 %, catalyst dosage of 0.15 g/L, SPC concentration of 0.8 mM, and initial pH of 3.0, achieving complete SMX removal within 30 min. After five cycle tests, the leaching rates of copper and iron ions were 0.179 mg/L and 0.376 mg/L, respectively, significantly lower compared to the use of CuFe2O4 alone as the catalyst (Cu: 0.46 mg/L, Fe: 1.43 mg/L). The radicals present in the system were identified, with their contribution rates ranked from highest to lowest as follows: OH > h(+)> O-2(-) > CO3(-) > O-1(2). Further mechanistic investigations revealed that the heterogeneous structures in CuFe2O4/ZIF-8 enhanced the efficiency of the photo-Fenton-like reaction by facilitating electron transfer. This study introduced an innovative approach for antibiotic treatment using the CuFe2O4/ZIF-8 composite under visible light irradiation and broadened the technical framework of SPC-based advanced oxidation processes (AOPs) for treating wastewater.
Keyword ：
CuFe2O4/ZIF-8 CuFe2O4/ZIF-8 Heterogeneous photo-Fenton-like Heterogeneous photo-Fenton-like Magnetic recovery Magnetic recovery Sodium percarbonate Sodium percarbonate Sulfonamide antibiotics Sulfonamide antibiotics
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| GB/T 7714 | Xu, Junge , Yu, Weihao , Zhang, Ziwei et al. Rhombic dodecahedral ZIF-8-supported CuFe2O4 triggers sodium percarbonate activation for enhanced sulfonamide antibiotics degradation: Synergistic roles of heterostructure and photocatalytic mechanisms [J]. | CHEMICAL ENGINEERING JOURNAL , 2024 , 501 . |
| MLA | Xu, Junge et al. "Rhombic dodecahedral ZIF-8-supported CuFe2O4 triggers sodium percarbonate activation for enhanced sulfonamide antibiotics degradation: Synergistic roles of heterostructure and photocatalytic mechanisms" . | CHEMICAL ENGINEERING JOURNAL 501 (2024) . |
| APA | Xu, Junge , Yu, Weihao , Zhang, Ziwei , Deng, Fubin , Wang, Shengkong , Zou, Rusen et al. Rhombic dodecahedral ZIF-8-supported CuFe2O4 triggers sodium percarbonate activation for enhanced sulfonamide antibiotics degradation: Synergistic roles of heterostructure and photocatalytic mechanisms . | CHEMICAL ENGINEERING JOURNAL , 2024 , 501 . |
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In this work, CoMn2O4 spinel catalyst was used for the first time to activate peroxyacetic acid (PAA) for the degradation of fluoroquinolone antibiotic levofloxacin (LVF). The results showed that the degradation efficiency of CoMn2O4/PAA system reached 93% within 15 min at initial LVF concentration of 20 mg/L. In addition, the bimetallic oxide CoMn2O4 with spinel structure showed significantly higher activation performance than the single metal oxide (Co3O4 and MnO2). The excellent PAA activation performance by CoMn2O4 was attributed to the redox cycles between Co3+/ Co2+, Mn3+/ Mn2+, and Mn4+/ Mn3+, as well as the synergistic interaction between Co and Mn species. Radical quenching and electron paramagnetic resonance (EPR) spectra results indicated that acetylperoxyl radical (CH3C(O)OO center dot) was the dominant radical species, and this work highlighted that O-1(2) played an important role in non-radical process in PAA-based AOPs for the first time. The production of O-1(2) may be attributed to the interaction between reactive oxygen (O*) and PAA. In addition, the CoMn2O4/PAA system has been proved to have great stability and reusability, and exhibit selective degradation of organic pollutants which contained electron-rich groups. Overall, this work presents perspective for the application of antibiotic remediation by CoMn2O4/PAA process.
Keyword ：
Advanced oxidation Advanced oxidation CoMn2O4 catalyst CoMn2O4 catalyst Degradation pathway Degradation pathway Peroxyacetic acid Peroxyacetic acid Selective degradation Selective degradation
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| GB/T 7714 | Fan, Gongduan , Yao, Lei , Wang, Yingmu et al. The dual pathway mechanisms of peroxyacetic acid activation by CoMn2O4 spinel for efficient levofloxacin degradation [J]. | JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING , 2023 , 11 (3) . |
| MLA | Fan, Gongduan et al. "The dual pathway mechanisms of peroxyacetic acid activation by CoMn2O4 spinel for efficient levofloxacin degradation" . | JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING 11 . 3 (2023) . |
| APA | Fan, Gongduan , Yao, Lei , Wang, Yingmu , Peng, Xiaoxu , Xu, Junge , Pang, Shenghua et al. The dual pathway mechanisms of peroxyacetic acid activation by CoMn2O4 spinel for efficient levofloxacin degradation . | JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING , 2023 , 11 (3) . |
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