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学者姓名:魏佳
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Abstract :
In this study, a calcination and boron-doping strategy was developed to construct a metal defect-rich B@Co1-xS catalyst for Fenton-like reaction. Density functional theory (DFT) calculation and mechanistic investigation confirmed that the enhanced Co vacancies could increase the adsorption of the terminal oxygen in the peroxymonosulfate (PMS) molecules to the surrounding Co atoms, resulting in the activation mechanism by highvalent cobalt-oxygen species (Co(IV)=O), boosting the reaction rate constant by 7.14 times. The B@Co1-xS/ PMS system possessed excellent interference resistance and renewability for efficient degradation of a wide range of contaminants. Moreover, a continuous flow reactor loaded with B@Co1-xS was developed, which could operate continuously and stably with ciprofloxacin (CIP) removal efficiency above 97 %, proving that the system was promising for applications. Taken all together, this study delved into how to rationally develop cation-deficient transition metal catalysts in Fenton-like systems at the molecular level, which was of critical meaning for wastewater treatment.
Keyword :
Peroxymonosulfate Peroxymonosulfate Multi-pathway degradation Multi-pathway degradation B doping B doping Cobalt sulfide Cobalt sulfide Cation vacancy Cation vacancy
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GB/T 7714 | Huo, Jiangkai , Wei, Jia , Li, Jiamei et al. Boron amplifies the cation vacancy effect to enhance multi-pathway degradation of organic pollutants [J]. | APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY , 2025 , 371 . |
MLA | Huo, Jiangkai et al. "Boron amplifies the cation vacancy effect to enhance multi-pathway degradation of organic pollutants" . | APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY 371 (2025) . |
APA | Huo, Jiangkai , Wei, Jia , Li, Jiamei , Jiang, Zijian , Ji, Wei , Wang, Linhao et al. Boron amplifies the cation vacancy effect to enhance multi-pathway degradation of organic pollutants . | APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY , 2025 , 371 . |
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Abstract :
A novel bimetallic heterojunction catalyst (Co2Mo3O8/Co9S8) with hydrangea-like structure was prepared by a straightforward one-pot hydrothermal and pyrolysis method, which was then applied for the efficient activation of peroxymonosulfate (PMS) in wastewater purification. Density functional theory (DFT) simulations revealed that the formation of the Co2Mo3O8/Co9S8 heterojunction increased the adsorption energy of PMS and elongated the O-O bond within PMS. Moreover, an internal electric field generated within the heterojunction further activated PMS through electron-deficient centers, establishing a degradation mechanism primarily dominated by non-radical pathways. Meanwhile, the exist Co(II) and Mo(IV) involved as active sites for enhanced catalytic performance through the redox cycling of metal valence states. In the optimized Co2Mo3O8/Co9S8-PMS system, the target pollutant doxycycline (DOX) was rapidly and efficiently degraded, with a relatively low activation energy (3.93 kJ & sdot;mol- 1). Furthermore, the system demonstrated strong adaptability to interference from inorganic anions, humic acid, and pH variations, while effectively removing various pollutants. It consistently maintained a relatively high DOX removal efficiency in cyclic experiments and continuous flow reaction experiments. The present study provided new insights for improving the rational design of bimetallic heterojunction catalysts, and contributed to a more effective and sustainable solution for environmental remediation.
Keyword :
Singlet oxygen Singlet oxygen Peroxymonosulfate Peroxymonosulfate Antibiotic Antibiotic Bimetal Bimetal Heterojunction Heterojunction
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GB/T 7714 | Li, Jiamei , Wei, Jia , Sun, Jihong et al. Building the bimetallic site of Co2Mo3O8/Co9S8 heterojunction via interface electronic reconfiguration to enhance peroxymonosulfate activation for singlet oxygen formation [J]. | CHEMICAL ENGINEERING JOURNAL , 2025 , 505 . |
MLA | Li, Jiamei et al. "Building the bimetallic site of Co2Mo3O8/Co9S8 heterojunction via interface electronic reconfiguration to enhance peroxymonosulfate activation for singlet oxygen formation" . | CHEMICAL ENGINEERING JOURNAL 505 (2025) . |
APA | Li, Jiamei , Wei, Jia , Sun, Jihong , Huo, Jiangkai , Li, Yanan , Cui, Nan et al. Building the bimetallic site of Co2Mo3O8/Co9S8 heterojunction via interface electronic reconfiguration to enhance peroxymonosulfate activation for singlet oxygen formation . | CHEMICAL ENGINEERING JOURNAL , 2025 , 505 . |
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Abstract :
Herein, an electron-optimized core-shell CoFe alloy-carbon composite (CoFeC) was developed from prepared CoFe Prussian blue analogues (CoFe PBAs) through pyrolysis and applied for peracetic acid (PAA) activation. Characterization analysis and theoretical calculations indicated that the Co sites as the primary active centers, with the presence of C and Fe in CoFeC significantly narrowed the difference between the d-band center (epsilon d) and the Fermi level (EF), thereby reducing PAA adsorption energy on Co sites and enhancing electron transfer. The identification of reactive species confirmed that acetylperoxy radicals (CH3C(O)OO.) and singlet oxygen (1O2) were the dominant species driving the reaction. The CoFeC/PAA system demonstrated exceptional pollutant degradation efficiency, achieving nearly 100 % removal within 30 min, along with strong interference resistance and high durability in continuous-flow reactors. This work provided novel insights into the activation of PAA by bimetallic carbon catalysts and offered guidance for the development of efficient and sustainable water treatment technologies.
Keyword :
Emerging micropollutants Emerging micropollutants Fenton-like Fenton-like Prussian blue analogues Prussian blue analogues Heterogeneous catalysis Heterogeneous catalysis Peracetic acid Peracetic acid
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GB/T 7714 | Wang, Linhao , Wei, Jia , Huo, Jiangkai et al. Harnessing electronically core-shell CoFe alloy-carbon from Prussian blue analogues for efficient pollutant abatement via peracetic acid activation: Dual reactive species generation and synergistic mechanisms [J]. | APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY , 2025 , 371 . |
MLA | Wang, Linhao et al. "Harnessing electronically core-shell CoFe alloy-carbon from Prussian blue analogues for efficient pollutant abatement via peracetic acid activation: Dual reactive species generation and synergistic mechanisms" . | APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY 371 (2025) . |
APA | Wang, Linhao , Wei, Jia , Huo, Jiangkai , Ji, Wei , Zhang, Xiaohui , Li, Yanan et al. Harnessing electronically core-shell CoFe alloy-carbon from Prussian blue analogues for efficient pollutant abatement via peracetic acid activation: Dual reactive species generation and synergistic mechanisms . | APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY , 2025 , 371 . |
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Abstract :
Interfacial engineering, which efficiently modulates the electron density and optimizes the electronic structure, has rapidly emerged as a promising strategy to facilitate Fenton-like reaction processes. Here, an interfacial catalyst with Fe7S8 coupled tubular g-C3N4 (TCN) was crafted for peroxymonosulfate (PMS) activation. Density functional theory (DFT) calculations revealed that the introduction of TCN in the interfacial engineering facilitated the d-band center of Fe7S8 to be closer to the Fermi energy level, enlarged the contribution of Fe-3d orbitals and raised the number of conductive carriers, resulting in higher PMS activation ability and electron utilization efficiency. S species promote valence cycling of Fe and improve catalytic efficiency as well. 5 mg & sdot;L- 1 tetracycline (TC) was efficiently eliminated with a high rate (0.49 min- 1) under dark conditions at 25 degrees C in 10 min. Moreover, contaminants containing electron-donating groups were susceptible to effective degradation. Given DFT calculations and experiments, the intermediate (*O) was the key precursor for the generation of 1O2, determining the reaction rate, while electron transfer process (ETP) was proposed. This work sheds new insights for interfacial engineering to manipulate the electronic structure of catalysts and enhanced catalytic performance, facilitating practical ecological remediation.
Keyword :
Nonradical mechanism Nonradical mechanism Peroxymonosulfate Peroxymonosulfate Emerging contaminants Emerging contaminants Theoretical calculation Theoretical calculation Interfacial engineering Interfacial engineering
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GB/T 7714 | Jiang, Zijian , Wei, Jia , Yan, Wenhao et al. Modulating the electronic structure of Fe7S8@TCN enhancing peroxymonosulfate activation for efficient water decontamination: Importance of interfacial engineering [J]. | SEPARATION AND PURIFICATION TECHNOLOGY , 2025 , 362 . |
MLA | Jiang, Zijian et al. "Modulating the electronic structure of Fe7S8@TCN enhancing peroxymonosulfate activation for efficient water decontamination: Importance of interfacial engineering" . | SEPARATION AND PURIFICATION TECHNOLOGY 362 (2025) . |
APA | Jiang, Zijian , Wei, Jia , Yan, Wenhao , Niu, Xiruo , Cui, Xueru , Li, Shizhao et al. Modulating the electronic structure of Fe7S8@TCN enhancing peroxymonosulfate activation for efficient water decontamination: Importance of interfacial engineering . | SEPARATION AND PURIFICATION TECHNOLOGY , 2025 , 362 . |
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Abstract :
Peracetic acid (PAA) as emerging oxidant in advanced oxidation processes (AOPs) has attracted widespread attention in purifying water pollution. In this research, the removal of target contaminant (sulfamethoxazole, SMX) was investigated through PAA activation by a facile catalyst (Co@C), and the active sites of catalyst were identified as sp(3)-C, O-ads, and Co-0 by correlation analysis. Especially, different pH adjustment strategies were designed, including System A (adjusting pH after adding PAA) and System B (adjusting pH before adding PAA), to investigate the impact of oxidant acidity and alkalinity on solution microenvironment as well as effect and mechanism of pollutant removal. The results showed that HO and CH3C(O)OO dominated in System A, while Co(IV)O2+ was also observed in System B. Both systems showed optimal SMX degradation (98 %). However, System A exhibited excellent water quality tolerance (efficiency > 78 %), superior sustained catalyst activation (efficiency > 80 % in 40 h), less ion leaching (41 mu g L-1), and lower products toxicity. Moreover, the pH of solution after reaction in System B was intensely acidic, requiring costly pH adjustments for discharge. This study unveils the strategy of adjusting pH after adding PAA is preferable for water purification, enriching the emerging research of PAA-based AOPs for the remediation of environments.
Keyword :
Peracetic acid Peracetic acid Emerging contaminants Emerging contaminants pH -dependent removal pH -dependent removal Radical oxidation process Radical oxidation process Co -based catalyst Co -based catalyst
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GB/T 7714 | Niu, Xiruo , Wei, Jia , Jiang, Zijian et al. New insights into the pH-dependent removal of sulfamethoxazole in peracetic acid activation systems: From mechanistic exploration to practical application potentials [J]. | JOURNAL OF HAZARDOUS MATERIALS , 2024 , 474 . |
MLA | Niu, Xiruo et al. "New insights into the pH-dependent removal of sulfamethoxazole in peracetic acid activation systems: From mechanistic exploration to practical application potentials" . | JOURNAL OF HAZARDOUS MATERIALS 474 (2024) . |
APA | Niu, Xiruo , Wei, Jia , Jiang, Zijian , Cui, Xueru , Li, Yanan , Cui, Nan et al. New insights into the pH-dependent removal of sulfamethoxazole in peracetic acid activation systems: From mechanistic exploration to practical application potentials . | JOURNAL OF HAZARDOUS MATERIALS , 2024 , 474 . |
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Abstract :
The pervasive presence of antibiotics in the environment poses ecological risks and jeopardizes human health. Herein, a simple one-step hydrothermal method was used to prepare a boron-doped (B-doped) bimetallic carbon felt as a cathode for the heterogeneous electro-Fenton (HEF) system. In the HEF process, the modified electrode (B-Co/Fe@CF) demonstrated exceptional efficiency in degrading the target pollutant doxycycline (DOX), owing to its maximal degree of defect and minimal electrochemical impedance. In addition, XPS and structure-activity relationship analysis results revealed that the superior performance of the modified electrode stemmed from the predominant influence of sp(3)/sp(2), C=O and metal-boron (M-B) groups in initiating the production of H2O2 and the consequent formation of reactive oxygen species (ROS). Meanwhile, the introduction of non-metallic boron species significantly accelerated the sustainable cycling of Co(II)/Co(III) and Fe(II)/Fe(III). The quenching and probe experiments suggested that the radicals center dot O-2(-) and center dot OH significantly contributed to the elimination of DOX. Moreover, the advanced B-Co/Fe@CF-HEF system exhibited remarkable versatility, stability and effectiveness throughout the degradation process. Three pathways for the degradation of the pollutants were identified using density functional theory (DFT) calculations and LC-MS detection. Additionally, the treated DOX solution significantly reduced the toxicity to the growth of E. coli and mung bean in actual toxicity experiments. This research presented a novel outlook on developing the B-doped metal catalysts for efficient degradation of pollutants and showcased promising applications in organic wastewater treatment.
Keyword :
Heterogeneous electro-Fenton Heterogeneous electro-Fenton Organic contaminants Organic contaminants Degradation Degradation Bimetal Bimetal Boron-doped Boron-doped
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GB/T 7714 | Ji, Wei , Wei, Jia , Xu, Mengdie et al. Enhanced organic contaminant eradication using boron-doped bimetallic cathodes in electro-Fenton: Unveiling structure-activity relationship [J]. | CHEMICAL ENGINEERING JOURNAL , 2024 , 496 . |
MLA | Ji, Wei et al. "Enhanced organic contaminant eradication using boron-doped bimetallic cathodes in electro-Fenton: Unveiling structure-activity relationship" . | CHEMICAL ENGINEERING JOURNAL 496 (2024) . |
APA | Ji, Wei , Wei, Jia , Xu, Mengdie , Wang, Linhao , Huo, Jiangkai , Li, Yanan et al. Enhanced organic contaminant eradication using boron-doped bimetallic cathodes in electro-Fenton: Unveiling structure-activity relationship . | CHEMICAL ENGINEERING JOURNAL , 2024 , 496 . |
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Abstract :
本发明公开了一种八硫化七铁负载生物炭催化剂的制备方法及应用,属于污水处理技术领域。该催化剂的制备方法为:将生物炭原料、六水合氯化铁、硫脲在乙二醇中完全溶解,通过溶剂热法得到八硫化七铁负载生物质前驱体,经热解法后得到八硫化七铁负载生物炭催化剂,将该催化剂和过一硫酸盐加入含有抗生素的水体中,通过以单线态氧为主的非自由基途径实现水体中抗生素的去除,本发明的催化剂制备方法简单,对抗生素去除效率高,pH、温度适用范围广泛,具有较大的比表面积,易回收利用,适合工业化生产。
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GB/T 7714 | 魏佳 , 姜子建 . 一种八硫化七铁负载生物炭催化剂的制备方法及应用 : CN202310170156.3[P]. | 2023-02-27 . |
MLA | 魏佳 et al. "一种八硫化七铁负载生物炭催化剂的制备方法及应用" : CN202310170156.3. | 2023-02-27 . |
APA | 魏佳 , 姜子建 . 一种八硫化七铁负载生物炭催化剂的制备方法及应用 : CN202310170156.3. | 2023-02-27 . |
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Abstract :
Recently, atomically dispersed dual-metal sites carbocatalysts (DMSCs) make a wave in the field of persulfate-based advanced oxidation processes (PS-AOPs) in light of their approximate to 100% atomic utilization efficiency, high density of active sites, and superior catalytic activity. This review aims to provide a state-of-the-art overview on the development of DMSCs for activating PS. Initially, the types and properties of DMSCs are summarized, as well as the role of doping different heteroatoms is discussed. Subsequently, the properties of different carbon carriers and the methods for the synthesis of DMSCs are outlined. After that, the mechanism and application of DMSCs for the activation of PS toward organic contaminants degradation are revealed. Particularly, the mechanism of nonradical pathway is described, and the necessity of coupling DMSCs-based PS-AOPs to other processes for practical water treatment is emphasized. Finally, the formidable challenges and future research directions of DMSCs are proposed. This review is expected to provide insight into the preparation of DMSCs in the field of nanomaterials and to broaden the path for their environmental applications.
Keyword :
dual-metal sites dual-metal sites persulfate persulfate organic contaminants organic contaminants advanced oxidation processes advanced oxidation processes carbocatalysts carbocatalysts
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GB/T 7714 | Li, Yanan , Wei, Jia , Cui, Nan et al. Recent Advance of Atomically Dispersed Dual-Metal Sites Carbocatalysts: Properties, Synthetic Materials, Catalytic Mechanisms, and Applications in Persulfate-Based Advanced Oxidation Process [J]. | ADVANCED FUNCTIONAL MATERIALS , 2023 , 33 (30) . |
MLA | Li, Yanan et al. "Recent Advance of Atomically Dispersed Dual-Metal Sites Carbocatalysts: Properties, Synthetic Materials, Catalytic Mechanisms, and Applications in Persulfate-Based Advanced Oxidation Process" . | ADVANCED FUNCTIONAL MATERIALS 33 . 30 (2023) . |
APA | Li, Yanan , Wei, Jia , Cui, Nan , Li, Jiamei , Xu, Mengdie , Pan, Guoping et al. Recent Advance of Atomically Dispersed Dual-Metal Sites Carbocatalysts: Properties, Synthetic Materials, Catalytic Mechanisms, and Applications in Persulfate-Based Advanced Oxidation Process . | ADVANCED FUNCTIONAL MATERIALS , 2023 , 33 (30) . |
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Abstract :
In recent years, metal-free catalysts for persulfate-mediated oxidation processes have been widely applied to remove contaminants in the aquatic environment. Herein, a simple pyrolysis approach was used to synthesize the boron doped biochars (B@TBCs) derived from boric acid mixed with tea seed shells powders. The obtained B@TBCs exhibited fantastic capability to boost PMS (0.5 mM) activation for 90%~ removal of oxytetracycline (OTC) within 20 min. Through the correlation analysis and DFT calculations, it was concluded that the apparent rate constant of pollutants removal was greatly related to the-O-B -O-groups on the biochars, which could improve the electron-donating capacity of the biochar. In addition, the degradation process of OTC was pH -dependent because of the changed roles of ROSs under different pH. Finally, according to the DFT calcula-tion, LC-MS and toxicological analysis, the degradation pathways of pollutants and the toxicity changes during the degradation process were obtained. These findings consolidated the theoretical basis for further boosting the catalytic activity of B-doped biochars and expanded the imagination for the modification of other metal-free biochar catalysts for PMS activation.
Keyword :
-O-B-O-moieties -O-B-O-moieties Density function theory Density function theory Antibiotic Antibiotic Peroxymonosulfate activation Peroxymonosulfate activation Boron doped biochar Boron doped biochar
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GB/T 7714 | Pan, Guoping , Wei, Jia , Xu, Mengdie et al. Insight into boron-doped biochar as efficient metal-free catalyst for peroxymonosulfate activation: Important role of-O-B-O- moieties [J]. | JOURNAL OF HAZARDOUS MATERIALS , 2023 , 445 . |
MLA | Pan, Guoping et al. "Insight into boron-doped biochar as efficient metal-free catalyst for peroxymonosulfate activation: Important role of-O-B-O- moieties" . | JOURNAL OF HAZARDOUS MATERIALS 445 (2023) . |
APA | Pan, Guoping , Wei, Jia , Xu, Mengdie , Li, Jiamei , Wang, Linhao , Li, Yanan et al. Insight into boron-doped biochar as efficient metal-free catalyst for peroxymonosulfate activation: Important role of-O-B-O- moieties . | JOURNAL OF HAZARDOUS MATERIALS , 2023 , 445 . |
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Abstract :
Electro-Fenton is one of the promising clean and renewable technologies for refractory pollutants control. Herein, a ternary metal-layered double hydroxide (CoFeCe-LDH) nanoparticle in situ growth on carbon felt (CF) was prepared to fabricate heterogeneous electro-Fenton (HEF) cathode via one-pot hydrothermal strategy. The optimal CoFeCe-LDH@CF cathode demonstrated high oxygen reduction activity, low resistance and efficient degradation of DOX over a wide pH range (pH = 1-9). On one hand, the introduction of Ce resulted in the generation of plenty of oxygen vacancies (O-alpha) on the electrode surface. On the other hand, the coexistence of Co2+/Co3+, Fe2+/Fe3+ and Ce3+/Ce4+ redox pairs significantly enhanced interfacial electron transfer and promoted the generation and decomposition of in situ H2O2, which in turn boosted the production of reactive radicals ((OH)-O-center dot, O-2(center dot-) and O-1(2)). The Estimation Program Interface (EPI) certificated that intermediates resulted from DOX degradation in the system were relatively low in toxicity to typical aquatic organisms. Meanwhile, the effect experiments of various ions, types of wastewater and pollutants were carried out in the CoFeCe-LDH@CFs-HEF system and all showed excellent pollutant degradation, proving that the developed cathode had special applicability and reusability. Thus, this paper gave a global contribution to develop the high-performance cathode by exploring the synergistic effects of trimetals in LDH and proposed a reliable strategy for enhanced degradation of contaminant by HEF system.
Keyword :
Heterogeneous electro-Fenton Heterogeneous electro-Fenton Oxygen vacancies Oxygen vacancies Antibiotic Antibiotic Layered double hydroxide Layered double hydroxide Cerium Cerium
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GB/T 7714 | Xu, Mengdie , Wei, Jia , Cui, Xueru et al. High-efficiency electro-Fenton process based on in-situ grown CoFeCe-LDH@CFs free-standing cathodes: Correlation of cerium and oxygen vacancies with H2O2 [J]. | CHEMICAL ENGINEERING JOURNAL , 2022 , 455 . |
MLA | Xu, Mengdie et al. "High-efficiency electro-Fenton process based on in-situ grown CoFeCe-LDH@CFs free-standing cathodes: Correlation of cerium and oxygen vacancies with H2O2" . | CHEMICAL ENGINEERING JOURNAL 455 (2022) . |
APA | Xu, Mengdie , Wei, Jia , Cui, Xueru , Li, Jiamei , Pan, Guoping , Li, Yanan et al. High-efficiency electro-Fenton process based on in-situ grown CoFeCe-LDH@CFs free-standing cathodes: Correlation of cerium and oxygen vacancies with H2O2 . | CHEMICAL ENGINEERING JOURNAL , 2022 , 455 . |
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