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学者姓名：方圣琼
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Abstract ：
Building an effective heterogeneous Fenton catalyst over a broad pH range without the requirement for external energy input is still challenging. Herein, a vanadium-cobalt bimetallic catalyst (Co-V-8) are employed to extended a pH range of 3-9 by activating H2O2 as a Fenton-like catalyst. The Co-based Co-V-8 catalysts demonstrate high diclofenac sodium deterioration efficiency (98.2%) under both acidic and alkaline environments, and the kinetic reaction rate within 15 min could reach 0.288 min-1. Crucially, density functional theory (DFT) calculations imply that the Co-V-8 owned a narrower band gap and a higher Fermi level, which beneficial for quickening the electron transfer process. Results showed that the catalyst modified by V could introduce abundant oxygen vacancies, promote the decomposition of H2O2 via V3+ and V4+, and enhance the conversion of Co3+ and Co2+, accelerating the formation of center dot OH, center dot OOH, center dot O2 and electron transfer process. Additionally, Co-V-8 promoted the utilization rate of H2O2 exceeding 90% and exhibited exceptional catalytic ability in cleaning actual pharmaceutical wastewater. This research offers a sustainable separable and purification technology for wastewater remediation.
Keyword ：
DFT DFT Electron transfer process Electron transfer process Heterogeneous Fenton Heterogeneous Fenton Oxygen vacancy Oxygen vacancy V modification V modification
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| GB/T 7714 | Huang, Xiaoyi , Wu, Qiangqiang , Tang, Jingwen et al. Unraveling the role of V modified CoO in a wide pH range Fenton-like process [J]. | JOURNAL OF ENVIRONMENTAL MANAGEMENT , 2025 , 375 . |
| MLA | Huang, Xiaoyi et al. "Unraveling the role of V modified CoO in a wide pH range Fenton-like process" . | JOURNAL OF ENVIRONMENTAL MANAGEMENT 375 (2025) . |
| APA | Huang, Xiaoyi , Wu, Qiangqiang , Tang, Jingwen , Ning, Rongsheng , Yuan, Jiang , Fang, Shengqiong et al. Unraveling the role of V modified CoO in a wide pH range Fenton-like process . | JOURNAL OF ENVIRONMENTAL MANAGEMENT , 2025 , 375 . |
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Transition metals are frequently used to create catalysts that activate peroxymonosulfate (PMS) to degrade water contaminants. However, the degradation efficiency may be decreased if metal ions are released into the solution. In this work, a one-step calcination method was used to modify graphitic carbon nitride (CN) in the presence of Co and S. The synthesis of CoS2was notably aided by the doping of S, which also improved the degradation efficiency of CBZ by penetrating the tri-s-triazine ring of CN, which alters the electron distribution and speeds up the electron transfer efficiency between Co2+ and Co3+. The Fenton-like reaction mechanism degrades carbamazepine (CBZ, C = 20 mg/L) by 98 % within 40 min when paired with PMS. When the pH value ranges between 5 and 9, the degradation efficiency of CBZ remains above 90 % even in the presence of humic acid and other anions. Sulphate radicals (SO4- center dot) and superoxide radicals (O2- center dot) were identified as the primary reactive oxygen species (ROS) involved in the reaction process. A believable CBZ degradation route was suggested. Additionally, the entire reaction process is environmentally safe due to the toxicity calculation.
Keyword ：
Carbamazepine Carbamazepine CN-S-Co CN-S-Co Fenton-like Fenton-like Graphite carbon nitride (CN) Graphite carbon nitride (CN) Peroxmonosulfate Peroxmonosulfate
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| GB/T 7714 | Huang, Lili , Ge, Yao , Zheng, Zhi et al. Co and S co-doped graphitic carbon nitride synergistically degrades carbamazepine in water with peroxymonosulfate [J]. | JOURNAL OF WATER PROCESS ENGINEERING , 2025 , 71 . |
| MLA | Huang, Lili et al. "Co and S co-doped graphitic carbon nitride synergistically degrades carbamazepine in water with peroxymonosulfate" . | JOURNAL OF WATER PROCESS ENGINEERING 71 (2025) . |
| APA | Huang, Lili , Ge, Yao , Zheng, Zhi , Wang, Dong , Wang, Xinlei , Yang, Liu et al. Co and S co-doped graphitic carbon nitride synergistically degrades carbamazepine in water with peroxymonosulfate . | JOURNAL OF WATER PROCESS ENGINEERING , 2025 , 71 . |
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Ciprofloxacin (CIP) is widely used in the aquaculture and medical fields. The discharge of unused residual CIP into the environment poses a threat to humans and the ecology. In this work, we successfully synthesized a composite catalyst (called PSBC-0.1) using a peanut shell to degrade the refractory antibiotic ciprofloxacin (CIP) in water. In addition, compared with that of biochar and CuFeO2, the specific surface area of the surface area of the PSBC-0.1 catalyst was greatly greater, which increased the contact area between the pollutant and the catalyst. The combined effect of iron and copper increases the rate of electron transport, while the abundance of functional groups on the biochar surface helps anchor the catalyst onto the substrate. As a result, the degradation efficiency of CIP was 95 % under optimal conditions (1.2 g & sdot;L-1 of PSBC-0.1, H2O2 dosage of 12 mM and pH = 7.0); moreover, it effectively degraded carbamazepine (CBZ), diclofenac (DF), sulfafurazole (SIZ), and tetracycline (TC). The intermediates and final products of the degradation process was investigated using liquid chromatography-mass spectrometry (LC-MS). Toxicity analysis revealed that the intermediates and final products of the degradation process are environmentally friendly. The active sites of the CIP were also analyzed using density functional theory (DFT) calculations. The catalyst not only prevented a decrease in degradation efficiency due to metal compound agglomeration but also enhanced the cyclic synergy of Fe3+/Fe2+ and Cu2+/ Cu+.
Keyword ：
Ciprofloxacin Ciprofloxacin CuFeO2 CuFeO2 Heterogeneous Fenton process Heterogeneous Fenton process Peanut shell biochar Peanut shell biochar
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| GB/T 7714 | Ge, Yao , Wang, Dong , Zheng, Zhi et al. High efficiency heterogeneous fenton-like catalyst biochar modified CuFeO2 for the degradation of ciprofloxacin: Catalytic performance and mechanism [J]. | JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING , 2025 , 13 (2) . |
| MLA | Ge, Yao et al. "High efficiency heterogeneous fenton-like catalyst biochar modified CuFeO2 for the degradation of ciprofloxacin: Catalytic performance and mechanism" . | JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING 13 . 2 (2025) . |
| APA | Ge, Yao , Wang, Dong , Zheng, Zhi , Huang, Lili , Wang, Junjie , Fang, Shengqiong . High efficiency heterogeneous fenton-like catalyst biochar modified CuFeO2 for the degradation of ciprofloxacin: Catalytic performance and mechanism . | JOURNAL OF ENVIRONMENTAL CHEMICAL ENGINEERING , 2025 , 13 (2) . |
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Substantial discharge of industrial oily wastewater calls for an efficient and sustainable treatment for resource recovery. Superwetting membranes offer a feasible approach to fractionate oil species and water from oily wastewater for addressing this technical challenge. In this study, we proposed a useful strategy for constructing a superhydrophilic membrane with superior antibacterial properties through rapid co-deposition of dopamine and 3-aminopropyltriethoxysilane (APTS) initiated by ammonium persulfate on the Cu nanoparticles-loaded porous PVDF substrate. The resultant superhydrophilic membrane yielded an underwater oil contact angle of 163.5(degrees), enabling a fast and robust gravity-driven filtration for various oil-in-water emulsions with a separation efficiency of >99.9 %. Additionally, incorporating of Cu nanoparticles and polydopamine endowed the superhydrophilic membrane with superior antibacterial activity (100 % inhibition efficiency against Escherichia coli), and thereby remarkably enhancing the anti-biofouling performance. This study provides a viable approach to design highperformance membranes for separation of oil-in-water emulsions, with promising applications in the industrial and environmental sectors.
Keyword ：
Antibacteria Antibacteria Cu nanoparticles Cu nanoparticles Mussel-inspired polydopamine coating Mussel-inspired polydopamine coating Oil -in -water emulsions Oil -in -water emulsions Superhydrophilic membrane Superhydrophilic membrane
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| GB/T 7714 | Lin, Yingying , Yu, Fan , Yu, Zijian et al. Mussel-inspired superhydrophilic and antibacterial membranes for effective gravity-driven separation of oil-in-water emulsions [J]. | SEPARATION AND PURIFICATION TECHNOLOGY , 2024 , 341 . |
| MLA | Lin, Yingying et al. "Mussel-inspired superhydrophilic and antibacterial membranes for effective gravity-driven separation of oil-in-water emulsions" . | SEPARATION AND PURIFICATION TECHNOLOGY 341 (2024) . |
| APA | Lin, Yingying , Yu, Fan , Yu, Zijian , Lin, Xiaoyan , Lin, Fang , Liu, Riri et al. Mussel-inspired superhydrophilic and antibacterial membranes for effective gravity-driven separation of oil-in-water emulsions . | SEPARATION AND PURIFICATION TECHNOLOGY , 2024 , 341 . |
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For the efficient degradation of organic pollutants with the goal of reducing the water environment pollution, we employed an alkaline hydrothermal treatment on primeval g-C 3 N 4 to synthesize a hydroxyl -grafted g-C 3 N 4 (CN0.5) material, from which we engineered a novel Fenton -like catalyst, known as Cu-CN-0.5. The introduction of numerous hydroxyl functional groups allowed the CN-0.5 substrate to stably fix active copper oxide particles through surface complexation, resulting in a low Cu leaching rate during a Cu-CN-0.5 Fenton -like process. A sequence of characterization techniques and theoretical calculations uncovered that interfacial complexation induced charge redistribution on the Cu-CN-0.5 surface. Specifically, some of the 7C electrons in the tris-s-triazine units were transferred to the copper oxide particles along the newly formed chemical bonds (C (7C) -O-Cu), forming a 7C -deficient area on the tris-s-triazine plane near the complexation site. In a typical Cu-CN-0.5 Fenton -like process, a stable 7C -7C interaction was established due to the favorable positive -negative match of electrostatic potential between the aromatic pollutants and 7C -deficient areas, leading to a significant improvement in Cu-CN0.5's adsorption capacity for aromatic pollutants. Furthermore, pollutants also delivered electrons to the Cu-CN0.5 Fenton -like system via a "through -space" approach, which suppressed the futile oxidation of H 2 O 2 in reducing the high-valent Cu 2 + and significantly improved the generation efficiency of center dot OH with high oxidative capacity. As expected, Cu-CN-0.5 not only exhibited an efficient Fenton degradation for several typical aromatic organic pollutants, but also demonstrated both a low metal leaching rate (0.12 mg/L) and a H 2 O 2 utilization rate exceeding 80%. The distinctive Fenton degradation mechanism substantiated the potential of the as -prepared material for effective wastewater treatment applications.
Keyword ：
Alkaline hydrothermal treatment Alkaline hydrothermal treatment Fenton Fenton Interfacial regulation Interfacial regulation
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| GB/T 7714 | Zhou, Bin , Liu, Qingsong , Zheng, Caihong et al. Enhanced Fenton-like catalysis via interfacial regulation of g-C3N4 for efficient aromatic organic pollutant degradation [J]. | ENVIRONMENTAL POLLUTION , 2024 , 356 . |
| MLA | Zhou, Bin et al. "Enhanced Fenton-like catalysis via interfacial regulation of g-C3N4 for efficient aromatic organic pollutant degradation" . | ENVIRONMENTAL POLLUTION 356 (2024) . |
| APA | Zhou, Bin , Liu, Qingsong , Zheng, Caihong , Ge, Yao , Huang, Lili , Fu, Haoyang et al. Enhanced Fenton-like catalysis via interfacial regulation of g-C3N4 for efficient aromatic organic pollutant degradation . | ENVIRONMENTAL POLLUTION , 2024 , 356 . |
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Poor water removal of low-molecular-weight anthropogenic contaminants is always a key problem in lowpressure membrane filtration process. In this work, we successfully designed and fabricated a novel cobaltbased bimetallic catalytic ceramic membrane (CoFe2O4@CM-2) with peroxymonosulfate (PMS) activation and membrane filtration dual functionality, employing a facile impregnation-filtration-calcination method. The resulting CoFe2O4@CM-2/PMS filtration system was specifically tailored for the removal of carbamazepine (CBZ). Our results demonstrate that the CoFe2O4@CM-2/PMS system achieved efficient removal of CBZ from contaminated waters. Under optimal conditions (PMS dosage of 0.5 mM and an operating flux of 40 L center dot m- 2 center dot h- 1), the CoFe2O4@CM-2/PMS system exhibited remarkable CBZ removal efficiency, reaching up to 96.5 %. This efficiency was 32.2 and 19.3 times higher than that achieved by ceramic membrane filtration alone and PMS treatment alone, respectively. Additionally, the CoFe2O4@CM-2/PMS system facilitated 37.0 % mineralization of CBZ and up to 87 % utilization of PMS in the permeate. Furthermore, the CoFe2O4@CM-2/PMS system demonstrated robust performance, removing over 91 % of CBZ across a pH range of 3-9 and maintaining stability stability in the presence of humic acid (HA) interference. Its exceptional anti-fouling ability effectively mitigates membrane flux loss compared to single membrane filtration process. Quenching test, electron paramagnetic resonance (EPR), and X-ray photoelectron spectroscopy (XPS) analyses revealed that 1O2, SO-4 center dot and center dot OH were the primary active substances in the system, while the redox cycle of Co2+/Co3+ played a crucial role in PMS activation. Moreover, the presence of iron (Fe) in the CoFe2O4@CM-2 expedited the Co2+/Co3+ cycle and enhanced PMS activation. This study introduces an innovative approach for fabricating ceramic membranes with catalytic degradation capabilities for organic pollutants and suggests promising avenues for integrating separation and advanced oxidation processes (AOPs) in future applications.
Keyword ：
Carbamazepine Carbamazepine Catalytic ultrafiltration ceramic membrane Catalytic ultrafiltration ceramic membrane Cobalt-based catalyst Cobalt-based catalyst Peroxymonosulfate Peroxymonosulfate
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| GB/T 7714 | Ge, Yao , Zhong, Xincheng , Wang, Kai et al. CoFe2O4-catalytic ceramic membrane for efficient carbamazepine removal via peroxymonosulfate activation [J]. | SEPARATION AND PURIFICATION TECHNOLOGY , 2024 , 357 . |
| MLA | Ge, Yao et al. "CoFe2O4-catalytic ceramic membrane for efficient carbamazepine removal via peroxymonosulfate activation" . | SEPARATION AND PURIFICATION TECHNOLOGY 357 (2024) . |
| APA | Ge, Yao , Zhong, Xincheng , Wang, Kai , Huang, Lili , Zheng, Zhi , Wu, Chenzhi et al. CoFe2O4-catalytic ceramic membrane for efficient carbamazepine removal via peroxymonosulfate activation . | SEPARATION AND PURIFICATION TECHNOLOGY , 2024 , 357 . |
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In order to overcome the low catalytic efficiency of conventional single cobalt-based catalysts, a cobalt-based peroxymonosulfate (PMS) heterogeneous catalyst, named P-Co@C, was synthesized by introducing phosphorus. The degradation rate of diclofenac (DCF) was increased by 5-fold from 0.076 min-1 (Co@C) to 0.426 min-1 (P-Co@C). The enhanced catalytic behavior was ascribed to the increased specific area, promotional hydrophilicity, reduced resistance to electron transfer and improved electron donor of reductive phosphorus. Density functional theory (DFT) calculations suggest that the doped P further facilitates the adsorbability and charge transfer intensity between catalyst and PMS, which benefits the generation of hydroxyl radical, sulfate radical and singlet oxygen. Furthermore, toxicity assessment of the intermediates revealed that the P-Co@C/ PMS/DCF system was a diminishing toxicity process, revealing the practicability and eco-friendly of P-Co@C in PMS-based oxidation process. This work provides a new strategy for exploring the cation and anion co-activation of the PMS heterogeneous catalytic systems.
Keyword ：
DFT DFT Diclofenac Diclofenac Electron transfer Electron transfer P-Co@C P-Co@C Peroxymonosulfate Peroxymonosulfate
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| GB/T 7714 | Huang, Xiaoyi , Fang, Shengqiong , Yu, Shuili et al. Unraveling the role of P doped Co@C in diclofenac degradation [J]. | SEPARATION AND PURIFICATION TECHNOLOGY , 2024 , 353 . |
| MLA | Huang, Xiaoyi et al. "Unraveling the role of P doped Co@C in diclofenac degradation" . | SEPARATION AND PURIFICATION TECHNOLOGY 353 (2024) . |
| APA | Huang, Xiaoyi , Fang, Shengqiong , Yu, Shuili , Yang, Junwei , You, Qinglun . Unraveling the role of P doped Co@C in diclofenac degradation . | SEPARATION AND PURIFICATION TECHNOLOGY , 2024 , 353 . |
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In recent studies, carbon nanotube (CNTs) materials and their composites have demonstrated remarkable catalytic activity in the activation of persulfate (PS), facilitating the efficient degradation of organic pollutants. In this study, a novel Co loaded carbon nanotubes (CoO@CNT) catalyst was prepared to promote PDS activation for the degradation of sulfafurazole (SIZ). Experimental results, the CNT as a carrier effectively reduces the leaching of cobalt ions and improves the electron transport capacity ,whereas the introduced Co effectively activates the PDS, promoting the generation of highly reactive radicals to degrade SIZ. Under optimized conditions (a catalyst dose of 0.2 g/L, a PDS dose of 1 g/L and an initial pH = 9.0), the obtained CoO@CNT demonstrated favorable Fenton-like performance, reaching a degradation efficiency of 95.55% within 30 min. Furthermore, density functional theory (DFT) calculations demonstrate that the introduction of cobalt (Co) accelerates electron transfer, promoting the decomposition of PDS while facilitating the Co 2 + /Co 3 + redox cycling. We further employed the environmental chemistry and risk assessment system (ECOSAR) to evaluate the ecological toxicity of intermediate products, revealing a significant reduction in ecological toxicity associated with this degradation process, thereby confirming its environmental harmlessness. Through batch experiments and studies, we gained a comprehensive understanding of the mechanism and influencing factors of CoO@CNT in the role of SIZ degradation, and provided robust support for evaluating the ecological toxicity of degradation products. This study provides a significant strategy for the development of efficient catalysts incorporating Co for the environmentally friendly degradation of organic pollutants.
Keyword ：
CoO CoO DFT DFT Ecotoxicity Ecotoxicity Persulfate activation Persulfate activation Sulfisoxazole Sulfisoxazole
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| GB/T 7714 | Liu, Qingsong , Zhou, Bin , Zheng, Caihong et al. The CoO-doped carbon nanotubes enhance electronic performance and effectively activate persulfate for the degradation of sulfafurazole [J]. | ENVIRONMENTAL RESEARCH , 2024 , 251 . |
| MLA | Liu, Qingsong et al. "The CoO-doped carbon nanotubes enhance electronic performance and effectively activate persulfate for the degradation of sulfafurazole" . | ENVIRONMENTAL RESEARCH 251 (2024) . |
| APA | Liu, Qingsong , Zhou, Bin , Zheng, Caihong , Wang, Dong , Ge, Yao , Fang, Shengqiong . The CoO-doped carbon nanotubes enhance electronic performance and effectively activate persulfate for the degradation of sulfafurazole . | ENVIRONMENTAL RESEARCH , 2024 , 251 . |
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Numerous superwetting separation membranes have been designed for the management of oily wastewater due to their highly efficient oil/water separation efficiency. However, the long-term stability of these developed membranes is still restricted by membrane fouling. In this study, we synthesized multifunctional superhydrophilic membranes with superior anti-adhesive and anti-biofouling properties through simple co-deposition of dopamine, polyethyleneimine and CoFe2O4 (CFO) photocatalyst on the porous PVDF substrates for sustainable management of oil-in-water emulsion. The resultant optimal composite membranes showed the superhydropilicity with an underwater oil contact angle of 162.4 degrees and achieved ca. 99.51 % oil/water separation efficiency with a maximum permeability of 232.2 Lm(-2)h(-1) in the treatment of oil-in-water emulsions driven by gravity. Moreover, the outstanding antibacterial performance of composite membrane was demonstrated by a nearly 100 % antibacterial rate during the exposure in 120-min visible light irradiation. Based on the synergistic effect of superhydrophilicity and photocatalysis, the fabricated composite membranes experienced a stable gravity-driven oil/water separation (oil rejection: >99.46 %) even after a 50-cycle filtration. Such an impressive filtration performance of the polydopamine/PEI/CFO composite membranes highlights their promising potential for sustainable and efficient treatment of oily wastewater.
Keyword ：
CoFe2 O(4 )nanoparticles CoFe2 O(4 )nanoparticles Dopamine Dopamine Fouling Fouling Oil/Water separation Oil/Water separation Photocatalysis Photocatalysis Superhydrophilicity Superhydrophilicity
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| GB/T 7714 | Yu, Fan , Liu, Riri , Chen, Lianxin et al. Facile fabrication of multifunctional superhydrophilic composite membranes for efficient oil-in-water emulsion separation [J]. | SEPARATION AND PURIFICATION TECHNOLOGY , 2024 , 356 . |
| MLA | Yu, Fan et al. "Facile fabrication of multifunctional superhydrophilic composite membranes for efficient oil-in-water emulsion separation" . | SEPARATION AND PURIFICATION TECHNOLOGY 356 (2024) . |
| APA | Yu, Fan , Liu, Riri , Chen, Lianxin , Yuan, Weishuang , Chen, Qin , Fang, Shengqiong et al. Facile fabrication of multifunctional superhydrophilic composite membranes for efficient oil-in-water emulsion separation . | SEPARATION AND PURIFICATION TECHNOLOGY , 2024 , 356 . |
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Conventional membrane processes, e.g., microfiltration and ultrafiltration, suffer from severe permeation flux decline and fouling during the oily wastewater treatment. The superhydrophilic surface decoration provides an important and effective strategy to address this challenge. Herein, a surperhydrophilic/underwater superoleophobic nanocomposite surface with the photocatalytic properties was constructed via one-step facile vacuum-assisted filtration of a g-C3N4 nanosheet/SiO2 nanoparticle dispersion onto a microfiltration membrane substrate. Specifically, with the intercalation of 20 mg.L-1 SiO2 nanoparticles into the g-C3N4 nanosheets, the g-C3N4/SiO2 composite membrane showed the superhydrophilic/underwater superoleophobic properties with an underwater oil contact angle of 170.0 +/- 0.3 degrees. Such a g-C3N4/SiO2 composite membrane yielded a permeation flux of >1290 LMH.bar(-1) with an oil rejection of >99.91% during the vacuum filtration of oil-in-water emulsions. The g-C3N4/SiO2 composite membrane significantly outperformed the pristine microfiltration substrate that had severe fouling caused by oil blockage. Additionally, the g-C3N4/SiO2 composite membrane not only effectively retained the E. coli bacteria through size exclusion effect, but also promoted the inactivation of bacteria via visible-light photocatalysis. Therefore, our membrane has a great promise in practical oily wastewater treatment due to its excellent separation performance and biofouling resistance.
Keyword ：
Bacteria inactivation Bacteria inactivation g-C3N4/SiO2 nanocomposite g-C3N4/SiO2 nanocomposite Oil-in-water emulsion separation Oil-in-water emulsion separation Superhydrophilic membrane Superhydrophilic membrane Visible-light photocatalysis Visible-light photocatalysis
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| GB/T 7714 | Ye, Wenyuan , Chen, Jinjie , Kong, Na et al. Superhydrophilic photocatalytic g-C3N4/SiO2 composite membranes for effective separation of oil-in-water emulsion and bacteria removal [J]. | SEPARATION AND PURIFICATION TECHNOLOGY , 2022 , 290 . |
| MLA | Ye, Wenyuan et al. "Superhydrophilic photocatalytic g-C3N4/SiO2 composite membranes for effective separation of oil-in-water emulsion and bacteria removal" . | SEPARATION AND PURIFICATION TECHNOLOGY 290 (2022) . |
| APA | Ye, Wenyuan , Chen, Jinjie , Kong, Na , Fang, Qingyuan , Hong, Mingqiu , Sun, Yuxiang et al. Superhydrophilic photocatalytic g-C3N4/SiO2 composite membranes for effective separation of oil-in-water emulsion and bacteria removal . | SEPARATION AND PURIFICATION TECHNOLOGY , 2022 , 290 . |
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