Journal of Water Chemistry and Technology
·
2023
·Vol. 45
·期 2
·164-175
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IF 0.6
Jing Meng,Geng Cong,Guan Yinyan,Gao Weichun,Ming Hao,Li Dan,Wang Nan,Liu Shiyue,Jiang Wei,Liang Jiyan,Wang Xueying
Abstract The sol-gel approach was utilized to make a copper-doped Ti/SnO 2 -Sb anode for electrochemical oxidation of norfloxacin (NOR). Sycanning electron microscopy (SEM), energy dispersive spectrometry (EDS), X-ray diffraction (XRD), linear scan voltammograms (LSV), and cyclic voltammetry (CV) were used to examine the anode’s surface morphology and electrochemical characteristics. The results show that the doped metal makes the anode coating denser and smoother, which is more conducive to resistance to electrochemical corrosion. The electrochemical degradation of NOR utilizing the constructed anode was examined in relation to reaction circumstances such as current density, pH value, and initial NOR concentration. Within the selected range of reaction conditions, the removal rate of NOR using Ti/SnO 2 –Sb–Cu electrode was significantly higher than that of blank electrode. The following were the shifting trends: NOR removal efficiencies grew with applied current density and initial NOR concentration, and reduced with increasing pH value. Water samples with different reaction times were taken and tested by UV-Vis spectrum. As can be seen from the results, with the progress of the reaction, the intensity of the characteristic peak decreased, indicating that NOR is degraded gradually. The electrochemical degradation pathways of NOR were studied using liquid chromatography coupled with mass spectrometry (LC-MS). Six intermediates were detected and a possible reaction pathway for the degradation of NOR by electrochemical oxidation was proposed.
研究领域:
环境科学
·
电化学工程
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产品关联
DOI
高影响因子
JOURNAL OF SOLID STATE ELECTROCHEMISTRY
·
2021
·Vol. 25
·期 5
·1541-1553
·
IF 2.647
Zeng Laiyuan,Wei Xuefeng,Miao Juan,Zhang Ruichang,Zhang Jun,Zhou Ming,Lu Weiwei
A Sb-doped SnO 2 anode modified with Ni and B was fabricated by the sol–gel method. The effect of major operation parameters of electrode preparation, such as Ni content, B content, and calcination temperature, on the mineralization degree of phenol was investigated. Response surface methodology was used to optimize the experimental conditions and evaluate the association between various operation parameters. The morphology, crystal structure, and electrocatalytic performance of the prepared SnO 2 –Sb–Ni–B anodes were studied by scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), linear sweep voltammetry (LSV), and cyclic voltammetry (CV). The optimized sol–gel preparation ratio of citric acid, ethylene glycol, tin tetrachloride, antimony trichloride, nickel chloride, and boric acid was 650:200:100:6.5:0.5:2, and the calcination temperature of the electrode was 550 °C. The SnO 2 –Sb–Ni–B anode has the highest oxygen evolution potential of 1.63 V (vs. Hg 2 /Hg 2 SO 4 ). The removal degree of phenol reached 58% within 2 h on the SnO 2 –Sb–Ni–B anode. The accelerated lifetime of the selected SnO 2 –Ni–B anode was 720 min, which was carried out in a 3-mol/L sulfuric acid solution with a current density of 500 mA/cm 2 .
研究领域:
环境科学
·
材料科学
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DOI
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2022
·Vol. 46
·期 37
·17767-17775
·
IF 3.925
Ji-Ping Jia,Yu-Lu Zhang,Jin-Yu Gou,Yi-Xuan Zhang,Yu-Ke Dai,Hong-Hua Ge,Yu-Zeng Zhao,Xin-Jing Meng
A Ti/SnO2–Sb–Cu–Zn electrode was prepared for the electrocatalytic oxidation of Acid Red 18 (AR18). The addition of Zn to the coating results in smaller surface cracks and greater roughness. When Cu and Zn coexist, high-index crystal planes are generated on smaller-sized grains formed on the coating surface, which allows the coating surface to adsorb oxygen. Sb5+ and the adjacent Cu2+–Zn2+ on the surface of the Cu–Zn co-doped coating are the advantageous active sites for adsorbed oxygen. The electrode exhibits a larger electrochemically active surface area and smaller electrochemical reaction resistance. The appearance of high-index crystal planes is beneficial to improve the electrocatalytic activity of the electrode, although the oxygen evolution potential of the electrode is not greatly improved. Cu–Zn co-doping produces synergistic mineralisation and enhances the ability to degrade AR18, and ˙OH is the main active species. During the thermal decomposition of the coating, Zn induces Cu to form more active sites on the high-index crystal planes of SnO2, a phenomenon that may be responsible for the synergistic production of more reactive oxygen species on the electrode surface.
研究领域:
环境科学
·
材料科学
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DOI
高影响因子
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2023
·
IF 5.8
Li Yang,Ma Hairun,Li Qianwei,Yan Guangxu,Guo Shaohui
Ti/SnO 2 -Sb electrodes possess high catalytic activity and efficiently degrade nitrobenzene (NB); however, their low service life limits their wide application. In this study, we used one-step hydrothermal synthesis to successfully prepare Pt-Nd co-doped Ti/SnO 2 -Sb nanosphere electrodes. Scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy were applied to characterize the surface morphology, microstructure, and chemical composition of the electrodes, respectively. The electrochemical activity and stability of the electrodes were characterized via linear sweep and cyclic voltammetry, electrochemical impedance spectroscopy, and an accelerated service life test; their performance for NB degradation was also studied. An appropriate amount of Pt-Nd co-doping refined the average grain size of SnO 2 and formed a uniform and compact coating on the electrode surface. The oxygen evolution potential, total voltammetric charge, and electron transfer resistance of the Ti/SnO 2 -Sb-Nd-Pt electrodes were 1.88 V, 3.77 mC/cm 2 , and 11.50 Ω, respectively. Hydroxy radical was the main active radical species during the electrolytic degradation of nitrobenzene with Ti/SnO 2 -Sb-Nd-Pt. After Pt-Nd co-doping, the accelerated service life of the electrodes was extended from 8.0 min to 78.2 h (500 mA/cm 2 ); although the NB degradation rate decreased from 94.1 to 80.6%, the total amount of theoretical catalytic degradation of NB in the effective working time increased from 17.4 to 8754.1 mg/cm 2 . These findings reveal good application potential for the electrodes and provide a reference for developing efficient and stable electrode materials.
研究领域:
环境科学
·
材料科学
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DOI
PubMed
高影响因子
RSC Advances
·
2017
·Vol. 7
·期 60
·37806-37814
·
IF 3.108
Anlin Xu,Xiang Dai,Kajia Wei,Weiqing Han,Jiansheng Li,Xiuyun Sun,Jinyou Shen,Lianjun Wang
The broad application of highly electrocatalytic SnO2–Sb electrodes for wastewater treatment is limited by their short service lifetime. Herein, a novel substrate structure, tubular porous titanium, was applied to prepare a TiO2-NT/SnO2–Sb electrode, which could greatly improve the stability of the electrode for electrochemical oxidation process. Based on the analysis conducted using a field emission scanning electron microscope (FE-SEM), linked with an energy dispersive spectrometer (EDS), it was demonstrated that a solid solution between Sn and Sb presented a smooth surface of the tubular porous electrode. The crystalline structure and chemical composition of the electrode coating are determined by X-ray diffraction (XRD). Accelerated service life test reveals that under the 0.2 A cm−2 current density in a 0.5 M H2SO4 solution, the TiO2-NT/SnO2–Sb tubular porous electrode has the longest accelerated service lifetime of 68.9 h, which is 10.9 times that of the TiO2-NT/SnO2–Sb plate electrode. Cyclic voltammetry curves (CVs) and linear sweep voltammetry curves (LSVs) reveal the enhanced electroactive surface area and higher oxygen evolution potential (OEP = 1.85 V vs. Ag/AgCl) of the electrode. Moreover, the TiO2-NT/SnO2–Sb tubular porous electrode has the larger outer voltammetric charge q*. During the electrochemical oxidation of pyrimidine, the tubular system constructed using the TiO2-NT/SnO2–Sb tubular porous electrode as the anode also exhibited best electrocatalytic performance, and 97.9% pyridimine removal efficiency and 79.4% COD removal efficiency at 6 h were achieved.
研究领域:
环境科学
·
材料科学
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产品关联
DOI
高影响因子
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