The laponite pillared by the CeO2 modified TiO2 (Ce-Ti-lap) were prepared by microwave intercalation reaction with laponite as the layered clay, tetrabutyl titanate and cerium chloride as the Ce-Ti composite pillaring...The laponite pillared by the CeO2 modified TiO2 (Ce-Ti-lap) were prepared by microwave intercalation reaction with laponite as the layered clay, tetrabutyl titanate and cerium chloride as the Ce-Ti composite pillaring agent, and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and Brumauer-Emmett-Teller (BET) surface area. The photocatalytic activities of Ce-Ti-lap were investigated by the degradation of methyl orange (MO). The results showed that Ce and Ti could be introduced to...展开更多
The binary composite photo-catalysts CeO2/ZiO2, ZrO2/ZiO2 and the ternary composite photo-catalysts H3PW12040-CeO2/TiO2, H3PW12O40-ZrO2/TiO2 were prepared by sol-gel method. The catalysts were characterized by thermog...The binary composite photo-catalysts CeO2/ZiO2, ZrO2/ZiO2 and the ternary composite photo-catalysts H3PW12040-CeO2/TiO2, H3PW12O40-ZrO2/TiO2 were prepared by sol-gel method. The catalysts were characterized by thermogravimetric-differential thermal analysis （TG-DTA）, scanning electron microscopy （SEM） and X-ray diffraction （XRD）. The photocatalytic elimination of methanol was used as model reaction to evaluate the photocatalytic activity of the composite catalysts under ultraviolet light irradiation. The effects of doped content, activation temperature, time, initial concentration of methanol and gas flow rate on the catalytic activity were investigated. The results showed that after doping a certain amount of CeO2 and ZrO2, crystallization process of TiO2 was restrained, particles of catalysts are smaller and more uniform. Doping ZrO2 not only significantly improved the catalytic activity, but also increased thermal stability. Doping H3PW12O40 alSO enhanced the catalytic activity. The catalytic activities of binary and ternary composite photocatalysts were significantly higher than un-doped TiO2. The dynamics law of photocatalytic reaction over the binary CeO2/TiO2 and ZrO2/TiO2 catalysts has been studied. The activation energy 15.627 and 15.631 kJ/mol and pre-exponential factors 0.5176 and 0.9899 s^-1 over each corresponding catalyst were obtained. This reaction accords to the first order dynamics law.展开更多
CeO2 was synthesized via sol-gel process and used as supporter to prepare CuO/CeO2, Cu/CeO2 catalysts by impregnation method. The catalytic properties and characterization of CeO2, CuO/CeO2 and Cu/CeO2 catalysts were ...CeO2 was synthesized via sol-gel process and used as supporter to prepare CuO/CeO2, Cu/CeO2 catalysts by impregnation method. The catalytic properties and characterization of CeO2, CuO/CeO2 and Cu/CeO2 catalysts were examined by means of a microreactor-GC system, HRTEM, XRD, TPR and XPS techniques. The results show that CuO has not catalytic activity and the activity of CeO2 is quite low for CO oxidation. However, the catalytic activity of CuO/CeO2 and Cu/ CeO2 catalysts increases significantly. Furthermore, the activity of CuO/CeO2 is higher than that of Cu/CeO2 catalysts.展开更多
Elucidation of the CuOx-CeO2 interactions is of great interest and importance in understanding complex CuOx-CeO2 interfacial catalysis in various reactions. In the present work, we have investigated structures and cat...Elucidation of the CuOx-CeO2 interactions is of great interest and importance in understanding complex CuOx-CeO2 interfacial catalysis in various reactions. In the present work, we have investigated structures and catalytic activity in CO oxidation of CuOx species on CeO2 rods, cubes and polyhedra predominantly exposing {110}+{100}, {100} and {111} facets by the incipient wetness impregnation method with the lowest Cu loading of 0.025%. The structural evolution of CuOx species was found to depend on both the Cu loading and the CeO2 morphology. As the Cu loading increases, CuOx species are deposited preferentially on the surface defect of CeO2 and then aggregate and grow, accompanied by the formation of isolated Cu ions, CuOx clusters strongly/weakly interacting with the CeO2, highly dispersed Cu O nanoparticles, and large Cu O nanoparticles. The isolated Cu^+ species and CuOx clusters weakly interacting with the CeO2 were observed mainly on the O-terminated CeO2{100} facets. Meanwhile, more Cu(I) species are stabilized during CO reduction processes in CuOx/c-CeO2 catalysts than in CuOx/r-CeO2 and CuOx/p-CeO2 catalysts. The catalytic activities of various CuOx/CeO2 catalysts in CO oxidation vary with both the CuOx species and the CeO2 morphology. These results comprehensively elucidate the CuOx-CeO2 interactions and exemplify their morphology-dependence.展开更多
The electrochemical behavior of vitamin C（ascorbic acid or AA） is investigated on the surface of a carbon-paste electrode modified with TiO2 nanoparticles and 2,2＇-（1,2 butanediylbis（nitriloethylidyne））-bis-hyd...The electrochemical behavior of vitamin C（ascorbic acid or AA） is investigated on the surface of a carbon-paste electrode modified with TiO2 nanoparticles and 2,2＇-（1,2 butanediylbis（nitriloethylidyne））-bis-hydroquinone（BBNBH）.The prepared modified electrode showed an efficient catalytic role in the electrochemical oxidation of AA,leading to remarkable decrease in oxidation overpotential and enhancement of the kinetics of the electrode reaction.This modified electrode exhibits well-separated oxidation peaks for AA and uric acid（UA）.The modified electrode is successfully applied for the accurate determination of AA in pharmaceutical preparations.展开更多
Nafion as a universal polymer ionomer was widely applied for nanocatalysts electrode preparation.However,the effect of Nafion on electrocatalytic performance was often overlooked,especially for CO_(2)electrolysis.Here...Nafion as a universal polymer ionomer was widely applied for nanocatalysts electrode preparation.However,the effect of Nafion on electrocatalytic performance was often overlooked,especially for CO_(2)electrolysis.Herein,the key roles of Nafion for CO_(2)RR were systematically studied on Cu nanoparticles(NPs)electrocatalyst.We found that Nafion modifier not only inhibit hydrogen evolution reaction(HER)by decreasing the accessibility of H_(2)O from electrolyte to Cu NPs,and increase the CO_(2)concentration at electrocatalyst interface for enhancing the CO_(2)mass transfer process,but also activate CO_(2)molecule by Lewis acid-base interaction between Nafion and CO_(2)to accelerate the formation of^(*)CO,which favor of C–C coupling for boosting C_(2)product generation.Owing to these features,the HER selectivity was suppressed from 40.6%to 16.8%on optimal Cu@Nafion electrode at-1.2 V versus reversible hydrogen electrode(RHE),and as high as 73.5%faradaic efficiencies(FEs)of C_(2)products were achieved at the same applied potential,which was 2.6 times higher than that on bare Cu electrode(~28.3%).In addition,Nafion also contributed to the long-term stability by hinder Cu NPs morphology reconstruction.Thus,this work provides insights into the impact of Nafion on electrocatalytic CO_(2)RR performance.展开更多
With the service environment becoming more and more severe, WC-Co coatings are required to apply in high temperature wear condition. In the present study, the sliding wear tests of CeO_2 modified WC-12 Co coatings wer...With the service environment becoming more and more severe, WC-Co coatings are required to apply in high temperature wear condition. In the present study, the sliding wear tests of CeO_2 modified WC-12 Co coatings were conducted at temperature of 450, 550 and 650 ℃. The wear loss and friction coefficient were recorded. The morphologies of wear tracks were observed every 1 h to investigate the dynamic wear mechanisms. The results show that the volume wear loss decreases with temperature increasing.The lowest volume wear loss is obtained at the temperature of 650 ℃ due to oxide films generated in the process of wearing. The wear mechanism is different at the temperature of 450, 550 and 650 0 C. Micro cutting wear, abrasive wear and oxidation wear dominate the wear mechanism at 450, 550 and 650 ℃,respectively. Abrasive wear and oxidation wear are the wear mechanisms at various temperatures.展开更多
A new technique for preparing TiO2 modified film on carbon steel was accomplished by electroless plating and sol-gel composite process. The artificial neural network was applied to optimize the preparing condition of ...A new technique for preparing TiO2 modified film on carbon steel was accomplished by electroless plating and sol-gel composite process. The artificial neural network was applied to optimize the preparing condition of TiO2 modified film. The optimized condition for forming TiO2 modified film on carbon steel was that NiP plating for 50 min, dip-coating times as 4, heat treatment time for 2 h, and the molar ratio of complexing agent and Ti(OC4HZ9)4 kept 1.5:1. The results showed that TiO2 modified film have good corrosion resistance. The result conformed that it is feasible to design the preparing conditions of TiO2 modified film by artificial neural network.展开更多
Cu/CeO2-ZrO2 catalysts for water-gas shift （WGS） reaction were prepared with co-precipitation method, and the influence of ZrO2 content on the catalytic structure and properties was investigated by the techniques of...Cu/CeO2-ZrO2 catalysts for water-gas shift （WGS） reaction were prepared with co-precipitation method, and the influence of ZrO2 content on the catalytic structure and properties was investigated by the techniques of N2 physical adsorption analysis, XRD and H2-TPR. The results indicate that the BET surface areas of the catalysts are increased in varying degrees due to the presence of ZrO2. With increasing ZrO2 content, the pore size distribution is centered on 1.9 nm. ZrO2 can efficiently restrain the growth of Cu crystal particles. The appropriate amount of ZrO2 in the Cu/CeO2 catalysts can help the catalyst keep better copper dispersion in the WGS reaction, which can lead to both higher catalytic activity and better thermal stability. When ZrO2 content is 10% （atom fraction）, Cu/CeO2-Zr02 catalyst reaches a CO conversion rate of 73.7% at the reaction temperature of 200℃.展开更多
This work studied CuO/CeO2-Co3O4 with wt% Ce:Co ratio 95:5 for selective CO oxidation with effect of? wt% Cu loading. The catalysts were prepared by co-precipitation. Characterizations of catalysts were carried out by...This work studied CuO/CeO2-Co3O4 with wt% Ce:Co ratio 95:5 for selective CO oxidation with effect of? wt% Cu loading. The catalysts were prepared by co-precipitation. Characterizations of catalysts were carried out by XRD and BET techniques. The results showed a good dispersion of CuO for 5 wt% Cu loading catalysts and showed high specific surface area of catalyst. For selective CO oxidation, both 5CuO and 30CuO catalysts could remove completely CO in the presence of excess hydrogen at 423 K and 20CuO could eliminate CO completely at 443 K. Moreover, considering the selectivity to CO oxidation, the 5CuO catalyst has shown the highest selectivity of 85% while the 30CuO catalyst obtains the selectivity of 65% at the reaction temperature of 423 K.展开更多
A novel fly ash cenospheres（FACs）-supported CeO2 composite（CeO2/FACs） was successfully synthesized by the modified pyrolysis process.The prepared composites were characterized by X-ray diffraction（XRD）, scanning...A novel fly ash cenospheres（FACs）-supported CeO2 composite（CeO2/FACs） was successfully synthesized by the modified pyrolysis process.The prepared composites were characterized by X-ray diffraction（XRD）, scanning electron microscopy（SEM）, X-ray photoelectron spectroscopy（XPS）, and diffuse reflection spectra（DRS） techniques.XRD results indicated that the CeO2 film coated on cenospheres was a face-centered cubic structure.SEM images confirmed that the CeO2 film was relatively compact.XPS results showed that Ce was present as both Ce4＋ and Ce3＋ oxidation states in CeO2 film coated on FACs substrate.The bandgap of the composite was narrower compared with the pure CeO2.The as-prepared material exhibited good photocatalytic activity for the decolorization of methylene blue（MB） under visible light irradiation, and the first-order reaction rate constant（k） of 0.0028 min–1 for CeO2/FACs composite was higher than 0.0015 min–1 of pure CeO2.The fact that they floated on water meant that CeO2/FACs composites were easily recovered from water by filtration after the reaction.The recycling test revealed that the composites were quite stable during the MB photocatalytic decolorization.The CeO2/ FACs catalyst was therefore promising for practical use in the degradation of pollutants or water cleanup.展开更多
基金Project supported by China Postdoctoral Science Foundation (20090450868)
文摘The laponite pillared by the CeO2 modified TiO2 (Ce-Ti-lap) were prepared by microwave intercalation reaction with laponite as the layered clay, tetrabutyl titanate and cerium chloride as the Ce-Ti composite pillaring agent, and characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and Brumauer-Emmett-Teller (BET) surface area. The photocatalytic activities of Ce-Ti-lap were investigated by the degradation of methyl orange (MO). The results showed that Ce and Ti could be introduced to...
基金the Hunan Provin-cial Natural Science Foundationthe Scientific Research Fund of Education Department and the Organic Chemistry Key Subject
文摘The binary composite photo-catalysts CeO2/ZiO2, ZrO2/ZiO2 and the ternary composite photo-catalysts H3PW12040-CeO2/TiO2, H3PW12O40-ZrO2/TiO2 were prepared by sol-gel method. The catalysts were characterized by thermogravimetric-differential thermal analysis （TG-DTA）, scanning electron microscopy （SEM） and X-ray diffraction （XRD）. The photocatalytic elimination of methanol was used as model reaction to evaluate the photocatalytic activity of the composite catalysts under ultraviolet light irradiation. The effects of doped content, activation temperature, time, initial concentration of methanol and gas flow rate on the catalytic activity were investigated. The results showed that after doping a certain amount of CeO2 and ZrO2, crystallization process of TiO2 was restrained, particles of catalysts are smaller and more uniform. Doping ZrO2 not only significantly improved the catalytic activity, but also increased thermal stability. Doping H3PW12O40 alSO enhanced the catalytic activity. The catalytic activities of binary and ternary composite photocatalysts were significantly higher than un-doped TiO2. The dynamics law of photocatalytic reaction over the binary CeO2/TiO2 and ZrO2/TiO2 catalysts has been studied. The activation energy 15.627 and 15.631 kJ/mol and pre-exponential factors 0.5176 and 0.9899 s^-1 over each corresponding catalyst were obtained. This reaction accords to the first order dynamics law.
基金Projected supported by the National Natural Science Foundation of China (20271028) and Tianjin Natural Science Foundation(033602511)
文摘CeO2 was synthesized via sol-gel process and used as supporter to prepare CuO/CeO2, Cu/CeO2 catalysts by impregnation method. The catalytic properties and characterization of CeO2, CuO/CeO2 and Cu/CeO2 catalysts were examined by means of a microreactor-GC system, HRTEM, XRD, TPR and XPS techniques. The results show that CuO has not catalytic activity and the activity of CeO2 is quite low for CO oxidation. However, the catalytic activity of CuO/CeO2 and Cu/ CeO2 catalysts increases significantly. Furthermore, the activity of CuO/CeO2 is higher than that of Cu/CeO2 catalysts.
文摘Elucidation of the CuOx-CeO2 interactions is of great interest and importance in understanding complex CuOx-CeO2 interfacial catalysis in various reactions. In the present work, we have investigated structures and catalytic activity in CO oxidation of CuOx species on CeO2 rods, cubes and polyhedra predominantly exposing {110}+{100}, {100} and {111} facets by the incipient wetness impregnation method with the lowest Cu loading of 0.025%. The structural evolution of CuOx species was found to depend on both the Cu loading and the CeO2 morphology. As the Cu loading increases, CuOx species are deposited preferentially on the surface defect of CeO2 and then aggregate and grow, accompanied by the formation of isolated Cu ions, CuOx clusters strongly/weakly interacting with the CeO2, highly dispersed Cu O nanoparticles, and large Cu O nanoparticles. The isolated Cu^+ species and CuOx clusters weakly interacting with the CeO2 were observed mainly on the O-terminated CeO2{100} facets. Meanwhile, more Cu(I) species are stabilized during CO reduction processes in CuOx/c-CeO2 catalysts than in CuOx/r-CeO2 and CuOx/p-CeO2 catalysts. The catalytic activities of various CuOx/CeO2 catalysts in CO oxidation vary with both the CuOx species and the CeO2 morphology. These results comprehensively elucidate the CuOx-CeO2 interactions and exemplify their morphology-dependence.
文摘The electrochemical behavior of vitamin C（ascorbic acid or AA） is investigated on the surface of a carbon-paste electrode modified with TiO2 nanoparticles and 2,2＇-（1,2 butanediylbis（nitriloethylidyne））-bis-hydroquinone（BBNBH）.The prepared modified electrode showed an efficient catalytic role in the electrochemical oxidation of AA,leading to remarkable decrease in oxidation overpotential and enhancement of the kinetics of the electrode reaction.This modified electrode exhibits well-separated oxidation peaks for AA and uric acid（UA）.The modified electrode is successfully applied for the accurate determination of AA in pharmaceutical preparations.
基金financially supported by the Natural Science Foundation of Guangdong Province (2022A1515012359)the National Natural Science Foundation of China (21902121)+1 种基金the STU Scientific Research Foundation for Talents (NTF21020)the 2020 Li Ka Shing Foundation Cross-Disciplinary Research Grant (2020LKSFG09A)。
文摘Nafion as a universal polymer ionomer was widely applied for nanocatalysts electrode preparation.However,the effect of Nafion on electrocatalytic performance was often overlooked,especially for CO_(2)electrolysis.Herein,the key roles of Nafion for CO_(2)RR were systematically studied on Cu nanoparticles(NPs)electrocatalyst.We found that Nafion modifier not only inhibit hydrogen evolution reaction(HER)by decreasing the accessibility of H_(2)O from electrolyte to Cu NPs,and increase the CO_(2)concentration at electrocatalyst interface for enhancing the CO_(2)mass transfer process,but also activate CO_(2)molecule by Lewis acid-base interaction between Nafion and CO_(2)to accelerate the formation of^(*)CO,which favor of C–C coupling for boosting C_(2)product generation.Owing to these features,the HER selectivity was suppressed from 40.6%to 16.8%on optimal Cu@Nafion electrode at-1.2 V versus reversible hydrogen electrode(RHE),and as high as 73.5%faradaic efficiencies(FEs)of C_(2)products were achieved at the same applied potential,which was 2.6 times higher than that on bare Cu electrode(~28.3%).In addition,Nafion also contributed to the long-term stability by hinder Cu NPs morphology reconstruction.Thus,this work provides insights into the impact of Nafion on electrocatalytic CO_(2)RR performance.
基金Project supported by National Natural Science Foundation of China(51505393)the National Key Research and Development Program of China(2017YFB0305905)
文摘With the service environment becoming more and more severe, WC-Co coatings are required to apply in high temperature wear condition. In the present study, the sliding wear tests of CeO_2 modified WC-12 Co coatings were conducted at temperature of 450, 550 and 650 ℃. The wear loss and friction coefficient were recorded. The morphologies of wear tracks were observed every 1 h to investigate the dynamic wear mechanisms. The results show that the volume wear loss decreases with temperature increasing.The lowest volume wear loss is obtained at the temperature of 650 ℃ due to oxide films generated in the process of wearing. The wear mechanism is different at the temperature of 450, 550 and 650 0 C. Micro cutting wear, abrasive wear and oxidation wear dominate the wear mechanism at 450, 550 and 650 ℃,respectively. Abrasive wear and oxidation wear are the wear mechanisms at various temperatures.
文摘A new technique for preparing TiO2 modified film on carbon steel was accomplished by electroless plating and sol-gel composite process. The artificial neural network was applied to optimize the preparing condition of TiO2 modified film. The optimized condition for forming TiO2 modified film on carbon steel was that NiP plating for 50 min, dip-coating times as 4, heat treatment time for 2 h, and the molar ratio of complexing agent and Ti(OC4HZ9)4 kept 1.5:1. The results showed that TiO2 modified film have good corrosion resistance. The result conformed that it is feasible to design the preparing conditions of TiO2 modified film by artificial neural network.
文摘Cu/CeO2-ZrO2 catalysts for water-gas shift （WGS） reaction were prepared with co-precipitation method, and the influence of ZrO2 content on the catalytic structure and properties was investigated by the techniques of N2 physical adsorption analysis, XRD and H2-TPR. The results indicate that the BET surface areas of the catalysts are increased in varying degrees due to the presence of ZrO2. With increasing ZrO2 content, the pore size distribution is centered on 1.9 nm. ZrO2 can efficiently restrain the growth of Cu crystal particles. The appropriate amount of ZrO2 in the Cu/CeO2 catalysts can help the catalyst keep better copper dispersion in the WGS reaction, which can lead to both higher catalytic activity and better thermal stability. When ZrO2 content is 10% （atom fraction）, Cu/CeO2-Zr02 catalyst reaches a CO conversion rate of 73.7% at the reaction temperature of 200℃.
文摘This work studied CuO/CeO2-Co3O4 with wt% Ce:Co ratio 95:5 for selective CO oxidation with effect of? wt% Cu loading. The catalysts were prepared by co-precipitation. Characterizations of catalysts were carried out by XRD and BET techniques. The results showed a good dispersion of CuO for 5 wt% Cu loading catalysts and showed high specific surface area of catalyst. For selective CO oxidation, both 5CuO and 30CuO catalysts could remove completely CO in the presence of excess hydrogen at 423 K and 20CuO could eliminate CO completely at 443 K. Moreover, considering the selectivity to CO oxidation, the 5CuO catalyst has shown the highest selectivity of 85% while the 30CuO catalyst obtains the selectivity of 65% at the reaction temperature of 423 K.
基金Project supported by National Natural Science Foundation of China(51308282)the China Postdoctoral Science Foundation Funded Project(2012M511254)the Natural Science Research Project of Jiangsu Province’s Education Department(12KJD610004)
文摘A novel fly ash cenospheres（FACs）-supported CeO2 composite（CeO2/FACs） was successfully synthesized by the modified pyrolysis process.The prepared composites were characterized by X-ray diffraction（XRD）, scanning electron microscopy（SEM）, X-ray photoelectron spectroscopy（XPS）, and diffuse reflection spectra（DRS） techniques.XRD results indicated that the CeO2 film coated on cenospheres was a face-centered cubic structure.SEM images confirmed that the CeO2 film was relatively compact.XPS results showed that Ce was present as both Ce4＋ and Ce3＋ oxidation states in CeO2 film coated on FACs substrate.The bandgap of the composite was narrower compared with the pure CeO2.The as-prepared material exhibited good photocatalytic activity for the decolorization of methylene blue（MB） under visible light irradiation, and the first-order reaction rate constant（k） of 0.0028 min–1 for CeO2/FACs composite was higher than 0.0015 min–1 of pure CeO2.The fact that they floated on water meant that CeO2/FACs composites were easily recovered from water by filtration after the reaction.The recycling test revealed that the composites were quite stable during the MB photocatalytic decolorization.The CeO2/ FACs catalyst was therefore promising for practical use in the degradation of pollutants or water cleanup.
