The immobilization of catalysts on supporting substrates for the removal of organic pollutants is a crucial strategy for mitigating catalyst loss during wastewater treatment.This study presented a rapid and cost-effec...The immobilization of catalysts on supporting substrates for the removal of organic pollutants is a crucial strategy for mitigating catalyst loss during wastewater treatment.This study presented a rapid and cost-effective direct heating method for synthesizing MnO2 nanoflowers on coil substrates for the removal of organic pollutants.Traditional methods often require high power,expensive equipment,and long synthesis times.In contrast,the direct heating approach successfully synthesized MnO2 nanoflowers in just 10 min with a heating power of approximately 40 W·h after the heating power and duration were optimized.These nanoflowers effectively degraded 99%Rhodamine B in 60 min with consistent repeatability.The catalytic mechanisms are attributed to crystal defects in MnO2,which generate electrons to produce H2O2.Mn2+ions in the acidic solution further dissociate H2O2 molecules into hydroxyl radicals(·OH).The high efficiency of this synthesis method and the excellent reusability of MnO2 nanoflowers highlight their potential as a promising solution for the development of supporting MnO2 catalysts for organic dye removal applications.展开更多
In this paper, KMnO4 was used to pre-treat Co3 Fe-layered double hydroxides(LDH) precursor to prepare MnO2 decorated Co3Fe1Ox catalyst. The toluene oxidation performance of the catalyst was investigated systematically...In this paper, KMnO4 was used to pre-treat Co3 Fe-layered double hydroxides(LDH) precursor to prepare MnO2 decorated Co3Fe1Ox catalyst. The toluene oxidation performance of the catalyst was investigated systematically. The optimized 0.1 Mn CF-LDO catalyst exhibited the best catalytic performance, and the temperatures of 50% and 90% toluene conversion( T50 and T90) were 218 and 243 ℃, respectively. The apparent activation energy( Ea) was 31.6 k J/mol. The characterization results showed that the pre-redox reaction by KMnO4 could increase the specific surface area, Co^3+ species amount and oxygen defect concentration of the catalyst, which are the main reason of the improved toluene catalytic activity. Besides, this method was also applied to enhance toluene oxidation of iron mesh based monolithic catalyst. The 0.1 Mn CF-LDO/Iron mesh(IM) catalyst showed a 90% toluene conversion at around 316 ℃ which was much lower than that of without MnO2 addition(359 ℃). In addition, the water resistant of all the catalysts was studied as well, all the samples showed relatively good water resistance. The toluene conversion still remained to be over > 80% even in the presence of 10 vol.% water vapor.展开更多
A λ-MnO2 supported Pt nanocatalyst（5 wt.% Pt/λ-MnO2） was synthesized using a facile approach.X-ray diffraction（XRD）, X-ray photoelectron spectroscopy（XPS）, scanning electronic microscope（SEM）, transmission e...A λ-MnO2 supported Pt nanocatalyst（5 wt.% Pt/λ-MnO2） was synthesized using a facile approach.X-ray diffraction（XRD）, X-ray photoelectron spectroscopy（XPS）, scanning electronic microscope（SEM）, transmission electron microscopy（TEM）, and energy disperse spectroscopy（EDS） were used for catalyst structure and morphology characterization, which showed that the metallic Pt particles were attached on a λ-MnO2 surface through the interaction between Pt and λ-MnO2.Cyclic voltammetry（CV） was used to test the catalytic activity of Pt/λ-MnO2 toward methanol oxidation, which showed that Pt/λ-MnO2 catalyst has much higher catalytic activity than baseline Pt/C catalyst.展开更多
Carbonate-modified metal-support interfaces allow Ru/MnCO_(3) catalyst to exhibit over 99% selectivity,great specific activity and long-term anti-CO poisoning stability in atmospheric CO_(2) methanation.As a contrast,...Carbonate-modified metal-support interfaces allow Ru/MnCO_(3) catalyst to exhibit over 99% selectivity,great specific activity and long-term anti-CO poisoning stability in atmospheric CO_(2) methanation.As a contrast,Ru/MnO catalyst with metal-oxide interfaces prefers reverse water-gas shift rather than methanation route,along with a remarkably lower activity and a less than 15% CH_(4) selectivity.The carbonatemodified interfaces are found to stabilize the Ru species and activate CO_(2) and H_(2) molecules.Ru-CO^(4) species are identified as the reaction intermediates steadily formed from CO_(2) dissociation,which show moderate adsorption strength and high reactivity in further hydrogenation to CH_(4),Furthermore,carbonates of Ru/MnCO_(3) are found to be consumed by hydrogenation to form CH_(4) and replenished by exchange with CO_(2),which are in a dynamic equilibrium during the reaction.Modification with surface carbonates is proved as an efficient strategy to endow metal-support interfaces of Ru-based catalysts with unique catalytic functions for selective CO_(2) hydrogenation.展开更多
The preparation of immobilizing-catalysts for decomposing ozone by using dipping method was studied. XRD, XPS and TEM were used to characterize the catalysts. The three kinds of catalysts were selected preferentially,...The preparation of immobilizing-catalysts for decomposing ozone by using dipping method was studied. XRD, XPS and TEM were used to characterize the catalysts. The three kinds of catalysts were selected preferentially, and their catalytic activities were investigated. The results showed that the catalyst with activated carbon dipping acetate(active components are Mn:Cu=3:2, active component proportion in catalyst is 15%, calcination temperature is 200℃) has the best catalytic activity for ozone decomposing. One gram of catalyst can decompose 17.6 g ozone at initial ozone concentration of 2.5 g/m 3 and the residence time in reactor of 0.1 s. The experimental results also indicated that humidity of reaction system had negative effect on catalytic activity.展开更多
基金supported by Ministry of Higher Education,Malaysia,through the Fundamental Research Grant Scheme(FRGS)(Grant No.FRGS/1/2020/TK0/USM/02/27)。
文摘The immobilization of catalysts on supporting substrates for the removal of organic pollutants is a crucial strategy for mitigating catalyst loss during wastewater treatment.This study presented a rapid and cost-effective direct heating method for synthesizing MnO2 nanoflowers on coil substrates for the removal of organic pollutants.Traditional methods often require high power,expensive equipment,and long synthesis times.In contrast,the direct heating approach successfully synthesized MnO2 nanoflowers in just 10 min with a heating power of approximately 40 W·h after the heating power and duration were optimized.These nanoflowers effectively degraded 99%Rhodamine B in 60 min with consistent repeatability.The catalytic mechanisms are attributed to crystal defects in MnO2,which generate electrons to produce H2O2.Mn2+ions in the acidic solution further dissociate H2O2 molecules into hydroxyl radicals(·OH).The high efficiency of this synthesis method and the excellent reusability of MnO2 nanoflowers highlight their potential as a promising solution for the development of supporting MnO2 catalysts for organic dye removal applications.
基金supported by the Fundamental Research Funds for the Central Universities (No. 2019JQ03015)the National Natural Science Foundation of China (No. U1810209)+1 种基金the International Science and Technology Cooperation Project of Bingtuan (No. 2018BC002)the Beijing Municipal Educa-tion Commission for their financial support through Innova-tive Transdisciplinary Program “Ecological Restoration Engi-neering”。
文摘In this paper, KMnO4 was used to pre-treat Co3 Fe-layered double hydroxides(LDH) precursor to prepare MnO2 decorated Co3Fe1Ox catalyst. The toluene oxidation performance of the catalyst was investigated systematically. The optimized 0.1 Mn CF-LDO catalyst exhibited the best catalytic performance, and the temperatures of 50% and 90% toluene conversion( T50 and T90) were 218 and 243 ℃, respectively. The apparent activation energy( Ea) was 31.6 k J/mol. The characterization results showed that the pre-redox reaction by KMnO4 could increase the specific surface area, Co^3+ species amount and oxygen defect concentration of the catalyst, which are the main reason of the improved toluene catalytic activity. Besides, this method was also applied to enhance toluene oxidation of iron mesh based monolithic catalyst. The 0.1 Mn CF-LDO/Iron mesh(IM) catalyst showed a 90% toluene conversion at around 316 ℃ which was much lower than that of without MnO2 addition(359 ℃). In addition, the water resistant of all the catalysts was studied as well, all the samples showed relatively good water resistance. The toluene conversion still remained to be over > 80% even in the presence of 10 vol.% water vapor.
基金supported by the Funding Project for Academic Human Resources Development in Institutions of Higher Learning under the Jurisdiction of Beijing Municipality, Beijing Natural Science Foundation (No. 207001)the Major State Basic Research and Development Program of China (No. 2002CB211807)
文摘A λ-MnO2 supported Pt nanocatalyst（5 wt.% Pt/λ-MnO2） was synthesized using a facile approach.X-ray diffraction（XRD）, X-ray photoelectron spectroscopy（XPS）, scanning electronic microscope（SEM）, transmission electron microscopy（TEM）, and energy disperse spectroscopy（EDS） were used for catalyst structure and morphology characterization, which showed that the metallic Pt particles were attached on a λ-MnO2 surface through the interaction between Pt and λ-MnO2.Cyclic voltammetry（CV） was used to test the catalytic activity of Pt/λ-MnO2 toward methanol oxidation, which showed that Pt/λ-MnO2 catalyst has much higher catalytic activity than baseline Pt/C catalyst.
基金the National Key R&D Program of China(2018YFE0122600)the National Natural Science Foundation of China(21802070).
文摘Carbonate-modified metal-support interfaces allow Ru/MnCO_(3) catalyst to exhibit over 99% selectivity,great specific activity and long-term anti-CO poisoning stability in atmospheric CO_(2) methanation.As a contrast,Ru/MnO catalyst with metal-oxide interfaces prefers reverse water-gas shift rather than methanation route,along with a remarkably lower activity and a less than 15% CH_(4) selectivity.The carbonatemodified interfaces are found to stabilize the Ru species and activate CO_(2) and H_(2) molecules.Ru-CO^(4) species are identified as the reaction intermediates steadily formed from CO_(2) dissociation,which show moderate adsorption strength and high reactivity in further hydrogenation to CH_(4),Furthermore,carbonates of Ru/MnCO_(3) are found to be consumed by hydrogenation to form CH_(4) and replenished by exchange with CO_(2),which are in a dynamic equilibrium during the reaction.Modification with surface carbonates is proved as an efficient strategy to endow metal-support interfaces of Ru-based catalysts with unique catalytic functions for selective CO_(2) hydrogenation.
文摘The preparation of immobilizing-catalysts for decomposing ozone by using dipping method was studied. XRD, XPS and TEM were used to characterize the catalysts. The three kinds of catalysts were selected preferentially, and their catalytic activities were investigated. The results showed that the catalyst with activated carbon dipping acetate(active components are Mn:Cu=3:2, active component proportion in catalyst is 15%, calcination temperature is 200℃) has the best catalytic activity for ozone decomposing. One gram of catalyst can decompose 17.6 g ozone at initial ozone concentration of 2.5 g/m 3 and the residence time in reactor of 0.1 s. The experimental results also indicated that humidity of reaction system had negative effect on catalytic activity.
