In this study,we used a simple impregnation method to prepare Fe-Ce-O_x catalysts and tested them regarding their low-temperature(200-300 ℃) selective catalytic reduction(SCR) of NO using NH_3.We investigated the eff...In this study,we used a simple impregnation method to prepare Fe-Ce-O_x catalysts and tested them regarding their low-temperature(200-300 ℃) selective catalytic reduction(SCR) of NO using NH_3.We investigated the effects of Fe/Ce molar ratio,the gas hourly space velocity(GHSV),the stability and SO_2/H_2O resistance of the catalysts.The results showed that the FeCe(1:6)O_x(Ce/Fe molar ratio is 1:6) catalyst,which has some ordered parallel channels,exhibited good SCR performance.The FeCe(1:6)O_x catalyst had the highest NO conversion with an activity of 94-99%at temperatures between 200 and300 ℃ at a space velocity of 28,800 h^(-1).The NO conversion for the FeCe(1:6)O_x catalyst also reached 80-98%between 200 and 300 ℃ at a space velocity of204,000h^(-1).In addition,the FeCe(1:6)O_x catalyst demonstrated good stability in a 10-h SCR reaction at200-300 ℃.Even in the presence of SO_2 and H_2O,the FeCe(1:6)O_x catalyst exhibited good SCR performance.展开更多
Niobium oxide as the promoter was doped in the V/WTi catalyst for the selective catalytic reduction（SCR）of NO.The results showed that the addition of Nb2O5could improve the SCR activity at low temperatures and the 6...Niobium oxide as the promoter was doped in the V/WTi catalyst for the selective catalytic reduction（SCR）of NO.The results showed that the addition of Nb2O5could improve the SCR activity at low temperatures and the 6 wt.%additive was an appropriate dosage.The enhanced reaction activity of adsorbed ammonia species and the improved dispersion of vanadium oxide might be the reasons for the elevation of SCR activity at low temperatures.The resistances to SO2of 3V6Nb/WTi catalyst at different temperatures were investigated.FTIR spectrum and TG-FTIR result indicated that the deposition of ammonium sulfate species was the main deactivation reason at low temperatures,which still exhibited the reactivity with NO above 200℃ on the catalyst surface.There was a synergistic effect among NH3,H2O and SO2that NH3and H2O both accelerated the catalyst deactivation in the presence of SO2at 175℃.The thermal treatment at 400℃ could regenerate the deactivated catalyst and get SCR activity recovered.The particle and monolith catalysts both kept stable NOxconversion at 225℃ with high concentration of H2O and SO2during the long time tests.展开更多
Temperature-programmed reduction (H2-TPR) was employed to quantitatively characterize the active oxygen species generated from a high Fe-loading Fe/ZSM-5 catalyst exposed to N2O at 250 ℃. Fe-O-Fe2+ dimer was determin...Temperature-programmed reduction (H2-TPR) was employed to quantitatively characterize the active oxygen species generated from a high Fe-loading Fe/ZSM-5 catalyst exposed to N2O at 250 ℃. Fe-O-Fe2+ dimer was determined as the active iron complex for N2O decomposition to produce the active oxygen. Reduction of Fe3+ to Fe2+ by H2 in the dimer and removal of OH- groups from Fe2+ dimer by heating Fe/ZSM-5 to 700 ℃ were the prerequisites for the formation of this active Fe complex. A linear correlation with a slope of 1.0 between the amount of Fe-O-Fe2+ and that of active oxygen species was observed. Maximum amount of active oxygen species can be generated by reducing Fe/ZSM-5 catalyst with H2 at the temperatures over 500 ℃ and then heating the resulting product in Ar to 700 ℃, followed by N2O exposure at 250 ℃.The ratio of the total number of oxygen atoms (Ode) deposited by interaction of Fe-O-Fe2+ with N2O to the amount of Fe-O-Fe2+ was 2. However, not all the deposited oxygen atoms were active oxygen (Oa); the ratio of Oa and Ode was 0.5. The iron dimer complex composing active oxygen is a five-atom ion Fe2O32+; the most probable structure is as follows:展开更多
Ce Zr O solid solution was prepared by four different methods, i.e., decomposition of nitrate, coprecipiation, hydroxysuainic acid sol gel as well as citrate sol gel, and characterized by using X ray powder diffr...Ce Zr O solid solution was prepared by four different methods, i.e., decomposition of nitrate, coprecipiation, hydroxysuainic acid sol gel as well as citrate sol gel, and characterized by using X ray powder diffraction, Raman and temperature programmed reduction. The phase composition and the reduction properties of Ce Zr O depend on the preparation method. A cubic Ce 0.5 Zr 0.5 O 2 solid solution can be obtained by using the sol gel method. The Ce Zr O solid solution prepared by using decomposition or coprecipiation was composed of cubic Ce 0.8 Zr 0.2 O 2 and tetragonal Ce 0.2 Zr 0.8 O 2 solid solution. The Ce Zr O solid solution prepared with different methods shows the different reduction properties owing to different phase composition. Results of differential thermal analysis and XRD show that Ce 0.5 Zr 0.5 O 2 solid solution is formed during the decomposition or combustion of the gel.展开更多
A new method called ultrasonic-assisted membrane reaction(UAMR)was reported for the fabrication of ceria-zirconia solid solution.A series of ceria-zirconia solid solutions with different Ce/Zr molar ratios were prepar...A new method called ultrasonic-assisted membrane reaction(UAMR)was reported for the fabrication of ceria-zirconia solid solution.A series of ceria-zirconia solid solutions with different Ce/Zr molar ratios were prepared by the UAMR method and characterized by Xray diffraction(XRD),N2 adsorption,hydrogen temperature-programmed reduction(H2-TPR),scanning electron microscope(SEM),and transmission electron microscopy(TEM)techniques.The UAMR method proved to be superior,especially when the Ce/Zr molar ratio was lower than 1,in fabricating ceria-zirconia solid solutions with large BET surface area,high oxygen storage capacity(OSC),and low reduction temperature.展开更多
K＋-doped Bi0.02Co was investigated as catalyst for N2O decomposition. It was found that the catalytic performance of the Bi0.02Co catalyst, which was prepared by coprecipitation method, can be effectively modified by...K＋-doped Bi0.02Co was investigated as catalyst for N2O decomposition. It was found that the catalytic performance of the Bi0.02Co catalyst, which was prepared by coprecipitation method, can be effectively modified by potassium cations via impregnation. The optimized K0.01Bi0.02Co catalyst exhibited much higher activity compared with Bi0.02Co and K0.01Co for the reaction in feed gas 0.2% N2O/Ar, irrespective of the presence or absence of impurity gas（volume fraction） 5%02, 2%H20, 0.12%NO and 10%CO2. Characterization of the catalysts with H2 temperature programmed reduction（H2-TPR） and O2 temperature programmed desorption（O2-TPD） indicate that the Co--O bond in Bi0.02Co was weakened by the K＋ doping, and hence the K0.01Bi0.02Co catalyst has much higher turnover frequency（TOF） than CO3O4 spinel and Bi0.02Co for the reaction.展开更多
基金supported by the National Natural Science Foundation of China (No.21206108)Tianjin Municipal Science and Technology Commission (No.14JCYBJC21200)
文摘In this study,we used a simple impregnation method to prepare Fe-Ce-O_x catalysts and tested them regarding their low-temperature(200-300 ℃) selective catalytic reduction(SCR) of NO using NH_3.We investigated the effects of Fe/Ce molar ratio,the gas hourly space velocity(GHSV),the stability and SO_2/H_2O resistance of the catalysts.The results showed that the FeCe(1:6)O_x(Ce/Fe molar ratio is 1:6) catalyst,which has some ordered parallel channels,exhibited good SCR performance.The FeCe(1:6)O_x catalyst had the highest NO conversion with an activity of 94-99%at temperatures between 200 and300 ℃ at a space velocity of 28,800 h^(-1).The NO conversion for the FeCe(1:6)O_x catalyst also reached 80-98%between 200 and 300 ℃ at a space velocity of204,000h^(-1).In addition,the FeCe(1:6)O_x catalyst demonstrated good stability in a 10-h SCR reaction at200-300 ℃.Even in the presence of SO_2 and H_2O,the FeCe(1:6)O_x catalyst exhibited good SCR performance.
基金supported by the Policy-induced Project of Jiangsu Province for the Industry-University-Research Cooperation (No. BY2015070-21)the project was also supported by National Science and Technology Ministry (No. 2015BAA05B01)the Natural Science Fund Program of Jiangsu Province (No. BK20150749)
文摘Niobium oxide as the promoter was doped in the V/WTi catalyst for the selective catalytic reduction（SCR）of NO.The results showed that the addition of Nb2O5could improve the SCR activity at low temperatures and the 6 wt.%additive was an appropriate dosage.The enhanced reaction activity of adsorbed ammonia species and the improved dispersion of vanadium oxide might be the reasons for the elevation of SCR activity at low temperatures.The resistances to SO2of 3V6Nb/WTi catalyst at different temperatures were investigated.FTIR spectrum and TG-FTIR result indicated that the deposition of ammonium sulfate species was the main deactivation reason at low temperatures,which still exhibited the reactivity with NO above 200℃ on the catalyst surface.There was a synergistic effect among NH3,H2O and SO2that NH3and H2O both accelerated the catalyst deactivation in the presence of SO2at 175℃.The thermal treatment at 400℃ could regenerate the deactivated catalyst and get SCR activity recovered.The particle and monolith catalysts both kept stable NOxconversion at 225℃ with high concentration of H2O and SO2during the long time tests.
文摘Temperature-programmed reduction (H2-TPR) was employed to quantitatively characterize the active oxygen species generated from a high Fe-loading Fe/ZSM-5 catalyst exposed to N2O at 250 ℃. Fe-O-Fe2+ dimer was determined as the active iron complex for N2O decomposition to produce the active oxygen. Reduction of Fe3+ to Fe2+ by H2 in the dimer and removal of OH- groups from Fe2+ dimer by heating Fe/ZSM-5 to 700 ℃ were the prerequisites for the formation of this active Fe complex. A linear correlation with a slope of 1.0 between the amount of Fe-O-Fe2+ and that of active oxygen species was observed. Maximum amount of active oxygen species can be generated by reducing Fe/ZSM-5 catalyst with H2 at the temperatures over 500 ℃ and then heating the resulting product in Ar to 700 ℃, followed by N2O exposure at 250 ℃.The ratio of the total number of oxygen atoms (Ode) deposited by interaction of Fe-O-Fe2+ with N2O to the amount of Fe-O-Fe2+ was 2. However, not all the deposited oxygen atoms were active oxygen (Oa); the ratio of Oa and Ode was 0.5. The iron dimer complex composing active oxygen is a five-atom ion Fe2O32+; the most probable structure is as follows:
文摘Ce Zr O solid solution was prepared by four different methods, i.e., decomposition of nitrate, coprecipiation, hydroxysuainic acid sol gel as well as citrate sol gel, and characterized by using X ray powder diffraction, Raman and temperature programmed reduction. The phase composition and the reduction properties of Ce Zr O depend on the preparation method. A cubic Ce 0.5 Zr 0.5 O 2 solid solution can be obtained by using the sol gel method. The Ce Zr O solid solution prepared by using decomposition or coprecipiation was composed of cubic Ce 0.8 Zr 0.2 O 2 and tetragonal Ce 0.2 Zr 0.8 O 2 solid solution. The Ce Zr O solid solution prepared with different methods shows the different reduction properties owing to different phase composition. Results of differential thermal analysis and XRD show that Ce 0.5 Zr 0.5 O 2 solid solution is formed during the decomposition or combustion of the gel.
基金the National High-Tech Research and Development Program of China(Grant No.2006AA06Z347)the National Natural Science Foundation of China(Grant Nos.20877006 and 20833011).
文摘A new method called ultrasonic-assisted membrane reaction(UAMR)was reported for the fabrication of ceria-zirconia solid solution.A series of ceria-zirconia solid solutions with different Ce/Zr molar ratios were prepared by the UAMR method and characterized by Xray diffraction(XRD),N2 adsorption,hydrogen temperature-programmed reduction(H2-TPR),scanning electron microscope(SEM),and transmission electron microscopy(TEM)techniques.The UAMR method proved to be superior,especially when the Ce/Zr molar ratio was lower than 1,in fabricating ceria-zirconia solid solutions with large BET surface area,high oxygen storage capacity(OSC),and low reduction temperature.
基金Supported by the State Hi-tech Research and Development Project of the Ministry of Science and Technology of China（No. 2013AA030705） and the National Natural Science Foundation of China（Nos. 21177016, 21277019）.
文摘K＋-doped Bi0.02Co was investigated as catalyst for N2O decomposition. It was found that the catalytic performance of the Bi0.02Co catalyst, which was prepared by coprecipitation method, can be effectively modified by potassium cations via impregnation. The optimized K0.01Bi0.02Co catalyst exhibited much higher activity compared with Bi0.02Co and K0.01Co for the reaction in feed gas 0.2% N2O/Ar, irrespective of the presence or absence of impurity gas（volume fraction） 5%02, 2%H20, 0.12%NO and 10%CO2. Characterization of the catalysts with H2 temperature programmed reduction（H2-TPR） and O2 temperature programmed desorption（O2-TPD） indicate that the Co--O bond in Bi0.02Co was weakened by the K＋ doping, and hence the K0.01Bi0.02Co catalyst has much higher turnover frequency（TOF） than CO3O4 spinel and Bi0.02Co for the reaction.
