CeO2-Co3O4 catalysts for low-temperature CO oxidation were prepared by a co-precipitation method. In combination with the characterization methods of N2 adsorption/desorption, XRD, temperature-programmed reduction （...CeO2-Co3O4 catalysts for low-temperature CO oxidation were prepared by a co-precipitation method. In combination with the characterization methods of N2 adsorption/desorption, XRD, temperature-programmed reduction （TPR）, and FT-IR, the influence of the cerium content on the catalytic performance of CeO2-Co3O4 was investigated. The results indicate that the prepared CeO2-Co3O4 catalysts exhibit a better activity than that of pure CeO2 or pure Co3O4. The catalyst with the Ce/Co atomic ratio 1 ： 16 exhibits the best activity, which converts 77% of CO at room temperature and completely oxidizes CO at 45 ℃.展开更多
In order to develop a catalyst with high activity for catalytic wet oxidation （CWO） process at room temperature and atmospheric pressure, Fe2O3-CeO2-TiO2/γ-Al2O3 catalyst was prepared by consecutive impregnation me...In order to develop a catalyst with high activity for catalytic wet oxidation （CWO） process at room temperature and atmospheric pressure, Fe2O3-CeO2-TiO2/γ-Al2O3 catalyst was prepared by consecutive impregnation method and the prepared parameters were optimized. The structure of the catalyst was characterized by BET, XRF, SEM and XPS technologies, and the actual wastewater was used to investigate the catalytic activity of Fe2O3-CeO2-TiO2/γ-Al2O3 in CWO process. The experimental results showed that the prepared catalyst exhibited good catalytic activity when the doping amount of Ti was 1.0 wt% （the weight ratio of Ti to carriers）, and the middle product, Fe2O3-CeO2-TiO2/γ-Al2O3, was calcined in 450℃ for 2 h. The CWO experiment for treating actual dye wastewater indicated that the COD, color and TOC of actual wastewater were decreased by 62.23%, 50.12% and 41.26% in 3 h, respectively, and the ratio of BOD5/COD was increased from 0.19 to 0.30.展开更多
The Ni-Al2O3 catalyst was prepared by the mechanochemical method in combination with a planetary ballmilling machine.Effect of milling time on the crystal structure,the reduction characteristics and the catalytic perf...The Ni-Al2O3 catalyst was prepared by the mechanochemical method in combination with a planetary ballmilling machine.Effect of milling time on the crystal structure,the reduction characteristics and the catalytic performance of Ni-Al2O3 catalyst for hydrogenation of 1,4-butynediol to produce 1,4-butenediol were investigated.The catalysts were characterized by PSD,EDX,XRD,H2-TPR,BET,TEM,and NH3-TPD methods.Results showed that the MCt2.5 catalyst treated at a ball milling time of 2.5 h could form a smallest particle size of 191.0 nm.The evaluation experiments revealed that the activity of the prepared catalyst increased at first and then reached a constant value with the extension of ballmilling time.The BYD conversion,BED selectivity and yield on the MCt2.5 catalyst reached 35.63%,33.48%and 32.46%,respectively,which were higher than those obtained by other samples.The excellent performance of MCt2.5 sample is mainly related to the following three reasons from characterization results.Firstly,it has a smallest particle size of 191.0 nm;and then,the surface acidity(in terms of strong acids)of the catalyst was weaker than other catalysts;and eventually,the loading amount(23.84%)of the active component Ni exceeded the theoretical value(20%).展开更多
Alkali-promoted Pd/Al2O3 catalysts exhibit much higher activities in NO decomposition than Pd/Al2O3. FTIR study shows that on the alkali promoted catalyst.nitric oxide exists on the surface mainly in negatively charge...Alkali-promoted Pd/Al2O3 catalysts exhibit much higher activities in NO decomposition than Pd/Al2O3. FTIR study shows that on the alkali promoted catalyst.nitric oxide exists on the surface mainly in negatively charged form(NO-)at high temperatures.which is consistent with the activity improvement.展开更多
A series of polymer- supported Pd -Fe2O3 composite catalysts were prepared and their hydrogenation property mas investigated. It was found that the above catalysts have good catalytic hydrogenation activity for carbon...A series of polymer- supported Pd -Fe2O3 composite catalysts were prepared and their hydrogenation property mas investigated. It was found that the above catalysts have good catalytic hydrogenation activity for carbon - carbon double bonds systems and reusability. Furthermore, XPS and IR spectra shouted that active component in the composite catalysts is atomic Pd(0). An addition of a small amount of Fe2O3 has a promotive action upon hydrogenation activity of the catalysts, which indicated that there are some strong interactions (electron transfer) between Pd(0) and Fe(Ⅲ) species. Based on these results, a possible catalytic hydrogenation mechanism was also suggested.展开更多
The effects of ceria and zirconium oxides additions to alumina-supported palladium catalysts on methane combustion behavior were investigated. The structure and TPR/TPO properties were studied by XRD, TPR, TPO techniq...The effects of ceria and zirconium oxides additions to alumina-supported palladium catalysts on methane combustion behavior were investigated. The structure and TPR/TPO properties were studied by XRD, TPR, TPO techniques. The results show that the addition of Ce-Zr oxides improves the thermal stability of alumina and PdO. The Pd/Ce0.2Zr0.8/Al2O3 exhibits the highest activity and thermal stability for methane combustion.展开更多
The microwave radiation method was introduced to prepare the Fe_2O_3/SO solid superacid.Its structure and properties were investigated by means of X-ray diffraction and infrared spectrum analyses as well as measuremen...The microwave radiation method was introduced to prepare the Fe_2O_3/SO solid superacid.Its structure and properties were investigated by means of X-ray diffraction and infrared spectrum analyses as well as measurement of magnetic susceptibility and rate of esterification. The structure of the superacids prepared in microwave field can be crystalline or non-crystalline, the latter has not been reported yet in literatures. Comparing with the traditional superacid, the non-crystalline Fe2O3/SO superacid prepared in microwave field has the highest magnetic susceptibility and catalytic activity. The di-coordination of Fe2O3 and SO and the S=O bi-bond were reinforced by microwave radiation, which is favorable for increasing the acid intensity of the Fe2O3/SO catalyst展开更多
基金supported by Climate Change Response Project (NRF-2019M1A2A2065612)Brainlink Project (NRF-2022H1D3A3A01081140) funded by the Ministry of Science and ICT of Korea via National Research Foundation+1 种基金by research funds from Hanhwa Solutions Chemicals (2.220990.01) and UNIST (1.190013.01)supported by the Institute for Basic Science (IBS-R019-D1)。
文摘CeO2-Co3O4 catalysts for low-temperature CO oxidation were prepared by a co-precipitation method. In combination with the characterization methods of N2 adsorption/desorption, XRD, temperature-programmed reduction （TPR）, and FT-IR, the influence of the cerium content on the catalytic performance of CeO2-Co3O4 was investigated. The results indicate that the prepared CeO2-Co3O4 catalysts exhibit a better activity than that of pure CeO2 or pure Co3O4. The catalyst with the Ce/Co atomic ratio 1 ： 16 exhibits the best activity, which converts 77% of CO at room temperature and completely oxidizes CO at 45 ℃.
基金The National Basic Research Program (973) of China (No. 2004CB418505) the Foundation for Excellent Youth of HeilongjiangProvince
文摘In order to develop a catalyst with high activity for catalytic wet oxidation （CWO） process at room temperature and atmospheric pressure, Fe2O3-CeO2-TiO2/γ-Al2O3 catalyst was prepared by consecutive impregnation method and the prepared parameters were optimized. The structure of the catalyst was characterized by BET, XRF, SEM and XPS technologies, and the actual wastewater was used to investigate the catalytic activity of Fe2O3-CeO2-TiO2/γ-Al2O3 in CWO process. The experimental results showed that the prepared catalyst exhibited good catalytic activity when the doping amount of Ti was 1.0 wt% （the weight ratio of Ti to carriers）, and the middle product, Fe2O3-CeO2-TiO2/γ-Al2O3, was calcined in 450℃ for 2 h. The CWO experiment for treating actual dye wastewater indicated that the COD, color and TOC of actual wastewater were decreased by 62.23%, 50.12% and 41.26% in 3 h, respectively, and the ratio of BOD5/COD was increased from 0.19 to 0.30.
基金This work has been supported by the Xinjiang Uygur Autonomous Region Key R&D Program(2017B02012)the Xinjiang University Natural Science Foundation Project(BS160221).
文摘The Ni-Al2O3 catalyst was prepared by the mechanochemical method in combination with a planetary ballmilling machine.Effect of milling time on the crystal structure,the reduction characteristics and the catalytic performance of Ni-Al2O3 catalyst for hydrogenation of 1,4-butynediol to produce 1,4-butenediol were investigated.The catalysts were characterized by PSD,EDX,XRD,H2-TPR,BET,TEM,and NH3-TPD methods.Results showed that the MCt2.5 catalyst treated at a ball milling time of 2.5 h could form a smallest particle size of 191.0 nm.The evaluation experiments revealed that the activity of the prepared catalyst increased at first and then reached a constant value with the extension of ballmilling time.The BYD conversion,BED selectivity and yield on the MCt2.5 catalyst reached 35.63%,33.48%and 32.46%,respectively,which were higher than those obtained by other samples.The excellent performance of MCt2.5 sample is mainly related to the following three reasons from characterization results.Firstly,it has a smallest particle size of 191.0 nm;and then,the surface acidity(in terms of strong acids)of the catalyst was weaker than other catalysts;and eventually,the loading amount(23.84%)of the active component Ni exceeded the theoretical value(20%).
文摘Alkali-promoted Pd/Al2O3 catalysts exhibit much higher activities in NO decomposition than Pd/Al2O3. FTIR study shows that on the alkali promoted catalyst.nitric oxide exists on the surface mainly in negatively charged form(NO-)at high temperatures.which is consistent with the activity improvement.
文摘A series of polymer- supported Pd -Fe2O3 composite catalysts were prepared and their hydrogenation property mas investigated. It was found that the above catalysts have good catalytic hydrogenation activity for carbon - carbon double bonds systems and reusability. Furthermore, XPS and IR spectra shouted that active component in the composite catalysts is atomic Pd(0). An addition of a small amount of Fe2O3 has a promotive action upon hydrogenation activity of the catalysts, which indicated that there are some strong interactions (electron transfer) between Pd(0) and Fe(Ⅲ) species. Based on these results, a possible catalytic hydrogenation mechanism was also suggested.
文摘The effects of ceria and zirconium oxides additions to alumina-supported palladium catalysts on methane combustion behavior were investigated. The structure and TPR/TPO properties were studied by XRD, TPR, TPO techniques. The results show that the addition of Ce-Zr oxides improves the thermal stability of alumina and PdO. The Pd/Ce0.2Zr0.8/Al2O3 exhibits the highest activity and thermal stability for methane combustion.
文摘The microwave radiation method was introduced to prepare the Fe_2O_3/SO solid superacid.Its structure and properties were investigated by means of X-ray diffraction and infrared spectrum analyses as well as measurement of magnetic susceptibility and rate of esterification. The structure of the superacids prepared in microwave field can be crystalline or non-crystalline, the latter has not been reported yet in literatures. Comparing with the traditional superacid, the non-crystalline Fe2O3/SO superacid prepared in microwave field has the highest magnetic susceptibility and catalytic activity. The di-coordination of Fe2O3 and SO and the S=O bi-bond were reinforced by microwave radiation, which is favorable for increasing the acid intensity of the Fe2O3/SO catalyst
