The catalytic oxidation of ethyl acetate(EA)was studied over CuO/CeO_(2) catalysts which were prepared by ball milling with different precursors(copper oxide,cerium acetate,cerium dioxide,copper acetate and cerium hyd...The catalytic oxidation of ethyl acetate(EA)was studied over CuO/CeO_(2) catalysts which were prepared by ball milling with different precursors(copper oxide,cerium acetate,cerium dioxide,copper acetate and cerium hydroxide).The CuO/CeO_(2) catalyst(O-A)prepared with copper oxide and cerium acetate as precursors shows very high catalytic activity that 100%EA conversion is achieved at low temperature of 220℃.It is found that specific surface area(112.8 m^(2)/g),particle size of CuO(3.5 nm)and proportion of oxygen vacancies are prominent on the O-A catalyst.Oxygen vacancies in CeO_(2)support are beneficial to enhancing the adsorption and activation of the oxygen.More finely dispersed CuO particles and oxygen vacancies which are derived from the synergistic interaction of Cu-Ce species play an important role in the catalytic oxidation of EA.展开更多
In this paper,the CuO-CeO_(2) catalyst was prepared by a direct solvothermal method.The effects of different copper salt precursors(copper nitrate,copper acetate,copper sulfate) on the catalytic performa nce of the pr...In this paper,the CuO-CeO_(2) catalyst was prepared by a direct solvothermal method.The effects of different copper salt precursors(copper nitrate,copper acetate,copper sulfate) on the catalytic performa nce of the prepared catalyst fo r CO oxidation were investigated.The physical and chemical properties of the prepared catalysts were characterized by X-ray diffraction(XRD),Raman spectroscopy,N_(2)physical adsorption,inductively coupled plasma-atomic emission spectrometry(ICP-AES),X-ray photoelectron spectroscopy(XPS),temperature-programmed desorption analysis of CO(CO-TPD),in-situ diffuse reflectance infrared Fourier transform spectroscopy(DRIFTs),and temperature-programmed reduction with H_(2)(H_(2)-TPR).The results show that the CuO-CeO_(2)catalyst prepared with copper acetate as precursor(CC-A) exhibits the best catalytic activity for CO oxidation at low temperatures,with T50and T90values of 62 and 78℃ respectively,which is mainly attributed to its large specific surface area,pore volume,CO adsorption capacity,and large amount and strong reactivity of surface oxygen.However,the CuO-CeO_(2) catalyst prepared with copper nitrate as precursor(CC-N) displays better stability and resistance to water or CO_(2) poisoning than CC-A.展开更多
CuO-CeO_(2)nanocomposite as a green recyclable catalyst,catalyzed amination of aryl halides with aqueous am-monia in water.This catalyst can be easily recovered by simple filtration and recycled up to 5 consecutive ru...CuO-CeO_(2)nanocomposite as a green recyclable catalyst,catalyzed amination of aryl halides with aqueous am-monia in water.This catalyst can be easily recovered by simple filtration and recycled up to 5 consecutive runs with consistent activity.The procedure provides some advantages such as simple work-up,clean procedure,relatively short reaction times and high yields of the products.展开更多
The performances of CO selective oxidation in hydrogen-rich gas over fourcatalytic systems of CuO/ZrO_2, CuO/MnO_2, CuO/CoO and CuO/CeO_2 were compared. The reducibility ofthese catalysts and the effect of CuO and CeO...The performances of CO selective oxidation in hydrogen-rich gas over fourcatalytic systems of CuO/ZrO_2, CuO/MnO_2, CuO/CoO and CuO/CeO_2 were compared. The reducibility ofthese catalysts and the effect of CuO and CeO_2 molar ratio of CuO/CeO_2 catalysts on the activityof selective CO oxidation are investigated by XRD and TPR methods. The results show that thecatalysts with the exception of CuO/ZrO_2 have the interactions between CuO and CoO, CeO_2 or MnO_2,which result in a decrease in the reduction temperature. Among the catalysts studied, CuO/ZrO_2catalyst shows the lowest catalytic activity while CuO/CeO_2 catalyst exhibits the best catalyticperformance. The CuO(10%)/CeO_2 catalyst attains the highest CO conversion and selectivity at 140and 160℃. The addition of 9% H_2O in the reactant feed decreases the activity of CuO/CeO_2 catalystbut increases its CO selectivity.展开更多
基金Project supported by the Shanghai Rising-Star Program(21QA1406600)the NSFC-Zhejiang Joint Fund for Integration of Industrialization and Diversification(U1809214)Zhoushan City Science&Technology Research Project(2019C21012).
文摘The catalytic oxidation of ethyl acetate(EA)was studied over CuO/CeO_(2) catalysts which were prepared by ball milling with different precursors(copper oxide,cerium acetate,cerium dioxide,copper acetate and cerium hydroxide).The CuO/CeO_(2) catalyst(O-A)prepared with copper oxide and cerium acetate as precursors shows very high catalytic activity that 100%EA conversion is achieved at low temperature of 220℃.It is found that specific surface area(112.8 m^(2)/g),particle size of CuO(3.5 nm)and proportion of oxygen vacancies are prominent on the O-A catalyst.Oxygen vacancies in CeO_(2)support are beneficial to enhancing the adsorption and activation of the oxygen.More finely dispersed CuO particles and oxygen vacancies which are derived from the synergistic interaction of Cu-Ce species play an important role in the catalytic oxidation of EA.
基金Project supported by the National Natural Science Foundation of China (21273150)。
文摘In this paper,the CuO-CeO_(2) catalyst was prepared by a direct solvothermal method.The effects of different copper salt precursors(copper nitrate,copper acetate,copper sulfate) on the catalytic performa nce of the prepared catalyst fo r CO oxidation were investigated.The physical and chemical properties of the prepared catalysts were characterized by X-ray diffraction(XRD),Raman spectroscopy,N_(2)physical adsorption,inductively coupled plasma-atomic emission spectrometry(ICP-AES),X-ray photoelectron spectroscopy(XPS),temperature-programmed desorption analysis of CO(CO-TPD),in-situ diffuse reflectance infrared Fourier transform spectroscopy(DRIFTs),and temperature-programmed reduction with H_(2)(H_(2)-TPR).The results show that the CuO-CeO_(2)catalyst prepared with copper acetate as precursor(CC-A) exhibits the best catalytic activity for CO oxidation at low temperatures,with T50and T90values of 62 and 78℃ respectively,which is mainly attributed to its large specific surface area,pore volume,CO adsorption capacity,and large amount and strong reactivity of surface oxygen.However,the CuO-CeO_(2) catalyst prepared with copper nitrate as precursor(CC-N) displays better stability and resistance to water or CO_(2) poisoning than CC-A.
基金We are thankful to the Behbahn Khatam Alanbia University of Technology for the support of this work.
文摘CuO-CeO_(2)nanocomposite as a green recyclable catalyst,catalyzed amination of aryl halides with aqueous am-monia in water.This catalyst can be easily recovered by simple filtration and recycled up to 5 consecutive runs with consistent activity.The procedure provides some advantages such as simple work-up,clean procedure,relatively short reaction times and high yields of the products.
基金This work was financially supported by Guangdong Province Natural Science Foundation of China(000435), the Doctoral Program Foundation of the Ministry of Education (20010561003) Guangzhou Municipal Science and Technology Project(2001J1C0211)
文摘The performances of CO selective oxidation in hydrogen-rich gas over fourcatalytic systems of CuO/ZrO_2, CuO/MnO_2, CuO/CoO and CuO/CeO_2 were compared. The reducibility ofthese catalysts and the effect of CuO and CeO_2 molar ratio of CuO/CeO_2 catalysts on the activityof selective CO oxidation are investigated by XRD and TPR methods. The results show that thecatalysts with the exception of CuO/ZrO_2 have the interactions between CuO and CoO, CeO_2 or MnO_2,which result in a decrease in the reduction temperature. Among the catalysts studied, CuO/ZrO_2catalyst shows the lowest catalytic activity while CuO/CeO_2 catalyst exhibits the best catalyticperformance. The CuO(10%)/CeO_2 catalyst attains the highest CO conversion and selectivity at 140and 160℃. The addition of 9% H_2O in the reactant feed decreases the activity of CuO/CeO_2 catalystbut increases its CO selectivity.
