Pt/ZrO_(2)catalysts promoted with MoO_(3)and Nb_(2)O_(5)were tested for the combustion of short-chain alkanes(namely,methane,ethane,propane,and n-hexane).For short-chain alkane combustion,the inhibition of MoO_(3)(for...Pt/ZrO_(2)catalysts promoted with MoO_(3)and Nb_(2)O_(5)were tested for the combustion of short-chain alkanes(namely,methane,ethane,propane,and n-hexane).For short-chain alkane combustion,the inhibition of MoO_(3)(for the methane reaction)dramatically transformed to promotion(for the ethane,propane,and n-hexane reactions)as the carbon chain length increased,whereas the remarkable promotion of Nb_(2)O_(5)gradually weakened with an increase in the carbon chain length.Based on a detailed study of the oxidation reactions of methane and propane over the catalysts,the different roles of the promoters in the reactions were ascribed to differences in the acidic properties of the surface and the oxidation or reduction states of the Pt species.The MoO_(3)promoter could decorate the surface of the Pt species for a Pt-Mo/ZrO_(2)catalyst,whereas the Nb_(2)O_(5)promoter on the support could be partially covered by Pt particles for a Pt-Nb/ZrO_(2)catalyst.The formation of accessible Pt-MoO_(3)interfacial sites,a high concentration of metallic Pt species,and a high surface acidity in Pt-Mo/ZrO_(2)were responsible for the enhanced activity for catalytic propane combustion.The lack of enough accessible Pt-Nb_(2)O_(5)interfacial sites but an enhanced surface acid sites in Pt-Nb/ZrO_(2)explained the slight improvement in activity for catalytic propane combustion.However,the stabilized Pt^(n+)species in Pt-Nb/ZrO_(2)were responsible for the much-improved activity for methane combustion,whereas the Pt^(n+)species in Pt-Mo/ZrO_(2)could be reduced during the oxidation reaction,and the fewer exposed surface Pt species because of MoO_(3)decoration accounted for the inhibited activity for methane combustion.In addition,it can be concluded that MoO_(3)promotion is favorable for the activation of C-C bonds,whereas Nb_(2)O_(5)promotion is more beneficial for the activation of C-H bonds with high energy.展开更多
Superfine Mo/ZrO_2 catalysts were prepared for partial oxidation of methane to HCHO and characterized by BET, XRD, LRS, H2-TPR and XPS. Mo existed mainly in the form of Zr(MoO4)2, and the catalytic performance and phy...Superfine Mo/ZrO_2 catalysts were prepared for partial oxidation of methane to HCHO and characterized by BET, XRD, LRS, H2-TPR and XPS. Mo existed mainly in the form of Zr(MoO4)2, and the catalytic performance and physicochemical properties of the Mo/ZrO2 catalysts were closely related to this species.展开更多
Heavy oil is characterized by high viscosity.High viscosity makes it challenging to recover and transport.HZSM-5,MoO_(3)/HZSM-5,ZrO_(2)/HZSM-5 and MoO_(3)–ZrO_(2)/HZSM-5 catalysts were developed to promote in situ de...Heavy oil is characterized by high viscosity.High viscosity makes it challenging to recover and transport.HZSM-5,MoO_(3)/HZSM-5,ZrO_(2)/HZSM-5 and MoO_(3)–ZrO_(2)/HZSM-5 catalysts were developed to promote in situ desulfurization and viscosity reduction of heavy oil.The physical and chemical properties of catalysts were characterized by XPS,XRD,TEM,NH3-TPD,etc.The effects of temperature,catalyst type and addition amount on viscosity and composition of heavy oil were evaluated.The results showed that the presence of MoO_(3)–ZrO_(2)/HZSM-5 nanoparticles during aquathermolysis could improve the oil quality by reducing the heavy fractions.It reduced viscosity by 82.56%after the reaction at 280℃ and catalyst addition of 1 wt%.The contents of resins and asphaltic in the oil samples were 5.69%lower than that in the crude oil.Sulfur content decreased from 1.45%to 1.03%.The concentration of H2S produced by the reaction was 2225 ppm.The contents of sulfur-containing functional groups sulfoxide and sulfone sulfur in the oil samples decreased by 19.92%after the catalytic reaction.The content of stable thiophene sulfur increased by 5.71%.This study provided a basis for understanding the mechanism of heavy oil desulfurization and viscosity reduction.展开更多
Solid acid MoO_(3)/ZrO_(2)-TiO_(2)catalysts were prepared by impregnation method,and catalytic hydrolysis of difluorodichloromethane(CFC-12)over the catalyst was studied.The presence of MoO_(3)/ZrO_(2)-TiO_(2)catalyst...Solid acid MoO_(3)/ZrO_(2)-TiO_(2)catalysts were prepared by impregnation method,and catalytic hydrolysis of difluorodichloromethane(CFC-12)over the catalyst was studied.The presence of MoO_(3)/ZrO_(2)-TiO_(2)catalyst in polycrystalline state could be clearly observed by transmission electron microscopy(TEM).Mesopores were detected by N2 adsorption-desorption isotherms which further confirmed the MoO_(3)/ZrO_(2)-TiO_(2)structural characteristics of catalyst.The results of NH_(3)-TPD showed that the calcination temperatures had a great influence on the acidity of the catalyst,and the weak acidic site had a strong catalytic activity for the catalytic hydrolysis of CFC-12.Moreover,ZrO_(2)-TiO_(2)was highly dispersed in the MoO_(3)framework,suggested by powder X-ray diffraction(XRD)and N_(2)adsorption-desorption results.The effects of the catalyst calcination temperatures on the conversion rate of CFC-12 were studied.The effects of catalytic hydrolysis temperatures and water vapor concentration on the catalytic hydrolysis rate of CFC-12 were also studied.The solid acid MoO_(3)/ZrO_(2)-TiO_(2)was calcined at 500℃for 3 h at a catalytic hydrolysis temperature of 400℃and water vapor concentration of 83.18%,and catalytic hydrolysis rate of CFC-12 reached 98.65%.The hydrolysis rate of CFC-12 remained above 65.34%after 30 hours continuous reaction.展开更多
Herein,a simple synthetic approach is employed for the atomic dispersion of Rh atoms(Rh SAs)over the surface of interconnected Mo_(2)C nanosheets intimately embedded in a three-dimensional Ni_(x)MoO_(y)nanorod arrays(...Herein,a simple synthetic approach is employed for the atomic dispersion of Rh atoms(Rh SAs)over the surface of interconnected Mo_(2)C nanosheets intimately embedded in a three-dimensional Ni_(x)MoO_(y)nanorod arrays(Ni_(x)MoO_(y)NRs)framework;we found that the introduction of both isolated Rh SAs and Ni_(x)MoO_(y)NRs adjusts the electrocatalytic function of the host Mo_(2)C toward the direction of being an advanced and highly stable electrocatalyst for efficient hydrogen evolution at pH-universal conditions.As a result,the proposed catalyst outperforms most recently reported transition metal-based catalysts,and its performance even rivals that of commercial Pt/C,as demonstrated by its ultralow overpotentials of 31.7,109.7,and 95.4 mV at a current density of 10 mA cm^(-2),along with its small Tafel slopes of 42.4,51.2,and 46.8 mV dec^(-1)in acidic,neutral,and alkaline conditions,respectively.In addition,the catalyst shows remarkable long-term stability over all pH values with good maintenance of its catalytic activity and structural characteristics after continuous operation.展开更多
文摘Pt/ZrO_(2)catalysts promoted with MoO_(3)and Nb_(2)O_(5)were tested for the combustion of short-chain alkanes(namely,methane,ethane,propane,and n-hexane).For short-chain alkane combustion,the inhibition of MoO_(3)(for the methane reaction)dramatically transformed to promotion(for the ethane,propane,and n-hexane reactions)as the carbon chain length increased,whereas the remarkable promotion of Nb_(2)O_(5)gradually weakened with an increase in the carbon chain length.Based on a detailed study of the oxidation reactions of methane and propane over the catalysts,the different roles of the promoters in the reactions were ascribed to differences in the acidic properties of the surface and the oxidation or reduction states of the Pt species.The MoO_(3)promoter could decorate the surface of the Pt species for a Pt-Mo/ZrO_(2)catalyst,whereas the Nb_(2)O_(5)promoter on the support could be partially covered by Pt particles for a Pt-Nb/ZrO_(2)catalyst.The formation of accessible Pt-MoO_(3)interfacial sites,a high concentration of metallic Pt species,and a high surface acidity in Pt-Mo/ZrO_(2)were responsible for the enhanced activity for catalytic propane combustion.The lack of enough accessible Pt-Nb_(2)O_(5)interfacial sites but an enhanced surface acid sites in Pt-Nb/ZrO_(2)explained the slight improvement in activity for catalytic propane combustion.However,the stabilized Pt^(n+)species in Pt-Nb/ZrO_(2)were responsible for the much-improved activity for methane combustion,whereas the Pt^(n+)species in Pt-Mo/ZrO_(2)could be reduced during the oxidation reaction,and the fewer exposed surface Pt species because of MoO_(3)decoration accounted for the inhibited activity for methane combustion.In addition,it can be concluded that MoO_(3)promotion is favorable for the activation of C-C bonds,whereas Nb_(2)O_(5)promotion is more beneficial for the activation of C-H bonds with high energy.
基金This work is supported by the Ministry of Science and Technology(G199902240-06)
文摘Superfine Mo/ZrO_2 catalysts were prepared for partial oxidation of methane to HCHO and characterized by BET, XRD, LRS, H2-TPR and XPS. Mo existed mainly in the form of Zr(MoO4)2, and the catalytic performance and physicochemical properties of the Mo/ZrO2 catalysts were closely related to this species.
基金support provided by the National Science and Technology Major Project of the Ministry of Science and Technology of China(2016ZX05012-002-005)Shandong Provincial Natural Science Foundation(Grant no.:ZR2021QE051)+1 种基金National Natural Science Foundation of China(Grant no.:52206291)the Fundamental Research Funds for the Central Universities(Grant no.:22CX06030A).
文摘Heavy oil is characterized by high viscosity.High viscosity makes it challenging to recover and transport.HZSM-5,MoO_(3)/HZSM-5,ZrO_(2)/HZSM-5 and MoO_(3)–ZrO_(2)/HZSM-5 catalysts were developed to promote in situ desulfurization and viscosity reduction of heavy oil.The physical and chemical properties of catalysts were characterized by XPS,XRD,TEM,NH3-TPD,etc.The effects of temperature,catalyst type and addition amount on viscosity and composition of heavy oil were evaluated.The results showed that the presence of MoO_(3)–ZrO_(2)/HZSM-5 nanoparticles during aquathermolysis could improve the oil quality by reducing the heavy fractions.It reduced viscosity by 82.56%after the reaction at 280℃ and catalyst addition of 1 wt%.The contents of resins and asphaltic in the oil samples were 5.69%lower than that in the crude oil.Sulfur content decreased from 1.45%to 1.03%.The concentration of H2S produced by the reaction was 2225 ppm.The contents of sulfur-containing functional groups sulfoxide and sulfone sulfur in the oil samples decreased by 19.92%after the catalytic reaction.The content of stable thiophene sulfur increased by 5.71%.This study provided a basis for understanding the mechanism of heavy oil desulfurization and viscosity reduction.
基金Funded by the National Natural Science Foundation of China(No.51568068)the Young and Middle-aged Academic and Technical Leaders Reserve Talent Program(No.202105AC160054)。
文摘Solid acid MoO_(3)/ZrO_(2)-TiO_(2)catalysts were prepared by impregnation method,and catalytic hydrolysis of difluorodichloromethane(CFC-12)over the catalyst was studied.The presence of MoO_(3)/ZrO_(2)-TiO_(2)catalyst in polycrystalline state could be clearly observed by transmission electron microscopy(TEM).Mesopores were detected by N2 adsorption-desorption isotherms which further confirmed the MoO_(3)/ZrO_(2)-TiO_(2)structural characteristics of catalyst.The results of NH_(3)-TPD showed that the calcination temperatures had a great influence on the acidity of the catalyst,and the weak acidic site had a strong catalytic activity for the catalytic hydrolysis of CFC-12.Moreover,ZrO_(2)-TiO_(2)was highly dispersed in the MoO_(3)framework,suggested by powder X-ray diffraction(XRD)and N_(2)adsorption-desorption results.The effects of the catalyst calcination temperatures on the conversion rate of CFC-12 were studied.The effects of catalytic hydrolysis temperatures and water vapor concentration on the catalytic hydrolysis rate of CFC-12 were also studied.The solid acid MoO_(3)/ZrO_(2)-TiO_(2)was calcined at 500℃for 3 h at a catalytic hydrolysis temperature of 400℃and water vapor concentration of 83.18%,and catalytic hydrolysis rate of CFC-12 reached 98.65%.The hydrolysis rate of CFC-12 remained above 65.34%after 30 hours continuous reaction.
基金Supported from the Regional Leading Research Center Program(2019R1A5A8080326)through the National Research Foundation funded by the Ministry of Science and ICT of Republic of Korea.
文摘Herein,a simple synthetic approach is employed for the atomic dispersion of Rh atoms(Rh SAs)over the surface of interconnected Mo_(2)C nanosheets intimately embedded in a three-dimensional Ni_(x)MoO_(y)nanorod arrays(Ni_(x)MoO_(y)NRs)framework;we found that the introduction of both isolated Rh SAs and Ni_(x)MoO_(y)NRs adjusts the electrocatalytic function of the host Mo_(2)C toward the direction of being an advanced and highly stable electrocatalyst for efficient hydrogen evolution at pH-universal conditions.As a result,the proposed catalyst outperforms most recently reported transition metal-based catalysts,and its performance even rivals that of commercial Pt/C,as demonstrated by its ultralow overpotentials of 31.7,109.7,and 95.4 mV at a current density of 10 mA cm^(-2),along with its small Tafel slopes of 42.4,51.2,and 46.8 mV dec^(-1)in acidic,neutral,and alkaline conditions,respectively.In addition,the catalyst shows remarkable long-term stability over all pH values with good maintenance of its catalytic activity and structural characteristics after continuous operation.
