The performance of deep oxidation of methanol on supported Pd catalyst was exami ned by a chromatograph-micro-reactor. The results show that the add ition of La into γ-Al 2O 3 support can affect greatly the perform...The performance of deep oxidation of methanol on supported Pd catalyst was exami ned by a chromatograph-micro-reactor. The results show that the add ition of La into γ-Al 2O 3 support can affect greatly the performance of t he Pd catalyst. In the absence of CO, La can decrease the content of oxygen-c ontaining intermediate, although La can not lower the light-off temperature of methanol oxidation. In the presence of CO, La can lower the light-off tem perature, decrease the amount of CO adsorption, and weaken evidently 'CO inhibi tion' to the oxidation of methanol. By XPS technique, it is shown that La modi fies the electronic structure of Pd, which attributes to the modifications of th e catalytic performance.展开更多
Pd nanoparticles(Pd-NPs)were prepared and directly anchored on the surface of multi-walled carbon nanotubes(MWCNTs)in the absence of chemical reduction agent,where MWCNTs were used as both the chemical reduction agent...Pd nanoparticles(Pd-NPs)were prepared and directly anchored on the surface of multi-walled carbon nanotubes(MWCNTs)in the absence of chemical reduction agent,where MWCNTs were used as both the chemical reduction agent and the support substrate of Pd-NPs.Effect of various surfactants on the in situ deposition of PdNPs on MWCNTs was investigated.When MWCNTs were modified with a cationic surfactant(hexadecyl trimethyl ammonium bromide,CTAB),the amount of the Pd-NPs(Pd-NP/CTAB-MWCNT)generated by such an in situ deposition method gets a notable increase,and the size of the as-synthesized Pd-NPs becomes smaller,compared with those in the absence of any surfactant(Pd-NP/MWCNT)or in the presence of an anionic surfactant SDS(Pd-NP/SDS-MWCNT)and a neutral surfactant OP(PdNP/OP-MWCNT).Results show that the MWCNTs modified with CTAB are propitious to the in situ reduction of Pd2?.Among the prepared catalysts,Pd-NP/CTABMWCNT displays the highest electroactivity for ethanol oxidation in alkaline media.展开更多
文摘The performance of deep oxidation of methanol on supported Pd catalyst was exami ned by a chromatograph-micro-reactor. The results show that the add ition of La into γ-Al 2O 3 support can affect greatly the performance of t he Pd catalyst. In the absence of CO, La can decrease the content of oxygen-c ontaining intermediate, although La can not lower the light-off temperature of methanol oxidation. In the presence of CO, La can lower the light-off tem perature, decrease the amount of CO adsorption, and weaken evidently 'CO inhibi tion' to the oxidation of methanol. By XPS technique, it is shown that La modi fies the electronic structure of Pd, which attributes to the modifications of th e catalytic performance.
基金supported by the National Natural Science Foundation of China (Nos. 21376070 and 20876038)Scientific Research Fund of Hunan Provincial Edu- cation Department (No. 11K023)Hunan Provincial Natural Science Foundation of China (14JJ2096)
文摘Pd nanoparticles(Pd-NPs)were prepared and directly anchored on the surface of multi-walled carbon nanotubes(MWCNTs)in the absence of chemical reduction agent,where MWCNTs were used as both the chemical reduction agent and the support substrate of Pd-NPs.Effect of various surfactants on the in situ deposition of PdNPs on MWCNTs was investigated.When MWCNTs were modified with a cationic surfactant(hexadecyl trimethyl ammonium bromide,CTAB),the amount of the Pd-NPs(Pd-NP/CTAB-MWCNT)generated by such an in situ deposition method gets a notable increase,and the size of the as-synthesized Pd-NPs becomes smaller,compared with those in the absence of any surfactant(Pd-NP/MWCNT)or in the presence of an anionic surfactant SDS(Pd-NP/SDS-MWCNT)and a neutral surfactant OP(PdNP/OP-MWCNT).Results show that the MWCNTs modified with CTAB are propitious to the in situ reduction of Pd2?.Among the prepared catalysts,Pd-NP/CTABMWCNT displays the highest electroactivity for ethanol oxidation in alkaline media.
