The structure and catalytic desulfurization characteristics of CeO2-TiO2 mixed oxides were investigated by means ofX-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS） and catalytic activity tests. Acco...The structure and catalytic desulfurization characteristics of CeO2-TiO2 mixed oxides were investigated by means ofX-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS） and catalytic activity tests. According to the results, a CeO2-TiO2solid solution is formed when the mole ratio of cerium to titanium n（Ce）：n（Ti） is 5：5 or greater, and the most suitable n（Ce）：n（Ti） isdetermined as 7：3, over which the conversion rate of SO2 and the yield of sulfur at 500℃ reach 93% and 99%, respectively.According to the activity testing curve, Ce0.7Ti0.3O2 （n（Ce）：n（Ti）=7：3） without any pretreatment can be gradually activated by reagentgas after about 10 min, and reaches a steady activation status 60 min later. The XPS results of Ce0.7Ti0.3O2 after different time ofSO2＋CO reaction show that CeO2 is the active component that offers the redox couple Ce4＋/Ce3＋ and the labile oxygen vacancies, andTiO2 only functions as a catalyst structure stabilizer during the catalytic reaction process. After 48 h of catalytic reaction at 500℃,Ce0.7Ti0.3O2 still maintains a stable structure without being vulcanized, demonstrating its good anti-sulfur poisoning performance.展开更多
The corrosion behaviors of hafnium in Et4NBr isopropanol and acetonitrile(ACN)solutions were investigated usingelectrochemical measurements,ICP-AES and SEM techniques.Results revealed that the open circuit potential g...The corrosion behaviors of hafnium in Et4NBr isopropanol and acetonitrile(ACN)solutions were investigated usingelectrochemical measurements,ICP-AES and SEM techniques.Results revealed that the open circuit potential gets more positive dueto the increased passivity of the surface oxide film with increasing immersion time until it reaches a steady state value.Thepotentiodynamic anodic polarization curves did not exhibit an active dissolution region near corrosion potential due to the presenceof an oxide film on the electrode surface,which was followed by pitting corrosion.SEM images confirmed the existence of pits onthe electrode surface.Cyclic voltammetry and galvanostatic measurements allowed the pitting potential(φpit)and the repassivationpotential(φp)to be determined.φpit increased with increasing potential scanning rate but decreased with increasing temperature,Br-concentration and ACN concentration.The impedance spectra showed that the resistances of the solution and charge transferdecreased with the increase of ACN concentration.展开更多
文摘The structure and catalytic desulfurization characteristics of CeO2-TiO2 mixed oxides were investigated by means ofX-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS） and catalytic activity tests. According to the results, a CeO2-TiO2solid solution is formed when the mole ratio of cerium to titanium n（Ce）：n（Ti） is 5：5 or greater, and the most suitable n（Ce）：n（Ti） isdetermined as 7：3, over which the conversion rate of SO2 and the yield of sulfur at 500℃ reach 93% and 99%, respectively.According to the activity testing curve, Ce0.7Ti0.3O2 （n（Ce）：n（Ti）=7：3） without any pretreatment can be gradually activated by reagentgas after about 10 min, and reaches a steady activation status 60 min later. The XPS results of Ce0.7Ti0.3O2 after different time ofSO2＋CO reaction show that CeO2 is the active component that offers the redox couple Ce4＋/Ce3＋ and the labile oxygen vacancies, andTiO2 only functions as a catalyst structure stabilizer during the catalytic reaction process. After 48 h of catalytic reaction at 500℃,Ce0.7Ti0.3O2 still maintains a stable structure without being vulcanized, demonstrating its good anti-sulfur poisoning performance.
基金Project(51374254) supported by the National Natural Science Foundation of China
文摘The corrosion behaviors of hafnium in Et4NBr isopropanol and acetonitrile(ACN)solutions were investigated usingelectrochemical measurements,ICP-AES and SEM techniques.Results revealed that the open circuit potential gets more positive dueto the increased passivity of the surface oxide film with increasing immersion time until it reaches a steady state value.Thepotentiodynamic anodic polarization curves did not exhibit an active dissolution region near corrosion potential due to the presenceof an oxide film on the electrode surface,which was followed by pitting corrosion.SEM images confirmed the existence of pits onthe electrode surface.Cyclic voltammetry and galvanostatic measurements allowed the pitting potential(φpit)and the repassivationpotential(φp)to be determined.φpit increased with increasing potential scanning rate but decreased with increasing temperature,Br-concentration and ACN concentration.The impedance spectra showed that the resistances of the solution and charge transferdecreased with the increase of ACN concentration.
