Oxygen Storage Capacity and Adsorptive Property of Praseodymium Oxides

Oxygen storage and adsorptive properties of praseodymium oxides were investigated by pulse experiments and temperature - programmed desportion/reduction (TPD/TPR) experiments. Pr2O3 possesses the similar oxygen storage properties to CeO2, and its dynamic oxygen storage capacity is 14.9 mumol.g(-1). The studies on TPD Of O-2, H2O and CO and TPR show that Pr2O3 provides more active surface oxygen species and at a lower temperature than CeO2. It is suggested that Pr2O3 can be a well candidate as an oxygen storage component in automobile three-way catalyst.

Getting insights into gas-phase sulfation effect on catalytic performance of praseodymium oxides in NH_(3)-SCR of NO

Sulfation treatment has been widely used to promote the catalytic performance of ceria(CeO_(2))based catalysts for the selective catalytic reduction of NO by NH_(3)(NH_(3)-SCR of NO).Praseodymium oxide(PrO_(x)),another commonly used rare earth material with similar structural properties as CeO_(2),also shows satistactory redox properties due to the facile redox cycle of Pr^(3+)■Pr^(4+).In this work,gas phase sulfation treatment with varied duration was performed on PrO_(x) at 200℃,and the NH_(3)-SCR activity of sulfated PrO_(x) was evaluated.Based on the results of systematic characterizations(e.g.,N_(2)-physisorption,NH_(3) oxidation,NO oxidation,in situ diffuse Fourier transform infrared spectroscopy),it is revealed that the catalytic performance of sulfated PrO_(x)is highly dependent on the sulfation time(or the amount of sulfate species deposited on PrO_(x)),which has a significant impact on the competitive reaction between NH_(3) oxidation and NH_(3)-SCR of NO,thus determining the NH_(3)-SCR activity of PrO_(x).This work provides new insight into tuning the interaction between PrO_(x) surface and reactants(NO,NH_(3))via sulfation treatment,which cam guide the design and application of PrO_(x)based catalysts for NH_(3)-SCR of NO in the future.

Eco-friendly green synthesis of novel magnetic Fe3O4/SiO2/ZnO-Pr6O11 nanocomposites for photocatalytic degradation of organic pollutant

This study reports the successful so nochemical synthesis of novel Fe3O4/SiO2/ZnO-Pr6O11(Fe/Si/Zn-Pr6O11) nanocomposites using fructose as a green capping agent.The influence of various parameters containing capping agent,power and time of ultrasound irradiation was investigated to reach optimum morphology and size conditions.The products obtained were characterized by transmission electron microscopy(TEM),UV/Vis diffuse reflectance spectroscopy(DRS),Fourier transform infrared spectra(FT-IR),vibration sample magnetometer(VSM),scanning electron microscopy(SEM),energy dispersive X-ray microanalysis(EDS) and X-ray diffraction(XRD).The Fe3O4/SiO2/ZnO-Pr6O11 nanocomposites display remarkably enhanced photocatalytic activity towards rhodamine b degradation(89.6%)and Congo red(84.7%) under UV irradiation compared with the other products.The results illustrate that the photocatalytic efficiency of magnetic nanocomposites is very much higher than pure Pr6O11nanostructures.Magnetic photocatalyst still has good stability after five successive runs.So,these recyclable nanocomposites can play a role in the treatment of both industrial and domestic contaminated water.

Fabrication,characterization,and electrical conductivity properties of Pr_6O_(11) nanoparticles

PrrOll nanoparticles were obtained by subsequent thermal decomposition of the as-prepared precipitate formed under ambient temperature and pressure using NaOH as precipitant. The calcination process was affected, for 1 h in static air atmosphere, at 400-700 ℃ temperature range. The different samples were characterized using X-ray diffraction （XRD）, transmission electron microscopy （TEM）, field emission scanning electron microscopy （FE-SEM）, thermogravimetric analysis （TGA）, in situ electrical conductivity, and N2 adsorption/desorption. The obtained results demonstrated that nano-crystalline Pr6O11, with crystallites size of 6-12 nm, started to form at 500 ℃. Such value increased to 20-33 nm for the sample calcined at 700℃. The as-synthesized PrrOll nanoparticles presented high electrical conductivity due to electron hopping between Pr（III）-Pr（IV） pairs.