PREPARATION OF LEAD MAGNESIUM NIOBATE-LEAD ZIRCONATE TITANATE FILMS AND THEIR CRYSTALLIZATION BEHAVIORS

PREPARATION OF LEAD MAGNESIUM NIOBATE-LEAD ZIRCONATE TITANATE FILMS AND THEIR CRYSTALLIZATION BEHAVIORS. The thin films with composition near morpotropic phase boundary (MPB) of the system xPb(Mg1/3, Nb2/3)O3-yPbTiO3-zPbZrO3 (x = 0 – 0.35, y = 0.47 and z = 0.53), were prepared by sol-gel method. The starting materials were consisted of Pb(iso-OC3H7)2, Zr(n-OC4H9)4, Ti(iso-OC3H7)4, Mg(CH3COO)2 4H2O and Nb(OC2H5)5. The 1-propanol was used as solvent. The concentration of PMN-PT-PZ in coating solution was 0.7 M, and the pH of the solution was 4.5. The thin films were prepared by dipcoating and spincoating. The crystallization behaviors of the PMN-PT-PZ thin films showed that the formation of perovskite phase at low temperature becomes difficult with increasing the content of PMN. The amounts of pyrochlore and perovskite phase in PMN-PT-PZ films depended on the heating temperatures, and PMN contents. Single-phase perovskite was found for the coated films containing 0 and 12.5 mol% after calcinating at 600 oC, 21 mol% after calcinating at 700oC, and 30 mol% after calcinating at 750oC. Single-phase perovskite of coated films will never be found when the content of PMN was 35 mol%

THE STABILIZING OF ANATASE AEROGEL AT HIGH TEMPERATURE

Stable anatase is attractive to its notable functions for photo catalysis and photon-electron transfer.   Stable anatase TiO­2 containing amorphous SiO2 aerogel was prepared by hydrolysis of Ti (OC3H7)4 and Si (OC3H7)4 in a 2-propanol solution with acid catalyst. The solvent in wet gels was supercritically extracted in CO2 at 60 oC and 22 Mpa. Thermal evolutions of the microstructure of the gels were evaluated by TGA-DTA, N2 adsorption and XRD. A stable anatase TiO2 containing amorphous SiO2 aerogel with a BET specific surface area of 365 m2/g and a total pore volume of 0.20 cm3/g was obtained as prepared condition. The anatase phase was stable after calcination up to 1000 oC, and BET specific surface area, total pore volume and average pore diameter did not change significantly after calcination up to 900 oC.   Keywords: Supercritical extraction, sol-gel, aerogel, stable anatase structur

A Review on the Hydroisomerisasion of n-Parafins over Supported Metal Catalysts

Catalytic hydroisomerization of n-paraffin aims to produce branched paraffin isomers and suppress cracking reactions in the production of the low cloud point of biodiesel. The development of the type of metal and catalyst support, amount of metal loading, and reaction conditions are important to increase the catalyst activity. A high performace catalyst for hydroisomerization bears bifunctional characteristics with a high level of hydrogenation active sites and low acidity, maximizing the progress of hydroisomerization compared to the competitive cracking reaction. In addition, a catalyst support with smaller pore size can hinder large molecular structure isoparaffins to react on the acid site in the pore thus providing good selectivity for converting n-paraffin. Catalysts loaded with noble metals (Pt or Pd) showed significantly higher selectivity for hydroisomerization than non-noble transition metals such as Ni, Co, Mo and W. The reaction temperature and contact time are also important parameters in hydroisomerization of long chain paraffin, because long contact times and high temperatures tend to produce undesired byproducts of cracking. This review reports several examples of supported metal catalyst used in the hydroisomerization of long chain hydrocarbon n-paraffins under optimized reaction conditions, providing the best isomerization selectivity results with the lowest amount of byproducts. The role of various metals and their supports will be explained mainly for bifunctional catalysts

Sol-gel Process for the Manufacturing of Translucent Lead Zirconate Titanate Gel-monolith

Translucent Lead Zirconate Titanate (PZT) gel-monolith was prepared by partially hydrolyzing metal alkoxides solution which modified with acetylacetone(acacH). Metal alkoxides, lead di-i-propoxide, zirconium tetra-nbutoxide and titanium tetra-i-propoxide were used as starting materials. In Infrared spectra for the translucent monolithic gel after aging at room temperature for several days or drying at 90°C for 18h, the most significant feature is the presence of band at around 1554 cm-1 which can be assigned to the v (C-O) and v (C-C) vibrati-ons of acetylacetanate group coordinated to the metal cations Ti and Zr. The diffraction peaks of PbO were found after heating at 300°C for 2h. After heating at 450 °C for 2 h, diffraction peaks of pyrochlore Pb2 Ti206 and perovskite PZT phase were observed. The diffraction peaks of PbO and pyrochlore phase disappeared after heating at 600°C, and tetragonal perovskite phase was stable up to 1000 °C. The diffraction peaks of perovskite phase were also found after heating at 430 ° for 24 h. The density of the compacted pulverizedgel after heating at 1000°C for 30 min. was 6.9 g/cm3 , about 86% of the theoretical value