Highly crystallized anatase TiO2 nanoparticles were synthesized at a temperature as low as 120 °C through a glycothermal reaction using amorphous titanium hydrous gel as precursor and 1,4-butanediol and water as solvent. X-ray diffraction (XRD) and transmission electron microscopy (TEM) data support that the glycothermal processing method provides a simple low-temperature route for producing highly crystallized anatase TiO2 nanoparticles without pH adjustment. It is demonstrated that the shape and dispersability of TiO2 nanoparticles can be controlled by the reaction conditions, such as the reaction temperature and variation of the volume ratio of 1,4- butanediol/water (B/W). It was observed that TiO2 samples glycothermally prepared at 220 °C and the B/W ratio of 8/0 showed excellent photocatalytic behavior. The high activity is attributed to the high crystallinity and bipyramidal shape of the particles, which have fewer defects and more active {101} surfaces.

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Li 1+x Al x Ti 2-x (PO 4 ) 3 (LATP) is a promising solid electrolyte for all-solid-state Li ion batteries. In this study, LATP is prepared through a sol-gel method using relatively the inexpensive reagents TiCl 4 . The thermal behavior, structural characteristics, fractured surface morphology, ion conductivity, and activation energy of the LATP sintered bodies are investigated by TG-DTA, X-ray diffraction, FE-SEM, and by an impedance method. A gelation powder was calcined at 500 Key words Li 1+x Al x Ti 2-x (PO 4 ) 3 , sol-gel, ion conductivity, solid electrolyte, activation energy. 서 론

Oxide coatings were prepared on Al-1050 substrates by an environment-friendly plasma electrolytic oxidation (PEO) process using an electrolytic solution of Na 2 SiO 3 (8 g/L) and NaOH (3 g/L). The effects of three different duty cycles (20%, 40%, and 60%) and frequencies (50 Hz, 200 Hz, and 800 Hz) on the structure and micro-hardness of the oxide coatings were investigated. XRD analysis revealed that the oxides were mainly composed of α-Al 2 O 3 , γ-Al 2 O 3 , and mullite. The proportion of each crystalline phase depended on various electrical parameters, such as duty cycle and frequency. SEM images indicated that the oxide coatings formed at a 60% duty cycle exhibited relatively coarser surfaces with larger pore sizes and sintering particles. However, the oxides prepared at a 20% duty cycle showed relatively smooth surfaces. The PEO treatment also resulted in a strong adhesion between the oxide coating and the substrate. The oxide coatings were found to improve the micro-hardness with the increase of duty cycle. The structural and physical properties of the oxide coatings were affected by the duty cycles.

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The production of functional activated carbon materials starting from inexpensive natural precursors using environmentally friendly and economically effective processes has attracted much attention in the areas of material science and technology. In particular, the use of plant biomass to produce functional carbonaceous materials has attracted a great deal of attention in various aspects. In this study the preparation of activated carbon has been attempted from rice husks via a chemical activation-assisted microwave system. The rice husks were milled via attrition milling with aluminum balls, and then carbonized under purified N 2 .The operational parameters including the activation agents, chemical impregnation weight ratio of the calcined rice husk to KOH (1:1, 1:2 and 1:4), microwave power heating within irradiation time (3-5 min), and the second activation process on the adsorption capability were investigated. Experimental results were investigated using XRD, FT-IR, and SEM. It was found that the BET surface area of activated carbons irrespective of the activation agent resulted in surface area. The activated carbons prepared by microwave heating with an activation process have higher surface area and larger average pore size than those prepared by activation without microwave heating when the ratio with KOH solution was the same. The activation time using microwave heating and the chemical impregnation ratio with KOH solution were varied to determine the optimal method for obtaining high surface area activated carbon (1505 m 2 /g).

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