A citric acid functionalized graphene oxide nanocomposite was successfully synthesized and the structure and morphology of the nanocatalyst were comprehensively characterized by Fourier transform infrared spectroscopy, energy-dispersive X-ray analysis, X-ray diffraction patterns, atomic force microscopy images, scanning electron microscopy images, transmission electron microscopy images, and thermogravimetric analysis. The application of this nanocatalyst was exemplified in an important condensation reaction to give imidazole derivatives in high yields and short reaction times at room temperature. The catalyst shows high catalytic activity and could be reused after simple work up and easy purification for at least six cycles without significant loss of activity, which indicates efficient immobilizing of citrate groups on the surface of graphene oxide sheets.

We studied the initial reaction mechanism of Zn precursors, namely, di-methylzinc (Zn(CH3)2, DMZ) and diethylzinc (Zn(C2H5)2, DEZ), for zinc oxide thin-film growth on a Si (001) surface using density functional theory. We calculated the migration and reaction energy barriers for DMZ and DEZ on a fully hydroxylized Si (001) surface. The Zn atom of DMZ or DEZ was adsorbed on an O atom of a hydroxyl (-OH) due to the lone pair electrons of the O atom on the Si (001) surface. The adsorbed DMZ or DEZ migrated to all available surface sites, and rotated on the O atom with low energy barriers in the range of 0.00-0.13 eV. We considered the DMZ or DEZ reaction at all available surface sites. The rotated and migrated DMZs reacted with the nearest -OH to produce a uni-methylzinc (-ZnCH3, UMZ) group and methane (CH4) with energy barriers in the range of 0.53-0.78 eV. In the case of the DEZs, smaller energy barriers in the range of 0.21-0.35 eV were needed for its reaction to produce a uni-ethylzinc (-ZnC2H5, UEZ) group and ethane (C2H6). Therefore, DEZ is preferred to DMZ due to its lower energy barrier for the surface reaction.

The purpose of this study was to observe the histopathologic reaction in vital bone to various surface treated implants. For this purpose, ten New Zealand Albino rabbits, weighing 3.3 to 4kg were used as experimental animals. All the experimental groups divided into five groups; 1) Machined surface as control, 2) RBM(resorbable blast media), 3) RBM etched nitric acid solution, 4) RBM etched sodium hydroxide solution, 5) RBM etched acid, alkali, and heat treated group on each. All the surfaces of implants were examined under the scannning electron microscope to distinguish the differences between each experimental groups compare to that on the control group. All the rabbits were implanted into the tibial metaphyses of rabbits. On the 4th and 8th week after implantations, all the experimental rabbits were sacrificed. All the tissues containing each implanted materials were fixed in ethyl alcohol, and embedded in spurr resin as usual manner, sectioned in 10μm or more thickness, grinded, stained with the Villanuevaʼs osteochrome bone stain method and examined histopatholgically. For the fluorescence microscopic examination, three kind of fluorescence dyes, Oxytetracycline, Alizarin-Complexone, and Xylenol-Orange were injected to put into the bone to implant interface produced polychromatic fluorescence labelling on the 1st week, 2nd week, and 5th week on each. On the 8th week after experiments, the animals sacrificed, and the tissues containing the implants were taken, fixed in ethyl alcohol and embedded in spurr resin, sectioned, grounded 10um in thickness and examined under the fluorescence microscope. Following results were obtained; On the scanning electron microscopic examination of the implants, dull cracks, continuous linear indentations were revealed on the machined surface implant, irregular multiple leaflike eruptions on the RBM, and more sharp porous indentation with multiple complicated c rack s on the RBM acid etched surface, and more dull margins on complicated porous indentation on the RBM alkalic etched surface and more dull and less indented particles were noted on the RBM, acid, alkalic etched, heat treated surface, On the histopathologic examination, on the 4th week after experiment, complete osseointegation was noted between the implant and cortical bone on the collar and the apex lesion. and in parts, small newly formed bone spicules directly attached to the screws, and osteoid tissues were revealed in marrow tissues, in all experimental groups. On the histopathologic examination, on the 8th week after experiment, osseointegration is more increased compare to that on the 4th week group, the amount of bone trabeculae and osteoid tissues directly fused to screw of implants were markedly increased. On fluorescence examination, band or linear shape was witnessed on the boarder of compact bone and marrow tissues, and on bone trabeculae according to the formed age. and precipitated as granular and globular shape on the haversian canals. These results indicate that the surface treated method used for the present study render the implants compatible to bone tissue but the tissue compartibility is not different among the surface treated implants.

The objective of the present study is to investigate the increase in the functional characteristics of a substrate by the formation of a thin coating layer. Thin coating layers of have high potential because exhibits high hardness. Shock induced reaction synthesis is an attractive fabrication technique to synthesize uniform coating layer by controlling the shock wave. Ti and Si powders to form using shock induced reaction synthesis, were mixed using high-energy ball mill into small scale. The positive effect of this technique is highly functional coating layer on the substrate due to ultra fine substructure, which improves the bonding strength. These materials are in great demand as heat resisting, structural and corrosion resistant materials. Thin coating layer was successfully recovered and showed high Vickers' hardness (Hv=1183). Characterization studies on microstructure revealed a fairly uniform distribution of powders with good interfacial integrity between the powders and the substrate.

이 연구에서는 플라즈마 제염 기술의 실용화를 위해 , , 등의 반응성 플라즈마 기체를 이용하여 원자력 시설의 주요 오염원인 코발트 핵종에 대한 표면 제염 모의실험을 수행하였다. 디스크 형태의 금속코발트에 대하여 시편 표면 온도를 변수로 플라즈마 식각 실험을 수행한 결과 반응율은 에서 기체의 경우 그리고 와 기체의 경우 각각 과 이었으며, 이들 반응의 활성화에너지는 각각 39.4 kJ/mol, 42.1 kJ/mol, 116.0 kJ/mol이었다. 이와 함께 AES (Auger Electron Spectroscopy)를 이용하여 반응 생성물 성분 분석 결과 이들 반응의 주요 반응 기구는 코발트의 불화 반응임이 밝혀졌다. 이 연구를 통해 확보된 의 금속 표면 식각율은 주요 반도체 공정의 식각율을 뛰어넘는 높은 식각율로 플라즈마 제 염 기술의 실용화를 앞당길 수 있는 고무적인 결과라 할 수 있을 것이다.