Silicon carbide whiskers (SiCw) having the diameter in the range of 20-80 nm were synthesised from coconut fibres through sol-gel process. The coconut fibres were impregnated with tetraethoxysilane and methyltriethoxysilane derived sol and pyrolyzed at 1400℃ in argon. X-ray of the pyrolyzed samples showed the formation of β-SiC.

Field emission display(FED) is actively investigated in view of the development of full color flat-panel display, which can replace some cathode-ray tube(CRT). Thus, the development of new phosphors appropriate for FED is urgently needed and has been actively investigated. In this work, SrTiO3:Pr3+ phosphor was prepared by sol-gel method and the coating was applied by sol-gel method combined with sonication on these phosphor's surface into diluted precursor solution. It was found that very fine particles of coating material were formed on phosphor's surface. The luminescent intensity of SrTiO3:Pr3+ phosphor coated with SiO2 and Al2O3 was considerably increased without any noticeable change in color chromaticity. The optimum concentration of coating material was found to be 1wt% and the optimum pH value of the solution was 10.

본 연구의 목적은 침지형(YEF 750D-2) 모듈을 적용하여 공기유량에 따른 유체 유속과 간헐적인 세정공기의 공급에 의한 오염제거를 평가하는 것이다. 공기유량에 따라 모듈의 유체 유속은 선형적으로 증가하였으며, MLSS의 농도가 1,000 mg/L 증가할 때 마다 3times10-4m·min/sec·L 수식 이미지의 비율로 유체 유속이 감소하였다. 세정공기의 공급이 정지되는 시간에 전여과가 일어나 흡인여과 시간 동안 겔층 위에 케익층이 형성되었다. 20초 정지와 20초 공기공급의 간헐공기주입으로 형성된 케익층이 역세정에 의하여 제거되면서 압력증가율이 가장 낮게 나타났다. 겔층이 제거되는 메커니즘은 세정 공기공급을 교대로 하여 겔층 위에 케익층을 형성시켜 케익층이 제거될 때 겔층이 함께 제거되는 원리로 설명할 수 있다.

Synthesis of zinc oxide nanorods, sheets and flower like structure were done by the sol-gel method using zinc acetate dihydrate and sodium hydroxide at with 12 hours refluxing time nanorods, in case of as synthesized powder, with diameter of 20-60nm. Annealing at higher temperature (300 and ,) in air ambient changes the morphology to sheet and flower like structure. The standard peak of zinc oxide was observed in IR at . The UV-VIS spectroscopy of zinc oxide shows a characteristic peak at 375nm.

In this study, spherical pre-BaTiO3 particles are prepared by gelation and aging process in autoclave without catalysts. The (Ba-Ti) gel used as a starting material was prepared by aging mixtures of titanyl acylate with barium acetate aqueous solution([glacial acetic acid (AcOH)]/[titanium isopropoxide (TIP)] 4, [barium acetate]/[TIP] 1) at 45℃ for 48hrs. XRD and SEM results for the (Ba-Ti) gel sample at aging process showed that the gel was formed via aggregation of the fine particles. It seems to be the primary particles of bulk (Ba-Ti) gel amorphous, but the spatial arrangement of barium and titanium in the (Ba-Ti) gel is similar to that in crystalline BaTiO3 particles. From XRD and FT-IR. spectroscopy analysis it was found that the crystal structure of the prepared particles continuously transformed from amorphous to tetragonal as the calcination temperature increased, and crystallized spherical cubic and tetragonal BaTiO3 powder obtained at the very low calcination temperature between 500℃ and 900℃ after 1hrs of heat treatment respectively. According to BET analysis result, final particle have pore structure of ink bottle shape which is produced by aggregation of fine spherical particles with surface area of 280m2/g and average pore size of 130nm.

In the present study, silver-doped antibacterial hydroxyapatites were successfully prepared by the sol-gel method. For the starting solution, the molar ratio of was set to 0.075:0.045:20:0.135; was added to a ratio of Ag to total cation concentration of . The prepared sol was dried at for 48h and heat-treated at for 2h to obtain particles in the 200-500nm size range. The product from the synthesis of silver-doped hydroxyapatite was investigated through X-ray diffraction experiments and scanning electron microscopy. The product showed high antibacterial properties, with a disinfection ratio of Staphylococcus aureus (ATCC 6538) and Escherichia coli (ATCC 25922) over as calculated from an antimicrobial effects evaluation by the shake flask method.

본 연구는 사용 후 핵연료의 금속전환 공정에서 발생되는 폐용융염을 고형화하는 방법으로 GRSS(Gel-Route Slabilization/Solidifcation)개념을 이용한 전처 리법을 제안하였다. Sodium silicate와 H3p04로 구성된 물질계에서는 SiO에 의해 형성되는 반응모듈 내에서 휘발성 핵종은 열적으로 안정한 화합물로 전환된다. 얻어진 생성물은 붕규산 유리매질과의 반응을 통하여 Li는 LiPO 형태로 유지되며 Cs 및 Sr은 유리매질내에 포용될 수 있다. 또한 sodium silicate, HPO 및 ZrCl로 이루어진 물질계를 이용하여 내구성이 우수한 WZP 세라믹 고화매질을 합성하였다. 이상에서 NZP구조가 형성되며, Cs가 Li보다 우선하여 NZP구조를 형성하였다. 이상의 결과로부터, GRSS를 이용한 폐용융염의 전처리는 단순한 공정과 열적 안정성을 통하여 검증된 고화매질로 고형화가 가능토록하는 유효한 접근법이라 할 수 있으며, 수화학적 안정성의 검증을 통하여 ANL의 제올라이트를 이용한 고화법에 대한 대안이 될 것으로 기대된다.

The capacity and long life of gel electrolyte batteries is connected with gas recombination producting PbO2 and Pb electrode. We prepared with sulfuric acid gel electrolyte to know gel characteristics per density to assemble valve regulated lead-acid (VRLA) batteries. We studied on actions of sulphuric acid gel electrolyte by measuring electrolyte dispersion using Brewster-angle microscope (BAM), charge-discharge cycle, and electrode structure using scanning election microscope (SEM). Sulphuric acid density 1.210 showed excellent gel dispersion in sol condition, electrode condition after fifty cycles in this study.

An aqueous solution of a commercial liquid synthetic detergent for kitchen use was photodecomposed in the presence of titanium dioxides powder under an atmosphere of air at room temperature. Titanium dioxides were prepared by sol-gel method from titanium iso-propoxide at different R ratio(H2O/titanium iso-propoxide) and calcined at 500℃. All titanium dioxides were characterized by XRD, BET surface area analyzer and UV-VIS spectrometer. The surface area of titanium dioxides prepared at R ratio=6 appeared higher volume about 20% than commercial TiO2 catalysts. XRD patterns of titania particles were observed mixing phase together with rutile and anatase type. Titanium dioxides prepared by sol-gel method show higher activity about 6% than commercial TiO2 catalysts on the photocatalytic degradation of a commercial liquid synthetic detergent for kitchen. The concentration of the detergent decreased to about 90% of its initial value at illumination times of 2 hour. Illumination for 30 minutes decreased the concentration of oxygen to about one-fifth of the initial value.

동굴 내 정점별 세균 군집 구조를 분석하기 위하여 PCf amplified 16S rDNA denaturing gradient gel electrophoresis(DGGE)를 적용하였다. DGGE는 동일한 분자량을 갖는 dsDNA band라고 할지라도, 각각의 염기서열 차이에 따라 전기영동 상에서 고유한 band양상을 나타낼 수 있다. eubacteria의 16S rDNA V3region을 증폭하기 위해 GC341F와 PRUN518r을 primer로 사

BaTiO3, powders were prepared by sol-gel process from different aging time and reaction temperature. Particle shape, size and crystal structure of prepared BaTiO3 powders were analyzed by SEM, XRD and FT-IR. Effect of aging time alternation didn't particularly show up. Spherical nano-sized BaTiO3 powders were obtained from condition more than reaction temperature 55℃, and obtained sintered BaTiO3 powders of tetragonal phase from heat-treatment at 1,100℃.

The capacity and long life of gel electrolyte batteries is connected with gas recombination producting PbO2 and Pb electrode. We were prepared with phosphoric acid gel electrolyte to know gel characteristics per density to assemble VRLA batteries. We studied by measuring electrolyte dispersion using Brewster-angle microscope(BAM), charge-discharge cycle and electrode structure using scanning election microscope(SEM) per electrolyte density. As a results, phosphoric acid density 1.210 was excellent gel dispersion in sol condition, electrode condition after fifty cycles in this study.

The optimum polymer gel electrolyte composition ratio was 23 : 66 : 11 wt% of P(VdF-co-HFP) : PVP =20 : 3), (PC: EC =44 : 22) and TEABF4. And the optimal thickness of polymer gel electrolyte was 50um . The electrochemical characteristics result of unit cell were 31.41 Fig of specific capacitance, and 3.21x10-3 S/cm of ion conductivity. Ion conductivity of polymer gel electrolytes decreased according to added PVP through impedance analysis, and it was higher in 7 wt%, but electrochemical characteristics of unit cell were better in 3 wt% PVP. And for excellent ion conductivity of polymer gel electrolytes, the use of a thin layer electrolyte(20um) was an effective method, but with unit cell application, the best thickness was 50um . Unit cell showed higher capacitance and more stable electrochemical performance when hot pressed between polymer gel electrolyte and electrode. This results from enhancement of the physical contact between the electrode and the polymer gel electrolyte and good accessibility of the liquid electrolyte to the electrode surface.

한외여과막의 분획분자량을 결정하기 위하여 dead-end형 셀내에 평막을 설치하고 분자량 분포가 수천 내지 수백만의 혼합 dextran 수용액으로 투과 실험하였다. 원료 용액과 투과액을 GPC로 분석하여 각 분자량에 대한 배제율을 구하고 90% 배제율에 해당하는 dextran분자량을 분획분자량를 결정하였다. 투과압력을 0.5에서 2.0 bar까지 증가시킬 경우, Millipore사의 PBTK막은 63,000 내지 68,000 daltons로 10% 이내에서 변화하였지만 Millipore사의 PBQK 막 또는 (주)새한의 UE1812막의 분획분자량은 각각 3.5 및 4.3 배 증가하였다. 또한 투과액을 원료용액의 10내지 40%까지 분리막을 증가시키면서 배제율을 측정한 결과, PBTK의 분획분자량은 25% 증가하였다.

본 연구에서는 나노기술을 이용하여 에너지 감쇠 기능을 활용한 감쇠기 개발에 대한 연구를 하였다. 유체 감쇠기를 대체하는 완충역할을 하는 미로구조를 가지는 실리카 겔 입자를 사용하였으며, 입자에 관련한 작동 유체로는 물을 사용하여 그 효과를 검증하였다. 콜로이드 감쇠기를 구현하기 인해서는 형성된 실리카 겔 입자의 표면을 유기 실리콘 매질을 이용한 소수화 코팅 처리를 하였다. 정적 하중 상태에서의 가역적 콜로이드 감쇠기에 대한 실험을 수행하였다. 콜로이드 감쇠기내 다공질 입자의 나노 유로(pore)와 다공성 입자의 직경, 다공성 입자의 구조, 그리고 대기압 상태에서 유체의 출입을 통제하기 위한 코팅처리의 분자 간 길이와 같이 여러 가지 요인의 콜로이드 감쇠기 이력현상에 대한 영향을 평가하였다. 감쇠기의 소산 에너지양과 효율에 대해서도 조사하여 유압 감쇠기 보다 뛰어난 결과를 얻었으며 콜로이드 감쇠기로 사용 가능하다는 사실을 입증하였다.