목적 : 본 연구는 세륨(IV)-지르코늄(IV) 산화물 나노입자를 사용하여 콘택트렌즈를 제조한 후, 안의료용 기능성 렌즈로의 사용 가능을 확인 위해 제조된 렌즈의 물성을 비교 분석하였다. 방법 : 2-Hydroxyethyl methacrylate에 나노 세륨-지르코늄 산화물(cerium(IV)-zirconium(IV) oxide)을 첨가하여 공중합 한 후 물성을 측정하고, 친수성 단량체인 methacrylic acid(MA)를 추가로 첨가하여 물성을 측정, 비교하였다. 결과 : 다양한 비율의 세륨(IV)-지르코늄(IV) 산화물 나노입자와 MA를 첨가한 렌즈의 물성을 평가한 결과, UV-B 투과율은 40.95~66.26%, 굴절률 1.4163~1.4357, 함수율 37.44~47.18%, 접촉각 36.87~56.36°, 인장 강도 0.0612~0.561 kgf/mm², 표면거칠기 7.70~8.72 nm로 각각 측정되었다. 나노입자 및 MA 첨가는 습윤성, 인장강도 및 중합안정성을 향상시키고, UV-B 투과율과 표면거칠기를 감소시켰으며, 황색포도상구균에 대한 항균 성이 확인되었다. 결론 : 세륨(IV)-지르코늄(IV) 산화물 나노입자에 MA를 첨가하여 제조한 렌즈가 중합 안정성, 내구성, 습윤성 을 향상시키는 것을 확인하였으며, 따라서 안의료용 기능성 콘택트렌즈 소재로 활용할 수 있을 것으로 판단된다.

The separation of zirconium and hafnium using tributyl phosphate (TBP)-Dodecane extractants in nitric acid medium was performed. Zirconium oxychloride, used as extraction feed, was obtained from the synthesis of Kalimantan zircon sand concentrate smelted using NaOH. The extraction process was carried out by dissolving chloride-based metals in nitric acid media in the presence of sodium nitrate using TBP-Dodecane as an extractant. Some of the extraction parameters carried out in this study include variations in organic phase and aqueous phase (O/A), variations in contact time, and variations in nitric acid concentration. Extraction was carried out using a mechanical shaker according to the parameter conditions. X-ray fluorescence (XRF) was used for elemental (Zr and Hf) composition analysis of the aqueous solution. The results showed that zirconium was separated from hafnium at optimum conditions with an organic/aqueous ratio of 1:5, contact time of 75 min, and an HNO3 concentration of 7 M. The resulting separation factor of zirconium and hafnium using TBP-Dodecane was 14.4887.

Zirconium(Zr) nuclear fuel cladding tubes are made using a three-time pilgering and annealing process. In order to remove the oxidized layer and impurities on the surface of the tube, a pickling process is required. Zr is dissolved in HF and HNO3 mixed acid during the process and pickling waste acid, including dissolved Zr, is totally discarded after being neutralized. In this study, the waste acid was recycled by adding BaF2, which reacted with the Zr ion involved in the waste acid; Ba2ZrF8 was subsequently precipitated due to its low solubility in water. It is very difficult to extract zirconium from the as-recovered Ba2ZrF8 because its melting temperature is 1031 oC. Hence, we tried to recover Zr using an electrowinning process with a low temperature molten salt compound that was fabricated by adding ZrF4 to Ba2ZrF8 to decrease the melting point. Change of the Zr redox potential was observed using cyclic voltammetry; the voltage change of the cell was observed by polarization and chronopotentiometry. The structure of the electrodeposited Zr was analyzed and the electrodeposition characteristics were also evaluated.

The effects of Nb and Cr addition on the microstructure, corrosion and oxide characteristics of Zr based alloys wereinvestigated. The corrosion tests were performed in a pressurized water reactor simulated-loop system at 360oC. Themicrostructures were examined using OM and TEM, and the oxide properties were characterized by low-angle X-ray diffractionand TEM. The corrosion test results up to 360 days revealed that the corrosion rates were considerably affected by Cr contentbut not Nb content. The corrosion resistance of the Zr-xNb-0.1Sn-yCr quaternary alloys was improved by an increasing Nb/Cr ratio. The crystal structure of the precipitates was affected by a variation of the Nb/Cr ratio. The Zr-Nb beta-enrichedprecipitates were mainly formed in the high Nb/Cr ratio alloy while Zr(NbCr)2 precipitates were frequently observed in the lowNb/Cr ratio alloy. The studies of oxide characteristics revealed that the corrosion resistance was related to the crystal structureof the precipitate.

The coastal area of Republic of Korea is very clean compared to other countries. In this reason, west coastal area of our country is a good place for breeding up a fish such as shrimp. In winter season, the heating system is required for preventing shrimp death caused by freezing in the farm. The heater in the heating system for fishery's farm is operated very severe combating corrosion due to high accumulation by feeding material and high temperature in heated sea water. Almost all manufactured heaters of STS 316L and Ti material are scrapped every year due to heavy corrosion such a general and crevice corrosion. For comparing the general and galvanic corrosion in new heater material, the test material of Zirconium (Zr), Titanium (Ti) and STS 316L are tested by potentiodynamic polarization, electrochemical impedance spectroscopy (EIS), current density-time methods and microscopic examination in a 3.5% NaCl solution. The corrosion potential (Ecor) measured by potentiodynamic polarization for Zr, Ti and STS 316L reveals -198, -250 and -450mV, corrosion current density 0.5, 2.5 and 6.5μA/cm2 respectively. The film resistance measured by EIS are Zr 63,000, Ti 39,700 and 316L 3,150Ω, and the current of Zr-Ti couple is 0.03μA, whereas Zr-316L SS is 0.1μA. According to the result of this experiment in 3.5% NaCl solution, Zr is excellent corrosion resistance material than Ti and STS 316L.

The present study was focused on the synthesis of a zirconium-based alloyed nanopowder by the plasma arc discharge process. The chemical composition, phase structure, particle size and hydrogen sorption property of the synthesized powders under various synthesis conditions were analyzed using XRF, XRD, SEM, XPS and the ASTM-F798 method. The chemical composition of the synthesized Zr-V-Fe-based powders approached that of the raw material with an increasing hydrogen fraction in the powder synthesis atmosphere. The synthesized powder consist of a mixed phase structure of the phases. This powder has an average particle size of about 20 nm. The synthesized nanopowder showed getter characteristics, even though it had a lower hydrogen sorption speed than the getter powder. However, the synthesized Zr nanopowder with an average particle size of 20 nm showed higher hydrogen sorption speed than the getter powder.

본 연구는 직접메탄을 연료전지(Direct Methanol Fuel Cell)에 적용가능한 양이온교환막 개발에 관한 것으로 PVA/PAM/ZrP 막을 제조하여 PAM, ZrP의 함량 및 농도 변화에 따른 막의 특성을 연구하였다. PVA/PAM/ZrP 막은 PVA에 가교제인 PAM의 함량을 7∼11 wt%로 증가시켜 제조하였으며 그 각각의 막에 80℃에서 zirconyl chloride와 Phosphoric acid solution에 침적시켜 제조하였다. ZrP의 농도를 1, 2 M로 변화시켜 메탄을 투과도, 이온전도도, 함수율 및 이온교환용량을 측정하였다. PVA/PAM/ZrP 막의 메탄올 투과도는 10/-8∼l0-6 cm2/sec, 이온전도도는 10-3~10-2 S/cm 정도 나타내었으며 함수율은 0.26∼l.17 g H2O/g membrane, 이온교환용량은 2.59∼5.1 meq/g membrane의 결과를 보였는데 이는 PVA/PAM 막과 비교하여 메탄을 투과도, 이온전도도는 각각 18%, 23% 정도 증가한 것으로 관찰되었다.

Zirconium nitride powders were synthesized at a relatively lower temperature using methane as a reducing agent in the nitridation of zircoia. ZrO2 powder was prepared by a sol-gel technique. The resulting sol-gel was centrifuged, and the gel was washed with deionized water. Anhydrous ammonia was used as the nitrogen source and methane was used as the reducing agent. Conversion diagrams show the equilibrium solid phase as a function of reagent concentrations for a specific temperature and gas pressure for the reagent system NH3-ZrO2-CH4. The reagent concentration ranges within which pure ZrN is formed increase with increasing reaction temperature. Low pressure with an excess of hydrogen decreases the reaction temperature at which pure ZrN is formed. Low pressure together with the introduction of excess hydrogen into the reaction system increases Zr and N conversion efficiency and retards C deposition.

The -zirconium phosphate particles as fine as 20 nm were fabricated through solution technique using and as precursors. Stability of -Zirconium phosphate could be ensured by adding excess phosphoric acid to a stoichiometric composition Instead of using reflux route that resulted in coarsening of particles due to an inevitably long aging. The excess phosphorous incorporated in the crystal could be successfully eliminated afterwards through careful washing. Moreover, heavily agglomerated particles are observed before washing, but fairly dispersed state is found out after washing treatment. Thus, it is found that dispersed state as well as phase stability is ensured through proper washing treatment.

2원계 (Zr-xNb, Zr-xSnl 와 3원계 (Zr-O.8Sn-xNb, Zr-O.4Nb-xSnl Zr합금의 기계적 특성에 미치는 Nb와 Sn의 영향올 조사하기 위하여 인장시험 빛 마세조직 분석을 실시하였다. Nb와 Sn량이 많이 첨가될수록 2원계와 3원계 합금의 강도는 정진적으로 증가하는 경향을 보이는데, Nb와 Sn이 고용도 이상으로 첨가될 때 강도중가는 더욱 두드러진 것으로 냐타났다. 강도 증가현상을 고용강화, 석출강화, 결정립 미세화에 의한 강화, 집합조직에 의한 강화효과 관정에서 분석한 결과, 고용강화 효과가 가장 두드러지며 Nb와 Sn이 고용도 이상에서는 석출강화가 강도에 기여하는 것으로 냐타났다. 합금원소 첨가에 따른 결정립미세화도 강도에 약간은 영향을 미치는 것으로 사료된다. 그러나 집합조직은 합금원소 변화에 따라서 거의 변화가 없는 것으로 냐타났으므로 집합조직은 강도증가에 기여하지 않는 것으로 생각된다.

Zr-Si의 2원계 합금에서 Si함량 변화가 Zr의 부식특성에 미치는 영향을 알아보기 위해 Si 함량을 0.01-0.1wt.%로 조절하여 Zr-Si 2원계 합금을 제조하고 360˚C, 2660psi 물 분위기의 autoclave에서 100일동안 부식 실험을 수행하였다. 0.01wt.%, 0.05wt.%의 Si 첨가에서는 검은색의 균일한 산화막이 생성되었고, 부식속도의 천이는 발생하지 않았다. 그러나 0.01wt.%에서는 흰색의 산화막이 생성되었고, 70일에서 부식속도 천이가 발생하였다. Sigkafid이 0.01에서 0.01wt.%로 증가할수록 무게증가량은 증가하는 경향을 보였다. Si 첨가량 변화에 따라 산화막구조의 변화는 나타나지 않았지만, 산화막의 전기적 성질에 많은 영향을 주었다. Si 첨가량 변화에 따라 산화막구조의 변화는 나타나지 않았지만, 산화막의 전기적 성질에 많은 영향을 주었다. Zr-Si 2원계 합금에서 Si은 tetragonal 구조의 Zr3Si로 석출되었으며, Si 함량이 증가할수록 석출물의 크기와 부피분율이 증가하였고, 석출물의 크기와 부피분율 증가에 따라 석출물의 short-circuit 효과 때문에 무게증가량이 증가하는 경향을 보였다.