• 보존과학연구
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• 통권31호
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• pp.43-57
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• 2010

This study intends to provide quantitative data about the extraction characteristics of major elements of earthenware by executing soaking test of cleaning agents. It aims at providing basic data for the stability assessment when applying the cleaning agents for conserving earthenware. The data will be extracted from the analysis of co-relationship between the physical characteristics and the ion extraction characteristics. XRD analysis displayed that AT-1, AT-2 and AT-3 which did not generate mullite were fired at lower than 1,000 whereas AT-3 and AT-5 that included mullite were higher than 1,000. The degree of absorption was AT-4 > AT-2 > AT-1 > AT-3 > AT-5 in order and the correlation between the degree of absorption and firing temperature of earthenware displayed a positive correlation. Extraction amount of oxalic acid which was used for the removing iron oxide was AT-1 > AT-2 AT-4 > AT-3 > AT-5 in order. and the ion extraction data displayed that there is a positive correlation with absorption level. However AT-1 and AT-2 which were fired at lower temperature showed that there was no correlation between the ion extraction characteristics and absorption level. Ion extraction of citric acid produced little amount compared with the one of oxalic acid, yet it caused less damage to earthenware than oxalic acid when it applied. The result of ion extraction level in the absorption test displayed that Fe had higher level than in Si, Al from the test for both oxalic acid and citric acid. Based on the regression analysis of the data from the previous studies, the physical characteristics of the earthenware and ion extraction level, further studies will be conducted on the predicting technique on the extraction characteristics of major elements of earthenware samples for the conservation in future.

• 한국세라믹학회지
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• 제42권4호
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• pp.237-244
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• 2005

비정질알루미나와 기공형성제에 물을 혼합하여 원통형으로 성형하고 수화한 다음, 건조 및 소성하여 직경 5mm, 평균 길이 약 10mm의 $\gamma-$알루미나 펠릿을 제조하였다. 이를 $Fe(NO_{3})_{3}{\cdot}9H_{2}O$용액과 $CH_{3}COOH$ 혼합용액에 침척시켜 $200^{\circ}C$ 온도로 3시간 수열처리한 후, 건조하고 소성하여 촉매를 제조하였다. 이와 같이 수열법에 의해 제조된 $Fe_{2}O_{3}/\gamma-Al_{2}O_{3}$ 세라믹촉매를 환경촉매로 적용하기 위해, 아닐린과 같은 난분해성물질을 촉매를 사용하지 않는 오존단독공정과 촉매를 사용하는 촉매오존(catalytic ozonation)공정으로 구분하여 $OH^{\cdot}$ 라디칼 전환반응 개시제로서의 기능과 그 분해특성을 비교하였다.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2013년도 제44회 동계 정기학술대회 초록집
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• pp.130-131
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• 2013

Nanostructured oxides are widely used in heterogeneous catalysis where their catalytic properties are closely associated with the size and morphology at nanometer level. The effect of particle size has been well decumented in the past two decades, but the shape of the nanoparticles has rarely been concerned. Here we illustrate that the redox and acidic-basic properties of oxides are largely dependent on their shapes by taking $Co_3O_4$, $Fe_2O_3$, $CeO_2$ and $La_2O_3$ nanorods as typical examples. The catalytic activities of these rod-shaped oxides are mainly governed by the nature of the exposed crystal planes. For instance, the predominant presence of {110} planes which are rich in active $Co^{3+}$ on $Co_3O_4$ nanorods led to a much higher activity for CO oxidation than the nanoparticles that mainly exposed the {111} planes. The simultaneous exposure of iron and oxygen ions on the surface of $Fe_2O_3$ nanorods have significantly enhanced the adsorption and activation of NO and thereby promoted the efficiency of DeNOx process. Moreover, the exposed surface planes of these rod-shaped oxides mediated the reaction performance of the integrated metal-oxide catalysts. Au/$CeO_2$ catalysts exhibited outstanding stability under water-gas shift conditions owing to the strong bonding of gold particle on the $CeO_2$ nanorods where the formed gold-ceria interface was resistant towards sintering. Cu nanoparticles dispersed on $La_2O_3$ nanorods efficiently catalyzed transfer dehydrogenation of primary aliphatic alcohols based on the uniue role of the exposed {110} planes on the support. Morphology control at nanometer level allows preferential exposure of the catalytically active sites, providing a new stragegy for the design of highly efficient nanostructured catalysts.

• 보존과학회지
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• 제34권4호
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• pp.245-257
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• 2018

To investigate the deterioration of textiles with metal thread, I surveyed 40 textile objects, dating from the 11th to the 19th century from Korea, China, Japan, and Central Asia at the Metropolitan Museum of Art, New York. This survey included various types, widths, and thicknesses of metal thread. In addition, deterioration was examined under the microscope and color information was collected using the spectrophotometer. While investigating metal thread in the collections, I fabricated 12 different types of metal samples with metal leaf(24K gold, silver, and copper leaf), adhesive (hide animal glue and a mixture of hide animal glue and iron oxide red), and paper substrate(Korean mulberry and Taiwanese kozo paper). The accelerated deterioration process of those fabricated samples was carried out using a light box(UV and daylight), and a humidity cabinet. In the light experiment with blue scales textile fading card(aka, blue wool standard), the metal leaf began to peel off during the deterioration process with 756,000 lux-hours UV and daylight. In the temperature and humidity experiment, I could observe the reddish tarnish on copper, and some part of it began to peel off. Color reading on the light exposed samples showed that the degree of color change on the surface follows the amount of exposure as it increased over time. On the other hand, color change on the samples after artificial deterioration using temperature and humidity factors showed random change of color with occasional spikes. Distortion of original shape worsened in the samples exposed to temperature and humidity.

• 상하수도학회지
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• 제26권3호
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• pp.431-442
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• 2012

The purpose of this study, is to separate magnetic separation devices using permanent magnets by using magnetization characteristics remaining in treated water after adsorption and synthesizing phosphorus adsorbent capable of magnetic separation for efficient removal of phosphorus. The synthesis of the adsorbent which set Zirconium(Zr) having high friendly features for phosphorus as an element, and by synthesizing Iron Oxide($Fe_3O_4$, another name of $Fe_3O_4$ is magnetite) being able to grant magnetism to Zirconium Sulfate($Zr(SO_4)_2$), zirconium magnetic adsorbent(ZM) were manufactured. In order to consider the phosphorus adsorption characteristics of adsorbent ZM, batch adsorption experiment was performed, and based on the results, pH effect, adsorption isotherm, adsorption kinetics, and magnetic separation have been explore. As the experiment result, adsorbent ZM showed a tendency that the adsorption number was decreased rapidly at pH 13; however, it was showed a high amount of phosphorus removal in other range and it showed the highest amount of phosphorus removal in pH 6 of neutral range. In addtion, the Langmuir adsorption isotherm model is matched well, and D-R adsorption isotherm model is ranged 14.43kJ/mol indicating ion exchange mechanism. The result shown adsorption kinetics match well to the Pseudo-second-order kinetic model. The adsorbent ZM's capablility of regenerating NaOH and $H_2SO_4$, was high selectivity on the phosphorus without impacts on the other anions. The results of applying the treated water after adsorption of phosphorus to the magnetic separation device by using permanent magnets, shows that capture of the adsorbent by the magnetization filter was perfect. And they show the possibility of utilization on the phosphorus removal in water.

• 멤브레인
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• 제14권2호
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• pp.149-156
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• 2004

본 연구에서는 광촉매 반응과 막분리 기술을 접목시킨 혼성 고도 정수처리 공정에서 소독 부산물의 전구체로 알려진 자연산 유기물을 효과적으로 제거하고자 하였고 다양한 운전 조건에서 시스템의 성능을 비교 평가하였다. 자연산 유기물은 흡입여과 방식의 분리막과 TiO$_2$ 광촉매를 이용하여 광분해하였을 때 광촉매 투입량의 증가에 따라 반응속도가 증가하였지만 과량의 촉매 주입시에는 반응 속도 향상에 오히려 부정적으로 작용하였다. 자연산 유기물을 보다 효과적으로 제거하기 위해 산화철 주입, TiO$_2$ 표면처리, 분리막 표면코팅을 시도하여 제거특성 및 운전에 따른 막여과 특성을 평가하였다. 산화철 주입은 초기에 흡착작용으로 인해 제거율 증가를 보였으나 반응이 진행됨에 따라 산화철 입자에 의한 광산란으로 광분해 효율이 오히려 감소되었다. 산화철 입자에 의한 광산란을 제어하고자 TiO$_2$ 표면을 광처리와 열처리 방법을 이용해 철을 직접 부착시킨 경우 긍정적인 효과를 얻지 못했다. 그러나 산화철로 막표면을 코팅하여 광산란 효과를 배제시킨 경우에는 향상된 결과를 보였다 막투과 플럭스 15 L/$m^2$-h에서 정밀여과를 수행하였을 때 TiO$_2$나 산화철에 의한 막오염은 거의 일어나지 않았고 안정된 막투과도를 나타내었다.

• 한국광물학회지
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• 제24권1호
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• pp.31-36
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• 2011

운석은 모암인 소행성(asteroid)이나 미세소행성(planetesimal)에서 충돌에 의해 분리된 후, 태양계 내의 공간을 배회하다가 지구의 중력에 이끌려 지표에 떨어진 후 수집된 돌덩이다. 따라서 생성 초기의 지구를 포함하는 태양계 내 지구형 행성의 생성 초기와 진화과정을 규명하려면 원시 태양계의 정보를 간직하고 있는 운석의 물리/화학적 분석이 반드시 필요하다. 특히 열잔류자화(thermoremanent magnetization, TRM) 대비 포화등온잔류자화(saturation isothermal remanent magnetization, SIRM)의 비율과 자화를 유도하는 자기장 강도의 상관관계를 이용하면 운석이 함유하는 자성광물을 판별할 수 있다. TRM/SIRM 비를 이용하여 2종류의 미분화운석(H5 Richardton, LL6 St. Severin)과 2종류의 화성기원 분화운석(ALH84001, DaG476)에 대해 자성광물 판별을 시도하였다. 실험 결과 H5 Richardton, LL6 St. Severin, ALH84001, DaG476의 주 자성광물이 각각 카마사이트, 테트라테나이트, 자철석, 크롬티탄함유철석임을 판별하였다.

• 한국인터넷방송통신학회논문지
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• 제10권5호
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• pp.1-5
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• 2010

본 논문은 열연 공정을 거친 철강 강판에 형성된 산화철 층, 즉 scale 층의 두께를 유전체 렌즈 안테나를 이용하여 측정하는 방법을 소개하였다. 유전체 렌즈 안테나는 X 밴드 대역에서 주파수에 독립적인 특성을 가지며, 혼 안테나에서 방사되는 구면파를 초점이 형성되는 평면에 평면파를 형성하는 역할을 한다. 이러한 동작원리를 이용하여 철강 강판에 형성된 scale 층에 완전 도체와 유전체로 형성된 two-layer 구조에 직각 입사하는 평면파의 이론적 해석이 적용될 수 있다. Scale의 두께를 도출해 내는 과정에서 유전체 렌즈의 영향을 최소화하기 위한 calibration 과정이 삽입되었으며, 이로 인한 반사 계수 위상의 오차가 발생하였다. 이러한 위상 오차에 의한 scale 두께의 오차를 줄이기 위하여, 수치적으로 regression 방법을 사용하였으며, 기존의 iteration 방법과 비교하여, 주기적으로 얻어지는 두께의 값이 아닌 단일 두께 값을 얻어낼 수 있었다.

• 한국수소및신에너지학회논문집
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• 제19권6호
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• pp.505-513
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• 2008

The two-step thermochemical cycle was examined on the $CeO_2$, YSZ, and $ZrO_2$-supported $NiFe_2O_4$ to investigate the effects of support material addition. The supported $NiFe_2O_4$ was prepared by the aerial oxidation method. Thermal reduction was conducted at 1573K and 1523K while water-splitting was carried out at 1073K. Supporting $NiFe_2O_4$ on $CeO_2$, YSZ and $ZrO_2$ alleviated the high-temperature sintering of iron-oxide. As a result, the supported $NiFe_2O_4$ exhibited greater reactivity and repeatability in the water-splitting cycle as compared to the unsupported $NiFe_2O_4$. Especially, $ZrO_2$-supported $NiFe_2O_4$ showed better sintering inhibition effect than other supporting materials, but hydrogen production amount was decreased as cycle repeated. In case of $CeO_2$-supported $NiFe_2O_4$, improvement of hydrogen production was found when the thermal reduction was conducted at 1573K. It was deduced that redox reaction of $CeO_2$ activated above 1573K.

• 한국물환경학회지
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• 제22권6호
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• pp.991-995
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• 2006

The layered double hydroxide with the insertion of chloride ions (LDH-Cl), which was synthesized by the co-precipitation method, was applied to investigate the fundamental aspects of the absorptive agent for phosphate removal from wastewater. The adsorption capacity was best described by the Langmuir-FreundIich isotherm, and the estimated isotherm parameters indicate that the LDH-CI capacity for the phosphate removal is much higher than that observed using a natural adsorbent material such iron oxide tailing. The kinetic experiment also showed that the LDH-Cl adsorption reaction rapidly at the adsorptive rate of 0.55 mg-P/g-LDH/min, implying that this adsorbent can be of use in the full-scale applications. The pH had a minimal effect on the LDH adsorption capacity in the range of 5 to 11, although the capacity dropped at the low pHs because of the change in LDH surface properties. Furthermore, other anions such as $Cl^-$ and $NO_3{^-}$ commonly found in the wastewater streams insignificantly affected the phosphate removal efficiencies, while $HCO_3{^-}$ ions had a negative effect on the LDH adsorption capacity due to its high selectivity. The phosphate removal experiment using the actual secondary effluent from a wastewater treatment plant showed the similar decrease in adsorption capacity, indicating that the bicarbonate ions in the wastewater were competing with phosphate for the adsorptive site in the surface of the LDH-Cl. Overall, the synthetic adsorbent material, LDH-Cl, can be a feasible alternative over other conventional chemical agents, since the LDH-Cl exhibits the high phosphate removal capacity with the low sensitivity to other environmental conditions.