• Journal of the Korean Magnetics Society
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• v.23 no.4
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• pp.126-129
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• 2013

We have fabricated an ordered Ni nanodot structure using an alumina mask prepared via 2-step anodization technique under phosphoric acid. We have formed a porous structure with average pore size of 279 nm on $2{\mu}m$ thick alumina film and the thermal deposition of thin Ni film though the mask led to the formation of ordered Ni nanodot structure with an average dot size of 293 nm, following the pore structure on the mask. We further investigated the magnetic properties of the nanodot structure by measuring the hysteresis curve at room temperature. When compared to the magnetic properties of a continuous Ni film, we observed the decrease in the squareness and the increase in coercivity along the magnetization easy axis, due to the isolated nanodot structure. Our study suggests that the ordered nanodot structure can be easiy fabricated with thin film deposition technique using anodized alumina mask as a mask.

• Korean Chemical Engineering Research
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• v.47 no.5
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• pp.646-650
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• 2009

Hydrocarbon gases generated from the gasification of waste could be converted into $CO_2$ and $H_2$ using reforming catalysts and then $CO_2$ was selectively adsorbed and removed to obtain pure hydrogen. To optimize adsorption efficiency for $CO_2$ removal, $Na_2CO_3$ was supported on nanoporous alumina and the efficiency was compared with commercial alumina(Degussa). Nanoporous adsorbents formed more uniform pores and larger surface area compared to adsorbents using commercial alumina. The increase of $Na_2CO_3$ loading improved adsorption of $CO_2$. Finally, the highest adsorption capacity per unit mass of $Na_2CO_3$ could be achieved when the loading of $Na_2CO_3$ reached up to 20wt%. When the content of $Na_2CO_3$ increased above 20 wt%, it aggregated on the surface, and the pore volume was decreased. Used adsorbents could be recycled by the thermal treatment.

• Journal of the Korean Ceramic Society
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• v.41 no.12 s.271
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• pp.900-906
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• 2004

Solid oxide fuel cells have a limitation in their low-temperature application due to the low ionic conductivity of electrolyte materials and difficulties in thin film formation on porous gas diffusion layer. These problems can be solved by improvement of ionic conductivity through controlled nanostructure of electrolyte and adopting nanoporous electrodes as substrates which have homogeneous submicron pore size and highly flattened surface. In this study, ultra-thin oxide films having submicron thickness without gas leakage are deposited on nanoporous substrates. By oxidation of metal thin films deposited onto nanoporous anodic alumina substrates with pore size of $20nm{\sim}200nm$ using dc-magnetron sputtering at room temperature, ultra-thin and dense ionic conducting oxide films with submicron thickness are realized. The specific material properties of the thin films including gas permeation, grain/gran boundaries formation, change of crystalline structure/microstructure by phase transition are investigated for optimization of ultra thin film deposition process.

• Journal of the Korea Institute of Information and Communication Engineering
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• v.14 no.4
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• pp.923-928
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• 2010

Anodic aluminum oxide (AAO) nanotemplates for nano electronic device applications have been attracting increasing interest because of ease of fabrication, low cost process, and possible fabrication in large area. The size and density of the nanostructured materials can be controlled by changing the pore diameter and the pole density of AAO nanotemplate. In this paper, nano porous alumina films AAO nanotemplate was fabricated by second anodization method using sputterd Al films. In addition, effects of electrolyte temperature and anodization voltate on the microstructure of porous alumina films were investigated. As the electrolyte temperature was increased from $8^{\circ}C$ to $20^{\circ}C$, the growth rate of nanoporous alumina films was increased from 86.2 nm/min to 179.5 nm/min. The AAO nanotemplate fabricated with optimal condition had the mean pore diameter of 70 nm and the pore depth of $1\;{\mu}m$.

• Proceedings of the Korean Institute of Surface Engineering Conference
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• 2015.11a
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• pp.274-274
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• 2015

양극산화를 통해 생기는 다공성 알루미나 산화막의 기공은 전해질과 적절한 온도 등 제작 조건에서 자기 조립하여 고도로 정렬된 (Highly ordered) 나노기공을 가지는 AAO (AnodicAluminum Oxide)를 제조하는데 주로 쓰이고 있다. 본 연구에서는 다단계 산화방법으로 빛의 파장에 무관하게 빛의 반사를 매우 효과적으로 줄이는 포물선 형태의 Moth-eye 구조를 가지는 템플릿을 제조하였다. SEM 측정을 통해 구조체 다공성 알루미늄 산화막의 표면적 변화를 알 수 있었고, 일정한 크기와 모양의 pore가 규칙적으로 형성된 것을 확인하였다. 그리고 제조된 템플릿 내부에 고분자를 채워 포물선 형태의 나노핀을 갖는 필름을 제조할 수 있었다.

• Journal of the Korean Magnetics Society
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• v.22 no.1
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• pp.6-10
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• 2012

We have observed the change in the film resistance of thin nickel film up to 13 nm, which is deposited on a porous anodic alumina substrate, prepared by two-step anodization technique under phosphoric acid. The resulting film grows as a porous film, following the pore structure on the surface of the alumina substrate, and the value of the resistance lies above $150k{\Omega}$ within the range of thickness studied here, decreasing very slowly with the film thickness. The observed resistance value is much higher than the reported value of a uniform film at the same thickness. Since the observed value of the surface coverage with the pores is smaller than the critical value, expected from the percolation theory, the pore structure limits the formation of conduction channel across the film. In addition, by comparing to the typical model of thickness-dependent resistivity, we expect that the scattering at the pore edge further increases the film resistance.

• Applied Chemistry for Engineering
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• v.19 no.5
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• pp.466-470
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• 2008

The objective of this study is to convert methane into hydrogen using a nanoporous catalyst in the $CO_2$ containing syngas generated from the gasified waste. For the purpose, $Ni/Al_2O_3$ catalyst was prepared with the one-pot method. According to analyses of the catalyst, three dimensionally linked sponge shaped particles were created and the prepared nanoporous catalysts had larger surface area and smaller particle size and more uniform pores compared to the sphere shaped commercial catalyst. The catalyst for reforming reaction gave the highest $CH_4$ conversion of 91%, and $CO_2$ conversion of 92% when impregnated with 16 wt% of Ni at the reaction temperature of $750^{\circ}C$. At that time, the prepared catalyst remarkably improved the $CH_4$ and $CO_2$ conversion up to 20% compared to the commercial one.

• Journal of the Korean Ceramic Society
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• v.40 no.8
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• pp.791-797
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• 2003

The special binding mechanism developed provides higher density, lower porosity and higher strengths compared with conventional castables. $\rho$-alumina was employed as a binder materials and nano-sized clay colloidal was added to enhance the drying strength preparing for the alumina vibrated castable. Lower water requirement for casting results in a denser product. The mechanical properties with dimensional stability and corrosion resistance behaviors have been improved by controlling the matrix compositions of the castable. The modulus of rupture and compressive strength after heat treatment at 150$0^{\circ}C$ are 92.34 kgf/$\textrm{cm}^2$ and 370 kgf/$\textrm{cm}^2$ respectively. The activation energy of mullite formation is 11.47 kcal/mol.

• Applied Chemistry for Engineering
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• v.19 no.3
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• pp.249-258
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• 2008

Nanoporous alumina with highly ordered pore arrays, which is prepared based on electrochemical anodization under the controlled conditions, has attracted great attention due to the variety of its applications. In case of porous alumina, the manipulation of nanoporous structures under different electrochemical conditions and their formation mechanisms have been studied for a long time. Recently, its principles have been applied to other valve metals. Especially, there have been a big success in the preparation of titania nanotubes via the anodization of titanium. In this paper, we review the anodization of aluminum and recent trends in anodization of Ti and other valve metals based on the principles of aluminum anodization.

• 한국신재생에너지학회:학술대회논문집
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• 2010.06a
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• pp.231-231
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• 2010

아직까지 국내에서 사용하는 대부분의 에너지는 화석연료에 의존하고 있다. 지하자원에서 나오는 석탄, 석유와 같은 화석연료는 다른 에너지원에 비해 운송이 간편하고 쉽게 이용할 수 있는 장점이 있지만, 환경오염의 문제성과 오일가상승, 자원의양 및 저장장소가 한정되어 있다는 단점을 가지고 있다. 이에 따라 수소와 같은 대체에너지를 이용하여 환경오염을 예방하고 무한히 사용할 수 있는 에너지원을 개발하기 위한 대체 방안들이 연구되고 있다. 폐기물 가스화시 발생되는 합성가스(CO, $CO_2$, $CH_4$, $H_2$) 내 일차로 생성된 일산화탄소는 수증기와 반응함으로써 이산화탄소로 전환이 가능하다. 잔류 메탄은 이산화탄소를 이용하여 개질함으로써 합성가스내 수소농도를 높일 수 있다. 전환된 잔류가스(CO, $CO_2$, $H_2$)내 일산화탄소는 산소를 이용하여 이산화탄소로 산화시킬 수 있으며, 산화된 이산화탄소는 흡착제를 이용하여 제거가 가능하다. 본 연구에서는 실제 가스화시 발생되는 합성가스를 이용하기 위하여, RPF가스화시 발생되는 합성가스를 직접 포집하여 실험을 진행하였다. 합성가스내 소량의 메탄은 니켈촉매를 이용하여 수소로 전화시켰으며, 잔류하는 일산화탄소는 백금촉매, 이산화탄소는 탄산나트륨 흡착제를 이용하여 연속적으로 제거함으로써 순수한 수소를 제공하였다.