• 분석과학
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• 제22권3호
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• pp.247-253
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• 2009

단결정의 실리콘 웨이퍼를 hydrofluoric acid와 ethyl alcohol이 혼합된 용액에 담궈 적정한 전류를 흘려주면 웨이퍼 표면에 수많은 pore를 형성하면서 에칭되어진다. 이러한 pore의 형태와 porosity는 전류 값과 에칭 시간 및 주기를 변화시켜 쉽게 조절할 수 있는데, 이렇게 제작된 다공성 실리콘은 수백 $m^2/cm^3$의 큰 표면적을 가지게 된다. 이때 sin 파와 같은 모양으로 시간대별 가해지는 전류 밀도를 다르게 해주어 pore안쪽의 모양을 변화시켜 주어 가시광선 영역에서 하나의 spectrum을 나타나게 되는 rugate 박막을 제작 한다. 본 연구에서는 법과학적인 목적으로 코드화된 다공성 실리콘의 rugate film을 이용하여 nano particle을 제작한 다음 이 입자들을 페인트에 혼합, 차량에 도포하고, 회수 후에 이를 확인할 수 있는지 조사하였다. 본 연구에서는 또 다양하게 가해지는 전류 값을 변경 또는 혼합하여 다공성 실리콘에 다양한 코드화를 시도하였으며, 사고 시 탈착한 페인트에서 다공성 실리콘 nano particle을 회수 하기위해 다공성 실리콘 안에 magnetite를 삽입하여 자석을 이용한 미량 나노입자 시료를 응집시켜 스펙트럼을 확인하였다.

• KSBB Journal
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• 제24권6호
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• pp.533-540
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• 2009

본 연구에서는 난용성 약물인 5'-NIO의 가용화를 위해 초임계 유체 ASES 공정을 이용하여 PVP K-30과의 고체분산체를 제조하고 첨가제인 P188의 영향에 대해 고찰하였다. FE-SEM을 이용하여 초임계 유체 공정으로 제조된 고체분산체 미립자의 형상을 분석한 결과 100-200 nm 크기의 나노입자들이 응집된 형태를 나타내었으며, P188의 함량이 증가함에 따라 입자간의 응집이 증가하여 덩어리 형태로 전환되는 것을 확인할 수 있었다. XRD 분석 결과 5'-NIO 결정피크가 사라진 것을 확인하였으며, 이는 5'-NIO가 고분자 매질내에 분자 또는 나노 크기 수준으로 분산되었음을 의미한다. 또한 FT-IR 분석 결과 5'-NIO와 PVP K-30간에 수소결합과 같은 상호작용이 존재함을 학인할 수 있었다. 5'-NIO/PVP K-30 2성분계 고체분산체에 비이온성 계면활성제를 첨가한 경우 용출률이 현저히 향상되었으나, P188의 함량이 매우 큰 경우에는 오히려 용출률이 감소한 다는 것을 확인하였다. 본 연구를 통해 초임계 유체 공정이 기존의 고체분산체 제조 방법을 충분히 대체할 수 있다는 가능성을 확인할 수 있었다.

• Restorative Dentistry and Endodontics
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• 제24권1호
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• pp.156-165
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• 1999

The purpose of this study was to evaluate the effect of surface treatments on the shear bond strength between new and old composites. Circular cavities prepared on the center of acrylic resin mold and the prepared cavities were filled with composite resin. They randomly assigned into control group and 8 groups according to the difference in surface treatments of old composites; Control group: no surface treatment, Group 1: surface treated with #120 SiC paper & bonding agent, Group 2: surface treated with #400 SiC paper & bonding agent, Group 3: surface treated with #120 SiC paper, 32% $H_3PO_4$ & bonding agent, Group 4: surface treated with #400 SiC paper, 32% $H_3PO_4$ & bonding agent, Group 5: surface treated with #120 SiC paper, primer & bonding agent, Group 6: surface treated with #400 SiC paper, primer & bonding agent, Group 7: surface treated with #120 SiC paper, 32% $H_3PO_4$, primer & bonding agent, Group 8: surface treated with #400 SiC paper, 32% $H_3PO_4$, primer & bonding agent. New composites were applicated on the old composites of experimental groups. The shear bond strengths for the experimental specimen were measured and the results were analyzed by using one way ANOVA. The observations of surface morphology after SiC paper roughening and debonded surface morphology after shear bond strength test were done by SEM. The results were as follows; 1. Shear bond strengths for specimens roughened with #120 SiC paper matching with the particle size of coarse diamond bur were significantly higher than those for the specimens with #400 SiC paper(P<0.05). By SEM, the surface of the specimens roughened with #120 SiC paper was more irregular than the specimens with #400 SiC paper. 2. Shear bond strengths for specimens treated with 32% $H_3PO_4$ etchant, primer, bonding resin were significantly higher than those for specimens treated with 32% $H_3PO_4$ and bonding resin(P<0.05). 3. Shear bond strengths for the specimens treated with 32% $H_3PO_4$ etchant and bonding resin were significantly higher than those for specimens treated with only bonding resin(P<0.05). There was no remarkable change of surface morphology after 32% $H_3PO_4$ etching. 4. It was possible to observe mixed fracture patterns (the cohesive fracture of old composite and the adhesive fracture between old and new composite) in the specimens roughened with #120 SiC paper, but almost adhesive fracture in the specimens roughened with #400 SiC paper.

• 한국염색가공학회지
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• 제28권1호
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• pp.48-56
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• 2016

Improvement of heat sink technology related to the continuous implementation performance and extension of device-life in circumstance of easy heating and more compact space has been becoming more important issue as multi-functional integration and miniaturization trend of electronic gadgets and products has been generalized. In this study, it purposed to minimize of decline of the heat diffusivity by gluing polymer through compounding of inorganic particles which have thermal conductive properties. We used NH-9300 as base resin and used inorganic fillers such as silicon carbide(SiC), aluminum nitride(AlN), and boron nitride(BN) to improve heat diffusivity. After making film which was made from 100 part of acrylic resin mixed hardener(1.0 part more or less) with inorganic particles. The film was matured at $80^{\circ}C$ for 24h. Diffusivity were tested according to sorts of particles and density of particles as well as size and structure of particle to improve the effect of heat sink in view of morphology assessing diffusivity by LFA(Netzsch/LFA 447 Nano Flash) and adhesion strength by UTM(Universal Testing Machine). The correlation between diffusivity of pure inorganic particles and composite as well as the relation between density and morphology of inorganic particles has been studied. The study related morphology showed that globular type had superior diffusivity at low density of 25% but on the contarary globular type was inferior to non-globular type at high density of 80%.

• Korean Chemical Engineering Research
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• 제54권6호
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• pp.854-862
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• 2016

최근 화석연료를 대체할 친환경 신재생에너지에 대한 요구가 증가하면서 수소에너지가 미래 대체에너지원으로서 주목받고 있다. 수소를 생산하는 방법 중 수전해 기술은 에너지효율과 안정성이 뛰어난 장점이 있지만, 산소발생반응시 발생하는 높은 과전압은 여전히 단점으로 지적되고 있다. 본 연구에서는 분무열분해 공정을 통하여 Co 전구체로부터 $Co_3O_4$를 제조하였다. 또한, urea, sucrose, citric acid의 유기물첨가제를 사용하여 다양한 입자 크기와 표면형상을 가지는 $Co_3O_4$를 제조하였고, 필요에 따라 추가로 열처리를 실시하였다. 합성한 $Co_3O_4$의 물리적 특성을 분석하기 위해 X-선 회절 분석(XRD)으로 결정성을 조사하였고, 주사전자현미경(SEM)과 투과전자현미경(TEM)으로 입자형상 및 표면을 분석하였다. 질소 흡 탈착 시험을 통해 촉매의 비표면적 및 기공부피를 측정하였고, 질소도핑을 확인하기 위해 X-선 광전자 분광법(XPS)을 사용하였다. 촉매의 산소발생반응 활성을 알아보기 위해 3전극 셀에서 선형주사전위법(LSV)으로 전기화학적 거동을 분석하였다. 첨가제를 사용하지 않은 $Co_3O_4$가 가장 우수한 활성을 보였고, 이는 분무열분해법을 통하여 상대적으로 작은 입자형성과 높은 비표면적의 영향인 것으로 판단된다.

• 한국재료학회지
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• 제14권3호
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• pp.224-228
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• 2004

Respectively the powder made of ZnO added $SnO_2$ was prepared by coprecipitation method and the thick film gas sensor was fabricated by screen-printing technique, The morphology and phase of the powder and film was investigated by SEM and XRD. The specific area of the particle was linearly increased with ZnO contents. Target gas was di(propylene glycol) methylether ($CH_3$($OC_3$$H_{6}$ )$_2$OH, DPGME), which is simulant gas of blister gas. The gas sensing characteristics for DPGME were examined with flow type measurement system and the concentrations of target gas were controlled from 500 ppb to 1500 ppb. ZnO (2 wt%) added $SnO_2$ showed maximum sensitivity to DPGME at $300^{\circ}C$.

• Korean Chemical Engineering Research
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• 제54권1호
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• pp.75-80
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• 2016

Biologically stabilized gold nanoparticles were synthesized from the flower aqueous extract of T. divaricata. The synthesized nanoparticles were characterized by UV-Vis spectrophotometer, Zeta sizer, FTIR and TEM analysis. T. divaricata reduced gold nanoparticles having particle size and potential of 106.532 nm and -10.2 mV, respectively, with a characteristic peak of 550 nm in UV-visible spectrophotometer. FTIR graph after comparison between the crude flower extract and gold nanoparticles showed three major shifts in the functional groups. The morphology and size of the gold nanoparticles were examined by HRTEM analysis, which showed that most of the nanoparticles were nearly spherical with size of 100 nm. The gold nanoparticles synthesized demonstrated potent anticancer activity against MCF-7 cell line. The findings conclude that the antioxidant molecule present in T. divaricata may be responsible for both reduction and capping of gold nanoparticles which possess potential applications in medicine and pharmaceutical fields.

• 한국세라믹학회지
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• 제51권5호
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• pp.413-417
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• 2014

The effect of calcination treatment of raw powders prior to high temperature synthesis of Ca-${\alpha}$-SiAlON:$Eu^{2+}$ phosphor was investigated. Based on data acquired from thermogravimetric analysis, calcination temperatures were set at 600, 750, and $900^{\circ}C$. Compared to the photoluminescence (PL) intensity of direct synthesis without calcination, a similar intensity was found for the $600^{\circ}C$ treatment, a 19% increased PL intensity was found for the $750^{\circ}C$ treatment, and a 23% decreased PL intensity was found for the $900^{\circ}C$ treatment. Observation of the particle morphology of the synthesized phosphors revealed that the material transport promoted through the agglomerates formed by the $750^{\circ}C$ treatment led to enhanced PL intensity. On the other hand, the oxidation of the starting AlN particles during the $900^{\circ}C$ treatment resulted in decreased photoluminescence.

• 한국세라믹학회지
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• 제51권5호
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• pp.424-429
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• 2014

YAG:$Ce^{3+}$ phosphor powders were synthesized using $Al(OH)_3$ seeds by means of a PVA-polymer-solution route. Various types of PVA with different molecular weights (different polymerization) were used. All dried precursor gels were calcined at $500^{\circ}C$ and then heated at $1500^{\circ}C$ in a mix of nitrogen and hydrogen gases. The final powders were characterized via XRD, SEM, PSA, PL, and PKG analyses. The phosphor properties and morphologies of the synthesized powders were dependent on the PVA type. As the molecular weight of the PVA was increased, the particle size gradually decreased with agglomeration, and the luminous intensity of the phosphor increased. However, the phosphor powder prepared from the PVA exhibiting very high molecular weight, showed a 531 nm (blue) shift from the 541 nm (yellow) wavelength of the YAG:$Ce^{3+}$ phosphor. Finally, the synthesized YAG:$Ce^{3+}$ phosphor powder prepared from the PVA with 89,000 - 98,000 molecular weight showed phosphor properties similar to those of a commercial phosphor powder, but without a post-treatment process.

• 한국신재생에너지학회:학술대회논문집
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• 한국신재생에너지학회 2010년도 춘계학술대회 초록집
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• pp.138.2-138.2
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• 2010

Scandium-doped zirconium, ScSZ-based electrolyte, provides higher oxygen conductivity than YSZ and nano-based electrolyte materials are ideal for fabricating thin film electrolyte membrane of SOFC unit cell. Moreover, it may be applied to anode and cathode as well as electrolyte as ionic conductor. In this report, nano-based ScSZ-based electrolyte powder was prepared by co-precipitation synthesis. The particle size, surface area and morphology of the powder were observed by SEM and BET. Thin film electrolyte of under $10{\mu}m$ was fabricated by tape casting and co-firing using the synthesized ScSZ-based powders, and ionic conductivity and gas permeability of electrolyte film were evaluated. Finally, the SOFC unit cell was fabricated using the anode-supported electrolyte prepared by a tape casting method and co-sintering. Electrochemical evaluations of the SOFC unit cell, including measurements such as power density and impedance, were performed and analyzed.