• 한국진공학회지
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• 제22권4호
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• pp.204-210
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• 2013

임플란트와의 골융합을 향상시키기 위해서 세포와 임플란트 표면의 나노구조의 상호작용에 대한 이해가 중요하다. 본 연구에서는 Sn를 촉매로 이용하여 Vapor-Liquid-Solid 법을 이용하여 $TiO_2$ 나노와이어를 튜브 전기로 안에서 질소기체 조건하에서 합성하였다. 이 때 촉매로 사용된 Sn 박막의 두께에 따라 응집된 나노스피어를 이용하여 $TiO_2$ 나노와이어의 크기를 조절하였다. 골융합을 위한 예비 실험으로써, 만들어진 $TiO_2$ 나노와이어 샘플 위에서 조골전구세포(pre-osteoblast)를 1주일간 배양하였고, 세포가 $TiO_2$ 나노와이어에 잘 결합함을 볼 수 있었다.

• 한국세라믹학회지
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• 제27권2호
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• pp.274-282
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• 1990

SnO2 powder was prepared by hydroxide method and oxalate method. In hydroxide method, the pH dependence of powder characteristics was investigated by using buffer solution. As increasing the pH of solution, SnO2 powder size was decreased because nucleation rate was inctreased by more supersaturation of solution. Also, we found that the powder by our method has larger specific surface area in comaprison with other method. And the degree of agglomeration of precipitate with the change of precipitation temperature was investigated in oxalate method. The SnC2O4 was angular shape precipitate, and the size of the SnC2O4 was increased with the increase of precipitation temperature in methanol solvent.

• 한국재료학회지
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• 제12권3호
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• pp.225-230
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• 2002

Sn was selected as an alloying element of Cu. The Cu-Sn thin layers were deposited on the Si substrates by the electroplating method and their properties were studied. By rapidly thermal annealing(RTA) up to 40$0^{\circ}C$ after electroplating, sheet resistance decreased and adhesion strength increased, but that trend was reversed at the 50$0^{\circ}C$ RTA. Cu-Sn particles grew dense and the surface was uniform up to 40$0^{\circ}C$, but at 50$0^{\circ}C$, empty area was introduced and the surface became rough owing to oxidation and particle coarsening and agglomeration. Deposited layer contained significant amount of Si, while pure Cu-Sn layer with the composition ratio of 90:10 was present only on the top surface. However, no significant change in the Cu composition within alloy layers occured by the RTA regardless of its temperature. This indicates that the Cu diffusion into the Si was suppressed by the presence of Sn.

• 한국세라믹학회지
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• 제53권1호
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• pp.122-127
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• 2016

Tin oxide ($SnO_2$) nanoparticles have been synthesized by solution combustion method using citric acid as a fuel. The oxide to fuel ratio has been varied to obtain ultrafine nanoparticles with better surface area; such particles will be useful in many applications. With this synthesis method, spherical particles are formed having a particle size in the range of 11-30 nm and BET surface area of ~ $24m^2/g$. The degree of agglomeration of $SnO_2$ nanoparticles has been calculated.

• 한국재료학회지
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• 제24권11호
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• pp.578-584
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• 2014

To synthesize Sn nanoparticles (NPs) less than 30 nm in diameter, a modified polyol process was conducted at room temperature using a reducing agent, and the effects of different pH values of the initial solutions on the morphology and size of the synthesized Sn NPs were analyzed. tin(II) 2-ethylhexanoate, diethylene glycol, sodium borohydride, polyvinyl pyrrolidone (PVP), and sodium hydroxide were used as a precursor, reaction medium, reducing agent, capping agent, and pH adjusting agent, respectively. It was found by transmission electron microscopy that the morphology of the synthesized Sn NPs varied according to the pH of the initial solution. Moreover, while the size decreased to 11.32 nm with an increase up to 11.66 of the pH value, the size increased rapidly to 39.25 nm with an increase to 12.69. The pH increase up to 11.66 dominantly promoted generation of electrons and increased the amount of initial nucleation in the solution, finally inducing the reduced-size of the Sn particles. However, the additional increase of pH dominantly induced a decrease of PVP by neutralization, which resulted in acceleration of the agglomeration by collisions between particles.

• Bulletin of the Korean Chemical Society
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• 제35권7호
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• pp.1999-2003
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• 2014

Indium tin oxide ($In_2Sn_{1-x}O_{5-y}$) nanoparticles were synthesized by hydrothermal method from stable indium tin acetylacetone complexes and postannealing at $600^{\circ}C$. The absence of chlorine ions shortened the synthesis process, decreased the particle agglomeration and improved the particle purity. The introduced complexing ligand acetylacetone decreased the obtained nanoparticle size. The improved powder properties accelerated the sintering of the $In_2Sn_{1-x}O_{5-y}$ nanoparticles and reached a relative density of 96.4% when pressureless sintered at $1400^{\circ}C$.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 1999년도 춘계학술대회 논문집
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• pp.442-446
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• 1999

Melting behavior and bridge phenomenon of solder paste, which is essential for surface mount technology in packaging, were investigated. solder paste of Sn-37%Pb was printed on Sn-coated Cu-pattern of PCB, and heated over melting point. Melting behavior of the paste was observed using CCD-camera. In order to modelize the melting and agglomeration phenomena of the paste, two solder balls of 0.76mm diameter were used. As experimental results, the paste start to melt from the margin of the printed shape. The hight of the melted paste decreased from 270 $\mu$m to 200 $\mu$m firstly, and finally recovered to 250 $\mu$m. During the melting procedure, pores were evolved from the molten paste. Bridge Phenomenon of the molten Paste depends upon the pitch of the pattern.

• Journal of the Korean Physical Society
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• 제73권10호
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• pp.1437-1443
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• 2018

In this work, $SnO_2$ modified with reduced graphene oxide (rGO) and carbon nanotubes (CNTs) separately and combined sensitized by using the co-precipitation method and their sensing behavior toward ethanol vapor at room temperature were investigated. An interdigitated electrode (IDE) gold substrate is very expensive compared to a fluorine doped tin oxide (FTO) substrate; hence, we used the latter to reduce the fabrication cost. The structure and the morphology of the studied materials were characterized by using differential thermal analyses (DTA) and thermogravimetric analysis (TGA), transmission electron microscope (TEM), X-ray diffraction (XRD), Fourier transform infrared (FTIR) spectroscopy, Brunauer-Emmett-Teller surface area and Barrett-Joyner-Halenda (BJH) pore size measurements. The studied composites were subjected to ethanol in its gas phase at concentrations from 10 to 200 ppm. The present composites showed high-performance sensitivity for many reasons: the incorporation of $SnO_2$ and CNTs which prevents the agglomeration of rGO sheets, the formation of a 3D mesopourus structure and an increase in the surface area. The decoration with rGO and CNTs led to more active sites, such as vacancies, which increased the adsorption of ethanol gas. In addition, the mesopore structure and the nano size of the $SnO_2$ particles allowed an efficient diffusion of gases to the active sites. Based on these results, the present composites should be considered as efficient and low-cost sensors for alcohol.

• 한국재료학회지
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• 제8권9호
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• pp.813-818
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• 1998

공침법을 이용하여 $\textrm{In}_{2}\textrm{O}_{3}$가 0-10 wt.% 첨가된 $\textrm{SnO}_{2}$ 계 미세 분말을 합성한 후, 스크린 인쇄법(screen printing)으로 후막형 가스센서를 제조하고 탄화수소($\textrm{C}_{3}\textrm{H}_{8}$, $\textrm{C}_{4}\textrm{H}_{10}$) 가스에 대하여 가스 감응 특성을 조사하였다. $\textrm{In}_{2}\textrm{O}_{3}$는 $\textrm{SnO}_{2}$의 입자 성장을 억제시키기 위하여 첨가해 주었는데, $600^{\circ}C$에서 하소한 후에도 수 nm 크기의 미세한 입자를 얻을 수 있었다. 공침시 pH 값은 $\textrm{SnO}_{2}$ 의 입자 크기에 영향을 거의 미치지 않은 반면, $\textrm{In}_{2}\textrm{O}_{3}$ 첨가량은 입자 크기와 미세 구조에 큰 영향을 주었다. $\textrm{In}_{2}\textrm{O}_{3}$ 첨가량이 증가할수록 입자 크기는 감소하고 비표면적은 증가하였으며, 센세의 동작 온도를 약 $500^{\circ}C$로 하여 측정한 가스 감응 특성은 3wt.% 첨가했을 때 최대 감도를 나타내고 그 이상의 첨가량에서는 오히려 저하되었다. 3wt.%의 In2O3첨가시 $\textrm{SnO}_{2}$의 입자 크기와 비표면적은 각각 9.5nm, 38$\m^2$/g이었다. 임피던스 측정으로부터 얻은 단일 반원의 Nyquist curve와 선형의 전류-전압(1-V)특성 곡선으로부터, $\textrm{In}_{2}\textrm{O}_{3}$를 첨가하여 수nm로 입자 크기를 억제한 $\textrm{SnO}_{2}$ 계 가스센서는 미세 입자들끼리 형성한 치밀한 응집체와 이들 간의 계면(boundary)에 의해서 가스 감응 특성이 영향을 받음을 알 수 있었다.

• 마이크로전자및패키징학회지
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• 제8권1호
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• pp.5-11
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• 2001

SMT(Surface Mount Technology)패키징 공정에서 발생하는 솔더 페이스트의 용융거동과 브릿지 현상을 관찰하였다. 이를 위하여 Cu 패드위에 Sn-37%Pb 조성의 솔더 페이스트를 인쇄하였으며, 인쇄된 PCB기판을 솔더의 융점($183^{\circ}C$)이상으로 가열하였다. 이 때에 페이스트의 용융거동을 조사하기 위하여 CCD카메라를 이용하여 근접촬영하였다. 솔더링시 솔더 페이스트가 용융.응집되는 과정을 규명하기 위하여 동일한 조성의 0.76 mm직경을 갖는 두 개의 솔더 볼을 사용하여 모델링 하였다. 솔더 페이스트의 용융거동을 관찰한 결과 페이스트는 인쇄된 부분의 가장자리에서 안쪽으로 녹아들어가는 모습을 보였다. 또한, 페이스트의 높이는 가열 초기 270 $\mu\textrm{m}$에서 가열후 약 35초 경과시 200 $\mu\textrm{m}$로 줄어들었다가 최종적으로 250 $\mu\textrm{m}$로 다시 증가하였으며, 이 때 용융된 페이스트 내에서 기포가 방출되었다. 솔더볼의 용융모델에서 용융온도가 $280^{\circ}C$인 경우에 솔더볼의 접촉면적과 솔더링 시간 사이에는 $\chi^2/t=4r \; \gamma/\eta=7.56 m^2$/s의 관계식이 성립됨을 알 수 있었다.