• 치위생과학회지
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• 제14권2호
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• pp.140-149
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• 2014

본 연구에서는 지르코니아 에칭에 의한 표면변화가 지르코니아 코어와 도재 사이의 결합강도에 미치는 영향을 조사하기 위해 전단결합강도 실시하였고, 표면의 변화를 관찰하기 위한 SEM 측정, 에칭처리에 따른 지르코니아의 성분변화를 알아보기 위해 EDS 분석을 실시하였다. 그리고 구강상태에서 15~20년의 저온열화현상을 재현하기 위해 저온 열화 처리를 시행하여 전단결합강도 평가를 실시하여 다음과 같은 결과가 도출되었다. 1. 에칭처리를 시행하지 않은 시편과 에칭처리를 시행한 시편의 전단결합강도를 비교할 경우 에칭한 시편의 전단결합강도가 큰 것을 알 수 있다. 이는 에칭용액이 지르코니아코어 표면에 interlocking을 형성하여 기계적인 결합을 높여 주었을 것이라고 생각된다. 2. 전단결합강도의 결과(EZ>AEZ>NEZ>ANEZ)를 보았을 때 통계적으로는 유의한 차이를 보였으며, 저온열화처리를 하지 않고 에칭처리를 한 EZ군이 전단결합강도가 가장 큰 것을 알 수 있었다. 또한 파절 양상에서도 EZ군에서만 응집파절을 보여 가장 결합강도가 높다는 결과를 도출할 수 있다. 결론적으로 저온열화처리 여부에 관계없이 표면에칭처리를 한 시편의 전단결합강도가 큰 것으로 나타나 지르코니아 표면의 에칭처리로 인한 interlocking의 형성이 기계적인 결합을 향상시키는 요인이 되었다고 생각된다.

• Carbon letters
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• 제28권
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• pp.31-37
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• 2018

This paper examines a simple one-step and catalyst-free method for synthesizing carbon nanoparticles from aliphatic alcohols and n-hexane with linear molecule formations by using a stable solution plasma process with a bipolar pulse and an external resistor. When the external resistor is adopted, it is observed that the current spikes are dramatically decreased, which induced production of a more stable discharge. Six aliphatic linear alcohols (methanol-hexanol) containing carbon with oxygen sources are studied as possible precursors for the massive production of carbon nanoparticles. Additional study is also carried out with the use of n-hexane containing many carbons without an oxygen source in order to enhance the formation of carbon nanoparticles and to eliminate unwanted oxygen effects. The obtained carbon nanoparticles are characterized with field emission-scanning electron microscopy, energy dispersive X-ray spectroscopy, and Raman spectroscopy. The results show that with increasing carbon ratios in alcohol content, the synthesis rate of carbon nanoparticles is increased, whereas the size of the carbon nanoparticles is decreased. Moreover, the degree of graphitization of the carbon nanoparticles synthesized from 1-hexanol and n-hexane with a high carbon (C)/oxygen (O) ratio and low or no oxygen is observed to be greater than that of the carbon nanoparticles synthesized from the corresponding materials with a low C/O ratio.

• Korean Chemical Engineering Research
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• 제43권4호
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• pp.495-502
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• 2005

무전해 도금 용액을 이용하여 구리를 직접 텅스텐(Tungsten, W) 기판 위에 도금하였다. 도금 용액의 농도는 각각 $CuSO_4$ 7.615 g/L, EDTA 10.258 g/L, glyoxylic acid 7 g/L로 하였다. 도금 용액의 pH는 11.0에서 12.8까지 변화시켰으며, 용액의 온도는 $60^{\circ}C$로 유지하였다. 도금된 필름의 특성을 조사하기 위하여 X선 회절분석기, 전계 방출 주사 전자 현미경, 주사형 원자력 현미경, X선 광전자 분석기 및 Rutherford backscattering spectroscope(RBS)를 사용하였다. 구리 도금을 위한 가장 좋은 pH 조건은 11.8이였다. 이 용액에서 10분 동안 도금한 경우 둥근 모양의 구리 입자가 균일하게 도금되었으며, 불순물 peak이 없는 순수 구리 peak이였고, 근평균 제곱 표면 거칠기는 약 11 nm가 되었다. 또한, pH 11.8에서 12분 동안 도금한 필름의 두께는 140 nm이었고 도금속도는 약 12 nm/min였다. 무전해 도금 용액의 pH를 12.8로 증가시키면 도금된 구리 필름은 Cu peak 이외에 불순물 peak인 $Cu_2O$가 나타나고 구리 입자 모양도 기다란 직사각형 모양으로 변하였다. 순수 구리의 도금을 위해서는 도금 용액에서 적당한 pH를 유지하여야 한다. 도금된 구리의 농도는 RBS로 측정한 결과 99 atom％였다. 또한, Cu/W 필름은 전기 도금하는 동안 합금 형태를 이루기 때문에 접착성도 좋았다.

• 한국세라믹학회지
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• 제56권2호
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• pp.178-183
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• 2019

A process of fabricating the foamed glass that has closed pores with 8 ~ 580 ㎛ sizes without a blowing agent by sintering 10 ㎛ boron-free glass powder composed of CaO, MgO, SO₃, Al₂O₃-83 wt% SiO₂ at a molding pressure of 0 ~ 120 MPa and a sintering temperature of 750 ~ 1000℃ was investigated. To analyze the glass transition temperature of glass powder, thermogravimetric analysis-differential thermal analysis (TGA-DTA) method were used. The microstructure and pore size of foamed glass were examined using the optical microscopy and field emission scanning electron microscopy (FE-SEM). For the thermal diffusivity and color of the fabricated samples, a heat flow meter and ultraviolet-visible-near-infrared (UV-VIS-NIR)-colormetry were used, respectively. In the TGA-DTA result, the glass transition temperature of glass powder was confirmed to be 626℃. In the microstructure result, closed pores of 7 ~ 20 ㎛ were formed at 750 ~ 900℃, and they were not affected by the molding pressure and sintering temperature. However, at 1,000℃, when there was 0 MPa molding pressure, closed pores of 580 ㎛ were confirmed, and the pore size decreased as the molding pressure increased. Moreover, at a molding pressure of 30 MPa or higher, closed pores of approximately 400 ㎛ were formed. The porosity showed an increasing trend of smaller molding pressure and larger sintering temperature, and it was controllable in the range of 5.69 ~ 68.45%. In the thermal diffusivity result, there was no change according to the molding pressure, and, by increasing the sintering temperature, up to 0.115 W/m·K could be obtained. The Lab color index (CIE-Lab) results all showed a similar translucent white color regardless of molding pressure and sintering temperature. Therefore, based on the foamed glass without boron and blowing agent, it was confirmed that white foamed glass, which has closed pores of 8 ~ 580 ㎛ and a thermal diffusivity characteristic of 0.115 W/m·K, can be fabricated by changing the molding pressure and sintering temperature.

• 한국세라믹학회지
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• 제39권5호
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• pp.460-466
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• 2002

티타늄 임플란트의 표면을 열산화법을 이용하여 티타늄의 표면 위에 생체활성을 갖는 $TiO_2$ 박막을 생성시켜 다양한 의료분야의 응용 가능성을 검토하였다. 시판되고 있는 순수한 티타늄 디스크를 세척 공정을 거친 후, 공기와 아르곤 분위기에서 500, 550, 600, 650, 700${\circ}C$의 온도로 10분간 각각 열산화 처리를 실시하였다. 열처리된 시편의 인산칼슘 결정의 형성 능력을 시험하기 위하여 36.5${\circ}C$의 Eagle's minimum essential medium 용액에서 15일 동안 침적시험을 행하였다. 침적하기 전과 후의 시편의 표면 형상과 표면 조성을 Field Emission-Scanning Electron Microscopy(FE-SEM)와 Energy Dispersive X-ray Spectrometry(EDS)로 각각 분석하였다. In vitro 시험에서 미세한 $TiO_2$ 결정이 생성된 박막의 표면에는 탄소가 함유된 인산칼슘 결정이 생성됨을 확인하였다.

• Maxillofacial Plastic and Reconstructive Surgery
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• 제35권1호
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• pp.38-50
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• 2013

Purpose: The aim of this study is to evaluate the effect and potential of electron beam (E-beam) irradiation treatment to the synthetic bony mixtures composed of hydroxyapatite (HA; Bongros$^{(R)}$, Bio@ Co., Korea) and tricalcium phosphate (${\beta}$-TCP, Sigma-Aldrich Co., USA), mixed at various ratios and of type I collagen (Rat tail, BD Biosciences Co., Sweden) as an organic matrix. Methods: We used 1.0~2.0 MeV linear accelerator and 2.0 MeV superconductive linear accelerator (power 100 KW, pressure 115 kPa, temperature $-30{\sim}120^{\circ}C$, sensor sensitivity 0.1~1.2 mV/kPa, generating power sensitivity 44.75 mV/kPa, supply voltage $5{\pm}0.25$ V) with different irradiation dose, such as 1, 30 and 60 kGy. Structural changes in this synthetic bone material were studied in vitro, by scanning electron microscopy (SEM), elementary analysis and field emission scanning electron microscope (FE-SEM), attenuated total reflection (ATR), and electron spectroscopy for chemical analysis (ESCA). Results: The large particular size of HA was changed after E-beam irradiation, to which small particle of TCP was engaged with organic collagen components in SEM findings. Conclusion: The important new in vitro data to be applicable as the substitutes of artificial bone materials in dental and medical fields will be able to be summarized.

• 한국결정성장학회지
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• 제19권6호
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• pp.288-292
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• 2009

LPD법을 이용하여 유리 기판 위에 발수/친수 패터닝 기판을 제조하였다. 발수 표면은 거친 표면을 갖는 ZnO 박막을 FAS를 이용한 표면 개질에 의하여 만들어졌고, 친수 표면은 자외선을 조사하여 FAS를 제거함으로써 만들어졌다. Hexagonal ZnO rod는 LPD법에 의하여 ZnO seed 층이 코팅된 유리 기판 위에 수직으로 성장되었다. 침적시간이 증가함에 따라 ZnO rod의 직경과 두께는 증가하였다. 제조된 ZnO 박막의 표면구조, 두께, 결정구조, 투과율과 접촉각은 FE-SEM, XRD, UV-vis와 contact angle meter를 이용하여 측정하였다. $20^{\circ}{\sim}30^{\circ}$의 접촉각을 갖는 친수 ZnO 박막은 FAS 표면 처리에 의해 $145^{\circ}{\sim}161^{\circ}$의 접촉각을 갖는 표면으로 바뀌었다. 제조된 발수 표면은 $300\;{\mu}m$, 3 mm의 dot size를 갖는 shadow mask를 이용하여 자외선을 조사하여 패터닝 되었다. 최종적으로 자외선이 조사된 발수 표면은 친수 표면으로 바뀌었다.

• 한국결정성장학회지
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• 제20권6호
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• pp.267-271
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• 2010

Sol-gel법을 이용하여 초친수성이며 높은 투과율을 갖는 $TiO_2$ 박막을 UV를 조사하지 않고 제조하였다. 제조된 박막의 투과율을 높이기 위하여 계면활성제 Tween 80을 첨가하였다. $TiO_2$ 용액에서 Tween 80의 함량이 0.0, 1.0, 3.0, 5.0 wt%일 때, 파장 550 nm에서 측정된 $TiO_2$ 박막의 투과율은 각각 약 74.31%, 74.25%, 79.69%, 81.99%였다. Tween 80의 첨가유무에 따라 제조된 박막은 약 $4.0{\sim}4.5^{\circ}$의 초친수 접촉각을 나타내었다. $400^{\circ}C$ 이상에서 열처리된 $TiO_2$ 박막은 아나타제 타입의 결정구조를 보였으며, UV를 조사하였을 때 메틸 오렌지 용액을 분해시키는 광촉매 특성을 보였다. Tween 80의 함량에 따라 제조된 박막의 표면구조, 광학특성 및 접촉각을 FE-SEM, XRD, UV-Vis 분광기, 접촉각 측정기를 이용하여 평가하였다.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2010년도 하계학술대회 논문집
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• pp.264-264
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• 2010

Single-walled carbon nanotubes (SWCNTs) were grown on a Si wafer by using thermal chemical vapor deposition (t-CVD). We investigated the effect of the catalyst deposition rate on the types of CNTs grown on the substrate. In general, smaller islands of catalyst occur by agglomeration of a catalyst layer upon annealing as the catalyst layer becomes thinner, which results in the growth of CNTs with smaller diameters. For the same thickness of catalyst, a slower deposition rate will cause a more uniformly thin catalyst layer, which will be agglomerated during annealing, producing smaller catalyst islands. Thus, we can expect that the smaller-diameter CNTs will grow on the catalyst deposited with a lower rate even for the same thickness of catalyst. The 0.5-nm-thick Fe served as a catalyst, underneath which Al was coated as a catalyst support as well as a diffusion barrier on the Si substrate. The catalyst layers were. coated by using thermal evaporation. The deposition rates of the Al and Fe layers varied to be 90, 180 sec/nm and 70, 140 sec/nm, respectively. We prepared the four different combinations of the deposition rates of the AI and Fe layers. CNTs were synthesized for 10 min by flowing 60 sccm of Ar and 60 sccm of $H_2$ as a carrier gas and 20 sccm of $C_2H_2$ as a feedstock at 95 torr and $810^{\circ}C$. The substrates were subject to annealing for 20 sec for every case to form small catalyst islands prior to CNT growth. As-grown CNTs were characterized by using field emission scanning electron microscopy, high resolution transmission electron microscopy, Raman spectroscopy, UV-Vis NIR spectroscopy, and atomic force microscopy. The fast deposition of both the Al and Fe layers gave rise to the growth of thin multiwalled CNTs with the height of ${\sim}680\;{\mu}m$ for 10 min while the slow deposition caused the growth of ${\sim}800\;{\mu}m$ high SWCNTs. Several radial breathing mode (RBM) peaks in the Raman spectra were observed at the Raman shifts of $113.3{\sim}281.3\;cm^{-1}$, implying the presence of SWCNTs (or double-walled CNTs) with the tube diameters 2.07~0.83 nm. The Raman spectra of the as-grown SWCNTs showed very low G/D peak intensity ratios, indicating their low defect concentrations.

• 한국전기전자재료학회:학술대회논문집
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• 한국전기전자재료학회 2008년도 추계학술대회 논문집 Vol.21
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• pp.399-399
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• 2008

Synthesis and characterization of ZnO structure such as nanowires, nanorods, nanotube, nanowall, etc. have been studied to multifunctional application such as optical, nanoscale electronic and chemical devices because it has a room-temperature wide band gap of 3.37eV, large exiton binding energy(60meV) and various properties. Various synthesis methods including chemical vapor deposition (CVD), physical vapor deposition, electrochemical deposition, micro-emulsion, and hydrothermal approach have been reported to fabricate various kinds of ZnO nanostructures. But some of these synthesis methods are expensive and difficult of mass production. Wet chemical method has several advantage such as simple process, mass production, low temperature process, and low cost. In the present work, ZnO nanorods are deposited on ITO/glass substrate by simple wet chemical method. The process is perfomed by two steps. One-step is deposition of ZnO seeds and two-step is growth of ZnO nanorods on substrates. In order to form ZnO seeds on substrates, mixture solution of Zn acetate and Methanol was prepared.(one-step) Seed layers were deposited for control of morpholgy of ZnO seed layers by spin coating process because ZnO seeds is deposited uniformly by centrifugal force of spin coating. The seed-deposited samples were pre-annealed for 30min at $180^{\circ}C$ to enhance adhesion and crystallinnity of ZnO seed layer on substrate. Vertically well-aligned ZnO nanorods were grown by the "dipping-and-holding" process of the substrates into the mixture solution consisting of the mixture solution of DI water, Zinc nitrate and hexamethylenetetramine for 4 hours at $90^{\circ}C$.(two-step) It was found that density and morphology of ZnO nanorods were controlled by manipulation of ZnO seeds through rpm of spin coating. The morphology, crystallinity, optical properties of the grown ZnO nanostructures were carried out by field-emission scanning electron microscopy, high-resolution electron microscopy, photoluminescence, respectively. We are convinced that this method is complementing problems of main techniques of existing reports.