• 한국세라믹학회지
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• 제28권4호
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• pp.338-346
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• 1991

The alumina-titania composite powders coated with Al2O3 were prepared by the method of hydrolysis-deposition of mixed aluminium salt solution of Al2(SO)4-Al(NO3)3-Urea. The effects of coating-process parameters on the characteristics of coated composite powders were also investigated. As the content of TiO2 dispersed in deionized water increased, the coated composite powders were found to be more uniform in size and unagglomerated. When TiO2 powders were coated for 30 min, the optimum TiO2 content in the coating process was 400 mg/ι. The size of TiO2 particle was increased approximately from 0.7${\mu}{\textrm}{m}$ to 1.0${\mu}{\textrm}{m}$ through coating of Al2O3. The IEP of coated composite powders was pH=8.3 identical to the value of aluminium hydroxides and the zeta-potential showed nearly similar values each other. When heat treating coated composite powders at 130$0^{\circ}C$, only two phases of TiO2(rutile) and Al2TiO5 were observed. These results showed that the suface of TiO2 could be uniformly coated with the aluminium hydroxide.

• 한국세라믹학회지
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• 제47권1호
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• pp.92-96
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• 2010

Based on the differential electrode equilibria approach, potentiometric YSZ sensors with semiconducting oxide electrodes for CO detection are developed. To improve the selectivity, sensitivity and response-time of the sensor, our strategy includes (a) selection of an oxide with a semiconducting response to CO, (b) addition of other semiconducting materials, (c) addition of a catalyst (Pd), (d) utilization of combined p- and n-type electrodes in one sensor configuration, and (e) optimization of operating temperatures. Excellent sensing performance is obtained by a novel device structure incorporating $La_2CuO_4$ electrodes on one side and $TiO_2$-based electrodes on opposite substrate faces with Pt contacts. The resulting response produces additive effects for the individual $La_2CuO_4$ and $TiO_2$-based electrodes voltages, thereby realizing an even higher CO sensitivity. The device also is highly selective to CO versus NO with minor sensitivity for NO concentration, compared to a notably large CO sensitivity.

• Journal of Electrochemical Science and Technology
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• 제7권1호
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• pp.76-81
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• 2016

An anatase TiO₂ nanotube array (NTA) was fabricated by anodization and successive heat treatments. When the anatase TiO₂ NTA was cathodically polarized, its color changed to blue, and it could be used as an electrochemically active anode for an oxygen evolution reaction (OER) in alkaline water electrolysis. The structure of the blue anatase TiO₂ NTA was controlled by the anodization conditions and its catalytic activity increased with an increase of the surface area. The activity of the blue anatase TiO₂ NTA gradually reduced with the continued OER because of the partial oxidation of Ti³⁺ to Ti⁴⁺. However, an intermittent cathodic regeneration process could significantly slow its reduction rate. The blue anatase TiO₂ NTA could be an alternative anode for alkaline water electrolysis.

• 센서학회지
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• 제23권1호
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• pp.42-45
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• 2014

Recently, tremendous application utilizing electrospun nanofibers have been actively reported due to its several advantages, such as high surface to volume ratio, simple fabrication and high-throughput manufacturing. In this paper, we developed highly sensitive and consistent nanofiber humidity sensor by electrospinning. The humidity sensor was fabricated by rapid electrospinning (~2 sec) $TiO_2$/PVP/LiCl mixed solution on the micro-interdigitated electrode. In order to evaluate the humidity sensing performances, we measured current response using DC bias voltage under various relative humidity levels. The results show fast response / recovery time and marginal hysteresis as well as long-term stability. In addition, with the aid of micro-interdigitated electrode, we can reduce a total resistance of the sensor and increase the total reaction area of nanofibers across the electrodes resulting in high sensitivity and enhanced current level. Therefore, we expect that the electrospun nanofiber array for humidity sensor can be feasible and promising for diverse humidity sensing application.

• Carbon letters
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• 제16권4호
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• pp.247-254
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• 2015

To improve photocatalytic efficiency, graphene/Ag/TiO₂ nanotube catalyst was synthesized, and its surface characteristics and photocatalytic activity investigated. For deposition of Ag nanoparticles on the TiO₂ nanotubes, a polymer compound containing CH₃COOAg/poly(L-lactide) was utilized, and the silver particles were precipitated by reducing the silver ions during the annealing process. Graphene deposition on the Ag/TiO₂ nanotubes was achieved using an electrophoretic deposition process. Based on the dye degradation results, it was determined that the photocatalytic efficiency was significantly affected by deposition of silver particles and graphene on the TiO₂ catalyst. Highly efficient destruction of the dye was obtained with the new graphene/Ag/TiO₂ nanotube photocatalyst. This may be attributed to a synergistic effect of the graphene and Ag nanoparticles on the TiO₂ nanotubes.

• 한국재료학회지
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• 제25권5호
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• pp.247-252
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• 2015

The effect of precursor concentration on the structural, morphological, and optical properties of $TiO_2$nano-flowers was investigated in this study. An increase in crystallite size was observed with an increase in the concentration of the precursor (titanium butoxide). The FE-SEM micrographs of the as-prepared samples show a three-dimensional flower-like morphology. The flowers consist of several nanorods coming out of a single core and have very sharp edges. Also, the variation in the aspect ratio of the nanostructure was observed with the concentration of the precursor. The photocatalytic properties of the samples show that the sample that has a high aspect ratio (AR~9) has a much better photocatalytic activity compared to the nano-crystal with a low aspect ratio (AR~6.1). It is believed that the excellent photocatalytic performance and short time synthesis of $TiO_2$nano-flowers using the microwave hydrothermal method can have potential applications in the field of photocatalysis.

• 한국산학기술학회:학술대회논문집
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• 한국산학기술학회 2005년도 춘계학술발표논문집
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• pp.274-276
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• 2005

본 논문에서는 유동층 화학기상증착법(FB CVB; Fluidized Bed Chemical Vapor Deposition)으로 광촉매가 박막증착된 비드를 제조하였고 제조된 광촉매코팅비드의 광반응성을 연속식 반응기에서 아세트알데히드의 분해능력을 측정하여 분석하였다. 광촉매가 박막증착된 비드의 FE-SEM 분석 결과 글라스 비드 위의 티타니아는 비교적 매끄럽게 증착되었고, 실리카 위의 티타니아는 입자의 형태로 증착되었으며 알루미나 위의 티타니아는 결정상을 이루며 증착됨을 확인 할 수 있었다. Acetaldehyde 기체의 광촉매에 의한 분해 실험을 진행하기 위해 연속식 반응기를 설계 제작하였고, 이 반응기를 사용하여 제조된 광촉매 코팅입자의 광반응성을 살펴보았다. 반응기는 가스 주입구와 출구를 갖고 있으며, 중심부에 UV 램프가 설치되었다. 반응기는 내열유리(pyrex)로 제작하였으며, 체적은 100 ml이다. 반응기 내부의 중심부에 UV 램프가 설치되고 UV 램프와 반응기 외부사이에 유동층 화학기상증착법에 의해 티타니아가 박막증착된 광촉매입자가 위치하여 광반응성을 평가하였다. 유량변화에 따른 광반응성을 측정하였으며, 알루미나에 광촉매를 증착시킨 제품의 경우 가스유량 100cc/min에서는 acetaldehyde가 $100\%$ 분해되고, 가스유량 500cc/min에서는 $50\%$정도 분해되는 것을 알 수 있었다.

• 공업화학
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• 제16권4호
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• pp.542-548
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• 2005

몇 가지 금속 산화물에 플루오르르 치환된 카르복시산의 자기조립박막을 제조하였다. 사슬 길이의 영향을 비교하기 위하여 퍼플루오르도테칸 산과 퍼플루오르옥타데칸 산을 사용하였다. 사용된 금속 산화물은 알루미나, 탄탈리아, 티타니아, 지르코니아였다. 자기조립박막의 형성은 DRIFT (Diffuse Reflectance Infrared Fourier Transform) 분광법으로 확인하였다. 퍼플루오르탄화수소는 소수성을 가지므로 형성된 자기조립박막도 소수성을 지닐 것으로 예측된다. 형성된 자기조립박막의 DRIFT 스펙트럼의 품질은 금속산화물의 성분 원소뿐만 아니라 분말으 크기에 따라서도 달라졌다.

• 한국수소및신에너지학회논문집
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• 제18권2호
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• pp.151-156
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• 2007

Solar cell and nanofiltration membrane were utilized in a system of enzymatic hydrogen production through light-sensitized photoanode, which resembles photoelectrochemical(PEC) configuration. Solar cell uses no additional light energy to increase energy for electrons to reduce protons and for holes to oxidize water to oxygen, and nanofiltration membrane replaces a salt bridge successfully with increased ion transport capability. With this system configuration, optimized amount of enzyme(10.98 unit), and an anodized tubular $TiO_2$ electrode($5^{\circ}C$/1 hr in 0.5 wt% HF-$650^{\circ}C$/5 hr) hydrogen evolved at a rate of ca. $43\;{\mu}mol/(cm^2{\times}hr)$ in a cathodic compartment and oxygen generated at a rate of ca. $20\;{\mu}mol/(cm^2{\times}hr)$ in an anodic compartment. The stoichiometric evolution of gases indicated that water was splitted in the system.

• The Korean Journal of Ceramics
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• 제4권4호
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• pp.336-339
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• 1998

Bioactive titanium metal can be prepared by simple 5M-NaOH treatment and subsuquent heat treatment at $600^{\circ}C$ to form an amorphous sodium titanate on its surface. In the present study, mechanism of apatite formation on the titanium metal was investigated by examining its surface compositional and structural changes in a simulated body fluid. The apatite formation on the metal was found to proceed in the sequence of 1)$Na^+$ ion release from the sodium titanate to form hydrated titania abundant in Ti-OH groups, 2) early and selective binding of calcium ions with the Ti-OH groups to form a calcium titanate, and 3) late binding of phosphate ions to make apatite nucleation and growth. This indicates that Ti-OH groups do not directly induce the apatite nucleation, but via formation of a calcium titanate.