• 소성∙가공
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• 제16권1호
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• pp.42-47
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• 2007

LCD-BLU is one of kernel parts of LCD and it consists of several optical sheets: LGP, light source and mold frame. The LGP of LCD-BLU is usually manufactured by etching process and forming numerous dots with $50\sim300{\mu}m$ diameter on the surface. But the surface of the etched dots of LGP is very rough due to the characteristics of the etching process during the mold fabrication, so that its light loss is high along with the dispersion of light into the surface. Accordingly, there is a limit in raising the luminance of LCD-BLU. In order to overcome the limit of current etched dot patterned LGP, optical pattern with continuous microlens was designed using optical simulation CAE. Also, a mold with continuous micro-lens was fabricated by UV-LiGA reflow process and applied to 7 inch size of navigator LCD-BLU in the present study.

• 대한환경공학회지
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• 제37권1호
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• pp.34-44
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• 2015

본 연구는 기존의 광촉매 산화 기술에서 주로 사용된 자외선램프의 단점을 보완할 수 있는 대체 광원인 자외선 LED를 사용하여 자유 시안을 폐수로부터 제거하는 공정을 평가하고자 수행되었다. 특히 광촉매 산화 공정의 다양한 영향 인자들에 대해 살펴보았다. 연구 결과, 자외선 LED는 기존의 광원인 자외선램프를 대체할 수 있는 적용성을 확인할 수 있었다. 뿐만 아니라 LED 개수를 증가할수록 광촉매 산화 반응의 효율은 증가하였으나, 공정의 경제성과 효율성을 동시에 만족시키기 위해서는 최적의 LED의 개수를 선정할 필요가 있다는 것을 확인하였다. 광촉매로 이용된 아나타제(anatase), 루틸(rutile), Degussa P25 등 세 종류의 $TiO_2$ 중 Degussa P25가 가장 높은 성능을 보였으며, 아나타제(anatase)와 루틸(rutile)을 특별한 전처리 과정없이 단순하게 혼합하였을 때는 Degussa P25 만큼의 공정의 효율은 얻지 못했다. 또한 $TiO_2$의 입자 크기가 작을수록 광촉매 산화 반응이 더욱 활발하게 이루어졌다. 그리고 광촉매 산화 반응에 있어 주로 전자 수용체 역할을 수행하는 산소를 주입함으로써 공정의 효율이 증진되는 효과를 얻을 수 있었다.

• 전기화학회지
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• 제5권4호
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• pp.189-191
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• 2002

Reversible trans-cis isomerization of meta-bipyridylazobenzene coordinated to cobalt was achieved by a combination of photoirradiation with a single UV light source and a Co(II)/Co(III) redox reaction. The trans/cis conversion performance was significantly improved in the meta-form compared with the meta-form ligated to cobalt.

• 한국자동차공학회논문집
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• 제10권2호
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• pp.48-54
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• 2002

Since photocatalysts are activated by lights of UV wavelengths, plasma is alternatively used as a light source for a photocatalytic reactor. Light intensity generated by plasma is proportional to the surface area of catalytic material, and this, in many practical applications, is prescribed by the geometry of a plasma generator. Thus, it is crucial to increase the surface area far sufficient light intensity for photocatalytic reaction. For example, in a pack-bed type reactor, multitudes of beads are used as a substrate in order to increase the surface area. Honeycomb monolith type substrate, which has very good surface area to volume ratio, has been difficult to apply plasma as a light source due to the fact that light penetration depth through the honeycomb monolith was too short to cover sufficient area, thus resulting in poor intensity for photocatalytic reaction. In this study, nonthermal plasma generation through a photocatalytic reactor of honeycomb monolith substrate is investigated to lengthen this short penetration depth. The ceramic honeycomb monolith substrate used in this study has the same length as a three way catalyst used fur automotive applications, and it is shown that sufficient light intensity for photocatalytic reaction can also be obtained with honeycomb monolith type reactor.

• 한국전기전자재료학회논문지
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• 제29권4호
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• pp.237-240
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• 2016

The improvement of irradiation intensity and irradiation uniformity is essential for large area and high power UVA light source application. In this study, large number of chips bonded by micro soldering technique were driven by low current, and current limiting diodes were configured to supply constant current to parallel circuits consisting of large number of series strings. The dimension of light source module circuit board was $350{\times}90mm^2$ and 16,650 numbers of 385 nm flip chip LEDs were used with a configuration of 90 parallel and 185 series strings. The space between LEDs in parallel and series strings were maintained at 1.9 mm and 1.0 mm distance, respectively. The size of the flip chip was $750{\times}750{\mu}m^2$ were used with contact pads of $260{\times}669{\mu}m^2$ size, and SAC (96.5 Sn/3.0 Ag/0.5 Cu) solder was used for flip chip bonding. The fabricated light source module with 7.5 m A supply current showed temperature rise of $66^{\circ}C$, whereas irradiation was measured to be $300mW/cm^2$. Inaddition, 0.23% variation of the constant current in each series string was demonstrated.

• 센서학회지
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• 제16권4호
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• pp.307-312
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• 2007

The films of Er-doped ZnO (ZnO:Er) were prepared onto MgO wafers by ultrasonic spray pyrolysis at $550^{\circ}C$. The concentration of Er in the deposition source varied from 0.5 wt% to 3.0 wt%. The crystallographic properties and surface morphologies of the films were investigated by X-ray diffraction (XRD) and scanning electron microscope (SEM), respectively. The properties of photoluminescence (PL) for the films were investigated by dependence of PL spectra on the Er concentration in the films. The films were grown as polycrystalline with a dominant direction of [002]. The grain size of the films were reduced by Er-doping. Er-doping enhanced the ultraviolet emission of ZnO:Er films. The ZnO:Er films prepared with the deposition source of 2.0 wt% Er showed the strongest ultraviolet light emission peak among the films in this study.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2016년도 제50회 동계 정기학술대회 초록집
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• pp.374.2-374.2
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• 2016

Volatile organic compounds (VOCs) in the atmosphere are harmful materials which influence indoor air environment and human health. Titanium dioxide ($TiO_2$) is photocatalyst extensively used in degradation of organic compound. To improve the photocatalytic activity in the visible light region, doping with non-metals element or loading noble metals on the surface of $TiO_2$ is generally proposed. In this study, N- doped $TiO_2$ having photocatalytic activity in visible light region was attached noble metal such as Pt, Ag, Pd, Au by coupling method. Catalytic activities of Noble metal coupled $N-TiO_2$ powders were evaluated by the improvement of their photocatalytic activities and the degradation of VOC gas. A UV-Vis spectrophotometer was used to measure the diffuse reflectance spectra of coupled $N-TiO_2$ sample. The photocatlytic activities of as prepared samples were characterized by the decoloration of aqueous MB solution under Xenon light source (UV and visible light). To measure of decomposition VOCs, ethylbenzene was selected for target VOC material and the concentration was monitored under UVLED irradiation in a closed chamber system. Adjusting the initial concentration of 10~12 ppm, to evaluate the removal characteristics by using the coupled $N-TiO_2$.

• 원예과학기술지
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• 제34권4호
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• pp.596-606
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• 2016

본 연구의 공시품종은 적치마 상추(Lactuca sativa L., cv. 'Jeokchima')로서 파종 후 본엽이 4매일 때 식물공장 내에 설치된 DFT 재배시스템에 정식하였다. 본 연구에서는 피크파장이 각각 450nm, 660nm, 365nm인 청색 LED, 적색 LED, UV-A LED를 이용하여 청색 LED (B), 적색 LED (R), 청색+UV-A LED (BUV), 적색+UV-A LED (RUV) 등 4개의 처리구를 설정하였고, 대조구로서 3파장 백색형광등을 사용하였다. 또한 광주기(명기/암기)에 따른 효과를 분석하고자 3수준(12/12h, 16/8h, 20/4h)의 광주기를 설정하였다. 식물공장 내 환경 조건은 기온(명기/암기) $22/18^{\circ}C$, 상대습도 70%, $CO_2$ 농도 $800{\mu}mol{\cdot}mol^{-1}$로 조절하였다. 한편 광합성유효광양자속과 UV-A LED의 조사강도는 각각 $230{\pm}11{\mu}mol{\cdot}m^{-2}{\cdot}s^{-1}$, $80{\pm}3mW{\cdot}m^{-2}$이었다. 정식 후 28일째에 측정된 상추의 엽수, 엽장, 엽폭, 엽면적, 지상부 생체중 및 건물중은 본 연구에서 적용된 광질 및 광주기에 따라 유의차가 인정될 만큼 다르게 나타났다. 명기가 증가할수록 R 처리구에서의 엽수, 엽장, 엽폭, 엽면적, 지상부 생체중 및 건물중은 증가하였다. 한편 B 처리구에서는 잎의 신장이 억제되었으나, 엽록소함량은 증가하였다. UV-A의 부가 조사로 인하여 엽장, 엽폭, 엽면적 및 지상부 생체중이 감소하였다. 그러나 상추 잎의 안토시아닌 함량은 청색광 하에서 많이 증가하였으며, 명기가 짧아질수록 높게 축적되었다. 한편 UV-A의 부가 조사에 따른 안토시아닌 함량의 증가 효과는 R 처리구에서 높게 나타났다. 상추 잎의 아스코르빈산 함량은 광주기의 영향을 크게 받았다. 청색 또는 적색 LED에서 UV-A LED의 부가 조사에 따라 아스코르빈산 함량이 20-30% 증가하였다. 결론적으로 상추의 생장, 안토시아닌 및 아스코르빈산 함량에 미치는 UV-A LED의 조사 효과가 분명하게 나타났다. 향후 폐쇄형 시스템에서 엽채류의 영양성을 향상시키는 데 필요한 UV-A LED의 운용 조건을 제시하고자 할 때 본 연구 결과가 기초 자료로서 유용하게 활용될 것이다.

• 복식
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• 제34권
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• pp.109-120
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• 1997

The conservation of collections in muse-ums is an important aspect for our her-itage. The control of museum environment is a vital factor in the preservation of cool-lections. Inappropriate or fluctuating envi-ronmental conditions can cause irreparable damage to works of arts. In this research we investigated the ac-tual conditions of museum environment for old testiles using questionnaire and mea-sured dye fasing of old textiles on exhibi-tion for 2 months in a university museum the major results are as follows: 1. The control of temperature and rela-tive humidity is a vital factors I the preservation of old textiles in museum generally acceptable temperature and rel-ative humidity standards for old textiles are 18-23$^{\circ}C$ and 50-65% R. H and light level for textiles on exhibition should be limited to 30-50 lux. 2, In university museums the limate control system in exhibition and storage area is in an early stage. Therefore to minimize the deterioration of old textiles the best method of controlling the envi-ronment is to have centralized climate control system in sorage area as well as in display area. 3. Conservator is needed to maintain collections scientifically. Only professional conservator by combining scientific tech-nical and artistic training has the exper-tise needed to maintain the physical in-tegrity of old textiles. In order to solve the inferior environment of museums the staff should recognize the importance of the condition of exhibition and storage. 4. Old textiles are susceptible to damage by light and associated heat. Dyed textiles which have been exhibited under the light without any UV filter were faded notice-ably within two months of exhibition. Light levels for textiles on exhibition should be limited to 30-50 lux. It is de-sirable to use special light source that can absorb UV. and UV filter is also recom-mended to reduce photodegradation of old textiles.

• 한국대기환경학회지
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• 제24권1호
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• pp.91-99
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• 2008

A multilayer tower-type photoreactor, in which $TiO_2$-coated glass-tubes were installed, was used to measure the vapor-phase BTEX removal efficiencies by ozone oxidation ($O_3$/UV), photocatalytic oxidation ($TiO_2$/UV) and the combination of ozone and photocatalytic oxidation ($O_3/TiO_2$/UV) process, respectively. The experiments were conducted under various relative humidities, temperatures, ozone concentrations, gas flow rates and BTEX concentrations. As a result, the BTEX removal efficiency and the oxidation rate by $O_3/TiO_2$/UV system were highest, compared to $O_3$/UV and $TiO_2$/UV system. The $O_3/TiO_2$/UV system accelerated the low oxidation rate of low-concentration organic compounds and removed organic compounds to a large extent in a fixed volume of reactor in a short time. Therefore, $O_3/TiO_2$/UV system as a superimposed oxidation technology was developed to efficiently and economically treat refractory VOCs. Also, this study demonstrated feasibility of a technology to scale up a photoreactor from lab-scale to pilot-scale, which uses (i) a separated light-source chamber and a light distribution system, (ii) catalyst fixing to glass-tube media, and (iii) unit connection in series and/or parallel. The experimental results from $O_3/TiO_2$/UV system showed that (i) the highest BTEX removal efficiencies were obtained under relative humidity ranging from 50 to 55% and temperature ranging from 40 to $50^{\circ}C$, and (ii) the removal efficiencies linearly increased with ozone dosage and decreased with gas flow rate. When applying Langmuir-Hinshelwood model to $TiO_2$/UV and $O_3/TiO_2$/UV system, reaction rate constant for $O_3/TiO_2$/UV system was larger than that for $TiO_2$/UV system, however, it was found that adsorption constant for $O_3/TiO_2$/UV system was smaller than that for $TiO_2$/UV system due to competitive adsorption between organics and ozone.