• 정보저장시스템학회논문집
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• 제2권1호
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• pp.79-84
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• 2006

The next generation of optical storage systems requires higher numerical aperture(NA) objective lenses and shorter wavelength laser in order to improve the unit areal density. A blu-ray technology satisfies a miniaturization and a high capacity which are the requirements of the portable device. In this paper, we analyze the optical performance of hybrid micro lens and do active alignment. The hybrid micro lens is manufactured by using a wafer based fabrication technology. Optical components of hybrid micro lens are evaluated. The measurement of the optical power, the spot size and the wavefront error are performed to evaluate the hybrid micro lens with NA 0.85. Using the measured data, we estimate if the performance of hybrid micro lens corresponds to the designed performance. After the performance of hybrid micro lens is evaluated. the integrated optical pickup and the hybrid micro lens are assembled by active alignment using UV curing and the optical performance of SFFOP is satisfied with BD specifications.

• 한국화재소방학회논문지
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• 제33권1호
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• pp.85-91
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• 2019

이 연구는 불꽃파장 감지기술과 불꽃영상 감지기술을 융합한 도로터널용 자동소화설비의 화재감지성능을 평가하기 위한 실험이다. 화재감지성능을 향상시키기 위한 이 융합기술은 화재 시 화원의 위치를 파악하고, 노즐을 화원으로 향하여 화재가 발생한 장소에만 가압수를 방사함으로서 화재진압에 따른 수손피해를 줄이는 효과를 얻을 수 있었다. 도로터널의 화재 중 불꽃 및 연기가 선행되는 상황에서 각각 15 m, 20 m, 25 m, 30 m, 35 m 거리에 $70cm{\times}70cm$의 목표물을 두었을 때 화원의 위치를 파악하는지를 실험하였다. 실험결과 농연의 간섭으로 인해 자외선 및 삼파장적외선센서의 감지능력이 감쇠되는 결과를 확인하였다. 또한 농연으로 인해 불꽃이 가려진 경우 이미지센서가 농연을 감지하여 화재신호를 발신함을 확인하였다.

• 생약학회지
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• 제40권4호
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• pp.298-302
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• 2009

Samultang is one of traditional medicine composed of Paeonia lactiflora, Angelica gigas, Rehmannia glutinosa and Cnidium officinale. To develop simultaneous determination of paeoniflorin, decursin and 5-HMF in Samultang, a high performance liquid chromatography with diode array detector was used. To separate three marker components, Dionex $C_{18}$ column (5 ${\mu}m$, 120 ${\AA}$, 4.6 mm${\times}$150 mm) was used with a gradient elution system of water and methanol. UV wavelength of detector set at 230 nm and 280 nm. This method was validated by linearity, precision test and recovery test. Calibration curves of three standard components were showed good linear regression ($R^2$>0.9973). LOD and LOQ ranged from 0.08 ${\mu}g$/ml to 0.38 ${\mu}g$/ml and 0.25 ${\mu}g$/ml to 1.16 ${\mu}g$/ml, respectively. The relative standard deviations (RSDs) of data of the inter-day and intra-day experiments were less than 0.54% and 0.89%, respectively. The measured results of recovery test were varied from 93.36 to 107.79 with RSD values 0.01~1.45%. The established method was applied for separation of bio-conversion Samultang sample and compared with control sample.

• 생약학회지
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• 제41권4호
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• pp.323-327
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• 2010

A high performance liquid chromatographic (HPLC) method for the simultaneous determination of dictamine, obacunone and fraxinellone was established for the quality control of traditional herb Dictamnus dasycarpus cortex. Separation and quantification were successfully achieved with a Shiseido C18 column ($5\;{\mu}m$, 4.6 mm I.D. ${\times}$ 250 mm) by gradient elution of a mixture of methanol and water at a flow rate of 1.0 ml/min. The diode-array UV/Vis detector (DAD) was used for the detection and the wavelength for quantification was set at 236 nm. The presence of dictamine, obacunone and fraxinellone in this extract was ascertained by retention time, spiking with each authentic standard and UV spectrum. All three compounds showed good linearity ($r^2$ > 0.999) in relatively wide concentration ranges. The R.S.D. recovery of each compound was 101.0~103.7% with R.S.D. values less than 1.0%. This method was successfully applied to the determination of contents of dictamine, obacunone and fraxitnellone in three commercial products of D. dasycarpus cortex. These results suggest that the developed HPLC method is simple, effective and could be readily utilized as a quality control method for commercial products.

• Natural Product Sciences
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• 제14권3호
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• pp.147-151
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• 2008

A high performance liquid chromatographic (HPLC) method for the simultaneous determination of marker constituents, baicalin and glycyrrhizin was established for the quality control of traditional herbal medicinal preparation, Eul-Ja-Tang (EJT). Separation and quantification were successfully achieved with a Waters XTerra RP18 column ($5{\mu}m$, 4.6 mm I.D. ${\times}$ 150 mm) by gradient elution of a mixture of acetonitrile and water containing 0.03% phosphoric acid (pH 2.03) at a flow rate of 1.0 mL/min. The diode-array UV/VIS detector (DAD) was used for the detection and the wavelength for quantification was set at 250 nm. The presence of baicalin and glycyrrhizin in this decoction was ascertained by retention time, spiking with each authentic standard and UV spectrum. Both baicalin and glycyrrhizin showed good linearity ($r^2$ > 0.999) in a relatively wide concentration ranges. The R.S.D. for intra-day and inter-day precision was less than 5% and the limits of detection (LOD) were about 30 ng. The mean recovery of each compound was 99.5 - 101.2% with R.S.D. values less than 4.0%. This method was successfully applied to the determination of contents of baicalin and glycyrrhizin in three commercial products of EJT, which resulted in the difference in the contents of these compounds. These results suggest that the developed HPLC method is simple, effective and could be readily utilized as a quality control method for commercial EJT products.

• Journal of Pharmaceutical Investigation
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• 제39권1호
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• pp.23-27
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• 2009

A high performance liquid chromatographic (HPLC) method for the simultaneous determination of marker constituents, paeoniflorin and glycyrrhizin was established for the quality control of traditional herbal medicinal preparation, Sayuk-san (SYS). Separation and quantification were successfully achieved with a Waters XTerra RP18 column ($5{\mu}m$, $4.6mm\;I.D.{\times}150mm$) by gradient elution of a mixture of acetonitrile and water containing 0.03% phosphoric acid (pH 2.03) at a flow rate of 1.0 mL/min. The diode-array UV/vis detector (DAD) was used for the detection and the wavelength for quantification was set at 230 nm. The presence of paeoniflorin and glycyrrhizin in this decoction was ascertained by retention time, spiking with each authentic standard and UV spectrum. All two compounds showed good linearity ($r^2$>0.996) in a relatively wide concentration ranges. The R.S.D. for intra-day and inter-day precision was less than 7.3% and the limits of detection (LOD) were less than 55.7 ng. The mean recovery of each compound was $102.3{\sim}111.1%$ with R.S.D. values less than 4.6%. This method was successfully applied to the determination of contents of paeoniflorin and glycyrrhizin in three commercial products of SYS. These results suggest that the developed HPLC method is simple, effective and could be readily utilized as a quality control method for commercial SYS products.

• 대한전자공학회논문지SD
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• 제38권10호
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• pp.671-677
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• 2001

사파이어 기판 위에 성장된 GaN위에 RUO₂/GaN 쇼트키형 자외선 수광소자를 설계, 제작하였다. 자외선 빛의 흡수율을 높이기 위해, MOCVD 다층구조는 undoped GaN(0.5 ㎛)in￣-GaN(0.1 ㎛)/n＋-GaN(1.5 ㎛)로 성장하였다. 성장층은 3.8×10/sup 18/ cm￣³의 캐리어 농도와 283 ㎠/V· s의 이동도를 가진다. 500 ㎛내외의 직경을 가지는 메사구조를 형성하기 위해 ECR 식각한 후, n＋-GaN층위에 Al으로 저항성 접촉을 하였다. 저항성 및 쇼트키 접촉 사이에 Si₃/N₄ 박막으로 절연한 이후 undoped GaN 층위에 RuO₂ 쇼트키 접촉을 하였다. 제작된 쇼트키 다이오드는 1.15×10/sup -5/ ［Ω-㎠］의 접촉비저항을 가졌다. 제작된 다이오드는 역전압인 -5V에서 305pA의 낮은 누설전류를 확인하였는데, 이 값은 RuO₂ 쇼트키 금속증착에 의해 현저히 향상된 것이다. 광측정에서는 10/sup 5/의 자외선대가시광선 제거비와 365nm 파장에서 0.23A/W로 높은 응답도를 보인다.

• 분석과학
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• 제18권3호
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• pp.250-256
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• 2005

고속액체크로마토그라피를 이용하여 동물성 식품 중 테트라싸이클린계 항생물질의 동시분석을 시도하였다. 대상물질은 동물의 질병치료.예방, 성장촉진 및 사료효율 개선에 널리 사용되는 클로르테트라싸이클린, 독시싸이클린, 옥시테트라싸이클린 및 테트라싸이클린이었으며, 대상식품은 쇠고기, 돼지고기, 닭고기, 우유, 계란, 넙치, 우럭, 참돔, 뱀장어 및 바다가재이었다. 시료를 McIlvaine 완충액 및 20% 삼염화초산으로 추출한 후 $C_18$ 카트리지로 정제하여 고속액체크로마토그라피로 분석하였다. 이동상으로는 0.01M 수산과 아세토니트릴의 혼합용액을 85:15에서 60:40까지 기울기로 사용하였으며 UV의 검출파장은 365 nm 이었다. 평균 회수율은 71-98% 이었으며, 검출한계는 신호대 잡음비 3 이상에서 클로르테트라싸이클린은 0.022, 독시싸이클린은 0.012, 옥시테트라싸이클린은 0.012 및 테트라싸이클린은 0.009 mg/kg이었다. 대부분의 시료에서 클로르테트라싸이클린, 독시싸이클린 및 테트라싸이클린은 검출되지 않았으나, 돼지고기, 넙치 및 참돔(2시료)에서 옥시테트라싸이클린이 각각 0.04, 0.17, 0.05 및 0.08 mg/kg로 모두 잔류허용기준을 초과하지 않은 수준으로 검출되었다.

• 분석과학
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• 제20권1호
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• pp.84-90
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• 2007

식품중 설폰아마이드계 동물용의약품 11종을 분석하기 위하여 고속액체크로마토그라피를 이용하여 동시분석을 시도하였다. 대상물질은 설파클로로피리다진(SCP), 설파디아진(SDZ), 설파디메톡신(SDM), 설피속사졸(SSX), 설파메라진(SMZ), 설파메타진(SMT), 설파메톡사졸(SMX), 설파메톡시피리다진(SMP), 설파모노메톡신(SMM), 설파퀴녹살린(SQX) 및 설파치아졸(STZ)이었다. 대상식품은 축산식품인 소고기, 돼지고기, 닭고기, 우유 및 계란 5품목이었으며, 전국 6대도시인 서울, 부산, 대전, 인천, 목포, 강릉에서 수집하였다. 시료에 인산나트륨 및 아세토니트릴을 가하여 균질화한 후 핵산을 가하여 추출하고 고속액체크로마토그라피로 분석하였다. 이동상으로는 5 mM 제1인산칼륨용액(pH 3.25)과 메탄올의 혼합용액을 100:0에서 30:70까지 그래디언트로 사용하였으며 UV의 검출파장은 270 nm이었다. 평균 회수율은 75~95%이었으며, 검출한계는 신호대 잡음비 3 이상에서 대상물질에 따라 최저 SMT 0.004에서 최고 STZ 0.007 mg/kg로 나타났다. 대부분의 시료에서 설폰아미이드계 동물용의약품은 검출되지 않았으나, 소고기(2시료)에서 설파모노메톡신이 각각 0.03, 0.06 mg/kg 수준으로 검출되었으며 잔류허용기준 이하로 평가되었다.

• 생약학회지
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• 제41권4호
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• pp.313-318
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• 2010

Guibi-tang, a traditional herbal medicine, is used for anti-oxidant, anti-osteoporosis, hemostasis and gastroprotection. To develop an analysis method of simultaneous determination of six compounds, swertisin, decursinol, glycyrrhizin, 6-gingerol, costunolide and decursin in Guibi-tang, a high performance liquid chromatography was used with diode array detector. Six bioactive components were separated on a SHISEIDO $C_{18}$ column ($5\;{\mu}m$, 4.6 mm I.D.${\times}$250 mm) with column temperature $30^{\circ}C$. The gradient elution was composed of water with 0.1% trifluoroacetic acid (TFA) and acetonitrile. UV wavelength was set at 230 nm, 254 nm and 330 nm, respectively. Calibration curve showed good linear regression ($R^2$ > 0.9999). The limits of detection (LOD) and the limits of quantification (LOQ) ranged in 0.03 - 0.23 ${\mu}g/ml$ and 0.08 - $0.70\;{\mu}g/ml$, respectively. The RSD values of intra- and inter-day test were in the range of 0.03 ~ 0.96% and 0.01 ~ 1.46%, respectively. The evaluated results of accuracy test were varied from 92.28% ~ 105.14% with RSD < 1.60%. In conclusion, this developed simultaneous determination method was accuracy and sensitive to the quality evaluation of Guibi-tang.