• 전자공학회논문지
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• 제51권11호
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• pp.205-210
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• 2014

본 연구는 도자기의 표면에 무늬, 모양, 그림, 글씨 등의 문양을 움직이는 효과를 갖는 광응용 시스템에 관한 것으로, 도자기 표면 문양에 부착된 광섬유에 의한 LED광신호를 이용하여 문양의 움직임 효과를 실시간으로 표출하고, 도자기가 있는 장소의 조도와 회전판의 움직임을 수집하여 큐레이터가 응급조치를 취하고 문양의 표출효과를 관리하기 위한 광응용 시스템에 관한 것이다. 이와 같은 본 연구에 의하면, 도자기가 놓여져 있는 장소의 조도를 측정하여 문양의 표출효과를 큐레이터 및 응용프로그램이 실시간 관리할 수 있음과 동시에, 이상 발생 시에 자동으로 신호를 발생하여 조치할 수 있게한다. 또한, 본 연구은 일정기간 동안 광신호 전송데이터를 메모리에 저장하였다가, 데이터베이스화하여, 표출효과를 분석 후, 최적의 표출효과를 갖도록 적절한 조치를 취할 수 있도록 한다. 도자기가 있는 장소의 조도 상태를 감지 및 전달하고, 적정한 판단을 내릴 수 있는 일정한 조도수치를 데이터베이스화하고, 적절한 조건에 의거 문양 표출관련 광섬유 색체, 표출간격과 밝기에 대한 신호 데이터가 강제 혹은 의도에 의한 전달이 이루어지게 한다. 따라서 본 연구의 목적은 관제센터의 응용프로그램과 LED제어모듈에 의해 발생되는 광송출신호를 생성하여 색채, 조도, 표출간격을 측정하고 전송할 수 있는 문양을 움직이는 효과를 갖는 광응용시스템을 연구하였다.

• 한국전자파학회논문지
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• 제16권7호
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• pp.671-680
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• 2005

CQPSK(Compatible QPSK) 디지털 변조 기술을 이용하는 초협대역 단말기용 송신기에 가장 핵심적인 부품들 중의 하나인 카테지안 궤환 루프(CFL: Cartesian Feedback Loop) 선형화 칩을 $0.35{\mu}m$ CMOS 기술을 이용하여 설계 및 제작하였다. 직접 변환 방식 및 CFL칩을 이용하여 요구되는 부품 수를 줄임에 의하여 송신기의 저비용 및 소형화가 가능하고, 이를 통하여 송신 전력 효율 및 선형성을 향상시켰다. 또한 CMOS기술을 통하여 저전력 구동이 가능하도록 하였다. 송신 성능 시험 결과 PEP 37 dBm(5 W)의 출력 전력에서 CFL 칩을 구동하여 -25 dBc의 상호 변조 왜곡(@ 3 kHz주파수 오프셋) 개선을 통하여 FCC 47 CFR 90.210 E에 정의된 방사 마스크 규격을 만족함을 확인하였다. 또한 상기 언급된 송신 특성 개선에 가장 영 향을 미치는 성분들인 DC-offset 성분, 궤환 루프에서 발생하는 왜곡 성분을 보상하기 위한 루프 이득 및 위상 값들을 조정할 수 있도록 컴퓨터와의 외부 인터페이스를 구현하여 소프트웨어적으로 이러한 값들을 제어할 수 있도록 프로그램화 하였다.

• 한국환경과학회지
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• 제25권8호
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• pp.1065-1076
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• 2016

This study analyzes the $PM_{10}$ characteristics (particulate matter with aerodynamic diameter less than $10{\mu}m$), concentration, and emissions in eight large South Korean cities (Seoul, Incheon, Daejeon, Daegu, Gwangju, Ulsan, Busan, Jeju). The annual median of $PM_{10}$ concentration showed a decline of $0.02{\sim}1.97{\mu}g/m^3$ in the regions, except for Incheon, which recorded an annual $0.02{\mu}g/m^3$ increase. The monthly distribution levels were high in spring, winter, fall, and the summer, but were lower in summer for all regions except for Ulsan. These differences are thought to be due to the dust in spring and the cleaning effect of precipitation in summer. The variation in concentrations during the day (diurnal variation) showed that $PM_{10}$ levels were very high during the rush hour and that this was most extreme in the cities (10.00 and 18.00-21.00). The total annual $PM_{10}$ emissions analysis suggested that there had been a general decrease, except for Jeju. On-road mobile (OM) sources, which contributed a large proportion of the particulates in most regions, decreased, but fugitive dust (FD) sources increased in the remaining regions, except for Daegu. The correlation analysis between $PM_{10}$ concentrations and emissions showed that FD could be used as a valid, positive predictor of $PM_{10}$ emissions in Seoul (74.5% (p<0.05)), Dajeon (47.2% (p<0.05)), and Busan (59.1% (p<0.01)). Furthermore, industrial combustion (IC) was also a significant predictor in Incheon (61.7% (p<0.01)), and on-road mobile (OC) sources were a valid predictor in Daegu (24.8% (p<0.05)).

• Journal of Pharmaceutical Investigation
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• 제36권5호
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• pp.331-338
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• 2006

A rapid, selective and sensitive reverse-phase HPLC methods for the determination of atenolol and chlorthalidone in human serum and whole blood were validated, and applied to the pharmacokinetic study of atenolol and chlorthalidone combination therapy. Atenolol and an internal standard, pindolol, were extracted from human serum by liquid-liquid extraction, and analyzed on a $\mu$-Bondapak C18 $10-{\mu}$ column in a mobile phase of methanol-0.01 M potassium dihydrogenphosphate(30:70, v/v, adjusted to pH 3.5) and fluorescence detection(emission: 300 nm, excitation: 224 nm). Chlorthalidone and an internal standard, probenecid, were extracted form human whole blood by liquid-liquid extraction, and analyzed on a Luna C18 $5-{\mu}$ column in a mobile phase of acetonitrile containing 77% 0.01 M sodium acetate and UV detection at 214 nm. These analysis were performed at three different laboratories using the same quality control(QC) samples. The chromatograms showed good resolution, sensitivity, and no interference by human serum and whole blood, respectively. The methods showed linear responses over a concentration range of 10-1,000 ng/mL for atenolol and 0.05-20 ${\mu}g/mL$ for chlorthalidone, with correlation coefficients of greater than 0.999 at all the three laboratories. Intra- and inter-day assay precision and accuracy fulfilled international requirements. Stability studies(freeze-thaw, short-, long-term, extracted sample and stock solution) showed that atenolol and chlorthalidone were stable. The lower limit of quantitation of atenolol and chlorthalidone were 10 ng/mL and 0.05 ${\mu}g/mL$, respectively, which was sensitive enough for pharmacokinetic studies. These methods were applied to the pharmacokinetic study of atenolol and chlorthalidone in human volunteers following a single oral administration of Hyundai $Tenoretic^{\circledR}$ tablet(atenolol 50 mg and chlorthalidone 12.5 mg) at three different laboratories.

• 공업화학
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• 제21권6호
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• pp.632-637
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• 2010

현재 시행되고 있는 수질오염 총량관리제나 수질 TMS 등과 같은 수자원 보호에 대한 국가 관심도를 미루어 볼 때 자동채수기는 반드시 필요하다. 본 연구에서는 수입에 의존하는 자동채수기를 개발하여, 외화낭비를 줄이고 동시에 기능적 성능을 높이는 데 있다. 개발결과물들을 얻고자 몇 가지 노력을 하였다. 이를 위하여 현장측정용 유량센서, 즉, Flow Meter를 자동채수기에 설치하여 연동 운영될 수 있는 기술개발을 했으며, 개발된 현장측정용 센서에서 송신되는 데이터를 원격으로 모니터링 및 저장할 수 있는 원격 D/L 시스템을 개발하였다. 또한, 개발된 자동채수기를 실제 하수처리장에 설치하여 운전해 보았고, 그 결과 현장적용이 충분히 가능함을 확인할 수 있었다.

• 한국전자파학회논문지
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• 제21권5호
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• pp.510-518
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• 2010

본 논문에서는 UHF 대역(380~910 MHz)의 간이 무선 및 TRS(Trunked Radio System) 단말기에서 이용 가능한 CFL(Cartesian Feedback Loop) 선형화 칩을 Si 기반의 $0.6\;{\mu}m$ BiCMOS 공정을 이용하여 설계 및 제작한 결과를 보였다. 단말기의 송신 전력을 가변하기 위한 이득 제어 회로를 궤환 경로뿐만 아나라 순방향 경로에도 삽입함으로써 CFL의 안정성을 일정하게 유지하도록 하였으며, 무전기 PTT(Push-To-Talk) 동작에 적합하고 구현이 용이한 S/H(Sample & Hold) 구조를 이용한 DC-offset 제거 기능을 구현하였다. 송신 시험 결과, CQPSK(Compatible QPSK) 신호 인가 시, PEP(Peak Envelope Power) 3 W(34.8 dBm) 출력에서 FCC의 방사 마스크 규격을 만족함을 확인하였으며, Two-tone 인가 시, 30 dB 이상의 3차 IMD 성분 개선을 확인하였다.

• 한국환경농학회지
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• 제25권4호
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• pp.359-364
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• 2006

Reversed-phase high-performance liquid chromatography (HPLC) techniques were developed to quantify abamectin (ABM) in paprika (Capsicum annum). Separation was achieved on a $C_{18}$ ODS column with a mobile phase of acetonitrile/water (96/4, v/v) mixture in an isocratic elution at the flow tate of 1.2 mL/min for avermectins (AVMs). The retention times were 8.0 and 9.7mins for AVM $B_{lb}$ and AVM $B_{1a}$, respectively. Residual AVMs (sum of AVM $B_{1a}$, AVM $B_{1b}$ and 8,9-Z-AVM $B_{1a}$) in the vegetable were extracted with acetonitrile, and the silica solid-phase extraction cartridges were used to purify the extract. AVMs were derivatized using trifluoroacetic acid and 1-methylimidazole, and the derivatives were determined with a fluorescence detector (excitation at 365 nm and emission at 470 nm). High and consistent recoveries, ranging from 93% to 115%, were obtained for AVM $B_{1a}$ and 8, 9-Z-AVM $B_{1a}$ at fortified levels of $20{\mu}g/kg\;and\;200{\mu}g/kg$ for paprika. The limit of quantitation (LOQ) was $2{\mu}g/kg$. The residual levels of AVMs in paprika in a field experiment from one day to seven days after the last application decreased from 18.40 to $7.59{\mu}g/kg$. The half-life $(T_{1/2})$ of AVMs in paprika was 1.47 days.

• Journal of Pharmaceutical Investigation
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• 제35권1호
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• pp.51-55
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• 2005

A high-performance liquid chromatographic method was employed for the determination of bumetanide in human plasma. After addition of internal standard (IS, naproxen) and acidification of the plasma with 1 M hydrochloric acid, the drug and IS were extracted into dichloromethane. The organic phase was back-extracted into 1 M sodium bicarbonate solution and 50 ${\mu}l$ of the aqueous phase was injected onto a reversed-phase C18 column with a mobile phase consisting of methanol: water: glacial acetic acid = 65 : 35 : 1. The samples were detected utilizing a fluorescence detector (excitation wavelength 235 nm, emission wavelength 405 nm). The method was specific and validated with a lower limit of 5 ng/mL. Intra- and inter-day precision and accuracy were acceptable for all quality control samples including the lower limit of quantification. The applicability of the method was demonstrated by analysis of plasma after oral administration of a single 2 mg dose to 24 healthy subjects. From the plasma bumetanide concentration vs. time curves, the mean AUC was $246.5{\pm}73.8\;ng{\cdot}hr/mL$ and $C_{max}$ of $132.1{\pm}40.9$ ng/mL reached 1.2 hr after administration. The mean biological half-life of burnet ani de was $1.1{\pm}0.2$hr. Based on the results, this simple and validated assay method could readily be used in any pharmacokinetic or bioequivalence studies using humans.

• Journal of Pharmaceutical Investigation
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• 제35권6호
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• pp.431-436
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• 2005

A high-performance liquid chromatographic method was validated for quantitation of nadolol in human plasma. Nadolol and internal standard, pindolol, were extracted with tert-butyl methyl ether after addition of 10 M sodium hydroxide solution. The analytes were separated on a reverse phased C18 column using a mobile phase consisting of 0.05 M ammonium phosphate monobasic buffer, acetonitrile and methanol (81: 17:2 v/v/v) and detected using a fluorescence detector (excitation wavelength 230 nm, emission wavelength 294 nm). The method was specific and sensitive enough to detect as low as 3 ng/mL of nadolol in human plasma. Linear calibration range was 3-150 ng/mL with correlation coefficient greater than 0.999. The overall accuracy was in the range of 96.8 to 103% and precision C.V.(%) 7.30 to 12.2%. The recovery was approximately 100% and stability was confirmed during storage and sample preparation. The present HPLC method was successfully applied to study bioavailability after oral administration of 80 mg of nadolol in healthy Korean subjects. The mean $AUC_{t}$ was $1968{\pm}397\;ng{\cdot}hr/mL$ and $C_{max}$ of $186{\pm}79.3\;ng/mL$ was reached at $3.5{\pm}0.76\;hr$. The mean $t_{1/2}$ of nadolol was $17.3{\pm}2.59\;hr$.

• 한국동물위생학회지
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• 제29권2호
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• pp.111-122
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• 2006

A direct, accurate and sensitive chromatographic analytical method for quantitative determination of four fluoroquinolones (norfloxacin, cirprofloxacin, danofloxacin and enrofloxacin) in chicken, pork and beef edible muscle is proposed in the present study. The developed method was successfully applied to the determination of enrofloxacin, as the main component of commercially available veterinary drugs. The samples were homogenized and the antimicrobials were added, then they were extracted twice with dichloromethane. Fluoroquinolone antibiotics were separated on an agilent $250x4mm,\;C_{18},\;5{\mu}m$, analytical column, at $25^{\circ}C$. The mobile phase consisted of a mixture of DW : acetonitrile : triethylamine(80:19:1%, v/v, pH 3.0) leading to retention times less than 14 min. at a flow rate 0.5 ml/min. These fluoroquinolones were detected by liquid chromatography with fluorescence at 290 nm excitation and 465 nm emission. The limits of quantification in each edible muscle (chicken, pork, and beef) were 0.32-6.54 ng/g. Using 0.5 g of each sample, average recovery rates at fortification levels of 0.05, 0.1 and 0.2 ${\mu}g/ml$ ranged 70.14-71.71% for NFX, 71.87-73.89% for CFX, 82.16-92.35% for DFX, and 90.13-98.12 for EFX This is a simple and economic method to quantify the presence of NFX, CFX, EFX and DFX in edible muscle of animal origin.