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이원재,이재형,박경환,이정환,임규호,강형근,고봉진,박무훈,하판봉,김영희,Yi, Won-Jae,Lee, Jae-Hyung,Park, Kyung-Hwan,Lee, Jung-Hwan,Lim, Gyu-Ho,Kang, Hyung-Geun,Ko, Bong-Jin,Park, Mu-Hun,Ha, Pan-Bong,Kim, Young-Hee 한국정보통신학회 2006 한국정보통신학회논문지 Vol.10 No.3
본 논문에서 는 플래쉬 셀을 사용하여 수동형 UHF RFID 태그 칩에 사용되는 저전력 1Kb 동기식 EEPROM을 설계하였다. 저전력 EEPROM을 구현하기 위한 방법으로 다음과 같은 4가지 방법을 제안하였다. 첫째, VDD(=1.5V)와 VDDP(=2.5V)의 이중 전원 공급전압 방식을 사용하였고, 둘째, 동기식 회로 설계에서 클럭(clock) 신호가 계속 클럭킹(clocking)으로 인한 스위칭 전류(switching current)가 흐르는 것을 막기 위해 CKE(Clock Enable) 신호를 사용하였다. 셋째, 읽기 사이클에서 전류 센싱(current sensing) 방식 대신 저전력 소모를 갖는 clocked inverter를 사용한 센싱 방식을 사용하였으며, 넷째, 쓰기 모드시 Voltage-up 변환기(converter) 회로를 사용하여 기준전압 발생기(Reference Voltage Generator)에는 저전압인 VDD를 사용할 수 있도록 하여 전력 소모를 줄일 수가 있었다. $0.25{\mu}m$ EEPROM 공정을 이용하여 칩을 제작하였으며, 1Kb EEPROM을 설계한 결과 읽기 모드와 쓰기 모드 시에 소모되는 전력은 각각 $4.25{\mu}W$와 $25{\mu}W$이고, 레이아웃 면적(layout area)은 $646.3\times657.68{\mu}m^2$이다. In this paper, a low-power 1Kb synchronous EEPROM is designed with flash cells for passive UHF RFID tag chips. To make a low-power EEPROM, four techniques are newly proposed. Firstly, dual power supply voltages VDD(1.5V) and VDDP(2.5V), are used. Secondly, CKE signal is used to remove switching current due to clocking of synchronous circuits. Thirdly, a low-speed but low-power sensing scheme using clocked inverters is used instead of the conventional current sensing method. Lastly, the low-voltage, VDD for the reference voltage generator is supplied by using the Voltage-up converter in write cycle. An EEPROM is fabricated with the $0.25{\mu}m$ EEPROM process. Simulation results show that power dissipations are $4.25{\mu}W$ in the read cycle and $25{\mu}W$ in the write cycle, respectively. The layout area is $646.3\times657.68{\mu}m^2$.
안무영,고광균,이강순 순천향대학교 1992 논문집 Vol.15 No.2
A new plating medium from the extract of Solen gouldi has been developed as alternative to MacConkey agar for the isolation of Shigella. The new medium was tested for the growth of Shigella, Salmonella E. coli, Proteus, Vibrio, Pseudomonas, Staphylococcus and their ability form colonies, and that was compared with MacConkey and Brain Heart Infusion agar media. The following results were obtained. 1. Shigella dysenteriae and Escherichia coli grow best as large colonies on Solen agar medium. 2. Salmonella and Proteus grow well on Solen agar and Brain Heart Infusion agar but MacConkey agar was inhibited. 3. Vibrio parahaemolyticus and Vibric vulnificus was inhibited on Solen agar than thiosulfate-citrate-bilesalt-sucrose agar. 4. The growth of Staphylococcus aureus was highly inhibited on Solen agar media.
저전압 DRAM을 위한 2단 2위상 부스터 전압 발생기
김영희,박무훈,고봉진 국립7개대학공동논문집간행위원회 2002 공업기술연구 Vol.2 No.-
This paper proposes a new two-stage two-phase VPP charge pump configured in such a manner that the body effect and the threshold voltage loss are eliminated. The newly proposed circuit is fabricated using 0.18um triple-well CMOS process and the measurement result shows that the VPP level tracks 3VDD when VDD is above the threshold voltage.
2급 와동 수복시 사용방법에 따른 복합 레진 인레이의 변연누출에 관한 실험적 연구
박경준,계기성,고영무,김경남 大韓齒科器材學會 1993 대한치과재료학회지 Vol.20 No.1
The purpose of this in vitro study was to evaluate the marginal microleakage of Class Ⅱ composite resin inlay restoration and to compare the marginal leakage of inlay with indirectly placed composite restoration and that of direct filling composite restoration. MO or DO cavity preparations were cut in 60 extracted human permanent molars. The experimental group was restored with Herculite XR inlay, Clearfil inlay, and E.O.S. inlay with dual cement. The control group was directly filled with Herculite XR after being etched and applied with dentin bonding agent. The specimens were thermocycled 1,000 times between 5℃ and 55℃. Microleakage was evaluated by use of the Methylene bule staining technique. The depth of microleakage was measured with stereomicroscope after the teeth were sectioned. The obtained results were as follows : 1. The marginal leakage was reduced in the order of Clearfil inlay, Herculity XR-inlay, E.O.S. inlay, and Herculite XR-direct filling group at the occlusal margin. 2. The marginal leakage was reduced in the order of Clearfil inlay, Herculity XR-inlay, Herculite XR-direct filling group and E.O.S. inlay at the gingival margin. 3. Generally, the marginal leakage was more greatly showed at the gingival margin than at the occlusal margin. 4. The marginal leakage was greatest at the gingival margin of E.O.S. inlay, and was the least at the occlusal margin of Clearfil inlay.
중대산업사고 예방을 위한 종합위험관리체제(IRMS) 구축에 관한 연구
권혁면,성대현,김재현,임대식,김기영,편무욱,문일,고재욱,이영순,윤인섭 한국안전학회 2003 한국안전학회지 Vol.18 No.3
The Process Safety Management (PSM) by the Law of Industry, Safety and Health has been performed for preventing major accidents of chemical plants since 1996. In terms of preventing chemical accidents more precisely, it is essential to develop a tool for quantitative risk assessment. For this, KOSHA (Korea Occupational Safety and Health Agency) developed an Integrated Risk Management System (IRMS) . The system is designed to assimilate data on chemical plant hazards from external database, to integrate these data with location information (topographic and demographic), and to make them user-friendly accessible. The system consists of several main functions: display of five major Korean petrochemical complex layout, display of equipment layout with its information utilizing the external database, zonation of the hazard effected area with consequence analyses, the most probable accident scenario generation, accident/incident database and calculation of frequency of accident using equipment reliability database, etc. The highlight of IRMS is to provide the risk contours using GIS(Geographical Information System) technology. IRMS is intended to manage hazardous installation more systematically and effectively, to reduce the number of accident remarkably, further minimizing production loss in the plant. The system is now under application to about 500 PSM sites as well as and emergency authorities in Korea by KOSHA (Korea Occupational Safety and Health Agency)
KO, SANG-MU,VAIDYA, BIPIN,KWON, JOSEPH,LEE, HEE-MIN,OH, MYUNG-JOO,SHIN, TAI-SUN,CHO, SE-YOUNG,KIM, DUWOON International Association for Food Protection 2015 Journal of food protection Vol.78 No.5
<P>Outbreaks of hepatitis A virus (HAV) infections are most frequently associated with the consumption of contaminated oysters. A rapid and selective concentration method is necessary for the recovery of HAV from contaminated oysters prior to detection using PCR. In this study, ricin extracted from castor beans (Ricinus communis) was tested as an alternative to antibody used in immunomagnetic separation while concentrating HAV prior to its detection using reverse transcription PCR. Initially, the extracted proteins from castor beans were fractionated into 13 fractions by gel filtration chromatography. Pretreatment of different protein fractions showed a variation in binding of HAV viral protein (VP) 1 to oyster digestive tissue in the range of 25.9 to 63.9%. The protein fraction, which caused the highest reduction in binding of VP1 to the tissue, was identified as ricin A by quadrupole time-of-flight mass spectrometry. Ricin A could significantly inhibit binding of VP1 to the tissue with a 50% inhibitory concentration of 4.5 μg/ml and a maximal inhibitory concentration of 105.2%. The result showed that the rate of inhibition of HAV binding to tissue was higher compared to the rate of ricin itself binding to HAV (slope: 0.0029 versus 0.00059). However, ricin A concentration showed a higher correlation to the relative binding of ricin itself to HAV than the inhibition of binding of HAV to the tissue (coefficient of determination, R2: 0.9739 versus 0.6804). In conclusion, ricin A-linked magnetic bead separation combined with reverse transcription PCR can successfully detect HAV in artificially seeded oyster digestive tissue up to a 10−4 dilution of the virus stock (titer: 104 50% tissue culture infective dose per ml).</P>
Young-Min Kwon,Sung-Dong Lee,Hyun-Sook Kang,Mu-Gung Cho,Soon-Sun Hong,Chae-Kyu Park,Jong-Tae Lee,Byeong-Seon Jeon,Sung-Ryong Ko,Hyun-Joo Shon,Dal-Woong Choi 고려인삼학회 2008 Journal of Ginseng Research Vol.32 No.4
For evaluating the quality of ginseng, simple and fast analysis methods are needed to detennine the ginsenoside content of the ginseng products. The aim of this study was therefore to optimize conditions for fast analysis of the ginsenosides, the active ingredients in extracts of Korean red ginseng. When tandem HPLC mass spectrometry (HPLC-MS/ MS) was used, four fonns of ginsenoside, Rb1, Rb2, Rc, and Re, were readily separated in seven minutes using a gradient mobile phase (acetonitrile and water containing acetic acid). This is the shortest separation time reported among the studies of major ginsenoside analysis. When gradient HPLC with UV detection was used, the detection limit was high, but separation of these four ginsenosides required 25 minutes using acetonitrile and water containing formic acid as a mobile phase. HPLC-MS/MS was able to separate ginsenoside Rg1 easily regardless of the mobile phase condition, but the HPLC-UV could not separate Rg1 because acetonitrile concentration in the mobile phase had to be maintained below 20%. Ginsenoside peaks were clearer and had more sensitive detection limits when Korean red ginseng extract was analyzed by the HPLC-MS/MS, but the UV detection was useful for chromatographic fingerprinting of all four major ginsenosides of the extract: Rb1, Rb2, Rc, and Re. Extracts were found to contain 2.17 mg, 1.51 mg, 1.29 mg, and 0.46 mg of ginsenoside Rb1, Rb2. Rc, Re, respectively, per gram weight. The ratios of each ginsenoside in the extracts were 1.0 : 0.7 : 0.6 : 0.2, respectively. Taken together, the results indicate that HPLC-MS/MS spectrometIy could be the most useful method for rapid analysis of even small amounts of major ginsenosides, while HPLC with UV detection could also be used for rapid analysis of major ginsenosides and for quality control of ginseng products.
Ko, Yeong-Mu,Choi, Do-Young,Jung, Sang-Chul,Kim, Byung-Hoon American Scientific Publishers 2015 Journal of Nanoscience and Nanotechnology Vol.15 No.1
<P>Polycaprolactone (PCL) nanofibers (PCL-NF) with uniform fibrous structure were fabricated by electrospinning. However, PCL-NF has hydrophobic surface, lacks functional groups and hence it is not a good substrate for cell adhesion. To improve the cell adhesion, PCL-NF surfaces were modified by low pressure RF discharge plasma treatment using monomer such as acrylic acid or oxygen gas. The plasma treated PCL-NFs improved the wettability and cell proliferation.</P>