• Title/Summary/Keyword: Ah 측정법

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RF 스퍼터링법을 이용한 리튬이차전지용 Li[Li0.2Mn0.54Co0.13Ni0.13]O2 양극박막의 제조 및 전기적 특성

  • Im, Hae-Na;Gong, U-Yeon;Yun, Seok-Jin;Choe, Ji-Won
    • Proceedings of the Korean Vacuum Society Conference
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    • 2011.02a
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    • pp.413-413
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    • 2011
  • 최근 전기, 전자, 반도체 산업의 발전으로 전 고상 박막리튬전지는 초소형, 초경량의 마이크로 소자의 구현을 위한 고밀도 에너지원으로 각광받고 있다. 현재 양극박막은 대부분LCO(LiCoO2)계열이 이용되고 있으나, 코발트는 높은 가격과 인체 유해성 뿐만 아니라 상대적으로 낮은 용량(~140 mAh/g)등의 단점을 갖고 있어 향후 보다 고용량의 양극박막이 요구된다. 3원계 양극활물질 LiMO2(M=Co,Ni,Mn,etc.)은 우수한 충방전 효율 과 열적 안정성 뿐 아니라 277mAh/g의 높은 이론용량을 갖고 있어 고용량 양극박막으로의 적용시 고용량 박막이차전지 제작이 가능하다. 본 연구에서는 전 고상 박막 전지의 구현을 위하여 RF 스퍼터링법을 사용하여 Li[Li0.2Mn0.54Co0.13Ni0.13]O2 박막을 증착하였다. Li/MnCoNi의 몰 비율을 변화시켜 높은 전기화학적 특성을 갖는 분말을 합성하여 제조한 타겟으로 Pt/TiO2/SiO2/Si 기판위에 RF 스퍼터법을 이용하여 박막을 성장시켰다. 박막 증착 시 가스의 비율은 Ar:O2=3:1로 하고 증착 압력의 조절(0.005~0.02 torr)을 통하여 박막의 두께와 표면 특성을 조절하며 성장시켰다. 또한 박막을 다양한 온도에서($400{\sim}550^{\circ}C$) 열처리하여 결정화도와 전기화학적 특성을 측정하였다. 증착 된 박막의 구조적 특성은 X-ray diffraction(XRD) 과 scanning electron microscopy(SEM)로 관찰되었다. 박막의 전기화학적 특성 평가를 위하여 Cyclic voltammatry를 측정하여 가역성의 정도를 확인하고 WBC3000 battery cycler를 이용한 half-cell 테스트를 통하여 박막의 용량을 평가하였다.

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Protonation State of Norfloxacin and Their Interaction with DNA (pH에 따른 Norfloxacin의 형태 및 DNA와의 상호작용에 관한 연구)

  • Yeo, Jeong-Ah;Son, Gwan-Su;Kim, Jong-Moon;Moon, Hyung-Rang;Jun, Eun-Duk;Cho, Tae-Sub
    • Journal of the Korean Chemical Society
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    • v.44 no.1
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    • pp.4-9
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    • 2000
  • We investigated the self-association and protonation state of norfloxacin, a member of quinokme antibiotics, using electric absorption and potentiom,etric titration. Both nitrogen at the piperazine ring and carboxylic acid were protonated at a low pH (cationic norfloxacin), and deprotonated at a high pH (anionic norfloxacin). In the intermediate pH range, a neutral species was dominant with the possibility of forming a zwitter ion. We also observed that nortloxacin molecules can be sracked to form a dimer at an intermediate pH, The equilibrium constant of the norfloxacin-DNA complex formation, which was measured by Stem-Volmermethod, increases as the pH of the system is lowered. This observation indicates that it is the cationic nortloxacin that forms a complex with DNA among various norfloxacin species in aqueous solution.

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Analysis of Thiosultap in Hulled Rice by Derivatization (유도체화 반응에 의한 현미 중 thiosultap의 분석)

  • Choi, Jeong-Heui;Do, Jung-Ah;Yoon, Hae-Jung;Park, Yong-Chun;Kim, Jae-Hun;Choi, Dong-Mi
    • The Korean Journal of Pesticide Science
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    • v.14 no.1
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    • pp.16-20
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    • 2010
  • Thiosultap, a nereistoxin analog insecticide, registered in China has been used to control selected beetles and Lepidopteran pests on rice, vegetables and fruit trees. Although domestic use of thiosultap is not permitted, it is needed to monitor this insecticide from imported crops because that has been used on crops in many foreign countries, especially China. Thiosultap in hulled rice was determined as nereistoxin derived in basic condition by GC-FPD. This method accomplished ion-associated liquid-liquid partitioning for cleanup, and limit of quantification and linearity performed by the established method were 0.05 mg $kg^{-1}$ and 0.995$(r^2)$. The recoveries performed by control hulled rice fortified with thiosultap at 0.5 and 2.5 mg $kg^{-1}$ were $96.1{\pm}7.9\sim100.8{\pm}6.1%$.

Fundamental Investigation of Non-invasive Determination of Alcohol in Blood by Near Infrared Spectrophotometry (근적외선 분광분석법을 이용한 음주측정기술 개발에 관한 연구)

  • Chang, Soo-Hyun;Cho, Chang-Hee;Woo, Young-Ah;Kim, Hyo-Jin;Kim, Young-Man;Lee, Kang-Boong;Kim, Young-Woon;Park, Sung-Woo
    • Analytical Science and Technology
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    • v.12 no.5
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    • pp.375-381
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    • 1999
  • Near infrared spectrophotometry(NIR) was developed as a non-invasive determination of blood alcohol. The first pure alcohol/water samples were prepared with ethanol concentration from 0.01 to 0.1%(w/w). Analysis of the second-derivative data was accomplished with multilinear regression(MLR). The standard error of calibration(SEC) of ethanol in ethanol/water solutions was approximately 0.0039%. The calibration models were established from the blood alcohol spectra by MLR and PLSR analysis. The best calibration was built with the second-derivative spectra of 2266 and 2326 nm by MLR. Second-derivative spectra in the spectral ranges of 1100~1340, 1500~1796 and 2064~2300 nm with four PLSR factors provided the standard error of prediction(SEP) of 0.030%(w/w). These results indicate that NIR may be applied for a fast non-invasive determination of alcohol in the blood.

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Electrochemical Properties of Ionic Liquid Composite Poly(ethylene oxide)(PEO) Solid Polymer Electrolyte (이온성 액체 복합 Poly(ethylene oxide)(PEO) 고체 고분자 전해질의 전기화학적 특성)

  • Park, Ji-Hyun;Kim, Jae-Kwang
    • Journal of the Korean Electrochemical Society
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    • v.19 no.3
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    • pp.101-106
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    • 2016
  • In this study, we prepared an ionic liquid composite solid polymer electrolyte (PEO-LiTFSI-$Pyr_{14}TFSI$) with poly(ethylen oxide), lithium bis(trifluoromethanesulfonyl)imide, N-butyl-N-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide by blending-cross linking process. Although the PEO-LiTFSI-$Pyr_{14}TFSI$ composite solid polymer electrolyte displayed a small peak at 4.4 V, it had high electrochemical oxidation stability up to 5.7 V. Ionic conductivity of the PEO-LiTFSI-$Pyr_{14}TFSI$ composite solid polymer electrolyte increased with increasing temperature from $10^{-6}S\;cm^{-1}$ at $30^{\circ}C$ to $10^{-4}S\;cm^{-1}$ at $70^{\circ}C$. To investigate the electrochemical properties, the PEO-LiTFSI-$Pyr_{14}TFSI$ composite solid polymer electrolyte assembled with $LiFePO_4$ cathode and Li-metal anode. At 0.1 C-rate, the cell delivered $40mAh\;g^{-1}$ for $30^{\circ}C$, $69.8mAh\;g^{-1}$ for $40^{\circ}C$ and $113mAh\;g^{-1}$ for $50^{\circ}C$, respectively. The PEO-LiTFSI-$Pyr_{14}TFSI$ solid polymer electrolyte exhibited good charge-discharge performance in Li/SPE/$LiFePO_4$ cells at $50^{\circ}C$.

A Study on the Evaluation Method of New and Renewable Energy Human Resource Development Programs (신재생에너지 인력양성 평가 방법론 연구)

  • Lee, You-Ah;Kim, Jin-Soo;Heo, Eun-Nyeong
    • 한국신재생에너지학회:학술대회논문집
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    • 2008.05a
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    • pp.103-106
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    • 2008
  • 신재생에너지기술 개발인력 확보는 국가 에너지 안보의 확보 및 지속적인 성장을 가능하게 하는 주요 요인이다. 관련 사업추진에 있어 비효율성의 제거와 인적자원 개발 정책의 효과적인 추진을 위해서 신재생에너지 인력양성 사업에 대한 체계적인 성과평가가 요구되고 있다. 본 연구에서는 신재생에너지 인력양성의 평가를 위하여 적용가능한 방법론을 살펴 보았다. 기존 인력양성 방법론의 구분을 수정하여 인력 양성의 평가 방법을 성과점검, 요인통제분석, 사업의 파급효과 산출방법으로 분류하고 각 기준별 세부방법론을 제안하였다. 성과점검 방식에는 단순환산/일반질문법, 요인통제분석에는 AHP-DEA효율성 측정방법, 인적자본 축적모형방법이 포함될 수 있다. 마지막으로 사업의 파급효과 산출방법에는 산업연관분석 방법, 인력양성 산업연관도 작성 방법이 있다. 제안된 모형 중AHP-DEA효율성 측정방법은 신재생 에너지 인력양성 평가에 적용될 경우 DEA 모형의 객관성이라는 특징을 최대한 이용하는 동시에, 한계로 지적될 수 있는 변별력 분제를 체계적으로 보완하기위한 방편으로 AHP를 도입함으로써 적절한 인력양성 평가 방법론으로 적용될 수 있을 것이다.

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Flow Forecasting using Neural Networks Model in Nakdong River Basin (신경망 모형을 이용한 낙동강 유역에서의 유량 예측)

  • Han, Kun-Yeun;Kim, Dong-Il;Son, Ah-Long;Kim, Ji-Eun
    • Proceedings of the Korea Water Resources Association Conference
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    • 2009.05a
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    • pp.314-318
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    • 2009
  • 본 연구의 목적은 강우-유출자료 및 댐 방류량 자료의 비선형적인 특정을 가장 잘 반영할 수 있는 신경망모형을 적용하여 수질정책의 기초자료를 제공하기 위하여 신뢰성 있는 유량자료를 산정하는 모형을 개발하였고 이를 낙동강 유역에 적용하는 것이다. 이를 위해서 낙동강물환경연구소의 8일 측정 유량이 가지는 정확성을 이용하면서 상류 댐의 일 방류량자료와 유역별 강우자료 및 국토해양부 수위관측소의 수위자료를 연계하여 유량을 보간할 수 있는 유량 보간 신경망 모형을 개발하였다. 신경망 모형의 출력값은 낙동강물환경 연구소에서 측정하지 않은 기간에 대하여 유량을 보간할 수 있도록 구성하였으며 신경망 모형의 구조는 입력층과 출력층 사이에 하나의 은닉층이 존재하는 다층 신경망으로 구성하였으며, 학습단계에서는 오류 역전파 알고리듬 학습방법 중 모멘텀법을 사용하였다. 본 연구를 통하여 낙동강 전 유역에 대하여 유량 보간 모형을 적용한 결과 댐 방류량과 강우자료 및 상류 수위 관측소의 유량 자료를 이용한 유량 보간 신경망모형의 일 유량결과의 적용가능성을 검증할 수 있으며, 제시된 모형은 지속적인 수문자료의 질적 향상과 유출패턴의 축적으로 그 성능을 향상시킬 수 있을 것이며 또한 홍수기의 더 정확한 유량예측을 위한 적용사례의 확장 및 SWAT을 이용한 모형의 적용에 대한 연구가 병행되어야 할 것이다.

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Development and validation of an analytical method for the determination of lepimectin residues by HPLC-PDA (HPLC-PDA를 이용한 lepimectin 잔류량 분석법 개발 및 확인)

  • Do, Jung-Ah;Kwon, Ji-Eun;Kim, Mi-Ra;Lee, Eun-Mi;Kuk, Ju-Hee;Kwon, Kisung;Oh, Jae-Ho
    • Analytical Science and Technology
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    • v.26 no.2
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    • pp.142-153
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    • 2013
  • A new, rapid, and simple analytical method was developed and validated using high performance liquid chromatograph-photodiode array detector (HPLC-PAD) for the determination of lepimectin residues in agricultural commodities. The lepimectin residues in samples were extracted with methanol, partitioned with dichloromethane, and then purified with glass column filled with subsequently to aminopropyl ($NH_2$) solid phase extraction (SPE) cartridge. The purified samples were detected using HPLC-PAD. Correlation coefficient ($R^2$) of both lepimectin $A_3$ and $A_4$ solutions were 0.9999. The method was validated using cucumber spiked with lepimectin at 0.02 and 0.2 mg/kg and pepper, mandarin, hulled rice, potato, soybean at 0.02 and 0.5 mg/kg. Average recoveries were 76.0~114.8% with relative standard deviation less than 10%, and limit of detection (LOD) and limit of quantification (LOQ) were 0.005 and 0.01 mg/kg, respectively. The result of recoveries and overall coefficient of variation of a laboratory results in Gwangju regional KFDA and Daejeon regional KFDA was followed with Codex guideline (CAC/GL 40). Therefore, developed method in this study is accurate, rapid, and appropriate for lepimectin determination and will be used to keep safety of lepimectin residues in agricultural products.

Heart-Model-Based Automated Method for Left Ventricular Measurements in Cardiac MR: Comparison with Manual and Semi-automated Methods (자동화 방식 모델 기반 좌심방 파라미터 측정법: 수동 및 반자동 방식과의 비교)

  • Chae, Seung Hoon;Lee, Whal;Park, Eun-Ah;Chung, Jin Wook
    • Investigative Magnetic Resonance Imaging
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    • v.17 no.3
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    • pp.200-206
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    • 2013
  • Purpose : To assess the effect of applying an automated heart model based measurements of left ventricle (LV) and compare with manual and semi-automated measurements at Cardiovascular MR Imaging. Materials and Methods: Sixty-two patients who underwent cardiac 1.5T MR imaging were included. Steady state free precession cine images of 20 phases per cardiac cycle were obtained in short axis views and both 2-chamber and 4-chamber views. Epicardial and endocardial contours were drawn in manual, automated, and semi-automated ways. Based on these acquired contour sets, the end-diastolic (ED) and end-systolic (ES) volumes, ejection fraction (EF), systolic volume (SV) and LV mass were calculated and compared. Results: In EDV and ESV, the differences among three measurement methods were not statistically significant (P = .399 and .145, respectively). However, in EF, SV, and LV mass, the differences were statistically significant (P=.001, <001, <001, respectively) and the measured value from automated method tend to be consistently higher than the values from other two methods. Conclusion: An automatic heart model-based method grossly overestimate EF, SV and LV mass compared with manual or semi-automated methods. Even though the method saves a considerable amount of efforts, further manual adjustment should be considered in critical clinical cases.

Development and Validation of an Analytical Method for Flutianil Residue Identification Using Gas Chromatography-Electron Capture Detection (GC-ECD를 이용한 flutianil 잔류량 분석법 개발 및 확인)

  • Kwon, Ji-Eun;Do, Jung-Ah;Park, Hyejin;Lee, Ji-Young;Cho, Yoon-Jae;Oh, Jae-Ho;Rhee, Gyu-Seek;Lee, Sang-Jae;Chang, Moon-Ik
    • Korean Journal of Food Science and Technology
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    • v.46 no.1
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    • pp.7-12
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    • 2014
  • A sensitive and simple analytical method to identify flutianil residues in agricultural commodities was developed and validated using gas chromatography-electron capture detection (GC-ECD) and mass spectrometry (GC-MS). The flutianil residues were extracted with acetonitrile, partitioned with dichloromethane, and then purified using a silica solid-phase extraction (SPE) cartridge. The method was validated using pepper, sweet pepper, mandarin, hulled rice, soybean, and potato spiked with 0.02 or 0.2 mg/kg flutianil. The average recovery of flutianil was 76.5-108.0% with a relative standard deviation of less than 10%. The limit of detection and limit of quantification were 0.004 and 0.02 mg/kg, respectively. The result of recoveries and relative standard deviation were in line with Codex Alimentarius Commission Guidelines (CAC/GL 40). These results show that the method developed in this study is appropriate for flutianil identification and can be used to maintain the safety of agricultural products containing flutianil residues.