• 산업경영시스템학회지
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• 제23권55호
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• pp.85-96
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• 2000

This paper describes IDMS, a graph-based modeling system that supports problem structuring. We employs influence diagram as a problem representation tool, that is, a modeling tool. In particular, IDMS is designed as domain-independent shell. Therefore, a modeler can change the contents of the knowledge base to suit his/her own interested domain. Since the knowledge base of IDMS contains both modeling knowledge and domain knowledge, IDMS provides not only the syntactic support for modeling tool, but also the semantic support for problem domain. To apply the method in the real world context, we tested IDMS on the process selection problem in business reengineering, which is typical semi-structured problem.

• 대한전자공학회논문지TC
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• 제43권7호
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• pp.104-114
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• 2006

인터넷 서비스를 이용하기 위해서 사용자는 일반적으로 가입절차를 수행하고 서비스를 위한 id(identifier)를 등록하게 된다. 그러나 인터넷의 활용이 증가함에 따라, 사용자는 많은 id를 가지게 되었으며 이것은 사용자가 인터넷 서비스를 이용할 때마다, 매번 인증을 받아야 한다는 문제를 발생시키고 있다 또한 여러 사이트에 산재되어 관리되지 않은 id들은 사용자 개인정보의 침해 가능성을 높이고 있다. 본 논문에서는 이와 같은 문제를 해결하기 위해 ETRI에서 개발한 ID(IDentity) 연계 기반의 인터넷 ID 관리 시스템인 e-IDMS에 대하여 기술한다. e-IDMS는 ID 연계를 기반으로 복합 인증, 인터넷 SSG, ID 정보 관리, ID 정보 공유, 개인정보 보호 및 대화형 질의 기능을 제공한다. e-IDMS는 공공기관 통합 ID 관리 시스템 구축에 활용되고 있다.

• 전기학회논문지
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• 제58권9호
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• pp.1651-1657
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• 2009

In this paper, restoration solution algorithm to improve reliability better than restoration system of DAS(Distribution Automation System) is proposed in IDMS(Intelligent Distribution Management System). A strategy of IDMS restoration system to improve reliability and efficiency is proposed by analysis restoration system in DAS. Restoration sequence algorithm, distributed restoration solution algorithm considering a characteristic and a suitable restoration solution algorithm in IDMS are proposed. In the case study, algorithms have testified with example distribution network by C language

• Journal of information and communication convergence engineering
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• 제20권3호
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• pp.181-188
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• 2022

An intelligent distributed multi-agent system (IDMS) using reinforcement learning (RL) is a challenging and intricate problem in which single or multiple agent(s) aim to achieve their specific goals (sub-goal and final goal), where they move their states in a complex and cluttered environment. The environment provided by the IDMS provides a cumulative optimal reward for each action based on the policy of the learning process. Most actions involve interacting with a given IDMS environment; therefore, it can provide the following elements: a starting agent state, multiple obstacles, agent goals, and a cluttered index. The reward in the environment is also reflected by RL-based agents, in which agents can move randomly or intelligently to reach their respective goals, to improve the agent learning performance. We extend different cases of intelligent multi-agent systems from our previous works: (a) a proposed environment-clutter-based-index for agent sub-goal selection and analysis of its effect, and (b) a newly proposed RL reward scheme based on the environmental clutter-index to identify and analyze the prerequisites and conditions for improving the overall system.

• 분석과학
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• 제16권3호
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• pp.191-197
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• 2003

플루토늄 표준물 (NBL, CRM No.122)을 이용하여 정확한 농도의 플루토늄 용액을 만들고 이 용액에 대하여 동위원소희석 질량분석법과 조절전위 전기량법으로 플루토늄을 정량하였다. 동위원소희석 질량분석법에 의한 결과는 약 $0.9{\mu}g$-Pu 시료량의 크기에서 모액 플루토늄의 농도에 대하여 얻어진 측정값의 비는 $1.002176{\pm}0.000452$이었으며, 상대 표준편차 0.045%(신뢰도 95%)의 좋은 정밀도를 보였다. 조절전위 전기량법에 의한 측정값은 사용한 시료량에 따라 0.9923~0.9960의 비를 보였다. 두 방법 간의 차이는 0.6~1% 범위 내에서 잘 일치하는 결과를 보였다. 따라서 조절전위 전기량법보다 좋은 결과를 보인 동위원소희석 질량분석법을 이용하여, 조사된 하나로 연소 핵연료봉을 상, 중 및 하단부분으로 구분하여 시료를 취하여 이를 용해하고 음이온교환 칼람을 사용 분리한 플루토늄을 각각 정량 하였다. 이 결과 각각 그람(fuel+clad) 시료당 1.155 mg, 2.483 mg 및 1.920 mg의 플루토늄 값을 얻었다.

• Bulletin of the Korean Chemical Society
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• 제20권8호
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• pp.910-916
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• 1999

A current interest in chemistry concerns traceability of analytical measurements to the International System of Units (SI) and the proper estimation of their uncertainties in accordance with the internationally agreed guide provided by the International Organization for Standardization (ISO). Isotope dilution mass spectrometry (IDMS) is regarded as a primary method, which make the measurement results traceable to SI units without significant empirical correction factors. Our laboratory, as the national standards institute of Korea, participated in an intercomparison of environmental analysis, pp'-DDE in corn oil, which was organized by the CCQM under supervision of the CIPM to test feasibility of IDMS as a primary method for the trace analysis of organic compounds. In this report, we provide basic equations used for the calculation of the concentration of the analyte in a sample and a precise description of the processes for the evaluation of the uncertainties of the measurement results. Also, we report the experimental conditions adopted to improve the accuracy of the IDMS measurement. The principles contained in ？？Guide to the Expression of Uncertainty in Measurement'' provided by ISO are followed for the uncertainty evaluation.

• 분석과학
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• 제16권6호
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• pp.450-457
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• 2003

사용후핵연료 내 U 및 동위원소 정량분석을 동위원소 희석 질량분석법 (isotope dilution mass spectrometry, IDMS)으로 수행하였다. 시료는 산화우라늄 사용후핵연료 시료를 $HNO_3$(1+1) 또는 이 용액과 14 M $HNO_3-0.05M$ HF 혼합용액으로 용해한 후 막 거르게 ($1.2{\mu}m$)로 여과하여 준비하였다. 시료 및 스파이크를 첨가한 시료 중의 U은 AG lX8 음이온교환 수지관에서 0.1 M HCl 용액으로 용리하였다. 시료 중의 총 U 량과 성분 동위원소 ($^{234}U$, $^{235}U$, $^{236}U$ 및 $^{238}U$)의 조성은 $^{233}U$을 스파이크로 이용하는 동위원소 희석 질량분석법으로 정량하였다. 제조한 U-233 스파이크 용액은 천연 및 감손 U을 이용한 역동위원소 희석 질량분석법 (reverse isotope dilution mass spectrometry, R-IDMS)으로 표정하였다. 동위원소 희석 질량분석법에 의한 핵연료시료 중의 총 U 량 측정결과를 전위차 적정으로 측정한 결과와 비교하였을 때 0.34% 평균 상대오차 범위에서 일치하였다.

• Mass Spectrometry Letters
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• 제4권4호
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• pp.75-78
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• 2013

A gas chromatography/mass spectrometric (GC/MS) method was developed as a candidate reference method for the accurate determination of essential fatty acids (linoleic acid, ${\alpha}$- and ${\gamma}$-linolenic acids) in food supplemental oil products. Samples were spiked with three internal standards (stearic acid-$d_{35}$, $^{13}C_{18}$-linoleic acid, and $^{13}C_{18}$-${\alpha}$-linolenic acid). Samples were then subject to saponification, derivatization for methylation, and extraction by organic solvent. For GC/MS measurement, an Agilent HP-88 column, designed for the separation of fatty acid methyl esters, was selected after comparing with other columns as it provided better separation for target analytes. Target analytes and internal standards were detected by selected ion monitoring of molecular ions of their methyl ester forms. The GC/MS method was applied for the measurement of three botanical oils in NIST SRM 3274 (borage oil, evening primrose oil, and flax oil), and measurement results agreed with the certified values. Measurement results for target analytes which have corresponding isotope-labeled analogues as internal standard were calculated based on isotope dilution mass spectrometry (IDMS) approach, and compared with results calculated by using the other two internal standards. Results from the IDMS approach and the typical internal standard approach were in good agreement within their measurement uncertainties. It proves that the developed GC/MS method can provide similar metrological quality with IDMS methods for the measurement of fatty acids in natural oil samples if a proper fatty acid is used as an internal standard.

• Bulletin of the Korean Chemical Society
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• 제31권11호
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• pp.3139-3144
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• 2010

A model system has been established for the evaluation of the uncertainty of the value from measurements of multiple subsamples by isotope dilution mass spectrometry (IDMS). In this report, we apply this model system for the evaluation of measurement uncertainty in determination of folic acid in infant formula. Five subsamples were analyzed by IDMS. The mean of the measurement results of the five subsamples was assigned as the final measurement value. The standard deviation (s) of the results from five subsamples was attributable to repeatability of the measurement. The uncertainty components in the IDMS measurement methods were categorized into two groups. Group I includes uncertainty components which give common systematic effects to all subsamples and do not contribute to the variation among multiple measurements (repeatability). Group II includes uncertainty components that give random effects on the measurement results, and are related with the measurement repeatability. These random effects are attributed to s. Therefore, the uncertainty of the final value was calculated by combining the standard deviation of the mean of multiple measurements, $s/{\surd}n$ (where n = 5), and the measurement uncertainty associated with the uncertainty components that give systematic effects.

• Bulletin of the Korean Chemical Society
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• 제25권10호
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• pp.1508-1512
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• 2004

A gas chromatography/mass spectrometric (GC/MS) method has been developed for the determination of trace mono-n-butyltin (MBT), di-n-butyltin (DBT), and tri-n-butyltin (TBT) compounds in sediments. Samples were extracted by 10% acetic acid in methanol containing 0.03% tropolone and were then derivatized for GC/MS analysis. Ethylation by sodium tetraethylborate and phenylation by sodium tetraphenylborate were evaluated as a derivatization reaction of the organotins in sample extract. n-Hexane was added into reaction media in the beginning of the reaction for the continuous extraction of derivatized organotins. Ethylation requires less than 2 hours to get proper derivatization yields for MBT, DBT, and TBT altogether and produces relatively low amounts of side reaction products. Compared to ethylation, phenylation requires much longer time but provides relatively lower yield and produces considerable amounts of side reaction products. Therefore, the ethylation reaction was applied for the analysis of organotin compounds in sediment. An isotope dilution mass spectrometric (IDMS) method based on GC/MS has been applied to the accurate determination of DBT compounds in the sediments. The IDMS results from the analyses of sediment samples showed a reasonable repeatability and a good agreement with the values obtained by IDMS based on liquid chromatography/induced coupled plasma/mass spectrometry.