• 제목/요약/키워드: Karl Fischer Method

검색결과 9건 처리시간 0.019초

Karl Fischer를 통한 전력케이블용 반도전 Composite 특성 연구 (A Study on the Property of Semiconductive Shield Composite through Karl Fischer Method in Power Cable)

  • 양훈;박대희
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 2008년도 Techno-Fair 및 합동춘계학술대회 논문집 전기물성,응용부문
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    • pp.187-188
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    • 2008
  • In this paper, we have investigated water content of semiconductive shield materials for power cables, EEA(Ethylene Ethyl Acrylate) is used polymer matrix. And filler is used CNT(Carbon Nanotube) and CB(Carbon Black). EEA, CNT and CB is favor moisture. In case of EEA, it has polyolefin resin that strong polarity combination. To research water content, experimental method used KF(Karl Fischer). KF method is Electrochemical titration based on chemical reaction. As a result, specification by KEPCO(Korea Electric Power Corporation) is lower than 800ppm. CNT and CB ratio of 80 versus 20 is best specimen that had lowest moisture content. It seem likely to increase crosslinking rate, CNT between CB.

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진공건조오븐과 Karl-Fischer법을 이용한 담배의 최적 수분측정법 연구 (A Study on the Optimal Vacuum Drying Conditions of Tobacco for Moisture Measuring)

  • 박배식;김봉주;박흥진
    • 한국연초학회지
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    • 제19권2호
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    • pp.159-161
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    • 1997
  • A study on the optimal drying condition by a vacuum drying oven was done using shredded tobacco lamina and commercial cigarettes ('This'). Changes in the mass of the experimental material were monitored for about 50 hrs at 6 different temperatures (5$0^{\circ}C$~10$0^{\circ}C$, 1$0^{\circ}C$ stepwise) while continuously operating a vacuum pump. After 30 hrs, small amount of samples from each material were taken sequentially to monitor changes in moisture content using a Karl-Fischer method (Metrohm KF 701 Titrino). Absolute moisture contents calculated from the measurements indicated an ideal data distribution could be obtained by drying at temperatures between 7$0^{\circ}C$~8$0^{\circ}C$. Results from cigarette products which contains humectant and tobacco lamina without it were compared.

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Karl-Fischer법과 회복전압법을 이용한 수분량 검출 비교 특성 (Measurement of Moisture Contents using Recovery Voltage Method and Karl-Fischer Method)

  • 김형민;김재훈;김주한;한상옥;이세현
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 2005년도 제36회 하계학술대회 논문집 전기설비
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    • pp.76-78
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    • 2005
  • Moisture contents measurement is frequently used as one of parameters for degradation diagnosis of transformer insulation. In general Karl-Fisher method is mainly used for moisture contents till now. But this method is inconvenient because of dismounting transformer for sampling oil or paper, and also partial sampling. At latest Recovery Voltage Method(RVM) is noticed for complement of this method. RVM can directly estimate moisture contents of transformer insulations in field without dismounting transformer. In this paper the accelerated aging process of oil-paper samples have been investigated at a temperature up to 140$^{\circ}C$ for 500 hours. The oil-paper insulation samples have been measured at intervals of 100 hours. Next to, we have estimated moisture contents using both Karl-Fisher Titration Method and RVM. And we have compared with Karl-Fisher Titration Method and RVM for estimating moisture contents. At last we have verified reliability of RVM which is new measurement method.

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수분함유량에 따른 RVM 특성곡선의 특성 (The Characteristics of RVM Curve at Moisture Content)

  • 한희준;김주한;강석영;이세현;한상옥
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 2006년도 제37회 하계학술대회 논문집 전기설비
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    • pp.45-46
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    • 2006
  • 변압기 내부의 수분은 절연물의 절연내력에 악영향을 끼치므로 수분측정은 변압기 사고예방과 수명연장에 매우 중요하다. 변압기 내의 수분함유량을 검출하는 시험법으로 Karl-Fischer법과 Dew-Point법을 사용해 왔다. 그러나 이 시험법은 기기를 분해해야 하고, 국부적인 부분에 대한 정보일 뿐 아니라 분석을 즉시 현장에서 하지 못하는 단점이 있다. 따라서 기존 시험법의 단점을 보완하기 위해 회복전압법(RVM, Return Voltage Method)이 제안되었다. 본 논문에서는 모의 셀 내부에 수분을 강제로 주입하여 수분함유량 변화를 주고 Karl-Fischer법을 통한 수분함유량 측정 결과와 RVM 특성 곡선을 비교 분석하였다.

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Comparison of Oven-drying Methods for Determination of Moisture Content in Feed Ingredients

  • Ahn, J.Y.;Kil, D.Y.;Kong, C.;Kim, B.G.
    • Asian-Australasian Journal of Animal Sciences
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    • 제27권11호
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    • pp.1615-1622
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    • 2014
  • An accurate assessment of moisture content in feed ingredients is important because moisture influences the nutritional evaluation of feedstuffs. The objective of this study was to evaluate various methods for moisture content determination. In Exp. 1, the weight loss on drying (LOD) of corn, soybean meal (SBM), distillers dried grains with solubles (DDGS), whey permeate, whey powder, spray-dried porcine plasma (SDPP), fish meal, and a mixed diet of these 7 ingredients were measured by oven drying at $135^{\circ}C$ for 2 h. Additionally, the samples were dried at $105^{\circ}C$ for 3, 6, 9, 12, or 15 h. The LOD contents of the DDGS, whey permeate, and whey powder measured by drying at $135^{\circ}C$ for 2 h were greater than the values measured by drying at $105^{\circ}C$ for 3 h (p<0.05). All samples except SDPP (p = 0.70) dried at $105^{\circ}C$ for 6, 9, 12, or 15 h caused more LOD compared with the samples dried for at $105^{\circ}C$ for 3 h (p<0.05). The LOD contents of the individual ingredients were additive when dried at $105^{\circ}C$ regardless of drying time. In Exp. 2, moisture contents of corn, SBM, wheat, whey permeate, whey powder, lactose, and 2 sources of DDGS (DDGS1 and DDGS2) were measured by the Karl Fischer method, oven drying at $135^{\circ}C$ for 2 h, and oven drying at $125^{\circ}C$, $115^{\circ}C$, $105^{\circ}C$, or $95^{\circ}C$ for increasing drying time from 1 to 24 h. Drying samples at $135^{\circ}C$ for 2 h resulted in higher moisture content in whey permeate (7.5% vs 3.0%), whey powder (7.7% vs 3.8%), DDGS1 (11.4% vs 7.5%), and DDGS2 (13.1% vs 8.8%) compared with the Karl Fischer method (p<0.05). Whey permeate and whey powder were considerably darkened as the drying time increased. In conclusion, drying samples at $135^{\circ}C$ for 2 h is not appropriate for determining the moisture content in whey permeate, whey powder, or DDGS as well as the mixed diet containing these ingredients. The oven-drying method at $105^{\circ}C$ for 5 to 6 h appears to be appropriate for whey permeate and whey powder, and at $105^{\circ}C$ for 2 to 3 h for DDGS.

경년 열화에 따른 변압기 절연물의 회복전압 특성 (The Characteristics of RVM by Accelerated Aging in Insulating Materials of the Transformer)

  • 강석영;한상옥;김재훈;김주한;이세현
    • 대한전기학회:학술대회논문집
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    • 대한전기학회 2005년도 제36회 하계학술대회 논문집 전기설비
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    • pp.73-75
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    • 2005
  • In present measurement of moisture contents is used as one of method for estimating degradation of transformer. Most of people use Karl-Fischer titration method for detection moisture contents but this measurement is inconvenient method because we must analyze transformer oil-paper after dismounting transformer and sampling in field. Therefore we don't directly investigate them in field. In this paper we will introduce Recovery Voltage Method(RVM) that is new method for estimating measurement in field though dismounting facility. For measure of moisture contents using RVM in accordance with accelerated thermal aging we have made experimental test cell and aged at a temperature up to 140$^{\circ}C$ for 300 hours. And we have been measured at intervals of 100 hours using RVM 5462 made in fetter company.

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Mass Balance Method for Purity Assessment of Organic Reference Materials: for Thermolabile Materials with LC-UV Method

  • Lee, Joonhee;Kim, Byungjoo
    • Bulletin of the Korean Chemical Society
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    • 제35권11호
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    • pp.3275-3279
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    • 2014
  • A mass balance method for purity assessment of thermolabile organic reference materials was established by combining several techniques, including liquid chromatography with UV/VIS detector (LC-UV), Karl-Fischer (K-F) Coulometry, and thermal gravimetric analysis (TGA). This method was applied to three fluoroquinolones like enrofloxacin, norfloxacin and ciprofloxacin. LC-UV was used to analyze structurally related organic impurities based on UV/VIS absorbance spectra obtained in combination with LC separation. For all three organic reference materials, the UV/VIS spectra of the separated impurities were similar to that of the major component of the corresponding materials. This indicates that the impurities are structurally related to the respective reference material sharing common chromophores. Impurities could be quantified by comparing their absorbances at the wavelength of maximum absorbance (${\lambda}_{max}$). The water contents of the reference materials were measured by K-F Coulometry by an oven-drying method. The total inorganic impurities contents were assayed from ash residues in TGA analysis with using air as a reagent gas. The final purities estimated from results of those analytical techniques were assigned as ($99.91{\pm}0.06$), ($97.09{\pm}0.17$) and ($91.85{\pm}0.17$)% (kg/kg) for enrofloxacin, norfloxacin and ciprofloxacin, respectively. The assigned final purities would be applied to the reference materials which will be used as calibrators for the certification of those compounds in matrix CRMs as starting points for the traceability of their certified values to SI units.

Purity Assessment of Organic Reference Materials with a Mass Balance Method: A Case Study of Endosulfan-II

  • Kim, Seung-Hyun;Lee, Joonhee;Ahn, Seonghee;Song, Young-Sin;Kim, Dong-Kyum;Kim, Byungjoo
    • Bulletin of the Korean Chemical Society
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    • 제34권2호
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    • pp.531-538
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    • 2013
  • A mass balance method established in this laboratory was applied to determine the purity of an endosulfan-II pure substance. Gas chromatography-flame ionization detector (GC-FID) was used to measure organic impurities. Total of 10 structurally related organic impurities were detected by GC-FID in the material. Water content was determined to be 0.187% by Karl-Fischer (K-F) coulometry with an oven-drying method. Non-volatile residual impurities was not detected by Thermal gravimetric analysis (TGA) within the detection limit of 0.04% (0.7 ${\mu}g$ in absolute amount). Residual solvents within the substance were determined to be 0.007% in the Endosulfan-II pure substance by running GC-FID after dissolving it with two solvents. The purity of the endosulfan-II was finally assigned to be ($99.17{\pm}0.14$)%. Details of the mass balance method including interpretation and evaluating uncertainties of results from each individual methods and the finally assayed purity were also described.

새로운 Thorium (IV)-Crown Ether 착물형성 (Formation of New Thorium (IV) Complexes with Crown Ethers)

  • 정학진;정오진;서혁춘
    • 대한화학회지
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    • 제31권3호
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    • pp.258-270
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    • 1987
  • 여러 용매(methanol, ethanol, butanol, ethylether, methylacetate, acetone, THF 및 acetylacetone)중에서 아직 보고된 바 없는 공동을 달리한 crown ether들을 리간드로 한 토륨(IV) 고체 착물을 합성하였다. 이 고체 착물에 대한 배위 화학적인 정보를 얻기 위하여 원소분석(C.H.N) 및 ICPAS법에 의한 토륨분상, 열분석과 Karl-Fischer적정법에 의한 착물중의 결정수 분석에 의해서 고체 착물들의 조성을 결정하였다. 그리고 적외선, 자외선 분광분석, $^1H$-핵자기 공명 분석 및 X-선 회절분석법에 의하여 각 합성 착물들의 결합구조에 대한 정보들을 얻었고 각 합성 착물들에 대한 용매화 현상을 논의하였다. 그 결과 아세틸아세톤 용매하에서 합성된 착물들은 아세틸아세톤을 제외한 모든 실험 용매중에서 합성된 crown ether를 가지는 토륨(IV) 착물들은 용매화 반응이 일어나지 않았다. $Th^{4+}$금속이온에 대한 리간드 결합비는 고리의 크기에 주로 영향을 받으며 12-crown-4의 경우는 1:1([$Th^{4+}$]:[lig.]) 착물, 15-crown-5의 경우는 2:3 착물 및 18-crown-6와 dicyclohexano-18-crown-6의 경우는 1:1 착물이었다. 용매화가 일어나는 15-crown-5 와 18-crown-6 착물의 경우는 1:1:1([$Th^{4+}$]:[lig.]:$[CH_3COCH_2COCH_3]$)이었다. 용매화하지 않는 모든 착물들은 crown-ether의 n-${\sigma}^{\ast}$전자전이를, 그리고 용매화된 착물은 crown-ether n-${\sigma}^{\ast}$와 acac의 $n-{\pi}^{\ast}$전자전이를 동시에 나타냈다. 반양성자성 용매에서 모든 착물들은 1:1전해질로, 물에서는 1:4전해질로 각각 행동하는 9배위자 착물임을 알 수 있다.

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