• 제목/요약/키워드: extraction constant

검색결과 252건 처리시간 0.034초

질산유로퓸을 TBP 로 추출할때 TBP와 유로퓸착물의 활동도계수간의 관계 (The Activity Coefficients of Tri-n-butylphosphate and Europium Complex in the Extraction of Europium by Tri-n-butylphosphate in Nitric Acid Solution)

  • 강익균
    • 대한화학회지
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    • 제18권4호
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    • pp.272-277
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    • 1974
  • 분배계수와 용매의 용해도 파라미터 도표상의 추출포물선을 검토하여 질산산성에서 유로퓸을 TBP로 추출할 때 유로퓸착물과 TBP의 활동도 계수간의 관계를 알 수 있었고 이에 따라 TBP의 용해도 파라미터를 결정하는 가능성을 제시하였다. 용매로서는 cyclohexane, 벤젠, 톨루엔, chlorobenzene을 사용하였고 TBP의 농도를 용적백분율로 5에서 50까지 변화시켰다.

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웨이브렛 변환과 편광 필터를 이용한 차량번호판 축출 (Vehicle Plate Extraction Using Wavelet Transform and Polarized Light Filter)

  • 김옥규;이창윤;황형덕;강혜진;박영식
    • 융합신호처리학회 학술대회논문집
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    • 한국신호처리시스템학회 2003년도 하계학술대회 논문집
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    • pp.102-105
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    • 2003
  • Up to the present studies of the car number recognition system, it is generally known to have serious problems such as relatively long processing time due to the excessive length of data extracted from the number plate based on the current image characteristics, and the image blurring with the physical damage of the brightness and darkness signals of the number plate caused by external impulses with many difficulties in the extraction of the highlighted numbers. In this Paper we used the characteristics firstly having a constant brightness of number plate, and a high density to the horizontal axis, and the influences of highlighted signal could be reduced by making reflections less through the polarized filter on the camera for any highlighted signal. For the more, the data processing time and the noise reduction are effectively implemented by using the wavelet transform of time-space scale with the considerations on the physical loss and processing time.

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Tris(1,10-phenathroline) Fe(II) chelate에 의한 undecylenic acid의 흡광광도 정량법 (The spectrophotometric determination of undecylenic acid using tris (1,10-phenanthroline) Fe(II) chelate)

  • 강삼식;백남호
    • 약학회지
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    • 제16권4호
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    • pp.180-185
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    • 1972
  • A new spectrophotometric method was established for the determination of undecylenic acid. The method is based on the solvent extraction into nitrobenzene of the ion pair formed between tris(1,10-phenanthroline)Fe(II) chelate and the anion of undecylenic acid. The maximum absorbance of the extract in the organic phase was at 518nm. A maximum extraction was obtained at pH 9-11, when excess of at least 50-fold(molar) of the phenanthroline-Fe(II) chelate to undecylenic acid was present. The color intensity of the extracted species remained constant at room temperature for the several hours after separation of the organic layer. A linear relationship was obtained over the tested range of 5-20${\gamma}$/ml of undecylenic acid. The effect of several other fungicids on this method was investigated. The method was applied to the determination of undecylenic acid in preparations and the results were in good agreement with those added amounts.

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Removal of diesel hydrocarbons by microwave-enhanced soil vapor extraction (Focused on Loss and Kinetic constant for Diesel Hydrocarbons)

  • 김종운;박갑성
    • 한국지하수토양환경학회:학술대회논문집
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    • 한국지하수토양환경학회 2004년도 총회 및 춘계학술발표회
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    • pp.223-226
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    • 2004
  • In this paper, removal of diesel hydrocarbons (C$_{10}$-C$_{22}$) for dry and moist soil was investigated so that microwave-enhanced soil vapor extraction(SVE) reduced soil treatment time and raised remediation efficiency. Kinetic constants of diesel hydrocarbons with microwave energy were 7 times on dry soil and 1580 times on moist soil as much as those of SVE process without microwave energy. The diesel removals were 67.7~78.4% for $C_{10}$ and $C_{12}$, and 0~18.5% for $C_{14}$~C$_{22}$ for dry and moist soil with SVE process only. On the other hand, dry soil with microwave-enhanced SVE process showed 89.3~99.4% removal for $C_{10}$ and $C_{12}$ and 35.6~67.0% for hydrocarbons over $C_{14}$. All hydrocarbons(C$_{10}$~C$_{22}$) studied were significantly removed (93.6~99.8%) for moist soil with microwave-enhanced SVE process. Almost all diesel hydrocarbons were usually considered as semi-volatile compounds(SVOCs). Microwave-enhanced SVE process might have a great potential for remediation of soils contaminated with SVOCs.OCs.

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Liquid-liquid extraction process for gas separation from water in polymeric membrane: Mathematical modeling and simulation

  • Salimi, Nahid;Moradi, Sadegh;Fakhar, Afsaneh;Razavi, Seyed Mohammad Reza
    • Membrane and Water Treatment
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    • 제7권5호
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    • pp.463-476
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    • 2016
  • In this study, application of polypropylene hollow fiber membrane contactors for $CO_2$ removal from water in liquid-liquid extraction (LLE) mode was simulated. For this purpose, a steady state 2D mathematical model was developed. In this model axial and radial diffusion was considered to $CO_2$ permeation through the hollow fibers. $CO_2$ laden water is fed at a constant flow rate into the lumen side, permeated through the pores of membrane and at the end of this process, $CO_2$ solution in the lumen side was extracted by means of aqueous diethanolamine (DEA) and chemical reaction. The simulation results were validated with the experimental data and it was found a good agreement between them, which confirmed the reliability of the proposed model. Both simulation and experimental results confirmed the reduction in the percentage of $CO_2$ removal by increment of feed flow rate.

눈 영역에 적합한 에지 추출과 밝기값 정보를 이용한 눈 검출 (Detection of eye using optimal edge technique and intensity information)

  • 문원호;최연석;김철기;차의영
    • 한국정보통신학회:학술대회논문집
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    • 한국해양정보통신학회 2010년도 추계학술대회
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    • pp.196-199
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    • 2010
  • 사람의 눈동자는 얼굴 크기와 비교해 볼 때 상대적으로 일정한 거리를 가지고 있기 때문에 이미지 정규화에 있어서 중요한 지표로 사용된다. 이 논문은 이러한 특징을 이용해 최적화된 세그멘테이션 방법을 사용하여 눈동자 검출의 새로운 접근방법을 소개한다. 눈 검출 방법은 세 가지 중요한 단계로 나눌 수 있다. (1)흑백 영상에서 눈 영역에 적합한 에지 추출 방법, (2)레이블링(labeling) 기법을 이용한 눈 영역 추출, (3)밝기값 정보를 이용한 눈동자 위치 검출. 실험 결과로는 다양한 조명 환경과 얼굴표정을 가진 2408장의 FERET 영상을 이용하여 98.9%의 검출 성능을 보였다.

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The Characteristics of Soil Organic Matter

  • You Sun-Jae;Kim Jong-gu;Cho Eun-Il
    • 한국환경과학회지
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    • 제15권1호
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    • pp.1-7
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    • 2006
  • The purpose of this study is to illustrate the characteristics of soil organic matter (SOM) and partition coefficient $(K_{DOC})$. Humic substances (HS) from eight soils of varying properties were extracted by two different methods. The dissolved organic carbon (DOC) concentration was stabilized in 22hrs. The ratio of UV absorbance at 465nm and 665nm (E4/E6 ratio) for HS were similar pattern for 8 soils. The extraction with increasing pH increased dissolution of SON. The ratio of organic carbon (OC) associated with HA and FA (the HA:FA ratio) was varied widely in accordance with the soils and was highly correlated to OC $content(\%)$ of the soils. in modeling metal speciation in soils and soil solutions, assumptions that all DOC in soil solution is associated with FA and that HA:FA ratio in SOM is constant have been made. The results of this study indicate that the validity of these assumptions is questionable. By sequential pH extraction, the $K_{DOC}$ showed in a linear correlation with pH.

Extraction of Water-Soluble Porphyrin and Metalloporphyrins into Acetonitrile by Salting-out

  • Tabata, Masaaki;Kumamoto, Midori
    • 분석과학
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    • 제8권4호
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    • pp.511-517
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    • 1995
  • A cationic water soluble porphyrin (5,10,15,20-tetrakis (l-methyl-pyridinium-4-yl)porphyrin, $H_2tmpyp^{4+}$) and its metalloporphyrins (MP) were easily extracted into acetonitrile separated by addition of sodium chloride ($4mol\;dm^{-3}$) in the presence of sodium perchlorate, where M denotes $Zn^{2+}$, $Cu^{2+}$, $Co^{3+}$, $Fe^{3+}$, and $Mn^{3+}$ and $P^{2-}$ is porphyrinate ion. The extracted ion-pair complexes were completely dissociated to $[MP(ClO_4)_3]^+$, and $[MP(ClO_4)_2]^{2+}$. The extraction and the dissociation constants were determined by taking into account of the partition constant of sodium perchlorate ($K_D=1.82{\pm}0.01$). The chemical properties of the separated acetonitrile phase as $E_{T(30)}$ and $D_{II,I}$ were determined and compared with other water miscible solvents (acetone, actonitrile, 1,4-dioxane, tetrahydrofuran, 1-propanol and 2-propanol). Furthermore, a sensitive and selective method was proposed for the determination of a subnanogram amount of copper(II) in natural water samples by using the present salting-out method and the porphyrins.

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Headspace Hanging Drop Liquid Phase Microextraction and Gas Chromatography-Mass Spectrometry for the Analysis of Flavors from Clove Buds

  • Jung, Mi-Jin;Shin, Yeon-Jae;Oh, Se-Yeon;Kim, Nam-Sun;Kim, Kun;Lee, Dong-Sun
    • Bulletin of the Korean Chemical Society
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    • 제27권2호
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    • pp.231-236
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    • 2006
  • A novel sample pretreatment technique, headspace hanging drop liquid phase microextraction (HS-LPME) was studied and applied to the determination of flavors from solid clove buds by gas chromatography-mass spectrometry (GC-MS). Several parameters affecting on HS-LPME such as organic solvent drop volume, extraction time, extraction temperature and phase ratio were investigated. 1-Octanol was selected as the extracting solvent, drop size was fixed to 0.6 $\mu$L. 60 min extraction time at 25 ${^{\circ}C}$ was chosen. HS-LPME has the good efficiency demonstrated by the higher partition equilibrium constant ($K_{lh}$) values and concentration factor (CF) values. The limits of detection (LOD) were 1.5-3.2 ng. The amounts of eugenol, $\beta$-caryophyllene and eugenol acetate from the clove bud sample were 1.90 mg/g, 1.47 mg/g and 7.0 mg/g, respectively. This hanging drop based method is a simple, fast and easy sample enrichment technique using minimal solvent. HSLPME is an alternative sample preparation method for the analysis of volatile aroma compounds by GC-MS.

양이온 계면활성제로 형성된 역미셀을 이용한 초유 Immunoglobulin G의 분리 (Separation of Immunoglobulin G from Colostrum by Reverse Micelles of Cationic Surfactant)

  • 노경현;임지영
    • 한국축산식품학회지
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    • 제24권1호
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    • pp.80-85
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    • 2004
  • 본 연구에서는 역미셀을 이용한 단백질 추출공정에서 적극적으로 활용되지 못했던 양이온 계면활성제에 의한 단백질 추출 가능성을 제시하였으며 초유로부터 IgG의 분리를 위한 반응조건을 조사하였다. IgG의 분리에 적합한 조건은 반응 수용액상의 경우 pH 8, 50 mM KCl었으며 유기용매상의 계면활성제(CDAB) 농도는 100 mM로 나타났다. 위의 조건에서는 초기시료에 존재하는 IgG의 90%이상이 회수되었으며 회수된 단백질의 93%가 IgG로 나타났다. 또한 본 연구는 기존의 역미셀을 이용한 일반적인 단백질 추출공정인 정추출 및 역추출 공정을 이용하지 않고 정추출 공정만을 이용함으로써 추출과정을 단순화하였다.