• 제목/요약/키워드: Selective solution method

검색결과 206건 처리시간 0.035초

Spectrofluorimeteric Determination of Oxalate Based on Its Ternary Complex Between Eu3+ and Thenoyltrifluoroacetone

  • Cha, Ki-Won;Huang, Hua-Zi;Choi, Hyun Cheol
    • Bulletin of the Korean Chemical Society
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    • 제23권10호
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    • pp.1456-1458
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    • 2002
  • A simple, sensitive and selective determination method of oxalate has been investigated based on the fluorescence enhancement of $Eu^{3+}$-TTA complex due to the formation of $Eu^{3+}$-TTA-oxalate ternary complex. An emission peak of $Eu^{3+}$-TTA, which is increased linearly with addition of oxalate, occurs at 610 nm in aqueous solution with excitation at 306 nm. The linear range of the calibration curve is 1 ${\times}$$10^{-6}$-8 ${\times}$$10^{-6}$ M and the detection limit is 1 ${\times}$$10^{-6}$ M. The effects of foreign ions were studied. The present method was applied to determine oxalate of two synthetic samples.

Nicotinaldehyde-4-phenyl-3-thiosemicarbazone을 이용한 Hg(II)의 추출 흡광광도 정량 (Extraction-Spectrophotometric Determination of Mercury(II) using Nicotinaldehyde-4-phenyl-3-thiosemicarbazone)

  • 이진식;카츠야 우에스기;최원형;김재수;김도훈
    • 분석과학
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    • 제7권4호
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    • pp.455-460
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    • 1994
  • 새로운 합성 시약 nocotinaldehyde-4-phenyl-3-thiosemicarbazone(NPS)을 이용하여 Hg(II)의 추출 흡광광도 정량법을 검토하여 미량 Hg(II)의 최적 정량조건을 확립하였다. Hg(II)-NPS 착물은 pH가 3.0~10까지 넓은 범위에서 선택성을 가진 안정된 착물을 형성하며, chloroform을 추출용매로 사용하여 365nm에서 측정한 몰흡광계수는 $2.45{\times}10^4L\;mol^{-1}\;cm^{-1}$이며, Hg(II)의 농도가 $0.2{\sim}18{\mu}g\;mL^{-1}$까지 Beer의 법칙을 만족하였다. 또한 본 분석법을 이용하여 두발(표준시료) 중의 수은을 분석하여 양호한 결과를 얻었다.

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직접해법 기반의 FETI 알고리즘의 개선 (Further Improvement of Direct Solution-based FETI Algorithm)

  • 강승훈;공두현;신상준
    • 한국전산구조공학회논문집
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    • 제35권5호
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    • pp.249-257
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    • 2022
  • 본 논문은 직접해법 기반 FETI 알고리즘의 개선 방안을 제시하였다. 개선 대상은 FETI-local로, 해당 알고리즘은 국부 Lagrange 승수를 통해 부영역 간 경계 문제를 정의한다. 부영역 경계 강성 및 하중 계산 단계의 경우, 전체 역행렬 계산 등 과도한 비용을 요구했던 기존 알고리즘을 Boolean 행렬 특성을 활용한 선택적 역행렬 성분 계산으로 개선하였다. 전역 경계 행렬식 계산 단계의 경우, 기존 단일 프로세서 연산을 다중 프론탈 기법 기반 병렬 연산으로 대체하였다. 제시된 FETI-local 알고리즘의 성능 개선은 64만 자유도 수치 예제를 통해 검증되었으며, 기존 대비 최대 97.8%의 계산 시간 감소가 달성되었다. 또한, 기존 대비 안정적이고 개선된 확장성이 가속 지표를 통해 확인되었다. 추가로, 432만 자유도의 대용량 계산 성능 비교가 제시된 알고리즘과 상용 프로그램인 ANSYS 간에 수행되었다. 그 결과, 계산 시간 측면에선 ANSYS가 우수하였으나, 프로세서 수에 따른 가속 성능 증가율 측면에선 제시된 알고리즘이 우수한 것이 확인되었다.

동심축류가 유도되는 미세유체 소자 기반 Collagen Type I 미세섬유의 제작 (Fabrication of Collagen Type I Microfiber based on Co-axial Flow-induced Microfluidic Chip)

  • 이수경;이광호
    • 대한의용생체공학회:의공학회지
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    • 제37권5호
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    • pp.186-194
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    • 2016
  • In this study, a co-axial flow induced microfluidic chip to fabricate pure collagen type I microfiber via the control of collagen type I and Na-alginate gelation process. The pure collagen type I microfiber was generated by selective degradation of Ca-alginate from 'Core-Shell' structured hydrogel microfiber. To make 'Core-Shell' structure, collagen type I solution was introduced into core channel and 1.5% Na-alginate solution was injected into side channel in microfluidic chip. To evaluatethe 'Core-Shell' structure, the red and green fluorescence substances were mixed into collagen type I and Na-alginate solution, respectively. The fluorescence substances were uniformly loaded into each fiber, and the different fluorescence images were dependent on their location. By immoblizing EpH4-Ras and C6 cells within collagen type I and Na-alginate solution, we sucessfully demonstrated the co-culture of EpH4-Ras and C6 cells with 'Core-Shell' like hydrogel microfiber for 5 days. Only to produce pure collagen type I hydrogel fiber, tri-sodium citrate solution was used to dissolve the shell-like Ca-alginate hydrogel fiber from 'Core-Shell' structured hydrogel microfiber, which is an excellent advantage when the fiber is employed in three-dimensional scaffold. This novel method could apply various application in tissue engineering and biomedical engineering.

Application of Organized Media for Rapid Spectrofluorimetric Determination of Trace Amounts of Cr(VI) in the Presence of Cr(III)

  • Madrakian, Tayyebeh;Afkhami, Abbas;Mohammadnejad, Masoumeh
    • Bulletin of the Korean Chemical Society
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    • 제30권6호
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    • pp.1252-1256
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    • 2009
  • A simple, selective and sensitive fluorescence quenching method was developed to the determination Cr(VI). The method is based on the oxidation of $I^-\;to\;{{I_3}^-}$ by Cr(VI) in sulfuric acid solution followed by immediate formation of ion association compound between I3 − and rhodamine 6G in Tween-80 micellar media at room temperature. The influence of several surfactants on rhodamine 6G fluorescence signal was studied; particular attention was paid in the aggregation behavior of rhodamine 6G–Tween-80 system. The experimental parameters (e.g., type of surfactant, reagent concentration) were studied and the optimal conditions were established. The linear calibration graph was obtained in the range 2.0 - 100.0 ng m$L^{-1}$ Cr(VI). The detection limit of the method was 0.37 ng m$L^{-1}$. The relative standard deviation (R.S.D.) is less than 5% (n = 5). The efficiency of the method for the determination of Cr(VI) in the presence of Cr(III) in the sample was investigated. The method was applied successfully to the determination of Cr(VI) and total Cr in water, and liver tissue samples.

디지털 포렌식 관점에서 SSD TRIM 명령의 선별적 복구 (Selective Recovery of the SSD TRIM Command in Digital Forensics)

  • 황현호;박동주
    • 정보처리학회논문지:컴퓨터 및 통신 시스템
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    • 제4권9호
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    • pp.307-314
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    • 2015
  • 최근 보조기억장치 스토리지 시장 추세는 HDD와 SSD가 혼용되어 사용되고 있다. 미래에는 HDD보다 SSD가 보조기억장치 역할로 더욱 많이 사용될 것으로 예상되고 있다. SSD 기술이 발달하면서 이를 효율적으로 사용하기 위해 TRIM 명령기법이 나오게 되었다. TRIM 명령기법은 과거 SSD의 문제점인 Freezing 현상을 해결하기 위해 나온 명령으로 운영체제와 SSD가 협동하여 작동한다. TRIM 명령기법은 사용자가 데이터를 삭제하였을 때 SSD 내부에서도 실제로 삭제하는 기법으로 유휴시간에 수행한다. 하지만, 디지털 포렌식 관점에서 본다면 디지털 범죄는 매년 급증하지만 데이터 미복구로 인한 검거율은 미흡하다. 본 논문에서는 기존 TRIM 명령의 장점인 안정성(Freezing Solution)과 쓰기 속도를 최대한 지원하며 선별적으로 데이터를 관리하여 삭제하는 기법을 제안한다. 실험을 통해 기존 기법과 선별된 기법의 성능을 측정하여 검증한다.

${\beta}-Ag_3SI$ 단결정막 전극에 관한 연구 (${\beta}-Ag_3SI$ Single Crystal Membrane Electrode)

  • 신두순;이선천
    • 대한화학회지
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    • 제28권2호
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    • pp.86-94
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    • 1984
  • ${\beta}-Ag_3SI$의 단결정을 만들어 막전극으로의 응용을 살펴보았다. 그 결과 할로겐 이온들에 대해 감응함을 알았고, 분리용액법과 혼합용액법으로 할로겐 이온들에 대한 선택계수를 얻어 이론값과 비교검토 하였으며, 전위시간 곡선으로 부터 이 전극이 유리 전극기구에 의해 전도함을 알았고, 넓은 pH 범위에서 전위가 일정한 값을 가짐을 알았다. 한편 분석화학에의 응용을 살펴 본 결과 할로겐이온의 혼합용액에서 좋은 지시전극으로 사용할 수 있음을 알았다

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상 분리 폴리머 혼합액의 전기 방사에 의한 나노 포러스 탄소 파이버 제작 (Fabrication of Nanoporous Carbon Fibers by Electrospinning)

  • 김홍연;이대희;문주호
    • 한국재료학회지
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    • 제19권10호
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    • pp.562-568
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    • 2009
  • Electrospinning is a technique that produces sub-micron sized continuous fibers by electric force from polymer solutions or melts. Due to its versatile manufacturability and the cost effectiveness, this method has been recently adopted for the fabrication of one-dimensional materials. Here, we fabricated polyacrylonitrile (PAN) polymer fibers, from which uniform carbon fibers with diameters of 100-200 nm were obtained after carbonization at 800 $^{\circ}C$ in N$_2$. Special emphasis was directed to the influence of the phase separated polymer solution on the morphology and the microstructure of the resulting carbon fiber. The addition of poly(stylene-co-acrylonitile) (SAN) makes the polymer solution phase separated, which allows for the formation of internal pores by its selective elimination after electrospinning. XPS and Raman Spectroscopy were used to confirm the surface composition and the degree of carbonization. At the PAN:SAN = 50:50 in vol%, the uniform carbon fibers with diameters of 300$\sim$500 nm and surface area of 131.6 m$^2$g$^{-1}$ were obtained.

Complexation of Cadmium(Ⅱ) with Humic Acids: Effects of pH and Humic Acid Origin

  • Lee, Mee-Hae;Choi, Se-Young;Chung, Kun-Ho;Moon, Hi-Chung
    • Bulletin of the Korean Chemical Society
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    • 제14권6호
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    • pp.726-732
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    • 1993
  • A comparative study on cadmium(II) complexation with three well characterized humic acids (SHA: soil humic acid from the Okchun Metamorphic Belt; AqHA: aquatic humic acid from Gorleben underground aquifer, Germany; CoHA: commercially available humic acid from the Aldrich Co.) was carried out in 0.1 M $NaClO_4$ at different solution pH(5.0, 5.5, and 6.0) using the ultrafiltration technique. The maximum binding ability (MBA) of the humic acids for cadmium(II) was observed to vary with their origins and solution pH. The results suggest that 1 : 1 complex predominates within the experimental range, and the conditional stability constants were calculated based on the assumption of cooperative binding, yielding log K values that were quite similar (CoHA: 4.17${\pm}$0.08; AqHA: 4.14${\pm}$0.07; SHA: $4.06{\pm} 0.12\;l\;mol^{-1}$ at pH 6.0) irrespective of humic acid origins or pH. By contrast a nonlinear Schatchard plot was obtained, using the cadmium(II) ion selective electrode speciation analysis method, which indicated that humic acid may have two or more classes of binding sites, with $log\;K_1\;and\;log\;K_2$ of 4.73${\pm}$ 0.08 and $3.31{\pm}0.14\;l\;mol^{-1}$ respectively.

Utility of solid phase extraction for colorimetric determination of lead in waters, vegetables, biological and soil samples

  • Al-Mallah, Zakia;Amin, Alaa S.
    • Journal of Industrial and Engineering Chemistry
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    • 제67권
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    • pp.461-468
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    • 2018
  • A highly sensitive, selective and rapid method for the determination of lead based on the reaction of lead (II) with 5-(4'-chlorophenylazo)-6-hydroxypyrimidine-2,4-dione (CPAHPD) and the solid phase extraction of the Pb(II)-CPAHPD complex with Amberlite XAD-2000 was developed, in the presence of pH 5.6 buffer solution and Triton X-114 medium. CPAHPD reacts with lead to form a violet complex with a molar ratio of 2:1 (CPAHPD to lead). This complex was enriched by the solid phase extraction with Amberlite XAD-2000. An enrichment factor of 500 was obtained by elution of the complex from the resin with a minimal amount of isopentyl alcohol(0.2 mL). In isopentyl alcohol medium,the molar absorptivity of the complex is $1.13{\times}10^6L\;mol^{-1}cm^{-1}$ at 647 nm. Beer's law is obeyed in the range of $5.0-160ng\;mL^{-1}$ in the measured solution. The relative standard deviation for 10 replicate samples of $50ng\;mL^{-1}$ level is 1.26%. The detection and quantification limits reaches 1.5 and $4.7ng\;mL^{-1}$ in the original samples. The presented procedure was successfully applied for determination of lead content in real samples such as vegetables, waters, biological and soil samples with satisfactory results.