• 제목/요약/키워드: Atomic Absorption Spectrometry

검색결과 120건 처리시간 0.025초

질소이온주입된 초내식성 스테인리스강의 마모부식 특성 (Wear Corrosion Behaviour of Nitrogen Ion Implanted Super Stainless Steel)

  • 강선화;김철생
    • 대한의용생체공학회:학술대회논문집
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    • 대한의용생체공학회 1994년도 추계학술대회
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    • pp.175-177
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    • 1994
  • The wear corrosion behaviour of a nitrogen ion implanted super stainless steel (S.S.S, 22Cr - 20Ni - 6Mo - 0.25N) was compared with those of S.S.S, 316L SS and TiN coated 316L SS. The Cr and Ni amounts won out from the materials were investigated using an electrothermal atomic absorption spectrometry. We observed that the Cr dissolution rate of the S.S.S was similar to that of 316L SS, however, the Ni release of the S.S.S was feater than 316L SS. The metal ions released from the nitrogen ion implanted S.S.S surface were significantly reduced. The wear corrosion behaviour of the stainless steels was not correlated with the results shown by a static metal ion release test.

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휴/폐광 광산폐기물의 지구화학적 특성 (Geochemical Characteristics of Mine Wastes in Abandoned Mines in Korea)

  • 정명채;정영욱;민정식
    • 한국지하수토양환경학회:학술대회논문집
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    • 한국지하수토양환경학회 1998년도 공동 심포지엄 및 추계학술발표회
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    • pp.71-75
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    • 1998
  • The objective of this study is to investigate geochemical characteristics of mine wastes including tailings in various abandoned mines in Korea. Tailings and wastes were sampled in and around 39 metalliferous mines, and analysed heavy metal concentrations including Cd, Cu, Pb and Zn extracted by 0.1N HCl and aqua regia by Atomic Absorption Spectrometry. Measurements of paste pH and lime requirement were carried out to examine a general geochemical characteristics of the materials. Lots of mine wastes were characterized by very low pH values of 2 to 4 and high lime requirement to control neutralization of the wastes. In addition, elevated levels of heavy metals were found in various mine wastes extracted by both 0.lN HCl and aqua regia. Because the mine wastes can be dispersed into the downstream by clastic movement and wind-blow, it is necessary to control the materials with a proper method for their reclamation.

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Determination of Trace Metals in Waters by FAAS after Enrichment as Metal-HMDTC Complexes Using Solid Phase Extraction

  • Tokalioglu, Serife;Kartal, Senol;Elci, Latif
    • Bulletin of the Korean Chemical Society
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    • 제23권5호
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    • pp.693-698
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    • 2002
  • A method has been described for the determination of Cu(Ⅱ), Pb(Ⅱ), Ni(Ⅱ), Cd(Ⅱ), Mn(Ⅱ) and Fe(Ⅲ) by flame atomic absorption spectrometry (FAAS) after preconcentration on Amberlite XAD-16 resin, using hexamethyleneammonium-hexamethylenedithiocarbamate (HMA-HMDTC) as a chelating agent, and NH3/NH4Cl buffer solution (pH 9). Influences of various analytical parameters such as pH, concentration of nitric acid, amount of analytes, diverse ions and sample volume were investigated. The relative standard deviation (RSD) and the detection limit (LOD) were found in the range of 0.8-2.9% and 0.006-0.277 ㎍/mL,respectively. Recoveries obtained by the column method were quantitative ( >95%) at optimum conditions.The method was applied to the determination of some metal ions in seawater and wastewater samples. A high preconcentration factor (about 150 for seawater and 75 for wastewater samples) and simplicity are the main advantages of this suggested method.

Purification and Glycosylation Pattern of Human L-Ferritin in Pichia pastoris

  • Lee, Jong-Lim;Yang, Seung-Nam;Park, Cheon-Seok;Jeoung, Doo-Il;Kim, Hae-Yeong
    • Journal of Microbiology and Biotechnology
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    • 제14권1호
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    • pp.68-73
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    • 2004
  • Ferritin is an iron storage protein found in most living organisms. For expression and industrial use, human light chain ferritin (L-ferritin) was cloned from human liver cDNA library and expressed in Pichia pastoris strain GS115. The recombinant L-ferritin in Pichia pastoris was glycosylated. In a fed-batch culture, the cell mass reached about 57 g/l of dry cell weight, and the L-ferritin in the cell was increased to about 95 mg/l after 150 h. In an atomic absorption spectrometry analysis, the intracellular content of iron in the L-ferritin transformant was measured as $1,694{\pm}85\;\mu\textrm{g}g/g$, which is 5.4-fold more than that of the control strain. This L-ferritin transformant could serve as iron-fortified nutrients in animal feed stock.

Determination of Selenium and Tellurium by HG-AAS in Foods

  • Cha, Ki-Won;Park, Sang-Ho;Park, Kwang-Won
    • 분석과학
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    • 제8권4호
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    • pp.419-425
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    • 1995
  • A method has been investigated for the determination of selenium and tellurium in Ginseng, Ganoderma and Garlic using hydride generation atomic absorption spectrometry(HG-AAS). The concentration effects of hydrochloric acid and sodium tetrahydroborate on the hydride generation for the determination of selenium and tellurium were investigated. The method of sample decomposition was also investigated using various mineral acids, such as nitric, perchloric and sulfuric acid in the closed system, and foreign ion effects containing in the samples were studied. The calibration curves of selenium and tellurium were obtained in the range of 0~40 ppb. The detection limits(S/N=2) of selenium and tellurium are 0.1 and 0.2 ppb. Analytical data of selenium and tellurium in Garlic, Ganoderma and Ginseng are 289, 296 and 198 ng/g for selenium and 146, 127 and 110 ng/g for tellurium, respectively.

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FAAS를 이용한 혈중 Cisplatin의 분석법 개발 (The Development of Cisplatin Analysis Method in Plasma by Flameless Atomic Absorption Spectrometry)

  • 백만정;임호섭;정미진;이경옥;신호상
    • 분석과학
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    • 제11권4호
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    • pp.243-247
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    • 1998
  • 백금을 함유한 항암제로 신장과 신경계에 심각한 부작용을 일으키는 cisplatin의 혈중 농도를 flameless atomic absorption spectrometry법(FAAS)으로 분석하였다. 이 방법은 시료전처리 과정이 필요 없어 신속하고 간단한 분석법이다. 검정곡선에 대한 직선성을 조사한 결과 20~1000ng/mL 농도 범위에서 r=0.999로 나타났으며, 정확도는 50 ng/mL 이상의 농도에서 상대표준편차가 5.0% 이하 이었다. 그리고, 혈장시료 $200{\mu}L$에 대한 검출한계는 10 ng/mL 이었다. 본 방법은 cisplatin의 최적 치료 조건과 독성 경감을 위한 혈중 모니터링에 그 활용이 크게 기대된다.

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흑연로 원자흡수분광법에 의한 혈중 납분석시 매트릭스 변형제의 역할 (The role of matrix modifier for the determination of Lead (Pb) in blood by graphite furnace atomic absorption spectrometry)

  • 유광식;권진기
    • 분석과학
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    • 제5권4호
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    • pp.349-358
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    • 1992
  • 본 연구에서는 흑연로 원자흡수분광법을 이용하여 혈액을 1% Triton X-100을 5배 희석시킨 다음 납 함량을 직접 측정하였다. 혈액내 방해 성분을 제거하기 위하여 매트릭스 변형제를 사용하여 최적의 분석 조건을 조사하였다. 매트릭스 변형제로서 1% $(NH_4)_2HPO_4$와 0.1% $PdCl_2$를 같이 사용하고 700도에서 회화시켰을 때에, 일본 비교 분석 프로그램에 의해 제공된 혈중 납 함량에 대한 정도관리용 표준시료(우혈)의 공인값과 비교적 잘 일치하였다. 이 실험에서 얻은 표준편차는 $31{\mu}gPb/l$에서 $624{\mu}gPb/l$ 범위에서는 1% $(NH_4)_2HPO_4$ 및 1% $(NH_4)_2HPO_4$와 0.1% $PdCl_2$를 매트릭스 변형제로서 사용했을 경우 각각 2.2~6.3%, 3.1~9.1%였다.

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도금업 근로자의 혈청과 공기중 크롬 및 니켈 농도 (Chromium and nickel concentrations in air and in serum of workers in chromium and nickel electroplating plants)

  • 최호춘;김해정;정호근
    • 한국산업보건학회지
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    • 제1권2호
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    • pp.117-127
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    • 1991
  • The exposure level of chromium and nickel for chrome and nickel plating workers were evaluated. Chromium and nickel concentrations in serum from 82 exposed workers and 66 controls, who were not exposed occupationally to metals, were analyzed by flameless atomic absorption spectrophotometry. The results were as follows : 1. The recovery percent of chromium and nickel concentrations in personal air samples were 95-108.2%, 88.0-107.7%, precisions (C.V., %) were 2.7-3.1%, 2.1-4.4%. respectively. 2. The recovery percent of chromium and nickel concentrations in serum were 93.6-106.4%, 91.3-107.9% and precisions (C.V. %) were 1.1-7.6%, 2.4-5.4% respectively. 3. The exposure level of chromium and nickel concentrations in the place of preparation process were $2.0{\pm}2.00{\mu}g/m^3$, chromplating were $35.7{\pm}53.07{\mu}g/m^3$, $2.8{\pm}3.42{\mu}g/m^3$, nickelplating were $4.6.0{\pm}5.8{\mu}g/m^3$, $18.62{\pm}4.41{\mu}g/m^3$, and covering were $2.9{\pm}2.02{\mu}g/m^3$, $1.1{\pm}0.47{\mu}g/m^3$ respectively. There were significant difference of concentrations for chromium and nickel in workplaces by groups statistically. 4. Chromium concentrations in serum of exposed group and control were $0.68{\pm}0.399{\mu}g/l$, $1.41{\pm}0.748{\mu}g/l$, respectively. There were significant difference of concentrations for chromium and nickel in serum by groups statistically. 5. Chromium and nickel concentrations in serum of exposed group were not significant by workplaces.

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Determination of Cadmium(II) and Copper(II) by Flame Atomic Absorption Spectrometry after Preconcentration on Column with Pulverized Amberlite XAD-4 with Bismuthiol I

  • Park, Dong-Seok;Choi, Hee-Seon
    • Bulletin of the Korean Chemical Society
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    • 제28권8호
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    • pp.1375-1382
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    • 2007
  • A column preconcentration method with pulverized Amberlite XAD-4 loaded with bismuthiol I (BI) has been developed for the determination of trace Cd(II) and Cu(II) in various real samples by flame atomic absorption spectrophotometry. Various experimental conditions, such as the size of XAD-4, adsorption flow rate, amount of bismuthiol I, stirring time for adsorbing bismuthiol I on XAD-4, pH of sample solution, amount of XAD-4- BI, desorption solvent, and desorption flow rate, were optimized. Also, the adsorption capacity and the adsorption rate of Cd(II) and Cu(II) on XAD-4-BI were investigated. The interfering effects of various concomitant ions were investigated, Bi(III), Sn(II) and Fe(III) were found to affect the determination. But the interference by these ions was completely eliminated by adjusting the amount of XAD-4-BI resin to 0.70 g, although the adsorption flow rate was slower. For Cd(II) our proposed technique obtained a dynamic range of 0.5-40 ng mL-1, a correlation coefficient (R2) of 0.9913, and a detection limit of 0.3 ng mL-1. For Cu(II), the corresponding values were 2.0-120 ng mL-1, 0.9921 and 1.02 ng mL-1. To validate this proposed technique, the aqueous samples (stream water, reservoir water, tap water and wastewater), the diluted brass sample and the plastic sample, as real samples, were used. Recovery yields of 91-103% were obtained. These measured data were not different from ICP-MS data at 95% confidence level. Our proposed method was also validated using rice flour CRM (normal, fortified) samples. From the results of our experiment, we found that the technique we present here can be applied to the determination of Cd(II) and Cu(II) in various real samples.

HG-AAS에 의한 무기비소 분석 시 예비환원제의 최적화 조건과 분석에 미치는 영향 (Effects and optimum conditions of pre-reductant in the analysis of inorganic arsenic by hydride generation-atomic absorption spectrometry)

  • 송명진;박경수;김영만;이원
    • 분석과학
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    • 제18권5호
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    • pp.396-402
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    • 2005
  • 수소화물 발생법-원자흡수 분광계를 이용한 무기비소의 분석 시 예비환원제로써 L-Cysteine, KI, $FeSO_4$의 최적 조건을 찾고자 하였으며, 이들이 분석에 미치는 영향을 서로 비교 연구하였다. 이와 더불어 $H_2SO_4$-trap에 의하여 시료 중 공존 가능성이 있는 유기비소인 MMA(monomethylarsonate)와 DMA(dimethylarsinate)를 제거하여 무기비소만을 분리 분석하였다. 1.8 M 염산과 0.08 M 질산의 혼합산에서 비소 표준용액 20 ppb는 산을 넣지 않았을 때보다도, 높은 흡광도를 나타내었다. L-Cysteine의 경우 0.5 g 정도를 취하고 약 0.07 M의 질산이나 염산의 약 산성 조건에서 30 분 이상을 반응시켰을 경우에 완전히 As(V)는 As(III)로 환원되었다. KI의 경우, 3 g 정도를 취하고 약 0.8 M의 질산 조건에서 1시간 이상 반응시켰을 경우에 완전히 As(V)는 As(III)로 환원되었다. $FeSO_4$의 경우에는, 다른 예비환원제와 비교하여 NaBH4와 $Fe^{2+}$의 반응으로 인한 침전물의 생성으로 튜브내부가 막히게 되어, As(V)가 As(III)로 환원되는 효율의 재현성이 없었다. 분석결과의 정확도를 확인하기 위하여, NIST SRM 1643C Trace Elements in Water ($82.1{\pm}1.2ng/mL$)를 사용하였으며 그 결과는 KI를 예비환원제로 사용하였을 경우에는 97.5%의 회수율이고 L-Cysteine를 예비환원제로 사용하였을 경우에는 101.9%의 회수율로서 두 경우 모두 만족할 만한 수준이였다.