• 제목/요약/키워드: $Cu^{2+}$ detection

검색결과 185건 처리시간 0.026초

Cupferron과 Tetrabutylammonium ion을 이용한 Mn(II)의 상승용매 추출에 관한 연구 (Synergistic Solvent Extraction of Manganese(II) by using Cupferron and Tetrabutylammonium ion)

  • 인교;소진환;최종문;김영상
    • 분석과학
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    • 제17권1호
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    • pp.1-7
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    • 2004
  • N-nitroso-N-phenylhydroxylamineammonium salt(cupferron)과 tetrabutylammonium ion ($TBA^+$)을 사용하여 수용액 중 미량 Mn(II)을 상승 용매 추출하는 법에 대해서 연구하였다. $TBA^+$가 존재할 때 cupferron으로 수용액 중의 Mn(II)을 추출하면 용액의 pH 4-10 범위에서 95% 이상이 추출되지만 $TBA^+$가 존재하지 않으면 거의 추출되지 않았다. 이런 조건에서 Mn(II)의 추출은 $CH_2Cl_2$$CHCl_3$와 같은 유기용매를 사용 할 때가 다른 비극성 용매를 사용할 때 보다 현저히 잘 추출되었으므로 여기서는 chloroform을 사용하였다. 그리고 수용액의 pH는 5로 조절하였다. 실제시료 중 존재하는 극미량의 Mn(II)을 정량하기 위해서는 chloroform에 추출된 Mn(II)을 다시 0.1 mol/L $HNO_3$용액에 역 추출하여 GF-AAS로 Mn(II)의 흡광도를 측정하였다. 본 방법으로 얻은 Mn(II)의 검출한계는 0.37 ng/mL이었고, 이 방법을 응용하여 실험실 수돗물 중 Mn(II)을 정량한 결과는 0.4-1.01 ng/mL로 얻어졌다. 이 시료에 일정량의 Mn(II)용액을 첨가하여 얻은 회수율은 94-107%이었다. 그리고 Cu(II), Ca(II), Fe(III) 등 공존하는 다른 원소는 10 내지 $20{\mu}g/mL$까지 Mn(II) 정량에 방해를 하지 않았다. 이로서 본 방법이 극미량 Mn(II)의 새로운 분석법으로 사용될 수 있을 것으로 생각된다.

Detection of Heavy Metal Ions in Aqueous Solution Using Direct Dye Chemosensors

  • Heo, Eun-Yeong;Ko, Young-Il;Bae, Jin-Seok
    • 한국염색가공학회지
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    • 제21권5호
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    • pp.51-57
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    • 2009
  • Since heavy metal pollution is a significant global environmental problem and very dangerous to human health, the improved methods for detecting heavy metals are required recently. Colorimetric chemosensors are now considered as one of the most effective analytical method used in the environment monitoring. New direct dyes having the function of colorimetric chemosensors were synthesized. When metal ions such as $Al^{3+}$, $Ca^{2+}$, $Cd^{2+}$, $Cr^{3+}$, $Cu^{2+}$, $Fe^{2+}$, $Fe^{3+}$, $Hg^{2+}$, $Li^+$, $Mg^{2+}$, $Na^+$, $Ni^{2+}$, $Pb^{2+}$ and $Zn^{2+}$ were added each solution of new direct dyes, the color of solution was changed and can be easily detected with naked eyes without expensive experimental equipment such as atomic absorption spectrometer (AAS) or inductively coupled plasma?mass spectrometer (ICP-MS). The new benzidine analogues were diazotized and reacted with couplers such as H-acid, J-acid, Chromotropic acid, Nevill-winther acid and gamma acid to synthesize new direct dyes. The structures of the new direct dyes were confirmed by high resolution mass spectrometer (FAB ionization) and evaluated with UV-Vis spectroscopy. The UV-VIS spectroscopy was measured for the dye solutions by adding various concentrations of metal ions. It was observed that the absorbance in UV-Vis spectra was changed as the heavy metal ions were added.

Flotation-Spectrophotometric Determination of Ag(I) at the 10-7 mol L-1 Level Using Iodide and Ferroin as an Ion-associate

  • Hosseini, Mohammad Saeid;Hashemi-Moghaddam, Hamid
    • Bulletin of the Korean Chemical Society
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    • 제26권10호
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    • pp.1529-1532
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    • 2005
  • A simple and cost effective method for separation and preconcentration of Ag(I) at the $10^{-7}\;mol\;L^{-1}$ level in the environmental and mineral samples is present. The method is based on the flotation of Ag(I)-iodide complex as an ion-associate with ferroin in pH of 4 from a large volume of an aqueous solution (500 mL) using nheptane. The floated layer was then dissolved in dimethylsulfoxide (DMSO) for the subsequent spectrophotometric determination. Beer's law was obeyed over a range of 2.0 ${\times}$ $10^{-7}$-4.0 ${\times}$ $10^{-6}$ mol $L^{-1}$ with the apparent molar absorptivity of 2.67 ${\times}$ $10^5$ L $mol^{-1}\;cm^{-1}$. The detection limit (n = 5) was 4 ${\times}$ $10^{-8}$ mol $L^{-1}$, and RSD (n = 5) obtained for 2.0 ${\times}$ $10^{-6}$ mol $L^{-1}$ of Ag(I) was 2.2%. The interference effects of a number of elements was studied and found that only $Hg^{2+}$ at low concentration, and $Pb^{2+}$, $Cd^{2+}$, $Cu^{2+}$, and $Fe^{3+}$ ions at moderately high concentrations were interfered. To overcome on these interference effects, the solution was treated with EDTA at a buffering pH of 4 and passed through a column containing Amberlite IR-120 ionexchanger resin, just before the flotation process. The proposed method was applied to determine of Ag(I) in a synthetic waste water, a photographic washing sample and a geological sample and the results was compared with those obtained from the flame atomic absorption spectrometry. The results were satisfactorily comparable with together, so that the applicability of the proposed method was confirmed in encountering with the real samples.

조리용구용 석재의 기초 특성과 중금속 원소의 용출 특성 (Basic Properties of Stones used for Cooking Utensils and Their Leaching Characteristics for Heavy Metal Elements)

  • 진호일;김신자;김복란;민경원
    • 자원환경지질
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    • 제35권4호
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    • pp.347-353
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    • 2002
  • 현재 우리 나라에서 조리용구로 많이 사용되고 있는 석재에는 휘석암과 각력암, 흑운모섬록암 등이 있으며, 이중 유색광물이 상대적으로 많은 휘석암과 흑운모섬록암은 비중이 3.0으로 각력암(2.5)보다 약간 더 무거운 특징을 보였고, 흡수율은 각력암이 2.9%로 가장 높았으며, pH는 모두 9.7-9.9의 범위로 약알칼리성을 나타내었다. 또한 조리용구용 석재중 흑운모섬록암이 각력암이나 휘석암보다 마모에 대한 내구성과 강도가 가장 우수하석 다른 특별한 요인이 없는 한 가장 오랫동안 사용할 수 있음을 나타내었다. 용출시험 결과, Cu, Pb, Co, Cr Ni 등의 유독성 중금속 원소들은 연구대상 암석에서 모두 반응시간 및 용액의 초기 pH에 관계없이 모두 측정 한계값인 0.1 ppm 이하로 낮았으나, 철(Fe)은 암석의 종류 및 용출 조건에 따라 다소간의 용출량 차이를 보였는데, 대체로 중성보다는 산성용액을 첨가하였을 경우에 약 1.8-31배 정도 더 높은 용출량을 나타내었고, 반응용액이 중성인 조건에서는 각력암에서, 산성인 경우에는 흑운모섬록암에서 가장 높은 철(Fe)의 용출량을 보여 주었다. 석재를 인체에 해가 없는 고기능성 조리용구로 이용하기 위해서는 인체에 영향을 미칠 수 있는 중금속 및 다량 무기질 원소들에 대한 용출함량 기준이 먼저 마련되어야 하며, 또한 보다 많은 종류의 조리용구용 석재와 화학원소들을 대상으로 좀 더 체계적인 무기화학적 특성에 하한 연구가 필요할 것으로 생각한다.

4,5-Dihydroxy-1,3-Benzenedisulfonic Acid를 이용한 Fe(Ⅲ)의 분광형광법 정량 (Spectrofluorimetric Determination of Fe(Ⅲ) with 4,5-Dihydroxy-1,3-Benzenedisulfonic Acid)

  • 김혜선;최희선
    • 대한화학회지
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    • 제43권4호
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    • pp.423-429
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    • 1999
  • 형광체로서 4,5-dihydroxy-1,3-benzenedisulfonic acid(Tiron)를 이용하여 수용액속의 Fe(III)를 정량할 수 있는 분광형광법에 대해 연구하였다. 물에 잘 용해되는 Tiron은 좋은 형광시약이지만, Fe(III)와 착물을 이루면 소광 효과로 인해 형광의 세기가 Fe(III)의 농도에 비례하여 감소하였다. pH 4.5에서 Fe(III)에 의해 소광 효과를 보여주는 Tiron의 들뜸 및 형광 파장은 각각 312 nm와 341 nm이었다. 감도는 Tiron의 농도가 $1.0{\times}10^{-2}M$일 때 가장 좋았다. 소광효과를 증가시키기 위하여 Fe(III)-Tiron 착물 용액을 80$^{\circ}C$에서 90분 동안 가열하였다. Fe(III)의 경우 가장 방해하는 이온은 Cu(II) 이었는데, 이는 pH를 조절하거나 EDTA를 넣어주므로서 방해효과를 없앨 수 있었다. Fe(III)의 직선 농도범위는 $5.0{\times}10^{-7}M$ 에서 $6.0{\times}10^{-5}M$까지 이었다. 이 제시된 방법의 검출한계는 $2.8{\times}10^{-6}M$이었고, 합성시료에서 Fe(III)의 회수는 거의 정량적으로 이루어졌다. 실험결과를 종합하여 보면, 이 제시된 방법을 이용하면 실제 시료에 들어있는 Fe(III)을 정량할 수 있을 것이다.

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서울市 一部 水道栓水中 重金屬에 관한 調査硏究 (A Study on Heavy Metals at the Consumer s Tap in Seoul)

  • Lee, Byung Mu
    • 한국환경보건학회지
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    • 제10권2호
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    • pp.41-51
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    • 1984
  • This study was performed using samples collected at Myungryundong and at Reservoirs. The purpose of this study was to investigate the differences of water quality between tap and raw water, and to analyse drinking water quality by Fe, Zn from corroded galvanized steel pipe. Results were as follows 1. The older the pipe was, the higher the concentration of Ferrum and Zinc was (t-test : p<0.05). Ferrum and Zinc also exceeded the limits in the older galvanized steel pipe. I think that this comes from the corrosion of pipe. 2. Mercury, Arsenic, Cadmium, Lead, Chomium, Argentum and Aurum not detected in raw water were not detected in tap water. Cobalt, Bismuth and Molybudenum detected in raw water were not detected in tap water. I think that this comes from the quality of raw water, the result of water treatment and the improbability of detection of above metals in water delivery system. 3. Silicon measured 2.4698ppm in raw water, but it ranged from 0.4769ppm to 1.982 ppm in tap water. Manganese measured 0.0638ppm in raw water, but it ranged from 0.0026ppm to 0.0198ppm in 17cases(31%) out of 55samples in tap water. I think that this comes from the water treatment. 4. Aluminium not detected in raw water was found in 17 cases (31%) out of the samples (55cases). It may be considered as the use of coagulants $Al_2(SO_4)_3$. $18H_2O$ and PAC (Poly Aluminium Chloride). The concentration of copper in tap water was much higher in 2 cases(3.6%) out of the samples(55) than that of copper in raw water. I think that this may come from the use of ${CuSO}_4$, the preventive of algae growth, and the result of chlorination, but further study must be necoessary to support the proof.

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방풍통성산의 동시분석 및 항산화 효능 연구 (Simultaneous Analysis of Bangpungtongseong-san and Its Antioxidant Effect)

  • 서창섭;김온순;신현규
    • 대한한의학방제학회지
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    • 제21권2호
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    • pp.133-143
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    • 2013
  • Objectives : We carry out the simultaneous quantification for quality control of four components in Bangpungtongseong-san (BPTSS) sample. In addition, we assessed the antioxidant effects of BPTSS sample. Methods : The used column for separation and analysis of four compounds was Luna C18 column and column oven temperature was maintained at $40^{\circ}C$. The mobile phase for simultaneous determination consisted of two solvent systems, 1.0% acetic acid in water and 1.0% acetic acid in acetonitrile. High performance liquid chromatography-photodiode array (HPLC-PDA) method for analysis was performed at a flow rate of 1.0 mL/min with PDA detection at 254 and 280 nm. The injection volume was 10 ${\mu}L$. The antioxidant activities of BPTSS were evaluated by measuring free radical scavenging activities on 2,2'-Azinobis-3-ethyl-benzothiazoline-6-sulfonic acid (ABTS) and 1-1-diphenyl-2-picrylhydrazyl (DPPH). The inhibitory effects on low-density lipoprotein (LDL) oxidation were evaluated by the formation of thiobarbituric acid relative substances (TBARS) and relative electrophoretic mobility (REM). Results : Calibration curves were acquired with $r^2{\geq}0.9999$. The values of limit of detection (LOD) and quantification (LOQ) were 0.06-0.29 ${\mu}g/mL$ and 0.20-0.98 ${\mu}g/mL$, respectively. The amounts of geniposide, liquiritin, baicalin, and glycyrrhizin in BPTSS were 5.06, 7.33, 27.56, and 7.81 mg/g, respectively. The BPTSS showed the radical scavenging activity in a dose-dependent manner. The concentration required for 50% reduction (RC50) against ABTS and DPPH radicals were 72.51 ${\mu}g/mL$ and 128.49 ${\mu}g/mL$. Furthermore, GMGHT reduced the oxidation properties of LDL induced by CuSO4. Conclusions : The established HPLC-PDA method will be helpful to improve quality control of BPTSS. In addition, BPTSS has potentials as therapeutic agent on anti-atherosclerosis.

1,5,9,13-Tetrathiacyclohexadecane 수식전극을 사용한 Ag(I)의 전기화학적 정량 (Electrochemical Determination of Ag(I) Ion at Chemically Modified Carbon-Paste Electrode Containing 1,5,9,13-Tetrathiacyclohexadecane)

  • 하광수;장미경;서무룡
    • 분석과학
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    • 제10권3호
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    • pp.187-195
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    • 1997
  • [16]-ane-$S_4$/탄소분말 함량비를 50%로 하여 nujol oil과 혼합하여 수식전극을 제조하였다. $5.0{\times}10^{-4}M$ $Ag^+$를 포함하는 pH 4.5인 아세트 완충용액에 수식전극을 담가 $Ag^+$를 전극 표면에 흡착시켰다. 이 때 흡착시간을 15분으로 하고 전해환원시키는 시간은 -0.3V vs S.C.E에서 2분으로 하였다. 또한 0.1M $HNO_3$ 용액으로 전극을 활성화시켰으며 한번 활성화한 전극은 10회까지 사용이 가능하였다. 최적 분석조건에서 미분펄스 전압전류법으로 $5.0{\times}10^{-7}{\sim}1.5{\times}10^{-6}M$ 사이의 농도 범위에서 정량해 보았을 때 직선성이 잘 성립하였으며, 검출한계는 $2.0{\times}10^{-7}M$이었다. 대부분의 금속들은 방해를 주지 않았으나, Cu(II)은 방해를 나타내었다.

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구미강활탕의 성분 분석 및 LDL 산화억제 효능 연구 (Simultaneous Determination of Gumiganghwal-tang and Its Anti-atherosclerotic Effect)

  • 김온순;서창섭;신현규
    • 대한예방한의학회지
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    • 제17권3호
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    • pp.165-176
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    • 2013
  • Objective : The purpose of this study was to establish the simultaneous analysis for six compounds in Gumiganghwal-tang (GMGHT, Jiuweiqianghuo-tang) and to investigate the anti-atherosclerotic effects of GMGHT in vitro. Methods : The column for separation of six compounds was used Luna $C_{18}$ column and maintained at $40^{\circ}C$. The mobile phase for gradient elution consisted of two solvent systems, 1.0% acetic acid in water and 1.0% acetic acid in acetonitrile. The analysis was carried out at a flow rate of 1.0 mL/min with pothodiode array (PDA) detection at 254, 280, and 320 nm. The injection volume was 10 ${\mu}L$. The antioxidant activities of GMGHT were evaluated by measuring free radical scavenging activities on 2,2'-Azinobis-3-ethyl-benzothiazoline-6-sulfonic acid (ABTS) and 1-1-diphenyl-2-picrylhydrazyl (DPPH). The inhibitory effects on low-density lipoprotein (LDL) oxidation were evaluated by the formation of thiobarbituric acid relative substances (TBARS), relative electrophoretic mobility (REM), and fragmentation of apolipoprotein B (ApoB)-100. Results : Calibration curves were acquired with $r^2{\geq}0.9998$. The contents of liquiritin, ferulic acid, baicalin, baicalein, glycyrrhizin, and wogonin in GMGHT were 1.784, 1.693, 37.899, 0.258, 1.869, and 0.034 mg/g, respectively. The GMGHT showed the radical scavenging activity in a dose-dependent manner. The concentration required for 50% reduction ($RC_{50}$) against ABTS and DPPH radicals were 72.51 ${\mu}g/mL$ and 128.49 ${\mu}g/mL$. Furthermore, GMGHT reduced the oxidation properties of LDL induced by $CuSO_4$. Conclusion : HPLC-PDA is considered as an available and convenient method for quality control and standardization of GMGH and GMGHT has potentials on anti-atherosclerosis by anti-oxidative effect and suppressive effect on LDL oxidation.

Molecular and Morphological Evidence of Hepatotoxicity after Silver Nanoparticle Exposure: A Systematic Review, In Silico, and Ultrastructure Investigation

  • Sooklert, Kanidta;Wongjarupong, Asarn;Cherdchom, Sarocha;Wongjarupong, Nicha;Jindatip, Depicha;Phungnoi, Yupa;Rojanathanes, Rojrit;Sereemaspun, Amornpun
    • Toxicological Research
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    • 제35권3호
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    • pp.257-270
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    • 2019
  • Silver nanoparticles (AgNPs) have been widely used in a variety of applications in innovative development; consequently, people are more exposed to this particle. Growing concern about toxicity from AgNP exposure has attracted greater attention, while questions about nanosilver-responsive genes and consequences for human health remain unanswered. By considering early detection and prevention of nanotoxicology at the genetic level, this study aimed to identify 1) changes in gene expression levels that could be potential indicators for AgNP toxicity and 2) morphological phenotypes correlating to toxicity of HepG2 cells. To detect possible nanosilver-responsive genes in xenogenic targeted organs, a comprehensive systematic literature review of changes in gene expression in HepG2 cells after AgNP exposure and in silico method, connection up- and down-regulation expression analysis of microarrays (CU-DREAM), were performed. In addition, cells were extracted and processed for transmission electron microscopy to examine ultrastructural alterations. From the Gene Expression Omnibus (GEO) Series database, we selected genes that were up- and down-regulated in AgNPs, but not up- and down-regulated in silver ion exposed cells, as nanosilver-responsive genes. HepG2 cells in the AgNP-treated group showed distinct ultrastructural alterations. Our results suggested potential representative gene data after AgNPs exposure provide insight into assessment and prediction of toxicity from nanosilver exposure.