• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2000년도 추계학술대회
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• pp.294-297
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• 2000

Heavy metals are extracted from Chonju stream sediment, roadside soils and sediments along Honam expressway, soils and tailings from mining area using partial ectraction in Standard Method, partial ectraction method with maintaining 0.1N of extraction solution and acid digestion. In samples having buffer capacity against acid, 0.1N of extraction solution can not be maintained and pH of extraction solution increases up to 8.0 when partial extraction in Standard Method is used. The averages and ranges of (heavy metals extracted using partial extraction in standard method, HPE)/(heavy metals extracted using partial extraction method with maintaining 0.1N of extraction solution, HPEM) values are 0.506 and 0.145~1.126 in Cd, 0.534~ and 0.078~0.928 in Zn, 0.461 and 0.041~1.715 in Mn, 0.359 and 0.011~0.874 in Cu, 0.195 and 0.018~1.785 in Cr, 0.710 and 0.003~3.075 in Pb, and 0.088 and 1.73$\times$10$^{-5}$ ~0.303 in Fe. These data indicate that the difference between HPE and HPEM is big in the order of Fe, Cr, Cu, Mn, Cd, Zn and Pb. It is quite possible that the partial extraction method in Standard Method of soil in Korea is not adequate for an assessment of contamination in area where buffer capacity of soil will be decreased or lost after a long term exposure of soils to environmental damage.

• 대한환경공학회지
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• 제27권8호
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• pp.787-798
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• 2005

본 연구에서는 폐광산지역에서 발생되는 폐기물인 광미를 대상으로 토양세척공정을 이용하여 다양한 세척용매와 농도, 그리고 추출시간에 따른 중금속의 추출특성을 파악하였다. 세척용매로는 물, HCl(0.1, 0.3, 1.0 N), EDTA(0.01, 0.05, 0.1 M), SDS(0.1, 0.5, 1.0%)를 이용하였다. 그 결과, 물과 SDS 용매에서 Zn과 Cd이 Pb과 Cu보다 높은 추출효율을 보였지만, 전체적으로는 1%이하로 중금속의 추출에 효과적이지 못하였다. 그러나, SDS에서 Pb과 Cu의 추출효율은 추출시간이 길어질수록 증가하였다. HCl과 EDTA를 이용한 중금속의 추출은 물과 SDS보다 빠른 추출경향을 보였고, 대부분의 중금속이 6시간 이내에 추출되었으며 용매의 농도와 무관하였다. 6시간 이후에는 느린 추출경향을 보였지만 세척용매의 농도에 따라 좌우되었다. 또한, 용매의 농도가 증가할수록 추출경향은 빨라졌고, 추출 효율도 증가하였다. 추출효율은 1.0 N HCl에서 Cd>Pb>Zn>Cu로, 0.1M EDTA에서 Pb>Cd>Zn>Cu 순으로 높았다. 농도증가에 따른 추출효과는 HCl에서 Pb이, EDTA에서 Pb과 Cd이 가장 컸으며, 중금속제거를 위한 6시간이상의 추출은 비효과적이었다.

• 자원환경지질
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• 제36권3호
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• pp.159-170
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• 2003

전주시 하천 퇴적물시료, 호남고속도로 주변의 토양과 퇴적물 시료, 광산주변 광미 및 토양시료를 대상으로 토양오염 공정시험방법상의 용출법, 0.1N 유지용출법, Tessir et al.(1979)의 연속추출방법을 적용하여 중금속을 추출하고 그 결과를 비교하였다. 공정시험방법상의 용출법 사용시 산에 대한 완충능력이 있는 시료는 용출액의 pH 1(0.1N HCl)이 유지되지 못했고 용출액의 pH가 최고 8.0까지 증가하였다. 또한, 토양오염 공정시험방법상의 용출법 사용시 중금속 추출량(HPE)/0.1 N 유지용출법 사용시 중금속 추출량(HPEM) 값의 평균치와 범위는 Cd의 경우 0.479와 0.145~0.929, Zn의 경우 0.534와 0.078~0.928, Mn의 경우 0.432와 0.041~0.992, Cu의 경우 0,359와 0.011~0.874, Cr의 경우 0.150과 0.018~0.530, Pb의 경우 0.219와 0.003~0.853, 그리고 Fe의 경우 0.088과 1.73${\times}$$10^{-5}$~0.303이다. 이는 두 전처리 방법에 의해 추출된 중금속량의 차이가 Fe>Cr>Pb>Cu〉Mn>Cd>Zn 순임을 지시한다. HPE, HPEM과 연속추출법 비교시 Zn, Cd, Mn의 경우 추출량은 대체적으로 연속추출 3단계까지의 합$\geq$0.1N 유지용출법>연속추출 2단계까지의 합$\geq$용출법 순이었으며, Cr과 Fe의 경우 연속추출 3단계까지 합》0.1N 유지용출법>용출법 순이었으며 연속추출 2단계 까지 합은 Cr의 경우 0.1N 유지용출법의 추출량보다 낮았고 용출법의 추출량보다 높았다. Cu의 경우 연속추출 4단계까지의 합$\geq$0.1N 유지용출법>3단계까지의 합 용출법으로 나타났다. 0.1N유지위해 첨가된 염산의 양이 증가할수록, 즉 시료내의 산에 대한 완충능력이 증가할수록 HPE/HPEM 값이 감소하며, 완충능력이 큰 시료의 경우 모든 원소에서 HPE/HPEM이 0.2보다 낮다. 완충능력이 낮은 시료의 경우 Zn, Cd, Mn, Cu는 연속추출 1,2단계의 합과 연속추출 3단계의 중금속 추출함량간의 차이가 적고, 다른 원소에 비해서 상대적인 유동도가 높기 때문에 HPE/HPEM이 대채적으로 0.2보다 높으며 0.6이상의 값을 갖는 시료가 많다. 그러나, Fe, Cr의 경우는 상대적으로 Zn, Cd, Mn, Cu에 비해 유동도가 낮고, 연속추출 3단계의 함량이 1+2단계의 함량과 차이가 커 완충능력이 낮은 시료의 HPE/HPEM값도 전반적으로 0.2보다 낮다. 이러한 연구결과는 국내 토양오염 공정시험방법상의 전처리 방법인 용출법이 장래에 장기적으로 산성비와 같은 환경피해에 노출되어 토양의 완충능력이 감소하거나 상실될 수 있는 지역의 오염평가에 적합치 않을 가능성을 제시한다.

• 한국방사성폐기물학회:학술대회논문집
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• 한국방사성폐기물학회 2004년도 Proceedings of the 4th Korea-China Joint Workshop on Nuclear Waste Management
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• pp.245-256
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• 2004

The extraction of three kinds of amido podands, N,N,N'N'-tetrabutyl-3-oxa-pentanedi- amide (TBDGA), N,N,N'N'-tetra-isobutyl-3-oxa-pentanediamide(TiBDGA) and N,N,N'N'-tetra- butyl-3,6-dioxa-oct-anediam- ide(TBDOODA) on U(VI),Pu(IV), Am(III), Eu(III) and other metal ions is studied in nitric acid solutions. 40%octanol-kerosene is chosen as diluents to eliminate third phase and emulsion. TBDGA and TiBDGA show extraction selectivity to An(III) and Ln(III) much higher than to U(VI) and Pu(IV). Fe, Ru and Mo is poorly extracted by the three kinds of amid podands in 2~3mol/L $HNO_3$ solutions. Aiming to eliminate interface crude when using simulated HLLW solution in the system of 0.2mol/L TBDGA/Octanol＋kerosene, acetohydroxyamic acid was adapted. Distribution ratio of zirconium was decreased when adding acetohydroxyamic acid in aqueous solution, and interface crude disappeared as mixing extractant with HLLW. The counter-current extraction test is carried out in a set of miniature mixer-settler, with 0.2mol/L TBDGA/ 40% octanol-kerosene as extractant to separate U(VI), Pu(IV), Am(III) and Eu(III) from simulated high level liquid waste(HLLW) solution. In battery A, lanthanides and actinides are coextracted into organic phase with the recovery of 99.98% for U(Ⅵ), >99.99% for Pu(IV), and >99.99% for Am(III) and Eu(III) respectively. In battery R1, 99.99% U, 86.2% Pu and a part of Am or Eu are stripped into aqueous phase by 0.2mol/L acetohydroxyamic acid (AHA) in 0.01mol/L $HNO_3$ solution. In battery $R_2$, Am, Eu and remained Pu are completely back-extracted by 0.2mol/L AHA. This separation process contains no salt reagent, and it is not necessary to dilute HLLW feed.

• 한국식품영양학회지
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• 제22권1호
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• pp.8-13
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• 2009

Effects of microwave and ultrasonication on chitin extraction time were investigated in this study. Chitin was extracted from ground crab shell by demineralization in 1.0 N HCl solution at 25$^{\circ}C$ with or without ultrasonication and deproteinization in 1.0 NaOH solution at 100$^{\circ}C$ without ultrasonication and at 70$^{\circ}C$ with ultrasonication. Microwave treatment was also used for deproteinization with 5 min heating and 5 min standing without microwave. The changes in color difference, the contents of ash, calcium and nitrogen were measured during demineralization and deproteinization. Ultrasonication of 4 hr in 1.0 N HCl solution for removal of calcium and 1.5 hr of microwave heating in 1.0 N NaOH for deproteinization corresponded to 6 hr in 0.1 N HCl and 2 hr in 1.0 N NaOH of heating at 100$^{\circ}C$ without those treatments, respectively. The data obtained showed that these treatments were effective reduction of chitin extraction time by 25${\sim}$33% for chitin preparation. The chitin obtained from these ultrasonication and microwave treatments resulted 0.55% of ash, 0.25% of calcium, 2.47% of nitrogen and 20.64% of yield ratio. Those treatments selected were also reduced the darkness development time of the chitin solution during demineralization and deproteinization.

• Bulletin of the Korean Chemical Society
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• 제22권8호
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• pp.821-826
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• 2001

Solvent sublation has been studied for the separation and determination of trace Zn(Ⅱ) and Pb(Ⅱ) in water samples. A synergy producing method was utilized to improve the efficiency of extraction in the sublation using an ion-pair of metal-naphth oate {M-(Nph)3- } complexes and tetra-n-butylammonium (TBA+ ) ion. After the M-(Nph)3- complexes were formed by adding 1-naphthoic acid to the sample solution, tetra-n-butylammonium bromide was added in the solution to form the ion-pair. And sodium lauryl sulfate (SLS) was added to make the ion-pair hydrophobic. The ion-pairs of the metal complexes were floated and extracted into methylisobutyl ketone (MIBK) from the aqueous solution by bubbling with nitrogen gas in a flotation cell. Metal ions in MIBK solution were measured by graphite furnace-AAS. Experimental conditions were optimized as follow so. After the pH of a 1.0 L water sample was adjusted to 5.0, 6.0 mL of 0.1 M 1-HNph and 10 mL of 0.03 M TBA-bromide were added to the sample to form ion-pairs, and 2.0 mL of 0.2%(w/v) SLS was added to make the ion-pairs hydrophobic. The solution was bubbled with 30 mL/min N2 gas for 5 minutes in a flotation cell. Linear calibration curves were obtained for the determination of Zn(Ⅱ) and Pb(Ⅱ) in several water samples. Reproducible results of showing a relative standard deviation of < 10% and recoveries of 80-100% could be obtained.

• Journal of Industrial and Engineering Chemistry
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• 제67권
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• pp.109-122
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• 2018

This work highlights extraction and removal of Lignosulfonate using sunflower oil-Tri-n-octylamine (TOA) system in bulk liquid membrane transport. Maximum extraction and recovery percentages of 92.4% and 75.2% were achieved. Optimum manifold operating conditions were: 4 vol.% TOA, $2{\pm}0.1$ feed phase pH, 300 rpm stirring speed, at $40^{\circ}C$ with 0.2 (M) $Na_2SO_4$ solution. 1:2 (organic/aqueous) and 1:1 (aqueous/aqueous) phase ratios produced best results. Extraction (36.85 kJ/mol) was found to be intermediate controlled and stripping (54.79 kJ/mol) was chemical reaction controlled. Kinetic estimation of data with higher rate constants for stripping vis-${\grave{a}}$-vis extraction showed latter to be rate determining.

• 동아시아식생활학회지
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• 제15권1호
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• pp.100-105
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• 2005

This study was conducted to investigate the extraction characteristics of the polysaccharide from Jeseng mushroom (Fomitopsis pinicola Jeseng). Yields of the polysaccharide extracted from powdered mushroom by autoclaving(120, 30 min) with water at different pH and salt concentration were 8.2～9.2% in pH 5～11, 4.7～5.5% in 1～5% salt solution, respectively. The yield by the 0.05～1.0 N KOH-extraction was ranged 3.45～13.20%, while that by HAS-extraction(homogenizing after KOH swelling) using 1～2.5 N KOH 73.6～78.4%. Content of carbohydrate, protein, lipid and ash of the crude polysaccharide extracted from fruits body and its cultured mycelium by method of water extraction, KOH extraction(0.005～1N) and HAS-extraction were ranged 86.5～92.6%, 2.3～13.1%, 0.1～4.2% and 0.1～1.7%, respectively. The polysaccharide were composed of 62.0～77.8 g/g of pentose, 138.0～187.8 g/g of hexose and 21.2～117.3 mg/g of protein. From these results, the polysaccharide extracted was supposed to be a protein-bound polysaccharide.

• 분석과학
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• 제7권4호
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• pp.493-504
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• 1994

Nb steel에 있어서의 석출물의 형상과 구조를 SEM, TEM과 XRD를 이용하여 연구하였고 추출물들의 정량분석을 ICP-AES를 사용하여 실시하였다. 석출물 추출 방법으로는 정전위 전해추출법을 사용하였고 전해액으로는 10% AA-methanol 용액과 15% Na-citrate 용액을 사용하여 비교하였다. 전해추출 전위는 10% AA-methanol 용액에서는 -100mV, 15% Na-citrate 용액에서는 -250mV로 선택하였고 이 전위에서 Nb 석출물을 분리하는 데 적당하였다. 추출 잔사 중의 $Fe_3C$의 크기는 $0.2{\sim}1.0{\mu}m$ 정도였고 Nb 탄질화물의 크기는 $0.003{\sim}0.1{\mu}m$ 정도였다. 0.1% C-0.007% Nb-0.004% N의 조성을 가진 강에서 Nb 석출물의 조성은 $NbC_{0.65}N_{0.2}$인 것으로 나타나 입방정계의 탄질화물인 것으로 판명되었다.

• Environmental Analysis Health and Toxicology
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• 제16권3호
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• pp.121-126
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• 2001

Analytical method of benzophenone (BP) in sediment and soil was developed by gas chromatography/mass selective detector/selected ion monitoring (GC/MSD/SIM). The ultrasonic extraction of US EPA (method 3550B) method and liquid-liquid extraction for sediment and soil samples were used for the analysis of BP from sediment and soil. BP was extracted with n-hexane. Organic layer was washed with 5% sodium chloride solution. 1∼2 l of the concentrated solution of organic layer was applied to GC/MSD. The retention time of BP peak was 11.10 min. Recovery (％) of BP by ultrasonication from sediment and soil samples was 96.0∼100.6％ and 40.0∼83.0％, respectively. Recovery of BP by liquid-liquid extraction was 51∼59％ in soil samples. The detection limit of BP in sediment and soil samples were determined to 0.1 ng/g.