• 대한화학회지
• /
• 제26권5호
• /
• pp.326-332
• /
• 1982

플루오르화수소산 존재하에서 methylene blue의 양이온과 $BF_4^-$, 음이온이 이루는 착물을 1,2-dichloroethane과 nitrobenzene으로 용매추출하여 분광광도법으로 분석하였다. 적외선과 가시선 스펙트럼을 조사하여 이 착물은 1:1 조성비를 가지는 ion-pair로 존재하는 것으로 보이며 1,2-dichlorethane 중에서는 해리하지 않는 것을 알아냈다. 1,2-Dichlorethane에 대해서는 HF의 농도가 1.43${\times}10^{-2}$~ 2.86${\times}10^{-1}$M 범위에서 추출상수가 25$^{\circ}$C에서 1.1${\times}10^4M{-1}$로 일정한 값을 나타내었으며 nitrobenzene에 대하여는 대체로 10배 가량 큰 값을 가지지만 HF농도가 증가함에 약간씩 증가하였다.

• 한국진공학회:학술대회논문집
• /
• 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
• /
• pp.241.1-241.1
• /
• 2014

The large-area high-power radio-frequency (RF) driven ion sources based on the negative hydrogen (deuterium) ion beam extraction are the major components of neutral beam injection (NBI) systems in future large-scale fusion devices such as an ITER and DEMO. Positive hydrogen (deuterium) RF ion sources were the major components of the second NBI system on ASDEX-U tokamak. A test large-area high-power RF ion source (LAHP-RaFIS) has been developed for steady-state operation at the Korea Atomic Energy Research Institute (KAERI) to extract the positive ions, which can be used for the NBI heating and current drive systems in the present fusion devices, and to extract the negative ions for negative ion-based plasma heating and for future fusion devices such as a Fusion Neutron Source and Korea-DEMO. The test RF ion source consists of a driver region, including a helical antenna and a discharge chamber, and an expansion region. RF power can be transferred at up to 10 kW with a fixed frequency of 2 MHz through an optimized RF matching system. An actively water-cooled Faraday shield is located inside the driver region of the ion source for the stable and steady-state operations of RF discharge. The characteristics and uniformities of the plasma parameter in the RF ion source were measured at the lowest area of the expansion bucket using two RF-compensated electrostatic probes along the direction of the short- and long-dimensions of the expansion region. The plasma parameters in the expansion region were characterized by the variation of loaded RF power (voltage) and filling gas pressure.

• Nuclear Engineering and Technology
• /
• 제23권4호
• /
• pp.426-437
• /
• 1991

SNU 1.5-MV 직렬형 반데그라프 가속기의 $He^{++}$ 빔 수송계를 이온광학적으로 분석하였다. 각 이온광학요소의 최적운전조건을 결정하고, 이온빔 수송을 모사하기 위하여 프로그램 OPTRANS를 개발하였다. 일차행렬법을 사용하였으며, 공간전하효과는 무시하였다. 프로그램 OPTRANS를 사용하여 0.5~3.0 MeV $He^{++}$ 빔 수송을 위한 최적운전조건을 결정하였다. 초기 이온빔의 방사면량은 인출전극의 구조와 이온빔 인출실험에 의해 0.5$\times$80.0 mm.mrad으로 가정하였다. 운전조건의 변화에 따른 각 이온광학요소의 이온빔 수송 특성을 검토하였으며, 각 Slit과 Stripping Foil, 그리고 표적에서 빔 크기가 최소로 되도록 하는 운전조건을 계산하였다. 이온빔 수송 실험으로부터 얻어진 최적운전조건은 계산된 값과 오차 범위 15% 내에서 일치하였다. 이온빔 수송 모사와 실험을 통해, 계산된 최적운전조건의 타당성 및 프로그램 OPTRANS의 유용성을 입증하였다.

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

• Fisheries and Aquatic Sciences
• /
• 제15권3호
• /
• pp.203-207
• /
• 2012

The amount of fluoride removed from Antarctic krill via organic acid extraction depends on the extraction time, concentration, extraction volume, and the nature of the acid itself. The fluoride content in Euphausia superba was determined by measuring the concentration of fluoride ion in acidic extracts using an ion-selective electrode. The best results were obtained by adding 50 mL of 0.01 M citric acid to 0.3-0.5 g of krill and extracting for 5 min. Under these conditions, recoveries of fluoride from frozen whole krill and krill meat were 95.6-99.5% and 97.5-101.3%, respectively. The dry basis fluoride contents of krill by-product, krill meat and the boiled krill were 705, 298, and 575 ppm, respectively. These levels were significantly reduced by citric acid extraction.

• 한국환경과학회지
• /
• 제9권5호
• /
• pp.437-441
• /
• 2000

A study on the removal of Pb ion from Pb-contaminated soil was carried out using ex-site extraction process. Tartaric acid (TA) and iminodiacetic acid sodium salt(IDA) as a washing agent were evaluated as a function of concentration reaction time mixing ratio of washing agent and recycling of washing agent. TA showed a better extraction performance than IDA. The optimum washing condition of TA and IDA were in the ratio of 1:15 and 1:20 between soil and acid solution during 1 hr reaction. The total concentrations of Pb ion by TA and IDA at three repeated extraction were 368.8 ppm and 267.5 ppm respectively. The recovery of Pb ion from washing solution was achieved by adding calcium hydroxide and sodium sulfide form the precipitation of lead hydroxide and lead sulfide and optimum amounts of sodium sulfide and calcium hydroxide were 7 g/$\ell$ for the TA washing solution and 4 g/$\ell$, 5g/$\ell$ for the IDA washing solution respectively. The efficiency of recycle for TA and IDA washing solution were 78.8% , 95.1%, and 89.2%, 96.6% at third extractions under $Na_2S$ and $Ca(OH)_2$, respectively.

• 분석과학
• /
• 제8권4호
• /
• pp.511-517
• /
• 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.

• 유기물자원화
• /
• 제6권1호
• /
• pp.43-52
• /
• 1998

본 연구는 피혁 폐기물로부터 크롬 이온을 분리한 상태로 Collagen을 추출할 수 있는 최적 조건에 관한 것이다. Collagen 추출에 있어 온도, pH, 그리고 알칼리 용액 농도의 영향을 실험했다. 실험결과 점도측정에 의해 초기 변성온도는 $25^{\circ}C$, 완전 변성온도는 $31.5^{\circ}C$였다. Collagen 추출의 최적조건은 가용화 온도 $15^{\circ}C{\sim}20^{\circ}C$, pH 1.5, 알칼리 용액 3%였다. PH 1.5에서 크롬 이온이 거의 분리되었다. 탄닌 폐기물로부터 크롬 이온의 분리효율은 99.5% 이상이었다. 피혁 폐기물로부터 조단백질의 추출율은 89.%이었다. 추출된 조단백질내에 hydroxyprolne과 collagen의 함량은 각각 8.53%, 63.62%였다.

• 분석과학
• /
• 제6권3호
• /
• pp.289-296
• /
• 1993

자연수 중 극미량 몰리브덴[Mo(VI)]을 분리 정량하기 위하여 Mo(VI)의 킬레이트이온을 이온쌍으로 만들어 유기용매로 상승 용매추출시키는 방법에 대해 검토하였다. 자연수 시료 100mL를 분별 깔때기에 취하였다. pH 4.0인 시료에 0.01M alizarin red S 용액 0.5mL를 가하여 Mo(VI)-ARS의 킬레이트이온을 형성시킨 다음, aliquat-336을 0.2% 되게 녹인 chloroform 10mL를 가해 30초 정도 격렬하게 흔들어 모든 킬레이트이온이 이온쌍을 형성하여 용매층으로 분배되도록 하였다. 90분간 방치하여 두 쌍이 완전히 분리되면 chloroform층을 받아서 520nm에서 흡광도를 측정하여 검정곡선법으로 Mo(VI)을 정량하였다. 이상의 과정에서 용액의 pH, alizarin red S와 aliquat-336의 가해 주는 양, 흔들어 주고 방치하는 시간 등과 같은 추출조건에 대해서 검토하였다. 실제 시료인 강물과 수돗물의 분석에 응용하였다. 이들 시료에 Mo(VI)을 일정량 가하여 분석한 회수율은 모두 99% 이상으로 본 방법이 정량적임을 확인하였다.

• 한국재료학회지
• /
• 제12권11호
• /
• pp.860-864
• /
• 2002

$Li^{+}$ extraction reactions with ion-exchange type lithium manganese oxide in an aqueous phase were examined using chemical and x-ray diffraction (XRD) analysis. In the process of extraction reaction, the lithium manganese oxide showed a topotactic extraction of $Li^{+ }$ in the aqueous phase mainly through an ion-exchange mechanism, and the $Li^{+}$ extracted samples indicated a high selectivity and a large capacity for $Li^{+}$ . The electronic structures and chemical bonding properties were also studied using a discrete variational (DV)-X$\alpha$ molecular orbital method with cluster model of (Li$Mn_{12}$ $O_{40}$ )$^{27-}$ for tetrahedral sites and ($Li_{7}$ Mn $O_{38}$ )$^{3}$ for octahedral site in $Li_{1.33}$ $Mn_{1.67}$ / $O_{4}$ respectively. Li in the manganese oxides is highly ionized in both sites, but the net charge of Li was greater for tetrahedral sites than octahedral. These calculations suggest that the tetrahedral sites have higher $Li^{+}$ $H^{+}$ exchangeability than the octahedral sites, and are preferable for the selective adsorption for L $i^{+}$ ions.s.