• 제목/요약/키워드: Metal chloride solution

검색결과 130건 처리시간 0.031초

Dithiocarbamate 금속착물의 용매추출 및 분석적 응용(제2보) Dibenzylammonium dibenzyldithiocarbamate 금속착물의 추출평형 (Studies on Solvent Extraction and Analytical Application of Metal Dithiocarbamate Complexes(II). Extraction Equilibria of Metal-Dibenzylammonium dibenzyldithiocarbamate Complexes)

  • 이종선;최종문;최희선;김영상
    • 분석과학
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    • 제9권3호
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    • pp.221-234
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    • 1996
  • 흔적량 금속이온인 Ag(I), Pd(II), Au(III) 및 Pt(IV)의 dibenzylammonium dibenzyldithiocarbamate(DBADBDC) 착물을 용매추출하기 위한 기초적인 연구를 수행하였다. 클로로포름으로 리간드 및 금속착물을 추출하기 위한 pH의 영향을 조사한 결과, DBADBDC는 pH 2~9에서 일정하게 추출되었으며 금속착물의 경우 Ag(I)는 산성용액에서, Pd(II) 는 pH 4 이상에서, Au(III)는 모든 pH 영역에서, Pt(IV)는 pH 3 이상에서 일정하게 추출되었다. 금속-DBDC 착물의 수용액과 용매간 분배 및 추출평형에서 분포비와 추출률은 Ag(I)의 경우 pH 0에서 log D=4.226 : E(%)=99.9%, Pd(II)는 pH 4~7에서 log D=1.804 ; E(%)=98.5%, Au(III)는 pH 2~10에서 log D=3.755: E(%)=99.9%, Pt(IV)는 pH 8에서 log D=0.165 : E(%)=57.2%의 최대값을 나타내었다. 몰비법으로 금속이온과 리간드가 착물을 형성할 때의 결합비를 조사해 보았다. Ag(I)는 1 : 1, Pd(II), Au(III) 및 Pt(IV)는 1 : 2의 착물을 형성하였으며, Au(III) 와 Pt(IV)는 착물내에 염화이온이 포함되어 있었다. 수용액에 염화이온이 존재할 때의 금속-클로로 착물의 추출반응을 규명할 수 있었으며, 각 금속이온을 착화제인 DBADBDC로보 추출할 때 각각의 추출반응과 상수식을 얻을 수 있었다.

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중금속이 토양용액 중 화학종 변화에 미치는 영향 (Changes of Chemical Species in Soil Solution Induced by Heavy Metals)

  • 양재의;이기원;김정제;임형식
    • 한국환경농학회지
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    • 제14권3호
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    • pp.263-271
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    • 1995
  • 중금속에 의한 토양오염을 화학적으로 평가하기 위한 일환으로 토양을 중금속으로 오염시킨 후 토양용액을 추출하여 pH, 이온강도, 이온농도, 화합물형태 변화를 분석했다. 토양이 Cu와 Cd에 의해 오염될수록 토양용액의 이온강도는 증가했다. 이런 변화는 Cd보다 Cu에 의해 더 컸다. 토양용액 중의 Cu와 Cd의 농도는 가한 양(量)에 비해 소량으로 존재했으나 처리량에 비례하여 금속의 농도는 증가했다. 토양용액 중의 Cd의 농도는 Cu보다 훨씬 높았다. 토양용액 중의 Ca, Mg, K의 농도는 중금속에 의해 증가되었으나 주로 free ion상태로 존재했으며 화합물형태는 Cu나 Cd의 처리에 의해 변화되지 않았다. 토양용액 중 중금속이온의 화합물의 변화 경향은 Cu와 Cd이 달랐다. Cu의 경우 토성과 pH에 의해 영향을 받았는데 pH가 낮은 SiCL 및 SL 토양에서는 free $Cu^{2+}$가 95 molar % 이상으로 주된 화합물형태이었고 pH가 높은 LS토양의 경우 free $Cu^{2+}$과 Cu-hydroxide이 주된 화합물형태로 Cu처리량에 따라 이들 화학종의 molar %는 변화되었다. Cd의 경우 free $Cd^{2+}$과 Cd-chloride 화합물이 주된 화합물형태이었고 Cd처리량이 증가함에 따라 $Cd^{2+}$는 감소한 반면 Cd-chloride 화합물 형성은 증가했다. 중금속에 의한 토양용액의 pH감소, 중금속의 흡착에 따른 양이온의 일시적인 증가, 중금속의 화합물 변화들은 식물영양적 측면에서 볼 때 식물에 불리한 변화로 간주되며, 중금속의 생물유효성과 독성을 평가하는 자료로 활용될 수 있을 것이다.

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MWCNT, silver nanoparticles, CuBTC를 사용한 염소 이온 센서 합성

  • 곽병관;박수빈;유봉영
    • 한국표면공학회:학술대회논문집
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    • 한국표면공학회 2018년도 춘계학술대회 논문집
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    • pp.101-101
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    • 2018
  • Quantitative measurement of chloride ion concentration has an important role in various fields of electrochemistry, medical science, biology, metallurgy, architecture, etc. Among them, its importance of architecture is ever-growing due to unexpected degradations of building structure. These situations are caused by corrosion of reinforced concrete (RC) structure of buildings. And chloride ions are the most powerful factors of RC structure corrosion. Therefore, precise inspection of chloride ion concentration must be required to increase the accuracy of durability monitoring. Multi-walled Carbon nanotubes (MWCNTs) have high chemical resistivity, large surface area and superior electrical property. Thus, it is suitable for the channels of electrical signals made by the sensor. Silver nanoparticles were added to giving the sensing property. CuBTC, one of the metal organic frameworks (MOFs), was employed as a material to improve the sensing property because of its hydrophilicity and high surface area to volume ratio. In this study, sensing element was synthesized by various chemical reaction procedures. At first, MWCNTs were functionalized with a mixture of sulfuric acid and nitric acid because of enhancement of solubility in solution and surface activation. And functionalized MWCNTs, silver nanoparticles, and CuBTC were synthesized on PTFE membrane, one by one. Electroless deposition process was performed to deposit the silver nanoparticles. CuBTC was produced by room temperature synthesis. Surface morphology and composition analysis were characterized by scanning electron microscope (SEM), energy dispersive X-ray spectroscopy (EDS), respectively. X-ray photoelectron spectroscopy (XPS) was also performed to confirm the existence of sensing materials. The electrical properties of sensor were measured by semiconductor analyzer. The chloride ion sensing characteristics were confirmed with the variation of the resistance at 1 V.

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탄소강 볼트 체결된 GECM(Graphite Epoxy Composite Material)/Al 판재 간의 갈바닉 부식 거동 (Galvanic Corrosion Behavior between Carbon Steel Bolted GECM(Graphite Epoxy Composite Material)/Al plates)

  • 김영식;박수진;유영란
    • Corrosion Science and Technology
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    • 제12권1호
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    • pp.12-26
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    • 2013
  • This work focused on galvanic corrosion of carbon steel bolted GECM/Al plates by long-term test in tap water and NaCl solutions. Test product was carbon steel bolted between cross packed GECM and painted aluminium. Tests for the product and coupled parts determined corrosion rate in tap water and NaCl solutions. Also, using a potentiostat and salt water sprayer, galvanic test was done. In galvanic test on carbon steel bolted GECM/Al plates, corrosion of carbon steel bolt was faster in series of tap water>1% NaCl solution>3.5% NaCl solution. In galvanic couple between aluminium and carbon steel bolt, their corrosion rates were higher than those of single specimen. In galvanic couple between GECM, aluminium, and carbon steel bolt, corrosion behaviors of carbon steel bolt and aluminium were changed due to different corrosion mechanism in tap water and chloride solution.

사진폐액으로부터 용매추출에 의한 은의 제거 및 회수에 대한 기초연구 (Fundamental Studies for the Removal and Recovery of Silver from Waste Photo-Developing Solution by Solvent Extraction)

  • 이선화;김동수;이화영
    • 한국물환경학회지
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    • 제22권1호
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    • pp.122-127
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    • 2006
  • Fundamental studies were carried out for an effective removal and recovery of silver from waste photo-developing solution by solvent extraction. The organic solvents examined for silver-extraction were ALIQUAT 336, D2EHPA, KELEX 100, and TBP. ALIQUAT 336, which is an anionic exchanger, was found to be efficient for the extraction of silver and the reason for this was considered to be due to the chloride ion contained in its structure. The extent of silver extraction was examined to increase with the concentration of ALIQUAT 336 until it reached 0.6 M and no more extraction was observed above this concentration. The extraction of silver by ALIQUAT 336 was found to reach its pseudo-equilibrium within a few minutes after the reaction started and additional slight increase in silver extraction was observed until 30 minutes of reaction time. The observed differences in silver extraction for artificial and actual waste solutions were considered to be based upon the different ionic form of silver-containing species in these solutions.

Voltammetric Determination of Copper(II) at Chemically Modified Carbon Paste Electrodes Containing Alga

  • Bae, Zun-Ung;Kim, Young-Lark;Chang, Hye-Young
    • 분석과학
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    • 제8권4호
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    • pp.611-615
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    • 1995
  • The design of appropriate chemically modified electrodes should allow development of new voltammetric measurement schemes with enhanced selectivity and sensitivity. Microorganism like algae has high ability to trap toxic and heavy metal ions and different affinities for metal ions. A copper(II) ion-selective carbon paste electrode was constructed by incorporating alga Anabaena into a conventional carbon paste mixture, and then the film of 10% Nafion was coated to avoid the swelling of the electrode surface. Copper ion could be deposited at the 25% algamodified electrode for 15 min without the applied potential while stirring the solution by only immersing the electrode in a buffer (pH 4.0) cot1taining copper(II). Temperature was controlled at $35^{\circ}C$. After preconcentration was carried out the electrode was transferred to a 0.1 M potassium chloride solution and was reduced at -0.6 volt at $25^{\circ}C$. The differential pulse anodic stripping voltammetry was employed. A well-defined oxidation peak could be obtained at -0.1 volt (vs SCE). In five deposition / measurement / regeneration cycles, the responses were reproducible and relative standard deviations were 3.3% for $8.0{\times}10^{-4}M$ copper(II). Calibration curve for copper was linear over the range from $2.0{\times}10^{-4}M$ to $1.0{\times}10^{-3}M$. The detection limit was $7.5{\times}10^{-5}M$. Studies of the effect of diverse ions showed that the coexisting metal ions had little or no effect for the determination of copper. But anions such as cyanide. oxalate and EDTA seriously interfered.

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크라온에테르를 이용한 탈륨(I) 이온 선택성 전극 (Tallium(I) Ion-Selective Electrodes Based on Crown Ethers)

  • 김성민;정성욱;김진은;김재상
    • 대한화학회지
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    • 제37권8호
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    • pp.773-778
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    • 1993
  • Tl$^+$이온 센서로서 크라운 에테르 B15C5와 DB18C6를 중성운반체로 한 PVC 액체막 이온 선택성 전극을 제작하였다. 막용매로는 DOA, NPPE 및 NPOE를 사용하였으며 친유성 염, KTClPB의 농도를 변화시킨 여러가지 조성의 막을 시험하였다. B15C5와 DB18C6 막 전극의 감응전위는 농도범위, 10$^{-1}$∼10$^{-5}$M에서 직선으로 나타났으며 최대 기울기는 전극에 따라서 40∼55 mV/decade였다. 선택계수는 분리용액법으로 결정하였으며 알카리금속 이온, 알칼리토금속 이온 및 일부 전이금속 이온에 대하여 좋은 선택성을 나타냈다. 제작된 액체막 전극은 Ph > 3 에서 안정한 감응전위를 보였다.

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Sol-Gel and photoreduction 공정에 의한 Au 미립자분산 $TiO_{2}$ 박막 제조 (Preparation of Au fine particle dispersedf $TiO_{2}$ film by sol-gel and photoreduction process)

  • 현부성;김병일;강원호
    • 한국결정성장학회지
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    • 제9권1호
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    • pp.23-28
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    • 1999
  • Au 미립자가 분산된 $TiO_{2}$ 박막을 졸겔담금법과 열처리공정으로 실리카 유리기판위에 제조하였다. $TiO_{2}$ 박막제조는 titanium tetraisopropoxide-EtOH-HCl-$H_{2}O$-hydrogen tetrachloroaurat (III) tetrahydrate계를 이용하였다. 고농도로 Au 화합물을 함유하면서 투명한 코팅용액을 형성하는 조건을 검토하였다. Au 금속미립자의 크기를 조절하기 위하여 광환원공정을 채택하였다. UV 조사에 따른 Au 입자의 변화와 $TiO_{2}$ 매트릭스의 상전이과정을 XRD, SEM, TEM and UV-visible spectrophotometer로 관찰하였다. 분산제로서 CPCl (Cetylpyridinium chloride monohydrate)의 효과를 평가하였다.

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마그네슘환원에 의한 지르코늄-티타늄 합금분말 합성 (Synthesis of Zr-Ti Alloy Powder by Magnesium Reduction)

  • 이동원;박근태;임태수;이혜문;유지훈
    • 한국분말재료학회지
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    • 제18권4호
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    • pp.359-364
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    • 2011
  • Zr-Ti alloy powders were successfully synthesized by magnesium thermal reduction of metal chlorides. The evaporated and mixed gasses of $ZrCl_4+TiCl_4$ were injected to liquid magnesium and the chloride components were reduced by magnesium leading to the formation of $MgCl_2$. The released Zr and Ti atoms were then condensed to particle forms inside the mixture of liquid magnesium and magnesium chloride, which could be dissolved fully in post process by 1~5% HCl solution at room temperature. By the fraction-control of individually injected $ZrCl_4$ and $TiCl_4$ gasses, the final compositions of produced alloy powders were changed in the ranges of Zr-0 wt.%~20 wt.%Ti and their purity and particle size were about 99.4% and the level of several micrometers, respectively.

염산 독소루비신 주사액의 안정화 (Stabilization of Doxorubicin Hydrochloride in Injections)

  • 이상철;남상철;김춘성;신현종;백우현
    • Journal of Pharmaceutical Investigation
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    • 제24권3호
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    • pp.109-113
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    • 1994
  • Effects of various formulation factors using $L_8$ orthogonal arrays with the stability of doxorubicin hydrochloride injections(DHls) were investigated. The degradation of DHI may be occured by pH, temperature, light and metal ions. It is known that DHI should be stored on refrigerated condition of $4{\sim}8^{\circ}C$ because of its unstability on the room temperature. The employed factors were sodium chloride as isotonic solution, sodium bisulfite or sodium pyrosulfite as an antioxidant, disodium edetate as a chelating agent, methyl parahydroxybenzoate as a dissolution time shortening agent, and hydrochloric acid or citric acid as a pH adjusting agent at $22^{\circ}C$. From the results of $L_8$ orthogonal arrays, an optimal formula, including sodium chloride, disodium edetate, sodium bisulfite and hydrochloric acid, was obtained and the shelf-life of the formula was determined as 560 days approximately.

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