• 분석과학
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• 제24권4호
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• pp.298-303
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• 2011

셀레늄은 인체의 필수영양소로써 환경에서 또한 많은 관심을 가지고 있는 원소이다. 셀레늄은 자연수에서 주로 +4가의 selenite ($SeO_3^{-2}$)와 +6가의 selenate ($SeO_4^{2-}$)로 용해되어 있는데, 이들의 독성 및 화학적 성질은 매우 다르다. 따라서 자연수에서 셀레늄의 거동을 이해하기 위해서는 이들 두 화학종을 분리하는 것이 필요하다. 기존에 알려진 알루미나 충전 컬럼과 이온크로마토그래피를 이용한 selenite와 selenate의 분리방법들은 silicate 때문에 자연수에 직접 적용하기가 곤란하였다. 따라서 마그네타이트가 용액의 pH에 따라 selenite와 selenate를 흡착하는 정도가 다르므로 마그네타이트가 충전된 컬럼을 이용하여 이들의 분리를 수행한 결과, 성공적으로 분리할 수 있었다. 아울러 자연수에 존재하는 다른 음이온들 중에서 silicate는 selenite의 흡착을 방해하므로 silicate의 농도를 고려하여 충분한 양의 마그네타이트를 사용하여야만 한다.

• 공업화학
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• 제8권4호
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• pp.679-684
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• 1997

석유화학공업에서 사용된 유동접촉분해(FCC) 폐촉매의 주성분은 Si와 Al이며, 그외에 Fe, Zn, Ti 등의 기본금속과 알칼리금속 및 Ce, Nd, Ni, V 등의 희유금속이 함유되어 있다. $0.25mo1/dm^3-H_2SO_4$를 침출제로 폐촉매를 침출하였을 때 Ce가 640, Nd가 310, 그리고 V가 $450mg/dm^3$ 함유된 pH 1.0의 침출액을 얻었고, 아미노인산형 킬레이트수지에 의하여 Ce와 Nd를 선택흡착시킨 후, $4.0mol/dm^3-HCl$로 용리시켜 $1.2g/dm^3$의 Ce와 $0.75 g/dm^3$의 Nd 농축액을 얻었다. 농축액을 다시 옥살산 침전 및 공기산화법으로 처리하여 Ce와 Nd의 분리가 가능하였으며, 염소이온 공존하에 추출제 TOPO를 이용한 용매추출법으로 V와 Al을 각각 분리시켜, FCC 폐촉매로부터 순도가 99%인 Ce, Nd 및 V의 분리정제가 가능하였다.

• 대한전자공학회:학술대회논문집
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• 대한전자공학회 2001년도 The 6th International Symposium of East Asian Resources Recycling Technology
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• pp.259-263
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• 2001

There are several steps such as slicing, lapping, chemical etching and mechanical polishing in the silicon wafer production process. The chemical etching step is necessary to remove damaged layer caused In the slicing and lapping steps. The typical etching liquor is the acid mixture comprising nitric acid, acetic acid and hydrofluoric acid. At present, the waste acid is treated by a neutralization method with a high alkali cost and balky solid residue. A solvent extraction method is applicable to separate and recover each acid. Acetic acid is first separated from the waste liquor using 2-ethlyhexyl alcohols as an extractant. Then, nitric acid is recovered using TBP(Tri-butyl phosphate) as an extractant. Finally hydrofluoric acid is separated with the TBP solvent extraction. The expected recovered acids in this process are 2㏖/l acetic acid, 6㏖/1 nitric acid and 6㏖/l hydrofluoric acid. The yields of this process are almost 100% for acetic acid and nitric acid. On the other hand, it is important to recover and reuse the metal values contained in various industrial wastes in a viewpoint of environmental preservation. Most of industrial products are made through the processes to separate impurities in raw materials, solid and liquid wastes being necessarily discharged as industrial wastes. Chemical methods such as solvent extraction, ion exchange and membrane, and physical methods such as heavy media separation, magnetic separation and electrostatic separation are considered as the methods for separation and recovery of the metal values from the wastes. Some examples of the application of solvent extraction to the treatment of wastes such as Ni-Co alloy scrap, Sm-Co alloy scrap, fly ash and flue dust, and liquid wastes such as plating solution, the rinse solution, etching solution and pickling solution are introduced.

• Journal of Electrochemical Science and Technology
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• 제11권1호
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• pp.60-67
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• 2020

In this study, copper (II) oxide powder for electroplating was prepared by recovering CuCl₂ from NaClO₃ type etching wastes via recovered non-sintering two step chemical reaction. In case of alkali copper carbonate [mCuCo₃·nCu(OH)₂], first reaction product, CuCo₃ is produced more than Cu(OH)₂ when the reaction molar ratio of sodium carbonate is low, since m is larger than n. As the reaction molar ratio of sodium carbonate increased, m is larger than n and Cu(OH)₂ was produced more than CuCO₃. In the case of m has same values as n, the optimum reaction mole ratio was 1.44 at the reaction temperature of 80℃ based on the theoretical copper content of 57.5 wt. %. The optimum amount of sodium hydroxide was 120 g at 80℃ for production of copper (II) oxide prepared by using basic copper carbonate product of first reaction. At this time, the yield of copper (II) oxide was 96.6 wt.%. Also, the chloride ion concentration was 9.7 mg/L. The properties of produced copper (II) oxide such as mean particle size, dissolution time for sulfuric acid, and repose angle were 19.5 mm, 64 second, and 34.8°, respectively. As a result of the hole filling test, it was found that the copper oxide (II) prepared with 120 g of sodium hydroxide, the optimum amount of basic hydroxide for copper carbonate, has a hole filling of 11.0 mm, which satisfies the general hole filling management range of 15 mm or less.

• 한국응용과학기술학회지
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• 제32권1호
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• pp.116-126
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• 2015

본 연구에서는 이산화탄소 고정화에 있어 이산화탄소 전환을 위해 MEA를 이용한 습식화학흡수법의 셔틀메카니즘을 도입하였다. 또한 알칼리 무기물질을 다량 함유한 산업부산물을 습식탄산화법을 이용해 처리하고자 하였다. 즉, 산업부산물의 화학적 처리를 통해 칼슘이온을 용출하였다. 산성물질을 이용한 용출상징수를 ICP로 분석한 결과, 칼슘이온이 최대 17,900 ppm(1.79%)을 확보하였다. 또한 MEA를 이용한 습식 흡수공정을 통해 상온, 상압조건의 이산화탄소 분위기에서 94%의 전환률을 얻었다. 슬러지의 액상탄산화를 통해 슬러지 mg 당 0.175 mg의 이산화탄소를 고정하였으며, 최종생성물의 XRD 분석결과 일반적인 탄산칼슘의 결정구조인 calcite 형상을 확인하였다.

• 한국염색가공학회지
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• 제11권1호
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• pp.16-24
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• 1999

The effects of two-step fixation of steaming and baking on the dischargeability of cotton fabrics dyed with C.I. Reactive Black 5(Bl-5) were investigated when the concentrations of $K_2CO_3$ and benzaldehyde sodium bisulfite(BASB) were increased over 120/kg. Remarkably increased dischargeability resulted from baking for 3 min or more at 160t after steaming for 8 min or more at $102^\circ{C}$, but 120g/kg or more amounts of $K_2CO_3$ and BASB(50%) had little influence on dischargeability. Therefore the discharge mechanism can be suggested that covalent bonds between cellulose and Bl-5 undergo $S_N2$ attack by hydroxide ion formed by the reaction of $K_2CO_3$ and water in steaming at $102^\circ{C}$ first and then, through transition states they are cleavaged in baking at 160t to yield hydrolyzed Bl-S and compounds of BASB and Bl-5 isolated from fiber, which are undyeable and removed by washing. The effect of urea, one of the hydrotrope agents, on discharge printing was also studied. The result which dischargeability was greatly improved by increasing the steaming time from 8 min to 15 min at $102^\circ{C}$ or by increasing the amount of urea obviously shows that water in steaming and urea in print paste play an important role in discharge printing. And as an increase of the baking time from 5 min to 7 min at $160^\circ{C}$ makes it possible to improve dischargeability, it is once more confirmed that high temperature of about 160t is exactly required to discharge the dyed Bl-5. The colored discharge printing demands a more amount of urea because urea contributes to the putting color fixation as well as the discharge reaction.

• Journal of Microbiology and Biotechnology
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• 제16권2호
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• pp.247-255
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• 2006

Yeast cell wall matrix particles are composed entirely of mannoprotein and ${\beta}-glucan$. The mannoproteins of yeast cell wall can systemically enhance the immune system. We previously purified and analyzed alkali-soluble ${\beta}-glucans$ [${\beta}$-(1,3)- and ${\beta}$-(1,6)-glucans] [10]. In the present study, a wild-type strain was first mutagenized with ultraviolet light, and the cell wall mutants were then selected by treatment with 1.0 mg/ml laminarinase (endo-${\beta}$-(1,3)-D-glucanase). Mannoproteins of Saccharomyces cerevisiae were released by laminarinase, purified by concanavalin-A affinity and ion-exchange chromatography. The results indicated that the mutants yielded 3-fold more mannoprotein than the wild-type. The mannoprotein mass of mutant K48L3 was 2.25 mg/100 mg of yeast cell dry mass. Carbohydrate analysis revealed that they contained mannose, glucose, and N-acetylglucosamine. Saccharomyces cerevisiae cell wall components, mannoproteins, are known to interact with macrophages through receptors, thereby inducing release of tumor necrosis factor alpha ($TNF-{\alpha}$) and nitric oxide. Mannoprotein tractions in the present study had a higher macrophage activity of secretion of $TNF-{\alpha}$ and nitric oxide and direct phagocytosis than positive control ($1{\mu}g$ of lipopolysaccharide). In particular, F1 and F3 fractions in mannoproteins of K48L3 enhanced and upregulated the activity of nitric oxide secretion and macrophage phagocytosis by approximately two- and four-fold, respectively.

• 생약학회지
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• 제1권3호
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• pp.93-99
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• 1970

There have been reported by several workers for the isolation and determination of the amine derivatives as Metbylephedrine Hydrochloride and Ephedrine Hydrochloride adopting neutralization method, steam distillation method, non-aqous titration method, ion-exchange resin method, titration method after acetylation, colorimetric method, gravimetric method, iodine titration method and gas chromatography. Those methods mentioned in above, can be practically applied for the sample which is not mixed one mith the other amine compounds. Presently, it has not shown on the isolative determination of the mixed sample of amine derivatives. In this paper, it is discussed on the isolative determination of Methylephedrine Hydrochloride as the tertiary amine compound and Ephedrine Hydrochloride as the secondary amine compound. According to the results of the experiment, it could be summarized as follows: 1. There is no time-variation on the color reaction of Methylephedrine Hydrochloride and Ephedrine Hydrochloride with the color reagent, bromcresolgreen. And Methylephedrine Hydrochloride and Ephedrine Hydrochloride, respectively, can be determined spectrophotometrically by means oft his color reaction. 2. For the isolation of Methylephedrine Hydrochloride and Ephedrine Hydrochloride from the mixed sample, Methylephedrine Hydrochloride can be eluted by chloroform, while Ephedrine Hydrochloride by the mixed solvent of chloroform and ethylalcohol (2:1), from the celite column adsorbed at pH6.4 followed by extraction with ether undersodium hydroxide alkali re action. 3. When the sample is mixed with quinine hydrochloride, dihydrocodeine bitartate, and noscapine, these mixed compounds can be eliminated by means of stram distillation. 4. When the sample is mixed with chlorpheniramine maleate, dextromethorphan hydrobromide and diphenhydramine hydrochloride, the mixed compounds can be eliminated by means of steam distillation and celite adsorption column chromatography, In conclusion, the isolative determination method for Methylephedrine Hydrochloride and Ephedrine Hydrochloride studied in this paper, indicates with the excellent reproducibility and accuracy.

• 분석과학
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• 제8권4호
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• pp.675-682
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• 1995

Thin films of buckminsterfullerene($C_{60}$) formed by solution drop casting on Pt foil electrode surfaces were studied by cyclic voltammetry(CV) in acetonitrile(MeCN) containing quaternary ammonium or alkali-metal salts as supporting electrolyte. The electrochemical behaviors of $C_{60}$ films are found to be strongly dependent on the nature of the supporting electrolytes, especially with tetrabutyl ammonium perchlorate (TBAP, $NBu_4ClO_4$), and tetrabutyl ammonium tetrafluoroborate ($TBABF_4$, $NBu_4BF_4$). Reasonably stable films are formed into which electrons can be injected. The interaction of $C_{60}$ film with the quaternary ammonium cation may produce the fulleride salts $(TBA^+)(C{_{60}}^-)$ and $(TBA^+)_2(C{_{60}}^{2-})$. The bulk electroreduction with a controlled potential to generate the soluble $C{_{60}}^{3-}$ anions(dark red-brown color) is followed by electrooxidative deposition to produce a neutral $C_{60}$ film on the surface. The peak currents($I_{pc}$ and $I_{pa}$) of these thin film were dramatically decreased with repetitive potential scanning. These results could be explained by the adsorption-desorption phenomena and ion pairing interaction of reduced species($C{_{60}}^-$, and $C{_{60}}^{2-}$) onto the electrode surface. The peak current changes and peak potential shifts of the thin $C_{60}$ film in cyclic voltammograms formed from solution were observed by varying scan rates.

• 자원환경지질
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• 제29권4호
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• pp.483-493
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• 1996

중부 옥천대에 분포하는 대보 화강암질 저반의 주원소, 미량원소 조성으로부터 조구조환경과 기원물질의 특징을 연구하였다. 화강암류는 흑운모 화강암, 조립질 반상화강암 및 화강섬록암으로 나눌 수 있다. 화강암류의 불규칙적인 Na, K 함량변화는 분별정출작용만으로 설명될 수 없고 기원물질의 불균질성이나 다양한 기원물질의 불완전한 혼합을 반영하는 것으로 생각된다. 대보 화강암에서 나타나는 친석 원소(LIL element)의 부화와 낮은 Ta/Hf비는 정상적인 칼크 알칼리 계열의 대륙 연변부 호 화강암의 특징과 부합된다. 희토류원소 변화양상으로 보아 $SO_2$ 함량이 높은 흑운모 화강암을 보다 염기성인 화강섬록암의 후기 분화체로 보기는 어렵다. 대보 화강암의 ${\varepsilon}_{Nd}(t)$값과 친석 원소의 함량은 서로 체계적인 변화를 보이지 않아 그들의 지화학적 특징이 초생적인 용융체와 지각 물질 사이의 혼합에 의해 규정되었을 가능성을 배제한다. 대보 화강암의 지구화학적 특징은 주로 기원물질의 고유한 불균질성을 반영한다고 보아진다.