• 대한화학회지
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• 제15권4호
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• pp.199-203
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• 1971

The adsorption method for the determination of the formation constants of the metal complexes with organic acids was developed by using membrane filters. The adsorption method involved the measurements of radioactivities of the adsorbed metal on membrane filters and the filtrate solution after the radioactive metal ion were filtered through membrane filters in the presence of organic ions of varying concentration. Comparing the adsorption method with the ion exchange method, it was seen that the adsorption method was simpler and faster than the ion exchange method. As an example of the metal complex with organic acid yttrium citrate complex was chosen, and the formation constant of the complex obtained by the adsorption method showed $K_f=2.0{\times}10^{-4}(l. mole^{-1})$ at a pH of 7. Also the present study revealed that the carrierfree state of yttrium in aqueous solution was present in the completely ionized state.

• 대한화학회지
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• 제29권2호
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• pp.178-182
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• 1985

비철특수합금중 아연(II) 구리(II)와 마그네슘(II)을 양이온 교환수지(Dowex 50w${\times}$8, 80-100 mesh)와 음이온 교환수지(IRA-400)을 이용하여 이온교환크로마토그라프로서 분리하는 방법을 연구 하였다. 이온교환수지는 25 ${\times}$ 2cm ID 칼럼에 넣고 흐르는 속도는 0.30 ml/min으로 조절하였다. 아연(II), 구리(II), 마그네슘(II)와 같은 비철금속 이온들을 분리하기 위한 좋은 용리액의 조건은 다음과 같다. 0.5M $NaNO_3$ (pH 3.1), 0.2~0.5M HCl + 50~90% Acetone과 1M HAc + 0.1M NaAcf(pH 3.7)였으며 0.1M NaAc + 1M NaAc(pH 3.7), 0.5M HCl + 50% Acetone이 가장 좋은 용리액으로 판명되었다. 분리된 용출액은 원자흡광 광도계로 측정하였으며 특히 아연 (II)은 음이온 교환수지에서 0.12N HCl과 1.5N $NH_4OH$ 수용액으로 분리하고 E.D.T.A로 적정하였다.

• Carbon letters
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• 제4권1호
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• pp.21-23
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• 2003

In this work, the effect of anodic oxidation treatment on Cr(VI) ion adsorption behaviors of activated carbon fibers (ACFs) was investigated. The aqueous solutions of 10 wt% $H_3PO_4$ and $NH_4OH$ were used for acidic and basic electrolytes, respectively. Surface characteristics and textural properties of ACFs were determined by XPS and $N_2$ adsorption at 77 K. The heavy metal adsorption of ACFs was conducted by ICP. As a result, the adsorption amount of the anodized ACFs was improved in order of B-ACFs > A-ACFs > pristine-ACFs. In case of the anodized treated ACFs, the specific surface area was decreased due to the pore blocking or pore destroying by acidic electrolyte. However, the anodic oxidation led to an increase of the Cr(VI) adsorption, which can be attributed to an increase of oxygen-containing functional groups, such as, carboxylic, lactonic, and phenolic groups. It was clearly found that the Cr(VI) adsorption was largely influenced by the surface functional groups, in spite of the reduced specific surface area of the ACFs.

• Bulletin of the Korean Chemical Society
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• 제21권9호
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• pp.849-854
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• 2000

The protonation and divalent cation complexation equilibria of several quinolone antibiotics such as nalidixic acid (NAL),flumequine (FLU), oxolinic acid (OXO), ofloxacin (OFL), norfloxacin (NOR) and enoxacin (ENO) have been examined by potentiome tric titration and spectrophotometric method. The antibacterial activity of these drugs depends upon the pH and the concentration of metal cations such as Mg2+ , Ca2+ in solu-tion. The apparent ionization constants of NAL, FLU, OXO, OFL, NOR and ENO in aqueous solution were found to be 6.33, 6.51, 6.72, 7.18, 7.26, and 7.53, respectively. In aqueous solution, NAL, FLU and OXO were found to be present mainly as two chemical species : molecularand anionic; but OFL, NOR and ENO were present mainly as three chemical species : anionic, neutral zwitterionic and cationic form, in equilibrium. The pKa1 and pKa2are found to be 6.10 and 8.28 for OFL; 6.23 and 8.55 for NOR; 6.32 and8.62 for ENO, respec-tively. The complex formation constants between OFL, NOR or FLU and some divalent cations are measured at pH 7.5. The 1 : 1 complexes are formed mainly by ion-dipole interaction. FLU has somewhat larger Kf values than OFL and NOR because its molecular size is small and the FLU is present asanionic form at pH 7.5.

• 공업화학
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• 제3권1호
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• pp.100-110
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• 1992

수용액에서 amlne류와 arylsulfonyl carbamate류를 반응시켜 다음과 같은 arylsulfonyl urea유도체들을 좋은 수율로 쉽게 합성할 수 있다 : 1) N-Arylsulfonyl-N'-arylurea 유도체, 2) N-Arylsulfonyl-N'-alkyl urea 유도체, 3) N-Arylsulfonyl-N'-heterocyclic urea 유도체. Arylsulfonyl urea의 합성에 관한 반응메카니즘은, 먼저 산-염기 반응에 의해 ion-pair형태가 만들어지고, 그 다음 사면체형 중간체를 형성하는 친핵성첨가반응, 그리고 산촉매에 의한 alkoxide ion과 양성자의 제거반응에 따라 일어난다.

• 상하수도학회지
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• 제33권2호
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• pp.131-140
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• 2019

This study used a packed column reactor and a horizontal flow mesh reactor to examine the removal of copper ions from aqueous solutions using pine bark, a natural adsorbent prepared from Korean red pine (Pinus densiflora). Both equilibrium and nonequilibrium adsorption experiments were conducted on copper ion concentrations of 10mg/L, and the removals of copper ions at equilibrium were close to 95%. Adsorption of copper ions could be well described by both the Langmuir and Freundlich adsorption isotherms. The bark was treated with nitric acid to enhance efficiency of copper removal, and sorption capacity was improved by about 48% at equilibrium; mechanisms such as ion exchange and chelation may have been involved in the sorption process. A pseudo second-order kinetic model described the kinetic behavior of the copper ion adsorption onto the bark. Regeneration with nitric acid resulted in extended use of spent bark in the packed column. The horizontal flow mesh reactor allowed approximately 80% removal efficiency, demonstrating its operational flexibility and the potential for its practical use as a bark filter reactor.

• 공업화학
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• 제34권1호
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• pp.64-68
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• 2023

전기투석에서 농축 공정은 전기 에너지를 이용하여 전해질 수용액 상의 이온의 농도를 증가시키는 기술로, 이온교환막에서 일어나는 이온과 물 분자의 전달 현상에 대해 많은 연구들이 진행되고 있다. 본 연구에서는 전기투석 시스템에서 고농도 전해질 수용액의 전기 삼투에 의한 농축 현상에 대한 실험을 통해 한계 농축 현상에 대한 변수를 분석한다. 두 가지 전해질 수용액(NaCl 2M / 4M)에 대해 이온과 물 분자의 투과량을 측정해 전기 삼투 현상을 분석하였고, 농축조 대비 탈염조의 부피 비에 따른 한계 농축 현상을 관찰하였다. 실험 결과, 전해질 수용액의 농도가 높을수록 전기 삼투가 감소하였고, 부피 비가 클수록 탈염수의 농도가 높게 유지되기 때문에 한계 농축 농도가 증가하고 비에너지 소모가 감소됨을 확인하였다.

• 상하수도학회지
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• 제23권1호
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• pp.113-119
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• 2009

The feasibility of using cork oak bark for phosphorus removal from wastewater was evaluated in this study. Recently, development of more cost-effective media while maintaining high efficiency in pollutants removal has received concern. Barks have a negative surface charge and, hence, tend to show a high affinity to bind cations, and they need to undergo chemical modification to increase their adsorption capacity of anions. Bark was hydrolyzed by HCl solution and it received modification using an aqueous solution of high molecular weight polyethylenimine(PEI). Surface modification with HCl and PEI resulted in a decrease of specific surface area of the bark from $1.932 m^2/g$ to $1.094 m^2/g$. The adsorption experiments were carried out in batch tests and the data were fitted to the Langmuir isotherm and Freundlich isotherm equations. Phosphate removal rate was higher at the lower solution pH possibly due to the form of phosphate ion in solution. For the initial phosphate concentration of 10 mg/L, maximum adsorption was 20.88 mg P/g at pH 3 and 12.02 mg P/g at pH 5. Mechanism of phosphorus sorption onto the HCl-PEI bark was examined through FT-IR spectrometer. Ion exchange between $NH^+$ and $H_2PO_4{^-}$ appeared to be a key mechanism of phosphate adsorption onto the HCl-PEI bark surface.

• 한국대기환경학회지
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• 제24권6호
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• pp.674-681
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• 2008

Silver as a metal catalyst has been used to remove odorous compounds. In this study, silver particles in nano sizes ($5{\sim}30nm$) were prepared on the surface of $NaHCO_3$, the supporting material, using a sputtering method. The silver nano-particles were dispersed by dissolving $Ag-NaHCO_3$ into water, and the dispersed silver nano-particles in the aqueous phase was applied to remove inorganic odor compounds, $NH_3$ and ${H_2}O$, in a scrubbing reactor. Since ammonia has high solubility, it was removed from the gas phase even by spraying water in the scrubber. However, the concentration of nitrate (${NO_3}^-$) ion increased only in the silver nano-particle solution, implying that the silver nano-particles oxidized ammonia. Hydrogen sulfide in the gas phase was rapidly removed by the silver nano-particles, and the concentration of sulfate (${SO_4}^{2-}$) ion increased with time due to the oxidation reaction by silver. As a result, the silver nano-particles in the aqueous solution can be successfully applied to remove odorous compounds without adding additional energy sources and producing any harmful byproducts.

• 약학회지
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• 제43권3호
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• pp.289-293
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• 1999

Many poly (vinyl chloride : PVC) membrane electrodes were investigated for the determination of basic drugs, chlorpromazine, amitriptyline, nortriptyline, etc. These electrodes are based on the use of the ion-association complexes of the basic drugs with eriochrome cyanine R, chromoxane cyanine, chrome azurol S and picric acid as ion-exchange sites in a plasticized PVC matrix. All ion-exchangers except picrate complex were not proper for use, because those complexes in plasticized membrane were excluded into aqueous working solution. These drug electrodes show excellent Nernstian responses in the concentration ranges $10^{-2}~10^{-6}$ mol $dm^{-3}$. Their selectivity with respect to each other, as well as their work-able pH range have been investigated. The major advantages of the proposed methods are their simplicity and speed.