• 한국환경과학회지
• /
• 제16권8호
• /
• pp.907-912
• /
• 2007

Ion exchange resin was used to remove silica ion at ultralow concentration. The effects of temperature, type of ion exchange resin and single/mixed-resin systems on removal efficiency were estimated. As temperature increased, the slope of concentration profile became stiff, and the equilibrium concentration was higher. In the single resin system, the removal of silica was continued up to 400 min, but the silica concentration was recovered to initial concentration after 400 min due to the effect of dissolved $CO_2$. In the mixed-resin system it took about 600 min to reach equilibrium. Because of faster cation exchange reaction than anion exchange reaction, the effect of $CO_2$ could be removed. Based on the experimental results carried out in the mixed-resin system, the selectivity coefficients of silica ion for each ion exchange resin were calculated at some specific temperatures. The temperature dependency of the selectivity coefficient was expressed by the equation of Kraus-Raridon type.

• Bulletin of the Korean Chemical Society
• /
• 제22권4호
• /
• pp.405-408
• /
• 2001

New lipophilic triesters of calix[4]arene and calix[4]quinone are investigated as sodium ion-selective ionophores in poly(vinyl chloride) membrane electrodes. For an ion selective electrode based on calix[4]arene triester I, the linear response is 1 ${\times}$10-3.5 to 1 ${\times}$ 10-1 M of Na+ concentrations. The selectivity coefficients for sodium ion over alkali metal and ammonium ions are determined. The detection limit (logaNa+ = -4.50) and the selectivity coefficient (logKNa+,K+pot = -1.86) are obtained for polymeric membrane electrode containing calix[4]arene triester I.

• 한국안전학회지
• /
• 제6권4호
• /
• pp.13-20
• /
• 1991

Ion-selective electrode responsive to the thiocynate ion prepared by using the quaternary ammonium salts as a active material and PVC as a membrane matrix. The effect of chemical structure and composition of active material, and the membrane thickness on the linear response. the detection limit, and Nernstian slope of the electrode studied. Under the above optimum conditions of membrane, the effect of pH and the selectivity coefficients to various interfering anions were compared and investigated. It was concluded that the functions of thiocynate ion-selective electrode(ISE) were closely related to the chemical structure of the quaternary ammonium salts. The linear response, and the detection limit of the electrode potential increased with the increase of the carbon chain length of the alkyl group in the quaternary ammonium salts in the ascending order of Aliquat 336T, TOAT, TDAT, and TDDAT. The optimum membrane thickness was 0.3mm. The electrode characteristics was better with the decrease of the concentration of active material, and the best concentration was 3 weight percent. The membrane potential was independent of the pH variation in the region from pH 2 to 12. The order of the selectivity coefficients is as follows：Cl $O_4$$^{[-10]}$ ＞ $I^{[-10]}$ ＞N $O_3$$^{[-10]}$ ＞B $r^{[-10]}$ ＞ $F^{[-10]}$ ＞C $l^{[-10]}$ ＞O $A_{c}$ $^{[-10]}$ 〓S $O_4$$^{2-}$.

• Bulletin of the Korean Chemical Society
• /
• 제22권12호
• /
• pp.1345-1349
• /
• 2001

New quadruply-bridged calix[6]arenes (I-V) have been studied as cesium selective ionophores in poly(vinyl chloride) (PVC) membrane electrodes. PVC membranes were prepared with dioctyl sebacate (DOS) or 2-nitrophenyl octyl ether (o-NPOE) as the sol vent mediator and potassium tetrakis(p-chlorophenyl)borate as the lipophilic salt additive. These ionophores produced electrodes with near-Nernstian slope. The selectivity coefficients for cesium ion with respect to alkali, alkaline earth and ammonium ions have been determined. The lowest detection limit (logaCs+ = -6.3) and the higher selectivity coefficient (logkpotCs+,Rb+ = -2.1 by SSM, -2.3 by FIM for calix[6]arene I) for Cs+ have been obtained for membranes containing quadruply-bridged calix[6]arenes (I, Ⅱ, Ⅲ), which have no para t-butyl substituents on the bridging benzene ring.

• 환경위생공학
• /
• 제22권4호
• /
• pp.11-21
• /
• 2007

The recent investigation indicates that the kinetic constants for anionic ions were merely the result of ion exchange between the algae cell wall surface and the anionic ion. In this study, Zygnema sterile and Lepocinclism textra, floating flagellate alga as the dominant algae strains, were cultivated using HRABR(High Rate Algae Biomass Reactor) and the cultivation conditions were 24 hrs. and 12 hrs. irradiation and it was studied how this algal biomass acts on the biosorption mechanism of anionic N and P. Results are as follows : 1. Calculating the specific chl.-a growth rate using Michaelis-Menten model, the one of 24hrs. irradiation was about 55 times higher than the one of 12 hrs. irradiation 2. Calculating the specific chl.-a growth rate using Kuo model, the one of 24 hrs. irradiation was about 2.26 times higher than the one of 12 hrs. irradiation 3. Langmuir model can apply to the biosorption mechanism of anionic N and P in HRABP. 4. Regarding the chlorophyll-a concentration as unit weight of sorbent, the ion selectivity coefficients for N and P are as follows : $(NH_3-N)+(NO_3-N)$ in 24 hrs. irradiation ; 44.984 $PO_4-P$ in 24 hrs. irradiation ; 24.237 $(NH_3-N)+(NO_3-N)$ in 12 hrs. irradiation ; 1432.851 $PO_4-P$ in 12 hrs. irradiation ; 599.076

• Bulletin of the Korean Chemical Society
• /
• 제34권10호
• /
• pp.3088-3092
• /
• 2013

A novel PVC membrane sensor for perindopril based on perindopril-phosphotungstate ion pair complex was prepared. The influence of membrane composition (i.e. percent of PVC, plasticizer, ion-pair complex, and kind of plasticizer), inner solution, pH of test solution and foreign cations on the electrode performance was investigated. The optimized membrane demonstrates Nernstian response ($30.9{\pm}1.0$ mV per decade) for perindopril cations over a wide linear range from $9.0{\times}10^{-7}$ to $1{\times}10^{-2}$ M at $25^{\circ}C$. The potentiometric response is independent of the pH in the range of 4.0-9.5. The proposed sensor has the advantages of easy preparation, fast response time. The selectivity coefficients indicate excellent selectivity for perindopril over many common cations (e.g., $Na^+$, $K^+$, $Mg^{2+}$, $Cu^{2+}$, $Ni^{2+}$, rhamnose, maltose, glycine and benzamide. The practical applications of this electrode was demonstrated by measuring the concentrations of perindopril in pure solutions and pharmaceutical preparations with satisfactory results.

• 분석과학
• /
• 제8권1호
• /
• pp.33-40
• /
• 1995

미량의 hydroxide 이온은 Tetra-n-Butyl Ammonium(TBAC)에 의해 수액상에서 유기상으로 추출될 수 있다. 일차 알코올류, 특히 다이올류의 적은 양을 첨가하면 상전이 촉매계의 거동이 급격히 변하고 과량의 염기를 유기상에서 발견할 수 있다. 정량 측정은 유기상에서 1차, 2차 알콕사이드와 다이올 음이온들의 추출한 양에 대해 행하였다. 한편, 일차 알코올류와 벤질 알코올의 추출에 대한 선택상수들은 수액상과 유기상에서 $Q^+RO^-$($Q^+$ : quaternary 양이온, $RO^-$ : 알콕사이드 이온)와 $Q^+Cl^-$과 같은 이온쌍들의 평형상수와 이 두 상간의 분배계수로 분리되었다. 따라서 $Q^+RO^-$의 선택성에 대한 전제 특성을 본 연구결과에서 언급된 여러 상수들에 대하여 자유에너지에 상응하는 값들을 사용해서 더욱 상세하게 논하였다.

• 한국산학기술학회논문지
• /
• 제4권3호
• /
• pp.307-311
• /
• 2003

탈염기 혼합 이온교환 수지탑에서 양 ㆍ 음이온의 최적혼합비율을 결정하기 위해 실험을 수행하였다. 2, 3, 4, 5 성분 양ㆍ음이온 흡착은 많은 양이온 그리고 음이온의 선택도를 얻기 위하여 small-volume batch test로부터 실험 데이터를 얻기 위해 수행되었다. Quantitative run time은 반-실험적 질량 작용과 표면 착화 모델을 이용한 이온 교환 모델에 의해서 추정될 수 있었다. 탈염기 수지층의 음이온 교환수지에 대한 양이온 교환수지의 비율을 증가시킴으로써 더 길게 사용될 수 있다.

• 분석과학
• /
• 제5권1호
• /
• pp.33-39
• /
• 1992

리튬이온의 새로운 중성운반체로서 tetrahydrofuran 단위의 16고리형 crown-4를 퓨란과 아세톤으로부터 산 촉매하에서 합성하여 수소화시킨 후 리튬-이온과의 착물형성반응을 Li-7 NMR과 전기전도도법으로 조사했다. 합성한 리간드를 PVC-액체막 전극에 사용하여 분리용액법에 의한 리튬이온의 선택성을 결정하였다. 막용매, tris(2-ethylhexyl) phosphate에서 리튬이온의 선택계수는 알칼리금속이온 및 알칼리토금속이온에 대해 $2.4{\times}10^{-1}$에서 $2.3{\times}10^{-4}$ 범위의 값을 가졌으며, 산성용액(pH=2 이하, 0.1M LiCl)에서 액체막은 $H^+$ 이온의 방해로 불안정하였다.

• Bulletin of the Korean Chemical Society
• /
• 제31권10호
• /
• pp.2980-2984
• /
• 2010

A new poly (vinyl chloride) (PVC) membrane electrode that is highly selective to $Mn^{+2}$ ions was prepared using N,N'-bis(2'-pyridinecarboxamide)-1,2-ethane ($bpenH_2$) as a suitable neutral carrier. This concentration range ($1.0{\times}10^{-5}$ to $1.0{\times}10^{-1}\;M$) with Nernstian slope of $29.3{\pm}0.5\;mV$ per decade. The detection limit and the response time of electrode were $8.0{\times}10^{-6}\;M$ and (${\leq}15\;s$) respectively. The membrane can be used for more than two months without observing any divergence. The electrodes exhibited excellent selectivity for $Mn^{+2}$ ion over other mono-, di- and trivalent cations. Selectivity coefficients were determined by the matched potential method (MPM). The electrode can be used in the pH range from 4.0 - 9.0. The isothermal coefficient of this electrode amounted to 0.00023 V/$^{\circ}C$. The stability constant (log $K_s$) of the $Mn^{+2}$ - $bpenH_2$ complex was determined at $25^{\circ}C$ by potentiometric titration in mixed aqueous solution. The proposed electrode was applied to the determination of $Mn^{+2}$ ions in real samples.