• Title/Summary/Keyword: Ammonium ionophore

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Comparative Studies on Ammonium Ion Selective Electrodes Using Poly(Vinyl Chloride) and Polyurethane as Substrate Matrix Materials (Poly(Vinyl Chloride)와 Polyurethane을 지지체로 사용한 암모늄이온 선택성 전극의 특성비교)

  • Cho Chang-Ae;Park Su-Moon
    • Journal of the Korean Electrochemical Society
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    • v.7 no.3
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    • pp.148-154
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    • 2004
  • Ammonium ion selective electrodes have been prepared using nonactin as an ionophore and poly(vinyl chloride) (PVC) or polyurethane(PU) as a polymer matrix with or without a plasticizer, bis(2-ethylhexyl) adipate, and their performances have been evaluated. The reults indicate that PU-based electrodes can be designed to perform better although PVC-based electrodes generally show better performances. In efforts to explain the obervation, we also carried out atomic force microscopy as well as impedance studies, and the results suggests that islands of ion-ophores are formed in the PVC membranes through which ion transfers appear to be more facile than through the PU membranes. The PU membranes appear to have ionophores better dispersed throughout the film and are more resistive to ion mobilities in comparison to PVC films.

Tetrahydrofuran-Containing Crown Ethers as Ionophores for NH+4-Selective Electrodes

  • Jin, Hua-Yan;Kim, Tae-Ho;Kim, Jin-Eun;Lee, Shim-Sung;Kim, Jae-Sang
    • Bulletin of the Korean Chemical Society
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    • v.25 no.1
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    • pp.59-62
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    • 2004
  • The ammonium ion-selective electrodes ($NH^+_4$-ISEs) based on the tetrahydrofuran(THF)-containing-16-crown-4 derivatives,1,4,6,9,11,14,16,19-tetraoxocycloeicosane ($L^1$) and 5,10,15,20,-tetramethyl-1,4,6,9,11,14,16,19-tetraoxocycloeicosane ($L^2$), were prepared and the electrode characteristics were tested. The conditioned $NH_4^+$-ISEs (E1) based on $L^1$ with TEHP as a plasticising solvent mediator gave best results with near-Nernstian slope of 53.9 mV/decade of activity, detection limit of $10^{-4.9}$ M, and enhanced selectivity coefficients for the $NH^+_4$ ion with respect to an interfering $K^+$ ion (log $K^{pot}_{NH_4^+,K^+}$ = -1.84). This result was compared to other ammonium ionophores reported previously, for example, that of nonactin (log $K^{pot}_{NH_4^+,K^+}$ = -0.92). The proposed electrode showed no significant potential changes in the range of 3.0 < pH < 9.0.

Polymeric Membrane Cesium-Selective Electrodes Based on Quadruply-bridged Calix[6]arenes

  • Choe, Eun Mi;O, Hye Jin;Go, Seung Hwa;Choe, Yong Guk;Nam, Gye Chun;Jeon, Seung Won
    • Bulletin of the Korean Chemical Society
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    • v.22 no.12
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    • pp.1345-1349
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    • 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.

Lithium Ion Selective Electrode Based on a Synthetic Neutural Carrier (중성운반체를 이용한 리튬이온 선택 전극)

  • Kim, Jae Sang
    • Analytical Science and Technology
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    • v.5 no.1
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    • pp.33-39
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    • 1992
  • THF-based crown-4 of 16-membered rings having tetrahydrofuran unit was synthesized by an acid-catalyzed condensation of furan and acetone followed by hydrogenation in an effort to obtain highly elective ionophores for lithium ions. The new ionophore was compared with previously reported ionophores under similar measurement conditions with the same plasticizer, tris(2-ethylhexyl) phosphate in poly(vinyl chloride)(PVC) membrane electrodes. Separate solution method was used to determine relative selectivity coefficients for the electrode. The selectivity coefficients($K_{LiM}^{POT}$) of lithium over ammonium, alkali and alkaline earth metal ions go from about $2.4{\times}10^{-1}$ to $2.3{\times}10^{-4}$ to working range and pH dependence have also been studied.

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Culture Parameters for Nonactin Production by Streptomyces viridochromogenes JM-4151

  • Lee, Sang-Han;Lee, Dong-Sun;Lee, Jin-Man;Kim, Tae-Ho;Kim, Jong-Guk;Han, Kab-Cho;Lee, Jin-Sik;Kwon, Gi-Seok
    • Journal of Life Science
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    • v.11 no.1
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    • pp.7-10
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    • 2001
  • Nonactin is the parent compound of a group of ionophore antibiotics, that known as the macrotetrolides. In previous report, in th course of screening superoxide radical-generating compounds from microbial sources, we first screened Streptomyces viridochromogenes JM-4151 that produces nonactin. It was proved that nonactin is superoxide radical-producing compound. In present study, we examined the optimal culture conditions of nonacin. Th optimal culture conditions for nonactin production were as follows: 1% soluble starch, 1% yeast extract, 0.2% ammonium nitrate, 0.06% magnesium sulfate, 0.2% calcium carbonate, initial pH 7.0 at 28$^{\circ}C$ for 96 h. The highest nonactin production was achieved in the production medium of initial pH7.0 at 28$^{\circ}C$ for 96h. The threshold level of dissolved oxygen was found to be above 33.2% at 28$^{\circ}C$ when 1% soluble starch was used as a carbon source. These results suggest that S. viridochromogenes JM-4151 might be a possible strain for industrial nonactin producer.

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