• 제목/요약/키워드: Sodium ion selective electrode

검색결과 17건 처리시간 0.018초

Sodium Ion-Selective Membrane Electrode Based on Dibenzopyridino-18-Crown-6

  • Tavakkoli, Nahid
    • Bulletin of the Korean Chemical Society
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    • 제25권10호
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    • pp.1474-1476
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    • 2004
  • A sodium ion- selective electrode based on dibenzopyridino-18-crown-6 as membrane carrier was successfully prepared. The electrode exhibits a Nernstian response for $Na^+$ ions within the concentration range of $1.0\;{\times}\;10^{-4}-1.0\;{\times}\;10^{-1}$ M. The response time of the sensor is 20 s. The sodium ion-selective electrode exhibited comparatively good selectivities with respect to alkali, alkaline earth and some transition metal ions.

Pilymeric Membrane Sodium Ion-Selective Electrodes Based on Calix[4}arene Triesters

  • 김윤덕;정해상;강성옥;남계천;전승원
    • Bulletin of the Korean Chemical Society
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    • 제22권4호
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    • pp.405-408
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    • 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.

Silicone Rubber Blended with Polyurethane as the Matrix for Ion-Selective Membrane Electrodes

  • Lee, Hyun Jung;Rho, Kyung Lae;Kim, Chang Yong;Oh, Bong Kyun;Cha, Geun Sig;Nam, Hakhyun
    • 분석과학
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    • 제8권4호
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    • pp.623-630
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    • 1995
  • Silicone rubber-based sodium-selective membranes are developed for solid-state ion sensors. It was shown that the potetiometric performance of SR-based membranes are greatly dependent on the type of neutral carriers employed; among the three ionophores, N,N,N',N'-tetracyclohexyl-1,2-phenylenedioxydiacetamide (ETH 2120), bis[(12-crown-4)methyl]dodecylmethylmalonate (D12C4DMM) and monensin methyl ester (MME), examined, only ETH 2120 was compatible with the SR-based matrix. Addition of about 20 wt% plasticizer to the SR-based matrix provided the resulting membranes with potentiometric properties essentially equivalent to those of the corresponding PVC-based membranes. Owing to the strong adhesive strength of SR-based membranes, the CWEs coated \vith those membranes exhibited long lifetime with conventional electrode-like performance. Blending of PU into the SR matrix increased the lifetime of CWEs from two weeks to one month.

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거대고리 중성 운반체를 갖는 Hg(II)이온 선택성 전극 (Hg(II) ion- Selective Electrodes with Neutral Carriers of Macrocycles)

  • 정오진
    • 한국환경과학회지
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    • 제5권2호
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    • pp.211-220
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    • 1996
  • 두 개의 황과 셀렌의 주개원자를 포함한 새로운 thia 및 diselena 크라운에데르 화합물을 합성하였다. 그리고 이 화합들을 중성운반체로 하고 PVC-가소제 (STPB)를 포함한 Hg(ll) 선택성 전극을 제작하였다. 이 전극들을 이용하여 여러 이온들의 전기화학적 선택성, 중성운반체의 종류 및 농도와 선택막의 매질에 대한 효과 그리고 실험용액의 pH변화에 대한 전극의 선택적 감응성들의 영향을 각각 검토하였다. 1,10-diselena-18-crown-6-PVC-STPB의 중성운반체의 막전극은 $10^{-2}$-10- M $Hg^{2+}$ 이온의 농도범위에서 ${28.2}\pm{0.6}$의 Nernstian 기울기를 갖는 좋은 선형적 감응성을 갖는다. 그리고 이 전극은 pH 2.5~6.0 범 위에서 알칼리토 금속, 몇가지 중금속 및 희토류 금속 이온에 대하여 좋은 선택성을 갖는다. 특히 이 전극은 수용액 중에서.$1^-$ 이온으로 Hg^{2-}$ 이온을 전위차 적정할 수 있는 센서로서 응용할 수 있다.

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Lead-Selective Poly(vinyl chloride) Membrane Electrode Based on 1-Phenyl-2-(2-quinolyl)-1,2-dioxo-2-(4-bromo) phenylhydrazone

  • Zare, Hamid Reza;Ardakani, Mahammad Mazloum;Nasirizadeh, Navid;Safari, Javad
    • Bulletin of the Korean Chemical Society
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    • 제26권1호
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    • pp.51-56
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    • 2005
  • A PVC membrane electrode for lead ion based on 1-phenyl-2-(2-quinolyl)-1,2-dioxo-2-(4-bromo) phenylhydrazone (PQDBP) as ionophore was demonstrated. The optimum composition of the membrane was 30 wt% poly(vinyl chloride), 60 wt% dibutyl phthalate as a plasticizer, 4 wt% ionophore and 6 wt% sodium tetraphenylborate as additive. The electrode exhibits a Nernstian response (28.7 mV decade$^{-1}$) for Pb$^{2+}$ over a wide concentration range (1.0 ${\times}$ 10$^{-1}$ to 1 ${\times}$ 10$^{-6}$ M) with a detection limit of 6.0 ${\times}$ 10$^{-7}$ M. This sensor has a short response time and can be used for at least 2 months without any divergence in potentials. The proposed electrode could be used in a pH range of 3.0-6.0 and revealed good selectivities for Pb$^{+2}$ over a wide variety of other metal ions. It was successfully applied as an indicator electrode for the potentiometric titration of lead ion with potassium chromate and for the direct determination of lead in mine.

Synthesis of a New Hexadendates Schiff's Base and Its Application in the Fabrication of a Highly Selective Mercury(II) Sensor

  • Ganjali, M.R.;Norouzi, P.;Alizadeh, T.;Salavati-Niasari, M.
    • Bulletin of the Korean Chemical Society
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    • 제28권1호
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    • pp.68-72
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    • 2007
  • A new PVC membrane potentiometric sensor that is highly selective to Hg2+ ions was prepared, using bis(2-hydroxybenzophenone) butane-2,3-dihydrazone (HBBD) as an excellent hexadendates neutral carrier. The sensor works satisfactorily in the concentration range of 1.0 × 10-6 to 1.0 × 10-1 mol L-1 (detection limit 4 × 10-7 mol L-1) with a Nernstian slope of 29.7 mV per decade. This electrode showed a fast response time (~8 s) and was used for at least 12 weeks without any divergence. The sensor exhibits good Hg2+ selectivity for a broad range of common alkali, alkaline earth, transition and heavy metal ions (lithium, sodium, potassium, magnesium, calcium, copper, nickel, cobalt, zinc, cadmium, lead and lanthanum). The electrode response is pH independent in the range of 1.5-4.0. Furthermore, the developed sensor was successfully used as an indicator electrode in the potentiometric titration of mercury ions with potassium iodide and the direct determination of mercury in some binary and ternary mixtures.

용매 고분자막 상에 고정된 나트륨 이온선택성 물질의 착물형성상수 결정 (Determination of Complex Formation Constant of Sodium-Selective Ionophores in Solvent Polymeric Membranes)

  • 강태영;김성배;오현준;한상현;차근식;남학현
    • 분석과학
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    • 제13권4호
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    • pp.466-473
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    • 2000
  • 용매고분자막 상에 칼륨과 다양한 나트륨이온 선택성 중성 운반체의 착물형성상수(${\beta}_{MLn}$)를 고분자막형 광센서(optode)와 이온선택성 전극(ISE)을 이용하여 결정하였다. 수소이온선택성 발색물질(chromoionophore : ETH 5294)에 가장 널리 쓰이는 나트륨 이온선택성 물질들(4-tert-butylcalix[4]arenetetraacetic acid tetraethyl ester, ETH 2120, bis[(12-crown-4)methyl] dodecyl-methylmalonate 및 monensin methyl ester)을 첨가한 막과 첨가하지 않은 막으로 두 가지 다른 조성의 PVC 막을 제작하여, 일정 pH(0.05 M Tris-HCl, pH7.2)에서 알칼리금속 양이온(나트륨과 칼륨)의 농도 변화에 따른 광학적 감응을 측정하고, 또 일정한 알칼리금속 양이온 농도(0.1M)에서 pH변화에 따른 광학적 감응을 측정하였다. 또한 유사한 조성의 막을 각각 재래식 전극체에 장착하고 일정한 알칼리금속 양이온의 농도(0.1M)에서 pH 변화에 따른 전위치를 측정하였다. 양이온/수소이온의 활동도 비($a_{M^+}/a_{H^+}$)와 상대흡광도로 도시한 광센서 감응곡선과 수소이온농도에 따른 전위차 감응곡선으로부터 나트륨 이온선택성 리간드들의 착물형성상수를 결정하였다. 목적이온과 방해이온에 대한 착물형성상수들의 비로부터 얻어진 값은 실험적으로 얻어진 이온선택성 전극의 선택계수와 근접함을 확인하였다.

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Effect of Surfactants on the Electrochemical Performance of Cation-Selective Membrane Electrodes

  • Oh, Hyun-Joon;Cha, Geun-Sig;Nam, Hak-hyun
    • Bulletin of the Korean Chemical Society
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    • 제24권1호
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    • pp.37-44
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    • 2003
  • We examined the effect of polyether-type nonionic surfactants (Brij 35, Triton X-100, Tween 20 and Tween 80) on the potentiometric properties of sodium-, potassium- and calcium-selective membranes which are prepared with widely used ionophores and four kinds of polymer matrices [poly(vinyl chloride) (PVC), polyurethane (PU), PVC/PU blend, and silicone rubber (SR)]. It was found that the PVC-based membranes, which provide the best performance among all other matrix-based membranes in the absence of nonionic surfactants, exhibited larger change in their potentiometric properties when nonionic surfactants are added to the sample solution. On the other hand, the sodium-selective SR-based membrane with calix[4]arene, potassium-selective PVC/PU- or SR-based membrane with valinomycin, and the calcium-selective SR-based membrane with ETH 1001 provide almost identical analytical performance in the presence and absence of Tween 20 or Tween 80 surfactants. The origin of nonionic surfactants effect was also investigated by interpreting the experimental results obtained with various matrices and ionophores. The results suggest that the nonionic surfactant extracted into the membrane phase unselectively form complexes with the primary and interfering ions, resulting in increased background potential and lower binding ability for the ionophore. Such effects should result in deteriorated detection limits, reduced response slopes and lower selectivity for the primary ions.

전해질 첨가에 따른 키토산/Sodium Dodecyl Sulfate 상호작용의 변화 (The Change of Interactions of Chitosan/Sodium Dodecyl Sulfate in the Presence of Electrolytes)

  • 배현숙;강인숙
    • 한국의류학회지
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    • 제27권5호
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    • pp.523-523
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    • 2003
  • The change of interactions of anionic surfactants, sodium dodecyl sulfate(SDS) and sodium tetradecyl sulfate(575) in the presence of electrolytes, to the chitosan-based polyelectrolyte(sol'n and gel phase) were studied. The chitosan gel used in this study were crosslinked with epichlorohydrin(ECH). Binding isotherms were determined by potentiometric technique using a surfactant ion selective solid-state electrode and the results were represented by using the sequence generating function(SGF) method. The results of binding isotherm were shown comparatively high cooperativity. The addition of electrolytes in the chitosan/SDS system resulted in a shift of the binding to higher free surfactant concentration because of screen effect by the electrolytes. Degree of binding of chitosan gel was higher than that of chitosan sol'n. And also a conformational phase transition of the chitosan gel in the presence of electrolytes has been investigated.

전해질 첨가에 따른 키토산/Sodium Dodecyl Sulfate 상호작용의 변화 (The Change of Interactions of Chitosan/Sodium Dodecyl Sulfate in the Presence of Electrolytes)

  • 배현숙;강인숙
    • 한국의류학회지
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    • 제27권5호
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    • pp.524-532
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    • 2003
  • The change of interactions of anionic surfactants, sodium dodecyl sulfate(SDS) and sodium tetradecyl sulfate(575) in the presence of electrolytes, to the chitosan-based polyelectrolyte(sol'n and gel phase) were studied. The chitosan gel used in this study were crosslinked with epichlorohydrin(ECH). Binding isotherms were determined by potentiometric technique using a surfactant ion selective solid-state electrode and the results were represented by using the sequence generating function(SGF) method. The results of binding isotherm were shown comparatively high cooperativity. The addition of electrolytes in the chitosan/SDS system resulted in a shift of the binding to higher free surfactant concentration because of screen effect by the electrolytes. Degree of binding of chitosan gel was higher than that of chitosan sol'n. And also a conformational phase transition of the chitosan gel in the presence of electrolytes has been investigated.