Bis(2-hydroxyacetophenone)ethylenediimine as a neutral carrier in a coated-wire membrane electrode for lead(II).

A coated-wire ion-selective electrode (CWISE), based on a Schiff base as a neutral carrier, was successfully developed for the detection of Pb(II) in aqueous solution. CWISE exhibited a linear response with a Nernstian slope of 29.4 +/- 0.5 mV/decade within the concentration range of 1.0 x 10(-5) - 1.0 x 10(-1) M lead ion. CWISE has shown detection limits of 5.0 x 10(-6) M. The electrode exhibited good selectivity over a number of alkali, alkaline earth, transition and heavy metal ions. This sensor yielded a steady potential within 10 to 20 s at a linear dynamic range. The electrode was suitable for use in aqueous solutions in a pH range of 2.0 to 5.0. Applications of this electrode for the determination of lead in real samples and as indicator electrode for potentiometric titration of Pb2+ ion using K2CrO4 are reported.     

Silver(I)-selective coated-wire electrode based on an octahydroxycalix[4]arene derivative.

The performance of octahydroxycalix[4]arene derivative used as a neutral carrier for silver polymeric membrane electrode was studied. The sensor gave a good Nernstian response of 58 +/- 1 mV per decade for silver ion in the activity range 3.3 x 10(-6) to 3.3 x 10(-2) M Ag+. The limit of detection reached 2.1 x 10(-6) M Ag+ and exhibited high selectivity for silver ion against the alkali, alkaline earth and transition metal ions. The sensor can be used in wide pH range from 1.5 to 6.5. The response time of the sensor is less than 20 s. The potentiometric sensor was used as the indicator electrode in the titration of Ag+ ions by sodium chloride solution.     

Coated wire silver-ion selective electrode based on a N,N'-bis(2-thienylmethylene)-1,2-diaminobenzene.

A novel membrane coated platinum-wire electrode (MCPWE) based on N,N'-bis(2-thienylmethylene)-1,2-diaminobenzene (BTMD) for highly selective determination of Ag+ ion has been developed. The influences of membrane composition and pH on the potentiometric responses of electrode were investigated. The potentiometric responses are independent of the pH of the test solution in the range of 5.0 - 9.0. The electrode shows a linear response for Ag+ ion over the concentration range of 1.0 x 10(-60 to 1.0 x 10(-1) M with a lower detection limit of 6.0 x 10(-7) M. The electrode possesses a Nernstian slope of 59.7 mV decade(-1) and a fast response time of < or = 17 s and can be used for at least 2 months without any observable deviation. The proposed electrode displayed very good selectivity for Ag+ ion with respect to NH4+ and alkali, alkaline earth and some common transition metal ions. The practical utility of the electrode has been demonstrated by its use as the indicator electrode in the potentiometric titration of an AgNO3 solution with a NaI solution and in determination of the silver content of a developed radiological film.     

2,6-bis-methylsulfanyl-[1,3,5]thiadiazine-4-thione as a Ag+-selective ionophore.

A silver ion-selective electrode was prepared with a polymeric membrane incorporating 2,6-bis-methylsulfanyl-[1,3,5]thiadiazine-4-thione as an ionophore, tri-n-butylphosphate (TBP) as a plasticizer and sodium tetraphenylborate (NaTPB) as an additive. The electrode exhibited a near-Nernstian response of 52 mV/decade over a wide linear concentration range of 1.0 x 10(-5) - 1.0 x 10(-1) M with a lower detection limit of 9.77 x 10(-6) M. The electrode exhibited excellent selectivity for silver ion over many of the alkali, alkaline-earth and transition metal ions. The electrode worked well over a wide pH range of 1.77 - 7.13. The response time of the electrode was less than 20 s. The sensor can be applied as indicator electrode for the potentiometric titration of Ag+ ions with Cl- ions.     

Oxidation with permanganate in acid medium containing fluoride: determination of bisulphite

The factors affecting the success of both visual and potentiometric end-point detection in titration of bisulphite with permanganate in the presence of fluoride are examined. The optimum conditions are 0.02M H(2)SO(4) and 0.24-0.38M NaF. The oxidation product comprises dithionate and sulphate according to the overall reaction MnO(4)(-) + H(+) + 2HF(2)(-) + 3HSO(3)(-) right harpoon over left harpoon MnF(4)(-) + S(2)O(6)(2-) + SO(4)(2-) + 3H(2)O. The reverse titration is also satisfactory, but proceeds quantitatively according to MnO(4)(2-) + 2HF(2)(-) + 2HSO(3)(-) right harpoon over left harpoon MnF(4)(-) + 2SO(4)(2-) + 2H(2)O.     

Lead selective membrane electrode using cryptand(222) neutral carrier

The construction, performance characteristics and applications of a polymeric membrance electrode for lead(II) ion are reported. The electrode was prepared by incorporating cryptand(222) as the neutral carrier into a plasticized poly(vinyl chloride) membrane. The influence of membrane composition, pH and concentration of internal reference solution were investigated. The electrode exhibits a potentiometric response for Pb²⁺ ion over the concentration range 10^–1–10^–5 M with a detection limit of 5 × 10^–6 M Pb²⁺. It shows a relatively fast response time of about 30 s and can be used for about two months without any considerable divergence in potential. The proposed sensor revealed good selectivities for Pb²⁺ in the presence of several metal ions and could be used in the pH range of 2.5 to 7.5. It was used as an indicator electrode in the potentiometric titration of Pb²⁺ with EDTA. Received: 20 November 1998 / Revised: 26 March 1999 / Accepted: 31 March 1999     

Lead selective membrane electrode using cryptand(222) neutral carrier

The construction, performance characteristics and applications of a polymeric membrance electrode for lead(II) ion are reported. The electrode was prepared by incorporating cryptand(222) as the neutral carrier into a plasticized poly(vinyl chloride) membrane. The influence of membrane composition, pH and concentration of internal reference solution were investigated. The electrode exhibits a potentiometric response for Pb²⁺ ion over the concentration range 10^–1–10^–5 M with a detection limit of 5 × 10^–6 M Pb²⁺. It shows a relatively fast response time of about 30 s and can be used for about two months without any considerable divergence in potential. The proposed sensor revealed good selectivities for Pb²⁺ in the presence of several metal ions and could be used in the pH range of 2.5 to 7.5. It was used as an indicator electrode in the potentiometric titration of Pb²⁺ with EDTA. Received: 20 November 1998 / Revised: 26 March 1999 / Accepted: 31 March 1999     

Novel Copper(II)‐Selective Membrane Electrode Based on a New Synthesized Schiff Base

A PVC membrane electrode for copper(II) ion based on a recently synthesized Schiff base as a suitable ion carrier was constructed. The electrode exhibits a Nernstian slope of 28.3 ± 0.6 mV per decade of Cu²⁺ over a wide concentration range of 7.0 × 10^?6‐2.6 × 10^?2 M with a detection limit of 5.0 × 10^?6M in the pH range of 4.2–5.8. The response time is about 10s and it can be used for at least 1 month without any considerable divergence in potential. It was successfully applied as an indicator electrode in the potentiometric titration of copper ions.     

Coated-wire copper(II)-selective electrode based on phenylglyoxal-α-monoxime ionophore

A copper(II) ion-selective electrode based on a recently synthesized 2-quinolyl-2-phenylglyoxal-2-oxime (phenylglyoxal-alpha-monoxime) has been developed. The PVC-based membrane containing phenylglyoxal-alpha-monoxime, dibutyl phthalate as plasticizer, and sodium tetraphenylborate as anion excluder and membrane modifier, was directly coated on the surface of a platinum-wire electrode. The response of the electrode was linear with a near-Nernstian slope of 28.2 mV decade(-1) within the Cu2+ ion concentration range 1x10(-6)-1x10(-1) mol x L(-1). The response time for the proposed electrode to achieve a 95% steady potential for Cu2+ concentrations ranging from 1x10(-1) to 1x10(-6) mol x L(-1) is between 10 and 50 s, and the electrode is suitable for use within the pH range of 3 to 6.5. The electrode has a detection limit of 5x10(-7) mol x L(-1) Cu2+ and its selectivity relative to several alkali, alkaline earth, transition, and heavy metal ions was good. The coated-wire electrode could be used for at least two months without a considerable alteration of its potential. Applications of the electrode for determination of copper in milk powder samples and as an indicator electrode for potentiometric titration of Cu2+ ion using EDTA are reported.     

The mechanism of the platinum indicator electrode in argentometry

A study has been made of the behaviour of platinum and some other inert electrodes in silver nitrate titrations. Where the metal surface has been subjected to a reducing treatment, such as cathodic polarization, before use, the electrode will often function as a silver indicator electrode throughout the titration. It has been shown experimentally that this is due to the formation of a layer of metallic silver upon the electrode by interaction of the surface with silver ions in solution. If the metal surface undergoes such pretreatment that it is oxidized, then its potential normally remains at the oxide value during a silver nitrate titration until the silver ion concentration is sufficiently great for this value to be exceeded by the silver silver ion potential; formation of metallic silver then again takes place and from this point onwards the electrode behaves as a silver electrode. A detailed interpretation of the behaviour of platinum after various pretreatments has been made along these lines.     

Highly selective and sensitive copper(II) membrane coated graphite electrode based on a recently synthesized Schiff’s base

A PVC membrane electrode based on bis-2-thiophenal propanediamine (TPDA) coated directly on graphite is described. The electrode exhibits a Nernstian response for Cu²⁺ over a very wide concentration range (1.0×10⁻¹ to 6.0×10⁻⁸ M) with a detection limit of 3.0×10⁻⁸ M (2.56 ng ml⁻¹). It has a fast response time and can be used for at least 2 months without any major deviation. The proposed sensor revealed very good selectivities for Cu²⁺ over a wide variety of other metal ions and could be used in the pH range of 3.0–7.0. It was successfully used for direct determination of copper in black tea and as an indicator electrode in potentiometric titration of copper ion.     

Lead ion-selective membrane electrodes based on some recently synthesized 9,10-anthraquinone derivatives

Four different 9,10-anthraquinone derivatives were studied to characterize their abilities as lead ion carrier in PVC membrane electrodes. The electrode based on 1,8-dihydroxy-2,7-bis(prop-2′-enyl)-9,10-anthraquinone exhibits a Nernstian response for Pb²⁺ ions over a wide concentration range (2.0×10⁻³–2.0×10⁻⁶ M). The response time of the sensor is 30 s and the membrane can be used for more than four months without observing any deviation. The electrode revealed comparatively good selectivities with respect to alkali, alkaline earth and some transition and heavy metal ions. It was used as an indicator electrode in potentiometric titration of sulfate ions with a lead ion solution.     

Synthesis of N'-(1-pyridin-2-ylmethylene)-2-furohydrazide and its application in construction of a highly selective PVC-based membrane sensor for La(III) ions.

A highly La(III) ion-selective PVC membrane sensor based on N'-(1-pyridin-2-ylmethylene)-2-furohydrazide (NPYFH) as an excellent sensing material was successfully developed. The electrode shows a good selectivity for La(III) ion with respect to most common cations including alkali, alkaline earth, transition and heavy metal ions. The proposed sensor exhibits a wide linear response with slope of 19.2 +/- 0.6 mV per decade over the concentration range of 1.0 x 10(-6) - 1.0 x 10(-1) M, and a detection limit of 7.0 x 10(-7) M of La(III) ions. The sensor response is independent of pH in the range of 3.5-10.0. The proposed electrode was applied as an indicator electrode in potentiometric titration of La(III) ion with EDTA.     

Potentiometric determination of the standard potential of the As(V)/As(III) couple

The potential of the As(V)/As(III) half-cell was measured at 25 degrees with a glass electrode as reference electrode in order to eliminate the liquid-junction potential. Rapid and reproducible values could be obtained only in the presence of iodide, which increases the rate of electron-exchange between the two oxidation states of arsenic, but only at hydrogen-ion concentrations higher than about 0.5M. Extrapolation to zero ionic strength was therefore required to obtain the standard potential. A value of 573 +/- 2 mV was calculated for the half-reaction AsO(OH)(3) + 2e(-) + 2H(+) right harpoon over left harpoon As(OH)(3) + H(2)O.     

Hydroxy-thioxanthones as suitable neutral ionophores for the preparation of PVC-membrane potentiometric sensors for Al(III) ion.

The complexation of five recently synthesized hydroxy-thioxanthone derivatives with Al3+ ion was studied in a methanol solution spectrophotometrically, and the stepwise formation constants of the resulting 1:1 and 2:1 (ligand-to-metal) complexes were evaluated. The suitability of the thioxanthone derivatives as neutral ionophores for the preparation of a new Al3+ ion-selective PVC-membrane electrode was investigated, and 1-hydroxy-3-methyl-thiocanthone was selected as the best compound for this purpose. The prepared electrode exhibits a Nernstian response for Al3+ ions over a wide concentration range (2.0 x 10(-2) to 2.0 x 10(-6) M), with a limit of detection of 1.0 x 10(-6) M. It has a very fast response time of about 5 s and can be used for at least 3 months without any considerable divergence in the potentials. The proposed membrane sensor revealed very good selectivities for Al3+ over a wide variety of other metal ions, and could be used at a working pH range of 3.4 - 5.0. It was used as an indicator electrode in potentiometric titration of aluminum ions with EDTA, and in the determination of Al3+ in different real samples.     

Lead-Selective Membrane Potentiometric Sensor Based on a Recently Synthesized Bis(Anthraquinone) Sulfide Derivative

Abstract

A new PVC membrane electrode for lead ions, based on bis[(1-hydroxy-9,10-anthraquinone)-2-methyl]sulfide as membrane carrier, was prepared. The sensor exhibits a Nernstian response for Pb²⁺ over a wide concentration range (5.6 × 10^?3-4.0 × 10^?6 M). It has a response time of about 30 s and can be used for at least 3 months without any divergence in potentials. The proposed membrane sensor revealed good selectivities for Pb²⁺ over a wide variety of other metal ions. It was used as an indicator electrode in potentiometric titration of lead ion.     

Highly selective iodide membrane electrode based on a cerium salen.

A highly selective PVC membrane electrode based on a cerium-salen complex was prepared. The sensor displays an anti-Hofmeister selectivity sequence with a preference for iodide ion over many common organic and inorganic anions. The proposed electrode exhibits a near-Nernstian behavior over a wide concentration range (5.0 x 10(-2) - 8.0 x 10(-6) M) with a slope of 57.5 mV per decade, and a detection limit of 6.0 x 10(-6) M. The electrode has a very fast response time and can be used in the pH range of 3.0 - 1 1.0. It was applied, as an indicator electrode, in potentiometric titration of Ag+ ions.     

Lead(II)-Selective Membrane Electrode Based on Tetraphenylporphyrin

ABSTRACT

A PVC membrane electrode for Pb² ions based on tetraphenylporphyrin was prepared. The sensor exhibits a Nernstian response for lead ions over a wide concentration range (1.0 x 10^?5-1.0 x 10^?2 M). The limit of detection is 8.5 x 10^?6M. It has a response time of 15 s and can be used for at least three months without any divergence in potential. The proposed electrode shows a fairly good discriminating ability towards Pb² ion in comparison to some alkali, alkaline earth, transition and heavy metal ions. The electrode can be used in the pH range 5.0 to 7.5. It was used as an indicator electrode in potentiometric titration of lead ion.     

Mercury(II) ion-selective electrodes based on p-tert-butyl calix[4]crowns with imine units.

A PVC membrane incorporating p-tert-butyl calix[4]crown with imine units as an ionophore was prepared and used in an ion-selective electrode for the determination of mercury(II) ions. An electrode based on this ionophore showed a good potentiometric response for mercury(II) ions over a wide concentration range of 5.0 x 10(-5) - 1.0 x 10(-1) M with a near-Nernstian slope of 27.3 mV per decade. The detection limit of the electrode was 2.24 x 10(-5) M and the electrode worked well in the pH range of 1.3 - 4.0. The electrode showed a short response time of less than 20 s. The electrode also showed better selectivity for mercury(II) ions over many of the alkali (Na+, -1.69; K+, -1.54), alkaline-earth (Ca2+, -3.30; Ba2+, -3.32), and heavy metal ions (Co2+, -3.67; Ni2+, -3.43; Pb2+, -3.31; Fe3+, -1.82). Ag+ ion was found to be the strongest interfering ion. Also, sharp end points were obtained when the sensor was used as an indicator electrode for the potentiometric titration of mercury(II) ions with iodide and dichromate ions.