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Related Concept Videos

Potentiometry: Membrane Electrodes01:15

Potentiometry: Membrane Electrodes

Membrane electrodes, also known as p-ion electrodes, use membranes that selectively interact with free analyte ions, generating a potential difference across the membrane. The resulting membrane potential, known as the asymmetry potential, is not zero even when analyte concentrations on both sides of the membrane are equal. The membrane's response is typically not selective to a single analyte but proportional to the concentration of all ions in the sample solution capable of interacting at the...
Ion-Exchange Chromatography01:09

Ion-Exchange Chromatography

Ion-exchange chromatography, or IEC, is a technique for separating ions based on their affinity for the stationary phase. The stationary phase is a cross-linked polymer resin with covalently attached ionic functional groups. The functional groups can be either positively charged (cation exchangers) or negatively charged (anion exchangers). A cation exchanger consists of a polymeric anion and active cations, while an anion exchanger is a polymeric cation with active anions. The choice of...
Ion Exchange01:17

Ion Exchange

Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or basic...
Potentiometry: Types of Electrodes01:19

Potentiometry: Types of Electrodes

Reference electrodes serve as a stable reference point for potentiometric measurements, while indicator and working electrodes react to variations in the composition of a solution.
The Standard Hydrogen Electrode (SHE) is a widely used reference electrode that maintains zero potential across all temperatures. However, its need for a continuous hydrogen gas supply renders it impractical for everyday use.
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Factors Affecting Activity Coefficient01:17

Factors Affecting Activity Coefficient

The extended Debye-Hückel equation indicates that the activity coefficient of an ion in an aqueous solution at 25°C depends on three partially interdependent properties: the ionic strength of the solution, the charge of the ion, and the ion size. 
The activity coefficient value for an ion is close to one when the solution has almost zero ionic strength, i.e., when the solution shows close to ideal behavior. As the ionic strength of the solution increases from 0 to 0.1 mol/L, a decrease in the...
Ionic Strength: Effects on Chemical Equilibria01:19

Ionic Strength: Effects on Chemical Equilibria

The addition of an inert ionic compound increases the solubility of a sparingly soluble salt. For example, adding potassium nitrate to a saturated solution of calcium sulfate significantly enhances the solubility of calcium sulfate. Le Châtelier's principle cannot predict this shift in the equilibrium. Instead, this could be explained in terms of changes in the effective concentration of the ions in solution in the presence of added inert salt.
In this solution, the primary cation—the calcium...

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Multi-analyte Biochip (MAB) Based on All-solid-state Ion-selective Electrodes (ASSISE) for Physiological Research
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Variability of selectivity coefficients of solid-state ion-selective electrodes.

A Hulanicki1, A Lewenstam

  • 1Department of Chemistry, University of Warsaw, Warsaw, Poland.

Talanta
|August 1, 1982
PubMed
Summary

This study validates a model for ion-selective electrode selectivity, confirming its accuracy across various ion combinations and conditions like temperature and stirring.

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Area of Science:

  • Electrochemistry
  • Analytical Chemistry

Background:

  • Ion-selective electrodes (ISEs) are crucial for measuring specific ions.
  • Understanding ISE selectivity mechanisms is vital for accurate potentiometric measurements.

Purpose of the Study:

  • To experimentally verify a generalized model for the selectivity mechanism of solid-state ion-selective electrodes.
  • To assess the influence of interfering ions, temperature, and stirring on electrode performance.

Main Methods:

  • Experimental verification of the generalized selectivity model.
  • Investigated electrodes sensitive to chloride, bromide, iodide, silver, copper, and lead ions.
  • Varied concentrations of interfering ions, temperature, and stirring rates.

Main Results:

  • The generalized model was confirmed for most tested ion-selective electrode systems.
  • Model validation held true across different interfering ion concentrations, temperatures, and stirring conditions.
  • Exceptions were noted when metathesis ion concentrations at the electrode surface were too low to influence potential.

Conclusions:

  • The generalized model provides a reliable framework for predicting solid-state ion-selective electrode behavior.
  • Experimental conditions significantly impact electrode selectivity, as predicted by the model.
  • Further refinement of the model may be needed for scenarios with minimal metathesis ion formation.