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Commercial reference electrodes consist of a glass or plastic tube electrode body. The electrode consists of a metallic silver wire (Ag (s)) coated with a thin layer of silver chloride (AgCl), either physically by dipping the wire in molten silver chloride, chemically by electroplating the wire in concentrated hydrochloric acid (HCl) [3] or electrochemically by oxidising the silver at an anode ...
The chloride content of an aqueous solution can be determined quantitatively by weighing the precipitated AgCl, which conveniently is non-hygroscopic since AgCl is one of the few transition metal chlorides that are insoluble in water. Interfering ions for this test are bromide and iodide, as well as a variety of ligands (see silver halide).
Insert a piece of silver wire into concentrated HCl then allow the wire to dry on a lint-free cleaning cloth. This forms an insoluble layer of AgCl on the surface of the electrode and gives you an Ag/AgCl wire. Repeat dipping every few months or if the QRE starts to drift. Obtain a Vycor glass frit (4 mm diameter) and glass tubing of similar ...
In chemistry, a strong electrolyte is a solute that completely, or almost completely, ionizes or dissociates in a solution. These ions are good conductors of electric current in the solution. Originally, a "strong electrolyte" was defined as a chemical compound that, when in aqueous solution , is a good conductor of electricity.
The ability for ions to move freely through the solvent is a characteristic of an aqueous strong electrolyte solution. The solutes in a weak electrolyte solution are present as ions, but only in a small amount. [3] Nonelectrolytes are substances that dissolve in water yet maintain their molecular integrity (do not dissociate into ions).
The molar ionic strength, I, of a solution is a function of the concentration of all ions present in that solution. [3]= = where one half is because we are including both cations and anions, c i is the molar concentration of ion i (M, mol/L), z i is the charge number of that ion, and the sum is taken over all ions in the solution.
The cation of the indicator electrolyte should not move faster than the cation whose transport number is to be determined, and it should have same anion as the principle electrolyte. Besides the principal electrolyte (e.g., HCl) is kept light so that it floats on indicator electrolyte.
They adsorb on the AgCl surface, imparting a negative charge to the particles. Past the equivalence point, excess silver(I) ions adsorb on the AgCl surface, imparting a positive charge. Anionic dyes such as dichlorofluorescein are attracted to the particles, and undergo a colour change upon adsorption, representing the end-point.