Potential determining ion

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When placed into solution, salts begin to dissolve and form ions. This is not always in equal proportion, due to the preference of an ion to be dissolved in a given solution. The ability of an ion to preferentially dissolve (as a result of unequal activities) over its counterion is classified as the potential determining ion. The properties of this ion are strongly related to the surface potential present on a corresponding solid. [1]

This unequal property between corresponding ions results in a net surface charge. In some cases this arises because one of the ions freely leaves a corresponding solid and the other does not or it is bound to the solid by some other means. Adsorption of an ion to the solid may result in the solid acting as an electrode. (e.g., H+ and OH on the surfaces of clays).

In a colloidal dispersed system, ion dissolution arises, where the dispersed particles exist in equilibrium with their saturated counterpart, for example:

NaCl(s) Na+(aq) + Cl(aq)

The behavior of this system is characterised by the components activity coefficients and solubility product:

aNa+ · aCl = Ksp

In clay-aqueous systems the potential of the surface is determined by the activity of ions which react with the mineral surface. Frequently this is the hydrogen ion H+ in which case the important activity is determined by pH.

The simultaneous adsorption of protons and hydroxyls as well as other potential determining cations and anions, leads to the concept of point of zero charge or PZC, where the total charge from the cations and anions at the surface is equal to zero.

The charge must be zero, and this does not necessarily mean the number of cations versus anions in the solution are equal. For clay minerals the potential determining ions are H+ and OH and complex ions formed by bonding with H+ and OH.

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An acid is a molecule or ion capable of donating a proton (hydrogen ion H+) (a Brønsted–Lowry acid), or, alternatively, capable of forming a covalent bond with an electron pair (a Lewis acid).

Acid–base reaction chemical reaction

An acid–base reaction is a chemical reaction that occurs between an acid and a base. It can be used to determine pH. Several theoretical frameworks provide alternative conceptions of the reaction mechanisms and their application in solving related problems; these are called the acid–base theories, for example, Brønsted–Lowry acid–base theory.

Hydroxide family of the hydroxide salts

Hydroxide is a diatomic anion with chemical formula OH. It consists of an oxygen and hydrogen atom held together by a covalent bond, and carries a negative electric charge. It is an important but usually minor constituent of water. It functions as a base, a ligand, a nucleophile, and a catalyst. The hydroxide ion forms salts, some of which dissociate in aqueous solution, liberating solvated hydroxide ions. Sodium hydroxide is a multi-million-ton per annum commodity chemical. A hydroxide attached to a strongly electropositive center may itself ionize, liberating a hydrogen cation (H+), making the parent compound an acid.

Ionic bonding Chemical bonding involving attraction between ions

Ionic bonding is a type of chemical bonding that involves the electrostatic attraction between oppositely charged ions, and is the primary interaction occurring in ionic compounds. It is one of the main types of bonding along with covalent bonding and metallic bonding. Ions are atoms with an electrostatic charge. Atoms that gain electrons make negatively charged ions. Atoms that lose electrons make positively charged ions. This transfer of electrons is known as electrovalence in contrast to covalence. In the simplest case, the cation is a metal atom and the anion is a nonmetal atom, but these ions can be of a more complex nature, e.g. molecular ions like NH+
4
or SO2−
4
. In simpler words, an ionic bond results from the transfer of electrons from a metal to a non-metal in order to obtain a full valence shell for both atoms.

The isoelectric point (pI, pH(I), IEP), is the pH at which a molecule carries no net electrical charge or is electrically neutral in the statistical mean. The standard nomenclature to represent the isoelectric point is pH(I), although pI is also commonly seen, and is used in this article for brevity. The net charge on the molecule is affected by pH of its surrounding environment and can become more positively or negatively charged due to the gain or loss, respectively, of protons (H+).

An electrolyte is a substance that produces an electrically conducting solution when dissolved in a polar solvent, such as water. The dissolved electrolyte separates into cations and anions, which disperse uniformly through the solvent. Electrically, such a solution is neutral. If an electric potential is applied to such a solution, the cations of the solution are drawn to the electrode that has an abundance of electrons, while the anions are drawn to the electrode that has a deficit of electrons. The movement of anions and cations in opposite directions within the solution amounts to a current. This includes most soluble salts, acids, and bases. Some gases, such as hydrogen chloride, under conditions of high temperature or low pressure can also function as electrolytes. Electrolyte solutions can also result from the dissolution of some biological and synthetic polymers, termed "polyelectrolytes", which contain charged functional groups. A substance that dissociates into ions in solution acquires the capacity to conduct electricity. Sodium, potassium, chloride, calcium, magnesium, and phosphate are examples of electrolytes.

Solubility equilibrium is a type of dynamic equilibrium that exists when a chemical compound in the solid state is in chemical equilibrium with a solution of that compound. The solid may dissolve unchanged, with dissociation or with chemical reaction with another constituent of the solvent, such as acid or alkali. Each type of equilibrium is characterized by a temperature-dependent equilibrium constant. Solubility equilibria are important in pharmaceutical, environmental and many other scenarios.

Aqueous solution Solution in which the solvent is water

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Base (chemistry) substance that can react with an acid, accepting hydrogen ions (protons) or more generally, donating a pair of valence electrons

In chemistry, bases are substances that, in aqueous solution, release hydroxide (OH) ions, are slippery to the touch, can taste bitter if an alkali, change the color of indicators (e.g., turn red litmus paper blue), react with acids to form salts, promote certain chemical reactions (base catalysis), accept protons from any proton donor or contain completely or partially displaceable OH ions. Examples of bases are the hydroxides of the alkali metals and the alkaline earth metals (NaOH, Ca(OH)2, etc.—see alkali hydroxide and alkaline earth hydroxide).

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Ion exchange usually describes a processes of purification of aqueous solutions using solid polymeric ion exchange resin. More precisely, the term encompasses a large variety of processes where ions are exchanged between two electrolytes. Aside from its use to purify drinking water, the technique is widely applied for purification and separation of a variety of industrially and medicinally important chemicals. Although the term usually refers to applications of synthetic (man-made) resins, many materials, in particular soil.

Surface charge is a two-dimensional surface with non-zero electric charge. These electric charges are constrained on this 2-D surface, and surface charge density, measured in coulombs per square meter (C•m−2), is used to describe the charge distribution on the surface. The electric potential is continuous across a surface charge and the electric field is discontinuous, but not infinite; this is unless the surface charge consists of a dipole layer. In comparison, the potential and electric field both diverge at any Point Charge or Linear Charge.

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Reaction in which two compounds in their aqueous solution react to form two new product by interchanging their radicals or ions is called a double decomposition reaction or double displacement reaction

Point of zero charge

The point of zero charge (pzc) is generally described as the pH at which the net charge of total particle surface is equal to zero, which concept has been introduced in the studies dealt with colloidal flocculation to explain pH affecting the phenomenon.

Alkali soil soil type

Alkali, or Alkaline, soils are clay soils with high pH, a poor soil structure and a low infiltration capacity. Often they have a hard calcareous layer at 0.5 to 1 metre depth. Alkali soils owe their unfavorable physico-chemical properties mainly to the dominating presence of sodium carbonate, which causes the soil to swell and difficult to clarify/settle. They derive their name from the alkali metal group of elements, to which sodium belongs, and which can induce basicity. Sometimes these soils are also referred to as alkaline sodic soils.
Alkaline soils are basic, but not all basic soils are alkaline.

An ion is an atom or molecule that has a net electrical charge. Since the charge of the electron is equal and opposite to that of the proton, the net charge of an ion is non-zero due to its total number of electrons being unequal to its total number of protons. A cation is a positively charged ion, with fewer electrons than protons, while an anion is negatively charged, with more electrons than protons. Because of their opposite electric charges, cations and anions attract each other and readily form ionic compounds.

In analytical chemistry, argentometry is a type of titration involving the silver(I) ion. Typically, it is used to determine the amount of chloride present in a sample. The sample solution is titrated against a solution of silver nitrate of known concentration. Chloride ions react with silver(I) ions to give the insoluble silver chloride:

In chemistry, ion association is a chemical reaction whereby ions of opposite electrical charge come together in solution to form a distinct chemical entity. Ion associates are classified, according to the number of ions that associate with each other, as ion pairs, ion triplets, etc. Ion pairs are also classified according to the nature of the interaction as contact, solvent-shared or solvent-separated. The most important factor to determine the extent of ion association is the dielectric constant of the solvent. Ion associates have been characterized by means of vibrational spectroscopy. The concept was introduced by Niels Bjerrum.

A metal ion in aqueous solution or aqua ion is a cation, dissolved in water, of chemical formula [M(H2O)n]z+. The solvation number, n, determined by a variety of experimental methods is 4 for Li+ and Be2+ and 6 for elements in periods 3 and 4 of the periodic table. Lanthanide and actinide aqua ions have a solvation number of 8 or 9. The strength of the bonds between the metal ion and water molecules in the primary solvation shell increases with the electrical charge, z, on the metal ion and decreases as its ionic radius, r, increases. Aqua ions are subject to hydrolysis. The logarithm of the first hydrolysis constant is proportional to z2/r for most aqua ions.

Ion transport number, also called the transference number, is the fraction of the total electrical current carried in an electrolyte by a given ionic species ,

References

  1. Kenneth N. Han (2002). Fundamentals of Aqueous Metallurgy. SME. p. 157. ISBN   978-0-87335-215-4 . Retrieved 3 February 2014.

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