A factor relating the concentration of a species to its activity
For neutral species, the position of equilibrium is essentially independent of electrolyte concentration
Electrolyte effect
The effect of added electrolyte on equilibria, which depends on the ionic strength of the solution
The electrolyte effect results from the electrostatic attractive and repulsive forces between the ions of an electrolyte and the ions involved in an equilibrium
Chemists use the term 'activity' to account for the effects of electrolytes on chemical equilibria
Debye-Huckel equation
An equation that permits the calculation of activity coefficients of ions from their charge and average size
Aqueous solutions often contain species that interact with one another and water to yield two or more simultaneous equilibria
Mass-balance equations
Equations that relate the equilibrium concentrations of various species in a solution to one another and to the analytical concentrations of the various solutes
Charge-balance equations
Equations that express the equality of the number of moles per liter of positive and negative charges in an electrolyte solution
Electrolyte solutions are electrically neutral even though they may contain up to several moles per liter of charged ions
Gravimetric methods
Quantitative methods based on determining the mass of a pure compound to which the analyte is chemically related
Gravimetric methods of analysis are based on mass measurements with an analytical balance, an instrument that yields highly accurate and precise data
Precipitation gravimetry
The analyte is separated from a solution of the sample as a precipitate and is converted to a compound of known composition that can be weighed
Volatilization gravimetry
The analyte is separated from other constituents of a sample by converting it to a gas of known chemical composition, and the mass of the gas then serves as a measure of the analyte concentration
Electrogravimetry
The analyte is separated by deposition on an electrode by an electrical current, and the mass of this product then provides a measure of the analyte concentration
Gravimetric titrimetry
The mass of a reagent of known concentration required to react completely with the analyte provides the information needed to determine the analyte concentration
Atomic mass spectrometry
Uses a mass spectrometer to separate the gaseous ions formed from the elements making up a sample of matter
In precipitation gravimetry, the analyte is converted to a sparingly soluble precipitate
Colloidal suspensions
Suspensions with tiny particles invisible to the naked eye
Crystalline suspension
The temporary dispersion of colloidal particles in the liquid phase
Supersaturated solution
A solution that contains a higher solute concentration than a saturated solution
Coagulation
The process by which colloidal particles aggregate and precipitate out of the solution, which can be hastened by heating, stirring, or adding an electrolyte
Peptization
The process by which a coagulated colloid reverts to its original dispersed state
Crystalline precipitates are generally more easily filtered and purified than are coagulated colloids
Types of coprecipitation
Surface adsorption
Mixed-crystal formation
Occlusion
Mechanical entrapment
Adsorption is often the major source of contamination in coagulated colloids but of no significance in crystalline precipitates
Mixed-crystal formation
A type of coprecipitation in which a contaminant ion replaces an ion in the lattice of a crystal
Occlusion
A type of coprecipitation in which a compound is trapped within a pocket formed during rapid crystal growth
Mechanical entrapment
A type of coprecipitation that occurs when crystals lie close together during growth
The purity of many coagulated colloids is improved by digestion
Reprecipitation
A drastic but effective way to minimize the effects of adsorption, involving the precipitate being redissolved and reprecipitated
After filtration, a gravimetric precipitate is heated until its mass becomes constant