Buffer solution


A buffer solution is an aqueous solution consisting of a mixture of a weak acid and its conjugate base, or vice versa. Its pH changes very little when a small amount of strong acid or base is added to it. Buffer solutions are used as a means of keeping pH at a nearly constant value in a wide variety of chemical applications. In nature, there are many systems that use buffering for pH regulation. For example, the bicarbonate buffering system is used to regulate the pH of blood.

Principles of buffering

Buffer solutions achieve their resistance to pH change because of the presence of an equilibrium between the weak acid HA and its conjugate base A−:
When some strong acid is added to an equilibrium mixture of the weak acid and its conjugate base, hydrogen ions are added, and the equilibrium is shifted to the left, in accordance with Le Châtelier's principle. Because of this, the hydrogen ion concentration increases by less than the amount expected for the quantity of strong acid added.
Similarly, if strong alkali is added to the mixture, the hydrogen ion concentration decreases by less than the amount expected for the quantity of alkali added. The effect is illustrated by the simulated titration of a weak acid with pKa = 4.7. The relative concentration of undissociated acid is shown in blue, and of its conjugate base in red. The pH changes relatively slowly in the buffer region, pH = pKa ± 1, centered at pH = 4.7, where = . The hydrogen ion concentration decreases by less than the amount expected because most of the added hydroxide ion is consumed in the reaction
and only a little is consumed in the neutralization reaction
Once the acid is more than 95% deprotonated, the pH rises rapidly because most of the added alkali is consumed in the neutralization reaction.

Buffer capacity

Buffer capacity is a quantitative measure of the resistance to change of pH of a solution containing a buffering agent with respect to a change of acid or alkali concentration. It can be defined as follows:
where is an infinitesimal amount of added base, or
where is an infinitesimal amount of added acid. pH is defined as −log10, and d is an infinitesimal change in pH.
With either definition the buffer capacity for a weak acid HA with dissociation constant Ka can be expressed as
where is the concentration of hydrogen ions, and is the total concentration of added acid. Kw is the equilibrium constant for self-ionization of water, equal to 1.0. Note that in solution H+ exists as the hydronium ion H3O+, and further aquation of the hydronium ion has negligible effect on the dissociation equilibrium, except at very high acid concentration.
This equation shows that there are three regions of raised buffer capacity.
The pH of a solution containing a buffering agent can only vary within a narrow range, regardless of what else may be present in the solution. In biological systems this is an essential condition for enzymes to function correctly. For example, in human blood a mixture of carbonic acid and bicarbonate is present in the plasma fraction; this constitutes the major mechanism for maintaining the pH of blood between 7.35 and 7.45. Outside this narrow range, acidosis and alkalosis metabolic conditions rapidly develop, ultimately leading to death if the correct buffering capacity is not rapidly restored.
If the pH value of a solution rises or falls too much, the effectiveness of an enzyme decreases in a process, known as denaturation, which is usually irreversible. The majority of biological samples that are used in research are kept in a buffer solution, often phosphate buffered saline at pH 7.4.
In industry, buffering agents are used in fermentation processes and in setting the correct conditions for dyes used in colouring fabrics. They are also used in chemical analysis and calibration of pH meters.

Simple buffering agents

For buffers in acid regions, the pH may be adjusted to a desired value by adding a strong acid such as hydrochloric acid to the particular buffering agent. For alkaline buffers, a strong base such as sodium hydroxide may be added. Alternatively, a buffer mixture can be made from a mixture of an acid and its conjugate base. For example, an acetate buffer can be made from a mixture of acetic acid and sodium acetate. Similarly, an alkaline buffer can be made from a mixture of the base and its conjugate acid.

"Universal" buffer mixtures

By combining substances with pKa values differing by only two or less and adjusting the pH, a wide range of buffers can be obtained. Citric acid is a useful component of a buffer mixture because it has three pKa values, separated by less than two. The buffer range can be extended by adding other buffering agents. The following mixtures have a buffer range of pH 3 to 8.
A mixture containing citric acid, monopotassium phosphate, boric acid, and diethyl barbituric acid can be made to cover the pH range 2.6 to 12.
Other universal buffers are the Carmody buffer and the Britton–Robinson buffer, developed in 1931.

Common buffer compounds used in biology

For effective range see Buffer capacity, above.
Common name StructurepKa
at 25 °C		Temp. effect
Mol.
weight
TAPS 8.43−0.018243.3
Bicine 8.35−0.018163.2
Tris or 8.07*−0.028121.14
Tricine 8.05−0.021179.2
TAPSO 7.635259.3
HEPES 7.48−0.014238.3
TES 7.40−0.020229.20
MOPS 7.20−0.015209.3
PIPES 6.76−0.008302.4
Cacodylate 6.27138.0
MES 6.15−0.011195.2

Tris is a base, the pKa = 8.07 refers to its conjugate acid.

Calculating buffer pH

Monoprotic acids

First write down the equilibrium expression
This shows that when the acid dissociates, equal amounts of hydrogen ion and anion are produced. The equilibrium concentrations of these three components can be calculated in an ICE table.
The first row, labelled I, lists the initial conditions: the concentration of acid is C0, initially undissociated, so the concentrations of A− and H+ would be zero; y is the initial concentration of added strong acid, such as hydrochloric acid. If strong alkali, such as sodium hydroxide, is added, then y will have a negative sign because alkali removes hydrogen ions from the solution. The second row, labelled C for "change", specifies the changes that occur when the acid dissociates. The acid concentration decreases by an amount −x, and the concentrations of A− and H+ both increase by an amount +x. This follows from the equilibrium expression. The third row, labelled E for "equilibrium", adds together the first two rows and shows the concentrations at equilibrium.
To find x, use the formula for the equilibrium constant in terms of concentrations:
Substitute the concentrations with the values found in the last row of the ICE table:
Simplify to
With specific values for C0, Ka and y, this equation can be solved for x. Assuming that pH = −log10, the pH can be calculated as pH = −log10.

Polyprotic acids

Polyprotic acids are acids that can lose more than one proton. The constant for dissociation of the first proton may be denoted as Ka1, and the constants for dissociation of successive protons as Ka2, etc. Citric acid is an example of a polyprotic acid H3A, as it can lose three protons.
When the difference between successive pKa values is less than about 3, there is overlap between the pH range of existence of the species in equilibrium. The smaller the difference, the more the overlap. In the case of citric acid, the overlap is extensive and solutions of citric acid are buffered over the whole range of pH 2.5 to 7.5.
Calculation of the pH with a polyprotic acid requires a speciation calculation to be performed. In the case of citric acid, this entails the solution of the two equations of mass balance:
CA is the analytical concentration of the acid, CH is the analytical concentration of added hydrogen ions, βq are the cumulative association constants:
Kw is the constant for self-ionization of water. There are two non-linear simultaneous equations in two unknown quantities and . Many computer programs are available to do this calculation. The speciation diagram for citric acid was produced with the program HySS.