Buffer solution#Common buffer compounds used in biology

File:Buffer titration graph.svg of an acidified solution of a weak acid ({{math|1=pK_a = 4.7}}) with alkali]]

Buffer solutions resist pH change because of a chemical equilibrium between the weak acid HA and its conjugate base A⁻:

{{block indent|em=1.5|text=HA {{eqm}} H⁺ + A⁻}}

When some strong acid is added to an equilibrium mixture of the weak acid and its conjugate base, hydrogen ions (H⁺) are added, and the equilibrium is shifted to the left, in accordance with Le Chatelier'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. In Figure 1, the effect is illustrated by the simulated titration of a weak acid with pK_a = 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 = pK_a ± 1, centered at pH = 4.7, where [HA] = [A⁻]. The hydrogen ion concentration decreases by less than the amount expected because most of the added hydroxide ion is consumed in the reaction

{{block indent|em=1.5|text=OH⁻ + HA → H₂O + A⁻}}

and only a little is consumed in the neutralization reaction (which is the reaction that results in an increase in pH)

{{block indent|em=1.5|text=OH⁻ + H⁺ → H₂O.}}

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 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:

$$\backslash beta\; =\; \backslash frac\{dC\_b\}\{d(\backslash mathrm\{pH\})\},$$

where $dC\_b$ is an infinitesimal amount of added base, or

$$\backslash beta\; =\; -\backslash frac\{dC\_a\}\{d(\backslash mathrm\{pH\})\},$$

where $dC\_a$ is an infinitesimal amount of added acid. pH is defined as −log₁₀[H⁺], and d(pH) is an infinitesimal change in pH.

With either definition the buffer capacity for a weak acid HA with dissociation constant K_a can be expressed as{{cite book |last1=Butler |first1=J. N. |title=Ionic Equilibrium: Solubility and pH calculations |date=1998 |publisher=Wiley |pages=133–136 |isbn= 978-0-471-58526-8}}{{cite journal |last1=Urbansky |first1=Edward T. |last2=Schock |first2=Michael R.|title=Understanding, Deriving and Computing Buffer Capacity |journal=Journal of Chemical Education |date=2000 |volume=77 |issue=12 |pages=1640–1644 |doi=10.1021/ed077p1640 |bibcode=2000JChEd..77.1640U }}

$$\backslash beta\; =\; 2.303\; \backslash left([\backslash ce\{H+\}]\; +\; \backslash frac\{T\_\backslash ce\{HA\}\; K\_a[\backslash ce\{H+\}]\}\{(K\_a\; +\; [\backslash ce\{H+\}])^2\}\; +\; \backslash frac\{K\_\backslash text\{w\}\}\{[\backslash ce\{H+\}]\}\backslash right),$$

where [H⁺] is the concentration of hydrogen ions, and $T\_\backslash text\{HA\}$ is the total concentration of added acid. K_w is the equilibrium constant for self-ionization of water, equal to 1.0{{e|−14}}. 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.

File:Buffer Capacity 2.png

This equation shows that there are three regions of raised buffer capacity (see figure 2).

• In the central region of the curve (colored green on the plot), the second term is dominant, and $$\backslash beta\; \backslash approx\; 2.303\; \backslash frac\{T\_\backslash ce\{HA\}\; K\_a[\backslash ce\{H+\}]\}\{(K\_a\; +\; [\backslash ce\{H+\}])^2\}.$$ Buffer capacity rises to a local maximum at pH = pK_a. The height of this peak depends on the value of pK_a. Buffer capacity is negligible when the concentration [HA] of buffering agent is very small and increases with increasing concentration of the buffering agent. Some authors show only this region in graphs of buffer capacity.{{pb}} Buffer capacity falls to 33% of the maximum value at pH = pK_a ± 1, to 10% at pH = pK_a ± 1.5 and to 1% at pH = pK_a ± 2. For this reason the most useful range is approximately pK_a ± 1. When choosing a buffer for use at a specific pH, it should have a pK_a value as close as possible to that pH.{{cite book |last1=Skoog |first1=Douglas A. |last2=West |first2=Donald M. |last3=Holler |first3=F. James |last4=Crouch |first4=Stanley R. |title=Fundamentals of Analytical Chemistry |date=2014 |publisher=Brooks/Cole |isbn=978-0-495-55828-6 |pages=226 |edition=9th}}
• With strongly acidic solutions, pH less than about 2 (coloured red on the plot), the first term in the equation dominates, and buffer capacity rises exponentially with decreasing pH: $$\backslash beta\; \backslash approx\; 10^\{-\backslash mathrm\{pH\}\}.$$ This results from the fact that the second and third terms become negligible at very low pH. This term is independent of the presence or absence of a buffering agent.
• With strongly alkaline solutions, pH more than about 12 (coloured blue on the plot), the third term in the equation dominates, and buffer capacity rises exponentially with increasing pH: $$\backslash beta\; \backslash approx\; 10^\{\backslash mathrm\{pH\}\; -\; \backslash mathrm\{p\}K\_\backslash text\{w\}\}.$$ This results from the fact that the first and second terms become negligible at very high pH. This term is also independent of the presence or absence of a buffering agent.

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 (H{{su|b=2}}CO{{su|b=3}}) and bicarbonate (HCO{{su|b=3|p=−}}) 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 (7.40 ± 0.05 pH unit), 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.{{cite book |title=Fundamentals of Acids, Bases, Buffers & Their Application to Biochemical Systems |last=Scorpio |first=R. |year=2000 |publisher=Kendall/Hunt Publishing Company |isbn=978-0-7872-7374-3}} The majority of biological samples that are used in research are kept in a buffer solution, often phosphate buffered saline (PBS) 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{{cite book |last= Hulanicki |first= A. |title= Reactions of acids and bases in analytical chemistry |publisher= Horwood |year= 1987 |isbn=978-0-85312-330-9 |translator-first= Mary R.|translator-last= Masson}} and calibration of pH meters.

:

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.

By combining substances with pK_a 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 pK_a values, separated by less than two. The buffer range can be extended by adding other buffering agents. The following mixtures (McIlvaine's buffer solutions) have a buffer range of pH 3 to 8.{{cite journal |last=McIlvaine |first=T. C. |year=1921 |title=A buffer solution for colorimetric comparaison |journal=J. Biol. Chem. |volume=49 |pages=183–186 |url=http://www.jbc.org/content/49/1/183.full.pdf |issue=1 |doi=10.1016/S0021-9258(18)86000-8 |url-status=live |archive-url=https://web.archive.org/web/20150226111238/http://www.jbc.org/content/49/1/183.full.pdf |archive-date=2015-02-26|doi-access=free }}

:

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.{{cite book |title=Vogel's textbook of quantitative chemical analysis |last1=Mendham |first1=J. |last2=Denny|first2= R. C. |last3=Barnes |first3=J. D. |last4=Thomas|first4= M. |edition=5th|year=2000 |publisher=Pearson Education |location=Harlow |isbn=978-0-582-22628-9|chapter= Appendix 5}}

Other universal buffers are the Carmody buffer{{cite journal |last=Carmody |first=Walter R. |title=Easily prepared wide range buffer series |journal=J. Chem. Educ. |year=1961 |volume=38 |issue=11 |pages=559–560 |doi=10.1021/ed038p559 |bibcode = 1961JChEd..38..559C }} and the Britton–Robinson buffer, developed in 1931.

For effective range see Buffer capacity, above. Also see Good's buffers for the historic design principles and favourable properties of these buffer substances in biochemical applications.

{{noteslist}}

First write down the equilibrium expression

{{block indent|em=1.5|text=HA {{eqm}} A⁻ + H⁺}}

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 (ICE standing for "initial, change, equilibrium").

:

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:

$$K\_\backslash text\{a\}\; =\; \backslash frac\{[\backslash ce\{H+\}]\; [\backslash ce\{A-\}]\}\{[\backslash ce\{HA\}]\}.$$

Substitute the concentrations with the values found in the last row of the ICE table:

$$K\_\backslash text\{a\}\; =\; \backslash frac\{x(x\; +\; y)\}\{C\_0\; -\; x\}.$$

Simplify to $$x^2\; +\; (K\_\backslash text\{a\}\; +\; y)\; x\; -\; K\_\backslash text\{a\}\; C\_0\; =\; 0.$$

With specific values for C₀, K_a and y, this equation can be solved for x. Assuming that pH = −log₁₀[H⁺], the pH can be calculated as pH = −log₁₀(x + y).

File:Citric acid speciation.svg calculated for a 10-millimolar solution of citric acid]]

Polyprotic acids are acids that can lose more than one proton. The constant for dissociation of the first proton may be denoted as K_a1, and the constants for dissociation of successive protons as K_a2, etc. Citric acid is an example of a polyprotic acid H₃A, as it can lose three protons.

:

When the difference between successive pK_a 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:

$$\backslash begin\{align\}$$

C_\ce{A} &= [\ce{A^3-}]+ \beta_1 [\ce{A^3-}][\ce{H+}] + \beta_2 [\ce{A^3-}][\ce{H+}]^2 + \beta_3 [\ce{A^3-}][\ce{H+}]^3, \\

C_\ce{H} &= [\ce{H+}] + \beta_1 [\ce{A^3-}][\ce{H+}] + 2\beta_2 [\ce{A^3-}][\ce{H+}]^2 + 3\beta_3 [\ce{A^3-}][\ce{H+}]^3 - K_\text{w}[\ce{H+}]^{-1}.

\end{align}

C_A is the analytical concentration of the acid, C_H is the analytical concentration of added hydrogen ions, β_q are the cumulative association constants. K_w is the constant for self-ionization of water. There are two non-linear simultaneous equations in two unknown quantities [A³⁻] and [H⁺]. Many computer programs are available to do this calculation. The speciation diagram for citric acid was produced with the program HySS.{{cite journal | last1 = Alderighi | first1 = L. | last2 = Gans | first2 = P. | last3 = Ienco | first3 = A. | last4 = Peters | first4 = D. | last5 = Sabatini | first5 = A. | last6 = Vacca | first6 = A. | year = 1999 | title = Hyperquad simulation and speciation (HySS): a utility program for the investigation of equilibria involving soluble and partially soluble species | journal = Coordination Chemistry Reviews | volume = 184 | issue = 1 | pages = 311–318 | doi = 10.1016/S0010-8545(98)00260-4 | url = http://www.hyperquad.co.uk/hyss.htm | url-status = live | archive-url = https://web.archive.org/web/20070704083413/http://www.hyperquad.co.uk/hyss.htm | archive-date = 2007-07-04 }}

N.B. The numbering of cumulative, overall constants is the reverse of the numbering of the stepwise, dissociation constants.

:

Cumulative association constants are used in general-purpose computer programs such as the one used to obtain the speciation diagram above.

• Henderson–Hasselbalch equation
• Good's buffers
• Common-ion effect
• Metal ion buffer
• Mineral redox buffer

{{reflist}}

{{Cite web|title=Biological buffers |url=http://www.reachdevices.com/Protein/BiologicalBuffers.html |publisher=REACH Devices}}

{{Chemical equilibria}}

Category:Acid–base chemistry

Category:Acid–base physiology

Category:Equilibrium chemistry