Buffer Solution
Buffer Solution
1
2 2 APPLICATIONS
cologarithm of the hydrogen ion concentration. With this work only under very precise conditions; if the pH moves
definition the buffer capacity of a weak acid, with a dis- outside of a narrow range, the enzymes slow or stop work-
sociation constant Kₐ, can be expressed as ing and can denature. In many cases denaturation can
permanently disable their catalytic activity.[3] A buffer of
( ) carbonic acid (H
dn CA Ka [H ]+ 2 CO
= 2.303 2 3) and bicarbonate (HCO−
d(pH) (Ka + [H+ ])
3) is present in blood plasma, to maintain a pH between
7.35 and 7.45.
where CA is the analytical concentration of the acid.[1][2]
Industrially, buffer solutions are used in fermentation pro-
cesses and in setting the correct conditions for dyes used
in colouring fabrics. They are also used in chemical
analysis[2] and calibration of pH meters.
The majority of biological samples that are used in re-
search are made in buffers, especially phosphate buffered
saline (PBS) at pH 7.4.
there are three regions of raised buffer capacity. 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.
1. At very low p[H+ ] the [H+ ] term in the denominator
predominates and buffer capacity rises exponentially
with decreasing pH. 2.2 “Universal” buffer mixtures
2. The buffer capacity of a buffering agent is at a local
By combining substances with pKₐ values differing by
maximum when p[H+ ] = pKₐ. It falls to 33% of the
only two or less and adjusting the pH, a wide range of
maximum value at p[H+ ] = pKₐ ± 1 and to 10% at
buffers can be obtained. Citric acid is a useful component
p[H+ ] = pKₐ ± 1.5. For this reason the useful range
of a buffer mixture because it has three pKₐ values, sepa-
is approximately pKₐ ± 1. Buffer capacity is pro-
rated by less than two. The buffer range can be extended
portional to the concentration of the buffering agent,
by adding other buffering agents. The following mixtures
CA, so dilute solutions have little buffer capacity.
(McIlvaine’s buffer solutions) have a buffer range of pH
[4]
3. At very high p[H ] the second term in the denomi- 3 to 8.
+
3 Calculating buffer pH
HA ⇌ A− + H+
CH = [H+ ]+β1 [A3− ][H+ ]+2β2 [A3− ][H+ ]2 +3β3 [A3− ][H+ ]3 −Kw [H+ ]−1
x(x + y)
Ka =
C0 − x CA is the analytical concentration of the acid, CH is the
analytical concentration of added hydrogen ions, βq are
Simplify to:
the cumulative association constants
x2 + (Ka + y)x − Ka C0 = 0
log β1 = pKa3 , log β2 = pKa2 +pKa3 , log β3 = pKa1 +pKa2 +pKa3
With specific values for C 0 , Kₐ and y this equation can be
solved for x. Assuming that pH = −log10 [H+ ] the pH can K is the constant for self-ionization of water. There are
be calculated as pH = −log10 (x + y). two non-linear simultaneous equations in two unknown
quantities [A3− ] and [H+ ]. Many computer programs are
available to do this calculation. The speciation diagram
3.2 Polyprotic acids for citric acid was produced with the program HySS.[8]
Polyprotic acids are acids that can lose more than one pro-
ton. The constant for dissociation of the first proton may
be denoted as Kₐ₁ and the constants for dissociation of 4 See also
successive protons as Kₐ₂, etc. Citric acid, H3 A, is an
example of a polyprotic acid as it can lose three protons. • Henderson–Hasselbalch equation
4 6 EXTERNAL LINKS
• Buffering agent
• Good’s buffers
• Common-ion effect
5 References
[1] Butler, J. N. (1964). Ionic Equilibrium: A Mathematical
Approach. Addison-Wesley. p. 151.
[8] Alderighi, L.; Gans, P.; Ienco, A.; Peters, D.; Saba-
tini, A.; Vacca, A. (1999). “Hyperquad simulation and
speciation (HySS): a utility program for the investiga-
tion of equilibria involving soluble and partially soluble
species”. Coordination Chemistry Reviews. 184 (1): 311–
318. doi:10.1016/S0010-8545(98)00260-4.
6 External links
• “Biological buffers”. REACH Devices.
• Phosphate buffer
5
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