Buffer solution - Wikipedia, the free encyclopedia

Buffer solution

From Wikipedia, the free encyclopedia

For an individual weak acid or weak base component, see Buffering agent. For uses not related to acid-base chemistry, see Buffer (disambiguation).

Acids and bases:

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Buffer solutions are solutions that resist change in hydronium ion and the hydroxide ion concentration (and consequently pH) upon addition of small amounts of acid or base, or upon dilution. Buffer solutions consist of a weak acid and its conjugate base (more common) or a weak base and its conjugate acid (less common). The resistive action is the result of the equilibrium between the weak acid (HA) and its conjugate base (A⁻):

HA(aq) + H₂O(l) ↔ H₃O⁺(aq) + A⁻(aq)

Any alkali added to the solution is consumed by the hydronium ions. These ions are mostly regenerated as the equilibrium moves to the right and some of the acid dissociates into hydronium ions and the conjugate base. If a strong acid is added, the conjugate base is protonated, and the pH is almost entirely restored. This is an example of Le Chatelier's principle and the common ion effect. This contrasts with solutions of strong acids or strong bases, where any additional strong acid or base can greatly change the pH. This may be easier to see by comparing two graphs when an strong acid is titrated with a strong base the curve will have a large gradient throughout showing that a small addition of base/acid will have a large effect compared to a weak acid/strong base titration curve which will have a smaller gradient near the pKa.

When writing about buffer systems they can be represented as salt of conjugate base/acid, or base/salt of conjugate acid. It should be noted that here buffer solutions are presented in terms of the Brønsted-Lowry notion of acids and bases, as opposed to the Lewis acid-base theory (see acid-base reaction theories). Omitted here are buffer solutions prepared with solvents other than water.

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[edit] Calculating pH

Titration of a weak acid with a strong base the flat region at pKa is the buffering region.

Titration of a strong acid with a strong base. Note the sharp rise in pH: this solution can not buffer.

The equilibrium above has the following acid dissociation constant:

$\mathrm{K_a = \frac{[H^+][A^-]}{[HA]}}$

Simple manipulation with logarithms gives the Henderson-Hasselbalch equation, which describes pH in terms of pK_a:

$pH=pK_a+\log_{10}\frac{[A^-]}{[HA]}$

In this equation

[A−] is the concentration of the conjugate base. This may be considered as coming completely from the salt, since the acid supplies relatively few anions compared to the salt lyn.
[HA] is the concentration of the acid. This may be considered as coming completely from the acid, since the salt supplies relatively few complete acid molecules (A ⁻ may extract H ⁺ from water to become HA) compared to the added acid.

Maximum buffering capacity is found when pH = pKa, and buffer range is considered to be at a pH = pKa ± 1.

[edit] Illustration of buffering effect: Sodium acetate/acetic acid

The acid dissociation constant for acetic acid-sodium acetate is given by the equation:

$\mathrm{K_a = \frac{[H^+][CH_3COO^-]}{[CH_3COOH]}}$

Since this equilibrium only involves a weak acid and base, it can be assumed that ionization of the acetic acid and hydrolysis of the acetate ions are negligible. In a buffer consisting of equal amounts of acetic acid and sodium acetate, the equilibrium equation simplifies to

K_a = [H ⁺ ],

and the pH of the buffer as is equal to the pK_a.

To determine the effect of addition of a strong acid such as HCl, the following mathematics would provide the new pH. Since HCl is a strong acid, it is completely ionized in solution. This increases the concentration of H⁺ in solution, which then neutralizes the acetate by the following equation.

$\mathrm{CH_3COO^-_{(aq)}+H^+_{(aq)} \to CH_3COOH_{(aq)}}$

The consumed hydrogen ions change the effective number of moles of acetic acid and acetate ions:

$\mathrm{moles\ of\ CH_3COO^- = initial\ moles\ of\ CH_3COO^- - initial\ moles\ of\ HCl}$

$\mathrm{moles\ of\ CH_3COOH = initial\ moles\ of\ CH_3COOH + initial\ moles\ of\ HCl}$

After accounting for volume change to determine concentrations, the new pH could be calculated from the Henderson-Hasselbalch equation. Any neutralization will result in a small change in pH, since it is on a logarithmic scale.

[edit] Applications

Their resistance to changes in pH makes buffer solutions very useful for chemical manufacturing and essential for many biochemical processes. The ideal buffer for a particular pH has a pK_a equal to the pH desired, since a solution of this buffer would contain equal amounts of acid and base and be in the middle of the range of buffering capacity.

Buffer solutions are necessary to keep the correct pH for enzymes in many organisms to work. Many enzymes work only under very precise conditions; if the pH strays too far out of the margin, the enzymes slow or stop working and can denature, thus permanently disabling its catalytic activity. A buffer of carbonic acid (H₂CO₃) and bicarbonate (HCO₃⁻) is present in blood plasma, to maintain a pH between 7.35 and 7.45.

Industrially, buffer solutions 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.

[edit] Common buffer compounds used in biology

See also: Good's buffers

Common Name	pK_a at 25°C	Buffer Range	Temp Effect (pH / °C)**	Mol. Weight	Full Compound Name
TAPS	8.43	7.7 – 9.1	−0.018	243.3	3-{[tris(hydroxymethyl)methyl]amino}propanesulfonic acid
Bicine	8.35	7.6 – 9.0	−0.018	163.2	N,N-bis(2-hydroxyethyl)glycine
Tris	8.06	7.5 – 9.0	−0.028	121.14	tris(hydroxymethyl)methylamine
Tricine	8.05	7.4 – 8.8	−0.021	179.2	N-tris(hydroxymethyl)methylglycine
HEPES	7.48	6.8 – 8.2	−0.014	238.3	4-2-hydroxyethyl-1-piperazineethanesulfonic acid
TES	7.40	6.8 – 8.2	−0.020	229.20	2-{[tris(hydroxymethyl)methyl]amino}ethanesulfonic acid
MOPS	7.20	6.5 – 7.9	−0.015	209.3	3-(N-morpholino)propanesulfonic acid
PIPES	6.76	6.1 – 7.5	−0.008	302.4	piperazine-N,N′-bis(2-ethanesulfonic acid)
Cacodylate	6.27	5.0 – 7.4		138.0	dimethylarsinic acid
MES	6.15	5.5 – 6.7	−0.011	195.2	2-(N-morpholino)ethanesulfonic acid
Acetate	4.76	3.8 – 5.8		59.04	Deprotonated Ethanoic Acid (Non-IUPAC Name);

** Values are approximate

[edit] Making buffer solutions

In general, preparing a buffer solution requires either:

A weak acid and a salt of the acid's conjugate base
Or a weak base and a salt of the base's conjugate acid

Both of which in sufficient amounts to maintain the ability to buffer

[edit] Example: Citric acid-phosphate buffer

Make up 0.1M citric acid and 0.2M disodium phosphate solutions then mix as follows to make a 100 ml solution:

Citric acid-phosphate buffers
pH	0.2M Na₂HPO₄	0.1M Citric Acid
3.0	20.55 ml	79.45 ml
4.0	38.55 ml	61.45 ml
5.0	51.50 ml	48.50 ml
6.0	63.15 ml	36.85 ml
7.0	82.35 ml	17.65 ml
8.0	97.25 ml	2.75 ml

[edit] See also

[edit] External links

Derivation and discussion of Henderson-Hasselbalch equation
Buffer formulation and analysis free spreadsheet for calculation of pH, species distribution and titration of buffers (buffer capacity)
Sigma Aldrich Buffer Calculator - Useful tool to calculate weight, volume, or concentration from molecular weight.mansoor

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Categories: Acid-base chemistry

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4.26.2008

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