Everything about Acid-base Extraction totally explained
Acid-base extraction is a procedure using sequential
liquid-liquid extractions to purify
acids and
bases from mixtures based on their chemical properties. Acid-base extraction is routinely performed during the
work-up after
chemical syntheses and for the
isolation of compounds and
natural products like
alkaloids from crude
extracts. The product is largely free of neutral and acidic or basic impurities. It isn't possible to separate chemically similar acids or bases using this simple method.
Theory
The fundamental theory behind this technique is that salts, which are ionic, tend to be water-soluble while neutral molecules tend not to be.
The addition of an acid to a mixture of an organic acid and base will result in the acid remaining uncharged, while the base will be protonated. If the organic acid, such as a
carboxylic acid, is sufficiently strong, its self-ionization can be suppressed by the added acid.
Conversely, the addition of a base to a mixture of an organic acid and base will result in the base remaining uncharged, while the acid is deprotonated to give the corresponding salt. Once again, the self-ionization of a strong base is suppressed by the added base.
The acid-base extraction procedure can also be used to separate very weak acids from stronger acids and very weak bases from stronger bases as long as the difference of their
pKa (or pK
b) constants is large enough. Examples are:
Usually the pH is adjusted to a value roughly between the pK
a (or pK
b) constants of the compounds to be separated. Weak acids like
citric acid,
phosphoric acid, or diluted
sulfuric acid are used for moderately acidic pH values and
hydrochloric acid or more concentrated sulfuric acid is used for strongly acidic pH values. Similarly, weak bases like
ammonia or
sodium bicarbonate (NaHCO
3) are used for moderately basic pH values while stronger bases like
potassium carbonate (K
2CO
3) or
sodium hydroxide (NaOH) are used for strongly alkaline conditions.
Technique
Usually, the mixture is dissolved in a suitable solvent such as
dichloromethane or
ether, and poured into a
separating funnel. An aqueous solution of the acid or base is added, and the pH of the aqueous phase is adjusted to bring the compound of interest into its required form. After shaking and allowing for phase separation, the phase containing the compound of interest is collected. The procedure is then repeated with this phase at the opposite pH range. The order of the step isn't important and the process can be repeated to increase the separation. However, it's often convenient to have the compound dissolved the organic phase after the last step, so that
evaporation of the solvent yields the product.
Limitations
The procedure works only for acids and bases with a large difference in solubility between their charged and their uncharged form. The procedure doesn't work for:
Zwitterions with acidic and basic functional groups in the same molecule, for example glycine which tend to be water soluble at most pH.
Very lipophilic amines that don't easily dissolve in the aqueous phase in their charged form, e.g triphenylamine and trihexylamine.
Very lipophilic acids that don't easily dissolve in the aqueous phase in their charged form, e.g fatty acids.
Lower amines amines like ammonia, methylamine, or triethanolamine which are miscible or significantly soluble in water at most pH.
Hydrophilic acids like acetic acid, citric acid, and most inorganic acids like sulfuric acid or phosphoric acid.
Alternatives
Alternatives to acid-base extraction including:
filtering the mixture through a plug of silica gel or alumina — charged salts tend to remain strongly adsorbed to the silica gel or alumina
ion exchange chromatography can separate acids, bases, or mixtures of strong and weak acids and bases by their varying affinities to the column medium at different pH.Further Information
Get more info on 'Acid-base Extraction'.
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