Jump to content

Extraction (chemistry)

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Thisisnotcam (talk | contribs) at 01:48, 18 November 2016 (Reverted 1 edit by 2602:306:CE6B:C1E0:A94D:C935:9A34:2A7C (talk) to last revision by 140.113.206.9. (TW)). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

Laboratory-scale liquid-liquid extraction. Schematic of a separatory funnel used for laboratory scale (<2L combined volume) extractions of 2 immiscible liquid phases, where "oil" may be any phase less dense than water (typically an organic solvent) and "water" may be any less dense liquid phase, typically an aqueous phase.
Laboratory-scale liquid-liquid extraction. Photograph of a separatory funnel in a laboratory scale extraction of 2 immiscible liquids, see above; liquids are a diethyl ether upper phase, and a lower aqueous phase.

Extraction in chemistry is a separation process consisting in the separation of a substance from a matrix. It includes Liquid-liquid extraction, and Solid phase extraction.

Types of extraction

There exist several types of extraction, including: liquid-liquid extraction, solid-phase extraction, solid-phase microextraction, Soxhlet extraction, fizzy extraction.

Components of an extractive process

Extractions often use two immiscible phases to separate a solute from one phase into the other. Typical lab extractions are of organic compounds out of an aqueous phase and into an organic phase. Common extractants are arranged from ethyl acetate to water (ethyl acetate < acetone < ethanol < methanol < acetone:water (7:3) < ethanol:water (8:2) < methanol:water (8:2) < water) in increasing order of polarity according to the Hildebrand solubility parameter. The extract can be put back to dried form using a centrifugal evaporator or a freeze-drier.

Theory of an extraction between two phases

The distribution of a solute between two phases is an equilibrium condition described by partition theory. This is based on exactly how the analyte move from the water into an organic layer

Modern variations

Techniques include supercritical carbon dioxide extraction, ultrasonic extraction, heat reflux extraction, microwave-assisted extraction, instant controlled pressure drop extraction (DIC), and perstraction.

Applications

Boiling tea leaves in water extracts the tannins, theobromine, and caffeine out of the leaves and into the water. Solid-liquid extractions at laboratory scales can use Soxhlet extractors (such as oil from olive cakesee at right).

Soxhlet extractor

Further reading

  • Gunt Hamburg, 2014, Thermal Process Engineering: Liquid-liquid extraction and solid-liquid extraction, see [1], accessed 12 May 2014.
  • G.W. Stevens, T.C., Lo, & M. H. I. Baird, 2007, "Extraction, Liquid-Liquid", in Kirk-Othmer Encyclopedia of Chemical Technology, DOI: 10.1002/0471238961.120917211215.a01.pub2, see [2], accessed 12 May 2014.
  • T. Voeste, K. Weber, B. Hiskey & G. Brunner, 2006, "Liquid–Solid Extraction", in Ullmann's Encyclopedia of Industrial Chemistry, DOI: 10.1002/14356007.b03_07.pub2, see [3], accessed 12 May 2014.
  • R. J. Wakeman, 2000, "Extraction, Liquid-Solid", in Kirk-Othmer Encyclopedia of Chemical Technology, DOI: 10.1002/0471238961.1209172123011105.a01, see [4], accessed 12 May 2014.
  • M.J.M. Wells, 2000, "Essential guides to method development in solid-phase extraction," in Encyclopedia of Separation Science, Vol. 10 (I.D. Wilson, E.R. Adlard, M. Cooke, and C.F. Poole, eds.), London:Academic Press, London, 2000, pp. 4636–4643.
  • Colin Poole & Michael Cooke, 2000, Extraction, in Encyclopedia of Separation Science, 10 Vols., ISBN 9780122267703, see [5], accessed 12 May 2014.

See also

References