Difference between revisions of "Hydrolysis"

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'''Hydrolysis''' (/haɪˈdrɒlɪsɪs/; from Ancient Greek ''hydro-'' 'water', and ''lysis'' 'to unbind') is a chemical reaction in which a molecule of water breaks one or more chemical bonds. The term is used broadly for substitution, elimination, and solvation reactions in which water is the nucleophile.<ref>{{Cite web|year=2002|title=Hydrolysis|e-pub date=2002|date accessed=2021|url=https://en.wikipedia.org/wiki/Hydrolysis}}</ref>
'''Hydrolysis''' (/haɪˈdrɒlɪsɪs/; from Ancient Greek ''hydro-'' 'water', and ''lysis'' 'to unbind') is a chemical reaction in which a molecule of water breaks one or more chemical bonds. The term is used broadly for substitution, elimination, and solvation reactions in which water is the nucleophile.<ref>{{Cite web|year=2002|title=Hydrolysis|e-pub date=2002|date accessed=2021|url=https://en.wikipedia.org/wiki/Hydrolysis|Author=Wikipedia}}</ref> In lignocellulosic biomass, the cellulose and hemicellulose breaks down into individual sugars, where hemicellulose is easier to hydrolyse than cellulose.<ref>{{Cite journal|title=Dilute acid hydrolysis of lignocellulosic biomass|year=2010-01-15|author=P. Lenihan, A. Orozco, E. O’Neill, M.N.M. Ahmad, D.W. Rooney, G.M. Walker|journal=Chemical Engineering Journal|volume=156|issue=2|page=395–403|doi=10.1016/j.cej.2009.10.061}}</ref> The result of hydrolysing hemicellulose and cellulose is sugars (glucose, xylose, mannose, and galactose) and organic acids (formic acid and acetic acid).<ref>{{Cite journal|title=Acid Hydrolysis of Lignocellulosic Biomass: Sugars and Furfurals Formation|year=2020-04-17|author=Katarzyna Świątek, Stephanie Gaag, Andreas Klier, Andrea Kruse, Jörg Sauer, David Steinbach|journal=Catalysts|volume=10|issue=4|page=437|doi=10.3390/catal10040437}}</ref>


== Feedstock ==
== Feedstock ==
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=== Acid ===
=== Acid ===
'''Acid hydrolysis''' is a hydrolysis process in which a protic acid is used to catalyze the hydrolysis reaction. Dilute or concentrated acids help to break down the cellulose and hemicellulose into individual sugars.<ref>{{Cite journal|title=Dilute acid hydrolysis of lignocellulosic biomass|year=2010-01-15|author=P. Lenihan, A. Orozco, E. O’Neill, M.N.M. Ahmad, D.W. Rooney, G.M. Walker|journal=Chemical Engineering Journal|volume=156|issue=2|page=395–403|doi=10.1016/j.cej.2009.10.061}}</ref>
'''Acid hydrolysis''' is a hydrolysis process in which a protic acid is used to catalyze the hydrolysis reaction.  


=== Alkali ===
=== Alkali ===

Revision as of 12:27, 13 August 2021

Hydrolysis (/haɪˈdrɒlɪsɪs/; from Ancient Greek hydro- 'water', and lysis 'to unbind') is a chemical reaction in which a molecule of water breaks one or more chemical bonds. The term is used broadly for substitution, elimination, and solvation reactions in which water is the nucleophile.[1] In lignocellulosic biomass, the cellulose and hemicellulose breaks down into individual sugars, where hemicellulose is easier to hydrolyse than cellulose.[2] The result of hydrolysing hemicellulose and cellulose is sugars (glucose, xylose, mannose, and galactose) and organic acids (formic acid and acetic acid).[3]

Feedstock

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Process and technologies

Acid

Acid hydrolysis is a hydrolysis process in which a protic acid is used to catalyze the hydrolysis reaction.

Alkali

Alkaline hydrolysis refers to types of nucleophilic substitution reactions in which the attacking nucleophile is a hydroxide ion.

Salt

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Ionic liquids

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Sulphite salt

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Solvent

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Organosolv

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Product

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Technology providers

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Patents

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References

  1. Wikipedia, 2002: Hydrolysis 2002, Last access 2021. https://en.wikipedia.org/wiki/Hydrolysis
  2. P. Lenihan, A. Orozco, E. O’Neill, M.N.M. Ahmad, D.W. Rooney, G.M. Walker, 2010-01-15: Dilute acid hydrolysis of lignocellulosic biomass. Chemical Engineering Journal, Vol. 156, (2), 395–403. doi: https://doi.org/10.1016/j.cej.2009.10.061
  3. Katarzyna Świątek, Stephanie Gaag, Andreas Klier, Andrea Kruse, Jörg Sauer, David Steinbach, 2020-04-17: Acid Hydrolysis of Lignocellulosic Biomass: Sugars and Furfurals Formation. Catalysts, Vol. 10, (4), 437. doi: https://doi.org/10.3390/catal10040437