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Condensation polymer
Polymer produced via a condensation reaction

In polymer chemistry, condensation polymers are any kind of polymers whose process of polymerization involves a condensation reaction (i.e. a small molecule, such as water or methanol, is produced as a byproduct). Natural proteins as well as some common plastics such as nylon and PETE are formed in this way. Condensation polymers are formed by polycondensation, when the polymer is formed by condensation reactions between species of all degrees of polymerization, or by condensative chain polymerization, when the polymer is formed by sequential addition of monomers to an active site in a chain reaction. The main alternative forms of polymerization are chain polymerization and polyaddition, both of which give addition polymers.

Condensation polymerization is a form of step-growth polymerization. Linear polymers are produced from bifunctional monomers, i.e. compounds with two reactive end-groups. Common condensation polymers include polyesters, polyamides such as nylon, polyacetals, and proteins.

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Polyamides

One important class of condensation polymers are polyamides.3 They arise from the reaction of carboxylic acid and an amine. Examples include nylons and proteins. When prepared from amino-carboxylic acids, e.g. amino acids, the stoichiometry of the polymerization includes co-formation of water:

n H2N-X-CO2H → [HN-X-C(O)]n + (n-1) H2O

When prepared from diamines and dicarboxylic acids, e.g. the production of nylon 66, the polymerization produces two molecules of water per repeat unit:

n H2N-X-NH2 + n HO2C-Y-CO2H → [HN-X-NHC(O)-Y-C(O)]n + (2n-1) H2O

Polyesters

Another important class of condensation polymers are polyesters.4 They arise from the reaction of a carboxylic acid and an alcohol. An example is polyethyleneterephthalate, the common plastic PET (recycling #1 in the USA):

n HO-X-OH + n HO2C-Y-CO2H → [O-X-O2C-Y-C(O)]n + (2n-1) H2O

Safety and environmental considerations

Condensation polymers tend to be more biodegradable than addition polymers. The peptide or ester bonds between monomers can be hydrolysed, especially in the presence of catalysts or bacterial enzymes.5

See also

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References

  1. Introduction to Polymers 1987 R.J. Young Chapman & Hall ISBN 0-412-22170-5 /wiki/ISBN_(identifier)

  2. D. Margerison; G. C. East; J. E. Spice (1967). An Introduction to Polymer Chemistry. Pergamon Press. ISBN 978-0-08-011891-8. 978-0-08-011891-8

  3. B. Herzog; M. I. Kohan; S. A. Mestemacher; R. U. Pagilagan; K. Redmond (2013). "Polyamides". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a21_179.pub3. ISBN 978-3-527-30673-2. S2CID 241272519. 978-3-527-30673-2

  4. Horst Köpnick; Manfred Schmidt; Wilhelm Brügging; Jörn Rüter; Walter Kaminsky (2002). "Polyesters". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a21_227. ISBN 3-527-30673-0. 3-527-30673-0

  5. Wei, Ren; Zimmermann, Wolfgang (November 2017). "Microbial enzymes for the recycling of recalcitrant petroleum-based plastics: how far are we?". Microbial Biotechnology. 10 (6): 1308–1322. doi:10.1111/1751-7915.12710. PMC 5658625. PMID 28371373. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5658625