Poly(3-hydroxybutyrate) from carbon monoxide

Robert Reichardt, Bernhard Rieger

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

47 Scopus citations

Abstract

The potential applications of naturally occurring poly(3-hydroxybutyrate) (PHB) is demonstrated by a summary of its variable mechanical properties in comparison with different commercially available polymers. This comparison underlines the striking similarity to the most-produced materials in the world, the poly(olefin)s, which offers many possible applications depending on the correct polymer microstructure. However, there is a resulting competition with regard to product prices. When commercialization is addressed, low-cost raw materials as well as fast and simple polymer synthesis and purification are necessary. A brief look into today's biotechnological PHB synthesis is followed by a short discussion of potential raw materials. This clearly demonstrates that a non-fermentative synthesis is desirable. Therefore, this manuscript reviews the latest results of catalytic PHB synthesis. Besides alternating copolymerization of carbon monoxide and propylene oxide there is special focus on ring-opening polymerization of β-butyrolactone, which has gained increasing interest over the past decade. Since stereocontrol is relatively difficult to achieve during ring-opening polymerization, an outlook on stereoselective monomer synthesis concludes this article.

Original languageEnglish
Title of host publicationSynthetic Biodegradable Polymers
EditorsBernhard Rieger, Geoffrey Coates, Eckhard Dinjus, Thomas Zevaco, Andreas Kunkel, Robert Reichardt
Pages49-90
Number of pages42
DOIs
StatePublished - 2012

Publication series

NameAdvances in Polymer Science
Volume245
ISSN (Print)0065-3195

Keywords

  • Alternating copolymerization
  • Poly(3-hydroxybutyrate)
  • Propylene oxide and carbon monoxide
  • Ring-opening polymerization
  • Stereoselective carbonylation
  • β-Butyrolactone

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