Poly(methyl acrylate) explained

Poly(methyl acrylate) (PMA) is a family of organic polymers with the formula n. It is a synthetic acrylate polymer derived from methyl acrylate monomer. The polymers are colorless. This homopolymer is far less important than copolymers derived from methyl acrylate and other monomers. PMA is softer than polymethyl methacrylate (PMMA),[1] It is tough, leathery, and flexible.[2]

Copolymers

Far more important than PMA are copolymers produced from methyl acrylate and one or more of the following comonomers methyl methacrylate, styrene, acrylonitrile, vinyl acetate, vinyl chloride, vinylidene chloride, and butadiene.[3]

Properties

It has a low glass-transition temperature about 10°C (12.5°C in case of PMA38).[4] It is soluble in dimethyl sulfoxide (DMSO). PMA is water-sensitive and unlike PMMA, is not stable against alkalies.

High-energy radiation leads to cross linking in PMA. However in polymethyl methacrylate (PMMA), a compound similar to PMA, degradation occurs instead.

Uses

Also used in leather finishing and textiles.

Derivatives of this polymer are commonly used in orally administerd pharmaceutical formulations to target specific regions of the gastrointestinal tract.[5]

Notes and References

  1. Book: Peter A. Ciullo. Industrial Minerals and Their Uses: A Handbook and Formulary. 30 June 2012. 1996. Elsevier. 978-0-8155-1408-4. 115.
  2. Book: J. A. Brydson. Plastics Materials. 30 June 2012. 8 November 1999. Butterworth-Heinemann. 978-0-7506-4132-6. 423.
  3. Book: 10.1002/14356007.a21_157.pub2. Polyacrylates . Ullmann's Encyclopedia of Industrial Chemistry . 2018 . Penzel . Erich . Ballard . Nicholas . Asua . José M. . 1–20 . 9783527306732 .
  4. Book: Kyle B. Guice. Synthesis & Characterization of Temperature- and PH-responsive Nanostructures Derived from Block Copolymers Containing Statistical Copolymers of HEMA and DMAEMA.. 30 June 2012. 2008. 978-0-549-63651-9. 29.
  5. Web site: Eudragit a versatile polymer: A review .