Skip to main content

Copolymerization

  • Chapter

Abstract

In addition to forming polymers with molecules of their own kind, many monomers can form copolymers with other monomers. The scale of possibilities is thus widely extended. In free radical polymerization, for example, styrene is converted to poly(styrene), methyl methacrylate to poly(methyl methacrylate), and vinyl acetate to poly(vinyl acetate). A mixture of styrene and methyl methacrylate gives poly(styrene-co-methyl methacrylate) even at the lowest conversions. From a mixture of styrene and vinyl acetate, on the other hand, practically pure poly(styrene) is first formed, and then, when the styrene is exhausted, almost pure poly(vinyl acetate). This is therefore a mixture (blend) and not a copolymer. Whereas stilbene, free-radically initiated, does not give a unipolymer, and maleic anhydride gives one of only low molecular weight, a mixture of both monomers leads to a copolymer of the composition 1:1.

This is a preview of subscription content, log in via an institution.

Buying options

Chapter
USD   29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD   129.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD   169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Learn about institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

Literature

General

  • T. J. Alfrey, J. J. Bohrer, and H. Mark, Copolymerization, Interscience, New York, 1952.

    Google Scholar 

  • G. E. Ham, ed., Copolymerization, Interscience, New York, 1964.

    Google Scholar 

  • R. A. Patsiga, Copolymerization of vinyl monomers with ring compounds, J. Macromol. Sci. C (Rev. Macromol. Chem.) 1, 223 (1967).

    CAS  Google Scholar 

  • J. E. Herz and V. Stannett, Copolymerization in the crystalline solid state, Macromol. Rev. 3, 1 (1968).

    Article  CAS  Google Scholar 

  • P. W. Tidswell and G. A. Mortimer, Science of determining copolymerization reactivity ratios, J. Macromol. Sci. C (Rev. Macromol. Chem.) 4, 281 (1970)

    Article  Google Scholar 

  • H. Sawada, Thermodynamics of polymerization. V. Thermodynamics of copolymerization. Pt. I., J. Macromol. Sci. C (Rev. Macromol. Chem.) 11, 293 (1974).

    Google Scholar 

Section 22.2 Terpolymerization

  • A. Valvassori and G. Sartori, Present status of the multicopolymerization theory, Adv. Polym. Sci. 5, 28 (1967/1968).

    Google Scholar 

Section 22.4 Free Radical Copolymerization

  • S. Iwasuki and Y. Yamashita, Radical alternating copolymerizations, Prog. Polym. Sci. Japan 2, 1 (1971).

    Google Scholar 

  • J. Furukawa, Alternating copolymers of diolefins and olefinic compounds, Prog. Polym. Sci. Japan 5, 1 (1973).

    CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

Copyright information

© 1977 Springer Science+Business Media New York

About this chapter

Cite this chapter

Elias, HG. (1977). Copolymerization. In: Macromolecules. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-7364-7_22

Download citation

  • DOI: https://doi.org/10.1007/978-1-4615-7364-7_22

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4615-7366-1

  • Online ISBN: 978-1-4615-7364-7

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics