Powered by OpenAIRE graph
Found an issue? Give us feedback
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Gazi Üniversitesi - ...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Rubber Chemistry and Technology
Article . 2002 . Peer-reviewed
Data sources: Crossref
versions View all 2 versions
addClaim

The Modification of Butadiene-Acrylonitrile Rubber with Vinylcyclohexyl Ketone

Authors: Talu, M; Sari, BEKİR; Resulov, NS;

The Modification of Butadiene-Acrylonitrile Rubber with Vinylcyclohexyl Ketone

Abstract

Abstract Butadiene-acrylonitrile-vinylcyclohexyl ketone (BD-AN-VCHK) terpolymer was synthesized by radical polymerization. The structure of the synthesized terpolymer was elucidated by IR spectroscopy and physical and mechanical tests. BD-AN-VCHK terpolymer was stable at lower temperatures and exhibited good adhesive properties. It was also observed that the yield of terpolymer was dependent upon the initial concentration of VCHK and pH of the media. The percentage of conversion increased by increasing the initial concentration of VCHK. With addition of 10.8% VCHK to the BD-AN mixture, the glass transition temperature (Tg) value of the polymers decreased from −40 °C to −57 °C. However further increase of VCHK ratio (20.4%) resulted in the formation of the polymers with Tg value of −48 °C. It was shown that this was due to the fact that VCHK, entering the structure during polymerization process, converted the trans structure of butadiene sequences into the cis form.

Country
Turkey
Related Organizations
  • BIP!
    Impact byBIP!
    selected citations
    These citations are derived from selected sources.
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    0
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Average
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Average
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Average
Powered by OpenAIRE graph
Found an issue? Give us feedback
selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
0
Average
Average
Average
Related to Research communities
Upload OA version
Are you the author of this publication? Upload your Open Access version to Zenodo!
It’s fast and easy, just two clicks!