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 Bulletin of the Acad...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
Bulletin of the Academy of Sciences of the USSR Division of Chemical Science
Article . 1968 . Peer-reviewed
License: Springer TDM
Data sources: Crossref
versions View all 1 versions
addClaim

Polymerization of phenylacetylene on Ziegler-Natta catalysts

Authors: G. I. Bantsyrev; M. I. Cherkashin; A. A. Berlin;

Polymerization of phenylacetylene on Ziegler-Natta catalysts

Abstract

1. The kinetics of the polymerization of phenylacetylene on catalysts (α, δ-TiCl3)-(C3H5)3Al in heptane and benzene medium was studied by a dilatometric method. 2. The influence of the concentration of the components of the catalytic system on the rate of polymerization of phenylacetylene was investigated, and the observed constants, related to the concentration of the catalyst k′ (liters/g·sec), were determined. 3. The temperature dependences of the polymerization of phenylacetylene (40–70°) were studied and the observed activation energies (E) were calculated. The values of E and k′ for styrne were obtained for comparison. 4. In the polymerization of phenylacetylene in heptane, the formation of a substantial amount of cyclic trimer, the yield of which depends on the concentration of (C2H5)3Al, is observed; chiefly a linear polymer is formed in the case of polymerization in benzene. 5. A mechanism of the formation of cyclic products was proposed.

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!