Active Sites of Polymerization

Regular price €427.80
Title
Quantity:
In stock with our UK publisher. 14-28 days
Delivery/Collection within 10-20 working days
14 days return policy Shipping & Delivery
advanced polymerisation kinetics
catalytic site analysis
Category=PNNP
Category=PNRA
Category=PNRD
eq_bestseller
eq_isMigrated=1
eq_nobargain
eq_non-fiction
eq_science
molecular weight distribution
polymer microstructure
polymer reaction mechanisms
quantum chemical modelling
stereoregular polymers

Product details

  • ISBN 9789067644242
  • Weight: 764g
  • Dimensions: 156 x 234mm
  • Publication Date: 28 Mar 2005
  • Publisher: Brill
  • Publication City/Country: NL
  • Product Form: Hardback
Secure checkout Fast Shipping Easy returns
The monograph is intended to systematize data on active sites and their kinetic and stereospecific heterogeneity (polysite phenomenon) in olefin and diene monomer ion, ion-coordination and complex radical polymerization processes. Questions of molecular-mass distribution of polymers obtained by ion and ion-coordination polymerization methods are discussed together with composition and stereo regularity distribution of olefin copolymers. Data on the influence of transition and non-transition metal origin and their ligand ambience, conditions of catalytic system preparation and polymerization are shown. Various assessment methods of polymerization active site distribution by kinetic activity and stereospecific action are considered. In particular, an assessment method for kinetic activity distribution at ion-coordination diene polymerization is described, mathematical simulation parameters for polymerization processes are shown, taking into account the polysite structure of catalytic systems. Of special attention are geometrical and electron structure of active sites in the ion-coordination polymerization by the quantum chemistry method, interrelation between reactivity of some types of active sites and stereospecificity of their action in diene polymerization. The importance of ratio between specific time elementary act duration at the diene injection, coordinated on an active site, and time of propagating macrochain end unit existence in the s-state at polydiene microstructure formation is indicated. Questions of the polysite mechanism occurrence in complex radical polymerization processes are discussed. A possibility for polymerization to proceed in both free-radical and complex related chain propagation sites is shown.
Gennady Zaikov, Yuri Monakov, Natalia Sigaeva, Vadim Urazbaev