z-logo
open-access-imgOpen Access
Emulsion polymerization of butadiene, 3. Kinetic effects of stirring conditions and monomer/water ratio
Author(s) -
Weerts Pierre A.,
Van der Loos Jos L. M.,
German Anton L.
Publication year - 1991
Publication title -
die makromolekulare chemie
Language(s) - English
Resource type - Journals
ISSN - 0025-116X
DOI - 10.1002/macp.1991.021920909
Subject(s) - monomer , emulsion polymerization , polymerization , nucleation , diffusion , particle (ecology) , emulsion , phase (matter) , polymer chemistry , limiting , chemical engineering , kinetic energy , chemistry , polymer , materials science , thermodynamics , organic chemistry , physics , mechanical engineering , oceanography , quantum mechanics , engineering , geology
The stirring speed n influences the emulsion polymerization of butadiene, (1) by reducing the effective emulsifier concentration [E] eff available for particle nucleation and stabilization at high n , and (2) by limiting diffusion of monomer to the latex particles at low n . The large density difference between butadiene and water promotes the breaking up of droplets at high n , while the same condition constitutes a large driving force for (partial) phase separation at low n . Increasing the monomer/water ratio at constant [E] decreases [E] eff , and thus the final particle number. At monomer volume fractions >0,6 mixed emulsions are likely to be formed initially, reducing [E] eff even further. In the presence of mixed emulsions, polymerization in the monomer phase may no longer be neglected, giving rise to a complex kinetic behaviour.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom