THE INCORPORATION OF SIDE REACTIONS INTO PSEUDOSTATIONARY POLYMERIZATION .1. THE CLOSED SOLUTION OF A KINETIC SCHEME COMPRISING CHAIN-TRANSFER TO MONOMER OR SOLVENT
G. Zifferer et Of. Olaj, THE INCORPORATION OF SIDE REACTIONS INTO PSEUDOSTATIONARY POLYMERIZATION .1. THE CLOSED SOLUTION OF A KINETIC SCHEME COMPRISING CHAIN-TRANSFER TO MONOMER OR SOLVENT, Macromolecular theory and simulations, 5(5), 1996, pp. 901-921
A procedure is developed that allows the calculation of chain length d
istributions of polymers prepared by periodic modulation of the initia
tion process, considering termination by disproportionation and chain
transfer. For the case of a (pseudostationary) laser-pulse initiated p
olymerization process a closed solution can be derived for the chain l
ength distribution (cld) of dead polymer and its 0(th), 1(st) and 2(nd
) moments. By analysis of the detectability of the ''extra-peaks'' app
earing in the cld (which represent the key for the determination of pr
opagation constants) as a function of the parameters chosen the optimu
m conditions can be predicted for experiments.