Observation and Modeling of a Sharp Oxygen Threshold in Aqueous Free Radical and RAFT Polymerization

J Phys Chem B. 2022 Dec 29;126(51):10933-10947. doi: 10.1021/acs.jpcb.2c06067. Epub 2022 Dec 15.

Abstract

It is known that oxygen (O2) stops radical polymerization (RP). Here, it was found that the reaction turn-off occurs abruptly at a threshold concentration of O2, [O2]t, for both free RP and reversible addition-fragmentation chain-transfer polymerization (RAFT). In some reactions, there was a spontaneous re-start of conversion. Three cases were investigated: RP of (i) acrylamide (Am) and (ii) sodium styrene sulfonate (SS) and (iii) Am RAFT polymerization. A controlled flow of O2 into the reactor was employed. An abrupt turn-off was observed in all cases, where polymerization stops sharply at [O2]t and remains stopped when [O2] > [O2]t. In (i), Am acts as a catalytic radical-transfer agent during conversion plateau, eliminating excess [O2], and polymerization spontaneously resumes at [O2]t. In no reaction, the initiator alone was capable of eliminating O2. N2 purge was needed to re-start reactions (ii) and (iii). For (i) and (ii), while [O2] < [O2]t, O2 acts a chain termination agent, reducing the molecular weight (Mw) and reduced viscosity (RV). O2 acts as an inhibitor for [O2] > [O2]t in all cases. The radical-transfer rates from Am* and SS* to O2 are >10,000× higher than the initial chain propagation step rates for Am and SS, which causes [O2]t at very low [O2].

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acrylamide*
  • Free Radicals
  • Molecular Weight
  • Polymerization
  • Styrene*

Substances

  • Free Radicals
  • Styrene
  • Acrylamide