Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/37211
Title: Pulsed laser polymerization–size exclusion chromatography investigations into backbiting in ethylhexyl acrylate polymerization
Authors: QUINTENS, Greg 
JUNKERS, Tanja 
Issue Date: 2022
Publisher: ROYAL SOC CHEMISTRY
Source: POLYMER CHEMISTRY, 13 (14) , p. 2019 -2025
Abstract: Free radical acrylate polymerization is associated with a considerable number of side reactions occurring during chain growth. Most notably, secondary chain propagating radicals can undergo intramolecular transfer reactions, forming more stable, tertiary midchain radicals. These midchain radicals can transform back into rapidly propagating secondary radicals by monomer addition. In practice, under steady-state polymerization conditions, an average propagation rate will be observed that is described by three individual rate coefficients. These are the coefficients for secondary radical propagation, kSPR(p), the backbiting reaction, k(bb), and the tertiary radical monomer addition rate, ktert(p). Based on our previous work on tert-butyl acrylate, we determined these rate coefficients in the temperature range of 5 to 60 degrees C via pulsed laser polymerization experiments in a laser frequency range of 1 to 1000 Hz for the monomer 2-ethylhexyl acrylate. Parameter estimations via Predici allowed all rate coefficients to be determined directly from the apparent propagation rate coefficients determined at various frequencies. The obtained Arrhenius relations are E-A(kSPR(p)) = 16.0 kJ mol(-1) and ln(A(kSPR(p))/L mol(-1) s(-1)) = 16.1, E-A(k(bb)) = 32.2 kJ mol(-1) and ln(A(k(bb))/L mol(-1) s(-1)) = 16.5 and E-A(ktert(p)) = 33.3 kJ mol(-1) and ln(A(ktert(p))/L mol(-1) s(-1)) = 15.1.
Notes: Junkers, T (corresponding author), Monash Univ, Polymer React Design Grp, 19 Rainforest Walk, Clayton, Vic 3800, Australia.
tanja.junkers@monash.edu
Document URI: http://hdl.handle.net/1942/37211
DOI: 10.1039/d1py01533h
ISI #: WOS:000771681300001
Rights: This journal is © The Royal Society of Chemistry 2022Polym.Chem., 2022,13,2019–2025 |2019Published on 12 March 2022.
Category: A1
Type: Journal Contribution
Validations: ecoom 2023
Appears in Collections:Research publications

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