Initiators for Continuous Activator Regeneration (ICAR) Depolymerization

Chemical recycling of polymers synthesized by atom transfer radical polymerization (ATRP) typically requires high temperatures (i.e., 170 °C) to operate effectively, not only consuming unnecessary energy but also compromising depolymerization yields due to unavoidable end-group deterioration. To overcome this, the concept of initiators for continuous activator regeneration (ICAR) depolymerization is introduced herein as a broadly applicable approach to significantly reduce reaction temperatures for ATRP depolymerizations. Addition of commercially available free radical initiators enables the on-demand increase of depolymerization efficiency from <1% to 96%, achieving monomer generation at 120 °C, with conversions on par with thermal reversible addition-fragmentation chain transfer (RAFT) depolymerizations. Incubation studies confirm the elimination of deleterious side reactions at the milder temperatures employed, while the methodology can be scaled up to 1 g. The robustness and versatility of ICAR depolymerization is further demonstrated by the possibility to effectively depolymerize both chlorine and bromine terminated polymers and its compatibility with both copper and iron catalysts.

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Publication Details

Journal
Journal of the American Chemical Society
Published
2024-12-12
DOI
https://doi.org/10.1021/jacs.4c13785
Citations
6
Primary Topic
Mass Spectrometry Techniques and Applications
Type
article
Field-Weighted Citation Impact
1.44

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article

Initiators for Continuous Activator Regeneration (ICAR) Depolymerization

Nghia P. Truong, Glen R. Jones, Maria-Nefeli Antonopoulou, Athina Anastasaki
6 citations
Journal of the American Chemical Society
Mass Spectrometry Techniques and Applications
1.44
article

Initiators for Continuous Activator Regeneration (ICAR) Depolymerization

Nghia P. Truong, Glen R. Jones, Maria-Nefeli Antonopoulou, Athina Anastasaki
article en
6 citations

Abstract

Chemical recycling of polymers synthesized by atom transfer radical polymerization (ATRP) typically requires high temperatures (i.e., 170 °C) to operate effectively, not only consuming unnecessary energy but also compromising depolymerization yields due to unavoidable end-group deterioration. To overcome this, the concept of initiators for continuous activator regeneration (ICAR) depolymerization is introduced herein as a broadly applicable approach to significantly reduce reaction temperatures for ATRP depolymerizations. Addition of commercially available free radical initiators enables the on-demand increase of depolymerization efficiency from <1% to 96%, achieving monomer generation at 120 °C, with conversions on par with thermal reversible addition-fragmentation chain transfer (RAFT) depolymerizations. Incubation studies confirm the elimination of deleterious side reactions at the milder temperatures employed, while the methodology can be scaled up to 1 g. The robustness and versatility of ICAR depolymerization is further demonstrated by the possibility to effectively depolymerize both chlorine and bromine terminated polymers and its compatibility with both copper and iron catalysts.

Journal of the American Chemical SocietyVol. 146(51)
ETH Zurich (CH)
Australian Research Council, HORIZON EUROPE European Research Council
Openalex Percentile: Top 19%
Mass Spectrometry Techniques and Applications
1.44
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Initiators for Continuous Activator Regeneration (ICAR) Depolymerization — Nghia P. Truong, Glen R. Jones, et al. · Journal of the American Chemical Society (2024) | TGRS Research Map | TGRS