Ultrafast Thermal RAFT Depolymerization at HigherSolid Contents

Although thermal solution RAFT depolymerization has recently emerged as an efficient chemical recycling methodology, current approaches require specialized solvents (i.e., dioxane), typically suffer from extended reaction times, and operate exclusively under highly dilute conditions (i.e., 5 mM repeat unit concentration). To circumvent these limitations, a commercial radical initiator is introduced to kinetically untrap the depolymerization and promote chain-end activation. By varying the initiator concentration, a remarkable rate acceleration (up to 72 times faster) can be observed, enabling the completion of the depolymerization within 5 min. Notably, a 20-fold increase in the repeat unit concentration did not appreciably compromise the final depolymerization yield, while very high percentages of monomer could be recovered in a wide range of solvents, including dimethyl sulfoxide, anisole, xylene, acetonitrile, toluene, and trichlorobenzene. Our findings not only offer intriguing mechanistic aspects, but also significantly expand the scope and applications of thermal RAFT depolymerization.

Publication Details

Journal
Figshare
Published
2025-02-10
DOI
https://doi.org/10.1021/acsmacrolett.5c00009.s001
Primary Topic
Mycorrhizal Fungi and Plant Interactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Ultrafast Thermal RAFT Depolymerization at HigherSolid Contents

Figshare
Mycorrhizal Fungi and Plant Interactions
article

Ultrafast Thermal RAFT Depolymerization at HigherSolid Contents

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Abstract

Although thermal solution RAFT depolymerization has recently emerged as an efficient chemical recycling methodology, current approaches require specialized solvents (i.e., dioxane), typically suffer from extended reaction times, and operate exclusively under highly dilute conditions (i.e., 5 mM repeat unit concentration). To circumvent these limitations, a commercial radical initiator is introduced to kinetically untrap the depolymerization and promote chain-end activation. By varying the initiator concentration, a remarkable rate acceleration (up to 72 times faster) can be observed, enabling the completion of the depolymerization within 5 min. Notably, a 20-fold increase in the repeat unit concentration did not appreciably compromise the final depolymerization yield, while very high percentages of monomer could be recovered in a wide range of solvents, including dimethyl sulfoxide, anisole, xylene, acetonitrile, toluene, and trichlorobenzene. Our findings not only offer intriguing mechanistic aspects, but also significantly expand the scope and applications of thermal RAFT depolymerization.

Figshare
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Mycorrhizal Fungi and Plant Interactions
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Ultrafast Thermal RAFT Depolymerization at HigherSolid Contents · Figshare (2025) | TGRS Research Map | TGRS