Highly Selective, Catalyst‐Free, and Low Temperature Depolymerizable Styrene Copolymer With Incorporated <i>α</i>‐Methylstyrene Structural Units

ABSTRACT A simple strategy is proposed to offer styrene (St) copolymer with intrinsic and catalyst‐free upcycling capability by incorporating α ‐methylstyrene (AMS) units into the copolymer poly(AMS ‐co‐ St) (PAS). Compared to polystyrene (PS), the PAS is more susceptible to depolymerizing into St and AMS monomers with higher yields at relatively lower temperature. The yield of liquid chemicals of PAS‐4 (26.1 mol% AMS) is up to 93 wt% at 380°C, whereas that PS as control is 78 wt%. The reclaimed liquid chemicals of PAS‐4 contain 58.4 wt% St and 37.7 wt% AMS, while the chemicals of PS contain 81.8 wt% St and 4.1 wt% AMS. The introduction of AMS units in PAS leads to a reduction in the liquid chemicals other than St and AMS monomers. The blends of PS and PAMS do not demonstrate the synergistic effect regarding facilitating the PS depolymerization. In addition, the properties of the new PASs prepared with the reclaimed monomers are comparable with those of the virgin PASs. This work proves the concept that recycling efficiency could be boosted by incorporating liable structural units into the copolymer chains and demonstrates a closed‐loop of PS up‐cycling.

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Publication Details

Journal
Journal of Applied Polymer Science
Published
2024-12-27
DOI
https://doi.org/10.1002/app.56663
Citations
2
Primary Topic
biodegradable polymer synthesis and properties
Type
article
Field-Weighted Citation Impact
0.35
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article

Highly Selective, Catalyst‐Free, and Low Temperature Depolymerizable Styrene Copolymer With Incorporated α‐Methylstyrene Structural Units

Yucheng Zi, Guochen Wang, Wantai Yang, Dong Chen et al.
2 citations
Journal of Applied Polymer Science
biodegradable polymer synthesis and properties
0.35
article

Highly Selective, Catalyst‐Free, and Low Temperature Depolymerizable Styrene Copolymer With Incorporated α‐Methylstyrene Structural Units

Yucheng Zi, Guochen Wang, Wantai Yang, Dong Chen, Yuhong Ma
article en
2 citations

Abstract

ABSTRACT A simple strategy is proposed to offer styrene (St) copolymer with intrinsic and catalyst‐free upcycling capability by incorporating α ‐methylstyrene (AMS) units into the copolymer poly(AMS ‐co‐ St) (PAS). Compared to polystyrene (PS), the PAS is more susceptible to depolymerizing into St and AMS monomers with higher yields at relatively lower temperature. The yield of liquid chemicals of PAS‐4 (26.1 mol% AMS) is up to 93 wt% at 380°C, whereas that PS as control is 78 wt%. The reclaimed liquid chemicals of PAS‐4 contain 58.4 wt% St and 37.7 wt% AMS, while the chemicals of PS contain 81.8 wt% St and 4.1 wt% AMS. The introduction of AMS units in PAS leads to a reduction in the liquid chemicals other than St and AMS monomers. The blends of PS and PAMS do not demonstrate the synergistic effect regarding facilitating the PS depolymerization. In addition, the properties of the new PASs prepared with the reclaimed monomers are comparable with those of the virgin PASs. This work proves the concept that recycling efficiency could be boosted by incorporating liable structural units into the copolymer chains and demonstrates a closed‐loop of PS up‐cycling.

Journal of Applied Polymer ScienceVol. 142(13)
Beijing University of Chemical Technology (CN)
Openalex Percentile: Top 42%
biodegradable polymer synthesis and properties
0.35
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