Journal article
Solid-state chemical recycling of polycarbonates to epoxides and carbon dioxide using a heterodinuclear Mg(II)Co(II) catalyst
- Abstract:
- Polymer chemical recycling to monomers (CRM) could help improve polymer sustainability, but its implementation requires much better understanding of depolymerization catalysis, ensuring high rates and selectivity. Here, a heterodinuclear [Mg(II)Co(II)] catalyst is applied for CRM of aliphatic polycarbonates, including poly(cyclohexene carbonate) (PCHC), to epoxides and carbon dioxide using solid-state conditions, in contrast with many other CRM strategies that rely on high dilution. The depolymerizations are performed in the solid state giving very high activity and selectivity (PCHC, TOF = 25700 h–1, CHO selectivity >99 %, 0.02 mol %, 140 °C). Reactions may also be performed in air without impacting on the rate or selectivity of epoxide formation. The depolymerization can be performed on a 2 g scale to isolate the epoxides in up to 95 % yield with >99 % selectivity. In addition, the catalyst can be re-used four times without compromising its productivity or selectivity.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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- Files:
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(Preview, Version of record, pdf, 1.8MB, Terms of use)
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(Preview, Supplementary materials, pdf, 2.4MB, Terms of use)
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- Publisher copy:
- 10.1021/jacs.2c06937
Authors
+ Engineering and Physical Sciences Research Council
More from this funder
- Grant:
- RC-CH1302
- EP/S018603/1
- Publisher:
- American Chemical Society
- Journal:
- Journal of the American Chemical Society More from this journal
- Volume:
- 144
- Issue:
- 40
- Pages:
- 18444-18449
- Publication date:
- 2022-09-28
- Acceptance date:
- 2022-09-15
- DOI:
- EISSN:
-
1520-5126
- ISSN:
-
0002-7863
- Language:
-
English
- Keywords:
- Pubs id:
-
1280310
- Local pid:
-
pubs:1280310
- Deposit date:
-
2022-09-30
Terms of use
- Copyright holder:
- McGuire et al.
- Copyright date:
- 2022
- Rights statement:
- Copyright © 2022 The Author(s). This is an open access article published under CC BY 4.0.
- Licence:
- CC Attribution (CC BY)
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