Carbon-Resource Recovery from Vinyl Polymers of Cyclic Ketene Acetal Esters Using High-Temperature Water

19 June 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Vinyl polymer prepared from 2-methylene-4H-benzo[d][1,3]dioxin-4-one (MBDO), a cyclic ketene acetal ester, is a chemically recyclable polymer that is hydrolyzed to salicylic acid (SA) and acetic acid (AA). Despite this potential, the polymer, poly-MBDO required a strong acid or base in organic solvent for the hydrolysis. In this study, we report the quantitative conversion of poly-MBDO to phenol by treatment in high-temperature water. Hydrolysis of poly-MBDO afforded SA, which underwent rapid decarboxylation to phenol. For example, poly-MBDO quantitatively afforded phenol upon heating in water at 300 °C for 5 min and freeze-drying. Although the hydrolysis of the main chain was incomplete, the products were volatile and removed by drying the reaction mixture, leaving the residue of pure phenol. Since SA is industrially synthesized from phenol and CO2, the synthesis of poly-MBDO from phenol is in principle possible. The quantitative conversion of poly-MBDO to phenol can also be considered as upcycling, since phenol is a raw material for various fine chemicals.

Keywords

Dehydroaspirin
main-chain scission
polymer degradation
hydrolysis
chemical recycling
retro-Kolbe-Schmitt reaction
salicylic acid
phenol
hydrothermal reaction

Supplementary materials

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Figure S1. Calibration lines of SA (A), phenol (B), and AA (C). Figure S2. First-order kinetic plots of decarboxylation of SA at 125 (A), 150 (B), 175 (C), 200 (D), and 250 °C (E). Arrhenius plots of decarboxylation of SA (F).
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