# Aqueous Depolymerization of Polyethylene at Ambient Temperature: In Situ Generation of Permanganate Using Ozone

**Authors:** Michael S. Behrendt, Brandon D. Howard, Daniel Holmes, Scott Calabrese Barton, John R. Dorgan

PMC · DOI: 10.1021/acssuschemeng.5c12302 · ACS Sustainable Chemistry & Engineering · 2026-03-17

## TL;DR

Scientists developed a new method to break down polyethylene plastic into useful products using water and ozone at room temperature.

## Contribution

A novel ambient-temperature aqueous process for polyethylene depolymerization using in situ permanganate generation.

## Key findings

- LDPE is converted into carboxylic acids and wax using ozone and water at 30°C.
- Diacids with 4-6 carbon units are the main water-soluble products detected by HPLC.
- Oxidation occurs preferentially at branch points, forming linear acids and ketones.

## Abstract

The long sought-after
goal of chemically recycling polyolefins
at ambient temperature and pressure without the use of organic solvents
is realized. Using ozone to regenerate a permanganate oxidant in situ in an aqueous environment, low-density polyethylene
is converted to carboxylic acids and oligomeric wax. LDPE powder (with
average particle sizes between 150 and 250 μm) serves as the
substratereactions are conducted at atmospheric pressure and
30 °C. Water-soluble products are quantified using HPLC, with
diacids having 4, 5, and 6 carbon units as the primary products. The
remaining solid wax was analyzed for crystallinity by calorimetry
(DSC), for acid number by titration, and for molecular functionality
by ATR-IR and NMR spectroscopies. All three measured quantities increase
with increasing reaction time. The acid number of the residual wax
indicates a diacid carbon length of ∼30 (∼450 g/mol).
Polymer oxidation occurs preferentially at side-chain branch points.
Results suggest a two-reaction system in which branch-point tertiary
carbons are selectively oxidized to yield linear carboxylic acids
and ketones, followed by secondary depolymerization to yield water-soluble
diacids. Experimental yields were 10% at 144 h.

## Linked entities

- **Chemicals:** ozone (PubChem CID 24823), permanganate (PubChem CID 24401)

## Full-text entities

- **Chemicals:** carbon (MESH:D002244), Ozone (MESH:D010126), LDPE (MESH:D020959), Permanganate (MESH:C048856), carboxylic acids (MESH:D002264), diacid carbon (-), ketones (MESH:D007659), wax (MESH:D014885), polyolefins (MESH:C035051), Water (MESH:D014867)

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## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13040521/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC13040521/full.md

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Source: https://tomesphere.com/paper/PMC13040521