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Updated: Apr 4, 2026

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
Published on: December 16, 2022
Aqueous Depolymerization of Polyethylene at Ambient Temperature: In Situ Generation of Permanganate Using Ozone
Michael S Behrendt1, Brandon D Howard1, Daniel Holmes2
1Chemical Engineering and Materials Science Department, Michigan State University, 3900 Collins Rd, Lansing, Michigan 48910, United States.
None:
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 substratereactions 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.
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