4.6 Article

Tandem Heterogeneous Catalysis for Polyethylene Depolymerization via an Olefin-Intermediate Process

Journal

ACS SUSTAINABLE CHEMISTRY & ENGINEERING
Volume 9, Issue 2, Pages 623-628

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acssuschemeng.0c07612

Keywords

Olefin-intermediate process; Polyethylene; Plastics upcycling; Olefin cross metathesis; Dehydrogenation

Funding

  1. U.S. Department of Energy (DOE) [DE-AC36-08GO28308]
  2. Laboratory Directed Research and Development (LDRD) Program at NREL
  3. US Department of Energy, Office of Energy Efficiency and Renewable Energy, Advanced Manufacturing Office (AMO)
  4. Bioenergy Technologies Office (BETO)
  5. AMO
  6. BETO [DE-AC36-08GO28308]
  7. National Renewable Energy Laboratory (NREL)

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Recent research has developed a new chemical recycling technology that utilizes a heterogeneous catalyst system to depolymerize polyethylene feedstocks into a mixture of alkane products, offering a selective and versatile means to break down polyolefins at lower severity conditions.
The accumulation of plastic waste in the environment has prompted the development of new chemical recycling technologies. A recently reported approach employed homogeneous organometallic catalysts for tandem dehydrogenation and olefin cross metathesis to depolymerize polyethylene (PE) feedstocks to a mixture of alkane products. Here, we build on that prior work by developing a fully heterogeneous catalyst system using a physical mixture of SnPt/gamma-Al2O3 and Re2O7/gamma-Al2O3. This heterogeneous catalyst system produces a distribution of linear alkane products from a model, linear C-20 alkane, n-eicosane, and from a linear PE substrate (which is representative of high-density polyethylene), both in an n-pentane solvent. For the PE substrate, a molecular weight decrease of 73% was observed at 200 degrees C in 15 h. This type of tandem chemistry is an example of an olefin-intermediate process, in which poorly reactive aliphatic substrates are first activated through dehydrogenation and then functionalized or cleaved by a highly-active olefin catalyst. Olefin-intermediate processes like that examined here offer both a selective and versatile means to depolymerize polyolefins at lower severity than traditional pyrolysis or cracking conditions.

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