4.4 Article

Fast successive self-nucleation and annealing (SSA) thermal fractionation protocol for the characterization of polyolefin blends from mechanical recycling

Journal

JOURNAL OF POLYMER SCIENCE
Volume 60, Issue 24, Pages 3366-3378

Publisher

WILEY
DOI: 10.1002/pol.20220104

Keywords

polyethylene; polypropylene; recycling; thermal fractionation

Funding

  1. REPOL project
  2. European Union [860221]
  3. Marie Curie Actions (MSCA) [860221] Funding Source: Marie Curie Actions (MSCA)

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The sorting stage of mechanical recycling of post-consumer polyolefins faces challenges, and fast characterization is needed to assess the content of recycled pellets. Experiment shows that by increasing scanning rates and reducing sample mass, the thermal fractionation time can be shortened without losing resolution power.
The sorting stage of mechanical recycling of post-consumer polyolefins has severe challenges. Polypropylene (PP) is often contaminated with polyethylene (PE) and vice versa. To meet quality requirements, characterization of the recycled pellets is needed. To address this problem, fast characterization generating a statistical assessment of the content of the various batches from recycling is required. This investigation shows that the use of fast scanning rates (in a conventional Differential Scanning Calorimeter) in the successive self-nucleation and annealing (SSA) protocol can reduce the thermal fractionation time, without losing resolution power, as long as the increase in heating/cooling rate is compensated by reducing sample mass. Using a coupled SSA protocol for polypropylene and polyethylene fractions at a rate of 10 degrees C/min, the measurement time is approximately 420 min. Implementing mass compensation, faster heating rates (i.e., 30 degrees C/min) and using a single-fraction protocol, sufficient to determine the content of PP and high-density PE, reduced the time of the measurement to 75 min. Examples of fractionations of commercial post-consumer and post-industrial recycled polyolefin blends conducted at a faster rate are provided. The derived polyolefin content is compared with the standard temperature rising elution fractionation analysis to assess the validity of the proposed method.

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