Show simple item record

dc.contributor.authorGóra, Magdalena
dc.contributor.authorTranchida, Davide
dc.contributor.authorAlbrecht, Albert
dc.contributor.authorMüller Sánchez, Alejandro Jesús ORCID
dc.contributor.authorCavallo, Dario
dc.date.accessioned2024-04-08T16:36:07Z
dc.date.available2024-04-08T16:36:07Z
dc.date.issued2022-04-29
dc.identifier.citationJournal of Polymer Science 60(24) :3366-3378 (2022)es_ES
dc.identifier.issn2642-4169
dc.identifier.urihttp://hdl.handle.net/10810/66556
dc.description.abstractThe 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 °C/min, the measurement time is approximately 420 min. Implementing mass compensation, faster heating rates (i.e., 30 °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.es_ES
dc.description.sponsorshipThe authors acknowledge the financial support from the REPOL project; this project has received funding from the European Union's Horizon 2020 research and innovation program under the Marie Skłodowska-Curie Grant Agreement No. 860221. Furthermore, the authors would like to thank Enrico Carmeli for training M.G. and Vitor Barroso for supervision in the early stage of this study.es_ES
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/860221es_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectpolyethylenees_ES
dc.subjectpolypropylenees_ES
dc.subjectrecyclinges_ES
dc.subjectthermal fractionationes_ES
dc.titleFast successive self-nucleation and annealing (SSA) thermal fractionation protocol for the characterization of polyolefin blends from mechanical recyclinges_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2022 The Authors published by Wiley Periodicals LLC.This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.es_ES
dc.relation.publisherversionhttps://onlinelibrary.wiley.com/doi/10.1002/pol.20220104es_ES
dc.identifier.doi10.1002/pol.20220104
dc.contributor.funderEuropean Commission
dc.departamentoesQuímica aplicadaes_ES
dc.departamentoeuKimika aplikatuaes_ES


Files in this item

Thumbnail

This item appears in the following Collection(s)

Show simple item record

© 2022 The Authors published by Wiley Periodicals LLC.This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's license is described as © 2022 The Authors published by Wiley Periodicals LLC.This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.