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Data Publication

Unravelling Potential Reaction Intermediates during Catalytic Pyrolysis of Polypropylene with Microscopy and Spectroscopy

Ina Vollmer

Utrecht University

(2023)

Descriptions

While plastics-to-plastics recycling via melting and re-extrusion is often the preferred option due to a relatively low CO2 footprint, this technique requires a highly sorted waste stream and plastic properties can often not be maintained. Obtaining aromatics, such as benzene, toluene, and xylene (BTX), via catalytic pyrolysis of polyolefins, such as polypropylene and polyethylene, offers another attractive recycling technology. In this process, a discarded crude oil refinery catalyst (ECAT) was previously shown to lower the unwanted formation of deactivating coke species compared to a fresh crude oil refinery catalyst (FCC-cat), while yielding 20 wt.% aromatics from polypropylene. In this work, we study the underlying reaction mechanism for this chemical recycling process over the fresh and used refinery catalyst as well as a model system, not containing any zeolite material, using a combination of microscopy and spectroscopy. More specifically, by using in-situ fluorescence microscopy, in-situ infrared spectroscopy, in-situ ultraviolet-visible spectroscopy as well as ex-situ solid-state nuclear magnetic resonance, we observe highly fluorescent methylated aromatic intermediates that differ for the three catalyst materials under study both in their fluorescence, IR, UV-Vis, and NMR features. This detailed micro-spectroscopic comparison informs which potential reaction intermediates lead to increased coke formation. Our results suggests that a next generation of catalyst materials for this process would profit from a higher accessibility and a milder acidity compared to an FCC-cat and shows the great potential of using ECAT to reduce coking and obtain a BTX stream, which could be become the chemical building blocks for the manufacturing of e.g., plastics and coatings.

Keywords


Originally assigned keywords
Natural Sciences - Chemical sciences (1.4)
IR
CFM
UV-Vis
TGA
NMR

MSL enriched keywords
minerals
silicate minerals
tectosilicates
zeolite
analogue modelling material
elastic modelling material
synthetic elastic material
polyethylene (LDPE) foam
measured property
iridium (Ir)
Technique
chemical and mineralogical analysis
infrared spectroscopy

MSL enriched sub domains i

geochemistry
microscopy and tomography


Source publisher

Utrecht University


DOI

10.24416/uu01-90syai


Creators

Ina Vollmer

Utrecht University

ORCID:

https://orcid.org/0000-0001-9917-1499


Contributors

Jenks, Michael J. F.

DataCollector

Utrecht University

Rejman, Sebastian

DataCollector

Utrecht University

ORCID:

https://orcid.org/0000-0001-7976-6372

Meirer, Florian

RelatedPerson

Utrecht University

ORCID:

https://orcid.org/0000-0001-5581-5790

Gurinov, Andrei

DataCollector

Utrecht University

Baldus, Marc

Supervisor

Utrecht University

ORCID:

https://orcid.org/0000-0001-7068-5613

Weckhuysen, Bert M.

Supervisor

Utrecht University

ORCID:

https://orcid.org/0000-0001-5245-1426


References

added later


Citation

Vollmer, I. (2023). Unravelling Potential Reaction Intermediates during Catalytic Pyrolysis of Polypropylene with Microscopy and Spectroscopy (Version 1.0) [Data set]. Utrecht University. https://doi.org/10.24416/UU01-90SYAI


Dates

Updated:

2024-07-09T09:04:16


Language

en


Funding References

Funder name: NWO


Rights

Open - freely retrievable

Creative Commons Attribution 4.0 International Public License


Datacite version

1.0