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dc.contributor.author | Bezuidenhoudt, Anya![]() |
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dc.contributor.author | Sonnendecker, Paul W.![]() |
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dc.contributor.author | Crouse, Philippus L.![]() |
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dc.date.accessioned | 2017-09-18T08:15:49Z | |
dc.date.issued | 2017-08 | |
dc.description.abstract | The results of the depolymerisation of PTFE under steady operating conditions in a semi-automated, continuous depolymerisation system are presented. The influence of temperature and pressure on the selectivity of the three main products of depolymerisation (tetrafluoroethylene (TFE), hexafluoropropylene (HFP), and octafluorocyclobutane (OFCB)) was investigated via qualitative in-line FTIR analysis. No carrier gas was used, with the PTFE feed rate and experimental run time kept constant. The temperature and pressure ranges investigated were: 650 °C–750 °C and <10 kPa–40 kPa. The optimum operating conditions to maximise the three main products were determined using response surface methodology following a three-level face centered composite design. A TFE mole fraction of 0.95 and higher was achieved at operating conditions of ±675 °C and <10 kPa. HFP mole fractions of 0.19 and higher were achieved within the operating range of 744 °C–750 °C and 32 kPa up to 40 kPa. At operating conditions of 750 °C and 40 kPa, OFCB fractions of 0.5–0.55 were achieved. The OFCB and HFP mole fractions achieved differed from those previously mentioned in the literature. Analysis of the determined product specific kinetics indicates that the predominant HFP production pathway at low residence times (<3 s) is via the reaction of TFE with difluorocarbenes. At higher residence times the dominant reaction pathway is the dissociation OFCB. | en_ZA |
dc.description.department | Chemical Engineering | en_ZA |
dc.description.embargo | 2018-08-30 | |
dc.description.librarian | hj2017 | en_ZA |
dc.description.sponsorship | The National Research Foundation (NRF) and the Fluoro-expansion Initiative (FEI) which is supported by the South African Department of Science and Technology (DST). | en_ZA |
dc.description.uri | http://www.elsevier.com/locate/polydegstab | en_ZA |
dc.identifier.citation | Bezuidenhoudt, A., Sonnendecker, P.W. & Crouse, P.L. 2017, 'Temperature and pressure effects on the product distribution of PTFE pyrolysis by means of qualitative, in-line FTIR analysis', Polymer Degradation and Stability, vol. 142, pp. 79-88. | en_ZA |
dc.identifier.issn | 0141-3910 (print) | |
dc.identifier.issn | 1873-2321 (online) | |
dc.identifier.other | 10.1016/j.polymdegradstab.2017.05.025 | |
dc.identifier.uri | http://hdl.handle.net/2263/62271 | |
dc.language.iso | en | en_ZA |
dc.publisher | Elsevier | en_ZA |
dc.rights | © 2017 Elsevier Ltd.. All rights reserved. Notice : this is the author’s version of a work that was accepted for publication in Polymer Degradation and Stability. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. A definitive version was subsequently published in Polymer Degradation and Stability, vol. 142, pp. 79-88, 2017. doi : 10.1016/j.polymdegradstab.2017.05.025. | en_ZA |
dc.subject | Tetrafluoroethylene (TFE) | en_ZA |
dc.subject | Hexafluoropropylene (HFP) | en_ZA |
dc.subject | Octafluorocyclobutane (OFCB) | en_ZA |
dc.subject | Polytetrafluoroethylene (PTFE) | en_ZA |
dc.subject | PTFE depolymerisation | en_ZA |
dc.subject | In-line FTIR | en_ZA |
dc.subject | Regression analysis | en_ZA |
dc.subject | Product-specific kinetics | en_ZA |
dc.subject | Fourier transform infrared spectroscopy (FTIR) | en_ZA |
dc.subject | Waste | en_ZA |
dc.subject | Polymers | en_ZA |
dc.subject | Decomposition | en_ZA |
dc.subject | Thermogravimetry | en_ZA |
dc.title | Temperature and pressure effects on the product distribution of PTFE pyrolysis by means of qualitative, in-line FTIR analysis | en_ZA |
dc.type | Postprint Article | en_ZA |