Please use this identifier to cite or link to this item:
http://hdl.handle.net/10397/118378
| DC Field | Value | Language |
|---|---|---|
| dc.contributor | Department of Building Environment and Energy Engineering | en_US |
| dc.creator | Tian, C | en_US |
| dc.creator | Yuen, ACY | en_US |
| dc.creator | Chen, Q | en_US |
| dc.creator | De Cachinho Cordeiro, IM | en_US |
| dc.creator | Chen, TBY | en_US |
| dc.creator | Chan, QN | en_US |
| dc.creator | Huang, X | en_US |
| dc.date.accessioned | 2026-04-13T07:57:12Z | - |
| dc.date.available | 2026-04-13T07:57:12Z | - |
| dc.identifier.issn | 1383-5866 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10397/118378 | - |
| dc.language.iso | en | en_US |
| dc.publisher | Elsevier Ltd | en_US |
| dc.subject | Catalytic pyrolysis | en_US |
| dc.subject | HZSM-5 | en_US |
| dc.subject | Molecular dynamics | en_US |
| dc.subject | Polypropylene | en_US |
| dc.subject | ReaxFF | en_US |
| dc.subject | Recycling | en_US |
| dc.title | Parametric optimisation and mechanistic characterisation of polypropylene/HZSM-5 pyrolysis towards high-efficiency resource recycling | en_US |
| dc.type | Journal/Magazine Article | en_US |
| dc.identifier.volume | 380 | en_US |
| dc.identifier.doi | 10.1016/j.seppur.2025.135330 | en_US |
| dcterms.abstract | To achieve a plastic upcycling pyrolysis process with high conversion efficiency and low energy input, the pyrolysis conditions of polypropylene(PP)/HZSM-5 were optimised. Through reactive force field molecular dynamics (ReaxFF-MD) simulation techniques, it was discovered that the optimal pyrolysis temperature and catalyst loading of PP are 2000 K (748 K in the experiments) and 30 % respectively, with a conversion efficiency over 98 %. The catalytic efficiency of PP decreased by less than 2 % after 5 cycles for HZSM-5. Moreover, the catalytic effect can be breakdown down into two steps: Firstly, the HZSM-5 enhances the conversion of C3H5 and C3H7, and then these intermediate species have a higher tendency to form C3H6 as the final products. Furthermore, the deterioration mechanism of HZSM-5 was attributed to structural deformation on the active sites after numerous reactions with PP, and subsequently, a neutral hydroxyl group replaced the active site. Overall, this work demonstrated an in-depth characterisation approach using ReaxFF-MD in visualising the molecular breakdown process, revealing the catalytic and deactivation mechanism of HZSM-5 to PP. it presents an innovative framework for future research on the development of zeolite-based catalysts to improve the recycling efficiency of waste plastic | en_US |
| dcterms.abstract | Graphical abstract: [Figure not available: see fulltext.] | en_US |
| dcterms.accessRights | embargoed access | en_US |
| dcterms.bibliographicCitation | Separation and purification technology, 7 Feb. 2026, v. 380, pt. 2, 135330 | en_US |
| dcterms.isPartOf | Separation and purification technology | en_US |
| dcterms.issued | 2026-02-07 | - |
| dc.identifier.eissn | 1873-3794 | en_US |
| dc.identifier.artn | 135330 | en_US |
| dc.description.validate | 202604 bcch | en_US |
| dc.description.oa | Not applicable | en_US |
| dc.identifier.FolderNumber | a4370 | - |
| dc.identifier.SubFormID | 52648 | - |
| dc.description.fundingSource | RGC | en_US |
| dc.description.fundingSource | Others | en_US |
| dc.description.fundingText | This research work was sponsored by the PolyU UGC fundings (P0044994) and (P0052426). Additionally, it is also supported by the Hong Kong MTR Research Funding Scheme (PTU-23019), the Research Grant Council of the Hong Kong Special Administrative Region, China (CityU11214221) and the City University of Hong Kong Internal Grant (9610681). All funding and support are fully appreciated by the authors. | en_US |
| dc.description.pubStatus | Published | en_US |
| dc.date.embargo | 2028-02-07 | en_US |
| dc.description.oaCategory | Green (AAM) | en_US |
| Appears in Collections: | Journal/Magazine Article | |
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.



