Synthesis and characterization of natural rubber‐based telechelic oligomers via olefin metathesis. Issue 8 (10th September 2020)
- Record Type:
- Journal Article
- Title:
- Synthesis and characterization of natural rubber‐based telechelic oligomers via olefin metathesis. Issue 8 (10th September 2020)
- Main Title:
- Synthesis and characterization of natural rubber‐based telechelic oligomers via olefin metathesis
- Authors:
- Hu, Guangwei
Lin, Shaohui
Zhao, Boxin
Pan, Qinmin - Abstract:
- Abstract: Metathesis degradation and functionalization of natural rubber (NR) were conducted with 1‐hexene, 1‐octene, 1‐decene, 1‐dodecene, trans ‐stilbene, and 4, 4′‐dibromo‐ trans ‐stilbene as chain transfer agents (CTAs) in presence of Grubbs 2nd generation catalyst to generate NR‐based telechelic oligomers that had been a long‐lasting challenge due to the structure and compositions of NR with various impurities. Orthogonal experiments were applied and the effects of the CTA type, CTA concentration, catalyst concentration, reaction time, and reaction temperature on the formation of telechelic oligomers were studied, indicating that the catalyst concentration was the major factor influencing the number average molecular weights ( M n ) and polymer dispersity index (PDI) of telechelic oligomers. The structures of the oligomers were characterized using 1 H NMR, 13 C NMR, and MALDI‐TOF‐MS, which confirmed the formation of the designed terminal groups. The results showed that well‐defined telechelic oligomers with a M n of a few thousand and a PDI around 1.6 were obtained, with potential applications in binder, lubricant and many other fields. Abstract : Metathesis degradation and functionalization of natural rubber were conducted with asymmetric and symmetric olefins as chain transfer agents in presence of a Grubbs catalyst to generate various valuable natural rubber‐based telechelic oligomers, which also bring out a feasible life‐cycle route of natural/synthetic rubberAbstract: Metathesis degradation and functionalization of natural rubber (NR) were conducted with 1‐hexene, 1‐octene, 1‐decene, 1‐dodecene, trans ‐stilbene, and 4, 4′‐dibromo‐ trans ‐stilbene as chain transfer agents (CTAs) in presence of Grubbs 2nd generation catalyst to generate NR‐based telechelic oligomers that had been a long‐lasting challenge due to the structure and compositions of NR with various impurities. Orthogonal experiments were applied and the effects of the CTA type, CTA concentration, catalyst concentration, reaction time, and reaction temperature on the formation of telechelic oligomers were studied, indicating that the catalyst concentration was the major factor influencing the number average molecular weights ( M n ) and polymer dispersity index (PDI) of telechelic oligomers. The structures of the oligomers were characterized using 1 H NMR, 13 C NMR, and MALDI‐TOF‐MS, which confirmed the formation of the designed terminal groups. The results showed that well‐defined telechelic oligomers with a M n of a few thousand and a PDI around 1.6 were obtained, with potential applications in binder, lubricant and many other fields. Abstract : Metathesis degradation and functionalization of natural rubber were conducted with asymmetric and symmetric olefins as chain transfer agents in presence of a Grubbs catalyst to generate various valuable natural rubber‐based telechelic oligomers, which also bring out a feasible life‐cycle route of natural/synthetic rubber resources. … (more)
- Is Part Of:
- Journal of applied polymer science. Volume 138:Issue 8(2021)
- Journal:
- Journal of applied polymer science
- Issue:
- Volume 138:Issue 8(2021)
- Issue Display:
- Volume 138, Issue 8 (2021)
- Year:
- 2021
- Volume:
- 138
- Issue:
- 8
- Issue Sort Value:
- 2021-0138-0008-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2020-09-10
- Subjects:
- degradation -- recycling -- rubber
Polymers -- Periodicals
Polymerization -- Periodicals
668.9 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1097-4628 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/app.49899 ↗
- Languages:
- English
- ISSNs:
- 0021-8995
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4946.600000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 15015.xml