P‐Menthadienes as Biorenewable Feedstocks for a Monoterpene‐Based Biorefinery. (26th March 2021)
- Record Type:
- Journal Article
- Title:
- P‐Menthadienes as Biorenewable Feedstocks for a Monoterpene‐Based Biorefinery. (26th March 2021)
- Main Title:
- P‐Menthadienes as Biorenewable Feedstocks for a Monoterpene‐Based Biorefinery
- Authors:
- Tibbetts, Joshua D.
Bull, Steven D. - Abstract:
- Abstract: A terpene‐based biorefinery is described that uses crude sulfate turpentine (CST) and gum turpentine (GT) to produce mixtures of p ‐menthadienes ( p ‐MeDs) as biorenewable terpene feedstocks. An acid catalyzed ring opening reaction (6 m aq. H2 SO4, 90 °C) is first used to convert the major bicyclic monoterpenes (α‐pinene, β‐pinene, and 3‐carene) in untreated CST (or GT with 5 mol% Me2 S) into mixtures of monocyclic p ‐MeDs. These unpurified sulfurous p ‐MeD mixtures (α‐terpinene, γ‐terpinene, and isoterpinolene) are then used as feedstocks for oxidative aromatization (OA), ozonolysis, Diels–Alder, and hydrogenation reactions to produce p ‐cymene, fragrances, anti‐oxidants, drugs, biopolymers, and biofuels. Mechanistic studies of the OA reaction used to convert the p ‐MeDs into p ‐cymene reveal that p ‐cymene hydroperoxide acts as an initiator to produce polar radical intermediates that are stabilized by DMSO generated in situ through aerobic oxidation of Me2 S. This enables CST and GT to be converted into biorenewable p ‐cymene in 50–60% yields (two steps) using a process that only requires aqueous acid, oxygen, heat, and a final distillation step. Abstract : A terpene‐based biorefinery model is developed that is built around utilization of industrial waste streams (crude sulfate turpentine), with a view to transitioning toward a biobased chemical economy. Development of a sustainable route to a core intermediate, p ‐cymene, allows a range of valuable fragrances,Abstract: A terpene‐based biorefinery is described that uses crude sulfate turpentine (CST) and gum turpentine (GT) to produce mixtures of p ‐menthadienes ( p ‐MeDs) as biorenewable terpene feedstocks. An acid catalyzed ring opening reaction (6 m aq. H2 SO4, 90 °C) is first used to convert the major bicyclic monoterpenes (α‐pinene, β‐pinene, and 3‐carene) in untreated CST (or GT with 5 mol% Me2 S) into mixtures of monocyclic p ‐MeDs. These unpurified sulfurous p ‐MeD mixtures (α‐terpinene, γ‐terpinene, and isoterpinolene) are then used as feedstocks for oxidative aromatization (OA), ozonolysis, Diels–Alder, and hydrogenation reactions to produce p ‐cymene, fragrances, anti‐oxidants, drugs, biopolymers, and biofuels. Mechanistic studies of the OA reaction used to convert the p ‐MeDs into p ‐cymene reveal that p ‐cymene hydroperoxide acts as an initiator to produce polar radical intermediates that are stabilized by DMSO generated in situ through aerobic oxidation of Me2 S. This enables CST and GT to be converted into biorenewable p ‐cymene in 50–60% yields (two steps) using a process that only requires aqueous acid, oxygen, heat, and a final distillation step. Abstract : A terpene‐based biorefinery model is developed that is built around utilization of industrial waste streams (crude sulfate turpentine), with a view to transitioning toward a biobased chemical economy. Development of a sustainable route to a core intermediate, p ‐cymene, allows a range of valuable fragrances, biofuels, solvents, commodity chemicals, and polymers to be produced from biorenewable, turpentine‐derived p ‐menthadienes. … (more)
- Is Part Of:
- Advanced sustainable systems. Volume 5:Number 6(2021)
- Journal:
- Advanced sustainable systems
- Issue:
- Volume 5:Number 6(2021)
- Issue Display:
- Volume 5, Issue 6 (2021)
- Year:
- 2021
- Volume:
- 5
- Issue:
- 6
- Issue Sort Value:
- 2021-0005-0006-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2021-03-26
- Subjects:
- biorefinery -- CST -- monoterpenes -- terpenes -- turpentine
Sustainable living -- Periodicals
Sustainability -- Periodicals
Green technology -- Periodicals
Periodicals
628 - Journal URLs:
- http://resolver.library.ualberta.ca/resolver?ctx_enc=info%3Aofi%2Fenc%3AUTF-8&ctx_ver=Z39.88-2004&rfr_id=info%3Asid%2Fualberta.ca%3Aopac&rft.genre=journal&rft.object_id=3710000000966647&rft.issn=2366-7486&rft.eissn=2366-7486&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&url_ctx_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Actx&url_ver=Z39.88-2004 ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2366-7486/issues ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/adsu.202000292 ↗
- Languages:
- English
- ISSNs:
- 2366-7486
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0696.931975
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 17337.xml