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Biphasic valorization of byproducts from biodiesel synthesis using floating photochemo-enzymatic domino catalysis

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Peer-reviewed

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Abstract

We introduce a practical one-pot process for the full valorization of biodiesel byproducts via a photochemo-enzymatic domino approach in liquid|solid|liquid (L|S|L) photocatalysis. Sustainable chemical synthesis requires a cradle-to-cradle design strategy to upcycle waste streams with optimal atom and step economy. Here, we demonstrate the full valorization of vegetable oil using a scalable two-step process. First, transesterification of triglycerides (vegetable oil) with methanol in aqueous NaOH generates biodiesel, together with glycerol and unreacted unsaturated fatty acids as byproducts. Following separation of biodiesel, glycerol and fatty acids were valorized using a biphasic domino reaction at the liquid–liquid interface with a floating photochemo-enzymatic platform. Specifically, a floatable polymeric carbon nitride/polypropylene (CN x /PP) composite photo-catalyzes first the reduction of O 2 to H 2 O 2 using aqueous glycerol as the electron donor to produce glyceraldehyde and dihydroxyacetone. An immobilized lipase on a floating acrylic resin support subsequently utilizes the in situ generated aqueous H 2 O 2 for the conversion of unsaturated fatty acids into epoxides in ethyl acetate. This novel photochemo-enzymatic domino reaction enables the full valorization of waste cooking oil at 1 kg scale, producing biodiesel (550 g), epoxidized fatty acids (438 g) and glyceraldehyde (663 g) in a 100 mL scale reactor under blue LED ( λ = 450 nm, 40 ± 4 mW cm −2 ) and simulated solar light (AM1.5G) at 40 °C generated by solar heating. A comparative life cycle assessment indicates that our integrated solar-driven process with optimized catalyst recyclability over 100 cycles has an expected 39% lower global warming potential compared to a decentralized process for conventional biodiesel, epoxy fatty acids and glyceraldehyde synthesis.

Description

Acknowledgements: We gratefully acknowledge support by the Cambridge Trust (PhD scholarship to A.R.), UK Research and Innovation (EP/S022953/1 to A.R., ERC Advanced Grant EP/X030563/1 to E.R.), UK Department of Science, Innovation and Technology and the Royal Academy of Engineering Chair in Emerging Technologies program (CIET-2324-83 to E. R.). The XPS and UPS data collection was supported by the Henry Royce Institute for advanced materials through the Equipment Access Scheme enabling access to the Royce XPS facility at Cambridge; Cambridge Royce Facilities grant EP/P024947/1 and Sir Henry Royce Institute – recurrent grant EP/R00661X/1. The authors would like to acknowledge Dr Heather Greer for assistance with electron microscopy, Natalie Potter and the Melville Lab for assistance with contact angle analysis, Dongseok Kim for assistance with zeta potential measurements, and Flora Mammadova and Prof. Pawel Dydio for assistance with GC-MS analysis. The authors would also like to thank Dr Zhipeng Huang and Papa Kwarteng for helpful discussion.


Publication status: Published

Journal Title

Energy & Environmental Science

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Journal ISSN

1754-5692
1754-5706

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Publisher

Royal Society of Chemistry (RSC)

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Except where otherwised noted, this item's license is described as https://creativecommons.org/licenses/by/3.0/
Sponsorship
Engineering and Physical Sciences Research Council (EP/P024947/1)
Engineering and Physical Sciences Research Council (EP/S022953/1)
Engineering and Physical Sciences Research Council (EP/R00661X/1)