Publication: Biocatalytic hydrolysis of di-urethane model compounds in ionic liquid reaction media
| dc.contributor.author | Salas, Rebeca | |
| dc.contributor.author | Villa Aroca, Rocío | |
| dc.contributor.author | Cano, Sergio | |
| dc.contributor.author | Garcia Verdugo, Eduardo | |
| dc.contributor.author | Villa Aroca, Rocío | |
| dc.contributor.author | Lozano Rodríguez, Pedro | |
| dc.contributor.author | Nieto Cerón, Susana | |
| dc.contributor.department | Bioquímica y Biología Molecular B e Inmunología | |
| dc.date.accessioned | 2025-01-09T16:45:19Z | |
| dc.date.available | 2025-01-09T16:45:19Z | |
| dc.date.issued | 2024-03-15 | |
| dc.description | © 2024 The Author(s). This manuscript version is made available under the CC-BY 4.0 license http://creativecommons.org/licenses/by/4.0/ This document is the Published Manuscript version of a Published Work that appeared in final form in Catalysis Today. To access the final edited and published work see https://doi.org/10.1016/j.cattod.2024.114516 | |
| dc.description.abstract | The suitability of different enzymes to carry out the hydrolysis of two-different toluene-based urethane model compounds (i.e. bis(2-methoxyethyl) (4-methyl-1,3-phenylene)dicarbamate, and bis(2-methoxyethyl) (2-methyl-1,3-phenylene)dicarbamate) has been demonstrated for the first time by taking advantage of ionic liquid (IL) technologies. Toluene-based urethane compounds were prepared from usual substrates in polyurethane industrial synthesis. Afterwards, their carbamate groups were target of a biocatalytic hydrolysis by means of different commercial hydrolases (i.e. lipase, urease and proteases) in either water, hydrophilic organic solvents (i.e. ethylene glycol or 1,2-dimethyl-1,3-dioxolane-4-methanol, (solketal)), or hydrophobic ILs (e.g. [C4mim][NTf2], etc.) as reaction media. Because of the insolubility of these compounds in water, most of the enzymes were unable to catalyse the hydrolysis of the di-urethane substrates in pure water, being clearly improved (up to 31.6 mU/mg for the urease case) in solketal:water (90:10, v/v) reaction media. When hydrophobic ILs were added into this reaction medium, the urease activity increased by more than twice (74.1 mU/mg). The most promising results for the hydrolysis of these urethane compounds were obtained by combining lipase and urease biocatalysts in a IL:solketal:H2O (70:25:5, v/v/v) reaction medium. These results demonstrate a possible biocatalytic approach for the hydrolytic depolymerization of polyurethane foam wastes. | es |
| dc.format | application/msword | es |
| dc.format.extent | 7 | es |
| dc.identifier.citation | Catalysis Today, 2024, Vol. 430 : 114516 | |
| dc.identifier.issn | Print: 0920-5861 | |
| dc.identifier.issn | Electronic: 1873-4308 | |
| dc.identifier.uri | http://hdl.handle.net/10201/148180 | |
| dc.language | eng | es |
| dc.publisher | Elsevier | |
| dc.relation | This work was partially supported by MICINN-FEDER-AEI 10.13039/501100011033 (PID2021- 124695OB-C21/C22, and PDC2022-133313-C21/C22), MICINN –European Union Next Generation EU-PRTR (TED2021-129626B-C21/C22), and SENECA (21884/PI/22) for financial support. | es |
| dc.relation.publisherversion | https://www.sciencedirect.com/science/article/pii/S0920586124000105?via%3Dihub | |
| dc.rights | info:eu-repo/semantics/openAccess | es |
| dc.rights | Atribución 4.0 Internacional | * |
| dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | * |
| dc.subject | Urethane hydrolysis | es |
| dc.subject | Urease | |
| dc.subject | Lipase | |
| dc.subject | Ionic liquid | |
| dc.subject | Polyurethane wastes | |
| dc.title | Biocatalytic hydrolysis of di-urethane model compounds in ionic liquid reaction media | es |
| dc.type | info:eu-repo/semantics/article | es |
| dspace.entity.type | Publication | es |
| relation.isAuthorOfPublication | cf083d38-2b18-4a96-9e50-17022804a6c8 | |
| relation.isAuthorOfPublication | afd0ddee-9224-46b4-a275-0bb48476fccc | |
| relation.isAuthorOfPublication | ce9ba261-d6c0-4b1e-80fc-e220e72ba63d | |
| relation.isAuthorOfPublication.latestForDiscovery | cf083d38-2b18-4a96-9e50-17022804a6c8 |
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