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dc.contributor.authorIzaguirre Aróstegui, Nagore
dc.contributor.authorFernández Rodríguez, Javier
dc.contributor.authorRobles Barrios, José Eduardo
dc.contributor.authorLabidi Bouchrika, Jalel
dc.date.accessioned2024-01-17T16:40:47Z
dc.date.available2024-01-17T16:40:47Z
dc.date.issued2023-11
dc.identifier.citationGreen Chemistry 25(21) : 8808-8819 (2023)es_ES
dc.identifier.issn1463-9270
dc.identifier.urihttp://hdl.handle.net/10810/64067
dc.description.abstractKraft lignin (KL) was treated by employing mild oxidation conditions enhanced by ultrasound irradiation (US) for obtaining more functionalized particles, avoiding the undesired side reactions of degradation and depolymerization. The aim was to obtain products with plausible value for applications with a greater potential market, enabling the introduction of low-cost bio-based materials for technically advanced applications. In the present work, KL was oxidized in alkaline media, applying low temperatures (30–60 °C), short times (15 to 60 min), and US waves (20 kHz). The influence of incorporating hydrogen peroxide (H2O2) as an oxidizing agent was also studied, as well as the chemical composition, physicochemical, thermal, and morphological properties of the final lignin particles. It was observed from Quantitative Acid Hydrolysis (QAH), Elemental Analysis (EA), and molecular weights (Mw) that oxidized lignin particles (OxL) did not suffer any major degradation. Other techniques used to determine physicochemical properties, such as Fourier Transformed Infrared (FTIR), 31 Phosphorous Nuclear Magnetic Resonance (31P NMR), or Ultraviolet–visible (UV-vis) methods, corroborated oxidation reactions, evident by the increment of carboxylic groups. The most noticeable difference, however, was observed when the stability and morphology of the particles were observed by Dynamic Light Scattering (DLS) and Transmission Electron Microscopy (TEM). Some conditions greatly promoted the formation of more stable and nanosized particles. The best conditions were the mildest but with the highest reaction times (no addition of H2O2, 30 °C and 60 minutes). Moreover, all reactions had good recovery yields, above 70% of the original lignin.es_ES
dc.description.sponsorshipThe authors would like to acknowledge the Basque Government for the financial support of this research through project IT1498-22 and grant PIF19-183. E. R. wants to acknowledge the tenure track position “BOIS” part of E2S UPPA supported by the “Investissements d'Avenir” French program managed by ANR (ANR-16-IDEX-0002). The authors thank for the technical and human support provided by SGIker (UPV/EHU/ERDF, EU).es_ES
dc.language.isoenges_ES
dc.publisherRSCes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es/*
dc.titleSonochemical oxidation of technical lignin to obtain nanoparticles with enhanced functionalityes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderThis Open Access Article is licensed under a Creative Commons Attribution-Non Commercial 3.0 Unported Licence.es_ES
dc.rights.holderAtribución-NoComercial 3.0 España*
dc.relation.publisherversionhttps://pubs.rsc.org/en/content/articlehtml/2023/gc/d3gc01037fes_ES
dc.identifier.doi10.1039/d3gc01037f
dc.departamentoesIngeniería química y del medio ambientees_ES
dc.departamentoeuIngeniaritza kimikoa eta ingurumenaren ingeniaritzaes_ES


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This Open Access Article is licensed under a Creative Commons Attribution-Non Commercial 3.0 Unported Licence.
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