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hal.structure.identifierGéosciences Rennes [GR]
dc.contributor.authorTESFA, Marawit
dc.contributor.authorDIA, Aline
hal.structure.identifierInstitut de Recherche Mathématique de Rennes [IRMAR]
dc.contributor.authorMAHÉ, Fabrice
hal.structure.identifierInteractions Sol Plante Atmosphère [UMR ISPA]
dc.contributor.authorJANOT, Noémie
hal.structure.identifierGéosciences Rennes [GR]
dc.contributor.authorMARSAC, Remi
dc.date.accessioned2024-04-08T11:42:56Z
dc.date.available2024-04-08T11:42:56Z
dc.date.conference2023-07-09
dc.identifier.urihttps://oskar-bordeaux.fr/handle/20.500.12278/195088
dc.description.abstractEnNatural Organic Matter (NOM) holds a crucial role in major environmental issues such as soil quality and contamination, because of its ubiquity and high reactivity. Both NOM (1) adsorption onto mineral surfaces and (2) reactivity towards various contaminants are mainly related to NOM acid-base functional groups such as, carboxylic and phenolic ones. Although acid-base potentiometric titration is the most reliable approach to quantify these groups, it is time-consuming and often impossible to apply to environmentally relevant NOM concentrations, because it requires several hundreds of milligrams per liter of dissolved organic carbon [1]. Spectrophotometric acid-base titration is a simple and powerful technique to evaluate NOM proton binding sites properties at environmentally relevant concentrations [2]. However, the quantitative determination of NOM electrical charge (Q), from the measured absorbance (A), remains a great challenge. In a previous work [2], a linear relationship between Q and the UV-vis differential absorbance (∆Aλ) at a given wavelength (λ) was evidenced for a specific humic acid solution. Here, by using a simplified and efficient spectroscopic acid-base titration protocol [3], the present study proposes a novel method to extend this ∆Aλ vs Q relationship to various NOM samples. This approach deconvolutes the absorbance spectra into 3 components, proton-inert chromophores (A0,λ), a signal related to the deprotonation process of carboxylic (A1,λ) and phenolic groups (A2,λ). This method enabled to select a sample-specific wavelength (λmid) where both A1,λ and A2,λ significantly contribute to the variation of the absorbance with pH. By linear regression analysis of Aλmid,pH vs Q for various NOM reference samples, sample-specific slope (SNOM) and intercept (INOM) were found to be related to intrinsic sample spectroscopic properties (A0,λmid, A1,λmid and A2,λmid), allowing the approximation of Q values of NOM at environmentally relevant concentrations. This approach will improve the understanding and enable more accurate predictions of NOM role in the metal ion fate in natural systems.[1] Tesfa; Duval; Marsac; Dia; Pinheiro (2022), Environ. Sci. Technol. 56 (14), 10494–10503.[2] Janot; Reiller; Korshin; Benedetti (2010), Environ. Sci. Technol. 44 (17), 6782–6788.[3] Tesfa; Dia; Ollivier; Osorio-Leon; Marsac (2022), MethodsX. 56 (14), 9, 101721.
dc.language.isoen
dc.title.enEstimating organic matter acid-base properties and electrical charge by spectrophotometry
dc.typeAutre communication scientifique (congrès sans actes - poster - séminaire...)
dc.subject.halPlanète et Univers [physics]/Sciences de la Terre/Géochimie
dc.subject.halSciences de l'environnement
bordeaux.hal.laboratoriesInteractions Soil Plant Atmosphere (ISPA) - UMR 1391*
bordeaux.institutionBordeaux Sciences Agro
bordeaux.institutionINRAE
bordeaux.conference.titleGoldschmidt Conference 2023
bordeaux.countryFR
bordeaux.conference.cityLyon
bordeaux.peerReviewedoui
hal.identifierinsu-04187920
hal.version1
hal.invitednon
hal.proceedingsoui
hal.conference.end2023-07-14
hal.popularnon
hal.audienceInternationale
hal.origin.linkhttps://hal.archives-ouvertes.fr//insu-04187920v1
bordeaux.COinSctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.au=TESFA,%20Marawit&DIA,%20Aline&MAH%C3%89,%20Fabrice&JANOT,%20No%C3%A9mie&MARSAC,%20Remi&rft.genre=conference


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