Auswahl der wissenschaftlichen Literatur zum Thema „Réduction du dioxyde de carbone“
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Zeitschriftenartikel zum Thema "Réduction du dioxyde de carbone"
Mrabet Temsamani, Rabía. „Le détroit de Gibraltar et la mer d’Alboran : quels enjeux pour le déploiement des énergies marines renouvelables“. Revista de Estudios Internacionales Mediterráneos, Nr. 36 (24.06.2024): 293–327. http://dx.doi.org/10.15366/reim2024.36.012.
Der volle Inhalt der QuelleFielden, L. J., F. D. Duncan, J. R. B. Lighton und Y. Rechav. „Ventilation chez les adultes d’Amblyomma hebraeum et A. marmoreum (Acarina, Ixodidae), vecteurs de la cowdriose en Afrique australe“. Revue d’élevage et de médecine vétérinaire des pays tropicaux 46, Nr. 1-2 (01.01.1993): 335–38. http://dx.doi.org/10.19182/remvt.9388.
Der volle Inhalt der QuelleBinet, C., A. Jadi und JC Lavalley. „Étude par spectroscopie infrarouge de l’adsorption du dioxyde et du monoxyde de carbone sur la cérine ; influence de l’état de réduction de la cérine“. Journal de Chimie Physique 89 (1992): 1779–97. http://dx.doi.org/10.1051/jcp/1992891779.
Der volle Inhalt der QuelleAderinboye, R. Y., und A. O. Olanipekun. „An in-vitro evaluation of the potentials of turmeric as phytogenic feed additive for rumen modification“. Nigerian Journal of Animal Production 48, Nr. 3 (06.03.2021): 193–203. http://dx.doi.org/10.51791/njap.v48i3.2950.
Der volle Inhalt der QuelleTestud, F. „Dioxyde de carbone“. EMC - Pathologie professionnelle et de l 'environnement 5, Nr. 2 (Januar 2010): 1–5. http://dx.doi.org/10.1016/s1155-1925(10)71870-x.
Der volle Inhalt der QuelleMavouroulou Quentin, Moundounga, Ngomanda Alfred und Lepengue Nicaise Alexis. „Etat des Lieux des Incertitudes Liées à l’Estimation de la Biomasse des Arbres (Revue Bibliographique)“. European Scientific Journal, ESJ 19, Nr. 6 (28.02.2023): 60. http://dx.doi.org/10.19044/esj.2023.v19n6p60.
Der volle Inhalt der QuellePrud’homme, Rémy. „Dioxyde de carbone : raison garder“. Commentaire Numéro125, Nr. 1 (2009): 133. http://dx.doi.org/10.3917/comm.125.0133.
Der volle Inhalt der QuelleSoubeyran, Aurélien, Ahmed Rouabhi und Christophe Coquelet. „Étude du comportement thermodynamique du CO2 en stockage en cavité saline“. Revue Française de Géotechnique, Nr. 179 (2024): 1. http://dx.doi.org/10.1051/geotech/2024002.
Der volle Inhalt der QuelleSène, Matar, Maurice Ndeye und Alpha Oumar Diallo. „Le carbone 14 (14C) un traceur idéal pour la surveillance de la pollution atmosphérique en dioxyde de carbone (CO2) anthropogénique dans la zone de dakar“. Journal de Physique de la SOAPHYS 2, Nr. 2 (12.05.2021): C20A18–1—C20A18–8. http://dx.doi.org/10.46411/jpsoaphys.2020.02.18.
Der volle Inhalt der QuelleMastrodicasa, A., A. Cuenoud, M. Pasquier und P. N. Carron. „Intoxication aiguë au dioxyde de carbone“. Annales françaises de médecine d’urgence 8, Nr. 5 (17.09.2018): 326–31. http://dx.doi.org/10.3166/afmu-2018-0082.
Der volle Inhalt der QuelleDissertationen zum Thema "Réduction du dioxyde de carbone"
Gomes, Christophe. „Une approche diagonale pour la transformation catalytique du dioxyde de carbone“. Phd thesis, Université Paris Sud - Paris XI, 2013. http://tel.archives-ouvertes.fr/tel-00954408.
Der volle Inhalt der QuelleSahin, Nihat Ege. „Réduction électrochimique du dioxyde de carbone sur des électrocatalyseurs à base de cuivre“. Thesis, Poitiers, 2016. http://www.theses.fr/2016POIT2313/document.
Der volle Inhalt der QuelleThe anthropogenic emissions of carbon dioxide (CO2) are the major cause of global warming. The selective CO2 reduction reaction (CO2RR) of has been proposed as a promising, convenient and efficient method for sustainable energy conversion systems. The reduction of CO2 to energetically valuable products requires the use of an appropriate electrode material. This study focuses on the preparation of Cu-based electrocatalysts supported on different types of carbon materials such as Vulcan XC-72R, mesoporous carbon CMK-3, mesoporous carbon FDU-15 and tannin based mesoporous carbon IS2M for the CO2RR under mild conditions. Besides, Vulcan XC-72R carbon supported bimetallic copper/palladium alloy materials were prepared for increasing the Faradaic yield. These copper-based catalysts were electrochemically characterized and preparative electrolyses set at constant potential were carried out in order to investigate the reduction products distribution and Faradaic yields as a function of the applied potential and catalyst loading. Chemicals such as HCOOH, CO and H2 issued from the CO2RR, were determined with in-situ and ex-situ complementary (electro)analytical and spectroscopic techniques. The significant difference in the product distribution is probably due to the ensemble (geometry and ligand) effects in the bimetallic CuPd materials, and textural structure of the supporting substrates. Selective CO2 to-HCOOH conversion has been successfully undertaken on Cu50Pd50/C with 62 % Faradaic efficiency
Frogneux, Xavier. „Transformations réductrices du CO2 pour la formation de liaisons C-N et C-C“. Thesis, Paris 11, 2015. http://www.theses.fr/2015PA112136/document.
Der volle Inhalt der QuelleIn the current world, carbon dioxide (CO2) is the major waste of the massive utilization of fossil resources but only few applications have been developed using this compound. In order to take advantage of its abundancy, the development of novel chemical transformation of CO2 to produce fine chemicals is of high interest in the scientific community. In particular, the formation of C-N bond(s) from CO2 and amine compounds unlocks a new way to access high energy and value-added. A second type of highly desirable transformation is the formation of C-C bonds with CO2 so as to synthesize carboxylic acid derivatives. The utilization of hydrosilanes as mild reductants allows the reactions to proceed under 1 bar of CO2 with abundant and cheap metal-based catalysts (iron, zinc) or with organocatalysts. The synthesis of formamides, methylamines and aminals from CO2 are described herein. Ultimately, the catalytic carboxylation of carbosilanes has been achieved for the first time using copper-based complexes. In the specific case of 2-pyridylsilanes, the use of pentavalent fluoride salts allowed us to perform the reaction without catalyst
Christophe, Jennifer. „Etude de l'électroactivité du cuivre pour la réduction du dioxyde de carbone et pour la réduction de l'ion nitrate“. Doctoral thesis, Universite Libre de Bruxelles, 2007. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/210680.
Der volle Inhalt der QuelleDans la première partie du travail, nous avons comparé, à l’aide de la voltampérométrie, d’électrolyses à potentiel contrôlé et d’analyses chromatographiques, l'activité d'électrodes polycristalline et monocristallines de Cu et d'alliages AuxCuy de différentes orientations cristallines pour l'électroréduction de CO2.
Nous avons pu établir une étroite corrélation entre l'activité de l'électrode de Cu et l'arrangement atomique de sa surface. L'activité et la sélectivité pour CH4 de Cu décroissent selon la séquence :Cu (111) > Cu (100) > Cu (poly). La réduction du CO2 et la formation de CH4 sont favorisées sur les surfaces lisses et denses à l'échelle atomique.
La sélectivité des alliages AuxCuy est considérablement orientée vers CO quand la fraction superficielle de Au augmente. L'alliage de composition 50-50 conduit à la formation exclusive de CO.
La seconde partie de la thèse est consacrée à l'étude de l'activité d'électrodes massives de Cu polycristallin et monocristallin d’orientation (111) et de dispersions de Cu pour la réduction électrochimique de NO3-.
Nous avons mis en évidence l'importance des conditions de pH pour le déroulement des processus à l'électrode de cuivre. En milieu acide, NO3- est directement réduit en NH4+ alors qu’en milieu neutre, les réactions de réduction de NO3- en NO2- et de NO2- en NH4+ s’observent successivement en fonction du potentiel.
L'activité des dispersions de Cu dans un film de polyaniline dépend fortement des conditions de dépôt. Le cuivre incorporé au film sous sa forme réduite est plus actif que le cuivre incorporé au film initialement oxydé. Par ailleurs, nous avons montré que la concentration de H+ dans le polymère est limitée. En conséquence, le processus de réduction de NO3- sur le cuivre dispersé dans un film de polyaniline est modifié en milieu acide.
L’utilisation d’un film de poly-3,4-éthylènedioxythiophène déposé sur une surface de Pt s'est quant à elle révélée inadéquate comme support pour l'incorporation de Cu dans le cadre de l'étude de la réduction de NO3- en milieu acide.
Doctorat en Sciences
info:eu-repo/semantics/nonPublished
Stanbury, Matthew. „Réduction photo et électro-assistée sélective du dioxyde de carbone sur des catalyseurs moléculaires“. Thesis, Université Grenoble Alpes (ComUE), 2016. http://www.theses.fr/2016GREAV094/document.
Der volle Inhalt der QuelleThe general context of this thesis is on CO2 valorisation, and recounts fundamental research aimed at finding new molecular catalysts in order to achieve CO2 conversion. The results obtained provide additional knowledge in view of developing an efficient and selective catalytic CO2 reduction process. The first chapter begins with the general picture of CO2 utilisation and contains a bibliographical overview on the use of molecular catalysts for CO2 photo- and electroreduction. This short review demonstrates the wide variety of transition metal complexes used as catalysts, in particularly those based on rhenium. An analysis on the current state of CO2 reduction research using molecular catalyst complexes of the manganese carbonyl type is then reported. In Chapter II, the discussion begins with a brief overview of the research developed during this thesis relating to new complexes of the general formula: [Mn(L)(CO)3(X)] (X = Br, n = 0 ou CH3CN, n = 1; L = terpyridine derivatives). The interest in these complexes is twofold, as their physico-chemical properties give them potential catalytic CO2 reduction applications, as well as applications in the field relating to controlled CO release molecules. Developing new complexes based on ligands derived from terpy is one of the main routes that were chosen for catalyst performance optimisation and improvement. In this context, Mn complexes were synthesised, their photo- and electrochemical properties were studied in detail, before testing their activity with respect to catalytic CO2 reduction. The most remarkable result comes from the unique ability of these species to release one of their carbonyl ligands in a controlled fashion, which led to the discovery of novel Mn dicarbonyl complexes which are selective catalysts for CO2 reduction, and also to new molecules which are applicable in the release of small quantities of CO for therapeutic purposes.Chapter III covers the study of the complex [Mn(phen-dione)(CO)3(X)]n+ (X = Br, n = 0 ou CH3CN, n = 1). This complex was synthesised with the aim in mind of obtaining complexes soluble in aqueous media. While this objective was ambitious, it was soon found that these species showed no catalytic activity for CO2 reduction in the target aqueous medium. Nevertheless, electrocatalytic activity was demonstrated in hydro-organic media and photocatalytic applications in organic media proved promising. This work allowed us to gain a better understanding of the physicochemical properties and catalytic mechanisms of a Mn complex containing a redox-active ligand.The results presented in Chapter IV are based on the study of another new Mn carbonyl complex family. The study concentrated mainly on the complex [Mn(pyperNH)(CO)3(CH3CN)]+. The pyperNH ligand, with its aromatic system and NH functional group, plays a major role and is redox-active. After a section dedicated to its synthesis and characterisation, this chapter devotes a large part to the role that different experimental parameters can play on the efficiency of the catalytic CO2 reduction reaction. The Mn complexes described in this chapter have remarkable redox properties. A preliminary study of the catalytic activity of these complexes for CO2 reduction has allowed us to have an initial idea about the potential role of the N-H functional group of the ligand on the catalytic mechanism and reaction selectivity. This research was extended beyond the pyperNH ligand into a complex class of similar ligand structures, and the preliminary results obtained are original and promising, and open the way towards new perspectives
Routier, Mathilde. „Catalyse photochimique de la réduction du dioxyde de carbone par des porphyrines de fer“. Paris 7, 2014. http://www.theses.fr/2014PA077066.
Der volle Inhalt der QuelleThe transition from fossil fuels to renewable energy sources is a major challenge in today's society. The first step to address this challenge is to find a way to store and carry this energy, which can be done under the form of chemical bonds through the activation of small molecules like CO2, 02 and H2O. In this context, our work was focused on the catalytic photoreduction of carbon dioxide by three iron porphyrins showing remarkable electrocatalytic properties. We have first studied a homogeneous molecular photochemical approach. A careful analysis of the results, comparing the three porphyrins and the effect of the addition of a weak BrOnsted acid, allowed us to propose a reaction mechanism correlating the different behaviour of the porphyrins with their molecular structures. Furthermore, a detailed analysis of the experimental conditions required for the catalysis revealed that they induced the degradation of the porphyrins. To overcome these limits, we studied the use of a photosensitizer, resulting in improved catalytic performances and higher system stability. We also studied a homogeneous molecular photoelectrochemical approach, using p-type Si photoelectrodes. We observed the reduction of CO2 with a photovoltage of 350 mV, thus validating this strategy, but the process is limited by the sensitivity of the photoelectrodes towards 02. We are currently developing new electrodes made of copper oxide to obtain better catalytic performances and a higher stability
Gotico, Philipp. „Stratégies bio-inspirées pour la réduction catalytique et la valorisation du dioxyde de carbone“. Thesis, Université Paris-Saclay (ComUE), 2019. http://www.theses.fr/2019SACLS283/document.
Der volle Inhalt der QuelleThe criticality of global warming urges for the advancement of science to reduce carbon dioxide (CO₂) emissions in the atmosphere. At the heart of this challenge is the development of sustainable catalysts that can help capture, activate, reduce, and eventually valorize CO₂. This PhD work tried to respond to this call by developing molecular mimics inspired by natural systems in the larger scheme of artificial photosynthesis. Firstly, it involved tracking the journey of a photon of visible light and how it is transformed to a reducing power able to reduce CO₂. Secondly, in search for more efficient and stable catalysts, new mimics were synthesized inspired by the exceptional performance of CO dehydrogenase enzymes (CODH) in reducing CO₂. Lastly, further understanding of CODH also led to a proof-of-concept that directly valorizes the photo-produced CO for the synthesis of isotopically-labelled amide bonds, a common motif in pharmaceutically-relevant drugs
Bitar, Ziad. „Electrocatalyse de la réduction sélective du dioxyde de carbone sur électrodes à diffusion de gaz“. Thesis, Grenoble, 2014. http://www.theses.fr/2014GRENV030/document.
Der volle Inhalt der QuelleThis thesis concerns the valorization of CO2 by electrochemical means. It is largely devoted to the preparation and physico-chemical study of gas diffusion electrodes (GDE) in order to better understand the mechanisms and key parameters for electrocatalytic reduction of CO2 using this type of porous electrode. This study revolves around two main axes, the first is related to metal catalysts and the second is focused on molecular catalysts.The first axis deals with the preparation, characterization and electrochemical properties of Cu, Co, In, Zn, Bi, Pb and Fe catalysts supported on porous carbon powder. Their implementation to form GDE and their electrocatalytic activity toward CO2 reduction were studied. In aqueous medium, the GDE containing indium allowed obtaining the highest Faraday yields for electroreduction of CO2 to formic acid. In comparison with a metallic indium foil, the GDE-In/C showed improved catalytic performance and improved resistance to the electrolyte's impurities. We demonstrated that in the aqueous phase, a continuous flow of CO2 through a GDE resulted in an improved reactivity of the supported catalyst. This highlights the advantage of using dispersed metal particles on GDE rather than metal foil electrodes.The second axis of this study focuses on three dimeric ruthenium complexes with the general formula [Ru(L)(CH3CN)(CO)2]2(PF6)2. The study of the redox properties of these catalyst precursors containing variously substituted L (bipyridine) ligands, allowed the formation of polymer bonds of Ru-Ru by electroreduction to be demonstrated. The ligand with a pyrrole functional group allows for the prior formation of a polypyrrole film, conferring improved catalyst stability and enhancing the catalytic performance. Different ways of immobilizing the complex on porous carbon have been used to obtain modified GDE. This study provided insight into the interaction between the molecular catalyst and the catalyst carrier during the CO2 reduction. We have demonstrated that the electrocatalytic activity of the catalyst deposited on the GDE is maintained in an aqueous medium.Alongside this fundamental work, a laboratory pilot was developed to perform the electrocatalytic reduction of CO2 in the gas phase, in order to overcome limitations encountered in an aqueous medium, such as CO2 solubility and reaction products separation. This under development study has not only identified obstacles, including the nature of the ion exchange membrane, but has also identified the nature and proportion of the polymer electrolyte used in the formulation of the catalyst layer. This work has provided fundamental knowledge and concrete answers which probably allow one day that such a process as CO2 valorization may be viable on an industrial scale
Ruiz, Valencia Azariel. „A new microbiological way for CO2 reduction : from discovery to development“. Thesis, Montpellier, Ecole nationale supérieure de chimie, 2019. http://www.theses.fr/2019ENCM0002.
Der volle Inhalt der QuelleAt the European Institute of Membranes, a new microbiological process for CO2 reduction into formate was discovered. The first objective of this PhD work was to reproduce the CO2 reduction tests in reference conditions, with a new biocatalyst vial ordered to the same strain provider as for the prior trials at the Lab. However, these tests did not allow to reiterate the results obtained previously, i.e. formate production. A strain mutation was suspected and the strain that was stored during the preliminary tests was thus implemented. Nevertheless, new reproducibility problems were encountered. A biochemical analysis revealed finally that the strain assumed to catalyze the CO2 reduction was in consortium with other bacteria. In parallel, a reliable methodology based on CO2 labelling by 13C and NMR monitoring was developed at the Lab to follow 13CO2 assimilation. The different strains were isolated and tested separately regarding CO2 reduction. The NMR analysis demonstrated that the principal contamination, whose presence was unexpected, was the true biocatalyst of the 13CO2 reduction into 13C-formate.The 13C-formate was then quantified by a GC-MS method that was developed at the Lab. The effects of different reaction parameters on the reaction performances were thereafter investigated. These tests allowed notably to evidence an intracellular enzymatic system that could catalyze the CO2 reduction and to identify the possible electron donor. Indeed, addition of Poly-3-HydroxyButyrate (PHB) in the bacterial suspension enhanced significantly the formate production, suggesting that this energy storage polymer could be the electron source required for the CO2 reduction.Nevertheless, this intracellular PHB stock, formed during the bacteria culture step, is finite and can be exhausted during the reaction. This explains why the ability of the biocatalyst to recover electrons from a polarized cathode for CO2 reduction was assessed. Preliminary tests demonstrated the feasibility of this bio-electrochemical approach by the establishment of a CO2-dependant reduction current in a bio-electrolyzer. Current densities from 1.2 to 3.2 A·m-2 were obtained, which corresponds to volumetric flows of reduced CO2 ranging from 12 to 30 mL CO2·(g dry-cell)-1·d-1. Up to now, this new bioprocess was operated over 25 day. Regarding literature, this bioprocess is particularly interesting because (i) the volumetric flow of reduced CO2 is significant and (ii) no adding of cofactor, organic molecules, H2 or photons to the reaction medium is required
Innocent, Babette. „Etude des mécanismes réactionnels de l'électro-réduction du dioxyde de carbone sur le plomb en vue de sa transformation en des composés organiques“. Poitiers, 2008. http://www.theses.fr/2008POIT2308.
Der volle Inhalt der QuelleThe aim of this work was to promote the reduction of CO2 through its electrochemical conversion (electrosynthesis) on a lead electrode into high added value products. Depending on the nature of electrolyte, the electro-reduction of carbon dioxide leads to different products. Various electrolytes (aqueous or organic, protic or aprotic) were used to study two mechanisms: hydrogenation (formation of formate) and electrodimerization (synthesis of oxalate). Cyclic voltammetry studies have been carried out for electrochemically characterizing CO2 reduction on Pb. The electrochemical investigation of the electrode – electrolyte interface has shown that the process of CO2 electro-reduction is a mass transfer control both in the organic and aqueous media. Electrochemical experiments (cyclic voltammetry, chronoamperometry) coupled with in situ infrared reflectance spectroscopic techniques (SPAIRS, SNIFTIRS) have also shown that in aqueous medium (7
Bücher zum Thema "Réduction du dioxyde de carbone"
Brohé, Arnaud. Comptabilité carbone. Paris: La Découverte, 2013.
Den vollen Inhalt der Quelle findenHalmann, Martin M. Chemical fixation of carbon dioxide: Methods for recycling CO₂ into useful products. Boca Raton: CRC Press, 1993.
Den vollen Inhalt der Quelle findenMaroto-Valer, M. Mercedes. Developments and innovation in carbon dioxide (CO2) capture and storage technology. Boca Raton, Fla: CRC Press, 2010.
Den vollen Inhalt der Quelle findenBandyopadhyay, Amitava. Carbon capture and storage: CO2 management technologies. Toronto: Apple Academic Press, 2014.
Den vollen Inhalt der Quelle findenLecomte, Fabrice. CO₂ capture: Technologies to reduce greenhouse gas emissions. Paris, France: Editions Technip, 2010.
Den vollen Inhalt der Quelle findenHitchon, Brian. Pembina cardium CO2 monitoring pilot: A CO2-EOR project, Alberta, Canada : final report. Sherwood Park, Alta: Geoscience Publishing, 2009.
Den vollen Inhalt der Quelle findenMarkusson, Nils. The social dynamics of carbon capture and storage: Understanding CCS representations, governance and innovation. Abingdon, Oxon: Earthscan, 2012.
Den vollen Inhalt der Quelle findenRackley, Stephen A. Carbon capture and storage. Burlington, MA: Butterworth-Heinemann/Elsevier, 2010.
Den vollen Inhalt der Quelle finden1933-, Kohlmaier Gundolf H., Weber Michael 1952- und Houghton Richard A. 1943-, Hrsg. Carbon dioxide mitigation in forestry and wood industry. Berlin: Springer, 1998.
Den vollen Inhalt der Quelle findenLynas, Mark. Le compteur de carbone. Paris: Éditions First, 2007.
Den vollen Inhalt der Quelle findenBuchteile zum Thema "Réduction du dioxyde de carbone"
„Émissions de dioxyde de carbone“. In Panorama des statistiques de l'OCDE 2013. OECD, 2013. http://dx.doi.org/10.1787/factbook-2013-70-fr.
Der volle Inhalt der Quelle„Émissions de dioxyde de carbone (CO2)“. In Panorama de l'environnement 2013, 24–27. OECD, 2014. http://dx.doi.org/10.1787/9789264221802-6-fr.
Der volle Inhalt der QuelleBlanc, Guillaume, und Camille Noûs. „Chapitre 4 : L’énergie et le CO2“. In Physique et enjeux de société. Université Paris Cité, 2023. http://dx.doi.org/10.53480/physique-societe.8a7076.
Der volle Inhalt der QuelleGONTERO, Brigitte, und Stephen Christopher MABERLY. „Mécanismes biochimiques de concentration du dioxyde de carbone“. In Planète bleue, photosynthèse rouge et verte, 135–68. ISTE Group, 2023. http://dx.doi.org/10.51926/iste.9082.ch5.
Der volle Inhalt der QuelleRAPIN, Christophe, Eléonore DURAND und Marie-Alice SKAPER. „Recyclage et valorisation du matériau verre“. In Le recyclage, enjeu pour l’économie circulaire, 245–72. ISTE Group, 2023. http://dx.doi.org/10.51926/iste.9162.ch10.
Der volle Inhalt der QuelleAmouroux, Jacques, Paul Siffert, Jean Pierre Massué, Simeon Cavadias, Béatriz Trujillo, Koshi Hashimoto, Phillip Rutberg und Sergey Dresvin. „Chapitre 10 : Le dioxyde de carbone, la moléculeclé de la chimie du développement durable“. In La chimie et la nature, 209–30. EDP Sciences, 2020. http://dx.doi.org/10.1051/978-2-7598-0859-5-013.
Der volle Inhalt der QuelleAmouroux, Jacques, Paul Siffert, Jean Pierre Massué, Simeon Cavadias, Béatriz Trujillo, Koshi Hashimoto, Phillip Rutberg und Sergey Dresvin. „Chapitre 10 : Le dioxyde de carbone, la moléculeclé de la chimie du développement durable“. In La chimie et la nature, 209–30. EDP Sciences, 2020. http://dx.doi.org/10.1051/978-2-7598-0859-5.c013.
Der volle Inhalt der QuelleBasse, Diaga. „Recherches sur la Sustainability“. In Recherches sur la Sustainability, 213–32. EMS Editions, 2023. http://dx.doi.org/10.3917/ems.cheva.2023.01.0213.
Der volle Inhalt der QuelleMaaziz, Lyna. „Annuaire français de relations internationales“. In Annuaire français de relations internationales, 765–79. Éditions Panthéon-Assas, 2024. http://dx.doi.org/10.3917/epas.ferna.2024.01.0765.
Der volle Inhalt der QuelleKonferenzberichte zum Thema "Réduction du dioxyde de carbone"
Aukauloo, Ally. „S'inspirer de la nature pour produire de l'énergie. Photosynthèse artificielle à l'Université Paris-Saclay“. In MOlecules and Materials for the ENergy of TOMorrow. MSH Paris-Saclay Éditions, 2021. http://dx.doi.org/10.52983/nova3845.
Der volle Inhalt der QuelleBerichte der Organisationen zum Thema "Réduction du dioxyde de carbone"
Démonstrations de captage et de stockage de dioxyde de carbone (CO2) au Canada. Natural Resources Canada/ESS/Scientific and Technical Publishing Services, 2009. http://dx.doi.org/10.4095/261680.
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