Literatura académica sobre el tema "Catalyse or"
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Artículos de revistas sobre el tema "Catalyse or"
Rajesh, Nimmakuri y Dipak Prajapati. "Indium(iii) catalysed regio- and stereoselective hydrothiolation of bromoalkynes". RSC Adv. 4, n.º 61 (2014): 32108–12. http://dx.doi.org/10.1039/c4ra04359f.
Texto completoKhan, Mohammad Niyaz y Ibrahim Isah Fagge. "Kinetics and Mechanism of Cationic Micelle/Flexible Nanoparticle Catalysis: A Review". Progress in Reaction Kinetics and Mechanism 43, n.º 1 (marzo de 2018): 1–20. http://dx.doi.org/10.3184/146867818x15066862094905.
Texto completoAvigliano, L., V. Carelli, A. Casini, A. Finazzi-Agrò y F. Liberatore. "Oxidation of NAD dimers by horseradish peroxidase". Biochemical Journal 226, n.º 2 (1 de marzo de 1985): 391–95. http://dx.doi.org/10.1042/bj2260391.
Texto completoABBADI, Amine, Monika BRUMMEL, Burkhardt S. SCHüTT, Mary B. SLABAUGH, Ricardo SCHUCH y Friedrich SPENER. "Reaction mechanism of recombinant 3-oxoacyl-(acyl-carrier-protein) synthase III from Cuphea wrightii embryo, a fatty acid synthase type II condensing enzyme". Biochemical Journal 345, n.º 1 (17 de diciembre de 1999): 153–60. http://dx.doi.org/10.1042/bj3450153.
Texto completoOrtega-Caballero, Fernando y Mikael Bols. "Cyclodextrin derivatives with cyanohydrin and carboxylate groups as artificial glycosidases". Canadian Journal of Chemistry 84, n.º 4 (1 de abril de 2006): 650–58. http://dx.doi.org/10.1139/v06-039.
Texto completoJia, Yunhua, Takeo Tomita, Kazuma Yamauchi, Makoto Nishiyama y David R. J. Palmer. "Kinetics and product analysis of the reaction catalysed by recombinant homoaconitase from Thermus thermophilus". Biochemical Journal 396, n.º 3 (29 de mayo de 2006): 479–85. http://dx.doi.org/10.1042/bj20051711.
Texto completoLiu, Yansheng, Xinlin Li, Xuanduong Le, Wei Zhang, Hao Gu, Ruiwen Xue y Jiantai Ma. "Catalysis of the hydro-dechlorination of 4-chlorophenol by Pd(0)-modified MCM-48 mesoporous microspheres with an ultra-high surface area". New Journal of Chemistry 39, n.º 6 (2015): 4519–25. http://dx.doi.org/10.1039/c5nj00617a.
Texto completoGu, Nina X., Gaël Ung y Jonas C. Peters. "Catalytic hydrazine disproportionation mediated by a thiolate-bridged VFe complex". Chemical Communications 55, n.º 37 (2019): 5363–66. http://dx.doi.org/10.1039/c9cc00345b.
Texto completoBoucher, Guillaume, Bilal Said, Elizabeth L. Ostler, Marina Resmini, Keith Brocklehurst y Gerard Gallacher. "Evidence that the mechanism of antibody-catalysed hydrolysis of arylcarbamates can be determined by the structure of the immunogen used to elicit the catalytic antibody". Biochemical Journal 401, n.º 3 (12 de enero de 2007): 721–26. http://dx.doi.org/10.1042/bj20060551.
Texto completoGiger, Rudolf y Pascal Hoffmann. "Design and synthesis of a transition state analog of a metalloporphyrin-catalysed oxidation reaction". Journal of Porphyrins and Phthalocyanines 06, n.º 05 (mayo de 2002): 362–65. http://dx.doi.org/10.1142/s1088424602000439.
Texto completoTesis sobre el tema "Catalyse or"
Nguyen, Thi Xuan Phuong. "La catalyse hétérogène". Paris 5, 1994. http://www.theses.fr/1994PA05P039.
Texto completoRoudier, Mylène. "Catalyse duale pour une synthèse énantiosélective éco-compatible". Electronic Thesis or Diss., Aix-Marseille, 2016. http://www.theses.fr/2016AIXM4347.
Texto completoThis manuscript is focus on the development of multicatalyzed reactions involving iminium activation and reversible neutral hydrogen transfer reaction for the synthesis of complexe enantioenriched building blocks from allyl alcohols and 1,3-dicarbonyls.An unprecedented cascade catalysis combining an iron catalyst and a pyrrolidine-base catalyst is developed for the preparation of g-fonctionalized enantioenriched alcohols in a formal redox-, atom- and step-economical approach. The efficiency of this method involving a dual catalysis and a retro-Claisen xas further demonstrated in the short synthesis of several key fragments of biologically active natural products or odorant molecule. This methodolgy was then incremented by a experimental mechanistic study allowing a better understanding of the mechanism of this transformation and leading to a new catalytic systeminvolving three different catalysts (iron complex, copper and organocatalyst). Then, we focused on the development of a new synthetic approach to enantioenriched medium-sized lactones. This methodology is based on a 1,4-Michael addition of cycloalkane-1,3-diones to a,b-insaturated aldehydes. Then, a key chemoselective reductively triggered Claisen fragmentation occurred to generate desired lactones in a rapid manner.Finally, thanks to our methodology developed during this thesis, the total synthesis of floribundane B was studied
Sierra, salazar Andrés Felipe. "Waterborne catalytic materials with original design". Thesis, Montpellier, Ecole nationale supérieure de chimie, 2017. http://www.theses.fr/2017ENCM0014/document.
Texto completoLa catalyse est l'un des piliers pour le développement de procédés durables, car elle permet d'utiliser moins de ressources en accélérant les réactions chimiques. Afin de fournir des catalyseurs plus performants, cette étude propose une nouvelle méthode de préparation de catalyseurs pour contrôler la distribution de nanoparticules (NPs) métalliques au sein des catalyseurs hiérarchiquement poreux (méso et macro) en combinant la synthèse de latex, la réduction sonochimique et le procédé sol-gel. La première étape est la synthèse d'une empreinte porogène de billes de polystyrène (latex) obtenues par polymérisation en émulsion aqueuse. La deuxième étape est la synthèse et le dépôt de NPs de métaux nobles sur la surface des billes de polymère par voie sonochimique dans l’eau. La troisième étape est la synthèse du support catalytique par un procédé sol-gel en milieu aqueux en utilisant le latex décoré et l’orthosilicate de tétraéthyle (TEOS) dans des conditions contrôlées pour moduler la porosité finale de la matrice de silice (mésoporeuse). Toutes les étapes de cette approche sont effectuées dans l'eau, ce qui limite les impacts environnementaux de la préparation du catalyseur. L'élimination du porogène (latex) par calcination génère les macropores. Le matériau résultant possède alors une morphologie inédite pour un catalyseur, avec des macropores fonctionnalisés par des NPs métalliques, dans une matrice de silice mésoporeuse. Ainsi, il a été possible de synthétiser un latex monodisperse de polystyrène (~130 nm), lequel a été décoré avec des NPs de Pt (~2.3 nm) par réduction sonochimique. Le matériau final de silice a présenté des mésopores (2-15 nm) reliant les macropores (110-400 nm) contenant les NPs de Pt. Il a été possible d'obtenir des surfaces spécifiques et des volumes poreux totaux de 615 m2/g et 0,74 cm3/g, respectivement. Dans un premier cas d'étude, des catalyseurs de Pt/SiO2 à porosité hiérarchique ont été évalués dans l'hydrogénation sélective du p-chloronitrobenzene (p-CNB) pour produire la p-chloroaniline. Ils ont présenté des activités catalytiques allant jusqu'à 91,7 ± 2,9 molCNB/(min molPt) et des sélectivités jusqu'à 100 ± 2% à 80% de conversion, par rapport à 47,7 ± 2,9 molCNB/(min molPt) et 91 ± 2%, respectivement, obtenus dans les mêmes conditions avec un catalyseur commercial. Dans un deuxième cas d'étude, des catalyseurs à base de Pd, Pd-Pt et Pd-CeO2 supportés sur de la silice à porosité hiérarchique ont été préparés et testés dans la synthèse directe du peroxyde d'hydrogène. La meilleure productivité a été obtenue avec le catalyseur bimétallique Pd-Pt avec 32500 molH2O2/(h molmétal) en batch, et la meilleure sélectivité a été obtenue avec le catalyseur Pd-CeO2/SiO2 (63 ± 2%) en semi-continu. En résumé, cette thèse propose une nouvelle méthode de préparation dans l’eau de matériaux fonctionnels à porosité hiérarchique en combinant la synthèse de latex, la réduction sonochimique et le procédé sol-gel. Il a été démontré que cette technique de préparation fournit une boîte à outils très puissante et polyvalente pour la préparation et l'optimisation des catalyseurs. Des perspectives pour améliorer davantage les morphologies et la distribution contrôlée des sites actifs sont également proposées
Roudier, Mylène. "Catalyse duale pour une synthèse énantiosélective éco-compatible". Thesis, Aix-Marseille, 2016. http://www.theses.fr/2016AIXM4347.
Texto completoThis manuscript is focus on the development of multicatalyzed reactions involving iminium activation and reversible neutral hydrogen transfer reaction for the synthesis of complexe enantioenriched building blocks from allyl alcohols and 1,3-dicarbonyls.An unprecedented cascade catalysis combining an iron catalyst and a pyrrolidine-base catalyst is developed for the preparation of g-fonctionalized enantioenriched alcohols in a formal redox-, atom- and step-economical approach. The efficiency of this method involving a dual catalysis and a retro-Claisen xas further demonstrated in the short synthesis of several key fragments of biologically active natural products or odorant molecule. This methodolgy was then incremented by a experimental mechanistic study allowing a better understanding of the mechanism of this transformation and leading to a new catalytic systeminvolving three different catalysts (iron complex, copper and organocatalyst). Then, we focused on the development of a new synthetic approach to enantioenriched medium-sized lactones. This methodology is based on a 1,4-Michael addition of cycloalkane-1,3-diones to a,b-insaturated aldehydes. Then, a key chemoselective reductively triggered Claisen fragmentation occurred to generate desired lactones in a rapid manner.Finally, thanks to our methodology developed during this thesis, the total synthesis of floribundane B was studied
Chenneberg, Ludwig. "Nouvelles avancées en catalyse photoredox : applications en chimie radicalaire de synthèse et en catalyse duale". Thesis, Paris 6, 2016. http://www.theses.fr/2016PA066305/document.
Texto completoVisible-light photoredox catalysis has emerged as a very powerful strategy to generate radical species replacing more and more tin-mediated or stoichiometric redox methodologies. The main objective of the research described in this Ph. D. thesis is to develop new synthetic methodologies in radical and organometallic chemistry, and merge them in a dual catalysis process for the preparation of elaborated molecular building blocks. In a first study, we report a photocatalytic alternative of Barton-McCombie deoxygenation based on a visible-light photoreduction of O-thiocarbamates derived from secondary and tertiary alcohols. A mechanistic investigation is presented based on fluorescence quenching and cyclic voltammetry experiments. In a second study, a challenging method of generation of unstabilized alkyl radicals by photooxidation of borate salts or hypervalent silicon species is reported. These radicals are trapped by free radical scavengers or engaged in a photoredox/nickel dual catalysis
Dandachi, Hiba. "Nouveaux Complexes Oligomères Cycliques de Salens Chiraux pour la Catalyse Asymétrique". Thesis, Université Paris-Saclay (ComUE), 2015. http://www.theses.fr/2015SACLS106/document.
Texto completoThis thesis work takes place in the broad context of salen chemistry. A special attention is given to corresponding chiral complexes used as versatile enantioselective catalysts for a wide range of reactions of interest. In the context of heterogeneous asymmetric catalysis, we focus specifically on the development of polymeric, cyclic, chiral salen catalysts, named calixsalen complexes. Thus, we have developed an easy access to calixsalen cobalt (III) complexes by a facile polycondensation route. These calixsalens were used as catalysts to promote the dynamic hydrolytic kinetic resolution of epibromohydrin. They are easily recovered from the reaction mixture by a simple filtration. These cyclic complexes allowed the formation of homobimetallic species responsible for an efficient dual activation of both the epoxide and water, delivering the targeted product in both high yield and selectivity.We have also reported the use of a combination of cobalt and manganese calixsalen complexes in the hydrolysis of meso epoxydes. This dual heterobimetallic system proved to be even more selective than the homobimetallic one, in which cobalt complexes were only engaged. Based on these results, we have attempted preparing heterobimetallic salen complexes, wherein two different metals should be closely associated into the same macrocycle. Towards this aim, we explored click chemistry to couple alkyne- and azide-functionalized monomeric salen complexes coordinated to two different metals
Giuseppone, Nicolas. "Les iodures de lanthanides en catalyse et catalyse asymetrique". Paris 11, 2000. http://www.theses.fr/2000PA112122.
Texto completoCarrée, Fabien. "Catalyse et catalyse asymétrique par les dérivés des lanthanides". Paris 11, 2004. http://www.theses.fr/2004PA112208.
Texto completoThis work deals with the preparation of a novel class of lanthanides iodo-binaphtoxides complexes and their evaluation as lewis acid catalysts in various organic reactions. The structure of our complexes is very interesting since they bear ionic lanthanide-oxygen bonds. Various methods have been tested to carry out the synthesis of our catalysts. Among these, two of them involve the formation of a potassium binaphtoxide as an intermediar,. The other system uses a different strategy which consists in a ligand exchange. Among these methods, the bests results have been observed by using the diphenylmethane potassium salt as base for ligands deprotonation. Catalytic activity of lanthanides iodo-binaphtoxides has then been tested in the imino-aldol reaction involving a glyoxilic imine and ketene silyl dimethyl acetal (ksa). Very high enantiomeric excesses have been observed by optimising condition reactions. Our complexes have also shown an interesting catalytic activity in primary aromatic amines meso epoxides ring-opening reactions. Lanthanum as well as samarium iodo-binaphtoxides have allowed formation of ?-amino-alcohols with up to 90% enantiomeric excesses. Moreover, use of the samarium complex has furnished a wide range of amino-alcohols, also with very good enantiomeric excesses. Finally, non-linear temperature dependant variations of enantiomeric excesses have been highlighted in our system. It has been also shown that samarium diiodide as well as samarium iodo-binaphtoxides are efficient catalysts in addition of amines on n-acyloxazolidinones or ring-opening of aziridines by aromatic amines
Motos, Blanca. "Silices fonctionnalisées contenant des espèces ioniques pour la catalyse hétérogène". Thesis, Montpellier, Ecole nationale supérieure de chimie, 2011. http://www.theses.fr/2011ENCM0015.
Texto completoHeterogenous catalysis is an area in continuous development due to economical, health and environmental issues. This thesis deals with the preparation of i-silica materials for the posterior application in heterogeneous catalysis. First, di-aryl imidazolium containing silica materials were synthesized by post-grafting reactions on mesoporous SBA-15. Moreover, di-alkyl imidazolium containing PMO films were prepared in presence of an anionic surfactant. Then, supported copper and palladium N-heterocyclic carbenes were synthesized from di-aryl imidazolium silica and applied to A3 reactions (Cu-NHC) and Suzuki cross-coupling reactions (Pd-NHC). Imidazolium functionalized silicas were also utilized as heterogeneous organocatalysts in Henry reactions and in reactions of cycloaddition of carbon dioxide to epoxides. Finally, PMO type materials containing amine/ammonium and zwitterionic substructures were applied to Henry and Biginelli organocatalysed reactions, respectively
Leone, Matteo. "Development of novel synthetic methodologies in photocatalysis for the preparation of (a)chiral amine derivatives". Electronic Thesis or Diss., université Paris-Saclay, 2024. http://www.theses.fr/2024UPASF021.
Texto completoVisible light, known for being an abundant and economical energy source, has recently become crucial in advancing sustainable catalytic chemical processes. The scientific community's substantial contributions have disclosed a broad spectrum of transformations, as outlined in the initial chapter. Among the various synthetic applications developed so far, achieving photocatalysed reactions in an asymmetric fashion remains a considerable challenge. In this specific context, our focus extends beyond the creation of new sustainable and efficient light-mediated methodologies; we are also dedicated to pioneering innovative asymmetric processes. Within this manuscript, the second chapter is dedicated to introducing a novel category of visible-light-sensitive chiral organocatalysts. These catalysts feature a covalently linked backbone of BINOL-derived Chiral Phosphoric Acids (CPAs) with various photosensitizers, such as aryl ketones and phenothiazine. Several CPAs, incorporating one or two photosensitizer moieties, were easily synthesized in a few steps from BINOL. The photophysical and electrochemical properties of these C1- and C2-symmetric chiral photocatalysts were investigated. The ketone-based chiral photocatalysts were applied in an enantioselective multicomponent tandem process, enabling the efficient synthesis of fully substituted 1,2-diamines with excellent enantioselectivities. The third chapter presents an alternative strategy for the development of asymmetric processes through photocatalysis, exploiting chiral auxiliaries. It highlights the needs of a sustainable and efficient photocatalysed methodology specifically designed for the stereoselective radical alkylation of chiral sulfinyl-imines. By utilizing readily available non-prefunctionalized radical precursors and TBADT as a photocatalyst to generate radicals through direct hydrogen atom transfer (HAT), this method has enabled the synthesis of diverse chiral amines with high yields and excellent diastereoselectivities under mild conditions. This approach proves to be effective for accessing a varied range of medically relevant compounds, encompassing both natural and synthetic α-amino acids and other α-amino compounds commonly present in approved pharmaceuticals and natural products. The fourth chapter describes a deoxygenative cross-electrophile coupling technique that combines readily available carboxylic acid-derived redox-active esters (RAEs) with aldehyde derived sulfonyl hydrazones, employing Eosin Y as an organophotocatalyst under visible light irradiation. This methodology serves as a versatile, metal-free C(sp3)−C(sp3) cross-coupling platform. Its synthetic utility as a safer and widely applicable C1 homologation of carboxylic acids was demonstrated, providing an alternative to the traditional Arndt-Eistert reaction. Furthermore, the approach allows for the direct synthesis of cyclic and acyclic β-arylethylamines using various aldehyde-derived sulfonyl hydrazones. Notably, the method is compatible with late-stage functionalization of peptides on solid-phase, simplifying the modification of intricate peptides without the need for time demanding de novo synthesis
Libros sobre el tema "Catalyse or"
Pellissier, Hélène. Enantioselective titanium-catalysed transformations. New Jersey: Imperial College Press, 2015.
Buscar texto completoJ, Thomas W., ed. Principles and practice of heterogeneous catalysis. Weinheim: VCH, 1996.
Buscar texto completoRoss, J. R. H. Heterogeneous catalysis: Fundamentals and applications. Amsterdam: Elsevier, 2012.
Buscar texto completo1946-, Elshishini S. S., ed. Modelling, simulation, and optimization of industrial fixed bed catalytic reactors. Yverdon, Switzerland: Gordon and Breach Science Publishers, 1993.
Buscar texto completoFarrauto, Robert J. Fundamentals of industrial catalytic processes. 2a ed. Hoboken, N.J: Wiley, 2005.
Buscar texto completo1959-, Regalbuto John R., ed. Handbook of catalyst preparation. Boca Raton: Taylor & Francis, 2007.
Buscar texto completo1960-, Jacobsen Eric N., Pfaltz Andreas 1948- y Yamamoto Hisashi, eds. Comprehensive asymmetric catalysis. Berlin: Springer, 2004.
Buscar texto completoEley, D. D. Advances in catalysis. San Diego, Calif: Academic Press, 1998.
Buscar texto completoM, Starks Charles, American Chemical Society Meeting y American Chemical Society. Division of Petroleum Chemistry., eds. Phase-transfer catalysis: New chemistry, catalysts, and applications. Washington, DC: American Chemical Society, 1987.
Buscar texto completoL, Liotta Charles, Starks Charles M y Halpern Marc, eds. Phase-Transfer Catalysis: Fundamentals, Applications and Industrial Perspectives. New York: Chapman & Hall, 1993.
Buscar texto completoCapítulos de libros sobre el tema "Catalyse or"
Engel, Paul. "2. Making things happen—catalysis". En Enzymes: A Very Short Introduction, 12–26. Oxford University Press, 2020. http://dx.doi.org/10.1093/actrade/9780198824985.003.0002.
Texto completo"Catalyse". En Encyclopedia of Astrobiology, 262. Berlin, Heidelberg: Springer Berlin Heidelberg, 2011. http://dx.doi.org/10.1007/978-3-642-11274-4_5018.
Texto completo"3 Catalyse". En Chimie verte, 133–276. EDP Sciences, 2020. http://dx.doi.org/10.1051/978-2-7598-2002-3-004.
Texto completo"3 Catalyse". En Chimie verte, 133–276. EDP Sciences, 2020. http://dx.doi.org/10.1051/978-2-7598-2002-3.c004.
Texto completo"catalyse, v." En Oxford English Dictionary. 3a ed. Oxford University Press, 2023. http://dx.doi.org/10.1093/oed/8577801088.
Texto completoDobson, C. M., J. A. Gerrard y A. J. Pratt. "Proteins as catalysts". En Foundations of Chemical Biology. Oxford University Press, 2001. http://dx.doi.org/10.1093/hesc/9780199248995.003.0005.
Texto completoShao, Z. y Y. H. Deng. "2.1.1 General Principles of Metal/Organocatalyst Dual Catalysis". En Dual Catalysis in Organic Synthesis 2. Stuttgart: Georg Thieme Verlag, 2020. http://dx.doi.org/10.1055/sos-sd-232-00002.
Texto completo"8 Catalyse hétérogène". En Les agrégats, 327–56. EDP Sciences, 2020. http://dx.doi.org/10.1051/978-2-7598-2176-1-010.
Texto completo"8 Catalyse hétérogène". En Les agrégats, 327–56. EDP Sciences, 2020. http://dx.doi.org/10.1051/978-2-7598-2176-1.c010.
Texto completoMaskill, Howard. "Catalysis of organic reactions in solution by small molecules and ions". En Structure and Reactivity in Organic Chemistry. Oxford University Press, 1999. http://dx.doi.org/10.1093/hesc/9780198558200.003.0004.
Texto completoActas de conferencias sobre el tema "Catalyse or"
Kulić Mandić, Aleksandra, Milena Bečelić-Tomin, Đurđa Kerkez, Gordana Pucar Milidrag, Vesna Pešić y Miljana Prica. "A mini review: Optimal dye removal by fenton process catalysed with waste materials". En 10th International Symposium on Graphic Engineering and Design. University of Novi Sad, Faculty of technical sciences, Department of graphic engineering and design,, 2020. http://dx.doi.org/10.24867/grid-2020-p21.
Texto completoAppleyard, N. y Z. Lock. "Connect and catalyse - our strategy [innovation management]". En IET Seminar on the Directions and Funding of Robotics Research in the UK. IEE, 2008. http://dx.doi.org/10.1049/ic:20080553.
Texto completoBond, Gary, A. Halman, H. Eccles, R. Mao, S. Pollington, P. Hinde, V. Demidyuk y A. Gkelios. "A COMPARATIVE STUDY OF MICROWAVE AND BARRIER DISCHARGE PLASMA FOR THE REGENERATION OF SPENT ZEOLITE CATALYSTS". En Ampere 2019. Valencia: Universitat Politècnica de València, 2019. http://dx.doi.org/10.4995/ampere2019.2019.9936.
Texto completoAudhali, Nadia, Anna Moore, Tim Martin, Charlotte Munro y Florence Wedmore. "181 Harnessing staff values to catalyse workplace change". En Leaders in Healthcare Conference, 17–20 November 2020. BMJ Publishing Group Ltd, 2020. http://dx.doi.org/10.1136/leader-2020-fmlm.181.
Texto completoJobic, H. "Catalyse localisée : étude de molécules adsorbées et de systèmes catalytiques". En JDN 16 – Diffusion Inélastique des Neutrons pour l'Etude des Excitations dans la Matiére Condensée. Les Ulis, France: EDP Sciences, 2010. http://dx.doi.org/10.1051/sfn/2010018.
Texto completoAudhali, Nadia, Florence Wedmore, Anna Moore y Charlotte Monro. "1427 Harnessing staff values to catalyse workplace change. Towards 2040, NHS net-zero". En Royal College of Paediatrics and Child Health, Abstracts of the RCPCH Conference–Online, 15 June 2021–17 June 2021. BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health, 2021. http://dx.doi.org/10.1136/archdischild-2021-rcpch.636.
Texto completoOfosu, F. A., G. J. Modi, M. A. Blajchman, M. R. Buchanan y E. A. Johnson. "INCREASED SULFATION IMPROVES THE ABILITY OF VESSEL WALL GLYCOSA-MINOGLYCANS TO REGULATE THROMBIN ACTIVITY AND PROTHROMBIN ACTIVATION IN PLASMA". En XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1643252.
Texto completoLou, Diming, Yajuan Chen, Yunhua Zhang, Peng Wan, Piqiang Tan, Zhiyuan Hu, Liang Fang y Tong Wang. "Study on Soot Oxidation Characteristics of Ce and La Modified Pt-Pd CDPF Catalysts". En WCX SAE World Congress Experience. 400 Commonwealth Drive, Warrendale, PA, United States: SAE International, 2023. http://dx.doi.org/10.4271/2023-01-0390.
Texto completoZhang, Aihua. "EXPERIMENTAL STUDY ON THE APPLICATION OF MACHINE LEARNING METHOD IN CATALYTIC MATERIALS". En Topics In Chemical & Material Engineering (TCME). Volkson Press, 2023. http://dx.doi.org/10.26480/smmp.01.2023.24.27.
Texto completoHenriksen, Jesper, Susanne Bendsen, Tony Ao Han, Jin Wang, Tine Holmboe y Catherine Merlo. "Experience as Incentive: Promoting Sustainable Urban Mobility Through Bridge Design". En IABSE Congress, New Delhi 2023: Engineering for Sustainable Development. Zurich, Switzerland: International Association for Bridge and Structural Engineering (IABSE), 2023. http://dx.doi.org/10.2749/newdelhi.2023.0978.
Texto completoInformes sobre el tema "Catalyse or"
Olsen, Daniel, Bryan Hackleman y Rodrigo Bauza Tellechaea. PR-179-16207-R01 Oxidation Catalyst Degradation on a 2-Stroke Lean-Burn NG Engine - Washing. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), mayo de 2019. http://dx.doi.org/10.55274/r0011586.
Texto completoStevens y Olsen. PR-179-12214-R01 CO Sensor Experimental Evaluation for Catalyst Health Monitoring. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), septiembre de 2014. http://dx.doi.org/10.55274/r0010827.
Texto completoBadrinarayanan y Olsen. PR-179-11201-R01 Performance Evaluation of Multiple Oxidation Catalysts on a Lean Burn Natural Gas Engine. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), agosto de 2012. http://dx.doi.org/10.55274/r0010772.
Texto completoOlsen y Neuner. PR-179-12207-R01 Performance Measurements of Oxidation Catalyst on an Exhaust Slipstream. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), agosto de 2013. http://dx.doi.org/10.55274/r0010800.
Texto completoTaylor, Joe, Peter Taylor y Louise Clark. Covid Collective Learning Report. Institute of Development Studies, marzo de 2024. http://dx.doi.org/10.19088/cc.2024.001.
Texto completode Brauw, Alan, Shalini Roy y Mulugeta Tefera. Financial services in refugee hosting areas: Can they promote inclusion? Lessons from the SHARPE project in Ethiopia. Centre for Excellence and Development Impact and Learning (CEDIL), diciembre de 2022. http://dx.doi.org/10.51744/ceb4.
Texto completoDefoort, Willson y Olsen. L51849 Performance Evaluation of Exhaust Catalysts During the Initial Aging on Large Industrial Engines. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), junio de 2001. http://dx.doi.org/10.55274/r0011213.
Texto completode Brauw, Alan, Daniel Gilligan, Laura Leavens, Fekadu Moges, Shalini Roy y Mulugeta Tefera. Impact Evaluation of the SHARPE Programme in Ethiopia: Academic Report. Centre for Excellence and Development Impact and Learning (CEDIL), marzo de 2023. http://dx.doi.org/10.51744/crpp6.
Texto completoSwanson, Dr Larry y Christopher Samuelson. PR-362-06208-R01 Evaluation of Byproduct Emissions from Gas Turbine SCR Catalyst. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), febrero de 2009. http://dx.doi.org/10.55274/r0010978.
Texto completoBauza, Rodrigo y Daniel Olsen. PR-179-20200-R01 Improved Catalyst Regeneration Process to Increase Poison Removal. Chantilly, Virginia: Pipeline Research Council International, Inc. (PRCI), junio de 2021. http://dx.doi.org/10.55274/r0012106.
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