61 research outputs found

    Nowe wskazania do zastosowania terapii ECMO w ciągu ostatnich 5 lat

    Get PDF
    Nierecenzowany artykuł poglądowyPraca po krótkim wstępie historycznym, sięgającym połowy dwudziestego wieku, przedstawia metodę pozaustrojowego utlenowania krwi (ECMO). Artykuł wprowadza nas w dokładny opis tej metody leczenia, przedstawiając poszczególne etapy krążącej krwi od podłączenia układu do krwioobiegu pacjenta, po przepływ przez skomplikowany układ ECMO. Praca przedstawia aktualne wskazania, przeciwwskazania, możliwe powikłania oraz koszty prowadzenia terapii ECMO. Omawia także nowe zastosowania ECMO w Oddziałach Anestezjologii i Intensywnej Terapii w takich przypadkach jak ciężka hipotermia czy krwawienie śród-pęcherzykowe w płucach .The thesis, after a brief historical introduction, reaching half of the twentieth century concerning Extracorporeal Membrane Oxygenation, that is a therapy derived from cardiology, introduces us to the exact description of the treatment. It talks, among other things, about connecting the whole system to the patient's bloodstream, and what happens to the blood during each stage of the blood flow through the ECMO circuit. The thesis also aims at showing the current indications based primarily on the results of blood gas in ARDS, possible complications, contraindications, and the cost of doing the therapy. However that vast majority of the thesis is devoted to new applications of a treatment conducted by extracorporeal oxygenation. In this respect, we move from pandemic acute respiratory syndrome caused by A/H1N1 virus through treatment of ARDS in the diagnosed HIV infection and ending with severe hypothermia and diffuse alveolar hemorrhage

    Heterogeneous catalysis based on supramolecular association

    Full text link
    [EN] Heterogeneous catalysis is based mostly on materials built with strong covalent bonds. However, supramolecular aggregation in which individual components self-assemble due to non-covalent interactions to create a larger entity offers also considerable potential for the preparation of materials with application in catalysis. The present article provides a perspective on the use of supramolecular aggregation for the development of heterogeneous catalysts. One of the main advantages of this approach is that the preparation procedure based on spontaneous self-assembly is frequently simpler than those that require the formation of covalent bonds. The emphasis in this article has been placed on the use in the preparation of heterogeneous catalysts of not only carbon materials, particularly graphene and carbon nanotubes, but also dendrimers and organic capsules. Examples of hybrid organic-inorganic materials such as mesoporous organosilicas, metal-organic frameworks and heteropolyacids are also briefly described. The purpose is to illustrate the breadth of the field and the diverse array of possibilities already developed to apply the concepts of supramolecular association in heterogeneous catalysis.Financial support by the Spanish Ministry of Economy and Competitiveness (Severo Ochoa and CTQ2015-69153-CO2-R1) and Generalitat Valenciana (Prometeo 2017-083) is gratefully acknowledged. Prof Parvulescu thanks UEFISCDI for the Projects 121/2017 and 32PCCD1/2018.Parvulescu, VI.; García Gómez, H. (2018). Heterogeneous catalysis based on supramolecular association. Catalysis Science & Technology. 8(19):4834-4857. https://doi.org/10.1039/c8cy01295dS48344857819J.-M. Lehn , Supramolecular chemistry , Vch , Weinheim , 1995J. W. Steed , J. L.Atwood and P. A.Gale , Definition and emergence of supramolecular chemistry , Wiley Online Library , 2012Herbst, S., Soberats, B., Leowanawat, P., Stolte, M., Lehmann, M., & Würthner, F. (2018). Self-assembly of multi-stranded perylene dye J-aggregates in columnar liquid-crystalline phases. Nature Communications, 9(1). doi:10.1038/s41467-018-05018-6Würthner, F., Thalacker, C., & Sautter, A. (1999). Hierarchical Organization of Functional Perylene Chromophores to Mesoscopic Superstructures by Hydrogen Bonding and π-π Interactions. Advanced Materials, 11(9), 754-758. doi:10.1002/(sici)1521-4095(199906)11:93.0.co;2-5JELLEY, E. E. (1936). Spectral Absorption and Fluorescence of Dyes in the Molecular State. Nature, 138(3502), 1009-1010. doi:10.1038/1381009a0Wang, J., Liu, D., Zhu, Y., Zhou, S., & Guan, S. (2018). Supramolecular packing dominant photocatalytic oxidation and anticancer performance of PDI. Applied Catalysis B: Environmental, 231, 251-261. doi:10.1016/j.apcatb.2018.03.026Liebing, P., Pietrasiak, E., Otth, E., Kalim, J., Bornemann, D., & Togni, A. (2018). Supramolecular Aggregation of Perfluoroorganyl Iodane Reagents in the Solid State and in Solution. European Journal of Organic Chemistry, 2018(27-28), 3771-3781. doi:10.1002/ejoc.201800358Zhang, S. (2003). Fabrication of novel biomaterials through molecular self-assembly. Nature Biotechnology, 21(10), 1171-1178. doi:10.1038/nbt874Balzani, V., Gómez-López, M., & Stoddart, J. F. (1998). Molecular Machines. Accounts of Chemical Research, 31(7), 405-414. doi:10.1021/ar970340yBai, C., & Liu, M. (2012). Implantation of nanomaterials and nanostructures on surface and their applications. Nano Today, 7(4), 258-281. doi:10.1016/j.nantod.2012.05.002Lehn, J.-M. (2002). Toward complex matter: Supramolecular chemistry and self-organization. Proceedings of the National Academy of Sciences, 99(8), 4763-4768. doi:10.1073/pnas.072065599Lehn, J.-M. (2007). From supramolecular chemistry towards constitutional dynamic chemistry and adaptive chemistry. Chem. Soc. Rev., 36(2), 151-160. doi:10.1039/b616752gSanders, J. K. M. (1998). Supramolecular Catalysis in Transition. Chemistry - A European Journal, 4(8), 1378-1383. doi:10.1002/(sici)1521-3765(19980807)4:83.0.co;2-3A. Lützen , Supramolecular Catalysis , ed. P. W. N. M. van Leeuwen , Wiley Online Library , 2008Zhao, L., Sui, X.-L., Li, J.-Z., Zhang, J.-J., Zhang, L.-M., Huang, G.-S., & Wang, Z.-B. (2018). Supramolecular assembly promoted synthesis of three-dimensional nitrogen doped graphene frameworks as efficient electrocatalyst for oxygen reduction reaction and methanol electrooxidation. Applied Catalysis B: Environmental, 231, 224-233. doi:10.1016/j.apcatb.2018.03.020Wang, X., Liu, Q., Yang, Q., Zhang, Z., & Fang, X. (2018). Three-dimensional g-C3N4 aggregates of hollow bubbles with high photocatalytic degradation of tetracycline. Carbon, 136, 103-112. doi:10.1016/j.carbon.2018.04.059Yao, Y., Wei, X., Cai, Y., Kong, X., Chen, J., Wu, J., & Shi, Y. (2018). Hybrid supramolecular materials constructed from pillar[5]arene based host–guest interactions with photo and redox tunable properties. Journal of Colloid and Interface Science, 525, 48-53. doi:10.1016/j.jcis.2018.04.034Leung, F. C.-M., Leung, S. Y.-L., Chung, C. Y.-S., & Yam, V. W.-W. (2016). Metal–Metal and π–π Interactions Directed End-to-End Assembly of Gold Nanorods. Journal of the American Chemical Society, 138(9), 2989-2992. doi:10.1021/jacs.6b01382Lu, C., Zhang, M., Tang, D., Yan, X., Zhang, Z., Zhou, Z., … Stang, P. J. (2018). Fluorescent Metallacage-Core Supramolecular Polymer Gel Formed by Orthogonal Metal Coordination and Host–Guest Interactions. Journal of the American Chemical Society, 140(24), 7674-7680. doi:10.1021/jacs.8b03781Sun, Y., Li, S., Zhou, Z., Saha, M. L., Datta, S., Zhang, M., … Stang, P. J. (2017). Alanine-Based Chiral Metallogels via Supramolecular Coordination Complex Platforms: Metallogelation Induced Chirality Transfer. Journal of the American Chemical Society, 140(9), 3257-3263. doi:10.1021/jacs.7b10769Du, P., Jaouen, M., Bocheux, A., Bourgogne, C., Han, Z., Bouchiat, V., … Attias, A.-J. (2014). Surface-Confined Self-Assembled Janus Tectons: A Versatile Platform towards the Noncovalent Functionalization of Graphene. Angewandte Chemie, 126(38), 10224-10230. doi:10.1002/ange.201403572Georgakilas, V., Otyepka, M., Bourlinos, A. B., Chandra, V., Kim, N., Kemp, K. C., … Kim, K. S. (2012). Functionalization of Graphene: Covalent and Non-Covalent Approaches, Derivatives and Applications. Chemical Reviews, 112(11), 6156-6214. doi:10.1021/cr3000412Qu, S., Li, M., Xie, L., Huang, X., Yang, J., Wang, N., & Yang, S. (2013). Noncovalent Functionalization of Graphene Attaching [6,6]-Phenyl-C61-butyric Acid Methyl Ester (PCBM) and Application as Electron Extraction Layer of Polymer Solar Cells. ACS Nano, 7(5), 4070-4081. doi:10.1021/nn4001963Du, P., Bléger, D., Charra, F., Bouchiat, V., Kreher, D., Mathevet, F., & Attias, A.-J. (2015). A versatile strategy towards non-covalent functionalization of graphene by surface-confined supramolecular self-assembly of Janus tectons. Beilstein Journal of Nanotechnology, 6, 632-639. doi:10.3762/bjnano.6.64Chefetz, B., Deshmukh, A. P., Hatcher, P. G., & Guthrie, E. A. (2000). Pyrene Sorption by Natural Organic Matter. Environmental Science & Technology, 34(14), 2925-2930. doi:10.1021/es9912877Pan, B., & Xing, B. (2008). Adsorption Mechanisms of Organic Chemicals on Carbon Nanotubes. Environmental Science & Technology, 42(24), 9005-9013. doi:10.1021/es801777nChen, J., Chen, W., & Zhu, D. (2008). Adsorption of Nonionic Aromatic Compounds to Single-Walled Carbon Nanotubes: Effects of Aqueous Solution Chemistry. Environmental Science & Technology, 42(19), 7225-7230. doi:10.1021/es801412jPodeszwa, R. (2010). Interactions of graphene sheets deduced from properties of polycyclic aromatic hydrocarbons. The Journal of Chemical Physics, 132(4), 044704. doi:10.1063/1.3300064Peris, E. (2016). Polyaromatic N-heterocyclic carbene ligands and π-stacking. Catalytic consequences. Chemical Communications, 52(34), 5777-5787. doi:10.1039/c6cc02017hRuiz-Botella, S., & Peris, E. (2015). Unveiling the Importance of π-Stacking in Borrowing-Hydrogen Processes Catalysed by Iridium Complexes with Pyrene Tags. Chemistry - A European Journal, 21(43), 15263-15271. doi:10.1002/chem.201502948Sabater, S., Mata, J. A., & Peris, E. (2014). Immobilization of Pyrene-Tagged Palladium and Ruthenium Complexes onto Reduced Graphene Oxide: An Efficient and Highly Recyclable Catalyst for Hydrodefluorination. Organometallics, 34(7), 1186-1190. doi:10.1021/om501040xSabater, S., Mata, J. A., & Peris, E. (2014). Catalyst Enhancement and Recyclability by Immobilization of Metal Complexes onto Graphene Surface by Noncovalent Interactions. ACS Catalysis, 4(6), 2038-2047. doi:10.1021/cs5003959Wittmann, S., Schätz, A., Grass, R. N., Stark, W. J., & Reiser, O. (2010). A Recyclable Nanoparticle-Supported Palladium Catalyst for the Hydroxycarbonylation of Aryl Halides in Water. Angewandte Chemie International Edition, 49(10), 1867-1870. doi:10.1002/anie.200906166Keller, M., Collière, V., Reiser, O., Caminade, A.-M., Majoral, J.-P., & Ouali, A. (2013). Pyrene-Tagged Dendritic Catalysts Noncovalently Grafted onto Magnetic Co/C Nanoparticles: An Efficient and Recyclable System for Drug Synthesis. Angewandte Chemie International Edition, 52(13), 3626-3629. doi:10.1002/anie.201209969MISHRA, S., ARORA, S., NAGPAL, R., & SINGH CHAUHAN, S. M. (2014). Sulfonated graphenes catalyzed synthesis of expanded porphyrins and their supramolecular interactions with pristine graphene. Journal of Chemical Sciences, 126(6), 1729-1736. doi:10.1007/s12039-014-0731-8Xing, L., Xie, J.-H., Chen, Y.-S., Wang, L.-X., & Zhou, Q.-L. (2008). Simply Modified Chiral Diphosphine: Catalyst Recyclingvia Non-covalent Absorption on Carbon Nanotubes. Advanced Synthesis & Catalysis, 350(7-8), 1013-1016. doi:10.1002/adsc.200700617Che, G., Lakshmi, B. B., Fisher, E. R., & Martin, C. R. (1998). Carbon nanotubule membranes for electrochemical energy storage and production. Nature, 393(6683), 346-349. doi:10.1038/30694Zhu, Z., Su, D., Weinberg, G., & Schlögl, R. (2004). Supermolecular Self-Assembly of Graphene Sheets:  Formation of Tube-in-Tube Nanostructures. Nano Letters, 4(11), 2255-2259. doi:10.1021/nl048794tFukushima, T. (2003). Molecular Ordering of Organic Molten Salts Triggered by Single-Walled Carbon Nanotubes. Science, 300(5628), 2072-2074. doi:10.1126/science.1082289Tunckol, M., Durand, J., & Serp, P. (2012). Carbon nanomaterial–ionic liquid hybrids. Carbon, 50(12), 4303-4334. doi:10.1016/j.carbon.2012.05.017Subramaniam, K., Das, A., & Heinrich, G. (2011). Development of conducting polychloroprene rubber using imidazolium based ionic liquid modified multi-walled carbon nanotubes. Composites Science and Technology, 71(11), 1441-1449. doi:10.1016/j.compscitech.2011.05.018Chu, H., Shen, Y., Lin, L., Qin, X., Feng, G., Lin, Z., … Li, Y. (2010). Ionic-Liquid-Assisted Preparation of Carbon Nanotube-Supported Uniform Noble Metal Nanoparticles and Their Enhanced Catalytic Performance. Advanced Functional Materials, 20(21), 3747-3752. doi:10.1002/adfm.201001240Chun, Y. S., Shin, J. Y., Song, C. E., & Lee, S. (2008). Palladium nanoparticles supported onto ionic carbon nanotubes as robust recyclable catalysts in an ionic liquid. Chem. Commun., (8), 942-944. doi:10.1039/b715463aSalvo, A. M. P., La Parola, V., Liotta, L. F., Giacalone, F., & Gruttadauria, M. (2016). Highly Loaded Multi-Walled Carbon Nanotubes Non-Covalently Modified with a Bis-Imidazolium Salt and their Use as Catalyst Supports. ChemPlusChem, 81(5), 471-476. doi:10.1002/cplu.201600023Park, H. S., Choi, B. G., Yang, S. H., Shin, W. H., Kang, J. K., Jung, D., & Hong, W. H. (2009). Ionic-Liquid-Assisted Sonochemical Synthesis of Carbon-Nanotube-Based Nanohybrids: Control in the Structures and Interfacial Characteristics. Small, 5(15), 1754-1760. doi:10.1002/smll.200900128Noël, S., Léger, B., Ponchel, A., Philippot, K., Denicourt-Nowicki, A., Roucoux, A., & Monflier, E. (2014). Cyclodextrin-based systems for the stabilization of metallic(0) nanoparticles and their versatile applications in catalysis. Catalysis Today, 235, 20-32. doi:10.1016/j.cattod.2014.03.030Wyrwalski, F., Léger, B., Lancelot, C., Roucoux, A., Monflier, E., & Ponchel, A. (2011). Chemically modified cyclodextrins as supramolecular tools to generate carbon-supported ruthenium nanoparticles: An application towards gas phase hydrogenation. Applied Catalysis A: General, 391(1-2), 334-341. doi:10.1016/j.apcata.2010.07.006Jean-Marie, A., Griboval-Constant, A., Khodakov, A. Y., Monflier, E., & Diehl, F. (2011). β-Cyclodextrin for design of alumina supported cobalt catalysts efficient in Fischer–Tropsch synthesis. Chemical Communications, 47(38), 10767. doi:10.1039/c1cc13800fLéger, B., Menuel, S., Ponchel, A., Hapiot, F., & Monflier, E. (2012). Nanoparticle-Based Catalysis using Supramolecular Hydrogels. Advanced Synthesis & Catalysis, 354(7), 1269-1272. doi:10.1002/adsc.201100888Zhang, J.-J., Ge, J.-M., Wang, H.-H., Wei, X., Li, X.-H., & Chen, J.-S. (2016). Activating Oxygen Molecules over Carbonyl-Modified Graphitic Carbon Nitride: Merging Supramolecular Oxidation with Photocatalysis in a Metal-Free Catalyst for Oxidative Coupling of Amines into Imines. ChemCatChem, 8(22), 3441-3445. doi:10.1002/cctc.201601065Qi, W., Liu, W., Liu, S., Zhang, B., Gu, X., Guo, X., & Su, D. (2014). Heteropoly Acid/Carbon Nanotube Hybrid Materials as Efficient Solid-Acid Catalysts. ChemCatChem, 6(9), 2613-2620. doi:10.1002/cctc.201402270Willner, B., Katz, E., & Willner, I. (2006). Electrical contacting of redox proteins by nanotechnological means. Current Opinion in Biotechnology, 17(6), 589-596. doi:10.1016/j.copbio.2006.10.008Smalley, R. E., Li, Y., Moore, V. C., Price, B. K., Colorado, R., Schmidt, H. K., … Tour, J. M. (2006). Single Wall Carbon Nanotube Amplification:  En Route to a Type-Specific Growth Mechanism. Journal of the American Chemical Society, 128(49), 15824-15829. doi:10.1021/ja065767rJasti, R., Bhattacharjee, J., Neaton, J. B., & Bertozzi, C. R. (2008). Synthesis, Characterization, and Theory of [9]-, [12]-, and [18]Cycloparaphenylene: Carbon Nanohoop Structures. Journal of the American Chemical Society, 130(52), 17646-17647. doi:10.1021/ja807126uFort, E. H., Donovan, P. M., & Scott, L. T. (2009). Diels−Alder Reactivity of Polycyclic Aromatic Hydrocarbon Bay Regions: Implications for Metal-Free Growth of Single-Chirality Carbon Nanotubes. Journal of the American Chemical Society, 131(44), 16006-16007. doi:10.1021/ja907802gFort, E. H., & Scott, L. T. (2010). One-Step Conversion of Aromatic Hydrocarbon Bay Regions into Unsubstituted Benzene Rings: A Reagent for the Low-Temperature, Metal-Free Growth of Single-Chirality Carbon Nanotubes. Angewandte Chemie, 122(37), 6776-6778. doi:10.1002/ange.201002859Lu, D., Cui, S., & Du, P. (2017). Large π-Extension of Carbon Nanorings by Incorporating Hexa-peri-hexabenzocoronenes. Synlett, 28(14), 1671-1677. doi:10.1055/s-0036-1588830Niu, T., Wu, J., Ling, F., Jin, S., Lu, G., & Zhou, M. (2017). Halogen-Adatom Mediated Phase Transition of Two-Dimensional Molecular Self-Assembly on a Metal Surface. Langmuir, 34(1), 553-560. doi:10.1021/acs.langmuir.7b03796Lee, J. W., Samal, S., Selvapalam, N., Kim, H.-J., & Kim, K. (2003). Cucurbituril Homologues and Derivatives:  New Opportunities in Supramolecular Chemistry. Accounts of Chemical Research, 36(8), 621-630. doi:10.1021/ar020254kNi, X.-L., Xiao, X., Cong, H., Zhu, Q.-J., Xue, S.-F., & Tao, Z. (2014). Self-Assemblies Based on the «Outer-Surface Interactions» of Cucurbit[n]urils: New Opportunities for Supramolecular Architectures and Materials. Accounts of Chemical Research, 47(4), 1386-1395. doi:10.1021/ar5000133Wang, P., Wu, Y., Zhao, Y., Yu, Y., Zhang, M., & Cao, L. (2017). Crystalline nanotubular framework constructed by cucurbit[8]uril for selective CO2 adsorption. Chemical Communications, 53(40), 5503-5506. doi:10.1039/c7cc02074kJames, S. L. (2003). Metal-organic frameworks. Chemical Society Reviews, 32(5), 276. doi:10.1039/b200393gH.-C. Zhou , J. R.Long and O. M.Yaghi , Introduction to metal–organic frameworks , ACS Publications , 2012Dhakshinamoorthy, A., Asiri, A. M., & Garcia, H. (2017). Metal Organic Frameworks as Versatile Hosts of Au Nanoparticles in Heterogeneous Catalysis. ACS Catalysis, 7(4), 2896-2919. doi:10.1021/acscatal.6b03386Dhakshinamoorthy, A., & Garcia, H. (2014). Cascade Reactions Catalyzed by Metal Organic Frameworks. ChemSusChem, 7(9), 2392-2410. doi:10.1002/cssc.201402148Dhakshinamoorthy, A., Asiri, A. M., & Garcia, H. (2014). Catalysis by metal–organic frameworks in water. Chem. Commun., 50(85), 12800-12814. doi:10.1039/c4cc04387aDhakshinamoorthy, A., Asiri, A. M., & Garcia, H. (2016). Metal-Organic Frameworks as Catalysts for Oxidation Reactions. Chemistry - A European Journal, 22(24), 8012-8024. doi:10.1002/chem.201505141Noh, T. H., & Jung, O.-S. (2016). Recent Advances in Various Metal–Organic Channels for Photochemistry beyond Confined Spaces. Accounts of Chemical Research, 49(9), 1835-1843. doi:10.1021/acs.accounts.6b00291Tabacchi, G. (2018). Supramolecular Organization in Confined Nanospaces. ChemPhysChem, 19(11), 1249-1297. doi:10.1002/cphc.201701090Haldar, R., Reddy, S. K., Suresh, V. M., Mohapatra, S., Balasubramanian, S., & Maji, T. K. (2014). Flexible and Rigid Amine-Functionalized Microporous Frameworks Based on Different Secondary Building Units: Supramolecular Isomerism, Selective CO2Capture, and Catalysis. Chemistry - A European Journal, 20(15), 4347-4356. doi:10.1002/chem.201303610Tan, L.-L., Song, N., Zhang, S. X.-A., Li, H., Wang, B., & Yang, Y.-W. (2016). Ca2+, pH and thermo triple-responsive mechanized Zr-based MOFs for on-command drug release in bone diseases. Journal of Materials Chemistry B, 4(1), 135-140. doi:10.1039/c5tb01789kRimoldi, M., Howarth, A. J., DeStefano, M. R., Lin, L., Goswami, S., Li, P., … Farha, O. K. (2016). Catalytic Zirconium/Hafnium-Based Metal–Organic Frameworks. ACS Catalysis, 7(2), 997-1014. doi:10.1021/acscatal.6b02923Winter, A., Hager, M. D., Newkome, G. R., & Schubert, U. S. (2011). The Marriage of Terpyridines and Inorganic Nanoparticles: Synthetic Aspects, Characterization Techniques, and Potential Applications. Advanced Materials, 23(48), 5728-5748. doi:10.1002/adma.201103612Ding, X., Gao, Y., Ye, L., Zhang, L., & Sun, L. (2015). Assembling Supramolecular Dye-Sensitized Photoelectrochemical Cells for Water Splitting. ChemSusChem, 8(23), 3992-3995. doi:10.1002/cssc.201500313Tajima, T., Sakata, W., Wada, T., Tsutsui, A., Nishimoto, S., Miyake, M., & Takaguchi, Y. (2011). Photosensitized Hydrogen Evolution from Water Using a Single-Walled Carbon Nanotube/Fullerodendron/SiO2 Coaxial Nanohybrid. Advanced Materials, 23(48), 5750-5754. doi:10.1002/adma.201103472Ueda, Y., Takeda, H., Yui, T., Koike, K., Goto, Y., Inagaki, S., & Ishitani, O. (2014). A Visible-Light Harvesting System for CO2Reduction Using a RuII-ReIPhotocatalyst Adsorbed in Mesoporous Organosilica. ChemSusChem, 8(3), 439-442. doi:10.1002/cssc.201403194Yokoyama, T., Yokoyama, S., Kamikado, T., Okuno, Y., & Mashiko, S. (2001). Selective assembly on a surface of supramolecular aggregates with controlled size and shape. Nature, 413(6856), 619-621. doi:10.1038/35098059Barth, J. V., Costantini, G., & Kern, K. (2005). Engineering atomic and molecular nanostructures at surfaces. Nature, 437(7059), 671-679. doi:10.1038/nature04166Klasovsky, F., Hohmeyer, J., Brückner, A., Bonifer, M., Arras, J., Steffan, M., … Claus, P. (2008). Catalytic and Mechanistic Investigation of Polyaniline Supported PtO2 Nanoparticles: A Combined in situ/operando EPR, DRIFTS, and EXAFS Study. The Journal of Physical Chemistry C, 112(49), 19555-19559. doi:10.1021/jp805970eNishiyama, F., Yokoyama, T., Kamikado, T., Yokoyama, S., Mashiko, S., Sakaguchi, K., & Kikuchi, K. (2007). Interstitial Accommodation of C60 in a Surface-Supported Supramolecular Network. Advanced Materials, 19(1), 117-120. doi:10.1002/adma.200601364Shalom, M., Inal, S., Fettkenhauer, C., Neher, D., & Antonietti, M. (2013). Improving Carbon Nitride Photocatalysis by Supramolecular Preorganization of Monomers. Journal of the American Chemical Society, 135(19), 7118-7121. doi:10.1021/ja402521sSun, J., Xu, J., Grafmueller, A., Huang, X., Liedel, C., Algara-Siller, G., … Shalom, M. (2017). Self-assembled carbon nitride for photocatalytic hydrogen evolution and degradation of p-nitrophenol. Applied Catalysis B: Environmental, 205, 1-10. doi:10.1016/j.apcatb.2016.12.030Ishida, Y., Chabanne, L., Antonietti, M., & Shalom, M. (2014). Morphology Control and Photocatalysis Enhancement by the One-Pot Synthesis of Carbon Nitride from Preorganized Hydrogen-Bonded Supramolecular Precursors. Langmuir, 30(2), 447-451. doi:10.1021/la404101hZhang, J., Hao, J., Wei, Y., Xiao, F., Yin, P., & Wang, L. (2010). Nanoscale Chiral Rod-like Molecular Triads Assembled from Achiral Polyoxometalates. Journal of the American Chemical Society, 132(1), 14-15. doi:10.1021/ja907535gZheng, Y., Zhou, H., Liu, D., Floudas, G., Wagner, M., Koynov, K., … Ikeda, T. (2013). Supramolecular Thiophene Nanosheets. Angewandte Chemie, 125(18), 4945-4948. doi:10.1002/ange.201210090Lee, E., Kim, J.-K., & Lee, M. (2009). Reversible Scrolling of Two-Dimensional Sheets from the Self-Assembly of Laterally Grafted Amphiphilic Rods. Angewandte Chemie International Edition, 48(20), 3657-3660. doi:10.1002/anie.200900079Kambe, T., Sakamoto, R., Hoshiko, K., Takada, K., Miyachi, M., Ryu, J.-H., … Nishihara, H. (2013). π-Conjugated Nickel Bis(dithiolene) Complex Nanosheet. Journal of the American Chemical Society, 135(7), 2462-2465. doi:10.1021/ja312380bDong, R., Pfeffermann, M., Liang, H., Zheng, Z., Zhu, X., Zhang, J., & Feng, X. (2015). Large-Area, Free-Standing, Two-Dimensional Supramolecular Polymer Single-Layer Sheets for Highly Efficient Electro

    Contribution à l'optimisation par ajout d'éthylènediamine de catalyseurs supportés à base de cobalt destinés à l'oxydation de composés organiques volatils

    No full text
    Afin de limiter l'émission de composés organiques volatils (COV), des traitements de type récupératif ou destructif ont été développés. L'oxydation par voie catalytique est intéressante puisqu'elle permet un traitement à température relativement basse et une orientation de la réaction. Parmis les différents métaux de transition, l'oxyde de cobalt Co3O4 d'avère être une phase très active dans l'oxydation des COV. Cependant, dans le cas de catalyseurs supportés à fortes teneurs en cobalt, des méthodes de synthèse difficiles à réaliser sont nécessaires afin de minimiser la formation de grosses particules, moins actives en catalyse. Au cours de ce travail, des catalyseurs supportés à forte teneur en cobalt (5% en masse) ont été mis au point en utilisant la méthode classique d'imprégnationen excès de volume. Pour différents supports (cérine, titane, alumine et zircone), l'ajout d'éthylènediamine dans la solution d'imprégnation se traduit par un accroissement de l'activité catalytique lié à l'augmentation de la dispersion des espèces de cobalt. Dans le cas de la zircone, le gain observé est le plus marquant du fait de la présence d'espèces de cobalt fortement dispersées et très réductibles. Pour le solide Co/Zr, l'étude de la modification du support (ajout d'yttrium) et du précurseur (rapport en/Co = 1 ; 2 et 3) permet d'optimiser les conditions de synthèse de ce catalyseur et aussi d'éclaircir le rôle de l'éthylènediamine. Les bonnes capacités catalytiques du solide (Co-en1)/Zr ont été confirmées lors de l'oxydation de différents COV. Ce solide s'est également avéré plus stable sous flux réactionnel qu'un catalyseur conventionnel préparé en l'abscence d'éthylènediamine.In order to limit volatil organic compound (VOC), different treatments were developped. Catalytic oxydation is an interesting way since it allows a treatment at lower temperature and an orientation of the reaction. Amoung various transition metals , cobalt oxyde Co3O4 seems to be a very active phase for VOC's oxydation. However, in case of supported catalysts with hight cobalt contents, the use of synthesis' methods which are difficult to realize are necessary in order to minimize the formation of large particles, less active in catalysis. In this work, supported catalysts with hight cobalt content (5 weight %) were prepared by the traditional method (impregnatiooon in excess of volume). For different supports (ceria, titania, alumina and zirconia), addition of ethylenediamine during impregnation lead to a rise of cobalt species dispersion and therefore to an increase of the catalytic activity. In case of zirconia, the gain observed are most important due to the presence of cobalt species strongly dispersed and easier reducible. For Co/Zr samples, modifications of support (by yttrium addition) and precursor (ration en/Co = 1 ; 2 and 3) lead to an optimisation of synthesis' conditions and allow us to clear up the role of ethylenediamine. The good catalytic performances of the solid (Co-en1)/Zr were confirmed in oxydation reaction of different VOC. Moreover, this solid is proven more stable under reactional flow than the conventional catalyst prepared without ethylenediamine.DUNKERQUE-BU Lettres Sci.Hum. (591832101) / SudocSudocFranceF

    «Cyclodextrins as versatile tools for the preparation of heterogeneous catalysts»

    No full text
    International audienceno abstrac

    Modified Co3O4/ZrO2 catalysts for VOC emissions abatement.

    No full text
    The catalytic activity study of cobalt oxides dispersed on different supports evidenced first the highest performances of zirconia based catalysts in the reaction of toluene oxidn. The influence of the presence of ethylenediamine (en) during the prepn. of Co/ZrO2 and the ZrO2 support modification by Y2O3 were then studied and compared with ref. catalyst prepd. conventionally by impregnation of ZrO2 with an aq. soln. of Co(NO3)2. Addn. of an aq. soln. of ethylenediamine to a cobalt nitrate soln. led to a strong increase on the catalytic activity of the activated solids in the toluene deep oxidn. as compared with the ref. catalyst. The best catalytic results were explained in terms of cobalt oxides dispersion but also in terms of Co-support interaction. The generated cobalt species were reducible at much lower temps. and then were more active in the toluene total oxidn. Finally an efficient catalyst for VOC oxidn. was produced combining the modifications of ZrO2 by yttrium and of the precursor
    corecore