Дисертації з теми "Supported metal catalyst"
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Widyaningrum, Rosalia Nugraheni. "Mesoporous silica-supported catalysts to enhance hydrogen production during cellulose pyrolysis." Thesis, The University of Sydney, 2011. https://hdl.handle.net/2123/28917.
Повний текст джерелаIwanow, Melanie [Verfasser], and Burkhard [Akademischer Betreuer] König. "Supported Metal Catalyst Preparation using Deep Eutectic Solvents / Melanie Iwanow ; Betreuer: Burkhard König." Regensburg : Universitätsbibliothek Regensburg, 2020. http://d-nb.info/1215905971/34.
Повний текст джерелаMin, Byoung Koun. "Scanning tunneling microscopic studies of SiO2 thin film supported metal nano-clusters." Diss., Texas A&M University, 2004. http://hdl.handle.net/1969.1/2737.
Повний текст джерелаKamiuchi, Naoto. "Studies on Nano-structures and Catalytic Activities of Oxide-supported Precious Metal Catalysts." 京都大学 (Kyoto University), 2010. http://hdl.handle.net/2433/120878.
Повний текст джерелаWang, Shengye. "Algal and alginate based beads and foams as sorbents for metal sorption and catalyst supports for 3-nitrophenol hydrogenation." Thesis, Montpellier, 2019. http://www.theses.fr/2019MONTG001.
Повний текст джерелаThis work describes the synthesis of a series of materials based on alginate and algal biomass (AB); these materials have been designed under different shapes: beads and foams. Special processes have been developed for directly using the algal biomass (without adding other polymers) with the double objective of simple processing and environmentally-friendly manufacturing (reduced production of sub-products and without additional resources). These materials have been tested first for metal recovery for heavy metal decontamination (Pb(II) and Cu(II)) but also for the valorization of metals (platinum groups metals, PGMs: Pd(II) and Pt(IV)). These studies were performed investigating various operating conditions in order to evaluate sorption capacities and limiting steps but also to identify the processes to be used for improving sorption performance. The incorporation of poly(ethyleneimine), PEI, is a promising method for increasing the density of highly reactive groups (amine functions). Different processes have been tested: (a) the incorporation of particles of PEI crosslinked with glutaraldehyde (heterogeneous beads: ABA/PEI), and (b) the homogeneous grafting of PEI on alginate (followed by glutaraldehyde crosslinking) (HABA/PEI beads). Several techniques have been used for characterizing the sorption process and the structure of developed sorbents, including FTIR spectroscopy, SEM & SEM-EDX analysis. In a second step selected materials have been tested for supported catalysis using the simple reaction of hydrogenation of 3–nitrophenol (3-NP) as a test reaction. The results are structured in 3 parts successively developed: (a) synthesis of alginate, AB and AB/PEI beads and testing for sorption heavy metals and PGMs, (b) comparison of Pd(II) sorption properties of AB/PEI composite beads prepared by the homogeneous and the heterogeneous routes (and their application to supported catalytic tests), and (c) synthesis of highly porous foams (prepared by reaction of alginate with PEI) and the testing of Pd(II) sorption and Pd-supported catalysis (in fixed-bed reactor). While PEI hardly affects the sorption of heavy metals (due to direct interaction with carboxylic groups of alginate or algal biomass), the presence of PEI strongly improves metal binding in the case of PGMs (the protonated amine groups strongly bind chloro-anionic PGM species). All the sorbents have a preference for Pb(II) over Cu(II) and for Pd(II) over Pt(IV), especially for alginate and AB beads because the presence of PEI limits the selectivity of the material for Pb(II) and Pd(II). Both the sorption capacity and the stability of composite alginate/PEI beads were improved while using the homogeneous synthesis mode (the PEI polymer being homogeneously dispersed in the bead before glutaraldehyde crosslinking). The two supports (heterogeneous vs. homogeneous beads) loaded with Pd(II) and subsequently reduced gave comparable catalytic performance (lower than conventional catalysts) but the homogeneous mode improves the long-term stability. The conditioning of the catalytic support as a foam allows testing the catalytic reaction in fixed-bed system: the conditioning improves mass transfer properties compared to beads and the apparent rate constant is only slightly reduced after operating 30 cycles
CORVA, MANUEL. "Experimental modeling of nanostructured and single metal atom supported catalysts at close-to-ambient conditions." Doctoral thesis, Università degli Studi di Trieste, 2019. http://hdl.handle.net/11368/2991050.
Повний текст джерелаThis Thesis work deals with the growth and characterization of model nanostructured surface systems in ultra-high vacuum environment (UHV, <10−9 mbar) and with their evolution at near ambient pressure (NAP, 0.1 - 100 mbar) conditions. The investigations are performed with the aid of specific in situ techniques (IR-Vis SFG, NAP-XPS, etc.) in order to probe the structural, electronic, chemical and catalytic properties of the models. The latter span from ordered lattices of metal nanoparticles to 2D metallorganic crystals, where stabilized mono-metallic centers act as the active cores. These systems, based on single metal atom centers, represent the main topic of this manuscript and they will be referred to as Single Metal Atom Catalysts (SMAC). The discussion of the scientific findings will first focus on the evolution of graphene supported Pt nanoclusters in CO atmosphere, varying both surface temperature and CO pressure to test the stability of the nanostructures. As degradation of this nanosystem occurs at realistic reaction conditions, the attention was shifted to the design and synthesis of model SMAC systems, where the single metal atom is stabilized in a metallorganic cage, thus preventing structural degradation. A first, prototype SMAC model system consisted of a single layer of Nickel tetraphenyl porphyrins (Ni-TPPs) deposited on the Cu(100) surface. We proved that, following to NO exposure, a hyponitrite species (N2O2) readily forms at the Ni sites already at UHV conditions and is stable at room temperature. The NO conversion is observed only on the NiTPP monolayer interacting with the underlying copper surface, showing that the substrate plays a major role, governing the properties of the nanostructured system through trans-effects associated with a strong surface-to-molecule charge transfer. A single Iron Phthalocyanine (FePc) layer was instead considered for a model carbonylation reaction. The metalorganic molecules were deposited both on a single foil of graphene, grown on the Ir(111) surface (FePc/GR), and on an alumina ultra-thin film, grown on the Ni3Al(111) surface (FePc/alumina). In both cases, we exploited CO adsorption to probe the molecular active sites. On the FePc/GR layer, IR-Vis SFG evidenced unexpected CO stretching modes in 1-10 mbar CO at 300 K. We ascribe the observed vibrational features to the production of long-lived molecular excitons (induced by the visible radiation). The long lifetime of these excitons and their efficient production through singlet-fission mechanisms represent intriguing findings for innovative organic devices for solar energy conversion. We also investigated the interaction of the same system with gas-phase CO2 We found that oxidation of the underlying graphene support yields the control of the charge transfer to the active sites, thus reducing the threshold pressure for CO2 adsorption and activation at 300 K by at least two orders of magnitude. As CO2 catalytic conversion is hindered by its low reactivity, enhancing its adsorption to metal sites is crucial in the framework of the efficient conversion of this waste gas to valuable chemicals. A practical route to alter the mesoscopic properties of the single metal atom centers has been found, and in parallel we proved a novel graphene oxidation route employing molecular oxygen at near ambient pressure. Concerning instead the FePc/alumina film, we demonstrated that decoration by Cu nanoclusters tunes the surface potential energy, inducing a different symmetry in the molecular overlayer lattice, scarcely affecting the reactivity of the metallic sites, as proved by the vibrational modes of adsorbed CO molecules. Thus, we succeeded in tailoring the motif of a self-assembled metallorganic layer while preserving its active sites properties.
Xu, Chunbao. "Continuous and batch hydrothermal synthesis of metal oxide nanoparticles and metal oxide-activated carbon nanocomposites." Diss., Available online, Georgia Institute of Technology, 2006, 2006. http://etd.gatech.edu/theses/available/etd-07302006-231517/.
Повний текст джерелаTeja, Amyn, Committee Chair ; Kohl, Paul, Committee Member ; Liu, Meilin, Committee Member ; Nair,Sankar, Committee Member ; Rousseau, Ronald, Committee Member.
Verna, Frédérique. "Etude de l'interaction metal-compose sulfure en catalyse d'hydrogenation." Paris 6, 1988. http://www.theses.fr/1988PA066584.
Повний текст джерелаPrice, Robert. "Metal/metal oxide co-impregnated lanthanum strontium calcium titanate anodes for solid oxide fuel cells." Thesis, University of St Andrews, 2018. http://hdl.handle.net/10023/16018.
Повний текст джерелаAnderson, J. B. F. "Strong metal-support interactions in titania-supported metal catalysts." Thesis, University of Reading, 1986. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.372539.
Повний текст джерелаZheng, Zhanfeng. "Synthesis and modifications of metal oxide nanostructures and their applications." Thesis, Queensland University of Technology, 2009. https://eprints.qut.edu.au/31728/1/Zhanfeng_Zheng_Thesis.pdf.
Повний текст джерелаBoudouvas, Denis. "Effet du potassium sur un catalyseur composite Fe-Co-C en synthèse d'hydrocarbures." Grenoble INPG, 1989. http://www.theses.fr/1989INPG0092.
Повний текст джерелаWatts, Andrew M. "Polysiloxane supported metal catalysts." Thesis, University of Bath, 1986. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.370993.
Повний текст джерелаHickel, Probst Sonia Maria. "Propriétés catalytiques et caractérisation de catalyseurs au nickel déposé sur oxydes de terre rare : influence de l'intéraction métal-support." Poitiers, 1989. http://www.theses.fr/1989POIT2296.
Повний текст джерелаVenable, Margaret Hamm. "Syntheses, structures and support interactions of potential metal oxide catalyst precursors." Thesis, Georgia Institute of Technology, 1990. http://hdl.handle.net/1853/26940.
Повний текст джерелаBrown, Ronald. "A study of hydrocarbon reactions over supported metal catalysts : support and metal dependence." Thesis, University of Edinburgh, 1990. http://hdl.handle.net/1842/13013.
Повний текст джерелаHavil, Patrick. "Influence du vieillissement thermique sur les proprietes physico-chimiques et la reactivite des catalyseurs mono et bimetalliques a base de platine et/ou rhodium sur alumine ou sur cerine." Paris 6, 1988. http://www.theses.fr/1988PA066291.
Повний текст джерелаDerule, Hervé. "Influence du degré d'oxydation du métal sur la sélectivité des catalyseurs de synthèse Fischer-tropsch." Poitiers, 1989. http://www.theses.fr/1989POIT2268.
Повний текст джерелаKababji, Ala'a Hamed. "Effects of Diluent Addition and Metal Support Interactions in Heterogeneous Catalysis: SiC/VPO Catalysts for Maleic Anhydride Production and Co/Silica Supported Catalysts for FTS." Scholar Commons, 2009. https://scholarcommons.usf.edu/etd/2035.
Повний текст джерелаMessi, C. "Nanostructured catalytic metal oxides supported over oxide supports of various nature : the iron oxide system." Doctoral thesis, Università degli Studi di Milano, 2008. http://hdl.handle.net/2434/57081.
Повний текст джерелаBrimacombe, Lyn M. "Activation of methane on supported metal catalysts." Thesis, University of Ottawa (Canada), 1991. http://hdl.handle.net/10393/7805.
Повний текст джерелаNamijo, S. N. "Carbon dioxide hydrogenation over supported metal catalysts." Thesis, Brunel University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.379411.
Повний текст джерелаKennedy, David Rankin. "Hydrogenation of acetylenes over supported metal catalysts." Thesis, University of Glasgow, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.340756.
Повний текст джерелаMcLeod, Alistair Scott. "Monte Carlo studies of supported metal catalysts." Thesis, University of Cambridge, 1998. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.624870.
Повний текст джерелаBriquet, L. G. V. "Modelling active sites of supported metal catalysts." Thesis, University College London (University of London), 2010. http://discovery.ucl.ac.uk/19286/.
Повний текст джерелаAlvaro, Vasco Filipe Domingues. "Selective catalytic activity of metals supported on metal(IV) phosphates for heterogeneous reduction." Thesis, University of Liverpool, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.263780.
Повний текст джерелаPoupart, Romain. "Nanoparticules métalliques@polymères poreux : matériaux hybrides innovants pour la catalyse supportée." Thesis, Paris Est, 2017. http://www.theses.fr/2017PESC1174/document.
Повний текст джерелаPorous materials based on polymers have been the subject of intense and various researches since their discovery until now. Their unique and remarkable properties, like their easy functionalization or their large porosity range reachable for instance, coupled with their low production cost makes them attractive for numerous applications. Among them, supported catalysis is booming, especially since the rising of nanoparticles. During this Ph.D. contribution, we have developed different polymeric materials, which could be used as support, focusing mainly onto three types: bulky materials, porous polymeric matrixes into capillaries and porous polystyrene arising from the selective degradation of diblocks copolymers.Firstly, different strategies have been employed for the immobilization and the generation of nanoparticles onto bulk materials. On the one hand, the synthesis of a monomer, bearing a disulphide bridge which can, after a reduction step, free a thiol moiety allowing us to anchor gold nanoparticles. On the other hand, a new route to reduce nanoparticle has been employed using gaseous hydrogen. In another part, the syntheses of different polymeric matrixes into capillaries have been made. First, we used an already known matrix, based on N-acryloxysuccinimide -after modification step via thiol-ene reaction and nucleophilic substitution by amines- to anchor copper or gold nanoparticles, respectively. Also, a new matrix based on cyclic carbonates has been used, after modification, to immobilized platinum nanoparticles. Finally, starting from diblocks copolymers possessing different junctions between both blocks (disulphide bridge or acetal), porous polystyrenes have been obtained. The copolymers bearing an acetal have been implemented to immobilized gold nanoparticles, catalysing several reactions like nitro reduction, boronic homocoupling as well as the cascade reaction of both
Roberts, Mark Stephen. "Catalysis by semiconductor supported metal clusters." Thesis, University of Hull, 1987. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.327805.
Повний текст джерелаSwaminathan, Sneha. "Metal Oxide Nanofibers as Filters, Catalyst and Catalyst Support Structures." University of Akron / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=akron1279564885.
Повний текст джерелаCairns, Graham R. "Hydrogenation catalysts from supported palladium complexes." Thesis, University of Glasgow, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.360177.
Повний текст джерелаAbdoullah, Mohamad. "Supported transition metal oxides as solid base catalysts." Thesis, University of Huddersfield, 2016. http://eprints.hud.ac.uk/id/eprint/28325/.
Повний текст джерелаChambers, Nick. "Asymmetric heterogeneous reduction over modified supported metal catalysts." Thesis, Keele University, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.323719.
Повний текст джерелаTsui, Li-Hsin. "Supported metal catalysts for water-gas shift conversion." Master's thesis, University of Cape Town, 2014. http://hdl.handle.net/11427/13384.
Повний текст джерелаThe interests in an alternative, sustainable power generation method has greatly increased in the past decade due to increases in greenhouse gases and its impact on global climate change. The use of fuel cells as a form of energy generation is extremely promising as it converts chemical potential energy directly to electrical energy, bypassing the Carnot cycle limitations. Various types of fuel cells have been developed, with the proton exchange membrane fuel cell (PEMFC) being most promising for mobile and small-scale stationary uses under transient conditions. The PEMFC uses hydrogen and oxygen to generate electrical energy. While oxygen can be obtained from air, hydrogen does not exist in its elemental form; hence a process train is required to refine fuels (such as fossil fuels and bio-fuels) into pure hydrogen. This has been successfully achieved by large-scale industrial plants. A typical fuel processing train consists of a steam reforming stage converting the fuel into syngas. This is followed by a water-gas shift (WGS) stage to convert carbon monoxide, which is a poison for the platinum catalysts within fuel cells, into carbon dioxide. If the CO concentration required is extremely low, a methanation or preferential oxidation stage can be used subsequent to the WGS stage. This study focuses on the water-gas shift stage of the fuel processing train. Industrial base metal WGS catalysts are not suitable for a miniaturized fuel processing train due to the catalysts being developed for continuous operations, as miniaturized fuel processing trains are expected to operate at transient conditions. A slow and controlled reduction process is also required prior to operation, as well as the pyrophoricity of industrial catalysts after reduction. These can pose safety issues with non-technical personnel in household applications (e.g. CHP). PGM-based catalysts have shown high activities for the water-gas shift reaction in literature, are not pyrophoric and do not require lengthy and sensitive reduction processes prior to operation. The objective of this study was to investigate and compare two base metal catalysts (high temperature (HT) shift Fe₃O₄/Cr₂O₃ and low temperature (LT) shift CuO/ZnO/Al₂O₃ catalyst) with a PGM based counterpart, as well as to investigate whether the catalysts are able to achieve a required 1 vol% CO via the water-gas shift reaction. For these investigations a synthetic feedstock was used, based on typical exit concentrations of a steam methane reformer.
Pellegrini-Bonneau, Laurence. "Vaporeformage d'hydrocarbures lourds en présence de composés soufres." Poitiers, 1988. http://www.theses.fr/1988POIT2318.
Повний текст джерелаGogolieva, Ganna. "Catalyseurs greffés sur support et libérés sous stimulus externe." Phd thesis, Toulouse, INPT, 2014. http://oatao.univ-toulouse.fr/11916/1/gogolieva.pdf.
Повний текст джерелаHuang, Wei. "Selective hydrogenation on zeolite-supported bimetallic catalysts." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file 0.90 Mb., p. 76, 2005. http://proquest.umi.com/pqdlink?did=1037889271&Fmt=7&clientId=8331&RQT=309&VName=PQD.
Повний текст джерелаHuang, Wei. "Selective hydrogenation of acetylene on zeolite-supported bimetallic catalysts." Access to citation, abstract and download form provided by ProQuest Information and Learning Company; downloadable PDF file, 173 p, 2008. http://proquest.umi.com/pqdweb?did=1459913421&sid=16&Fmt=2&clientId=8331&RQT=309&VName=PQD.
Повний текст джерелаBrandmair, Maria. "Autothermal reforming of n-hexane over supported metal catalysts." [S.l.] : [s.n.], 2005. http://deposit.ddb.de/cgi-bin/dokserv?idn=978997700.
Повний текст джерелаKeegan, Michael Bernard Thomas. "Supported metal catalysts : some aspects of characterisation and function." Thesis, University of Hull, 1991. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.384806.
Повний текст джерелаWells, Peter Philip. "Controlled surface modification of supported platinum group metal catalysts." Thesis, University of Southampton, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.438652.
Повний текст джерелаHayward, James. "Supported metal catalysts for the production of chemical precursors." Thesis, Cardiff University, 2013. http://orca.cf.ac.uk/53589/.
Повний текст джерелаSewell, Gary Stanton. "The reductive animation of ethanol using supported metal catalysts." Doctoral thesis, University of Cape Town, 1996. http://hdl.handle.net/11427/18294.
Повний текст джерелаSilica supported cobalt, nickel and copper are efficient catalysts for the reductive amination of ethanol using ammonia. High selectivity to ethylamine product was obtained between reaction temperatures of 140 and 200°C, between ammonia to ethanol molar ratios ranging from 1 to 4 and between hydrogen to ethanol molar ratios ranging from 2 to 5. Depending on the partial pressures of the ethanol, ammonia and hydrogen feeds, different ethylamine selectivities were obtained. The degree of amine substitution was decreased (i.e. increasing MEA and decreasing DEA and TEA selectivities) by increasing the ammonia partial pressure or by decreasing either the ethanol or hydrogen partial pressures.
Reynhardt, Jan Petrus Karel. "Carbonylation catalysts based on metal complexed PAMAM-dendrimers supported on mesoporous and periodic mesoporous silica supports." Thesis, University of Ottawa (Canada), 2005. http://hdl.handle.net/10393/29253.
Повний текст джерелаZhao, Yanyan. "Dinuclear Heterogeneous Catalysts on Metal Oxide Supports:." Thesis, Boston College, 2020. http://hdl.handle.net/2345/bc-ir:109003.
Повний текст джерелаAtomically dispersed catalysts refer to substrate-supported heterogeneous catalysts featuring one or a few active metal atoms that are separated from one another. They represent an important class of materials ranging from single atom catalysts (SACs) and nanoparticles (NPs). The study of SACs has brought an attention of understanding the reaction mechanism at the molecular level. SACs is a promising field, however, there are still many challenges and opportunities in developing the next generation of catalysts. Catalysts featuring two atoms with well-defined structures as active sites are poorly studied. It is expected that this class of catalysts will show uniqueness in activity, selectivity, and stability. However, the difficulty in synthesizing such structures has been a critical challenge. I tackled this challenge by using a facile photochemical method to generate active metal centers consisting of two iridium metal atoms bridged by O ligands and bound to a support by stripping the ligands of the organometallic complex. My research also unveiled the structure of this dinuclear heterogeneous catalysts (DHCs) by integrating various characterization resources. Direct evidence unambiguously supporting the dinuclear nature of catalysts anchored on metal oxides is obtained by aberration-corrected scanning transmission electron microscopy. In addition, different binding modes have been achieved on two categories of metal oxides with distinguishable surface oxygen densities and interatomic distances of binding sites. Side-on bound DHCs was demonstrated on iron oxide and ceria where both Ir atoms are affixed to the surface with similar coordination environment. The binding sites on the OH-terminated surface of Fe2O3 and CeO2 anchor the catalysts to provide outstanding stability against detachment, diffusion and aggregation. The competing end-on binding mode, where only one Ir atom is attached to the substrate and the other one is dangling was observed on WO3. Evidence supporting the binding modes was obtained by in situ diffuse reflectance infrared Fourier transform spectroscopy. In addition, the synergistic effect between two adjacent Ir atoms and the uniqueness of different coordinative oxygen atoms around Ir atoms were investigated by a series of operando spectroscopy such as X-ray absorption spectroscopy and microscopy at atomic level under the reaction condition. The resulting catalysts exhibit high activities and stabilities toward H2O photo-oxidation and preferential CO oxidation. Density functional theory calculations provide additional support for atomic structure, binding sites modes on metal oxides, as well as insights into how DHCs may be beneficial for these catalytic reactions. This research has important implications for future studies of highly effective heterogeneous catalysts for complex chemical reactions
Thesis (PhD) — Boston College, 2020
Submitted to: Boston College. Graduate School of Arts and Sciences
Discipline: Chemistry
Castro, Cevallos Ursula Isabel. "Phenol oxidation catalysed by polymer-supported metal complexes." Doctoral thesis, Universitat Rovira i Virgili, 2009. http://hdl.handle.net/10803/8577.
Повний текст джерелаEntre los tratamiento de efluentes industriales con alto contenido de material orgánico, se encuentran los procesos de oxidación avanzada (AOPs) que desarrollan tecnologías como la oxidación húmedo catalítica con peroxido de hidrógeno de compuestos orgánicos (CWPO). El mejoramiento de éste proceso está basado en la variación tanto del catalizador como de la fuente oxidante. El presente trabajo de investigación propone aprovechar la actividad catalítica de catalizadores homogéneos, evitando la contaminación por metal del efluente mediante la heterogeneización de iones de Cu(II) sobre matrices poliméricas, para luego ser usados como catalizadores en la CWPO del fenol. Del grupo de catalizadores sintetizados, se identificaron dos catalizadores: Cu(II) adsorbido sobre poly(4-vinylpyridine) con 2% de entrecruzamiento y Cu(II) soportado en poli (DVB-co-VBC) funcionalizado con ácido aminodiacetico. Ambos catalizadores demostraron alta actividad catalítica sin liberación de Cu(II), concluyendo que la heterogeneización de catalizadores homogéneos para la CWPO es una decisión acertada cuando se desea promover la degradación del fenol.
Niemelä, Marita. "Reactions of synthesis gas on silica supported transition metal catalysts /." Espoo : Technical Research Centre of Finland, 1997. http://www.vtt.fi/inf/pdf/publications/1997/P310.pdf.
Повний текст джерелаGeorgiades, G. C. "A study of cyclohexene reactions on supported characterised metal catalysts." Thesis, Brunel University, 1988. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.233346.
Повний текст джерелаRollins, K. "The preparation and characterisation of supported metal chloride oxychlorination catalysts." Thesis, Brunel University, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.370138.
Повний текст джерелаHermans, S. "Mixed-metal clusters as precursors for bimetallic supported nanoparticle catalysts." Thesis, University of Cambridge, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.603977.
Повний текст джерелаKennedy, Mark James. "Catalytic combustion of benzene vapour using carbon supported metal catalysts." Thesis, University of Newcastle Upon Tyne, 2007. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.436172.
Повний текст джерела