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dc.contributor.authorSavva, Petros G.en
dc.contributor.authorPolychronopoulou, Kyriakien
dc.contributor.authorRyzkov, V. A.en
dc.contributor.authorEfstathiou, Angelos M.en
dc.creatorSavva, Petros G.en
dc.creatorPolychronopoulou, Kyriakien
dc.creatorRyzkov, V. A.en
dc.creatorEfstathiou, Angelos M.en
dc.date.accessioned2019-11-21T06:22:44Z
dc.date.available2019-11-21T06:22:44Z
dc.date.issued2010
dc.identifier.urihttp://gnosis.library.ucy.ac.cy/handle/7/56112
dc.description.abstractThe present work reports on the production of H2 and secondary carbon nanotubes (CNTs) during catalytic decomposition of ethylene over a novel catalytic system, namely, nickel supported on carbon nanotubes (Ni/CNTs) at remarkably low-temperatures, e.g. 400 °C. A number of catalyst parameters were investigated, namely the chemical nature of support, the Ni metal loading (0.1-10 wt%), the nature of nickel metal precursor (organometallic vs. inorganic) used during catalyst synthesis, and the nature of transition metal used (e.g. Co, Fe, Cu, Ni). Among the different Ni/CNT supported catalysts investigated, 0.5 wt% Ni/Ros1-B1 (Ros1-B1 a commercial CNT) presented the highest activity in terms of H2 production (296 mol H2/gNi) and carbon capacity (3552 gC/gNi). In terms of transition metal used as active catalytic phase, the activity (moles H2 per gram of metal) was found to decrease in the order Co ≫ Fe > Cu. The activity of supported Ni and Co catalysts was found to strongly depend on the metal loading. The structural and morphological features of primary (catalytic support) and secondary carbon nanotubes produced during ethylene decomposition at 400 °C were studied using X-ray Diffraction (XRD), scanning electron microscopy (SEM), High-resolution Transmission Electron Microscopy (HRTEM), and X-ray Photoelectron Spectroscopy (XPS). The production of secondary carbon nanotubes at 400 °C was confirmed after using HRTEM and after a comparison with the primary carbon nanotubes of catalyst support was made. Different regeneration conditions (use of oxygen or steam) were investigated in order to remove by gasification the amorphous carbon deposited under reaction conditions. Oxygen appeared to be a better regeneration reagent than steam, where after ten consecutive reaction/regeneration cycles the 0.5 wt% Ni/Ros1-B1 catalyst showed high and stable activity with time on stream. © 2009 Elsevier B.V. All rights reserved.en
dc.sourceApplied Catalysis B: Environmentalen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-72649097019&doi=10.1016%2fj.apcatb.2009.10.005&partnerID=40&md5=ed50f3c305800de4cf6c60c5f523141e
dc.subjectCarbon nanotubesen
dc.subjectOxygenen
dc.subjectLow temperaturesen
dc.subjectX ray diffractionen
dc.subjectX ray photoelectron spectroscopyen
dc.subjectNickelen
dc.subjectXPSen
dc.subjectHigh resolution transmission electron microscopyen
dc.subjectTransition metalsen
dc.subjectAmorphous carbonen
dc.subjectScanning electron microscopyen
dc.subjectSEMen
dc.subjectNickel alloysen
dc.subjectEthyleneen
dc.subjectCatalysisen
dc.subjectCatalytic supportsen
dc.subjectOrganometallicsen
dc.subjectCatalyst supportsen
dc.subjectH2 productionen
dc.subjectCatalyst regenerationen
dc.subjectHRTEMen
dc.subjectCatalytic systemen
dc.subjectChemical natureen
dc.subjectTime on streamsen
dc.subjectReaction conditionsen
dc.subjectStructural metalsen
dc.subjectMetal precursoren
dc.subjectCatalyst synthesisen
dc.subjectCatalytic decompositionen
dc.subjectCo catalystsen
dc.subjectEthylene decompositionen
dc.subjectInsectivoraen
dc.subjectMetal loadingsen
dc.subjectMorphological featuresen
dc.subjectNi metalen
dc.subjectPrimary carbonen
dc.subjectStable activityen
dc.subjectSupported catalystsen
dc.titleLow-temperature catalytic decomposition of ethylene into H2 and secondary carbon nanotubes over Ni/CNTsen
dc.typeinfo:eu-repo/semantics/article
dc.identifier.doi10.1016/j.apcatb.2009.10.005
dc.description.volume93
dc.description.issue3-4
dc.description.startingpage314
dc.description.endingpage324
dc.author.faculty002 Σχολή Θετικών και Εφαρμοσμένων Επιστημών / Faculty of Pure and Applied Sciences
dc.author.departmentΤμήμα Χημείας / Department of Chemistry
dc.type.uhtypeArticleen
dc.description.notes<p>Cited By :14</p>en
dc.source.abbreviationAppl.Catal.B Environ.en
dc.contributor.orcidEfstathiou, Angelos M. [0000-0001-8393-8800]
dc.contributor.orcidPolychronopoulou, Kyriaki [0000-0002-0723-9941]
dc.contributor.orcidSavva, Petros G. [0000-0001-6390-315X]
dc.gnosis.orcid0000-0001-8393-8800
dc.gnosis.orcid0000-0002-0723-9941
dc.gnosis.orcid0000-0001-6390-315X


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