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dc.contributor.advisorDalai, Ajay K.en_US
dc.creatorAkande, Abayomi Johnen_US
dc.date.accessioned2005-03-09T21:51:27Zen_US
dc.date.accessioned2013-01-04T04:26:20Z
dc.date.available2005-03-11T08:00:00Zen_US
dc.date.available2013-01-04T04:26:20Z
dc.date.created2005-02en_US
dc.date.issued2005-02-25en_US
dc.date.submittedFebruary 2005en_US
dc.identifier.urihttp://hdl.handle.net/10388/etd-03092005-215127en_US
dc.description.abstractThe purpose of this work was to design and to develop a high performance catalyst for the production of hydrogen from reforming of crude ethanol and also, to develop the kinetics and reactor model of crude ethanol reforming process. Crude ethanol reforming is an endothermic reaction of ethanol and other oxygenated hydrocarbons such as (lactic acid, glycerol and maltose) with water present in fermentation broth to produce hydrogen (H2) and carbon dioxide (CO2). Ni/Al2O3 catalysts were prepared using different preparation methods such as coprecipitation, precipitation and impregnation methods with different Ni loadings of 10 – 25 wt.%, 10-20 wt.%, and 10-20 wt.% respectively.All catalysts were characterised by thermogravimetric/differential scanning calorimetry (TG/DSC), X-ray diffraction (XRD), (including X-ray line broadening), temperature programmed reduction (TPR), BET surface area measurements, pore volume and pore size distribution analysis. TG/DSC analyses for the uncalcined catalysts showed the catalyst were stable up from 600oC. XRD analyses showed the presence of NiO, NiAl2O4 and Al2O3 species on the calcined catalysts whereas Ni, NiAl2O4, and Al2O3 were present on reduced catalysts. BET surface area decreased and average pore diameter reached a maximum and then decreased as the Ni loading increased. The temperature programmed reduction profiles showed peaks corresponding to the reduction of NiO between 400-600oC and reduction of NiAl2O4 between 700-800oC. Catalyst screening was performed in a micro reactor with calcination temperature, reaction temperature and the ratio of catalyst weight to crude ethanol flow rate (W/Fcrude-C2H5OH) of 600 oC, 400oC and 0.59 h respectively. Maximum crude-ethanol conversion of 85 mol% was observed for catalyst with 15wt% Ni loading prepared by precipitation method (PT15), while maximum hydrogen yield (= 4.33 moles H2 / mol crude-ethanol feed) was observed for catalyst with 15wt% Ni loading prepared by coprecipitation (CP15). Performance tests were carried out on (CP15) in which variables such as space velocity (WHSV) 1.68h-1to 4.68h-1, reduction temperature 400 to 600oC and reaction temperature 320 to 520 oC, were changed for optimum performance evaluation of the selected catalyst. The catalyst deactivated over first three hours of 11 hours time-on-stream (TOS) before it stabilized, the reaction conditions resulted in a drop of ethanol conversion from 80 to 70mol%.The compounds identified in the liqiud products in all cases were ethanoic acid, butanoic acid, butanal, propanone, propanoic acid, propylene glycol and butanedioic acid. The kinetic analysis was carried out for the rate data obtained for the reforming of crude ethanol reaction that produced only hydrogen and carbon dioxide. These data were fitted to the power law model and Eldey Rideal models for the entire temperature range of 320-520 oC. The activation energy found were 4405 and 4428 kJ/kmol respectively. Also the simulation of reactor model showed that irrespective of the operating temperature, the benefit of an increase in reactor length is limited. It also showed that by neglecting the axial dispersion term in the model the crude ethanol conversion is under predicted. In addition the beneficial effects of W/FAO start to diminish as its value increases (i.e. at lower flow rates).en_US
dc.language.isoen_USen_US
dc.subjectNickel alumina catalysten_US
dc.subjectCrude ethanolen_US
dc.subjectReformingen_US
dc.titleProduction of hydrogen by reforming of crude ethanolen_US
thesis.degree.departmentChemical Engineeringen_US
thesis.degree.disciplineChemical Engineeringen_US
thesis.degree.grantorUniversity of Saskatchewanen_US
thesis.degree.levelMastersen_US
thesis.degree.nameMaster of Science (M.Sc.)en_US
dc.type.materialtexten_US
dc.type.genreThesisen_US
dc.contributor.committeeMemberIdem, Raphaelen_US
dc.contributor.committeeMemberHill, Gordon A.en_US
dc.contributor.committeeMemberFoley, Stephen R.en_US
dc.contributor.committeeMemberBakhshi, Narendra N.en_US


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