Please use this identifier to cite or link to this item: http://repository.futminna.edu.ng:8080/jspui/handle/123456789/16220
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dc.contributor.authorEterigho, E. J.-
dc.contributor.authorLee, J. G. M.-
dc.contributor.authorHarvey, A. P.-
dc.date.accessioned2022-12-29T05:12:23Z-
dc.date.available2022-12-29T05:12:23Z-
dc.date.issued2011-09-25-
dc.identifier.citation8th European Congress of Chemical Engineering Berlin, Germanyen_US
dc.identifier.urihttp://repository.futminna.edu.ng:8080/jspui/handle/123456789/16220-
dc.description.abstractConventional wet-precipitation method was used to synthesis sulphated zirconia using two different molar ratios of sulphating agents. (1) the first was using a molar ratio of 1: 45 of ZrOCI,.8H₂O impregnated with 1 M H2SO4, (wp) and (2) a molar ratio of 1: 6 was used for the modified conventional wet-precipitation method. (mwp). The properties of both catalysts were examined by various techniques: EDX, XPS, FTIR, SEM, XRDP, Py-DRIFTS and BET nitrogen adsorption techniques. The variation in the molar ratio of the sulphating agent used during preparation led to sulphated zircomas that exhibited different properties in terms of specific surface areas, acid sites, thermal stability and surface sulphate. Both catalysts were catalytically active for triglycerides cracking for fatty acid methyl esters in a thermocatalytic reaction. The SZI not only exhibited higher conversion of triglycerides but higher FAMEs yield, approximately 50% after 3 h, as compared to SZ2 (39%). Interestingly, SZ1 was selective towards unsaturated esters whereas SZ2 was towards saturated esters.en_US
dc.description.sponsorshipNewcastle University upon Tyne, UKen_US
dc.language.isoenen_US
dc.publisher8th European Congress of Chemical Engineering Berlin, Germanyen_US
dc.subjectconventional method, sulphated zirconia, saturated and unsaturated FAMEs, thermocatalytic crackingen_US
dc.titleEvaluation of Catalytic Activity of Two Forms of Synthesized Sulphated Zirconia for Triglyceride Crackingen_US
dc.typePresentationen_US
Appears in Collections:Chemical Engineering



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