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DC Field | Value | Language |
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dc.contributor.author | Eterigho, E. J. | - |
dc.contributor.author | Lee, J. G. M. | - |
dc.contributor.author | Harvey, A. P. | - |
dc.date.accessioned | 2022-12-29T08:19:35Z | - |
dc.date.available | 2022-12-29T08:19:35Z | - |
dc.date.issued | 2011-02-08 | - |
dc.identifier.citation | doi:10.1016/j.biortech.2011.02.040 | en_US |
dc.identifier.uri | www.elsevier.com/locate/biortech | - |
dc.identifier.uri | http://repository.futminna.edu.ng:8080/jspui/handle/123456789/16240 | - |
dc.description | Elsevier publication | en_US |
dc.description.abstract | In this study, sulphated zirconia was directly synthesised and compared to the conventional wet method of preparation. The surface areas and pore sizes were 169 m2/g, 0.61 lm (directly synthesized) and 65 m2/g, 0.24 lm (conventional method), respectively. Directly synthesized sulphated zirconia was amorphous, whereas conventionally prepared sulphated zirconia is polycrystalline. Their IR spectra were broadly similar, although the area of the 1250 to 950 cm1 band was larger for directly synthesised sulphated zirconia. Not only were conversions greater for directly synthesised sulphated zirconia (63% vs. 42% after 4 h), but it exhibited significantly greater yield for fatty acid methyl esters. The percentage yield (after 1 h) of methyl esters was 43% for the directly synthesised catalyst and 15% for the conventionally synthesised. | en_US |
dc.description.sponsorship | Self | en_US |
dc.language.iso | en | en_US |
dc.publisher | Bioresource Technology Journal | en_US |
dc.relation.ispartofseries | Vol. 102;No 10 | - |
dc.subject | Catalyst preparation Sulphated zirconia Thermocatalytic cracking Biodiesel | en_US |
dc.title | Triglyceride cracking for biofuel production using a directly synthesised sulphated zirconia catalyst | en_US |
dc.type | Article | en_US |
Appears in Collections: | Chemical Engineering |
Files in This Item:
File | Description | Size | Format | |
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BIORESOURCES JORNAL.pdf | 200.33 kB | Adobe PDF | View/Open |
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