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dc.contributor.authorNjagi, Eric C. a
dc.contributor.authorGenuino, Homer C. a
dc.contributor.authorKuo, Chung-Hao a
dc.contributor.authorDharmarathna, Saminda a
dc.contributor.authorSteven, AntonGudza
dc.contributor.authorSuib, L. a,b
dc.date.accessioned2020-10-30T05:11:00Z
dc.date.available2020-10-30T05:11:00Z
dc.date.issued2015-01
dc.identifier.citationJournal of Environment sustainability Advancement Research Vol. 202, 15, pages 68-72en_US
dc.identifier.urihttps://doi.org/10.1016/j.micromeso.2014.09.044
dc.identifier.urihttp://repository.chuka.ac.ke/handle/chuka/4911
dc.description.abstractMesoporous sulfated-metal oxides and mixed-metal oxides prepared by a facile coprecipitation method employing titanium oxysulfate–sulfuric acid complex as a precursor of both titanium and sulfate are highly active and selective for direct methanolysis of carbohydrates to methyl levulinate. The most active sulfated TiO2–ZrO2 catalyst selectively converted fructose to methyl levulinate with a remarkably high yield (71%) after 1 h at 200 °C. Significant amounts of methyl levulinate were also obtained from sucrose (54%) and glucose (23%) after 1 h at 200 °C. The used catalyst was easily recovered and recycled without any loss of selectivity although activity decreased due to humin deposition on the surface. The spent catalysts were easily rejuvenated through calcination in air. The formation of ethers during dehydration was negligible suggesting that methanol can be recycled after distillation.en_US
dc.language.isoenen_US
dc.titleSelective conversion of fructose to methyl levulinate using sulphateden_US
dc.typeArticleen_US


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