Please use this identifier to cite or link to this item: https://repository.unej.ac.id/xmlui/handle/123456789/76845
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dc.contributor.authorRasrendra, Carolus B.-
dc.contributor.authorFachri, Boy Arief-
dc.contributor.authorMakertihartha, I. Gusti B. N.-
dc.contributor.authorAdisasmito, Sanggono-
dc.contributor.authorHeeres, Hero J.-
dc.date.accessioned2016-08-31T05:43:07Z-
dc.date.available2016-08-31T05:43:07Z-
dc.date.issued2016-08-31-
dc.identifier.issn1864-5631; e-ISSN : 1864-564X-
dc.identifier.urihttp://repository.unej.ac.id/handle/123456789/76845-
dc.description.abstractWe herein present a study on the application of homogeneous catalysts in the form of metal salts on the conversion of trioses, such as dihydroxyacetone (DHA), and glyceraldehyde (GLY) to lactic acid (LA) in water. A wide range of metal salts (26 in total) were examined. Al salts were identified as the most promising and essentially quantitative LA yields (>90 mol%) were obtained at 1408C and a reaction time of 90 min. A reaction pathway is proposed and a kinetic model using the power law approach was developed for the conversion of DHA to LA with pyruvaldehyde (PRV) as the intermediate. Good agreement between experimental data and the model was obtained. Model predictions, supported by experiments, indicate that a high yield of LA is favoured in dilute solutions of DHA (0.1 m) at elevated temperatures (180 8C) and reaction times less than 10 min.en_US
dc.language.isoenen_US
dc.subjectDihydroxyacetoneen_US
dc.subjectLactic Aciden_US
dc.subjectMetal Salts in Wateren_US
dc.titleCatalytic Conversion of Dihydroxyacetone to Lactic Acid Using Metal Salts in Wateren_US
dc.typeArticleen_US
Appears in Collections:LSP-Jurnal Ilmiah Dosen

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