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Reactive membrane extraction in biorefineries

dc.contributor.authorGrzenia, David Lukas, author
dc.contributor.authorWickramasinghe, Sumith Ranil, advisor
dc.contributor.authorKipper, Matthew J., committee member
dc.contributor.authorSmith, T. Gordon, committee member
dc.contributor.authorQian, Xianghong, committee member
dc.contributor.authorSchell, Daniel, committee member
dc.date.accessioned2007-01-03T05:15:57Z
dc.date.available2007-01-03T05:15:57Z
dc.date.issued2011
dc.description.abstractSeparations account for 60-80% of the processing costs of most mature chemical processes. Membrane based separations offer several advantages over conventional technology such as lower energy costs and easy scale up. Here we focus on membrane extraction for removal of acetic acid, sulfuric acid, furfural, HMF and other toxic compounds from biomass hydrolysates. As membrane extraction is non-dispersive it overcomes the disadvantages of conventional extraction. Experiments have been conducted using dilute sulfuric acid pretreated corn stover (hydrolysate). Acetic acid, in its protonated form, is extracted into an organic phase consisting of octanol/oleyl alcohol and Alamine 336, a tertiary amine, containing aliphatic chains of 8-10 carbon atoms. Co-extraction of sulfuric acid leads to an increase in hydrolyste pH. The effect of aqueous and organic phase flow rates and temperature, on the rate of extraction of acetic acid and sulfuric acid has been investigated. Changes in the rates of acetic and sulfuric acid extraction may be explained by considering the structure of the complexes formed in the organic phase. We conducted computational modeling to elucidate the extraction process of Alamine 336 in different solvents. Extraction of carboxylic acids, Furfural and HMF in water and octanol was simulated using the Gaussian 03 package. In the past the extraction process has been explained by the direct interaction of the carboxylic acid with the Alamine 336 to form an ion pair. More carboxylic acids could be extracted through hydrogen bonding forming a dimer or trimer complex form with the Alamine 336, stabilized by the organic solvent. Hydrolysates treated by membrane extraction and conventional conditioning technologies were fermented using a glucose-xylose fermenting bacteria to determine the viability of membrane technology to detoxify biomass hydrolysates. Membrane extraction could be a viable hydrolysate detoxification technology because the other conditioning technologies do not remove acetic acid.
dc.format.mediumborn digital
dc.format.mediumdoctoral dissertations
dc.identifierGrzenia_colostate_0053A_10437.pdf
dc.identifier.urihttp://hdl.handle.net/10217/47390
dc.languageEnglish
dc.language.isoeng
dc.publisherColorado State University. Libraries
dc.relation.ispartof2000-2019
dc.rightsCopyright and other restrictions may apply. User is responsible for compliance with all applicable laws. For information about copyright law, please see https://libguides.colostate.edu/copyright.
dc.subjectbio-ethanol
dc.subjectrenewable energy
dc.subjectreactive membranes
dc.subjectbiomass
dc.titleReactive membrane extraction in biorefineries
dc.typeText
dcterms.rights.dplaThis Item is protected by copyright and/or related rights (https://rightsstatements.org/vocab/InC/1.0/). You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).
thesis.degree.disciplineChemical and Biological Engineering
thesis.degree.grantorColorado State University
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy (Ph.D.)

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