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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/123576
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dc.contributor.authorRatti, Regiane-
dc.contributor.authorBotta, Livea-
dc.contributor.authorMaintinguer, Sandra Imaculada-
dc.contributor.authorLazaro, Carolina Zampol-
dc.contributor.authorVaresche, Maria Bernadete Amâncio-
dc.date.accessioned2015-05-15T13:30:26Z-
dc.date.accessioned2016-10-25T20:48:44Z-
dc.date.available2015-05-15T13:30:26Z-
dc.date.available2016-10-25T20:48:44Z-
dc.date.issued2011-
dc.identifierhttp://www.periodicos.rc.biblioteca.unesp.br/index.php/holos/article/view/4893-
dc.identifier.citationHOLOS Environment, v. 11, n. 1, p. 22-22, 2011.-
dc.identifier.issn1519-8634-
dc.identifier.urihttp://hdl.handle.net/11449/123576-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/123576-
dc.description.abstractHydrogen is known as a clean energy resource. The biological production of hydrogen has been attracting attention as an environmentally friendly processs that does not consume fossil fuels. Cellulosic plant and waste materials are potential resources for fermentative hydrogen production. Cellulose is a linear biopolymer of glucose molecules, connected by β-1,4-glycosidic bonds. Enzymatic hydrolysis of cellulose requires the presence of cellulase. The present study aimed to investigate the efficiency of acid pretreatment on ruminal fluid in order to enrich H2 producing bacteria consortia to enhance biohydrogen rate and substrate removal efficiency. In this study, fermentative hydrogen producers were enriched on cellulose (2g/L) in a modificated Del Nery medium (DNM) at 37ºC and initial pH 7.0 using rumen fluid (10% v/v) as inoculum. To increase the hydrogen production it was added cellulose (10mL) to the medium. The gas products (mainly H2 and CO2) was analyzed by gas chromatography (Shimadzu GC 2010) using a thermal conductivity detector. The volatile fatty acids and ethanol were also detected by GC using a flame ionization detector. Cellulose degradation was quantified by using the phenolsulfuric acid method. Analysis showed that the biogas produced from the anaerobic fermentation contained only hydrogen and carbon dioxide, without detectable methane after acid pretreatment test. On DNM the hydrogen production started with 4 h (5,3 x 105 mmol H2/L) of incubation, and the maximum H2 concentration was observed with 34 h (7,1 x 106 mmol H2/L) of incubation. During the process, it was observed a predominance of acetic acid and butyric acid as well as a low production of acetone, ethanol and nbutanol in all experimental phases. Butyrate accounted for more than 77% of total. As a result of the accumulation of volatile fatty acids (VFAs), the pH value in anaerobic digestion system was reduced to 4,0. On microscopy analyses there were observed rods with endospores. The batch anaerobic fermentation assays performed on anaerobic mixed inoculum from rumen fluid demonstrated the feasibility of H2 generation utilizing cellulose as substrate. Based on the results, it can be concluded that the acid treatment was efficient to inhibit the methanogenic archaea cells present in rumen fluid. The rumen fluid cells present a potential route in converting renewable biomass such as cellulose into hydrogen energy.en
dc.format.extent22-22-
dc.language.isoeng-
dc.sourceCurrículo Lattes-
dc.subjectcellulaseen
dc.subjectanaerobic bacteriaen
dc.subjectacid treatmenten
dc.titleBioconversion of Cellulose to Hydrogen by dark fermentationen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.description.affiliationUnespUniversidade Estadual Paulista Júlio de Mesquita Filho, Instituto de Química de Araraquara, Araraquara, Rua Prof. Francisco Degni nº 55, Quitandinha, CEP 14800900, SP, Brasil-
dc.rights.accessRightsAcesso aberto-
dc.identifier.fileISSN1519-8634-2011-11-01-22-22.pdf-
dc.relation.ispartofHOLOS Environment-
dc.identifier.lattes2967035823175406-
dc.identifier.lattes2291054769194665-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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