Publicação: Determination of Electroactive Organic Acids in Sugarcane Vinasse by High Performance Anion-Exchange Chromatography with Pulsed Amperometric Detection Using a Nickel Nanoparticle Modified Boron-Doped Diamond
dc.contributor.author | Sedenho, Graziela C. [UNESP] | |
dc.contributor.author | Da Silva, José Luiz [UNESP] | |
dc.contributor.author | Beluomini, Maísa A. [UNESP] | |
dc.contributor.author | De Sá, Acelino C. [UNESP] | |
dc.contributor.author | Stradiotto, Nelson R. [UNESP] | |
dc.contributor.institution | Universidade Estadual Paulista (Unesp) | |
dc.contributor.institution | Universidade de São Paulo (USP) | |
dc.date.accessioned | 2018-12-11T17:11:30Z | |
dc.date.available | 2018-12-11T17:11:30Z | |
dc.date.issued | 2017-03-16 | |
dc.description.abstract | Ethanol production process generates a huge quantity of vinasse. A suitable destination for this byproduct may be its utilization as source of chemical substances, by recovery within the biorefinery process. Vinasse is rich in organic acids, which present value-added due to their many industrial applications. In this context, the present work aimed the development of an anion-exchange chromatographic method with pulsed amperometric detection, using oxidized nickel nanoparticle modified boron-doped diamond electrode, to determine industrially interesting electroactive organic acids, such as lactic acid, malic acid, and tartaric acid, in sugarcane vinasse. The chromatographic separation was carried out in a CarboPac PA 1 column under gradient elution employing different proportions of 0.10 mol L-1 NaOH in 0.25 mol L-1 CH3COONa and deionized water. Under these conditions, lactic acid, malic acid, and tartaric acid were separated in 27 min. The limits of detection were 1.2 × 10-4 mol L-1 for lactic acid, 6.1 × 10-5 mol L-1 for malic acid, and 2.8 × 10-5 mol L-1 for tartaric acid. The concentration of each organic acid in sugarcane vinasse was determined to be (1.2 ± 0.3) × 10-1 mol L-1 lactic acid, (2.7 ± 0.6) × 10-3 mol L-1 malic acid, and (9.9 ± 1.0) × 10-4 mol L-1 tartaric acid. The values of recovery between 97.4 and 107.6% indicated the method has excellent accuracy. Our results showed the present method is attractive for routine analysis during the ethanol production process because of the not costly and not time-consuming sample preparation, no need for organic solvent, rapid run time, and satisfactory separation. Thus, it can contribute to the process of utilization of sugarcane vinasse as a source of value-added chemical substances. | en |
dc.description.affiliation | Department of Analytical Chemistry Institute of Chemistry of Araraquara Universidade Estadual Paulista (UNESP), Rua Prof. Francisco Degni, 55 | |
dc.description.affiliation | Institute of Chemistry of São Carlos Universidade de São Paulo (USP), Avenida Trabalhador São-carlense, 400 | |
dc.description.affiliationUnesp | Department of Analytical Chemistry Institute of Chemistry of Araraquara Universidade Estadual Paulista (UNESP), Rua Prof. Francisco Degni, 55 | |
dc.description.sponsorship | Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) | |
dc.description.sponsorshipId | FAPESP: 2013/09833-5 | |
dc.description.sponsorshipId | FAPESP: 2014/23846-5 | |
dc.format.extent | 2865-2870 | |
dc.identifier | http://dx.doi.org/10.1021/acs.energyfuels.6b02783 | |
dc.identifier.citation | Energy and Fuels, v. 31, n. 3, p. 2865-2870, 2017. | |
dc.identifier.doi | 10.1021/acs.energyfuels.6b02783 | |
dc.identifier.issn | 1520-5029 | |
dc.identifier.issn | 0887-0624 | |
dc.identifier.scopus | 2-s2.0-85018462768 | |
dc.identifier.uri | http://hdl.handle.net/11449/174513 | |
dc.language.iso | eng | |
dc.relation.ispartof | Energy and Fuels | |
dc.relation.ispartofsjr | 1,159 | |
dc.relation.ispartofsjr | 1,159 | |
dc.rights.accessRights | Acesso restrito | |
dc.source | Scopus | |
dc.title | Determination of Electroactive Organic Acids in Sugarcane Vinasse by High Performance Anion-Exchange Chromatography with Pulsed Amperometric Detection Using a Nickel Nanoparticle Modified Boron-Doped Diamond | en |
dc.type | Artigo | |
dspace.entity.type | Publication | |
unesp.author.orcid | 0000-0001-8696-5978[1] | |
unesp.author.orcid | 0000-0002-7130-9684[2] | |
unesp.author.orcid | 0000-0003-3441-1572[3] | |
unesp.author.orcid | 0000-0002-9811-4879[4] | |
unesp.campus | Universidade Estadual Paulista (UNESP), Instituto de Química, Araraquara | pt |
unesp.department | Química Analítica - IQAR | pt |