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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/131318
Title: 
Determination of furanic aldehydes in sugarcane bagasse by high-performance liquid chromatography with pulsed amperometric detection using a modified electrode with nickel nanoparticles
Author(s): 
Institution: 
Universidade Estadual Paulista (UNESP)
ISSN: 
1615-9314
Abstract: 
A glassy carbon electrode chemically modified with nickel nanoparticles coupled with reversed-phase chromatography with pulsed amperometric detection was used for the quantitative analysis of furanic aldehydes in a real sample of sugarcane bagasse hydrolysate. Chromatographic separation was carried out in isocratic conditions (acetonitrile/water, 1:9) with a flow rate of 1.0 mL/min, a detection potential of -50 mV vs. Pd, and the process was completed within 4 min. The analytical curves presented limits of detection of 4.0 × 10(-7) mol/L and 4.3 × 10(-7) mol/L, limits of quantification of 1.3 × 10(-6) and 1.4 × 10(-6) mol/L, amperometric sensitivities of 2.2 × 10(6) nA mol/L and 2.7 × 10(6) nA mol/L for furfural and 5-hydroxymethylfurfural, respectively. The values obtained in this sample by the standard addition method were 1.54 ± 0.02 g/kg for 5-hydroxymethylfurfural and 11.5 ± 0.2 g/kg for furfural. The results demonstrate that this new proposed method can be used for the quick detection of furanic aldehydes without the interference of other electroactive species, besides having other remarkable merits that include excellent peak resolution, analytical repeatability, sensitivity, and accuracy.
Issue Date: 
2015
Citation: 
Journal Of Separation Science, 2015.
Publisher: 
Wiley-Blackwell
Keywords: 
  • Electrochemical detection
  • Furfural
  • Hydroxymethylfurfural
  • Nickel nanoparticles
  • Sugarcane bagasse
Source: 
http://dx.doi.org/10.1002/jssc.201500253
URI: 
Access Rights: 
Acesso restrito
Type: 
outro
Source:
http://repositorio.unesp.br/handle/11449/131318
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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