2009
DOI: 10.1080/02773810903096025
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Determination of Furfural and Hydroxymethylfurfural Formed From Biomass Under Acidic Conditions

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Cited by 51 publications
(30 citation statements)
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“…Phenolics absorb at 280 nm due to aromatic rings; however, also heterocyclic aldehydes, particularly furfural and hydroxymethylfurfural, absorb considerably at around 280 nm (but only little at 205 nm). These aldehydes are common products of hot acid degradation of pentoses and hexoses (Hatfield and Fukushima 2005;Chi et al 2009). Hence, greater absorbance at 280 nm relative to 205 nm (i.e.…”
Section: Chemical Stability Parametersmentioning
confidence: 99%
“…Phenolics absorb at 280 nm due to aromatic rings; however, also heterocyclic aldehydes, particularly furfural and hydroxymethylfurfural, absorb considerably at around 280 nm (but only little at 205 nm). These aldehydes are common products of hot acid degradation of pentoses and hexoses (Hatfield and Fukushima 2005;Chi et al 2009). Hence, greater absorbance at 280 nm relative to 205 nm (i.e.…”
Section: Chemical Stability Parametersmentioning
confidence: 99%
“…For this purpose the used methods were the same for the initial characterization above mentioned. Furfural production was determined by spectrophotometry methods at 277 nm of wavelength (Chi et al, 2009). …”
Section: Chemical Compositionmentioning
confidence: 99%
“…The recovered PEG200 fraction was diluted by dioxane/0.2 M NaOH (v/v = 1:1) and reduced by NaBH4 for one week to eliminate UVabsorbing furans (Chi et al 2009). The reduced sample was adjusted to pH 5.0 with acetic acid, and the absorbance at 280 nm was measured as described above.…”
Section: Measurement Of Lignin Content and Phenolic Hydroxyl Group Comentioning
confidence: 99%