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1.
J Agric Food Chem ; 61(47): 11494-501, 2013 Nov 27.
Artículo en Inglés | MEDLINE | ID: mdl-24228787

RESUMEN

Biorefinery of sugar cane is the first economic activity of Reunion Island. Some sugar cane manufactured products (juice, syrup, molasses) have antioxidant activities and are sources of both phenolic compounds and Maillard Reaction Products (MRP). The study aimed to highlight the global antioxidant activity of sugar cane stillage and understand its identity. Chromatographic fractionation on Sephadex LH-20 resin allowed the recovery of a MRP-rich fraction, responsible for 58 to 66% of the global antioxidant activity according to the nature of the sugar cane stillage (DPPH test), and a phenolic compounds-rich fraction for 37 to 59% of the activity. A good correlation was recorded between the antioxidant activity of the sugar cane stillage and its content in total reducing compounds amount (Folin-Ciocalteu assay), among them 2.8 to 3.9 g/L of phenolic compounds (in 5-caffeoylquinic acid equivalent). Preliminary experiments by HPLC-DAD-MS allowed to identify several free phenolic acids and gave clues to identify esters of quinic acids.


Asunto(s)
Antioxidantes/análisis , Saccharum/química , Antioxidantes/farmacología , Fraccionamiento Químico/instrumentación , Fraccionamiento Químico/métodos , Manipulación de Alimentos , Hidroxibenzoatos/análisis , Hidroxibenzoatos/química , Hidroxibenzoatos/farmacología , Reacción de Maillard
2.
J Agric Food Chem ; 55(21): 8576-84, 2007 Oct 17.
Artículo en Inglés | MEDLINE | ID: mdl-17867642

RESUMEN

Sisal fibers have one of the greatest potentials among other lignocellulosic fibers to reinforce polymer matrices in composites. Sisal fibers have been modified to improve their compatibility with phenolic polymer matrices using furfuryl alcohol (FA) and polyfurfuryl alcohols (PFA) that can be obtained from renewable sources. The modification corresponded first to oxidation with ClO 2, which reacts mainly with guaiacyl and syringyl units of lignin, generating o- and p-quinones and muconic derivatives, followed by reaction with FA or PFA. The FA and PFA modified fibers presented a thin similar layer, indicating the polymer character of the coating. The untreated and treated sisal fibers were characterized by (13)C CP-MAS NMR spectrometry, thermal analysis, and scanning electron microscopy. Furthermore, for a better understanding of the reactions involved in the FA and PFA modifications, the sisal lignin previously extracted was also submitted to those reactions and characterized. The characterization of isolated lignin and hemicellulose provides some information on the chemical structure of the main constitutive macrocomponents of sisal fibers, such information being scarce in the literature.


Asunto(s)
Lignina/química , Polisacáridos/química , Saccharum/química , Fenómenos Químicos , Química Física , Furanos/química , Indicadores y Reactivos , Espectroscopía de Resonancia Magnética , Microscopía Electrónica de Rastreo
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