2006
DOI: 10.1007/s00217-006-0346-5
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Adsorptive recovery of phenolic compounds from apple juice

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Cited by 79 publications
(52 citation statements)
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“…The effect of temperature on the desorption yields depends on the resin and does not present a definite trend. Similar recovery yields have been reported during the alkaline elution of resins used for the simultaneous removal of phenolic compounds and polar anions from citrus peel juice and molasses [5] and for ethanol elution of phenolics from apple juice [15]. The range of phenolic content of the desorbed products was 44-51% for HP20, 35-51% for SP207 and between 30-47% for XAD16 HP.…”
Section: Desorptionsupporting
confidence: 78%
“…The effect of temperature on the desorption yields depends on the resin and does not present a definite trend. Similar recovery yields have been reported during the alkaline elution of resins used for the simultaneous removal of phenolic compounds and polar anions from citrus peel juice and molasses [5] and for ethanol elution of phenolics from apple juice [15]. The range of phenolic content of the desorbed products was 44-51% for HP20, 35-51% for SP207 and between 30-47% for XAD16 HP.…”
Section: Desorptionsupporting
confidence: 78%
“…Liquid chromatography was applied for identification and quantification of phenolic compounds in apple [53,59,60], nectarin, peaches and plums [61].…”
Section: Raw Materials Biomarkersmentioning
confidence: 99%
“…Thus, desorption experiments were performed with all resins with the exception of XAD4, which essentially differs from XAD16 for pore diameter dimensions (Table 1) and offered slightly lower adsorption performances. The use of ethanol as a non-toxic solvent for polyphenol recovery from organic residues was demonstrated to represent a feasible and effective approach [49,50]: in this research, basified and acidified ethanol were also tested as desorbing agents, with the aim of enhancing the desorption of the adsorbed phenolic acids from non-(or weakly) polar resins and from the polar IRA96, respectively. In fact, alkaline conditions favour the deprotonation of the phenolic acids adsorbed onto the non-polar matrices, thus decreasing the compounds affinity towards such matrices (and vice versa).…”
Section: Desorption Experimentsmentioning
confidence: 99%