2016
DOI: 10.1016/j.foodchem.2016.04.034
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Olive mill wastewater microconstituents composition according to olive variety and extraction process

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Cited by 86 publications
(37 citation statements)
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“…The amount of hydroxytyrosol (1.2 g/L) appeared to be in agreement with the value reported by De Marco et al (2007) and Fki, Allouche, and Sayadi (2005). High concentrations of tyrosol (12.9 g/L) and oleuropein (2.1 g/L) were detected in the extract, according to Aggoun et al (2016). Several studies reported a lower concentration of oleuropein in extract from OMWW (El-Abbassi et al, 2011;…”
Section: Pe Characterizationsupporting
confidence: 86%
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“…The amount of hydroxytyrosol (1.2 g/L) appeared to be in agreement with the value reported by De Marco et al (2007) and Fki, Allouche, and Sayadi (2005). High concentrations of tyrosol (12.9 g/L) and oleuropein (2.1 g/L) were detected in the extract, according to Aggoun et al (2016). Several studies reported a lower concentration of oleuropein in extract from OMWW (El-Abbassi et al, 2011;…”
Section: Pe Characterizationsupporting
confidence: 86%
“…Moreover, different values were found in literature studies for three‐phase olive wastewaters: De Marco et al () reported a value of 3,481 mg/L of extract, while other authors detected a range of values between 6,110 and 9,820 mg/L of extract for OMWW collected from semi‐modern and modern three‐phase processes (El‐Abbassi, Khayet, & Hafidi, ). In addition, the differences in total phenolic content can be explained by the impact of geographic and climatic conditions (Piscopo, Bruno, Zappia, Ventre, & Poiana, ), period of harvest (Piscopo, Zappia, Bruno, & Poiana, ), and olive variety (Aggoun et al, ; Dermeche, Nadour, Larroche, Moulti‐Mati, & Michaud, ).…”
Section: Resultsmentioning
confidence: 99%
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“…At pH = 7.0, oleuropein unveils a very low dissociation (0.2%) according to calculated values for its p K a1 = 9.70 ± 0.10, which involves the 3-OH on the aryl group as performed adopting the Hammett-type equation. This allowed utilization of apparent p K a values, thus mimicking the experimental order of deprotonation in the hydroxytyrosol residue of oleuropein in water solution [63,64]. The earlier p K a1 = 9.07 ± 0.02 and p K a2 = 9.98 ± 0.06 showed for catechol were 9.25 and 13.0, respectively [30,65].…”
Section: Computational Mapping Of Oleuropeinmentioning
confidence: 99%