Journal
CANADIAN JOURNAL OF CHEMICAL ENGINEERING
Volume 92, Issue 5, Pages 810-815Publisher
WILEY-BLACKWELL
DOI: 10.1002/cjce.21898
Keywords
thermal stability; decarboxylation; polyphenol; flavonoids; superheated water
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Funding
- Thailand Research Fund, Office of the Higher Education Commission
- Faculty of Engineering and Industrial Technology, Silpakorn University [MRG5380123]
- Silpakorn University Research and Development Institute [SURDI 53/01/06]
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The degradation of 10 phenolic compounds including 9 phenolic acids (caffeic, chlorogenic, p-coumaric, gallic, gentisic, p-hydroxybenzoic, protocatechuic, syringic and vanillic acids) and one flavanol (catechin) in subcritical water at the initial concentration of 100 mg/L was investigated in a temperature range of 100-250 degrees C for 30-120 min in a batch-type vessel. The degradation process followed the first-order kinetics model. After treatment at 250 degrees C for 30 min, all the compounds completely disappeared. We also demonstrated that the subcritical water treatment of some phenolic compounds, especially, caffeic acid, resulted in products that were quite stable at high temperature and exhibited a high DPPH radical scavenging activity, that is retaining about 50% of the DPPH radical scavenging activity compared to the original caffeic acid solution after the treatment at 250 degrees C for 120 min.
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