Continuous extraction of phenolic compounds from pomegranate peel using high voltage electrical discharge
•A continuous HVED extraction system was designed for the first time.•Response surface methodology was used to optimize the process variables.•The optimal conditions were: 12mL/min, 3.1mm and 35mL/g.•The predicted yield of phenolic compounds was 199.83mg/g.•The experimental values were in close agre...
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Published in: | Food chemistry Vol. 230; pp. 354 - 361 |
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Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
England
Elsevier Ltd
01-09-2017
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Subjects: | |
Online Access: | Get full text |
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Summary: | •A continuous HVED extraction system was designed for the first time.•Response surface methodology was used to optimize the process variables.•The optimal conditions were: 12mL/min, 3.1mm and 35mL/g.•The predicted yield of phenolic compounds was 199.83mg/g.•The experimental values were in close agreement with predicted values.
Pomegranate peel, a waste generated from fruit processing industry, is a potential source of phenolic compounds that are known for their anti-oxidative properties. In this study, a continuous high voltage electrical discharge (HVED) extraction system was for the first time designed and optimized for phenolic compounds from pomegranate peel. The optimal conditions for HVED were: flow rate of materials 12mL/min, electrodes gap distance 3.1mm (corresponding to 29kV/cm of electric field intensity) and liquid to solid ratio 35mL/g. Under these conditions, the experimental yield of phenolic compounds was 196.7±6.4mg/g, which closely agreed with the predicted value (199.83mg/g). Compared with the warm water maceration, HVED method possessed higher efficiency for the extraction of phenolic compounds. The results demonstrated that HVED technique could be a very effective method for continuous extraction of natural compounds. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0308-8146 1873-7072 |
DOI: | 10.1016/j.foodchem.2017.03.072 |