scholarly journals Evaluation of Tomato Processing By-Products: A Comparative Study in a Pilot Scale Setup

2014 ◽  
Vol 37 (3) ◽  
pp. 299-307 ◽  
Author(s):  
Anwesha Sarkar ◽  
Purnima Kaul
2014 ◽  
Author(s):  
Νικόλαος Ξυνός

The experimental work of this PhD thesis has been scheduled on a three-axis base. Theaims that were set, they concerned the optimal exploitation of four different by-products of the table olive, olive oil and olive kernel oil industries, for the recovery of specific highadded-value compounds with well-known biological properties. Those natural productswere desired either in the form of enriched fractions or pure compounds. The prerequisitewas to utilize as eco-friendly technologies as possible for extraction and purification and tooptimize the processes in laboratory as well as in pilot scale. Thus, trustworthy estimationof industrial feasibility is provided. The main technologies that were implicated for therecovery of the target compounds are: Supercritical fluid extraction Pressurized liquid (and subcritical water) extraction Liquid/liquid extraction Adsorption resin technology Centrifugal Partition ChromatographyThe by-products that were the subject of the tracing/ extraction/ enrichment/identification/ quantification on studies for this PhD thesis were the following: Olive leaves (by-products of the pruning of the trees and of the olive fruit harvest) Olive mill pomace waste (biphasic process) Table olive process wastewater (by-product of the debittering process for theproduction of table olives) Olive kernel oil deodorization distillates (by-product of the refining process for theproduction of olive kernel oil from olive pomace)The natural compounds that were targeted for their recovery, enrichment and isolation dueto their well-established (and still under research) biological properties and theirapplication in pharmaceutical, phytotherapeutical, nutraceutical, cosmetic andcosmeceutical industries were respectively: Oleuropein Hydroxytyrosol SqualeneIn all cases, not only biomarkers’ content but also the overall chemical profile of theextracts was studied. The applied scientific interest of this work was that novel green extraction technologies and combinatorial processes as well as experimental design wereimplemented in lab and pilot scale for the exploitation of certain by-products that occur invery large quantities every year as a result of the agricultural/ industrial processing of theolive tree, with the aim of recovering high added value natural products.


2005 ◽  
Vol 57 (3-4) ◽  
pp. 134-144 ◽  
Author(s):  
Hatairat Puchongkavarin ◽  
Saiyavit Varavinit ◽  
Wolfgang Bergthaller

2014 ◽  
Vol 57 (5) ◽  
pp. 192-198 ◽  
Author(s):  
H. P. Tiwari ◽  
P. K. Banerjee ◽  
R. Sharma ◽  
S. K. Haldar ◽  
P. C. Joshi

2022 ◽  
pp. 1-32
Author(s):  
George Liadakis ◽  
Maria Katsouli ◽  
Sofia Chanioti ◽  
Virginia Giannou ◽  
Constantina Tzia

2015 ◽  
Vol 74 ◽  
pp. 810-816 ◽  
Author(s):  
G.J.M. Rocha ◽  
A.R. Gonçalves ◽  
S.C. Nakanishi ◽  
V.M. Nascimento ◽  
V.F.N. Silva

2018 ◽  
Vol 73 (4) ◽  
pp. 268-277 ◽  
Author(s):  
Katalin Szabo ◽  
Adriana-Florinela Cătoi ◽  
Dan Cristian Vodnar

2010 ◽  
Vol 7 (3) ◽  
pp. 225 ◽  
Author(s):  
Janey V. Camp ◽  
Dennis B. George ◽  
Martha J. M. Wells ◽  
Pedro E. Arce

Environmental context.Potentially toxic disinfection by-products form when water containing humic and fulvic acids is chlorinated to destroy pathogenic microorganisms. A pulsed electrical discharge was examined for its ability to destroy an aquatic fulvic acid by oxidation. Spectroscopically, changes in the organic structures were observed, but carbon content and disinfection by-products were not reduced. Abstract.A pilot-scale pulsed electrical discharge (PED) system was used to treat Suwannee River fulvic acid (SRFA) as a representative precursor material for the formation of disinfection by-products (DBPs), specifically trihalomethane compounds. Ultraviolet-visible and fluorescence spectroscopy, dissolved organic carbon (DOC), and the trihalomethane formation potential (THMFP) were used as analytical parameters to monitor the effects of treatment on the substrate. The potential for SRFA degradation (5 mg L–1 DOC) was examined over 60 min at each of four operational configurations, varying pulse energy and frequency (0.15 J and 60 Hz, 0.15 J and 120 Hz, 0.4 J and 60 Hz, and 0.4 J and 120 Hz) in a factorial design. Statistically significant changes occurred for UV254, EX254EM460, and EX328EM460 under selected conditions; however, concomitant changes in DOC and THMFP were not observed. The composition of SRFA changed, but organic carbon was not mineralised to carbon dioxide. In addition to showing degradation by PED, the significance of the preliminary findings of this research was to demonstrate that spectroscopic monitoring of precursor degradation alone can be misleading, and that whereas ultraviolet-visible and fluorescence spectroscopy indicated degradation of precursor compounds, DOC and THMFP measurements were unchanged and did not support the occurrence of mineralisation in this system.


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