Coupling Solvent Extraction Units to Cyclic Adsorption Units

The possibility of regenerating the solvent of extraction units by cyclic adsorption was analyzed. This combination seems convenient when extraction is performed with a high solvent-to-impurity ratio, making other choices of solvent regeneration, typically distillation, unattractive. To our knowledg...

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Main Authors: Mariana Busto, Enrique Eduardo Tarifa, Carlos Román Vera
Format: Article
Language:English
Published: Wiley 2018-01-01
Series:International Journal of Chemical Engineering
Online Access:http://dx.doi.org/10.1155/2018/1620218
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author Mariana Busto
Enrique Eduardo Tarifa
Carlos Román Vera
author_facet Mariana Busto
Enrique Eduardo Tarifa
Carlos Román Vera
author_sort Mariana Busto
collection DOAJ
description The possibility of regenerating the solvent of extraction units by cyclic adsorption was analyzed. This combination seems convenient when extraction is performed with a high solvent-to-impurity ratio, making other choices of solvent regeneration, typically distillation, unattractive. To our knowledge, the proposed regeneration scheme has not been considered before in the open literature. Basic relations were developed for continuous and discontinuous extraction/adsorption combinations. One example, deacidification of plant oil with alcohol, was studied in detail using separate experiments for measuring process parameters and simulation for predicting performance at different conditions. An activated carbon adsorbent was regenerated by thermal swing, making cyclic operation possible. When extracting the acid with methanol in a spray column, feed = 4 L min−1, solvent = 80 L min−1, feed impurity level 140 mmol L−1, and extract concentration 7.6 mmol L−1, the raffinate reaches a purity of 1.2 mmol L−1, the solvent being regenerated cyclically in the adsorber (364 kg) to an average of 0.7 mmol L−1. Regeneration of the solvent by cyclic adsorption had a low heat duty. Values of 174 kJ per litre of solvent compared well with the high values for vaporization of the whole extract phase (1011 kJ L−1).
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series International Journal of Chemical Engineering
spelling doaj-art-7d8c5b3ba0e6416ab56db00d4423895f2025-02-03T06:00:36ZengWileyInternational Journal of Chemical Engineering1687-806X1687-80782018-01-01201810.1155/2018/16202181620218Coupling Solvent Extraction Units to Cyclic Adsorption UnitsMariana Busto0Enrique Eduardo Tarifa1Carlos Román Vera2Institute of Research on Catalysis and Petrochemistry, INCAPE, FIQ-UNL, CONICET, Collecting Ring, National Road 168 Km 0, El Pozo, 3000 Santa Fe, ArgentinaFaculty of Chemical Engineering, Universidad Nacional de Jujuy, CONICET, Ítalo Palanca No. 10, San Salvador de Jujuy, ArgentinaInstitute of Research on Catalysis and Petrochemistry, INCAPE, FIQ-UNL, CONICET, Collecting Ring, National Road 168 Km 0, El Pozo, 3000 Santa Fe, ArgentinaThe possibility of regenerating the solvent of extraction units by cyclic adsorption was analyzed. This combination seems convenient when extraction is performed with a high solvent-to-impurity ratio, making other choices of solvent regeneration, typically distillation, unattractive. To our knowledge, the proposed regeneration scheme has not been considered before in the open literature. Basic relations were developed for continuous and discontinuous extraction/adsorption combinations. One example, deacidification of plant oil with alcohol, was studied in detail using separate experiments for measuring process parameters and simulation for predicting performance at different conditions. An activated carbon adsorbent was regenerated by thermal swing, making cyclic operation possible. When extracting the acid with methanol in a spray column, feed = 4 L min−1, solvent = 80 L min−1, feed impurity level 140 mmol L−1, and extract concentration 7.6 mmol L−1, the raffinate reaches a purity of 1.2 mmol L−1, the solvent being regenerated cyclically in the adsorber (364 kg) to an average of 0.7 mmol L−1. Regeneration of the solvent by cyclic adsorption had a low heat duty. Values of 174 kJ per litre of solvent compared well with the high values for vaporization of the whole extract phase (1011 kJ L−1).http://dx.doi.org/10.1155/2018/1620218
spellingShingle Mariana Busto
Enrique Eduardo Tarifa
Carlos Román Vera
Coupling Solvent Extraction Units to Cyclic Adsorption Units
International Journal of Chemical Engineering
title Coupling Solvent Extraction Units to Cyclic Adsorption Units
title_full Coupling Solvent Extraction Units to Cyclic Adsorption Units
title_fullStr Coupling Solvent Extraction Units to Cyclic Adsorption Units
title_full_unstemmed Coupling Solvent Extraction Units to Cyclic Adsorption Units
title_short Coupling Solvent Extraction Units to Cyclic Adsorption Units
title_sort coupling solvent extraction units to cyclic adsorption units
url http://dx.doi.org/10.1155/2018/1620218
work_keys_str_mv AT marianabusto couplingsolventextractionunitstocyclicadsorptionunits
AT enriqueeduardotarifa couplingsolventextractionunitstocyclicadsorptionunits
AT carlosromanvera couplingsolventextractionunitstocyclicadsorptionunits