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Electrochemical recovery of zinc from the spent pickling baths coming from the hot dip galvanizing industry. Potentiostatic operation

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Electrochemical recovery of zinc from the spent pickling baths coming from the hot dip galvanizing industry. Potentiostatic operation

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dc.contributor.author Carrillo Abad, Jorge es_ES
dc.contributor.author García Gabaldón, Montserrat es_ES
dc.contributor.author Ortega Navarro, Emma María es_ES
dc.contributor.author Pérez-Herranz, Valentín es_ES
dc.date.accessioned 2015-11-03T10:17:49Z
dc.date.available 2015-11-03T10:17:49Z
dc.date.issued 2011-09
dc.identifier.issn 1383-5866
dc.identifier.uri http://hdl.handle.net/10251/56920
dc.description.abstract An electrochemical reactor was developed to recover zinc from the spent pickling solutions coming from the hot dip galvanizing industry. These solutions mainly contain ZnCl2 and FeCl2 in aqueous HCl media. The effect of the applied potential on the figures of merit (fractional conversion, current efficiency, space-time yield and specific energy consumption) of the electrochemical reactor was analysed. Voltammetric experiments were performed previously in order to select the optimum conditions to be applied in the electrolysis experiments. From the I-V curves it was inferred that bulk zinc deposition started from potential values more cathodic than -0.99 V. The hydrogen evolution reaction (HER) appeared from -0.45 V and masked the zinc cathodic peak C1, related to bulk zinc deposition, at high HCl concentrations. The presence of HCl inhibited iron deposition in synthetic samples. The additives present in the real baths, which diminish the massive hydrogen generation, allowed the observation of peak C1. The potential values to be applied in the electrolysis experiments were chosen from the voltammetric experiments and ranged between -1 V and -1.75 V. In the absence of iron in solution, as the electrode potential was shifted towards more negative values, the space-time yield of zinc and its fractional conversion increased because of the increase in the electrode roughness and the hydrogen turbulence-promoting action. Simultaneously, the specific energy consumption decreased initially due to the increase in the zinc conversion rate but decreased for the most cathodic potential value due to HER. The presence of iron in synthetic solutions led to a decrease in current efficiency associated with the reverse redox Fe 2+/Fe3+ system and to the enhancement of the HER, which also induced increments in the local pH and the subsequent zinc redissolution for the most cathodic potential values. On the contrary, the additives present in the real spent pickling baths avoided the adverse effects of iron, and zinc electrodeposition was possible even at high cathodic potential values. In fact, a potential value of -1.75 V was selected as the optimum since the conversion, the current efficiency and the space time yield obtained in the real baths were relatively high. es_ES
dc.description.sponsorship Authors want to express their gratitude to the Universidad Politecnica de Valencia for the economical support in the project reference PAID-06-08, and to the Generalitat Valenciana for the financing of the project reference GV/2010/029. en_EN
dc.language Inglés es_ES
dc.publisher Elsevier es_ES
dc.relation.ispartof Separation and Purification Technology es_ES
dc.rights Reserva de todos los derechos es_ES
dc.subject Electrochemical deposition es_ES
dc.subject Hydrogen evolution reaction es_ES
dc.subject Iron es_ES
dc.subject Pickling solutions es_ES
dc.subject Zinc electrodeposition es_ES
dc.subject Adverse effect es_ES
dc.subject Applied potentials es_ES
dc.subject Cathodic peak es_ES
dc.subject Cathodic potentials es_ES
dc.subject Conversion rates es_ES
dc.subject Current efficiency es_ES
dc.subject Electrochemical reactor es_ES
dc.subject Electrochemical recovery es_ES
dc.subject Electrode potentials es_ES
dc.subject Figures of merits es_ES
dc.subject Fractional conversion es_ES
dc.subject Hot-dip galvanizing es_ES
dc.subject Hydrogen evolution reactions es_ES
dc.subject Hydrogen generations es_ES
dc.subject I - V curve es_ES
dc.subject Iron deposition es_ES
dc.subject Negative values es_ES
dc.subject Optimum conditions es_ES
dc.subject Pickling baths es_ES
dc.subject Potential values es_ES
dc.subject Potentiostatic operations es_ES
dc.subject Re-dissolution es_ES
dc.subject Space time yield es_ES
dc.subject Specific energy consumption es_ES
dc.subject Synthetic solutions es_ES
dc.subject Voltammetric experiments es_ES
dc.subject Electric reactors es_ES
dc.subject Electrodeposition es_ES
dc.subject Electrolysis es_ES
dc.subject Energy efficiency es_ES
dc.subject Energy utilization es_ES
dc.subject Experiments es_ES
dc.subject Galvanizing es_ES
dc.subject Hydrochloric acid es_ES
dc.subject Hydrogen es_ES
dc.subject Hydrogen production es_ES
dc.subject Pickling es_ES
dc.subject Reduction es_ES
dc.subject Value engineering es_ES
dc.subject Zinc deposits es_ES
dc.subject Zinc es_ES
dc.subject.classification INGENIERIA QUIMICA es_ES
dc.title Electrochemical recovery of zinc from the spent pickling baths coming from the hot dip galvanizing industry. Potentiostatic operation es_ES
dc.type Artículo es_ES
dc.identifier.doi 10.1016/j.seppur.2011.07.029
dc.relation.projectID info:eu-repo/grantAgreement/UPV//PAID-06-08/ es_ES
dc.relation.projectID info:eu-repo/grantAgreement/GVA//GV%2F2010%2F029/ es_ES
dc.rights.accessRights Abierto es_ES
dc.contributor.affiliation Universitat Politècnica de València. Departamento de Ingeniería Química y Nuclear - Departament d'Enginyeria Química i Nuclear es_ES
dc.description.bibliographicCitation Carrillo Abad, J.; García Gabaldón, M.; Ortega Navarro, EM.; Pérez-Herranz, V. (2011). Electrochemical recovery of zinc from the spent pickling baths coming from the hot dip galvanizing industry. Potentiostatic operation. Separation and Purification Technology. 81(2):200-207. https://doi.org/10.1016/j.seppur.2011.07.029 es_ES
dc.description.accrualMethod S es_ES
dc.relation.publisherversion http://dx.doi.org/10.1016/j.seppur.2011.07.029 es_ES
dc.description.upvformatpinicio 200 es_ES
dc.description.upvformatpfin 207 es_ES
dc.type.version info:eu-repo/semantics/publishedVersion es_ES
dc.description.volume 81 es_ES
dc.description.issue 2 es_ES
dc.relation.senia 193567 es_ES
dc.contributor.funder Generalitat Valenciana es_ES
dc.contributor.funder Universitat Politècnica de València es_ES


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