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Recovery of Mo and V from the Spent Catalyst Using Organophosphorus Extractants

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dc.contributor.author Nayak, A.K.
dc.contributor.author Devi, N.
dc.contributor.author Sarangi, K.
dc.date.accessioned 2023-07-28T05:00:39Z
dc.date.available 2023-07-28T05:00:39Z
dc.date.issued 2021
dc.identifier.citation Transactions of the Indian Institute of Metals, 74(12), 2021: 3155-3162
dc.identifier.issn 0972-2815
dc.identifier.uri http://ore.immt.res.in/handle/2018/2876
dc.description.abstract The extraction and separation of Mo and V from sulphate media were investigated with phosphorus-based extractants such as D2EHPA, PC88A and Cyanex 272. The extraction was maximum within pH 1-3 and decreased after that pH. After pH 6.0, there was no extraction of Mo and V with the above extractants. The FTIR spectra indicated the bonding of hydroxyl group attached to phosphorus atom in each case which is due to the reaction of the cationic form of Mo (H3MoO4+) with the extractants. The highest separation factor was obtained with PC 88A. Hence, PC 88A was used for the separation of Mo and V from sulphate leach liquor of hydrodesulphurization spent catalyst. The McCabe-Thiele plot with 0.5 M PC 88A indicated three stages at A/O ratio of 2:1. Vanadium was selectively stripped with 0.5% H2SO4 followed by Mo stripping with NH4OH + (NH4)(2)CO3.
dc.language en
dc.publisher Springer
dc.relation.isreferencedby SCI
dc.rights Copyright [2021]. All efforts have been made to respect the copyright to the best of our knowledge. Inadvertent omissions, if brought to our notice, stand for correction and withdrawal of document from this repository.
dc.subject Materials Sciences
dc.title Recovery of Mo and V from the Spent Catalyst Using Organophosphorus Extractants
dc.type Journal Article
dc.affiliation.author AcSIR-IMMT, Bhubaneswar 751013, Odisha, India


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