Scholarly record
COMPARISON OF EXTRACTION METHODS FOR EXTRACTION OF IRON, ALUMINUM, MANGANESE AND TITANIUM USING CARBOXYLIC ACIDS AND NATURAL VEGETABLE OILS FROM WATER-SALT SYSTEMS
Abstract
The parameters of extraction from aqueous solutions into the organic phase of iron, aluminum, manganese and titanium are determined from the pH and concentration of the extractant when they are extracted with oleic and naphthenic acids, as well as olive and sunflower oils. The values of the thermodynamic functions of extraction equilibria with the participation of carboxylic acids and natural oils are taken as the basis for constructing the extractability series, which makes it possible to determine the thermodynamic capability and theoretical indicators of separation and extraction of elements. A principal technological scheme is proposed for the extraction of iron, aluminum, manganese and titanium during complex processing of eudialyte concentrates, which allows to reduce the number of equipment units and improve the ecological safety of the extraction process. To achieve the maximum extraction rates of elements, extraction with carboxylic acids or natural oils should be used when the pH is increased from 4.0 to 5.5, which creates good conditions for effective separation and extraction of metals. It was shown that all investigated vegetable oils such as olive and sunflower, either oleic or naphthenic acid exhibited a similar trend of extractability for iron, aluminum, manganese and titanium from aqueous solutions. A sigmoid curve was obtained for all the pH-extraction isotherms of iron, aluminum, manganese and titanium investigated with various types of vegetable oils. The extraction was the lowest at pH of 4.0, but increased sharply from 4.7 to 5.5, and achieved its maximum from 5.5 to 6.0
Publication Impact Profile
Publication details
References10
Chirkst D.E., Lutsky D.S., Lutskaya V.A., Zhukov S.V., Litvinova T.E., Separation of samarium, europium and erbium with naphthenic acid at the stoichiometric consumption of the extractant. High technologies, fundamental research, economics. vol. 1, 2011, pp 305-308;
Watson J.S., Separation Methods for Waste and Environmental Applications, Marcel Dekker, Inc., The United States of America, 1999;
Singh D.K., Singh H., Mathur J.N., Extraction of rare earths and yttrium with high molecular weight carboxylic acids. Elsevier, Hydrometallurgy, vol. 81, 2006, pp 174–181;
Gindin L.M. Extraction processes and their using. M.: Science, 1984, P 144.
Jaycock M.J., Jones A.D., Robinson C. Solvent extraction using carboxylic acids and their salts as extractants. Journal of Inorganic and Nuclear Chemistry, vol. 36, 1974. pp 887-898;
Miller F., Carboxylic acids as metal extractants. Talanta rev., vol. 2, 1974, pp 685- 703;
Preston J.S., Solvent extraction of metals by carboxylic acids. Hydrometallurgy. vol. 14, pp. 171 – 188;
Ren Z.Q., Zhang W., Dai Y., Yang Y., Hao Z., Modeling of effect of pH on mass transfer of copper(II) extraction by hollow fiber renewal liquid membrane, Ind. Eng. Chem. Res., vol. 47, 2008, pp 4256-4262;
Memon S., Akceylan E., Sap B., Tabakci M., Roundhill D. M., Yilmaz M., Polymer supported calix[4]arene derivatives for the extraction of metals and dichromate anions, J. Polym. Environ, vol. 11, 2003, pp 67-69;
Simonin J. P., Hendrawan H., Dardoize F., Clodic G. Study of salt effects on the kinetics of extraction of cobalt(II) and zinc(II) at trace level by D2EHPA in n-dodecane, Hydrometallurgy, vol. 69, 2003, pp 23-25.
Citing literature
Number of times cited according to Crossref: 2
View or Download full articleAccess options
SWS access login
Login as SWS Scientific CommitteeLogin as SWS Scientific PartnerLogin as SWS AuthorAuthors and approved SWS contributors will read and export their own linked papers after identity matching by SWS profile, email and SGEM GlobalID.
For librarian assistance: [email protected]
Purchase Instant Access
- Article can be downloaded after successful payment.
- Article may be used according to SWS library access terms.
- Article cannot be redistributed.


