Mass transfer modeling on the separation of tantalum and niobium from dilute hydrofluoric media through a hollow fiber supported liquid membrane
- 1. Department of Chemical Engineering, Faculty of Engineering, Chulalongkorn University, Bangkok 10330 (Thailand)
- 2. Department of Chemical Engineering, Faculty of Engineering and Industrial Technology, Silpakorn University, Nakhon Pathom 73000 (Thailand)
- 3. Chromatography and Separation Research Unit, Department of Chemistry, Faculty of Science, Chulalongkorn University, Patumwan, Bangkok 10330 (Thailand)
Description
Highlights: → Simultaneous separation of tantalum and niobium from the mixture solution. → An extraction through a hollow fiber supported liquid membrane (HFSLM). → The effect on tantalum removal found from Aliquat 336. → The mathematical model focusing on the extraction side of the liquid membrane system was presented. → The mass transfer coefficients of the aqueous feed (ki) and the organic membrane phase (km) for the system were estimated as 1.19 x 10-5 and 1.39 x 10-7 cm/s, respectively. → Experimental data and theoretical values were found to be in good agreement when the concentration of Aliquat336 in the membrane phase was below 4% (v/v). - Abstract: The separation of a mixture of tantalum and niobium in dilute hydrofluoric media via hollow fiber supported liquid membrane (HFSLM) was examined. Quaternary ammonium salt (Aliquat336) diluted in kerosene was used as a carrier. The various effects on the transport and separation of tantalum and niobium were studied: concentration of hydrofluoric acid in the feed solution, concentration of the carrier (Aliquat336) in the membrane phase, types of stripping solutions (NaClO4, thiourea and HCl) and their concentration. The extraction of tantalum in the membrane phase from 0.3 M hydrofluoric acid (HF) by 3% (v/v) Aliquat336 was achieved by leaving niobium in the feed solution. Quantitative recovery of tantalum was achieved by 0.2 M NaClO4. Furthermore, a mathematical model focusing on the extraction side of the liquid membrane system was presented in order to predict the concentration of tantalum at different times. The mass transfer coefficients of the aqueous feed (ki) and the organic membrane phase (km) were estimated as 1.19 x 10-5 and 1.39 x 10-7 cm/s, respectively. Therefore, the mass transfer limiting step is the diffusion of tantalum-Aliquat336 through the liquid membrane. Moreover, mass transfer modeling was performed and the validity of the developed model evaluated. Experimental data and theoretical values were found to be in good agreement when the concentration of Aliquat336 in the membrane phase was below 4% (v/v).
Availability note (English)
Available from http://dx.doi.org/10.1016/j.jallcom.2011.07.078Additional details
Identifiers
- DOI
- 10.1016/j.jallcom.2011.07.078;
- PII
- S0925-8388(11)01574-X;
Publishing Information
- Journal Title
- Journal of Alloys and Compounds
- Journal Volume
- 509
- Journal Issue
- 39
- Journal Page Range
- p. 9549-9557
- ISSN
- 0925-8388
- CODEN
- JALCEU
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 43047887
- Subject category
- S37: INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY; S36: MATERIALS SCIENCE;
- Descriptors DEI
- EXTRACTION; FIBERS; HYDROFLUORIC ACID; KEROSENE; LIQUIDS; MASS TRANSFER; MATHEMATICAL MODELS; NIOBIUM; SIMULATION; SODIUM PERCHLORATES; SUPPORTED LIQUID MEMBRANES; TANTALUM; THIOUREA
- Descriptors DEC
- ALKALI METAL COMPOUNDS; ANTITHYROID DRUGS; CARBONIC ACID DERIVATIVES; CHLORINE COMPOUNDS; DISTILLATES; DRUGS; ELEMENTS; ENERGY SOURCES; FLUIDS; FLUORINE COMPOUNDS; FOSSIL FUELS; FUELS; GAS OILS; HALOGEN COMPOUNDS; HYDROGEN COMPOUNDS; INORGANIC ACIDS; INORGANIC COMPOUNDS; LIQUID FUELS; MEMBRANES; METALS; ORGANIC COMPOUNDS; ORGANIC SULFUR COMPOUNDS; OXYGEN COMPOUNDS; PERCHLORATES; PETROLEUM; PETROLEUM DISTILLATES; PETROLEUM FRACTIONS; PETROLEUM PRODUCTS; REFRACTORY METALS; SEPARATION PROCESSES; SODIUM COMPOUNDS; THIOUREAS; TRANSITION ELEMENTS
Optional Information
- Copyright
- Copyright (c) 2011 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.