Separation Iron(III)-Manganese(II) via Supported Liquid Membrane Technology in the Treatment of Spent Alkaline Batteries

In this paper, the transport of iron(III) from iron(III)-manganese(II)-hydrochloric acid mixed solutions, coming from the treatment of spent alkaline batteries through a flat-sheet supported liquid membrane, is investigated (the carrier phase being of Cyanex 923 (commercially available phosphine oxide extractant) dissolved in Solvesso 100 (commercially available diluent)). Iron(III) transport is studied as a function of hydrodynamic conditions, the concentration of manganese and HCl in the feed phase, and the carrier concentration in the membrane phase. A transport model is derived that describes the transport mechanism, consisting of diffusion through a feed aqueous diffusion layer, a fast interfacial chemical reaction, and diffusion of the iron(III) species-Cyanex 923 complex across the membrane phase. The membrane diffusional resistance (Δm) and feed diffusional resistance (Δf) are calculated from the model, and their values are 145 s/cm and 361 s/cm, respectively. It is apparent that the transport of iron(III) is mainly controlled by diffusion through the aqueous feed boundary layer, this being the thickness of this layer calculated as 2.9 × 10−3 cm. Since manganese(II) is not transported through the membrane phase, the present system allows the purification of these manganese-bearing solutions.

Separation Fe(III)-Mn(II) via Supported Liquid Membrane Technology in the Treatment of Spent Alkaline Batteries

The transport of iron(III) from Fe(III)-Mn(II)-HCl mixed solutions through a flat-sheet supported liquid membrane is investigated, being the carrier phase of Cyanex 923 (commercially available phosphine oxide extractant) dissolved in Solvesso 100 (commercially available diluent), as a function of hydrodynamic conditions, concentration of manganese and HCl in the feed phase, and carrier concentration in the membrane phase. A transport model is derived that describes the transport mechanism, consisting of diffusion through a feed aqueous diffusion layer, a fast interfacial chemical reaction, and diffusion of the Fe(III)-Cyanex 923 complex across the membrane phase. The membrane diffusional resistance (Δm) and feed diffusional resistance (Δf) are calculated from the model, and their values are 145 s/cm and 361 s/cm, respectively. It is apparent that the transport of iron(III) is mainly controlled by diffusion through the aqueous feed boundary layer, being the thickness of this layer calculated as 2.9x10-3 cm. Since Mn(II) is not transported through the membrane phase, the present system allows to the purification of this manganese-bearing solutions.

Removal of Copper Ions from Aqueous Solution Using Liquid Surfactant Membrane Technique

Liquid Surfactant Membrane (LSM) as an alternative extraction technique shows many advantages without altering the chemistry of the oil process in terms of efficiency, cost effectiveness and fast demulsification post extraction. Copper (Cu) extraction from aqueous solution using Liquid Membrane (LM) technology is more efficient than the sludge-forming precipitation process and has to be disposed of in landfills. In this chapter, a liquid surfactant membrane (LSM) was developed that uses kerosene oil as LSM ‘s key diluent to extract copper ions as a carrier from the aqueous waste solution through di-(2-ethylhexyl) phosphoric acid (D2EHPA). This technique has several benefits, including extracting one-stage extracts. The LSM process was used to transport Cu (II) ions from the feed phase to the stripping phase, which was prepared, using H2SO4. For LSM process, various parameters have been studied such as carrier concentration, treat ratio (TR), agitating speed and initial feed concentration. After finding the optimum parameters, it was possible to extract Cu up to 95% from the aqueous feed phase in a single stage extraction.

Pertraction of Co(II) through Novel Ultrasound Prepared Supported Liquid Membranes Containing D2EHPA. Optimization and Transport Parameters

Pertraction of Co(II) through novel supported liquid membranes prepared by ultrasound, using bis-2-ethylhexyl phosphoric acid as carrier, sulfuric acid as stripping agent and a counter-transport mechanism, is studied in this paper. Supported liquid membrane characterization through scanning electron microscopy, energy-dispersive X-ray spectroscopy and Fourier transform infrared spectroscopy shows the impregnation of the microporous polymer support by the membrane phase by the action of ultrasound. The effect on the initial flux of Co(II) of different experimental conditions is analyzed to optimize the transport process. At these optimal experimental conditions (feed phase pH 6, 0.5 M sulfuric acid in product phase, carrier concentration 0.65 M in membrane phase and stirring speed of 300 rpm in both phases) supported liquid membrane shows great stability. From the relation between the inverse of Co(II) initial permeability and the inverse of the square of carrier concentration in the membrane phase, in the optimized experimental conditions, the transport resistance due to diffusion through both the aqueous feed boundary layer (3.7576 × 104 s·m−1) and the membrane phase (1.1434 × 1010 s·m−1), the thickness of the aqueous feed boundary layer (4.0206 × 10−6 m) and the diffusion coefficient of the Co(II)-carrier in the bulk membrane (4.0490 × 10−14 m2·s−1), have been determined.

Computational modeling of drug separation from aqueous solutions using octanol organic solution in membranes

Continuous membrane separation of pharmaceuticals from an aqueous feed was studied theoretically by development of high-performance mechanistic model. The model was developed based on mass and momentum transfer to predict separation and removal of ibuprofen (IP) and its metabolite compound, i.e. 4-isobutylacetophenone (4-IBAP) from aqueous solution. The modeling study was carried out for a membrane contactor considering mass transport of solute from feed to organic solvent (octanol solution). The solute experiences different mass transfer resistances during the removal in membrane system which were all taken into account in the modeling. The model’s equations were solved using computational fluid dynamic technique, and the simulations were carried out to understand the effect of process parameters, flow pattern, and membrane properties on the removal of both solutes. The simulation results indicated that IP and 4-IBAP can be effectively removed from aqueous feed by adjusting the process parameters and flow pattern. More removal was obtained when the feed flows in the shell side of membrane system due to improving mass transfer. Also, feed flow rate was indicated to be the most affecting process parameter, and the highest solute removal was obtained at the lowest feed flow rate.

Permeation of AuCl4− Across a Liquid Membrane Impregnated with A324H+Cl− Ionic Liquid

In the system Au(III)-HCl-A324H+Cl−, liquid-liquid extraction experiments were used to define the extraction equilibrium and the corresponding extraction constant; furthermore, the facilitated transport of this precious metal from HCl solutions across a flat-sheet supported liquid membrane was investigated using the same ionic liquid as a carrier, and as a function of different variables: hydrodynamic conditions, concentration of gold(III) (0.01–0.1 g/L), and HCl (0.5–6 M) in the feed phase, and carrier concentration (0.023–0.92 M) in the membrane. An uphill transport equation was derived considering aqueous feed boundary layer diffusion and membrane diffusion as controlling steps. The aqueous diffusional resistance (Δf) and the membrane diffusional resistance (Δm) were estimated from the proposed equation with values of 241 s/cm and 9730 s/cm, respectively. The performance of the present carrier was compared against results yielded by other ionic liquids, and the influence that other metals had on gold(III) transport from both binary or quaternary solutions was also investigated. Gold was finally recovered from receiving solutions as zero valent gold nanoparticles.