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Selection of the Best Process Stream to Remove Ca2+ Ion Using Electrodialysis from Sugar Solution

DOI: 10.1155/2014/304296

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Abstract:

Electrodialytic removal of calcium chloride (CaCl2, 25–50?mol·m?3) from 5% sugar solution was executed in batch recirculation mode. Calcium ion removal rate was monitored with (i) applied potential, (ii) feed flow rate, (iii) solution viscosity and conductivity, and (iv) catholyte streams (NaOH or sodium salt of ethylene diamine tetraacetic acid-acetic acid, Na2EDTA-AA). Unsteady state model for ion concentration change was written for the ED cell used. Linearized Nernst-Planck equation instead of Ohm’s law was applied to closely obtain the current density and concentration change theoretically. The model developed could closely predict the experimental observation. Mass transfer coefficients and specific energy densities were estimated for each combination of catholyte stream used. NaOH showed better performance for a short duration over Na2EDTA-acetic acid combination. 1. Introduction In cane based sugar industry the sugar concentration in the extracted juice after lime (CaO + H2O) treatment and color removal (clarification step) usually reaches around 5% (mass basis). This stream subsequently enters into series of evaporators to get concentrated. Presence of excess calcium in the postfloculation and precipitation stage of clarified sugar juice creates series of nuisance [1] to the subsequent stages (evaporators, etc.) in sugar industries affecting product quality as follows.(1)Scale formation in the evaporators.(2)Improper crystallization.(3)Molasses percentage may increase due to inversion of sugar in alkaline medium.(4)Storage is hampered because of hygroscopic nature of these metals ions.(5)Excess calcium is not hygienic as well. Therefore, removal of it at appropriate stage would drastically reduce operation and maintenance (evaporator scaling) cost and improve product quality. Electrodialysis (ED) was chosen to remove CaCl2 from its sugar solution. ED was applied earlier in sugar industry to recover tartrate and malate from grape sugar [2] and in demineralisation of beet sugar syrup, juice, and molasses [3, 4]. The technological difficulties arise due to fouling of ion exchange membranes mainly due to deposition of organic/inorganic molecules (sugars, proteins, Ca2+, Mg2+, etc.). With increase in solution viscosity fouling becomes even severe and affects the current efficiency and ion removal rate. The concentration polarization occurs around membrane surface leading to increase in ion resistance, and this is minimized with the help of suitable spacer design, temperature, pH, and flow rates applied [5–11]. A batch recirculation ED process having

References

[1]  R. B. L. Mathur, Handbook of Cane Sugar Technology, Oxford and IBH Publishing, New Delhi, India, 1978.
[2]  F. Smagghe, J. Mourgues, J. L. Escudier, T. Conte, J. Molinier, and C. Malmary, “Recovery of calcium tartrate and calcium malate in effluents from grape sugar production by electrodialysis,” Bioresource Technology, vol. 39, no. 2, pp. 185–189, 1992.
[3]  A. Elmidaoui, L. Chay, M. Tahaikt et al., “Demineralisation of beet sugar syrup, juice and molasses using an electrodialysis pilot plant to reduce melassigenic ions,” Desalination, vol. 165, p. 435, 2004.
[4]  G. Tr?g?rdh and V. Gekas, “Membrane technology in the sugar industry,” Desalination, vol. 69, no. 1, pp. 9–17, 1988.
[5]  H. Strathmann, Ion-Exchange Membrane Separation Processes, Elsevier, 2004.
[6]  J. J. Krol, M. Wessling, and H. Strathmann, “Concentration polarization with monopolar ion exchange membranes: current-voltage curves and water dissociation,” Journal of Membrane Science, vol. 162, no. 1-2, pp. 145–154, 1999.
[7]  V. Geraldes and M. D. Afonso, “Limiting current density in the electrodialysis of multi-ionic solutions,” Journal of Membrane Science, vol. 360, no. 1-2, pp. 499–508, 2010.
[8]  H. Strathmann, J. J. Krol, H.-J. Rapp, and G. Eigenberger, “Limiting current density and water dissociation in bipolar membranes,” Journal of Membrane Science, vol. 125, no. 1, pp. 123–142, 1997.
[9]  H.-J. Lee, H. Strathmann, and S.-H. Moon, “Determination of the limiting current density in electrodialysis desalination as an empirical function of linear velocity,” Desalination, vol. 190, no. 1–3, pp. 43–50, 2006.
[10]  Y. Tanaka, “Limiting current density of an ion-exchange membrane and of an electrodialyzer,” Journal of Membrane Science, vol. 266, no. 1-2, pp. 6–17, 2005.
[11]  A. Elmidaoui, F. Lutin, L. Chay, M. Taky, M. Tahaikt, and M. R. A. Hafidi, “Removal of melassigenic ions for beet sugar syrups by electrodialysis using a new anion-exchange membrane,” Desalination, vol. 148, no. 1–3, pp. 143–148, 2002.
[12]  Y. Tanaka, “Irreversible thermodynamics and overall mass transport in ion-exchange membrane electrodialysis,” Journal of Membrane Science, vol. 281, no. 1-2, pp. 517–531, 2006.
[13]  S. Chattopadhyay, Removal of Calcium Ion from Sugar Solution through Electrodialysis, Department of Chemical Engineering, Indian Institute of Technology Kanpur, Kanpur, India, 1994.
[14]  B. E. Poling, J. M. Prausnitz, and J. P. O’Connell, The Properties of Gases and Liquids, McGraw-Hill, New York, NY, USA, 5th edition, 2000.
[15]  L. Yuan-Hui and S. Gregory, “Diffusion of ions in sea water and in deep-sea sediments,” Geochimica et Cosmochimica Acta, vol. 38, no. 5, pp. 703–714, 1974.
[16]  http://www.sugartech.co.za/viscosity/index.php.
[17]  M. S. Isaacson and A. A. Sonin, “Sherwood number and friction factor correlations for electrodialysis systems, with application to process optimization,” Industrial & Engineering Chemistry Process Design and Development, vol. 15, no. 2, pp. 313–321, 1976.
[18]  J. M. Ortiz, J. A. Sotoca, E. Expósito et al., “Brackish water desalination by electrodialysis: batch recirculation operation modeling,” Journal of Membrane Science, vol. 252, no. 1-2, pp. 65–75, 2005.
[19]  F. S. Rohman, M. R. Othman, and N. Aziz, “Modeling of batch electrodialysis for hydrochloric acid recovery,” Chemical Engineering Journal, vol. 162, no. 2, pp. 466–479, 2010.
[20]  R. E. Treybal, Mass-Transfer Operations, McGraw-Hill, New York, NY, USA, 3rd edition, 1980.
[21]  R. B. Bird, W. E. Stewart, and E. N. Lightfoot, Transport Phenomenon, John Wiley & Sons, 2nd edition, 2002.
[22]  J. Balster, M. H. Yildirim, D. F. Stamatialis et al., “Morphology and microtopology of cation-exchange polymers and the origin of the overlimiting current,” The Journal of Physical Chemistry B, vol. 111, no. 9, pp. 2152–2165, 2007.
[23]  O. V. Grigorchuk, V. I. Vasil'eva, and V. A. Shaposhnik, “Local characteristics of mass transfer under electrodialysis demineralization,” Desalination, vol. 184, no. 1–3, pp. 431–438, 2005.
[24]  V. M. Barragán and C. Ruíz-Bauzá, “Current-voltage curves for ion-exchange membranes: a method for determining the limiting current density,” Journal of Colloid and Interface Science, vol. 205, no. 2, pp. 365–373, 1998.
[25]  J. Koryta, J. Dvorak, and L. Kavan, Principles of Electrochemistry, John Wiley & Sons, New York, NY, USA, 2nd edition, 1993.
[26]  N. Kabay, M. Demircioglu, E. Ers?z, and I. Kurucaovali, “Removal of calcium and magnesium hardness of electrodialysis,” Desalination, vol. 149, no. 1–3, pp. 343–349, 2002.
[27]  M. Araya-Farias and L. Bazinet, “Electrodialysis of calcium and carbonate high-concentration solutions and impact on membrane fouling,” Desalination, vol. 200, no. 1–3, p. 624, 2006.
[28]  http://www4.ncsu.edu/~franzen/public_html/CH201/data/Solubility_Product_Constants.pdf.

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