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Reactive Extraction of Propionic Acid: Equilibrium and Kinetic Studies

Received: 30 May 2022    Accepted: 24 June 2022    Published: 5 July 2022
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Abstract

Reactive extraction is an efficient, economical and environmentally friendly method for separating acids from waste streams. The separation of organic residues from aqueous waste streams released from industries is essential from the point of view of pollution control and recovery of useful materials. Propionic acid has become an important feedstock in chemical industries for manufacturing biodegradable polymers and synthetic resins. The disposal of wastewater containing propionic acid has been recognized as a significant expense to the industry and the environment. This study used reactive extraction to separate propionic acid from an aqueous solution using Tri-n-Pentyl Amine and Tri-n-Butyl Amine with different diluents. Kinetic variables such as order of reaction, mass transfer coefficient and rate constants were determined by conducting kinetic studies using a stirred cell in a batch-type reactive system. Physical equilibrium experiments showed that 1-Octanol has the highest extractable strength compared to chloroform and dimethylene chloride. The distribution coefficient of chemical extraction is higher than that of physical extraction. Effect of acid (0.1 to 0.4 N), amine concentration (10% to 40%) is noticed in terms of Distribution coefficient KD in the range of 3 to 19 for TPA and KD in the range of 1.5 to 5.67 for TBA at 0.1N. The Equilibrium complexion constant (KE1) was calculated using the loading ratio (Z) at 10% to 40% amine in 1-octanol. At 40% maximum Equilibrium complexion constants for TPA KE1=10.28 and TBA KE1=5.94 were obtained. The reaction regime depended on the Hatta number value, with TPA being instantaneous and TBA being a fast reaction. The enhancement factors for TPA and TBA were found to be 5.1 and 3.8, respectively.

Published in American Journal of Chemical Engineering (Volume 10, Issue 4)
DOI 10.11648/j.ajche.20221004.11
Page(s) 63-71
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Equilibrium, Kinetics, Reactive Extraction, Propionic Acid

References
[1] Keshav, and S. Chand, "Extraction of propionic acid using different extractants (tri-n-butyl phosphate, tri-n-octylamine, and Aliquat 336)," Industrial and Engineering Chemistry Research, vol. 47, no. 16, page: 6192–6196, 2008.
[2] Guocheng Du, Long Liu, Jian Chen “White Biotechnology for organic acids” Industrial Biorefineries and white Biotechnology, page: 409-444, 2015.
[3] A. S. Kertes and C. J. King, “Extraction chemistry of fermentation product carboxylic acids,” Biotechnology and Bioengineering, vol. 28, no. 2, pp. 269–282, 1986.
[4] Dipaloy Datta, Sushil Kumar, and Hassan Uslu Status of the Reactive Extraction as a Method of Separation”, Journal of Chemistry Volume, Article ID 853789, page: 16, 2015.
[5] R. Wennersten, “Extraction of carboxylic acid from fermentation broth in using solution of tertiary amine,” Journal of Chemical Technology and Biotechnology, no. 2, page. 85–94, 1983.
[6] J. A. Tamada, A. S. Kertes, and C. J. King, Extraction of carboxylic acids with amine extractants. 1. Equilibria and law of mass action modeling,” Industrial and Engineering Chemistry Research, vol. 29, no. 7, page. 1319–1326, 1990.
[7] Sumalatha Eda, T. Pratap kumar, and B. satyavathi"Recovery of succinic acid by Reactive extraction using tri-n-octylamine in 1-decanol: Equilibrium optimization using Response suraface method and kinetic studies" International Journal of chemical separation technology, vol. 2, no 2, 2016.
[8] J. Hartl and R. Marr, “Extraction processes for bioproduct separation,” Separation Science and Technology, vol. 28, no. 1–3, page. 805–819, 1993.
[9] J. M. Wardell and C. J. King, “Solvent equilibria for extraction of carboxylic acids from water,” Journal of Chemical & Engineering Data, vol. 23, no. 2, page. 144–148, 1978.
[10] T. Prathap kumar, B. Vishwanadham, K. N. Prasanna Rani, and V. V. Basavarao, "Reactive extraction of Levulinic acid from aqueous solutions with tri-n-octylamine (TOA) in 1-octanol: Equilibria, kinetics, and model development" chemical engineering communication, 198: 572-589, 2011.
[11] V. Bízek, J. Horáček, R. Řeřicha, and M. Koušová, “Amine extraction of hydroxycarboxylic acids. 1. Extraction of citric acid with 1-octanol/n-heptane solutions of trialkylamine,” Industrial & Engineering Chemistry Research, vol. 31, no. 6, page. 1554–1562, 1992.
[12] Doraiswamy, L. K., and Sharma, M. M. "Heterogeneous Reaction Analysis, Examples and Reactor Design, Fluid-Fluid-Solid-Reactions, John Wiley, New York, vol. 2, 1984.
[13] Dharmapala, and Keshav, A. “kinetics of reactive extraction for the separation of pyruvic acid using Tri-n-butylamine dissolved in butyl acetate” International journal of chemical reactor engineering, vol 13, page: 63-69, 2015.
[14] Madhumala, M. et al., Extraction of acetic acid from aquoeus media using indigenous Liquid-Liquid membrane contactor system, Journal of chemical Engineering Research Studies, vol. 2, Page: 1-9, 2015.
[15] Octave levenspiel "Chemical Reaction Engineering", Jhon Wiley & sons, third edition, Singapore, Chapter 23, page: 529, 2001.
[16] Mustafa, E., Marti, Turker Gurkan, “Equilibrium and kinetic studies on reactive extraction of pyruvic acid with Tri- octylamine in 1-octanol”. Industrial and Engineering Chemistry Research, vol. 50, page: 13518–13525, 2011.
[17] Shitanshu Pandey and Sushil Kumar. "Reactive Extraction of Gallic Acid Using Aminic and Phosphoric Extractants Dissolved in Different Diluents: Effect of Solvent’s Polarity and Column Design", Industrial & Engineering Chemistry Research, vol. 57 (8), page: 2976-2987, 2018.
[18] Sunderlal, P., Diwaker, Z. S., Shahida, A., Rathore, A. K. "Reactive extraction of Itaconic acid Using Tri-n- Butyl phosphate in 1- Butanol, 1-Octanol and 1-Dodecanol", International Journal of Research in Science, Engineering and Technology, vol. 5, page: 14251433, 2016.
[19] Uslu, H., Dipaloy data, Hisham S., Bamufleh, "Reactive Extraction of phenol from aqueous solution using tri octyl methyl ammonium chloride and tri octylamine in nonane and isoamyl alcohol", Article in water air and soil pollution, vol. 227, page: 804–809, 2016.
[20] Vicky, R. Dhongde, Biswajit, S. De., Wasewar, K. L. Experimental Study on Reactive Extraction of Malonic Acid with Validation by Fourier Transform Infrared Spectroscopy. Journal of Chemical & Engineering Data, vol. 64 (3), page: 1072-1084, 2019.
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  • APA Style

    Sunitha Palleti, Sadam Ilaiah, Vudata Venkata Basava Rao. (2022). Reactive Extraction of Propionic Acid: Equilibrium and Kinetic Studies. American Journal of Chemical Engineering, 10(4), 63-71. https://doi.org/10.11648/j.ajche.20221004.11

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    ACS Style

    Sunitha Palleti; Sadam Ilaiah; Vudata Venkata Basava Rao. Reactive Extraction of Propionic Acid: Equilibrium and Kinetic Studies. Am. J. Chem. Eng. 2022, 10(4), 63-71. doi: 10.11648/j.ajche.20221004.11

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    AMA Style

    Sunitha Palleti, Sadam Ilaiah, Vudata Venkata Basava Rao. Reactive Extraction of Propionic Acid: Equilibrium and Kinetic Studies. Am J Chem Eng. 2022;10(4):63-71. doi: 10.11648/j.ajche.20221004.11

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  • @article{10.11648/j.ajche.20221004.11,
      author = {Sunitha Palleti and Sadam Ilaiah and Vudata Venkata Basava Rao},
      title = {Reactive Extraction of Propionic Acid: Equilibrium and Kinetic Studies},
      journal = {American Journal of Chemical Engineering},
      volume = {10},
      number = {4},
      pages = {63-71},
      doi = {10.11648/j.ajche.20221004.11},
      url = {https://doi.org/10.11648/j.ajche.20221004.11},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajche.20221004.11},
      abstract = {Reactive extraction is an efficient, economical and environmentally friendly method for separating acids from waste streams. The separation of organic residues from aqueous waste streams released from industries is essential from the point of view of pollution control and recovery of useful materials. Propionic acid has become an important feedstock in chemical industries for manufacturing biodegradable polymers and synthetic resins. The disposal of wastewater containing propionic acid has been recognized as a significant expense to the industry and the environment. This study used reactive extraction to separate propionic acid from an aqueous solution using Tri-n-Pentyl Amine and Tri-n-Butyl Amine with different diluents. Kinetic variables such as order of reaction, mass transfer coefficient and rate constants were determined by conducting kinetic studies using a stirred cell in a batch-type reactive system. Physical equilibrium experiments showed that 1-Octanol has the highest extractable strength compared to chloroform and dimethylene chloride. The distribution coefficient of chemical extraction is higher than that of physical extraction. Effect of acid (0.1 to 0.4 N), amine concentration (10% to 40%) is noticed in terms of Distribution coefficient KD in the range of 3 to 19 for TPA and KD in the range of 1.5 to 5.67 for TBA at 0.1N. The Equilibrium complexion constant (KE1) was calculated using the loading ratio (Z) at 10% to 40% amine in 1-octanol. At 40% maximum Equilibrium complexion constants for TPA KE1=10.28 and TBA KE1=5.94 were obtained. The reaction regime depended on the Hatta number value, with TPA being instantaneous and TBA being a fast reaction. The enhancement factors for TPA and TBA were found to be 5.1 and 3.8, respectively.},
     year = {2022}
    }
    

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  • TY  - JOUR
    T1  - Reactive Extraction of Propionic Acid: Equilibrium and Kinetic Studies
    AU  - Sunitha Palleti
    AU  - Sadam Ilaiah
    AU  - Vudata Venkata Basava Rao
    Y1  - 2022/07/05
    PY  - 2022
    N1  - https://doi.org/10.11648/j.ajche.20221004.11
    DO  - 10.11648/j.ajche.20221004.11
    T2  - American Journal of Chemical Engineering
    JF  - American Journal of Chemical Engineering
    JO  - American Journal of Chemical Engineering
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    EP  - 71
    PB  - Science Publishing Group
    SN  - 2330-8613
    UR  - https://doi.org/10.11648/j.ajche.20221004.11
    AB  - Reactive extraction is an efficient, economical and environmentally friendly method for separating acids from waste streams. The separation of organic residues from aqueous waste streams released from industries is essential from the point of view of pollution control and recovery of useful materials. Propionic acid has become an important feedstock in chemical industries for manufacturing biodegradable polymers and synthetic resins. The disposal of wastewater containing propionic acid has been recognized as a significant expense to the industry and the environment. This study used reactive extraction to separate propionic acid from an aqueous solution using Tri-n-Pentyl Amine and Tri-n-Butyl Amine with different diluents. Kinetic variables such as order of reaction, mass transfer coefficient and rate constants were determined by conducting kinetic studies using a stirred cell in a batch-type reactive system. Physical equilibrium experiments showed that 1-Octanol has the highest extractable strength compared to chloroform and dimethylene chloride. The distribution coefficient of chemical extraction is higher than that of physical extraction. Effect of acid (0.1 to 0.4 N), amine concentration (10% to 40%) is noticed in terms of Distribution coefficient KD in the range of 3 to 19 for TPA and KD in the range of 1.5 to 5.67 for TBA at 0.1N. The Equilibrium complexion constant (KE1) was calculated using the loading ratio (Z) at 10% to 40% amine in 1-octanol. At 40% maximum Equilibrium complexion constants for TPA KE1=10.28 and TBA KE1=5.94 were obtained. The reaction regime depended on the Hatta number value, with TPA being instantaneous and TBA being a fast reaction. The enhancement factors for TPA and TBA were found to be 5.1 and 3.8, respectively.
    VL  - 10
    IS  - 4
    ER  - 

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Author Information
  • Department of Chemical Engineering, University College of Technology, Osmania University, Hyderabad, India

  • Department of Chemical Engineering, University College of Technology, Osmania University, Hyderabad, India

  • Department of Chemical Engineering, University College of Technology, Osmania University, Hyderabad, India

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