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Immobilizing Different Carbon Sources in Alginate Beads for Melanoidins Removal from Yeast Effluents

Received: 21 January 2017    Accepted: 21 February 2017    Published: 22 March 2017
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Abstract

Presently work describes a new method for melanoidins removal encountered in yeast industry effluents. Three different kinds of carbon sources were inmobilized in alginate beads and include rubber tire pyrolysis, activated carbon and multiwalled nanotubes. The yeast effluent was obtained through aerobic fermentation with 40 g/L of molasses. The effluent was separated through filtration. The alginate beads consisted in 3 g of alginate and 4 g of the carbon sources, which were dissolved in one liter of distilled water. The last was added drop by drop into a solution of CaCl2 (15 g/L). The alginate beads were used in different proportions (w/v) in the effluent (1:6, 1:3.5, 1:2.6 and 1:1). The melanoidins amount adsorbed was determined through a spectrophotometer UV vis (600 nm). At 1:1, the concentration of melanoidins at the equilibrium (qe) for rubber pyrolysis was 3.5 mg/g, for the activated carbon was 5.0 mg/g, for multiwalled nanotubes qe was 5.3 mg/g and when the alginate beads probed alone qe was only 1.5 mg/g. In order to predict the adsorption capacity in a continuous stirred tank we assessed the saturation constant (Ks) in the batch treatments. The continuous fermenter was simulated from 0.01 to 1.0 h-1 dilution rates. At the lowest proportion (w/v) 1:6 the maximum sorbtion capacity was at 0.427 g/L.h obtained with the rubber pyrolysis at 0.26 h-1. When we used a proportions (w/v) of 1:3.5, 1:2.6 and 1:1, the maximum adsorption capacity were 0.77, 1.04 and 1.13 g/L.h, respectively and these values were obtained with multiwalled nanotubes.

Published in Journal of Chemical, Environmental and Biological Engineering (Volume 1, Issue 1)
DOI 10.11648/j.jcebe.20170101.13
Page(s) 14-21
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

Carbon Sources, Alginate Beads, Melanoidins, Removal, Continuous Treatment, Batch Treatment, Simulations

References
[1] Zub S., Kurissoo T., Manert A., Blonkaja V., (2008). Combined biological treatment of high sulphate wastewater from yeast production. Water and Environmental Journal. 22, 274-286.
[2] Liang, Z., Wang, Y., Zhou, Y., Liu, H., Wu, Z. (2009). Variables affecting melanoidin containing wastewater by coagulation/flocculation. Separation and Purification Technology 68 (3): 382-389.
[3] Kalyuzhnyi S., Gladchenko M., Starostina E., Shcherbakov S., Versprille A., (2005). Combined biological and physico-chemical treatment of baker's yeast wastewater. Water Science and Technology, 52, 175–181.
[4] Gengec E., Kobya M., Demirbas E., Akyol A., Oktor K. (2012). Optimization of baker's yeast wastewater using response surface methodology by electrocoagulation. Desalination, 286, 200–209.
[5] Wedzicha B. L., Kaputo M. T., (1992). Melanoidins from glucose and glycine: composition, characteristics and reactivity towards sulphite ion. Food Chemistry, 43, 359–367.
[6] Braccini, I., Grasso, R. P. and Perez S. (1999). Alginate uses: a review. Carbohidrate Research, 317: 119-130.
[7] Wojtowick, M. A., & Serio M. A. (1996). Pyrolysis of scrap tires: Can it be profitable? Chemtech, 48-54.
[8] Liakos, T. I., & Lazaridis, N. K. (2016). Melanoidin removal from molasses effluents by adsorption. Journal of Water Process Engineering, 10: 156-164.
[9] Ho, Y. S., & McKay, G. (1999). Pseudo-second order model for sorption processes. Process Biochemistry, 34: 451-465.
[10] Ojijo, V. O., Onyango, M. S., Ochieng, A., Otieno F. A. O. (2010). Decolourization of Melanoidin Containing Wastewater Using South African Coal Fly Ash. International Journal of Chemical, Molecular, Nuclear, Materials and Metallurgical Engineering, 4 (1): 58-64.
[11] Figaro, S., Avril, J., Brouers, F., Ouensanga, A., Gaspard, S. (2009). Adsorption studies of molasse`s wastewaters on activated carbon: modeling with a new fractal kinetic equation and evaluation of kinetic models. Journal of Hazardous Materials, 161: 649-656.
[12] Dunn, I. J., Heinzle, E., Inham, J. Bioreaction Engineering Principles. Biological Reaction Engineering: Dynamic Modeling Fundamentals with Simulation Examples. 2th Ed. Wiley-VCH & kGaA, Weinheim. 2011.
[13] Onyango, M. S., Kittinya, J., Hadebe, N, Ojijo, V. O., Ochieng, A. (2011). Sorption of melanoidin onto surfactant modified zeolite. CI&CEQ 17 (4): 385−395.
[14] Satyawali, Y., & Balakrishnan M. (2007). Removal of color from biomethanated distillery spentwash by treatment with activated carbons. Bioresource Technology, 98: 2629-2635.
[15] Venkat, S. M., Krishna, S. M., Karthikeyan, J. (2000). Adsorption mechanism of the acid-azo dye from aqueous solution on to coal based sorbents and activated carbon. Analytical techniques in monitoring the Environment. Tiruphathi, India, pp. 97-103.
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    César Reyes-Reyes, Hebert Jair Barrales-Cureño, Petra Andrade-Hoyos, Rocío Fuentes-Galvan, Fernando Michel Zamora-Espinoza, et al. (2017). Immobilizing Different Carbon Sources in Alginate Beads for Melanoidins Removal from Yeast Effluents. Journal of Chemical, Environmental and Biological Engineering, 1(1), 14-21. https://doi.org/10.11648/j.jcebe.20170101.13

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    César Reyes-Reyes; Hebert Jair Barrales-Cureño; Petra Andrade-Hoyos; Rocío Fuentes-Galvan; Fernando Michel Zamora-Espinoza, et al. Immobilizing Different Carbon Sources in Alginate Beads for Melanoidins Removal from Yeast Effluents. J. Chem. Environ. Biol. Eng. 2017, 1(1), 14-21. doi: 10.11648/j.jcebe.20170101.13

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    AMA Style

    César Reyes-Reyes, Hebert Jair Barrales-Cureño, Petra Andrade-Hoyos, Rocío Fuentes-Galvan, Fernando Michel Zamora-Espinoza, et al. Immobilizing Different Carbon Sources in Alginate Beads for Melanoidins Removal from Yeast Effluents. J Chem Environ Biol Eng. 2017;1(1):14-21. doi: 10.11648/j.jcebe.20170101.13

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  • @article{10.11648/j.jcebe.20170101.13,
      author = {César Reyes-Reyes and Hebert Jair Barrales-Cureño and Petra Andrade-Hoyos and Rocío Fuentes-Galvan and Fernando Michel Zamora-Espinoza and Omar Alberto Hernández-Aguirre and Ketzasmin Armando Terrón-Mejía and Juan Antonio Cortes-Ruíz and Jordi Orlando González Osuna and Luis Germán López-Valdez and Salvador Chávez-Salinas},
      title = {Immobilizing Different Carbon Sources in Alginate Beads for Melanoidins Removal from Yeast Effluents},
      journal = {Journal of Chemical, Environmental and Biological Engineering},
      volume = {1},
      number = {1},
      pages = {14-21},
      doi = {10.11648/j.jcebe.20170101.13},
      url = {https://doi.org/10.11648/j.jcebe.20170101.13},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.jcebe.20170101.13},
      abstract = {Presently work describes a new method for melanoidins removal encountered in yeast industry effluents. Three different kinds of carbon sources were inmobilized in alginate beads and include rubber tire pyrolysis, activated carbon and multiwalled nanotubes. The yeast effluent was obtained through aerobic fermentation with 40 g/L of molasses. The effluent was separated through filtration. The alginate beads consisted in 3 g of alginate and 4 g of the carbon sources, which were dissolved in one liter of distilled water. The last was added drop by drop into a solution of CaCl2 (15 g/L). The alginate beads were used in different proportions (w/v) in the effluent (1:6, 1:3.5, 1:2.6 and 1:1). The melanoidins amount adsorbed was determined through a spectrophotometer UV vis (600 nm). At 1:1, the concentration of melanoidins at the equilibrium (qe) for rubber pyrolysis was 3.5 mg/g, for the activated carbon was 5.0 mg/g, for multiwalled nanotubes qe was 5.3 mg/g and when the alginate beads probed alone qe was only 1.5 mg/g. In order to predict the adsorption capacity in a continuous stirred tank we assessed the saturation constant (Ks) in the batch treatments. The continuous fermenter was simulated from 0.01 to 1.0 h-1 dilution rates. At the lowest proportion (w/v) 1:6 the maximum sorbtion capacity was at 0.427 g/L.h obtained with the rubber pyrolysis at 0.26 h-1. When we used a proportions (w/v) of 1:3.5, 1:2.6 and 1:1, the maximum adsorption capacity were 0.77, 1.04 and 1.13 g/L.h, respectively and these values were obtained with multiwalled nanotubes.},
     year = {2017}
    }
    

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  • TY  - JOUR
    T1  - Immobilizing Different Carbon Sources in Alginate Beads for Melanoidins Removal from Yeast Effluents
    AU  - César Reyes-Reyes
    AU  - Hebert Jair Barrales-Cureño
    AU  - Petra Andrade-Hoyos
    AU  - Rocío Fuentes-Galvan
    AU  - Fernando Michel Zamora-Espinoza
    AU  - Omar Alberto Hernández-Aguirre
    AU  - Ketzasmin Armando Terrón-Mejía
    AU  - Juan Antonio Cortes-Ruíz
    AU  - Jordi Orlando González Osuna
    AU  - Luis Germán López-Valdez
    AU  - Salvador Chávez-Salinas
    Y1  - 2017/03/22
    PY  - 2017
    N1  - https://doi.org/10.11648/j.jcebe.20170101.13
    DO  - 10.11648/j.jcebe.20170101.13
    T2  - Journal of Chemical, Environmental and Biological Engineering
    JF  - Journal of Chemical, Environmental and Biological Engineering
    JO  - Journal of Chemical, Environmental and Biological Engineering
    SP  - 14
    EP  - 21
    PB  - Science Publishing Group
    SN  - 2640-267X
    UR  - https://doi.org/10.11648/j.jcebe.20170101.13
    AB  - Presently work describes a new method for melanoidins removal encountered in yeast industry effluents. Three different kinds of carbon sources were inmobilized in alginate beads and include rubber tire pyrolysis, activated carbon and multiwalled nanotubes. The yeast effluent was obtained through aerobic fermentation with 40 g/L of molasses. The effluent was separated through filtration. The alginate beads consisted in 3 g of alginate and 4 g of the carbon sources, which were dissolved in one liter of distilled water. The last was added drop by drop into a solution of CaCl2 (15 g/L). The alginate beads were used in different proportions (w/v) in the effluent (1:6, 1:3.5, 1:2.6 and 1:1). The melanoidins amount adsorbed was determined through a spectrophotometer UV vis (600 nm). At 1:1, the concentration of melanoidins at the equilibrium (qe) for rubber pyrolysis was 3.5 mg/g, for the activated carbon was 5.0 mg/g, for multiwalled nanotubes qe was 5.3 mg/g and when the alginate beads probed alone qe was only 1.5 mg/g. In order to predict the adsorption capacity in a continuous stirred tank we assessed the saturation constant (Ks) in the batch treatments. The continuous fermenter was simulated from 0.01 to 1.0 h-1 dilution rates. At the lowest proportion (w/v) 1:6 the maximum sorbtion capacity was at 0.427 g/L.h obtained with the rubber pyrolysis at 0.26 h-1. When we used a proportions (w/v) of 1:3.5, 1:2.6 and 1:1, the maximum adsorption capacity were 0.77, 1.04 and 1.13 g/L.h, respectively and these values were obtained with multiwalled nanotubes.
    VL  - 1
    IS  - 1
    ER  - 

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Author Information
  • Ingeniería en Biotecnología, Universidad Politécnica del Valle de Toluca, Almoloya de Juárez, México

  • División de Procesos Naturales, Ingeniería Forestal Comunitaria, Universidad Intercultural del Estado de Puebla, Lipuntahuaca, Huehuetla, Puebla

  • Ingeniería en Biotecnología, Universidad Politécnica del Valle de Toluca, Almoloya de Juárez, México

  • Ingeniería en Biotecnología, Universidad Politécnica del Valle de Toluca, Almoloya de Juárez, México

  • Ingeniería en Biotecnología, Universidad Politécnica del Valle de Toluca, Almoloya de Juárez, México

  • Ingeniería en Biotecnología, Universidad Politécnica del Valle de Toluca, Almoloya de Juárez, México

  • Ingeniería Bioquímica, Instituto Tecnológico de Mazatlán, México

  • Ingeniería en Biotecnología, Universidad Politécnica del Valle de Toluca, Almoloya de Juárez, México

  • Laboratorio de Productos Naturales, área de Química, Departamento de Preparatoria Agricola, Universidad Autónoma Chapingo, Texcoco, Estado de México

  • Ingeniería en Biotecnología, Universidad Politécnica del Valle de Toluca, Almoloya de Juárez, México

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