American Journal of Quantum Chemistry and Molecular Spectroscopy

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Kinetic and Thermodynamic Studies of the Oxidation of Xylose in the Presence and Absence of Catalysts by Peroxdisuphate

Received: 05 August 2019    Accepted: 27 January 2020    Published: 06 July 2020
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Abstract

Sugars containing either aldehyde (aldose), ketone (ketose) or hemiacetal groups can be oxidized and are classified as reducing sugars. As oxidation of carbohydrates is widely studied under the field of organic chemistry, the present work deals with the study of the redox reactions between peroxodisulphate and xylose underuncatalyzed and catalyzed conditions. The kinetic study of the above reactions showed that these reactions followed first order with respect to peroxodisulphate and the silver nitrate ion catalyst and a fractional order of (0.2) with respect to xylose. Ag catalyst was used to increase the rate of reaction in case of xylose where reactions proceed very slowly with respect to time as compared to other sugars used. The oxidation showed that configuration of sugars has some bearing on rate of oxidation. At lower concentration of oxidants, the linear dependence of reaction rate tends towards new order at their higher concentration. The rate of reaction was affected at elevated temperature where thermodynamic activation parameters like activation energy (Ea), enthalpy change of activation (∆H#), free energy change of activation (∆G#) and entropy change of activation (∆S#) were determined by Arrhenius and Erying equations. The analysis of the reaction products using IR revealed the presence of formaldehyde and formic acid. A mechanism of the reactions was proposed to explain the experimentally observed rate law and the products.

DOI 10.11648/j.ajqcms.20200401.11
Published in American Journal of Quantum Chemistry and Molecular Spectroscopy (Volume 4, Issue 1, June 2020)
Page(s) 1-6
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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

Oxidation, Kinetic, Xylose, Peroxodisulphate

References
[1] Finar L. L., Organic Chemistry Vol. 1: The Fundamental Principles, Sixth Edition (1973).
[2] Brand Hans, Brand Elzbieta, Goliath Buissness Knowledge on Demand (2002).
[3] Singh M. P., Singh H. S., Tiwari S. C., Gupta K. C., Singh A. K., Singh V. P. and Singh R. K., (1975). Oxidation of D-glucose, D-xylose, D-fructose, L-arabinose and L- sorbose by ammoniacal silver nitrate, Ind. J. of Chem. 13, 819-22.
[4] Prashanth P. A., Mantelingu K., Anandamurthy A. S., Anitha N., Rangaswamy and Rangappa K. S., (2001). Kinetics and mechanism of oxidation of hexoses by bromamine-T in alkaline medium, J. Ind. Chem. Soc., 78.
[5] Chandrashekar, Venkatesha B. M. and Ananda S., (2012). Kinetics of Oxidation of Vitamin-B3 (Niacin) by Sodium N-bromo benzenesulphonamide (Bromamine-B) in HCl Medium and Catalysis by Rum (III) ion, Res. J. chem. sci., 2 (8), 26-30.
[6] Sarasan Geetha and Pathak Namrata, (2014). Effect of Acetic Acid on Chlorination of some Phenols by Chloramine-T: A Kinetic Approach, Res. J. chem. sci., 4 (3), 86-89.
[7] Johnson, R. L., Tratnyek, P. G. and Johnson, R. O. (2008). Persulfate persistence under thermal activation conditions”, Environ. Sci. Technol., 42 (24), 9350-9356.
[8] Huie, R. E. and Neta, P. (1984). Chemical behavior of SO3- and SO5- radicals in aqueous solutions”, J. Phys. Chem., 88 (23), 5665-5669.
[9] Deepa D. and Chandramohan G., (2012). Kinetic and Mechanistic Study on the Oxidation of Indole-3-Propionic Acid in Acetic Acid Medium Res. J. Chem. Sci., 2 (10), 70-74.
[10] Ghosh Manoj Kumar and Rajput Surendra K., (2012) Unanalyzed Oxidation of Dextrose by Cerium (IV) in Aqueous Acidic Medium-A Kinetic and Mechanistic Study, Res. J. Chem. Sci., 2 (11), 55-60.
[11] Junlian Qiao, Liying Feng, Hongyu Dong, Zhiwei Zhao, Xiaohong Guan. Overlooked Role of Sulfur-Centered Radicals During Bromate Reduction by Sulfite. Environmental Science & Technology 2019, 53 (17), 10320-10328. DOI: 10.1021/acs.est.9b01783.
[12] Rama Rao. K, Rambabu. R, Raghu Babu. K. International Journal of Innovative Research in Science Engineering and Technology Vol 2, Issue 11, 2013. Titrimetric estimation of ascorbic acid, hydrazine, sodium sulphite, thiosulphate and vanadium (II) with chloramine-Tas an acidimetric reagent in EDTA medium.
Author Information
  • Department of Chemistry, Faculty of Science and Technology, Merowe University of Technology, Merowe, Sudan; Department of Chemistry, College of Science, Beijing University of Chemical Technology, Beijing, China

  • Department of Chemistry, Faculty of Education, Dalanj University, Dalanj, Sudan

  • Department of Chemistry, Faculty of Education, University of Khartoum, Khartoum, Sudan

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    Mawia Hassan Elsaim, Jubrallah Elhaj, Ibrahim Mukhtar. (2020). Kinetic and Thermodynamic Studies of the Oxidation of Xylose in the Presence and Absence of Catalysts by Peroxdisuphate. American Journal of Quantum Chemistry and Molecular Spectroscopy, 4(1), 1-6. https://doi.org/10.11648/j.ajqcms.20200401.11

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    Mawia Hassan Elsaim; Jubrallah Elhaj; Ibrahim Mukhtar. Kinetic and Thermodynamic Studies of the Oxidation of Xylose in the Presence and Absence of Catalysts by Peroxdisuphate. Am. J. Quantum Chem. Mol. Spectrosc. 2020, 4(1), 1-6. doi: 10.11648/j.ajqcms.20200401.11

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    AMA Style

    Mawia Hassan Elsaim, Jubrallah Elhaj, Ibrahim Mukhtar. Kinetic and Thermodynamic Studies of the Oxidation of Xylose in the Presence and Absence of Catalysts by Peroxdisuphate. Am J Quantum Chem Mol Spectrosc. 2020;4(1):1-6. doi: 10.11648/j.ajqcms.20200401.11

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  • @article{10.11648/j.ajqcms.20200401.11,
      author = {Mawia Hassan Elsaim and Jubrallah Elhaj and Ibrahim Mukhtar},
      title = {Kinetic and Thermodynamic Studies of the Oxidation of Xylose in the Presence and Absence of Catalysts by Peroxdisuphate},
      journal = {American Journal of Quantum Chemistry and Molecular Spectroscopy},
      volume = {4},
      number = {1},
      pages = {1-6},
      doi = {10.11648/j.ajqcms.20200401.11},
      url = {https://doi.org/10.11648/j.ajqcms.20200401.11},
      eprint = {https://download.sciencepg.com/pdf/10.11648.j.ajqcms.20200401.11},
      abstract = {Sugars containing either aldehyde (aldose), ketone (ketose) or hemiacetal groups can be oxidized and are classified as reducing sugars. As oxidation of carbohydrates is widely studied under the field of organic chemistry, the present work deals with the study of the redox reactions between peroxodisulphate and xylose underuncatalyzed and catalyzed conditions. The kinetic study of the above reactions showed that these reactions followed first order with respect to peroxodisulphate and the silver nitrate ion catalyst and a fractional order of (0.2) with respect to xylose. Ag catalyst was used to increase the rate of reaction in case of xylose where reactions proceed very slowly with respect to time as compared to other sugars used. The oxidation showed that configuration of sugars has some bearing on rate of oxidation. At lower concentration of oxidants, the linear dependence of reaction rate tends towards new order at their higher concentration. The rate of reaction was affected at elevated temperature where thermodynamic activation parameters like activation energy (Ea), enthalpy change of activation (∆H#), free energy change of activation (∆G#) and entropy change of activation (∆S#) were determined by Arrhenius and Erying equations. The analysis of the reaction products using IR revealed the presence of formaldehyde and formic acid. A mechanism of the reactions was proposed to explain the experimentally observed rate law and the products.},
     year = {2020}
    }
    

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    T1  - Kinetic and Thermodynamic Studies of the Oxidation of Xylose in the Presence and Absence of Catalysts by Peroxdisuphate
    AU  - Mawia Hassan Elsaim
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    AU  - Ibrahim Mukhtar
    Y1  - 2020/07/06
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    T2  - American Journal of Quantum Chemistry and Molecular Spectroscopy
    JF  - American Journal of Quantum Chemistry and Molecular Spectroscopy
    JO  - American Journal of Quantum Chemistry and Molecular Spectroscopy
    SP  - 1
    EP  - 6
    PB  - Science Publishing Group
    SN  - 2994-7308
    UR  - https://doi.org/10.11648/j.ajqcms.20200401.11
    AB  - Sugars containing either aldehyde (aldose), ketone (ketose) or hemiacetal groups can be oxidized and are classified as reducing sugars. As oxidation of carbohydrates is widely studied under the field of organic chemistry, the present work deals with the study of the redox reactions between peroxodisulphate and xylose underuncatalyzed and catalyzed conditions. The kinetic study of the above reactions showed that these reactions followed first order with respect to peroxodisulphate and the silver nitrate ion catalyst and a fractional order of (0.2) with respect to xylose. Ag catalyst was used to increase the rate of reaction in case of xylose where reactions proceed very slowly with respect to time as compared to other sugars used. The oxidation showed that configuration of sugars has some bearing on rate of oxidation. At lower concentration of oxidants, the linear dependence of reaction rate tends towards new order at their higher concentration. The rate of reaction was affected at elevated temperature where thermodynamic activation parameters like activation energy (Ea), enthalpy change of activation (∆H#), free energy change of activation (∆G#) and entropy change of activation (∆S#) were determined by Arrhenius and Erying equations. The analysis of the reaction products using IR revealed the presence of formaldehyde and formic acid. A mechanism of the reactions was proposed to explain the experimentally observed rate law and the products.
    VL  - 4
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