IDEAS home Printed from https://ideas.repec.org/a/gam/jsusta/v16y2024i2p858-d1322298.html
   My bibliography  Save this article

Microwave-Assisted Production of 5-Hydroxymethylfurfural from Fructose Using Sulfamic Acid as a Green Catalyst

Author

Listed:
  • Vinícius Bertoncello Molon

    (Laboratório de Biotecnologia de Produtos Naturais e Sintéticos, Universidade de Caxias do Sul, Caxias do Sul 95070-560, RS, Brazil)

  • Bruno Luís Ferreira

    (Laboratório de Biotecnologia de Produtos Naturais e Sintéticos, Universidade de Caxias do Sul, Caxias do Sul 95070-560, RS, Brazil)

  • Carolina Colombo Tedesco

    (Laboratório de Biotecnologia de Produtos Naturais e Sintéticos, Universidade de Caxias do Sul, Caxias do Sul 95070-560, RS, Brazil)

  • Maria Gabriele Delagustin

    (Laboratório de Biotecnologia de Produtos Naturais e Sintéticos, Universidade de Caxias do Sul, Caxias do Sul 95070-560, RS, Brazil)

  • Thiago Barcellos

    (Laboratório de Biotecnologia de Produtos Naturais e Sintéticos, Universidade de Caxias do Sul, Caxias do Sul 95070-560, RS, Brazil)

Abstract

The development of safe-by-design synthesis of valuable chemicals from biomass derivatives is a key step towards sustainable chemical transformations in both academia and industry. 5-Hydroxymethylfurfural (5-HMF) is a biomass derivative chemical of high commercial interest due to its wide range of chemical and biofuel applications. In this scenario, the present work contributes to a methodology for producing 5-hydroxymethylfurfural (5-HMF) through fructose dehydration reaction under microwave irradiation. The proposed protocol uses a simple sodium chloride–saturated aqueous- i -PrOH biphasic system and catalysis of sulfamic acid, a low-cost solid Brønsted–Lowry inorganic acid, which presents pivotal features of a sustainable catalyst. A 2 3 full factorial design was applied to achieve the highest conversion and 5-HMF yield, allowing the identification of the main factors involved in the process. Under the optimized conditions, fructose at the concentration of 120 g L −1 was converted with 91.15 ± 6.98% after 20 min at 180 °C, using 10 mol% of catalyst. 5-HMF was produced in 80.34 ± 8.41% yield and 73.20 ± 8.23% selectivity. Thus, the present contribution discloses a new optimized methodology for converting the biomass derivative fructose to 5-hydroxymethylfurfural (5-HMF).

Suggested Citation

  • Vinícius Bertoncello Molon & Bruno Luís Ferreira & Carolina Colombo Tedesco & Maria Gabriele Delagustin & Thiago Barcellos, 2024. "Microwave-Assisted Production of 5-Hydroxymethylfurfural from Fructose Using Sulfamic Acid as a Green Catalyst," Sustainability, MDPI, vol. 16(2), pages 1-12, January.
  • Handle: RePEc:gam:jsusta:v:16:y:2024:i:2:p:858-:d:1322298
    as

    Download full text from publisher

    File URL: https://www.mdpi.com/2071-1050/16/2/858/pdf
    Download Restriction: no

    File URL: https://www.mdpi.com/2071-1050/16/2/858/
    Download Restriction: no
    ---><---

    References listed on IDEAS

    as
    1. Torres-Olea, Benjamín & Fúnez-Núñez, Inmaculada & García-Sancho, Cristina & Cecilia, Juan Antonio & Moreno-Tost, Ramón & Maireles-Torres, Pedro, 2023. "Influence of Lewis and Brønsted acid catalysts in the transformation of hexoses into 5-ethoxymethylfurfural," Renewable Energy, Elsevier, vol. 207(C), pages 588-600.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Zhu, Jishen & Jiang, Weiqiang & Yuan, Zong & Lu, Jie & Ding, Jincheng, 2024. "Esterification of tall oil fatty acid catalyzed by Zr4+-CER in fixed bed membrane reactor," Renewable Energy, Elsevier, vol. 221(C).
    2. Chai, Yu & Tian, Xin-Yu & Zheng, Xiao-Ping & Du, Ya-Peng & Zhang, Yu-Cang & Zheng, Yan-Zhen, 2024. "An effective approach for chitosan conversion to 5-hydroxymethylfurfural catalyzed by bio-based organic acid with ionic liquids additive," Renewable Energy, Elsevier, vol. 221(C).

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:gam:jsusta:v:16:y:2024:i:2:p:858-:d:1322298. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: MDPI Indexing Manager (email available below). General contact details of provider: https://www.mdpi.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.