IDEAS home Printed from https://ideas.repec.org/a/gam/jeners/v15y2022i17p6231-d898826.html
   My bibliography  Save this article

Effects of Solubilizer and Magnetic Field during Crystallization Induction of Ammonium Bicarbonate in New Ammonia-Based Carbon Capture Process

Author

Listed:
  • Linhan Dong

    (School of Energy Science and Engineering, Harbin Institute of Technology, Harbin 150001, China)

  • Dongdong Feng

    (School of Energy Science and Engineering, Harbin Institute of Technology, Harbin 150001, China)

  • Yu Zhang

    (School of Energy Science and Engineering, Harbin Institute of Technology, Harbin 150001, China)

  • Heming Dong

    (School of Energy Science and Engineering, Harbin Institute of Technology, Harbin 150001, China)

  • Zhiqi Zhao

    (School of Energy Science and Engineering, Harbin Institute of Technology, Harbin 150001, China)

  • Jianmin Gao

    (School of Energy Science and Engineering, Harbin Institute of Technology, Harbin 150001, China)

  • Feng Zhang

    (School of Mechatronics Engineering, Harbin Institute of Technology, Harbin 150001, China)

  • Yijun Zhao

    (School of Energy Science and Engineering, Harbin Institute of Technology, Harbin 150001, China)

  • Shaozeng Sun

    (School of Energy Science and Engineering, Harbin Institute of Technology, Harbin 150001, China)

  • Yudong Huang

    (School of Chemical Engineering and Technology, Harbin Institute of Technology, Harbin 150001, China)

Abstract

As a chemical absorption method, the new ammonia carbon capture technology can capture CO 2 . Adding ethanol to ammonia can reduce the escape of ammonia to a certain extent and increase the absorption rate of CO 2 . The dissolution and crystallization of ethanol can realize the crystallization of ammonium bicarbonate and generate solid products. The induction of the crystallization process is influenced by many parameters, such as solution temperature, supersaturation, and solvating precipitant content. The basic nucleation theory is related to the critical size of nucleation. Accurate measurement of the induction period and investigating relevant factors can help to assess the nucleation kinetics. The effects of solubilizer content, temperature, and magnetic field on the induction period of the crystallization process of ammonium bicarbonate in the ethanol–H 2 O binary solvent mixture and determining the growth mechanism of the crystal surface by solid–liquid surface tension and surface entropy factor are investigated. The results indicate that under the same conditions of mixed solution temperature, the crystallization induction period becomes significantly longer, the solid–liquid surface tension increases, and the nucleation barrier becomes more significant and less likely to form nuclei as the content of solvating precipitants in the components increases. At the same solubilizer content, there is an inverse relationship between the solution temperature and the induction period, and the solid–liquid surface tension decreases. The magnetic field can significantly reduce the induction period of the solvate crystallization process. This gap tends to decrease with an increase in supersaturation; the shortening reduces from 96.9% to 84.0%. This decreasing trend becomes more and more evident with the rise of solvent content in the solution. The variation of surface entropy factor under the present experimental conditions ranges from 0.752 to 1.499. The growth mode of ammonium bicarbonate in the ethanol–H 2 O binary solvent mixture can be judged by the surface entropy factor as continuous growth.

Suggested Citation

  • Linhan Dong & Dongdong Feng & Yu Zhang & Heming Dong & Zhiqi Zhao & Jianmin Gao & Feng Zhang & Yijun Zhao & Shaozeng Sun & Yudong Huang, 2022. "Effects of Solubilizer and Magnetic Field during Crystallization Induction of Ammonium Bicarbonate in New Ammonia-Based Carbon Capture Process," Energies, MDPI, vol. 15(17), pages 1-13, August.
  • Handle: RePEc:gam:jeners:v:15:y:2022:i:17:p:6231-:d:898826
    as

    Download full text from publisher

    File URL: https://www.mdpi.com/1996-1073/15/17/6231/pdf
    Download Restriction: no

    File URL: https://www.mdpi.com/1996-1073/15/17/6231/
    Download Restriction: no
    ---><---

    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:jeners:v:15:y:2022:i:17:p:6231-:d:898826. 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.

    We have no bibliographic references for this item. You can help adding them by using 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.