IDEAS home Printed from https://ideas.repec.org/a/oup/ijlctc/v13y2018i3p292-297..html
   My bibliography  Save this article

Energy distribution function based universal adsorption isotherm model for all types of isotherm

Author

Listed:
  • Muhammad Burhan
  • Muhammad Wakil Shahzad
  • Kim Choon Ng

Abstract

Based upon the adsorbate–adsorbent interactions due to pore size distribution and surface heterogeneity, as characterized by the adsorption isotherms, the adsorption phenomenon has many industrial and environmental applications. These adsorption isotherms are very important to define the information related to the equilibrium uptake of adsorbate–adsorbent pair. Due to the presence of different energy distribution of adsorption sites, pore size distribution, surface area availability and surface heterogeneity, of each of the adsorbent–adsorbate pair, these isotherms are categorized into six types by the International Union of Pure and Applied Chemistry and so far, in the literature, there is no generalized adsorption isotherm model available that can define and predict the behavior of all adsorption isotherm types. In this study, a universal adsorption isotherm model is developed based upon the energy distribution function of the available adsorption sites and the pore size. The proposed model is able to define all adsorption isotherm characteristics, irrespective of their multi- or monolayer formations and micro- or meso-pore distribution.

Suggested Citation

  • Muhammad Burhan & Muhammad Wakil Shahzad & Kim Choon Ng, 2018. "Energy distribution function based universal adsorption isotherm model for all types of isotherm," International Journal of Low-Carbon Technologies, Oxford University Press, vol. 13(3), pages 292-297.
  • Handle: RePEc:oup:ijlctc:v:13:y:2018:i:3:p:292-297.
    as

    Download full text from publisher

    File URL: http://hdl.handle.net/10.1093/ijlct/cty031
    Download Restriction: Access to full text is restricted to subscribers.
    ---><---

    As the access to this document is restricted, you may want to search for a different version of it.

    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:oup:ijlctc:v:13:y:2018:i:3:p:292-297.. 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: Oxford University Press (email available below). General contact details of provider: https://academic.oup.com/ijlct .

    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.