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Research Article Open access CC BY 4.0

Development of a New Type-I Isotherm for Correction of Langmuir Isotherm’s Over-estimation of Adsorption at Higher Pressures

Adeolu J. Alawode, Olugbenga A. Falode

Physical Science International Journal · pp. 1–26 · Published 17 Oct 2019

10.9734/psij/2019/v23i330157

Abstract

Different gas equilibrium adsorption models (or isotherms) with various theoretical frameworks have been applied to quantify adsorbed volume (V) of gas (or fluid) through pressure-volume behaviour at a constant temperature. Most often, Langmuir isotherm (representing Type I Isotherm) has been used in modelling monolayer adsorption even though it yields over-estimation at higher pressures thus contradicting the description of Type I isotherm. Here, higher pressures refer to pressures above the adsorption saturation pressure(Ps) . Hence, in this work, a new Type I adsorption isotherm involving pressure(P), adsorption saturation pressure(Ps) , maximum adsorbed volume  and adsorbate-adsorbent resistance parameter  was developed using kinetic approach. The developed adsorption isotherm is V=  and it shows that Vmax is attained when pressure increases to Ps , above which no further gas adsorption occurs. The developed isotherm can be used to model all cases of monolayer adsorptions of gases (or fluids) on adsorbents. The developed and Langmuir isotherms were used in modelling secondary low-pressure gas adsorption data of different adsorbents and the qualities of fit were statistically assessed. For laboratory methane adsorption on Turkey’s shale sample at 25°C, the developed isotherm yields a correlation with an R2 value of 0.997 and predicts a maximum adsorption volume of 0.0450 mmol g-1 at a Ps  of 2,005 psia. However, Langmuir isotherm yields a correlation with an R2 value of 0.989 and predicts a maximum adsorption volume (Langmuir volume,VL ) of 0.0548 mmol g-1 at infinite Ps. At the higher-pressure range, the developed isotherm reveals that Langmuir isotherm is not a Type I isotherm but a "pseudo-Type I” isotherm.

Type I isotherm adsorption saturation pressure Langmuir isotherm monolayer adsorption.

References (17)

  1. 1 The constitution and fundamental properties of solids and liquids [DOI]
  2. 2 A Useful Adsorption Isotherm [DOI]
  3. 3 The Potential Theory of Adsorption of Gases and Vapors for Adsorbents with Energetically Nonuniform Surfaces. [DOI]
  4. 4 The Equation of the Characteristic Curve of Activated Charcoal
  5. 5 Kinetics of ammonia synthesis on promoted iron catalysts
  6. 6 Description of Adsorption Equilibria of Vapors on Zeolites over Wide Ranges of Temperature and Pressure [DOI]
  7. 7 ADSORPTION ISOTHERMS FOR PURE HYDROCARBONS [DOI]
  8. 8 THE ADSORPTION OF GAS MIXTURES BY SILICA [DOI]
  9. 9 Langmuir Isotherm Models Applied to the Multicomponent Sorption of Acid Dyes from Effluent onto Activated Carbon [DOI]
  10. 10 Equilibrium isotherm studies for the sorption of benzene, toluene, and phenol onto organo-zeolites and as-synthesized MCM-41 [DOI]
  11. 11 Comparison of isotherm models for hydrocarbon adsorption on activated carbon [DOI]
  12. 12 Quantification of the limitation of Langmuir model used in adsorption research on sediments via site energy heterogeneity [DOI]
  13. 13 An adsorption isotherm of multi-site occupancy model for heterogeneous surface. [DOI]
  14. 14 Gas Adsorption Equilibria: Experimental Methods and Adsorption Isotherms
  15. 15 Application of Langmuir and Dubinin–Radushkevich models to estimate methane sorption capacity on two shale samples from the Upper Triassic Chang 7 Member in the southeastern Ordos Basin, China [DOI]
  16. 16 Adsorption of Pb(II) ion from aqueous solution onto Chitosan/silica/polyethylene glycol (Ch/Si/P) composites membrane [DOI]
  17. 17 Surface Area and Porosity [DOI]

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