Potential Theory In Analysis Of Equilibrium Data

POTENTIAL THEORY IN ANALYSIS OF EQUILIBRIUM DATA

FOR SUPERCRITICAL ADSORPTION

L. Czepirski, B. Laciak

University of Mining and Metallurgy, Faculty of Fuels and Energy,

al. Mickiewicza 30, 30-059 Cracow, Poland

High pressure adsorption is of particular use for the characterization of microporous materials. Low temperature adsorption on such materials is frequently complicated by excessive equilibration times due to activated diffusion. The use of adsorbates with small kinetic molecule diameter at temperatures above the critical temperature help to alleviate this problem. p>

Examples of adsorption isotherms for active carbon – gases systems at supercritical temperatures are presented.

The evaluation of some correlations that describe adsorption equilibria was carried out and the hypothesis that equilibrium data could be represented by the potential theory was tested.

Application of potential theory to the systems under study results in temperature – invariant characteristic curves. Using the molar volumes of gases in adsorbed state as an affinity coefficient to each adsorbate, it was demonstrated that characteristic curves for various adsorbates on a given adsorbent at different temperatures are superimposable on single reduced characteristic curve.

Experimental isotherms were also interpreted by the use of the Dubinin – Radushkevich equation. All of the D-R plots show linearity which demonstrates the possibility of application of D-R equation for analysis the microporous structure of carbonaceous adsorbents.

Modification of the Dubinin – Astakhov equation is given and discussed. The proposed form of D-A equation is preserved and physical background of its parameters is modified in accordance with the behavior of the adsorbate at supercritical temperature.

The equilibrium data can be directly related to gases separation to provide essential for contribution process modeling, such as pressure swing adsorption accomplished by selective adsorption.



Related articles::

  • Analysis Of Supercritical Adsorption Equilibrium Data For Active Carbons
  • Prediction Of Monolayer Adsorption Equilibrium Characteristics On The Basis Of Similarity Theory
  • H+-mg2+ And H+-ca2+ Exchange Onto Carboxylic Ionites In Terms Of The Exchange Equilibrium Theory
  • A New Quantitative Analysis Of The Surface Energetic Heterogeneity Of Catalyst
  • Analysis Of Potentiometric Titration Of Weakly Basic Anionites Curves
  • Method Of Observation Initial Stage
  • Hco3–cl Equilibrium On Strongly–basic Anionites
  • Prediction Of Henry’s Law Constants
  • Modified Langmuir Isotherm For Description Of Gas Adsorption Isotherms On Active Carbon
  • Group Energetic Characteristics Of Non-ionic Surfactants Adsorption Process
  • Analysis Of Water Vapour Sorption Isotherms
  • The New Mechanism Of Corrosion In Pore
  • A New Approach To Determination
  • Analysis Of The Excess Adsorption Isotherms For Solid/liquid Systems In Order To Determine The Surface Phase Capacity
  • Theoretical And Experimental Studies
  • Determination Of The Composition
  • Analysis Of Energetic Heterogeneity Of Hgba2ca2cu3o8+ Based On Programmed Thermodesorption Under The Quasi-isothermal Conditions From The Q-tg And Q-dtg Data
  • Surface Phenomena In Food Disperse Systems
  • About Some Properties Of Highly Dispersive Oxide Of A Titanium (iv) And Adsorption On It
  • Adsorption Features Of Polyfunctional Oligomers
  • Influence Of N-butanol And N-nonanol Concentration On Profiles Of The Local Velocities Of Bubbles
  • Regeneration Of Adsorbents By Using Liquid, Subcritical And Supercritical Carbon Dioxide
  • Theoretical And Experimental Studies
  • Regeneration Of Carboxylic Acrylic Cationexchange Resins By Stochiometric Amount
  • Zoning Of The North-western Part Of The Black Sea
  • Adsorption Investigations Of Toluidine Isomers And Toluidine Derivatives From Liquid Ammoniates
  • Extension Of The Applicability Of Jntti`s Method For Fast Calculation Of Adsorption Data
  • Biosorption Phenomenon On A Porous Carbon Surface
  • Influence Of Functional Group Of The Polymer
  • Electroregeneration Of Ni (ii) -loaded