Page 105 - Adsorption by Powders and Porous Solids
P. 105

ADSORPTION BY POWDERS AND POROUS SOLIDS

               Table 3.2.  Correction  for  non-ideality for  a  few  gases  com-
               monly used in adsorption experiments.
               Gas            Fonnula   T (K)   a = % correction
               Nitrogen       N2       77.3       4.0
                                       90.0       3.1
               Argon          Ar       77.3       4.8
                                       90.0       3.6
               Oxygen         02       77.3       5.1
                                       90.0       3.8
               Helium         He       77.3       0.2
               Carbon monoxide   CO    77.3       1.3
               Ammonia        NH3     273.15      1.5
                                      298.15      1.2
               Neopentane     (CH3),C   273.15    4.4
                                      298.15      3.9
               n-Butane       C,H,,   273.15      4.1
                                      298.15      3.2


   discontinuous manometric procedure (see Section 3.3.1).  the dosing volume being
   made up of the gas capacitance cell at the temperature of the adsorbent.

   3.4.9.  Presentation and use of the experimental data
   The raw experimental data (temperatures, pressures, flow-rates, equilibration times,
   sample treatment) should be stored, together with all calibration data of the set-up. It
   is highly desirable to plot the adsorption isotherm as soon as possible and preferably
   during the experiment itself.
     The commercial software generally includes a smoothing procedure in the first
   processing stage of the experimental data. This certainly improves the appearance of
   the data and may be useful for routine measurements, but the smoothing tends to hide
   systematically small events (including small phase changes) which may be  highly
   informative about the mechanism of adsorption. It is therefore preferable to store
   the  data in  their raw  form,  before any  smoothing has  been  applied,  so that  the
   experimental results are available for subsequent analysis.


   References

   Ajot H., Joly J.F., Raatz F. and Russmann C. (1991) In: Studies insurface Science and Catalysis, vol. 62,
     Elsevier, Amsterdam, p.  161.
   Atkins J.H. (1964) Aml. Chem. 36,579.
   Beebe R.A., Low G.W. andGoldwasser S. (1936) 1. Am. Chem. Soc. 58,2196.
   Bose T.K., Chahie R., Marchildon L.  and St Amaud J.M. (1988) Rev. Sci. Instrwn. 58(12), 2279.
   Bunsen R.W. (1870) Am. Phys 141, 1.
   Calvet E. and Pnt H. (1958) Rdcents Progrks en Microcalorimetrie, Dunod. Paris.
   Calvet E. and Rat H. (1963) Recent Progress in Microcalorimetry, Pergamon Press, Oxford.
   Camp R.W. andstanley H.D. (1991) American Labormory September, p. 34.
   Dash J.G. (197511 Films on Solid Surfaces, Academic Press, New York.
   100   101   102   103   104   105   106   107   108   109   110