Page 22 - Adsorption by Powders and Porous Solids
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CHAPTER 1  INTRODUCTION                                          7

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   Table 1.2.  Defirut~ons powders
   Tern             Defin~tlon
   powder           Dry  matenal  composed of  discrete parhcles  with  maxlmum dunens~on less
                    than about 1 mm
   Fme powder       Powder with particle slze below about 1 pm
   Aggregate        Loose, unconsohdated  assemblage of particles
   Agglomerate      bgld, consol~dated assemblage or parhcles
   compact          Agglomerate formed by compression of powder
   Ac~cul~          Needle-shaped
   surface area     Extent of avalable surface as detemed by a glven method under stated con-
                    dtlons
   Specific surface area   Surface area of umt mass of powder, as determmed under stated condibons
   External surface   Area of external surface of particles, as takmg account  of roughness  (1 e  all
                    cavrtles whlch are wlder than they are deep). but not porosity
   Roughness factor   Ratlo of external surface area to area of smoothed envelope around particles
   Divided sohd     Solid made up of more or less independent pamcles wh~ch may be m the form
                    of a powder, aggregate or agglomerate



   imprecise manner, but it seems reasonable to apply it to a material consisting of par-
   ticles less than about 1  p.rn (i.e. particles of colloidal dimensions). The unit mass of a
   fine powder contains a large number of small particles and hence exhibits an appre-
   ciable surface area. For example, in the simplest case of an assemblage of  spherical
   particles, all with the same diameter, d, the specific surface area, a, is given by  the
   relation


   where p is the particle absolute density. Thus, a powder composed of smooth spher-
   ical particles of d = 1 p.rn and p  = 3 g cm-3 would have a specific surface of 2 mZ g-'.
   The same calculation would apply to cubic particles, but in this case d would equal
   the edge length of the cube. In fact, an area of  about 2 mZg-' turns out to be of the
   same order of magnitude as the lower limit amenable to investigation by  the tech-
   niques most often used in routine adsorption measurements.
     It is evident that it is more difficult to &fine particle size if the particle shape is not
   spherical or cubic. With some other simple geometric forms, a single linear dimen-
   sion, d,  may be used to calculate the surface area. In particular, when the particle
   aspect ratio is sufficiently large, d, is taken as the minimum dimension. Thus, if the
   particles are thin or long (i.e. plates or rods), it is the thickness which mainly deter-
   mines the magnitude of the specific surface area (Gregg and Sing, 1982).
     Perfect spheres are rare, but spheroidal particles are present in some powders pro-
   duced at high temperature (e.g. pyrogenic silicas) or by the sol-gel process. The term
   sphericity is useful for some purposes. Sphericity has been defined in various ways,
   the simplest definition being the ratio of  the surface area of  a sphere of  the same
   volume as a given particle to the actual surface area of that particle (Allen, 1990).
     The individual particles (pnrnary particles) in a fine powder are usually clustered
   together in  the form  of  aggregates  or agglomerates.  Loosely bonded  aggregates
   are  unconsolidated  and  non-rigid,  but  they  may  be  converted  into  more  ng~d,
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