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8                              ADSORPTION BY POWDERS AND POROUS SOLIDS

   Table 13.  Definitions: porous solids
                                                                      2
   Term             Definition
   Porous solid     Solid with cavities or channels which are deeper than they are wide
   open PO=         Cavity or channel with access to the surface
   Interconnected pore   Pore which communicates with da pores
   Blind pore'      Pore with a single connection to the surface
     (Deadend pore)
   Closed pore      Cavity not connected to the surface
   Void             Space between particles
   Miclopore        Pore of internal width less than 2 nm
   Mesopore         Pore of internal width between 2 and 50 nm
                    Pore of internal width greater than 50 nm
   ~0~
   Pore size        Porc width (diameter of cylindrical porc or distance between opposite walls of
                    slit)
   Pon volume       Volume of pores determined by stated method
   Porosity         Ratio of total pore volume to apparent volume of particle or powder
   Total porosity   Ratio of volume of voids and pores (open and closed) to volume occupied by
                    solid
   Open porosity    Ratio of volume of voids and open pores to volume occupied by solid
   Surface area     Extent of  total  surface area  as  determined by  given  method  under  stated
                    conditions
   External surface area   Area of surface outside pores
   Intemal surface area   Area of pore walls
   Tme density      Density of solid, excluding pores and voids
   Apparent density   Density of material including closed and inaccessible pores, as determined by
                    stated method
     In the sense of the French word 'borgru'.

   consolidated agglomerates as a  result of  sintering or ageing.  The breakdown, or
   partial breakdown, of  the consolidated material can be  achieved by  grinding. The
   process  of  agglomeration involves  the  bridging  or  cementation  of  particles  and
   should not be confused with Osfwald ripening, which involves the growth of larger
   particles at the expense of  smaller ones. It is evident that an agglomerate may be
   regarded as a  'secondary'  particle, which always contains within it some internal
   surface. In many  cases the internal surface area is much larger than the external
   surface area and the agglomerate then possesses a well-defined pore structure.
     The classification of pores according to size has been under discussion for many
  . years, but in the past the terms micropore and macropore have been applied in dif-
   ferent ways by  physical chernists and some other scientists. In an attempt to clarify
   this situation, the limits of size of the different categories of pores included in Table
    1.3 have been proposed by the International Union of Pure and Applied Chemistry
   (Everett, 1972; Sing et al., 1985). As indicated, the pore size is generally specified as
   the  pore width, i.e. the available distance between the two opposite walls. Obviously,
   pore  size  has  a  precise  meaning  when  the  geometrical shape  is  well  defined.
   Nevertheless, for most purposes the limiting size is that of  the smallest dimension
   and  this  is  generally  taken to  represent the  effective pore  size. Micropores  and
   mesopores are especially important in the context of adsorption.
     The hypothetical types of pores shown in Figure 1.1 relate to the definitions in
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