Page 97 - Origin and Prediction of Abnormal Formation Pressures
P. 97

~] 8                      A. GUREVICH, G.V. CHILINGAR, J.O. ROBERTSON AND E AMINZADEH

               It  is  obvious  that  for  flat  areas  or,  more  precisely,  for  areas  with  a  nearly  flat water
             table,  p*  can  be  obtained just  by  subtraction  of hydrostatic  pressure  from  the  actually
             measured pressures.



             SOME  MAJOR  FACTORS  OF  UNDERGROUND  FLUID  FORCED  CONVECTION  AND
             CHARACTERISTICS  FOR  CORRELATION
               Characteristics  and parameters  for correlation  with the forced  convection component
             of  formation  pressure  should  be  selected  on  the  basis  of  thorough  causal  analysis  of
             each  phenomenon  and  its  impact  on  pressure  changes.  It  is  convenient  in  many  cases
             to  select  separately  characteristics  (1)  of  rock  properties  that  provide  a  possibility  of
             compression  and  pressure  change  resulting  from  an  external  influence,  and  (2)  of such
             an influence.  For example, porosity characterizes  the ability of pore  space to be reduced
            under  the  impact  of  external  influence,  and  overburden  weight  is  such  an  influence.
            Pressure increase is a superposition  of (1) a rock ability to respond to external influence,
             (2)  external  influence,  and  (3)  permeability.  The  first  two  characterize  the  pressure
            increase and the third one characterizes pressure dissipation.  There is a possibility, using
             characteristics  of these  three  types,  to  form  a  kind  of generalized  parameter  similar to
            the  similitude  criterion  and  correlate  it with  the  forced  convection  pressure  component.
            This possibility  should be thoroughly  explored  and tested on some regional  data.
               A preliminary analysis of several major factors  is given below.

             Compaction (~'granular sediments

               Compaction  of  granular  sediments  is  a  complex  process  strongly  dependent  on  the
            intensity  of  external  influences  (Athy,  1930;  Hedberg,  1936;  Dickinson,  1953;  Weller,
             1959;  Mukhin,  1965;  Rieke and Chilingarian,  1974;  Chilingarian  and Wolf,  1975,  1976;
            Gurevich,  1980;  and  many others).  It has two  major mechanical  components  (Gurevich,
             1980):  (1)  compaction  due  to  increase  in  the  effective  stress,  and  (2)  compaction  due
            to  changes  in  sand  matrix  strength  caused  by  external  influences  at  a  constant  or
            decreasing  effective  stress.  Alternating  stress  and  temperature  changes  and  especially
            vibrations  weaken  bonds  between  grains  and  help  their  rearrangement  at  points  of
            highest  stress.  The  third component  is a physicochemical  one:  filling of pore space with
            secondary minerals. The relative role of each one of these three contributions  to porosity
            reduction  varies  with  the  type  of geologic  formation,  intensity  of tectonic  deformation,
            and  geochemical  processes  including  migration  of mineral  solutions.  It  is  obvious  that
            porosity  and permeability of a sediment change  in time quite unevenly.
               Three  of  the  above-mentioned  components  of consolidation  pertain  to  sands.  Com-
            paction  of  clays  involves  both  of  the  mentioned  mechanical  components  and,  to  a
            lesser  degree,  the  geochemical,  but  is  more  complicated  because  other  processes  are
            also involved.  Clay minerals,  especially montmorillonite,  have large quantities  of water.
            This  water  partially  is  represented  by  bound  water  adsorbed  on  the  surfaces  of  clay
            minerals  and  contained  in-between  aluminosilicate  layers.  The  density  of bound  water
            is  approximately  equal  to  up  to  1.4  g/cm 3 immediately  near  the  clay  mineral  surface.
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