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Gas geochemistry surveys for petroleum                                223

           evolved  in  the  laboratory  by  heating  to  high  temperatures  and  their  concentrations  are
           determined  instrumentally.



           Soil

              Soil  samples  are  usually  collected  at the  surface  proper  or  at  depths  of up  to  several
           metres  below  the  surface.  As  far as  possible,  samples  are  kept  in their original  condition
           until  they  are  prepared  for  analysis  in  the  laboratory.  The  analytical  procedures  are
           invariably  partial  extraction  techniques.  This  approach  has  been  widely  used  in  other
           branches  of  exploration  geochemistry,  but  assumes  particular  importance  in  gas
           geochemical  surveys  for petroleum.
              For  gases  adsorbed  on  soils,  the  essential  requirement  is  to  regulate  desorption
           parameters,  so  that  variations  in  these  parameters  do  not  introduce  variations  into  the
           concentrations  desorbed.  In  order  to  prevent  production  of  new  gas  species  during  the
           thermal  desorption,  the  heating  temperature  is  usually  kept  under  200~   or applied  only
           for  milliseconds  (Kiusman  et  al.,  1986).  Stable  thermal  desorption  conditions  can  be
           attained  by  using  a  metal  heating  block  maintained  at  a  fixed  temperature,  into  which  a
           tube  containing  the  soil  sample  is  placed  for  a  fixed  time.  The  gases  released  are  then
           condensed  in  a  loop  held  in  liquid  N2,  which  subsequently  acts  as  the  input  to  the  gas
           chromatograph  (Fig.  6-4).  If the  soil  samples  are  in sealed  containers,  simple  vibration  at
           elevated  temperature  produces  an  equilibrium  concentration  of  gases  in  the  container
           headspace  that  can  be  taken  as  a  measurement  proportional  to  the  concentration  of
           adsorbed  hydrocarbons.
              For  the  extraction  of  hydrocarbons  in  carbonate  minerals  and  microbubbles,  the
           method  widely  used  is  acid  treatment  under  vacuum,  for  which  most  laboratories  in
           China  use the  apparatus  shown  in  Fig. 6-5.  The  soil  sample  is heated to 40~  in tile flask,
           then  1:6  HCI  is  added  until  its  reaction  with  the  warm  sample  ceases.  The  mixture  of
           gases  evolved  is  filtered  through  NaOH  solution  to  remove  CO2  (which  makes  up  the
           bulk  of  tile  evolved  gases)  and  the  remaining  gases  are  injected  into  a  gas
           chromatograph.
              A  selective  method  to  flush  out  microbubbles  is  hydrogen  stripping.  This  was  first
           proposed  by  Schaefer  et  ai.  (1978)  and  has  been  developed  by  Ruan  and  Cheng  (1991).
           Soil  samples  are  kept  in  a  natural  wet  state  and  an  aliquot  of saturated  NaCI  solution  is
           added  to make  a slurry,  through  which  H2 is passed.  The  gases  stripped  from  the  sample
           are  condensed  in  a  liquid  N2 cold  trap,  which  is then  used  as  the  gas  sample  loop  in  the
           carrier gas  line to a gas chromatograph  (Fig.  6-6).
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