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VII



               Thesis Title        Optimization  of  Hydrogen  and  Methane  Production  with  a  Two-Stage
                                   Anaerobic  Co-digestion  of  Skim  Latex  Serum  (SLS)  and  Palm  Oil  Mill
                                   Effluents (POME) under Thermophilic Condition
               Author              Mr. Kullachat  Sama
               Major Program       Applied Chemistry
               Academic Year       2014

                                                           ABSTRACT

                       Determination of  biohydrogen  production  potential (BHP) at  various mixing ratios  of
               skim latex serum (SLS) to palm oil mill effluent (POME) at initial concentration of 7 g-VS added/L
               and 21 g-VS added/L was conducted in batch dark fermentation at thermophilic conditions. At the
               organic  concentration  of  7  g-VS added/L  and  SLS:  POME  mixing  ratio  of  55:45  (%v/v),  high
               hydrogen  production  yield  of  71.8±1.7  mL  H 2/g-VS added  was  achieved.  Acetic  and  propionic
               acids were the major soluble end-products with concentrations of 26.83±0.40 mM and 7.59±1.14
               mM, respectively. Furthermore, buffer and nutrients optimization were then investigated through
               response surface methodology (RSM) with a central composite design (CCD) at initial organic
               concentration  of  7  g-VS added/L,  and  55:45  (%v/v)  SLS:POME  mixing  ratio.  Although,  the
               hydrogen production yield achieved from  optimization  is higher than that obtained from  non-
               optimization, approx. 22%. However, the increased yield is not uneconomical for the industrial
               scale when considering cost of the external buffer and nutrients supplemented. Afterwards, the
               effluents achieved from H 2 production phase, consisting of SLS and POME at the mixing ratio of
               55:45 (%v/v) and 7 g-VS added/L was further used as substrate for biomethane potential (BMP) in
               the second anaerobic stage. The methane production yield of 418±10 mL CH 4/g-VS added, which
               was 2 times greater than that achieved from sole anaerobic digestion of SLS was obtained.
                       The  two-stage  anaerobic  process  for  sequential  production  of  hydrogen  and  methane
               from thermophilic dark co-digestion of SLS with POME at a mixing ratio of 55:45 (%V/V) was
               investigated.  The  first  stage  was  operated  in  a  continuously  stirred  tank  reactor  (CSTR)  for
               producing at the hydraulic retention times (HRTs) of 2.25 days and 4.50 days, corresponding to
               organic  loading  rate  of  20  g-VS/  L reactor  d  and  10  g-VS/  L reactor  d,  respectively.  Hydrogen
               production  was  achieved  at  the  HRT  of  4.50  days  with  the  hydrogen  production  rate  and
               hydrogen  production  yield  was  341±19  mL  H 2/L reactor  d  and  1533±88  mL  H 2/L substrate,
               respectively,  which  is  higher  than  that  obtained  from  the  HRT  of  2.25  days.  Under  the
               operational conditions at the 4.50-day HRT, soluble metabolites were dominated with acetic acid
               (14.7-24.1 mM),  butyric acid  (15.8-28.7  mM), propionic  acid  (12.7-26.5 mM),  ethanol  (13.2-
               21.0 mM), and lactic acid (99.1-138.1 mM). Subsequently, the homogenized effluents collected
               the first stage hydrogen production operated at 4.50-day HRT was further fed into the second
               stage at the HRT of 18 days, corresponding to the organic loading rate of 2 g-VS/L reactor d. The
               average methane production rate and methane production yield was 79±12 mL CH 4/L reactor d and
               1517±199  mL  CH 4/L substrate,  respectively.  Further  optimization  for  the  second  stage  UASB  is
               necessary due to acetic acid accumulated in rather high concentration (63-150 mM).
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