In the marine environment, the rate of corrosion 
increase rapidly, due to the seawater contain solution 
that  are  able  to  dissolve other  substances  in  greater 
quantities  than  other  liquids.  Those  substances 
include  inorganic  salts,  organic  compounds  derived 
from living organisms (bacteria) and dissolved gases. 
One of  the  causes  of  corrosion  is  bacteria.  Bacteria 
live  in  the  marine  environment  extensively  in  their 
habitats  and  form  colonies  and  attach  to  the  metal 
surfaces in the form of thin layers. Factors that affect 
the occurrence of bio-corrosion are temperature, pH, 
and  oxygen  levels.  Based  on  our  previous  study,  3 
species  of  bacteria  Escherichia  coli,  Pseudomonas 
fluorescens, and Thiobacillus ferroxidans can caused 
bio-corrosion on steel structures of ASTM A106 and 
A53  in  deep  seawater  (salinity  of  33‰),  medium 
seawater  (salinity  of  35‰),  and  shallow  seawater 
(salinity of 37‰) (Pratikno and Titah, 2016). The bio-
corrosion rate by P. fluorescens on Aluminium Alloy 
6063 at salinity of 37‰ increased by one point six-
fold  compared  with  the  condition  without  bacteria 
addition  at  the  same  salinity  (Pratikno  and  Titah, 
2016). 
Corrosion  can  occur  rapidly  if  neither 
environmental  control  or  prevention.  The  usage  of 
aluminium in the maritime industry is high such as in 
ship  building.  So  that  aluminium  should  treat  with 
suitable  treatment  to  increase  the  resistance  of 
corrosion or decrease the corrosion rate. The aim of 
the  research  was  to  determine  the  effects  of 
Aluminium  AA6063  aging  treatment  on  bacterial 
corrosion.  The  material  was  be  treated  by  heat 
treatment  (Aging  Treatment)  before  the  bacterial 
corrosion test was conducted. 
2  MATERIALS AND METHODS  
2.1  Preparation of Specimen  
Material cut with area of ± 2 cm2 with diameter ± 
1mm  with  thickness  1-2  mm.  After  that,  the 
hardening  process  was  conducted  by  heating  the 
specimen  with  temperature  of  535  ºC  for  6  h.  This 
process was called as Solution Heat Treatment. After 
that,  the  specimen  was  immersed  in  water  or 
quenching phase, then re-heat it at 200 ºC for 5 h. This 
process  was  called  as  Aging  Treatment.  After  the 
aging treatment, the hardness test was conducting to 
all  specimens  using  Vickers  method.  Vickers 
Hardness Test is the standard method for measuring 
the  hardness  of  metals,  particularly  those  with 
extremely hard surfaces: the surface is subjected to a 
standard  pressure  for  a  standard  length  of  time  by 
means of a pyramid-shaped diamond. The diagonal of 
the  resulting  indention  is  measured  under  a 
microscope. 
2.2  Preparation of Artificial Seawater 
This research used a chemical solution instead of sea 
water with a salinity of 35 ‰. Salinity of 35‰ is the 
salinity in the ocean of medium depths, where in the 
microorganism  commonly  found  at  this  depth, 
including  bacteria.  The  chemical  composition  of 
seawater  replacement  is  in  accordance  with  ASTM 
D1141-90, 1994 (ASTM, 2004). 
2.3  Preparation of Bacteria  
The preparation of bacteria was conducted based on 
Pratikno and  Titah  (Pratikno  and  Titah,  2017).  The 
pure  culture  of  Thiobacillus  ferrooxidans, 
Pseudomonas fluorescens and Escherichia coli, were 
be  inoculated  onto  nutrient  agar  (NA)  media  using 
streak plate technique based on Harley and Prescott 
(Harley and Prescott, 2002). The age of bacteria for 
the test was 24 h. After that, one colony of bacteria 
was  transferred  to  nutrient  borth  (NB)  and  keep  in 
shaker  incubator  of  Innova  2000  (New  Brunswick-
Eppendorf,  Germany)  at  150  rpm  and  room 
temperature, 33 oC for 24 h. The cell suspension of 
selected bacteria was prepared by harvesting the cells 
at the middle of the logarithmic phase, based on the 
typical of growth rate graph for the selected bacteria. 
At this time, the OD at 600 nm was 1.0 was 
determined using UV spectrophotometer Genesys 20 
(Thermo,  USA).  The  cells  were  harvested  through 
centrifugation of  Jouan E82 (Thermo, USA) at 4,000 
rpm for 15 min. The obtained pellet was then washed 
twice  using  8.5  g  NaCl/1000  mL  solution.The 
suspension of bacteria was ready to be used  in bio-
corrosion test.  
2.4  Immersion Method for  
Bio-corrosion Test 
The specimen was tested by immersion tehnique in a 
prepared  seawater solution with salinity  33‰, 35‰ 
and  37‰  using  ASTM  G31-72  standard  (ASTM, 
2004). There were two different treatments, namely 
treatment without bacterial addition as a control and 
treatment with bacterial addition Testing was carried 
out for 4 weeks. Immersion testing was conducted in 
beaker  glass  with  size  of  300  mL  and  the  artificial 
seawater was 250 mL for each beker glass.