Oil related microbiology Oil related microbiology
Terje Torsvik
UNI - CIPR
CENTRE FOR INTEGRATED PETROLEUM RESEARCH
Important microbial processes in oil production:
Reservoir souring Reservoir souring
Microbial Influenced Corrosion (MIC) Produced water reinjection (PWRI) Microbial Enhanced Oil Recovery
VFB
VFA
Reservoir souring in offshore oil production Reservoir souring in offshore oil production
Sea water is injected into the reservoir as Sea water is injected into the reservoir as
pressure support
Oxygen is removed to reduce corrosion Sea water contains 28 mM sulphatep
Sea water injection promotes growth of SRB in the water injection system and in the
reservoir
SRB use sulphate for respiration
:
SO
2H S SO
42-→ H
2S
H S bl b it i t i d i
H2S cause problems because it is toxic and corrosive Traditionally biocides have been used to inhibit SRB
An alternative method based on nitrate injection have been developed in collaboration with Statoil and Hydro
in collaboration with Statoil and Hydro
Microbial production of H
2S in the oil reservoir Microbial production of H
2S in the oil reservoir
•H
2S production increases dramatically over the
lifetime of a production well.
•High H
2S levels may lt i h t d f th result in shut down of the well and reduced oil and gas production.
•H
2S is toxic and corrosive
Ref. : Sunde et al. (1993). Field related mathematical
• Strong restrictions on H
2S concentration in
export gas
Ref. : Sunde et al. (1993). Field related mathematical model to predict and reduce reservoir souring. SPE 25197 (1993)export gas
Laboratory experiments:
Effect of nitrate injection on H 2 S production
Sulphide production and nitrate injectin in column.
1,2 1,4
mM H2S mM NO3
0,4 0,6 0,8 1,0
mM H2S, NO3-
0,0 0,2
100 300 500 700 900 1100
Time (days)
Ref : Myhr et al (2002) Inhibition of microbial H2S production in an oil reservoir Ref.: Myhr et al. (2002). Inhibition of microbial H2S production in an oil reservoir model column. Appl. Microbiol Biotechnol 58: 400-408.
Monitoring SRB in the field:
Gullfaks Water injection system
Monitoring SRB in the field:
Biofilm sampling
Sampling point
Sampling point
Biocoupons collected from pipiline Biocoupons collected from pipiline Placed in box for anaerobic transportation Filled up with anaerobic injection sea water
Metal coupons incubated in pipeline
Measuring microbial activity in the water injection system
The biofilm is analyzed for microbial activity
GAB SRB NRB
Water injection system at Gullfaks.
Bacteria in biofilm before and after nitrate treatment Bacteria in biofilm before and after nitrate treatment
1,0E+09 1,0E+10
1 0E 06 1,0E+07 1,0E+08 1,0E 09
m2
1,0E+04 1,0E+05 1,0E+06
Log cells/cm
1,0E+01 1,0E+02 1,0E+03
1,0E+00 ,
feb.89 jun.90 dec.91 mar.93 apr.94 nov.94 jul.95 jun.96 feb.97 mar.98 may.99 feb.00 aug.00 may.01 mar.02 feb.03
Time (months)
SRB FA
Biocide (glutaraldehyde) Nitrate (start oct. 99)
SRB-FA SRB-MPN NRB
Total bacteria
Detection limit FA method: 1e+05 cells/cm2 Detection limit MPN method: 6 cells/cm2
SRB activity and corrosion rate at GFB
ay)
Nitrate added
year)
1,0 1,2
H2S/cm2 /da
20 25
rate (mm/y
0,6 0,8
n rate (µg H
15
Corrosion 0,2 0,4
e respiration
5 10
r.94 p.94 v.94 r.95 ul.95 ct.95 r.96 n.96 p.96 c.96 b.97 r.97 y.97 g.97 v.97 n.98 b.98 r.98 y.98 p.98 s.98 y.99 g.99 v.99 b.00 n.00 g.00 v.00 s.00 b.01 y.01 g.01 v.01 r.02 ul.02 ct.02 b.03 n.03
0,0
Sulphate
0
Time (month)
ap sep nov ma ju oc ma jun sep dec feb ma may aug nov jan feb ma may sep des may aug nov feb jun aug nov des feb may aug nov ma ju oc feb jun
Corrosion rate SRBactivity SRB activity
H2S in produced water on Gullfaks C H2S in produced water on Gullfaks C
9 10
6 7 8
e water
3 4 5
mg H2S/litre
measured mg H2S in water Theoretical H2S development
0 1 2
m 3
Start of nitrate injection
0
nov-97 sep-98 jul-99 mai-00 feb-01 des-01 okt-02 aug-03
Date
Sunde, Egil; Lillebø, Bente-Lise Polden; Bødtker, Gunhild; Torsvik, Terje; Thorstenson, Tore. H2S inhibition by nitrate injection on the Gullfaks field.NACE Corrosion 2004, Paper No 04760; 2004
Produced Water Reinjection (PWRI) Produced Water Reinjection (PWRI)
Produced Water Reinjection (PWRI) has been used on platforms, mainly due to requirements from the Norwegian Pollution Agency regulating release of hydrocarbons to the sea.
regulating release of hydrocarbons to the sea.
In the event of permission to produce oil in the Barents Sea, there must be zero release of hydrocarbons to the environment.y
Challenges:
High temperature stimulate growth of thermophilic SRB
Increased supply of VFA in the injected water stimulate reservoir souring
PWRI at Statfjord PWRI at Statfjord
Injection water:
Cold sea water (StA) Hot produced water (StC)
Microboal analysis of back flooded injection water
Ocean floor
Injection well Production well
Injection water Injection water
St A and B: Sea water St C: Produced water
Oil reservoir
St C: Produced water
Samples p
• Back-flooded injection water from wells 3000 meters below sea floor.
• From each injector: 9 samples taken at different times (0 – 96 hours)
• From each injector: 9 samples taken at different times (0 – 96 hours) of back-flooding.
Sample Statfjord A Statfjord B Statfjord C
Injected with Sea water Sea water Produced water
Temperature 30 °C 30 °C 60 °C
Temperature 30 C 30 C 60 C
Treatment Deoxygenated,
biocide treatment
Deoxygenated, nitrate treatment
Deoxygenated,
75 % produced water 75 % produced water 25 % seawater
Souring potential H2S mg/liter
(calculated by Statoil)
30 <1 200-400
epsilon
Principal component analysis of native populations at St A and C
Statfjord A (StA) Statfjord C (StC) Produced water (PW)
1.0
epsilon
Archaeog Thermoc
StC
Actinob Deferrib
Archaeog
Backflow delta
StA
beta Firmic
PW
-0 6 1 2
-1.0
alpha
0.6 1.2
K. Lysnes, G. Bødtker, T. Torsvik, E. Ø. Bjørnestad & Egil Sunde:
Appl Microbiol Biotechnol (2009) 83:1143–1157
MEOR
Principles – reservoir effects
BACTERIA + OIL + N + P + O
2DU CED
CIAL ON
RE DU
CE WAT PE REDU
INTERFACIA TEN
SION CE
D ATER PERME
ABI LITY
MOBILISED RESIDUAL OIL ENHANCED SWEEP EFFICIENCY
Y
MOBILISED RESIDUAL OIL ENHANCED SWEEP EFFICIENCY
Microbial biofilm on oil
crude oil
Bacterial colony surrounded by water
IFT laser light scattering IFT laser-light scattering
• Best suited for low values (< 30 mN/m)
• Measurement range is 10
2– 10
-5mN/m
• Method has been successfully applied down to 10
-4mN/m
Bacterum: Dietsia maris
D d k bi th ti t
100
OW IFT
Dodekan, aerobic synthetic sea water
10
OW IFT OWB IFT 4.0 ml/h 0.9 ml/h 1.8 ml/h
0,1 1
IFT (mN/m) 1.8 ml/h
2.7 ml/h 5.4 ml/h
0,01
0,001
0 2 4 6 8 10 12 14 16 18 20 22 24 26 28
Run time (days)
Kowalewski, E., Rueslåtten, I., Gilje, E., Sunde, E., Bødtker, G., Lillebø, B.L.P., Torsvik, T., Stensen, J.Å., Bjørkvik, B.
and Strand K A 2005 "Interpretation of Microbial Oil Recovery from Laboratory Experiments" Paper presented at the and Strand, K.A., 2005, Interpretation of Microbial Oil Recovery from Laboratory Experiments , Paper presented at the 13th European Symposium on Improved Oil Recovery, Budapest, Hungary, Apr 25-27
Hopeman sandstone core
L b t i t
45 cm long, 5 cm diameterStatfjord model oil
Fl t 0 1 l/ i 1 PV/d
Laboratory experiments
Flow rate: 0,1 ml/min = 1 PV/d
Anoxic synthetic Sor0,38 Anoxic synthetic
seawater
Microbes, O2, N, P 0,36
, , ,
0,34
0,32
0 5 10 15 20
Time (days)
MEOR at Norne
Injection of aerobic seawater from start in 1997
1997
MEOR implemented in January 2001 by
adding N and P to the injection water to
adding N and P to the injection water to
stimulate bacterial growth in the reservoir
Nitrate is also added in order to inhibit
reservoir souring
MEOR at Norne MEOR at Norne
2002: Increased oil production from MEOR at Norne – 900 000 m
3– 1 % of producible oil p
– At an oil price 20 $ per barrel and 1$= 5 NOK this amounts to approximately 750 000 000 NOK. pp y
(Reported from Norne to OD in 2002)
( p )