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Transcript of petrolem geology geochemistry
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G EOCH EM 1C A L CONSU LTANTS
COMPANY INCORPORATED IN U.K. NO. 1509402VAT REGISTRATION NO. 354021394
DIRECTORS: T. DORANV.L. ROVEDAS P LOWE
D.R. WHITBREAD
UNIT 14 PARAMOUNT INDUSTRIAL ESTATESANDOWN ROAD WATFORD WD24XA.TEL: 43196 TELEX: 8812973
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P A L E O C H E M
Contents.
Page No,
Summary
1. Introduction ^
2. Samples and Techniques 1 - 3
3. Results and Discussion 3 - 1 2
(a) Maturity
(b) Source Potential
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PA L E O C H E M
Summary
Twenty-two potentially rich sediment sidewall coresand three sandstone sidewall cores, containing oil shows
were used to complete a detailed geochemical source rockand reservoired hydrocarbons study. Maturity estimations
using Vitrinite Reflectance measurements and Spore Colourationratings, suggested all the sediments examined to be immaturefor any hydrocarbon generation.
The hydrocarbon potential of the 22 sediment sampleswere found to be extremely varied, but good source sectionswere identified in the Kimmeridgian and Early Jurassic sections
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PALEOCHEM
1. Introduction
A detailed geochemical study was completed ontwenty-five sidewall cores from the depth interval1835 - 3447.5 m of Well: 6507/12-2, Offshore Norway.Three of the sidewall cores contained oil shows andwere treated differently from the other twenty-two.The section examined extended from the Late Cretaceousto Late Triassic. The main emphasis of the study wasplaced on establishing reliable geochemical parameters
for use as well-to-well correlation parameters, inaddition to the more traditional tools available tothe hydrocarbon explorationist.
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P A L E O C H E M
any trace of drilling mud and then air dried under
controlled conditions at 40C. It was noted that themajority of the samples smelled strongly of hydrocarbons.(
Samples for Visual Kerogen Description were treatedwith mineral acid. The remaining debris was sedimented
onto a microscope slide and examined using a transmittedlight microscope. The results of the Visual Kerogendescriptions and assessments of Spore Colouration areshown in Table 1. The range of the Spore Colouration isfrom 1 - 7 and the colour taken as representing the onsetof liquid hydrocarbon generation is 3/4.
Samples for Total Organic Carbon measurements werefinely ground and sieved to achieve homogeneity then
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PALEOCHEM
Ground Samples from two cores at 1874 and 1875 milsed for Soluble Extract Studies were extracted withgeochemical grade dichloromethane, using a high velocityliquid mixer. Excess solvent was removed by evaporation
and the remaining extracts were separated on activatedsilica/ to provide saturate alkane and aromatic fractionsfor gas chromatographic analysis. The saturate alkane
fractions were examined by quartz capillary gas chromatography
using a Carlo Erba 2151 gas chromatograph with Grob-type
splitless injector system. The results of these measurementsare represented in Table 4. The saturate alkane fractionswere then examined by CGCMS using a modified Finnigan 9500with Grob-type injector. The aromatic fractions were alsoexamined by CGCMS, as above.
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4
PA L E O C H E M
None of the spore colours shown in Table 1 aregreater than 2 and the highest reflectivity value seen
* ' > :- * - ' . , - . - C . ;'U*' ' t - ; in sediments from the Late Trias was 0.47%. No sporefluorescence colours were available for supporting theimmature reflectivity values and spore colour ratings/but the sterane distributions shown in Fig.1 from the
Kimmeridgian sediment at 1873 m are typical of an immaturesediment extract.
(b) Source Potential
(i) Hydrocarbon Potential
Samples having total organic carbon values below
0.5% are generally regarded as containing insufficient
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The first peak (PI) is often considered as representative
of the quantity of free hydrocarbons that were present in the
sediment at the time of sampling. The second peak (P2) is
considered to be representative of the quantity of hydrocarbonspresent in the sediment and yet to be generated. The P2 peak
is produced by conversion of the Kerogen in the rock sampleby thermal cracking in the instrument. This is generally
considered to be a reasonable estimate of the amount ofhydrocarbons, which could theoretically be generated by
complete conversion of the Kerogen in sediments under
natural conditions throughout their geological lifetime.
Both the PI and P2 yields are expressed in Kg./tonne.
Comparison of pyrolysis data with conventional
h i l d id i l i
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-6-
measurements and Screening Pyrolysis. It was noted
that these sediments, similar to those from the Late
Cretaceous, had significant quantities of in situhydrocarbons (PI), in relation to the amount of Kerogen
breakdown products (P2). It is unfortunate, but during
conventional pyrolysis some of the PI can be eluted withthe P2 fraction (5). It is Paleochem practise to extractsamples, where the PI is above a threshold value of 10%
of the P2 value and to repeat the measurement of P2 a f ter_extraction, to obtain a more accurate measure of hydrocarbonpotential.
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significantly by extraction (Table 3) and the potentialmeasured on the unextracted sample was over optimistic.
There was insufficient sediment available from the1889 m sidewall core to complete TOG measurements, butScreening Pyrolysis demonstrated this sediment to haveonly poor hydrocarbon potential. The one sediment examinedfrom the Late/Middle Jurassic had a moderate TOG value of1.17%, but only a poor pyrolysis yield of only 0.3 Kg./tonne.This discrepancy in hydrocarbon potential ratings is thought
to be due to the presence of significant quantities of re-
worked material and/or inertinite in these sediments, whichwe would expect to have been evident during the Vitrinite
Reflectance Studies.
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The sidewall cores supplied were not spread evenly overstratigraphic intervals. It is suggested that the inter-pretation of the trends could be improved substantially bythe examination of further cores or cuttings/ filling inthe missing intervals.
'' . '
(ii) Hydrocarbon Type
Hydrocarbon typing using Visual Kerogen Descriptionsshowed a wide variation in both the type and quantity ofplant debris present in the sediments examined (Table 1).These variations suggested the likely hydrocarbon products
from the organic rich intervals in the Jurassic section ofthis well, to be varying proportions of both gas and liquids.Soluble Extract Studies completed on sediments from the
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I PALEQCHEM
and typical of a diesel fuel distribution. This diesel-likerange of hydrocarbons was also observed in the n-alkane dis-tributions of the reservoir sandstones at 3062, 3080.5 and3143 m as illustrated below.
' IX t^c -,j it ^ ^ - ^ . - , . < ; - . . . ; . .
6507/12-2.306
JV jV
2m
J
17
A
u " j ' 'T ^ r '
A A ^ ^iLLi i i^_ .... ^ ,
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PALEOCHEM
6507/12-2,1875mCP2 P E A K )
6507/12-2,1875m(PI P E A K )
L U B R I C AT I N G OIL
BOILING POINT DISTRIBUTION
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PALEOCHEM
GASES
G S O L I N E
KEROSENE DIESEL
H E V Y
GAS
O I L
s
L U B R I C T I N G
OIL
G S E S
G S O L I N E
KEROSENE DIESEL
H E V Y
GAS
OIL
L U B R I C T I N G
O I L
2235
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-12-
PA L E O C H E M
(c) Sediment/Oil Shows Correlation ' * -
T V ; i 'A sediment to oil show correlation study was completed
by CGCMS examination of the extracts from the two Kimmeridgiansediments (1873 and 1875 m) and oil shows from the reservoir
sandstones (3062, 3080.5 and 3143 m). The sediment from 1873was considered to be the least affected by hydrocarbon con-tamination, judged by Screening Pyrolysis measurements andwas therefore used in the following comparison. The extractfrom the reservoir sandstone at 3062 m was also chosen forcomparison, as it was the largest extract obtained (Table 4).
Detailed comparison was made between the sterane and
hopane distributions, together with the distributions of the
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PA L E O C H E M
References
1. Dow W.G. J. Geochem Expl. 1 _ , pp 79 (1977).
2. Ronov A.B. Geochemistry No.5., pp.510(1958) .
3. Hunt J.M. The Origin of PetroleumCarbonate Rocks .Elsevier Ch.7 (1967).
Clementz D.M. ,Demaison G. J.,Daly A.R.
OTC (1979) page 465.
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Well: 6507/12-2
VISUAL KEROGEN DATA
Depth Cuticle Brownm Wood
3305 Trace
3360 Trace
3447.5 Trace
Black Wood Amorphous& Inertinite
Trace
Trace
Trace
PredominantSource Type
None
None
None
ColourMaturationRating
2
Barren
2
Table 1 - continued.
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PALEOCHEM
Well: 6507/12-2
General Well Data
Sample Type Stratigraphy(by
Paleoservi ces)
SWC Late Cretaceous
SWC Late Cretaceous
SWC Kimmeridgian
SWC i ' Ki mme r dgi an
Depthm.
1835
1865
1873
1875
Lithology
Grey Claystone
Grey Claystone
Dark GreymicaceousSiltstone
Dark GreymicaceousSiltstone
Total OCarbon(TOC) %
1.
0.8
9.3
5.7
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1 PALEOCHEM -
Well: 6507/12-2
General
Sample Type Stratigraphy(by
Paleoservices)
swc Late Triassic
SWC Late Triassic
SWC Late Triassic
SWC Late Triassic
SWC Late Triassic
SWC Late Triassic
Well Data
Depthm.
3 1 7 5
3280
3305
3320
3360
3378
Lithology
Red ClaystoneRed Claystone(+Evaporite?)
Grey Claystone
Red Claystone
Pale GreyClaystone
White Sand-stone (+Rust?)
Total OrganicCarbon Cont(TOC) w
0.20
0.15
0.15
0.14
0.19
005
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PALEOCHEM
Well: 6507/12-2
Pyrolvsis Data
Depthm.
1835
1865
1873
1875
1873*
1875*
1889
Yield (Kg/tonne)PI Peak
0.3
0.2 (0.1 Rpt)
2.3
2.4
0.6
0.7
0.2 (0.2 Rpt)
P2 Peak
1.10.4 (0.4
10.8
10.3
7.6
6.9
0.7 (0.6
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Well No: 6507/12-2
SOLUBLE EXTRACT DATA
Depthm.
1873
1875
3062
3080.5 , , j
3143
Total SolubleExtract (TSE) wt.
0.199
0.217
0.706
0.607
0.170
Saturate AlkaneContent (SAC) of
TSE ( :/;,r
47.0f
46.8 ?
28.9 / ?
41.1 / > -
15.7 - 6 , t , 3
Aromat i csContent (AC) of TSE
0.2
1.2
15.3
20.7
26.1
Carbon PrefereceIndex (CPI)
N P - V '
NP /
NP
NP
NP -- - > .
NP - CPI values could not be calculated due to short range of saturate alkanes presentin samples.
Table 4.
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Sediment Extract 1873
I - . m M / i e / ic - - ,
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P A L E O C H E M
DI
Sediment Extract 1 8 7 3
V?
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Sediment Extract 1873
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PALEOCHEM
Sediment Extract 1873
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PLEGG H r: M
Sediment Extract
1873 m
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