Search

This study reports a laboratory pyrolysis experimental study on oil and n-hexadecane to rationalise the thermal stability of oil in deep petroleum reservoirs. Using a 25 ml Hastelloy pressure vessel, a 35° API North Sea oil (Oseberg) and n-hexadecane (n-C16), were pyrolysed separately under non-hydrous (20 bar), low pressure hydrous (175 bar) and high liquid water pressure (500 and 900 bar) at 350 °C for 24 h. This study shows that the initial cracking of oil and n-hexadecane to hydrocarbon gases was retarded in the presence of water (175 bar hydrous conditions) compared to low pressures in the absence of water (non-hydrous conditions). At 900 bar water pressure, the retardation of oil and n-hexadecane cracking was more significant compared to 175 bar hydrous and 500 bar water pressure conditions. Combination reactions have been observed for the first time in pressurised water experiments during the initial stages of cracking, resulting in the increased abundance of heavier n-alkane hydrocarbons (> C20), the amount of unresolved complex material (UCM), as well as the asphaltene content of the oil. These reactions, favoured by increasing water pressure provide a new mechanism for rationalising the thermal stability of oils, and for producing heavy oils at temperatures above which biodegradation can occur. Indeed, we demonstrate that bitumen from the high pressure Gulf of Mexico basin has been formed from lighter oil components and it possesses similar characteristics to the laboratory oils generated.

This study investigates the effect of water pressure on hydrocarbon generation and source rock maturation at high maturities for a perhydrous Tertiary Arctic coal, Svalbard. Using a 25 ml Hastalloy vessel, the coal was pyrolysed under low water pressure (230–300 bar) and high water pressure (500, 700 and 900 bar) conditions between 380 °C and 420 °C for 24 h. At 380 °C and 420 °C, gas yields were not affected by pressure up to 700 bar, but were reduced slightly at 900 bar. At 380 °C, the expelled oil yield was highest at 230 bar, but reduced significantly at 900 bar. At 420 °C cracking of expelled oil to gas was retarded at 700 and 900 bar. As well as direct cracking of the coal, the main source of gas generation at high pressure at both 380 °C and 420 °C is from bitumen trapped in the coal, indicating that this is a key mechanism in high pressure geological basins. Vitrinite reflectance (VR) was reduced by 0.16 %Ro at 380 °C and by 0.27 %Ro at 420 °C at 900 bar compared to the low pressure runs, indicating that source rock maturation will be more retarded at higher maturities in high pressure geological basins.

This study investigates the effect of water pressure on hydrocarbon generation and maturation of coals. Using a 25 ml Hastalloy pressure vessel, two high-volatile coals (Longannet, UK 0.75% Ro, and perhydrous Svalbard (Spitsbergen), Norway 0.68% Ro) were pyrolysed under non-hydrous, hydrous at 175 bar pressure, and high water pressure hydrous (500 bar and 900 bar) conditions at 350 °C for 24 h. The bitumen yield obtained during pyrolysis, together with the Rock–Eval S2, hydrogen index (HI) and vitrinite reflectance (VR) results from the pyrolysed coal residues indicated that water under relatively low pressure (175 bar) hydrous conditions promoted hydrocarbon generation and coal maturation in relation to non-hydrous conditions, consistent with previous work. However, under high water pressure (500 and 900 bar) conditions, a combination of the hydrocarbon gas (C1–C4) and bitumen yields, Rock–Eval S2, HI, VR and solid state 13C NMR results demonstrated that the changes in reaction pathways occurring with increasing pressure resulted in both hydrocarbon generation and maturation being retarded. The observed effect of pressure implies that for Type III source rocks, hydrocarbon generation will be retarded in high pressure geological basins, with gas yields being proportionally reduced more than bitumen yields. Source rock maturation (or coalification) is also retarded, with the decreases in vitrinite reflectance and carbon aromaticity being relatively small but significant in terms of explaining retardation in geological basins.

Central Tertiary Basin (CTB) coals from a variety of palaeogeographic conditions within the Longyear and Verkhnij seams, were sampled to assess the relationship between the petroleum present, the remaining generation potential and coal geochemistry in order to improve the spatial predictability of petroleum resources within the basin. Vitrinite reflectance (VR) values from the CTB coals have been shown to be suppressed (Marshall et al., 2015a). This study attempts to quantify and correct for this suppression effect by applying the Lo (1993) method (LoVR), which uses Hydrogen Index (HI) values to modify VR data, and the coal Rank(Sr) scale of Suggate (2000, 2002), a technique not affected by suppression. In addition, the oil generation and expulsion thresholds for the CTB coals were investigated.

This study reports a laboratory pyrolysis experimental study on oil and n-hexadecane to rationalise the thermal stability of oil in deep petroleum reservoirs. Using a 25 ml Hastelloy pressure vessel, a 35° API North Sea oil (Oseberg) and n-hexadecane (n-C16), were pyrolysed separately under non-hydrous (20 bar), low pressure hydrous (175 bar) and high liquid water pressure (500 and 900 bar) at 350°C for 24 h. This study reports a laboratory pyrolysis experimental study on oil and n-hexadecane to rationalise the thermal stability of oil in deep petroleum reservoirs. Using a 25 ml Hastelloy pressure vessel, a 35° API North Sea oil (Oseberg) and n-hexadecane (n-C16), were pyrolysed separately under non-hydrous (20 bar), low pressure hydrous (175 bar) and high liquid water pressure (500 and 900 bar) at 350 °C for 24 h. This study shows that the initial cracking of oil and n-hexadecane to hydrocarbon gases was retarded in the presence of water (175 bar hydrous conditions) compared to low pressures in the absence of water (non-hydrous conditions). At 900 bar water pressure, the retardation of oil and n-hexadecane cracking was more significant compared to 175 bar hydrous and 500 bar water pressure conditions. Combination reactions have been observed for the first time in pressurised water experiments during the initial stages of cracking, resulting in the increased abundance of heavier n-alkane hydrocarbons (> C20), the amount of unresolved complex material (UCM), as well as the asphaltene content of the oil. These reactions, favoured by increasing water pressure provide a new mechanism for rationalising the thermal stability of oils, and for producing heavy oils at temperatures above which biodegradation can occur. Indeed, we demonstrate that bitumen from the high pressure Gulf of Mexico basin has been formed from lighter oil components and it possesses similar characteristics to the laboratory oils generated.

This study presents results for pyrolysis experiments conducted on immature Type II and IIs source rocks (Kimmeridge Clay, Dorset UK, and Monterey shale, California, USA respectively) to investigate the impact of high water pressure on source rock maturation and petroleum (oil and gas) generation. Using a 25 ml Hastalloy vessel, the source rocks were pyrolysed at low (180 and 245 bar) and high (500, 700 and 900 bar) water pressure hydrous conditions at 350 °C and 380 °C for between 6 and 24 h. For the Kimmeridge Clay (KCF) at 350 °C, Rock Eval HI of the pyrolysed rock residues were 30–44 mg/g higher between 6 h and 12 h at 900 bar than at 180 bar. Also at 350 °C for 24 h the gas, expelled oil, and vitrinite reflectance (VR) were all reduced by 46%, 61%, and 0.25% Ro respectively at 900 bar compared with 180 bar. At 380 °C the retardation effect of pressure on the KCF was less significant for gas generation. However, oil yield and VR were reduced by 47% and 0.3% Ro respectively, and Rock Eval HI was also higher by 28 mg/g at 900 bar compared with 245 bar at 12 h. The huge decrease in gas and oil yields and the VR observed with an increase in water pressure at 350 °C for 24 h and 380 °C for 12 h (maximum oil generation) were also observed for all other times and temperatures investigated for the KCF and the Monterey shale. This shows that high water pressure significantly retards petroleum generation and source rock maturation. The retardation of oil generation and expulsion resulted in significant amounts of bitumen and oil being retained in the rocks pyrolysed at high pressures, suggesting that pressure is a possible mechanism for retaining petroleum (bitumen and oil) in source rocks. This retention of petroleum within the rock provides a mechanism for oil-prone source rocks to become potential shale gas reservoirs. The implications from this study are that in geological basins, pressure, temperature and time will all exert significant control on the extent of petro

This study investigates the effect of water pressure on hydrocarbon generation and source rock maturation at high maturities for a perhydrous Tertiary Arctic coal, Svalbard. Using a 25 ml Hastalloy vessel, the coal was pyrolysed under low water pressure (230–300 bar) and high water pressure (500, 700 and 900 bar) conditions between 380 °C and 420 °C for 24 h. At 380 °C and 420 °C, gas yields were not affected by pressure up to 700 bar, but were reduced slightly at 900 bar. At 380 °C, the expelled oil yield was highest at 230 bar, but reduced significantly at 900 bar. At 420 °C cracking of expelled oil to gas was retarded at 700 and 900 bar. As well as direct cracking of the coal, the main source of gas generation at high pressure at both 380 °C and 420 °C is from bitumen trapped in the coal, indicating that this is a key mechanism in high pressure geological basins. Vitrinite reflectance (VR) was reduced by 0.16 %Ro at 380 °C and by 0.27 %Ro at 420 °C at 900 bar compared to the low pressure runs, indicating that source rock maturation will be more retarded at higher maturities in high pressure geological basins.

Central Tertiary Basin (CTB) coals from a variety of palaeogeographic conditions within the Longyear and Verkhnij seams, were sampled to assess the relationship between the petroleum present, the remaining generation potential and coal geochemistry in order to improve the spatial predictability of petroleum resources within the basin. Vitrinite reflectance (VR) values from the CTB coals have been shown to be suppressed (Marshall et al., 2015a). This study attempts to quantify and correct for this suppression effect by applying the Lo (1993) method (LoVR), which uses Hydrogen Index (HI) values to modify VR data, and the coal Rank(Sr) scale of Suggate (2000, 2002), a technique not affected by suppression. In addition, the oil generation and expulsion thresholds for the CTB coals were investigated.

This study investigates the effect of water pressure on hydrocarbon generation and source rock maturation at high maturities for a perhydrous Tertiary Arctic coal, Svalbard. Using a 25 ml Hastalloy vessel, the coal was pyrolysed under low water pressure (230–300 bar) and high water pressure (500, 700 and 900 bar) conditions between 380 °C and 420 °C for 24 h. At 380 °C and 420 °C, gas yields were not affected by pressure up to 700 bar, but were reduced slightly at 900 bar. At 380 °C, the expelled oil yield was highest at 230 bar, but reduced significantly at 900 bar. At 420 °C cracking of expelled oil to gas was retarded at 700 and 900 bar. As well as direct cracking of the coal, the main source of gas generation at high pressure at both 380 °C and 420 °C is from bitumen trapped in the coal, indicating that this is a key mechanism in high pressure geological basins. Vitrinite reflectance (VR) was reduced by 0.16 %Ro at 380 °C and by 0.27 %Ro at 420 °C at 900 bar compared to the low pressure runs, indicating that source rock maturation will be more retarded at higher maturities in high pressure geological basins.

This study presents results for pyrolysis experiments conducted on immature Type II and IIs source rocks (Kimmeridge Clay, Dorset UK, and Monterey shale, California, USA respectively) to investigate the impact of high water pressure on source rock maturation and petroleum (oil and gas) generation. Using a 25 ml Hastalloy vessel, the source rocks were pyrolysed at low (180 and 245 bar) and high (500, 700 and 900 bar) water pressure hydrous conditions at 350 °C and 380 °C for between 6 and 24 h. For the Kimmeridge Clay (KCF) at 350 °C, Rock Eval HI of the pyrolysed rock residues were 30–44 mg/g higher between 6 h and 12 h at 900 bar than at 180 bar. Also at 350 °C for 24 h the gas, expelled oil, and vitrinite reflectance (VR) were all reduced by 46%, 61%, and 0.25% Ro respectively at 900 bar compared with 180 bar. At 380 °C the retardation effect of pressure on the KCF was less significant for gas generation. However, oil yield and VR were reduced by 47% and 0.3% Ro respectively, and Rock Eval HI was also higher by 28 mg/g at 900 bar compared with 245 bar at 12 h. The huge decrease in gas and oil yields and the VR observed with an increase in water pressure at 350 °C for 24 h and 380 °C for 12 h (maximum oil generation) were also observed for all other times and temperatures investigated for the KCF and the Monterey shale. This shows that high water pressure significantly retards petroleum generation and source rock maturation. The retardation of oil generation and expulsion resulted in significant amounts of bitumen and oil being retained in the rocks pyrolysed at high pressures, suggesting that pressure is a possible mechanism for retaining petroleum (bitumen and oil) in source rocks. This retention of petroleum within the rock provides a mechanism for oil-prone source rocks to become potential shale gas reservoirs. The implications from this study are that in geological basins, pressure, temperature and time will all exert significant control on the extent of petro

This study reports a laboratory pyrolysis experimental study on oil and n-hexadecane to rationalise the thermal stability of oil in deep petroleum reservoirs. Using a 25 ml Hastelloy pressure vessel, a 35° API North Sea oil (Oseberg) and n-hexadecane (n-C16), were pyrolysed separately under non-hydrous (20 bar), low pressure hydrous (175 bar) and high liquid water pressure (500 and 900 bar) at 350°C for 24 h. This study reports a laboratory pyrolysis experimental study on oil and n-hexadecane to rationalise the thermal stability of oil in deep petroleum reservoirs. Using a 25 ml Hastelloy pressure vessel, a 35° API North Sea oil (Oseberg) and n-hexadecane (n-C16), were pyrolysed separately under non-hydrous (20 bar), low pressure hydrous (175 bar) and high liquid water pressure (500 and 900 bar) at 350 °C for 24 h. This study shows that the initial cracking of oil and n-hexadecane to hydrocarbon gases was retarded in the presence of water (175 bar hydrous conditions) compared to low pressures in the absence of water (non-hydrous conditions). At 900 bar water pressure, the retardation of oil and n-hexadecane cracking was more significant compared to 175 bar hydrous and 500 bar water pressure conditions. Combination reactions have been observed for the first time in pressurised water experiments during the initial stages of cracking, resulting in the increased abundance of heavier n-alkane hydrocarbons (> C20), the amount of unresolved complex material (UCM), as well as the asphaltene content of the oil. These reactions, favoured by increasing water pressure provide a new mechanism for rationalising the thermal stability of oils, and for producing heavy oils at temperatures above which biodegradation can occur. Indeed, we demonstrate that bitumen from the high pressure Gulf of Mexico basin has been formed from lighter oil components and it possesses similar characteristics to the laboratory oils generated.

Central Tertiary Basin (CTB) coals from a variety of palaeogeographic conditions within the Longyear and Verkhnij seams, were sampled to assess the relationship between the petroleum present, the remaining generation potential and coal geochemistry in order to improve the spatial predictability of petroleum resources within the basin. Vitrinite reflectance (VR) values from the CTB coals have been shown to be suppressed (Marshall et al., 2015a). This study attempts to quantify and correct for this suppression effect by applying the Lo (1993) method (LoVR), which uses Hydrogen Index (HI) values to modify VR data, and the coal Rank(Sr) scale of Suggate (2000, 2002), a technique not affected by suppression. In addition, the oil generation and expulsion thresholds for the CTB coals were investigated.

This study presents results for pyrolysis experiments conducted on immature Type II and IIs source rocks (Kimmeridge Clay, Dorset UK, and Monterey shale, California, USA respectively) to investigate the impact of high water pressure on source rock maturation and petroleum (oil and gas) generation. Using a 25 ml Hastalloy vessel, the source rocks were pyrolysed at low (180 and 245 bar) and high (500, 700 and 900 bar) water pressure hydrous conditions at 350 °C and 380 °C for between 6 and 24 h. For the Kimmeridge Clay (KCF) at 350 °C, Rock Eval HI of the pyrolysed rock residues were 30–44 mg/g higher between 6 h and 12 h at 900 bar than at 180 bar. Also at 350 °C for 24 h the gas, expelled oil, and vitrinite reflectance (VR) were all reduced by 46%, 61%, and 0.25% Ro respectively at 900 bar compared with 180 bar. At 380 °C the retardation effect of pressure on the KCF was less significant for gas generation. However, oil yield and VR were reduced by 47% and 0.3% Ro respectively, and Rock Eval HI was also higher by 28 mg/g at 900 bar compared with 245 bar at 12 h. The huge decrease in gas and oil yields and the VR observed with an increase in water pressure at 350 °C for 24 h and 380 °C for 12 h (maximum oil generation) were also observed for all other times and temperatures investigated for the KCF and the Monterey shale. This shows that high water pressure significantly retards petroleum generation and source rock maturation. The retardation of oil generation and expulsion resulted in significant amounts of bitumen and oil being retained in the rocks pyrolysed at high pressures, suggesting that pressure is a possible mechanism for retaining petroleum (bitumen and oil) in source rocks. This retention of petroleum within the rock provides a mechanism for oil-prone source rocks to become potential shale gas reservoirs. The implications from this study are that in geological basins, pressure, temperature and time will all exert significant control on the extent of petro

This study investigates the effect of water pressure on hydrocarbon generation and source rock maturation at high maturities for a perhydrous Tertiary Arctic coal, Svalbard. Using a 25 ml Hastalloy vessel, the coal was pyrolysed under low water pressure (230–300 bar) and high water pressure (500, 700 and 900 bar) conditions between 380 °C and 420 °C for 24 h. At 380 °C and 420 °C, gas yields were not affected by pressure up to 700 bar, but were reduced slightly at 900 bar. At 380 °C, the expelled oil yield was highest at 230 bar, but reduced significantly at 900 bar. At 420 °C cracking of expelled oil to gas was retarded at 700 and 900 bar. As well as direct cracking of the coal, the main source of gas generation at high pressure at both 380 °C and 420 °C is from bitumen trapped in the coal, indicating that this is a key mechanism in high pressure geological basins. Vitrinite reflectance (VR) was reduced by 0.16 %Ro at 380 °C and by 0.27 %Ro at 420 °C at 900 bar compared to the low pressure runs, indicating that source rock maturation will be more retarded at higher maturities in high pressure geological basins.

This study reports a laboratory pyrolysis experimental study on oil and n-hexadecane to rationalise the thermal stability of oil in deep petroleum reservoirs. Using a 25 ml Hastelloy pressure vessel, a 35° API North Sea oil (Oseberg) and n-hexadecane (n-C16), were pyrolysed separately under non-hydrous (20 bar), low pressure hydrous (175 bar) and high liquid water pressure (500 and 900 bar) at 350°C for 24 h. This study reports a laboratory pyrolysis experimental study on oil and n-hexadecane to rationalise the thermal stability of oil in deep petroleum reservoirs. Using a 25 ml Hastelloy pressure vessel, a 35° API North Sea oil (Oseberg) and n-hexadecane (n-C16), were pyrolysed separately under non-hydrous (20 bar), low pressure hydrous (175 bar) and high liquid water pressure (500 and 900 bar) at 350 °C for 24 h. This study shows that the initial cracking of oil and n-hexadecane to hydrocarbon gases was retarded in the presence of water (175 bar hydrous conditions) compared to low pressures in the absence of water (non-hydrous conditions). At 900 bar water pressure, the retardation of oil and n-hexadecane cracking was more significant compared to 175 bar hydrous and 500 bar water pressure conditions. Combination reactions have been observed for the first time in pressurised water experiments during the initial stages of cracking, resulting in the increased abundance of heavier n-alkane hydrocarbons (> C20), the amount of unresolved complex material (UCM), as well as the asphaltene content of the oil. These reactions, favoured by increasing water pressure provide a new mechanism for rationalising the thermal stability of oils, and for producing heavy oils at temperatures above which biodegradation can occur. Indeed, we demonstrate that bitumen from the high pressure Gulf of Mexico basin has been formed from lighter oil components and it possesses similar characteristics to the laboratory oils generated.

Central Tertiary Basin (CTB) coals from a variety of palaeogeographic conditions within the Longyear and Verkhnij seams, were sampled to assess the relationship between the petroleum present, the remaining generation potential and coal geochemistry in order to improve the spatial predictability of petroleum resources within the basin. Vitrinite reflectance (VR) values from the CTB coals have been shown to be suppressed (Marshall et al., 2015a). This study attempts to quantify and correct for this suppression effect by applying the Lo (1993) method (LoVR), which uses Hydrogen Index (HI) values to modify VR data, and the coal Rank(Sr) scale of Suggate (2000, 2002), a technique not affected by suppression. In addition, the oil generation and expulsion thresholds for the CTB coals were investigated.

This study investigates the effect of water pressure on hydrocarbon generation and source rock maturation at high maturities for a perhydrous Tertiary Arctic coal, Svalbard. Using a 25 ml Hastalloy vessel, the coal was pyrolysed under low water pressure (230–300 bar) and high water pressure (500, 700 and 900 bar) conditions between 380 °C and 420 °C for 24 h. At 380 °C and 420 °C, gas yields were not affected by pressure up to 700 bar, but were reduced slightly at 900 bar. At 380 °C, the expelled oil yield was highest at 230 bar, but reduced significantly at 900 bar. At 420 °C cracking of expelled oil to gas was retarded at 700 and 900 bar. As well as direct cracking of the coal, the main source of gas generation at high pressure at both 380 °C and 420 °C is from bitumen trapped in the coal, indicating that this is a key mechanism in high pressure geological basins. Vitrinite reflectance (VR) was reduced by 0.16 %Ro at 380 °C and by 0.27 %Ro at 420 °C at 900 bar compared to the low pressure runs, indicating that source rock maturation will be more retarded at higher maturities in high pressure geological basins.

This study reports a laboratory pyrolysis experimental study on oil and n-hexadecane to rationalise the thermal stability of oil in deep petroleum reservoirs. Using a 25 ml Hastelloy pressure vessel, a 35° API North Sea oil (Oseberg) and n-hexadecane (n-C16), were pyrolysed separately under non-hydrous (20 bar), low pressure hydrous (175 bar) and high liquid water pressure (500 and 900 bar) at 350°C for 24 h. This study reports a laboratory pyrolysis experimental study on oil and n-hexadecane to rationalise the thermal stability of oil in deep petroleum reservoirs. Using a 25 ml Hastelloy pressure vessel, a 35° API North Sea oil (Oseberg) and n-hexadecane (n-C16), were pyrolysed separately under non-hydrous (20 bar), low pressure hydrous (175 bar) and high liquid water pressure (500 and 900 bar) at 350 °C for 24 h. This study shows that the initial cracking of oil and n-hexadecane to hydrocarbon gases was retarded in the presence of water (175 bar hydrous conditions) compared to low pressures in the absence of water (non-hydrous conditions). At 900 bar water pressure, the retardation of oil and n-hexadecane cracking was more significant compared to 175 bar hydrous and 500 bar water pressure conditions. Combination reactions have been observed for the first time in pressurised water experiments during the initial stages of cracking, resulting in the increased abundance of heavier n-alkane hydrocarbons (> C20), the amount of unresolved complex material (UCM), as well as the asphaltene content of the oil. These reactions, favoured by increasing water pressure provide a new mechanism for rationalising the thermal stability of oils, and for producing heavy oils at temperatures above which biodegradation can occur. Indeed, we demonstrate that bitumen from the high pressure Gulf of Mexico basin has been formed from lighter oil components and it possesses similar characteristics to the laboratory oils generated.

This study presents results for pyrolysis experiments conducted on immature Type II and IIs source rocks (Kimmeridge Clay, Dorset UK, and Monterey shale, California, USA respectively) to investigate the impact of high water pressure on source rock maturation and petroleum (oil and gas) generation. Using a 25 ml Hastalloy vessel, the source rocks were pyrolysed at low (180 and 245 bar) and high (500, 700 and 900 bar) water pressure hydrous conditions at 350 °C and 380 °C for between 6 and 24 h. For the Kimmeridge Clay (KCF) at 350 °C, Rock Eval HI of the pyrolysed rock residues were 30–44 mg/g higher between 6 h and 12 h at 900 bar than at 180 bar. Also at 350 °C for 24 h the gas, expelled oil, and vitrinite reflectance (VR) were all reduced by 46%, 61%, and 0.25% Ro respectively at 900 bar compared with 180 bar. At 380 °C the retardation effect of pressure on the KCF was less significant for gas generation. However, oil yield and VR were reduced by 47% and 0.3% Ro respectively, and Rock Eval HI was also higher by 28 mg/g at 900 bar compared with 245 bar at 12 h. The huge decrease in gas and oil yields and the VR observed with an increase in water pressure at 350 °C for 24 h and 380 °C for 12 h (maximum oil generation) were also observed for all other times and temperatures investigated for the KCF and the Monterey shale. This shows that high water pressure significantly retards petroleum generation and source rock maturation. The retardation of oil generation and expulsion resulted in significant amounts of bitumen and oil being retained in the rocks pyrolysed at high pressures, suggesting that pressure is a possible mechanism for retaining petroleum (bitumen and oil) in source rocks. This retention of petroleum within the rock provides a mechanism for oil-prone source rocks to become potential shale gas reservoirs. The implications from this study are that in geological basins, pressure, temperature and time will all exert significant control on the extent of petro

Central Tertiary Basin (CTB) coals from a variety of palaeogeographic conditions within the Longyear and Verkhnij seams, were sampled to assess the relationship between the petroleum present, the remaining generation potential and coal geochemistry in order to improve the spatial predictability of petroleum resources within the basin. Vitrinite reflectance (VR) values from the CTB coals have been shown to be suppressed (Marshall et al., 2015a). This study attempts to quantify and correct for this suppression effect by applying the Lo (1993) method (LoVR), which uses Hydrogen Index (HI) values to modify VR data, and the coal Rank(Sr) scale of Suggate (2000, 2002), a technique not affected by suppression. In addition, the oil generation and expulsion thresholds for the CTB coals were investigated.

This study reports a laboratory pyrolysis experimental study on oil and n-hexadecane to rationalise the thermal stability of oil in deep petroleum reservoirs. Using a 25 ml Hastelloy pressure vessel, a 35° API North Sea oil (Oseberg) and n-hexadecane (n-C16), were pyrolysed separately under non-hydrous (20 bar), low pressure hydrous (175 bar) and high liquid water pressure (500 and 900 bar) at 350°C for 24 h. This study reports a laboratory pyrolysis experimental study on oil and n-hexadecane to rationalise the thermal stability of oil in deep petroleum reservoirs. Using a 25 ml Hastelloy pressure vessel, a 35° API North Sea oil (Oseberg) and n-hexadecane (n-C16), were pyrolysed separately under non-hydrous (20 bar), low pressure hydrous (175 bar) and high liquid water pressure (500 and 900 bar) at 350 °C for 24 h. This study shows that the initial cracking of oil and n-hexadecane to hydrocarbon gases was retarded in the presence of water (175 bar hydrous conditions) compared to low pressures in the absence of water (non-hydrous conditions). At 900 bar water pressure, the retardation of oil and n-hexadecane cracking was more significant compared to 175 bar hydrous and 500 bar water pressure conditions. Combination reactions have been observed for the first time in pressurised water experiments during the initial stages of cracking, resulting in the increased abundance of heavier n-alkane hydrocarbons (> C20), the amount of unresolved complex material (UCM), as well as the asphaltene content of the oil. These reactions, favoured by increasing water pressure provide a new mechanism for rationalising the thermal stability of oils, and for producing heavy oils at temperatures above which biodegradation can occur. Indeed, we demonstrate that bitumen from the high pressure Gulf of Mexico basin has been formed from lighter oil components and it possesses similar characteristics to the laboratory oils generated.

This study investigates the effect of water pressure on hydrocarbon generation and source rock maturation at high maturities for a perhydrous Tertiary Arctic coal, Svalbard. Using a 25 ml Hastalloy vessel, the coal was pyrolysed under low water pressure (230–300 bar) and high water pressure (500, 700 and 900 bar) conditions between 380 °C and 420 °C for 24 h. At 380 °C and 420 °C, gas yields were not affected by pressure up to 700 bar, but were reduced slightly at 900 bar. At 380 °C, the expelled oil yield was highest at 230 bar, but reduced significantly at 900 bar. At 420 °C cracking of expelled oil to gas was retarded at 700 and 900 bar. As well as direct cracking of the coal, the main source of gas generation at high pressure at both 380 °C and 420 °C is from bitumen trapped in the coal, indicating that this is a key mechanism in high pressure geological basins. Vitrinite reflectance (VR) was reduced by 0.16 %Ro at 380 °C and by 0.27 %Ro at 420 °C at 900 bar compared to the low pressure runs, indicating that source rock maturation will be more retarded at higher maturities in high pressure geological basins.

This study presents results for pyrolysis experiments conducted on immature Type II and IIs source rocks (Kimmeridge Clay, Dorset UK, and Monterey shale, California, USA respectively) to investigate the impact of high water pressure on source rock maturation and petroleum (oil and gas) generation. Using a 25 ml Hastalloy vessel, the source rocks were pyrolysed at low (180 and 245 bar) and high (500, 700 and 900 bar) water pressure hydrous conditions at 350 °C and 380 °C for between 6 and 24 h. For the Kimmeridge Clay (KCF) at 350 °C, Rock Eval HI of the pyrolysed rock residues were 30–44 mg/g higher between 6 h and 12 h at 900 bar than at 180 bar. Also at 350 °C for 24 h the gas, expelled oil, and vitrinite reflectance (VR) were all reduced by 46%, 61%, and 0.25% Ro respectively at 900 bar compared with 180 bar. At 380 °C the retardation effect of pressure on the KCF was less significant for gas generation. However, oil yield and VR were reduced by 47% and 0.3% Ro respectively, and Rock Eval HI was also higher by 28 mg/g at 900 bar compared with 245 bar at 12 h. The huge decrease in gas and oil yields and the VR observed with an increase in water pressure at 350 °C for 24 h and 380 °C for 12 h (maximum oil generation) were also observed for all other times and temperatures investigated for the KCF and the Monterey shale. This shows that high water pressure significantly retards petroleum generation and source rock maturation. The retardation of oil generation and expulsion resulted in significant amounts of bitumen and oil being retained in the rocks pyrolysed at high pressures, suggesting that pressure is a possible mechanism for retaining petroleum (bitumen and oil) in source rocks. This retention of petroleum within the rock provides a mechanism for oil-prone source rocks to become potential shale gas reservoirs. The implications from this study are that in geological basins, pressure, temperature and time will all exert significant control on the extent of petro