Temperature-Dependent Oxygen Effect on NMR D-$$T_2$$ Relaxation-Diffusion Correlation of n-Alkanes
Abstract Nuclear magnetic resonance (NMR) diffusion-relaxation correlation experiments (D-$$T_2$$) are widely used for the petrophysical characterisation of rocks saturated with petroleum fluids both in situ and for laboratory analyses. The encoding for both diffusion and relaxation offers increased...
Ausführliche Beschreibung
Autor*in: |
Shikhov, Igor [verfasserIn] |
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Sprache: |
Englisch |
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2016 |
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Anmerkung: |
© The Author(s) 2016 |
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Übergeordnetes Werk: |
Enthalten in: Applied magnetic resonance - Springer Vienna, 1990, 47(2016), 12 vom: 19. Sept., Seite 1391-1408 |
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Übergeordnetes Werk: |
volume:47 ; year:2016 ; number:12 ; day:19 ; month:09 ; pages:1391-1408 |
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DOI / URN: |
10.1007/s00723-016-0830-4 |
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Katalog-ID: |
OLC2043929569 |
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520 | |a Abstract Nuclear magnetic resonance (NMR) diffusion-relaxation correlation experiments (D-$$T_2$$) are widely used for the petrophysical characterisation of rocks saturated with petroleum fluids both in situ and for laboratory analyses. The encoding for both diffusion and relaxation offers increased fluid typing contrast by discriminating fluids based on their self-diffusion coefficients, while relaxation times provide information about the interaction of solid and fluid phases and associated confinement geometry (if NMR responses of pure fluids at particular temperature and pressure are known). Petrophysical interpretation of D-$$T_2$$ correlation maps is typically assisted by the “standard alkane line”—a relaxation-diffusion correlation valid for pure normal alkanes and their mixtures in the absence of restrictions to diffusing molecules and effects of internal gradients. This correlation assumes fluids are free from paramagnetic impurities. In situations where fluid samples cannot be maintained at air-free state the diffusion-relaxation response of fluids shift towards shorter relaxation times due to oxygen paramagnetic relaxation enhancement. Interpretation of such a response using the “standard alkane line” would be erroneous and is further complicated by the temperature-dependence of oxygen solubility for each component of the alkane mixture. We propose a diffusion-relaxation correlation suitable for interpretation of low-field NMR D-$$T_2$$ responses of normal alkanes and their mixtures saturating rocks over a broad temperature range, in equilibrium with atmospheric air. We review and where necessary revise existing viscosity-relaxation correlations. Findings are applied to diffusion-relaxation dependencies taking into account the temperature dependence of oxygen solubility and solvent vapour pressure. The effect is demonstrated on a partially saturated carbonate rock. | ||
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10.1007/s00723-016-0830-4 doi (DE-627)OLC2043929569 (DE-He213)s00723-016-0830-4-p DE-627 ger DE-627 rakwb eng 530 620 VZ UA 2242.9 VZ rvk 53.00 bkl 33.00 bkl Shikhov, Igor verfasserin aut Temperature-Dependent Oxygen Effect on NMR D-$$T_2$$ Relaxation-Diffusion Correlation of n-Alkanes 2016 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © The Author(s) 2016 Abstract Nuclear magnetic resonance (NMR) diffusion-relaxation correlation experiments (D-$$T_2$$) are widely used for the petrophysical characterisation of rocks saturated with petroleum fluids both in situ and for laboratory analyses. The encoding for both diffusion and relaxation offers increased fluid typing contrast by discriminating fluids based on their self-diffusion coefficients, while relaxation times provide information about the interaction of solid and fluid phases and associated confinement geometry (if NMR responses of pure fluids at particular temperature and pressure are known). Petrophysical interpretation of D-$$T_2$$ correlation maps is typically assisted by the “standard alkane line”—a relaxation-diffusion correlation valid for pure normal alkanes and their mixtures in the absence of restrictions to diffusing molecules and effects of internal gradients. This correlation assumes fluids are free from paramagnetic impurities. In situations where fluid samples cannot be maintained at air-free state the diffusion-relaxation response of fluids shift towards shorter relaxation times due to oxygen paramagnetic relaxation enhancement. Interpretation of such a response using the “standard alkane line” would be erroneous and is further complicated by the temperature-dependence of oxygen solubility for each component of the alkane mixture. We propose a diffusion-relaxation correlation suitable for interpretation of low-field NMR D-$$T_2$$ responses of normal alkanes and their mixtures saturating rocks over a broad temperature range, in equilibrium with atmospheric air. We review and where necessary revise existing viscosity-relaxation correlations. Findings are applied to diffusion-relaxation dependencies taking into account the temperature dependence of oxygen solubility and solvent vapour pressure. The effect is demonstrated on a partially saturated carbonate rock. Nuclear Magnetic Resonance Alkane Normal Alkane Nuclear Magnetic Resonance Relaxation Paramagnetic Relaxation Enhancement Arns, Christoph H. (orcid)0000-0003-1721-3996 aut Enthalten in Applied magnetic resonance Springer Vienna, 1990 47(2016), 12 vom: 19. Sept., Seite 1391-1408 (DE-627)13092427X (DE-600)1054553-0 (DE-576)02803757X 0937-9347 nnns volume:47 year:2016 number:12 day:19 month:09 pages:1391-1408 https://doi.org/10.1007/s00723-016-0830-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-PHY GBV_ILN_65 GBV_ILN_70 GBV_ILN_2010 UA 2242.9 53.00 VZ 33.00 VZ AR 47 2016 12 19 09 1391-1408 |
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10.1007/s00723-016-0830-4 doi (DE-627)OLC2043929569 (DE-He213)s00723-016-0830-4-p DE-627 ger DE-627 rakwb eng 530 620 VZ UA 2242.9 VZ rvk 53.00 bkl 33.00 bkl Shikhov, Igor verfasserin aut Temperature-Dependent Oxygen Effect on NMR D-$$T_2$$ Relaxation-Diffusion Correlation of n-Alkanes 2016 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © The Author(s) 2016 Abstract Nuclear magnetic resonance (NMR) diffusion-relaxation correlation experiments (D-$$T_2$$) are widely used for the petrophysical characterisation of rocks saturated with petroleum fluids both in situ and for laboratory analyses. The encoding for both diffusion and relaxation offers increased fluid typing contrast by discriminating fluids based on their self-diffusion coefficients, while relaxation times provide information about the interaction of solid and fluid phases and associated confinement geometry (if NMR responses of pure fluids at particular temperature and pressure are known). Petrophysical interpretation of D-$$T_2$$ correlation maps is typically assisted by the “standard alkane line”—a relaxation-diffusion correlation valid for pure normal alkanes and their mixtures in the absence of restrictions to diffusing molecules and effects of internal gradients. This correlation assumes fluids are free from paramagnetic impurities. In situations where fluid samples cannot be maintained at air-free state the diffusion-relaxation response of fluids shift towards shorter relaxation times due to oxygen paramagnetic relaxation enhancement. Interpretation of such a response using the “standard alkane line” would be erroneous and is further complicated by the temperature-dependence of oxygen solubility for each component of the alkane mixture. We propose a diffusion-relaxation correlation suitable for interpretation of low-field NMR D-$$T_2$$ responses of normal alkanes and their mixtures saturating rocks over a broad temperature range, in equilibrium with atmospheric air. We review and where necessary revise existing viscosity-relaxation correlations. Findings are applied to diffusion-relaxation dependencies taking into account the temperature dependence of oxygen solubility and solvent vapour pressure. The effect is demonstrated on a partially saturated carbonate rock. Nuclear Magnetic Resonance Alkane Normal Alkane Nuclear Magnetic Resonance Relaxation Paramagnetic Relaxation Enhancement Arns, Christoph H. (orcid)0000-0003-1721-3996 aut Enthalten in Applied magnetic resonance Springer Vienna, 1990 47(2016), 12 vom: 19. Sept., Seite 1391-1408 (DE-627)13092427X (DE-600)1054553-0 (DE-576)02803757X 0937-9347 nnns volume:47 year:2016 number:12 day:19 month:09 pages:1391-1408 https://doi.org/10.1007/s00723-016-0830-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-PHY GBV_ILN_65 GBV_ILN_70 GBV_ILN_2010 UA 2242.9 53.00 VZ 33.00 VZ AR 47 2016 12 19 09 1391-1408 |
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10.1007/s00723-016-0830-4 doi (DE-627)OLC2043929569 (DE-He213)s00723-016-0830-4-p DE-627 ger DE-627 rakwb eng 530 620 VZ UA 2242.9 VZ rvk 53.00 bkl 33.00 bkl Shikhov, Igor verfasserin aut Temperature-Dependent Oxygen Effect on NMR D-$$T_2$$ Relaxation-Diffusion Correlation of n-Alkanes 2016 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © The Author(s) 2016 Abstract Nuclear magnetic resonance (NMR) diffusion-relaxation correlation experiments (D-$$T_2$$) are widely used for the petrophysical characterisation of rocks saturated with petroleum fluids both in situ and for laboratory analyses. The encoding for both diffusion and relaxation offers increased fluid typing contrast by discriminating fluids based on their self-diffusion coefficients, while relaxation times provide information about the interaction of solid and fluid phases and associated confinement geometry (if NMR responses of pure fluids at particular temperature and pressure are known). Petrophysical interpretation of D-$$T_2$$ correlation maps is typically assisted by the “standard alkane line”—a relaxation-diffusion correlation valid for pure normal alkanes and their mixtures in the absence of restrictions to diffusing molecules and effects of internal gradients. This correlation assumes fluids are free from paramagnetic impurities. In situations where fluid samples cannot be maintained at air-free state the diffusion-relaxation response of fluids shift towards shorter relaxation times due to oxygen paramagnetic relaxation enhancement. Interpretation of such a response using the “standard alkane line” would be erroneous and is further complicated by the temperature-dependence of oxygen solubility for each component of the alkane mixture. We propose a diffusion-relaxation correlation suitable for interpretation of low-field NMR D-$$T_2$$ responses of normal alkanes and their mixtures saturating rocks over a broad temperature range, in equilibrium with atmospheric air. We review and where necessary revise existing viscosity-relaxation correlations. Findings are applied to diffusion-relaxation dependencies taking into account the temperature dependence of oxygen solubility and solvent vapour pressure. The effect is demonstrated on a partially saturated carbonate rock. Nuclear Magnetic Resonance Alkane Normal Alkane Nuclear Magnetic Resonance Relaxation Paramagnetic Relaxation Enhancement Arns, Christoph H. (orcid)0000-0003-1721-3996 aut Enthalten in Applied magnetic resonance Springer Vienna, 1990 47(2016), 12 vom: 19. Sept., Seite 1391-1408 (DE-627)13092427X (DE-600)1054553-0 (DE-576)02803757X 0937-9347 nnns volume:47 year:2016 number:12 day:19 month:09 pages:1391-1408 https://doi.org/10.1007/s00723-016-0830-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-PHY GBV_ILN_65 GBV_ILN_70 GBV_ILN_2010 UA 2242.9 53.00 VZ 33.00 VZ AR 47 2016 12 19 09 1391-1408 |
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10.1007/s00723-016-0830-4 doi (DE-627)OLC2043929569 (DE-He213)s00723-016-0830-4-p DE-627 ger DE-627 rakwb eng 530 620 VZ UA 2242.9 VZ rvk 53.00 bkl 33.00 bkl Shikhov, Igor verfasserin aut Temperature-Dependent Oxygen Effect on NMR D-$$T_2$$ Relaxation-Diffusion Correlation of n-Alkanes 2016 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © The Author(s) 2016 Abstract Nuclear magnetic resonance (NMR) diffusion-relaxation correlation experiments (D-$$T_2$$) are widely used for the petrophysical characterisation of rocks saturated with petroleum fluids both in situ and for laboratory analyses. The encoding for both diffusion and relaxation offers increased fluid typing contrast by discriminating fluids based on their self-diffusion coefficients, while relaxation times provide information about the interaction of solid and fluid phases and associated confinement geometry (if NMR responses of pure fluids at particular temperature and pressure are known). Petrophysical interpretation of D-$$T_2$$ correlation maps is typically assisted by the “standard alkane line”—a relaxation-diffusion correlation valid for pure normal alkanes and their mixtures in the absence of restrictions to diffusing molecules and effects of internal gradients. This correlation assumes fluids are free from paramagnetic impurities. In situations where fluid samples cannot be maintained at air-free state the diffusion-relaxation response of fluids shift towards shorter relaxation times due to oxygen paramagnetic relaxation enhancement. Interpretation of such a response using the “standard alkane line” would be erroneous and is further complicated by the temperature-dependence of oxygen solubility for each component of the alkane mixture. We propose a diffusion-relaxation correlation suitable for interpretation of low-field NMR D-$$T_2$$ responses of normal alkanes and their mixtures saturating rocks over a broad temperature range, in equilibrium with atmospheric air. We review and where necessary revise existing viscosity-relaxation correlations. Findings are applied to diffusion-relaxation dependencies taking into account the temperature dependence of oxygen solubility and solvent vapour pressure. The effect is demonstrated on a partially saturated carbonate rock. Nuclear Magnetic Resonance Alkane Normal Alkane Nuclear Magnetic Resonance Relaxation Paramagnetic Relaxation Enhancement Arns, Christoph H. (orcid)0000-0003-1721-3996 aut Enthalten in Applied magnetic resonance Springer Vienna, 1990 47(2016), 12 vom: 19. Sept., Seite 1391-1408 (DE-627)13092427X (DE-600)1054553-0 (DE-576)02803757X 0937-9347 nnns volume:47 year:2016 number:12 day:19 month:09 pages:1391-1408 https://doi.org/10.1007/s00723-016-0830-4 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-PHY GBV_ILN_65 GBV_ILN_70 GBV_ILN_2010 UA 2242.9 53.00 VZ 33.00 VZ AR 47 2016 12 19 09 1391-1408 |
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Shikhov, Igor ddc 530 rvk UA 2242.9 bkl 53.00 bkl 33.00 misc Nuclear Magnetic Resonance misc Alkane misc Normal Alkane misc Nuclear Magnetic Resonance Relaxation misc Paramagnetic Relaxation Enhancement Temperature-Dependent Oxygen Effect on NMR D-$$T_2$$ Relaxation-Diffusion Correlation of n-Alkanes |
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530 620 VZ UA 2242.9 VZ rvk 53.00 bkl 33.00 bkl Temperature-Dependent Oxygen Effect on NMR D-$$T_2$$ Relaxation-Diffusion Correlation of n-Alkanes Nuclear Magnetic Resonance Alkane Normal Alkane Nuclear Magnetic Resonance Relaxation Paramagnetic Relaxation Enhancement |
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Temperature-Dependent Oxygen Effect on NMR D-$$T_2$$ Relaxation-Diffusion Correlation of n-Alkanes |
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Temperature-Dependent Oxygen Effect on NMR D-$$T_2$$ Relaxation-Diffusion Correlation of n-Alkanes |
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temperature-dependent oxygen effect on nmr d-$$t_2$$ relaxation-diffusion correlation of n-alkanes |
title_auth |
Temperature-Dependent Oxygen Effect on NMR D-$$T_2$$ Relaxation-Diffusion Correlation of n-Alkanes |
abstract |
Abstract Nuclear magnetic resonance (NMR) diffusion-relaxation correlation experiments (D-$$T_2$$) are widely used for the petrophysical characterisation of rocks saturated with petroleum fluids both in situ and for laboratory analyses. The encoding for both diffusion and relaxation offers increased fluid typing contrast by discriminating fluids based on their self-diffusion coefficients, while relaxation times provide information about the interaction of solid and fluid phases and associated confinement geometry (if NMR responses of pure fluids at particular temperature and pressure are known). Petrophysical interpretation of D-$$T_2$$ correlation maps is typically assisted by the “standard alkane line”—a relaxation-diffusion correlation valid for pure normal alkanes and their mixtures in the absence of restrictions to diffusing molecules and effects of internal gradients. This correlation assumes fluids are free from paramagnetic impurities. In situations where fluid samples cannot be maintained at air-free state the diffusion-relaxation response of fluids shift towards shorter relaxation times due to oxygen paramagnetic relaxation enhancement. Interpretation of such a response using the “standard alkane line” would be erroneous and is further complicated by the temperature-dependence of oxygen solubility for each component of the alkane mixture. We propose a diffusion-relaxation correlation suitable for interpretation of low-field NMR D-$$T_2$$ responses of normal alkanes and their mixtures saturating rocks over a broad temperature range, in equilibrium with atmospheric air. We review and where necessary revise existing viscosity-relaxation correlations. Findings are applied to diffusion-relaxation dependencies taking into account the temperature dependence of oxygen solubility and solvent vapour pressure. The effect is demonstrated on a partially saturated carbonate rock. © The Author(s) 2016 |
abstractGer |
Abstract Nuclear magnetic resonance (NMR) diffusion-relaxation correlation experiments (D-$$T_2$$) are widely used for the petrophysical characterisation of rocks saturated with petroleum fluids both in situ and for laboratory analyses. The encoding for both diffusion and relaxation offers increased fluid typing contrast by discriminating fluids based on their self-diffusion coefficients, while relaxation times provide information about the interaction of solid and fluid phases and associated confinement geometry (if NMR responses of pure fluids at particular temperature and pressure are known). Petrophysical interpretation of D-$$T_2$$ correlation maps is typically assisted by the “standard alkane line”—a relaxation-diffusion correlation valid for pure normal alkanes and their mixtures in the absence of restrictions to diffusing molecules and effects of internal gradients. This correlation assumes fluids are free from paramagnetic impurities. In situations where fluid samples cannot be maintained at air-free state the diffusion-relaxation response of fluids shift towards shorter relaxation times due to oxygen paramagnetic relaxation enhancement. Interpretation of such a response using the “standard alkane line” would be erroneous and is further complicated by the temperature-dependence of oxygen solubility for each component of the alkane mixture. We propose a diffusion-relaxation correlation suitable for interpretation of low-field NMR D-$$T_2$$ responses of normal alkanes and their mixtures saturating rocks over a broad temperature range, in equilibrium with atmospheric air. We review and where necessary revise existing viscosity-relaxation correlations. Findings are applied to diffusion-relaxation dependencies taking into account the temperature dependence of oxygen solubility and solvent vapour pressure. The effect is demonstrated on a partially saturated carbonate rock. © The Author(s) 2016 |
abstract_unstemmed |
Abstract Nuclear magnetic resonance (NMR) diffusion-relaxation correlation experiments (D-$$T_2$$) are widely used for the petrophysical characterisation of rocks saturated with petroleum fluids both in situ and for laboratory analyses. The encoding for both diffusion and relaxation offers increased fluid typing contrast by discriminating fluids based on their self-diffusion coefficients, while relaxation times provide information about the interaction of solid and fluid phases and associated confinement geometry (if NMR responses of pure fluids at particular temperature and pressure are known). Petrophysical interpretation of D-$$T_2$$ correlation maps is typically assisted by the “standard alkane line”—a relaxation-diffusion correlation valid for pure normal alkanes and their mixtures in the absence of restrictions to diffusing molecules and effects of internal gradients. This correlation assumes fluids are free from paramagnetic impurities. In situations where fluid samples cannot be maintained at air-free state the diffusion-relaxation response of fluids shift towards shorter relaxation times due to oxygen paramagnetic relaxation enhancement. Interpretation of such a response using the “standard alkane line” would be erroneous and is further complicated by the temperature-dependence of oxygen solubility for each component of the alkane mixture. We propose a diffusion-relaxation correlation suitable for interpretation of low-field NMR D-$$T_2$$ responses of normal alkanes and their mixtures saturating rocks over a broad temperature range, in equilibrium with atmospheric air. We review and where necessary revise existing viscosity-relaxation correlations. Findings are applied to diffusion-relaxation dependencies taking into account the temperature dependence of oxygen solubility and solvent vapour pressure. The effect is demonstrated on a partially saturated carbonate rock. © The Author(s) 2016 |
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Temperature-Dependent Oxygen Effect on NMR D-$$T_2$$ Relaxation-Diffusion Correlation of n-Alkanes |
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https://doi.org/10.1007/s00723-016-0830-4 |
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