Multi-dimensional nuclear magnetic resonance methods for characterizing fluids
US-2015268323-A1 · Sep 24, 2015 · US
US9851315B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9851315-B2 |
| Application number | US-201414567364-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 11, 2014 |
| Priority date | Dec 11, 2014 |
| Publication date | Dec 26, 2017 |
| Grant date | Dec 26, 2017 |
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A method for determining the concentration of asphaltenes in a solution is described. A model is first established for estimating the concentration of asphaltenes in a solution based on multiple samples of solutions of asphaltenes in the solvent in which the concentrations are known. The multiple samples have varying concentrations of asphaltenes. The diffusivity and relaxation time are measured for each sample using two-dimensional NMR. The ratio of diffusivity to relaxation time for each sample is then calculated. A linear equation is determined to fit the relationship between the ratio of diffusivity to relaxation time and the asphaltene concentration by weight for the multiple samples, thus creating the model. For a given solution sample for which the concentration of asphaltenes is desired to be determined, diffusivity and relaxation time are determined using two-dimensional NMR, and the ratio of diffusivity to relaxation time is calculated. This ratio is then used with the model, so that the linear equation can be solved for the asphaltene concentration in the given solution sample.
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What is claimed is: 1. A method for determining a concentration of asphaltenes in a solution, comprising: a. establishing a model for estimating the concentration of the asphaltenes in the solution, comprising the steps of: i. preparing a plurality of samples of solutions of the asphaltenes in a solvent wherein the solutions have varying concentrations of the asphaltenes and wherein concentrations of the asphaltenes are known for each sample within the plurality of samples; ii. exciting and detecting NMR signals from each sample within the plurality of samples using a two-dimensional NMR spectrometer; iii. measuring a diffusivity of an at least one response signal that is an NMR signal from the two-dimensional NMR spectrometer corresponding to each sample within the plurality of samples; iv. measuring a relaxation time of the at least one response signal that is the NMR signal from the two-dimensional NMR spectrometer corresponding to each sample within the plurality of samples; v. calculating a ratio of the diffusivity to the relaxation time for each sample within the plurality of samples; vi. fitting a linear equation to describe a relationship between the ratio of the diffusivity to the relaxation time and an asphaltene concentration by weight for each sample within the plurality of samples; and b. measuring the diffusivity and the relaxation time of the at least one response signal that is the NMR signal from the two-dimensional NMR spectrometer corresponding to a given solution sample for which the concentration of the asphaltenes is desired to be determined; c. calculating the ratio of the diffusivity to the relaxation time for the given solution sample; d. solving the linear equation as determined in step (a) (vi) using the ratio of the diffusivity to the relaxation time for the given solution sample as determined in step (c) to determine the asphaltene concentration in the given solution sample. 2. The method of claim 1 , wherein the solvent comprises toluene. 3. The method of claim 1 , wherein the diffusivity and the relaxation time measured in step (b) are received from an NMR probe located downhole in a hydrocarbon producing reservoir. 4. A system, comprising: a. an NMR probe located proximate a fluid solution for determining a diffusivity and a relaxation time of the fluid solution using exciting and detecting NMR signals from each sample in a two-dimensional NMR spectrometer; b. a computer processor that performs: i. receiving the diffusivity and the relaxation time of the fluid solution from the NMR probe; ii. calculating a ratio of the diffusivity to the relaxation time for the fluid solution; iii. accessing a linear equation describing a relationship between the ratio of the diffusivity to the relaxation time and an asphaltene concentration by weight; and iv. solving the linear equation to determine the asphaltene concentration by weight in the fluid solution based on the ratio of the diffusivity to the relaxation time for the fluid solution. 5. The system of claim 4 , wherein the NMR probe is located downhole in a hydrocarbon producing reservoir. 6. The method of claim 1 , where the asphaltene concentration that is determined in step (d) is determined by weight with an accuracy of R 2 >0.95. 7. The method of claim 1 , wherein the diffusivity and the relaxation time of the given solution sample are obtained simultaneously in step (b) using a D-T2 two-dimensional sequence. 8. The method of claim 1 , wherein the relaxation time is a transverse relaxation time. 9. The method of claim 1 , wherein the solvent is an extracted crude oil, wherein the asphaltenes were removed by a hot heptane filtration. 10. The system of claim 4 , wherein the NMR probe is configured to be surrounded by the fluid solution. 11. The system of claim 4 , wherein the NMR probe contains the fluid solution therein. 12. The method of claim 1 , wherein the two-dimensional NMR spectrometer is a low-frequency two-dimensional NMR spectrometer. 13. The method of claim 12 , additionally comprising performing a data inversion with a multidimensional inverse Laplace transformation. 14. The system of claim 4 , wherein the two-dimensional NMR spectrometer is a low-frequency two-dimensional NMR spectrometer.
Relaxometry, i.e. quantification of relaxation times or spin density (G01R33/50 takes precedence) · CPC title
for hydrocarbon content · CPC title
MR involving a non-standard magnetic field B0, e.g. of low magnitude as in the earth's magnetic field or in nanoTesla spectroscopy, comprising a polarizing magnetic field for pre-polarisation, B0 with a temporal variation of its magnitude or direction such as field cycling of B0 or rotation of the direction of B0, or spatially inhomogeneous B0 like in fringe-field MR or in stray-field imaging · CPC title
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operating with electron or nuclear magnetic resonance · CPC title
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