scholarly journals Investigating the effect of internal gradients on static gradient nuclear magnetic resonance diffusion measurements

Geophysics ◽  
2017 ◽  
Vol 82 (5) ◽  
pp. D293-D301
Author(s):  
Emily L. Fay ◽  
Denys J. Grombacher ◽  
Rosemary J. Knight

Nuclear magnetic resonance (NMR) methods can be used to measure the diffusion coefficient [Formula: see text] of fluids. In porous materials, diffusion of the pore fluid is restricted by pore boundaries, such that [Formula: see text] may be smaller than the diffusion coefficient of the bulk fluid. This reduction in [Formula: see text] provides information about the geometry of the pore space. Significant overestimates of [Formula: see text] can, however, occur due to internal gradients caused by magnetic susceptibility contrasts between the pore fluid and the solid phase. We have investigated the way in which internal gradients can impact the measured diffusion coefficient and obscure the link to pore geometry in unconsolidated sediments. We focus on measurements of [Formula: see text] obtained with a static gradient diffusion-editing sequence, which can be used with NMR logging tools to measure [Formula: see text] in subsurface sediments. Laboratory measurements of [Formula: see text] measured with a diffusion-editing [Formula: see text]-[Formula: see text] sequence indicate significant impacts from internal gradients, including [Formula: see text] values several orders of magnitude larger than [Formula: see text] of bulk water. The log-mean [Formula: see text] values were found to be highly correlated with estimated internal gradient magnitudes and indicate no clear relationship to pore size. Samples with heterogeneous magnetic susceptibility of the solid phase indicate [Formula: see text] distributions with multiple peaks, reflecting the nonuniform distribution of internal gradients in the sediment. We found evidence of high internal gradients impacting a majority of our samples, resulting in increased [Formula: see text] values that do not reflect pore size even in samples with low magnetic susceptibility.

2015 ◽  
Vol 3 (1) ◽  
pp. SA77-SA89 ◽  
Author(s):  
John Doveton ◽  
Lynn Watney

The T2 relaxation times recorded by nuclear magnetic resonance (NMR) logging are measures of the ratio of the internal surface area to volume of the formation pore system. Although standard porosity logs are restricted to estimating the volume, the NMR log partitions the pore space as a spectrum of pore sizes. These logs have great potential to elucidate carbonate sequences, which can have single, double, or triple porosity systems and whose pores have a wide variety of sizes and shapes. Continuous coring and NMR logging was made of the Cambro-Ordovician Arbuckle saline aquifer in a proposed CO2 injection well in southern Kansas. The large data set gave a rare opportunity to compare the core textural descriptions to NMR T2 relaxation time signatures over an extensive interval. Geochemical logs provided useful elemental information to assess the potential role of paramagnetic components that affect surface relaxivity. Principal component analysis of the T2 relaxation time subdivided the spectrum into five distinctive pore-size classes. When the T2 distribution was allocated between grainstones, packstones, and mudstones, the interparticle porosity component of the spectrum takes a bimodal form that marks a distinction between grain-supported and mud-supported texture. This discrimination was also reflected by the computed gamma-ray log, which recorded contributions from potassium and thorium and therefore assessed clay content reflected by fast relaxation times. A megaporosity class was equated with T2 relaxation times summed from 1024 to 2048 ms bins, and the volumetric curve compared favorably with variation over a range of vug sizes observed in the core. The complementary link between grain textures and pore textures was fruitful in the development of geomodels that integrates geologic core observations with petrophysical log measurements.


2010 ◽  
Vol 106 (6) ◽  
pp. 928-937 ◽  
Author(s):  
Ryan S. Renslow ◽  
Paul D. Majors ◽  
Jeffrey S. McLean ◽  
Jim K. Fredrickson ◽  
Bulbul Ahmed ◽  
...  

2018 ◽  
Vol 37 (1) ◽  
pp. 412-428
Author(s):  
Feng Zhu ◽  
Wenxuan Hu ◽  
Jian Cao ◽  
Biao Liu ◽  
Yifeng Liu ◽  
...  

Nuclear magnetic resonance cryoporometry is a newly developed technique that can characterize the pore size distribution of nano-scale porous materials. To date, this technique has scarcely been used for the testing of unconventional oil and gas reservoirs; thus, their micro- and nano-scale pore structures must still be investigated. The selection of the probe material for this technique has a key impact on the quality of the measurement results during the testing of geological samples. In this paper, we present details on the nuclear magnetic resonance cryoporometric procedure. Several types of probe materials were compared during the nuclear testing of standard nano-scale porous materials and unconventional reservoir geological samples from Sichuan Basin, Southwest China. Gas sorption experiments were also carried out on the same samples simultaneously. The KGT values of the probe materials octamethylcyclotetrasiloxane and calcium chloride hexahydrate were calibrated using standard nano-scale porous materials to reveal respective values of 149.3 Knm and 184 Knm. Water did not successfully wet the pore surfaces of the standard controlled pore glass samples; moreover, water damaged the pore structures of the geological samples, which was confirmed during two freeze-melting tests. The complex phase transition during the melting of cyclohexane introduced a nuclear magnetic resonance signal in addition to that from liquid in the pores, which led to an imprecise characterization of the pore size distribution. Octamethylcyclotetrasiloxane and calcium chloride hexahydrate have been rarely employed as nuclear magnetic resonance cryoporometric probe materials for the testing of an unconventional reservoir. Both of these materials were able to characterize pore sizes up to 1 μm, and they were more applicable than either water or cyclohexane.


2018 ◽  
Vol 20 (44) ◽  
pp. 28185-28192 ◽  
Author(s):  
Christian F. Pantoja ◽  
Y. Mauricio Muñoz-Muñoz ◽  
Lorraine Guastar ◽  
Jadran Vrabec ◽  
Julien Wist

Nuclear magnetic resonance (NMR) spectroscopy can also be used for the measurement of the Fick diffusion coefficient.


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