Experimental determination of porosity and methane sorption capacity of organic-rich shales as a function of effective stress: Implications for gas storage capacity

AAPG Bulletin ◽  
2021 ◽  
Vol 105 (2) ◽  
pp. 309-328
Author(s):  
Garri Gaus ◽  
Reinhard Fink ◽  
Alexandra Amann-Hildenbrand ◽  
Bernhard M. Krooss ◽  
Ralf Littke
2021 ◽  
Vol 14 (8) ◽  
Author(s):  
Harinandan Kumar ◽  
Manoj Kumar Mishra ◽  
Susmita Mishra ◽  
M. Muralidhar Singh ◽  
Dilip Kumar Srivastava

1998 ◽  
Vol 1 (01) ◽  
pp. 57-63 ◽  
Author(s):  
Theodore Klimentos ◽  
Abdallah Harouaka ◽  
Bechir Mtawaa ◽  
Salih Saner

Summary We developed an experimental method to obtain the Biot elastic constant of rocks from laboratory dynamic and static measurements. The Biot constant often has been calculated with various empirical equations. The experimental determination of the Biot elastic constant is very important to engineering problems associated with sand control, hydraulic fracturing, wellbore stability, earth stresses, sonic porosity, and estimation of compressional-, P, and shear-, S, wave velocity. Both the dynamic and static moduli of actual reservoir sandstone core samples, jacketed and mounted in a triaxial cell under vacuum, were measured at various confining and overburden stresses. The results obtained show that the Biot constant is a complex function of porosity, permeability, pore-size distribution, and overburden and confining stress, which means that it is not really a constant. Also, the static Biot constant is greater than the dynamic one and their difference increases with increasing overburden stress according to the equation astatic =[1+0.05*(sz)ef]*adynamic (where sz is in Ksi). Moreover, both the experimental static and dynamic Biot constants may be significantly different from values calculated with empirical equations. This study suggests that quantifying the Biot constant in the laboratory may enhance the determination of rock-strength/fracturing, earth stresses, rock subsidence, sanding predictions, P- and S-wave velocities, porosity, and pore fluid from sonic and seismic data. Introduction The Biot1–7 elastic constant, a, of a rock is an important poroelastic parameter that relates stress and pore pressure and describes how compressible the dry skeletal frame is with respect to the solid material composing the dry skeletal frame of the rock. Biot1 measures the ratio of the fluid volume squeezed out to the volume change of the rock if the latter is compressed while allowing the fluid to escape. It is described as Because the petroleum-related rocks are usually saturated, it is important to know how the saturation and pore pressure affect their mechanical and flow properties. Terzaghi's8 effective-stress principle for soils states that we can obtain the effective stress by simply subtracting the fluid pressure from the total stress; i.e., se=st -ap, which means that a=1. This implies that increasing the external stress by some amount produces the same volume change of the porous material as reducing the pore pressure with the same amount. This principle appears to be valid for most properties of soils. However, in petroleum-related rocks, Terzaghi's effective-stress principle may not be valid. Then, a modified effective stress is a function of the Biot constant, a, and given by sef=st -ap. Despite the great significance of a, only a limited amount of laboratory work on its determination has been reported in the literature.9–13 The failure criteria for a saturated rock with a pore pressure are obtained by introducing the effective stress into the dry form of the failure criteria. This means that all rock failure and sand-production prediction models require a known static Biot constant value. So far, researchers, engineers, and geophysicists quite often assume that a=1 (Terzaghi's principle), which is not necessarily true. Alternatively, for the determination of a, they may use various empirical equations.14–17 These equations, however, yield different values that may vary by up to 100% or more depending on the equation used. The primary objective of this study was to determine the Biot elastic constant experimentally, both by dynamic and static measurements, and to establish a correlation between the dynamic and static a. Another objective was to identify any rock properties controlling the Biot elastic constant. Experimental Determination of the Biot Constant In this experimental method, we determined both the dynamic and static moduli of actual reservoir sandstone core samples under high vacuum (<0.15 mbar) and at various confining (s2=s3=sx) and axial (s1=sx) stresses. The vacuum was obtained and maintained in-situ while the rock sample was mounted and tested with a triaxial system. The rock sample is prepared, jacketed, and mounted in the triaxial cell. Then, the cell is closed firmly to prevent leaks and filled with the confining fluid. Vacuum is then pulled out of the sample with a high-power vacuum pump. Once the desired vacuum condition (<0.15 mbar) is established, a multistage triaxial compression test is performed, as discussed in details elsewhere.18 Axial and confining stresses were applied hydraulically. The dynamic and static data were generated at various axial and confining stresses. At each confining-stress stage, several P and S waveforms were recorded as the axial (overburden) stress was increased. The measured P - and S-wave velocities were used to calculate the dynamic Poisson's ratio and the dynamic Bulk, Shear, and Young's moduli of the dry skeletal frame of the rock, Ksk.


Geofluids ◽  
2020 ◽  
Vol 2020 ◽  
pp. 1-13 ◽  
Author(s):  
Garri Gaus ◽  
Anton Kalmykov ◽  
Bernhard M. Krooss ◽  
Reinhard Fink

Crushing and grinding of carbonaceous shale samples is likely to enhance the accessibility of pores and embedded organic matter as compared to the intact rock. This may lead to an overestimation of the total (volume and sorptive) gas storage capacity. In order to investigate the importance of these effects we have measured unconfined apparent grain densities (helium pycnometry) and methane sorption capacities (high-pressure methane excess sorption) of four carbonaceous shales (Cambro-Ordovician Alum Shale, Jurassic Kimmeridge Clay, Jurassic/Cretaceous Bazhenov Shale, and Late Cretaceous Eagle Ford Shale) as a function of particle size. Measurements were first conducted on 38 mm diameter core plugs, which then were crushed and milled to successively smaller particle sizes (<10 mm, <2 mm, <64 μm, and <1 μm). Apparent grain densities of the smallest particle fractions of the Alum, Bazhenov and Kimmeridge samples were consistently higher by 0.5 to 1% than apparent grain densities of the original sample plugs. Methane excess sorption capacity increased significantly for particle sizes <64 μm for the Alum and <1 μm for the Bazhenov and Kimmeridge samples while no significant changes upon grinding were observed for the Eagle Ford Shale. For the Bazhenov Shale, the apparent grain density increased slightly from 2.446 g/cm3 to 2.450 g/cm3 upon particle size reduction from <64 μm to <1 μm while the maximum sorption capacity (“Langmuir volume”) increased substantially from 0.11 mmol/g to 0.19 mmol/g. Similarly, for the Kimmeridge Clay and Alum Shale, a slight increase of the apparent grain density from 1.546 g/cm3 to 1.552 g/cm3 and from 2.362 g/cm3 to 2.385 g/cm3, respectively, was accompanied by increases in sorption capacity from 0.37 mmol/g to 0.45 mmol/g and from 0.14 mmol/g to 0.185 mmol/g, respectively. The increase in sorption capacity indicates an opening of a considerable amount of micropores with large internal surface area upon physical disruption of the rock fabric and/or removal of included fluids. It may also be due to increased swelling abilities of clay minerals and organic matter upon destruction of the stabilizing rock fabric with decreasing particle size. Grain density and sorption isotherms measured on small particle sizes are likely to overestimate the gas storage capacities and the amounts of producible gas-in-place since under field conditions (largely undisrupted rock fabric), significant portions of this storage capacity are essentially inaccessible. Poor interconnectivity of the pore system and slow, diffusion-controlled transport will massively retard gas production. Based on these findings, particle sizes >64 μm should be used for porosity and sorption measurements because they are more likely to retain the properties of the rock fabric in terms of accessible pore volume and sorptive storage capacity.


1999 ◽  
Vol 96 (6) ◽  
pp. 1111-1116 ◽  
Author(s):  
E. Falcon ◽  
S. Fauve ◽  
C. Laroche

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