A Relationship Between Pore Structure and Residual Oil Saturation in Tertiary Surfactant Floods

1972 ◽  
Vol 12 (04) ◽  
pp. 289-296 ◽  
Author(s):  
F.A.L. Dullien ◽  
G.K. Dhawan ◽  
Nur Gurak ◽  
L. Babjak

Abstract Photomicrography and mercury porosimetry have been used jointly to determine the pore-size distributions of various sandstone samples. The two curves differed drastically from each other for all samples. Two unconsolidated packs consisting of uniform 250u glass beads and mixed 44-250u beads, respectively, as well as the sinters prepared from them, were also investigated. An index, D, measuring the difficulty of recovering waterflood residuals in tertiary surfactant floods has been constructed from the two different porosimetry curves. Reasonably good correlation porosimetry curves. Reasonably good correlation bas been obtained between D and residual oil saturations found in tertiary surfactant floods. Introduction This paper presents our first results in a continuing study of pore structure and oil recovery. The problem of how pore structure might influence oil recovery has been discussed by several authors. There is, however, no known method whereby one could rank various porous media (e.g., different sandstones) on the basis of pore structure in the order of decreasing amounts of expected residual oil saturations assuming identical conditions of flooding (identical oil, water, wetting and pressure gradient for the various sands. In this pressure gradient for the various sands. In this work we have taken an initial step toward this ideal objective. The prime target of the treatment has been the problem of correlating the extent of recovery of waterflood residuals by tertiary surfactant floods with the pore structure. The degree of difficulty presented by the pore structure in the way of recovering the isolated oil masses left behind by a waterflood has been expressed in the form of an index that is calculated from a mercury porosimetry and a photomicrographic pore-size distribution curve obtained on the sample. pore-size distribution curve obtained on the sample. The degree of correlation obtained amounts to a promising start in the case of tertiary surfactant promising start in the case of tertiary surfactant floods, and there also appears to be some correlation between the residual oil saturations found in the waterfloods and the pore structure. In this paper we are considering only the case of water-wet formations and moderate viscosity ratios. THEORY The term "pore structure" ordinarily means the distribution of pore volume by some linear pore dimension (pore-size distribution) and the topographical sequence of pores. Pore-size distributions have been determined by various methods. However, for reservoir rocks the most popular method has been mercury porosimetry. In a typical reservoir rock pore necks alternate with bulges. As the meniscus of penetrating mercury advances past a pore neck, it continues to advance in a nonequilibrium manner, until it comes to an even narrower neck. Since the capillary pressure of penetration of mercury into the pore pressure of penetration of mercury into the pore space between the two necks is determined by the size of the first neck, the pore diameters corresponding to the space between the two necks remain undetected by this method. Let us consider an arbitrary pore segment in the sample and approach it from the outside surface of the sample. Somewhere between the pore segment and the outside, there is a controlling cross-section in the pore space that is defined as follows: once the meniscus of the invading mercury has passed that cross-section, there is no narrower neck in its path all the way to the segment considered. The path all the way to the segment considered. The pore neck is the segment considered the controlling pore neck is the segment considered the controlling cross-section as defined above, even if the pore neck is far removed from the controlling crosssection. Denoting the radius of the pore segment by re and that of the controlling pore neck by r'e we have re greater than r'e. JPT P. 289

Author(s):  
Petra Foerst ◽  
M. Lechner ◽  
N. Vorhauer ◽  
H. Schuchmann ◽  
E. Tsotsas

The pore structure is a decisive factor for the process efficiency and product quality of freeze dried products. In this work the two-dimensional ice crystal structure was investigated for maltodextrin solutions with different concentrations by a freeze drying microscope. The resulting drying kinetics was investigated for different pore structures. Additionally the three-dimensional pore structure of the freeze dried samples was measured by µ-computed tomography and the pore size distribution was quantified by image analysis techniques. The two- and three-dimensional pore size distributions were compared and linked to the drying kinetics.Keywords: pore size distribution; freeze drying; maltodextrin solution; freeze drying microscope   


Materials ◽  
2019 ◽  
Vol 12 (9) ◽  
pp. 1454 ◽  
Author(s):  
Yong Zhang ◽  
Bin Yang ◽  
Zhengxian Yang ◽  
Guang Ye

Capturing the long-term performance of concrete must be underpinned by a detailed understanding of the pore structure. Mercury intrusion porosimetry (MIP) is a widely used technique for pore structure characterization. However, it has been proven inappropriate to measure the pore size distribution of cementitious materials due to the ink-bottle effect. MIP with cyclic pressurization–depressurization can overcome the ink-bottle effect and enables a distinction between large (ink-bottle) pores and small (throat) pores. In this paper, pressurization–depressurization cycling mercury intrusion porosimetry (PDC-MIP) is adopted to characterize the pore structure in a range of cementitious pastes cured from 28 to 370 days. The results indicate that PDC-MIP provides a more accurate estimation of the pore size distribution in cementitious pastes than the standard MIP. Bimodal pore size distributions can be obtained by performing PDC-MIP measurements on cementitious pastes, regardless of the age. Water–binder ratio, fly ash and limestone powder have considerable influences on the formation of capillary pores ranging from 0.01 to 0.5 µm.


1988 ◽  
Vol 137 ◽  
Author(s):  
Yahia Abdel-Jawad ◽  
Will Hansen

AbstractThe pore structure (i.e. total pore volume, surface area and pore-size distribution curves) was measured using mercury porosimetry and nitrogen sorption. Hydrated portland cement (type I) of water-cement (w/c) ratios 0.3, 0.4 and 0.6 by weight was analyzed at three degrees of hydration (i.e., 30%, 50% and 80%; 70% for the 0.3 w/c system) corresponding to low, intermediate and high levels of hydration. The effect of curing temperature (3°, 23°, and 43°C) on pore structure was also studied. The two techniques were evaluated as well on porous Vycor glass, which has a narrow pore size distribution in the size range accessible to both. Results obtained by both techniques on porous Vycor glass agreed well. However neither technique can be used alone to study the entire pore structure in well-hydrated cement due to the wide range in pore sizes and the presence of micropores. Due to the unstable pore structure in cement a specimen treatment procedure such as methanol replacement, combined with volume-thickness (V-t) analysis, is necessary in order to measure the micropores. At low hydration values the pore structure can be estimated by mercury intrusion porosimetry (MIP). At higher hydration values, however, this technique underestimates total pore volume and surface area due to the presence of micropores which MIP cannot determine. In the pore size range of overlap, higher pore volumes were obtained with MIP. Nitrogen V-t analysis shows that micropores are more pronounced with lower w/c ratios. This finding is consistent with pore size distribution curves obtained by MIP. For a given w/c ratio and degree of hydration the total pore volume measured by MIP was found to be independent of curing temperature in the temperature range studied. At any w/c ratio, capillary porosity is controlled by degree of hydration alone.


2017 ◽  
Vol 16 (01) ◽  
pp. 1750008 ◽  
Author(s):  
Bendegúz Dezső Bak ◽  
Tamás Kalmár-Nagy

Mercury porosimetry is utilized primarily in the oil industry to determine the pore size distribution of rock samples. During the process, mercury is forced into the sample with gradually increasing pressure and the volume of the injected mercury is measured vs. the applied pressure (the saturation curve). In practice, the saturation curve is assumed to be directly related the cumulative pore size distribution. However, this distribution does not coincide with the real one because of the “nonaccessibility” of pores at a given pressure. This motivates our goal to determine a more accurate cumulative pore size distribution. To achieve this, we treat the propagation of mercury as a percolation process (dubbed “porcolation” after PORosimetry perCOLATION). Porcolation is an external pressure-driven access-limited invasion percolation model where resistance values are assigned to sites/vertices. As pressure increases, the invading mercury occupies sites with smaller resistance values along paths that are connected to the “boundaries” of the network. Simulations are carried out on regular lattices, as well as on random graphs with prescribed degree distributions (representing the pore network of rock samples). An assumed pore size distribution is considered as an input/parameter of the simulations resulting in an output saturation curve. We determine the input–output mapping (homeomorphism) and utilize its inverse to correct the discrepancies between the assumed and actual pore size distributions. The results show nice agreement between experimental saturation curves and those obtained from our homeomorphism method.


2021 ◽  
Vol 11 (5) ◽  
pp. 2113-2125
Author(s):  
Chenzhi Huang ◽  
Xingde Zhang ◽  
Shuang Liu ◽  
Nianyin Li ◽  
Jia Kang ◽  
...  

AbstractThe development and stimulation of oil and gas fields are inseparable from the experimental analysis of reservoir rocks. Large number of experiments, poor reservoir properties and thin reservoir thickness will lead to insufficient number of cores, which restricts the experimental evaluation effect of cores. Digital rock physics (DRP) can solve these problems well. This paper presents a rapid, simple, and practical method to establish the pore structure and lithology of DRP based on laboratory experiments. First, a core is scanned by computed tomography (CT) scanning technology, and filtering back-projection reconstruction method is used to test the core visualization. Subsequently, three-dimensional median filtering technology is used to eliminate noise signals after scanning, and the maximum interclass variance method is used to segment the rock skeleton and pore. Based on X-ray diffraction technology, the distribution of minerals in the rock core is studied by combining the processed CT scan data. The core pore size distribution is analyzed by the mercury intrusion method, and the core pore size distribution with spatial correlation is constructed by the kriging interpolation method. Based on the analysis of the core particle-size distribution by the screening method, the shape of the rock particle is assumed to be a more practical irregular polyhedron; considering this shape and the mineral distribution, the DRP pore structure and lithology are finally established. The DRP porosity calculated by MATLAB software is 32.4%, and the core porosity measured in a nuclear magnetic resonance experiment is 29.9%; thus, the accuracy of the model is validated. Further, the method of simulating the process of physical and chemical changes by using the digital core is proposed for further study.


1988 ◽  
Vol 5 (3) ◽  
pp. 168-190 ◽  
Author(s):  
Bruce D. Adkins ◽  
Burtron H. Davis

The pore distributions calculated from nitrogen desorption and from mercury penetration data are similar for the four materials utilized in this study. While there are small differences in the distributions calculated using different models (Cohan. Foster or Broekhoff-deBoer) with nitrogen adsorption or desorption isotherm data, all three show reasonable agreement with distributions calculated from mercury penetration data. Frequently practical catalysts have such a broad pore size distribution that neither method alone is adequate to measure the total pore size range. The present results suggest a direct comparison, without recourse to a scaling factor, is appropriate when comparing results from the two methods even though the pore size distribution maximum may vary by at least 50% depending upon the model chosen for the calculation. Better agreement may be obtained between the two experimental techniques by adjusting either the nitrogen adsorption data using a packed sphere model or the mercury penetration data by an earlier reported correction ratio. The difference between the two methods becomes less than 20% when a correction procedure is used; however, further studies are needed to define the range of material shaped that these procedures are applicable to.


Polymers ◽  
2020 ◽  
Vol 12 (10) ◽  
pp. 2247
Author(s):  
Claire Delaroa ◽  
René Fulchiron ◽  
Eric Lintingre ◽  
Zoé Buniazet ◽  
Philippe Cassagnau

The impact of polypropylene and high-density polyethylene backbone binders on the structure of organic matrix, feedstock, and ceramic parts is investigated in terms of morphology in this paper. The miscibility of wax with polyethylene and polypropylene is investigated in the molten state via a rheological study, revealing wax full miscibility with high-density polyethylene and restricted miscibility with polypropylene. Mercury porosimetry measurements realized after wax extraction allow the characterization of wax dispersion in both neat organic blends and zirconia filled feedstocks. Miscibility differences in the molten state highly impact wax dispersion in backbone polymers after cooling: wax is preferentially located in polyethylene phase, while it is easily segregated from polypropylene phase, leading to the creation of large cracks during solvent debinding. The use of a polyethylene/polypropylene ratio higher than 70/30 hinders wax segregation and favors its homogeneous dispersion in organic binder. As zirconia is added to organic blends containing polyethylene, polypropylene, and wax, the pore size distribution created by wax extraction is shifted towards smaller pores. Above zirconia percolation at 40 vol%, the pore size distribution becomes sharp attesting of wax homogeneous dispersion. As the PP content in the organic binder decreases from 100% to 0%, the pore size distribution is reduced of 30%, leading to higher densification ability. In order to ensure a maximal densification of the final ceramic, polyethylene/polypropylene ratios with a minimum content of 70% of high-density polyethylene should be employed.


2009 ◽  
Vol 25 (6) ◽  
pp. 729-735 ◽  
Author(s):  
Elsa Vennat ◽  
Christine Bogicevic ◽  
Jean-Marie Fleureau ◽  
Michel Degrange

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