Effects of Impurities on Minimum Miscibility Pressures and Minimum Enrichment Levels for CO2 and Rich-Gas Displacements

1982 ◽  
Vol 22 (02) ◽  
pp. 219-225 ◽  
Author(s):  
R.S Metcalfe

Abstract Multicontact miscible displacement processes are becoming increasingly popular as a means of recovering secondary and tertiary oil reserves in the U.S. and Canada. Economics of multicontact miscible flooding are governed to some extent by the availability of large sources of high purity CO2 or suitable liquefied petroleum gas (LPG) streams. This is because achievement of miscibility depends on the solvent composition as well as the system temperature and pressure. Atypical components in a CO2 or solvent stream therefore may increase the required pressure or enrichment levels for achievement of miscibility. Several papers have been published discussing the pressure (for CO2) and composition (for rich gas) levels required for miscible displacement. The potential CO2 supply could be increased if complicated cleanup procedures for injected and produced fluids were not required. For engineering studies it is important that CO2 streams containing H2S and hydrocarbons be evaluated for their miscible flooding potential. It is also important to evaluate the effects of CO2 and C5+ components in rich gas mixtures to determine whether they can be used to reduce calculated enrichment levels for solvent systems. This paper presents results of studies using mixtures of CO2, H2S, and C1, CO2-LPG, and rich gas solvents containing CO2 or C5 to displace oil miscibly in slimtube experiments. The purpose of this work is to show the effects of various components on pressure and compositions required for miscibility. As expected, the changes in CO2 miscibility pressure are direct functions of temperature. It is reported that the addition of H2S and C2+ hydrocarbons lowers the miscibility pressure for CO2, whereas the presence of C1 in a CO2 solvent increases it. More important, the results give a quantitative measure of the degree of reduction/elevation in miscibility pressure to be expected with impure CO2 streams. The paper also presents similar results from displacements with typical rich gas solvents mixed with CO2 and/or C5. It is reported that CO2 increases the minimum enrichment required, while a heavier hydrocarbon component actually can reduce anticipated enrichment levels. Introduction The use of miscible gas flooding as an improved oil recovery technique is increasing rapidly. CO2 in particular is being tested in at least 16 pilot or fieldwide floods. Multicontact miscible (CO2 and rich gas) processes are pressure and/or composition dependent - i.e., a certain pressure is required before a gas of given composition can miscibly displace a given crude oil. The pressure level required for mlticontact miscibility is therefore an important control variable. Control of this pressure can help to increase the number of economically feasible miscible projects. Of more importance, perhaps, is the ability to select a CO2 or LPG stream of less than 100% purity with the assurance that some minor concentration of H2, N2, C1, H2S, or C2 through C4 will not affect the performance adversely. Benham,1 Rutherford,2 and Jacobson,3 by monitoring recovery from slim-tube or core tests, have looked at ways in which C1, C2, C3, or C4 concentrations affect miscibility pressure. This research was important for understanding the compositional relationships between solvent and oil in the hydrocarbon multicontact miscible process. Jacobson also studied effects of H2S on displacement efficiencies of a C1 drive gas. Generally, these papers considered rather large concentrations of hydrocarbons, H2S, or CO2 in C1. The effects of N2 or C1 contaminants on the pressure required for CO2 flooding have been discussed most recently by Graue and Zana.4

2021 ◽  
Vol 73 (06) ◽  
pp. 65-66
Author(s):  
Judy Feder

This article, written by JPT Technology Editor Judy Feder, contains highlights of paper SPE 200460, “A Case Study of SACROC CO2 Flooding in Marginal Pay Regions: Improving Asset Performance,” by John Kalteyer, SPE, Kinder Morgan, prepared for the 2020 SPE Improved Oil Recovery Conference, originally scheduled to be held in Tulsa, 18–22 April. The paper has not been peer reviewed. As one of the first fields in the world to use carbon dioxide (CO2) in enhanced oil recovery (EOR), the Scurry Area Canyon Reef Operators Committee (SACROC) unit of the Kelly-Snyder field in the Midland Basin of Texas provides a unique opportunity to study, learn from, and improve upon the development of CO2 flood technology. The complete paper reviews the history of EOR at SACROC, discusses changes in theory over time, and provides a look at the field’s future. Field Overview and Development History The first six pages of the paper discuss the field’s location, geology, and development before June 2000, when Kinder Morgan acquired the SACROC unit and took over as operator. Between initial gas injection in 1972 and 2000, approximately 1 TCF of CO2 had been injected into the Canyon Reef reservoir. Since 2000, cumulative CO2 injection has sur-passed 7 TCF and yielded cumulative EOR of over 180 million bbl. The reservoir is a primarily limestone reef complex containing an estimated original oil in place (OOIP) of just under 3 billion bbl. The reservoir ranges from 200 ft gross thickness in the south to 900 ft in the north, where the limestone matrix averages 8% porosity and 20-md permeability. The Canyon Reef structure is divided into four major intervals, of which the Upper Canyon zone provides the highest-quality pay. The field was discovered in 1948 at a pressure of 3,122 psi. By late 1950, 1,600 production wells had been drilled and the reservoir pressure plummeted, settling as low as 1,700 psi. Waterflooding begun in 1954 enabled the field to continue producing for nearly 20 years, at which time the operators deter-mined that another recovery mechanism would be needed to maximize recovery and reach additional areas of the field. The complete paper discusses various CO2 injection programs that were developed and applied—including a true tertiary response from a miscible CO2 flood in 1981—along with their outcomes. Acquisition and CO2-Injection Redevelopment In June 2000 Kinder Morgan acquired the SACROC Unit and took over as operator. Approximately 6.7 billion bbl of water and 1.3 TCF of CO2 had been injected across the unit to that date, but the daily oil rate of 8,700 B/D was approaching the field’s economic limit. An estimated 40% of the OOIP had been produced through the combination of recovery methods that each previous operator had used. Expanding on the conclusions of its immediate predecessor, the operator initiated large-scale CO2-flood redevelopment in a selection of project areas. These redevelopments were based on several key distinctions differentiating them from previous injection operations.


1979 ◽  
Vol 19 (04) ◽  
pp. 242-252 ◽  
Author(s):  
R.S. Metcalfe ◽  
Lyman Yarborough

Abstract Carbon dioxide flooding under miscible conditions is being developed as a major process for enhanced oil recovery. This paper presents results of research studies to increase our understanding of the multiple-contact miscible displacement mechanism for CO2 flooding. Carbon dioxide displacements of three synthetic oils of increasing complexity (increasing number of hydrocarbon components) are described. The paper concentrates on results of laboratory flow studies, but uses results of phase-equilibria and numerical studies to support the conclusions.Results from studies with synthetic oils show that at least two multiple-contact miscible mechanisms, vaporization and condensation, can be identified and that the phase-equilibria data can be used as a basis for describing the mechanism. The phase-equilibria change with varying reservoir conditions, and the flow studies show that the miscible mechanism depends on the phase-equilibria behavior. Qualitative predictions with mathematical models support our conclusions.Phase-equilibria data with naturally occurring oils suggest the two mechanisms (vaporization and condensation) are relevant to CO2 displacements at reservoir conditions and are a basis for specifying the controlling mechanisms. Introduction Miscible-displacement processes, which rely on multiple contacts of injected gas and reservoir oil to develop an in-situ solvent, generally have been recognized by the petroleum industry as an important enhanced oil-recovery method. More recently, CO2 flooding has advanced to the position (in the U.S.) of being the most economically attractive of the multiple-contact miscibility (MCM) processes. Several projects have been or are currently being conducted either to study or use CO2 as an enhanced oil-recovery method. It has been demonstrated convincingly by Holm and others that CO2 can recover oil from laboratory systems and therefore from the swept zone of petroleum reservoirs using miscible displacement. However, several contradictions seem to exist in published results.. These authors attempt to establish the mechanism(s) through which CO2 and oil form a miscible solvent in situ. (The solvent thus produced is capable of performing as though the two fluids were miscible when performing as though the two fluids were miscible when injected.) In addition, little experimental work has been published to provide support for the mechanisms of multiple-contact miscibility, as originally discussed by Hutchinson and Braun.One can reasonably assume that the miscible CO2 process will be related directly to phase equilibria process will be related directly to phase equilibria because it involves intimate contact of gases and liquids. However, no data have been published to indicate that the mechanism for miscibility development may differ for varying phase-equilibria conditions.This paper presents the results of both flow and phase-equilibria studies performed to determine the phase-equilibria studies performed to determine the mechanism(s) of CO2 multiple-contact miscibility. These flow studies used CO2 to displace three multicomponent hydrocarbon mixtures under first-contact miscible, multiple-contact miscible, and immiscible conditions. Results are presented to support the vaporization mechanism as described by Hutchinson and Braun, and also to show that more than one mechanism is possible with CO2 displacements. The reason for the latter is found in the results of phase-equilibria studies. SPEJ P. 242


1982 ◽  
Vol 22 (06) ◽  
pp. 805-815 ◽  
Author(s):  
William F. Yellig

Yellig, William F., SPE, Amoco Production Co. Abstract This paper presents results of an extensive study to understand CO2 displacement of Levelland (TX) reservoir oil. The work was conducted to support Levelland CO2 pilots currently in progress. Experimental displacement tests were conducted at various pressures, core lengths, and CO2 frontal advance rates. The experimental system included a novel analytical technique to obtain effluent compositional profiles within the oil-moving zone at test conditions. The results of this study show that at pressures greater than the CO2 minimum miscibility pressure (MMP), a multicontact miscible displacement mechanism predominates. Miscibility is developed in situ by vaporization or extraction-type mass transfer. The laboratory lengths required for CO2 to develop miscibility and exhibit miscible displacement efficiency were found dependent on the phase equilibria of the CO2/Levelland oil system. Displacements requiring the greatest length to develop miscibility were at pressures where single-contact mixtures of CO2 and Levelland oil form two liquid phases. A companion paper demonstrates the use of the analytical technique developed in this study to obtain process data from a CO2 field pilot test. In addition, the mechanistic information obtained from this study is used to interpret the process data from the pilot test. The results have application to other reservoir oils whose phase equilibria with CO2 are similar to the CO2/ Levelland oil system. Introduction Miscible CO2 flooding is developing rapidly as a commercial enhanced oil-recovery process. The successful design and interpretation of CO2 pilot tests and fieldwide floods are dependent on a good knowledge of the reservoir and the CO2 displacement process. The overall CO2 displacement process is shown schematically in Fig. 1. The main focus of this study concerned the oil moving zone (OMZ) and particularly the mechanisms by which this zone formed and by which CO2 displaced Levelland oil. Levelland oil was chosen because it is typical of many west Texas reservoir oils being considered for CO2 flooding. In addition, the CO2 pilot tests currently conducted in the Levelland field provide a direct application of this research. Several authors have discussed the displacement of reservoir oil by CO2. These discussions have centered around three primary displacement mechanisms: immiscible, multicontact or developed miscible, and contact miscible. In addition, two basic types of mass transfer have been postulated as responsible for the development of miscibility in a multicontact process: transfer of hydrocarbons from the in-place oil to the displacing CO2 (i.e., vaporization or extraction) and transfer of CO2 to the in-place oil (i.e., condensation). Vaporization and extraction are the same basic mass-transfer process. Vaporization refers to mass transfer from a liquid oil phase to a CO2-rich vapor phase and extraction refers to mass transfer from a liquid oil phase to a CO2-rich liquid phase. The distinction between vaporization and extraction is somewhat arbitrary in describing the CO2 process since it reflects the types of phases present only on first contact. One purpose of this paper is to present results of a comprehensive study to determine the mechanism by which CO2 displaces Levelland oil at reservoir conditions. SPEJ P. 805^


Energies ◽  
2021 ◽  
Vol 14 (4) ◽  
pp. 1077
Author(s):  
Tinuola Udoh ◽  
Jan Vinogradov

In this paper, a thorough experimental investigation of enhanced oil recovery via controlled salinity-biosurfactant injection under typical reservoir temperature conditions is reported for the first time. Sixteen core flooding experiments were carried out with four displacing fluids in carbonate rock samples and the improved oil recovery was investigated in secondary, tertiary and quaternary injection modes. The temperature effect on oil recovery during floodings was compared at two temperatures (23 °C and 70 °C) on similar rock samples and fluids using two types of biosurfactants: GreenZyme® and rhamnolipids. The results of this study show that injection of controlled salinity brine (CSB) and controlled salinity biosurfactant brine (CSBSB) improve oil recovery relative to injection of high salinity formation brine (FMB) at both high and low temperatures. At 23 °C, CSBSB improved oil recovery by 15–17% OIIP compared with conventional FMB injection, and by 4–8% OIIP compared with CSB injection. At 70 °C, the injection of CSBSB increased oil recovery by 10–13% OIIP compared with injection of FMB, and by 2–6% OIIP compared with CSB injection. Furthermore, increase in the system temperature generally resulted in increased oil recovery, irrespective of the type of the injection brine. The results of this study have demonstrated for the first time the enhanced oil recovery potential of combined controlled salinity brine and biosurfactant applications at temperature relevant to hydrocarbon reservoirs. The results of this study are significant for the design of controlled salinity and biosurfactant flooding in carbonate reservoirs.


Author(s):  
Jinju Han ◽  
Youngjin Seo ◽  
Juhyun Kim ◽  
Sunlee Han ◽  
Youngsoo Lee

This present study indicates experimental investigation about the impact of CO2 flooding on oil recovery and rock’s properties alteration in carbonate reservoir under the miscible condition. In order to compare the effect to initial pore characteristic, two type of carbonate rock was used; an Edward white represents homogeneous mainly consisted micropore, whereas an Indiana limestone represented heterogeneous mainly consisted macropore in this study. Under the miscible condition (9.65 MPa and 40°C), five pore volume of CO2 were injected into oil-wet carbonate rock, which was fully saturated with oil and connate water. After CO2 flooding, several analyses for each sample conducted to investigate oil recovery and rock properties change in porosity, permeability, and pore structure by chemical and physical reaction between CO2, water, and carbonate mineral before and after CO2 flooding by using core analysis, MICP, SEM, ICP, and X-ray CT techniques. From the results of oil recovery, it was more effective and larger in Edward white than in Indiana limestone. Because homogeneous characteristic with a large ratio of low permeable micropore in Edward white contributed to occur long reaction time between oil and CO2 for enough miscibility as well as to displace stably oil by CO2. Conversely, heterogeneous pore structure mainly consisted of high permeable conduit (macropore) in Indiana limestone has brought ineffective and low oil production. From the analysis of rock’s properties alteration, we found that, for the homogeneous sample, dissolution dominantly changed pore structure and became better flow path by improving permeability and reducing tortuosity. While plugging by precipitation of mineral particles was not critically affected rock’ properties, despite the sample mainly consisted small pores. In the case of the heterogeneous sample, both dissolution and precipitation critically affected change of rock’s properties and pore structure. In particular, superior precipitation in complex pore network seriously damaged flow path and change of rock’s properties. The largest porosity change markedly appeared in inlet section because of exposing rock surface from fresh CO2 during a long time. In conclusion, it shows that CO2 miscible flooding in carbonate reservoirs significantly affected to alteration of rock’s properties such as porosity, permeability, tortuosity, and pore connectivity, in particular in heterogeneous system compared with in homogeneous system. These experimental results can be useful to characterize carbonate rock as well as to study rock properties alteration on CO2 EOR and CCS processes.


2017 ◽  
Vol 3 (3) ◽  
pp. 33-38 ◽  
Author(s):  
А.V. Аntuseva ◽  
Е.F. Kudina ◽  
G.G. Pechersky ◽  
Y.R. Kuskildina ◽  
А.V., Melgui ◽  
...  

2020 ◽  
Vol 7 ◽  
pp. 116-119
Author(s):  
R.N. Fakhretdinov ◽  
◽  
D.F. Selimov ◽  
A.A. Fatkullin ◽  
S.A. Tastemirov ◽  
...  

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