Experimental Analysis of Alkali-Brine-Alcohol Phase Behavior with High Acid Number Crude Oil

2021 ◽  
pp. 1-19
Author(s):  
D. Magzymov ◽  
T. Clemens ◽  
B. Schumi ◽  
R. T. Johns

Summary A potential enhanced oil recovery technique is to inject alkali into a reservoir with a high-total acid number (TAN) crude to generate soap in situ and reduce interfacial tension (IFT) without the need to inject surfactant. The method may be cost-effective if the IFT can be lowered enough to cause significant mobilization of trapped oil while also avoiding formation of gels and viscous phases. This paper investigates the potential field application of injecting alkali to generate in-situ soap and favorable phase behavior for a high-TAN oil. Oil analyses show that the acids in the crude are a complex mixture of various polar acids and not mainly carboxylic acids. The results from phase behavior experiments do not undergo typical Winsor microemulsion behavior transition and subsequent ultralow IFTs below 1×10−3 mN/m that are conventionally observed. Instead, mixing of alkali and crude/brine generate water-in-oil macroemulsions that can be highly viscous. For a specific range of alkali concentrations, however, phases are not too viscous, and IFTs are reduced by several orders of magnitude. Incremental coreflood recoveries in this alkali range are excellent, even though not all trapped oil is mobilized. The viscous phase behavior at high alkali concentrations is explained by the formation of salt-crude complexes, created by acids from the crude oil under the alkali environment. These hydrophobic molecules tend to agglomerate at the oil-water interface. Together with polar components from the crude oil, they can organize into a highly viscous network and stabilize water droplets in the oleic phase. Oil-soluble alcohol was added to counter those two phenomena at large concentrations, but typical Winsor phase behavior was still not observed. A physicochemical model is proposed to explain the salt-crude complex formation at the oil-water interface that inhibits classical Winsor behavior.

SPE Journal ◽  
2020 ◽  
Vol 25 (04) ◽  
pp. 1812-1826
Author(s):  
Subhash Ayirala ◽  
Zuoli Li ◽  
Rubia Mariath ◽  
Abdulkareem AlSofi ◽  
Zhenghe Xu ◽  
...  

Summary The conventional experimental techniques used for performance evaluation of enhanced oil recovery (EOR) chemicals, such as polymers and surfactants, have been mostly limited to bulk viscosity, phase behavior/interfacial tension (IFT), and thermal stability measurements. Furthermore, fundamental studies exploring the different microscale interactions instigated by the EOR chemicals at the crude oil/water interface are scanty. The objective of this experimental study is to fill this existing knowledge gap and deliver an important understanding on underlying interfacial sciences and their potential implications for oil recovery in chemical EOR. Different microscale interactions of EOR chemicals, at crude oil/water interface, were studied by using a suite of experimental techniques, including an interfacial shear rheometer, Langmuir trough, and coalescence time measurement apparatus at both ambient (23°C) and elevated (70°C) temperatures. The reservoir crude oil and high-salinity injection water (57,000 ppm total dissolved solids) were used. Two chemicals, an amphoteric surfactant (at 1,000 ppm) and a sulfonated polyacrylamide polymer (at 500 and 700 ppm) were chosen because they are tolerant to high-salinity and high-temperature conditions. Interfacial viscous and elastic moduli (viscoelasticity), interface pressures, interface compression energies, and coalescence time between crude oil droplets are the major experimental data measured. Interfacial shear rheology results showed that surfactant favorably reduced the viscoelasticity of crude oil/water interface by decreasing the elastic and viscous modulus and increasing the phase angle to soften the interfacial film. Polymers in brine either alone or together with surfactant increased the viscous and elastic modulus and decreased the phase angle at the oil/water interface, thereby contributing to interfacial film rigidity. Interfacial pressures with polymers remained almost in the same order of magnitude as the high-salinity brine. In contrast, a significant reduction in interfacial pressures with surfactant was observed. The interface compression energies indicated the same trend and were reduced by approximately two orders of magnitude when surfactant was added to the brine. The surfactant was also able to retain similar interface behavior under compression even in the presence of polymers. The coalescence times between crude oil droplets were increased by polymers, while they were substantially decreased by the surfactant. These consistent findings from different experimental techniques demonstrated the adverse interactions of polymers at the crude oil/water interface to result in more rigid films, while confirming the high efficiency of the surfactant to soften the interfacial film, promote the oil droplets coalescence, and mobilize substantial amounts of residual oil in chemical EOR. This experimental study, for the first time, characterized the microscale interactions of surfactant-polymer chemicals at the crude oil/water interface. The applicability of several interfacial experimental techniques has been demonstrated to successfully understand underlying interfacial sciences and oil mobilization mechanisms in chemical EOR. These techniques and methods can provide potential means to efficiently screen and optimize EOR chemical formulations for better oil recovery in both sandstone and carbonate reservoirs.


1979 ◽  
Vol 19 (02) ◽  
pp. 116-128 ◽  
Author(s):  
Surendra P. Gupta ◽  
Scott P. Trushenski

Abstract Key variables that govern oil displacement in a micellar flood are capillary number (velocity x viscosity/interfacial tension) and chemical loss. At high capillary numbers, oil displacement is very efficient if various phases propagate at the same velocity. Chemical loss, however, is not always low when oil displacement efficiency is high. Compositions developed in situ often alter the ability of the micellar fluid to displace oil. Oil recovery can be predicted from static equilibrium fluid properties, providing the in situ compositions are known.The displacement of the wetting phase requires a capillary number of 10 times higher than that required to displace the nonwetting phase. This implies less efficient oil displacement in oil-wet systems. The correlation of oil recovery vs capillary number also varies with rock structure and wettability. Hence, for field application, immiscible oil displacement with micellar fluids should be determined in reservoir rocks. The decrease in final oil saturation with increase in capillary number indicates that relative permeability changes with capillary number. A numerically study showed that both the end-points and the shape of the relative permeability curves affect oil recovery at high permeability curves affect oil recovery at high capillary number in a slug process. The shape of the relative-permeability curves also affects the design of micellar slug viscosity. Thus, for field application, it is important to know the shape of relative-permeability curves at anticipated capillary numbers. Introduction In a micellar flood, the injected fluid banks interact with one another and with the reservoir brine, crude oil, and reservoir rock. This places stringent requirements on the design of the micellar flood. Initially, the micellar fluid may be miscible with crude oil and reservoir brine. However, because of dilution and surfactant adsorption, the flood can degenerate to an immiscible displacement. If low interfacial tension (IFT), or more specifically, high capillary number (velocity x viscosity/IFT) is maintained between all the phases, the displacement efficiency is good.There are many phenomena that can decrease oil recovery efficiency. The most important are chemical (surfactant or sulfonate) losses from adsorption by the rock, precipitation by high-salinity and high-hardness brines, interaction with polymer, partitioning into an immobile phase, and trapping of partitioning into an immobile phase, and trapping of the surfactant-rich phase. Recovery efficiency also can be poor when unfavorable in situ compositions develop. This occurs when the micellar fluid is diluted, develops undesirable salinity and hardness environment, experiences selective adsorption of surfactant, or undergoes selective partitioning of components into phases moving at different velocities.A micellar phase (or microemulsion) can exist in equilibrium with excess oil, water, or both. Winsor designated such phase behavior as Type I, II, and III, respectively. More recently, Healy et al. identified this behavior as lower phase (where the micellar phase is in equilibrium with excess oil), upper phase (where the micellar phase is in equilibrium with excess water), and middle phase (where the micellar phase is in equilibrium with excess oil and water). The importance of phase behavior has been the subject of considerable discussion in the literature.Since the function of the micellar fluid is to displace crude oil, not water, it would be desirable if the micellar fluid remained miscible with oil and immiscible with water during the immiscible displacement portion of a flood. This is achieved with upper-phase micellar systems. Since only a small bank of micellar fluid is injected, it must be displaced effectively by the succeeding polymer water bank. However, the upper-phase micellar fluid is not miscible with the polymer water; therefore, some of the micellar phase may be trapped as an immobile saturation (much as residual oil is trapped). SPEJ p. 116


1982 ◽  
Vol 22 (02) ◽  
pp. 245-258 ◽  
Author(s):  
E.F. deZabala ◽  
J.M. Vislocky ◽  
E. Rubin ◽  
C.J. Radke

Abstract A simple equilibrium chemical model is presented for continuous, linear, alkaline waterflooding of acid oils. The unique feature of the theory is that the chemistry of the acid hydrolysis to produce surfactants is included, but only for a single acid species. The in-situ produced surfactant is presumed to alter the oil/water fractional flow curves depending on its local concentration. Alkali adsorption lag is accounted for by base ion exchange with the reservoir rock. The effect of varying acid number, mobility ratio, and injected pH is investigated for secondary and tertiary alkaline flooding. Since the surface-active agent is produced in-situ, a continuous alkaline flood behaves similar to a displacement with a surfactant pulse. This surfactant-pulse behavior strands otherwise mobile oil. It also leads to delayed and reduced enhanced oil recovery for adverse mobility ratios, especially in the tertiary mode. Caustic ion exchange significantly delays enhanced oil production at low injected pH. New, experimental tertiary caustic displacements are presented for Ranger-zone oil in Wilmington sands. Tertiary oil recovery is observed once mobility control is established. Qualitative agreement is found between the chemical displacement model and the experimental displacement results. Introduction Use of alkaline agents to enhance oil recovery has considerable economic impetus. Hence, significant effort has been directed toward understanding and applying the process. To date, however, little progress has been made toward quantifying the alkaline flooding technique with a chemical displacement model. Part of the reason why simulation models have not been forthcoming for alkali recovery schemes is the wide divergence of opinion on the governing principles. Currently, there are at least eight postulated recovery mechanisms. As classified by Johnson and Radke and Somerton, these include emulsification with entrainment, emulsification with entrapment, emulsification (i.e., spontaneous or shear induced) with coalescence, wettability reversal (i.e., oil-wet to water-wet or water-wet to oil-wet), wettability gradients, oil-phase swelling (i.e., from water-in-oil emulsions), disruption of rigid films, and low interfacial tensions. The contradictions among these mechanisms apparently reside in the chemical sensitivity of the crude oil and the reservoir rock to reaction with hydroxide. Different crude oils in different reservoir rock can lead to widely disparate behavior upon contact with alkali under varying environments such as temperature, salinity, hardness concentration, and pH. The alkaline process remains one of the most complicated and least understood. It is not surprising that there is no consensus on how to design a high-pH flood for successful oil recovery. One theme, however, does unify all present understanding. The crude oil must contain acidic components, so that a finite acid number (i.e., the milligrams of potassium hydroxide required to neutralize 1 gram of oil) is necessary. Acid species in the oil react with hydroxide to produce salts, which must be surface active. It is not alkali per se that enhances oil recovery, but rather the hydrolyzed surfactant products. Therefore, a high acid number is not a sufficient recovery criterion, because not all the hydrolyzed acid species will be interfacially active. That acid crude oils can produce surfactants upon contact with alkali is well documented. The alkali technique must be distinguished from all others by the fundamental basis that the chemicals promoting oil recovery are generated in situ by saponification. SPEJ P. 245^


2019 ◽  
Author(s):  
Subhash Ayirala ◽  
Zuoli Li ◽  
Rubia Mariath Mariath ◽  
Abdulkareem AlSofi ◽  
Zhenghe Xu ◽  
...  

Processes ◽  
2020 ◽  
Vol 8 (7) ◽  
pp. 762 ◽  
Author(s):  
Mohd Sofi Numin ◽  
Khairulazhar Jumbri ◽  
Anita Ramli ◽  
Noorazlenawati Borhan

Injection of alkaline (A), polymer (P), and surfactant (S) chemicals in enhanced oil recovery (cEOR) processes increases output by changing the properties of the injected fluid. In this work, micellar fluid interactions were studied via microemulsion rheological analysis. Crude oil and stimulated brine with ASP or SP was used for bottle testing. The results revealed that no microemulsion was produced when ASP (Alkaline, Surfactant, and Polymer) or SP (Surfactant and Polymer) was left out during the bottle testing phase. The addition of ASP and SP led to the formation of microemulsions—up to 29% for 50% water cut (WC) ASP, and 36% for 40% WC SP. This shows that the addition of ASP and SP can be applied to flooding applications. The results of the rheological analysis show that the microemulsions behaved as a shear-thinning micellar fluid by decreasing viscosity with increase in shear rate. As per the power-law equation, the ASP micellar fluid viscoelastic behavior shows better shear-thinning compared to SP, suggesting more efficiency in fluid mobility and sweep efficiency. Most of the microemulsions exhibited viscoelastic fluid behavior (G’ = G”) at angular frequency of 10 to 60 rad s−1, and stable elastic fluid behavior (G’ > G’’) below 10 rad s−1 angular frequency. The viscosity of microemulsion fluids decreases as temperature increases; this indicates that the crude oil (i.e., alkanes) was solubilized in core micelles, leading to radial growth in the cylindrical part of the wormlike micelles, and resulting in a drop in end-cap energy and micelle length. No significant difference was found in the analysis of viscoelasticity evaluation and viscosity analysis for both ASP and SP microemulsions. The microemulsion tendency test and rheology test show that the addition of ASP and SP in the oil-water interface yields excellent viscoelastic properties.


SPE Journal ◽  
2018 ◽  
Vol 23 (05) ◽  
pp. 1817-1832 ◽  
Author(s):  
Subhash C. Ayirala ◽  
Ali A. Al-Yousef ◽  
Zuoli Li ◽  
Zhenghe Xu

Summary Smart waterflooding (SWF) through tailoring of injection-water salinity and ionic composition is receiving favorable attention in the industry for both improved and enhanced oil recovery (EOR) in carbonate reservoirs. Surface/intermolecular forces, thin-film dynamics, and capillary/adhesion forces at rock/fluid interfaces govern crude-oil liberation from pores. On the other hand, stability and rigidity of oil/water interfaces control the destabilization of interfacial film to promote coalescence between released oil droplets and to improve the oil-phase connectivity. As a result, the dynamics of oil recovery in smart waterflood is caused by the combined effect of favorable interactions occurring at both oil/brine and oil/brine/rock interfaces across the thin film. Most of the laboratory studies reported so far have been focused on only studying the interactions at rock/fluid interfaces. However, the other important aspect of characterizing water ion interactions at the crude oil/water interface and their impact on film stability and oil-droplet coalescence remains largely unexplored. A detailed experimental investigation was conducted to understand the effects of different water ions at the crude-oil/water interface by using several instruments such as Langmuir trough, interfacial shear rheometer, Attension tensiometer, and coalescence time-measurement apparatus. The reservoir crude oil and four different water recipes with varying salinities and individual ion concentrations were used. Interfacial tension (IFT), interface pressures, compression energy, interfacial viscous and elastic moduli, oil-droplet crumpling ratio, and coalescence time between crude-oil droplets are the major experimental data measured. The IFTs are found to be the largest for deionized (DI) water, followed by the 10-times-reduced-salinity seawater and 10-times-reduced-salinity seawater enriched with sulfates. Interfacial pressures gradually increased with compressing surface area for all the brines and DI water. The compression energy (integration of interfacial pressure over the surface-area change) is the highest for DI water, followed by the lower-salinity brine containing sulfate ions, indicating rigid interfaces. The transition times of interfacial layer to become elastic-dominant from viscous-dominant structures are found to be much shorter for brines enriched with sulfates, once again confirming the rigidity of interface. The crumpling ratios (oil drop wrinkles when contracted) are also higher with the two recipes of DI water and sulfates-only brine to indicate the same trend and to confirm elastic rigid skin at the interface. The coalescence time between oil droplets was the least in brines containing sufficient amounts of magnesium and calcium ions, while the highest in DI water and sulfate-rich brine, respectively. These results, therefore, showed a good correlation of coalescence times with the rigidity of oil/water interface, as interpreted from different measurement techniques. This study, thereby, integrates consistent results obtained from different measurement techniques at the crude-oil/water interface to demonstrate the importance of both salinity and certain ions, such as magnesium and calcium, on crude-oil-droplets coalescence, and to improve oil-phase connectivity in smart waterflood.


2001 ◽  
Vol 4 (06) ◽  
pp. 455-466 ◽  
Author(s):  
A. Graue ◽  
T. Bognø ◽  
B.A. Baldwin ◽  
E.A. Spinler

Summary Iterative comparison between experimental work and numerical simulations has been used to predict oil-recovery mechanisms in fractured chalk as a function of wettability. Selective and reproducible alteration of wettability by aging in crude oil at an elevated temperature produced chalk blocks that were strongly water-wet and moderately water-wet, but with identical mineralogy and pore geometry. Large scale, nuclear-tracer, 2D-imaging experiments monitored the waterflooding of these blocks of chalk, first whole, then fractured. This data provided in-situ fluid saturations for validating numerical simulations and evaluating capillary pressure- and relative permeability-input data used in the simulations. Capillary pressure and relative permeabilities at each wettability condition were measured experimentally and used as input for the simulations. Optimization of either Pc-data or kr-curves gave indications of the validity of these input data. History matching both the production profile and the in-situ saturation distribution development gave higher confidence in the simulations than matching production profiles only. Introduction Laboratory waterflood experiments, with larger blocks of fractured chalk where the advancing waterfront has been imaged by a nuclear tracer technique, showed that changing the wettability conditions from strongly water-wet to moderately water-wet had minor impact on the the oil-production profiles.1–3 The in-situ saturation development, however, was significantly different, indicating differences in oil-recovery mechanisms.4 The main objective for the current experiments was to determine the oil-recovery mechanisms at different wettability conditions. We have reported earlier on a technique that reproducibly alters wettability in outcrop chalk by aging the rock material in stock-tank crude oil at an elevated temperature for a selected period of time.5 After applying this aging technique to several blocks of chalk, we imaged waterfloods on blocks of outcrop chalk at different wettability conditions, first as a whole block, then when the blocks were fractured and reassembled. Earlier work reported experiments using an embedded fracture network,4,6,7 while this work also studied an interconnected fracture network. A secondary objective of these experiments was to validate a full-field numerical simulator for prediction of the oil production and the in-situ saturation dynamics for the waterfloods. In this process, the validity of the experimentally measured capillary pressure and relative permeability data, used as input for the simulator, has been tested at strongly water-wet and moderately water-wet conditions. Optimization of either Pc data or kr curves for the chalk matrix in the numerical simulations of the whole blocks at different wettabilities gave indications of the data's validity. History matching both the production profile and the in-situ saturation distribution development gave higher confidence in the simulations of the fractured blocks, in which only the fracture representation was a variable. Experimental Rock Material and Preparation. Two chalk blocks, CHP8 and CHP9, approximately 20×12×5 cm thick, were obtained from large pieces of Rørdal outcrop chalk from the Portland quarry near Ålborg, Denmark. The blocks were cut to size with a band saw and used without cleaning. Local air permeability was measured at each intersection of a 1×1-cm grid on both sides of the blocks with a minipermeameter. The measurements indicated homogeneous blocks on a centimeter scale. This chalk material had never been contacted by oil and was strongly water-wet. The blocks were dried in a 90°C oven for 3 days. End pieces were mounted on each block, and the whole assembly was epoxy coated. Each end piece contained three fittings so that entering and exiting fluids were evenly distributed with respect to height. The blocks were vacuum evacuated and saturated with brine containing 5 wt% NaCl+3.8 wt% CaCl2. Fluid data are found in Table 1. Porosity was determined from weight measurements, and the permeability was measured across the epoxy-coated blocks, at 2×10–3 µm2 and 4×10–3 µm2, for CHP8 and CHP9, respectively (see block data in Table 2). Immobile water saturations of 27 to 35% pore volume (PV) were established for both blocks by oilflooding. To obtain uniform initial water saturation, Swi, oil was injected alternately at both ends. Oilfloods of the epoxy-coated block, CHP8, were carried out with stock-tank crude oil in a heated pressure vessel at 90°C with a maximum differential pressure of 135 kPa/cm. CHP9 was oilflooded with decane at room temperature. Wettability Alteration. Selective and reproducible alteration of wettability, by aging in crude oil at elevated temperatures, produced a moderately water-wet chalk block, CHP8, with similar mineralogy and pore geometry to the untreated strongly water-wet chalk block CHP9. Block CHP8 was aged in crude oil at 90°C for 83 days at an immobile water saturation of 28% PV. A North Sea crude oil, filtered at 90°C through a chalk core, was used to oilflood the block and to determine the aging process. Two twin samples drilled from the same chunk of chalk as the cut block were treated similar to the block. An Amott-Harvey test was performed on these samples to indicate the wettability conditions after aging.8 After the waterfloods were terminated, four core plugs were drilled out of each block, and wettability measurements were conducted with the Amott-Harvey test. Because of possible wax problems with the North Sea crude oil used for aging, decane was used as the oil phase during the waterfloods, which were performed at room temperature. After the aging was completed for CHP8, the crude oil was flushed out with decahydronaphthalene (decalin), which again was flushed out with n-decane, all at 90°C. Decalin was used as a buffer between the decane and the crude oil to avoid asphalthene precipitation, which may occur when decane contacts the crude oil.


2021 ◽  
Author(s):  
Alexey V. Vakhin ◽  
Irek I. Mukhamatdinov ◽  
Firdavs A. Aliev ◽  
Dmitriy F. Feoktistov ◽  
Sergey A. Sitnov ◽  
...  

Abstract A nickel-based catalyst precursor has been synthesized for in-situ upgrading of heavy crude oil that is capable of increasing the efficiency of steam stimulation techniques. The precursor activation occurs due to the decomposition of nickel tallate under hydrothermal conditions. The aim of this study is to analyze the efficiency of in-situ catalytic upgrading of heavy oil from laboratory scale experiments to the field-scale implementation in Boca de Jaruco reservoir. The proposed catalytic composition for in-reservoir chemical transformation of heavy oil and natural bitumen is composed of oil-soluble nickel compound and organic hydrogen donor solvent. The nickel-based catalytic composition in laboratory-scale hydrothermal conditions at 300°С and 90 bars demonstrated a high performance; the content of asphaltenes was reduced from 22% to 7 wt.%. The viscosity of crude oil was also reduced by three times. The technology for industrial-scale production of catalyst precursor was designed and the first pilot batch with a mass of 12 ton was achieved. A «Cyclic steam stimulation» technology was modified in order to deliver the catalytic composition to the pay zones of Boca de Jaruco reservoir (Cuba). The active forms of catalyst precursors are nanodispersed mixed oxides and sulfides of nickel. The pilot test of catalyst injection was carried out in bituminous carbonate formation M, in Boca de Jaruco reservoir (Cuba). The application of catalytic composition provided increase in cumulative oil production and incremental oil recovery in contrast to the previous cycle (without catalyst) is 170% up to date (the effect is in progress). After injection of catalysts, more than 200 samples from production well were analyzed in laboratory. Based on the physical and chemical properties of investigated samples and considering the excellent oil recovery coefficient it is decided to expand the industrial application of catalysts in the given reservoir. The project is scheduled on the fourth quarter of 2021.


2021 ◽  
Author(s):  
Ahmed Almadhaji ◽  
Mohammed Saeed ◽  
Hitham Ibrahim ◽  
Anas Ahmed ◽  
Ragaei Maher

Abstract One of Sudanese fields has a heavy crude oil which has a high Total Acid Number (TAN) and high viscosity, can cause a lot of problems in production operation, transport, and storage facilities. The effect of ethanol dilution on the rheological properties of crude (especially the kinematic viscosity) was studied and presented. Moreover, the consequence of blending Trona (NaHCO3.Na2CO3) with a specified amount of Ethanol in the crude can reduce (TAN) to acceptable limits for solving corrosion and flowability problems. The approach is based on the experiments and laboratory works on the crude's samples after blending with a certain amount of Trona and Ethanol. It depends on the results of apparatuses, that are used to measure the samples, for instance, Calibrated glass capillary viscometer and ASTM D664 titration volume Total Acid Number tester which are employed to get the values of kinematic viscosity and TAN, respectively. The tests are established with crude have kinematic viscosity (187 cst) at temperature 75°C and TAN almost (8.51). While increasing the dosage of Trona at the ambient temperature (38°C) with the certain mass percentage of Ethanol (5%), TAN is decreased from (8.51 to 4.00 mgKOH/g). Also, the kinematic viscosity is declined from (187 cst to 96.75 cst) after increasing the volume of Ethanol at 75°C. These outcomes indicated that Ethanol could reduce Sudanese heavy crude's viscosity, and the Trona could decrease the TAN. This reduction occurred due to Ethanol dilution. The Ethanol molecules disturb the molecular structure of the crude, which forms polar bond within the hydrocarbon chain that leads to lower the friction between molecules of hydrocarbon in the crude. Also, Trona shrinks TAN because the Hydroxide ions (OH+) that founded in Trona neutralize the Hydrogen ions (H−) in Naphthenic acid in Sudanese heavy crude. This study can be summarized in the ability to solve the difficulty of transporting and processing the heavy crude oil in refineries; maintains the quality of the crude while utilizing it with friendly environmental materials and low cost.


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