An Experimental Investigation of Polymer Mechanical Degradation at the Centimeter and Meter Scale

SPE Journal ◽  
2019 ◽  
Vol 24 (04) ◽  
pp. 1700-1713 ◽  
Author(s):  
Siv Marie Åsen ◽  
Arne Stavland ◽  
Daniel Strand ◽  
Aksel Hiorth

Summary In this work, we examine the common understanding that mechanical degradation of polymers takes place at the rock surface or within the first few millimeters of the rock. The effect of core length on mechanical degradation of synthetic enhanced-oil-recovery (EOR) polymers was investigated. We constructed a novel experimental setup for studying mechanical degradation at different flow velocities as a function of distances traveled. The setup enabled us to evaluate degradation in serial mounted core segments of 3, 5, 8, and 13 cm individually or combined. By recycling, we could also evaluate degradation at effective distances up to 20 m. Using low-velocity reinjection of a polymer solution previously degraded at a higher rate, we simulated the effect of radial flow on degradation. Experiments were performed with two different polymers [high-molecular-weight (MW) hydrolyzed polyacrylamide (HPAM) and low-MW acrylamide tertiary butyl sulfonic acid (ATBS)] in two different brines [0.5% NaCl and synthetic seawater (SSW)]. In the linear flow at high shear rates, we observed a decline in degradation rate with distance traveled. Even after 20 m, some degradation occurred. However, the observed degradation was associated with high pressure gradients of 100 bar/m, which at field scale is not realistic. It is possible that oxidative degradation played a significant role during our experiments, where the polymer was cycled many times through a core. This occurrence could significantly affect our suggestion that mechanical degradation still occurs after 20 m or more of flow through a porous medium. The MW of the degraded polymer could be matched with a power-law dependency, MWD ≈ L–x, where x for the HPAM was 0.07 and x for the ATBS was 0.03. In the radial flow, where the velocity decreases by length, the mechanical degradation occurs close to the sandface with only minor degradation deeper in the formation. The length at which degradation reaches a stable condition is not determined. We confirmed previous findings that degradation depends on salinity (Maerker 1975) and MW (Stavland et al. 2010), and results show that in all experiments with significant degradation, most of the degradation takes place in the first core segment. Moreover, the higher the shear rate and degradation, the higher the fraction of degradation that occurs in the first core segment.

SPE Journal ◽  
2017 ◽  
Vol 23 (01) ◽  
pp. 18-33 ◽  
Author(s):  
S.. Jouenne ◽  
H.. Chakibi ◽  
D.. Levitt

Summary A key challenge in polymer-flood forecasting is the prediction of polymer stability far from the injector. Degradation may result from various mechanical-degradation events in surface facilities and at the wellbore interface, as well as possible oxidative degradation caused by the presence of oxygen and reduced transition metals. All these steps must be closely examined to minimize degradation and ensure propagation of a viscous polymer solution. In this paper, polymer solutions are pushed toward degradation rates that would be unacceptable for enhanced-oil-recovery applications to better understand the underlying physics. Multistep degradation events are induced in various geometries, such as capillaries, blenders, and porous media. For the geometries and range of polymer and salt concentrations investigated, degradation (as defined here) approaches an asymptotic value as the number of degrading events increases. An empirical normalization method is proposed, allowing superimposition of curves of viscosity loss vs. time across multiple possible geometries. The normalization procedure is applied to predict the extent of degradation during a field injection in which near-wellbore degradation occurs after degradation in surface facilities. We predict that degradation in the porous medium reaches a stable value after passing through approximately 6 mm of rock. Finally, degradation is proposed as a tool to probe the molecular-weight distribution and to narrow the polydispersity of polymers, which can be used for maximizing both viscosifying power and injectivity simultaneously.


1975 ◽  
Vol 15 (04) ◽  
pp. 311-322 ◽  
Author(s):  
J.M. Maerker

Abstract Partially hydrolyzed polyacrylamide solutions are highly shear degradable and may lose much of their effectiveness in reducing water mobility when sheared by flow through porous rock in the vicinity of an injection well. Degradation is investigated by forcing polymer solutions, prepared in brines of various salinities, through consolidated sandstone plugs differing in length and permeability, over a plugs differing in length and permeability, over a wide range of flow rates. A correlation for degradation based on a theoretical viscoelastic fluid model is developed that extends predictive capability to situations not easily reproduced in the laboratory. Mobility-reduction losses in field cores at reservoir flow rates are measured following degradation and are found to depend strongly on formation permeability. Consideration of field applications shows that injection into typical wellbore geometries can lead to more than an 80-percent loss of the mobility reduction provided by undegraded solutions. Also discussed are consequences for incremental oil recovery and the possibility of injecting through propped fractures. possibility of injecting through propped fractures Introduction Susceptibility of commercially available, partially hydrolyzed polyacrylamides to mechanical, or shear, degradation represents a serious problem regarding their applicability as mobility-control fluids for secondary and tertiary oil recovery applications. The approach taken in this work assumes that surface handling equipment in the field (pumps, flow controllers, etc.) have been adequately designed to minimize effects of shear degradation in all operations preceding actual delivery of the polymer solution to the sand face. The remaining problem is to assess the mechanical degradation a polymer solution experiences when it enters the porous matrix at the high fluxes prevailing around injection wells. Ability to predict the degree of mobility-control loss based on a laboratory investigation of the relevant parameters is desirable. White et al. were the first to attempt prediction of matrix-induced degradation, but the result was only a recommended injection-rate limit for minimizing polymer degradation for two specific wellbore completions. More recent papers offer limited data supporting the contention that matrix-induced degradation of polyacrylamide solutions results in significant loss polyacrylamide solutions results in significant loss of mobility control . This paper investigates the cause of mechanical degradation in dilute polymer solutions and presents experimental data on the effects of polymer concentration, water salinity, permeability, flow rate, and flow distance. permeability, flow rate, and flow distance. Several interesting and unexpected conclusions are drawn from the results. BACKGROUND - THEORETICAL CONCEPT The mechanical degradation of polymer solutions occurs when fluid stresses developed during deformation, or flow, become large enough to break the polymer molecular chains. Historically, the feeling has been that shearing stresses in laminar shear flow or turbulent pipe flow were responsible for chain scission. However, recent data reported by Culter et al. suggest that degradation of viscoelastic polymer solutions in capillary tubes may be dominated by large elongational or normal caresses occurring at the entrance to the squared-off capillaries. Such stresses result from Lagrangian unsteady flow, or elongational deformation, at the tube entrance. Flow through porous media also generates velocity fields that are sufficiently unsteady, in the Lagrangian sense, to lead one to anticipate large viscoelastic normal stresses. Viscoelastic fluids are materials that behave like viscous liquids at low rates of deformation and partially like elastic solids at high rates of partially like elastic solids at high rates of deformation. Several constitutive models are available for describing the stress-strain behavior of such fluids. SPEJ P. 311


2008 ◽  
Vol 2 (4) ◽  
pp. 295-303
Author(s):  
Maria de Melo ◽  
◽  
Elizabete Lucas ◽  

Polymer flooding has been applied for petroleum recovery and the main results of this method are the effective increasing in oil production and the reduction of water circulation The objective of this work is to present a methodology for pre-selecting a polymer to be used in future research on enhanced oil recovery (EOR) by injecting polymer solution. A reservoir was selected and characterized. Seven samples of commercial partially hydrolyzed polyacrylamide (PHPA) were also selected and characterized. Polymer solutions were prepared and characterized in terms of filterability, viscosity, stability (under reservoir conditions) and mechanical degradation. Polymer-reservoir interaction was also investigated. The results showed that it is very useful to establish a methodology to pre-select the more suitable polymer for fluid injection operations in oil field. Besides, for the conditions used in this study, the best polymer presents hydrolysis degree of 30%, molar mass of 5106 and intrinsic viscosity of 10 ml/g.


SPE Journal ◽  
2010 ◽  
Vol 16 (01) ◽  
pp. 35-42 ◽  
Author(s):  
R.S.. S. Seright ◽  
Tianguang Fan ◽  
Kathryn Wavrik ◽  
Rosangela de Carvalho Balaban

Summary This paper clarifies the rheology of xanthan and partially hydrolyzed polyacrylamide (HPAM) solutions in porous media, especially at low velocities. Previous literature reported resistance factors (effective viscosities in porous media) and an apparent shear thinning at low fluxes that were noticeably greater than what is expected on the basis of viscosity measurements. The polymer component that causes the latter behavior is shown to propagate quite slowly and generally will not penetrate deep into a formation. Particularly for HPAM solutions, this behavior can be reduced or eliminated for solutions that experience mechanical degradation or flow through a few feet of porous rock. Under practical conditions where HPAM is used for enhanced oil recovery (EOR), the degree of shear thinning is slight or nonexistent, especially compared to the level of shear thickening that occurs at high fluxes.


2011 ◽  
Vol 236-238 ◽  
pp. 2135-2141
Author(s):  
Qi Cheng Liu ◽  
Yong Jian Liu

Molecular film displacement is a new nanofilm EOR technique. A large number of experiments show that the mechanism of molecular film displacement is different from conventional chemical displacement (polymer, surfactant, alkali and ASP displacement etc). With water solution acting as transfer medium, molecules of the filming agent develop the force to form films through electrostatic interaction, with efficient molecules deposited on the negatively charged rock surface to form ultrathin films at nanometer scale. This change the properties of reservoir surface and the interaction condition with crude oil, making the oil easily be displaced as the pores swept by the injected fluid. Thus oil recovery is enhanced. The mechanism of molecular filming agent mainly includes absorption, wettability alteration, diffusion and capillary imbibition etc.


Author(s):  
H. Samara ◽  
T. V. Ostrowski ◽  
F. Ayad Abdulkareem ◽  
E. Padmanabhan ◽  
P. Jaeger

AbstractShales are mostly unexploited energy resources. However, the extraction and production of their hydrocarbons require innovative methods. Applications involving carbon dioxide in shales could combine its potential use in oil recovery with its storage in view of its impact on global climate. The success of these approaches highly depends on various mechanisms taking place in the rock pores simultaneously. In this work, properties governing these mechanisms are presented at technically relevant conditions. The pendant and sessile drop methods are utilized to measure interfacial tension and wettability, respectively. The gravimetric method is used to quantify CO2 adsorption capacity of shale and gas adsorption kinetics is evaluated to determine diffusion coefficients. It is found that interfacial properties are strongly affected by the operating pressure. The oil-CO2 interfacial tension shows a decrease from approx. 21 mN/m at 0.1 MPa to around 3 mN/m at 20 MPa. A similar trend is observed in brine-CO2 systems. The diffusion coefficient is observed to slightly increase with pressure at supercritical conditions. Finally, the contact angle is found to be directly related to the gas adsorption at the rock surface: Up to 3.8 wt% of CO2 is adsorbed on the shale surface at 20 MPa and 60 °C where a maximum in contact angle is also found. To the best of the author’s knowledge, the affinity of calcite-rich surfaces toward CO2 adsorption is linked experimentally to the wetting behavior for the first time. The results are discussed in terms of CO2 storage scenarios occurring optimally at 20 MPa.


2012 ◽  
Vol 5 (1) ◽  
pp. 37-44 ◽  
Author(s):  
Gustavo-Adolfo Maya-Toro ◽  
Rubén-Hernán Castro-García ◽  
Zarith del Pilar Pachón-Contreras. ◽  
Jose-Francisco Zapata-Arango

Oil recovery by water injection is the most extended technology in the world for additional recovery, however, formation heterogeneity can turn it into highly inefficient and expensive by channeling injected water. This work presents a chemical option that allows controlling the channeling of important amounts of injection water in specific layers, or portions of layers, which is the main explanation for low efficiency in many secondary oil recovery processes. The core of the stages presented here is using partially hydrolyzed polyacrylamide (HPAM) cross linked with a metallic ion (Cr+3), which, at high concentrations in the injection water (5000 – 20000 ppm), generates a rigid gel in the reservoir that forces the injected water to enter into the formation through upswept zones. The use of the stages presented here is a process that involves from experimental evaluation for the specific reservoir to the field monitoring, and going through a strict control during the well intervention, being this last step an innovation for this kind of treatments. This paper presents field cases that show positive results, besides the details of design, application and monitoring.


2021 ◽  
Vol 874 ◽  
pp. 45-49
Author(s):  
Ihsan Arifin ◽  
Grandprix Thomryes Marth Kadja ◽  
Cynthia L. Radiman

Enhanced Oil Recovery (EOR) is a promising technology for increasing crude oil production, especially from old wells. Polymer flooding is one of the techniques used in EOR in which the water-soluble polymer is added to increase the viscosity of the injected fluid. However, this technique has not been implemented in Indonesia due to the unavailability of locally-synthesized polymers. Therefore, this research aims to synthesize polyacrylamides and their partially-hydrolyzed derivatives and to study the possibility of their utilization for the EOR application. Various polymerization conditions using potassium persulfate (KPS) as initiators have been realized and the resulting polymers were characterized using FTIR spectroscopy and rheology measurement. It was found that higher monomer concentration resulted in higher viscosity-average molecular weight of polyacrylamide. Further study revealed that the hydrolysis of polyacrylamide by alkaline solution significantly increased the viscosity of 1000 ppm solution from 1.5 to 145.40 cP at room temperature, which is comparable to one of the commercial products. These results showed that the simple synthesis and hydrolysis method could be effectively used to produce water-soluble polymers for the EOR application.


2021 ◽  
Author(s):  
Xurong Zhao ◽  
Tianbo Liang ◽  
Jingge Zan ◽  
Mengchuan Zhang ◽  
Fujian Zhou ◽  
...  

Abstract Replacing oil from small pores of tight oil-wet rocks relies on altering the rock wettability with the injected fracturing fluid. Among different types of wettability-alteration surfactants, the liquid nanofluid has less adsorption loss during transport in the porous media, and can efficiently alter the rock wettability; meanwhile, it can also maintain a certain oil-water interfacial tension driving the water imbibition. In the previous study, the main properties of a Nonionic nanofluid-diluted microemulsion (DME) were evaluated, and the dispersion coefficient and adsorption rate of DME in tight rock under different conditions were quantified. In this study, to more intuitively show the change of wettability of DME to oil-wet rocks in the process of core flooding experiments and the changes of the water invasion front, CT is used to carry out on-line core flooding experiments, scan and calculate the water saturation in time, and compare it with the pressure drop in this process. Besides, the heterogeneity of rock samples is quantified in this paper. The results show that when the DME is used as the fracturing fluid additive, fingering of the water phase is observed at the beginning of the invasion; compared with brine, the fracturing fluid with DME has deeper invasion depth at the same time; the water invasion front gradually becomes uniform when the DME alters the rock wettability and triggers the imbibition; for tight rocks, DME can enter deeper pores and replace more oil because of its dominance. Finally, the selected nanofluids of DME were tested in two horizontal wells in the field, and their flowback fluids were collected and analyzed. The results show that the average droplet size of the flowback fluids in the wells using DME decreases with production time, and the altered wetting ability gradually returns to the level of the injected fracturing fluid. It can be confirmed that DME can migrate within the tight rock, make the rock surface more water-wet and enhance the imbibition capacity of the fracturing fluid, to reduce the reservoir pressure decline rate and increase production.


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