Dendritic Pattern Formation and Contact Line Forces during Dewetting of Dilute Polymer Solutions on a Hydrophobic Surface

The micro-scale morphology of the receding contact line of dilute polyethylene oxide solution drops (c ∼ 100 ppm) after impact and inertial spreading on a fluorinated hydrophobic surface is investigated. One can observe the formation of transient liquid filaments and dendritic structures that evolve into a bead-on-a-string structure similar to the well-known capillary breakup mechanism of dilute polymer solutions, which confirm the interaction between stetched polymer coils and the receding three-phase contact line. The estimation of the average polymer force per unit contact line lenght provides a quantitative explanation for the reduction of the contact line retraction velocity reduction observed experimentally.

Field Demonstration of the Impact of Fractures on Hydrolyzed Polyacrylamide Injectivity, Propagation, and Degradation

Summary During a polymer flood, the field operator must be convinced that the large chemical investment is not compromised during polymer injection. Furthermore, injectivity associated with the viscous polymer solutions must not be reduced to where fluid throughput in the reservoir and oil production rates become uneconomic. Fractures with limited length and proper orientation have been theoretically argued to dramatically increase polymer injectivity and eliminate polymer mechanical degradation. This paper confirms these predictions through a combination of calculations, laboratory measurements, and field observations (including step-rate tests, pressure transient analysis, and analysis of fluid samples flowed back from injection wells and produced from offset production wells) associated with the Kalamkas oil field in Western Kazakhstan. A novel method was developed to collect samples of fluids that were back-produced from injection wells using the natural energy of a reservoir at the wellhead. This method included a special procedure and surface-equipment scheme to protect samples from oxidative degradation. Rheological measurements of back-produced polymer solutions revealed no polymer mechanical degradation for conditions at the Kalamkas oil field. An injection well pressure falloff test and a step-rate test confirmed that polymer injection occurred above the formation parting pressure. The open fracture area was high enough to ensure low flow velocity for the polymer solution (and consequently, the mechanical stability of the polymer). Compared to other laboratory and field procedures, this new method is quick, simple, cheap, and reliable. Tests also confirmed that contact with the formation rapidly depleted dissolved oxygen from the fluids—thereby promoting polymer chemical stability.

Injectivity and Propagation of Sulfonated Acrylamide-Based Copolymers in Low Permeability Carbonate Reservoir Cores in Harsh Salinity and Temperature Conditions : Challenges and Learnings from a Middle East Onshore Case Study

Polymer flooding is one of the most mature EOR technology applied successfully in a broad range of reservoir conditions. The last developments made in polymer chemistries allowed pushing the boundaries of applicability towards higher temperature and salinity carbonate reservoirs. Specifically designed sulfonated acrylamide-based copolymers (SPAM) have been proven to be stable for more than one year at 120°C and are the best candidates to comply with Middle East carbonate reservoir conditions. Numerous studies have shown good injectivity and propagation properties of SPAM in carbonate cores with permeabilities ranging from 70 to 150 mD in presence of oil. This study aims at providing new insights on the propagation of SPAM in carbonate reservoir cores having permeabilities ranging between 10 and 40 mD. Polymer screening was performed in the conditions of ADNOC onshore carbonate reservoir using a 260 g/L TDS synthetic formation brine together with oil and core material from the reservoir. All the experiments were performed at residual oil saturation (Sor). The experimental approach aimed at reproducing the transport of the polymer entering the reservoir from the sand face up to a certain depth. Three reservoir coreflood experiments were performed in series at increasing temperatures and decreasing rates to mimic the progression of the polymer in the reservoir with a radial velocity profile. A polymer solution at 2000 ppm was injected in the first core at 100 mL/h and 40°C. Effluents were collected and injected in the second core at 20 mL/h and 70°C. Effluents were collected again and injected in the third core at 4 mL/h and 120°C. A further innovative approach using reservoir minicores (6 mm length disks) was also implemented to screen the impact of different parameters such as Sor, molecular weight and prefiltration step on the injectivity of the polymer solutions. According to minicores data, shearing of the polymer should help to ensure good propagation and avoid pressure build-up at the core inlet. This result was confirmed through an injection in a larger core at Sor and at 120°C. When comparing the injection of sheared and unsheared polymer at the same concentration, core inlet impairment was suppressed with the sheared polymer and the same range of mobility reduction (Rm) was achieved in the internal section of the core although viscosity was lower for the sheared polymer. Such result indicates that shearing is an efficient way to improve injectivity while maximizing the mobility reduction by suppressing the loss of product by filtration/retention at the core inlet. This paper gives new insights concerning SPAM rheology in low permeability carbonate cores. Additionally, it provides an innovative and easier approach for screening polymer solutions to anticipate their propagation in more advanced coreflooding experiments.

Characterizing the Influence of Organic Polymers on the Specific Reactivity of Particulate Remedial Amendments

Commercially available particulate amendments demonstrate high reactivity for effective treatment of water soluble organic and inorganic contaminants in laboratory studies; however, transport of these particles is constrained in the subsurface. In many field applications, particulate amendments are mixed with organic polymers to enhance mobility for direct push applications or stabilize suspensions for high mass loadings. As such, the interactions between particulate amendments, organic polymers and contaminant species need to be systematically investigated to properly understand mechanistic processes that facilitate predictive performance metrics for specific applications in situ. In this study, batch experiments were conducted to quantify the effects of organic polymers (xanthan gum, guar gum, and sodium alginate), polymer concentration (800 and 4,000 mg/L), and aging (up to 28 days) on chromate treatment rate and capacity by two classes of amendments: reductants [granular zero-valent iron (gZVI), micron-ZVI (mZVI), sulfur modified iron (SMI)], and an adsorbent (bismuth sub-nitrate). When particulate amendments were suspended in polymer solutions, reductants retained between 84–100% of the amendment treatment capacity. Conversely, the adsorbent maintained 63–97% relative treatment capacity of the no-polymer control. Polymer solutions had a more pronounced impact on the rate of chromate removal; first order rates of chemical reduction decreased by as much as 70% and adsorption by up to 81% relative to the no-polymer controls. Polymer–amendment aging experiments also showed decreased Cr(VI) treatment capacity; reductants decreased by as much as 24% and adsorption decreased by as much as 44% after 28 days of incubation. While polymer suspensions are needed to aid the injection of particulate amendments into the subsurface, the results from this study indicate potential losses of treatment capacity and a decrease in the rate of remedial performance due to the physical and chemical interactions between polymer suspensions and reactive particulate amendments. Simple batch systems provide baseline characterization of tripartite interactions for the removal of Cr(VI). Additional work is needed to quantify the full impact of polymers on remedial outcomes under site relevant conditions at field scale.

Analysis of Transient Boiling Processes during Steel Quenching in Water PAG Solutions to Decrease Distortion

The paper discusses results of testing standard cylindrical probe 12.5 mm diameter in water polymer solutions which was additionally instrumented with a surface thermocouple. It is shown that central thermocouple cannot depict many physical phenomena taking place during quenching in polymer solutions such as shoulder formation, self- regulated thermal process establishing, surface temperature transient from film boiling to nucleate boiling process. Moreover, it is shown that experimental data depicted by central thermocouple cannot be used for solving inverse problem to analyze quenching process in liquid media. Along with analyzing film and nucleate boiling processes during quenching, the paper discusses the possibility of quality quench process control via using sonar system. It is established an equation for evaluating duration of transient nucleate boiling process. As an example, the cooling characteristics of fresh and old polyalkylene glycol (PAG) polymer solutions are analyzed. It is shown that with passing time the critical heat flux density of polymer decreases and inverse solubility effect disappears. That is while the method and apparatus were developed to control in industrial condition the quality of quenched steel parts during hardening in liquid media.