Gelation and Plugging Performance of Low-Concentration Partially Hydrolyzed Polyacrylamide/Polyethyleneimine System at Moderate Temperature and in Fractured Low-Permeability Reservoir.

HPAM/PEI gel is a promising material for conformance control in hydrocarbon reservoirs. However, its use in low-permeability reservoirs is limited by the high polymer concentrations present. In this study, the gelation performance of an HPAM/PEI system with HPAM < 2.0 wt.% was systematically investigated. The gelation time for HPAM concentrations ranging from 0.4 to 2.0 wt.% varied from less than 1 h to 23 days, with the highest gel strength identified as grade H. The hydrodynamic radius manifested the primary effect of HPAM on the gelation performance. Branched PEI provided superior gelation performance over linear PEI, and the gelation performance was only affected when the molecular weight of the PEI varied significantly. The optimal number ratio of the PEI-provided imine groups and the HPAM-provided carboxylic acid functional groups was approximately 1.6:1~5:1. Regarding the reservoir conditions, the temperature had a crucial effect on the hydrodynamic radius of HPAM. Salts delayed the gelation process, and the order of ionic influence was Ca2+ > Na+ > K+. The pH controlled the crosslinking reaction, primarily due to the protonation degree of PEI and the hydrolysis degree of HPAM, and the most suitable pH was approximately 10.5. Plugging experiments based on a through-type fracture showed that multi-slug plugging could significantly improve the plugging performance of the system, being favorable for its application in fractured low-permeability reservoirs.

New Allosteric Modulators of AMPA Receptors: Synthesis and Study of Their Functional Activity by Radioligand-Receptor Binding Analysis.

The synthetic approaches to three new AMPA receptor modulators-derivatives of 1,11-dimethyl-3,6,9-triazatricyclo[7.3.1.13,11]tetradecane-4,8,12-trione-had been developed and all steps of synthesis were optimized. The structures of the compounds contain tricyclic cage and indane fragments necessary for binding with the target receptor. Their physiological activity was studied by radioligand-receptor binding analysis using [3H]PAM-43 as a reference ligand, which is a highly potent positive allosteric modulator of AMPA receptors. The results of radioligand-binding studies indicated the high potency of two synthesized compounds to bind with the same targets as positive allosteric modulator PAM-43 (at least on AMPA receptors). We suggest that the Glu-dependent specific binding site of [3H]PAM-43 or the receptor containing this site may be one of the targets of the new compounds. We also suggest that enhanced radioligand binding may indicate the existence of synergistic effects of compounds 11b and 11c with respect to PAM-43 binding to the targets. At the same time, these compounds may not compete directly with PAM-43 for its specific binding sites but bind to other specific sites of this biotarget, changing its conformation and thereby causing a synergistic effect of cooperative interaction. It can be expected that the newly synthesized compounds will also have pronounced effects on the glutamatergic system of the mammalian brain.

Polymer Screening for Efficient Water Cut Reduction in a Sandstone Oilfield in Kazakhstan.

Polymer flooding is one of the most widely used and effective enhanced oil recovery techniques. It can improve the macroscopic sweep efficiency of a reservoir by controlling the fractional flow of water. The applicability of polymer flooding for one of the sandstone fields in Kazakhstan was evaluated in this study and polymer screening was carried out to choose the most appropriate polymer among four hydrolyzed polyacrylamide polymer samples. Polymer samples were prepared in Caspian seawater (CSW) and assessed based on rheology, thermal stability, sensitivity to non-ionic materials and oxygen, and static adsorption. All the tests were performed at a reservoir temperature of 63 °C. Based on the results of the screening study, tolerance of a polymer towards high-temperature reservoir conditions, resistance to bacterial activity and dissolved oxygen present in make-up brine, chemical degradation, and reduced adsorption on rock surface were considered the most important screening parameters. As a result of this screening study, one out of four polymers was selected for the target field as it showed a negligible effect of bacterial activity on thermal stability. The results of static adsorption also showed 13-14% lower adsorption of the selected polymer compared to other polymers tested in the study. The results of this study demonstrate important screening criteria to be followed during polymer selection for an oilfield as the polymer should be selected based on not only polymer characteristics but also the polymer interactions with the ionic and non-ionic components of the make-up brine.

Silica Nanoparticles in Xanthan Gum Solutions: Oil Recovery Efficiency in Core Flooding Tests.

Polymer flooding is one of the enhanced oil recovery (EOR) methods that increase the macroscopic efficiency of the flooding process and enhanced crude oil recovery. In this study, the effect of silica nanoparticles (NP-SiO2) in xanthan gum (XG) solutions was investigated through the analysis of efficiency in core flooding tests. First, the viscosity profiles of two polymer solutions, XG biopolymer and synthetic hydrolyzed polyacrylamide (HPAM) polymer, were characterized individually through rheological measurements, with and without salt (NaCl). Both polymer solutions were found suitable for oil recovery at limited temperatures and salinities. Then, nanofluids composed of XG and dispersed NP-SiO2 were studied through rheological tests. The addition of nanoparticles was shown to produce a slight effect on the viscosity of the fluids, which was more remarkable over time. Interfacial tension tests were measured in water-mineral oil systems, without finding an effect on the interfacial properties with the addition of polymer or nanoparticles in the aqueous phase. Finally, three core flooding experiments were conducted using sandstone core plugs and mineral oil. The polymers solutions (XG and HPAM) with 3% NaCl recovered 6.6% and 7.5% of the residual oil from the core, respectively. In contrast, the nanofluid formulation recovered about 13% of the residual oil, which was almost double that of the original XG solution. The nanofluid was therefore more effective at boosting oil recovery in the sandstone core.

Rheological Performance of High-Temperature-Resistant, Salt-Resistant Fracturing Fluid Gel Based on Organic-Zirconium-Crosslinked HPAM.

Development of low-cost, high-temperature-resistant and salt-resistant fracturing fluids is a hot and difficult issue in reservoir fluids modification. In this study, an organic zirconium crosslinker that was synthesized and crosslinked with partially hydrolyzed polyacrylamide (HPAM) was employed as a cost-effective polymer thickener to synthesize a high-temperature-resistant and salt-resistant fracturing fluid. The rheological properties of HPAM in tap water solutions and 2 × 104 mg/L salt solutions were analyzed. The results demonstrated that addition of salt reduced viscosity and viscoelasticity of HPAM solutions. Molecular dynamics (MD) simulation results indicated that, due to electrostatic interaction, the carboxylate ions of HPAM formed an ionic bridge with metal cations, curling the conformation, decreasing the radius of rotation and thus decreasing viscosity. However, optimizing fracturing fluids formulation can mitigate the detrimental effects of salt on HPAM. The rheological characteristics of the HPAM fracturing fluid crosslinking process were analyzed and a crosslinking rheological kinetic equation was established under small-amplitude oscillatory shear (SAOS) test. The results of a large-amplitude oscillation shear (LAOS) test indicate that the heating effect on crosslinking is stronger than the shear effect on crosslinking. High-temperature-resistant and shear-resistant experiments demonstrated good performance of fracturing fluids of tap water and salt solution at 200 °C and 180 °C.

Effect of partially hydrolyzed polyacrylamide (HPAM) on the bacterial communities of wetland rhizosphere soils and their efficiency in HPAM and alkane degradation.

The effect of partially hydrolyzed polyacrylamide (HPAM) on structure and function of rhizosphere soil bacterial communities in constructed wetlands has been largely underinvestigated. In this study, we compare the effect of 250, 500, and 1000 mg/L of HPAM on bacterial community composition of Phragmites australis associated rhizosphere soils in an experimental wetland using MiSeq amplicon sequencing. Rhizosphere soils from the HPAM-free and the 500-mg/L-exposed treatments were used for laboratory experiments to further investigate the effect of HPAM on the soil's degradation and respiration activities. Soils treated with HPAM showed differences in bacterial communities with the dominance of Proteobacteria and the enrichment of potential hydrocarbon and HPAM-degrading bacteria. CO2 generation was higher in the HPAM-free soils than in the HPAM pre-exposed soil, with a noticeable increase in both soils when oil was added. The addition of HPAM at different concentrations had a more pronounced effect on CO2 evolution in the HPAM-pre-exposed soil. Soils were able to degrade between 37 ± 18.0 and 66 ± 6.7% of C10 to C30 alkanes after 28 days, except in the case of HPAM-pre-exposed soil treated with 500 mg/L where degradation reached 92 ± 4.3%. Both soils reduced HPAM concentration by 60 ± 15% of the initial amount in the 500 mg/L treatment, but by only ≤ 21 ± 7% in the 250-mg/L and 1000-mg/L treatments. In conclusion, the rhizosphere soils demonstrated the ability to adapt and retain their ability to degrade hydrocarbon in the presence of HPAM.

Preparation of Preformed Submicron Crosslinked Polymer Coils for Conformance Control in Low-Permeability Reservoirs.

With the increasing development of low-permeability reservoirs, the significance of conformance control treatment has risen considerably. To address the conflict between injectability and plugging performance, as well as to enhance the deep migration capacity of conformance control agents, preformed submicron crosslinked polymer coils (SCPCs) have been manufactured using aqueous solution dispersion polymerization. Fourier transform infrared and scanning electron microscopy were employed to examine the chemical structure and micromorphology, while particle size distribution, zeta potential, rheological, and filtration properties were analyzed. The effectiveness of conformance control was confirmed through the parallel core displacement. The effective particle size of SCPCs was at a submicron level (500~800 nm). SCPCs exhibit a transitional threshold concentration between gel and sol states (0.25 wt%~0.5 wt%). SCPCs can efficiently block the 1.2 µm microporous filter membrane. The filtration time is up to 67.8 min. SCPCs can improve the water absorption rate of lower permeability cores from 21.21% to 57.89% with a permeability difference of 5. Therefore, SCPCs have good injectability, plugging performance, and deep migration capacity and can be used for conformance control in low-permeability reservoirs.

A Systematic Investigation of Polymer Influence on Core Scale Wettability Aided by Positron Emission Tomography Imaging.

Polymers have been used as viscosifying agents in enhanced oil recovery applications for decades, but their influence on rock surface wettability is rarely discussed relative to its importance: wettability largely controls fluid flow in porous media and changes in wettability may significantly influence subsequent system performance. This paper presents a two-part systematic investigation of wettability alteration during polymer injection into oil-wet limestone. The first part of the paper determines wettability and wetting stability on the core scale. The well-established Amott-Harvey method is used, and five full cycles performed with repeated spontaneous imbibition and forced displacements. Wettability alterations are measured in a polymer/oil system, to determine polymer influence on wettability, and evaluated towards simpler brine/oil and glycerol/oil systems, to determine reproducibility and uncertainty related to the method and fluid/rock system. Polymer injection into oil-wet limestone core plugs is shown to repeatedly and reproducibly reverse the core wettability towards water-wet. Wettability changed both quicker and towards stronger water-wet conditions with polymer solution as the aqueous phase compared to brine and glycerol. The second part of the paper attempts to explain the observed behavior; by utilizing in situ imaging by Positron Emission Tomography, an emerging imaging technology within the geosciences. High resolution imaging provides insight into fluid flow dynamics during water and polymer injections, identifying uneven displacement fronts and significant polymer adsorption.

Comparative Study of Oil Recovery Using Amphoteric Terpolymer and Hydrolyzed Polyacrylamide.

This paper presents the viscosifying and oil recovery efficiencies of a novel high-molecular-weight ternary polyampholyte (TPA), composed of 80 mol.% acrylamide (AAm) (a nonionic monomer), 10 mol.% 2-acrylamido-2-methyl-1-propanesulfonic acid sodium salt (AMPS) (an anionic monomer), and 10 mol.% (3-acrylamidopropyl) trimethylammonium chloride (APTAC) (a cationic monomer), in various high-salinity brines as compared to the efficiency of hydrolyzed poly(acrylamide) (HPAM), which is the most commonly used polymer in oil production. The results show that, in a range of salinity from 200 to 300 g∙L-1, the viscosity of the TPA solution is rather high and relatively stable, whereas that of HPAM severely decreases. The ability of TPA to increase its viscosity in extremely high salinity brines is explained by the antipolyelectrolyte effect, resulting in the unfolding of macromolecular chains of charge-balanced polyampholytes at a quasi-neutral state, which occurs due to the screening of the electrostatic attraction between oppositely charged moieties. The novelty of this research is that, in high-salinity reservoirs, the amphoteric terpolymer Aam-AMPS-APTAC may surpass HPAM in oil displacement capability.

New Insights and Experimental Investigation of High-Temperature Gel Reinforced by Nano-SiO2.

The properties of a reinforced gel with partially hydrolyzed polyacrylamide (HPAM) as the main agent, water-soluble phenolic resin (WSPR) as the crosslinker, and nano-SiO2 as the stabilizer were evaluated in terms of gelation time, gel strength and thermal stability under the conditions of 110 °C and 12.124 g/L salinity in water. The results showed that the gelation time of the gel with high strength was adjustable from 3 to 23 h, remaining stable for more than 180 days under stratigraphic conditions, although with a certain degree of early dehydration in the gel. Cryo-scanning electron microscopy (cryo-SEM) and dynamic light scattering (DLS) analysis revealed that nano-SiO2 improves the dispersion of the polymer in water, resulting in a more homogeneous structure of the formed gel and thus improving the strength of the gels. In addition, rheological tests and cryo-SEM showed that the interaction between nano-SiO2 and the polymer could inhibit the degradation of polymer to a certain extent and improve the thermal stability of the gel. However, the oxidative degradation of the gel is still the main cause of early dehydration of water-soluble phenolic resin gel, and the addition of a small amount of hydroquinone to the gelants can significantly improve the antioxidative degradation properties of phenolic resin gel.

Biodegradation of anionic polyacrylamide by manganese peroxidase: docking, virtual mutation based on affinity, QM/MM calculation and molecular dynamics simulation.

Manganese peroxidase (Mn P) is capable of effectively degrading anionic polyacrylamide (HPAM). However, the interaction of Mn P with HPAM at molecular level is lacking until now. Here, the HPAM model compounds, HPAM-2, HPAM-3, HPAM-4, and HPAM-5, were selected to reveal their binding mechanisms with Mn P. The results showed that the most suitable substrate for Mn P was HPAM-5, and the main reason for MnP-HPAM-5 with maximal affinity was strong hydrogen bond. LYS96 was the important key residue in all complexes, and the number of key residue was largest in MnP-HPAM-5. The optimal THR27ILE mutant may enhance the affinity of Mn P to HPAM-4. The stability of Mn P binding to HPAM-4 was the optimal. These results were helpful in designing highly efficient Mn P against HPAM to protect the ecological environment.

Syneresis Behavior of Polymer Gels Aged in Different Brines from Gelants.

Gel syneresis is a common problem in gel treatment for oil recovery applications. In this study, a stable gel was prepared in a soft brine by using a water-soluble phenolic resin as a crosslinker, nanoparticles as a stabilizer, and partially hydrolyzed polyacrylamide (HPAM) or copolymers with different contents of 2-acrylamido-2-methylpropane sulfonic acid (AMPS) groups as polymers. The syneresis behavior of the gels formed in a soft brine was evaluated upon aging in hard brines. The results show that when the salinity of the hard brine is lower than 30,000 mg/L, the gel expands, and its strength decreases; when the salinity of the hard brine is higher than 50,000 mg/L, the gel exhibits syneresis, and its strength increases. The effects of various influencing factors on the gel syneresis behavior were also evaluated. It was found that optimizing the polymer structure and adding nanoparticles can effectively overcome gel syneresis and enhance gel stability. Based on the research described in this paper, some proposals for designing salt-resistant polymer gels are presented.

Optimization of physico-chemical and membrane filtration processes to remove high molecular weight polymers from produced water in enhanced oil recovery operations.

Polymer flooding is an enhanced oil recovery technique to extract the large portion of leftover subsurface oil following conventional extraction methods. In the flooding process, a long-chain polymer, such as partially hydrolyzed polyacrylamide (HPAM), is added to the displacing fluid to increase the mobility and extraction of the oil phase. Nevertheless, the challenge of managing produced water from polymer flooding operations is high because residual HPAM results in significantly high viscosity and organic content in the stream. Commonly used methods for produced water treatment, such as gravity settling and flotation, cannot be applied to obtain a purified stream efficiently, while innovative techniques are not yet feasible in practical operations. In this work, a simple method of polymer precipitation prompted by divalent ions is evaluated, optimized, and compared to membrane ultrafiltration. The physico-chemical properties of the HPAM are investigated and polymer precipitation tests are conducted by varying the main operational parameters, including pH, salinity, temperature, calcium and/or magnesium concentration, and polymer concentration. Response surface developed by central composite design method is used to optimize the process and identify the correct dosage of divalent cations coagulants and pH, the two main factors promoting HPAM separation. The removal of HPAM is well-described and maximized (>85%) by the model, which is also validated on three synthetic samples representing real wastewaters from polymer flooding applications. Optimized ultrafiltration, using ceramic membranes with surface pore size of 15 kDa, also shows the ability to remove HPAM effectively from water, but the precipitation method seems to be more versatile and easier to apply. The two processes, precipitation and ultrafiltration, may potentially be used in sequence as they complement each other in several ways.

Impacts of partially hydrolyzed polyacrylamide (HPAM) on microbial mats from a constructed wetland treating oilfield produced water.

Constructed wetlands have been successfully used in the treatment of produced water brought to the surface in large quantities during oil extraction activities. However, with the increasing use of partially hydrolyzed polyacrylamide (HPAM) in enhancing oil recovery, the impacts of HPAM on the biological processes of wetlands is still unknown. Microbial mats in wetlands play a key role in hydrocarbon degradation. Here, we compared the bacterial communities of four wetland microbial mats after flooding with different concentrations of HPAM. Two mats (i.e. the HPAM-free and the 500 ppm HPAM pre-exposed mats) were selected to further investigate the effect of HPAM on respiration and biodegradation activities. The field mats exhibited clear differences in their bacterial community structure, where Cyanobacteria and Alphaproteobacteria became dominant in the presence of HPAM. In the laboratory experiments, the generated CO2 by the HPAM-free and the 500 ppm HPAM pre-exposed mats did not vary significantly when HPAM was added, although CO2 values were slightly higher in the presence of oil. Both mats were still able to degrade between 15 ± 14.4 to 50 ± 13.0% of C10 to C30 alkanes in 28 days, and this degradation was not affected by HPAM addition. The HPAM concentration decreased by 22-34% of the initial amount after 28 days of incubation in the HPAM-free mat, versus only 7-18.4% decrease in the 500 ppm HPAM pre-exposed mat. We conclude that the wetland microbial mats seem to have become well adapted to HPAM and could maintain their respiration and hydrocarbon degradation activities.

Polymer-assisted modification of metal-organic framework MIL-96 (Al): influence of HPAM concentration on particle size, crystal morphology and removal of harmful environmental pollutant PFOA.

A new synthesis method was developed to prepare an aluminum-based metal organic framework (MIL-96) with a larger particle size and different crystal habits. A low cost and water-soluble polymer, hydrolyzed polyacrylamide (HPAM), was added in varying quantities into the synthesis reaction to achieve >200% particle size enlargement with controlled crystal morphology. The modified adsorbent, MIL-96-RHPAM2, was systematically characterized by SEM, XRD, FTIR, BET and TGA-MS. Using activated carbon (AC) as a reference adsorbent, the effectiveness of MIL-96-RHPAM2 for perfluorooctanoic acid (PFOA) removal from water was examined. The study confirms stable morphology of hydrated MIL-96-RHPAM2 particles as well as a superior PFOA adsorption capacity (340 mg/g) despite its lower surface area, relative to standard MIL-96. MIL-96-RHPAM2 suffers from slow adsorption kinetics as the modification significantly blocks pore access. The strong adsorption of PFOA by MIL-96-RHPAM2 was associated with the formation of electrostatic bonds between the anionic carboxylate of PFOA and the amine functionality present in the HPAM backbone. Thus, the strongly held PFOA molecules in the pores of MIL-96-RHPAM2 were not easily desorbed even after eluted with a high ionic strength solvent (500 mM NaCl). Nevertheless, this simple HPAM addition strategy can still chart promising pathways to impart judicious control over adsorbent particle size and crystal shapes while the introduction of amine functionality onto the surface chemistry is simultaneously useful for enhanced PFOA removal from contaminated aqueous systems.

Comparative Study of Green and Synthetic Polymers for Enhanced Oil Recovery.

Several publications by authors in the field of petrochemical engineering have examined the use of chemically enhanced oil recovery (CEOR) technology, with a specific interest in polymer flooding. Most observations thus far in this field have been based on the application of certain chemicals and/or physical properties within this technique regarding the production of 50-60% trapped (residual) oil in a reservoir. However, there is limited information within the literature about the combined effects of this process on whole properties (physical and chemical). Accordingly, in this work, we present a clear distinction between the use of xanthan gum (XG) and hydrolyzed polyacrylamide (HPAM) as a polymer flood, serving as a background for future studies. XG and HPAM have been chosen for this study because of their wide acceptance in relation to EOR processes. To this degree, the combined effect of a polymer's rheological properties, retention, inaccessible pore volume (PV), permeability reduction, polymer mobility, the effects of salinity and temperature, and costs are all investigated in this study. Further, the generic screening and design criteria for a polymer flood with emphasis on XG and HPAM are explained. Finally, a comparative study on the conditions for laboratory (experimental), pilot-scale, and field-scale application is presented.

Characterization of a New Positive Allosteric Modulator of AMPA Receptors - PAM-43: Specific Binding of the Ligand and its Ability to Potentiate AMPAR Currents.

BACKGROUND: Currently, the most dynamic areas in the glutamate receptor system neurobiology are the identification and development of positive allosteric modulators (PAMs) of glutamate ionotropic receptors. PAM-based drugs are of great interest as promising candidates for the treatment of neurological diseases, such as epilepsy, Alzheimer's disease, schizophrenia, etc. Understanding the molecular mechanisms underlying the biological action of natural and synthetic PAMs is a key point for modifying the original chemical compounds as well as for new drug design. OBJECTIVE: We are trying to elaborate a system of molecular functional screening of ionotropic glutamate receptor probable PAMs. METHODS: The system will be based on the radioligand - receptor method of analysis and will allow rapid quantification of new AMPAR probable PAMs molecular activity. We plan to use a tritiumlabeled analogue of recently elaborated ionotropic GluR probable PAM ([3H]PAM-43) as the main radioligand. RESULTS: Here, we characterized the specific binding of the ligand and its ability to potentiate ionotropic GluR currents. The existence of at least two different sites of [3H]PAM-43 specific binding has been shown. One of the above sites is glutamate-dependent and is characterized by higher affinity. "Patchclamp" technique showed the ability of PAM-43 to potentiate ionotropic GluR currents in rat cerebellar Purkinje neurons in a concentration-dependent manner. CONCLUSION: The possibility of using PAM-43 as a model compound to study different allosteric effects of potential regulatory drugs (AMPAR allosteric regulators) was shown. [3H]PAM-43 based screening system will allow rapid selection of new AMPAR probable PAM structures and quantification of their molecular activity.

Synergetic activation of persulfate by heat and Fe(II)-complexes for hydrolyzed polyacrylamide degradation at high pH condition: Kinetics, mechanism, and application potential for filter cake removal during cementing in CO2 storage wells.

The long-term integrity of the interface between cement and formation rock in CO2-capture and storage wells is crucial to avoid leakage of CO2 in/along wells. However, the interface can be easily damaged by the filter cake, which is a compressed composite of bentonite, polymers such as hydrolyzed polyacrylamide (HPAM), and barite, on the wellbore rock. Therefore, removing the filter cake during the cementing process by degrading HPAM in an efficient way is essential. In this study, chelated-Fe2+ activated potassium persulfate (KPS) was used for HPAM degradation and filter-cake removal. Ethylenediaminetetraacetic acid disodium salt dihydrate (EDTA-2Na) and diethylenetriaminepentaacetic acid (DTPA) were adopted to control the precipitation of Fe2+/Fe3+. A mixture of 0.4 mM Fe2+, 0.8 mM DTPA, and 4 mM KPS at a pH of 10.0 at 70 °C reduced the molecular weight of HPAM significantly from 3.0 × 106 to (3.6-10) × 104 Da. Electron paramagnetic resonance (EPR) analysis suggested that HO was the dominant radical and that SO4- and O2- were responsible for the degradation. The reactions conformed to continuous distribution kinetics with an activation energy of 38.36 kJ mol-1. A possible degradation pathway was proposed based on analyses via infrared spectroscopy (IR) and time-of-flight liquid chromatography-mass spectrometry (TOF-LC/MS). >90 wt% of the filter cake was removed by the system. The results suggest that the proposed DTPA-Fe2+ activated KPS system exhibits promising potential for in situ degradation of high molecular weight HPAM and for the removal of filter cake in downhole wells.

A review of polymer nanohybrids for oil recovery.

As oil fields go into their final stage of production, new technologies are necessary to sustain production and increase the recovery of the hydrocarbon. Chemical injection is an enhanced recovery technique, which focuses on increasing the effectiveness of waterfloods. However, the use of chemical flooding has been hampered by its relatively high cost and the adsorption of the injected chemicals onto the reservoir rocks. In recent years, nanofluids have been launched as an overall less expensive and more efficient alternative to other chemical agents. Nanoparticle inclusion is also proposed to mitigate polymer flooding performance limitations under harsh reservoir conditions. This review presents a comprehensive discussion of the most recent developments of polymer nanohybrids for oil recovery. First, the preparation methods of polymer nanohybrids are summarized and explained. Then, an explanation of the different mechanisms leading to improved oil recovery are highlighted. Finally, the current challenges and opportunities for future development and application of polymer nanohybrids for chemical flooding are identified.

Experimental and mechanism study: Partially hydrolyzed polyacrylamide gel degradation and deplugging via ultrasonic waves and chemical agents.

Partially hydrolyzed Polyacrylamide (PHPAM) crosslinked by Cr+3 is frequently applied to plug thief zone for the better water management in matured oil reservoir. However, PHPAM gel may certainly cause inevitable formation damage nearby the wellbore. Although various kinds of chemical agents, such as hydrogen peroxide (H2O2), sodium hypochlorite (NaOCl), and chlorine dioxide (ClO2) were employed to mitigate the nearby wellbore damage. But, huge financial investment, poor degelation efficiency, environmentally insecure, corrosion problem, and long time span requirement persuade researchers to look for other effective technique. In this connection, ultrasonic waves is characterized by reliable, environment friendly, and cost effective technology. Current work involves comparative study of PHPAM gel degradation by the individual means of chemical agent and ultrasonic waves. Subsequently, the best-performed ultrasonic parameters and well-performed chemical agent were used independently and then simultaneously to deplug (PHPAM gel) the core sample. Results showed that 20 KHz frequency (1000 W) effectively reduced gel viscosity from original (2495 mPa.s) to 1.37 mPa.s after 10 min irradiation. This degradation is attributed to cavitation, heat energy, and hydroxyl radical (HO∙). However, after 2 min further exposure, the viscosity grew back to 3.29 mPa.s (18 KHz), 1.42 mPa.s (20 KHz), and 3.74 mPa.s (25 KHz). This adverse behavior is owing to hydroxyl radical (HO∙) annihilation. In chemical treatment, H2O2 among other chemicals efficiently degelled the PHPAM gel's original viscosity to 2.64 mPa.s after 24 h reaction. Similarly, NaOCl and ClO2 brought down original viscosity to 6.5 mPa.s and 159 mPa.s respectively. SEM of the samples before and after treatment was performed for the better understanding of PHPAM gel morphology. Considering dynamic experiment, maximum 23.5% and 19.80% damaged permeability recovery (30 × 10-3 µm2 gas permeability) were obtained by applying ultrasonic waves (20 KHz, 1000 W, and 100 min irradiation) and chemical agent (H2O2) respectively. Permeability recovery was further increased to 40.90% by the simultaneous application of ultrasonic waves and chemical agent.