Copolymerization Of Acrylamide Research Articles

Synthesis of bi-functional amphiphilic acrylamide copolymers based on polymerizable spans for prospective EOR

Abstract Three polymerizable spans based on sorbitan monoesters were synthesized and copolymerized with the acrylamide at different ratios to prepare nine amphiphilic copolymers via the inverse emulsion copolymerization technique. The FTIR, 1H-NMR, and viscosity average molecular weight ways characterized the synthesized monomers and copolymers. The general designation for the copolymers is PSnSs. Surface active and thickening properties for the aqueous solutions of the prepared copolymers were investigated. The influence of salts' concentration and temperature variation on the apparent viscosity and surface/interfacial activity was studied for the selected copolymers, and their emulsification ability was also examined. The results showed that the attached polymerizable spans enhanced the properties and capabilities of the acrylamide copolymers. This enhancement increased with increasing the attached monomers' ratio and lipophilic chain length. The copolymer PS60S-3 displayed the best values and capabilities with values at 0.2 wt% in distilled water for the γ ST, γ IFT, and η app equal 42.25 mN.m−1, 13.3 mN.m−1, and 495.76 mPa.s, respectively. It has the potential to be used as a bi-functional flooding agent.

Synthesis of novel composite hydrogel based on carboxymethyl cellulose/acrylamide/β-cyclodextrin for drug delivery.

Polysaccharide-based hydrogels have attracted significant attention in fields such as drug delivery, tissue engineering, and wound healing, primarily due to their excellent water-retention capacity, biocompatibility, and biodegradability. This study reports the preparation of a hydrogel through the copolymerization of acrylamide (AM) and carboxymethyl cellulose (CMC) using a simple free-radical polymerization method. β-cyclodextrin (β-CD), capable of encapsulating hydrophobic drugs, was chemically modified with double bonds (Ac-β-CD) and incorporated as a pendant unit in the polymerization reaction, forming a ternary copolymer hydrogel with CMC, AM, and Ac-β-CD. Ibuprofen, a model hydrophobic drug, was incorporated with Ac-β-CD through high-pressure steam sterilization and was successfully loaded into the hydrogel. The hydrogel exhibited excellent water absorption and biocompatibility. Cytotoxicity and in vivo studies confirmed its non-toxic profile. The porous hydrogel achieved an encapsulation efficiency of 97.83 % for drug-loading by autoclaving. The hydrogel showed a cumulative release rate of 87.3 % over 12 h under simulated physiological pH (pH 7.4). The CMC/AM/Ac-β-CD hydrogel system developed here thus demonstrates potential as a carrier for hydrophobic drugs.

Wood adhesive based on polyvinyl alcohol stabilized polyvinyl acetate, vinyl neodecanoate, vinyl trimethoxy silane, and N-methylol acrylamide copolymer emulsion: synthesis and characterization

To improve a polyvinyl acetate (PVAc) emulsion-based glue’s water resistance, this study aims to offer it a controlled ability for cross-linking. Emulsion polymerization was used to synthesize PVAc-vinyl neodecanoate-vinyl trimethoxy silane-n-methyl acrylamide poly (VAc-VeoVa10-VTMO-NMA) copolymers with polyvinyl alcohol (PVA) stabilization. Using Fourier transform infrared spectroscopy and differential scanning calorimetry (DSC), the copolymerization and glass transition temperatures (Tg) of film were analyzed. To assess the effectiveness of the cross-linked emulsions-based adhesive, the tensile shear strength of wood joints under dry and wet conditions was measured in compliance with the EN 204 and EN 205 standards. The experimental results showed that the copolymer-based poly (VAc-VeoVa10-VTMO-NMA) adhesive significantly increased Tg and film hardness when compared to poly (VAc-VeoVa10-VTMO). Tensile shear strength increased by ∼9% in a dry environment after 24 h of bonding (per EN 204) and by ∼18% in a wet environment with poly (VAc-VeoVa10-VTMO-NMA) adhesive, in comparison to a poly (VAc-VeoVa10-VTMO) adhesive. A contact angle test confirmed that cross-linked poly (VAc-VeoVa10-VTMO-NMA) copolymer adhesives performed somewhat better in wet and heat-resistant conditions than cross-linked poly (VAc-VeoVa10-VTMO) copolymer adhesives. The method proposed provides an easy-to-use route to emulsions with enhanced water resistance and bonding strength by including NMA as a reactive co-monomer.

High-Strength, Self-Healing Copolymers of Acrylamide and Acrylic Acid with Co(II), Ni(II), and Cu(II) Complexes of 4'-Phenyl-2,2':6',2″-terpyridine: Preparation, Structure, Properties, and Autonomous and pH-Triggered Healing.

The utilization of self-healing polymers is a promising way of solving problems associated with the wear and tear of polymer products, such as those caused by mechanical stress or environmental factors. In this study, a series of novel self-healing, high-strength copolymers of acrylamide, acrylic acid, and novel acrylic complexes of 4'-phenyl-2,2':6',2″-terpyridine [Co(II), Ni(II), and Cu(II)] was prepared. A systematic study of the composition and properties of the obtained polymers was carried out using a variety of physicochemical techniques (elemental analysis, gel permeation chromatography (GPC), attenuated total reflectance Fourier transform infrared spectroscopy (ATR/FT-IR), ultraviolet-visible spectroscopy (UV-vis), small-angle X-ray scattering (SAXS), wide-angle X-ray scattering (WAXS), differential scanning calorimetry (DSC), thermogravimetric analysis (TGA), dynamic mechanical analysis (DMA), confocal laser scanning microscopy (CLSM), and tensile testing). All metallopolymer samples exhibit autonomous intrinsic healing along with maintaining high tensile strength values (for some samples, the initial tensile strength exceeded 100 MPa). The best values of healing efficiency are possessed by metallopolymers with a nickel complex (up to 83%), which is most likely due to the highest lability of the metal-heteroatom coordination bonds. The example of this system shows the ability to re-heal with negligible deterioration of the mechanical properties. The possibility of tuning the mechanical properties of self-healing films through the use of different metal ions has been demonstrated.

Effects of hydrodynamic shear during formation of paper sheets with the addition of nanofibrillated cellulose, cationic starch, and cationic retention aid

Laboratory tests were conducted to evaluate effects of hydrodynamic shear levels on papermaking process variables and paper handsheet properties. The furnish was from 100% recycled copy paper, to which was added nanofibrillated cellulose (NFC) at the 5% level following its optional pretreatment with cationic starch. A cationic copolymer of acrylamide (cPAM) was used as the retention aid. Different levels of hydrodynamic shear were applied both after mixing the NFC with the cationic starch (pre-shearing) or after all the furnish components had been combined (final shearing). The presence or absence of pre-shearing was found to have little effect on the measured outcomes. By contrast, increasing final shear hurt filler retention and made the resulting paper more uniform. However, the final shear level did not have a significant effect on the tensile strength of the resulting handsheets. Medium-charge density cationic starch, used in pretreating the NFC, consistently gave greater strength in comparison to a high-charge cationic starch. The significance of these findings is that though the relatively high hydrodynamic shear levels associated with modern paper machines can have some beneficial effects, they do not necessarily overcome all challenges associated with wet-end addition of nanocellulose in combination with other additives.

Synthesis of grafted copolymers of cod collagen and acrylamides in the presence of alkylborane – p-quinone system

The graft polymerization of acrylamide and N-isopropylacrylamide onto collagen in the presence of triethylborohexamethylenediamine complex and a number of p-quinones, including benzoquinone, naphthoquinone, 2,5-di-tretbutyl-p-benzoquinone, and duroquinone, was studied. In all cases, p-quinones act as polymerization retarders, reducing monomer conversion. An exception is the graft polymerization of acrylamide onto collagen in the presence of benzoquinone, which acts as a polymerization inhibitor. The proportion of the synthetic fragment in the obtained copolymers is determined by the structure of the monomer and p-quinone. The molecular weight distribution curves contain modes related to unreacted collagen, which differ significantly from those of the initial collagen in terms of intensity. This is related to the formation of a grafted copolymer of cross-linked structure, which cannot be analyzed by gel permeation chromatography. The degradation of copolymers under the action of enzymes was controlled by gel permeation chromatography. Enzymatic hydrolysis of copolymers proceeds slower than that of collagen, which confirms the formation of a copolymer. Following three hours after the onset of hydrolysis, the molecular weight distribution curves contain low-molecular weight modes of collagen and low-intensity modes related to polyacrylamide. The morphology of copolymers differs from that of collagen and polyacrylamides. Cytotoxicity evaluation of copolymers is an important research stage, determining their prospects as the basis of materials for regenerative medicine. An analysis of extracts obtained from the copolymers using culture medium by MTT assay showed a high rank of their toxicity, which can be reduced by dilution of collagen and N-isopropylacrylamide copolymer extracts with aqueous solutions. For the copolymers of collagen and acrylamide, the toxicity is maintained due to the high toxicity of the monomer. Their toxicity can be reduced by extraction of unreacted acrylamide with chloroform.

Insight into the corrosion inhibition performance of dimethyldiallylammonium chloride acrylamide copolymer for mild steel in acidic solution

Dimethyldiallylammonium chloride acrylamide (DADMAC-AAM) copolymer was firstly applied as a novel corrosion inhibitor for carbon steel in acidic solution. Electrochemical, theoretical and computational methods were performed to illustrate the corrosion inhibition mechanism of DADMAC-AAM. Results of electrochemical tests indicated that DADMAC-AAM effectively slowed down corrosion rate of mild steel in HCl solution as a mixed-type corrosion inhibitor. Its corrosion inhibition efficiency increased with dosage, and the maximum value reached about 92.44 % with adding 100 mg/L. In-situ scanning vibration electrode technique illustrated that the corrosion inhibition performance of DADMAC-AAM increased with immersion time. Metal surface was covered with a dense hydrophobic film due to the physical-chemical adsorption of DADMAC-AAM molecules, and the adsorption behavior obeyed to the Langmuir adsorption isothermal model. Theoretical calculations were carried out to explain the corrosion inhibition mechanism, and the increase of active energy indicated that the strong inhibitive action of DADMAC-AAM molecule could be due to the increase of activation energy barrier of corrosion reaction. Results obtained from computational simulations proved that DMDMAC-AAM molecules adsorbed on metal surface through interactions between N or O and Fe atoms. This adsorption film could retard the invasion of corrosive species, thus protecting metal from corrosion.

Fabrication of Flexible Wearable Mechanosensors Utilizing Piezoelectric Hydrogels Mechanically Enhanced by Dipole-Dipole Interactions.

Conductive hydrogels have been increasingly employed to construct wearable mechanosensors due to their excellent mechanical flexibility close to that of soft tissues. In this work, piezoelectric hydrogels are prepared through free radical copolymerization of acrylamide (AM) and acrylonitrile (AN) and further utilized in assembling flexible wearable mechanosensors. Introduction of the polyacrylonitrile (PAN) component in the copolymers endows the hydrogels with excellent piezoelectric properties. Meanwhile, significant enhancement of mechanical properties has been accessed by forming dipole-dipole interactions, which results in a tensile strength of 0.51 MPa. Flexible wearable mechanosensors are fabricated by utilizing piezoelectric hydrogels as key signal converting materials. Self-powered piezoelectric pressure sensors are assembled with a sensitivity (S) of 0.2 V kPa-1. Additionally, resistive strain sensors (gauge factor (GF): 0.84, strain range: 0-250%) and capacitive pressure sensors (S: 0.23 kPa-1, pressure range: 0-8 kPa) are fabricated by utilizing such hydrogels. These flexible wearable mechanosensors can monitor diverse body movements such as joint bending, walking, running, and stair climbing. This work is anticipated to offer promising soft materials for efficient mechanical-to-electrical signal conversion and provides new insights into the development of various wearable mechanosensors.

Preparation of sodium alginate grafted polyelectrolyte by adiabatic polymerization and study on its solution properties

In order to improve the salt resistance and shear resistance of partially hydrolyzed polyacrylamide-based oil displacement agents (they are all anionic polyelectrolytes), this paper proposes the preparation of branched low hydrophobic monomer content sodium alginate grafted hydrophobically modified partially hydrolyzed polyacrylamide P(AM-SA-MO8) using acrylamide (AM), sodium alginate (SA), and non-ionic hydrophobic monomer (MO8) as main raw materials through the method of adiabatic polymerization followed by hydrolysis. The polymerization conditions of P(AM-SA-MO8) were optimized, and the solution properties and oil displacement performance of P(AM-SA-MO8) and P(AM-MO8) (copolymer of AM and MO8) were compared. It was found that the viscosity, resistance to Ca2+/Mg2+, shear resistance, resistance factor (RF), residual resistance factor (RRF), and enhanced oil recovery performance of P(AM-SA-MO8) solution were better than those of P(AM-MO8). Especially in seawater, at 75 ℃, the viscosity of 1500 mg/L P(AM-SA-MO8) solution was 6.5 mpa.s, RF was 6.08, RRF was 2.28, and the enhanced oil recovery was 26.28 % with a injection rate of 4.9 ft/day.

Preparation and Performance Evaluation of a Supramolecular Polymer Gel-Based Temporary Plugging Agent for Heavy Oil Reservoir.

When encountering heavy oil reservoirs during drilling, due to the change in pressure difference inside the well, heavy oil will invade the drilling fluid, and drilling fluid will spill into the reservoir along the formation fractures, affecting the drilling process. A supramolecular polymer gel-based temporary plugging agent was prepared using acrylamide (AM), butyl acrylate (BA), and styrene (ST) as reacting monomers, N, N-methylenebisacrylamide (MBA) as a crosslinking agent, ammonium persulfate (APS) as an initiator, and poly(vinyl alcohol) (PVA) as a non-covalent component. A supermolecular polymer gel with a temperature tolerance of 120 °C and acid solubility of 90% was developed. The experimental results demonstrated that a mechanically robust, thermally stable supramolecular polymer gel was successfully synthesized through the copolymerization of AM, BA, and ST, as well as the in situ formation hydrogen bonding between poly (AM-co-BA-co-ST) and PVA, leading to a three-dimensional entangled structure. The gel-forming solution possessed excellent gelling performance even in the presence of a high content of salt and heavy oil, demonstrating superior resistance to salt and heavy oil under harsh reservoir conditions. High-temperature and high-pressure plugging displacement experiments proved that the supramolecular polymer gel exhibited high pressure-bearing capacity, and the blocking strength reached 5.96 MPa in a wedge-shaped fracture with a length of 30 cm. Furthermore, the dissolution rate of the supramolecular polymer gel was as high as 96.2% at 120 °C for 48 h under a 15% HCl solution condition.

Impact of hydrolysis on the quantification of sulfonated acrylamide copolymers by size exclusion chromatography with UV detection

AbstractSize exclusion chromatography with UV detection (SEC‐UV) is a precise method for quantifying polyacrylamides in water. However, its accuracy can be compromised in complex matrices due to chemical degradation of the polymer. This study focuses on the impact of hydrolysis on quantifying sulfonated polyacrylamide copolymers (PAM‐AMPS) via SEC‐UV, analyzing key influencing factors. Using controlled hydrolysis, hydrolyzed copolymer (HPAM‐AMPS) standards with varying hydrolysis degree (HD) (HD = 7%–33%) were prepared without significant changes in polymer chain size. SEC‐UV analysis revealed that quantification accuracy is highly dependent on hydrolysis extent. Errors are minimal for HD up to 10%, but significantly higher for HDs of 22%–33%. Furthermore, this effect is modulated by polymer concentration. Our findings indicate that there are two compensating factors for the decrease in molar absorptivity due to amide‐to‐carboxylate substitution: the sulfonate group acting as an additional chromophore, and a redshift in absorption spectra due to hydrogen bonding at higher concentrations. This interplay between HD and concentration in this type of sulfonated polyacrylamide can help reduce quantification errors in complex aqueous samples prone to chemical degradation, like those found in environmental and subsurface applications.

Performance analysis and degradation mechanism of acrylamide co-polymer as rheology and filtrate reducers in different salt aqueous-based drilling mud systems at high-temperature conditions

To maintain performance of an aqueous-based drilling muds (ABDMs), it was imperative to understand the decay mechanism of the incorporated synthetic polymers, when exposed to the elevated temperatures. The understanding of the decay mechanism could provide a polymer replenishment strategy for the fluid to retain a specific rheology and filtrate control performance. In this context, thermal-degradation of various acrylamide co-polymers was investigated in different monovalent brines. The acrylamide co-polymers were custom synthesized, and their molecular weight and % sulfonic substitution was verified using the capillary viscometer and nuclear magnetic resonance spectroscopy techniques respectively. The co-polymer thermal degradation mechanism (i.e., polymer hydrolysis) in various monovalent brines (KCl, NaCl and NaBr) was quantified by novel titration for temperature range {121 °C, 177 °C}. The degradation response of the co-polymers was then correlated with their rheology and HPHT (high-pressure-high-temperature) filtrate performance; for instance, the titration studies showed that co-polymer degradation was 12–15% and 44–47% after sixteen hours aging at 121 °C and 177 °C respectively; correspondingly the co-polymer performance in ABDM, exhibited HPHT filtrate of 12–18 mL and 38–40 mL at those respective temperatures after sixteen hours of aging. The quantified understanding of the co-polymer thermal degradation was used to device a new approach for co-polymer replenishment strategy; it was illustrated that a 7% replenishment of the co-polymer for every eight hours, at 121 °C, enabled sustained HPHT filtrate of 12–18 mL for the studied evaluation period of thirty-two hours. The replenishment approach presented in the study would provide a valuable tool for drilling automation to ensure sustained fluid performance.

Mechanically Robust and Electrically Conductive Hybrid Hydrogel Electrolyte Enabled by Simultaneous Dual In Situ Sol-Gel Technique and Free Radical Copolymerization.

Mechanically robust and ionically conductive hydrogels poly(acrylamide-co-2-acrylamido-2-methylpropanesulfonate-lithium)/TiO2/SiO2 (P(AM-co-AMPSLi)/TiO2/SiO2) with inorganic hybrid crosslinking are fabricated through dual in situ sol-gel reaction of vinyltriethoxysilane (VTES) and tetrabutyl titanate (TBOT), and in situ radical copolymerization of acrylamide (AM), 2-acrylamide-2-methylpropanesulfonate-lithium (AMPSLi), and vinyl-SiO2. Due to the introduction of the sulfonic acid groups and Li+ by the reaction of AMPS with Li2CO3, the conductivity of the ionic hydrogel can reach 0.19Sm-1. Vinyl-SiO2 and nano-TiO2 are used in this hybrid hydrogel as both multifunctional hybrid crosslinkers and fillers. The hybrid hydrogels demonstrate high tensile strength (0.11-0.33MPa) and elongation at break (98-1867%), ultrahigh compression strength (0.28-1.36MPa), certain fatigue resistance, self-healing, and self-adhesive properties, which are due to covalent bonds between TiO2 and SiO2, as well as P(AM-co-AMPSLi) chains and SiO2, and noncovalent bonds between TiO2 and P(AM-co-AMPSLi) chains, as well as the organic frameworks. Furthermore, the specific capacitance, energy density, and power density of the supercapacitors based on ionic hybrid hydrogel electrolytes are 2.88Fg-1, 0.09Whkg-1, and 3.07kWkg-1 at a current density of 0.05Ag-1, respectively. Consequently, the ionic hybrid hydrogels show great promise as flexible energy storage devices.

Self-Crosslinking AuNPs Composite Hydrogel Bolus for Radiophotothermal Therapy.

Radiophotothermal therapy is a promising treatment for superficial tumors. Traditional radiotherapy requires tissue boluses on the patient's skin to increase therapeutic effectiveness due to the dose-buildup effect of high-energy radiation. However, combining radiotherapy with photothermal therapy leads to uncertainties as the low-penetration near-infrared light dose is reduced after penetrating the bolus. To enhance precision and effectiveness, this study introduces a novel bolus made of AuNPs@poly(AM-THMA-DMAEMA) composite hydrogel. This hydrogel is prepared through a one-pot method involving the reduction of trihydrate chloroauric acid (HAuCl4·3H2O) and copolymerization of acrylamide (AM) and N-[Tris(hydroxymethyl)methyl]acrylamide (THMA) in a redox system with dimethylaminoethyl methacrylate (DMAEMA) and potassium persulfate (KPS). The gold nanoparticles (AuNPs) improve the mechanical strength (tensile strength of 320.84 kPa, elongation at break of 830%) and antibacterial properties (>99% against Staphylococcus aureus). The local surface plasmon resonance (LSPR) effect of AuNPs enables the hydrogel to absorb near-infrared light for precise monitoring of the infrared radiation dose. The hydrogel's biocompatibility is enhanced by the absence of additional crosslinking agents, and its excellent surface adhesion strength is due to numerous hydrogen bonds and electrostatic interactions. This study offers new possibilities for nanoparticle composite hydrogels as tissue boluses, achieving high precision and efficiency in radiophotothermal therapy.

Highly effective removal of basic fuchsin dye using carboxymethyl konjac glucomannan grafted acrylic acid-acrylamide/montmorillonite composite hydrogel

This study developed a nanocomposite hydrogel, CAM4-MMT, for efficiently removing basic fuchsin dye from water. The hydrogel was prepared by grafting a copolymer of acrylic acid (AA) and acrylamide (AM) onto carboxymethyl konjac glucomannan (CMKGM), and doped with montmorillonite (MMT), exhibited excellent thermal stability, a porous inner structure, large specific surface area (1.407 m2/g), and high swelling capacity (107.3 g/g). The hydrogel achieved a maximum adsorption capacity of 694.1 mg/g and a removal rate of 99.5 %. The Langmuir isotherm and pseudo-second-order kinetic model best described the adsorption process. Regeneration and reuse tests confirmed that the hydrogel has excellent recyclability. In conclusion, the CAM4-MMT composite hydrogel efficiently removed basic fuchsin from water solutions, offering a new scheme for eliminating basic fuchsin using natural polysaccharides with promising applications.

Amphiphilic acrylamide copolymers using polymerizable tweens for potential use in chemical-enhanced oil recovery

Amphiphilic acrylamide copolymers using polymerizable tweens for potential use in chemical-enhanced oil recovery

Highly adhesive hydrogel electrolytes driven by adenosine monophosphate and Fe3+ for high-voltage asymmetric flexible zinc-air batteries

Flexible zinc-air batteries (ZABs) are a promising power source for wearable electronics, owing to their high energy density and low cost. However, the limited operating voltage of about 1.4 V and the complex external packaging of conventional ZABs hinder their practical application. Herein, a hydrogel electrolyte (PAMA-ANa/Fe3+) is rapidly prepared for flexible ZABs using copolymers of acrylamide and acrylic acidic (PAMA), along with sodium adenosine-5′-monophosphate (AMPNa) and Fe3+. By leveraging the synergistic effects of exceptional mechanical properties, strong adhesion and the acidic-alkaline decoupling of the PAMA-ANa/Fe3+ hydrogel electrolyte, an asymmetric flexible ZAB (AF-ZAB) based on an acidic-alkaline double-layer PAMA-ANa/Fe3+ hydrogel electrolyte is assembled in a simple and rapid manner. This AF-ZAB achieves an excellent operating voltage of 2.15 V and a high power density of 75.86 mW cm−2. This study provides a new method and strategy for the development and assembly of novel high-voltage flexible quasi-solid-state batteries and other energy storage devices.

Experimental Study of the Swelling and Rheological Properties of a High-Strength Preformed Particle Gel Lost Circulation Material

Summary Preformed particulate gel (PPG) has emerged as a widely utilized lost circulation material in deep oil and gas drilling operations. The objective of our study was to devise a high-strength preformed particle gel (HSPPG) specifically designed to address drilling fluid loss in high-temperature fractured formations. To achieve this, a comprehensive set of laboratory experiments was conducted to assess the swelling and rheological properties of HSPPG under various conditions, and these investigations aimed to provide deeper insights into the pressure-bearing mechanism exhibited by HSPPG. The synthesis of HSPPG involved the copolymerization of acrylamide (AM) and N-hydroxymethacrylamide (NMA) molecular chains, catalyzed by organic peroxides, to form the primary network. Additionally, to enhance its temperature resistance, urea-formaldehyde (UF) resin, known for its superior thermal stability, was incorporated into the secondary network. This unique combination of primary and secondary networks imparted remarkable thermal endurance and structural stability to the resulting HSPPG. The swelling and rheological experiments revealed that HSPPG, with a particle size of 1000 µm, exhibited an equilibrium swelling rate (SR) value of 30.55 and a storage modulus (G’) of 1050 Pa at 120℃. These findings attested to its excellent temperature resistance and structural stability. Furthermore, when subjected to a sodium chloride solution at a temperature of 120℃ and a concentration of 25.0%, HSPPG achieved equilibrium swelling with an SR value of 24.93 and a G’ of approximately 7000 Pa. This significant increase in structural strength was attributed to charge shielding within the highly concentrated brine environment. In the plugging experiments, a wedge-shaped slit with an inlet of 3 mm and an outlet of 1 mm was successfully blocked using a concentration of 4% of HSPPG with a particle size of 1000 μm. The blocking strength achieved was 8.06 MPa. The results of these experiments, as well as the observed filling and plugging state of HSPPG in steel fractured cores, indicated that HSPPG possesses the properties of water absorption, swelling, and extrusion filling. These attributes facilitate the effective formation of a dense blocking layer within the fracture space, exhibiting excellent pressure-bearing capacity. In conclusion, the HSPPG developed in this study represents an advanced swellable granular plugging agent with excellent swelling capacity and structural strength at high temperatures. It offers an ideal solution to mitigate drilling fluid loss from fractured formations under high-temperature and high-salinity conditions.

Surface properties of systems based on amines and (co)polymers of acrylamide at the liquid–air interface

Surface properties of the systems based on amines and acrylamide (co)polymers have been studied depending on the molecular structure of the components in aqueous and saline (sodium chloride) solutions. For the systems of amines with an anionic acrylamide copolymer, a change in the shape of the surface tension isotherm was found. The tendency to change the surface properties is enhanced in systems with an anionic acrylamide copolymer, aliphatic amine and in the presence of a low molecular weight electrolyte.

An Innovative Approach for Tailoring Molecularly Imprinted Polymers for Biosensors-Application to Cancer Antigen 15-3.

This work presents a novel approach for tailoring molecularly imprinted polymers (MIPs) with a preliminary stage of atom transfer radical polymerization (ATRP), for a more precise definition of the imprinted cavity. A well-defined copolymer of acrylamide and N,N'-methylenebisacrylamide (PAAm-co-PMBAm) was synthesized by ATRP and applied to gold electrodes with the template, followed by a crosslinking reaction. The template was removed from the polymer matrix by enzymatic/chemical action. The surface modifications were monitored via electrochemical impedance spectroscopy (EIS), having the MIP polymer as a non-conducting film designed with affinity sites for CA15-3. The resulting biosensor exhibited a linear response to CA15-3 log concentrations from 0.001 to 100 U/mL in PBS or in diluted fetal bovine serum (1000×) in PBS. Compared to the polyacrylamide (PAAm) MIP from conventional free-radical polymerization, the ATRP-based MIP extended the biosensor's dynamic linear range 10-fold, improving low concentration detection, and enhanced the signal reproducibility across units. The biosensor demonstrated good sensitivity and selectivity. Overall, the work described confirmed that the process of radical polymerization to build an MIP material influences the detection capacity for the target substance and the reproducibility among different biosensor units. Extending this approach to other cancer biomarkers, the methodology presented could open doors to a new generation of MIP-based biosensors for point-of-care disease diagnosis.