Vinylpyrrolidone Research Articles

Gamma-ray shielding effectiveness, optical, mechanical, dielectric properties of nanofiller-reinforced PVA/PVP polymeric blend nanocomposites

The aqueous solution cast method was used to create the biodegradable polymer nanocomposite (PNC) films from a blend of poly (vinyl alcohol) PVA and poly (vinyl pyrrolidone) PVP (70/30 wt %) and Fe2O3 nanoparticles (NPs). These PNC films were characterized using X-ray diffraction, scanning electron microscopy SEM, Fourier transform infrared spectroscopy FTIR, and ultraviolet-visible spectroscopy. XRD and FTIR results indicate that Fe+ 3 NPs interact with the host polymer. Optical, electrical, mechanical, and radiation shielding measurements were performed on the PNC films. From the optical measurements, the indirect optical band gap drops from 4.86 eV for the pure blend to 4.26 eV at the greatest NPs concentration. Optical limiting characterization shows that the output power of He-Ne and solid-state green laser beams is reduced from 22.98 to 3.6 mW and 6.59 to 1.4 mW, respectively, when the Fe2O3 NPs content in the blend matrix is increased to 6 wt %. The NGCal software was utilized to calculate nuclear radiation shielding properties. The findings demonstrated that when the concentration of Fe2O3 rose, the PNC films half-value layer and mean free path decreased. Mechanical measurements demonstrate that increasing the Fe2O3 content significantly improves nanocomposite films’ yield and tensile strength. Tensile strength is measured at 27.03 MPa for the composite film containing 6 wt % Fe2O3, which is significantly higher than the 8.66 MPa of the pure (PVA-PVP) film. Compared to the other samples under examination, the 6 wt % Fe2O3 sample yielded the best results (based on the analyzed optical, electrical, mechanical, and radiation shielding properties).

Novel foam‐draining and anti‐polymerization integrated agent for gas well application

AbstractIn this article, surfactants such as cetyl trimethyl ammonium chloride (CTAC) and coconut oil amide propyl betaine (CAB) were compounded (TCJ) and used as a double function with foam drainage and hydrate anti‐polymerization. According to the result it was found that 0.05% of CTAC and 0.7% of CAB exhibited both excellent foam property and hydrate anti‐polymerization property. For further clarifying the stability characteristic of foam, the foam half‐life, drainage process, microcosmic liquid film structure, and stability mechanism were investigated in this article. The high initial foam volume of 415 mL with relatively long half‐life time of 5.5 min under high‐speed agitation at 50°C after 25 min indicated a good temperature resistance. The excellent foam properties still remained even amount of methanol and NaCl was added, which indicated its well stability and salt resistance. Furthermore, it was found that TCJ exhibited high liquid carrying rate of 62.5% at 65°C and good compatibility with poly vinyl pyrrolidone (PVP), which played great potential to the application in oil field. By the results of DSC curves, it can be found that the phase transformation point of hydrate decreases after addition of TCJ, which indicates the inhibition to the formation of hydrate as thermodynamic inhibitors.

Research and Application of Thermally Activated Gel for Control of Lost Circulations

Summary Thermally activated gel (TAG) for control of lost circulations was evaluated, which is based on acrylamide (AM) and N-vinylpyrrolidone (NVP) copolymers crosslinked by polyethyleneimine (PEI). Viscoelasticity, pumpable time, breakthrough pressures, thermal tolerance, and fluid compatibility were tested in this paper, and then field applications in Missan Oilfield, Iraq, were introduced. Laboratory results showed that the strain limit in the linear viscoelastic region was 169% and storage modulus was 870 Pa. Pumpable time of TAG varies with pH values, so pumpable time can be controlled above 60 minutes by adjusting pH values in the temperature ranges of 100°C to 140°C. Breakthrough pressures were tested in 5-mm (inner diameter) and 10-mm (inner diameter) simulating pipes.The breakthrough pressure gradients were 1.172 psi/cm and 1.200 psi/cm at 0.5 mL/min and 1.0 mL/min, respectively, for 10-mm simulating pipes, 1.872 psi/cm and 2.200 psi/cm for 5-mm simulating pipes. TAG maintained morphologies completely and dehydrated slightly after 30 days of aging at 140°C, transformed into a degraded and low-viscosity fluid after 45 days of aging. Tests proved that invasions of inorganic electrolytes, drilling fluid additives, and drilling fluids can lengthen the pumpable time of TAG, so flash settings due to invasions could not occur. Applications in Missan Oilfield verified the performances of TAG mentioned above.

Integrating an antimicrobial nanocomposite to bioactive electrospun fibers for improved wound dressing materials

This study investigates the fabrication and characterization of electrospun poly (ε-caprolactone)/poly (vinyl pyrrolidone) (PCL/PVP) fibers integrated with a nanocomposite of chitosan, silver nanocrystals, and graphene oxide (ChAgG), aimed at developing advanced wound dressing materials. The ChAgG nanocomposite, recognized for its antimicrobial and biocompatible properties, was incorporated into PCL/PVP fibers through electrospinning techniques. We assessed the resultant fibers’ morphological, physicochemical, and mechanical properties, which exhibited significant enhancements in mechanical strength and demonstrated effective antimicrobial activity against common bacterial pathogens. The findings suggest that the PCL/PVP-ChAgG fibers maintain biocompatibility and facilitate controlled therapeutic delivery, positioning them as a promising solution for managing chronic and burn-related wounds. This study underscores the potential of these advanced materials to improve healing outcomes cost-effectively, particularly in settings plagued by high incidences of burn injuries. Further clinical investigations are recommended to explore these innovative fibers’ full potential and real-world applicability.

Exploring the Role of Poly (N-vinyl pyrrolidone) in Drug Delivery

Exploring the Role of Poly (N-vinyl pyrrolidone) in Drug Delivery

PTFE-based antistatic coatings by incorporating modified carbon black

A kind of antistatic coatings which were applied to nonconductive surfaces were prepared with Polytetrafluoroethylene (PTFE) as matrix, modified carbon black (CB) as conductive filler. Compared to sodium dodecyl sulfate, poly(vinyl pyrrolidone), the TMN-10 modified CB has better wettability, dispersion, stability and re-disperse. When CBTMN-10content is 5 wt.%, the surface resistivity of coating reach to 106Ω*cm, which denotes the coating performance good antistatic behavior. The antistatic coating of 5 wt.% CBTMN-10content is found to exhibit excellent hydrophobicity and high HV hardness. Meanwhile, the low average friction coefficients and wear rate were achieved in antistatic coating of 5 wt.% CBTMN-10content. Furthermore, compared to MXene, reduced graphene oxide, carbon nanotube, the modified CB as conductive material in PTFE antistatic materials could be an useful way not only excellent properties but also large-scale production as well as a reduction in unit cost in antistatic materials.

Chitosan/Fibroin Biopolymer-Based Hydrogels for Potential Angiogenesis in Developing Chicks and Accelerated Wound Healing in Mice.

Potential therapies for wound management remain one of the most challenging affairs to date. Biopolymer hydrogels possess inherent properties that facilitate the healing of damaged tissue by creating a supportive and hydrated environment. Chitosan/fibroin hydrogels were formulated with poly (vinyl pyrrolidone) and cross-linked using 3-aminopropyl (diethoxy) methylsilane (APDEMS) for the aforementioned function. The hydrogels were characterized through Fourier transform infrared spectroscopy, thermogravimetric analysis, and scanning electron microscopy, and their swelling response was observed using a variety of solvents. Additionally, hydrogels were investigated for biomedical applications. As the amount of fibroin added to the hydrogels increased, the swelling ratio decreased. The analysis of chorioallantoic membrane (CAM) assay revealed that higher concentrations of fibroin in the hydrogel were directly correlated with increased angiogenesis. The intragroup comparison showed that the vascular number in the CPF5 group was significantly increased (p ≤ 0.05) compared to other hydrogel groups. The wound healing efficiency of the prepared hydrogels showed that the rate of wound reduction (99.06%) was remarkably (p ≤ 0.05) high in the hydrogel group with a greater fibroin content against control (67.03%). Histological findings of wounded tissues corroborate the abovementioned results, showing dense fibrous connective tissues in the fibroin group compared to the control. The results of this work provide thorough preclinical evidence that chitosan-fibroin biopolymers are involved in enhanced angiogenesis in growing chicks and speed up wound healing in mice without any obvious toxicity.

H2O2 Self-Supplied MoS2/CaO2 Nanozyme Hydrogel with Near-Infrared Photothermal Synergetic Cascade Peroxidase-Like Activity for Wound Disinfection.

In wound healing and clinical anti-infection therapy, the current feasibility of nanocatalysts is extremely limited because of inadequate reactive oxygen species (ROS) generation. Herein, a novel H2O2 self-supplying nanocomposite (M/C/AEK) consists of molybdenum disulfide (MoS2) decorated with calcium peroxide (CaO2) prepared at ambient temperature and encapsulated in AEK hydrogel. In the presence of H2O2 and poly(vinyl pyrrolidone) (PVP), CaO2 nanoclusters, ≈30nm, are anchored on the MoS2 surface. MoS2/CaO2 can induce both a cascaded peroxidase (POD)-like and catalase (CAT)-like catalytic activity to produce toxic hydroxyl radicals through self-supplied H2O2 and O2 responsive to the faintly acidic environment of acute wounds. The POD-like activity is increased under acidic compared with neutral conditions, allowing selective treatment of acute, slightly acidic wounds while avoiding the side effects of high-concentration antibacterial agents on normal tissues. The high near-infrared photothermal effect synergistically with POD-like/CAT-like activity of MoS2/CaO2 boosts the production of more ROS to eradicate Staphylococcus aureus and Escherichia coli bacteria (98.6% and 98.9%) effectively and selectively stimulate wound healing. The porous M/C/AEK hydrogel in the wound microenvironment can efficiently capture bacteria, and its Ca2+ ions and keratin stimulate healing, revealing excellent potential in advanced wound care and infection control therapies.

Magnetic Nanoparticles in Biopolymer Fibers: Fabrication Techniques and Characterization Methods.

Hybrid nanocomposites combining biopolymer fibers incorporated with nanoparticles (NPs) have received increasing attention due to their remarkable characteristics. Inorganic NPs are typically chosen for their properties, such as magnetism and thermal or electrical conductivity, for example. Meanwhile, the biopolymer fiber component is a backbone, and could act as a support structure for the NPs. This shift towards biopolymers over traditional synthetic polymers is motivated by their sustainability, compatibility with biological systems, non-toxic nature, and natural decomposition. This study employed the solution blow spinning (SBS) method to obtain a nanocomposite comprising poly(vinyl pyrrolidone), PVA, and gelatin biodegradable polymer fibers incorporated with magnetic iron oxide nanoparticles coated with poly(acrylic acid), PAA2k, coded as γ-Fe2O3-NPs-PAA2k. The fiber production process entailed a preliminary investigation to determine suitable solvents, polymer concentrations, and spinning parameters. γ-Fe2O3-NPs were synthesized via chemical co-precipitation as maghemite and coated with PAA2k through the precipitation-redispersion protocol in order to prepare γ-Fe2O3-NPs-PAA2k. Biopolymeric fibers containing coated NPs with sub-micrometer diameters were obtained, with NP concentrations ranging from 1.0 to 1.7% wt. The synthesized NPs underwent characterization via dynamic light scattering, zeta potential analysis, and infrared spectroscopy, while the biopolymer fibers were characterized through scanning electron microscopy, infrared spectroscopy, and thermogravimetric analysis. Overall, this study demonstrates the successful implementation of SBS for producing biopolymeric fibers incorporating iron oxide NPs, where the amalgamation of materials demonstrated superior thermal behavior to the plain polymers. The thorough characterization of the NPs and fibers provided valuable insights into their properties, paving the way for their potential applications in various fields such as biomedical engineering, environmental remediation, and functional materials.

Eutectogel adhesives with underwater-enhanced adhesion to hydrophilic surfaces and strong adhesion in harsh environments

It has been a challenge to achieve strong adhesion strength for gel adhesives in water. In this study, a novel eutectogel adhesive is synthesized via one-step photoinitiated polymerization of N-vinylpyrrolidone (NVP) in deep eutectic solvent (DES). The abundant hydrogen bonding interactions and the hydrophilic polyvinylpyrrolidone network structure endow the eutectogel with excellent adhesion to both hydrophilic and hydrophobic surfaces in air and underwater. Moreover, for hydrophilic substrates, the underwater adhesion strength of the eutectogel adhesives is 1.3 times larger than that in air, demonstrating an underwater-enhanced adhesion effect. In contrast, for hydrophobic substrates, the underwater adhesion strength is lower than in air. Furthermore, strong adhesion performance is maintained even in boiling water, strong acidic medium, strong basic medium, and organic solvents. The experimental and simulation results have unveiled the underwater adhesion enhancement mechanism of the eutectogel. It is believed that the designed eutectogel will show great promise in the development of the next-generation of gel adhesives with underwater adhesion capabilities and high environmental adaptability.

Synthesis of MnO@Fe2O3 core-shell doped PVA/PVP polymeric nanocomposites for electronic and optoelectronic devices: Mechanical, electrical, and optical properties

Abstract The aqueous solution cast method was utilized to create biodegradable nanocomposite of polymers (PNC) films from a poly (vinyl alcohol) / poly (vinyl pyrrolidone) blend (70/30 wt%) and MnO@Fe2O3 nFs. The dislocation density, particle size, and interplanar distance were all calculated. The PNC films' surface shape changes from smooth to porous and somewhat rough because of the nanosized MnO@Fe2O3 particles' dispersion in the blend matrix, which diminishes the blended crystallites' size. The composite film's tensile strength increased from 9.45 MPa for the pure (PVA-PVP) film to 22.35 MPa due to the addition of 6 wt% MnO@ Fe2O3. The optical band gap decreases from 5.26 and 4.84 eV for pure (PVA/PVP) blend direct and indirect energy band gap to 5.18 and 4.71 eV for comparable values of 6wt% MnO@Fe2O3 nFs. Up to 6 wt% MnO@Fe2O3 concentration, PNC films' dielectric permittivity first declines, but it is substantially identical to the pure polymer blend matrix. The PNC sheet's dielectric permittivity increases nonlinearly with temperature, although its DC conductivity follows the Arrhenius law. Laser power was attenuated by (PVA- PVP)/MnO@Fe2O3 for both He-Ne and solid-state green laser beams. When the MnO@Fe2O3 concentration in the blend matrix rises to 6 wt%, the output power for lasers with 532 nm and 650 nm wavelengths drops from 5.49 to 2.4 mW and 19.8 to 9.4 mW, respectively. The findings suggest that nanocomposites exist and are widely recommended for optoelectronics, microelectronics, radiation detection, and several other uses.

Double-layer dissolving microneedles for delivery of mesenchymal stem cell Secretome: Formulation, characterisation and skin irritation study

Regenerative therapy based on stem cells have been developed, focusing on either stem cell or secretome delivery. Most marketed cellular and gene therapy products are available as injectable dosage forms, leading to several limitations requiring alternative routes, such as the intradermal route. Microneedles, capable of penetratingthe stratum corneumbarrier, offer a potential alternative for intradermal delivery. This present study aimed to develop double-layer dissolving microneedles (DMN) for the delivery of freeze-dried mesenchymal stem cell secretome. DMNs were fabricated using a two-step casting method and composed of two polymer combinations: poly(vinyl pyrrolidone) (PVP) with poly(vinyl alcohol) (PVA) or PVP with sodium hyaluronate (SH). The manufactured DMNs underwent assessments for morphology, mechanical strength, in skin dissolution, protein content, in vitro permeation, in vivo skin irritation, and physical stability. Based on evaluations of morphology and mechanical strength, two formulas (F5 and F12) met acceptance criteria. Evaluation of protein content revealed that F12 (PVP-SH combination) had a higher protein content than F5 (PVP-PVA combination), 99.02 ± 3.24 μg and 78.36 ± 3.75 μg respectively. In vitro permeation studies showed that F5 delivered secretome protein by 100.84 ± 0.88%, while F12 delivered 99.63 ± 9.21% in 24 h. After four days of observation onSprague-Dawleyrat’s skin, no signs of irritation, such as oedema and redness, was observed after applying both formulations. The safety of using PVP-PVA and PVP-SH combinations as excipients for DMN secretome delivery has been confirmed, promising significant advancements in biotherapeutic development in the future.

Design and mediated hydrogen bonding strength of Poly(styrene-alt- N–(ethyl–4–hydroxyphenyl)maleimide) copolymer to enhance miscibility with hydrogen bonded acceptor homopolymers

In this study, the monomer N–(ethyl–4–hydroxyphenyl)maleimide (TyHPMI) was synthesized from tyramine and maleic anhydride. Subsequently, free radical copolymerization was used to prepare the poly(S–alt–TyHPMI) alternating copolymer by reacting TyHPMI with styrene. We confirmed the chemical structure using Fourier transform infrared (FTIR), 1H and 13C nuclear magnetic resonance (NMR). The sequence distribution of the poly(S–alt–TyHPMI) alternating copolymer was analyzed using mass–analyzed laser desorption ionization/time–of–flight (MALDI–TOF) mass spectrometry. Differential scanning calorimetry (DSC) measurements showed a single glass transition temperature (Tg) across various weight fractions of binary blended systems containing strong hydrogen–bonded acceptors, such as poly(S–alt–TyHPMI)/poly(4–vinyl pyridine) (P4VP) and poly(vinyl pyrrolidone) PVP, implying full miscibility. The Tg values predicted by kwei equation for the poly(S–alt–TyHPMI)/P4VP and poly(S–alt–TyHPMI)/PVP blends show a positive deviation from linearity. This deviation is due to the short alkyl chain reinforcing the addition of acidic TyHPMI units, which enhances intermolecular hydrogen bonding between the pyridyl or C=O groups and the OH units of the TyHPMI segment. As a result, FTIR spectral analyses indicate that the intermolecular hydrogen bonding between pyridyl and C=O groups is stronger in the poly(S–alt–TyHPMI) copolymer compared to the poly(S–alt–HPMI) copolymer. This is supported by the larger ratio of the inter/self-association equilibrium constant (KA/KB) value.

Physico-Chemical Studies of Anionic Surface Active Ionic Liquid in Aqueous Poly(vinyl pyrrolidone) (PVP) Solutions: Density and Speed of Sound Measurements

Physico-Chemical Studies of Anionic Surface Active Ionic Liquid in Aqueous Poly(vinyl pyrrolidone) (PVP) Solutions: Density and Speed of Sound Measurements

Block Copolymers of Poly(N-Vinyl Pyrrolidone) and Poly(Vinyl Esters) Bearing n-alkyl Side Groups via Reversible Addition-Fragmentation Chain-Transfer Polymerization: Synthesis, Characterization, and Thermal Properties.

Amphiphilic block copolymers of N-vinyl pyrrolidone (NVP) and various vinyl esters (VEs), PNVP-b-PVEs, namely vinyl butyrate (VBu), vinyl decanoate (VDc), and vinyl stearate (VSt), were synthesized through RAFT polymerization techniques. The sequential addition of the monomers methodology was employed starting from the polymerization of NVP followed by the polymerization of the Ves' monomer. The polymerization of NVP was conducted at 60 °C in benzene solution using AIBN as the initiator and O-ethyl S-(phthalimidylmethyl) xanthate as the CTA. The resulting PNVP macro-CTA was further applied for the polymerization of the vinyl ester in dioxane solution at 80 °C using, again, AIBN as the initiator. The block copolymers were characterized through size-exclusion chromatography (SEC) and NMR spectroscopy. The thermal behavior of the copolymers was studied by Differential Scanning Calorimetry (DSC), whereas their thermal stability via Thermogravimetric Analysis (TGA) and Differential Thermogravimetry (DTG).

Study on synthesis and mechanism of high temperature resistant suspension stabilizer for spacer fluid

With 2-acrylamido-2-methylpropanesulfonic acid (AMPS), YX-1 (a monomer containing an amide group) as the main chain, DX-2 (a monomer containing a hydrophobic group), N-vinylpyrrolidone (NVP) as the side chain, the high temperature resistant suspension stabilizer for spacer was prepared by free radical aqueous solution polymerization and characterized. The structure was characterized by fourier transform infrared (FTIR) spectroscopy and thermogravimetry-differential thermal analysis (TG-DTA), which proved that the synthesized product was the target product. The performance of the copolymer was evaluated. The experimental results showed that it could be used in the spacer fluid at 30 ∼ 210 °C, and its sedimentation performance could also meet the requirements in the spacer fluid system containing saturated brine. In order to explore the mechanism of the polymer, the polymer solution was tested by six-speed rotational viscometer, pyrene fluorescence probe test, environmental scanning electron microscopy (ESEM) test, and the isolation solution containing the copolymer was tested by Zeta potential test and X-ray diffraction (XRD). Based on the above test results, it is shown that the suspension stabilizer synthesized in this paper has the characteristics of thickening, physical plugging, chemical and physical adsorption, which can effectively ensure that the spacer fluid has excellent suspension performance at high temperature.

Synthesis of suspension stabilizers for isolation fluids by response surface methodology and study of their properties

In order to solve the problem of unstable settling of isolation fluid at high temperatures, high-temperature-resistant suspension stabilizers for isolation fluids were prepared. Using the free radical aqueous solution method with 2-acrylamido-2-methylpropanesulfonic acid (AMPS), YX-1 (a monomer containing an amide group) as the main chain of the molecule, and N-Vinylpyrrolidone (NVP) and DX-2 (monomer containing hydrophobic groups) as the side chains of the molecule. We innovate the suspension stabilizer synthesis process, the synthesis conditions of the suspension stabilizer were optimized by using the one-factor experimental design and response surface analysis. The elemental composition and structure of the polymer suspension stabilizers were tested and analyzed by using X-ray spectroscopy (XPS), infrared spectroscopy (FTIR) and nuclear magnetic resonance hydrogen spectroscopy (H NMR). The hydrophobic aggregation behaviour of the polymer molecular chains was demonstrated from a microscopic point of view using fluorescence spectroscopy tests and size analysis of polymer molecular aggregates. Oscillation experiments on the isolation solution with suspension stabiliser showed that the hydrophobic groups contained in the polymers can undergo the effect of joining and bridging, and can also form a strong spatial network structure at 220°C, leading to the enhanced elasticity of the isolation fluid, which helps to alleviate the sedimentation of barite. Sedimentation stability and compatibility were evaluated for the isolation fluid containing suspension stabilizers. It was found that the isolation solution suspension performance is good under the condition of 90–220℃, its density difference is less than 0.10 g/cm3. It can also effectively prevent the contact contamination of the drilling fluid cement slurry, which is conducive to the improvement of the quality of the deep well cementing.

Modelling insertion behaviour of PVP (Polyvinylpyrrolidone) and PVA (Polyvinyl Alcohol) microneedles

A comprehensive investigation into the effects of nonlinear material behaviour of polymeric (MN) and skin on the dynamics of the MN insertion in skin was undertaken in this study using experiments and numerical simulations. The nonlinearity of the material behaviour was incorporated by employing the Ramberg–Osgood and neo-Hookean equations for stress–strain relationships for the MN materials and skin, respectively. For this purpose, a characteristic type of dissolving MN array was selected. This type of MN is made by a combination of poly(vinyl alcohol) and poly(vinyl pyrrolidone). The numerical simulations were validated using experimental investigations where the MNs were fabricated using laser-engineered silicone micromould templates technology. Young’s modulus, Poisson’s ratio, and compression breaking force for the MN polymers were determined using a texture analyser. The alignment between experimental findings and simulation data underscores the accuracy of the parameters determined through mechanical testing and mathematical calculations for both MN materials (PVP/PVA) and skin behaviour during the MN insertion. This study has demonstrated a strong alignment between the experimental findings and computational simulations, confirming the accuracy of the established parameters for MNs and skin interactions for modelling MN insertion behaviour in skin, providing a solid foundation for future research in this area.

Maltodextrin polymer nanospheres as a filtrate reducer for filtration control in water-based drilling fluids

With the development of deep and ultra-deep wells, there is a need to enhance the rheological and filtration properties of water-based drilling fluids under high temperature and salinity conditions. In this study, maltodextrin polymer nanospheres (MDPN) were synthesized through cross-linking maltodextrin and methylene bisacrylamide (MBA) via inverse emulsion polymerization. Then, the polymer MDPN-DAN was synthesized via aqueous solution polymerization, using maltodextrin polymer nanospheres, N, N-dimethylacrylamide (DMAA), 2-acrylamide-2-methylpropanesulfonic acid (AMPS), and N-vinylpyrrolidone (NVP) as raw materials. Structural characterization confirmed the successful synthesis of the polymer MDPM-DAN, with a median particle size of 234.4 nm. Thermogravimetric analysis revealed a thermal decomposition temperature of 242 °C for MDPM-DAN. This polymer demonstrated excellent settling stability at 220 °C in high-temperature and weakly alkaline environments. Rheological assessments demonstrated a 754 % enhancement in the drilling fluid’s rheological properties when MDPM-DAN was added compared to the base mud. MDPM-DAN demonstrated significant reduction in filtration loss, with polymer mud aged at 220 °C showing only 5.6 mL of loss, and polymer mud aged at 220 °C with 15 wt% NaCl exhibiting 8.9 mL loss. The filtration loss reduction mechanism elucidated that MDPM-DAN could adsorb onto bentonite particles via hydrogen bonds, while nanoparticles filled the micropores of the filter cake, promoting the formation of a dense filter cake. Furthermore, plugging experiments showcased MDPM-DAN’s ability to block nano-pore throats, with the molecular chain’s amide groups reinforcing the plugging through hydrogen bonding with rocks, while bentonite coats the micro-pore throats.

-Effects and mechanisms of acrylamide-based polymer containing N-vinylpyrrolidone on drilling fluids at high temperature

The exploration of ultra-deep oil and gas presents higher temperature resistance requirements for water-based drilling fluids. However, the lack of temperature resistance mechanism of drilling fluid polymers limits the development of key materials and drilling fluids. In this paper, by comparing the preparation of acrylamide polymers for drilling fluids, the influence of cyclic monomer N-vinylpyrrolidone (NVP) on the properties of polymers for drilling fluids was investigated, and the mechanism of NVP was deeply discussed. The results show that the NVP-containing copolymer PAAN has superior viscosity enhancement and filtration control in high-temperature drilling fluids. This is mainly due to the fact that PAAN has a more stable and complex polymer chain structure than PAA, the polymer that does not contain NVP, and its thermal stability is improved by 18.6 % up to 268°C. At the same time, NVP provides more adsorption spots, and the high-temperature clay adsorption capacity of PAAN in drilling fluids is increased by more than 66.9 % compared with that of PAA, which improves clay hydration and promotes clay dispersion, and ultimately reduces filtration of drilling fluids and stabilizes drilling fluids at high temperatures by more than 23.7 %. The introduction of NVP and the in-depth analysis of its action mechanism supplemented the anti-temperature mechanism of drilling fluid polymers, aiming to support the research and development of ultra-deep drilling fluid technology.