Aqueous Polymer Solutions Research Articles

Preparation and properties of a new type of temperature-resistant and salt-resistant fluid loss additive ADIM for oil well cement

In order to adapt to the deep high temperature and high salt cementing operation environment, itaconic acid (IA), N,N-dimethylacrylamide (DMAA), 2-acrylamido-2-methylpropanesulfonic acid (AMPS) and heterocyclic alkenes (R) were used as polymerization monomers in this paper. A temperature-resistant and salt-resistant fluid loss additive named ADIM was successfully prepared by free radical aqueous solution polymerization and orthogonal experiment. Thermogravimetric, infrared, nuclear magnetic resonance, and elemental analysis have been utilized for assessing the copolymers' structure and heat resistance. The results showed that the target copolymers with thermal decomposition temperature up to 300 ℃ were successfully prepared. A methodical evaluation was conducted on ADIM's application performance. The results show that when the ADIM content is 5 %, the water loss of fresh water cement slurry is only 44 mL at 220 ℃, and the water loss of saturated brine cement slurry is only 64 mL at 180 ℃.In addition to the excellent temperature resistance and salt resistance, the overall performance of ADIM is also good. The mechanism of ADIM was studied by mercury intrusion experiment, scanning electron microscope and TOC test. The results show that ADIM can be adsorbed on the cement particles, effectively reducing the porosity and pore size of the filter cake, thereby reducing the water loss of the cement slurry. ADIM has excellent temperature and salt resistance, which is of great significance for guiding the development of deep oil and gas resources.

Adsorption behavior and mechanism of lead by starch/tobermorite composite hydrogel.

Tobermorite (TOB) is a synthetic inorganic mineral material with a montmorillonite-like layered structure that removes heavy metals from water, and its incorporation into starch-based hydrogels can optimize the stability and adsorption properties of the hydrogels; it can also significantly reduce the storage pressure of fly ash (FA) and reduce environmental pollution. This study utilized starch/tobemolite/acrylic acid (LR/TOB/AA) as the raw material, successfully synthesizing a starch-tobemolite composite hydrogel (LR-TOB/AA) using aqueous solution polymerization. The hydrogel exhibits excellent water absorption and retention capabilities, as well as a significant adsorption effect on Pb(II). The influence of adsorption duration, starting concentration, temperature, and hydrogel incorporation on Pb(II) adsorption was examined by intermittent adsorption experiments. The maximal adsorption capacity of Pb(II) was 900.25 mg/g, surpassing the majority of reported hydrogel adsorbents, as determined by Langmuir isothermal adsorption model fitting. Following five adsorption-desorption cycles, the hydrogel's adsorption of Pb(II) persisted above 90 %.

Preparation, optimization, and modification of urea‐formaldehyde resin for used as a plugging agent in fractured and caved oil and gas reservoirs

AbstractBased on the requirements of resin‐based plugging agents on initial viscosity, gel time and cost, the urea‐formaldehyde resin Poly‐UF was synthesized via aqueous solution polymerization. Subsequently, the Poly‐UF was further modified by using melamine, polyvinyl alcohol (PVA), and oxidized starch to enhance its application performances, which were marked by Poly‐UF‐M, Poly‐UF‐PVA and Poly‐UF‐OS, respectively. Simultaneously, the relationship between the preparation process, structural, and performance characteristics of the different resin types was investigated using a single‐factor experimental approach, specifically, the solid content, viscosity, and free formaldehyde content were evaluated to gauge its application performance. In this study, the chemical structure, thermal stability and microscopic morphology of Poly‐UF‐M, Poly‐UF‐PVA and Poly‐UF‐OS were studied by using FTIR, TG‐DTG and SEM. As a result, it was confirmed that the Poly‐UF was successfully modified, and the thermal stability was obviously improved, and the microstructure was further enhanced by melamine, PVA and oxidized starch. The outcomes revealed a notable reduction in free formaldehyde content and a significant increase in solid content for Poly‐UF‐M, Poly‐UF‐PVA, and Poly‐UF‐OS, specifically, the free formaldehyde content decreased by 47.15%, 36.59%, and 32.52%, respectively, while the solid content increased by 3.47%, 1.62%, and 1.39%, respectively. Moreover, the acid and alkali solubility, mechanical strength of cured Poly‐UF‐M, Poly‐UF‐PVA and Poly‐UF‐OS were improved attribute to excellent membrane‐forming performance. The innovation of this study is that the systematic investigation and optimization of urea‐formaldehyde resin are presented, providing technical insights on its utilization as a plugging agent in fractured and caved oil and gas reservoirs.

Flow Field Analysis within Industrial Quenching Tanks Operated with Aqueous Polymer Solutions in the Steel Industry

Abstract Quenching with polymer solutions for steel heat treatment offers adjustable performance and improved ecological impact compared to conventional water or oil quenching. The submersion cooling operation poses challenges due to the intense vapor/polymer film collapse on the component surface, potentially destabilizing batch components. Therefore, controlled recirculation is critical to preventing tank and specimen damage during cooling and ensuring effective steel hardening. However, flow structure analysis is often overlooked and disregarded in industrial tank design. Thus, this study evaluates the tank geometries of two partner industries to determine if they provide the necessary homogeneous flow for optimal quenching. The analysis combines experimental velocity measurements with a numerical model, with the identification of different flow intensity regions being the main outcome of this work. The results suggest that geometric modifications could improve flow recirculation, enhancing quenching performance.

Preparation and performance evaluation of a low‐damage fracturing fluid for unconventional reservoirs

AbstractThe characteristics of tight matrix, underdeveloped natural fractures, small pore throat radius, poor pore connectivity, and abundant clay minerals result in a high potential for damage to the tight sandstone reservoirs of the Shaximiao Formation in the Qiulin Block in the Sichuan Basin. In order to reduce the retention damage caused by fracturing fluid to the tight sandstone reservoir, a low damage fracturing fluid system applicable to the target reservoir is developed in this work, and the indoor performance meets the requirements of on‐site fracturing operation. A low‐damage, heat‐resistant, shear‐stable amphiphilic polyacrylamide (PAAD) was prepared by free radical polymerization in aqueous solution using acrylamide, acrylic acid, and methacryloyloyloxyethyl dimethyloctadecyl ammonium bromide (DM18) as the monomers. The amphoteric polyacrylamide was characterized by Fourier infrared spectroscopy, nuclear magnetic resonance spectroscopy (1H NMR), light scattering molecular weight determination, and thermogravimetric analysis. Fracturing fluids were formulated with the amphiphilic hydrophobic associative polymer PAAD as a drag‐reducing agent, the fluorine‐containing and nonionic complex surfactant FD1 as a clean‐up additive, CT10‐4B as a bactericide and CT1‐12 as an emulsion breaker. The fracturing fluid formulation was preferred, and the performance of the fracturing fluid was evaluated in terms of temperature resistance and shear resistance, drag reduction, anti‐expansion, and core damage. The fracturing fluid showed good temperature and shear resistance, with a viscosity retention of 58.4% at 120°C and 170 s−1 shear for 1 h. At a loading of 0.1%, the drag reduction rate reaches 72.3%, the anti‐expansion rate of the gel‐breaking fluid is 86.04%, and the damage rate to the tight sandstone core is 16.25%. The results show that the fracturing fluid has good heat resistance and shear stability, as well as low damage and good resistance reduction and anti‐expansion properties. This work can provide new strategies for designing polymeric fracturing fluids with low damage, good heat resistance and shear stability.

Development of Slow-Release Fertilizers with Function of Water Retention Using Eco-Friendly Starch Hydrogels

Over the past two decades, the development and commercialization of slow-release fertilizers (SRFs) have significantly advanced, with the primary aim of mitigating environmental issues associated with excessive fertilizer use. A range of methodologies, including chemical and physical reactions, incorporation into carriers with porous and layered structures, and coating techniques, have been explored and refined. On the other hand, global challenges such as drought and desertification further underscore the need for SRFs that not only control nutrient release but also improve soil moisture retention. This paper reviews the development and application of eco-friendly starch hydrogels as fertilizer carriers and water retention for SRFs, particularly starch-based superabsorbent polymers (SAPs) produced through grafting copolymerization with acrylamide. This review explores both scientific issues, such as the microstructures and releasing mechanisms of SAPs, and technical development, involving copolymerization technologies, multi-initialization processes, methods of loading fertilizer into hydrogel, etc. Starch, as both a biodegradable and renewable carbohydrate polymer, offers distinct advantages due to its excellent chemical stability and high reactivity. The fabrication techniques of SAPs have been developed from traditional batch polymerization in aqueous solutions to more efficient, solvent-free reactive extrusion. The benefits of SRFs based on SAPs encompass enhanced soil aeration, the prevention of soil deterioration, the minimization of water evaporation, environmental pollution control, reduction in plant mortality, and prolonged nutrient retention within soil. In this review, we summarize the current progress, identify limitations in existing technologies, and propose future research directions to further enhance the performance of starch-based SRFs.

Influence of excipients on solubility of oxcarbazepine: Modeling and prediction based on thermodynamic models

In this work, the solubility of oxcarbazepine in polymers (PEG 6000, PEG 20,000, PVP K25, and PVP K30) and their aqueous solutions was investigated by experimental measurement and thermodynamic modeling. Firstly, the solubility of oxcarbazepine in water and polymers was modeled and the corresponding binary interaction parameters (oxcarbazepine + water and oxcarbazepine + polymer) were determined based on the experimental phase equilibrium data. Furthermore, the solubility of oxcarbazepine in the polymer aqueous solution (the mass ratios of polymers in water were 2 %, 4 %, and 6 %) was predicted by the solid-liquid equilibrium (SLE) coupled with the Perturbed-Chain Statistical Associating Fluid Theory (PC-SAFT). It was observed that the predicted results agreed well with the experimental data, and the average relative deviation (ARD) was <7 %. In this study, the solubility of oxcarbazepine in polymer aqueous solution was successfully predicted through the SLE coupled with the PC-SAFT, which was expected to provide theoretical guidance for the selection of pharmaceutical excipients and the rational design of preparations.

Application of the Thermal Analysis of Frozen Aqueous Solutions to Assess the Miscibility of Hyaluronic Acid and Polymers Used for Dissolving Microneedles.

Background: The combination of multiple polymers is anticipated to serve as a means to diversify the physical properties and functionalities of dissolving microneedles. The mixing state of components is considered as a crucial factor in determining their suitability. Objectives: The purpose of this study was to elucidate whether thermal analysis of frozen aqueous solutions can appropriately predict the miscibility of hyaluronic acid (HA) and other polymers used for dissolving microneedles prepared by a micromolding method. Methods: Aliquots of aqueous polymer solutions were applied for thermal analysis by heating the samples from -70 °C at 5 °C/min to obtain the transition temperature of amorphous polymers and/or the crystallization/melting peaks of polymers (e.g., polyethylene glycol (PEG)). Films and dissolving microneedles were prepared by air-drying of the aqueous polymer solutions to assess the polymer miscibility in the solids. Results: The frozen aqueous single-solute HA solutions exhibited a clear Tg' (the glass transition temperature of maximally freeze-concentrated solutes) at approximately -20 °C. The combination of HA with several polymers (e.g., dextran FP40, DEAE-dextran, dextran sulfate, and gelatin) showed a single Tg' transition at temperatures that shifted according to their mass ratio, which strongly suggested the mixing of the freeze-concentrated solutes. By contrast, the observation of two Tg' transitions in a scan strongly suggested the separation of HA and polyvinylpyrrolidone (PVP) or HA and polyacrylic acid (PAA) into different freeze-concentrated phases, each of which was rich in an amorphous polymer. The combination of HA and PEG exhibited the individual physical changes of the polymers. The polymer combinations that showed phase separation in the frozen solution formed opaque films and microneedles upon their preparation by air-drying. Coacervation occurring in certain polymer combinations was also suggested as a factor contributing to the formation of cloudy films. Conclusions: Freezing aqueous polymer solutions creates a highly concentrated polymer environment that mimics the matrix of dissolving microneedles prepared through air drying. This study demonstrated that thermal analysis of the frozen solution offers insights into the mixing state of condensed polymers, which can be useful for predicting the physical properties of microneedles.

Environmentally friendly molecularly imprinted polymers as an insert for SPE type columns in the gentamicin monitoring process

The quantity and variety of micro-pollutants infiltrating water resources have increased rapidly in recent times. The appearance of many harmful substances in the waters has resulted in so-called chemical cocktails which significantly contribute to the deterioration of water quality. Additionally, the variety of these compounds, often similar to each other in terms of molecular weights, makes their separation and identification very difficult. In this paper we present the possibility of using self-regenerating mechanism of molecularly imprinted polymers to measure the concentration of micropollutants in the aquatic environment. Molecularly imprinted polymers toward gentamicin were prepared by monomer polymerization in aqueous solution at ambient temperature. Results from computer-based molecular modelling demonstrated potential binding sites between gentamicin and functional monomers in water. Various compositions of polymerization mixtures were tested. The ratio of monomers to each other was 1.1:1.4:0.0015 and 1:1:1 for N-isopropylacrylamine:acrylamide:acrylic acid, respectively. For each composition, various amounts of the standard were tested: 0, 3, 5, 7, 10,15 mol% in relation to monomers. The best results were obtained for 5 % gentamicin with an excess of acrylamide in relation to the other monomers. Sorption for this system was 0.783 mg/g at ambient temperature and desorption 0.593 at 4 °C. The synthesized materials, thanks to the incorporation of thermosensitive poly(N-isopropylacrylamide) into their structures, were able to release 89 % of adsorbed gentamicin. This made it possible to use the designed SPE columns repeatably with similar efficiency. The prepared materials were selective in the presence of other antibiotics like amoxicillin and norfloxacin.

Gas hydrate inhibition by urea and its blends with vinyl lactam polymer: Paving the way to green hybrid inhibitors

Urea is an environmentally benign substance considered a promising gas hydrate inhibitor in flow assurance. Nevertheless, its effect on gas hydrate formation kinetics remains poorly understood. This study investigates the impact of urea and hybrid urea/polymer KHI samples on the nucleation and growth kinetics of sII natural gas hydrates. Hydrate formation was observed at a lower onset temperature with increasing urea and polymer concentration. The nucleation of sII hydrate in aqueous urea solutions occurred at a higher subcooling (7.50 ± 0.58 K at 30 mass%) than in pure water (5.17 ± 0.69 K). These findings indicate that urea acts as a nucleation inhibitor of sII hydrates, although its capacity is not as potent as that of polymer KHI.The analysis of the hydrate nucleation probability distributions revealed that the sII hydrate nucleation rate exhibited a significant decline, approximately one order of magnitude, at subcooling of 5.3–6 K for 20 mass% urea compared to water. A similar behavior was noticed in an aqueous solution of polymer KHI. Urea has succeeded in providing a total benefit of up to 10 K in hydrate onset temperature due to a shift in the hydrate stability zone and nucleation retardation.Consequently, urea is a green dual-acting anti-hydrate chemical that inhibits the formation of sII hydrates by thermodynamic and kinetic mechanisms. Besides, adding 10 mass% urea increases the cloud point temperature of vinyl lactam polymer Luvicap 55W by 14 K. Urea is an additive that considerably augments the stability of the polymer in aqueous solutions at elevated temperatures. These findings make urea an effective and environmentally friendly top-up inhibitor that significantly enhances the anti-hydrate properties of polymer KHI.

CMC-Na and Laponite dual network reinforced P (AM-co-NVCL) hydrogel with pH/temperature dual sensitivity

In this paper, poly (acrylamide-co-N-vinylcaprolactam) [poly(AM-co-NVCL)] hydrogels were modified by aqueous solution polymerization using sodium carboxymethyl cellulose (CMC-Na) and Laponite. Their properties were characterized by infrared spectroscopy (FT-IR), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), X-ray diffraction (XRD), rheological testing, and scanning electron microscopy (SEM). The swelling kinetics showed that the equilibrium swelling ratio of the xerogel was influenced by the monomer ratio, crosslinking agent, and modifier content. As the Laponite and CMC-Na content increased, the compressive strength of the composite hydrogel increased, while the elongation at break decreased. The modified composite hydrogel exhibited dual sensitivity to pH and temperature. DSC and rheological tests indicated that CMC-Na functioned as a physical crosslinking agent in the system, and with the increase in CMC-Na content, the crosslinking effect was enhanced. SEM demonstrated that the addition of Laponite and CMC-Na increased the number of pores in the hydrogel and decreased the pore size.

Realizing the Rapid Release of Drag Reducers via pH-Induced Oil Phase Transition of Inverse Emulsion.

As a key component of slickwater fracturing fluids, emulsion drag reducers play a vital role. The dissolving capacity of traditional emulsion drag reducers is improved by adding hydrophilic surfactants, which leads to poor stability of the emulsion drag reducer. In order to eliminate the contradiction between stability and release of the emulsion drag reducer, here, pH-responsive polymer emulsion was fabricated using the switching solvent (HA) and white oil as the continuous phase. Monomer emulsions exhibit obvious pH-responsive behavior. This is because the deprotonation of HA by pH stimulation leads to a change in the oil-water ratio of the emulsion, thereby facilitating the demulsification of emulsion. The remarkable stability of the monomer emulsion benefits the preparation of inverse emulsion polymers (P(AM-AA-AMPS)). The obtained P(AM-AA-AMPS) polymer emulsion features remarkable stability even after 15 days of storage. Importantly, the P(AM-AA-AMPS) polymer was released from the emulsion efficiently by pH stimulation instead of introducing an extra hydrophilic surfactant, which confirmed the improvement of polymer release by pH stimulation. The viscosity of the P(AM-AA-AMPS) polymer aqueous solution reaches a maximum value of 96 mPa s within 80 s at a pH value of 9.2. The release efficiency of P(AA-AM-AMPS) polymer emulsion is increased by 33% in comparison with that of traditional polymer emulsion (2 min). The P(AM-AA-AMPS) emulsion demonstrated remarkable drag-reduction performance by achieving a drag-reduction rate of 73% at a concentration of 0.05 wt %. P(AM-AA-AMPS) polymer emulsion with pH responsiveness eliminates the contradiction between the stability and release of emulsion drag reducers. Research based on pH-responsive P(AM-AA-AMPS) polymer emulsion provides other ideas for the development of quickly dissolving and long-term storage drag reducers, which is helpful for the development of low-permeability oil and gas resources.

Fluorogenic in-situ Labelling of Gelatin Polymer in Aqueous Solution and Hydrogel.

Gelatin polymers made from partially degraded collagen are important biomaterials, but their in-situ analysis suffers from uncontrollable covalent labelling and poor spatial-temporal imaging resolution. Herein, three tetrazolate-tagged tetraphenylethylene fluorophores (TPE-TAs) are introduced for practical fluorogenic labelling of gelatin in aqueous phase and hydrogels. These probes with aggregation-induced emission characteristics offer negligible background and elicit turn-on fluorescence by simply mixing with the gelatin in aqueous phase, giving a detection limit of 0.15 mg/L over a linear dynamic range up to 100 mg/L. This method does not work for collagens and causes minimal interference with gelatin properties. Mechanistic studies reveal a key role for multivalent electrostatic interactions between the abundant basic residues in gelatin (e. g., lysine, hydroxylysine, arginine) and anionic tetrazolate moieties of the lipophilic fluorophore synergistically in spatially rigid macromolecular encapsulation to achieve fluorogenic labelling. The AIE strategy by forming non-covalent fluorophore-gelatin complexes was developed for novel hydrogels that exhibited reversible fluorescence in response to dynamic microstructural changes in the hydrogel scaffold upon salting-in/out treatments, and enabled high spatial-temporal imaging of the fiber network in lyophilized samples. This work may open up avenues for in-situ imaging analysis and evaluation of gelatin-based biomaterials during processes such as in vivo degradation and mineralization.

Synthesization and characterizations of coal fly ash-coffee grounds-based composite as super-absorbent for application in soil

To recycle and utilize two types of harmful solid waste, coffee grounds (CG) and coal fly ash (CFA), a novel and low-cost superabsorbent composite (MCG-PAA/CFA) was synthesized by aqueous solution polymerization with modified coffee grounds (MCG), acrylic acid (AA) and CFA as raw materials, and it was applied to soil to improve its drought resistance. Various reaction conditions were comprehensively investigated and analyzed to assess their influence on the water absorbency of the superabsorbent composite (SAC). After optimization, the MCG-PAA/CFA exhibited water absorbency capacities of 1260(±10.6) g/g and 82(±1.4) g/g in deionized water and physiological saline, respectively. After adding 3 wt% MCG, the water absorption of SAC was improved from 415 to 746 g/g. After further introduction of 2 wt% CFA, the water absorption of SAC increased from 746 to 1260 g/g. Fourier Transform Infrared (FTIR) analysis confirmed that the grafting reaction was successful and that CFA participated in the reaction, while scanning electron microscope (SEM) and thermogravimetric analysis (TGA) results revealed that the grafting reaction and the introduction of CFA improved the surface morphology and thermal stability of the SAC. Kinetic analysis was conducted to investigate how the grafting reaction and the introduction of CFA affected the swelling and water retention kinetics of the superabsorbent composite. In the soil experiment, adding only 0.1 wt% MCG-PAA/CFA can improve the water holding capacity of sandy soil, loam soil and clay soil by 6.65%, 4.42%, and 3.76% respectively This SAC composite has great potential in soil drought resistance.

Effects of Dye Addition on the Rheological Properties of Aqueous Polymer Solutions.

In many commercial applications, polymer-dye interactions are frequently encountered from food to wastewater treatment, and while shear rheology has been well characterized, the extensional properties are not well known. The extensional viscosity ηE and relaxation time λE are the extensional rheological parameters that provide valuable insights into how aqueous polymers respond during deformation, and this study investigated the effect of dyes on the extensional rheology of three different aqueous polymer solutions (e.g., anionic, cationic, and neutral) paired with two different dye salts (e.g., anionic and cationic) using drop pinch-off experiments. We have found that the influence of dyes on the pinch-off dynamics is complex but generally leads to a decrease in, for example, the apparent extensional relaxation time. We have utilized the dripping-onto-substrate method to probe the uniaxial deformation of widely used polymers such as xanthan gum (XG), poly(diallyldimethylammonium chloride) (PDADMAC), and poly(ethylene oxide) (PEO) as the anionic, cationic, and neutral polymers, respectively, paired with either fluorescein (Fl) or methylene blue (MB) as the anionic and cationic dyes, respectively. Polymer-dye pairs with opposite charges (e.g., XG-MB and PDADMAC-Fl) displayed a pronounced decrease in pinch-off times, but even PEO, which is a neutral polymer, resulted in decreased pinch-off times, which was restored by the addition of NaCl. The pinch-off times for the Boger fluid (mixture of poly(ethylene glycol) and PEO), however, were surprisingly uninfluenced by dyes. These results showed that not only did the small addition of dyes strongly decrease the polymer relaxation times, but the relative importance of the dye salts on the polymer pinch-off dynamics was also different from that of pure salts such as NaCl.

Application of a UV-vis spectrometer to investigate the effect of dissolution media on the diffusivity of small molecules and proteins

To date, the commonly used methods for diffusion coefficient measurements have some hurdles that prevent them from being widely applied in pharmaceutical laboratories. This study aimed to modify a method developed by di Cagno et al. based on the use of a UV-Vis spectrometer and apply the method to investigate the effect of dissolution media on the diffusivity of small molecules and proteins. A total of five small molecules and two proteins in different aqueous media and polymer solutions were investigated in this study. By attaching a 3D-printed cover with an open slit to a standard UV-Vis cuvette, the incident UV light could only pass through the open slit to measure the local drug concentration. During the diffusion experiment, drug molecules diffused from the cuvette bottom to the slit. According to the concentration measured as a function of time, diffusion coefficient was calculated based on Fick's law of diffusion using the analytical and numerical approaches. As a result, diffusion coefficients could be accurately measured with high reproducibility. The results also suggested that different media could affect the diffusion coefficients of small molecules by < 10% and proteins by < 15%. Since the UV-Vis spectrometer is a routine instrument, this method can potentially be employed by many pharmaceutical laboratories for diffusion coefficient measurements.

Capillary wave-assisted collapse of non-Newtonian droplets

Understanding the peripheral capillary wave propagation during droplet impact is crucial for comprehending the physics of wetting onset and droplet fragmentation. Although Newtonian droplets have been extensively studied, we show how capillary waves deform non-Newtonian droplets in such a way that rheological features, such as the critical concentrations for the overlap (c*) and entangled polymer molecules (c**), may be directly obtained from the deformation history. Determining these critical concentrations is essential as they mark transitions in the rheological behavior of aqueous polymeric solutions, influencing viscosity, elasticity, and associated fluid dynamics. We have also compared capillary waves among Newtonian, shear-thinning, and Boger fluid droplets and found that although the fluid kinematics appear to be purely biaxial extensional flow, the infinite-shear properties of the droplets dominate the physics of capillary wave formation and propagation.

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.

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.

Mesoporous silica stabilized perovskite quantum dots for the preparation of ultra-stable green flexible film.

CsPbBr3 perovskite quantum dots (QDs) have attracted much attention in the optical field because of their low band gap, wide absorption spectrum and high color purity. However, their poor stability in extreme environments such as water, light and heat severely limits their application in optical fields. Here, we prepared m-SiO2/CsPbBr3 composite luminescent material using an aqueous phase method combined with high temperature calcination. The material can retain 87% of the initial photoluminescence quantum efficiency after 60 days of storage under ambient conditions (humidity ∼80%; temperature ∼25 °C), its photoluminescence intensity only decreased by 33% after immersion in water for 90 min. This indicates that the material retains good stability under a high humidity environment. Finally, PMMA@m-SiO2/CsPbBr3 flexible films were prepared by aqueous solution polymerization. The flexible film has excellent green light emission properties and exhibits (0.092, 0.625) CIE coordinates.