Search Results (266)

The dynamic self-assembly and phase separation of donor–acceptor blends are processes that dictate the nanoscale morphology in organic solar cells. Here, we employ a fluidics-inspired framework, integrating dissipative particle dynamics simulations with percolation theory, to investigate the morphogenesis of two non-fullerene systems: P3HT-PPerAcr and P3HT-PFTBT. We analyze monomeric and homopolymer blends, and copolymer macrostructures, focusing on how key parameters such as temperature and polymer chain flexibility govern the dynamic evolution towards percolating networks. Our simulations captured the fundamental fluidic behavior and universal scaling near the critical percolation threshold (χ_c). The critical exponent β revealed distinct universality classes dictated by system compatibility and flexibility: monomeric and flexible homopolymer blends below the critical temperature (T_c) exhibit mean field behavior (β ≈ 1). In contrast, monomeric systems above χ_c and flexible copolymers below χ_c display 3D percolation behavior (β ≈ 0.45). In the case of flexible copolymeric macromolecules, above percolation threshold a quasi-bidimensional behavior emerge with (β ≈ 0.1). Notably, semi-rigid and rigid homopolymeric and copolymeric linear architectures induce a dimensional crossover, yielding quasi-2D (β ≈ 0.14) and quasi-1D (β ≈ 0.0) morphologies. These findings establish a direct link between tunable fluidic interactions, chain dynamics, and the emergence of optimal bicontinuous percolation networks. Full article

This study investigates how the composition and synthesis sequence affect the structure and responsive behavior of single-network (SN) and double-network (DN) hydrogels composed of poly(N,N’-diethylacrylamide) (PDEAAm) and polyacrylamide (PAAm). DN hydrogels were prepared in two configurations, PDEAAm/PAAm and PAAm/PDEAAm, and compared with SN copolymer hydrogels of varying DEAAm/AAm ratios. ¹H NMR spectroscopy revealed that DN hydrogels exhibit significant heterogeneity due to polymer-rich domains, impacting the accuracy of compositional determination and leading to broad NMR signals. Temperature-dependent NMR and gravimetric swelling analyses were used to quantify thermoresponsive behavior, showing that SN copolymer hydrogels exhibit composition-dependent phase transition parameters, while DN hydrogels show relatively constant transition parameters due to heterogeneous structures. NMR relaxation studies of water molecules identified “free” and “bound” molecules whose dynamics differ markedly above the transition temperature, especially in DN systems. Finally, the swelling behavior in water–acetone mixtures was examined, revealing distinct responses depending on hydrogel composition and thermal state. PAAm-rich hydrogels showed abrupt deswelling near 40 vol% acetone, while PDEAAm-based hydrogels responded more gradually. The findings demonstrate that both composition and network formation order critically influence the structural, thermal, and solvent-responsive properties of hydrogels, offering insights for the design of stimuli-responsive materials. Full article

We reported a simplified one-step emulsification strategy to prepare bi-continuous emulsions with a gel-like property using the pH-responsive self-assembled aggregates of an amphiphilic random copolymer poly (styrene-co-methacrylic acid) (P(St-co-MAA)) as the interfacial stabilizers. Using caprylic/capric triglyceride (GTCC) as the oil phase, 1.0% P(St-co-MAA) aqueous solution with a pH between 7.0 and 8.0 as the water phase, and an oil/water phase ratio of 6:4, bi-continuous emulsions could be formed directly through one-step emulsification. Systematic characterization with a fluorescence microscope, scanning electron microscope, and confocal laser scanning microscope confirmed the formation of the bi-continuous emulsions. The three-phase contact angle measurements confirmed that the surface wettability of the self-assembled aggregates changed with pH, and the three-phase contact angles of the bi-continuous emulsions formed at a pH between 7.0 and 8.0 were close to 90°. Furthermore, rheological analysis of the bi-continuous emulsion showed the storage modulus (G′) dominating over the loss modulus (G″), which verified that the bi-continuous emulsion was attributed to the existence of a three-dimensional elastic gel network. The pH-dependent wettability of the self-assembled aggregates as the stabilizers enabled pH to control the emulsion type from O/W to bi-continuous to W/O. The work provides a simple, rapid, and robust approach to preparing bi-continuous emulsions without intricate particle modifications and cumbersome procedures. Full article

Polymer gels are widely used for profile control and water shutoff in mature reservoirs, while conventional gels are limited under high temperature due to poor thermal stability. This study develops a high-temperature-resistant gel based on acrylamide/vinylpyrrolidone copolymer (P(AM/NVP)), crosslinked with hydroquinone-hexamethylenetetramine (HQ-HMTA). At 150 °C, the gel achieves a Sydansk strength code of H with a gelation time of 9.5 h, and shows excellent thermal stability, maintaining over 90% weight after 180 days. Rheological and microscopic analyses confirm a dense, stable network with high storage modulus (G′). Core flooding tests demonstrate good injectivity with resistance factors of 3.99~129.93, while the plugging rate exceeds 98%. All the experimental results indicate that the P(AM/NVP)-based gel has great potential for water plugging in high temperature oil reservoirs. Full article

To address the lack of systematic comparison regarding rheological properties and the unclear structure–property relationships among three core fracturing fluid materials including synthetic polymers, vegetable gums, and microbial polysaccharides, this study selected acrylamide-based polymers, hydroxypropyl guar gum and xanthan gum as the representative systems. The steady-state viscosity, rheological curves, thixotropy, viscoelasticity, and temperature-shear resistance of the three samples were systematically characterized at concentrations ranging from 0.1 to 0.7 wt% using an MCR301 rotational rheometer. The outcomes indicate that the structural strength values of all three materials increase with rising concentration, but their rheological behaviors and stability differ significantly due to distinct molecular structures. The acrylamide-based copolymer forms a temporary network via weak hydrogen bonds (amide-carboxyl or amide-amide) and physical entanglements, exhibiting thixotropy and a stress pre-elastic response. The most significant effects occur at 0.7 wt%, with a thixotropic loop area of 2.874 Pa·s⁻¹ and a stress overshoot of 4.97 Pa.; hydroxypropyl guar gum has insufficient thermal stability and poor heat resistance. Its viscosity retention rate is as low as 31%, and it always exhibits a solution-type rheological property of G′ < G″; the xanthan gum exhibits elastic gel properties with tanδ < 1 due to its double-helix molecular structure. It has excellent temperature shear tolerance and the viscosity retention value can reach up to 98.6 mPa·s. Two mathematical models were established and demonstrated strong applicability: a modified Carreau model for flow curve fitting yielded a coefficient of determination (R²) greater than 0.95, enabling accurate description of fluid-type transitions; a four-parameter equation for temperature–shear resistance curves also achieved an R² above 0.95, effectively characterizing viscosity evolution with temperature. Full article

This study addresses the challenge of high-temperature gas channeling in injection–production wells of karst-fractured reservoirs by developing a high-temperature-resistant resin–gel plugging system capable of withstanding up to 150 °C. The system employs an AMPS/NVP copolymer (molar ratio 3:1) as the polymer matrix, reinforced with phenolic resin to enhance the crosslinked network. Additionally, a polyamide microcapsule was utilized to encapsulate the gel breaker, enabling controlled release. The optimized formulation consists of 0.5% NEP, 0.5% DEP, 0.6% HMTA, 0.3% catechol, and 25% resin curing agent. Experimental results demonstrate that the system exhibits excellent stability at 150 °C, with a G′ ≥ 125 Pa and compressive strength > 18 MPa. It also displays strong contamination resistance, showing a viscosity reduction of <9.7% and a storage modulus retention rate > 87% after mixing with drilling fluid. Furthermore, the gel-breaking performance is controllable, achieving a gel-breaking rate ≥ 99.7% within 21 days. Under high-temperature and high-pressure conditions (150 °C), the system demonstrates a plugging efficiency > 92% for simulated fractures with widths ranging from 0.1 to 2 mm. This technology effectively suppresses gas channeling in complex high-temperature formations, making it suitable for gas injection wells in karst-fractured reservoirs. It also holds promise for extension to shale gas wells and geothermal reservoir sealing applications. Full article

This study synthesizes two highly water-soluble copolymers, p(SA-co-SMAS) and p(SA-co-SMAS-co-AMPS) using sodium alginate (SA), sodium 2-methylprop-2-ene-1-sulfonate (SMAS), and 2-acrylamido-2-methylpropane sulfonic acid (AMPS, with or without addition) as precursors. Under ball milling, these copolymers are blended with aluminum sulfate and glass fibers to produce two series of cement admixtures. Compared to systems without admixtures or with pure aluminum sulfate as sole admixture, the admixture obtained from p(SA-co-SMAS) and aluminum sulfate significantly shortens the initial setting time (4.47 vs. 33.59 and 29.51 min) and final setting time (8.46 vs. 45.26 and 35.12 min), while markedly improving compressive strength (9.2 vs. 3.5 and 4.3 MPa) and flexural strength (3.5 vs. 1.0 and 1.1 MPa). This enhancement is attributed to the formation of a unique boehmite (AlO(OH)) phase in synthesized admixture, which rapidly reacts with tricalcium silicate, gypsum, and water in cement to form ettringite (Ca₆Al₂(SO₄)₃(OH)₁₂·26H₂O). The ettringite interlocks with the two-dimensional C–S–H gel, creating a stable three-dimensional network. Further blending this admixture with 200-mesh glass fibers yields a new admixture containing Al₄SO₄(OH)₁₀·36H₂O. Compared to boehmite, this phase further reduces setting times and increases average compressive strength (10.2 vs. 9.2 MPa). The admixture derived from p(SA-co-SMAS-co-AMPS) and aluminum sulfate shows even better performance: setting times are further shortened and flexural strength is significantly enhanced, owing to the presence of the more effective Al₄SO₄(OH)₁₀·36H₂O phase. Incorporating 200-mesh glass fibers into this system results in the shortest setting times (initial: 2.24 min, final: 5.73 min) and an excellent 24 h compressive strength (9.4 MPa), likely due to a unique and unexpected pore-filling effect. In contrast to conventional uses of sodium alginate as a retarder, glass fibers as mere reinforcements, and aluminum sulfate as a strength-impairing accelerator, this work demonstrates a synergistic strategy, which enables an ultra-rapid and high-strength cement setting process, offering highly significant scientific and practical value. Full article

Superabsorbent polymers (SAPs) are materials that can absorb and retain water solutions with a mass of several hundred times greater than their own. This work aimed to synthesise and evaluate the effects of highly absorbent starch phosphate-g-poly(acrylic acid) copolymers on the microbiological activity of soils previously used for agriculture. The biopolymers studied were obtained by thermal and chemical oxidation of starch phosphates and copolymerized with potassium salts of acrylic acid. Basic physicochemical parameters were determined in the applied soil. Following SAP application, the basal respiration rate was measured at 22 °C with a constant soil moisture content of 60% WHC. The incubation time in constant temperature and moisture conditions was 78 days. After this period, their microbiological activity (microbial and organic phosphorus fractions) was assessed, thereby enabling the determination of the direction of change in the soil environment. The addition of SAP increases the soil’s water-holding capacity and respiration. The SP-g-PAA polymers serve as slow-release sources of potassium and phosphorus ions. These elements were bound to the polymer network by ionic and covalent bonds. Analysis of the results shows that within two weeks, 47–80% of the starch hydrogel undergoes microbial degradation. No differences were found in the content of labile forms of phosphorus in soils with SAP additions compared to soils without polymer additions. The use of modified starch reduces the consumption of vinyl monomers, while the resulting product is characterised by high absorbency and low water content, which reduces the amount of energy needed to obtain the finished product, thus contributing to sustainable development. Full article

Conventional lithium-ion batteries face issues like electrolyte leakage and interface instability. Solid-state lithium batteries with solid electrolytes address these, while solid-state polymer electrolytes (SPEs) offer safety and flexibility. This study primarily aimed to develop and synthesize a graft copolymer, PVA-g-SBMA, which was successfully synthesized by grafting [2-(methacryloyloxy)ethyl] dimethyl-(3-sulfopropyl)ammonium hydroxide (SBMA) onto poly(vinyl alcohol) (PVA). PVA provided excellent film-forming ability and mechanical strength, enhancing flexibility and stability in solid-state devices. Meanwhile, SBMA’s zwitterionic structure promoted efficient ion transport, improving ionic conductivity and solid electrolyte performance in energy storage applications. From the results, the proton assignment of the PVA-g-PSBMA zwitterionic graft copolymers was investigated via ¹H NMR spectra. The molecular weight of the graft copolymer was determined through aqueous GPC; the number average molecular weight (Mn) was 15,755, and the PDI was 1.17. The grafting efficiency of SBMA was calculated as 25%. However, the material lacked sufficient mechanical properties, leading to brittle membranes. To address this issue, we crosslinked the film to improve its mechanical properties. The grafted copolymer was crosslinked with the PEDOT:PSS as a crosslinkable sulfonated component using (3-glycidyloxypropyl)trimethoxysilane (GOPS) as the crosslinker and dimethyl sulfoxide (DMSO) as solvent to complete the crosslinking reaction. The crosslinking mechanism involved the reaction between hydroxyl groups on PVA and PSS, while the GOPS bonded with PSS, forming a robust crosslinked network. The crosslinking process was completed by heating the mixture to 120 °C. We also compared different crosslinking ratios to discuss the film performance. Lithium salts were incorporated to investigate the effect of varying lithium salt concentrations. According to EIS measurements, the best-performing system was crosslinked PVA-g-SBMA with PEDOT:PSS 0.1 wt% and LiTFSI 0.015 wt%, which reached conductivities of 4.9 × 10⁻⁴ S/cm at room temperature. We also explored the film’s thermal properties, morphologies, and chain interactions in this research. Full article

Controlling CO₂ channeling in heterogeneous reservoirs remains a major challenge for both enhanced oil recovery (EOR) and secure geological storage. AMPS-HPAM copolymers exhibit high-temperature resistance and brine tolerance compared with conventional HPAM gels, making them well suited for the harsh environments associated with CO₂ injection. Chromium-based crosslinkers (CrAc and CrCl₃) were investigated because sulfonic acid groups in AMPS can coordinate with trivalent chromium ions, enabling dual ionic crosslinking and the formation of a robust gel network. While organic crosslinked AMPS-HPAM gels have been widely studied, the behavior of chromium-crosslinked AMPS-containing systems, particularly their gelation kinetics under CO₂ exposure, remains less explored. This experimental study evaluates the gelation behavior and stability of chromium-crosslinked AMPS-HPAM gels by examining the effects of the polymer concentration, molecular weight, polymer–crosslinker ratio, temperature, pH, salinity, and dissolved CO₂. The results clarify the crosslinking behavior across a range of formulations and environmental conditions and establish criteria for designing robust gel systems. Gelation times can be controlled from 5 to 10 h, and the resulting gels maintained structural integrity under CO₂ exposure with less than 3.6% dehydration. Long-term thermal testing has shown that the gel remains stable after 10 months at 100 °C, with evaluation still ongoing. These results demonstrate that chromium-crosslinked AMPS-HPAM gels provide both durability and tunability for diverse subsurface conditions. Full article

As a non-invasive diagnostic technique, evolved gas analysis (EGA) holds significant value in assessing the insulation conditions of critical equipment such as power cables. Current analytical methods face two major challenges: insulation materials may undergo multiple aging mechanisms simultaneously, leading to interfering characteristic gases; and traditional approaches lack the multi-label recognition capability to address concurrent fault patterns when processing mixed-gas data. These limitations hinder the accuracy and comprehensiveness of insulation condition assessment, underscoring the urgent need for intelligent analytical methods. This study proposes a deep convolutional neural network (DCNN)-based multi-label classification framework to accurately identify the gas generation characteristics of five typical power cable insulation materials—ethylene propylene diene monomer (EPDM), ethylene-vinyl acetate copolymer (EVA), silicone rubber (SR), polyamide (PA), and cross-linked polyethylene (XLPE)—under fault conditions. The method leverages concentration data of six characteristic gases (CO₂, C₂H₄, C₂H₆, CH₄, CO, and H₂), integrating modern data analysis and deep learning techniques, including logarithmic transformation, Z-score normalization, multi-scale convolution, residual connections, channel attention mechanisms, and weighted binary cross-entropy loss functions, to enable simultaneous prediction of multiple degradation states or concurrent fault pattern combinations. By constructing a gas dataset covering diverse materials and operating conditions and conducting comparative experiments to validate the proposed DCNN model’s performance, the results demonstrate that the model can effectively learn material-specific gas generation patterns and accurately identify complex label co-occurrence scenarios. This approach provides technical support for improving the accuracy of insulation condition assessment in power cable equipment. Full article

Herein, we report the synthesis via controlled reversible addition-fragmentation chain transfer (RAFT) polymerization of amphiphilic 2-vinylpyridine-b-styrene (2VPy-b-Sty) diblock copolymers of high molar masses (range: 52,100–304,000 g mol⁻¹) and various compositions (range: 2VP content 11.6–59.2 mol%) and their use for the fabrication of nanoporous membranes. The successful synthesis of the amphiphilic diblock copolymers was confirmed through the characterization of their molar masses, molar mass distribution, and composition using GPC and ¹H-NMR spectroscopy, respectively. Subsequently, membranes of the diblock copolymers were fabricated following the “phase inversion” technique. The resulting membranes were characterized via scanning electron microscopy which revealed the presence of sphere percolation networks morphology for all diblock copolymers with M_n ranging from 120 to 300 kDa and 2VPy content between 10 and 15 mol% at the optimal conditions. Afterward, the developed membranes were evaluated in terms of their permeability towards water and in terms of their ability to retain two different microorganisms, namely, Enterococcus faecalis and Escherichia coli, that are known to be harmful to human health. The experimental water flux for a membrane with pore size around 60 nm was equal to 31,400 L h⁻¹ m² and expectedly decreased with the decrease in membrane pore diameter. The retention ability of membranes for Enterococcus faecalis and Escherichia coli was higher than 90%. In particular, the retention ability for Enterococcus faecalis was equal to 98.9% and for Escherichia coli was 91.4%. The toxicity of the produced membrane was also determined, and the measured value was relatively low, at 17%. Full article

A spring–dashpot model, consisting of a spring branch and two Maxwell (named long- and short-term) branches, was used to simulate stress drop during the relaxation stages of multi-relaxation (MR) tests. This work shows that the stress drop at relaxation in a deformation range around the peak stress could be closely simulated without changing the parameter values for the short-term branch. This possibility was confirmed using three ethylene/1-hexene copolymers and one ethylene homo-polymer, among which the main differences are mass density and short-chain branch (SCB) content. The work examined the influence of SCB content and mass density on the stiffness of the two Maxwell branches, and the results showed that, unlike the long-term branch counterpart, stiffness of the short-term branch is not a monotonic function of the SCB content or the mass density. This led to a discussion on the possible relationship between the stiffness of the two Maxwell branches and the deformation resistance of the amorphous phase at different locations of the microstructure, i.e., in the interlamellar region and as part of the network structure. The paper concludes that a combination of the MR test and the spring–dashpot model could provide information that is related to the stiffness in different parts of PE’s amorphous phase, though further work is needed to verify this conclusion. Full article

Temperature-responsive hydrogels are sophisticated stimuli-responsive biomaterials that undergo rapid, reversible sol–gel phase transitions in response to subtle thermal stimuli, most notably around physiological temperature. This inherent thermosensitivity enables non-invasive, precise spatiotemporal control of material properties and bioactive payload release, rendering them highly promising for advanced biomedical applications. This review critically surveys recent advances in the design, synthesis, and translational potential of thermo-responsive hydrogels, emphasizing nanoscale and hybrid architectures optimized for superior tunability and biological performance. Foundational systems remain dominated by poly(N-isopropylacrylamide) (PNIPAAm), which exhibits a sharp lower critical solution temperature near 32 °C, alongside Pluronic/Poloxamer triblock copolymers and thermosensitive cellulose derivatives. Contemporary developments increasingly exploit biohybrid and nanocomposite strategies that incorporate natural polymers such as chitosan, gelatin, or hyaluronic acid with synthetic thermo-responsive segments, yielding materials with markedly enhanced mechanical robustness, biocompatibility, and physiologically relevant transition behavior. Cross-linking methodologies—encompassing covalent chemical approaches, dynamic physical interactions, and radiation-induced polymerization are rigorously assessed for their effects on network topology, swelling/deswelling kinetics, pore structure, and degradation characteristics. Prominent applications include on-demand drug and gene delivery, injectable in situ gelling systems, three-dimensional matrices for cell encapsulation and organoid culture, tissue engineering scaffolds, self-healing wound dressings, and responsive biosensing platforms. The integration of multi-stimuli orthogonality, nanotechnology, and artificial intelligence-guided materials discovery is anticipated to deliver fully programmable, patient-specific hydrogels, establishing them as pivotal enabling technologies in precision and regenerative medicine. Full article

The paper analyses the effect of the solvent amount and nature on the structure and mechanical properties of hydrogels based on copolymers of 2-hydroxyethylmethacrylate (HEMA) with polyvinylpyrrolidone (PVP). The synthesis of pHEMA-gr-PVP copolymers was carried out by the copolymerization method in the presence of metal ions of variable oxidation states in solvents with various nature: water, dimethyl sulfoxide (DMSO), diethylene glycol (DEG), and cyclohexanol (HOCy). The structure of the copolymers was evaluated by the PVP grafting efficiency, its actual content in the copolymer, and the molecular weight between crosslinks (M_C). Taking the example of water, an increase in the solvent content up to 50 mass parts causes an increase in the efficiency of PVP grafting, which occurs due to enhanced macromolecule mobility through the dilution of the starting composition, hence the decrease in its viscosity. It was established that the nature of the solvent significantly affects the crosslinking density of the polymer network in the series H₂O, DEG, DMSO, HOCy, an increase in the M_C is observed causing a decrease in the hardness and elasticity of hydrogels and an increase in their water-retention capacity and swelling coefficient. The obtained results prove the possibility of targeted regulation within wide limits of the structure and properties of hydrogels based on pHEMA-gr-PVP copolymers through control of polymerization conditions (selection of the type and concentration of solvent). Full article