Search Results (1,471)

Monitoring trace nitrophenol pollutants in water has garnered considerable attention. A porous organic polymer-modified cellulose nanofiber membrane (COP-99@DCA) was fabricated via in situ growth of a porous organic polymer on an electrospun cellulose nanofiber membrane. The resulting brown COP-99@DCA composite possessed abundant functional groups, including C-F, C-O, and hydroxyl groups, and exhibited excellent thermal and chemical stability. Furthermore, when employed as a sorbent in dispersive solid-phase microextraction (d-SPME), COP-99@DCA efficiently enriched trace nitrophenols in water. Under optimal enrichment and desorption conditions, the enrichment efficiencies for five nitrophenol congeners ranged from 97.24% to 102.46%. Mechanistic investigations revealed that the efficient enrichment of trace nitrophenols by COP-99@DCA was primarily governed by hydrogen bonding, π-π stacking, and hydrophobic interactions. Coupled with solid-phase extraction (SPE) pre-treatment, high-performance liquid chromatography (HPLC) enabled the sensitive detection of trace nitrophenols. The established calibration curves exhibited favorable linearity, with low limits of quantitation (LOQs) ranging from 0.5 to 1 μg/L and low limits of detection (LODs) between 0.08 and 0.1 μg/L. Moreover, practical applications in real water samples confirmed the outstanding enrichment performance of COP-99@DCA. At spiked concentrations of 5 and 10 μg/L, the recovery rates were 85.35–113.55% and 92.17–110.46%, respectively. These results demonstrate the great potential of COP-99@DCA for practical water sample analysis. Collectively, these findings provide a novel strategy for the design of pre-treatment materials for the analysis of trace organic pollutants. Full article

Declining recovery factors from mature oil fields, coupled with the technical challenges of recovering residual oil under harsh reservoir conditions, necessitate the development of advanced enhanced oil recovery (EOR) techniques. While promising, chemical EOR often faces economic and technical hurdles in high-salinity, high-temperature environments where conventional polymers like hydrolyzed polyacrylamide (HPAM) degrade and fail. This study presents a comprehensive numerical investigation that addresses this critical industry challenge by applying a rigorously calibrated simulation framework to evaluate a novel hybrid EOR process that synergistically combines an ionic liquid (IL) with HPAM polymer. Utilizing core-flooding data from a prior study that employed the same Berea sandstone core plug and Saudi medium crude oil, supplemented by independently measured interfacial tension and contact angle data for the same chemical system, we built a core-scale model that was history-matched with RMSE < 2% OOIP. The calibrated polymer transport parameters—including a low adsorption capacity (~0.012 kg/kg-rock) and a high viscosity multiplier (4.5–5.0 at the injected concentration)—confirm favorable polymer propagation and effective in -situ mobility control. Using this validated model, we performed a systematic optimization of key process parameters, including IL slug size, HPAM concentration, salinity, temperature, and injection rate. Simulation results identify an optimal design: a 0.4 pore volume (PV) slug of IL (Ammoeng 102) reduces interfacial tension and shifts wettability toward water-wet, effectively mobilizing residual oil. This is followed by a tailored HPAM buffer in diluted formation brine (20% salinity, 500 ppm), which enhances recovery by up to 15% of the original oil in place (OOIP) over IL flooding alone by improving mobility control and enabling in-depth sweep. This excellent history match confirms the dual-displacement mechanism: microscopic oil mobilization by the IL, followed by macroscopic conformance improvement via HPAM-induced flow diversion. This integrated simulation-based approach not only validates the technical viability of the hybrid IL–HPAM flood but also delivers a predictive, field-scale-ready framework for heterogeneous reservoir systems. The work provides a robust strategy to unlock residual oil in such challenging reservoirs. Full article

Wellbore instability in shale formations represents a worldwide challenge in drilling engineering. The development of high-performance shale stabilizers is crucial for enhancing wellbore stability. A core–shell structured shale stabilizer, designated AAD-CaCO₃, was synthesized via inverse emulsion polymerization using acrylamide (AM), 2-acrylamido-2-methylpropanesulfonic acid (AMPS), and dimethyl diallyl ammonium chloride (DMDAAC) as monomers. Nano-CaCO₃ was generated in situ by reacting calcium chloride and sodium carbonate. Sodium bisulfite and ammonium persulfate were used as initiators. The product was characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and thermogravimetric analysis (TGA). Its effects on the rheological properties and filtration performance of a bentonite-based mud were evaluated. The stabilizer’s efficacy in inhibiting shale hydration swelling and dispersion was evaluated through linear swelling tests and shale rolling dispersion experiments, while its plugging performance was examined via a filtration loss test with a nanoporous membrane and spontaneous imbibition tests. The results indicated that AAD-CaCO₃ possesses a core–shell structure with the nano-CaCO₃ encapsulated by the polymer. It moderately improved the rheology of the bentonite-based mud and significantly reduced both the low-temperature and low-pressure (LTLP) filtration loss and the high-temperature and high-pressure (HTHP) filtration loss. AAD-CaCO₃ could be adsorbed onto shale surfaces through electrostatic attraction, resulting in substantially reduced clay hydration swelling and an increased shale cutting recovery rate. Effective plugging of micro-nanopores in shale was achieved, demonstrating a dual mechanism of chemical inhibition and physical plugging. Full article

The catalyst in methanol oxidation plays a pivotal role in direct fuel cell reaction. The aim of this work is to study the influence of polypyrrole polymer (PPy) added in the carbon Vulcan support for the methanol oxidation reaction. The catalytic active phase synthesized was nickel-based materials, which have been demonstrated to exhibit remarkable chemical stability in alkaline solutions. The metallic-active phase was supported at the PPy-carbon Vulcan matrix. PPy is a conductor polymer and the research of electric conduction in synergy with a carbon Vulcan and a Ni catalyst is scarcely reported. The morphology characterization of composite catalytic material was carried out by XRD, XPS, and TEM techniques. In turn, the catalytic activity of the composite is characterized by means of cyclic voltammetry (CV). Electrochemical impedance spectroscopy (EIS) showed the influence of PPy on the charge transfer resistance (Rch. t.). The results indicate that a decrease in the Rch. t. was associated with an increase in methanol oxidation; therefore, higher amounts of charge transfer is produced. Furthermore, the DEMS technique corroborates the EIS results, confirming elevated conversion toward oxidation products. In turn, the selectivity of the composite-catalytic support on the methanol oxidation was elucidated using in situ Raman spectroscopy. Full article

The discharge of dye-contaminated effluents from textile industries into water bodies poses a severe threat to aquatic ecosystems and human health. To address this challenge, cellulose and interpenetrating polymer network (IPN) hydrogels based on cellulose and poly(vinyl alcohol) (PVA) were developed via an in situ synthesis method. The cellulose solution was obtained by cold dissolving the polysaccharide in NaOH, then dissolving PVA. The IPN hydrogels were obtained by co-cross-linking the two polymers in an alkaline medium using ECH. To optimize the hydrogels, synthesis parameters like time (4–7 h), temperature (50–80 °C), and cross-linking ratio (ECH = 50–125% w/w) were varied. Different hydrogel compositions (Cel/PVA = 90/10 to 60/40 w/w) were tested for their absorption efficiency in removing Tubantin Blue (DB 78) dye under varying initial concentrations and temperatures. Hydrogels exhibit varying adsorption capacities for DB78, depending on their IPN composition, synthesis parameters, and dye concentration. Specifically, IPN adsorption capacity ranges from 8.8 to 38.1 mg DB78/g hydrogel (7.5–36.2% efficiency). At high effluent concentrations, IPN can reach a retention capacity of 217.7 mg/g, achieving a retention efficiency of 58.4%. Cellulose and cellulose/PVA IPN hydrogels show promise as sustainable adsorbents for treating dye-contaminated wastewater. Full article

Water quality observations are vital for effectively managing coastal resources and influencing decisions from emergency beach closures to aquaculture leasing agreements. This study focuses on deriving two water quality parameters—Chlorophyll a (Chl-a) and suspended particulate matter (SPM)—through the high-resolution multispectral imager (MSI) onboard the Sentinel 2A&B satellites, specifically for the Ningde coastal region, which is a crucial aquaculture hub in China. Since more than 90% of the signals captured by satellites are affected by atmospheric interference, it is crucial to apply a process called “atmospheric correction” (AC) to isolate the water contribution, known as water leaving reflectance, from the radiance measured at the top of the atmosphere. Our research assesses five published AC models and various algorithms designed to accurately estimate Chl-a and SPM from water leaving reflectance. We determine the most effective combination by comparing these findings against in situ data gathered from eleven locations in the Ningde coastal region (POLYMER-SOLID with lowest metric RMSLE (0.29), and MAE (1.68) and POLYMER-MDN with the lowest metric RMSLE (0.59), and MAE (0.56)). Our study underscores the importance of selecting locally validated AC models and algorithms for generating water quality products, as this enhances the utility of remote sensing data in monitoring water quality. Moreover, we conduct a spatiotemporal analysis of the water quality parameters from 2016 to 2021, revealing significant interannual variability that underlines the need for continuous monitoring and robust data analysis in coastal management efforts. Full article

Traditional flexible polyurethane (PU) foams frequently exhibit limited mechanical support and suboptimal moisture–heat regulation, which can compromise the microenvironmental comfort required for high-quality sleep. In this study, natural luffa fibers (LF) were incorporated as a microstructural modifier to simultaneously enhance the mechanical and moisture–heat regulation performance of PU foams. PU/LF composite foams with varying LF loadings were prepared via in situ polymerization, and their foaming kinetics, cellular morphology evolution, and physicochemical characteristics were systematically investigated. The results indicate that LF functions both as a reinforcing skeleton and as a heterogeneous nucleation site, thereby promoting more uniform bubble formation and controlled open-cell development. At an optimal loading of 4 wt%, the composite foam developed a highly interconnected porous architecture, leading to a 7.9% increase in tensile strength and improvements of 19.4% and 22.6% in moisture absorption and moisture dissipation rates, respectively, effectively alleviating the heat–moisture accumulation typically observed in unmodified PU foams. Ergonomic pillow prototypes fabricated from the optimized composite further exhibited enhanced pressure-relief performance, as evidenced by reduced peak cervical pressure and improved uniformity of contact-area distribution in human–pillow pressure mapping, together with an increased SAG factor, indicating improved load-bearing adaptability under physiological sleep postures. Collectively, these findings elucidate the microstructural regulatory role of biomass-derived luffa fibers within porous polymer matrices and provide a robust material basis for developing high-performance, sustainable, and ergonomically optimized sleep products. Full article

Severe reservoir heterogeneity in offshore oilfields often leads to dominant flow channels, high water cut, and low sweep efficiency during long-term water flooding. In this study, an in situ self-assembled composite foam system combining soft polymer particles with a low-interfacial-tension foaming agent was developed for profile control and enhanced oil recovery (EOR) in offshore heterogeneous reservoirs. The self-assembly characteristics and physicochemical properties of different particle systems were evaluated to optimize the composite foam structure. Static and dynamic experiments were conducted to assess foam stability, plugging performance, injectivity behavior, and oil displacement efficiency. Results show that the optimized composite foam undergoes in situ self-assembly under reservoir conditions, forming a stable particle–foam structure that enhances selective plugging and mobility control. Core flooding experiments demonstrate that the system increases oil recovery by up to 27.2% across a wide permeability range. Field application further confirms its effectiveness in regulating interlayer water absorption, stabilizing injection pressure, and reducing water cut. These results indicate that the proposed in situ self-assembled composite foam is a promising technique for integrated profile control and enhanced oil recovery in offshore heterogeneous reservoirs. Full article

Polymeric microfiltration membranes are among the most utilized pressure-driven membranes due to their excellent permeation flux, moderate removal efficiency, low operating pressure, low cost, as well as their potential for reusability and cleanability. Therefore, these membranes are used in different crucial sectors, including the water and wastewater, dairy, beverage, and pharmaceutical industries. However, well-known polymeric microfiltration membranes suffer from their poor hydrophilic properties, causing fouling phenomenon. A reduction in permeate flux, a shortened operational lifespan, and increased energy consumption are the primary negative consequences of membrane fouling. Over the years, a broad spectrum of studies has been performed to modify polymeric microfiltration membranes to improve their hydrophilic, transport, and antifouling characteristics. Despite extensive research, this issue remains a subject of ongoing discussion and scrutiny within the scientific community. This review article provides promising information about different physical and chemical modification methods—such as polymer blending, the incorporation of nanomaterials, surface coating, chemical crosslinking, in situ nanoparticle immobilization, and chemical surface functionalization—for polymeric microfiltration membranes. The physical and chemical modification methods are comparatively evaluated, highlighting their positive and negative aspects, supported by findings from recent investigations. Moreover, promising ideas and future-oriented techniques were proposed to obtain polymeric microfiltration membranes containing superior efficiency, extended service life, and mechanical strength. Full article

A new method of in situ hydrothermal reduction of graphene oxide (GO) to reduced graphene oxide (rGO) in polymer bulk was developed, which involves heating GO/polyacrylonitrile (PAN) composite membranes (0.5; 1.0; 2.0% w/w of GO/PAN) in the presence of water vapor at a temperature of 120 °C and a pressure of 0.2 MPa. As a result of this process, membranes containing rGO were obtained, as confirmed by FTIR, Raman, WAXS and TGA studies. The composite membranes obtained after hydrothermal reduction of GO to rGO (B60, C60, D60) were substantially different from the initial membranes containing unreduced GO (B0, C0, D0). The hydrothermal reduction process clearly influenced the physicochemical properties (reduction of apparent density, water sorption, and increase in the contact angle) and transport properties of the B60, C60, and D60 membranes (decrease in water flux by ~104 [dm³/m² × h] and even ~348 [dm³/m² × h] compared to the initial membranes). Full article

In this study, we report a reproducible in situ photochemical method for the simultaneous synthesis of metallic and hybrid metal/metal oxide nanoparticles (NPs) within a UV–curable polymer matrix. A series of epoxy diacrylate-based formulations (BEA) was prepared, consisting of Epoxy diacrylate, Di(Ethylene glycol)ethyl ether acrylate (DEGEEA), and Phenylbis (2,4,6-trimethylbenzoyl) phosphine oxide (BAPO), which served as a Type I photoinitiator. These formulations were designed to enable the simultaneous photopolymerization and photoreduction of metal precursors at various Ag⁺/Co²⁺ ratios, resulting in nanocomposites containing in situ-formed Ag NPs, cobalt oxide NPs, and hybrid Ag–Co₃O₄ nanostructures. The photochemical, magnetic, and dielectric properties of the resulting nanocomposites were evaluated in comparison with those of the pure polymer using UV–Vis and Fourier Transform Infrared Spectroscopy (FT-IR), Photo-Differential Scanning Calorimetry (Photo-DSC), Thermogravimetric Analysis (TGA), Scanning Electron Microscopy (SEM), X-Ray Diffraction (XRD), Impedance Analysis, and Vibrating Sample Magnetometry (VSM). Photo-DSC studies revealed that the highest conversion values were obtained for the BEA-Ag₁Co₁, BEA-Co, and BEA-Ag₁Co₂ samples, demonstrating that the presence of Co₃O₄ NPs enhances polymerization efficiency because of cobalt species participating in redox-assisted radical generation under UV irradiation, increasing the number of initiating radicals and leading to faster curing and higher final conversion. On the other hand, the Ag NPs, due to the SPR band formation at around 400 nm, compete with photoinitiator absorbance and result in a gradual decrease in conversion values. Crystal structures of the NPs were confirmed by XRD analyses. The dielectric and magnetic characteristics of the nanocomposites suggest potential applicability in energy-storage systems, electromagnetic interference mitigation, radar-absorbing materials, and related multifunctional electronic applications. Full article

Conductive polymers (CPs), such as polypyrrole (PPy), have shown promising properties for use as electro-responsive bioactive scaffolds for tissue regeneration. PPy can be synthesized by chemical electrosynthesis and doped with biomolecules such as hyaluronic acid (HA). Taking advantage of the electrochemical synthesis versatility, nanofibers for surface-modified indium tin oxide (ITO) electrodes can be used as templates to produce tridimensional HA-doped PPy scaffolds. In this study, polyvinyl alcohol/chitosan (PVA/CTS) electrospun nanofibers deposited on ITO electrodes were used as a 3D template for the in situ electrosynthesis of HA-doped PPy to produce a bioactive scaffold for tissue engineering. The final material gathers the advantages of each biopolymer, the porous morphology of the nanofiber, and the conductivity of the electrosynthetized polymer. Furthermore, the biological activity of the NF-PVA/CTS@PPy:HA composite was evaluated in NIH-3T3 fibroblasts by MTT, resulting in a cell viability of 146 ± 40% and wound-healing capacity of 97 ± 1.9% at 24 h of culture. Full article

The optical properties, electronic structure and morphology of thin films of the polymer donor PTB7-Th blended with either the fullerene acceptor PC70BM or the non-fullerene acceptor ZY-4Cl were systematically investigated to evaluate their annealing-induced evolution. Thin films were characterized using UV–Vis–NIR absorption spectroscopy, spectroscopic ellipsometry, ATR-FTIR spectroscopy, atomic force microscopy (AFM), and nano-IR analysis. In situ stepwise thermal annealing revealed distinct changes in absorption edge parameters, indicating thermally induced modifications in the electronic structure of the blend films. Ellipsometric analysis showed that elevated temperatures significantly affect the refractive index and extinction coefficient spectra. AFM measurements demonstrated markedly different surface morphology evolution for the two blend systems, with pronounced needle-shaped crystallites formation observed in PTB7-Th:ZY-4Cl films after annealing at 100 °C. Nano-IR characterization identified these crystallites as predominantly PTB7-Th, indicating phase separation driven by thermal treatment. The combined optical and structural results reveal distinct annealing-induced changes in the blend. Finally, BHJ solar cells, based on PTB7-Th:PC70BM and PTB7-Th:ZY-4Cl active layers, were fabricated, and their photovoltaic response was demonstrated. Full article

In this study, we aimed to develop a high-performance, anti-fouling ultrafiltration membrane by integrating photocatalytic and Fenton-like functions into a polymer matrix, in order to address the critical challenge of membrane fouling and achieve simultaneous separation and degradation of organic pollutants. To this end, a novel Fe-V_O-TiO₂-embedded polyethersulfone (PES) composite membrane was designed and fabricated using a facile phase inversion method. The key innovation lies in the incorporation of Fe-V_O-TiO₂ nanoparticles containing abundant bulk-phase single-electron-trapped oxygen vacancies, which not only modulate membrane morphology and hydrophilicity but also enable sustained generation of reactive oxygen species for the pollutant degradation under light irradiation and H₂O₂. The optimized Fe-V_O-TiO₂-PES-0.04 membrane exhibited a significantly enhanced pure water flux of 222.6 L·m⁻²·h⁻¹ (2.2 times higher than the pure PES membrane) while maintaining a high bovine serum albumin (BSA) retention of 93% and an improved hydrophilic surface. More importantly, the membrane demonstrated efficient and stable synergistic Photocatalytic-Fenton activity, achieving 82% degradation of norfloxacin (NOR) and retaining 75% efficiency after eight consecutive cycles. A key finding is the membrane’s Photocatalytic-Fenton-assisted self-cleaning capability, with an 80% flux recovery after methylene blue (MB) fouling, which was attributed to in situ reactive oxygen species (·OH) generation (verified by ESR). This work provides a feasible strategy for designing multifunctional membranes with enhanced antifouling performance and extended service life through built-in catalytic self-cleaning. Full article

This study investigates water-based gel and gel-like cleaning treatments on Superficie 553, an oil painting on canvas by Giuseppe Capogrossi, using portable NMR to assess their impact. The objective was to evaluate the effects of four cleaning systems composed of a buffer solution released in free form and combined with xanthan gum, a cross-linked silicone polymer gel, and an agar gel matrix. Two distinct NMR experiments were conducted. The first involved the acquisition of ¹H depth profiles to detect the distribution of the cleaning solution within the painted layer and the thickness variations resulting from cleaning procedures. The second employed the acquisition of relaxation times, facilitating the investigation of molecular mobility within the organic components of the paint layer. NMR results indicated that the agar gel system caused negligible structural changes, whereas the silicone gel induced rigidification, and the other systems permanently increased molecular mobility. These measurements provided insights into alterations in the dynamic behavior of the polymerized oil. A key strength of this investigation lies in the direct application of diagnostic methods on Superficie 553, made possible by the non-invasive nature and portability of the NMR-MOUSE system. Additionally, portable FTIR was used to detect residues and obtain chemical information, confirming that the silicone gel left detectable residues and identifying the agar gel as the most conservative cleaning method. This enabled in situ analysis of the original artwork without sampling or relocation—a crucial advantage given the difficulty of replicating the complex physicochemical conditions of historical paint surfaces under laboratory constraints. Such real-time, on-site monitoring ensured an authentic evaluation of the treatment effects, preserving the integrity of the artwork throughout the conservation process. Full article