Search Results (593)

This review surveys recent advances and emerging prospects in phase-transfer catalysis (PTC) for fuel desulfurization. In response to increasingly stringent environmental regulations, the removal of sulfur from transportation fuels has become imperative for curbing SO_x emissions. Conventional hydrodesulfurization (HDS) operates under severe temperature–pressure conditions and displays limited efficacy toward sterically hindered thiophenic compounds, motivating the exploration of non-hydrogen routes such as oxidative desulfurization (ODS). Within ODS, PTC offers distinctive benefits by shuttling reactants across immiscible phases, thereby enhancing reaction rates and selectivity. In particular, PTC enables efficient migration of organosulfur substrates from the hydrocarbon matrix into an aqueous phase where they are oxidized and subsequently extracted. The review first summarizes the deployment of classic PTC systems—quaternary ammonium salts, crown ethers, and related agents—in ODS operations and then delineates the underlying phase-transfer mechanisms, encompassing reaction-controlled, thermally triggered, photo-responsive, and pH-sensitive cycles. Attention is next directed to a new generation of catalysts, including quaternary-ammonium polyoxometalates, imidazolium-substituted polyoxometalates, and ionic-liquid-based hybrids. Their tailored architectures, catalytic performance, and mechanistic attributes are analyzed comprehensively. By incorporating multifunctional supports or rational structural modifications, these systems deliver superior desulfurization efficiency, product selectivity, and recyclability. Despite such progress, commercial deployment is hindered by the following outstanding issues: long-term catalyst durability, continuous-flow reactor design, and full life-cycle cost optimization. Future research should, therefore, focus on elucidating structure–performance relationships, translating batch protocols into robust continuous processes, and performing rigorous environmental and techno-economic assessments to accelerate the industrial adoption of PTC-enabled desulfurization. Full article

Polymer blending techniques enable the tailoring of desired properties for diverse applications. This study investigates the effect of PMMA content on the thermomechanical, chemical, mechanical, and fatigue life properties of PC/ABS/PMMA (polycarbonate/acrylonitrile–butadiene–styrene/polymethylmethacrylate) ternary blends. To this end, various characterization analyses, as well as tensile, impact, and fatigue tests, were conducted. The results indicate that the viscoelastic modulus improves with increasing PMMA content in ternary blends. Furthermore, PC/ABS/PMMA blends exhibit an immiscible phase morphology. The elastic modulus, yield strength, and tensile strength increase with higher PMMA content, while the elongation at break and impact strength decrease. Fatigue strength and the fatigue strength exponent were found to vary nonlinearly with PMMA content. Compared to PC/ABS blends, PC/ABS/PMMA blends demonstrated improvements of approximately 12% to 58% and 26% to 117% in hysteresis energy and the dynamic elastic modulus, respectively. Additionally, fatigue life cycles improved by 5% to 11% at low stress amplitudes. This experimental study provides comprehensive insight into the complex interplay among the chemical, thermomechanical, mechanical, and fatigue properties of ternary PC/ABS/PMMA blends, highlighting their potential for applications requiring balanced or tailored structural and material characteristics. Full article

Electrochemical sensors, particularly those based on ion transfer at the interface between two immiscible electrolyte solutions (ITIES), offer significant advantages such as high selectivity, ease of fabrication, and cost effectiveness for toxic metal ion detection. However, distinguishing between cyclic voltammograms (CVs) of analytes with closely spaced half-wave potentials, such as Cd²⁺ and Cu²⁺, remains a challenge, especially for non-expert users. In this work, we present a novel methodology that integrates advanced artificial intelligence (AI) models with ITIES-based sensing to automate and enhance metal ion detection. Our approach first employed a convolutional neural network to classify CVs as either ideal or faulty with an accuracy exceeding 95 percent. Ideal CVs were then further analyzed for metal ion identification, achieving a classification accuracy of 99.15 percent between Cd²⁺ and Cu²⁺ responses. Following classification, an artificial neural network was used to quantitatively predict metal ion concentrations, yielding low mean absolute errors of 0.0158 for Cd²⁺ and 0.0127 for Cu²⁺. This integrated AI–ITIES system not only provides a scientific methodology for differentiating analyte responses based on electrochemical signatures but also substantially lowers the expertise barrier for sensor signal interpretation. To our knowledge, this is the first report of the AI-assisted differentiation and quantification of metal ions from ITIES-based CVs, establishing a robust framework for the future development of user-friendly, automated electrochemical sensing platforms for environmental and biological applications. Full article

Solid polymer electrolytes (SPEs) have garnered significant attention due to their potential in all-solid-state batteries (ASSBs). However, adoption remains constrained by challenges such as low thermal stability and limited ionic conductivity. Here, we report on an electrospun (PAN/PEO)- conductive salt (LiBF₄) system, where the influence of varying polyacrylonitrile (PAN) and polyethylene oxide (PEO) ratios, along with different plasticizer concentrations, is evaluated. Notably, the 50:50 PAN/PEO sample exhibited the highest ionic conductivity, reaching 1∙10⁻² S/cm at 55 °C. This system also balanced conductivity and processability. Succinonitrile (SN) significantly influenced the morphology and conductivity. Samples with increased SN content showed enhanced capacity in symmetrical cells, achieving ~140 mAs/cm² for an 18:9:1 polymer (PAN/PEO):SN:conductive salt (LiBF₄) composition. The enhanced lithium-ion conductivity of the electrospun blend is attributed to the deliberate use of an unmixable PAN–PEO system. Their immiscibility creates well-defined interfacial regions within fibers, acting as efficient lithium-ion pathways. These findings support electrospun polymer blends as promising candidates for high-performance SPEs for ASSB development. Full article

Many granitic enclaves are developed in the volcanic channel of the Xiangshan volcanic basin. To explore their genesis, this study examined the petrography, geochemistry, LA-ICP-MS zircon U–Pb chronology, and zircon Hf isotopes of the granitic enclaves and compared them with the porphyroclastic lavas. In general, the granitic enclaves and porphyroclastic lavas have similar structures, and the rock-forming minerals and accessory minerals have relatively close compositions. In terms of rock geochemical characteristics, the granitic enclaves are richer in silicon and alkalis but have lower abundances of aluminum, magnesium, iron, and calcium than the porphyroclastic lavas. Rb, Th, K, Sm, and other elements are more enriched, whereas Ba, Ti, Nb, P, and other elements are more depleted. The granitic enclaves have lower rare earth contents (195.53 × 10⁻⁶–271.06 × 10⁻⁶) than the porphyroclastic lavas (246.67 × 10⁻⁶–314.27 × 10⁻⁶). The rare earth element distribution curves of the two are generally consistent, both right-leaning, and enriched with light rare earth patterns. The weighted average zircon U–Pb ages of two granitic enclave samples were 135.45 ± 0.54 Ma (MSWD = 0.62, n = 17) and 135.81 ± 0.60 Ma (MSWD = 0.40, n = 20), respectively, which are consistent with the weighted average age of a single porphyroclastic lava sample of 134.01 ± 0.53 Ma (MSWD = 2.0, n = 20). The zircons of the two kinds of rocks crystallize at almost the same temperature. The consistent trend of the rare earth element distribution curve of zircons in the granitic enclaves and the porphyroclastic lava samples indicates that the zircons of the two samples were formed in the same stage. The formation process of granitic enclaves may be that the lower crustal melt is induced to rise, and the crystallization differentiation occurs in the magma reservoir and is stored in the form of crystal mush, forming a shallow crystal mush reservoir. The crystal mush reservoir is composed of a large number of rock-forming minerals such as quartz, feldspar, and biotite, as well as accessory mineral crystals such as zircon and flowable intergranular melt. In the later stage of magma high evolution, a small and short-time magmatic activity caused a large amount of crystalline granitic crystal mush to pour into the volcanic pipeline. In the closed system of volcanic pipeline, the pressure and temperature decreased rapidly, and the supercooling degree increased, and the immiscibility finally formed pale granitic enclaves. Full article

Coacervate is a form of liquid–liquid phase separation (LLPS) in which a solution containing one or more charged components spontaneously separates into two immiscible liquid phases. Due to their ability to mimic membraneless cellular environments and their high biocompatibility, coacervates have found broad applications across various fields of life sciences. This review provides a comprehensive overview of recent advances in biomolecule-based coacervation for biotechnological and biomedical applications. Encapsulation via biomolecule-based coacervation enables high encapsulation efficiency, enhanced stability, and the sustained release of cargos. In the field of tissue engineering, coacervates not only support cell adhesion and proliferation but also serve as printable bioinks with tunable rheological properties for 3D bioprinting. Moreover, biomolecule-based coacervates have been utilized to mimic membraneless organelles, serving as experimental models to understand the origin of life or investigate the mechanisms of biochemical compartmentalization. This review discusses the mechanisms of coacervation induced by various types of biomolecules, evaluates their respective advantages and limitations in applied contexts, and outlines future research directions. Given their modularity and biocompatibility, biomolecule-based coacervates are expected to play a pivotal role in next-generation therapeutic development and the construction of controlled tissue microenvironments, especially when integrated with emerging technologies. Full article

The increasing accumulation of plastic waste—especially from packaging and post-consumer sources—calls for the development of sustainable recycling strategies. Due to the challenges associated with sorting mixed waste, directly processing waste streams offers a practical approach. Polyethylene terephthalate (PET) and high-density polyethylene (HDPE) are common consumer plastics, but they are difficult to recycle together due to immiscibility and degradation. In mixed waste, recycled HDPE (r-HDPE) often contaminates the recycled PET (r-PET) stream. Additive manufacturing (AM) offers a promising solution to upcycle these mixed polymers into functional products with minimal waste. This study investigates the processing and characterization of r-PET/r-HDPE blends for AM, focusing on the role of compatibilizers in enhancing their properties. Blends were melt-compounded using a twin-screw extruder to improve dispersion, followed by direct pellet-based 3D printing. A compatibilizer (0–7 php) was incorporated to improve miscibility. Rheological testing showed that the 5 php compatibilizer optimized viscosity and elasticity, ensuring smoother extrusion. Thermal analysis revealed a 30 °C increase in crystallization temperature and a shift in decomposition temperature from 370 °C to 400 °C, indicating improved thermal stability. Mechanical testing showed a tensile strength of 35 MPa and 17% elongation at break at optimal loading. Scanning electron microscopy (SEM) confirmed reduced phase separation and improved morphology. This work demonstrates that properly compatibilized r-PET/r-HDPE blends enable sustainable 3D printing without requiring polymer separation. The results highlight a viable path for the conversion of plastic waste into high-value, customizable components, contributing to landfill reduction and advancing circular economy practices in polymer manufacturing. Full article

Residual oil saturation in reservoirs is primarily influenced by viscous and capillary forces, with interfacial tension (IFT) being a critical factor in fluid distribution due to capillary pressure. Adjusting IFT is essential for enhancing oil recovery, particularly in waterflooding, which is the most common secondary recovery technique after primary production. The salinity of injected water directly affects the IFT between crude oil and brine, making it a crucial factor in optimizing recovery. However, limited studies have examined IFT using live oil samples under actual reservoir conditions. In this study, a high-pressure, high-temperature (HPHT) drop shape analyzer was used to measure the IFT between live oil and brine under reservoir conditions. Five live oil samples and two sodium chloride (NaCl) brine concentrations (30,000 and 100,000 ppm) were tested at a reservoir temperature of 180 °F. Measurements were conducted above the bubble points of the oils, replicating undersaturated reservoir conditions. The results revealed that the impact of pressure on IFT was more complex than that of salinity. IFT generally decreased with increasing pressure but showed mixed behavior across different samples. Conversely, IFT consistently increased with higher salinity. These findings enhance the understanding of IFT behavior under reservoir conditions, supporting improved reservoir simulations and oil recovery strategies. Full article

Natural deep eutectic solvents (NaDESs) are emerging solvents for their yield when used for extraction of different molecules, including polyphenols. NaDESs are a cutting-edge technology that offers numerous advantages, including cheap cost, safety, effectiveness and environmental friendliness. However, due to NaDES’ high boiling point, the recovery and separation of compounds after the extraction is the bottleneck of the process. In this work, two affordable methods were tested for the recovery of phenolic compounds from three binary NaDESs (composed of choline chloride mixed separately with lactic acid, tartaric acid or glycerol as hydrogen bond donors): the antisolvent and the liquid–liquid extraction methods. The former was assessed by diluting the extracts with different aliquots of water, employed as antisolvent, which was ineffective. For the liquid–liquid extraction method, ethyl acetate (EtOAc), acetonitrile (ACN), 2-chlorobutane (2-CB) and 2-methyltetrahydrofuran (2-MeTHF) were compared. Except for ACN, all solvents were perfectly immiscible with the three NaDESs, forming biphasic systems that were analyzed by colorimetric assays and HPLC/MS. 2-MeTHF applied on a 10-fold water dilution of the NaDES extract reached recovery percentages higher than 90% for most of the non-anthocyanin phenols and good recovery (up to 80%) for some anthocyanins. 2-MeTHF appears to be the first known solvent capable of extracting anthocyanins from NaDESs. Finally, a two-step liquid–liquid extraction performed firstly with EtOAc and subsequently with 2-MeTHF is proposed for the separation of different phenolic fractions. Full article

This study investigates pegmatites with exceptionally rare mineralogical and chemical signatures, hosted by the 1.8 Ga peralkaline albite-enriched granite, which corresponds to the renowned Madeira Sn-Nb-Ta-F (REE, Th, U) deposit in Pitinga, Brazil. Four distinct pegmatite types are identified: border pegmatites, pegmatitic albite-enriched granite, miarolitic pegmatite, and pegmatite veins. The host rock itself has served as the source for the fluids that gave rise to all these pegmatites. Their mineral assemblages mirror the rare-metal-rich paragenesis of the host rock, including pyrochlore, cassiterite, riebeckite, polylithionite, zircon, thorite, xenotime, gagarinite-(Y), genthelvite, and cryolite. These pegmatites formed at the same crustal level as the host granite and record a progressive magmatic–hydrothermal evolution driven by various physicochemical processes, including tectonic decompressing, extreme fractionation, melt–melt immiscibility, and internal fluid exsolution. Border pegmatites crystallized early from a F-poor, K-Ca-Sr-Zr-Y-HREE-rich fluid exsolved during solidification of the pluton’s border and were emplaced in contraction fractures between the pluton and country rocks. Continued crystallization toward the pluton’s core produced a highly fractionated melt enriched in Sn, Nb, Ta, Rb, HREE, U, Th, and other HFSE, forming pegmatitic albite-enriched granite within centimetric fractures. A subsequent pressure quench—likely induced by reverse faulting—triggered the separation of a supercritical melt, further enriched in rare metals, which migrated into fractures and cavities to form amphibole-rich pegmatite veins and miarolitic pegmatites. A key process in this evolution was melt–melt immiscibility, which led to the partitioning of alkalis between two phases: a K-F-rich aluminosilicate melt (low in H₂O), enriched in Y, Li, Be, and Zn; and a Na-F-rich aqueous melt (low in SiO₂). These immiscible melts crystallized polylithionite-rich and cryolite-rich pegmatite veins, respectively. The magmatic–hydrothermal transition occurred independently in each pegmatite body upon H₂O saturation, with the hydrothermal fluid composition controlled by the local degree of melt fractionation. These highly F-rich exsolved fluids caused intense autometasomatic alteration and secondary mineralization. The exceptional F content (up to 35 wt.% F in pegmatite veins), played a central role in concentrating strategic and critical metals such as Nb, Ta, REEs (notably HREE), Li, and Be. These findings establish the Madeira system as a reference for rare-metal magmatic–hydrothermal evolution in peralkaline granites. Full article

CO₂ flooding technology has been established as a key technique that is both economically viable and environmentally sustainable, achieving enhanced oil recovery (EOR) while advancing CCUS objectives. This study addresses the challenge of optimizing CO₂ flooding well patterns in tight oil reservoirs through a geological–engineering integrated approach. A semi-analytical model incorporating startup pressure gradients and miscible/immiscible two-phase flow was developed to dynamically adjust injection intensity. An effective driving coefficient model considering reservoir heterogeneity and fracture orientation was proposed to determine well pattern boundaries. Field data from Blocks A and B were used to validate the models, with the results indicating optimal injection intensities of 0.39 t/d/m and 0.63 t/d/m, respectively. Numerical simulations confirmed that inverted five-spot patterns with well spacings of 240 m (Block A) and 260 m (Block B) achieved the highest incremental oil production (3621.6 t/well and 4213.1 t/well) while reducing the gas channeling risk by 35–47%. The proposed methodology provides a robust framework for enhancing recovery efficiency in low-permeability reservoirs under varying geological conditions. Full article

The Cuyu gold deposit in central Jilin Province in Northeast China is located in the eastern segment of the northern margin of the North China Craton (NCC), as well as the eastern segment of the Xing’an–Mongolian Orogenic Belt (XMOB). Gold ore-bodies are controlled by NW-trending faults and mainly occur in late Hercynian granodiorite. The mineralization process in the Cuyu deposit can be divided into three stages: quartz + coarse grained arsenopyrite + pyrite (stage I), quartz + sericite + pyrite + arsenopyrite + electrum + chalcopyrite + sphalerite (stage II), and quartz + calcite ± pyrite (stage III). Stage II is the most important for gold mineralization. We conducted analyses including petrography, microthermometry, laser Raman spectroscopy of fluid inclusions, and H–O–S–Pb isotopic analysis to elucidate the mineralization processes in the Cuyu deposit. Five types of primary fluid inclusions (FIs) are present in the hydrothermal quartz and calcite grains of the ore: liquid-rich two-phase aqueous fluid inclusions (L-type), vapor-rich two-phase aqueous fluid inclusions (V-type), CO₂-bearing two- or three-phase inclusions (C1-type), CO₂-rich two- or three-phase inclusions (C2-type), and pure CO₂ mono-phase inclusions (C3-type). From stages I to III, the fluid inclusion assemblages changed from L-, C2-, and C3-types to L-, V-, C1-, C2-, and C3-types and, finally, to L-types only. The corresponding homogenization temperatures for stages I to III were 242–326 °C, 202–298 °C, and 106–188 °C, and the salinities were 4.69–9.73, 1.63–7.30, and 1.39–3.53 wt.% NaCl equiv., respectively. The ore-forming fluid system evolved from a NaCl-H₂O-CO₂ ± CH₄ ± H₂S fluid system in stage I and II with immiscible characteristics to a homogeneous NaC-H₂O fluid system in stage III. Microthermometric data for stages I to III show a decreasing trend in homogenization temperatures and salinities. The mineral assemblages, fluid inclusions, and H–O–S–Pb isotopes indicate that the initial ore-forming fluids of stage I were exsolved from diorite porphyrite and characterized by a high temperature and low salinity. The addition of meteoric water in large quantities led to decreases in temperature and pressure, resulting in a NaCl-H₂O-CO₂ ± CH₄ ± H₂S fluid system with significant immiscibility in stage II, facilitating the deposition of gold and associated polymetallic sulfides. The Cuyu gold deposit has a similar ore genesis to those of gold deposits in the Jiapigou–Haigou gold belt (JHGB) of southeastern Jilin Province indicating potential for gold prospecting in the northwest-trending seam of the JHGB. Full article

Miniaturization and reliable, real-time, non-invasive monitoring are essential for investigating microfluidic processes in Lab-on-a-Chip (LoC) systems. Progress in this field is driven by three complementary approaches: analytical modeling, computational fluid dynamics (CFD) simulations, and experimental validation techniques. In this study, we present an on-chip experimental method for estimating the slug-flow velocity in microchannels through in situ optical monitoring. Slug flow involving two immiscible fluids was investigated under both liquid–liquid and gas–liquid conditions via an extensive experimental campaign. The measured velocities were used to determine the slug length and key dimensionless parameters, including the Reynolds number and Capillary number. A comparison with analytical models and CFD simulations revealed significant discrepancies, particularly in gas–liquid flows. These differences are mainly attributed to factors such as gas compressibility, pressure fluctuations, the presence of a liquid film, and leakage flows, all of which substantially affect flow dynamics. Notably, the percentage error in liquid–liquid flows was lower than that in gas–liquid flows, largely due to the incompressibility assumption inherent in the model. The high-frequency monitoring capability of the proposed method enables in situ mapping of evolving multiphase structures, offering valuable insights into slug-flow dynamics and transient phenomena that are often difficult to capture using conventional measurement techniques. Full article

The lattice Boltzmann method (LBM) is widely applied to model the pore-scale two-phase flow of immiscible fluids through porous media, and one common variant of the LBM is the color gradient method (CGM). However, in the literature, many competing algorithms have been proposed for accomplishing different steps in the CGM. Therefore, this paper is the first in a series that aims to critically review and evaluate different algorithms and methodologies that have been proposed for use in the CGM. Specifically, in this paper, we (1) provide a brief introduction to the LBM and CGM that enables and facilitates consideration of more sophisticated topics subsequently; (2) compare three methods for modeling the behavior of fluids of moderately different viscosities; (3) compare two methods for calculating the color gradient; and (4) compare two methods for modeling external forces or accelerations acting upon the fluids of interest. These topics are selected for the first paper in the series because proper selection of these algorithms is necessary and sufficient to perform two common “benchmark” simulations, namely bubble tests and layered Poiseuille flow. Future papers in the series will build upon these topics, considering more challenging conditions or phenomena. By systematically reviewing key aspects, features, capabilities, and limitations of the CGM, this series of papers will extend our collective ability to apply the method to a variety of important fluid flow problems in geosciences and engineering. Full article

The immiscibility of thermoplastic starch (TPS) and polybutylene succinate (PBS) complicates the thermal processing of these materials. This study provides the first comparative assessment of two compatibilizers with differing reaction mechanisms, Joncryl^® ADR 4468 and epoxidized linseed oil (ELO), for the optimization of biobased TPS/PBS blends. A total of 13 batches, varying in compatibilizer and blend composition, were processed via hot melt extrusion and injection molding to produce pellets. Blends were analyzed using tensile and impact testing, differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FTIR), rheology, and scanning electron microscopy (SEM). The findings suggest that both compatibilizers can improve the compatibility of these blends, as evidenced by higher glass transition temperatures (T_g) compared to the reference batch (100-0-N/A). Joncryl^® ADR 4468 batches exhibit superior tensile strength and Young’s moduli, while ELO batches demonstrate greater elongation at break. The enhanced processability observed in Joncryl^® ADR 4468 is attributed to the increased polymer chain entanglement and molecular weight, whereas ELO facilitates greater chain mobility due to its plasticizing effect. These differences arise from the distinct mechanisms of action: Joncryl^® ADR 4468 promotes chain extension and crosslinking, whereas ELO mainly enhances flexibility through plasticization. Overall, this study provides a comparative assessment of these compatibilizers in TPS/PBS blends, laying the groundwork for future investigations into optimizing compatibilizer concentration and blend composition. Full article