Search Results (533)

High-entropy perovskite oxides attract considerable attention due to their outstanding properties and extensive applications. In this work, the lattice distortion and the mechanical, thermal and electronic structure properties of high-entropy (Ca_0.2Sr_0.2Ba_0.2La_0.2Pb_0.2)TiO₃ (CSBLPT) are investigated through first-principles calculations. The results suggest that the influence of O atoms on lattice distortion is predominant, and the effect of overall A-site atoms plays a distinctly greater role than that of the B-site atoms. The mechanical results show that the high-entropy CSBLPT has a lower Young’s modulus and higher fracture toughness than ternary SrTiO₃. The Debye temperature also indirectly indicates that the thermal expansion coefficient of the studied high-entropy perovskite is greater than that of SrTiO₃. As for thermal conductivity, the obtained result of CSBLPT is also appreciably lower than that of SrTiO₃, and the lowest thermal conductivity is along the [100] direction. The Fermi level of high-entropy CSBLPT is transferred to the conduction band, exhibiting a degenerate n-type semiconductor behavior with metallic-like characteristics, and the Bader charge values are also related to the local lattice distortion, which may cause differences in thermomechanical properties between high-entropy CSBLPT and SrTiO₃. Above all, high-entropy CSBLPT is a preferable TBC material with excellent performance under working conditions compared to SrTiO₃. Full article

The Akseki–Kuyucak bauxite deposits, located in the Western Taurus Belt in southwestern Türkiye, represent karst-type bauxite mineralization derived from carbonate platform phases. This work integrates field observations, X-ray diffraction (XRD) analysis, and extensive geochemical data, including major, trace, and rare earth elements (REEs), to clarify the mineralogical characteristics, geochemical processes, and genetic implications of the deposits. Field and petrographic investigations indicate that the bauxite deposits occur as irregular fills and lens-shaped formations on paleokarstic surfaces of carbonate substrates. The XRD examination reveals that the major minerals in the bauxite samples are boehmite, hematite, and anatase, with some samples exhibiting a predominance of calcite, indicating a strong genetic relationship between the ore bodies and the carbonate host rocks. Major oxide analysis reveals a distinct compositional disparity between bauxitic and carbonate-dominated materials: bauxitic samples exhibit elevated Al₂O₃ and Fe₂O₃ levels, with reduced SiO₂ and CaO concentrations. In contrast, carbonate-rich samples show higher CaO and loss-on-ignition values. Ternary discrimination diagrams categorize most bauxitic samples into the ferritic bauxite and robust lateritization domains, indicating substantial weathering and residual enrichment processes. The trace element and REE studies reveal ΣLREE values ranging from 22.3 to 240.2 ppm, with a right-skewed distribution indicating heterogeneous enrichment. Correlation studies indicate that ΣLREE has a positive correlation with SiO₂ and K₂O, suggesting that the enrichment of REEs is more closely associated with silicate/clay minerals than with iron oxide phases. Furthermore, spider diagrams and the study of immobile components emphasize the significance of residual concentration processes in bauxitization. In contrast, modest TiO₂ levels indicate a composite source derived from both insoluble carbonate remnants and detrital siliciclastic materials. In summary, the Akseki–Kuyucak deposits are categorized as intricate karst bauxite systems, characterized by significant lateritization, regulated accumulation governed by paleokarst characteristics, and a complex geochemical evolution. The results demonstrate that integrating mineralogical, geochemical, and statistical methods provides a thorough framework for evaluating REE behaviors and the effects of source-related factors in karst bauxite deposits. Full article

To overcome the inherent drawbacks of poly(propylene carbonate) (PPC), such as poor thermal stability, low mechanical strength, and high surface energy, this study introduced, for the first time, 1,1,1-trifluoro-2,3-epoxypropane (TF-PO) as a third monomer into the metal-free TEB/PPNCl catalytic system for the terpolymerization with carbon dioxide (CO₂) and propylene oxide (PO), successfully synthesizing a series of fluorinated PPC (PPCF). The optimal polymerization conditions ($60 °C$, 2.0 MPa, 12 h, n(PO):n(TF-PO) = 100:4) were determined through systematic optimization. Comprehensive structural characterization (FT-IR, NMR, XPS) confirmed the successful incorporation of TF-PO into the polymer backbone. Property evaluation revealed that the PPCF materials exhibited substantial improvements in thermal stability, mechanical strength, hydrophobicity, and dielectric properties compared to unmodified PPC. The optimal sample, PPCF4, achieved a $5\%$ weight-loss temperature ($T_{d,-5\%}$) of $242 °C$, a glass transition temperature ($T_{\mathrm{g}}$) of $42 °C$, a tensile strength of 21.5 MPa, and a Young modulus of 296 MPa. With a $5\%$ TF-PO feed ratio, the material’s water contact angle increased to 102°, and its dielectric constant reached 6.01 at ${10}^4$ Hz. Furthermore, density functional theory (DFT) calculations elucidated the Lewis acidity of the TEB catalyst and the reactive sites of the monomers, leading to a proposed mechanism for the ternary alternating copolymerization. This work provides an effective synthetic strategy and theoretical foundation for preparing high-performance and functionalized PPC materials through molecular structure design. Full article

With the rapid development of electronic devices and wireless communication systems, electromagnetic interference pollution has become a critical concern, driving the urgent demand for high-performance, lightweight, and flexible electromagnetic interference (EMI) shielding materials. To endow fabrics with excellent electromagnetic shielding, a Fe₃O₄/Ag/RGO ternary nanocomposite-coated cotton fabric for electrical conductivity and EMI shielding application was developed. The cotton fabric pretreated with dopamine was coated with graphene oxide (GO), followed by silver nanoparticles (Ag) via a microwave-assisted chemical reduction method, and Ag/reduced graphene oxide (RGO)-coated cotton. Subsequently, nano-ferroferric oxide was deposited on Ag/RGO-coated cotton fabric using a coprecipitation method. The results show that the surface resistance of Fe₃O₄/Ag/RGO-coated cotton fabric arrives at 1.68 Ω/sq, demonstrating excellent electrically conductive performance. Fe₃O₄/Ag/RGO-coated cotton fabric demonstrates outstanding electromagnetic shielding performance, with SE values exceeding 45 dB across the entire 1–18 GHz range. The flexibility and superior electromagnetic shielding performance of Fe₃O₄/Ag/RGO-coated cotton fabric render it a promising candidate for applications in wearable electronics, aerospace, advanced protective systems, and military protective clothing. Full article

The rational design of oxygen carriers (OCs) is critical for enhancing biomass chemical looping gasification (BCLG) performance. This work systematically investigated the effects of different supports (Al₂O₃, ZrO₂, TiO₂, SiO₂) on the performance of NiFe-based OCs with oxidation and catalytic reforming functions. The gasification reactivity and support-active phase interaction of OCs in both oxidized and reduced states were evaluated. XRD, H₂-TPR, XPS, and SEM techniques were employed to characterize the phase composition, synergistic interactions, and surface morphology. The results showed that NiFeAl exhibited the optimal gasification performance in both oxidized and reduced states, achieving a syngas (H₂ + CO) yield of approximately 1.4 m³/kg (dry walnut shell). NiFeAl featured a higher Fe binding energy, abundant cavity structures, and the uniform dispersion of Ni and Fe on Al₂O₃, which confirm the formation of an appropriately strong Ni-Fe-Al ternary system. In contrast, NiFeZr suffered from the higher CO₂ yield, attributed to the over-oxidation caused by the weak interactions. NiFeTi and NiFeSi had lower syngas yields due to their poor reducibility induced by excessively strong interactions. This work verifies that moderate support-active phase interactions in OCs are optimal for BCLG. Full article

A ternary CdS–MoS₂–rGO photocathode was developed to enhance visible light-driven hydrogen evolution through interfacial heterostructure engineering. The composite was fabricated via a solution-based deposition method followed by thermal conversion, resulting in crystalline CdS and MoS₂ phases that were uniformly integrated within a conductive reduced graphene oxide (rGO) framework. Structural and surface analyses (XRD and XPS) confirmed the coexistence of Cd²⁺, Mo⁴⁺, and S²⁻ chemical states without detectable secondary phases. Photoelectrochemical measurements revealed that the ternary architecture significantly improves charge separation efficiency and interfacial charge-transfer kinetics compared to binary and single-component films. The CdS–MoS₂–rGO photocathode exhibited the highest photocurrent density, reduced charge-transfer resistance, and favorable Tafel slope under visible-light irradiation (0.25 sun, neutral electrolyte). Gas chromatography measurements verified that these electrochemical enhancements translate into increased hydrogen production rates, following the trend: CdS–MoS₂–rGO > CdS–rGO > MoS₂–rGO >> rGO. Applied bias photon-to-current efficiency (ABPE) analysis further confirmed improved photon utilization efficiency in the ternary system. The enhanced performance is attributed to synergistic integration of CdS (light harvesting), rGO (rapid electron transport), and MoS₂ (catalytic edge sites), which suppresses recombination and accelerates proton reduction kinetics. These findings demonstrate that rational multi-component heterostructure design is an effective strategy for improving hydrogen evolution rate under mild operating conditions. Full article

The peripheries of rare-metal metallogenic systems frequently host skarn-type or hydrothermal vein-type Pb-Zn deposits, though their genetic connections with parental systems remain debated. The newly identified Gariatong W-Mo polymetallic metallogenic system in the Lhasa Terrane displays well-defined Nb-Ta-Rb, Mo-W, W-Mo, W-Bi, and Pb-Zn-Ag metallogenic zoning, establishing it as an exemplary site for investigating genetic relationships between Pb-Zn and rare-metal mineralization. This investigation targets skarn-type Pb-Zn deposits spatially associated with rare-metal orebodies at Gariatong, utilizing integrated analytical approaches, including in situ LA-ICP-MS trace-element analysis of sulfides, sulfur isotope geochemistry, and LA-ICP-MS elemental mapping of sphalerite, to constrain metal sources, characterize fluid evolution, and establish genetic correlations with the rare-metal system. Key findings include the following: (1) sphalerite shows enrichment in Fe, Mn, Co, and Cd, while pyrite contains elevated As, Pb, Co, Cu, and Mn. Fe, Cd, and Mn primarily occur as solid solutions or nanoparticles, whereas As and Pb exist as micro-inclusions. (2) Sphalerite Zn/Cd ratios (73.6–184) and Co-Ni-As ternary diagrams confirm a magmatic–hydrothermal skarn origin. (3) Mineralization occurred under moderate-temperature, mildly oxidized conditions, as constrained by sphalerite Fe contents and mineral assemblages. Sulfur isotope compositions (δ³⁴S = −1.0‰ to 3.2‰; mean: 1.9‰) indicate a magmatic sulfur source. This study reveals that the Nb-Ta-Rb mineralization, quartz-vein- and greisen-type W-Mo deposits, and skarn-type Pb-Zn orebodies—all genetically associated with highly fractionated granites—constitute an integrated magmatic–hydrothermal system with vertical (depth-related) zoning relative to the granitic intrusion. These results provide critical constraints for understanding rare-metal–Pb-Zn genetic associations and suggest that Pb-Zn mineralization may serve as a key exploration indicator for rare metals in the Lhasa Terrane. Full article

Chelating agents can extend the operational pH range of iron-based advanced oxidation processes, yet comprehensive studies on chelated Fe-activated persulfate systems for textile dye degradation remain scarce. This study establishes an integrated framework for optimizing Fe(II)/persulfate (PS) systems using chelating ligands and hybrid energy inputs under near-neutral conditions. Among the tested systems, Fe(II)/PS complexed with citric acid (CA) exhibited superior performance, achieving ~91% dye removal within 20 min at pH 6.5 under optimized conditions (1.25 mM Fe(II), 10 mM PS, 0.1 mM CA). Chelation stabilized Fe redox cycling and prevented precipitation, enabling effective catalysis across pH 3–10. Optimal CA/Fe and Fe/PS ratios (0.1:1.25 and 1.25:10) yielded ~96% decolorization and 67.65% TOC removal in 60 min, while excessive chelation reduced activity. Transition metal screening (Mn(II), Zn(II), Cu(II), Co(II), and Ni(II) confirmed Fe(II) as the most effective activator, providing removal efficiencies up to 3.2-fold higher than competing metals. Mixed-dye experiments showed competitive degradation, with >37% color removal after 60 min for ternary dye mixtures. Mineralization reached ~92% TOC reduction after 120 min, indicating deep oxidation beyond chromophore cleavage. Reactive species quenching revealed a mixed oxidation mechanism involving ^•OH radicals and high-valent Fe(IV) species. Hybrid assistance improved mineralization, with UVC increasing TOC removal by 15.6%, while solar irradiation provided moderate enhancement under low-energy input. In contrast, low-power ultrasound (40 kHz, 60 W) delivered only 17.6 W acoustic power to the solution and did not improve performance due to limited cavitation and mixing. This work thus contributes a robust platform for advancing chelated iron-persulfate oxidation systems toward practical, effective treatment of recalcitrant dye-contaminated wastewaters under near-neutral conditions. Full article

Constructing efficient conductive networks is essential to overcome the intrinsically low electronic conductivity of LiFePO₄ cathodes. Previous studies have demonstrated that different conductive agents possess distinct electrical conduction mechanisms. The synergistic integration of multiple types of conductive agents can achieve more favorable conductive performance. Nevertheless, most relevant studies are still limited to binary conductive systems, and the synergistic mechanism among various conductive agents has not been systematically investigated and deeply analyzed. In this work, a multidimensional ternary conductive system composed of Super P carbon black (SP), graphene (GN), and carbon nanotubes (CNTs) was systematically optimized to regulate electron and ion transport pathways. By adjusting the relative proportions of SP, GN, and CNTs, the evolution of conductive network structure and its impact on electrochemical performance were investigated, and the optimized composition (SP/GN/CNTs = 50/15/35, denoted as S5GC37) was identified. The results reveal that the multidimensional conductive framework formed by S5GC37 effectively integrates short-range ion diffusion with long-range electron transport, leading to reduced polarization, suppressed surface oxidation, and enhanced charge transport kinetics. As a result, the LiFePO₄ electrode with S5GC37 delivers an initial discharge capacity of 164.8 mAh·g⁻¹ and maintains 151.9 mAh·g⁻¹ after 200 cycles at 1C. Even at 3C, a capacity retention of 83.2% is achieved after 200 cycles, demonstrating excellent rate capability and cycling stability. These findings highlight the importance of multidimensional conductive network design for high-performance LiFePO₄ batteries. Full article

This study addresses the challenges associated with deep-well drilling mud cuttings, including large waste volumes, high transportation costs, and complex organic pollutants. A low-cost synergistic technology was developed for the resource utilization of pyrolyzed drilling waste residue (PDWR) and the in situ remediation of oil-contaminated drill cuttings. A ternary photocatalytic system consisting of PDWR, H₂O₂, and oxalic acid was proposed and demonstrated to effectively degrade total petroleum hydrocarbons (TPH) in drill cuttings under solar irradiation. Systematic optimization identified optimal dosages of PDWR, H₂O₂, and oxalic acid as 250 mg, 280 mg, and 90 mg, respectively. The addition of oxalic acid significantly enhanced photocatalytic oxidation performance, increasing H₂O₂ utilization by 63.8% and improving the TPH degradation rate by a factor of 3.03. Under optimal conditions and 7 days of solar irradiation, TPH degradation efficiencies of 65.19–88.66% were achieved for initial TPH concentrations ranging from 5000 to 12,000 mg kg⁻¹. Mechanistic analysis revealed that a Fenton-like reaction between transition metals in PDWR and H₂O₂ dominated the photocatalytic process, while oxalic acid facilitated metal redox cycling through coordination and electron transfer, promoting sustained generation of reactive oxygen species (·OH). This study demonstrates a feasible and sustainable approach for high-value utilization of drilling waste residue and solar-driven in situ remediation of oil-contaminated drill cuttings, highlighting its strong potential for practical application. Full article

As a ternary metal oxide, indium gallium zinc oxide (IGZO) has gathered much attention for various applications, including gas sensors, due to its remarkable semiconducting properties, even in amorphous phases and at a low process temperature. For gas sensing applications, as surface area is an important factor affecting the response and performance of a gas sensor, nanofibers (NFs) with 1D morphology are expected to have good sensing performance. In this research, IGZO NFs were synthesized using an electrospinning process, which is a suitable technique for the large-scale and low-cost fabrication of NFs. Various characterizations were performed on the synthesized IGZO NFs, and the desired NF morphology and chemical composition were confirmed. Gas sensing experiments showed that the sensor was sensitive and selective to H₂S gas at 250 °C with a response of 40.5 to 100 ppm gas. This study demonstrates the strong potential of IGZO for use in sensitive and selective H₂S gas sensors. Full article

Landfill leachate, a byproduct of municipal solid waste treatment, typically contains hazardous substances such as toxic metals (e.g., lead) and eutrophication agents (e.g., phosphate). This study addresses the pressing challenge of polishing complex wastewater, such as landfill leachate, through the development of a novel ternary layered double hydroxide (LDH). As CaFe-LDHs are known to have an affinity for anions, and CoFe-LDHs have shown an affinity for toxic metal cations, CoCaFe-LDH was proposed to integrate both functionalities. The LDH was anchored on activated biochar to synthetize the novel composite adsorbent CoCaFe-LAB. Key operational parameters (including initial pH, adsorbent dosage, contact time, initial adsorbate concentration, presence of coexisting ions, and regeneration capability) were systematically evaluated. Kinetic and equilibrium analyses revealed that Elovich and Sips models, respectively, best described the adsorption behavior of Pb²⁺ and PO₄³⁻, indicating a heterogeneous adsorption system. Maximum adsorption capacities in synthetic solutions reached 140.81 mg Pb²⁺ g⁻¹ and 25.19 mg PO₄³⁻ g⁻¹ at 45 °C. The CoCaFe-LAB composite proved highly effective, particularly for lead removal. In real effluent tests, the adsorbent achieved complete phosphate removal (100%) from electro-oxidized landfill leachate at a dosage of 2.0 g L⁻¹, confirming its practical applicability and efficiency. Full article

Plutella xylostella (L.) (Lepidoptera: Plutellidae), the diamondback moth (DBM), is a cosmopolitan pest of brassicas. To validate and compare the performance of yeast-derived sex pheromone components with chemically synthesized ones, we studied the behavioral and electrophysiological responses (EAGs) of male DBM adults. In addition, using gas chromatography coupled with electroantennographic detection (GC-EAD), we examined whether any residual impurities present in yeast-derived pheromone components can be perceived by the insects’ antennae and are thus capable of interfering with normal behavior. Furthermore, we assessed the performance of the yeast-derived pheromones under field conditions through monitoring trials conducted in cabbage crops in Greece. Electrophysiological and behavioral assays revealed equivalent responses from the insects to both the yeast-derived (BIO) and chemically synthesized (CHEM) pheromone blends. Consistent with this, GC-EAD results showed no significant differences in antennal response to minor impurities present in the BIO blend compared to the CHEM blend. Finally, it was demonstrated that the binary pheromone blend—comprising (Z)-11-hexadecenal and (Z)-11-hexadecenyl acetate derived from (Z)-11-hexadecen-1-ol produced by yeast cell-factories—was as efficient and specific for trapping male moths in cabbage fields as the conventional ternary synthetic blend [(Z)-11-hexadecenal and (Z)-11-hexadecenyl acetate and (Z)-11-hexadecen-1-ol]. The yeast-derived mixture contained small amounts of unoxidized (Z)-11-hexadecen-1-ol due to incomplete oxidation. Full article

This study presents a straightforward process for producing a hybrid ternary composite of silver nanoparticles (Ag NPs), small graphene oxide (s-GO), and zirconia (ZrO₂) and its use as an electrode material for electrochemical sensing. The physico-chemical properties of the ternary composite were analyzed by means of field emission scanning electron microscopy (FE-SEM), ultraviolet-visible (UV-vis) and FTIR spectroscopy, X-ray Photoelectron Spectrometry (XPS) and contact angle (CA) measurements. The synthesized hybrid nanomaterial was employed as an electrode modifier in the fabrication of a modified screen-printed carbon electrode (SPCE) and used for the simultaneous electrochemical sensing of key environmental pollutants such as hydroquinone (HQ) and catechol (CAT). The developed sensor exhibited linearity in the range of 0–100 µM for both HQ and CAT, with sensitivity values of 2640 µA·mM⁻¹·cm⁻² for HQ and 5120 µA·mM⁻¹·cm⁻² for CAT. The limits of detection (LOD) were 1.5 µM for HQ and 0.72 µM for CAT, respectively. The synergistic enhancement of electron transfer kinetics, the increased electroactive surface area, the strong anti-interference capability, and excellent reproducibility and stability establish these modified electrodes as promising candidates for environmental monitoring and real sample analysis. Full article

Quaternary Ni-Zn-Mg-Al metallic mixed oxide (MMO) catalysts were synthesized by co-precipitation from layered double hydroxide precursors. The effect of varying Zn content on physicochemical properties and catalytic performance was evaluated. Mg-Al and ternary Ni-Mg-Al and Zn-Mg-Al catalysts were synthetized for comparative purposes. XRD, N₂ sorption, MP-AES, CO₂-TPD, NH₃-TPD, SEM, and EDS characterized the materials’ physicochemical properties. The tested reaction was the transesterification between glycerol and dimethyl carbonate to obtain glycerol carbonate to improve the biodiesel industry. The catalyst containing both Ni and Zn showed the highest glycerol conversion among the evaluated materials. This was related to the increased number and strength of surface basic and acid active sites. Specifically, a high density of strong basic sites and acid ones in the quaternary catalysts was required for the reaction mechanism. The catalyst with 20 at% of Zn (MMO-Ni₁₅Zn₂₀) achieved the highest glycerol carbonate yield (89.6%) under mild reaction conditions and was solvent-free. MMO-Ni₁₅Zn₂₀ catalytic performance was associated with its high total basicity and predominance of strong basic sites and a moderate amount of acid sites. The differences observed between catalytic performances suggest that these results depend on the influence of structural, textural, acid, and basic properties. Reuse tests of the MMO-Ni₁₅Zn₂₀ catalyst showed moderate stability, with a progressive decrease in activity due to the loss of strong basic sites and the formation of agglomerated regions. Nevertheless, MMO-Ni₁₅Zn₂₀ maintained a GC selectivity of 100% in the successive cycles. Full article