Search Results (339)

Dual fuel engines utilize two different fuels consisting of a high reactivity fuel (HRF) injected into the cylinder and a low reactivity fuel (LRF), typically fumigated into the intake manifold. To reduce engine-out emissions of oxides of nitrogen (NO_x), early start of injection (SOI) of HRF may be employed in dual fuel combustion, albeit at the expense of higher engine-out emissions of unburned hydrocarbons (HC) and carbon monoxide (CO). This study compares performance and emissions of diesel–propane and poly-oxy methylene dimethyl ether (POMDME)-propane dual fuel combustion for a heavy-duty single-cylinder research engine (SCRE) platform based on a production PACCAR MX-11 engine at a low load of 5 bar IMEPg and a constant speed (“B Speed”) of 1339 rpm. While POMDME-natural gas combustion has been explored in previous work, the novelty of the present work lies in the direct comparison of diesel–propane and POMDME–propane combustion for the same SCRE under fixed constraints of NO_x < 1 g/kWh, COV of IMEP < 5%, and a maximum pressure rise rate < 10 bar/CAD. By optimizing HRF injection parameters, boost pressure, and propane energy substitution, the present work demonstrates diesel–propane HC and CO emissions improvements of ~86% and ~67%, respectively, while POMDME–propane HC and CO emissions improved by ~91% and ~86% respectively, compared to the corresponding unoptimized baseline values. These improvements were obtained while achieving very low engine-out NO_x emissions (diesel–propane ~0.7 g/kWh, POMDME–propane ~0.1 g/kWh) and very good gross indicated fuel conversion efficiencies (diesel–propane ~51%, POMDME–propane ~48%). Additionally, POMDME–propane demonstrated near-zero measurable smoke emissions for all engine operating conditions. Full article

Nitrous oxide (N₂O) has attracted increasing attention as an oxidizer for space propulsion systems due to its non-toxic nature and favorable handling characteristics. Its relatively high vapor pressure allows self-pressurization, while its wide storage temperature range makes it attractive for a range of space applications. In parallel with broader efforts to identify alternatives to conventional toxic propellants, numerous studies have investigated liquid propulsion systems based on N₂O combined with hydrocarbon fuels, spanning both premixed fuel blends and non-premixed bipropellant configurations. This review summarizes experimental and system-level studies on N₂O–hydrocarbon propellant combinations, including ethylene, ethane, ethanol, propane, acetylene, methane, dimethyl ether, and propylene. Results reported by different research groups reveal clear differences among propellant combinations in terms of vapor pressure, thermal stability, chemical reactivity, and ignition delay. These differences have direct implications for injector design, mixing strategies, ignition mechanism, and system safety. By bringing together recent results from the literature, this paper aims to clarify the practical trade-offs associated with fuel selection in N₂O-based premixed and bipropellant systems and to provide a useful reference for the design and development of future space propulsion concepts. Full article

In recent years, interest in carbon dioxide (CO₂) hydrogenation technologies has intensified. Driven by the continuous rise in greenhouse gas emissions and the unprecedented negative impacts of global warming, these technologies offer a viable pathway toward sustainability and support the development of low-carbon industrial processes. In addition to methanol and methane, other possible hydrogenation products (i.e., hydrocarbons, formic acid, acetic acid, dimethyl ether, and dimethyl carbonate) are of industrial relevance due to their wide range of applications. Therefore, this review aims to provide a comprehensive overview of the various aspects associated with thermocatalytic CO₂ hydrogenation processes, from thermodynamic and kinetic studies to upscaled reactor modeling and process synthesis and optimization. The review proceeds to examine different integration strategies and optimization approaches for multi-product systems, with the objective of evaluating how distinct technologies may be combined in an integrated flowsheet. It then concludes by outlining future research opportunities in this field, particularly those related to developing comprehensive kinetic rate expressions and reactor modeling studies for routes with low technology readiness levels, the exploration of prospective reaction pathways, strategies to mitigate the dependence on green hydrogen (which, today, exhibits high costs), and the consideration of market price or product demand fluctuations in optimization studies. Overall, this review provides a solid base to support other decarbonization studies focused on hydrogenation technologies. Full article

In order to solve the problems of high volatility and insufficient absorption effect when using chemical by-product washing oil to treat benzene-containing waste gas, this study innovatively proposed a composite solvent screening method based on the solvation free energy (ΔGsol), and reasonably predicted the absorption performance of 26 solvents for benzene. Through theoretical calculation and experimental verification, tetraethylene glycol dimethyl ether (TGDE) was finally determined to be the optimal composite component of washing oil. The absorption efficiency of the composite solvent reached 96.2%, and the regeneration efficiency was stable after 12 cycles with a mass loss of only 2.4%. Quantum computing simulation revealed that the dispersion force is dominant between benzene and the solvent, and TGDE enhances the electrostatic interaction through weak hydrogen bonds. The synergistic effect of the two improves the absorption performance. This study provides theoretical and technical support for the development of efficient and renewable benzene waste gas recovery solvent systems. Full article

As global efforts to combat climate change and promote sustainable development intensify, PODEn, as an innovative type of clean, sustainable fuel, has gained growing attention for its potential to support eco-friendly energy transitions, especially concerning the spray characteristics of its blended fuels. Environmental conditions are crucial in the fuel spraying process, which is essential for optimizing combustion efficiency and reducing emissions—key elements of sustainable energy use and climate action. In this study, the parameters of spray morphology, droplet size distribution, and velocity were accurately measured using a constant-volume combustor and high-speed photography. The results demonstrate that as ambient pressure increases, both the spray cone angle and boundary gas entrainment volume increase, while the spray penetration distance and spray volume decrease. These changes, driven by pressure differences and variations in gas density that influence droplet movement and fragmentation, are critical for optimizing fuel injection strategies to enhance combustion efficiency and reduce environmental impact. This aligns closely with the Sustainable Development Goals focused on clean energy, responsible consumption, and climate mitigation. Conversely, as ambient temperature rises, the penetration distance and spray volume increase, whereas the entrainment volume decreases and the spray cone angle narrows. This phenomenon results from the combined effects of temperature on gas density, viscosity, evaporation rate, and convective flow, underscoring the need for adaptive engine designs that leverage these characteristics to improve fuel efficiency and reduce carbon emissions—an essential step toward sustainable development in the energy and automotive sectors. Full article

The methanol oxidation reaction was investigated on Co- and/or Ag-based γ-Al₂O₃ catalysts, which were prepared by different methods (WI: wet impregnation and SI: spray impregnation) and further doped with noble metals (Pd, Pt). During the present study, three different reaction pathways were revealed. The complete oxidation of methanol to CO₂ and H₂O was achieved on Pd-doped catalysts prepared by the spray impregnation method (Pd-Co/Al-SI and Pd-Ag/Al-SI), while partial oxidation to intermediates such as formaldehyde was observed for Ag/alumina catalysts. The dehydration reaction of methanol to dimethyl ether was carried out on Co/alumina, Ag-Co/alumina, and Pt-Co/alumina catalysts. The improved reducibility of the 5Co/Al-SI catalyst with the incorporation of Pd, combined with the easier surface oxygen desorption, resulted in higher catalytic activity compared to the Pt-doped catalyst. On the other hand, the incorporation of Pd into Ag/Al-SI enhanced the well-dispersed Ag₂O species, mainly affecting the structural properties of the catalyst, thus resulting in partial oxidation of methanol. The 0.5 wt.% Pd-5 wt.% Co/γ-Al₂O₃ catalyst, prepared by the spray impregnation method, exhibited the highest methanol oxidation efficiency (T₅₀: 43 °C) and was further evaluated in the presence of H₂O and CO in the feed for several hours on stream and at reaction temperature of 230 °C. The presence of impurities initially reduced the catalyst’s activity from 100% methanol conversion (in the absence of H₂O and CO in the feed) to 80%; however, over time complete methanol oxidation was regained (achieving again 100% methanol conversion after 12 h on stream). Characterization of the used catalyst (after the stability experiment) revealed that in addition to the Co₃O₄ phase, initially formed in the fresh, as-prepared catalyst, some Co₃O₄ species were reduced to CoO under the reaction conditions, suggesting that the active phase of the 0.5Pd-5Co/Al-SI catalyst for the methanol oxidation reaction in the presence of the impurities (such as H₂O and CO) is probably a mixture of Co₃O₄ and CoO phases. Full article

The integrated injection of low-salinity water (LSW) and carbon dioxide (CO₂) into the water-alternating-gas (WAG) process offers advantages, primarily increasing oil recovery and reducing operating costs. However, CO₂ has challenges in sweep efficiency due to significant differences in density and viscosity compared with oil. While LSW and dimethyl ether (DME) have shown promise in improving recovery through wettability alteration and reducing minimum miscible pressure, interfacial tension (IFT), and CO₂ mobility, their synergistic integration with CO₂-WAG remains poorly understood. Existing DME-based enhanced oil recovery (EOR) studies have not explored low-salinity water injection as a cost-effective alternative to mitigate high DME operating costs. This study introduces the CO₂/DME-LSWAG method, systematically evaluating the effect of DME concentrations (0%, 10%, 25%) and LSWs (seawater, twice-diluted seawater, ten-times-diluted seawater) on sweep and displacement efficiencies, oil recovery, and CO₂ storage in a 2D cross-sectional carbonate reservoir model. Results showed that DME dramatically reduces IFT (67% and 95% at 10% and 25% DME solvent, respectively) while salinity effects are relatively small. Compared with CO₂-LSWAG, the oil recovery factor improved by 5.2–13.1% depending on DME concentration and water salinity, with DME performance maximized at higher salinity water. CO₂ storage efficiency showed opposing trends. Structural trapping decreased, while solubility trapping increased with lower salinity. The sensitivity analysis identified DME concentration as the dominant factor for CO₂ storage. The composition modeling and simulation of the CO₂/DME-LSWAG process provide critical engineering guidance for the design of future EOR and CO₂ storage projects that utilize DME in carbonate reservoirs. Full article

Magnesium metal boasts a high theoretical volumetric specific capacity and abundant reserves. Magnesium batteries offer high safety and environmental friendliness. In recent years, magnesium-ion batteries (MIBs) with Mg or Mg alloys as anodes have garnered extensive interest and emerged as promising candidates for next-generation competitive energy storage technologies. However, MIBs are plagued by issues such as sluggish desolvation kinetics and slow migration kinetics, which lead to limitations including a limited electrochemical window and poor magnesium storage reversibility. Herein, the sodium vanadium phosphate @ carbon (Na₃V₂(PO₄)₃@C, hereafter abbreviated as NVP@C) cathode material was synthesized via a sol–gel method. The electrochemical performance and magnesium storage mechanism of NVP@C in a 0.5 M magnesium bis(trifluoromethanesulfonyl)imide/ethylene glycol dimethyl ether (Mg(TFSI)₂/DME) electrolyte were investigated. The as-prepared NVP@C features a pure-phase orthorhombic structure with a porous microspherical morphology. The discharge voltage of NVP@C is 0.75 V vs. activated carbon (AC), corresponding to 3.5 V vs. Mg/Mg²⁺. The magnesium storage process of NVP@C is tentatively proposed to follow a ‘sodium extraction → magnesium intercalation → magnesium deintercalation’ three-step intercalation–deintercalation mechanism, based on the characterization results of ICP-OES, ex situ XRD, and FTIR. No abnormal phases are generated throughout the process, and the lattice parameter variation is below 0.5%. Additionally, the vibration peaks of PO₄ tetrahedrons and VO₆ octahedrons shift reversibly, and the valence state transitions between V³⁺ and V⁴⁺/V⁵⁺ are reversible. These results confirm the excellent reversibility of the material’s structure and chemical environment. At a current density of 50 mA/g, NVP@C delivers a maximum discharge specific capacity of 62 mAh/g, with a capacity retention rate of 66% after 200 cycles. The observed performance degradation is attributed to the gradual densification of the CEI film during cycling, leading to increased Mg²⁺ diffusion resistance. This work offers valuable insights for the development of high-voltage MIB systems. Full article

Background/Objectives: Lavandula stoechas has reported bioactivities, but its selective anticancer potential in human models remains insufficiently defined. This study aimed to compare cytotoxicity and selectivity of ethanol and methanol extracts prepared from fresh and dried L. stoechas and to profile candidate bioactive metabolites. Methods: Aerial parts Lavandula stoechas L. subsp. stoechas (L. stoechas L.) were extracted with ethanol or methanol from fresh (LsFE, LsFM) and dried (LsDE, LsDM) material. Cytotoxicity was assessed in cancer (MDA-MB-231, T98G, RT4) and non-malignant (hGF, ARPE-19) cells using Hoechst 33342-stained nuclear counts and MTS viability at 24–48 h. Metabolite identification was performed using LC–QTOF–MS in both positive and negative ESI modes, supported by database search results. Results: All extracts reduced viability in a dose- and time-dependent manner. Among them, the ethanol extract from fresh material (LsFE) displayed the highest cytotoxic potency and the most favorable selectivity profile, markedly reducing viability in breast (MDA-MB-231) and glioblastoma (T98G) cells while exerting only mild effects on non-malignant fibroblast (hGF) and retinal epithelial (ARPE-19) cells. In contrast, extracts from dried material, particularly LsDE, showed broader cytotoxicity across both cancerous and non-cancerous lines. LC–MS highlighted sesquiterpenoids (Kikkanol A; 3(4→5)-Abeo-4,11:4,12-diepoxy-3-eudesmanol), phenolics (tyrosol; 3,4-dihydroxybenzoic acid), flavonoid/ionone derivatives (luteolin 5,3′-dimethyl ether; 3-hydroxy-β-ionone), oxidized fatty acids (9(S)-HpODE, α-EpODE, 5,12-dihydroxy-eicosatetraenoic acid), and jasmonates (12-hydroxyjasmonic acid; dihydrojasmonic acid methyl ester), especially enriched in LsFE. Conclusions: Ethanol extracts of L. stoechas L., especially LsFE, demonstrated selective cytotoxicity against cancer cells while exerting relatively mild effects on non-malignant cells. The metabolite profile of L. stoechas L. extracts revealed a diverse composition, including phenolics, terpenoids, flavonoids, and oxidized lipids, which are commonly associated with biological activity. These results suggest that LsFE is a promising candidate for further studies focusing on compound isolation and mechanistic analysis. Full article

There are many obstacles to the industrial application of CO₂ hydrogenation reduction technology, the most important of which is the high economic cost. The purpose of this study is to explore the interaction mechanism between the active component CuO-ZnO-Al₂O₃(CZA) and the zeolite carrier Zeolite Socony Mobil-5(ZSM-5), screen the simplified preparation method of catalysts with high catalytic performance, and further promote the industrial application of CO₂ hydrogenation reduction technology. In this study, the effects of the gas velocity of the feedstock, the reaction temperature, the content of acidic sites in the carrier, the filling amount of active component, and the mixing mode of the active component and the carrier on catalytic CO₂ hydrogenation reduction were investigated. The structure of the catalysts was analyzed by X-ray diffractometer (XRD), Brunauer-Emmett-Teller (BET), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscope (SEM) and transmission electron microscopy (TEM). The catalyst surface properties were analyzed by X-ray photoelectron spectroscopy (XPS), ammonia temperature programmed desorption (NH₃-TPD), hydrogen temperature programed reduction (H₂-TPR) and other characterization methods. The research found that the grinding treatment led to the insertion of CZA between ZSM-5 zeolite particles in CZA@HZ5-20-GB, which was prepared via grinding both CZA and H-ZSM-5 with an Si/Al ratio of 20, inhibiting the action of strongly acidic sites in the zeolite, resulting in only CO and MeOH in the catalytic products, with no Dimethyl Ether (DME) generation. Full article

Ammonia (NH₃) is a promising zero-carbon fuel to eliminate carbon footprint while the high autoignition temperature and low combustion rate of NH₃ remain challenging for practical implementation. Using dimethyl ether (DME) as pilot ignition fuel can substantially promote the reactivity of NH₃, thus paving the way for a widespread application of NH₃. In this study, the ignition process and nitrogen oxides (NO_x) emissions of the NH₃ liquid spray ignited by liquid DME spray were numerically investigated using Converge software. The ambient temperatures (T_amb) ranging from 900 K to 1100 K were used to mimic the in-cylinder temperature typically encountered in turbocharger engines. The effect of ammonia energy ratio (AER) and fuel injection timing was examined as well. It is found that only half of NH₃ is consumed at T_amb = 900 K while 97.4% of NH₃ is burned at T_amb = 1100 K. Nitric oxide (NO) and nitrogen dioxide (NO₂) formation also have strong correlation with T_amb and NO₂ is usually formed around the periphery of NO through these two channels HO₂ + NO = NO₂ + OH and NO + O(+M) = NO₂(+M). Extremely high nitrous oxide (N₂O, formed by NH + NO = H + N₂O) and carbon monoxide (CO) are produced with the presence of abundant unburned NH₃ at T_amb = 900 K. Additionally, increasing AER from 60% to 90% results in slightly declined combustion efficiency of NH₃ from 98.7% to 94%. NO emission has a non-monotonical relationship with AER owing to the ‘trade-off’ relationship between HNO concentration and radical pool at varying AERs. A higher AER of 95% leads to failed ignition of NH₃. Advancing DME injection not only increases combustion efficiency, but also reduces NO_x and CO emissions. Full article

Collagen, as the predominant structural protein in vertebrates, represents a promising biomimetic material for scaffold development. Fibre-based scaffolds produced through textile technologies enable precise modulation of structural characteristics to closely mimic the extracellular matrix architecture using wet-spun collagen fibres. However, this in vitro fibre formation lacks natural crosslinking, resulting in collagen fibres with compromised mechanical strength, enzymatic resistance, and thermal stability compared to their native counterparts, thus restricting their biomedical applicability. Post-fabrication crosslinking is therefore imperative to enhance the durability and functional performance of collagen fibre-based scaffolds. Although traditional crosslinkers like glutaraldehyde effectively improve mechanical strength and stability, their clinical utility is hindered by cytotoxicity and associated adverse biological responses. Alternative synthetic crosslinking agents, such as hexamethylene diisocyanate, 1-Ethyl-3-(3’-dimethyl amino propyl) carbodiimide, and 1,4-Butanediol diglycidyl ether, have demonstrated superior cytocompatibility while effectively improving collagen fibre properties. Nonetheless, synthetic compounds may induce more pronounced foreign body reaction than natural agents, necessitating further investigation into their cytocompatibility across varying concentrations. In contrast, plant-based crosslinking offers a promising, cytocompatible alternative, significantly enhancing the thermal and mechanical stability of collagen fibres, provided that potential fibre discolouration is acceptable for intended biomedical applications. Full article

Understanding how solvents influence the luminescence behavior of Cu(I) complexes is crucial for designing advanced optical sensors. This study reports the synthesis, structures and photophysical investigation of an 8-hydroxyquinoline-functionalized 1H-imidazo[4,5-f][1,10]phenanthroline ligand, ipqH₂, and its four Cu(I) complexes with diphosphine co-ligands. Photoluminescence studies demonstrated distinct solvent-dependent excited-state mechanisms. In DMSO/alcohol mixtures, free ipqH₂ exhibited excited-state proton transfer (ESPT) and enol-keto tautomerization, producing dual emission at about 447 and 560 nm, while the complexes resisted ESPT due to hydrogen bond blocking by PF₆⁻ anions and Cu(I) coordination. In DMSO/H₂O, aggregation-caused quenching (ACQ) and high-energy O–H vibrational quenching dominated, but complexes 1 and 2 showed a significant red-shifted emission (569–574 nm) with high water content due to solvent-stabilized intra-ligand charge transfer and metal-to-ligand charge transfer ((IL+ML)CT) states. In DMSO/DMF, hydrogen bond competition and solvation-shell reorganization led to distinct responses: complexes 1 and 3, with flexible bis[(2-diphenylphosphino)phenyl]ether (POP) ligands, displayed peak splitting and (IL + ML)CT redshift emission (501 ⟶ 530 nm), whereas complexes 2 and 4, with rigid 9,9-dimethyl-4,5-bis(diphenylphosphino)-9H-xanthene (xantphos), showed weaker responses. The flexibility of the diphosphine ligand dictated DMF sensitivity, while the coordination, the hydrogen bonds between PF₆⁻ anions and ipqH₂, and water solubility governed the alcohol/water responses. This work elucidates the multifaceted solvent-responsive mechanisms in Cu(I) complexes, facilitating the design of solvent-discriminative luminescent sensors. Full article

Surface roughness influences biofilm adhesion on denture base materials, impacting oral health. Despite advances in polymeric denture materials, the effects of common cleaning protocols on their surface texture remain inadequately characterized. This study investigated the influence of toothbrush abrasion on the surface texture of dimethyl methacrylate-based (DMA, printed: V-Print dentbase), polymethyl methacrylate (PMMA, milled: VITA Vionic Base, pressed: IvoBase Hybrid), polyamide (PA, pressed: Bre.flex), and polyether ether ketone (PEEK, milled: Juvora Disc). The specimens were fabricated as polished discs. The Vickers and Martens hardness, indentation modulus, elastic and plastic part of indentation work, and indentation creep were determined. Toothbrushing simulation and surface texture analysis were conducted in three steps: 1800, 1800, and 3600 cycles using water, dish detergent, or toothpaste slurry. The surface texture parameters Sa, Sal, Sdr, Sku, and Ssk were determined using confocal laser scanning microscopy and suitable filtering (S-F and S-L surface). Sa, Sal, and Sdr showed significant changes depending on the choice of medium and the material used. The duration had a small effect (three-way ANOVA; all p < 0.001). DMA showed minor surface changes. Milled and pressed PMMA exhibited similar surface deformities due to wide valleys that were not considered critical for biofilm adhesion. PA showed the lowest and PEEK the highest Vickers and Martens hardness. However, both PA and PEEK exhibited surface changes that could promote biofilm development. These findings suggest that denture cleaning recommendations should remain material-specific. Regular surface inspections and repolishing are necessary to reduce the risk of biofilm formation on PA or PEEK-containing dentures. Full article

The aim of this study was to investigate the metabolites in Aspergillus subramanianii 1901NT-1.40.2 extract using UPLC-MS, isolate and elucidate the structure of individual compounds, and study the antimicrobial and cytotoxic activities of the isolated compounds. The structures of two previously unreported ergostane triterpenoid aspersubrin A (1) and pyrazine alkaloid ochramide E (2) were established using NMR and HR ESI-MS. The absolute configuration of 1 was determined using quantum chemical calculations. Moreover, the known polyketides sclerolide (3) and sclerin (4); the indolediterpene alkaloid 10,23-dihydro-24,25-dehydroaflavinine (5); the bis-indolyl benzenoid alkaloids kumbicin D (6), asterriquinol D dimethyl ether (7), petromurin C (8); and the cyclopentenedione asterredione (9) were isolated. The effects of compounds 3-9 on the growth and biofilm formation of the yeast-like fungus Candida albicans and the bacteria Staphylococcus aureus and Escherichia coli were investigated. Compounds 5 and 6 inhibited C. albicans growth and biofilm formation at an IC₅₀ of 7–10 µM. Moreover, the effects of compounds 3-9 on non-cancerous H9c2 cardiomyocytes, HaCaT keratinocytes, MCF-10A breast epithelial cells, and breast cancer MCF-7 and MDA-MB-231 cells were also investigated. Compound 8 (10 µM) significantly decreased the viability of MCF-7 cells, inhibited colony formation, and arrested cell cycle progression and proliferation in monolayer culture. Moreover, 8 significantly decreased the area of MCF-7 3D spheroids by approximately 30%. A competitive test with 4-hydroxytamoxyfen and molecular docking showed that estrogen receptors (ERβ more than ERα) were involved in the anticancer effect of petromurin C (8). Full article