Search Results (81)

Climate-sensitive ice-covered reservoirs are critical components of methane (CH₄) release. To reveal the spatial characteristics of CH₄ concentrations, diffusive fluxes and bubble fluxes during the ice-covered and ice-free periods in northern reservoirs, and in order to clarify the critical influences on their variations. We selected Dongfeng Reservoir, a large reservoir in Northeast China, and conducted six field investigations of CH₄ concentrations and emissions in deep and shallow waters during the ice-covered (January 2022 and January 2023) and ice-free (July 2022, October 2022, March 2023, and September 2023) periods. The results showed that spatially, surface CH₄ concentration and diffusive flux were significantly higher in shallow water than those in deep water. CH₄ bubble flux had the largest range of variation in shallow water, while there was no obvious spatial difference in the proportion of CH₄ in bubbles. Temporally, surface CH₄ concentration, diffusive flux, bubble flux, and the proportion of CH₄ in bubbles were generally high in summer and low in autumn. The surface CH₄ concentration had the largest range of variation in winter, and the CH₄ concentration under the ice was significantly higher in shallow water than those in deep water. Water depth determines the release of CH₄ bubbles from sediments and is the basis for determining deep and shallow water based on bubbles. Ice cover leads to significant differences in CH₄ production and transport compared with ice-free periods by indirectly changing the water environment and directly altering the CH₄ release. CH₄ accumulated under the ice and in the ice will greatly increase the CH₄ release potential during the spring ice-melt period. Overall, this study improves the understanding of CH₄ emissions from reservoirs characterized by ice-covered periods and provides theoretical basis for comprehensive estimation of CH₄ emissions from reservoirs. Full article

A strategy allowing for the application of orange waste (OW) in anaerobic co-digestion with municipal sewage sludge (MSS) has been proposed. For this purpose, the introduction of an additional component represented by ice-cream processing waste (IPW) has been chosen. The experiment was conducted in batch mode at a temperature of 37 °C. Four series were conducted: S1—the mono-digestion of MSS; S2—two-component co-digestion of MSS and 1.5 g of OW; S3—two-component co-digestion of MSS and 1.0 g of IPW; and S4—three-component co-digestion of MSS, 1.0 g of IPW, and 1.5 g of OW. The obtained results indicate that the highest methane production was achieved in the presence of IPW in two- and three-component mixtures (S3 and S4). It was also accompanied by improved kinetics, enhanced organic removal, and stable process performance. The related methane yields were 407.6 and 401.6 mL/g VS in S3 and S4, respectively. In turn, in S1 and S2, this parameter was established at the level of 351.3 and 344.3 mL/g VS. Additionally, as compared to MSS mono-digestion (S1), the energy profit was enhanced by 54 and 62% in S3 and S4, respectively. The obtained results indicate the possibility of effective management of OW with energy recovery in the anaerobic digestion process (AD). Full article

Background/Objectives: The study aims to investigate an improved version of lipid nanocarriers (NLCs) (formulated with functional coconut butter and marula oil) by designing hyaluronic acid (HA) decorated NLC co-loaded with dual UVA (butyl methoxy dibenzoyl methane, BMDBM), UVB absorbers (ethyl-hexyl-salicylate, EHS) and a Raspberry rich polyphenols fraction (RPRF) for development of more natural NLC-based to-pical formulations. Methods: Quality and quantitative attributes of classic- and HA-NLC have been assigned based on particle size, electrokinetic potential, encapsulation efficiency, spectroscopic characteristics, and high-resolution mass spectrometry. To establish the performance profile of antioxidant activity, release of active substances, sun blocking action, and photostability, in vitro studies were conducted. Results: NLC with an average size of ~150 nm and zeta potentials < −39.5 mV showed 80% and 93.1% of encapsulation efficiency for BMDBM and EHS, and up to 83% for natural RPRF. A long-lasting release of absorbers, with a maximum cumulative release of 2.1% BMDBM and 4.6% EHS was detected. NLC-UV Abs-RPRF-HA assured 72.83% radical scavenging activity. The IC₅₀ for HA-NLC-UV Abs-RPRF was 6.25-fold lower than NLC-UV Abs-HA, which reflects the greater free radical scavenging action. The conditioned NLC–UV Abs-RPRF-HA cream was able to provide a sun protection factor value of 52 and UVA-PF value of 81, which underlines an impressive removal of both categories of UVA and UVB radiation. A significant photoprotective upregulation, four-fold for the topical formulation with NLC-UV Abs-RPRF-HA, resulted after a simulated irradiation process. Conclusions: HA decorated-NLC-conditioned creams might provide a useful platform for developing na-tural and sophisticated dermal delivery systems, for influencing skin permeability, and for synergistically imparting antioxidant and photoprotective actions to cosmetic pro-ducts. Full article

In the endeavor to accomplish a fully de-carbonized globe, sparkling interest is growing towards using natural gas (NG) having as vastly major component methane (CH₄). This has the lowest carbon/hydrogen atom ratio compared to other conventional fossil fuels used in engines and power-plants hence mitigating carbon dioxide (CO₂) emissions. Given that using neat hydrogen (H₂) containing nil carbon still possesses several issues, blending CH₄ with H₂ constitutes a stepping-stone towards the ultimate goal of zero producing CO₂. In this context, the current work investigates the exergy terms development in high-speed spark-ignition engine (SI) fueled with various hydrogen/methane blends from neat CH₄ to 50% vol. fraction H₂, at equivalence ratios (EQR) from stoichiometric into the lean region. Experimental data available for that engine were used for validation from the first-law (energy) perspective plus emissions and cycle-by-cycle variations (CCV), using in-house, comprehensive, two-zone (unburned and burned), quasi-dimensional turbulent combustion model tracking tightly the flame-front pathway, developed and reported recently by authors. The latter is expanded to comprise exergy terms accompanying the energy outcomes, affording extra valuable information on judicious energy usage. The development in each zone, over the engine cycle, of various exergy terms accounting too for the reactive and diffusion components making up the chemical exergy is calculated and assessed. The correct calculation of species and temperature histories inside the burned zone subsequent to entrainment of fresh mixture from the unburned zone contributes to more exact computation, especially considering the H₂ percentage in the fuel blend modifying temperature-levels, which is key factor when the irreversibility is calculated from a balance comprising all rest exergy terms. Illustrative diagrams of the exergy terms in every zone and whole charge reveal the influence of H₂ and EQR values on exergy terms, furnishing thorough information. Concerning the joint content of both zones normalized exergy values over the engine cycle, the heat loss transfer exergy curves acquire higher values the higher the H₂ or EQR, the work transfer exergy curves acquire slightly higher values the higher the H₂ and slightly higher values the lower the EQR, and the irreversibility curves acquire lower values the higher the H₂ or EQR. This exergy approach can offer new reflection for the prospective research to advancing engines performance along judicious use of fully friendly ecological fuel as H₂. This extended and in-depth exergy analysis on the use of hydrogen in engines has not appeared in the literature. It can lead to undertaking corrective actions for the irreversibility, exergy losses, and chemical exergy, eventually increasing the knowledge of the SI engines science and technology for building smarter control devices when fueling the IC engines with H₂ fuel, which can prove to be game changer to attaining a clean energy environment transition. Full article

The present work addresses the production of nitrogen oxides in ICEs burning hydrogen mixed with methane. A mathematical model that allows the calculation of nitrogen oxide emissions from such combustion was built; this model uses the extended chemical kinetic mechanism of Zeldovich. Numerical simulations were carried out on the production of NO, varying the following variables: proportion of H₂ to CH₄, the equivalence ratio of the reactant mixture, the compression ratio, and the engine speed. The essential purpose was to assess how NO production is affected by the mentioned variables. The main assumptions were (i) Otto cycle; (ii) instantaneous combustion; (iii) chemical equilibrium reached just at the end of combustion; (iv) the formation of NO only during the expansion stroke of pistons. Results were obtained for various proportions of hydrogen and methane, various equivalence ratios, speeds of rotation, and compression ratios of an engine. In short, the results obtained in the current work show that the lowering of the equivalence ratio leads to a lower concentration of NO; that increasing the compression ratio also lowers the concentration of NO; that NO production occurs until shortly after the beginning of the expansion stroke; and finally, that the NO concentration in the engine exhaust is not very sensitive to the H₂/CH₄ ratio in the fuel mixture. Full article

A family of bifunctional dihetarylmethanes and dibenzoxanthenes is assembled via a reaction of acetals containing a 2-chloroacetamide moiety with phenols and related oxygen-containing heterocycles. These compounds demonstrated selective antitumor activity associated with the induction of cell apoptosis and inhibition of the process of glycolysis. In particular, bis(heteroaryl)methane containing two 4-hydroxy-6-methyl-2H-pyran-2-one moieties combine excellent in vitro antitumor efficacy with an IC₅₀ of 1.7 µM in HuTu-80 human duodenal adenocarcinoma models with a high selectivity index of 73. Overall, this work highlights the therapeutic potential of dimeric compounds assembled from functionalized acetals and builds a starting point for the development of a new family of anticancer agents. Full article

Methane (CH₄), a non-polar molecule characterized by a tetrahedral structure, stands as the simplest organic compound. Predominantly constituting conventional natural gas, shale gas, and combustible ice, it plays a pivotal role as a carbon-based resource and a key raw material in the petrochemical industry. In natural formations, CH₄ and H₂O coexist in a synergistic system. This interplay necessitates a thorough examination of the phase equilibrium in the CH₄-H₂O system and CH₄’s solubility under extreme conditions of temperature and pressure, which is crucial for understanding the genesis and development of gas reservoirs. This study synthesizes a comprehensive solubility database by aggregating extensive solubility data of CH₄ in both pure and saline water. Utilizing this database, the study updates and refines the key parameters of Henry’s law. The updated Henry’s law has a prediction error of 22.86% at less than 40 MPa, which is an improvement in prediction accuracy compared to before the update. However, the modified Henry’s law suffers from poor calculation accuracy under certain pressure conditions. To further improve the accuracy of solubility prediction, this work also trains a BP (Back Propagation) neural network model based on the database. In addition, MSE (Mean-Square Error) is used as the model evaluation index, and pressure, temperature, compression coefficient, salinity, and fugacity are preferred as input variables, which finally reduces the mean relative error of the model to 16.32%, and the calculation results are more accurate than the modified Henry’s law. In conclusion, this study provides a novel and more accurate method for predicting CH₄ solubility by comparing modified Henry’s law to neural network modeling. Full article

Gas hydrates represent an attractive opportunity for gas storage. These ice-like structures can be produced both for the final disposal of greenhouse gases such as carbon dioxide in the solid form and for the storage of energy gases, such as methane, propane, and others, with the possibility of reaching energy densities comparable with those of pressurised vessels, but at lower pressures. In addition, gas hydrates can be directly produced for their capability to act as phase change materials at temperatures higher than 0 °C. This research deals with cold energy storage via the production of gas hydrate into a lab-scale apparatus. Hydrates were produced with pure carbon dioxide and with CO₂/N₂ mixtures (70/30 and 50/50 vol%). For each mixture, the amount of energy spent for hydrates production and cold energy stored were calculated, and the results were compared among each other. The addition of nitrogen to the system allowed us to maximise the energy stored/energy spent ratio, which passed from 78.06% to 109.04%; however, due to its molecular size and the consequent impossibility to stabilise the occupied water cages, nitrogen caused a reduction in the total quantity of hydrates produced, which was obviously proportional to the energy stored. Therefore, the concentration of nitrogen in the mixtures need to be carefully determined in order to optimise the Estored/Espent ratio. Full article

Modern integrated circuits (ICs) take advantage of three-dimensional (3D) nanostructures in devices and interconnects to achieve high-speed and ultra-low-power performance. The choice of electrical insulation materials with excellent dielectric strength, electrical resistivity, strong mechanical strength, and high thermal conductivity becomes critical. Diamond possesses these properties and is recently recognized as a promising dielectric material for the fabrication of advanced ICs, which are sensitive to detrimental high-temperature processes. Therefore, a high-rate low-temperature deposition technique for large-grain, high-quality diamond films of the thickness of a few tens to a few hundred nanometers is desirable. The diamond growth rate by microwave plasma chemical vapor deposition (MPCVD) decreases rapidly with lowering substrate temperature. In addition, the thermal conductivity of non-diamond carbon is much lower than that of diamond. Furthermore, a small-grain diamond film suffers from poor thermal conductivity due to frequent phonon scattering at grain boundaries. This paper reports a novel MPCVD process aiming at high growth rate, large grain size, and high sp³/sp² ratio for diamond films deposited on silicon. Graphite paste containing nanoscale graphite and oxy-hydrocarbon binder and solvent vaporizes and mixes with gas feeds of hydrogen, methane, and carbon dioxide to form plasma. Rapid diamond growth of diamond seeds at 450 °C by the plasma results in large-grained diamond films on silicon at a high deposition rate of 200 nm/h. Full article

Climate-induced changes contribute to the thawing of ice-rich permafrost in the Arctic, which leads to the release of large amounts of organic carbon into the atmosphere in the form of greenhouse gases, mainly carbon dioxide and methane. Ground ice constitutes a considerable volume of the cryogenically sequestered labile dissolved organic carbon (DOC) subjected to fast mineralization upon thawing. In this work, we collected a unique geochemical database of the ground and glacier ice comprising the samples from various geographic locations in the Russian Arctic characterized by a variety of key parameters, including ion composition, carbon-bearing gases (methane and carbon dioxide), bulk biogeochemical indicators, and fluorescent dissolved organic matter (DOM) fractions. Our results show that interaction with solid material—such as sediments, detritus, and vegetation—is likely the overriding process in enrichment of the ground ice in all the dissolved compounds. Terrigenous humic-like dissolved organic matter was predominant in all the analyzed ice samples except for glacier ice from Bolshevik Island (the Severnaya Zemlya archipelago) and pure (with low sediment content) tabular ground ice from western Yamal. The labile protein-like DOM showed no correlation to humic components and was probably linked to microbial abundance in the ground ice. The sum of the fluorophores deconvoluted by PARAFAC strongly correlates to DOC, which proves the potential of using this approach for differentiation of bulk DOC into fractions with various origins and biogeochemical behaviors. The pure tabular ground ice samples exhibit the highest rate of fresh easily degradable DOM in the bulk DOC, which may be responsible for the amplification of permafrost organic matter decomposition upon thawing. Full article

Bis-indole derived compounds such as 1,1-bis(3′-indolyl)-1-(3,5-disubstitutedphenyl) methane (DIM-3,5) and the corresponding 4-hydroxyl analogs (DIM8-3,5) are NR4A1 ligands that act as inverse NR4A1 agonists and are potent inhibitors of tumor growth. The high potency of several DIM-3,5 analogs (IC₅₀ < 1 mg/kg/day), coupled with the >60% similarity of the ligand-binding domains (LBDs) of NR4A1 and NR4A2 and the pro-oncogenic activities of both receptors lead us to hypothesize that these compounds may act as dual NR4A1 and NR4A2 ligands. Using a fluorescence binding assay, it was shown that 22 synthetic DIM8-3,5 and DIM-3,5 analogs bound the LBD of NR4A1 and NR4A2 with most K_D values in the low µM range. Moreover, the DIM-3,5 and DIM8-3,5 analogs also decreased NR4A1- and NR4A2-dependent transactivation in U87G glioblastoma cells transfected with GAL4-NR4A1 or GAL4-NR4A2 chimeras and a UAS-luciferase reporter gene construct. The DIM-3,5 and DIM8-3,5 analogs were cytotoxic to U87 glioblastoma and RKO colon cancer cells and the DIM-3,5 compounds were more cytotoxic than the DIM8-3,5 compounds. These studies show that both DIM-3,5 and DIM8-3,5 compounds previously identified as NR4A1 ligands bind both NR4A1 and NR4A2 and are dual NR4A1/2 ligands. Full article

Coal penetration enhancement technology is the key to increase the production of coalbed methane. Coal bodies are subjected to different peripheral pressures in the in situ strata, and the study of the changes in the mechanical strength of coal bodies under different peripheral pressures after the action of liquid nitrogen is crucial for the penetration enhancement of liquid nitrogen (LN₂)-fractured coal. In this paper, an MTS universal testing machine was utilized to carry out experiments to obtain the stress–strain curves of the coal under different freezing times under 1 MPa surrounding pressure and different surrounding pressures after 50 min of LN₂ action. The experimental results showed the following: (1) the uniaxial compressive strength and peak strain of coal samples in a frozen state are positively correlated under two conditions. The modulus of elasticity decreased before 100 min at different times of LN₂ action, and the modulus of elasticity was maximum at 5 MPa at different peripheral pressure actions; (2) the uniaxial compressive strength and peak strain of the frozen-thawed coal samples decreased before 100 min of LN₂ action at different times, and the modulus of elasticity continued to decrease. The uniaxial compressive strength and modulus of elasticity of coal samples in freeze–thaw state under different peripheral pressures were the largest at 5 MPa, and the peak strain was negatively correlated. (3) The elastic strain energy of the frozen coal samples under the action of LN₂ at different times was positively correlated with the freezing time before 80 min, and negatively correlated after 80 min. The elastic strain energy of the frozen coal samples was positively correlated with the freezing time. The elastic strain energy and freezing time of the two coal samples under different circumferential pressures were positively correlated before 5 MPa and negatively correlated after 5 MPa, with opposite dissipation energies. (4) The water–ice phase transition and temperature–thermal stresses on the internal structure of the coal in the presence of LN₂ cause significant damage. The degradation of coal samples in the freeze–thaw state is even higher under in situ ground pressure. Full article

Noctilucent clouds (NLC) are sensitive indicators in the upper mesosphere, reflecting changes in the background atmosphere. Studying NLC responses to the solar cycle is important for understanding solar-induced changes and assessing long-term climate trends in the upper mesosphere. Additionally, it enhances our understanding of how increases in greenhouse gas concentration in the atmosphere impact the Earth’s upper mesosphere and climate. This study presents long-term trends in the response of NLC and the background atmosphere to the 11-year solar cycle variations. We utilised model simulations from the Leibniz Institute Middle Atmosphere (LIMA) and the Mesospheric Ice Microphysics and Transport (MIMAS) over 170 years (1849 to 2019), covering 15 solar cycles. Background temperature and water vapour (H₂O) exhibit an apparent response to the solar cycle, with an enhancement post-1960, followed by an acceleration of greenhouse gas concentrations. NLC properties, such as maximum brightness (β_max), calculated as the maximum backscatter coefficient, altitude of β_max (referred to as NLC altitude) and ice water content (IWC), show responses to solar cycle variations that increase over time. This increase is primarily due to an increase in background water vapour concentration caused by an increase in methane (CH₄). The NLC altitude positively responds to the solar cycle mainly due to solar cycle-induced temperature changes. The response of NLC properties to the solar cycle varies with latitude, with most NLC properties showing larger and similar responses at higher latitudes (69° N and 78° N) than mid-latitudes (58° N). Full article

Bis(indolyl)methanes (BIMs) are a class of compounds that have been recognized as an important core in the design of drugs with important pharmacological properties, such as promising anticancer and antiparasitic activities. Here, we explored the biological activity of the BIM core functionalized with different (hetero)aromatic moieties. We synthesized substituted BIM derivatives with triphenylamine, N,N-dimethyl-1-naphthylamine and 8-hydroxylquinolyl groups, studied their photophysical properties and evaluated their in vitro antiproliferative and antiparasitic activities. The triphenylamine BIM derivative 2a displayed an IC₅₀ of 3.21, 3.30 and 3.93 μM against Trypanosoma brucei, Leishmania major and HT-29 cancer cell line, respectively. The selectivity index demonstrated that compound 2a was up to eight-fold more active against the parasites and HT-29 than against the healthy cell line MRC-5. Fluorescence microscopy studies with MRC-5 cells and T. brucei parasites incubated with derivative 2a indicate that the compound seems to accumulate in the cell’s mitochondria and in the parasite’s nucleus. In conclusion, the BIM scaffold functionalized with the triphenylamine moiety proved to be the most promising antiparasitic and anticancer agent of this series. Full article

The relaxation processes induced by exposure of the Ar matrices doped with CH₄ (0.1–10%) to an electron beam were studied with a focus on the dynamics of radiolysis products—H atoms, H₂ molecules, CH radicals, and energy transfer processes. Three channels of energy transfer to dopant and radiolysis products were discussed, including free charge carriers, free excitons and photons from the “intrinsic source” provided by the emission of the self-trapped excitons. Radiolysis products along with the total yield of desorbing particles were monitored in a correlated manner. Analysis of methane transformation reactions induced by free excitons showed that the CH radical can be considered a marker of the CH₃ species. The competition between exciton self-trapping and energy transfer to the dopant and radiolysis products has been demonstrated. A nonlinear concentration behavior of the H atoms in doped Ar matrices has been established. Real-time correlated monitoring of optical emissions (H atom and CH₃ radicals), particle ejection, and temperature revealed a nonmonotonic behavior of optical yields with a strong luminescence flash after almost an hour of exposure, which correlated with the explosive pulse of particle ejection and temperature. The connection of this phenomenon with the processes of energy transfer and recombination reactions has been established. It is shown that the delayed explosive ejection of particles is driven by both the recombination of H atoms and CH₃ radicals. This occurs after their accumulation to a critical concentration in matrices at a CH₄ content C ≥ 1%. Full article