Search Results (8,592)

The exceptionally strong geomagnetic storm of 10–11 May 2024 injected new energetic protons and electrons into the terrestrial radiation belts, creating extraordinary conditions to study the loss mechanisms scattering these particles into the atmosphere after the storm. For the first time, four electron belts were observed during several weeks. We show that this structure was due to electron loss, highly dependent on specific positions. Using the proton and electron fluxes measured by the Energetic Particle Telescope, EPT, on board PROBA-V, we determine the lifetimes of these populations depending on their energy ranges and positions. We show that the lifetimes are much longer for protons than for electrons, which enables us to determine their time variations independently. For electrons, the wave–particle loss mechanisms depend on the background ionosphere–plasmasphere density. The lifetimes determined after the May 2024 and 10 October 2024 big events are compared with average ones to understand their unusual specificity for the formation of four and three belts, respectively. For the injected protons of 9.5 to 13 MeV, the lifetime is minimum at L~1.9, where the fluxes are maximum, showing a lifetime depending on the flux intensity. Loss is due to pitch angle diffusion and collisions with electrons and nuclei in the ambient plasma and neutral atmosphere. At the outer edge of the proton belt, the flux is depleted at all energies after the geomagnetic perturbation, and we determine that the progressive time of refilling after the storm generally reaches more than 40 days. There is an excellent discrimination between the different populations of energetic electrons (0.5–8 MeV) and the injected protons (9.5–13 MeV) that are still observed several months after the event. Such results contribute to advancing understanding of the interactions between the terrestrial atmosphere and space radiation. Full article

Kavalactones are psychoactive substances that naturally occur in some plants, such as Piper methysticum, Alpinia zerumbet, and Achyrocline satureioides, which are considered to have a significantly positive effect on human organisms. For example, Alpinia zerumbet is classified as a life-expanding plant. Although high-pressure liquid chromatography–mass spectrometry has been used for kavalactone analysis in plant material, the fragmentation pathways of protonated kavalactone molecules are not fully known and require further detailed study. In this paper, the fragmentation pathways of [M+H]⁺ ions of twelve kavalactones, including three pairs of isomers, are discussed in detail. Special emphasis has been placed on diagnostic product ions, which are characteristic of kavalactone structures. It has been demonstrated that diagnostic ions and structure–fragmentation relationships enable the differentiation of isomeric kavalactones and may be useful for the identification of other kavalactone conjugates, such as kavalactone dimers or kavalactone glycosides. Full article

Carbon dioxide emissions from fossil fuel burning remains a severe environmental challenge that needs to be addressed. Deep eutectic solvents (DESs) have emerged as promising alternatives to conventional alkanolamines for CO₂ capture applications due to their lower volatility and reduced corrosion potential. In this work, two tetrabutylammonium bromide (TBAB)-based systems were synthesized using different hydrogen bond donors: 2-amino-2-methyl-1-propanol (AMP) at a 1:1 molar ratio and p-toluenesulfonic acid (PTSA) at a 1:2 molar ratio. FTIR spectroscopic analysis confirmed that TBAB-AMP (1:1) forms a true DES through hydrogen bonding interactions, whereas TBAB-PTSA (1:2) undergoes proton transfer to form an ionic salt. CO₂ solubility measurements were conducted using the pressure drop method up to 15 bar at 30 °C. The TBAB-AMP system exhibited a CO₂ uptake of 0.194 mol CO₂/mol DES at 14.7 bar, approximately 2.5-fold higher than the TBAB-PTSA system, which achieved 0.079 mol/mol at 14.5 bar. Critical and thermophysical properties were estimated using the modified Lydersen–Joback–Reid, Lee–Kesler, and Haghbakhsh group-contribution methods. Viscosity measurements conducted from 30 to 50 °C revealed that TBAB-AMP exhibited significantly lower viscosity, ranging from 163 to 46 mPa·s, compared to TBAB-PTSA, which showed viscosity values between 536 and 155 mPa·s. The superior CO₂ capture performance of the amine-functionalized DES was attributed to favorable hydrogen-bonding interactions, lower viscosity, which enabled better mass transfer, and enhanced chemical affinity toward CO₂ through carbamate formation. Full article

Conventional phenolic-resin-based carbon fiber paper (CFP) typically suffers from low mechanical strength, poor toughness, insufficient pore interconnectivity, and a reliance on extreme high-temperature graphitization to attain high conductivity. This study employs a novel melamine-hexamethylenediamine (MH) thermosetting resin as the binder to fabricate MH resin-based CFP (MHCFP). Through the synergistic effects of robust interfacial bonding, triazine-ring-induced low-temperature formation of sp² carbon clusters, and nitrogen doping, the MHCFP achieves comprehensive performance superiority over the phenol-formaldehyde (PF)-based CFP (PFCFP) at moderate carbonization temperatures (500–700 °C): MHCFP exhibits superior toughness, tensile strengths of 23–45 MPa (vs. PFCFP’s 8–18 MPa), and in-plane resistivity of 24–39 mΩ·cm (vs. PFCFP’s 54–83 mΩ·cm). Furthermore, MHCFP possesses a highly open macroporous structure (porosity > 78%), ensuring excellent gas permeability and water management capability. This work presents a promising low-temperature strategy for developing high-performance CFP, showing great potential for next-generation proton exchange membrane fuel cell gas diffusion layers. Full article

A correct description of quarkonia production and kinematics is still one of the most challenging assignments for Quantum Chromodynamics. This document presents a study of the ${\rm Y}$(1S), (2S) and (3S) mean transverse momentum ($⟨p_{\mathrm{T}}^{{\rm Y}}⟩$) as a function of the charged particle multiplicity ($N_{\mathrm{Track}}$) in proton–proton collisions at $\sqrt{s}$ = 7 TeV generated with Pythia 8.312 CUETP8M1 tune. The comparison to real data collected by the CMS experiment indicates that the agreement is much better for the excited states than for the ground state. The observed fast increase in the $⟨p_{\mathrm{T}}^{{\rm Y}}⟩$ at small values of $N_{\mathrm{Track}}$ is mainly due to the contribution from the away region. Furthermore, when computing the $⟨p_{\mathrm{T}}^{{\rm Y}}⟩$ from jetty and isotropic events, a clear $p_{\mathrm{T}}$ hardening is observed in jetty events. Finally, analyzing the fragmentation of jets containing an ${\rm Y}$(nS), a new method is proposed to test the new quarkonia shower present in the Monte Carlo event generator. Full article

The conformational properties and intrinsic reactivity of unsaturated CH₂=C(R)XH systems (R = –H, –CH=CH₂, –C≡CH, –C≡N, –Cl, –phenyl, –cyclopentadienyl, –pyrrole; X = O, S, Se)—namely enols, enethiols, and eneselenols—have been investigated using G4 and CCSD(T) calculations. All compounds exhibit antiperiplanar (ap) and anticlinal (ac)-conformers that are nearly isoenergetic, as their relative stabilities are governed by subtle noncovalent interactions, which are analyzed in detail. Both conformers are therefore expected to coexist in the gas phase, and because the rotational barriers are very low, their interconversion is effectively barrierless under typical conditions. In contrast, the corresponding protonated species display significantly higher barriers, approximately three to five times larger. The keto–enol tautomerization involves activation barriers exceeding 180 kJ·mol⁻¹, confirming that, as in other keto–enol rearrangements, the process is not monomolecular. Protonation generally occurs at the methylene carbon, with the exceptions of the –C≡CH and –C≡N derivatives. Strong linear correlations are found among the proton affinities of the three families studied, which follow the trend: enols > enethiols > eneselenols. All systems behave as strong carbon bases; some are predicted to be 20–21 orders of magnitude more basic than ketene and 3–5 orders of magnitude more basic than vinylimine in terms of equilibrium constants. Deprotonation preferentially occurs at the X–H group in nearly all cases. The only exception is the cyclopentadienyl-substituted enol, for which deprotonation of the cyclopentadienyl moiety is favored due to enhanced aromatic stabilization of the resulting anion. Overall, acidity increases along the series O < S < Se. Full article

In this work the feasibility of fully autonomous hydrogen homes designed for complete off-grid operation is presented. A detailed mathematical modeling and optimization model is developed to evaluate the technical performance and economic feasibility of hydrogen fuel cell-powered residential systems with no grid connection or fallback. The system integrates primary and standby Proton Exchange Membrane (PEM) fuel cells, multi-day hydrogen storage, advanced power conditioning, and comprehensive controls to achieve reliable year-round power supply. The analysis encompasses a complete 20-year lifecycle cost assessment. The results demonstrate that fully autonomous hydrogen homes achieve 99.85% system availability with 13.1 h of potential downtime annually, providing reliable energy independence. The levelized cost of electricity over the 20-year system lifetime is calculated at 0.4543 US$/kWh at baseline hydrogen prices of 6 US$/${\mathrm{kg}}_{{\mathrm{H}}_2}$, substantially higher than grid-connected alternatives. The analysis identifies critical sensitivity to hydrogen pricing and demonstrates that at hydrogen costs below 3 US$/${\mathrm{kg}}_{{\mathrm{H}}_2}$ (achievable with mature green hydrogen production), competitive payback periods of 12–15 years are possible in high-cost electricity regions. This study concludes that hydrogen-based autonomous homes represent a viable long-term solution for residential energy independence, particularly in remote or off-grid locations where grid connection is impractical or in regions with high electricity tariffs and developing green hydrogen production capacity. Full article

Structural optimization of the cathode flow field is a viable approach to homogenize multi-physical field distributions and boost the output of air-cooled proton exchange membrane fuel cells (PEMFCs). This work develops a three-dimensional non-isothermal model to systematically evaluate the performance of graded flow channel designs. The results indicate that the graded structure promotes fluid transport in the central zone, thereby improving oxygen distribution uniformity at the gas diffusion layer/catalyst layer (GDL/CL) interface. Compared to the traditional parallel flow channel (with an average oxygen mass fraction of 0.051% and a uniformity index of 0.779), this configuration yields a 6.4% increase in the average oxygen mass fraction and a 0.96% enhancement in distribution uniformity. However, increased gradient flow reduces the flow velocity within the channels and raises the operating temperature, posing challenges for water and thermal management. The curved channel design, featuring longer channels at the ends and shorter channels in the center, compensates for the uneven air supply caused by the fan, thus balancing the flow distribution. Among the tested configurations, the 10° curved structure exhibits optimal performance, achieving the best compromise between gas distribution and liquid water removal. It effectively promotes oxygen diffusion and uniform water distribution, significantly alleviating mass transfer polarization and yielding a more uniform interface temperature distribution due to evaporative cooling. Both excessively small and large curvature angles lead to performance degradation, primarily due to inadequate water removal and flow separation, accompanied by excessive pressure drop, respectively. In contrast, the 10° curved channel strikes an optimal balance, offering significant advantages in overall cell performance and water–thermal management, which provides critical guidance for optimizing PEMFC flow field designs. Full article

We report on laser fusion research with nanotechnology-improved targets embedded in special polymers. The results of the last three years are reviewed here, including laser matter interaction craters, laser infrared breakdown spectroscopy, and Raman spectroscopy results, as well as a selected Thomson parabola image showing protons accelerated up to 300 keV. In this paper, we focus on proton acceleration and plasmonic enhancement mechanisms rather than on the direct demonstration of sustained fusion reactions. Full article

Micropropagated plantlets, after removal from controlled laboratory conditions, require an acclimatization period. Adaptation to the new environment induces anatomical and physiological changes controlled by cellular processes. This study investigated the involvement of the primary proton transport systems of total membranes in pineapple root colonization by diazotrophic bacteria and in the development of plantlets treated with different nitrogen doses, allowing an understanding of nutrient absorption and accumulation dynamics. The experiment followed a randomized block design (RBD) in a factorial scheme (2 × 3 × 2), with two inocula (a mixture of diazotrophic bacteria containing Burkholderia sp. UENF 114111, Burkholderia silvatlantica UENF 117111, and Herbaspirillum seropedicae HRC 54, and another without bacteria), three urea doses (0, 5, and 10 g L⁻¹), and two evaluation (90 and 150 days) and bacterial counting times (30 and 150 days), with three blocks. Diazotrophic bacterial populations were lower in older plantlets. H⁺ transport mediated by P H⁺-ATPases changed with acclimatization time. Inoculation did not induce transport; however, the F_max of V H⁺-ATPase was lower without nitrogen fertilization. Nitrogen fertilization affected V H⁺-ATPase proton transport activity in root membranes. The presence of diazotrophic bacteria did not induce proton transport. On the other hand, nitrogen fertilization and acclimatization time affected the proton transport activity mediated by H⁺-ATPases isolated from roots of micropropagated pineapple. Full article

Percentage depth–dose (PDD) distributions are fundamental to characterizing radiation beams in radiotherapy. This review provides an overview of both methods and sensor technologies for measuring PDD in photon, electron, proton, and carbon-ion beams. We summarize conventional dosimetry techniques, including water-phantom scanning with ionization chambers (cylindrical and parallel-plate) and radiochromic film, and discuss their strengths (established accuracy, calibration traceability) and limitations (volume averaging, delayed readout). We then examine emerging sensor technologies designed to improve spatial resolution, speed, and radiation hardness: multi-layer ionization chambers and Faraday cups for one-shot PDD acquisition; scintillator-based detectors (liquid, plastic, and fiber-optic) enabling real-time and high-resolution depth–dose measurements; advanced semiconductor detectors including silicon carbide diodes; as well as novel approaches such as ionoacoustic range sensing for proton beams. For each modality and detector type, we emphasize clinical relevance, measurement accuracy, spatial resolution, radiation durability, and suitability for high dose-per-pulse environments (e.g., FLASH radiotherapy). Current challenges, such as detector response in regions of steep dose gradient, saturation or recombination at ultra-high dose rates, and energy-dependent sensitivity in mixed radiation fields, are analyzed in detail. We also highlight the limitations of each technique and discuss ongoing improvements and prospects for clinical implementation. In summary, no single detector technology fully satisfies all requirements for fast, high-accuracy, high-resolution, radiation-hard PDD measurement, but the integration of emerging sensor innovations into clinical dosimetry promises to enhance the precision and efficiency of radiotherapy quality assurance. Full article

Pt-based catalysts remain the most effective materials for the oxygen reduction reaction (ORR) at the cathode of proton exchange membrane fuel cells (PEMFCs); however, platinum scarcity and high cost severely limit the large-scale deployment of the technology. Improving catalytic activity and durability through precise control of nanoparticle morphology is therefore crucial for reducing costs and enhancing sustainability, enabling PEMFC widespread adoption. In this context, carbon-supported Pt-based nanoparticles with a 30 wt.% Pt loading were synthesized by an organometallic chemistry approach using hexadecylamine (HDA) as a stabilizer, allowing fine control over nanoparticle morphology. Two distinct synthesis pathways (one-pot and two-step procedures) were used to prepare platinum catalysts supported on KetjenBlack EC-300J (KB), and their influence on the electrocatalytic activity of the obtained nanomaterials was studied. Furthermore, the effect of HDA stabilization on catalyst performance was investigated. Directly synthesized Pt/KB catalysts exhibited similar ORR mass activity, regardless of whether or not HDA was present. Pt/KB prepared by the two-step procedure showed a significantly lower performance. Additionally, despite a larger loss of electrochemical surface area during an accelerated stress test compared to a commercial Pt/C reference, Pt^HDA/KB and Pt/KB catalysts maintained stable mass activity and limited specific activity degradation, highlighting the beneficial effect of nanoparticle stabilization in the presence of HDA on prolonged electrocatalyst cycling. Full article

Background: Pancreatic trauma (PT) in children is rare and associated with significant morbidity. The optimal form of management—operative versus non-operative—remains controversial, particularly in the presence of acute post-traumatic peripancreatic fluid collection, which may later evolve into pancreatic pseudocysts. Isolated pancreatic injuries without associated organ damage are uncommon and pose diagnostic and therapeutic challenges. Case Presentation: We report a 5-year-old boy who sustained an isolated grade IB blunt pancreatic head contusion following blunt abdominal trauma after falling onto a wooden fence. He presented with epigastric pain, repeated emesis, and an abdominal wall bruise. Initial ultrasound (US) findings were subtle; however, serial imaging and contrast-enhanced computed tomography (CECT) revealed focal contusion of the pancreatic head/uncinate process with a small peripancreatic fluid collection. Pancreatic enzymes were markedly elevated, with peak serum lipase reaching approximately 6579 U/L. The child remained hemodynamically stable and was managed conservatively with bowel rest, intravenous fluids, octreotide, proton-pump inhibition, pancreatic enzyme replacement therapy (PERT), and antibiotics. Serial US demonstrated the dynamic evolution of an acute peripancreatic fluid collection (APFC) (~2 cm), which remained stable without complications. Clinical and biochemical parameters gradually improved, and no invasive intervention was required. The patient was discharged on hospital day 16 with planned outpatient imaging follow-up. Conclusions: This case demonstrates that isolated pediatric pancreatic contusions complicated by small, evolving peripancreatic fluid collections can be safely managed non-operatively in hemodynamically stable patients. Serial ultrasound plays a key role in monitoring lesion evolution and guiding management decisions. In accordance with current pediatric trauma guidelines, careful observation with structured follow-up may prevent unnecessary invasive interventions while achieving excellent clinical outcomes. Full article

While many [FeFe]-hydrogenase biomimetics are effective proton-reduction catalysts, few are active for H₂ oxidation, and examples containing both a pendant amine group, able to act as a proton relay, and a second redox center, both essential features of the enzymes, are rare. Here we report the preparation and oxidation chemistry of two ferrocene-functionalized amino-diphosphines (PCNCP), (CH₂PR₂)₂NCH₂Fc (R = Ph (1), Cy (2)), and their ethylenedithiolate (edt) diiron complexes, [Fe₂(CO)₄(μ-edt){κ²-(R₂PCH₂)₂NCH₂Fc}] (R = Ph (3), Cy (4)). Their crystallographic characterization shows that PCNCP occupies an apical–basal position. CV responses are slightly R-dependent, showing for 3 and 4 in three separate oxidative processes assigned to successive one-electron oxidation of the diiron core (quasireversible), appended Fc (reversible), and the amine–diiron moiety (irreversible), as confirmed by IR and UV–Vis spectroelectrochemical studies supported by Density Functional Theory (DFT) and Time-dependent Density Functional Theory (TDDFT) calculations. The first oxidation results in a structural rearrangement of the Fe(PNP)(CO) unit and the formation of a semi-bridging carbonyl. Slow protonation of 3 with HBF₄∙Et₂O affords the corresponding N-protonated cation in acetone, whilst μ-hydride products dominate for both 3 and 4 in CD₂Cl₂. A preliminary H₂ oxidation study was carried out with 3, and while there was some evidence of activity, it was much lower than reported for alkyl-functionalized PCNPC diiron derivatives. Full article

5-Methoxymethyl-2-furfural (MMF) serves as a crucial biobased platform molecule that can be transformed into various high-value chemicals and biobased polyester monomers. However, the current production of MMF still faces several challenges, such as low yield and prolonged reaction time. In this study, we prepared a series of amide-modified strongly acidic resin catalysts and discovered that they have a higher efficiency in converting fructose to prepare MMF in 1-Butyl-3-methylimidazolium chloride ([BMIM]Cl) and methanol. Among the synthesized catalysts, DB757-NMP demonstrated superior performance, achieving an MMF yield of approximately 61.5% under the optimized conditions, with a combined yield of HMF and MMF reaching about 66.6%. The catalyst formation mechanism was analyzed using FTIR, and NMR, confirming the transformation of proton between NMP and the sulfonic acid groups of the resin, which collectively promoted the conversion of fructose to MMF. In addition, we investigated main reasons for catalyst deactivation and successfully restored catalytic activity through regeneration. The regenerated catalyst could be reused for three times with only a slight decrease in MMF yield. The results suggested that DB757-NMP is a more sufficient and recyclable catalyst for the production of MMF from fructose. This work presented a simple and environmentally benign approach for the synthesis of MMF. Full article