69,553 research outputs found

    Chemical Lake Restoration Methods: From Alum to Innovative Composite Materials

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    This chapter evaluated a spectrum of chemical restoration approaches of eutrophic water systems, highlighting the key role of internal nutrient loads to guide remediation methods that control eutrophication. The usage of P- and joint P-/N-inactivation agents have been considered as feasible restoration tools through capacity and application methods in alignment with a wide spectrum of individuallyexamined nature-contexts, including that of water quality, algal blooms, flora, and fauna. Moreover, an integrated approach was developed to evaluate those restoration tools of degraded waters through specified conditions when P-inactivation agent was applied

    Novel Composite Materials as P-Adsorption Agents and Their Potential Applications as Fertilizers

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    In a world with high demand in P for the maintenance of soil fertility and crop productivity, this chapter introduced the types and sources of P fertilizers in soil. Specifically chemical fertilizers were discussed, with phosphate rock being the primary source of phosphate, versus organic phosphate fertilizers, such as P humates and organominerals. Moreover, novel composite materials that have been used as P-adsorption agents are proposed as an alternative source of soil P fertilizers, which could be effective soil conditioners, slowly releasing macro- and micro-nutrients in agricultural soils

    New performing GC columns with unmatched separation capabilities

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    Gas chromatography (GC) is widely used for qualitative and quantitative analysis in numerous fields, such as petroleum, chemical industry, agriculture, environmental protection, medicine, and so on, due to its high versatility, high selectivity, simplicity of use, analysis speed, and low sample consumption. The column is the heart of a GC instrumentation, which allows the analyte separation and their recognition and quantification. Commercial columns do not always allow a complete peak separation when compounds (i.e., isomers) are very similar in molecular weight, polarity, and vapor pressure. The choice of the correct stationary phase, with high selectivity towards target analytes, is the key to obtaining the required chromatographic separation and the subsequent qualitative and quantitative analysis. Considering the rapid polymer science development and the growing demand for new columns with improved resolution capabilities, in this work novel stationary phases for capillary GC have been designed, synthesized, and characterized in terms of polarity range, resolution, column efficiency, thermal stability, filmforming properties, and support-deactivating capacity1-5. The separation features of these novel stationary phases allow high-resolution performances for a wide range of compounds, like aromatic anilines, xylenes, aromatic amines, halogenated benzenes, and aromatic aldehydes, with marked capabilities toward isomer separations.References: [1] T. Sun, M. Ba, Y. Song, W. Li, Y. Zhang, Z. Cai, S. Hu, X. Liu, D. Nardiello, M. Quinto, Analytica Chimica Acta, 2024, 1291, art. no. 342221. [2] T. Sun, R. Chen, Q. Huang, M. Ba, Z. Cai, H. Chen, Y. Qi, H. Chen, X. Liu, D. Nardiello, M. Quinto, Analytica Chimica Acta, 2023, 1251, art. no. 340979. [3] T. Sun, R. Chen, Q. Huang, M. Ba, Z. Cai, S. Hu, X. Liu, D. Nardiello, M. Quinto, ACS Applied Materials and Interfaces, 2022, 14 50, pp. 56132-56142 [4] R. Chen, Z. Cai, W. Li, Q. Huang, D. Nardiello, M. Quinto, X. Liu, S. Hu, T. Sun, Chemistry and Biodiversity, 2022, 19, art. no. e202200829 [5] Q. Huang, Z. Cai, R. Chen, W. Zhang, D. Nardiello, M. Quinto, X. Liu, S. Hu, T. Sun, Microchemical Journal, 2022, 183, art. no. 10808

    A 2 h periodic variation in the low-mass X-ray binary Ser X-1

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    Spectroscopy of the low-mass X-ray binary Ser X-1 using the Gran Telescopio Canarias have revealed a ?2 h periodic variability that is present in the three strongest emission lines. We tentatively interpret this variability as due to orbital motion, making it the first indication of the orbital period of Ser X-1. Together with the fact that the emission lines are remarkably narrow, but still resolved, we show that a main-sequence K dwarf together with a canonical 1.4 M? neutron star gives a good description of the system. In this scenario, the most likely place for the emission lines to arise is the accretion disc, instead of a localized region in the binary (such as the irradiated surface or the stream-impact point), and their narrowness is due instead to the low inclination (?10°) of Ser X-1

    Extension of the sun-synchronous Orbit

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    Through careful consideration of the orbit perturbation force due to the oblate nature of the primary body a secular variation of the ascending node angle of a near-polar orbit can be induced without expulsion of propellant. Resultantly, the orbit perturbations can be used to maintain the orbit plane in, for example, a near-perpendicular (or at any other angle) alignment to the Sun-line throughout the full year of the primary body; such orbits are normally termed Sun-synchronous orbits [1, 2]. Sun-synchronous orbits about the Earth are typically near-circular Low-Earth Orbits (LEOs), with an altitude of less than 1500 km. It is normal to design a LEO such that the orbit period is synchronised with the rotation of the Earth‟s surface over a given period, such that a repeating ground-track is established. A repeating ground-track, together with the near-constant illumination conditions of the ground-track when observed from a Sun-synchronous orbit, enables repeat observations of a target over an extended period under similar illumination conditions [1, 2]. For this reason, Sun-synchronous orbits are extensively used by Earth Observation (EO) platforms, including currently the Environmental Satellite (ENVISAT), the second European Remote Sensing satellite (ERS-2) and many more. By definition, a given Sun-synchronous orbit is a finite resource similar to a geostationary orbit. A typical characterising parameter of a Sun-synchronous orbit is the Mean Local Solar Time (MLST) at descending node, with a value of 1030 hours typical. Note that ERS-1 and ERS-2 used a MLST at descending node of 1030 hours ± 5 minutes, while ENVISAT uses a 1000 hours ± 5 minutes MLST at descending node [3]. Following selection of the MLST at descending node and for a given desired repeat ground-track, the orbit period and hence the semi-major axis are fixed, thereafter assuming a circular orbit is desired it is found that only a single orbit inclination will enable a Sun-synchronous orbit [2]. As such, only a few spacecraft can populate a given repeat ground-track Sun-synchronous orbit without compromise, for example on the MLST at descending node. Indeed a notable feature of on-going studies by the ENVISAT Post launch Support Office is the desire to ensure sufficient propellant remains at end-of-mission for re-orbiting to a graveyard orbit to ensure the orbital slot is available for future missions [4]. An extension to the Sun-synchronous orbit is considered using an undefined, non-orientation constrained, low-thrust propulsion system. Initially the low-thrust propulsion system will be considered for the free selection of orbit inclination and altitude while maintaining the Sun-synchronous condition. Subsequently the maintenance of a given Sun-synchronous repeat-ground track will be considered, using the low-thrust propulsion system to enable the free selection of orbit altitude. An analytical expression will be developed to describe these extensions prior to then validating the analytical expressions within a numerical simulation of a spacecraft orbit. Finally, an analysis will be presented on transfer and injection trajectories to these orbits

    INNOVATIVE PILLAR[6]ARENE-BASED STATIONARY PHASES FOR HIGH-RESOLUTION GAS CHROMATOGRAPHIC ANALYSES

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    In this work, the synthesis, fabrication, and characterization of new stationary phases based on pillar[6]arene derivative modified by long alkyl chains (P6A-C10) for high-resolution gas chromatographic (GC) analyses are reported. Pillar[n]arenes are a new class of macrocyclic hosts that can accommodate specific guests due to their highly symmetrical and rigid pillar architectures with π-electron rich cavities. Quantum chemistry calculations have been performed, showing a difference in non-covalent interactions with the P6A-C10 pillar framework, which leads to specific selectivity for aromatic compounds. The GC columns prepared with these innovative stationary phases exhibited a medium polarity, and good reproducibility for run-to-run, day-to-day, and column-to-column analyses [1], demonstrating great potential as new stationary phases in separation science. Furthermore, peculiar advantages are achieved if compared with the commercial HP-5, HP-35, DB-17, and PEG-20M columns, showing unmatched resolving capabilities toward chloroaniline, bromoaniline, iodoaniline, toluidine, and xylene isomers [2]. References: 1. Sun, T., Chen, R., Huang, Q., Ba, M., Cai, Z., Hu, S., Liu, X., Nardiello, D., & Quinto, M., ACS Appl. Mater. Interfaces 14 (2022) 56132−56142. 2. Sun, T., Chen, R., Huang, Q., Ba, M., Cai, Z., Chen, H., Qi, Y., Chen, H., Liu, X., Nardiello, D., & Quinto, M., Anal. Chim. Acta 1251 (2023) 340979

    Operando X-ray absorption spectroscopy investigations on NaxNi1/3Fe1/3Mn1/3O2 positive electrode materials for sodium and sodium ion batteries

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    NaxMn1/3Fe1/3Ni1/3O2 (x = 2/3 and 1) layered oxides are synthesized and applied as positive electrode materials for sodium batteries. The crystal structure of the material changes from the O3 single phase to P2/O3 mixed phases as the Na content decreases from 1 to 2/3. The mixed-phases Na2/3Mn1/3Fe1/3Ni1/3O2 shows superior cycling performance compared to the single-phase NaMn1/3Fe1/3Ni1/3O2 due to different redox process and structural change that are demonstrated by operando X-ray absorption spectroscopy (XAS). The Na2/3Mn1/3Fe1/3Ni1/3O2 experiences redox reactions of Ni3+|Ni4+ and Fe3+|Fe4+ with inactive Mn ions during the charge/discharge processes, while the NaMn1/3Fe1/3Ni1/3O2 undergoes deeper redox reactions from Ni2+|Ni3+|Ni4+ and Fe3+|Fe4+ that Mn ions are irreversibly oxidized to Mn4+ in the 1st charge process. In addition, the mixed-phases material has smaller changes in the transition metal oxygen bond lengths during cycling, corresponding to less distortions of TMO6 units in the crystal structure. The better reversibility of the redox reactions and the occurrence of less structural changes are both responsible for the enhanced cycling performance obtained from the mixed-phases material compared to the single-phase material. These results strengthen the understanding of interactions of transition metals in the layered cathode and provide guidelines for designing positive electrode materials for sodium batteries

    Small scale energy release driven by supergranular flows on the quiet Sun

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    In this article we present data and modelling for the quiet Sun that strongly suggest a ubiquitous small-scale atmospheric heating mechanism that is driven solely by converging supergranular flows. A possible energy source for such events is the power transfer to the plasma via the work done on the magnetic field by photospheric convective flows, which exert drag of the footpoints of magnetic structures. In this paper we present evidence of small scale energy release events driven directly by the hydrodynamic forces that act on the magnetic elements in the photosphere, as a result of supergranular scale flows. We show strong spatial and temporal correlation between quiet Sun soft X-ray emission (from <i>Yohkoh</i> and <i>SOHO</i> MDI-derived flux removal events driven by deduced photospheric flows. We also present a simple model of heating generated by flux submergence, based on particle acceleration by converging magnetic mirrors. In the near future, high resolution soft X-ray images from XRT on the <i>Hinode</i> satellite will allow definitive, quantitative verification of our results

    Latest results on Jovian disk X-rays from XMM-Newton

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    We present the results of a spectral study of the soft X-ray emission (0.2–2.5 keV) from low-latitude (‘disk’) regions of Jupiter. The data were obtained during two observing campaigns with XMM-Newton in April and November 2003. While the level of the emission remained approximately the same between April and the first half of the November observation, the second part of the latter shows an enhancement by about 40% in the 0.2–2.5 keV flux. A very similar, and apparently correlated increase, in time and scale, was observed in the solar X-ray and EUV flux. The months of October and November 2003 saw a period of particularly intense solar activity, which appears reflected in the behavior of the soft X-rays from Jupiter's disk. The X-ray spectra, from the XMM-Newton EPIC CCD cameras, are all well fitted by a coronal model with temperatures in the range 0.4–0.5 keV, with additional line emission from Mg XI (1.35 keV) and Si XIII (1.86 keV): these are characteristic lines of solar X-ray spectra at maximum activity and during flares. The XMM-Newton observations lend further support to the theory that Jupiter's disk X-ray emission is controlled by the Sun, and may be produced in large part by scattering, elastic and fluorescent, of solar X-rays in the upper atmosphere of the planet

    Development of Ti/Au Transition-Edge Sensors for Single-Photon Detection

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    Transition-edge sensors (TESs) have shown remarkable energy resolution and photon-number resolving ability. In this paper, we report the fabrication and characterization of Ti/Au optical TESs for the detection of single photon at the telecommunication wavelength 1550 nm. A SiO2/SiNx antireflection coating is deposited on top of TESs by an inductively coupled plasma-assisted plasma-enhanced chemical vapor deposition (ICP-PECVD) process to improve the detection efficiency. Ti/Au (50/60 nm) TES with a small sensitive area 10 mu mx 10 mu m shows an energy resolution of 0.12 eV. The TES with a large sensitive area 20 mu mx 20 mu m can discriminate up to 55 incident photons and the detection efficiency is 46%
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