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The DESTINY+(Demonstration and Experiment of Space Technology for INterplanetary voYage with Phaethon fLyby and dUst Science) Dust Analyser (DDA) is a state-of-the-art dust telescope for the in situ analysis of cosmic dust particles. As the primary scientific payload of the DESTINY+ mission, it serves the purpose of characterizing the dust environment within the Earth-Moon system, investigating interplanetary and interstellar dust populations at 1 AU from the Sun and studying the dust cloud enveloping the asteroid (3200) Phaethon. DDA features a two-axis pointing platform for increasing the accessible fraction of the sky. The instrument combines a trajectory sensor with an impact ionization time-of-flight mass spectrometer, enabling the correlation of dynamical, physical and compositional properties for individual dust grains. For each dust measurement, a set of nine signals provides the surface charge, particle size, velocity vector, as well as the atomic, molecular and isotopic composition of the dust grain. With its capabilities, DDA is a key asset in advancing our understanding of the cosmic dust populations present along the orbit of DESTINY+. In addition to providing the scientific context, we are presenting an overview of the instrument's design and functionality, showing first laboratory measurements and giving insights into the observation planning. This article is part of a theme issue 'Dust in the Solar System and beyond'.
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BACKGROUND: The purpose of this study was to determine the effects of high tibial osteotomy (HTO) on varus thrust during gait in patients with medial compartment knee osteoarthritis (KOA), and to identify factors that influence thrust before and one year after surgery. METHODS: HTO was performed in 60 KOA patients (70 knees, including 56 knees by open wedge and 14 by closed wedge). The control group comprised 28 normal, control subjects. Several parameters were evaluated before surgery and one year thereafter. Varus thrust was defined as acceleration of the thigh relative to the lower leg in the coronal plane. Knee-injury-and-osteoarthritis-outcome scores (KOOSs), knee joint angles, radiography, and mediolateral knee acceleration during free speed gait were measured and analyzed. RESULTS: One-year after HTO, KOOSs, knee extension angles, and range of knee motion were improved (p < 0.001). The hip-knee-ankle angle and joint-line-convergent angle (JLCA) had decreased (p < 0.001), and walking speed had increased (p < 0.001). Preoperatively, patient acceleration was significantly (p < 0.05) higher than that of controls, and it did not change after HTO. However, it was reduced significantly (p < 0.05) after adjusting for walking speed. Walking speed correlated significantly with acceleration preoperatively, postoperatively, and among controls. Surgical methods (open-wedge/closed-wedge HTO) and correction angle did not affect postoperative acceleration. There was a low correlation between acceleration and KOOSs (KOOSa, KOOSp), knee joint angles, or JLCA postoperatively, but no relationship was found between acceleration and these parameters in the preoperative or the control group. CONCLUSIONS: Walking speed correlated significantly with acceleration preoperatively, postoperatively, and with those of controls. Mediolateral acceleration of the thigh relative to the lower leg in patients with KOA was significantly higher than that of normal controls before surgery, and it did not change after HTO. However, after surgery it was reduced significantly after adjusting for walking speed.
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Sunlight-driven photocatalytic dinitrogen (N2) fixation with water at ambient conditions is of vital importance for a sustainable energy society. The efficiency of this reaction, however, is still low because of the difficulty in promoting both water oxidation and N2 reduction reactions. Herein, we report that a high-phosphorus-doped carbon nitride with surface nitrogen vacancies (PCN(V)) synthesized by thermal condensation under a hydrogen (H2) atmosphere using phosphorus oxide (P2O5) as a phosphorus source efficiently promotes N2 fixation. The large numbers of the doped P atoms on the PCN(V)-P2O5 catalysts enhance the oxidation of water, while the N vacancies reduce N2, facilitating efficient ammonia (NH3) generation with an apparent quantum yield at 420 nm of 3.4%. Simulated sunlight illumination of the catalyst in water under N2 bubbling produces NH3 with a solar-to-chemical conversion efficiency of 0.16%, which is the highest efficiency among the previously reported powder photocatalysts.
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The generation of hydrogen peroxide (H2O2) from water and dioxygen by sunlight-driven heterogeneous photocatalysis is a promising method for the artificial photosynthesis of a liquid solar fuel. We previously found that resorcinol-formaldehyde (RF) resin powders prepared by high-temperature hydrothermal synthesis act as highly active semiconductor photocatalysts for H2O2 generation. Herein, we report that RF resin powders doped with poly(3-hexylthiophene-2,5-diyl) (RF/P3HT) exhibit enhanced photocatalytic activities. The highly dispersed P3HT within the resin particles created charge transfer complexes with the conduction band of the resin via electron donation, facilitating efficient transfer of the photogenerated conduction band electrons through P3HT. This enhanced charge separation promoted efficient water oxidation and O2 reduction. The solar-to-chemical conversion efficiency for H2O2 generation on the RF/P3HT resin in water under simulated sunlight irradiation with atmospheric pressure of O2 was â¼1.0%, which is the highest efficiency reported for powder catalysts in artificial photosynthesis.
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Ammonia is an indispensable chemical. Photocatalytic NH3 production via dinitrogen fixation using water by sunlight illumination under ambient conditions is a promising strategy, although previously reported catalysts show insufficient activity. Herein, we showed that ultraviolet light irradiation of a semiconductor, bismuth oxychloride with surface oxygen vacancies (BiOCl-OVs), in water containing chloride anions (Cl-) under N2 flow efficiently produces NH3. The surface OVs behave as the N2 reduction sites by the photoformed conduction band electrons. The valence band holes are consumed by self-oxidation of interlayer Cl- on the catalyst. The hypochloric acid (HClO) formed absorbs ultraviolet light and undergoes photodecomposition into O2 and Cl-. These consecutive photoreactions produce NH3 with water as the electron donor. The Cl- in solution compensates for the removed interlayer Cl- and inhibits catalyst deactivation. Simulated sunlight illumination of the catalyst in seawater stably generates NH3 with 0.05% solar-to-chemical conversion efficiency, thus exhibiting significant potential of the seawater system for artificial photosynthesis.
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Artificial photosynthesis is a critical challenge in moving towards a sustainable energy future. Photocatalytic generation of hydrogen peroxide from water and dioxygen (H2O + [Formula: see text]O2 â H2O2, ΔG° = 117 kJ mol-1) by sunlight is a promising strategy for artificial photosynthesis because H2O2 is a storable and transportable fuel that can be used directly for electricity generation. All previously reported powder photocatalysts, however, have suffered from low efficiency in H2O2 generation. Here we report that resorcinol-formaldehyde resins, widely used inexpensive polymers, act as efficient semiconductor photocatalysts to provide a new basis for H2O2 generation. Simple high-temperature hydrothermal synthesis (~523 K) produces low-bandgap resorcinol-formaldehyde resins comprising π-conjugated and π-stacked benzenoid-quinoid donor-acceptor resorcinol couples. The resins absorb broad-wavelength light up to 700 nm and catalyse water oxidation and O2 reduction by the photogenerated charges. Simulated sunlight irradiation of the resins stably generates H2O2 with more than 0.5% solar-to-chemical conversion efficiency. Therefore, this metal-free system shows significant potential as a new artificial photosynthesis system.
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Photocatalytic N2 reduction with water by sunlight irradiation is a challenging issue toward sustainable energy society, but previously reported photocatalysts had suffered from low stability and low activity. We prepared a boron-doped carbon nitride (BCN) semiconductor powder loaded with nickel phosphide particles (Ni2P) as cocatalysts. The Ni2P/BCN catalyst, when photoirradiated in pure water by simulated sunlight under N2 flow, successfully produces NH3 at room temperature. The B doping leads to a positive shift of the valence band level and enhances water oxidation by the photoformed holes. The Ni2P particles efficiently receive the conduction band electrons of BCN, leading to enhanced charge separation of the photoformed hole and electron pairs, and behave as N2 reduction sites. Simulated sunlight irradiation of the catalyst in water stably generates NH3 with 0.010% solar-to-chemical conversion efficiency. This noble-metal-free system therefore shows a significant potential for N2 photofixation.
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Au nanoparticles loaded on semiconductor TiO2 absorb visible light due to their surface plasmon resonance (SPR) and inject the photogenerated hot electrons (ehot-) into the conduction band of TiO2. The separated charges promote oxidation and reduction reactions. The step that determines the rate of the plasmonic photocatalysis on the Au/TiO2 system is the ehot- injection through the Schottky barrier created at the Au-TiO2 interface. In the present work, niobium (Nb5+) oxide species were doped at the Au-TiO2 interface by loading Nb5+ onto the TiO2 surface followed by deposition of Au particles (2 wt % of TiO2). Visible light irradiation of the Au/Nb5+/TiO2 catalysts promotes aerobic oxidation of alcohols with much higher efficiency than that of undoped Au/TiO2. Lewis acidity of the Nb5+ species located at the interface cancels the negative charges of Au and creates a barrier with a narrower depletion layer, promoting tunneling ehot- injection. Efficiency of the ehot- injection depends on the amount of Nb5+ doped. Loading small amounts of Nb5+ (â¼0.1 wt % of TiO2) creates mononuclear NbO4 species and shows large activity enhancement. In contrast, loading larger amounts of Nb5+ creates aggregated polynuclear Nb2O5 species. They decrease the electron density of Au particles and weaken their SPR absorption. This suppresses the ehot- generation on the Au particles and decreases the activity of plasmonic photocatalysis.
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Ammonia (NH3) is an essential chemical in modern society. It is currently manufactured by the Haber-Bosch process using H2 and N2 under extremely high-pressure (>200 bar) and high-temperature (>673 K) conditions. Photocatalytic NH3 production from water and N2 at atmospheric pressure and room temperature is ideal. Several semiconductor photocatalysts have been proposed, but all suffer from low efficiency. Here we report that a commercially available TiO2 with a large number of surface oxygen vacancies, when photoirradiated by UV light in pure water with N2, successfully produces NH3. The active sites for N2 reduction are the Ti3+ species on the oxygen vacancies. These species act as adsorption sites for N2 and trapping sites for the photoformed conduction band electrons. These properties therefore promote efficient reduction of N2 to NH3. The solar-to-chemical energy conversion efficiency is 0.02%, which is the highest efficiency among the early reported photocatalytic systems. This noble-metal-free TiO2 system therefore shows a potential as a new artificial photosynthesis for green NH3 production.
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Photoreductive synthesis of colloidal gold nanoparticles (AuNPs) from Au3+ is one important process for nanoprocessing. Several methods have been proposed; however, there is no report of a method capable of producing AuNPs with inexpensive reagents acting as both reductant and surface stabilizer, promoted solely under photoirradiation. We found that UV irradiation of water with Au3+ and benzoic acid successfully produces monodispersed AuNPs, where thermal reduction does not occur in the dark condition even at elevated temperatures. Photoexcitation of a benzoate-Au3+ complex reduces Au3+ while oxidizing benzoic acid. The benzoic acid molecules are adsorbed on the AuNPs and act as surface stabilizers. Change in light intensity and benzoic acid amount successfully creates AuNPs with controllable sizes. The obtained AuNPs can easily be redispersed in an organic solvent or loaded onto a solid support by simple treatments.
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Solar-to-chemical energy conversion is a challenging subject for renewable energy storage. In the past 40 years, overall water splitting into H2 and O2 by semiconductor photocatalysis has been studied extensively; however, they need noble metals and extreme care to avoid explosion of the mixed gases. Here we report that generating hydrogen peroxide (H2O2) from water and O2 by organic semiconductor photocatalysts could provide a new basis for clean energy storage without metal and explosion risk. We found that carbon nitride-aromatic diimide-graphene nanohybrids prepared by simple hydrothermal-calcination procedure produce H2O2 from pure water and O2 under visible light (λ > 420 nm). Photoexcitation of the semiconducting carbon nitride-aromatic diimide moiety transfers their conduction band electrons to graphene and enhances charge separation. The valence band holes on the semiconducting moiety oxidize water, while the electrons on the graphene moiety promote selective two-electron reduction of O2. This metal-free system produces H2O2 with solar-to-chemical energy conversion efficiency 0.20%, comparable to the highest levels achieved by powdered water-splitting photocatalysts.
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We synthesized a coumarin-spiropyran dyad with a hydrogenated pyran moiety (2), behaving as an off-on type fluorescent receptor for rapid, selective, and sensitive detection of cyanide anion (CN(-)) in aqueous media. The receptor itself shows almost no fluorescence with a quantum yield < 0.01, due to the delocalization of π-electrons over the molecule. Selective nucleophilic addition of CN(-) to the spirocarbon of the molecule rapidly promotes spirocycle opening within only 3 min. This leads to localization of π-electrons on the coumarin moiety and exhibits strong light-blue fluorescence at 459 nm with very high quantum yield (0.52). As a result of this, the receptor facilitates rapid, selective, and sensitive fluorometric detection of CN(-) as low as 1.0 µM.
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Previous studies have established the rationale for NK105, a nanomicellar formulation of paclitaxel, administered every 3 weeks. The aim of this phase I study was to determine the recommended dose and pharmacokinetics of weekly administered NK105. NK105 was administered by a 30-min infusion once weekly for three consecutive weeks in each 4-week cycle. In the dose-escalation phase, three to seven patients with solid tumors were enrolled to each of the four dose levels (50-100 mg/m2; n = 16). At a dose level of 100 mg/m2, predefined dose-limiting toxicity (DLT) manifested in only one out of six evaluable patients, whereas a dose delay due to neutropenia during the first course occurred two patients. None of the three patients given 80 mg/m2 had a dose reduction, while a dose delay occurred in two. NK105 exhibited linear pharmacokinetics at doses of 50-100 mg/m2, and approximately 5 % of total paclitaxel was released from micelles. Thus, the recommended dose was set at 80 mg/m2, and an additional 10 advanced breast cancer (ABC) patients were given this dose in the dose-expansion phase. DLT manifested in two patients, and grade ≥ 3 neutropenia was found in eight patients. Among the nine patients who completed the first cycle, four had a dose reduction, mostly because of neutropenia. Of the 10 patients, six achieved partial response (PR), and four achieved stable disease (SD) status. Overall, weekly NK105 was well tolerated and had a desirable antitumor activity profile. Further investigations of NK105 in ABC patients are currently underway.
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Antineoplásicos Fitogênicos/uso terapêutico , Neoplasias/tratamento farmacológico , Paclitaxel/análogos & derivados , Adulto , Idoso , Idoso de 80 Anos ou mais , Antineoplásicos Fitogênicos/farmacocinética , Esquema de Medicação , Feminino , Seguimentos , Humanos , Masculino , Dose Máxima Tolerável , Pessoa de Meia-Idade , Estadiamento de Neoplasias , Neoplasias/patologia , Paclitaxel/farmacocinética , Paclitaxel/uso terapêutico , Prognóstico , Taxa de Sobrevida , Distribuição TecidualRESUMO
Aerobic oxidation on a heterogeneous catalyst driven by visible light (λ >400 nm) at ambient temperature is a very important reaction for green organic synthesis. A metal particles/semiconductor system, driven by charge separation via an injection of "hot electrons (e(hot)(-))" from photoactivated metal particles to semiconductor, is one of the promising systems. These systems, however, suffer from low quantum yields for the reaction (<5% at 550 nm) because the Schottky barrier created at the metal/semiconductor interface suppresses the e(hot)(-) injection. Some metal particle systems promote aerobic oxidation via a non-e(hot)(-)-injection mechanism, but require high reaction temperatures (>373 K). Here we report that Pt nanoparticles (â¼5 nm diameter), when supported on semiconductor Ta2O5, promote the reaction without e(hot)(-) injection at room temperature with significantly high quantum yields (â¼25%). Strong Pt-Ta2O5 interaction increases the electron density of the Pt particles and enhances interband transition of Pt electrons by absorbing visible light. A large number of photogenerated e(hot)(-) directly activate O2 on the Pt surface and produce active oxygen species, thus promoting highly efficient aerobic oxidation at room temperature.
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We synthesized an indoliumcoumarin dyad (1) and its derivatives with Cl (2), N(CH3)2 (3), or NO2 (4) substituent, and used them for fluorometric detection of cyanide anions (CN(-)) in aqueous media. All of the dyads exhibit fluorescence enhancement by CN(-) via a nucleophilic interaction of CN(-) with the indolium carbon atoms. Their fluorescence response and selectivity to CN(-), however, depend strongly on the substituents. Ab initio calculation and kinetic analysis were performed to verify the behaviors. Substitution of electron-withdrawing groups (2 and 4) increases the electrophilicity of the indolium carbon. This decreases the activation enthalpy for the nucleophilic interaction with CN(-) and facilitates rapid CN(-) sensing. Compound 4 with very high electrophilicity, however, also promotes nucleophilic interaction with OH(-) in the solution, resulting in decreased CN(-) selectivity. As a result of this, the Cl-substituted compound 2 containing the indolium carbon with appropriate electrophilicity facilitates rapid (within 1 min) and selective CN(-) detection.
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Cumarínicos/química , Cianetos/análise , Indóis/química , Espectrometria de Fluorescência , Ânions/química , Corantes Fluorescentes/síntese química , Corantes Fluorescentes/química , Cinética , Espectroscopia de Ressonância Magnética , Teoria QuânticaRESUMO
Design of optical molecular probes for selective detection of aromatic thiols has attracted much attention. Although several types of probes have been proposed, all of them exhibit colorimetric or fluorometric response via irreversible reaction with aromatic thiols and cannot be reused. Here we report that a spiropyran dye is the first example of a reusable chemosensor for aromatic thiols. A colorless spiropyran dye () dissolved in aqueous media containing aromatic thiols is selectively isomerized to the colored merocyanine form in the dark. In contrast, visible light irradiation of the merocyanine form promotes successful reversion to the colorless spirocyclic form. Kinetic absorption analysis and ab initio calculations of the transition states revealed that this colorimetric response in the dark is ascribed to the decrease in activation energy for isomerization via the nucleophilic interaction between the aromatic thiol and the olefinic carbon of the dye.
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Benzopiranos/química , Colorimetria/métodos , Indóis/química , Nitrocompostos/química , Compostos de Sulfidrila/análise , IsomerismoRESUMO
Design of green, safe, and sustainable process for the synthesis of hydrogen peroxide (H2 O2 ) is a very important subject. Early reported processes, however, require hydrogen (H2 ) and palladium-based catalysts. Herein we propose a photocatalytic process for H2 O2 synthesis driven by metal-free catalysts with earth-abundant water and molecular oxygen (O2 ) as resources under sunlight irradiation (λ>400â nm). We use graphitic carbon nitride (g-C3 N4 ) containing electron-deficient aromatic diimide units as catalysts. Incorporating the diimide units positively shifts the valence-band potential of the catalysts, while maintaining sufficient conduction-band potential for O2 reduction. Visible light irradiation of the catalysts in pure water with O2 successfully produces H2 O2 by oxidation of water by the photoformed valence-band holes and selective two-electron reduction of O2 by the conduction band electrons.
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The photocatalytic reduction of harmful nitrates (NO3-) in strongly acidic wastewater to ammonia (NH3) under sunlight is crucial for the recycling of limited nitrogen resources. This study reports that a naturally occurring Cl--containing iron oxyhydroxide (akaganeite) powder with surface oxygen vacancies (ß-FeOOH(Cl)-OVs) facilitates this transformation. Ultraviolet light irradiation of the catalyst suspended in a Cl--containing solution promoted quantitative NO3--to-NH3 reduction with water under ambient conditions. The photogenerated conduction band electrons promoted the reduction of NO3--to-NH3 over the OVs. The valence band holes promoted self-oxidation of Cl- as the direct electron donor and eliminated Cl- was compensated from the solution. Photodecomposition of the generated hypochlorous acid (HClO) produced O2, facilitating catalytic reduction of NO3--to-NH3 with water as the electron donor in the entire system. Simulated sunlight irradiation of the catalyst in a strongly acidic nitric acid (HNO3) solution (pH â¼ 1) containing Cl- stably generated NH3 with a solar-to-chemical conversion efficiency of â¼0.025%. This strategy paves the way for sustainable NH3 production from wastewater.
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The carbon spheres synthesized by pyrolysis of resorcinol-formaldehyde (RF) semiconducting resins exhibit enhanced activity for electrocatalytic oxygen reduction. The spheres consist of narrow reticulated carbon layers, which are derived from the donor-acceptor π-stacking interaction of the resins, and show high electron conductivity.
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(1) Background: There is controversy regarding stent placement for unresectable malignant hilar biliary obstruction (UMHBO). We mainly use the partial stent-in-stent (PSIS) method with an uncovered self-expandable metallic stent (UCSEMS) based on the drainage area and patency period. In this study, we investigated the usefulness and safety of the PSIS method. (2) Methods: In total, 59 patients who underwent the PSIS method for UMHBO at our hospital were included in the study. The technical success rate, clinical success rate, time to recurrent biliary obstruction (TRBO) and overall survival (OS) from the first placement, factors affecting TRBO and OS, and early complications within 30 days after the procedure were evaluated retrospectively. (3) Results: The technical and clinical success rates were 100% and 96.6%, respectively, with a TRBO of 121 days [95% confidence interval: 82-231] and an OS of 194 days [95% confidence interval: 113-305] after the first placement. Early complications occurred in nine patients (15.3%), including five cases of cholangitis, three cases of pancreatitis, and one case of cholecystitis. (4) Conclusions: The PSIS method for UMHBO is safe and useful with high technical and clinical success rates.