arXiv subjects

Hiroshi Hidaka

Publications and source records attributed to Hiroshi Hidaka.

10 recordsLinked to original sources

arXiv2026

Methanol Formation via the Radical-radical Reaction of OH and CH3 Radicals Undergoing Transient Diffusion on Ice at 10 to 60 K

Methanol (CH3OH) is thought to form on interstellar ice dust via successive hydrogenation reactions. The reaction between CH3 and OH radicals could also conceivably generate methanol at temperatures above approximately 20 K, at which temperature hydrogen atoms will not adhere to the ice surface. However, this process has not been verified by well-controlled experiments. Using a newly-developed Cs+ ion pickup technique, the authors investigated the reaction between CH3 and OH radicals on the surface of amorphous solid water, an ice dust analogue, at temperatures from 10 to 60 K. In the present experiments, OH radicals were generated by UV photolysis of water molecules, following which methane (CH4) gas was deposited on the ice substrate. The results show that CH3OH was formed on the ice surface through the sequential reactions CH4 + OH -> CH3 + H2O and CH3 + OH -> CH3OH even at 10 K. Considering the very low surface coverage of reactants in the experimental condition, the second reaction was found to occur as a result of transient diffusion of CH3 due to the heat of the first reaction.

astro-ph.GA↗

arXiv2025

Hydrogenation of HOCO and formation of interstellar CO$_2$: A not so straightforward relation

Carbon dioxide (CO$_2$) is one of the most important interstellar molecules. While it is considered that it forms on the surface of interstellar dust grains, the exact contribution of different chemical mechanisms is still poorly constrained. Traditionally it is deemed that the CO + OH reaction occurring on top of ices is the main reaction path for its formation. Recent investigations showed that in reality the reaction presents a more complex mechanism, requiring an additional H-abstraction step. Building on our previous works, we carried out a detailed investigation of such H abstraction reactions with the hydrogen atom as a reactant for the abstraction reaction. We found an unconventional chemistry for this reaction, markedly depending on the isomeric form of the HOCO radical prior to reaction. The favored reactions are t-HOCO + H -> CO + H$_2$O, c-HOCO + H -> CO$_2$ + H$_2$ and t/c-HOCO + H -> c/t-HCOOH. We estimate bounds for the rate constants of the less favored reaction channels, t-HOCO + H -> CO$_2$ + H and c-HOCO + H -> CO + H$_2$O, to be approximately 10$^{4-6}$ s$^{-1}$. However, these estimates should be interpreted cautiously due to the significant role of quantum tunneling in these reactions and the complex electronic structure of the involved molecules, which complicates their study. Our findings underscore the need for detailed investigation into the chemistry of interstellar CO$_2$ and pave the way for a reevaluation of its primary formation mechanisms in the interstellar medium.

astro-ph.GA↗

arXiv2024

The Ni isotopic composition of Ryugu reveals a common accretion region for carbonaceous chondrites

The isotopic compositions of samples returned from Cb-type asteroid Ryugu and Ivuna-type (CI) chondrites are distinct from other carbonaceous chondrites, which has led to the suggestion that Ryugu and CI chondrites formed in a different region of the accretion disk, possibly around the orbits of Uranus and Neptune. We show that, like for Fe, Ryugu and CI chondrites also have indistinguishable Ni isotope anomalies, which differ from those of other carbonaceous chondrites. We propose that this unique Fe and Ni isotopic composition reflects different accretion efficiencies of small FeNi metal grains among the carbonaceous chondrite parent bodies. The CI chondrites incorporated these grains more efficiently, possibly because they formed at the end of the disk's lifetime, when planetesimal formation was also triggered by photoevaporation of the disk. Isotopic variations among carbonaceous chondrites may thus reflect fractionation of distinct dust components from a common reservoir, implying CI chondrites and Ryugu may have formed in the same region of the accretion disk as other carbonaceous chondrites.

astro-ph.EP↗

arXiv2024

Proposed importance of HOCO chemistry: Inefficient formation of CO$_2$ from CO and OH reactions on ice dust

With the advent of JWST ice observations, dedicated studies on the formation reactions of detected molecules are becoming increasingly important. One of the most interesting molecules in interstellar ice is CO$_2$. Despite its simplicity, the main formation reaction considered, CO + OH -> CO$_2$ + H through the energetic HOCO* intermediate on ice dust, is subject to uncertainty because it directly competes with the stabilization of HOCO as a final product which is formed through energy dissipation of HOCO* to the water ice. When energy dissipation to the surface is effective during reaction, HOCO can be a dominant product. In this study, we experimentally demonstrate that the major product of the reaction is indeed not CO$_2$, but rather the highly reactive radical HOCO. The HOCO radical can later evolve into CO$_2$ through H-abstraction reactions, but these reactions compete with addition reactions, leading to the formation of carboxylic acids (R-COOH). Our results highlight the importance of HOCO chemistry and encourage further exploration of the chemistry of this radical.

astro-ph.GA↗

arXiv2023

Determination of the branching ratio of CH$_3$OH + OH reaction on water ice surface at 10 K

The CH$_3$O and CH$_2$OH radicals can be important precursors of complex organic molecules (COMs) in interstellar dust. The COMs presumably originating from these radicals were abundantly found in various astronomical objects. Because each radical leads to different types of COMs, determining the abundance ratio of CH$_3$O to CH$_2$OH is crucial for a better understanding of the chemical evolution to various COMs. Recent work suggested that the reaction between CH$_3$OH and OH on ice dust plays an important role in forming CH$_3$O and CH$_2$OH radicals. However, quantitative details on the abundance of these radicals have not been presented to date. Herein, we experimentally determined the branching ratio (CH$_3$O/CH$_2$OH) resulting from the CH$_3$OH + OH reaction on the water ice surface at 10 K to be 4.3 $\pm$ 0.6. Furthermore, the CH$_3$O product in the reaction would participate in subsequent diffusive reactions even at a temperature as low as 10 K. This fact should provide critical information for COMs formation models in cold molecular clouds.

astro-ph.GA↗

arXiv2022

Presolar stardust in asteroid Ryugu

We have conducted a NanoSIMS-based search for presolar material in samples recently returned from C-type asteroid Ryugu as part of JAXA's Hayabusa2 mission. We report the detection of all major presolar grain types with O- and C-anomalous isotopic compositions typically identified in carbonaceous chondrite meteorites: 1 silicate, 1 oxide, 1 O-anomalous supernova grain of ambiguous phase, 38 SiC, and 16 carbonaceous grains. At least two of the carbonaceous grains are presolar graphites, whereas several grains with moderate C isotopic anomalies are probably organics. The presolar silicate was located in a clast with a less altered lithology than the typical extensively aqueously altered Ryugu matrix. The matrix-normalized presolar grain abundances in Ryugu are 4.8$^{+4.7}_{-2.6}$ ppm for O-anomalous grains, 25$^{+6}_{-5}$ ppm for SiC grains and 11$^{+5}_{-3}$ ppm for carbonaceous grains. Ryugu is isotopically and petrologically similar to carbonaceous Ivuna-type (CI) chondrites. To compare the in situ presolar grain abundances of Ryugu with CI chondrites, we also mapped Ivuna and Orgueil samples and found a total of SiC grains and 6 carbonaceous grains. No O-anomalous grains were detected. The matrix-normalized presolar grain abundances in the CI chondrites are similar to those in Ryugu: 23 $^{+7}_{-6}$ ppm SiC and 9.0$^{+5.3}_{-4.6}$ ppm carbonaceous grains. Thus, our results provide further evidence in support of the Ryugu-CI connection. They also reveal intriguing hints of small-scale heterogeneities in the Ryugu samples, such as locally distinct degrees of alteration that allowed the preservation of delicate presolar material.

astro-ph.EP↗

arXiv2021

Transmission Electron Microscopy Study of the Morphology of Ices Composed of H2O, CO2, and CO on Refractory Grains

It has been implicitly assumed that ices on grains in molecular clouds and proto planetary disks are formed by homogeneous layers regardless of their composition or crystallinity. To verify this assumption, we observed the H2O deposition onto refractory substrates and the crystallization of amorphous ices (H2O, CO2, and CO) using an ultra-high-vacuum transmission electron microscope. In the H2O-deposition experiments, we found that three-dimensional islands of crystalline ice (Ic) were formed at temperatures above 130 K. The crystallization experiments showed that uniform thin films of amorphous CO and H2O became three-dimensional islands of polyhedral crystals; amorphous CO2, on the other hand, became a thin film of nano crystalline CO2 covering the amorphous H2O. Our observations show that crystal morphologies strongly depend not only on the ice composition, but also on the substrate. Using experimental data concerning the crystallinity of deposited ices and the crystallization timescale of amorphous ices, we illustrated the criteria for ice crystallinity in space and outlined the macroscopic morphology of icy grains in molecular clouds as follows: amorphous H2O covered the refractory grain uniformly, CO2 nano-crystals were embedded in the amorphous H2O, and a polyhedral CO crystal was attached to the amorphous H2O. Furthermore, a change in the grain morphology in a proto-planetary disk is shown. These results have important implications for the chemical evolution of molecules, non-thermal desorption, collision of icy grains, and sintering.

astro-ph.GA↗

arXiv2020

Diffusive hydrogenation reactions of CO embedded in amorphous solid water at elevated temperatures ~70 K

The surface processes on interstellar dust grains have an important role in the chemical evolution in molecular clouds. Hydrogenation reactions on ice surfaces have been extensively investigated and are known to proceed at low temperatures mostly below 20 K. In contrast, information about the chemical processes of molecules within an ice mantle is lacking. In this work, we investigated diffusive hydrogenation reactions of carbon monoxide (CO) embedded in amorphous solid water (ASW) as a model case and discovered that the hydrogenation of CO efficiently proceeds to yield H2CO and CH3OH even above 20 K when CO is buried beneath ASW. The experimental results suggest that hydrogen atoms diffuse through the cracks of ASW and have a sufficient residence time to react with embedded CO. The hydrogenation reactions occurred even at temperatures up to ~70 K. Cracks collapse at elevated temperatures but the occurrence of hydrogenation reactions means that the cracks would not completely disappear and remain large enough for penetration by hydrogen atoms. Considering the hydrogen-atom fluence in the laboratory and molecular clouds, we suggest that the penetration of hydrogen and its reactions within the ice mantle occur in astrophysical environments. Unified Astronomy

astro-ph.GA↗

arXiv2002

Nuclear Data in Oklo and Time-Variability of Fundamental Coupling Constants

We re-examined Shlyakhter's analysis of the Sm data in Oklo. With a special care of minimizing contamination due to the inflow of the isotope after the end of the reactor activity, we confirmed that his result on the time-variability of the fine-structure constant, $|\dotα/α|\lsim 10^{-17}{\rm y}^{-1}$, was basically correct. In addition to this upper bound, however, we obtained another result that indicates a different value of $α$ 2 billion years ago. We add comments on the recent result from QSO's.

hep-ph↗

arXiv2000

The nuclear interaction at Oklo 2 billion years ago

We re-examine the effort to constrain the time-variability of the coupling constants of the fundamental interactions by studying the anomalous isotopic abundance of Sm observed at the remnants of the natural reactors which were in operation at Oklo about 2 billion years ago, in terms of a possible deviation of the resonance energy from the value observed today. We rely on new samples that were carefully collected to minimize natural contamination and also on a careful temperature estimate of the reactors. We obtain the upper bound $(-0.2\pm 0.8)\times 10^{-17}$ ${\rm y}^{-1}$ on the fractional rate of change of the electromagnetic as well as the strong interaction coupling constants. Our result basically agrees with and even suggests some improvement of the result due recently to Damour and Dyson. Strictly speaking, however, we find another range of the resonance energy shift indicating a nonzero time variation of the constants. We find a rather strong but still tentative indication that this range can be ruled out by including the Gd data, for which it is essential to take the effect of contamination into account.

hep-ph↗