Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userSulphur chemistry in the L1544 pre-stellar core
67
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
The L1544 pre-stellar core has been observed as part of the ASAI IRAM 30m Large Program as well as follow-up programs. These observations have revealed the chemical richness of the earliest phases of low-mass star-forming regions. In this paper we focus on the twenty-one sulphur bearing species (ions, isotopomers and deuteration) that have been detected in this spectral-survey through fifty one transitions: CS, CCS, C3S, SO, SO2, H2CS, OCS, HSCN, NS, HCS+, NS+ and H2S. We also report the tentative detection (4 {sigma} level) for methyl mercaptan (CH3SH). LTE and non-LTE radiative transfer modelling have been performed and we used the nautilus chemical code updated with the most recent chemical network for sulphur to explain our observations. From the chemical modelling we expect a strong radial variation for the abundances of these species, which mostly are emitted in the external layer where non thermal desorption of other species has previously been observed. We show that the chemical study cannot be compared to what has been done for the TMC-1 dark cloud, where the abundance is supposed constant along the line of sight, and conclude that a strong sulphur depletion is necessary to fully reproduce our observations of the prototypical pre-stellar core L1544.
rate research
Read More
Context: The study of dust emission at millimeter wavelengths is important to shed light on the dust properties and physical structure of pre-stellar cores, the initial conditions in the process of star and planet formation. Aims: Using two new continuum facilities, AzTEC at the LMT and MUSTANG-2 at the GBO, we aim to detect changes in the optical properties of dust grains as a function of radius for the well-known pre-stellar core L1544. Methods: We determine the emission profiles at 1.1 and 3.3 mm and examine whether they can be reproduced in terms of the current best physical models for L1544. We also make use of various tools to determine the radial distributions of the density, temperature, and the dust opacity in a self-consistent manner. Results: We find that our observations cannot be reproduced without invoking opacity variations. With the new data, new temperature and density profiles, as well as opacity variations across the core, have been derived. The opacity changes are consistent with the expected variations between uncoagulated bare grains, toward the outer regions of the core, and grains with thick ice mantles, toward the core center. A simple analytical grain growth model predicts the presence of grains of ~3-4 um within the central 2000 au for the new density profile.
Pre-stellar cores represent the initial conditions in the process of star and planet formation, therefore it is important to study their physical and chemical structure. Because of their volatility, nitrogen-bearing molecules are key to study the dense and cold gas present in pre-stellar cores. The NH_3 rotational transition detected with Herschel-HIFI provides a unique combination of sensitivity and spectral resolution to further investigate physical and chemical processes in pre-stellar cores. Here we present the velocity-resolved Herschel-HIFI observations of the ortho-NH_3(1_0-0_0) line at 572 GHz and study the abundance profile of ammonia across the pre-stellar core L1544 to test current theories of its physical and chemical structure. Recently calculated collisional coefficients have been included in our non-LTE radiative transfer code to reproduce Herschel observations. A gas-grain chemical model, including spin-state chemistry and applied to the (static) physical structure of L1544 is also used to infer the abundance profile of ortho-NH_3 . The hyperfine structure of ortho-NH_3(1_0-0_0) is resolved for the first time in space. All the hyperfine components are strongly self-absorbed. The profile can be reproduced if the core is contracting in quasi-equilibrium, consistent with previous work, and if the NH_3 abundance is slightly rising toward the core centre, as deduced from previous interferometric observations of para-NH_3(1,1). The chemical model overestimates the NH_3 abundance at radii between ~ 4000 and 15000 AU by about two orders of magnitude and underestimates the abundance toward the core centre by more than one order of magnitude. Our observations show that chemical models applied to static clouds have problems in reproducing NH_3 observations.
Towards the pre-stellar core L1544, the methanol (CH$_3$OH) emission forms an asymmetric ring around the core centre, where CH$_3$OH is mostly in solid form, with a clear peak 4000~au to the north-east of the dust continuum peak. As part of the NOEMA Large Project SOLIS (Seeds of Life in Space), the CH$_3$OH peak has been spatially resolved to study its kinematics and physical structure and to investigate the cause behind the local enhancement. We find that methanol emission is distributed in a ridge parallel to the main axis of the dense core. The centroid velocity increases by about 0.2~km~s$^{-1}$ and the velocity dispersion increases from subsonic to transonic towards the central zone of the core, where the velocity field also shows complex structure. This could be indication of gentle accretion of material onto the core or interaction of two filaments, producing a slow shock. We measure the rotational temperature and show that methanol is in local thermodynamic equilibrium (LTE) only close to the dust peak, where it is significantly depleted. The CH$_3$OH column density, $N_{tot}({rm CH_3OH})$, profile has been derived with non-LTE radiative transfer modelling and compared with chemical models of a static core. The measured $N_{tot}({rm CH_3OH})$ profile is consistent with model predictions, but the total column densities are one order of magnitude lower than those predicted by models, suggesting that the efficiency of reactive desorption or atomic hydrogen tunnelling adopted in the model may be overestimated; or that an evolutionary model is needed to better reproduce methanol abundance.
The detection of complex organic molecules (COMs) toward cold sources such as pre-stellar cores (with T<10 K), has challenged our understanding of the formation processes of COMs in the interstellar medium. Recent modelling on COM chemistry at low temperatures has provided new insight into these processes predicting that COM formation depends strongly on parameters such as visual extinction and the level of CO freeze out. We report deep observations of COMs toward two positions in the L1544 pre-stellar core: the dense, highly-extinguished continuum peak with Av>=30 mag within the inner 2700 au; and a low-density shell with average Av~7.5-8 mag located at 4000 au from the cores center and bright in CH3OH. Our observations show that CH3O, CH3OCH3 and CH3CHO are more abundant (by factors ~2-10) toward the low-density shell than toward the continuum peak. Other COMs such as CH3OCHO, c-C3H2O, HCCCHO, CH2CHCN and HCCNC show slight enhancements (by factors <=3) but the associated uncertainties are large. This suggests that COMs are actively formed and already present in the low-density shells of pre-stellar cores. The modelling of the chemistry of O-bearing COMs in L1544 indicates that these species are enhanced in this shell because i) CO starts freezing out onto dust grains driving an active surface chemistry; ii) the visual extinction is sufficiently high to prevent the UV photo-dissociation of COMs by the external interstellar radiation field; and iii) the density is still moderate to prevent severe depletion of COMs onto grains.
We have carried out observations of CCH ($N=1-0$), CH$_{3}$CN ($J=5-4$), and three $^{13}$C isotopologues of HC$_{3}$N ($J=10-9$) toward three massive young stellar objects (MYSOs), G12.89+0.49, G16.86--2.16, and G28.28--0.36, with the Nobeyama 45-m radio telescope. Combined with previous results on HC$_{5}$N, the column density ratios of $N$(CCH)/$N$(HC$_{5}$N), hereafter the CCH/HC$_{5}$N ratios, in the MYSOs are derived to be $sim 15$. This value is lower than that in a low-mass warm carbon chain chemistry (WCCC) source by more than one order of magnitude. We compare the observed CCH/HC$_{5}$N ratios with hot-core model calculations (Taniguchi et al. 2019). The observed ratios in the MYSOs can be best reproduced by models when the gas temperature is $sim 85$ K, which is higher than in L1527, a low-mass WCCC source ($sim 35$ K). These results suggest that carbon-chain molecules detected around the MYSOs exist at least partially in higher temperature regions than those in low-mass WCCC sources. There is no significant difference in column density among the three $^{13}$C isotopologues of HC$_{3}$N in G12.89+0.49 and G16.86-2.16, while HCC$^{13}$CN is more abundant than the others in G28.28--0.36. We discuss carbon-chain chemistry around the three MYSOs based on the CCH/HC$_{5}$N ratio and the $^{13}$C isotopic fractionation of HC$_{3}$N.
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
