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Cecilia Ceccarelli

Publications and source records attributed to Cecilia Ceccarelli.

At least 91 records · Page 5Linked to original sources

Chemical and Physical Picture of IRAS 16293-2422 Source B at a Sub-arcsecond Scale Studied with ALMA

We have analyzed the OCS, H$_2$CS, CH$_3$OH, and HCOOCH$_3$ data observed toward the low-mass protostar IRAS 16293--2422 Source B at a sub-arcsecond resolution with ALMA. A clear chemical differentiation is seen in their distributions; OCS and H$_2$CS are extended with a slight rotation signature, while CH$_3$OH and HCOOCH$_3$ are concentrated near the protostar. Such a chemical change in the vicinity of the protostar is similar to the companion (Source A) case. The extended component is interpreted by the infalling-rotating envelope model with a nearly face-on configuration. The radius of the centrifugal barrier of the infalling-rotating envelope is roughly evaluated to be ($30-50$) au. The observed lines show the inverse P-Cygni profile, indicating the infall motion with in a few 10 au from the protostar. The nearly pole-on geometry of the outflow lobes is inferred from the SiO distribution, and thus, the infalling and outflowing motions should coexist along the line-of-sight to the protostar. This implies that the infalling gas is localized near the protostar and the current launching points of the outflow have an offset from the protostar. A possible mechanism for this configuration is discussed.

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The genealogical tree of ethanol: gas-phase formation of glycolaldehyde, acetic acid and formic acid

Despite the harsh conditions of the interstellar medium, chemistry thrives in it, especially in star forming regions where several interstellar complex organic molecules (iCOMs) have been detected. Yet, how these species are synthesised is a mystery. The majority of current models claim that this happens on interstellar grain surfaces. Nevertheless, evidence is mounting that neutral gas-phase chemistry plays an important role. In this article, we propose a new scheme for the gas-phase synthesis of glycolaldehyde, a species with a prebiotic potential and for which no gas-phase formation route was previously known. In the proposed scheme, the ancestor is ethanol and the glycolaldehyde sister species are acetic acid (another iCOM with unknown gas-phase formation routes) and formic acid. For the reactions of the new scheme with no available data, we have performed electronic structure and kinetics calculations deriving rate coefficients and branching ratios. Furthermore, after a careful review of the chemistry literature, we revised the available chemical networks, adding and correcting several reactions related to glycolaldehyde, acetic acid and formic acid. The new chemical network has been used in an astrochemical model to predict the abundance of glycolaldehyde, acetic acid and formic acid. The predicted abundance of glycolaldehyde depends on the ethanol abundance in the gas phase and is in excellent agreement with the measured one in hot corinos and shock sites. Our new model overpredicts the abundance of acetic acid and formic acid by about a factor of ten, which might imply a yet incomplete reaction network.

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Laboratory measurements and astronomical search for cyanomethanimine

C-cyanomethanimine (HNCHCN), existing in the two $Z$ and $E$ isomeric forms, is a key prebiotic molecule, but, so far, only the $E$ isomer has been detected toward the massive star-forming region. Sagittarius B2(N) using transitions in the radio wavelength domain. With the aim of detecting HNCHCN in Sun-like-star forming regions, the laboratory investigation of its rotational spectrum has been extended to the millimeter-/submillimeter-wave (mm-/submm-) spectral window in which several unbiased spectral surveys have been already carried out. High-resolution laboratory measurements of the rotational spectrum of C-cyanomethanimine were carried out in the 100-420 GHz range using a frequency-modulation absorption spectrometer. We then searched for the C-cyanomethanimine spectral features in the mm-wave range using the high-sensitivity and unbiased spectral surveys obtained with the IRAM 30-m antenna in the ASAI context, the earliest stages of star formation from starless to evolved Class I objects being sampled. For both the $Z$ and $E$ isomers, the spectroscopic work has led to an improved and extended knowledge of the spectroscopic parameters, thus providing accurate predictions of the rotational signatures up to $\sim$700 GHz. So far, no C-cyanomethanimine emission has been detected toward the ASAI targets, and upper limits of the column density of $\sim$ 10$^{11}$--10$^{12}$ cm$^{-2}$ could only be derived. Consequently, the C-cyanomethanimine abundances have to be less than a few 10$^{-10}$ for starless and hot-corinos. A less stringent constraint, $\leq$ 10$^{-9}$, is obtained for shocks sites. The combination of the upper limits of the abundances of C-cyanomethanimine together with accurate laboratory frequencies up to $\sim$ 700 GHz poses the basis for future higher sensitivity searches around Sun-like-star forming regions.

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First measurement of the 14N/15N ratio in the analogue of the Sun progenitor OMC-2 FIR4

We present a complete census of the 14N/15N isotopic ratio in the most abundant N-bearing molecules towards the cold envelope of the protocluster OMC-2 FIR4, the best known Sun progenitor. To this scope, we analysed the unbiased spectral survey obtained with the IRAM-30m telescope at 3mm, 2mm and 1mm. We detected several lines of CN, HCN, HNC, HC3N, N2H+, and their respective 13C and 15N isotopologues. The lines relative fluxes are compatible with LTE conditions and moderate line opacities have been corrected via a Population Diagram method or theoretical relative intensity ratios of the hyperfine structures. The five species lead to very similar 14N/15N isotopic ratios, without any systematic difference between amine and nitrile bearing species as previously found in other protostellar sources. The weighted average of the 14N/15N isotopic ratio is 270 +/- 30. This 14N/15N value is remarkably consistent with the [250-350] range measured for the local galactic ratio but significantly differs from the ratio measured in comets (around 140). High-angular resolution observations are needed to examine whether this discrepancy is maintained at smaller scales. In addition, using the CN, HCN and HC3N lines, we derived a 12C/13C isotopic ratio of 50 +/- 5.

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Detection of the HC$_3$NH$^+$ and HCNH$^+$ ions in the L1544 pre-stellar core

The L1544 pre-stellar core was observed as part of the ASAI (Astrochemical Surveys At IRAM) Large Program. We report the first detection in a pre-stellar core of the HCNH$^+$ and HC$_3$NH$^+$ ions. The high spectral resolution of the observations allows to resolve the hyperfine structure of HCNH$^+$. Local thermodynamic equilibrium analysis leads to derive a column density equal to (2.0$\pm$0.2)$\times$10$^{13}$cm$^{-2}$ for HCNH$^+$ and (1.5$\pm$0.5)$\times$10$^{11}$cm$^{-2}$ for HC$_3$NH$^+$. We also present non-LTE analysis of five transitions of HC$_3$N, three transitions of H$^{13}$CN and one transition of HN$^{13}$C, all of them linked to the chemistry of HCNH$^+$ and HC$_3$NH$^+$. We computed for HC$_3$N, HCN, and HNC a column density of (2.0$\pm$0.4)$\times$10$^{13}$cm$^{-2}$, (3.6$\pm$0.9)$\times10^{14}$cm$^{-2}$, and (3.0$\pm$1.0)$\times$10$^{14}$cm$^{-2}$, respectively. We used the gas-grain chemical code Nautilus to predict the abundances all these species across the pre-stellar core. Comparison of the observations with the model predictions suggests that the emission from HCNH$^+$ and HC$_3$NH$^+$ originates in the external layer where non-thermal desorption of other species was previously observed. The observed abundance of both ionic species ([HCNH$^+$]$\,\simeq3\times10^{-10}$ and [HC$_3$NH$^+$]$\,\simeq[1.5-3.0]\times10^{-12}$, with respect to H$_2$) cannot be reproduced at the same time by the chemical modelling, within the error bars of the observations only. We discuss the possible reasons for the discrepancy and suggest that the current chemical models are not fully accurate or complete. However, the modelled abundances are within a factor of three consistent with the observations, considering a late stage of the evolution of the pre-stellar core, compatible with previous observations.

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Vertical Structure of the Transition Zone from Infalling Rotating Envelope to Disk in the Class 0 Protostar, IRAS04368+2557

We have resolved for the first time the radial and vertical structure of the almost edge-on envelope/disk system of the low-mass Class 0 protostar L1527. For that, we have used ALMA observations with a spatial resolution of 0.25$^{\prime\prime}$$\times$0.13$^{\prime\prime}$ and 0.37$^{\prime\prime}$$\times$0.23$^{\prime\prime}$ at 0.8 mm and 1.2 mm, respectively. The L1527 dust continuum emission has a deconvolved size of 78 au $\times$ 21 au, and shows a flared disk-like structure. A thin infalling-rotating envelope is seen in the CCH emission outward of about 150 au, and its thickness is increased by a factor of 2 inward of it. This radius lies between the centrifugal radius (200 au) and the centrifugal barrier of the infalling-rotating envelope (100 au). The gas stagnates in front of the centrifugal barrier and moves toward vertical directions. SO emission is concentrated around and inside the centrifugal barrier. The rotation speed of the SO emitting gas is found to be decelerated around the centrifugal barrier. A part of the angular momentum could be extracted by the gas which moves away from the mid-plane around the centrifugal barrier. If this is the case, the centrifugal barrier would be related to the launching mechanism of low velocity outflows, such as disk winds.

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L483: Warm Carbon-Chain Chemistry Source Harboring Hot Corino Activity

The Class 0 protostar, L483, has been observed in various molecular lines in the 1.2 mm band at a sub-arcsecond resolution with ALMA. An infalling-rotating envelope is traced by the CS line, while a very compact component with a broad velocity width is observed for the CS, SO, HNCO, NH$_2$CHO, and HCOOCH$_3$ lines. Although this source is regarded as the warm carbon-chain chemistry (WCCC) candidate source at a 1000 au scale, complex organic molecules characteristic of hot corinos such as NH$_2$CHO and HCOOCH$_3$ are detected in the vicinity of the protostar. Thus, both hot corino chemistry and WCCC are seen in L483. Although such a mixed chemical character source has been recognized as an intermediate source in previous single-dish observations, we here report the first spatially-resolved detection. A kinematic structure of the infalling-rotating envelope is roughly explained by a simple ballistic model with the protostellar mass of 0.1--0.2 $M_\odot$ and the radius of the centrifugal barrier (a half of the centrifugal radius) of 30--200 au, assuming the inclination angle of 80\degr\ (0\degr\ for a face-on). The broad line emission observed in the above molecules most likely comes from the disk component inside the centrifugal barrier. Thus, a drastic chemical change is seen around the centrifugal barrier.

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Discovery of a Hot Corino in the Bok Globule B335

We report the first evidence of a hot corino in a Bok globule. This is based on the ALMA observations in the 1.2 mm band toward the low-mass Class 0 protostar IRAS 19347+0727 in B335. Saturated complex organic molecules (COMs), CH$_3$CHO, HCOOCH$_3$, and NH$_2$CHO, are detected in a compact region within a few 10 au around the protostar. Additionally, CH$_3$OCH$_3$, C$_2$H$_5$OH, C$_2$H$_5$CN, and CH$_3$COCH$_3$ are tentatively detected. Carbon-chain related molecules, CCH and c-C$_3$H$_2$, are also found in this source, whose distributions are extended over a few 100 au scale. On the other hand, sulfur-bearing molecules CS, SO, and SO$_2$, have both compact and extended components. Fractional abundances of the COMs relative to H$_2$ are found to be comparable to those in known hot-corino sources. Though the COMs lines are as broad as 5-8 km s$^{-1}$, they do not show obvious rotation motion in the present observation. Thus, the COMs mainly exist in a structure whose distribution is much smaller than the synthesized beam (0."58 x 0."52).

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The problematic growth of dust in high redshift galaxies

Dust growth via accretion of gas species has been proposed as the dominant process to increase the amount of dust in galaxies. We show here that this hypothesis encounters severe difficulties that make it unfit to explain the observed UV and IR properties of such systems, particularly at high redshifts. Dust growth in the diffuse ISM phases is hampered by (a) too slow accretion rates; (b) too high dust temperatures, and (c) the Coulomb barrier that effectively blocks accretion. In molecular clouds these problems are largely alleviated. Grains are cold (but not colder than the CMB temperature, (Tcmb = 20 K at redshift z=6). However, in dense environments accreted materials form icy water mantles, perhaps with impurities. Mantles are immediately photo-desorbed as grains return to the diffuse ISM at the end of the cloud lifetime, thus erasing any memory of the growth. We conclude that dust attenuating stellar light at high-$z$ must be ready-made stardust largely produced in supernova ejecta.

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A Search for O_2 in CO-depleted Molecular Cloud Cores with Herschel

The general lack of molecular oxygen in molecular clouds is an outstanding problem in astrochemistry. Extensive searches with SWAS, Odin and Herschel have only produced two detections; upper limits to the O_2 abundance in the remaining sources observed are about 1000 times lower than predicted by chemical models. Previous atomic oxygen observations and inferences from observations of other molecules indicated that high abundances of O atoms might be present in dense cores exhibiting large amounts of CO depletion. Theoretical arguments concerning the oxygen gas-grain interaction in cold dense cores suggested that, if O atoms could survive in the gas after most of the rest of the heavy molecular material has frozen out on to dust, then O_2 could be formed efficiently in the gas. Using Herschel HIFI we searched a small sample of four depletion cores - L1544, L694-2, L429, Oph D - for emission in the low excitation O_2 N_J=3_3-1_2 line at 487.249 GHz. Molecular oxygen was not detected and we derive upper limits to its abundance in the range N(O_2)/N(H_2) = (0.6 - 1.6)x10^{-7}. We discuss the absence of O_2 in the light of recent laboratory and observational studies.

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H2S in the L1157-B1 Bow shock

Sulfur-bearing molecules are highly reactive in the gas phase of the ISM. However, the form in which most of the sulfur is locked onto interstellar dust grains is unknown. By taking advantage of the short time-scales of shocks in young molecular outflows, one could track back the main form of sulfur in the ices. In this paper, six transitions of H$_2$S and its isotopologues in the L1157-B1 bowshock have been detected using data from the Herschel-CHESS survey and the IRAM-30m ASAI large program. These detections are used to calculate the properties of H$_2$S gas in L1157-B1 through use of a rotation diagram and to explore the possible carriers of sulfur on the grains. The isotopologue detections allow the first calculation of the H$_2$S deuteration fraction in an outflow from a low mass protostar. The fractional abundance of H$_2$S in the region is found to be 6.0$\times$10$^{-7}$ and the deuteration fraction is 2$\times$10$^{-2}$. In order to investigate the form of sulfur on the grains, a chemical model is run with four different networks, each with different branching ratios for the freeze out of sulfur bearing species into molecules such as OCS and H$_2$S. It is found that the model best fits the data when at least half of each sulfur bearing species hydrogenates when freezing. We therefore conclude that a significant fraction of sulfur in L1157-B1 is likely to be locked in H$_2$S on the grains.

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Abundance of HOCO+ and CO2 in the outer layers of the L1544 prestellar core

The L1544 prestellar core has been observed as part of the ASAI IRAM Large Program at 3 mm. These observations led to the detection of many complex molecules. In this Letter, we report the detection of two lines, at 85.5 GHz (4,0,4-3,0,3) and 106.9 GHz (5,0,5-4,0,4), respectively, of the protonated carbon dioxide ion, HOCO+. We also report the tentative detection of the line at 100.4 GHz (5,0,5-4,0,4) of DOCO+. The non-LTE analysis of the detected lines shows that the HOCO+ emission originates in the external layer where non-thermal desorption of other species has previously been observed. Its abundance is (5 +/- 2) e-11. Modelling of the chemistry involved in the formation and destruction of HOCO+ provides a gaseous CO2 abundance of 2e-7 (with respect to H2) with an upper limit of 2e-6.

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Infalling-Rotating Motion and Associated Chemical Change in the Envelope of IRAS 16293-2422 Source A Studied with ALMA

We have analyzed rotational spectral line emission of OCS, CH3OH, HCOOCH3, and H2CS observed toward the low-mass Class 0 protostellar source IRAS 16293-2422 Source A at a sub-arcsecond resolution (~0".6 x 0".5) with ALMA. Significant chemical differentiation is found at a 50 AU scale. The OCS line is found to well trace the infalling-rotating envelope in this source. On the other hand, the CH3OH and HCOOCH3 distributions are found to be concentrated around the inner part of the infalling-rotating envelope. With a simple ballistic model of the infalling-rotating envelope, the radius of the centrifugal barrier (a half of the centrifugal radius) and the protostellar mass are evaluated from the OCS data to be from 40 to 60 AU and from 0.5 to 1.0 Msun, respectively, assuming the inclination angle of the envelope/disk structure to be 60 degrees (90 degrees for the edge-on configuration). Although the protostellar mass is correlated with the inclination angle, the radius of the centrifugal barrier is not. This is the first indication of the centrifugal barrier of the infalling-rotating envelope in a hot corino source. CH3OH and HCOOCH3 may be liberated from ice mantles due to weak accretion shocks around the centrifugal barrier, and/or due to protostellar heating. The H2CS emission seems to come from the disk component inside the centrifugal barrier in addition to the envelope component. The centrifugal barrier plays a central role not only in the formation of a rotationally-supported disk but also in the chemical evolution from the envelope to the protoplanetary disk.

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Geometric and Kinematic Structure of the Outflow/Envelope System of L1527 Revealed by Subarcsecond-resolution Observation of CS

Subarcsecond-resolution images of the rotational line emissions of CS and c-C$_3$H$_2$ obtained toward the low-mass protostar IRAS 04368$+$2557 in L1527 with the Atacama Large Millimeter/submillimeter Array are investigated to constrain the orientation of the outflow/envelope system. The distribution of CS consists of an envelope component extending from north to south and a faint butterfly-shaped outflow component. The kinematic structure of the envelope is well reproduced by a simple ballistic model of an infalling rotating envelope. Although the envelope has a nearly edge-on configuration, the inclination angle of the rotation axis from the plane of the sky is found to be 5$^\circ$, where we find that the western side of the envelope faces the observer. This configuration is opposite to the direction of the large-scale ($\sim$ 10$^4$ AU) outflow suggested previously from the $^{12}$CO ($J$=3$-$2) observation, and to the morphology of infrared reflection near the protostar ($\sim$ 200 AU). The latter discrepancy could originate from high extinction by the outflow cavity of the western side, these discrepancies or may indicate that the outflow axis is not parallel to the rotation axis of the envelope. Position-velocity diagrams show the accelerated outflow cavity wall, and its kinematic structure in the 2000 AU scale is explained by a standard parabolic model with the inclination angle derived from the analysis of the envelope. The different orientation of the outflow between the small and large scale implies a possibility of precession of the outflow axis. The shape and the velocity of the outflow in the vicinity of the protostar are compared with those of other protostars.

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The (impossible?) formation of acetaldehyde on the grain surfaces: insights from quantum chemical calculations

Complex Organic Molecules (COMs) have been detected in the interstellar medium (ISM). However, it is not clear whether their synthesis occurs on the icy surfaces of interstellar grains or via a series of gas-phase reactions. As a test case of the COMs synthesis in the ISM, we present new quantum chemical calculations on the formation of acetaldehyde (CH3CHO) from the coupling of the HCO and CH3 radicals, both in gas phase and on water ice surfaces. The binding energies of HCO and CH3 on the amorphous water ice were also computed (2333 and 734 K, respectively). Results indicate that, in gas phase, the products could be either CH3CHO, CH4 + CO, or CH3OCH, depending on the relative orientation of the two radicals. However, on the amorphous water ice, only the CH4 + CO product is possible due to the geometrical constraints imposed by the water ice surface. Therefore, acetaldehyde cannot be synthesized by the CH3 + HCO coupling on the icy grains. We discuss the implications of these results and other cases, such as ethylene glycol and dimethyl ether, in which similar situations can occur, suggesting that formation of these molecules on the grain surfaces might be unlikely.

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Subarcsecond Analysis of Infalling-Rotating Envelope around the Class I Protostar IRAS 04365+2535

Sub-arcsecond images of the rotational line emission of CS and SO have been obtained toward the Class I protostar IRAS 04365$+$2535 in TMC-1A with ALMA. A compact component around the protostar is clearly detected in the CS and SO emission. The velocity structure of the compact component of CS reveals infalling-rotating motion conserving the angular momentum. It is well explained by a ballistic model of an infalling-rotating envelope with the radius of the centrifugal barrier (a half of the centrifugal radius) of 50 AU, although the distribution of the infalling gas is asymmetric around the protostar. The distribution of SO is mostly concentrated around the radius of the centrifugal barrier of the simple model. Thus a drastic change in chemical composition of the gas infalling onto the protostar is found to occur at a 50 AU scale probably due to accretion shocks, demonstrating that the infalling material is significantly processed before being delivered into the disk.

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Detectability of deuterated water in prestellar cores

Water is an important molecule in the chemical and thermal balance of dense molecular gas, but knowing its history through-out the various stages of the star formation is a fundamental problem. Its molecular deuteration provides us with a crucial clue to its formation history. H$_2$O has recently been detected for the first time towards the prestellar core L1544 with the Herschel Space Observatory with a high spectral resolution (HIFI instrument). Prestellar cores provide the original reservoir of material from which future planetary systems are built, but few observational constraints exist on the formation of water and none on its deuteration before the collapse starts and a protostar forms at the centre. We report on new APEX observations of the ground state 1$_{0,1}$-0$_{0,0}$ HDO transition at 464 GHz towards the prestellar core L1544. The line is undetected, and we present an extensive study of the conditions for its detectability in cold and dense cloud cores. The water and deuterated water abundances have been estimated using an advanced chemical model simplified for the limited number of reactions or processes that are active in cold regions (< 15 K). We use the LIME radiative transfer code to compute the expected intensity and profile of both H$_2$O and HDO lines and compare them with the observations. We present several ad hoc profiles that best-fit the observations and compare the profiles with results from an astrochemical modelling, coupling gas phase and grain surface chemistry. Our comparison between observations, radiative transfer, and chemical modelling shows the limits of detectability for singly deuterated water, through the ground-state transitions 1$_{0,1}$-0$_{0,0}$ and 1$_{1,1}$-0$_{0,0}$ at 464.9 and 893.6 GHz, respectively, with both single-dish telescope and interferometric observations.

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Abundance Anomaly of the $^{13}$C Isotopic Species of c-C$_3$H$_2$ in the Low-Mass Star Formation Region L1527

The rotational spectral lines of c-C$_3$H$_2$ and two kinds of the $^{13}$C isotopic species, c-$^{13}$CCCH$_2$ ($C_{2v}$ symmetry) and c-CC$^{13}$CH$_2$ ($C_s$ symmetry) have been observed in the 1-3 mm band toward the low-mass star-forming region L1527. We have detected 7, 3, and 6 lines of c-C$_3$H$_2$, c-$^{13}$CCCH$_2$ , and c-CC$^{13}$CH$_2$, respectively, with the Nobeyama 45 m telescope, and 34, 6, and 13 lines, respectively, with the IRAM 30 m telescope, where 7, 2, and 2 transitions, respectively, are observed with the both telescopes. With these data, we have evaluated the column densities of the normal and $^{13}$C isotopic species. The [c-C$_3$H$_2$]/[c-$^{13}$CCCH$_2$] ratio is determined to be $310\pm80$, while the [c-C$_3$H$_2$]/[c-CC$^{13}$CH$_2$] ratio is determined to be $61\pm11$. The [c-C$_3$H$_2$]/[c-$^{13}$CCCH$_2$] and [c-C$_3$H$_2$]/[c-CC$^{13}$CH$_2$] ratios expected from the elemental $^{12}$C/$^{13}$C ratio are 60-70 and 30-35, respectively, where the latter takes into account the statistical factor of 2 for the two equivalent carbon atoms in c-C$_3$H$_2$. Hence, this observation further confirms the dilution of the $^{13}$C species in carbon-chain molecules and their related molecules, which are thought to originate from the dilution of $^{13}$C$^+$ in the gas-phase C$^+$ due to the isotope exchange reaction: $\mathrm{^{13}C^++CO\rightarrow{}^{13}CO+C^+}$. Moreover, the abundances of the two $^{13}$C isotopic species are different from each other. The ratio of c-$\mathrm{^{13}CCCH_2}$ species relative to c-$\mathrm{CC^{13}CH_2}$ is determined to be $0.20\pm0.05$. If $^{13}$C were randomly substituted for the three carbon atoms, the [c-$\mathrm{^{13}CCCH_2}$]/[c-$\mathrm{CC^{13}CH_2}$] ratio would be 0.5. Hence, the observed ratio indicates that c-$\mathrm{CC^{13}CH_2}$ exists more favorably. Possible origins of the different abundances are discussed.

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