arXiv subjects

J. A. Noble

Publications and source records attributed to J. A. Noble.

24 records · Page 2Linked to original sources

arXiv2015

The electronic spectra of protonated PANH molecules

Aims. This study was designed to examine the viability of protonated nitrogen-substituted polycyclic aromatic hydrocarbons (H+PANHs) as candidates for the carriers of the diffuse interstellar bands (DIBs). Methods. We obtained the electronic spectra of two protonated PANH cations, protonated acridine and phenanthridine, using parent ion photo-fragment spectroscopy and generated theoretical electronic spectra using ab initio calculations. Results. We show that the spectra of the two species studied here do not correspond to known DIBs. However, based on the general properties derived from the spectra of these small protonated nitrogen-substituted PAHs, we propose that larger H+PANH cations represent good candidates for DIB carriers due to the expected positions of their electronic transitions in the UV-visible and their narrow spectral bands.

astro-ph.SR↗

arXiv2015

Hydrogenation at low temperatures does not always lead to saturation: the case of HNCO

Context. It is generally agreed that hydrogenation reactions dominate chemistry on grain surfaces in cold, dense molecular cores, saturating the molecules present in ice mantles. Aims. We present a study of the low temperature reactivity of solid phase isocyanic acid (HNCO) with hydrogen atoms, with the aim of elucidating its reaction network. Methods. Fourier transform infrared spectroscopy and mass spectrometry were employed to follow the evolution of pure HNCO ice during bombardment with H atoms. Both multilayer and monolayer regimes were investigated. Results. The hydrogenation of HNCO does not produce detectable amounts of formamide (NH2CHO) as the major product. Experiments using deuterium reveal that deuteration of solid HNCO occurs rapidly, probably via cyclic reaction paths regenerating HNCO. Chemical desorption during these reaction cycles leads to loss of HNCO from the surface. Conclusions. It is unlikely that significant quantities of NH2CHO form from HNCO. In dense regions, however, deuteration of HNCO will occur. HNCO and DNCO will be introduced into the gas phase, even at low temperatures, as a result of chemical desorption.

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arXiv2013

A survey of H$_2$O, CO$_2$ and CO ice features towards background stars and low mass YSOs using AKARI

We present near infrared spectroscopic observations of 19 molecular clouds made using the AKARI satellite, and the data reduction pipeline written to analyse those observations. The 2.5 --~5 $μ$m spectra of 30 objects -- 22 field stars behind quiescent molecular clouds and eight low mass YSOs in cores -- were successfully extracted using the pipeline. Those spectra are further analysed to calculate the column densities of key solid phase molecular species, including H$_2$O, CO$_2$, CO, and OCN$^-$. The profile of the H$_2$O ice band is seen to vary across the objects observed and we suggest that the extended red wing may be an evolutionary indicator of both dust and ice mantle properties. The observation of 22 spectra with fluxes as low as $<$~5 mJy towards background stars, including 15 where the column densities of H$_2$O, CO and CO$_2$ were calculated, provides valuable data that could help to benchmark the initial conditions in star-forming regions prior to the onset of star formation.

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arXiv2012

The thermal reactivity of HCN and NH3 in interstellar ice analogues

HCN is a molecule central to interstellar chemistry, since it is the simplest molecule containing a carbon-nitrogen bond and its solid state chemistry is rich. The aim of this work was to study the NH3 + HCN -> NH4+CN- thermal reaction in interstellar ice analogues. Laboratory experiments based on Fourier transform infrared spectroscopy and mass spectrometry were performed to characterise the NH4+CN- reaction product and its formation kinetics. This reaction is purely thermal and can occur at low temperatures in interstellar ices without requiring non-thermal processing by photons, electrons or cosmic rays. The reaction rate constant has a temperature dependence of k(T) = 0.016+0.010-0.006 s-1.exp((-2.7+-0.4 kJmol-1)/(RT)) when NH3 is much more abundant than HCN. When both reactants are diluted in water ice, the reaction is slowed down. We have estimated the CN- ion band strength to be A_CN- = 1.8+-1.5 x10-17 cm molec-1 at both 20 K and 140 K. NH4+CN- exhibits zeroth-order multilayer desorption kinetics with a rate of k_des(T) = 10^28 molecules cm-2 s-1.exp((-38.0+-1.4 kJmol-1)/(RT)). The NH3 + HCN -> NH4+CN- thermal reaction is of primary importance because (i) it decreases the amount of HCN available to be hydrogenated into CH2NH, (ii) the NH4+ and CN- ions react with species such as H2CO, or CH2NH to form complex molecules, and (iii) NH4+CN- is a reservoir of NH3 and HCN, which can be made available to a high temperature chemistry.

astro-ph.EP↗

arXiv2011

AKARI observations of ice absorption bands towards edge-on YSOs

To investigate the composition and evolution of circumstellar ice around low-mass YSOs, we observed ice absorption bands in the near infrared (NIR) towards eight YSOs ranging from class 0 to class II, among which seven are associated with edge-on disks. We performed slit-less spectroscopic observations using the grism mode of the Infrared Camera (IRC) on board AKARI, which enables us to obtain full NIR spectra from 2.5 $μ$m to 5 $μ$m. The spectra were fitted with polynomial baselines to derive the absorption spectra. The molecular absorption bands were then fitted with the laboratory database of ice absorption bands, considering the instrumental line profile and the spectral resolution of the grism dispersion element. Towards the class 0-I sources (L1527, IRC-L1041-2, and IRAS04302), absorption bands of H$_2$O, CO$_2$, CO, and XCN are clearly detected. Column density ratios of CO$_2$ ice and CO ice relative to H$_2$O ice are 21-28% and 13-46%, respectively. If XCN is OCN$^-$, its column density is as high as 2-6% relative to H$_2$O ice. The HDO ice feature at 4.1 $μ$m is tentatively detected towards the class 0-I sources and HV Tau. Non-detections of the CH-stretching mode features around 3.5 $μ$m provide upper limits to the CH$_3$OH abundance of 26% (L1527) and 42% (IRAS04302) relative to H$_2$O. We tentatively detect OCS ice absorption towards IRC-L1041-2. Towards class 0-I sources, the detected features should mostly originate in the cold envelope, while CO gas and OCN$^-$ could originate in the region close to the protostar, where there are warm temperatures and UV radiation. We detect H$_2$O ice band towards ASR41 and 2MASSJ1628137-243139, which are edge-on class II disks. We also detect H$_2$O ice and CO$_2$ ice towards HV Tau, HK Tau, and UY Aur, and tentatively detect CO gas features towards HK Tau and UY Aur.

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arXiv2011

Thermal desorption characteristics of CO, O2 and CO2 on non-porous water, crystalline water and silicate surfaces at sub-monolayer and multilayer coverages

The desorption characteristics of molecules on interstellar dust grains are important for modelling the behaviour of molecules in icy mantles and, critically, in describing the solid-gas interface. In this study, a series of laboratory experiments exploring the desorption of three small molecules from three astrophysically relevant surfaces are presented. The desorption of CO, O2 and CO2 at both sub-monolayer and multilayer coverages was investigated from non-porous water, crystalline water and silicate surfaces. Experimental data was modelled using the Polanyi-Wigner equation to produce a mathematical description of the desorption of each molecular species from each type of surface, uniquely describing both the monolayer and multilayer desorption in a single combined model. The implications of desorption behaviour over astrophysically relevant timescales are discussed.

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