Organic Acid Chemistry in ISM: Detection of Formic Acid and its Prebiotic Chemistry in Hot Core G358.93$-$0.03 MM1
Arijit Manna, Sabyasachi Pal, Sekhar Sinha, Sushanta Kumar Mondal
TL;DR
This study reports the first ALMA Band 7 detection of the $trans$ form of formic acid ($t$-HCOOH) toward the hot core G358.93--0.03 MM1, deriving $N_T=(8.10 ext{±}1.12) imes10^{15}$ cm$^{-2}$, $T_{rot} ext{≈}116$ K, and a fractional abundance $X(t ext{-HCOOH}) ext{≈}(2.62 ext{±}0.29) imes10^{-9}$; MM3 remains undetected for $t$-HCOOH. A three-phase warm-up chemical model using UCLCHEM shows that the observed abundances are reproduced within a factor of 0.89, supporting grain-surface formation of HCOOH via the HCO + OH reaction followed by desorption. The work also characterizes the dust continuum structure (eight cores, with MM1/MM3 as hot cores) and maps the spatial distribution of $t$-HCOOH, finding emission co-located with the dense inner region but unresolved at the current resolution. Correlation analyses reveal weak or non-significant links between HCOOH and proposed precursors CH$_3$OH and H$_2$CO, suggesting a more complex chemical network. Overall, the results underscore the role of $t$-HCOOH as a tracer of hot-core chemistry and its potential relevance to prebiotic molecule formation in high-mass star-forming regions.
Abstract
In the interstellar medium, formic acid (HCOOH) plays a significant role in the synthesis of the simplest amino acid, glycine (NH$_{2}$CH$_{2}$COOH). The presence of HCOOH suggests that oxygen-bearing molecules may be directly involved in the chemical and physical evolution of star formation regions, particularly in hot molecular cores. This paper presents the first detection of the rotational emission lines of the $trans$-conformer of HCOOH toward the hot molecular core G358.93$-$0.03 MM1, located in the massive star formation region G358.93$-$0.03. This study employed high-resolution observations from the Atacama Large Millimeter/submillimeter Array (ALMA) in Band 7. The column density and excitation temperature of $t$-HCOOH are determined as $(8.13\pm0.72)\times10^{15}$ cm$^{-2}$ and $120\pm15$ K, respectively. The fractional abundance of $t$-HCOOH relative to H$_{2}$ is $(2.62\pm 0.29)\times 10^{-9}$. The column density ratios of $t$-HCOOH/CH$_{3}$OH and $t$-HCOOH/H$_{2}$CO are $(1.56 \pm 0.12)\times 10^{-2}$ and $(1.16 \pm 0.12)$, respectively. We computed a three-phase warm-up chemical model of HCOOH using the gas-grain chemical code UCLCHEM. We found that the observed and modelled abundances of HCOOH are almost identical, within a factor of 0.89. Based on chemical modelling, we showed that HCOOH may be formed through the reaction between HCO and OH on the grain surface, which is further released in the gas-phase.
