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Namrata Rani

Publications and source records attributed to Namrata Rani.

2 recordsLinked to original sources

A Comprehensive Sulfur Chemistry Network Including Excited S(1D) and SO(1Δ) for the XODIAC Photochemical Model: Accounting for Missing Sulfur Processes in Venus and Exo-Venus Analogs

Sulfur chemistry plays a central role in controlling the atmospheric structure, cloud formation, and composition of Venus and Venus-like exoplanets. However, key reactions involving ground- and excited-state sulfur species remain poorly constrained, and existing photochemical models often rely on incomplete or uncertain kinetic data under high-temperature, CO2-rich conditions. In this work, we compute kinetic parameters for reactions of ground-state S(3P) and excited-state S(1D) with CO2 under Venus-like conditions, forming SO(3Sigma), SO(1Delta), and CO. We characterize the underlying potential energy surfaces, identify intermediate complexes, and derive temperature-dependent rate coefficients using a master-equation framework based on the chemically significant eigenvalue method. We also provide NASA 7-term polynomial coefficients for S and SO in both ground and excited states to enable consistent incorporation into photochemical models. Incorporating these reactions into the one-dimensional photochemical model XODIAC for Venus produces only minor effects above 60 km due to competing pathways. While the model reproduces most observed sulfur species, discrepancies remain for S3 and S4. Introducing a 1 ppm near-surface atomic sulfur source, representing unresolved deep-atmosphere or surface processes, enhances S3 and S4 abundances by 1-2 orders of magnitude and improves agreement with observations. For exo-Venus analogs, the updated chemistry produces modest changes under isothermal conditions. In contrast, in strongly irradiated atmospheres with a high-altitude isotherm and a near-surface sulfur source, it leads to pronounced changes in most sulfur-bearing species, along with significant enhancements in S(1D) and SO(1Delta). These results highlight missing sulfur pathways, including excited states and deep sources, and potential implications for shaping Venus and exo-Venus atmospheres.

astro-ph.EP

Pathways to Interstellar Amides via Carbamoyl (NH2CO) Isomers by Radical-Neutral Reactions on Ice Grain Mantles

Explaining the formation pathways of amides on ice-grain mantels is crucial to understanding the prebiotic chemistry in an interstellar medium. In this computational study, we explore different radical-neutral formation pathways for some of the observed amides (formamide, acetamide, urea, and N-methylformamide) via intermediate carbamoyl (NH2CO) radical precursors and their isomers. We assess the relative energy of four NH2CO isomers in the gas phase and evaluate their binding energy on small water clusters to discern the affinity that the isomers present to an ice model. We consider three possible reaction pathways for the formation of the carbamoyl radicals, namely, the OH + HCN, CN + H2O, and NH2 + CO reaction channels. We computed the binding energy distribution for the HCN and CH3CN precursors on an ice model consisting of a set of clusters of 22 water molecules each to serve as a starting point for the reactivity study on the ice surface. The computations revealed that the lowest barrier to the formation of an NH2CO isomer corresponds to the NH2 + CO reaction (12.6 kJ/mol). The OH + HCN reaction pathway results in the exothermic formation of the N-radical form of carbamoyl HN(C=O)H with a reaction barrier of 26.7 kJ/mol. We found that the CN + H2O reaction displays a high energy barrier of 70.6 kJ/mol. Finally, we also probed the direct formation of the acetamide radical precursor via the OH + CH3CN reaction and found that the most probable outcome on interstellar ices is the H-abstraction reaction to yield CH2CN and H2O. Based on these results, we believe that including alternative reaction pathways, leading to the formation of amides via the N-radical form of carbamoyl, would provide an improvement in the prediction of the amide abundances in astrochemical models, especially regarding the chemistry of star-forming regions.

astro-ph.GA