Chemical study of intermediate-mass (IM) Class 0 protostars. CO depletion and N2H+ deuteration

TL;DR

This study investigates the chemical composition of intermediate-mass Class 0 protostars, focusing on CO depletion and N2H+ deuteration, revealing insights into molecular processes and chemical modeling limitations in early star formation stages.

Contribution

It provides detailed observational and chemical modeling analysis of CO and N2H+ in IM Class 0 protostars, highlighting discrepancies in deuterium fractionation modeling.

Findings

C18O abundance decreases inward until CO evaporation temperature.

N2H+ deuterium fractionation is 0.005-0.014, higher than ISM D/H ratio.

Chemical models require lower CO abundance and cannot fully explain deuteration.

Abstract

We are carrying out a physical and chemical study of the protostellar envelopes in a representative sample of IM Class 0 protostars. In our first paper (Crimier et al. 2010), we determined the physical structure (density-temperature radial profiles) of the protostellar envelopes. Here, we study the CO depletion and N2H+ deuteration. We observed the millimeter lines of C18O, C17O, N2H+ and N2D+ toward the protostars using the IRAM 30m telescope. Based on these observations, we derived the C18O, N2H+ and N2D+ radial abundance profiles across their envelopes using a radiative transfer code. In addition, we modeled the chemistry of the protostellar envelopes. All the C18O 1-0 maps are well fit assuming that the C18O abundance decreases inwards within the protostellar envelope until the gas and dust reach the CO evaporation temperature, 20-25K, where the CO is released back to the gas phase. The N2H+ deuterium fractionation in Class 0 IMs is [N2D+]/[N2H+]=0.005-0.014, two orders of magnitude higher than the elemental [D/H] value in the interstellar medium, but a factor of 10 lower than in pre-stellar clumps. Chemical models account for the C18O and N2H+ observations if we assume the CO abundance is 2 times lower than the canonical value in the inner envelope. This could be the consequence of the CO being converted into CH3OH on the grain surfaces prior to the evaporation and/or the photodissociation of CO by the stellar UV radiation. The deuterium fractionation is not fitted by chemical models. This discrepancy is very likely caused by the simplicity of our model that assumes spherical geometry and neglects important phenomena like the effect of bipolar outflows and UV radiation from the star. More important, the deuterium fractionation is dependent on the ortho-to-para H2 ratio, which is not likely to reach the steady-state value in the dynamical time scales of these protostars.