Pith. sign in

REVIEW

OD + CO -> D + CO2 Branching Kinetics Probed with Time-Resolved Frequency Comb Spectroscopy

Not yet reviewed by Pith; the record is open.

This paper has not been read by Pith yet. Machine review is queued; the pith claim, tier, and objections will appear here once it completes.

SPECIMEN: schema-true, not a live event

T0 review · schema-true

One-sentence machine reading of the paper's core claim.

pith:XXXXXXXX · record.json · timestamp

arxiv 1701.00832 v1 pith:T3AULBJ3 submitted 2017-01-03 physics.chem-ph physics.optics

OD + CO -> D + CO2 Branching Kinetics Probed with Time-Resolved Frequency Comb Spectroscopy

classification physics.chem-ph physics.optics
keywords branchingformationkineticsmeasurementsrateactivatedcombfrequency
verification ladder T0 review T1 audit T2 compute T3 formal T4 reserved
0 comments
Share X Bluesky LinkedIn Reddit HN
read the original abstract

Time-resolved direct frequency comb spectroscopy (TRFCS) was used to study the kinetics of the deuterated analogue of the OH+CO->H+CO2 reaction, which is important for atmospheric and combustion chemistry. Complementing our recent work on quantifying the formation rate of the transient trans-DOCO radical, we report measurements of the kinetics of the activated product channel, D+CO2, at room temperature. Simultaneous measurements of the time-dependence of OD and CO2 concentrations allowed us to directly determine the formation rate, branching yield, and dependence on pressure and bath gas of the activated product. Together with the trans-DOCO formation rate, these new measurements provide absolute yields of branching channels for both products of OD+CO in the low-pressure limit.

discussion (0)

Sign in with ORCID, Apple, or X to comment. Anyone can read and Pith papers without signing in.