A direct sampling mass spectrometer investigation of oxidation mechanisms for acetic acid in supercritical water

Citation
Sp. Maharrey et Dr. Miller, A direct sampling mass spectrometer investigation of oxidation mechanisms for acetic acid in supercritical water, J PHYS CH A, 105(24), 2001, pp. 5860-5867
Citations number
33
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF PHYSICAL CHEMISTRY A
ISSN journal
10895639 → ACNP
Volume
105
Issue
24
Year of publication
2001
Pages
5860 - 5867
Database
ISI
SICI code
1089-5639(20010621)105:24<5860:ADSMSI>2.0.ZU;2-3
Abstract
A quartz capillary microreactor:is directly coupled to a mass spectrometer utilizing the exit of the reactor as a standard high-pressure free-jet mole cular beam source. This direct sampling mass spectrometry (DSMS) design is used to-probe the reaction mechanism for the oxidation of acetic acid in su percritical water. The DSMS system is able to probe reactor conditions and to detect reaction intermediates, radicals, and product species during the early stages of reaction at the extreme pressures (> 23 MPa) and temperatur es (400-500 OC)of interest to supercritical water oxidation; The oxidation of acetic acid with hydrogen peroxide in supercritical water was selected a s a prototypical oxidation reaction to validate:our DSMS design. We report on our initial results, which include (1) the complete decomposition of the ,hydrogen peroxide to oxygen before 450 degreesC, (2) the subsequent onset of reaction at 470 degreesC, (3) the identification and measurement of the HO2* radical, indicating hydrogen abstraction by oxygen as the dominate ini tiation step, and (4) the lack of any bulk water incorporation into the rea ction mechanism up to 500 degreesC.