Optimization of two methods for the analysis of hydrogen peroxide: High performance liquid chromatography with fluorescence detection and high performance liquid chromatography with electrochemical detection in direct current mode

• Published in: Journal of Chromatography A Vol. 1217; no. 48; pp. 7564 - 7572
• Main Authors: Tarvin, Megan, McCord, Bruce, Mount, Kelly, Sherlach, Katy, Miller, Mark L.
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 26-11-2010; Amsterdam; New York: Elsevier; Elsevier
• Subjects: Analytical chemistry; Chemistry; Chromatographic methods and physical methods associated with chromatography; Chromatography, High Pressure Liquid - instrumentation; Chromatography, High Pressure Liquid - methods; Electrochemical detection; Electrochemistry; Exact sciences and technology; Fluorescence; Fluorescence detection; HPLC; Hydrogen peroxide; Hydrogen Peroxide - analysis; Other chromatographic methods; Hydrogen peroxide; Electrochemical detection; HPLC; Fluorescence detection; Trace analysis; Fluorescence detector; Chemical analysis; HPLC chromatography; Explosions; Derivatization; Optimization; Postcolumn; Electrochemical detector; Reversed phase chromatography; Hemin; Residue; Metalloporphyrin; Quantitative analysis
• ISSN: 0021-9673; 1873-3778
• DOI: 10.1016/j.chroma.2010.10.022

Two complementary methods were optimized for the separation and detection of trace levels of hydrogen peroxide. The first method utilized reversed-phase high-performance liquid chromatography with fluorescence detection (HPLC–FD). With this approach, hydrogen peroxide was detected based upon its participation in the hemin-catalyzed oxidation of
p-hydroxyphenylacetic acid to yield the fluorescent dimer. The second method utilized high performance liquid chromatography with electrochemical detection (HPLC–ED). With this approach, hydrogen peroxide was detected based upon its oxidation at a gold working electrode at an applied potential of 400
mV vs. hydrogen reference electrode (Pd/H
2). Both methods were linear across the range of 15–300
μM, and the electrochemical method was linear across a wider range of 7.4–15,000
μM. The limit of detection for hydrogen peroxide was 6
μM by HPLC/FD, and 0.6
μM by HPLC/ED. A series of organic peroxides and inorganic ions were evaluated for their potential to interfere with the detection of hydrogen peroxide. Studies investigating the recovery of hydrogen peroxide with three different extraction protocols were also performed. Post-blast debris from the detonation of a mixture of concentrated hydrogen peroxide with nitromethane was analyzed on both systems. Hydrogen peroxide residues were successfully detected on this post-blast debris.