"Gas-Phase Reactions of Methamphetamine with Hydroxyl Radicals and Ozon" by Crystal D. Forester

Semester

Spring

Date of Graduation

2013

Document Type

Thesis

Degree Type

MS

College

Eberly College of Arts and Sciences

Department

Chemistry

Committee Chair

Suzanne Bell

Committee Co-Chair

Jonathan Boyd

Committee Member

Harry Finklea

Abstract

Gas-phase reactions involving methamphetamine, the hydroxyl radical (OH·), and ozone (O3) at (297 +/- 3) K and 1 atmosphere total pressure were investigated. A bimolecular rate constant, kOH·+methamphetamine, (960 +/- 100) x 10 -12 cm3molecule-1s-1, was measured using the relative rate technique for reactions of methamphetamine with OH·. Pseudo first-order techniques were used to measure the bimolecular rate constant, kO3+methamphetamine , (2.7 +/- 0.5) x 10-17 cm3molecule -1s-1 for reactions of methamphetamine with O 3. Product studies to determine the degradation of methamphetamine in the gasphase were conducted and the products of these reactions were identified. The positively identified methamphetamine/OH· and methamphetamine/O 3 reaction products were: benzaldehyde, ethanedial (glyoxal), and 2-oxopropanal (methylglyoxal). The use of derivatizing agent O-(2,3,4,5,6-pentafluorobenzyl)hydroxylamine (PFBHA) was used to propose phenyl-2-propanone as the other major methamphetamine/OH· and methamphetamine/O3 reaction product. The elucidation of this other reaction product was facilitated by mass spectrometry of the derivatized reaction products coupled with plausible methamphetamine/OH· and methamphetamine/O 3 reaction mechanisms based on previously published volatile organic compound/OH· and volatile organic compound/O3 gas-phase reaction mechanisms.

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