Hydroxyl radical oxidation of phospholipid-coated NaCl particles

Literature Information

Publication Date 2013-05-02
DOI 10.1039/C3CP51237A
Impact Factor 3.676
Authors

Christopher W. Dilbeck, Barbara J. Finlayson-Pitts


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Abstract

Biological organic compounds mixed with NaCl and other inorganic compounds in sea-salt aerosol particles react in air with oxidants such as ozone and hydroxyl (OH) radicals. Laboratory studies of model systems can provide insight into these reactions. We report here studies of the kinetics and mechanism of oxidation of unsaturated 1-palmitoyl-2-oleoyl-sn-glycero-3-phosphocholine (POPC) on NaCl by gas phase OH in air at room temperature and 1 atm pressure using diffuse reflection infrared Fourier transform spectrometry (DRIFTS) and matrix-assisted laser desorption/ionization-time-of-flight-mass spectrometry (MALDI-TOF-MS) to identify possible structures of surface-bound reaction products. For comparison, some studies were also carried out on the saturated 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) on NaCl. The calculated concentration of hydroxyl radicals, generated by photolysis of isopropyl nitrite, was (1.6–6.4) × 108 radicals cm−3. Surface-bound aldehydes, ketones, organic nitrates and nitrate ions were identified as products of these reactions and structures of potential products were proposed based on mechanistic considerations combined with the MALDI-TOF-MS and DRIFTS spectra. The loss rate of vinyl hydrogen, C–H, at 3008 cm−1 was used to obtain a lower limit for the rate constant (k1) for addition of OH to the double bond, k1 > (3 ± 1) × 10−13 cm3 molecule−1 s−1 (1s), corresponding to a reaction probability of γadd > (4 ± 1) × 10−3 (1s). Assuming that abstraction from –CH2– groups in POPC is the same as for DPPC, the percentage of the reaction that occurs by addition is ∼80%. This is similar to the percent addition predicted using structure–reactivity relationships for gas-phase reactions. Decreasing the amount of POPC relative to NaCl resulted in more nitrate ion formation and less relative loss of POPC, and increasing the OH concentration resulted in a more rapid loss of POPC and faster product formation. These studies suggest that under atmospheric conditions with an OH concentration of 5 × 106 radicals cm−3, the lifetime of POPC with respect to OH is <6 days.

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
CiteScore: 5.5
Self-citation Rate: 10.3%
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Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.

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