Mechanistic studies on gas-phase negative ion unimolecular decompositions. Alkoxide anions

1988 ◽  
Vol 110 (9) ◽  
pp. 2714-2722 ◽  
Author(s):  
William. Tumas ◽  
Robert F. Foster ◽  
John I. Brauman
Keyword(s):  
Gas Phase ◽  
Negative Ion ◽  
Mechanistic Studies

scholarly journals Negative ion photoelectron spectroscopy confirms the prediction that D3h carbon trioxide (CO3) has a singlet ground state

2016 ◽  
Vol 7 (2) ◽  
pp. 1142-1150 ◽  
Author(s):  
David A. Hrovat ◽  
Gao-Lei Hou ◽  
Bo Chen ◽  
Xue-Bin Wang ◽  
Weston Thatcher Borden
Keyword(s):  
Gas Phase ◽  
Ground State ◽  
Photoelectron Spectroscopy ◽  
Radical Anion ◽  
Negative Ion ◽  
Singlet Ground State

The CO3 radical anion (CO3˙−) has been formed by electrospraying carbonate dianion (CO32−) into the gas phase.

scholarly journals Observation of HClO3 and HClO4 in the Arctic atmosphere

2020 ◽  
Author(s):  
Yee Jun Tham ◽  
Nina Sarnela ◽  
Carlos A. Cuevas ◽  
Iyer Siddharth ◽  
Lisa Beck ◽  
...  
Keyword(s):  
Gas Phase ◽  
Ozone Depletion ◽  
Surface Ozone ◽  
Negative Ion ◽  
The Arctic ◽  
Research Station ◽  
Visible Absorption ◽  
Data Set ◽  
Near Surface ◽  
Arctic Atmosphere

<p>Atmospheric halogens chemistry like the catalytic reaction of bromine and chlorine radicals with ozone (O<sub>3</sub>) has been known to cause the springtime surface-ozone destruction in the polar region. Although the initial atmospheric reactions of chlorine with ozone are well understood, the final oxidation steps leading to the formation of chlorate (ClO<sub>3</sub><sup>-</sup>) and perchlorate (ClO<sub>4</sub><sup>-</sup>) remain unclear due to the lack of direct evidence of their presence and fate in the atmosphere. In this study, we present the first high-resolution ambient data set of gas-phase HClO<sub>3</sub> (chloric acid) and HClO<sub>4</sub> (perchlorate acid) obtained from the field measurement at the Villum Research Station, Station Nord, in high arctic North Greenland (81°36’ N, 16°40’ W) during the spring of 2015. A state-of-the-art chemical ionization atmospheric pressure interface time-of-flight mass spectrometer (CI-APi-TOF) was used in negative ion mode with nitrate ion as the reagent ion to detect the gas-phase HClO<sub>3</sub> and HClO<sub>4</sub>. We measured significant level of HClO<sub>3</sub> and HClO<sub>4</sub> only during the springtime ozone depletion events in the Greenland, with concentration up to 9x10<sup>5</sup> molecule cm<sup>-3</sup>. Air mass trajectory analysis shows that the air during the ozone depletion event was confined to near-surface, indicating that the O<sub>3</sub> and surface of sea-ice/snowpack may play important roles in the formation of HClO<sub>3</sub> and HClO<sub>4</sub>. We used high-level quantum-chemical methods to calculate the ultraviolet-visible absorption spectra and cross-section of HClO<sub>3</sub> and HClO<sub>4</sub> in the gas-phase to assess their fates in the atmosphere. Overall, our results reveal the presence of HClO<sub>3</sub> and HClO<sub>4</sub> during ozone depletion events, which could affect the chlorine chemistry in the Arctic atmosphere.</p>

scholarly journals Identifying precursors and aqueous organic aerosol formation pathways during the SOAS campaign

2016 ◽  
Vol 16 (22) ◽  
pp. 14409-14420 ◽  
Author(s):  
Neha Sareen ◽  
Annmarie G. Carlton ◽  
Jason D. Surratt ◽  
Avram Gold ◽  
Ben Lee ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Gas Phase ◽  
Aqueous Phase ◽  
Organic Aerosol ◽  
Water Soluble ◽  
Negative Ion ◽  
Anthropogenic Sources ◽  
Ionization Mass ◽  
Aqueous Mixtures ◽  
Aerosol Formation

Abstract. Aqueous multiphase chemistry in the atmosphere can lead to rapid transformation of organic compounds, forming highly oxidized, low-volatility organic aerosol and, in some cases, light-absorbing (brown) carbon. Because liquid water is globally abundant, this chemistry could substantially impact climate, air quality, and health. Gas-phase precursors released from biogenic and anthropogenic sources are oxidized and fragmented, forming water-soluble gases that can undergo reactions in the aqueous phase (in clouds, fogs, and wet aerosols), leading to the formation of secondary organic aerosol (SOAAQ). Recent studies have highlighted the role of certain precursors like glyoxal, methylglyoxal, glycolaldehyde, acetic acid, acetone, and epoxides in the formation of SOAAQ. The goal of this work is to identify additional precursors and products that may be atmospherically important. In this study, ambient mixtures of water-soluble gases were scrubbed from the atmosphere into water at Brent, Alabama, during the 2013 Southern Oxidant and Aerosol Study (SOAS). Hydroxyl (OH⚫) radical oxidation experiments were conducted with the aqueous mixtures collected from SOAS to better understand the formation of SOA through gas-phase followed by aqueous-phase chemistry. Total aqueous-phase organic carbon concentrations for these mixtures ranged from 92 to 179 µM-C, relevant for cloud and fog waters. Aqueous OH-reactive compounds were primarily observed as odd ions in the positive ion mode by electrospray ionization mass spectrometry (ESI-MS). Ultra high-resolution Fourier-transform ion cyclotron resonance mass spectrometry (FT-ICR-MS) spectra and tandem MS (MS–MS) fragmentation of these ions were consistent with the presence of carbonyls and tetrols. Products were observed in the negative ion mode and included pyruvate and oxalate, which were confirmed by ion chromatography. Pyruvate and oxalate have been found in the particle phase in many locations (as salts and complexes). Thus, formation of pyruvate/oxalate suggests the potential for aqueous processing of these ambient mixtures to form SOAAQ.

Negative Ion Chemistry of Ozone in the Gas Phase

2002 ◽  
Vol 106 (6) ◽  
pp. 997-1003 ◽  
Author(s):  
Skip Williams ◽  
Meghann F. Campos ◽  
Anthony J. Midey ◽  
Susan T. Arnold ◽  
Robert A. Morris ◽  
...  
Keyword(s):  
Gas Phase ◽  
Negative Ion ◽  
Ion Chemistry

Negative ion chemistry of triflic anhydride in the gas phase and the electron affinity of trifluoromethanesulfonate ion

1987 ◽  
Vol 91 (11) ◽  
pp. 3031-3032 ◽  
Author(s):  
A. A. Viggiano ◽  
John F. Paulson ◽  
Fred. Dale ◽  
Michael. Henchman
Keyword(s):  
Gas Phase ◽  
Electron Affinity ◽  
Negative Ion ◽  
Ion Chemistry
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