Effect of Polar Molecules on Reaction of Negative Ions in Radiolysis of Hydrocarbon + Nitrous Oxide Systems in the Gas Phase

1969 ◽  
Vol 73 (9) ◽  
pp. 2809-2814 ◽  
Author(s):  
J Redpath ◽  
M Simic
Keyword(s):  
Nitrous Oxide ◽  
Gas Phase ◽  
Negative Ions ◽  
Polar Molecules ◽  
Oxide Systems

Ion chemistry of second-row transition metals in hydrocarbon flames: cations and anions of Y, Zr, Nb, and Mo

1995 ◽  
Vol 73 (12) ◽  
pp. 2263-2271 ◽  
Author(s):  
Christine C.Y. Chow ◽  
John M. Goodings
Keyword(s):  
Transition Metals ◽  
Gas Phase ◽  
Atmospheric Pressure ◽  
Chemical Ionization ◽  
Negative Ions ◽  
Ion Concentration ◽  
Oxidation States ◽  
Metallic Ions ◽  
Ion Chemistry ◽  
Hydrocarbon Flames

A pair of laminar, premixed, CH4–O2 flames above 2000 K at atmospheric pressure, one fuel-rich (FR) and the other fuel-lean (FL), were doped with ~10−6 mol fraction of the second-row transition metals Y, Zr, Nb, and Mo. Since these hydrocarbon flames contain natural ionization, metallic ions were produced in the flames by the chemical ionization (CI) of metallic neutral species, primarily by H3O+ and OH− as CI sources. Both positive and negative ions of the metals were observed as profiles of ion concentration versus distance along the flame axis by sampling the flames through a nozzle into a mass spectrometer. For yttrium, the observed ions include the YO+•nH2O (n = 0–3) series, and Y(OH)4−. With zirconium, they include the ZrO(OH)+•nH2O (n = 0–2) series, and ZrO(OH)3−. Those observed with niobium were the cations Nb(OH)3+ and Nb(OH)4+, and the single anion NbO2(OH)2−. For molybdenum, they include the cations MoO(OH)2+ and MoO(OH)3+, and the anions MoO3− and MoO3(OH)−. Not every ion was observed in each flame; the FL flame tended to favour the ions in higher oxidation states. Also, flame ions in higher oxidation states were emphasized for these second-row transition metals compared with their first-row counterparts. Some ions written as members of hydrate series may have structures different from those of simple hydrates; e.g., YO+•H2O = Y(OH)2+ and ZrO(OH)+•H2O = Zr(OH)3+, etc. The ion chemistry for the production of these ions by CI in flames is discussed in detail. Keywords: transition metals, ions, flame, gas phase, negative ions.

Symmetry of negative ions of polar molecules

1973 ◽  
Vol 26 (1) ◽  
pp. 139-143 ◽  
Author(s):  
Oakley H. Crawford
Keyword(s):  
Negative Ions ◽  
Polar Molecules

Gas-phase chemistry of the negative ions derived from azo- and hydrazobenzene

1991 ◽  
Vol 56 (2) ◽  
pp. 607-612 ◽  
Author(s):  
Steen Ingemann ◽  
Roel H. Fokkens ◽  
Nico M. M. Nibbering
Keyword(s):  
Gas Phase ◽  
Negative Ions ◽  
Gas Phase Chemistry ◽  
Phase Chemistry

Formation of gas-phase negative ions in vinylene carbonate

1983 ◽  
Vol 49 (2) ◽  
pp. 113-122 ◽  
Author(s):  
R.N. Compton ◽  
P.W. Reinhardt ◽  
H.C. Schweinler
Keyword(s):  
Gas Phase ◽  
Negative Ions ◽  
Vinylene Carbonate

Carbanion Rearrangements in the Gas Phase: The Unusual Claisen Rearrangement of Deprotonated Allyl Vinyl Ether

1990 ◽  
Vol 43 (9) ◽  
pp. 1479 ◽  
Author(s):  
PCH Eichinger ◽  
JH Bowie
Keyword(s):  
Gas Phase ◽  
Vinyl Ether ◽  
Condensed Phase ◽  
Claisen Rearrangement ◽  
Negative Ions ◽  
Marked Contrast ◽  
Wittig Rearrangement ◽  
Major Reaction

Allyl vinyl ether is reported to undergo a facile Wittig rearrangement to yield penta-1,4-dien-3-ol under base- catalysed conditions in the condensed phase. In marked contrast, the Wittig rearrangement is not a major reaction in the gas phase. Instead, initial rearrangement occurs by a Claisen process and subsequent fragmentations involve some of the most complex interconversions yet proposed for negative ions.

scholarly journals COHERENT SYNCHRONIZATION OF PYRIDINE DIMERIZATION REACTIONS AND DECOMPOSITION OF “GREEN OXIDANTS” – H2O2 AND N2O

2021 ◽  
Vol 0 (4) ◽  
pp. 6-11
Author(s):  
I.T. Nagieva ◽  
◽  
N.I. Ali-zadeh ◽  
T.М. Nagiev ◽  
◽  
...  
Keyword(s):  
Hydrogen Peroxide ◽  
Nitrous Oxide ◽  
Gas Phase ◽  
Atmospheric Pressure ◽  
Raw Materials ◽  
Oxidizing Agent ◽  
Optimal Conditions ◽  
Pyridine Bases ◽  
Pharmaceutical Industries ◽  
Oxidation By Hydrogen Peroxide

In recent years, hydrogen peroxide and nitrous oxide (1) "green oxidants" – have attracted much attention of researchers as a selective oxidizing agent for the catalytic oxidation of pyridine bases. In this regard, the reaction of pyridine oxidation by hydrogen peroxide and nitrous oxide under homogeneous conditions, in the gas phase, without the use of catalysts, at atmospheric pressure, has been experimentally investigated. Areas of selective oxidation of pyridine with hydrogen peroxide and nitrous oxide have been established, and optimal conditions have been found for obtaining valuable raw materials required in the petrochemical, chemical, and pharmaceutical industries

Moisture effects on gas-phase biofilter ammonia removal efficiency, nitrous oxide generation, and microbial communities

2014 ◽  
Vol 271 ◽  
pp. 292-301 ◽  
Author(s):  
Liangcheng Yang ◽  
Angela D. Kent ◽  
Xinlei Wang ◽  
Ted L. Funk ◽  
Richard S. Gates ◽  
...  
Keyword(s):  
Nitrous Oxide ◽  
Microbial Communities ◽  
Gas Phase ◽  
Removal Efficiency ◽  
Ammonia Removal ◽  
Moisture Effects

ChemInform Abstract: GAS PHASE REACTIONS OF ANIONS WITH NITROUS OXIDE AND CARBON DIOXIDE

1977 ◽  
Vol 8 (47) ◽  
pp. no-no
Author(s):  
V. M. BIERBAUM ◽  
C. H. DEPUY ◽  
R. H. SHAPIRO
Keyword(s):  
Carbon Dioxide ◽  
Nitrous Oxide ◽  
Gas Phase ◽  
Gas Phase Reactions
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