Gas phase photolysis of hydrogen iodide. Part 1.—Inhibition with nitric oxide at 25°C

1966 ◽  
Vol 62 (0) ◽  
pp. 910-917 ◽  
Author(s):  
J. L. Holmes ◽  
E. V. Sundaram
Keyword(s):  
Nitric Oxide ◽  
Gas Phase ◽  
Hydrogen Iodide

The gas-phase photolysis of 2-methyl-1,3-butadiene at 123.6 nm

1984 ◽  
Vol 62 (9) ◽  
pp. 1731-1735
Author(s):  
Valerie I. Lang ◽  
Richard D. Doepker
Keyword(s):  
Nitric Oxide ◽  
Hydrogen Sulfide ◽  
Gas Phase ◽  
Quantum Efficiency ◽  
Hydrogen Iodide ◽  
Quantum Yields ◽  
Primary Decomposition ◽  
Radical Scavengers ◽  
Molecule Reaction ◽  
Reaction Channels

The gas-phase photolysis of 2-methyl-1,3-butadiene has been investigated using krypton (123.6 nm) resonance radiation. The observed neutral products of the primary decomposition were vinylacetylene, ethylene, acetylene, methylacetylene, propylene, allene, 2-methy-1-buten-3-yne, pentatriene/1-penten-3-yne, 1,3-butadiene, 2-butyne and butatriene, listed in decreasing order of concentration. There was also evidence of the presence of several radical fragments: CH2/CH3, C2H3, C3H3, and C4H5. Quantum yields for each of the products were determined in the photolysis of 2-methyl-1,3-butadiene, performed both in the presence and the absence of additives. Nitric oxide and oxygen were employed as radical scavengers, while hydrogen sulfide and hydrogen iodide were used as radical interceptors. Twelve primary, neutral molecule, reaction channels were proposed and the quantum efficiency assigned for each. The ionization efficiency of 2-methyl-1,3-butadiene was established as n = 0.55 at 10.03 eV. No products formed exclusively via an ion–molecule pathway were identified and therefore the fate of the C5H8+ ion was not determined.

Gas-phase photolysis of spiropentane at 147.0 nm

1985 ◽  
Vol 63 (12) ◽  
pp. 3593-3596 ◽  
Author(s):  
M. Paller ◽  
R. D. Doepker
Keyword(s):  
Nitric Oxide ◽  
Hydrogen Sulfide ◽  
Gas Phase ◽  
Hydrogen Iodide ◽  
Radical Scavenger ◽  
Relative Importance ◽  
Molecular Processes ◽  
Primary Reaction ◽  
Reaction Channels

The gas-phase photolysis of spiropentane has been investigated using xenon (147.0 nm) resonance radiation. Major products observed in order of decreasing importance are ethylene, aliène, methylacetylene, 1,2-butadiene, acetylene, propylene, and vinylacetylene. Nitric oxide was used as a radical scavenger while hydrogen sulfide and hydrogen iodide were employed as radical interceptors in the determination of the relative importance of radical and molecular processes. CH3/CH2 and CH3C=C• radicals were identified and quantified. Seven primary reaction channels were postulated of which those involving the "elimination" of ethylene were the most predominant accounting for 71% of the photodecomposition.

Kinetics of the gas-phase reaction between nitric oxide, ammonia and oxygen

1992 ◽  
Vol 70 (5) ◽  
pp. 1014-1020 ◽  
Author(s):  
W. Duo ◽  
K. Dam-Johansen ◽  
K. Østergaard
Keyword(s):  
Nitric Oxide ◽  
Gas Phase ◽  
Phase Reaction ◽  
Gas Phase Reaction ◽  
Kinetics Of

scholarly journals Gas-phase reaction products and yields of terpinolene with ozone and nitric oxide using a new derivatization agent

2015 ◽  
Vol 122 ◽  
pp. 513-520 ◽  
Author(s):  
Jason E. Ham ◽  
Stephen R. Jackson ◽  
Joel C. Harrison ◽  
J.R. Wells
Keyword(s):  
Nitric Oxide ◽  
Gas Phase ◽  
Phase Reaction ◽  
Reaction Products ◽  
Gas Phase Reaction

scholarly journals The Determination of Nitric Oxide in Gas Phase Cigarette Smoke by Non-dispersive Infrared Analysis

1980 ◽  
Vol 10 (2) ◽  
Author(s):  
T. B. Williams
Keyword(s):  
Nitric Oxide ◽  
Gas Phase ◽  
Cigarette Smoke ◽  
Relative Error ◽  
Dead Volume ◽  
High Yield ◽  
Infrared Analysis ◽  
Colorimetric Analysis ◽  
Standard Gas

AbstractNitric oxide in cigarette smoke was conveniently determined by non-dispersive infrared analysis (NDIR). Recoveries of 95 % were obtained with standard gas-air mixtures but recoveries from smoke increased from 87% for high-yield to 91 % for low-yield cigarettes. Relative error was about 4 %. A reduction in the dead volume of Cambridge filter cassettes, to reduce the amount of NO reacted between puffs, increased NO deliveries of cigarettes by 4%. Deliveries of NO were estimated to average 4 % lower due to oxidation, but reaction with other smoke components reduced them further depending upon concentrations. The NO deliveries of cigarettes increased as blend nitrate increased and as the flow of air around cigarettes decreased. Nitric oxide in smoke and in standard gas-air mixtures, determined by non-dispersive infrared (NDIR) spectroscopy, was substantiated by an automated colorimetric analysis. Interfering smoke species were determined and circumvented in both methods.

Gas-phase reactions of nitric oxide with atomic lanthanide cations: Room-temperature kinetics and periodicity in reactivity

2006 ◽  
Vol 249-250 ◽  
pp. 385-391 ◽  
Author(s):  
Voislav Blagojevic ◽  
Eric Flaim ◽  
Michael J.Y. Jarvis ◽  
Gregory K. Koyanagi ◽  
Diethard K. Bohme
Keyword(s):  
Nitric Oxide ◽  
Gas Phase ◽  
Room Temperature ◽  
Gas Phase Reactions ◽  
Lanthanide Cations

Wilzbach Tritation studies. III. A study of physical variables affecting exchange in the polycyclic aromatics

1967 ◽  
Vol 20 (9) ◽  
pp. 1875 ◽  
Author(s):  
JL Garnett ◽  
SW Law
Keyword(s):  
Nitric Oxide ◽  
Gas Phase ◽  
Polycyclic Hydrocarbon ◽  
Simple Relationship ◽  
Polycyclic Aromatics ◽  
Radical Scavengers ◽  
Effect Of Particle Size ◽  
Labelling Process ◽  
Physical Variables ◽  
Radical Processes

The effect of particle size of substrate and tritium gas pressure on the efficiency of Wilzbach tritiation of crystalline polycyclic hydrocarbons has been investigated. The hydrocarbons studied included naphthalene, biphenyl, phenanthrene, chrysene, pyrene, m- and p-terphenyls, and acridine. No simple relationship between ionization potential and tritium incorporation was observed. The effect of radical scavengers such as nitric oxide and moderators such as helium on the labelling process have been examined. Tritium incorporation in a polycyclic hydrocarbon is enhanced lf gas exposure occurs in the presence of benzoic acid. The results are discussed in terms of current theories proposed for tritium labelling based on gas-phase studies. In the condensed phase present data show that radical processes are important in Wilzbach labelling. This has been confirmed by a preliminary e.s.r. examination of naphthalene and anthracene in the presence of tritium gas.

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