Spectroscopic measurement of the rate of the gas-phase combination of methyl radicals with nitric oxide and oxygen at 295 K

1971 ◽  
Vol 67 ◽  
pp. 2017 ◽  
Author(s):  
H. E. van den Bergh ◽  
A. B. Callear
Keyword(s):  
Nitric Oxide ◽  
Gas Phase ◽  
Spectroscopic Measurement ◽  
Methyl Radicals ◽  
Phase Combination

The photochemical decomposition of methyl iodide in presence of nitric oxide - II. Reactions of nitrosomethane

1959 ◽  
Vol 249 (1257) ◽  
pp. 258-269 ◽  
Keyword(s):  
Nitric Oxide ◽  
Gas Phase ◽  
Methyl Iodide ◽  
Initial Rate ◽  
Wavelength Region ◽  
Order Reaction ◽  
Methyl Radicals ◽  
Second Order Reaction ◽  
Photochemical Decomposition ◽  
Rate Method

A product of the photolysis, in presence of a small quantity of nitric oxide, of methyl iodide reacts with excess nitric oxide to form a substance(s), Y , which absorbs light throughout the wavelength region 2300 to 5300 Å. The initial products of the photolysis, in presence of small quantities of nitric oxide, of both acetone and acetaldehyde react similarly. The species undergoing the reaction is believed to be monomeric nitrosomethane, formed by the association of methyl radicals with nitric oxide. The order of the reaction to form Y , as determined by the initial rate method, is one with respect to nitrosomethane and two with respect to nitric oxide. The extent of the reaction, which can be used as a measure of nitrosomethane concentration, depends on the concentration of nitric oxide. In absence of excess nitric oxide the monomer disappears slowly from the gas phase in a second-order reaction, which is thought to be the dimerization to nitrosomethane dimer.

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

Detection of gas-phase methyl radicals using multiphoton ionization

1981 ◽  
Vol 82 (2) ◽  
pp. 267-269 ◽  
Author(s):  
T.G. Digiuseppe ◽  
Jeffrey W. Hudgens ◽  
M.C. Lin
Keyword(s):  
Gas Phase ◽  
Multiphoton Ionization ◽  
Methyl Radicals

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.

The Reaction of Methyl Radicals with Nitric Oxide

1964 ◽  
Vol 86 (10) ◽  
pp. 1929-1934 ◽  
Author(s):  
A. Maschke ◽  
B. S. Shapiro ◽  
F. W. Lampe
Keyword(s):  
Nitric Oxide ◽  
Methyl Radicals

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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