Gas phase dosimetry based on nitrogen yield from nitrous oxide

1974 ◽  
Vol 25 (2) ◽  
pp. 87-93 ◽  
Author(s):  
K.G. McLaren
Keyword(s):  
Nitrous Oxide ◽  
Gas Phase ◽  
Nitrogen Yield

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

Gas-Phase Oxidation and Nitration of First-, Second-, and Third-Row Atomic Cations in Reactions with Nitrous Oxide:  Periodicities in Reactivity

2004 ◽  
Vol 108 (26) ◽  
pp. 5610-5624 ◽  
Author(s):  
Vitali V. Lavrov ◽  
Voislav Blagojevic ◽  
Gregory K. Koyanagi ◽  
Galina Orlova ◽  
Diethard K. Bohme
Keyword(s):  
Nitrous Oxide ◽  
Gas Phase ◽  
Phase Oxidation ◽  
Gas Phase Oxidation

scholarly journals Structural isomers and low-lying electronic states of gas-phase M+(N2O)n (M = Co, Rh, Ir) ion–molecule complexes

2019 ◽  
Vol 21 (26) ◽  
pp. 13959-13967 ◽  
Author(s):  
Ethan M. Cunningham ◽  
Alexander S. Gentleman ◽  
Peter W. Beardsmore ◽  
Stuart R. Mackenzie
Keyword(s):  
Density Functional Theory ◽  
Nitrous Oxide ◽  
Gas Phase ◽  
Density Functional ◽  
Electronic States ◽  
Structural Isomers ◽  
Functional Theory ◽  
Phase Group ◽  
Ion Molecule Complexes ◽  
Metal Ligand

The structures of gas-phase group nine cation–nitrous oxide metal–ligand complexes, M+(N2O)n (M = Co, Rh, Ir; n = 2–7) have been determined by a combination of infrared photodissociation spectroscopy and density functional theory.

Gas-phase radiolysis of nitrous oxide. Effect of the addition of several hydrocarbons

1971 ◽  
Vol 75 (20) ◽  
pp. 3178-3182 ◽  
Author(s):  
Satoshi Takao ◽  
Yoshihiko Hatano ◽  
Shoji Shida
Keyword(s):  
Nitrous Oxide ◽  
Gas Phase

Borierungsreaktionen an den N-Oxiden und -Iminen ungesättigter Stickstoffbasen / Boration Reactions with the N-Oxides and m-Imines of Unsaturated Nitrogen Bases

1980 ◽  
Vol 35 (5) ◽  
pp. 568-577 ◽  
Author(s):  
Peter Paetzold ◽  
Günther Schimmel
Keyword(s):  
Nitrous Oxide ◽  
Liquid Phase ◽  
Gas Phase ◽  
The Other ◽  
Double Bonds ◽  
Similar Reduction ◽  
Nitrogen Bases ◽  
Other Hand

1,3-Dipolar reagents with an unsaturated CNO- or CNN-skeleton undergo 1,3-organoboration by triorganoboranes. On the other hand, the unsaturated NNO-skeletons in azoxybenzene or nitrous-oxide are reduced to the corresponding NN-fragment by trialkylboranes. The 1,3-addition of aminoborane Cl2BNMe2 to the aldimineoxide PhHC = NMe-0 represents one of the rare examples of analogous reactivity of BN- and CC-double bonds. O-Borylhydroxylamines PhHCR-NMe-OBR2 are reduced by BR′3 to PhHCR-NMe-BR′2 and R′0-BR2. Similar reduction products are isolated from liquid-phase thermolysis of PhHCEt-NMe-OBEt2 (16), whereas gas-phase thermolysis of 16 gives PhCH = NMe, (EtBO)3, and C4H10.

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