## Abstract The reaction of CH~2~O with NO~2~ has been studied with a shock tube equipped with two stabilized ew CO lasers. The production of CO, NO, and H~2~O has been monitored with the CO lasers in the temperature range of 1140β1650 K using three different Arβdiluted CH~2~OβNO~2~ mixtures. Kinet
A spectroscopic and gravimetric study of the soot-NO2N2O4 reaction at various temperatures
β Scribed by A.R Chughtai; W.F Welch; D.M Smith
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- English
- Weight
- 988 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0008-6223
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β¦ Synopsis
A study of the hexane soot-NOJN,O, reaction. with and without water vapor, over a range of concentrations and temperatures has been conducted. Two types of reaction are evident: activated chemisorption and redox. In the case of activated chemisorption. nitrogen-containing species are formed on the soot resulting in an increase in its mass. The other reaction in which 82-95% of the soot is converted into CO2 and CO is the major redox reaction, during which NO and NzO also are formed. This redox reaction commences at temperatures near 60Β°C. The major redox and activated chemisorption reactions are competitive in the sense that, if activated chemisorption is initiated, it precludes the major redox reaction. The presence of water vapor and dilution of NO,/N,O, by Nz or air inhibit the major redox reaction and the irreversible activated chemisorption reaction dominates. In addition, a third reaction termed the minor redox reaction occurs under all conditions with the evolution of CO and CO:. The quantities of effluent gases from this reaction are significantly lower than those evolved during the major redox reaction. The rate equations for the formation of CO: from the major redox reaction. and CO? and CO from the minor redox reaction, have been determined. A mechanism for the major redox reaction is presented. A determining role of NO, monomer in redox reactions of soot and NO>/ N,O, is indicated.
π SIMILAR VOLUMES
The kinetics of the reaction of 0 atoms with NO2 was investigated in the temperature range 199-357 K. The value of the rate constant can be expressed by k, = (5.21 kO.50) x lo-'\* exp [(202\*27)lT] cm3 s-' (3~ error). At temperatures below 230 K, the formation of equilibrium concentrations of N204 a
The gas-phase reaction of the NOa radical with NO, was investigated, using a flash photolysis-visible absorption technique, over the total pressure range 25-400 Torr of nitrogen or oxygen diluent a t 298 2 2 K. The absolute rate constants determined (in units of em3 molecule-' s-') a t 25, 100, and
The equilibrium constant, K,, of the reaction NO2 + NO3 + M N z O ~ + M has been determined for a small range of temperatures around room temperature in air at 740 torr by direct spectroscopical measurements of NOz, NOS, and NzOs. At 298 K, K, was determined as (3.73 2 0.61) x lo-'' cm3 molecule-'.
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