Nitrogen methane reactions

Methane-Nitrogen Reactions. Products of Reaction. A quantitative analysis of the gas stream withdrawn through the quenching probe was made for each run. Over the entire range of stoichiometries studied, the methane fed to the plasma reacted completely no methane was detected in the quenched gas stream. The following major reaction products were identified HCN, C2H2, H2. Also present were Ar and unreacted N2. 

There has been a great deal of research on the combustion of small hydrocarbons, including nitrogen-cycle chemistry leading to nitric-oxide formation and abatement [138]. There are a number of methane-air reaction mechanisms that have been developed and validated [274,276,278], the most popular one being GRI-Mech [366]. There is also active research on the kinetics of large hydrocarbon combustion [81,88,171,246,328-330,426]. 

All the elementary steps in the hydrogenation of carbon to methane, nitrogen to ammonia, and oxygen to water on Pt(lll) were investigated, i.e., reaction pathways for the following reactions were determined ... 

Figure 12 Major reduction-oxidation reactions involving nitrogen. The reactions are numbered as follows (1) mineralization, (2) ammonium assimilation, (3) nitrification, (4) assimilatory or dissimilatory nitrate reduction, (5) ammonium oxidation, (6) nitrite oxidation, (7) assimilatory or dissimilatory nitrate reduction, (8) assimilatory or dissimilatory nitrite reduction, (9) denitrification, (10) chemodenitrification, (11) anaerobic ammonium oxidation, and (12) dinitrogen fixation (after Capone, 1991) (reproduced by permission of ASM Press from Microbial Production and Consumption of Greenhouse Gases Methane, Nitrogen Oxides, and Halomethanes, 1991).

Figure 3. Scheme of apparatus used in the research on methane-nitrogen and methane-ammonia reactions to produce hydrogen cyanide with acetylene as a... 

Fig. 12.19 Methane oxidation reaction data for microreactor ACT-G2-4 channel B with a feed gas flow rate of 10.1 ml min". The feed composition was 14.9% methane, 10.3% oxygen, 39.8% nitrogen, and balance helium. This microreactor was placed in Reactor Board 2. Error bars represent the 95% confidence interval of each value.

Lewisite is reduced to elementary arsenic by reaction with ammonia up at temperatures of 1000-1100 C. Besides elementary arsenic, the products are non-toxic compounds, such as methane, nitrogen, and ammonium chloride. 

Irradiation of ethyleneimine (341,342) with light of short wavelength ia the gas phase has been carried out direcdy and with sensitization (343—349). Photolysis products found were hydrogen, nitrogen, ethylene, ammonium, saturated hydrocarbons (methane, ethane, propane, / -butane), and the dimer of the ethyleneimino radical. The nature and the amount of the reaction products is highly dependent on the conditions used. For example, the photoproducts identified ia a fast flow photoreactor iacluded hydrocyanic acid and acetonitrile (345), ia addition to those found ia a steady state system. The reaction of hydrogen radicals with ethyleneimine results ia the formation of hydrocyanic acid ia addition to methane (350). Important processes ia the photolysis of ethyleneimine are nitrene extmsion and homolysis of the N—H bond, as suggested and simulated by ab initio SCF calculations (351). The occurrence of ethyleneimine as an iatermediate ia the photolytic formation of hydrocyanic acid from acetylene and ammonia ia the atmosphere of the planet Jupiter has been postulated (352), but is disputed (353). 

Only 20—40% of the HNO is converted ia the reactor to nitroparaffins. The remaining HNO produces mainly nitrogen oxides (and mainly NO) and acts primarily as an oxidising agent. Conversions of HNO to nitroparaffins are up to about 20% when methane is nitrated. Conversions are, however, often ia the 36—40% range for nitrations of propane and / -butane. These differences ia HNO conversions are explained by the types of C—H bonds ia the paraffins. Only primary C—H bonds exist ia methane and ethane. In propane and / -butane, both primary and secondary C—H bonds exist. Secondary C—H bonds are considerably weaker than primary C—H bonds. The kinetics of reaction 6 (a desired reaction for production of nitroparaffins) are hence considerably higher for both propane and / -butane as compared to methane and ethane. Experimental results also iadicate for propane nitration that more 2-nitropropane [79-46-9] is produced than 1-nitropropane [108-03-2]. Obviously the hydroxyl radical attacks the secondary bonds preferentially even though there are more primary bonds than secondary bonds. 

Hydrogenolysis is analogous to hydrolysis and ammonolysis, which involve the cleavage of a bond induced by the action of water and ammonia, respectively. Chemical bonds that are broken by hydrogenolysis reactions include carbon—carbon, carbon—oxygen, carbon—sulfur, and carbon—nitrogen bonds. An example of hydrogenolysis is the hydrodealkylation of toluene to form benzene and methane ... 

---