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Methane water reactions

Commercial-scale processes have been developed for the production of hydrogen sulfide from heavy fuel oils and sulfur as well as from methane, water vapor, and sulfur. The latter process can be carried out in two steps reaction of methane with sulfur to form carbon disulfide and hydrogen sulfide followed by hydrolysis of carbon disulfide (116). [Pg.135]

This reaction equation describes the combustion of methane, a reaction you might expect to release heat. The enthalpy change listed for the reaction confirms this expectation For each mole of methane that combusts, 802 kJ of heat is released. The reaction is highly exothermic. Based on the stoichiometry of the equation, you can also say that 802 kJ of heat is released for every 2 mol of water produced. (Flip to Chapter 9 for the scoop on stoichiometry.)... [Pg.214]

We examine, as an example, the exergy vector diagram for methanol synthesis to estimate the minimum exergy loss thermodynamically required for the synthesis reaction of methanol from methane [Ref. 16.]. First, we consider a direct (single step) synthesis of methanol from methane through a coupled-and-coupling reaction consisting of the oxidation of methane (objective reaction) and the dissociation of water molecule (coupled reaction) shown, respectively, as follows ... [Pg.134]

For the reaction rates of Equations 14 to 17 global expressions from the literature were adopted. For reactions 14, 16, and 17, the overall correlations of Dryer and Glassman (1) were used, expressing respectively the methane disappearance" rate, the rate of reaction of carbon monoxide with oxygen in the presence of water, and the appearance rate of carbon dioxide in the methane-oxygen reaction ... [Pg.132]

In particular, the excited oxygen atom quickly attacks methane, water vapor or molecular hydrogen present in stratosphere, see Figure 3.1, producing hydroxyl radicals according to reactions [4]... [Pg.24]

Reaction of CO with hydroxyl radicals (OH ) is the major method of removing CO from the atmosphere (IPCS, 1999). The cycle of hydroxyl radicals is coupled to cycles of CO, methane, water, and ozone they are produced by the photolysis of ozone followed by the reaction of the excited oxygen atoms with water vapor to produce two hydroxyl radicals (0( D) + H2O —> OH + OH ). A small proportion of atmospheric CO is removed by the sod. [Pg.277]

The crude trimethylolnitromethane from the condensation commonly contains a small amount. of mono- and dimethylolnitro methane from reactions involving one and two molecules of formaldehyde respectively. It is recrystalHzed from water to a melting point of 150, and is then nitrated. Stettbacher reports that the pure substance after many recrystallizations melts at 164-165 .,.The nitratiop is carried out either with the same mix acid as is used for the nitration of glycerin nitric acid,... [Pg.420]

Chloromethane can be produced by either chlorination of methane or reaction of methanol with hydrogen chloride. In an integrated production of silicones hydrogen chloride obtained by hydrolysis of methylchlorosilanes is recycled to the Direct Process via a chloromethane synthesis. The losses are compensated by make-up chloromethane or hydrogenchloride. Impurities, tike water, methanol, dimethyl ether or oxygen, must be kept at as low a level as possible. [Pg.481]

Reeburgh, W.S. and Heggie, D.T., 1977. Microbial methane consumption reactions and their effect on methane distributions in fresh water and marine environments. Limnol. Oceanogr., 22 1—9. [Pg.25]

WGS), reverse water-gas shift (RWGS), CO disproportionation (Boudouard reaction), and methane decomposition reactions as described in Equations 22-2.5 ... [Pg.18]

Fig. 12 Methane reforming reaction at the anode of a molten carbonate fuel cell. The reaction between fuel and water takes place in the outer part of the anode, the produced hydrogen reacts at the interface anode-electrolyte. Fig. 12 Methane reforming reaction at the anode of a molten carbonate fuel cell. The reaction between fuel and water takes place in the outer part of the anode, the produced hydrogen reacts at the interface anode-electrolyte.
The products of these endothermic reactions, which are not necessarily primary products, can be equilibrated by the water-gas shift reaction (4) and methane-steam reactions (5) and (6) ... [Pg.39]

Tar cracking reactions to produce simpler gases also occur, as long as the residenee time in the reactor is sufficient. Gaseous eomponents can rearrange via the water gas shift or methane formation reactions ... [Pg.542]

Initially acetic acid desorbed unaltered. However, as the tenperature increased, products of thermal decomposition and further reaction were observed. At 240°C there was a large 002 peak, some ethene, methane, water and acetone. Integration of the desorption peaks, followed by scaling by their respective sensitivity factors, gave the following mole percentages of products desorbed CO2 39, ethene 15.4, H2O 25.8, CH4 9.9 and acetone 9.9. A mass balance of the C, 0 and H atoms evolved gave a ratio of C 0 H of 109 114 212, approximately the ratio for acetic acid (2 2 4). This implies that the products desorbed were from the decomposition of acetic acid only. This supports the hypothesis that acetic acid was sorbed intact (i.e. equation 2 rather them equation 1). If water had been eliminated upon sorption on an acid site then the desorption products could not include acetic acid, as any water evolved would have rapidly desorbed from the zeolite at 150°C. [Pg.591]

From a consideration of the equilibrium of reaction (3) as a function of temperature (Fig. 14), it is noticed that this reaction occurs readily to the right at temperatures of 900° to 1000° C. The (COa - - CH4) reaction is catalyzed by substances similar to those used for the methane-steam reaction, i.e., 90 per cent nickel oxide-10 per cent thoria, etc. A combination of reaction (2) and reactions (3) and (4) may, hence, be considered as a means of producing hydrogen and carbon monoxide mixtures or by use of the water-gas catalytic reaction, (6), of producing hydrogen. A combination of these reactions thus becomes ... [Pg.268]

The methane-steam reaction requires an active catalyst even at temperatures of 1000° to 1100° C. as has been pointed out already. With a suitable catalyst and time of contact it is possible to obtain practically complete conversion of the methane to hydrogen and carbon monoxide at this temperature. Excess steam above that required for suppression of carbon deposition, about 60 mols total steam to 40 mols of methane, forces the water-gas reaction and carbon dioxide formation may result. [Pg.276]


See other pages where Methane water reactions is mentioned: [Pg.622]    [Pg.622]    [Pg.1178]    [Pg.273]    [Pg.442]    [Pg.195]    [Pg.206]    [Pg.176]    [Pg.355]    [Pg.284]    [Pg.125]    [Pg.144]    [Pg.219]    [Pg.182]    [Pg.97]    [Pg.849]    [Pg.2825]    [Pg.169]    [Pg.810]    [Pg.126]    [Pg.2013]    [Pg.385]    [Pg.170]    [Pg.237]    [Pg.399]    [Pg.132]    [Pg.261]    [Pg.275]    [Pg.84]    [Pg.498]    [Pg.23]    [Pg.133]   
See also in sourсe #XX -- [ Pg.392 ]




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