dc.contributor.author |
Megalofonos, SK |
en |
dc.contributor.author |
Papayannakos, NG |
en |
dc.date.accessioned |
2014-03-01T01:08:23Z |
|
dc.date.available |
2014-03-01T01:08:23Z |
|
dc.date.issued |
1991 |
en |
dc.identifier.issn |
03603199 |
en |
dc.identifier.uri |
https://dspace.lib.ntua.gr/xmlui/handle/123456789/10455 |
|
dc.subject |
Hydrogen Production |
en |
dc.subject |
Hydrogen Sulphide |
en |
dc.subject |
Natural Gas |
en |
dc.subject.other |
Catalysts--Deactivation |
en |
dc.subject.other |
Chemical Reactions--Thermodynamics |
en |
dc.subject.other |
Chemical Reactors--Efficiency |
en |
dc.subject.other |
Hydrogen Sulfide--Methanation |
en |
dc.subject.other |
Thermodynamics--Phase Equilibria |
en |
dc.subject.other |
Catalytic Tubular Reactors |
en |
dc.subject.other |
Equilibrium Gas Mixture Composition |
en |
dc.subject.other |
Hydrogen Sulfide/Methane Reaction |
en |
dc.subject.other |
Natural Gas Based Hydrogen Production |
en |
dc.subject.other |
Thermal Noncatalytic Reactors |
en |
dc.subject.other |
Hydrogen |
en |
dc.title |
Hydrogen production from natural gas and hydrogen sulphide |
en |
heal.type |
journalArticle |
en |
heal.identifier.primary |
10.1016/0360-3199(91)90168-I |
en |
heal.identifier.secondary |
http://dx.doi.org/10.1016/0360-3199(91)90168-I |
en |
heal.publicationDate |
1991 |
en |
heal.abstract |
A promising method for hydrogen production from the reaction of hydrogen sulphide and methane is studied. The equilibrium composition of the gaseous mixture CH4/H2S/H2/CS2/S2/C2H6/C2H4 is calculated over a temperature range of 973 to 1098 K under 0.1 MPa pressure. It is shown that at equilibrium state the gas mixture practically contains CH4, H2S, H2 and CS2 when the initial gas mixture contains 10-90% mole/mole hydrogen sulphide. Experiments were carried out in a thermal non-catalytic and in a MoS2 catalytic tubular reactor. A comparison of the experimental data is presented. It is shown that the catalytic reaction rates are much greater than the thermal ones. The catalyst is irreversibly deactivated but after 240 × 103 s in operation it reaches a level of constant, about 50%, remaining activity. An economic evaluation of the process is also presented. © 1991. |
en |
heal.journalName |
International Journal of Hydrogen Energy |
en |
dc.identifier.doi |
10.1016/0360-3199(91)90168-I |
en |
dc.identifier.volume |
16 |
en |
dc.identifier.issue |
5 |
en |
dc.identifier.spage |
319 |
en |
dc.identifier.epage |
327 |
en |