Cyclic process for producing methane with catalyst regeneration

Claim 2

In a cyclic process for the production of methane from carbon monoxide-containing gas streams in which a carbon monoxide-containing gas stream is passed over a catalyst present in a metal state and capable of catalyzing the disproportionation of carbon monoxide at a pressure of from about 1 to about 100 atmos and a temperature of from about 100° C. to about 350° C., with said carbon monoxide thereby being decomposed to form carbon dioxide and an active surface carbon that is deposited on said catalyst, and with said gas stream being passed over the catalyst for a time sufficient to deposit a surface layer of said active surface carbon on the catalyst essentially without the subsequent formation of inactive coke thereon, and in which said layer of active surface carbon deposited on said catalyst present in a metal state is contacted with steam or a steam-containing gas stream at a pressure of from about 1 to about 100 atmos and a temperature of from about 100° C. to about 400° C., thereby converting said active surface carbon to methane and carbon dioxide, with said methane being at least about 50% of the stoichiometric amount, with the carbon thus recovered in the form of methane being at least about 12.5% of the carbon in said carbon monoxide decomposed upon contact with said disproportionation catalyst and in which additional carbon monoxide-containing gas is passed over said catalyst and said steps are repeated on a two step cyclic basis, a process for the periodic regeneration of the catalyst employed in said cyclic process comprising: (a) withdrawing said catalyst from use in said cyclic methanation process, on a periodic basis, upon reduction of the efficiency of the catalyst as a result of the deposition of inactive carbon thereon over the course of repeated use in said cyclic process; (b) contacting said catalyst having inactive carbon deposited thereon with a CO 2 -rich gas at a temperature in excess of about 500° F. but less than the degradation temperature of said catalyst, thereby converting said inactive carbon to CO, said regeneration reaction being endothermic and resulting in a decrease in the temperature of the gaseous regeneration effluent and the catalyst; and (c) withdrawing said gaseous regeneration effluent from contact with said catalyst, whereby the inactive carbon deposited on said catalyst is effectively removed therefrom, the endothermic regeneration reaction eliminating the temperature control problems inherent in conventional burn off operations, the oxidation of the catalyst from its metal state being minimized and the long term stability of the catalyst being enhanced as the bulk thereof is not switched between the oxide form and the active metal form as the result of each said periodic regeneration of the catalyst.

Claim 3

The process of claim 1 in which said catalyst is taken from the group consisting of nickel, cobalt, ruthenium, rhenium and alloys thereof.

Claim 4

The process of claim 1 in which said regeneration temperature is initially about 1000° F.

Claim 5

The process of claim 3 in which said catalyst comprises nickel.

Claim 6

The process of claim 2 in which said catalyst comprises nickel.

Claim 7

The process of claim 1 in which said CO 2 -rich stream comprises by-product CO 2 separated from product methane produced in said cyclic methanation process.

Claim 8

The process of claim 6 in which said by-product CO 2 is employed with CO-hd 2-containing effluent from said disproportionation step of said cyclic methanation process.

Claim 9

The process of claim 6 in which said catalyst comprises nickel and said regeneration temperature is initially about 1,000° F.

Claim 10

The process of claim 1 in which said catalyst is mixed with a catalyst support additive in the amount of from about 0.1 to about 50% by weight based on the weight of said catalyst composition mixture of catalyst and additive, said catalyst having a surface area of at least about 10 m 2 /gr.

Claim 11

The process of claim 9 in which said additive comprises zirconia and said catalyst comprises nickel.

Claim 12

The process of claim 10 in which said regeneration temperature is initially about 1000° F.

Claim 13

A cyclic process for the production of methane from carbon monoxide-containing gas streams with effective and advantageous periodic regeneration of the methanation catalyst comprising: (a) passing a carbon-monoxide-containing gas stream over a catalyst present in a metal state and capable of catalyzing the disproportionation of carbon monoxide at a pressure of from about 1 to about 100 atmos. and a temperature of from about 100° C. to about 350° C., said carbon monoxide thereby being decomposed to form carbon dioxide and an active surface carbon that is deposited on said catalyst, which is taken from the group consisting of nickel, cobalt, ruthenium, rhenium, and alloys thereof, said gas stream being passed over the catalyst for a time sufficient to deposit a surface layer of said active surface carbon on the catalyst essentially without the subsequent formation of inactive coke thereon; (b) contacting said layer of active surface carbon deposited on said catalyst present in a metal state with steam or a steam-containing gas stream at a pressure of from about 1 to about 100 atmos. and a temperature of from about 100° C. to about 400° C., thereby converting said active surface carbon to product methane and by-product carbon dioxide, said methane being at least about 50% of the stoichiometric amount, the carbon thus recovered in the form of methane being at least about 12.5% of the carbon in said carbon monoxide decomposed upon contact with said disproportionation catalyst; (c) separating product methane from by-product carbon dioxide; (d) passing additional carbon monoxide-containing gas over said catalyst from step (b), and repeating said steps (a) and (b) on a two step cyclic basis; (e) contacting CO 2 -rich gas from said cyclic methanation process with additional amounts of said catalyst withdrawn from use in said cyclic process at a temperature in excess of about 500° F. but less than the degradation temperature of said catalyst, said catalyst having been withdrawn from use, on a periodic basis, upon reduction of the efficiency of the catalyst as a result of the deposition of inactive carbon thereon over the course of repeated use in said cyclic process, said inactive carbon being converted to CO, said regeneration reaction being endothermic and resulting in a decrease in the temperature of the gaseous regeneration effluent and the catalyst; and (f) withdrawing said gaseous regeneration effluent from contact with said catalyst, whereby the inactive carbon deposited on said catalyst being regenerated is effectively removed therefrom, the endothermic regeneration reaction eliminating the temperature control problems inherent in conventional burn-off operations, the long term stability of said catalyst is enhanced and the oxidation of said regenerated catalyst is minimized by the use of the carbon dioxide produced in said advantageous cyclic methanation operation for regeneration of said catalyst withdrawn from use.

Claim 14

A cyclic process for the production of methane from carbon monoxide-containing gas streams with effective and advantageous periodic regeneration of the methanation catalyst comprising: (a) passing a carbon-monoxide-containing gas stream over a catalyst present in a metal state and capable of catalyzing the disproportionation of carbon monoxide at a pressure of from about 1 to about 100 atmos. and a temperature of from about 100° C. to about 350° C., said carbon monoxide thereby being decomposed to form carbon dioxide and an active surface carbon that is deposited on said catalyst, which is taken from the group consisting of nickel, cobalt, ruthenium, rhenium, and alloys thereof, said gas stream being passed over the catalyst for a time sufficient to deposit a surface layer of said active surface carbon on the catalyst essentially without the subsequent formation of inactive coke thereon; (b) contacting said layer of active surface carbon deposited on said catalyst present in a metal state with steam or a steam-containing gas stream at a pressure of from about 1 to about 100 atmos. and a temperature of from about 100° C. to about 400° C., thereby converting said active surface carbon to product methane and by-product carbon dioxide, said methane being at least about 50% of the stoichiometric amount, the carbon thus recovered in the form of methane being at least about 12.5% of the carbon in said carbon monoxide decomposed upon contact with said disproportionation catalyst; (c) separating product methane from by-product carbon dioxide; (d) passing additional carbon monoxide-containing gas over said catalyst from step (b), and repeating said steps (a) and (b) on a two step cyclic basis; (e) contacting CO 2 -rich gas from said cyclic methanation process with additional amounts of said catalyst withdrawn from use in said cyclic process at a temperature in excess of about 500° F. but less than the degradation temperature of said catalyst, said catalyst having been withdrawn from use, on a periodic basis, upon reduction of the efficiency of the catalyst as a result of the deposition of inactive carbon thereon over the course of repeated use in said cyclic process, said inactive carbon being converted to CO, said regeneration reaction being endothermic and resulting in a decrease in the temperature of the gaseous regeneration effluent and the catalyst; and (f) withdrawing said gaseous regeneration effluent from contact with said catalyst, whereby the inactive carbon deposited on said catalyst being regenerated is effectively removed therefrom, the endothermic regeneration reaction eliminating the temperature control problems inherent in conventional burn-off operations, the long term stability of said catalyst is enhanced and the oxidation of said regenerated catalyst is minimized by the use of the carbon dioxide produced in said advantageous cyclic methanation operation for regeneration of said catalyst withdrawn from use.

Claim 15

The process of claim 12 in which said regeneration temperature is initially about 1000° F.

Claim 16

The process of claim 13 in which said catalyst comprises nickel.

Claim 17

The process of claim 12 in which said CO 2 -rich gas contacting said catalyst to be regenerated comprises by-product carbon dioxide formed during the conversion of said active surface carbon to product methane.

Claim 18

The process of claim 15 and including the contacting of said catalyst to be regenerated with additional carbon dioxide formed during the disproportionation of CO to form said active surface carbon on the disproportionation catalyst.

Claim 19

The process of claim 15 in which said catalyst being regenerated comprises nickel and said regeneration temperature is initially on the order of about 1,000° F.

Claim 20

The process of claim 12 in which said disproportionation of CO, said active surface carbon conversion to methane and said catalyst regeneration are each carried out in separate reaction zones, said zones being switched during the course of said methanation operation so that said cyclic methanation process is carried out continuously in two such zones while the catalyst in a third zone is being regenerated, on a periodic basis, to assure its effectiveness in subsequent use in the cyclic methanation process.

Claim 21

The process of claim 18 in which said regeneration temperature is initially about 1,000° F.

Claim 22

The process of claim 18 in which said catalyst comprises nickel.

Claim 23

The process of claim 18 in which said CO 2 -rich gas contacting said catalyst to be regenerated comprises by-product carbon dioxide formed during the conversion of said active surface carbon to product methane.

Claim 24

The process of claim 21 in which the CO-containing gaseous regeneration effluent is recycled to said disproportionation zone for conversion to active surface carbon therein.

Claim 25

The process of claim 21 and including the contacting of said catalyst to be regenerated with additional carbon dioxide formed during the disproportionation of CO to form active surface carbon on the disproportionation catalyst.

Claim 26

The process of claim 23 in which said regeneration temperature is initially about 1000° F. and said catalyst comprises nickel.