Production of liquid hydrocarbons

Abstract

The invention relates to a process for the conversion of hydrogen and one or more oxides of carbon to hydrocarbons, which process comprises: contacting hydrogen and one or more oxides of carbon with a catalyst in a reaction zone; removing from the reaction zone an outlet stream comprising unreacted hydrogen, unreacted one or more oxides of carbon and one or more hydrocarbons and feeding the outlet stream to a separation zone in which the outlet stream is divided into at least three fractions, in which; a first fraction predominantly comprises unreacted hydrogen, unreacted one or more oxides of carbon and hydrocarbons having from 1 to 4 carbon atoms; a second fraction predominantly comprises hydrocarbons having 5 to 9 carbon atoms, at least a portion of which hydrocarbons having from 5 to 9 carbon atoms are olefinic; and a third fraction predominantly comprises hydrocarbons having 10 or more carbon atoms; characterised in that at least a portion of the second fraction is recycled to the reaction zone.

1 . A process for the conversion of hydrogen and one or more oxides of carbon to hydrocarbons, which process comprises:
 contacting hydrogen and one or more oxides of carbon with a catalyst in a reaction zone; removing from the reaction zone an outlet stream comprising unreacted hydrogen, unreacted one or more oxides of carbon and one or more hydrocarbons and feeding the outlet stream to a separation zone in which the outlet stream is divided into at least three fractions, in which;   a first fraction predominantly comprises unreacted hydrogen, unreacted one or more oxides of carbon and hydrocarbons having from 1 to 4 carbon atoms;   a second fraction predominantly comprises hydrocarbons having 5 to 9 carbon atoms, at least a portion of which hydrocarbons having from 5 to 9 carbon atoms are olefinic; and   a third fraction predominantly comprises hydrocarbons having 10 or more carbon atoms; characterised in that at least a portion of the second fraction is recycled to the reaction zone.   
     
     
         2 . A process as claimed in  claim 1 , in which the reaction zone is maintained at a temperature in the range of from 150 to 400° C. and a pressure in the range of from 10 to 100 bara (1.0 to 10.0 MPa), preferably a temperature in the range of from 150 to 400° C. and a pressure in the range of from 10 to 85 bara (1.0 to 8.5 MPa), more preferably at a temperature in the range of from 170 to 400° C. and a pressure in the range of from 35 to 85 bara (3.5 to 8.5 MPa), and more preferably at a temperature in the range of from 250 to 400° C. and a pressure in the range of from 45 to 85 bara (4.5 to 8.5 MPa). 
     
     
         3 . A process as claimed in  claim 1 , in which the reaction zone comprises a solid, fixed bed Fischer-Tropsch catalyst. 
     
     
         4 . A process as claimed in  claim 1 , in which the catalyst comprises iron. 
     
     
         5 . A process as claimed in  claim 4 , in which the catalyst comprises one or more promoters selected from a manganese promoter, a potassium promoter, a lanthanide promoter such as a cerium promoter, and a copper promoter. 
     
     
         6 . A process as claimed in  claim 5 , in which the catalyst comprises a manganese promoter, a potassium promoter, a cerium promoter and a copper promoter. 
     
     
         7 . A process as claimed in  claim 1 , in which the separation zone comprises a flash separation zone and a fractionation zone, in which the outlet stream from the reaction zone is fed to the flash separation zone to produce a gaseous fraction which is the first fraction, and a liquid fraction predominantly comprising hydrocarbons having 5 or more carbon atoms, which liquid fraction is fed to the fractionation zone to produce the second fraction predominantly comprising hydrocarbons having 5 to 9 carbon atoms at least a portion of which are olefinic, and a third fraction comprising hydrocarbons having 10 or more carbon atoms. 
     
     
         8 . A process as claimed in  claim 1 , in which at least a portion, but not all, of the first fraction is recycled to the reaction zone. 
     
     
         9 . A process as claimed in  claim 1 , in which a portion of the first fraction is separated into C 3 -C 4  fraction which comprises an increased concentration of C 3 -C 4  hydrocarbons compared to the first fraction, and a lights fraction, which comprises an increased concentration of hydrogen, one or more oxides of carbon and C 1 -C 2  hydrocarbons compared to the first fraction. 
     
     
         10 . A process as claimed in  claim 9 , in which at least a portion of the C 3 -C 4  fraction is fed to a dehydrogenation zone which is maintained under conditions such that C 3 -C 4  alkanes can be converted to corresponding olefins, to produce a C 3   ═ -C 4   ═  fraction that has an increased concentration of C 3 -C 4  olefins compared to the C 3 -C 4  fraction, at least a portion of which C 3   ═ -C 4   ═  fraction is fed to the reaction zone. 
     
     
         11 . A process as claimed in  claim 9 , in which at least a portion of the lights fraction is fed to a reforming zone, in which at least a portion of the C 1 -C 2  hydrocarbons and CO 2  are converted to CO and H 2  to produce a reformed fraction, at least a portion of which reformed fraction is fed to the reaction zone. 
     
     
         12 . A process as claimed in  claim 1 , in which at least a portion of the unrecycled second fraction is used to make gasoline, or is used to produce hydrocarbons that are blended with gasoline. 
     
     
         13 . A process as claimed in  claim 12 , in which the portion of the unrecycled second fraction is isomerised and/or alkylated before being used as or blended with gasoline. 
     
     
         14 . A process as claimed in  claim 1 , in which at least a portion of the third fraction is used to make jet fuel and/or diesel fuel, or is used to produce hydrocarbons that can be blended with jet fuel and/or diesel fuel. 
     
     
         15 . A process as claimed in  claim 14 , in which the portion of the third fraction is hydrogenated before being used as or blended with jet fuel and/or diesel fuel. 
     
     
         16 . A process as claimed in  claim 15 , in which the portion of the third fraction is isomerised either prior to or during hydrogenation. 
     
     
         17 . A diesel fuel or aviation fuel as made by the process of  claim 14 . 
     
     
         18 . A gasoline fuel as made by the process of  claim 12 .