EP0583836B2 - Process for the preparation of hydrocarbon fuels - Google Patents

Process for the preparation of hydrocarbon fuels Download PDF

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Publication number
EP0583836B2
EP0583836B2 EP93202395A EP93202395A EP0583836B2 EP 0583836 B2 EP0583836 B2 EP 0583836B2 EP 93202395 A EP93202395 A EP 93202395A EP 93202395 A EP93202395 A EP 93202395A EP 0583836 B2 EP0583836 B2 EP 0583836B2
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EP
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Prior art keywords
process according
catalyst
hydrocarbon
hydrogen
hydroconversion
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German (de)
English (en)
French (fr)
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EP0583836A1 (en
EP0583836B1 (en
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Jacobus Eilers
Sytze Abel Posthuma
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Shell Internationale Research Maatschappij BV
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Shell Internationale Research Maatschappij BV
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    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G2/00—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon
    • C10G2/30—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G65/00—Treatment of hydrocarbon oils by two or more hydrotreatment processes only
    • C10G65/02—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only
    • C10G65/12—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only including cracking steps and other hydrotreatment steps

Definitions

  • the present invention relates to a process for the preparation of gasoil, in particular to a process for the preparation of gasoil from a mixture of carbon monoxide and hydrogen.
  • the preparation of hydrocarbons from a mixture comprising carbon monoxide and hydrogen by contacting the mixture with a suitable synthesis catalyst at elevated temperatures and pressures is known in the art as the Fischer-Tropsch synthesis. It is known in the art to apply Fischer-Tropsch synthesis processes in the preparation of a range of principly aliphatic hydrocarbons having a wide range of molecular weights. Of particular interest, however, is the use of the Fischer-Tropsch synthesis to prepare hydrocarbons suitable for use as fuels, for example hydrocarbons having boiling points within the boiling point ranges of naphtha and the middle distillates.
  • mishtha is a reference to hydrocarbons or hydrocarbon mixtures having a boiling point or boiling point range substantially corresponding to that of the naphtha (sometimes referred to as the gasoline) fractions obtained during the conventional atmospheric distillation of crude oil.
  • the following fractions are consecutively recovered from the crude oil: one or more naphtha fractions boiling in the range of from 30 to 220 °C, one or more kerosine fractions boiling in the range of from 120 to 300 °C and one or more gasoil fractions boiling in the range of from 170 to 370°C.
  • hydrocarbon fuel is to be taken as a reference to either one of or a mixture of naphtha and middle distillates.
  • US-A-4,478,955 discloses a process scheme comprising contacting the effluent of a Fischer-Tropsch synthesis process with hydrogen in the presence of a suitable hydrogenation catalyst.
  • the effluent of the Fischer-Tropsch synthesis is described in US-A-4,478,955 as comprising predominantly olefins and carboxylic acids.
  • useful fuel components comprising alkanes, alcohols and esters are produced.
  • the present invention provides a process for the preparation of gasoil comprising the steps of:
  • the products of the hydrocarbon synthesis stage are subjected to a hydroconversion treatment.
  • the primary objective of the hydro-conversion is to convert, by hydrocracking, the high molecular weight, paraffinic products of the synthesis stage into the desired hydrocarbon fuels, for example middle distillates.
  • the hydroconversion treatment serves to isomerise a portion of the linear paraffinic hydrocarbons, which in turn improves the properties of the hydrocarbon fuels.
  • the action of the hydroconversion treatment is to hydrogenate the minor quantities of olefinic and oxygen-containing compounds formed during the hydrocarbon synthesis reactions and which are undesirable components in hydrocarbon fuels.
  • the hydrocarbons prepared in the first stage, stage (a), of the process of the present invention are subjected to a hydroconversion in two separate and distinct stages.
  • the olefinic and oxygen-containing compounds are hydrogenated, followed by removal of the C 4 - fraction from the higher molecular weight fraction.
  • the operating conditions of the first hydroconversion stage are selected so as to substantially prevent hydrocracking and/or hydroisomerisation reactions from occurring.
  • stage (c) the desired hydrocarbon fuels are prepared by subjecting at least a part of the higher molecular weight product of the first hydroconversion stage to a second hydroconversion treatment, in which the high molecular weight paraffinic hydrocarbons are hydroisomerised and hydrocracked using a catalyst not containing any crystalline zeolite.
  • water is formed as a product of the hydrogenation of the oxygen-containing hydrocarbons. It has been found that water produced during this reaction adversely affects certain hydroconversion catalysts, leading to a reduction in catalyst performance.
  • milder operating conditions are required in the second hydroconversion stage to achieve the desired degree of hydrocracking and hydroisomerisation than required in the single hydroconversion stage of the prior art process. This results in an improved lifetime of the hydroconversion catalyst and, most surprisingly, leads to a markedly improved product.
  • the process of the present invention most surprisingly exhibits an improved selectivity to gasoil, compared with the processes of the prior art.
  • substantially paraffinic when used in connection with hydrocarbon products refers to a hydrocarbon mixture comprising at least 70 %wt paraffins, preferably at least 80 %wt paraffins.
  • Gasoil produced by the process of this invention comprises at least 95 %wt paraffins.
  • a feed comprising a mixture of carbon monoxide and hydrogen is contacted at elevated temperature and pressure with a catalyst active in the synthesis of paraffinic hydrocarbons.
  • Suitable processes for the preparation of the mixture of carbon monoxide and hydrogen are well known in the art and include such processes as the partial oxidation of methane, typically in the form of natural gas, and the steam reforming of methane.
  • the relative amounts of carbon monoxide and hydrogen present in the feed may vary over a wide range and may be selected according to the precise catalyst and process operating conditions being employed.
  • the feed contacting the catalyst comprises carbon monoxide and hydrogen in a hydrogen/carbon monoxide molar ratio of below 2.5, preferably below 1.75. More preferably, the hydrogen/carbon monoxide ratio is in the range of from 0.4 to 1.5, especially from 0.9 to 1.3.
  • Unconverted carbon monoxide and hydrogen may be separated from the synthesis product and recycled to the inlet of the synthesis reactor.
  • the catalyst comprises, as the catalytically active component, a metal from Group VIII of the Periodic Table of Elements.
  • a metal from Group VIII include ruthenium, iron, cobalt and nickel.
  • a catalyst comprising cobalt as the catalytically active metal is preferred.
  • the catalytically active metal is preferably supported on a porous carrier.
  • the porous carrier may be selected from any suitable refractory metal oxide or silicate or mixture thereof. Particular examples of preferred carriers include silica, alumina, titania, zirconia and mixtures thereof. Carriers comprising silica and/or alumina are especially preferred.
  • the catalytically active metal may be applied to the carrier by any of the techniques known in the art, for example comulling, impregnation or precipitation. Impregnation is a particularly preferred technique, in which the carrier is contacted with a compound of the catalytically active metal in the presence of a liquid, most conveniently in the form of a solution of the metal compound.
  • the compound of the active metal may be inorganic or organic, with inorganic compounds being preferred, in particular nitrates.
  • the liquid employed may also be either organic or inorganic. Water is a most convenient liquid.
  • the amount of catalytically active metal present on the carrier is typically in the range of from 1 to 100 parts by weight, preferably 10 to 50 parts by weight, per 100 parts by weight of carrier material.
  • the catalytically active metal may be present in the catalyst together with one or more metal promoters or cocatalysts.
  • the promoters may be present as metals or as the metal oxide, depending upon the particular promoter concerned. Suitable metal oxide promoters include oxides of metals from Groups IIA, IIIB, IVB, VB or VIB of the Periodic Table, oxides of the lanthanides and/or the actinides.
  • the catalyst comprises an oxide of an element in Group IVB of the Periodic Table, in particular titanium or zirconium. Catalysts comprising zirconium are especially preferred.
  • the catalyst may comprise a metal promoter selected from Groups VIIB and/or VIII of the Periodic Table.
  • Preferred metal promoters include platinum and palladium.
  • a most suitable catalyst comprises cobalt as the catalytically active metal and zirconium as a promoter.
  • the promoter may be incorporated in the catalyst using any of the methods discussed hereinbefore with respect to the catalytically active component.
  • the promoter if present in the catalyst, is typically present in an amount of from 1 to 60 parts by weight, preferably from 2 to 40 parts by weight, per 100 parts by weight of carrier material.
  • the hydrocarbon synthesis is conducted under conditions of elevated temperature and pressure. Typically, the synthesis is effected at a temperature in the range of from 125 to 300 °C, preferably from 175 to 250 °C.
  • the reaction pressure is typically in the range of from 5 to 100 bar, preferably from 12 to 50 bar.
  • the synthesis may be conducted using a variety of reactor types and reaction regimes, for example in a fixed bed regime, a slurry phase regime or an ebullating bed regime.
  • the hydrocarbon product of the synthesis stage is subjected to a two-stage hydroconversion treatment in stages (b) and (c) of the process of the present invention.
  • the entire effluent of the synthesis stage may be led directly to the first hydroconversion stage.
  • the low molecular weight products of the synthesis stage in particular the C 4 - fraction, for example methane, ethane and propane, may also be removed prior to the hydroconversion treatment.
  • the separation is conveniently effected using distillation techniques well known in the art.
  • the hydrocarbon product is contacted with hydrogen in the presence of a hydrogenation catalyst.
  • a hydrogenation catalyst Suitable catalysts for use in this stage are known in the art.
  • the catalyst comprises as catalytically active component one or more metals selected from Groups VIB and VIII of the Periodic Table of Elements, in particular one or more metals selected from molybdenum, tungsten, cobalt, nickel, ruthenium, iridium, osmium, platinum and palladium.
  • the catalyst comprises on or more metals selected from nickel, platinum and palladium as the catalytically active component.
  • a particularly suitable catalyst comprises nickel as a catalytically active component.
  • Catalysts for use in the first hydroconversion stage typically comprise a refractory metal oxide or silicate as a carrier.
  • Suitable carrier materials include silica, alumina, silica-alumina, zirconia, titania and mixtures thereof.
  • Preferred carrier materials for inclusion in the catalyst for use in the process of this invention are silica, alumina and silica-alumina.
  • the catalyst may comprise the catalytically active component in an amount of from 0.05 to 80 parts by weight, preferably from 0.1 to 70 parts by weight, per 100 parts by weight of carrier material.
  • the amount of catalytically active metal present in the catalyst will vary according to the specific metal concerned.
  • One particularly suitable catalyst for use in the first hydroconversion stage comprises nickel in an amount in the range of from 30 to 70 parts by weight per 100 parts by weight of carrier material.
  • a second particularly suitable catalyst comprises platinum in an amount in the range of from 0.05 to 2.0 parts by weight per 100 parts by weight of carrier material.
  • Suitable catalysts for use in the first hydroconversion stage of the process of this invention are available commercially, or may be prepared by methods well known in the art, for example the methods discussed hereinbefore with reference to the preparation of the hydrocarbon synthesis catalyst.
  • the hydrocarbon product is contacted with hydrogen at elevated temperature and pressure.
  • the operating temperature may typically range from 100 to 300 °C, more preferably from 150 to 275 °C, in particular from 175 to 250 °C.
  • the operating pressure ranges from 5 to 150 bars, preferably from 10 to 50 bars.
  • Hydrogen may be supplied to the hydroconversion stage at a gas hourly space velocity in the range of from 100 to 10000 Nl/l/hr, more preferably from 250 to 5000 Nl/l/hr.
  • the hydrocarbon product being treated is typically supplied to the hydroconversion stage at a weight hourly space velocity in the range of from 0.1 to 5 kg/l/hr, more preferably from 0.25 to 2.5 kg/l/hr.
  • the ratio of hydrogen to hydrocarbon product may range from 100 to 5000 Nl/kg and is preferably from 250 to 3000 Nl/kg.
  • the first hydroconversion stage is operated under conditions such that substantially no isomerisation or hydrocracking of the feed occurs.
  • the precise operating conditions required to achieve the desired degree of hydrogenation without substantial hydrocracking or hydroisomerisation occurring will vary according to the composition of the hydrocarbon product being fed to the hydroconversion stage and the particular catalyst being employed.
  • the degree of conversion of the feed hydrocarbon may be determined. In this respect, conversion, in percent, is defined as the percent weight of the fraction of the feed boiling above 370 °C which is converted during the hydroconversion to a fraction boiling below 370 °C.
  • the conversion of the first hydroconversion stage is below 20%, preferably below 10%, more preferably below 5%.
  • the hydrocarbon product leaving the first hydroconversion stage substantially consists of high molecular weight, paraffinic hydrocarbons having a boiling point range above that of the middle distillates. At least a part of this hydrocarbon product is subjected to a second hydroconversion in stage (c) of the process of this invention, to yield the desired hydrocarbon fuel product.
  • the C 4 -fraction is separated from the higher molecular weight hydrocarbons prior to the second hydroconversion stage. The separation may be conveniently achieved using distillation techniques well known in the art. At least a part of the remaining C 5 + fraction of the hydrocarbon product is then used as feed for the second hydroconversion stage.
  • the catalyst comprises as catalytically active component one or more metals selected from Groups VIB and VIII of the Periodic Table of Elements, in particular one or more metals selected from molybdenum, tungsten, cobalt, nickel, ruthenium, iridium, osmium, platinum and palladium.
  • the catalyst comprises one or more metals selected from nickel, platinum and palladium as the catalytically active component. Catalysts comprising platinum as the catalytically active component have been found to be particularly suitable for use in the second hydroconversion stage.
  • Catalysts for use in the second hydroconversion stage typically comprise a refractory metal oxide or silicate as a carrier.
  • the carrier material may be amorphous or crystalline.
  • Suitable carrier materials include silica, alumina, silica-alumina, zirconia, titania and mixtures thereof.
  • Preferred carrier materials for inclusion in the catalyst for use in the process of this invention are silica, alumina and silica-alumina.
  • a particularly preferred catalyst comprises platinum supported on a silica-alumina carrier.
  • the catalyst may comprise the catalytically active component in an amount of from 0.05 to 80 parts by weight, preferably from 0.1 to 70 parts by weight, per 100 parts by weight of carrier material.
  • the amount of catalytically active metal present in the catalyst will vary according to the specific metal concemed.
  • a particularly preferred catalyst for use in the second hydroconversion stage comprises platinum in an amount in the range of from 0.05 to 2 parts by weight, more preferably from 0.1 to 1 parts by weight, per 100 parts by weight of carrier material.
  • Suitable catalysts for use in the second hydroconversion stage of the process of this invention are available commercially, or may be prepared by methods well known in the art, for example the methods discussed hereinbefore with reference to the preparation of the hydrocarbon synthesis catalyst.
  • the hydrocarbon product of the first hydroconversion stage is contacted with hydrogen in the presence of the catalyst at elevated temperature and pressure.
  • the temperatures necessary to yield the hydrocarbon fuels will lie in the range of from 175 to 400 °C, preferably from 250 to 375 °C.
  • the pressure typically applied ranges from 10 to 250 bars, more preferably from 25 to 250 bars.
  • Hydrogen may be supplied at a gas hourly space velocity of from 100 to 10000 Nl/l/hr, preferably from 500 to 5000 Nl/l/hr.
  • the hydrocarbon feed may be provided at a weight hourly space velocity of from 0.1 to 5 kg/l/hr, preferably from 0.25 to 2 kg/l/hr.
  • the ratio of hydrogen to hydrocarbon feed may range from 100 to 5000 Nl/kg and is preferably from 250 to 2500 Nl/kg.
  • the degree of hydrocracking and isomerisation occurring in the second hydroconversion stage may be measured by determining the degree of conversion of the fraction boiling above 370 °C, as hereinbefore defined.
  • the second hydroconversion stage is operated at a conversion of at least 40%.
  • the hydrogen required for the operation of both the first and the second hydroconversion stages may be generated by processes well known in the art, for example by the steam reforming of a refinery fuel gas.
  • the hydrocarbon fuel produced in the second hydroconversion stage will typically comprise hydrocarbons having boiling points lying in a number of different fuel fractions, for example the naphtha, kerosine and gasoil fractions discussed hereinbefore. Separation of the hydrocarbon fuel into the appropriate fractions may be conveniently achieved using distillation techniques well known in the art.
  • a mixture comprising silica (precipitated silica, average particle size 50 ⁇ m, surface area 450 m 2 /g), ammonium zirconium carbonate ("Bacote" 20, 20 %wt equivalent of ZrO 2 ) and water was mulled for a period of about 20 minutes.
  • Acetic acid 5% aqueous solution
  • water were added and the mixture mulled for a further period of about 30 minutes.
  • Polyelectrolyte (“Nalco”: as a 4% aqueous solution) was added and the resulting mixture mulled for a further 5 minutes to yield a final mixture having a pH of about 8.4 and a loss on ignition of about 70%.
  • the resulting mixture was extruded using a 2.54 cm (1 inch) "Bonnot” extruder having a 1.7 mm “Delrin” trilobe dieplate insert to yield trilobe extrudates.
  • the extrudates were dried at a temperature of about 120 °C and finally calcined at a temperature between 500 and 550 °C for 2 hours.
  • the calcined extrudates were washed using an aqueous solution of ammonium acetate and thereafter calcined as hereinbefore described.
  • An aqueous solution was prepared by dissolving cobalt nitrate (Co(NO 3 ) 2 . 6H 2 O; sufficient to yield an 18% aqueous solution) in water and heated to a temperature of 80 °C.
  • the extrudates were impregnated by immersion in the cobalt nitrate solution for a period of 8 hours at 80 °C.
  • the thus impregnated extrudates were dried and finally calcined at a temperature of 500 °C for from 1 to 2 hours.
  • the catalyst prepared in (i) hereabove was loaded into a reaction vessel.
  • the catalyst was first activated by reduction by being contacted with a mixture of hydrogen and nitrogen at a temperature of 250 °C, a pressure of 5 bar and a gas hourly space velocity of from 500 to 600 Nl/l/hr.
  • the activated catalyst was then contacted with a mixture of carbon monoxide and hydrogen having a hydrogen/carbon monoxide ratio of 1.1 at a gas inlet pressure of from 35 to 40 bars and a gas hourly space velocity of from 1000 to 1200 Nl/l/hr.
  • a heavy wax was produced.
  • a mixture comprising amorphous silica-alumina (ex Grace Davison, pore volume (H 2 O) 1.10 ml/g, 13 %wt alumina (dry basis)), and alumina (ex Criterion Catalyst Co.) was placed in a mulling machine and mulled for a period of about 10 minutes.
  • Acetic acid (10 %wt solution) and water were added and the resulting mixture mulled for a further 10 minutes.
  • polyacrylamide (“Superfloc" A1839, 2 %wt aqueous solution) was added and mulling continued for a further 10 minutes.
  • polyelectrolyte (“Nalco", 4 %wt aqueous solution) was added and the mixture mulled for a final period of about 5 minutes.
  • the resulting mixture was extruded using a 5.72 cm (2.25 inch) "Bonnot" extruder through a dieplate, yielding 2.5 mm trilobe extrudates.
  • the resulting extrudates were dried at a temperature of 120 °C for about 2 hours and subsequently calcined at a temperature of 600 °C for 2 hours.
  • aqueous solution comprising hexachloroplatinic acid (H 2 PtCl 6 , 2.45 %wt) and nitric acid (7.66 %wt) having a pH of below 1.
  • the extrudates were impregnated using this aqueous solution via the Pore Impregnation technique to give a final platinum loading on the carrier of 0.8 %wt.
  • the thus impregnated extrudates were finally calcined at a temperature of 500 °C for about 2 hours.
  • the catalyst prepared in (i) hereabove was loaded into a reaction vessel
  • the C 5 + hydrocarbon product of the hydrocarbon synthesis stage was fed to the reaction vessel at a weight hourly space velocity of 0.88 kg/l/hr, a temperature of 315 °C and a pressure of 35 bars.
  • Hydrogen was supplied to the reaction vessel at a gas hourly space velocity of 660 Nl/l/hr (that is a hydrogen to hydrocarbon ratio of 750 Nl/kg).
  • the conversion achieved in terms of percent weight of the fraction of the feed having a boiling point above 370 °C converted to products having a boiling point of below 370 °C, was 16%, indicating that substantially no cracking or isomerisation of the feed hydrocarbon occurred.
  • a catalyst was prepared following the procedure described in Example 1(B)(i) hereabove.
  • the catalyst prepared in (i) was loaded into a reaction vessel.
  • the C 5 + hydrocarbon product of the first hydroconversion stage was fed to the reaction vessel at a weight hourly space velocity of 1.046 kg/l/hr and a pressure of 31 bars.
  • Hydrogen was supplied to the reaction vessel at a gas hourly space velocity of 660 NI/I/ hr (that is a hydrogen to hydrocarbon ratio of 630 Nl/kg).
  • a liquid recycle rate of 0.17 kg/l/hr was applied.
  • a conversion target of 55% (as defined in Example 1(B) (ii) hereabove) was set and was achieved by adjusting the operating temperature of the second hydroconversion stage. It was found that an operating temperature of 330 °C was required.
  • the effluent of the reaction vessel was collected and separated by means of distillation into a number of fractions.
  • the properties of a gasoil fraction boiling in the temperature range of from 170 to 340 °C recovered from the effluent are given in Table 1.
  • Example 1(C)(i) hereabove A sample of the catalyst prepared as described in Example 1(C)(i) hereabove was loaded into a reaction vessel.
  • the C 5 + hydrocarbon product of the hydrocarbon synthesis stage was fed to the reaction vessel at a weight hourly space velocity of 1.103 kg/l/hr and a pressure of 31 bars.
  • Hydrogen was supplied to the reaction vessel at a gas hourly space velocity of 660 Nl/l/hr (that is a hydrogen to hydrocarbon ratio of 596 Nl/kg).
  • a liquid recycle rate of 0.23 kg/l/hr was applied.
  • a conversion of 55% (as defined in Example 1(B) (ii) hereabove) was achieved at an operating temperature of 338 °C.
  • the effluent of the reaction vessel was collected and separated by means of distillation into a number of fractions.
  • the properties of a gasoil fraction boiling in the temperature range of from 170 to 340 °C recovered from the effluent are given in Table 1.
  • Example 1(A) hereabove product from the hydrocarbon synthesis stage as described in Example 1(A) hereabove was treated to a single hydroconversion stage, operated to yield hydrocarbon fuels as in Example 2, but operated as follows:
  • a sample of the catalyst prepared as described in Example 1(C)(i) hereabove was loaded into a reaction vessel.
  • the C 5 + hydrocarbon product of the hydrocarbon synthesis stage was fed to the reaction vessel at a weight hourly space velocity of 1.01 kg/l/hr and a pressure of 31.4 bars.
  • Hydrogen was supplied to the reaction vessel at a gas hourly space velocity of 660 Nl/l/hr (that is a hydrogen to hydrocarbon ratio of 655 Nl/kg).
  • a liquid recycle rate of 0.13 kg/l/hr was applied.
  • a conversion of 39% (as defined in Example 1(B) (ii) hereabove) was achieved at an operating temperature of 334 °C.
  • a catalyst was prepared using the general method outlined in Example 1(A)(i) hereabove and used to prepare a C 5 + hydrocarbon product following the general procedure described in Example 1(A) (ii) hereabove.
  • a commercially available nickel-containing hydrogenation catalyst (60 %wt nickel; ex Harshaw Catalysts) was loaded into a reaction vessel.
  • the C 5 + hydrocarbon product of the hydrocarbon synthesis stage was fed to the reaction vessel at a weight hourly space velocity of 1.0 kg/l/hr, a temperature of 220 °C and a pressure of 30 bars.
  • Hydrogen was supplied to the reaction vessel at a gas hourly space velocity of 1000 Nl/l/hr (that is a hydrogen to hydrocarbon ratio of 1000 Nl/kg).
  • a catalyst was prepared following the procedure described in Example 1(B)(i) hereabove.
  • the catalyst prepared in (i) was loaded into a reaction vessel.
  • the C 5 + hydrocarbon product of the first hydroconversion stage was fed to the reaction vessel at a weight hourly space velocity of 1.25 kg/l/hr and a pressure of 30 bars.
  • Hydrogen was supplied to the reaction vessel at a gas hourly space velocity of 1000 NI/ l/hr (that is a hydrogen to hydrocarbon ratio of 800 Nl/kg).
  • a conversion target of 60% (as defined in Example 4(B) hereabove) was set and achieved by adjusting the operating temperature of the second hydroconversion stage. It was found that an operating temperature of 334 °C was required.
  • the effluent of the reaction vessel was collected and separated by means of distillation into a number of fractions.
  • the selectivity of the second hydroconversion stage to a gasoil fraction boiling in the temperature range of from 220 to 370 °C was 50%.
  • Catalyst prepared as described in Example 1 (B)(i) was loaded into a reaction vessel.
  • the C 5 + hydrocarbon product of the hydrocarbon synthesis stage was fed to the reaction vessel at a weight hourly space velocity of 1.25 kg/l/hr and a pressure of 30 bars.
  • Hydrogen was supplied to the reaction vessel at a gas hourly space velocity of 1000 Nl/l/hr (that is a hydrogen to hydrocarbon ratio of 800 Nl/kg).
  • a conversion target of 60% (as defined in Example 4(B) hereabove) was set and achieved by adjusting the operating temperature of the second hydroconversion stage. It was found that an operating temperature of 338 °C was required.
  • the effluent of the reaction vessel was collected and separated by means of distillation into a number of fractions.
  • the selectivity of the second hydroconversion stage to a gasoil fraction boiling in the temperature range of from 220 to 370 °C was 40%.
EP93202395A 1992-08-18 1993-08-16 Process for the preparation of hydrocarbon fuels Expired - Lifetime EP0583836B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP93202395A EP0583836B2 (en) 1992-08-18 1993-08-16 Process for the preparation of hydrocarbon fuels

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP92202537 1992-08-18
EP92202537 1992-08-18
EP93202395A EP0583836B2 (en) 1992-08-18 1993-08-16 Process for the preparation of hydrocarbon fuels

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EP0583836A1 EP0583836A1 (en) 1994-02-23
EP0583836B1 EP0583836B1 (en) 1997-10-29
EP0583836B2 true EP0583836B2 (en) 2002-02-13

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EP (1) EP0583836B2 (da)
JP (1) JP3522797B2 (da)
AU (1) AU666960B2 (da)
CA (1) CA2104158C (da)
DE (1) DE69314879T3 (da)
DK (1) DK0583836T4 (da)
DZ (1) DZ1708A1 (da)
ES (1) ES2110051T5 (da)
MY (1) MY108862A (da)
NO (1) NO305288B1 (da)
NZ (1) NZ248415A (da)
RU (1) RU2101324C1 (da)
ZA (1) ZA935964B (da)

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US7875670B2 (en) 2002-08-12 2011-01-25 Exxonmobil Chemical Patents Inc. Articles from plasticized polyolefin compositions
US7985801B2 (en) 2002-08-12 2011-07-26 Exxonmobil Chemical Patents Inc. Fibers and nonwovens from plasticized polyolefin compositions
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RU2656601C1 (ru) * 2017-08-08 2018-06-06 Публичное акционерное общество "Нефтяная компания "Роснефть" (ПАО "НК "Роснефть") Способ получения синтетической нефти

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CA2104158C (en) 2005-11-15
DE69314879T3 (de) 2002-07-18
ZA935964B (en) 1994-03-15
MY108862A (en) 1996-11-30
RU2101324C1 (ru) 1998-01-10
NO305288B1 (no) 1999-05-03
DE69314879D1 (de) 1997-12-04
DK0583836T3 (da) 1998-03-02
NO932905L (no) 1994-02-21
ES2110051T3 (es) 1998-02-01
EP0583836A1 (en) 1994-02-23
DK0583836T4 (da) 2002-03-11
CA2104158A1 (en) 1994-02-19
JP3522797B2 (ja) 2004-04-26
DZ1708A1 (fr) 2002-02-17
NZ248415A (en) 1995-03-28
EP0583836B1 (en) 1997-10-29
ES2110051T5 (es) 2002-10-01
NO932905D0 (no) 1993-08-16
DE69314879T2 (de) 1998-03-12
AU4467693A (en) 1994-02-24
AU666960B2 (en) 1996-02-29
JPH06158058A (ja) 1994-06-07

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