WO2016091691A1

WO2016091691A1 - Fischer-tropsch process using supported reduced cobalt catalyst

Info

Publication number: WO2016091691A1
Application number: PCT/EP2015/078415
Authority: WO
Inventors: Ewen Ferguson; Piotr KRAWIEC; Matthew James WELLS
Original assignee: Bp P.L.C.; Johnson Matthey Davy Technologies Limited
Priority date: 2014-12-12
Filing date: 2015-12-02
Publication date: 2016-06-16

Abstract

A process for the conversion of a feed comprising a mixture of hydrogen and carbon monoxide to hydrocarbons, the hydrogen and carbon monoxide in the feed being present in a ratio of from 1 :9 to 9:1 by volume, the process comprising the step of contacting the feed at elevated temperature and atmospheric or elevated pressure with a catalyst comprising zinc oxide and cobalt, wherein the catalyst initially comprises from 20% to 95% metallic cobalt by weight of cobalt.

Description

FISCHER-TROPSCH PROCESS USING SUPPORTED REDUCED COBALT

CATALYST

This invention relates to Fischer-Tropsch (FT) processes for the conversion of a feed comprising a mixture of carbon monoxide gas and hydrogen gas (e.g. synthesis gas

(syngas)) to hydrocarbons over a cobalt catalyst comprising a zinc oxide support, catalysts therefor and uses of said catalysts.

Known FT processes typically utilise a stable catalyst comprising oxidic cobalt, such as cobalt(II) dicobalt(III) oxide (also known as cobalt oxide or cobalt(II,III) oxide, i.e. Co₃0₄) which may be supported on zinc oxide, and employ a reduction step in order to activate the catalyst by reducing the cobalt(II,III) oxide to elemental (or metallic) cobalt (Co⁰) which is understood to be the catalytically active species. It has thus been thought desirable to reduce as much of the cobalt present as possible in order to improve the activity of the resultant catalyst, in other words to obtain a degree of reduction of the cobalt as near to 100% as possible. See Bartholomew et al, Journal of Catalysis 128, 231-247

(1991). EP0261870 discloses an FT process utilising a reduced cobalt catalyst comprising a zinc oxide support. There remains an ongoing need to improve the properties of such FT catalysts, most notably in relation to their activity, i.e. enabling greater conversion of syngas to hydrocarbons for the same temperature (or equal or greater conversion at lower temperatures) and enabling more desirable selectivity, such as selectivity towards producing hydrocarbons having at least 5 carbon atoms (C₅₊), or selectivity away from producing methane. Surprisingly, it has now been found that a limited degree (or extent) of reduction of a zinc oxide supported cobalt catalyst, (commensurately the extent of reduction of the catalyst when it is subsequently exposed to the feed) actually improves the catalyst activity and C₅₊ selectivity in an FT process.

According to a first aspect, the present invention thus relates to a process for the conversion of a feed comprising a mixture of hydrogen and carbon monoxide to hydrocarbons, the hydrogen and carbon monoxide in the mixture being present in a ratio of from 1 :9 to 9:1 by volume, the process comprising the step of contacting the feed at elevated temperature and atmospheric or elevated pressure with a catalyst comprising zinc oxide and cobalt, wherein the catalyst initially comprises from 20% to 95% metallic cobalt by weight of cobalt. This aspect may also desirably include a step of pre-treating a catalyst composition comprising zinc oxide support and cobalt oxide or a cobalt compound decomposable thereto by reduction to produce the catalyst above.

Advantageously, the catalyst initially comprises from 25% to 90% metallic cobalt by weight of cobalt, preferably from 30% to 80% metallic cobalt by weight of cobalt, such as from 30% to 70% metallic cobalt by weight of cobalt. Within these preferred ranges, the selectivity/activity is surprisingly further improved. As used herein, the general term "cobalt" includes cobalt either in metallic (elemental) form or as part of a cobalt compound (i.e. referring to the total cobalt present), so for example where the catalyst is referred to as "comprising cobalt", it is intended to mean that the catalyst comprises metallic/elemental cobalt and/or at least one cobalt compound. Commensurately, the mass of cobalt includes the total mass of cobalt atoms and ions present, i.e. ignoring any other ions in any cobalt compounds. As used herein, the more specific terms "metallic cobalt" or "elemental cobalt" mean cobalt in an oxidation state of zero, i.e. Co⁰.

The percentage metallic cobalt by weight of cobalt (herein interchangeable with the degree of reduction) of the catalyst according to the present invention applies to the catalyst initially, which refers to process startup, i.e. the point in time at which the catalyst is first contacted with the feed. Accordingly, the percentage metallic cobalt by weight of cobalt applies to the catalyst immediately prior to, and/or substantially at the time of, introducing the feed to the catalyst to produce hydrocarbons, or may additionally or alternatively refer to the degree of reduction achieved by a reduction step, especially if such a reduction step is carried out in situ. Notably, it is thus recognised that exposing the catalyst to the feed itself at elevated temperature may further impact the degree of reduction, for example to a level outside the claimed range, such as complete reduction. However, even if further reduction of the catalyst occurs upon, or following exposure to the feed, it has been found that the benefits of the present invention remain, and this is specifically included within the scope of the present invention.

The catalyst employed in the present invention may be obtained by pre-treating a catalyst composition comprising zinc oxide support and oxidic cobalt or a cobalt compound decomposable thereto, with a reducing agent. Accordingly, a pre-treatment, or reduction step, may be used to obtain the degree of reduction, i.e. by reducing the catalyst. That pre-treatment is not particularly limited by the present invention.

Suitably, a pre-treatment step which may be a gaseous reduction, i.e. using a reducing gas stream, may be employed. If a reducing gas stream is used, it advantageously comprises at least 25 vol.% of a reducing gas, preferably at least 50 vol.% of a reducing gas, more preferably at least 75 vol.% reducing gas, even more preferably at least 90 vol.% reducing gas, even more preferably still at least 95 vol.% reducing gas and yet further preferably is substantially entirely made up of reducing gas. Any remainder may comprise, or be, inert diluents such as argon, helium, nitrogen and/or water vapour, or minor components such as hydrocarbons (e.g. methane) or carbon dioxide. The reducing gas referred to above may particularly be carbon monoxide or hydrogen.

Advantageously, as such gases are readily available where processes using a feed comprising a mixture of hydrogen gas and carbon monoxide gas are located, the catalyst may be pre-treated using reducing gases such as a gas comprising molecular hydrogen (hydrogen gas) and/or a gas comprising carbon monoxide (carbon monoxide gas). If hydrogen gas is used then it is suitable that the reducing gas stream comprises less than 10%) carbon monoxide gas (by volume of hydrogen gas and carbon monoxide gas) in order to prevent premature reaction start-up and a resultant poorly performing catalyst.

Similarly, if carbon monoxide gas is used then it is suitable that the reducing gas stream comprises less than 10% hydrogen gas (by volume of hydrogen gas and carbon monoxide gas). For the avoidance of any doubt, the upper limit of hydrogen which may be present in the reducing gas stream as reported herein is relative only to the volume of carbon monoxide in the gaseous stream, and not relative to the combined volume of carbon monoxide and any inert diluents or other components. Correspondingly, the upper limit of carbon monoxide which may be present in the reducing gas as reported herein is relative only to the volume of molecular hydrogen in the gaseous stream, and not relative to the combined volume of hydrogen and any inert diluents or other components.

Suitably, the pre-treating step may be performed at a temperature of from 100 °C to 500 °C, preferably from 200 °C to 350 °C, and/or at any desired pressure, for instance from 10 to 5500 kPa, preferably from 20 to 3000 kPa, more preferably from 50 to 1000 kPa, and even more preferably from 100 to 800 kPa. During this step, reducing gas (such as hydrogen gas or carbon monoxide gas) is suitably passed over the catalyst bed at a gas hourly space velocity (GHSV) in the range from 100 to 10000 h^"1, preferably from 250 to 5000 h^"1, such as from 250 to 3000 h^"1 and more preferably from 250 to 2000 h^"1, for example 1000 h^"1. As used herein, unless otherwise specified, GHSV means gas hourly space velocity on gas volumes converted to standard temperature and pressure based on the catalyst bed volume.

In order to efficiently obtain the desired level of metallic cobalt in the catalyst, the pre-treating step of reducing a catalyst advantageously occurs at a temperature of from 200°C to 300°C, preferably from 220°C to 280°C, more preferably from 230°C to 250°C. These temperature ranges particularly apply (non-exclusively) in combination with using carbon monoxide gas and/or hydrogen gas to reduce the catalyst. Within these temperature ranges, it is thought to be easier to control the degree of reduction. As used herein, temperatures may refer to feed temperatures, applied temperatures and/or catalyst bed temperatures.

The precise duration of the pre-treatment step is important only insofar as to obtain the desired degree of reduction. Exemplary durations of the pre-treatment step, which may be in combination with any of the temperature ranges specified above, include from 0.1 to 100 hours, preferably from 1 to 50 hours, more preferably from 5 to 35 hours, even more preferably from 7 to 20 hours, and even more preferably still from 10 to 15 hours.

For convenience, the pre-treatment step may desirably occur in the same reactor used for the subsequent conversion of syngas to hydrocarbons ("in situ") in order to reduce the time and effort required loading and unloading catalysts. Reducing in situ also mitigates the need for any steps to ensure the degree of reduction achieved during the pre-treatment step remains present when the conversion of syngas to hydrocarbons is commenced. The pre-treatment step may, however, also be carried out in another location apart from the FT reactor ("ex situ").

As used herein, the degree of reduction may be measured using temperature programmed reduction (TPR). TPR is a technique for the characterisation of solid materials in which a catalyst (e.g. cobalt(II,III) oxide) is subjected to a programmed temperature increase while a reducing gas is passed over the sample. The effluent gas may be analysed by a thermal conductivity detector (TCD) or mass spectrometer (MS) to determine the decrease in reductant gas concentration or evolution of other species, such as water.

In order to determine the degree of reduction herein, a standard data set is produced by drying a sample and conducting TPR through to 100% reduction of the cobalt atoms present in the catalyst (e.g. corresponding to 100% reduction of C03O₄ to Co⁰). The standard data may thus be obtained in situ (i.e. within the TPR unit) by initially exposing the sample to a drying step including contacting the sample with argon gas at a GHSV of 1800 h^"1, ramping the temperature from 20°C to 120°C at a rate of 5°C/min then dwelling at 120°C for 15 min before cooling back to 20°C also under argon gas. The TPR itself may be performed utilising 4% H₂ gas (in Argon), at a gas hourly space velocity (GHSV) of 3800 h^"1 and ramping the temperature from 20°C to 800°C at a rate of 5°C/min. Sample data is generally produced by conducting the drying step as above, followed by the reduction step desired (for example 10 hours under 100% hydrogen gas at 240, 260, 280 or 300°C at a GHSV of 1800 h^"1) and then conducting TPR through to 100% reduction. The sample data may thus be obtained in situ (i.e. within the TPR unit) by initially exposing the sample to a drying step including contacting the sample with argon gas at a GHSV of 1800 h^"1, ramping the temperature from 20°C to 120°C at a rate of 5°C/min then dwelling at 120°C for 15 min before cooling back to 20°C also under argon gas. For the reduction step itself, 100%) H₂ gas may be utilised, also at a GHSV of 1800 h^"1 and the temperature ramped from 20°C to 150°C at a rate of 2°C/min followed by slower ramping from 150°C to the desired reduction temperature at a rate of l°C/min before dwelling at the desired reduction temperature for 10 hours and cooling to 20°C under argon gas. The TPR itself is then conducted as described above. Utilising a TCD, a graph of thermal conductivity against temperature may be produced, with the conductivity approaching a baseline value at complete reduction. Comparison of the area under the TCD graph (relative to the baseline) obtained in the sample TPR data against the corresponding area of the standard TPR data allows the calculation of the relative amount of hydrogen consumed during prereduction between the sample and standard data. In practice, this involves subtracting the integrated area under the TCD graph obtained for the sample data from the area under the TCD graph for the standard data, then expressing the resultant value as a percentage of the integrated area from the standard data. Expressed as an equation, this is:

[Area of standard TPR data]— [Area of sample TPR data] %H2 consumed = 100 x

[Area of standard TPR data] Equation 1 : Method of calculating relative hydrogen consumption using TPR data TPR is an advantageous technique to utilise for determining degree of reduction because the technical measurements on a sample are made following the reduction step.

Accordingly, while the % H consumed is calculated via the formula above, the data obtained is applicable even if another reducing gas (for example, carbon monoxide) has been used, merely being expressed as the equivalent % H₂ consumed and enabling the stoichiometry from hydrogen reduction to be used in calculating the degree of reduction i.e. the percentage of cobalt atoms present as Co⁰. This is a preferred approach because determining simply the percentage H₂ consumed may correspond to a different relative amount of Co⁰ produced by reduction for different catalysts, but Co⁰ is understood to be the catalytically active species so in the context of the present invention it is desirable to understand the actual amount of Co⁰ produced by reduction.

The complete reduction of cobalt oxide (Co₃0₄) is a two-step process (firstly the reduction to cobalt(II) oxide, also known as cobaltous oxide, and then the reduction of cobalt(II) oxide to metallic cobalt) as shown by the chemical equations below:

Co₃0₄ + H₂→ 3CoO + H₂0

CoO + H₂→ Co⁰ + H₂0

Equations 2 and 3 : Step-wise reduction of cobalt(II,III) oxide to metallic cobalt

The overall reduction may alternatively be represented as a single stoichiometric equation:

Co₃0₄ + 4H₂→ 3CoO + H₂0 + 3H₂→ 3Co° + 4H₂0 Equation 4: Overall reduction of cobalt(II,III) oxide to metallic cobalt

Accordingly, in the first step, 1 equivalent of H₂ is consumed without producing any metallic cobalt, while in the second, 3 equivalents are consumed. In total, therefore, complete reduction requires 4 equivalents of ¾ to reduce the 3 equivalents Co to Co⁰. However, the first step is believed to be much faster than the second so herein is assumed to proceed to completion before any formation of Co⁰ occurs. The amount of hydrogen required to produce the metallic cobalt is thus higher per mole of metallic cobalt when the degree of reduction is lower, and tends towards the stoichiometric ratio of 4 moles of H₂ for every 3 moles of Co as 100% reduction is approached.

Taking this into account, the degree of reduction achieved in the sample may be calculated using the formula below:

4 [Area of sample TPR data]

% Degree of Reduction = 100 * (1—— p- — ,

3 [Area of standard TPR data]

Equation 5: Calculation of degree of reduction from TPR data.

More generally, for a reduction having stoichiometry whereby x equivalents of H₂ are required before the rate determining step of the reduction, and y equivalents of H₂ are required during and after the rate determining step, the degree of reduction may be calculated using the formula below:

(x + y) [Area of sample TPR data]

% Degree of Reduction = 100 * (1 p- — . __,„„ , =— )

y [Area of standard TPR data] ^J

Equation 6: General Calculation of degree of reduction from TPR data

Using TPR as described above, the degree of reduction may thus be determined for a catalyst that has been reduced ex situ, e.g. following any period in storage, transport or other intermediate steps that may occur before the catalyst is used to produce

hydrocarbons, in order to be assured that the amount of cobalt metal present by weight of cobalt remains within the range of the present invention. If not, additional measures may be taken in order to achieve the required degree of reduction, for example additional reduction in situ or avoiding exposing the catalyst to an oxidising atmosphere during storage and transport. Such avoidance of oxidising atmospheres may be achieved by packing the catalyst in an inert (e.g. nitrogen) atmosphere, packing the catalyst in a reducing atmosphere (e.g. 5%> ¾, 95% nitrogen by volume), passivating by creating a thin, protective oxide layer on the surface of the catalyst, or wax-coating the catalyst for storage and transport. The catalyst used in accordance with the present invention may comprise a cobalt compound intended to be reduced to metallic cobalt. The identity of the cobalt compound is not particularly limited except that the cobalt compound should be decomposable (either directly or indirectly (e.g. via intermediates) to metallic cobalt, including mixtures of such compounds. Preferably, the cobalt compound is oxidic cobalt, a cobalt compound decomposable thereto or mixtures thereof, for example cobalt(III) oxide, cobalt(II,III) oxide, and/or cobalt(II) oxide, compounds decomposable to cobalt(III) oxide, cobalt(II,III) oxide, and/or cobalt(II) oxide, and mixtures thereof. More preferably, the cobalt compound is cobalt(II,III) oxide, cobalt(II) oxide, a cobalt compound that is decomposable to cobalt(II,III) oxide and/or cobalt(II) oxide, or mixtures thereof, for example cobalt(II,III) oxide, cobalt(II) oxide, cobalt nitrate (e.g. cobalt nitrate hexahydrate), cobalt acetate or cobalt hydroxide. Even more preferably, the cobalt compound is cobalt(II,III) oxide, cobalt(II) oxide or mixtures thereof, as this removes the need for additional

calcination/oxidation/decomposition steps to prepare the oxide, and even more preferably still the cobalt compound is cobalt(II,III) oxide. If a cobalt compound other than oxidic cobalt is used, this may be referred to herein as a catalyst precursor, from which the calcination/oxidation/decomposition step used to form cobalt oxide may be carried out in situ or ex situ with respect to the hydrocarbon synthesis reactor or with respect to the reduction step. For the avoidance of doubt, it is accepted that the cobalt compound may be a mixed oxide, e.g. one formed by reaction with the zinc oxide support. Examples include mixed spinels, e.g. cobalt(III) zinc (II) oxide. Such mixed oxides are also considered examples of oxidic cobalt and understood to be decomposable to at least cobalt(II) oxide. The amount of cobalt compound present in the catalyst is not particularly limited.

According to some embodiments of the present invention, the catalyst comprises from 5% to 30%, preferably from 10% to 20%, cobalt compound by weight of the catalyst.

The catalyst also comprises zinc oxide as a supporting material for the cobalt compound. The catalyst may further comprise one or more promoters in order to improve the activity of the catalyst. Non-limiting examples of promoters include: chromium, nickel, iron, molybdenum, tungsten, manganese, boron, zirconium, gallium, thorium, lanthanum, cerium, ruthenium, rhodium, rhenium, palladium, platinum and/or mixtures thereof. The one or more promoters may be present as the elemental metal or as a compound, for example an oxide. In some embodiments, the promoter comprises, or is selected from platinum, molybdenum or mixtures thereof. Such promoters may be present in an amount up to 15% by weight of the catalyst but may be present in an amount of from 0% to 5% by weight of the catalyst, from 0.1% to 2% by weight of the catalyst, or from 0.5% to 1.5% by weight of the catalyst, such as from 0.0001% to 1.5% or from 0.001% to 0.5%.

The catalyst may be prepared by any known method, including impregnation, precipitation or gelation. A suitable method, for example, comprises impregnating zinc oxide with a compound of cobalt that is thermally decomposable to metallic cobalt (e.g. via the oxide), such as cobalt nitrate, cobalt acetate or cobalt hydroxide. Any suitable impregnation technique including the incipient wetness technique or the excess solution technique, both of which are well-known in the art, may be employed. The incipient wetness technique is so-called because it requires that the volume of impregnating solution be predetermined so as to provide the minimum volume of solution necessary to just wet the entire surface of the support, with no excess liquid. The excess solution technique as the name implies, requires an excess of the impregnating solution, the solvent being thereafter removed, usually by evaporation. The impregnation solution may suitably be either an aqueous solution or a nonaqueous, organic solution of the cobalt compound. Suitable nonaqueous organic solvents include, for example, alcohols, ketones, liquid paraffinic hydrocarbons and ethers. Alternatively, aqueous organic solutions, for example an aqueous alcoholic solution, of the thermally decomposable cobalt compound may be employed.

Following preparation, the catalyst may also be formed by any known technique including extrusion, pulverisation, powderisation, pelletisation, granulation and/or coagulation. Preferably, the catalyst is extruded, for example to enable less pressure drop in a reactor and highly consistent diameter of the catalyst. In extrusion, an extrudable paste may be formed, such as from a mixture of the catalyst components in water, which is then extruded into the desired shape and dried to form the catalyst. Alternatively, an extrudable paste of zinc oxide may be formed from a mixture of powdered zinc oxide and water. This paste may then be extruded and typically dried and/or calcined to form the desired shape, which may then be contacted with a solution of a cobalt compound in order to impregnate the extruded support material with the cobalt compound. The resultant impregnated support material may then be dried to form the catalyst, which if not already comprising oxidic cobalt such as cobalt(III) oxide, cobalt(II,III) oxide or cobalt(II) oxide may also be calcined.

As indicated above, the present invention provides, in a first aspect, a process for the conversion of a feed comprising a mixture of hydrogen and carbon monoxide, preferably in the form of a synthesis gas mixture, to hydrocarbons, which process comprises contacting the feed with a reductively activated catalyst composition as hereinbefore described.

In the hydrocarbon synthesis processes described herein, the volume ratio of hydrogen to carbon monoxide (H₂:CO) in the feed is in the range of from 1 :9 to 9:1 preferably in the range of from 0.5 : 1 to 5 : 1 , more preferably from 1 :1 to 3: 1 , and most preferably from 1.6: 1 to 2.2: 1. Such ratios especially apply as regards the feed to the reactor, e.g. at the reactor inlet. The feed may also comprise other gaseous components, such as nitrogen, carbon dioxide, water, methane and other saturated and/or unsaturated light hydrocarbons, each preferably being present at a concentration of less than 30% by volume. The temperature of the reaction (or reactor) is elevated, preferably in the range from 100 to 400 °C, more preferably from 150 to 350 °C, and most preferably from 150 to 250 °C. The pressure of the reaction (or reactor) is atmospheric or elevated, preferably in the range from 1 to 100 bar (from 0.1 to 10 MPa), more preferably from 5 to 75 bar (from 0.5 to 7.5 MPa), and most preferably from 10 to 50 bar (from 1.0 to 5 .0 MPa). As used herein "elevated" in relation to conditions refers to conditions greater than standard conditions, for example, temperatures and pressures greater than standard temperature and pressure (STP).

The gaseous reactants (feed) for the present process may be fed into the reactor either separately or pre-mixed (e.g. as in the case of syngas). They may initially all contact the solid catalyst at the same portion of the solid catalyst, or they may be added at different positions of the solid catalyst. The ratio of hydrogen gas to carbon monoxide gas may thus be determined from the relative flow rates when both streams are flowing. Preferably, the one or more gaseous reactants flow co-currently over the solid catalyst.

The feed used for the present process may also comprise recycled materials extracted from elsewhere in the process, such as unreacted reactants separated from any reduction steps associated with the process of the invention.

The mixture of hydrogen and carbon monoxide is suitably passed over the catalyst bed at a gas hourly space velocity (GHSV) in the range from 100 to 10000 h^"1 (gas volumes converted to standard temperature and pressure), preferably from 250 to 5000 h^"1, such as from 250 to 3000 h^"1, and more preferably from 250 to 2000 h^"1.

As is well known in the art, synthesis gas, which is preferably used as the feed for the present process, principally comprises carbon monoxide and hydrogen and possibly also minor amounts of carbon dioxide, nitrogen and other inert gases depending upon its origin and degree of purity. Methods of preparing synthesis gas are established in the art and usually involve the partial oxidation of a carbonaceous substance, e.g. coal. Alternatively, synthesis gas may be prepared, for example by the catalytic steam reforming of methane. The ratio of carbon monoxide to hydrogen present in the synthesis gas may be altered appropriately by the addition of either carbon monoxide or hydrogen, or may be adjusted by the so-called shift reaction well known to those skilled in the art.

The process of the invention may be carried out batch wise or continuously in a fixed bed, fluidised bed or slurry phase reactor. When using the catalyst as described in the present invention in a fixed bed process, the particle size should be of such shape and dimension that an acceptable pressure drop over the catalyst bed is achieved. A person skilled in the art is able to determine the particle dimension optimal for use in such fixed bed reactors. Particles of the desired shape and dimension may be obtained by extrusion of a paste to which optionally extrusion aids and/or binders may be optionally added.

According to second and third aspects, the present invention relates to uses of a catalyst comprising zinc oxide support and cobalt, wherein the catalyst comprises from

20% to 95% metallic cobalt by weight of cobalt, for the conversion of a feed comprising a mixture of hydrogen gas and carbon monoxide gas to hydrocarbons, and to increase the selectivity and/or productivity of a process for the conversion of a feed comprising a mixture of hydrogen gas and carbon monoxide gas to hydrocarbons. As the catalyst so used is in a process for the conversion of a feed comprising a mixture of hydrogen gas and carbon monoxide gas to hydrocarbons (to which the first aspect of the invention relates), any features of the catalyst or any process relating to it described above in relation to the first aspect are applicable to these second and third aspects, either individually or in any combination.

In a fourth aspect, the present invention relates to a Fischer-Tropsch catalyst comprising zinc oxide support and cobalt, wherein the catalyst comprises from 20% to 95% metallic cobalt by weight of cobalt. As the catalyst is intended for use in a process for the conversion of a feed comprising a mixture of hydrogen gas and carbon monoxide gas to hydrocarbons (to which the first aspect of the invention relates), any features of the catalyst or any process relating to it described above in relation to the first aspect are applicable to this fourth aspect, either individually or in any combination.

In a fifth aspect, the present invention relates to a process for making a Fischer-

Tropsch catalyst according to the fourth aspect, comprising the step of reducing a catalyst comprising zinc oxide support and oxidic cobalt or a cobalt compound decomposable thereto to produce the Fischer-Tropsch catalyst. As the catalyst is intended for use in a process for the conversion of a feed comprising a mixture of hydrogen gas and carbon monoxide gas to hydrocarbons (to which the first aspect of the invention relates), any features of the catalyst or any process relating to it described above in relation to the first aspect are applicable to this fifth aspect, either individually or in any combination.

In a sixth aspect, the present invention also provides a product (preferably a fuel) comprising hydrocarbons obtained from a process according to the first aspect. As the product results from a process for the conversion of a feed comprising a mixture of hydrogen gas and carbon monoxide gas to hydrocarbons (to which the first aspect of the invention relates), any features of the process described above in relation to the first aspect are applicable to this sixth aspect, either individually or in any combination.

Examples

Examples 1-4

Cobalt oxide supported on zinc oxide was manufactured as a catalyst by

impregnating zinc oxide powder with an aqueous solution of cobalt nitrate hexahydrate, followed by extrusion of the formed paste, and then drying and calcining to yield catalyst extrudates with a cobalt loading of 10.5% by weight of catalyst. 0.82g of the catalyst was loaded into the quartz u-tube reactor of a TPR unit and subjected to reduction under 100% hydrogen gas (at a GHSV of 1800 h^"1) for 10 hours at the temperatures in Table 1 below. As described hereinabove, the degree of reduction was determined using TPR via comparison of the integrated areas of the TCD graphs of the samples against a standard that had been subject to TPR with no reduction step, in order to obtain the percentage hydrogen consumption, and calculation of the degree of reduction as percentage of Co present as Co⁰ using Equation 5 detailed hereinabove.

Table 1. Temperature Programmed Reduction (TPR) of cobalt oxide on zinc oxide support

Examples 5-7 The catalyst sample was cobalt oxide on zinc oxide support, 10.5 wt.% cobalt loading, 125-160 μηι sieve-fraction. 0.74 ml of catalyst sample was loaded into a metal liner of a multi-channel catalyst-screening microreactor. Each channel of the microreactor underwent the same drying procedure in parallel, before the catalysts were activated according to the following protocols under 100% H₂ gas at a GHSV 1800 h^"1 and pressure of l atm:

Example 5 (inventive): From room temperature ramped to 150 °C at a rate of 2°C/min, then ramped to 260 °C at a rate of l°C/min, before dwelling at 260°C for 10 hours.

Example 6 (comparative): From room temperature ramped to 150 °C at a rate of 2°C/min, then ramped to 300 °C at a rate of 1 °C/min, before dwelling at 300°C for 15 hours.

Example 7 (comparative): From room temperature ramped to 150 °C at a rate of 2°C/min, then ramped to 400 °C at a rate of l°C/min, before dwelling at 400°C for 15 hours.

The liners were then cooled, purged with argon, and temperature ramped identically under a 1.8: 1 H₂:CO molar stream of syngas at 30 barg total pressure. Each example was operated at a temperature of 194-195°C under identical operating conditions other than GHSV with results presented in Table 2. The data clearly shows superior selectivity to C₅₊ and away from CH₄, and increased CO conversion for the example according to the invention over the comparative examples (noting that the CO conversion is expected to be inversely proportional to the GHSV but selectivity is not understood to be dependent on this variable). Example 5 6 7

Pre-reduction Temperature (°C) 260 300 400

GHSV (h^_1) 1 130 1736 1326

Time Period on Stream (h) 49-70 77-109 48-105

Temperature (°C) 195 194 194

CO Conversion (%) 54.6 12.3 2.04

C₅₊ Selectivity (%) 80.1 66.4 45.2

CH₄ Selectivity (%) 6.2 11.1 21.4

C₅₊ Productivity (g.L^'l.K^l) 148.0 22.8 2.1

CH₄ Productivity (g.L^"1.!!^"1) 11.4 3.7 0.9

Table 2. Performance data of examples 5-7 in conversion of syngas to hydrocarbons Examples 8-13

The catalyst sample was cobalt oxide on zinc oxide support, 10.5 wt.% cobalt loading, 125-160 μηι sieve-fraction.

1.1000 g of each catalyst sample was loaded into a metal liner of a multi-channel catalyst-screening microreactor. Each channel of the microreactor underwent the same drying procedure in parallel, before the catalysts were activated according to the following protocols under 100% H₂ gas at a GHSV 1800 h^"1 and pressure of 1 atm:

From room temperature, ramped to 150 °C at a rate of 2°C/min, then ramped to 260 °C (examples 8-10 ) or 240 °C (examples 1 1 -13) at a rate of l°C/min, before dwelling at this final temperature for 10 hours.

The liners were then cooled, purged with argon, and temperature ramped identically under a 1.8: 1 H₂:CO molar stream of syngas at 30 barg total pressure. Each example was operated at a temperature of 195°C under identical operating conditions with results presented in Table 3. The data clearly shows very similar selectivity to C₅₊ and away from CH₄, and increased CO conversion between the two examples according to the invention and superior to the comparative examples of Tables 2 and 4.

a e 3. Per ormance ata o examples 8-13 n convers on o syngas to y rocar ons Examples 14-15

The catalyst sample was cobalt oxide on zinc oxide support, 10.5 wt.% cobalt loading, 125-160 μπι sieve-fraction.

1.1000 g of each catalyst sample was loaded into a metal liner of a multi-channel catalyst-screening microreactor. Each channel of the microreactor underwent the same drying procedure in parallel, before the catalysts were activated according to the following protocols under 100% H₂ gas at a GHSV 5000 h^"1 and pressure of 1 atm:

From room temperature, ramped to 150 °C at a rate of 2°C/min, then ramped to 250 °C (example 14, inventive ) or 300 °C (example 15, comparative ) at a rate of l°C/min, before dwelling at this final temperature for 15 hours.

The liners were then cooled, purged with argon, and temperature ramped identically under a 1.8:1 H₂:CO molar stream of syngas at 30 barg total pressure. Each example was operated at a temperature of 195°C under identical operating conditions with results presented in Table 4. The data clearly shows superior selectivity to C₅₊ and away from CH₄, and increased CO conversion for the example according to the invention over the comparative examples.

Table 4. Performance data of examples 14-15 in conversion of syngas to hydrocarbons The dimensions and values disclosed herein are not to be understood as being strictly limited to the exact numerical values recited. Instead, unless otherwise specified, each such dimension is intended to mean both the recited value and a functionally equivalent range surrounding that value. For example, a dimension disclosed as "40 mm" is intended to mean "about 40 mm."

Every document cited herein, including any cross referenced or related patent or application, is hereby incorporated herein by reference in its entirety unless expressly excluded or otherwise limited. The citation of any document is not an admission that it is prior art with respect to any invention disclosed or claimed herein or that it alone, or in any combination with any other reference or references, teaches, suggests or discloses any such invention. Further, to the extent that any meaning or definition of a term in this document conflicts with any meaning or definition of the same term in a document incorporated by reference, the meaning or definition assigned to that term in this document shall govern.

While particular embodiments of the present invention have been illustrated and described, it would be obvious to those skilled in the art that various other changes and modifications can be made without departing from the spirit and scope of the invention. It is therefore intended to cover in the appended claims all such changes and modifications that are within the scope and spirit of this invention.

Claims

1. A process for the conversion of a feed comprising a mixture of hydrogen and carbon monoxide to hydrocarbons, the hydrogen and carbon monoxide in the feed being present in a ratio of from 1 :9 to 9: 1 by volume, the process comprising the step of :

a. contacting the feed at elevated temperature and atmospheric or elevated pressure with a catalyst comprising zinc oxide and cobalt;

wherein the catalyst initially comprises from 20% to 95% metallic cobalt by weight of cobalt.

2. A process according to claim 1 , further comprising the step of:

i. pre-treating a catalyst composition comprising:

a) zinc oxide support, and

b) oxidic cobalt or a cobalt compound decomposable thereto, to reduce the oxidic cobalt or cobalt compound decomposable thereto, before step a of claim 1.

3. A process according to either preceding claim, wherein the catalyst initially comprises from 25% to 90%, preferably from 30% to 80%, and more preferably from 30%) to 70%) metallic cobalt by weight of cobalt.

4. A process according to either claim 2 or claim 3 wherein step i is conducted by exposing the catalyst to a hydrogen gas-containing stream, wherein the hydrogen gas- containing stream comprises less than 10% carbon monoxide gas by volume of carbon monoxide gas and hydrogen gas.

5. A process according to either claim 2 or claim 3 wherein step i is conducted by exposing the catalyst to a carbon monoxide gas-containing stream, wherein the carbon monoxide gas-containing stream comprises less than 10% hydrogen gas by volume of carbon monoxide gas and hydrogen gas.

6. A process according to any preceding claim wherein the mixture of hydrogen and carbon monoxide is in the form of synthesis gas, preferably wherein the synthesis gas comprises hydrogen gas and carbon monoxide gas at a ratio in the range of from 0.5: 1 to 5: 1 by volume, preferably in the range of from 1 : 1 to 3 : 1 by volume, more preferably in the range of from 1.6 to 2.2: 1 by volume.

7. A process according to any preceding claim, wherein the catalyst comprises from 5% to 30%, preferably from 10% to 20%, cobalt by weight of the catalyst.

8. A process according to any preceding claim, wherein the catalyst comprises one or more promoters selected from chromium, nickel, iron, molybdenum, tungsten, manganese, boron, zirconium, gallium, thorium, lanthanum, cerium, ruthenium, rhenium, palladium, platinum, compounds and/or mixtures thereof.

9. A process according to any preceding claim, wherein the catalyst has been produced by extrusion, pulverisation, powderisation, pelletisation, granulation, coagulation or combinations thereof, preferably wherein the catalyst has been produced by extrusion.

10. A process according to claim 2 or any claim dependent therefrom, wherein the oxidic cobalt or a cobalt compound decomposable thereto is selected from cobalt(III) oxide, cobalt(II,III) oxide, cobalt(II) oxide, compounds decomposable thereto, or mixtures thereof.

11. A process according to claim 2 or any claim dependent therefrom , wherein the step of pre-treating a catalyst composition occurs at a temperature of from 200°C to 300°C, preferably from 220°C to 280°C, more preferably from 240°C to 260°C.

12. Use of a catalyst comprising zinc oxide support and cobalt, wherein the catalyst comprises from 20% to 95%, preferably from 25% to 90%, more preferably from 30%) to 80%, and even more preferably from 30% to 70% metallic cobalt by weight of cobalt, for the conversion of a mixture of hydrogen and carbon monoxide to hydrocarbons.

13. Use of a catalyst comprising zinc oxide support and cobalt, wherein the catalyst comprises from 20% to 95%, preferably from 25% to 90%, more preferably from 30%) to 80%, and even more preferably from 30% to 70% metallic cobalt by weight of cobalt, to increase the selectivity and/or productivity of a process for the conversion of a feed comprising a mixture of hydrogen and carbon monoxide to hydrocarbons.

14. A Fischer-Tropsch catalyst comprising:

i. zinc oxide support, and

ii. cobalt wherein the catalyst comprises from 20% to 95%», preferably from 25% to 90%>, more preferably from 30%> to 80%, even more preferably from 30%> to 70%> metallic cobalt by weight of cobalt.

15. A process for making a Fischer-Tropsch catalyst according to claim 14, comprising the step of:

I. reducing a catalyst composition comprising:

a) zinc oxide support, and

b) oxidic cobalt or a cobalt compound decomposable thereto, to produce the Fischer-Tropsch catalyst.

16. A product, preferably a fuel, comprising hydrocarbons obtained from a process according to any of claims 1 to 11.