EP1421157A1 - Procede de production de distillats moyens par hydroisomerisation et hydrocraquage de 2 fractions issues de charges provenant du procede fischer-tropsch - Google Patents
Procede de production de distillats moyens par hydroisomerisation et hydrocraquage de 2 fractions issues de charges provenant du procede fischer-tropschInfo
- Publication number
- EP1421157A1 EP1421157A1 EP02755093A EP02755093A EP1421157A1 EP 1421157 A1 EP1421157 A1 EP 1421157A1 EP 02755093 A EP02755093 A EP 02755093A EP 02755093 A EP02755093 A EP 02755093A EP 1421157 A1 EP1421157 A1 EP 1421157A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- fraction
- hydrocracking
- catalyst
- fractions
- boiling
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
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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
- C10G65/00—Treatment of hydrocarbon oils by two or more hydrotreatment processes only
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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
- C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
- C10G45/58—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to change the structural skeleton of some of the hydrocarbon content without cracking the other hydrocarbons present, e.g. lowering pour point; Selective hydrocracking of normal paraffins
- C10G45/60—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to change the structural skeleton of some of the hydrocarbon content without cracking the other hydrocarbons present, e.g. lowering pour point; Selective hydrocracking of normal paraffins characterised by the catalyst used
- C10G45/62—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to change the structural skeleton of some of the hydrocarbon content without cracking the other hydrocarbons present, e.g. lowering pour point; Selective hydrocracking of normal paraffins characterised by the catalyst used containing platinum group metals or compounds thereof
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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
- C10G47/00—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions
- C10G47/02—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions characterised by the catalyst used
- C10G47/10—Cracking of hydrocarbon oils, in the presence of hydrogen or hydrogen- generating compounds, to obtain lower boiling fractions characterised by the catalyst used with catalysts deposited on a carrier
- C10G47/12—Inorganic carriers
- C10G47/14—Inorganic carriers the catalyst containing platinum group metals or compounds thereof
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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
- C10G65/00—Treatment of hydrocarbon oils by two or more hydrotreatment processes only
- C10G65/14—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural parallel stages only
-
- 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
- C10G69/00—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process
- C10G69/14—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process plural parallel stages only
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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
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/1022—Fischer-Tropsch products
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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
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/20—Characteristics of the feedstock or the products
- C10G2300/30—Physical properties of feedstocks or products
- C10G2300/301—Boiling range
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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
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/40—Characteristics of the process deviating from typical ways of processing
- C10G2300/4018—Spatial velocity, e.g. LHSV, WHSV
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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
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/40—Characteristics of the process deviating from typical ways of processing
- C10G2300/4081—Recycling aspects
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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
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/04—Diesel oil
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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
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/06—Gasoil
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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
- C10G2400/00—Products obtained by processes covered by groups C10G9/00 - C10G69/14
- C10G2400/08—Jet fuel
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S208/00—Mineral oils: processes and products
- Y10S208/95—Processing of "fischer-tropsch" crude
Definitions
- the present invention relates to a treatment process and installation with hydrocracking and hydroisomerization, of charges originating from the Fischer-Tropsch process, making it possible to obtain middle distillates (gas oil, kerosene).
- the synthesis gas (CO + H 2 ) is catalytically transformed into oxygenated products and essentially linear hydrocarbons in gaseous, liquid or solid form.
- oxygenated products are generally free from heteroatomic impurities such as, for example, sulfur, nitrogen or metals. They also contain practically little or no aromatics, naphthenes and more generally rings, in particular in the case of cobalt catalysts.
- they can have a non-negligible content of oxygenated products which, expressed by weight of oxygen, is generally less than 5% by weight approximately and also a content of unsaturated (olefinic products in general) generally less than 10% by weight.
- Patent EP-635, 557 describes a process for the production of middle distillates having good properties at low temperatures, from a feed which is an Fischer-Tropsch process effluent.
- the process consists in separating said charge into at least a light fraction boiling below 260 ° C and a heavy fraction boiling above 260 ° C.
- Light and heavy fractions are processed separately.
- the light fraction is hydrotreated to remove the heteroatoms and then hydroisomerized.
- the heavy fraction optionally undergoes hydrotreatment (but preferably, there is no hydrotreatment), then hydroisomerization of the fraction obtained by hydrotreatment.
- the conversion of the products 371 ° C + to 371 ° C " is 35-80% by weight.
- the present invention provides an alternative process for the production of middle distillates.
- the invention relates to a process for the production of middle distillates from a paraffinic charge produced by Fischer-Tropsch synthesis, and comprising the following steps:
- step a Fractionation (step a) of the charge into at least 3 fractions: - at least one intermediate fraction having an initial boiling point T1 between 120 and 200 ° C, and a final boiling point T2 greater than 300 ° C and less than 410 ° C,
- step b Hydrotreatment of at least part of said intermediate fraction, then passage (step d) of at least part of the hydrotreated fraction over an amorphous hydroisomerization / hydrocracking catalyst.
- step f Passage (step f) of at least part of said heavy fraction over an amorphous hydrocracking / hydroisomerization catalyst with a conversion of products 370 ° C + to products 370 ° C greater than 80% by weight. 4. Distillation (steps e and g) of at least part of the hydrocracked / hydroisomeric fractions to obtain middle distillates.
- the paraffinic effluent from the Fischer-Tropsch synthesis unit is fractionated into at least three fractions:
- a light fraction comprising the compounds having boiling points below a temperature T1 of between 120 and 200 ° C, and preferably between 130 and 180 ° C and for example around 150 ° C.
- the cutting point T1 is located between 120 and 200 ° C.
- An intermediate fraction comprising the compounds whose boiling points are between the cutting point T1, previously defined, and a temperature T2 greater than 300 ° C, even more preferably greater than 350 ° C and less than 410 ° C or better, at 370 ° C. -
- a so-called heavy fraction comprising the compounds having boiling points higher than the cutting point T2 previously defined.
- the intermediate and heavy fractions generally have paraffin contents of at least 50% by weight.
- At least part (and preferably all) of the intermediate fraction is brought into contact with a hydrotreating catalyst, in the presence of hydrogen.
- the water formed during the hydrotreatment step is eliminated at least in part and preferably entirely.
- At least part (and preferably all) of the effluent from step (c) or (b) is brought into contact, in the presence of hydrogen and a hydroisomerization / hydrocracking catalyst in order to to produce at least one medium distillate cut (kerosene, diesel and preferably kerosene and diesel cut).
- step (d) The effluent leaving step (d) is subjected to a separation step in a distillation train so as to separate the light products inevitably formed during step (d), for example gases (C ⁇ - C 4 ) and a petrol cut and also so as to distill at least one diesel cut and at least one kerosene cut. A part of these fractions can be recycled, jointly or separately, at the top of the hydroisomerization / hydrocracking reactor of step (d).
- Said heavy fraction is brought into contact, in the presence of hydrogen, with a hydrocracking / hydroisomerization catalyst in order to produce middle distillates (kerosene, diesel), the conversion of the products 370 ° C + to 370 ° C " being greater than 80% wt.
- step (f) The effluent leaving step (f) is subjected to a separation step in a distillation train so as to separate on the one hand the light products inevitably formed during step (f) for example the gas (CrC 4 ) and a petrol cut and also so as to distill at least one diesel cut and at least one kerosene cut, and also to distill the non-hydrocracked fraction whose compounds which constitute it have boiling points higher than those middle distillates (kerosene + diesel).
- This non-hydrocracked fraction generally has an initial boiling point of at least 350 ° C, preferably greater than 370 ° C.
- This fraction, called the residual fraction is advantageously recycled at the top of the hydroisomerization / hydrocracking reactor of step (f).
- the yields of middle distillates (kerosene + diesel) from process according to the invention are higher than those of the prior art, in particular because the kerosene cut (generally initial boiling point from 150 to 160 ° C - final boiling point from 260 to 280 C C) could be optimized (and even maximized compared to the prior art EP-635, 557), and moreover, without being to the detriment of the diesel cut.
- this kerosene cut unexpectedly exhibits excellent cold properties (freezing point for example).
- the catalytic performances (activity, selectivity) and / or the cycle time of the hydrotreatment and hydroisomerization / hydrocracking catalysts used in the process according to the invention could be improved.
- the effluent from the Fischer-Tropsch synthesis unit mainly contains paraffins but also contains olefins and oxygenated compounds such as alcohols. It also contains water, CO 2 , CO and unreacted hydrogen as well as light hydrocarbon compounds C1 to C4 in the form of gas.
- the effluent from the Fischer-Tropsch synthesis unit arriving via line (1) is fractionated in a fractionation zone (2) into at least three fractions:
- the cutting point is between 120 and 200 ° C.
- At least one intermediate fraction comprising the compounds whose boiling points are between the cutting point T1, previously defined, and a temperature T2 greater than 300 ° C, even more preferably greater than 350 ° C and less than 410 ° C or better than 370 ° C.
- line 5 at least one so-called heavy fraction (line 5) comprising the compounds having boiling points greater than the cutting point T2 previously defined.
- a cut between a boiling point T1 between 120-200 ° C and T2 greater than 300 ° C and less than 370 ° C is preferred.
- the 370 C cut is even more preferred, that is to say the heavy fraction is a 370 ° C + cut.
- Cutting at 370 ° C makes it possible to separate at least 90% by weight of the oxygenates and olefins, and most often at least 95% by weight.
- the heavy cut to be treated is then purified and elimination of heteroatoms or unsaturated by hydrotreating is then not necessary.
- Fractionation is obtained here by distillation, but it can be carried out in one or more stages and by other means than distillation.
- This fractionation can be carried out by methods well known to those skilled in the art such as flash, distillation, etc.
- the effluent from the Fischer-Tropsch synthesis unit will be subjected to a flash, a decantation to remove the water and a distillation in order to obtain at least the 2 fractions described above.
- the light fraction is not treated according to the process of the invention but can for example constitute a good charge for a petrochemical unit and more particularly for a steam cracker (installation 6 of steam cracking).
- Said intermediate fraction is admitted via line (4), in the presence of hydrogen supplied by the pipe (7), in a hydrotreatment zone (8) containing a hydrotreatment catalyst.
- the objective of this hydrotreatment is to reduce the content of olefinic and unsaturated compounds as well as to hydrotreat the oxygenated compounds (alcohols) present.
- the catalysts used in this step (b) are non-cracking or slightly cracking hydrotreating catalysts comprising at least one metal from group VIII and / or group VI of the periodic table.
- the catalyst comprises at least one metal from the group of metals formed by nickel, molybdenum, tungsten, cobalt, ruthenium, indium, palladium and platinum and comprising at least one support.
- the hydro-dehydrogenating function is preferably provided by at least one metal or compound of group VIII metal such as nickel and cobalt in particular. It is possible to use a combination of at least one metal or compound of group VI metal (in particular molybdenum or tungsten) and of at least one metal or compound of group VIII metal (especially cobalt and nickel) of the classification of the elements.
- the concentration of non-noble group VIII metal, when it is used, is 0.01-15% by weight relative to the finished catalyst.
- At least one element chosen from P, B, Si is deposited on the support.
- This catalyst may advantageously contain phosphorus; in fact, this compound brings two advantages to hydrotreatment catalysts: ease of preparation during, in particular, the impregnation of nickel and molybdenum solutions, and better hydrogenation activity.
- the concentration of phosphorus oxide P205 will be less than 15% by weight and preferably less than 10% by weight. It is also possible to use a catalyst containing boron and phosphorus, advantageously boron and phosphorus are promoter elements deposited on the support, and for example the catalyst according to patent EP-297,949.
- the sum of the amounts of boron and phosphorus, expressed respectively by weight of boron trioxide and phosphorus pentoxide, relative to the weight of support, is approximately 5 to 5% and the atomic ratio boron to phosphorus is approximately 1 : 1 to 2: 1 and at least 40% of the total pore volume of the finished catalyst is contained in pores with an average diameter greater than 13 nanometers.
- the quantity of group VI metal such as molybdenum or tungsten is such that the phosphorus-to-metal atomic ratio of group VIB metal is approximately 0.5: 1 to 1.5: 1; the amounts of group VIB metal and group VIII metal, such as nickel or cobalt, are such that the group VIII metal to group VIB metal atomic ratio is approximately 0.3: 1 to 0.7 1.
- the quantities of group VIB metal expressed by weight of metal relative to the weight of finished catalyst is approximately 2 to 30% and the quantity of group VIII metal expressed by weight of metal relative to the weight of finished catalyst is about 0.01 to 15%.
- Another particularly advantageous catalyst contains promoter silicon deposited on the support.
- An interesting catalyst contains BSi or PSi.
- Ni alumina, NiMo on alumina, NiMo on alumina doped with boron and phosphorus and NiMo on silica-alumina are also preferred.
- the metal content is between 0.05 and 3% by weight relative to the finished catalyst and preferably between 0.1 and 2% by weight of the catalyst.
- These metals are deposited on a support which is preferably an alumina, but which can also be boron oxide, magnesia, zirconia, titanium oxide, clay or a combination of these oxides.
- a support which is preferably an alumina, but which can also be boron oxide, magnesia, zirconia, titanium oxide, clay or a combination of these oxides.
- These catalysts can be prepared by all the methods known to those skilled in the art or else can be acquired from companies specializing in the manufacture and sale of catalysts.
- the charge is brought into contact in the presence of hydrogen and of the catalyst at operating temperatures and pressures making it possible to carry out the hydrodeoxygenation (HDO) of the alcohols and the hydrogenation of the olefins present in load.
- the reaction temperatures used in the hydrotreatment reactor are between 100 and 350, preferably between 150 and 300 ° C, even more preferably between 150 and 275 ° C and better still between 175 and 250 ° C.
- the total pressure range used varies from 5 to 150 bars, preferably between 10 and 100 bars and even more preferably between 10 and 90 bars.
- the hydrogen which feeds the hydrotreatment reactor is introduced at a rate such that the hydrogen / hydrocarbon volume ratio is between 100 to 3000 Nl / l / h, preferably between 100 and 2000NI / l / h and even more preferred between 250 and 1500 Nl / l / h.
- the charge flow rate is such that the hourly volume speed is between 0.1 and 10h "1 , preferably between 0.2 and 5h " 1 and even more preferably between 0.2 and 3h "1. Under these conditions , the content of unsaturated and oxygenated molecules is reduced to less than 0.5% and to approximately less than 0.1% in general.
- the hydrotreatment step is carried out under conditions such as the conversion into products having dots 'Boiling greater than or equal to 370 ° C in products having boiling points less than 370 ° C is limited to 30% by weight, preferably is less than 20% and even more preferably is less than 10%.
- the effluent from the hydrotreatment reactor is optionally introduced into a water removal zone (9) which aims to remove at least part of the water produced during the hydrotreatment reactions.
- This elimination of water can be carried out with or without elimination of the gaseous fraction C less which is generally produced during the hydrotreatment step.
- elimination of water is understood the elimination of the water produced by the hydrodeoxygenation (HDO) reactions of the alcohols, but it can also include the elimination at least in part of the water saturated with hydrocarbons.
- Water removal can be achieved by all the methods and techniques known to those skilled in the art, for example by drying, passing over a desiccant, flash, decanting, etc.
- the fraction thus optionally dried is then introduced (line 10), as well as possibly a stream of hydrogen, (line 11) in the zone (12) containing the hydroisomerization / hydrocracking catalyst.
- Another possibility of the process also according to the invention consists in sending all the effluent leaving the hydrotreatment reactor (without drying) into the reactor containing the amorphous hydroisomerization / hydrocracking catalyst and preferably at the same time as 'a stream of hydrogen.
- the pressure is maintained between 2 and 150 bars and preferably between 5 and 100 bars and advantageously from 10 to 90 bars, the space speed is between 0.1 h “1 and 10 h “ 1 and preferably between 0.2 and 7h '1 is advantageously between 0.5 and 5.0h "1.
- the hydrogen rate is between 100 and 2000 Normal liters of hydrogen per liter of charge and per hour and preferably between 150 and 1500 liters of hydrogen per liter of charge.
- the temperature used in this step is between 200 and 450 ° C and preferably from 250 ° C to 450 ° C advantageously from 300 to 450 ° C, and even more advantageously above 320 C C or for example between 320-420 ° C .
- the two stages, hydrotreating and hydroisomerization-hydrocracking, can be carried out on the two types of catalyst in two or more different reactors, or / and in the same reactor.
- step (d) of hydroisomerization and hydrocracking is carried out under conditions such as pass conversion to point products.
- boiling point greater than or equal to 150 ° C. in products having boiling points below 150 ° C. is as low as possible, preferably less than 50%, even more preferably less than 30%, and allows d '' obtain middle distillates (diesel and kerosene) having cold properties (pour point and freezing point) good enough to meet the specifications in force for this type of fuel.
- step (d) it is sought to favor hydroisomerization rather than hydrocracking.
- Said heavy fraction is introduced via the line (5) into a zone (13) where it is brought into contact, in the presence of hydrogen (26).
- an amorphous hydroisomerization / hydrocracking catalyst in order to produce a middle distillate cut (kerosene + diesel) having good cold properties.
- the catalyst used in zone (13) of step (f) to carry out the hydrocracking and hydroisomerization reactions of the heavy fraction, defined according to the invention, is of the same type as that present in the reactor (12 ). However, it should be noted that the catalysts used in the reactors (12) and (13) may be the same or different.
- the fraction entering the reactor undergoes, in contact with the catalyst and in the presence of hydrogen, essentially hydrocracking reactions which, accompanied by hydroisomerization reactions of n-paraffins, will make it possible to improve the quality of the products formed and more particularly the cold properties of kerosene and diesel, and also to obtain very good distillate yields.
- the conversion into products with boiling points greater than or equal to 370 ° C. into products with boiling points less than 370 ° C. is greater than 80% by weight, often at least 85% and preferably greater than or equal to 88%.
- conversions of products with a boiling point greater than or equal to 260 ° C into products with a boiling point below 260 ° C is at most 90% by weight, generally at most 70% or 80%, and preferably at most 60% by weight.
- step (f) we will therefore seek to promote hydrocracking, but preferably by limiting the cracking of diesel.
- the choice of operating conditions makes it possible to finely adjust the quality of the products (diesel, kerosene) and in particular the cold properties of kerosene, while retaining a good yield of diesel and / or kerosene.
- the process according to the invention makes it entirely advantageous to produce both kerosene and diesel and which are of good quality.
- step (d) is sent to a distillation train, which incorporates atmospheric distillation and possibly vacuum distillation, and which aims to separate light products on the one hand inevitably formed during step (d) for example the gases (C 1 -C 4 ) (line 14) and a gasoline cut (line 19), and to distill at least one gas oil (line 17) and kerosene cut (line 16) ).
- the diesel and kerosene fractions can be partially recycled (line 25), jointly or separately, at the top of the hydroisomerization / hydrocracking reactor step (d).
- the effluent leaving step (f) is subjected to a separation step in a distillation train so as to separate on the one hand the light products inevitably formed during step (f), for example gases (CC 4 ) (line 18) and a gasoline cut (line 19), to distill a diesel cut (line 21) and kerosene (line 20) and to distill the fraction (line 22) boiling over diesel, it that is to say, the compounds which constitute it have higher boiling points than those of middle distillates (kerosene + diesel).
- This fraction, called the residual fraction generally has an initial boiling point of at least
- step (f) It may also be advantageous to recycle part of the kerosene and / or diesel in step (d), step (f) or both. Preferably, at least one of the kerosene and / or diesel fractions is partially recycled (line 25) in step (d) (zone 12). We have seen that it is advantageous to recycle part of the kerosene to improve its cold properties.
- the non-hydrocracked fraction is partially recycled in step (f) (zone 13).
- the diesel fuel (s) obtained has a pour point of at most 0 ° C, generally less than -10 ° C and often less than -15 ° C.
- the cetane number is greater than 60, generally greater than 65, often greater than 70.
- the kerosene (s) obtained have a freezing point of at most -35 ° C., generally less than - 40 ° C.
- the smoke point is more than 25 mm, generally more than 30 mm. In this process, the production of gasoline (not sought) is as low as possible. Fuel efficiency will always be
- the invention also relates to a plant for the production of middle distillates comprising: at least one zone (2) for fractionating the charge coming from a Fischer-Tropsch synthesis unit having: - at least one tube (1) for the introduction of the load,
- At least one hydrotreatment zone (8) provided with an inlet pipe for at least part of said intermediate fraction followed by at least one zone (12) containing a hydrocracking / hydroisomerization catalyst provided with a pipe for the introduction of at least part of said hydrotreated fraction,
- At least one distillation column (23, 24) provided with at least one tube for the introduction of at least part of the hydrocracked fractions and at least one tube (16, 17, 20, 21) for the exit of the middle distillates.
- it comprises a tube (23) for recycling part of at least one of the kerosene, diesel fractions obtained at the outlet of the column (s) (23, 24) for distilling the fractions hydrocracked, to at least one of the zones (12, 13) containing a hydrocracking / hydroisomerization catalyst.
- the catalysts can be the same or different.
- they will be chosen from the preferred catalysts described below.
- the majority of the catalysts currently used in hydroisomerization / hydrocracking are of the bifunctional type combining an acid function with a hydrogenating function.
- the acid function is provided by
- the hydrogenating function is provided either by one or more metals from group VIII of the periodic table of elements, such as iron, cobalt, nickel, ruthenium, rhodium, palladium, osmium, iridium and platinum, or by a combination of at least one group VI metal such as chromium, molybdenum and tungsten and at least one group VIII metal.
- group VIII of the periodic table of elements such as iron, cobalt, nickel, ruthenium, rhodium, palladium, osmium, iridium and platinum, or by a combination of at least one group VI metal such as chromium, molybdenum and tungsten and at least one group VIII metal.
- the balance between the two acid and hydrogenating functions is the fundamental parameter which governs the activity and the selectivity of the catalyst.
- a weak acid function and a strong hydrogenating function give catalysts which are not very active and selective towards isomerization whereas a strong acid function and a weak hydrogenating function give very active and selective catalysts towards cracking.
- a third possibility is to use a strong acid function and a strong hydrogenating function in order to obtain a very active catalyst but also very selective towards isomerization. It is therefore possible, by judiciously choosing each of the functions, to adjust the activity / selectivity pair of the catalyst.
- the hydroisomerization-hydrocracking catalysts are bifunctional catalysts comprising an amorphous acid support (preferably a silica-alumina) and a hydro-dehydrogenating metal function provided by at least one noble metal.
- the support is said to be amorphous, that is to say devoid of molecular sieves, and in particular of zeolite, as well as the catalyst.
- the amorphous acid support is advantageously a silica-alumina but other supports can be used.
- the catalyst preferably does not contain any added halogen, other than that which could be introduced for the impregnation, of the noble metal for example. More generally and preferably, the catalyst does not contain any added halogen, for example fluorine.
- the support has not been impregnated with a silicon compound.
- a catalyst is used comprising a particular silica-alumina which makes it possible to obtain catalysts which are very active but also very selective in the isomerization of effluents from Fischer synthesis units. Tropsch.
- the preferred catalyst comprises (and preferably consists essentially of) 0.05-10% by weight of at least one noble metal from group VIII deposited on an amorphous silica-alumina support (which preferably contains between 5 and 70% by weight of silica) which has a BET specific surface of 100-500m 2 / g and the catalyst has:
- a pore volume of the pores whose diameter is between the mean diameter as defined previously decreased by 3 nm and the mean diameter as defined previously increased by 3 nm is greater than ⁇ 0% of the total pore volume
- the preferred support used for the preparation of the catalyst is composed of silica SiO 2 and alumina AI 2 O 3 .
- the silica content of the support is generally between 1 and 95%, advantageously even between 5 and 95% and preferably between 10 and 80% and even more preferably between 20 and 70% and between 22 and 45%. This silica content is perfectly measured using X-ray fluorescence.
- the metallic function is provided by a noble metal from group VIII of the periodic table of the elements and more particularly platinum and / or palladium.
- the noble metal content is between 0.05 to 10 and more preferably between 0.1 and 5.
- the dispersion representing the fraction of metal accessible to the reagent relative to the total amount of metal in the catalyst, can be measured, for example, by H ⁇ / O tit titration.
- the metal is reduced beforehand, that is to say it undergoes treatment under a stream of hydrogen at high temperature under conditions such that all of the platinum atoms accessible to hydrogen are transformed into metallic form. Then, a flow of oxygen is sent under suitable operating conditions so that all of the reduced platinum atoms accessible to oxygen are oxidized in PtO 2 form.
- the dispersion is then equal to the ratio of the quantity of platinum accessible to oxygen to the total quantity of platinum in the catalyst. In our case, the dispersion is between 20% and 100% and preferably between 30% and 100%.
- the distribution of the noble metal represents the distribution of the metal inside the catalyst grain, the metal being able to be well or badly dispersed.
- platinum for example detected in a crown whose thickness is much less than the radius of the grain
- all the platinum atoms, located in crown will be accessible to reagents.
- the distribution of platinum is good, that is to say that the profile of platinum, measured according to the Castaing microprobe method, has a distribution coefficient greater than 0.1 and preferably greater than 0.2.
- the BET surface of the support is between 100 m 2 / g and 500 m 2 / g and preferably between 250 m 2 / g and 450m 2 / g and for supports based on silica-alumina, even more preferably between 310 m 2 / g and 450 m / g.
- the average pore diameter of the catalyst is measured from the porous distribution profile obtained using a mercury porosimeter.
- the average pore diameter is defined as being the diameter corresponding to the cancellation of the derivative curve obtained from the mercury porosity curve.
- the average pore diameter, thus defined is between 1 nm (1x10 "9 meters) and 12 nm (12x10 " 9 meters) and preferably between 1 nm (1x10 '9 meters) and 11 nm (11x10 ' 9 meters) ) and again more preferred between 3 nm (4x10 '9 meters) and 10.5 nm (10.5x10 ' 9 meters).
- the preferred catalyst has a porous distribution such that the pore volume of the pores whose diameter is between the mean diameter as defined previously decreased by 3 nm and the mean diameter as defined previously increased by 3 nm (ie the mean diameter ⁇ 3 nm) is greater than 40% of the total pore volume and preferably between 50% and 90% of the total pore volume and more advantageously still between 50% and 70% of the total pore volume.
- the preferred catalyst based on silica-alumina it is generally less than 1.0 ml / g and preferably between 0.3 and 0.9 ml / g and even more advantageously less than 0.85 ml / g.
- the preparation and the shaping of the support, and in particular of the silica-alumina (in particular used in the preferred embodiment) is done by usual methods well known to those skilled in the art.
- the support may undergo calcination such as for example a heat treatment at 300-750 ° C (600 ° C preferred) for 0.25-10 hours (2 hours preferred) under 0 -30% water vapor volume (for 7.5% alumina silica preferred).
- the noble metal salt is introduced by one of the usual methods used to deposit the metal (preferably platinum and / or palladium, platinum being more preferred) on the surface of a support.
- One of the preferred methods is dry impregnation which consists in introducing the metal salt into a volume of solution which is equal to the pore volume of the mass of catalyst to be impregnated.
- the catalyst may undergo calcination, for example a treatment in dry air at 300-750 ° C (520 ° C preferred) for 0.25-10 hours (2 hours preferred).
- the bifunctional catalyst comprises at least one noble metal deposited on an amorphous acid support, the dispersion in noble metal being less than 20%.
- the fraction of the noble metal particles having a size less than 2 nm represents at most 2% by weight of the noble metal deposited on the catalyst.
- noble metal particles have a size greater than 4 nm (% number).
- the support is amorphous, it does not contain a molecular sieve; the catalyst also does not contain a molecular sieve.
- the amorphous acid support is generally chosen from the group formed by a silica-alumina, a halogenated alumina (preferably fluorinated), an alumina doped with silicon (deposited silicon), an alumina titanium oxide mixture, a sulfated zirconia, a doped zirconia with tungsten, and their mixtures with each other or with at least one amorphous matrix chosen from the group formed by alumina, titanium oxide, silica, boron oxide, magnesia, zirconia, clay by example.
- the support consists of an amorphous alumina silica.
- a preferred catalyst comprises (preferably essentially consists of) 0.05 to 10% by weight of at least one noble metal from group VIII deposited on an amorphous support of silica-alumina.
- the preferred support used for the preparation of the catalyst is composed of silica Si0 2 and alumina Al 2 0 3 from the synthesis.
- the silica content of the support is generally between 1 and 95%, advantageously between 5 and 95% and preferably between 10 and 80% and even more preferably between 20 and 70% or even between 22 and 45%. This content is perfectly measured using X-ray fluorescence.
- the metallic function is provided by at least one noble metal from group VIII of the periodic table of the elements and more particularly platinum and / or palladium.
- the noble metal content expressed in% by weight of metal relative to the catalyst, is between 0.05 to 10 and more preferably between 0.1 and 5.
- the dispersion (measured in the same way as above) is less than 20%, they are generally greater than 1% or better than 5%.
- the catalyst sample is finely ground in an agate mortar and then it is dispersed in ethanol by ultrasound. Samples at different locations to ensure good size representativeness are taken and deposited on a copper grid covered with a thin carbon film. The grids are then air-dried under an infrared lamp before being introduced into the microscope for observation.
- the average size of the noble metal particles several hundred measurements are made from several tens of photographs. All of these measurements make it possible to produce a histogram of particle size distribution. Thus, we can accurately estimate the proportion of particles corresponding to each particle size range.
- the distribution of platinum is good, that is to say that the profile of platinum, measured according to the Castaing microprobe method, has a distribution coefficient greater than 0.1, advantageously greater than 0.2 and preferably greater than 0.5.
- the BET surface of the support is generally between 100 m 2 / g and 500 m 2 / g and preferably between 250 m / g and 450 m 2 / g and for supports based on silica alumina, even more preferably between 310 m 2 / g.
- the preparation and the shaping of the silica-alumina and of any support in general is done by usual methods well known to those skilled in the art.
- the support may undergo calcination such as for example a heat treatment at 300-750 ° C (600 ° C preferred) for a period of between 0.25 and 10 hours (2 hours preferred) under 0-30% water vapor volume (about 7.5% preferred for silica-alumina).
- the metal salt is introduced by one of the usual methods used to deposit the metal (preferably platinum) on the surface of a support.
- One of the preferred methods is dry impregnation which consists in introducing the metal salt into a volume of solution which is equal to the pore volume of the mass of catalyst to be impregnated.
- the catalyst undergoes calcination in humidified air at 300-750 ° C (550 ° C preferred) for 0.25-10 hours (2 hours preferred).
- the partial pressure of H2O during calcination is for example 0.05 bar to 0.50 bar (0.15 bar preferred).
- Other known treatment methods making it possible to obtain the dispersion of less than 20% are suitable in the context of the invention.
- Another preferred catalyst for the invention comprises at least one hydro-dehydrogenating element (preferably deposited on the support) and a support comprising (or preferably consisting of) at least one silica-alumina, said silica-alumina having the following characteristics : a content by weight of silica SiO 2 of between 10 and 60% preferably between 20 and 60% and even more preferably between 20 and 50% by weight or
- the porosity of said silica-alumina being as follows:
- the volume of the mesopores whose diameter is between 40 ⁇ and 150 ⁇ , and whose average diameter varies between 80 and 120 ⁇ represents between 30 and 80% of the total pore volume previously defined and preferably between 40 and 70%.
- the volume of macropores the diameter of which is greater than 500 ⁇ , and preferably between 1000 ⁇ and 10,000 ⁇ represents between 20 and 80% of the total pore volume and preferably between 30 and 60% of the total pore volume and way even more preferred the volume of the macropores represents at least 35% of the total pore volume.
- the diffractograms of the silica-aluminas of the invention correspond to a mixture of the silica and the alumina with a certain evolution between the gamma alumina and the silica as a function of the Si0 2 content. some samples. In these silica-aluminas an alumina is observed which is less well crystallized compared to the alumina alone.
- the 27 AI NMR spectra of the silica-aluminas show two distinct peak masses. Each massif can be broken down into at least two species. We observe a large dominance of species whose maximum resonates around 10 ppm and which extends between 10 and 60 ppm. The position of the maximum suggests that these species are essentially of the AI V ⁇ (octahedral) type. On all the spectra we observe a second type of species which resonates around 80-110 ppm. These species would correspond to the atoms of AI
- the silicon silica-alumina environment studied by 29 Si NMR shows the chemical shifts of the different silicon species such as Q 4 (-105ppm to - 120 ppm), Q 3 (-90ppm to -102 ppm) and Q 2 (-75ppm to - 93 ppm).
- the sites with a chemical shift at -102 ppm can be sites of type Q 3 or Q 4 , we call them in this work sites Q 3 "4.
- the silica-aluminas of the invention are composed of silicon of types Q 2 , Q 3 , Q 3 "4 and Q 4 . Many species are said to be Q 2 , approximately in the range of 30 to 50%. The proportion of species Q 3 is also significant, approximately of the order of 10 to 30%.
- sites Q 4 If linked to 4Si (or Al) sites
- Q 3 If linked to 3 Si (or Al) and 1 OH sites
- Q ⁇ If linked to 2 Si (or Al) and 2 OH;
- the homogeneity of the supports was evaluated by Transmission Electron Microscopy. We seek by this method to verify the homogeneity of the distribution of Si and Al on the nanometric scale. The analyzes are carried out on ultra-thin sections of the supports, using different size probes, 50nm or 15nm. For each solid studied, 32 spectra are recorded, including 16 with 50nm probe and 16 with 15nm probe.
- Si / Ai atomic ratios are then calculated, with the means of the ratios, the minimum ratio, the maximum ratio and the standard deviation of the series.
- the average of the Si / Ai ratios measured by Transmission Electron Microscopy for the different silica-aluminas are close to the Si / Ai ratio obtained by
- Fluorescence X The homogeneity criterion is evaluated on the value of the standard deviation.
- silica-aluminas of the present invention can be considered to be heterogeneous since they have atomic Si / Ai ratios with standard deviations of the order of 30-40%.
- the support can consist of pure silica-alumina or results from the mixture with said silica-alumina of a binder such as silica (Si0 2 ), alumina (Al 2 0 3 ), clays, titanium oxide (TiO 2 ), boron oxide (B 2 0 3 ) and zirconia (ZrO 2 ) and any mixture of the above-mentioned binders.
- a binder such as silica (Si0 2 ), alumina (Al 2 0 3 ), clays, titanium oxide (TiO 2 ), boron oxide (B 2 0 3 ) and zirconia (ZrO 2 ) and any mixture of the above-mentioned binders.
- the preferred binders are silica and alumina and even more preferably alumina in all of these forms known to those skilled in the art, for example gamma alumina.
- the content by weight of binder in the catalyst support is between 0 and 40%, more particularly
- the support can be prepared by shaping the silica-alumina in the presence or absence of a binder by any technique known to those skilled in the art.
- the shaping can be carried out, for example, by extrusion, by tableting, by the oil-drop coagulation method, by granulation on a turntable or by any other method well known to those skilled in the art.
- At least one calcination can be carried out after any of the stages of the preparation, it is usually carried out in air at a temperature of at least 150 ° C, preferably at least 300 ° C.
- the catalyst is a bifunctional catalyst in which a noble metal is supported by a support essentially consisting of an amorphous and micro / mesoporous silica-alumina gel with a pore size controlled, having an area of at least 500 m / g and a SiO 2 / AI 2 O 3 molar ratio of between 30/1 and 500/1, preferably between 40/1 and 150/1.
- the noble metal supported on the support can be chosen from the metals of groups 8, 9 and 10 of the periodic table, in particular Co, Ni, Pd and Pt. Palladium and platinum are preferably used.
- the proportion of noble metals is normally between 0.05 and 5.0% by weight relative to the weight of the support. Particularly advantageous results have been obtained using palladium and platinum in proportions of between 0.2 and 1.0% by weight.
- Said support is generally obtained from a mixture of tetraalkylated ammonium hydroxide, an aluminum compound which can be hydrolyzed to Al 2 0 3 , a silicon compound which can be hydrolyzed to SiO 2 and a sufficient amount of water to dissolve and hydrolyze these compounds, said tetraalkylated ammonium hydroxide having 2 to 6 carbon atoms in each alkyl residue, said hydrolyzable aluminum compound preferably being a trialkoxide of aluminum having 2 to 4 carbon atoms in each alkoxide residue and said hydrolyzable silicon compound being a tetraalkylorthosilicate having 1 to 5 carbon atoms for each alkyl residue.
- the tetraalkylated ammonium hydroxide which can be used in the context of the present invention is for example chosen from hydroxides of tetraethylammonium, propylammonium, isopropylammonium, butylammonium, isobutylammonium, terbutylammonium and pentylammonium, and preferably among the hydroxides of tetrapropylammonium, tetra-isopropylammonium and tetrabutyl-ammonium.
- the aluminum trialkoxide is for example chosen from triethoxide, propoxide, isopropoxide, butoxide, isobutoxide and aluminum terbutoxide, preferably from tripropoxide and aluminum tri-isopropoxide.
- the tetra-alkylated orthosilicate is chosen for example from tetramethyl-, tetraethyl-, propyl-, isopropyl-, butyl-, isobutyl-, terbutyl- and pentyl-orthosilicate, tetraethyl- orthosilicate being used preferably.
- an aqueous solution containing the tetraalkylated ammonium hydroxide and the aluminum trialkoxide is first prepared at a temperature sufficient to guarantee effective dissolution of the aluminum compound.
- the tetraalkylated orthosilicate is added to said aqueous solution.
- This mixture is brought to a temperature suitable for activating the hydrolysis reaction. This temperature depends on the composition of the reaction mixture (generally from 70 to 100 ° C).
- the hydrolysis reaction is exothermic, which guarantees a self-sustaining reaction after activation.
- the proportions of the constituents of the mixture are such that they respect the following molar ratios: Si0 2 / Al 2 O 3 from 30/1 to 500/1, tetraalkylated ammonium hydroxide / Si0 2 from 0.05 / 1 to 0.2 / 1, and H 2 0 / Si0 2 from 5/1 to 40/1.
- the preferred values for these molar ratios are as follows: Si ⁇ 2 / AI 2 0 3 from 40/1 to 150/1, tetraalkylated ammonium hydroxide / SiO 2 from 0.05 / 1 to 0.2 / 1, and H 2 O / SiO 2 from 10/1 to 25/1.
- the hydrolysis of the reagents and their gelation are carried out at a temperature equal to or higher than the boiling point, at atmospheric pressure, of any alcohol developed in the form of by-product of said hydrolysis reaction, without elimination or significant elimination. of these alcohols from the reaction medium.
- the hydrolysis and gelation temperature is therefore critical and is appropriately maintained at values above about 65 ° C, in the range of about 110 ° C.
- the hydrolysis and the gelling are carried out in the presence of an amount of alcohol greater than that developed in the form of by-product.
- a free alcohol preferably ethanol, is added to the reaction mixture in a proportion which can range up to a maximum molar ratio of added alcohol / Si0 2 of 8/1.
- the time required to carry out the hydrolysis and gelling under the conditions indicated above is normally between 10 minutes and 3 hours, preferably between 1 and 2 hours.
- the alcohol is finally extracted from the gel which is then dried, preferably under reduced pressure (from 3 to 6 kPa for example), at a temperature of 110 ° C.
- the dried gel is then subjected to a calcination process under an oxidizing atmosphere (normally in air), at a temperature between 500 and 700 ° C for 4 to 20 hours, preferably at 500-600 ° C for 6 to 10 hours.
- the silica and alumina gel thus obtained has a composition which corresponds to that of the reactants used, if one considers that the reaction yields are practically complete.
- the SiO 2 / AI 2 O 3 molar ratio is therefore between 30/1 and 500/1, preferably between 40/1 and 150/1, the preferred values being of the order of 100/1.
- This gel is amorphous, when subjected to an X-ray powder diffraction analysis, it has an area of at least 500 m 2 / g, generally between 600 and 850 m 2 / g, and a pore volume of 0.4 to 0.8 cm 3 / g.
- a metal chosen from the noble metals of groups 8, 9 or 10 of the periodic table is supported on the micro / mesoporous amorphous silica-alumina gel obtained as described above. As indicated above, this metal is preferably chosen from platinum or palladium, platinum being preferably used.
- the proportion of noble metal, in particular platinum, within the catalyst thus supported is between 0.4 and 0.8%, preferably between 0.6 and 0.8% by weight relative to the weight of the support.
- the porous support having the characteristics of the acid support (a) described above is brought into contact with an aqueous or alcohol solution of a compound of the desired metal for a sufficient time to allow a homogeneous distribution of the metal in the solid. This operation normally requires a few minutes to several hours, preferably with stirring.
- H 2 PtF 6 , H 2 PtCI 6 , [Pt (NH 3 )] CI 2 , [Pt (NH 3 ) 4 ] (OH) 2 constitute, for example, soluble salts suitable for this purpose, as well as analogous palladium salts ; mixtures of salts of different metals are also used in the context of the invention. It is advantageous to use the minimum quantity of aqueous liquid (usually water or an aqueous mixture with a second inert liquid or with an acid in a proportion of less than 50% by weight) necessary to dissolve the salt and to impregnate uniformly said support, preferably with a solution / support ratio of between 1 and 3. The amount of metal used is chosen according to the desired concentration in the catalyst, all of the metal being fixed on the support.
- the solution is evaporated and the solid obtained is dried and calcined under an inert or reducing atmosphere, under temperature and time conditions similar to those previously described for the calcination of the support.
- Another method of impregnation is carried out by means of an ion exchange.
- the support consisting of amorphous silica-alumina gel is brought into contact with an aqueous solution of a salt of the metal used, as in the previous case, but the deposition is carried out by ion exchange, under conditions made basic (pH between 8.5 and 11) by the addition of a sufficient amount of an alkaline compound, usually an ammonium hydroxide.
- the suspended solid is then separated from the liquid by filtration or decantation, then dried and calcined as described above.
- the salt of the transition metal can be included in the silica-alumina gel during the preparation phase, for example before hydrolysis for the formation of the wet gel, or before its calcination.
- the latter method is advantageously easier to implement, the catalyst thus obtained is slightly less active and selective than that obtained with the two previous methods.
- the supported catalyst described above can be used as it is during the hydrocracking step of the process according to the present invention, after activation according to one of the known methods and / or described below.
- said supported catalyst is reinforced by the addition with mixing of an appropriate amount of an inert mineral solid capable of improving its mechanical properties.
- the catalyst is preferably used in granular form rather than in powder form with a relatively tight particle distribution.
- Extrusion and shaping methods are also known which use a suitable inert additive (or binder) capable of providing the properties mentioned above, for example, according to the methods described in European patent applications EP-A 550.922 and EP-A 665.055, the latter preferably being implemented, their content being mentioned here for reference.
- a suitable inert additive or binder
- a typical method for preparing the catalyst in extruded form comprises the following steps: (a) the solution of hydrolysable components obtained as described above is heated to cause hydrolysis and gelling of said solution and for obtain a mixture A having a viscosity of between 0.01 and 100 Pa.sec;
- a binder belonging to the group of bohemites or pseudobohemites is first added to mixture A, in a weight ratio with mixture A of between 0.05 and 0.5, then a mineral or organic acid is added in a proportion between 0.5 and 8.0 g per 100 g of binder;
- Plasticizers such as methylcellulose are also preferably added during step (b) in order to promote the formation of a homogeneous mixture which is easy to process.
- a granular acid support comprising from 30 to 70% by weight of inert mineral binder is thus obtained, the remaining proportion consisting of amorphous silica-alumina having essentially the same characteristics of porosity, surface and structure as those described above for the same gel without binder.
- the granules are advantageously in the form of pellets about 2-5 mm in diameter and 2-10 mm long.
- the step of depositing the noble metal on the granular acid support is then carried out according to the same procedure as that described above.
- the metal contained in the catalyst must be reduced.
- One of the preferred methods for carrying out the reduction of the metal is the treatment under hydrogen at a temperature between 150 ° C and 650 ° C and a total pressure between 0.1 and 25 Mpa.
- a reduction consists of a plateau at 150 ° C for 2 hours and then a temperature rise up to 450 C C at a rate of 1 ° C / min and then a stage of 2 hours at 450 ° C; during this entire reduction step, the hydrogen flow rate is 1000 l hydrogen / l catalyst.
- any in situ or ex situ reduction method is suitable.
- a typical method implements the procedure described below:
- the pressure within the reactor is maintained between 30 and 80 atm.
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Abstract
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FR0108971 | 2001-07-06 | ||
FR0108971A FR2826973B1 (fr) | 2001-07-06 | 2001-07-06 | Procede de production de distillats moyens par hydroisomerisation et hydrocraquage de 2 fractions issues de charges provenant du procede fischer-tropsch |
PCT/FR2002/002207 WO2003004584A1 (fr) | 2001-07-06 | 2002-06-26 | Procede de production de distillats moyens par hydroisomerisation et hydrocraquage de 2 fractions issues de charges provenant du procede fischer-tropsch |
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FR2826972B1 (fr) * | 2001-07-06 | 2007-03-23 | Inst Francais Du Petrole | Procede de production de distillats moyens par hydroisomerisation et hydrocraquage d'une fraction lourde issue d'un effluent produit par le procede fischer-tropsch |
FR2826971B1 (fr) * | 2001-07-06 | 2003-09-26 | Inst Francais Du Petrole | Procede de production de distillats moyens par hydroisomerisation et hydrocraquage de charges issues du procede fischer-tropsch |
US6949180B2 (en) * | 2002-10-09 | 2005-09-27 | Chevron U.S.A. Inc. | Low toxicity Fischer-Tropsch derived fuel and process for making same |
NL1026215C2 (nl) * | 2003-05-19 | 2005-07-08 | Sasol Tech Pty Ltd | Koolwaterstofsamenstelling voor gebruik in CI motoren. |
US7354507B2 (en) * | 2004-03-17 | 2008-04-08 | Conocophillips Company | Hydroprocessing methods and apparatus for use in the preparation of liquid hydrocarbons |
US7323100B2 (en) * | 2004-07-16 | 2008-01-29 | Conocophillips Company | Combination of amorphous materials for hydrocracking catalysts |
US20080194901A1 (en) * | 2004-12-23 | 2008-08-14 | Michiel Cramwinckel | Process To Prepare Two Iso Paraffinic Products From A Fischer-Tropsch Derived Feed |
FR2888584B1 (fr) * | 2005-07-18 | 2010-12-10 | Inst Francais Du Petrole | Procede de production de distillats moyens par hydroisomerisation et hydrocraquage de charges issues du procede fischer-tropsch utilisant un lit de garde multifonctionnel |
DE102005035988B4 (de) * | 2005-07-28 | 2009-01-02 | Wolf, Bodo Max, Dr.-Ing. | Verfahren zur Erzeugung von flüssigen Kohlenwasserstoffen aus Gas |
US7776207B2 (en) * | 2006-10-05 | 2010-08-17 | Syntroleum Corporation | Process to produce middle distillate |
US20100108568A1 (en) * | 2007-04-10 | 2010-05-06 | Sasol Technology (Pty) Ltd | Fischer-tropsch jet fuel process |
US20080260631A1 (en) | 2007-04-18 | 2008-10-23 | H2Gen Innovations, Inc. | Hydrogen production process |
FR2917419B1 (fr) | 2007-06-12 | 2014-10-24 | Inst Francais Du Petrole | Procede de production de distillats moyens par hydroisomerisation et hydrocraquage d'une fraction lourde issue d'un effluent fischer-tropsch |
EP2188352A1 (fr) | 2007-09-10 | 2010-05-26 | Shell Internationale Research Maatschappij B.V. | Procede d'hydrocraquage et d'hydroisomerisation d'une charge de depart paraffinique |
FR2934794B1 (fr) * | 2008-08-08 | 2010-10-22 | Inst Francais Du Petrole | Procede de production de distillats moyens par hydrocraquage de charges issues du procede fischer-trospch en presence d'un catalyseur comprenant un solide izm-2 |
KR102321624B1 (ko) * | 2014-05-23 | 2021-11-04 | 에스케이이노베이션 주식회사 | 디젤 수율을 극대화할 수 있는 rfcc 공정용 접촉분해촉매 및 이의 제조방법 |
US10472581B2 (en) * | 2016-06-30 | 2019-11-12 | Uop Llc | Process and apparatus for hydrocracking and hydroisomerizing a hydrocarbon stream |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2617412B1 (fr) * | 1987-07-01 | 1993-05-14 | Inst Francais Du Petrole | Catalyseur comprenant un support mineral, du phosphore et du bore, methodes de preparation et utilisation en hydroraffinage de coupes petrolieres |
US4832819A (en) * | 1987-12-18 | 1989-05-23 | Exxon Research And Engineering Company | Process for the hydroisomerization and hydrocracking of Fisher-Tropsch waxes to produce a syncrude and upgraded hydrocarbon products |
US4919786A (en) * | 1987-12-18 | 1990-04-24 | Exxon Research And Engineering Company | Process for the hydroisomerization of was to produce middle distillate products (OP-3403) |
GB9119505D0 (en) * | 1991-09-12 | 1991-10-23 | Shell Int Research | Process for the preparation of middle distillates |
ES2110051T5 (es) * | 1992-08-18 | 2002-10-01 | Shell Int Research | Procedimiento de preparacion de combustibles hidrocarbonados. |
CA2104044C (fr) * | 1992-08-25 | 2004-11-02 | Johan W. Gosselink | Procede pour la preparation d'olefines inferieures |
US5378348A (en) * | 1993-07-22 | 1995-01-03 | Exxon Research And Engineering Company | Distillate fuel production from Fischer-Tropsch wax |
DE69711348T2 (de) * | 1996-12-17 | 2002-10-24 | Inst Francais Du Petrol | Bor und Silicium enthaltender Katalysator und Anwendung dieses in der Hydrobehandlung von Kohlenwasserstoffeinsätzen |
US6113775A (en) * | 1997-12-05 | 2000-09-05 | Uop Llc | Split end hydrocracking process |
DE69940483D1 (de) * | 1999-04-06 | 2009-04-09 | Sasol Tech Pty Ltd | Synthetischer Naphtha-Brennstoff |
FR2792851B1 (fr) * | 1999-04-29 | 2002-04-05 | Inst Francais Du Petrole | Catalyseur a base de metal noble faiblement disperse et son utilisation pour la conversion de charges hydrocarbonees |
EP1101813B1 (fr) * | 1999-11-19 | 2014-03-19 | ENI S.p.A. | Procédé pour la préparation de distillats moyens à partir de paraffines linéaires |
-
2001
- 2001-07-06 FR FR0108971A patent/FR2826973B1/fr not_active Expired - Lifetime
-
2002
- 2002-06-26 EP EP02755093A patent/EP1421157B1/fr not_active Expired - Lifetime
- 2002-06-26 RU RU2004103463/04A patent/RU2283858C2/ru not_active IP Right Cessation
- 2002-06-26 WO PCT/FR2002/002207 patent/WO2003004584A1/fr not_active Application Discontinuation
- 2002-07-03 MY MYPI20022514A patent/MY141718A/en unknown
- 2002-07-08 US US10/189,793 patent/US7156978B2/en not_active Expired - Lifetime
-
2003
- 2003-12-29 NO NO20035837A patent/NO335525B1/no not_active IP Right Cessation
Non-Patent Citations (1)
Title |
---|
See references of WO03004584A1 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US10487273B2 (en) | 2014-07-28 | 2019-11-26 | Sasol Technology Proprietary Limited | Production of oilfield hydrocarbons |
Also Published As
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MY141718A (en) | 2010-06-15 |
NO20035837L (no) | 2004-03-04 |
RU2004103463A (ru) | 2005-08-10 |
RU2283858C2 (ru) | 2006-09-20 |
FR2826973B1 (fr) | 2005-09-09 |
US20030057133A1 (en) | 2003-03-27 |
WO2003004584A1 (fr) | 2003-01-16 |
NO335525B1 (no) | 2014-12-22 |
EP1421157B1 (fr) | 2012-08-15 |
US7156978B2 (en) | 2007-01-02 |
FR2826973A1 (fr) | 2003-01-10 |
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