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WO1998004345A1 - Catalyseur, son utilisation et son procede de preparation - Google Patents

Catalyseur, son utilisation et son procede de preparation Download PDF

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Publication number
WO1998004345A1
WO1998004345A1 PCT/EP1997/004013 EP9704013W WO9804345A1 WO 1998004345 A1 WO1998004345 A1 WO 1998004345A1 EP 9704013 W EP9704013 W EP 9704013W WO 9804345 A1 WO9804345 A1 WO 9804345A1
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WO
WIPO (PCT)
Prior art keywords
catalyst
weight
carrier
alumina
catalyst according
Prior art date
Application number
PCT/EP1997/004013
Other languages
English (en)
Inventor
Guy Barre
Taous Grandvallet Mahtout
Sylvie Claude Lebigre
Original Assignee
Shell Internationale Research Maatschappij B.V.
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Shell Internationale Research Maatschappij B.V. filed Critical Shell Internationale Research Maatschappij B.V.
Priority to JP10508477A priority Critical patent/JP2000515914A/ja
Priority to BR9710608A priority patent/BR9710608A/pt
Priority to EP97934533A priority patent/EP0958047A1/fr
Priority to EA199900178A priority patent/EA199900178A1/ru
Priority to PL97331383A priority patent/PL331383A1/xx
Priority to AU37709/97A priority patent/AU725317B2/en
Publication of WO1998004345A1 publication Critical patent/WO1998004345A1/fr
Priority to NO990411A priority patent/NO990411L/no

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Classifications

    • 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
    • C10G49/00—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00
    • C10G49/02—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00 characterised by the catalyst used
    • C10G49/08—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00 characterised by the catalyst used containing crystalline alumino-silicates, e.g. molecular sieves
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/54—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
    • B01J23/56—Platinum group metals
    • B01J23/64—Platinum group metals with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
    • B01J23/656—Manganese, technetium or rhenium
    • 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
    • C10G49/00—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00
    • C10G49/02—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00 characterised by the catalyst used
    • C10G49/06—Treatment of hydrocarbon oils, in the presence of hydrogen or hydrogen-generating compounds, not provided for in a single one of groups C10G45/02, C10G45/32, C10G45/44, C10G45/58 or C10G47/00 characterised by the catalyst used containing platinum group metals or compounds thereof

Definitions

  • the present invention relates to a catalyst composition and to its use in hydroconversion processes, wherein a hydrocarbon oil comprising aromatic compounds is contacted with hydrogen in the presence of such a catalyst composition.
  • a process for the preparation of the catalyst composition also forma part of the present invention.
  • Hydrotreating catalysts are well known in the art.
  • Conventional hydrotreating catalysts comprise at least one Group VIII metal component and/or at least one Group VIB metal component supported on a refractory oxide support.
  • the Group VIII metal component may be either based on a non-noble metal, such as nickel (Ni) and/or cobalt (Co), or may be based on a noble metal, such as platinum (Pt) and/or palladium (Pd) .
  • Useful Group VIB metal components include those based on molybdenum (Mo) and tungsten (W) .
  • the most commonly applied refractory oxide support materials are inorganic oxides such as silica, alumina and silica-alumina and aluminosilicates, such as modified zeolite Y.
  • specific examples of conventional hydrotreating catalysts are NiMo/alumina, CoMo/alumina, NiW/silica-alumina, Pt/silica-alumina, PtPd/silica-alumina, Pt/modified zeolite Y and PtPd/modified zeolite Y.
  • Hydrotreating catalysts are normally used in processes wherein a hydrocarbon oil feed is contacted with hydrogen to reduce its content of aromatic compounds, sulphur compounds and/or nitrogen compounds.
  • hydrotreating processes wherein reduction of the aro atics content is the main purpose are referred to as hydrogenation processes, whilst processes predominantly focusing on reducing sulphur and/or nitrogen content are referred to as hydrodesulphurisation and hydrodenitrogenation, respectively.
  • Current environmental standards require that both aromatic content and sulphur and nitrogen content of oil products are very low and it is generally expected that specifications for aromatics, sulphur and nitrogen will become more and more severe in the future. Accordingly, in the refining of hydrocarbon oil fractions the ability to deeply hydrogenate, deeply hydrodesulphurise and deeply hydrodenitrogenate will become increasingly important .
  • the present invention aims to provide a hydrotreating catalyst which exhibits an excellent aromatics hydrogenation activity, whilst at the same time having an excellent hydrodesulphurisation and/or hydrodenitrogenation activity. This, consequently, implies that the catalyst composition should be able to effectively promote the hydrogenation of aromatics in the presence of substantial quantities of sulphur- and nitrogen-containing compounds.
  • the present invention moreover aims to provide a hydrotreating catalyst exhibiting an excellent hydrogenation activity towards monoaromatics . It will be understood that the use of such a catalyst in a hydrotreating process offers an increased potential for meeting future low-content specifications for (mono) aromatics, sulphur and nitrogen.
  • the present invention in a first aspect relates to a catalyst composition
  • a catalyst composition comprising from 0.1 to 15% by weight of a noble metal selected from one or more of platinum, palladium and iridium, and from 2 to 40% by weight of manganese and/or rhenium, said weight percentages indicating the amount of metal based on the total weight of carrier, supported on an acidic carrier.
  • a noble metal selected from one or more of platinum, palladium and iridium
  • manganese and/or rhenium both belong to Group VIIB of the Periodic Table of Elements.
  • the third Group VIIB metal, technetium is not useful due to its instability as will be appreciated by those skilled in the art.
  • the catalytically active metals i.e.
  • platinum and/or palladium and/or iridium on the one hand and manganese and/or rhenium on the other hand may be present in elemental form, as an oxide, as a sulphide or as a mixture of two or more of these forms.
  • a suitable preparation method used to prepare the present catalyst includes a final step of calcination in air, which will cause the catalytically active metals to be at least partially converted into their oxides. Usually such final calcination step will cause substantially all catalytically active metals to be converted into their oxides.
  • the catalyst is subsequently contacted with a sulphur-containing feed, then at least a part of these oxides will be sulphided and hence converted into the corresponding sulphides ("in situ" sulphidation) .
  • Very good catalyst performance has been observed in this situation and therefore it is considered a preferred embodiment of the present invention to have the catalytically active metals at least partly present in the catalyst as sulphides.
  • the catalyst may also be subjected to a separate presulphiding treatment prior to being contacted with the feed.
  • the degree of sulphidation of the metal oxides can be controlled by relevant parameters such as temperature and partial pressures of hydrogen, hydrogen sulphide, water and/or oxygen.
  • the metal oxides may be completely converted into the corresponding sulphides, but suitably an equilibrium state between the oxides and sulphides of the catalytically active metals will be formed, so that the catalytically active metals are present both as oxides and as sulphides.
  • the catalyst according to the present invention can suitably be used in a variety of hydroconversion processes.
  • the catalyst has been found to be particularly useful in the hydrotreatment of gas oils, thermally and/or catalytically cracked distillates (such as light cycle oils and cracked cycle oils) and mixtures of two or more of these. These oils usually contain a relatively large amount of aromatic compounds, sulphur-containing compounds and nitrogen-containing compounds. The amounts of such compounds must usually be reduced in view of environmental regulations.
  • Aromatic compounds reduction may also be desirable for reaching certain technical quality specifica ions, such as cetane number in the case of automotive gas oils, smoke point in the case of jet fuels and colour and stability in the case of lub oil fractions.
  • certain technical quality specifica ions such as cetane number in the case of automotive gas oils, smoke point in the case of jet fuels and colour and stability in the case of lub oil fractions.
  • the catalyst according to the present invention in the hydrotreatment of gas oils, thermally and/or catalytically cracked distillates and mixtures of two or more of these, the required reduction for e.g. meeting automotive gas oil specifications can be attained in a single stage. It has been found that the catalysts of the present invention are especially active in reducing the amount of mono-aromatics in the final product, even in the presence of substantial amounts of sulphur- and nitrogen-containing compounds.
  • the catalyst according to the present invention comprises as catalytically active metals from 0.1 to 15% by weight of platinum and/or palladium and/or iridium and from 2 to 40% by weight of manganese and/or rhenium. If lower amounts of catalytically active metals are applied, the activity of the catalyst becomes too low to be commercially attractive. If, on the other hand, the amount of catalytically active metals is higher than the upper limits indicated, the further increase in catalytic activity does not warrant the costs of the extra amount of metal. This applies in particular for platinum and palladium. Good results can be obtained with catalysts comprising from 3 to 10% by weight of noble metal, i.e. platinum and/or palladium and/or iridium and from 2, preferably from 5 to 30% by weight of manganese and/or rhenium.
  • a very much preferred catalyst is a catalyst comprising palladium and rhenium as the catalytically active metals.
  • the carrier used to support the catalytically active metals is an acidic carrier.
  • Acidic carriers are known in the art .
  • suitable carriers for the purpose of the present invention include acidic carriers comprising an aluminosilicate or silicoaluminophosphate zeolite, amorphous silica-alumina, alumina, fluorided alumina, phyllosilicate or a mixture of two or more of these.
  • the type of acidic carrier to be used largely depends on the intended application of the catalyst. For most applications it is, however, preferred that the carrier comprises a zeolite.
  • zeolites examples include silicoalumino- phosphates, such as SAPO-11, SAPO-31 and SAPO-41 and aluminosilicate zeolites like ferrierite, ZSM-5, ZSM-23, SSZ-32, mordenite, beta zeolite and zeolites of the faujasite type, such as faujasite and the synthetic zeolite Y.
  • silicoaluminophosphates may, for instance, be considered when using the present catalyst in a process for producing lubricating base oils which involves a hydroconversion step. In general, however, the use of aluminosilicate zeolites is preferred.
  • a particularly preferred aluminosilicate zeolite is zeolite Y, which is usually used in a modified, i.e. dealuminated, form. Particularly when using the catalyst according to the present invention as a hydrotreating catalyst for reducing the content of aromatics and sulphur- and nitrogen-containing compounds, the use of an acidic carrier comprising a modified zeolite Y is very much preferred.
  • a particularly useful modified zeolite Y is one having a unit cell size below 24.60 A, preferably from 24.20 to 24.45 A and even more preferably from 24.20 to 24.35 A, and a Si ⁇ 2/Al2 ⁇ 3 molar ratio in the range of from 5 or 10 to 150, e.g.
  • the carrier may also comprise a binder material.
  • binders in catalyst carriers are well known in the art and suitable binders, then, include inorganic oxides, such as silica, alumina, silica- alumina, boria, zirconia and titania, and clays. Of these, the use of silica and/or alumina is preferred for the purpose of the present invention.
  • the binder content of the carrier may vary from 5 to 95% by weight based on total weight of carrier. In a preferred embodiment, the carrier comprises 10 to 60% by weight of binder. A binder content of from 10 to 40% by weight has been found particularly advantageous.
  • the catalyst according to the present invention can be used in a variety of hydroconversion processes, wherein a hydrocarbon feedstock comprising aromatic compounds is contacted with the catalyst at elevated temperature and pressure in the presence of hydrogen.
  • hydroconversion processes wherein a hydrocarbon feedstock comprising aromatic compounds is contacted with the catalyst at elevated temperature and pressure in the presence of hydrogen.
  • specific examples of such processes are hydrocracking, lub oil manufacture (hydrocracking/hydroisomerization) and hydrotreating.
  • the present invention also relates to the use of the catalyst described above in a process wherein a hydrocarbon feedstock comprising aromatic compounds is contacted with the catalyst at elevated temperature and pressure in the presence of hydrogen. Since the present catalysts are active not only in hydrogenating aromatic compounds, but also in removing sulphur and/or nitrogen compounds, hydrocarbon feedstocks comprising sulphur and/or nitrogen containing compounds in addition to the aromatic compounds are particularly suitable .
  • the catalyst according to the present invention is, due to its excellent hydrotreating performance, particularly useful as the first stage catalyst in a two stage hydrocracking process.
  • the second stage catalyst is a dedicated hydrocracking catalyst.
  • the catalyst according to the present invention will preferably comprise a carrier comprising amorphous silica-alumina, fluorided alumina or a zeolite with silica and/or alumina as binder.
  • a hydroconversion step in a lubricating base oil manufacture process typically comprises contacting a luboil feedstock at a temperature of between 200 and 450 °C and a pressure up to 200 bar with a suitable catalyst in the presence of hydrogen. Examples of lubricating base oil manufacturing processes, wherein the catalyst according to the present invention may be used, are disclosed in GB-A-1, 546 , 504 and EP-A-0,178,710.
  • the catalyst according the present invention has been found to be particularly suitable for use in a hydrotreating process.
  • Suitable hydrotreating operating conditions are a temperature in the range of from 200 to
  • Suitable hydrotreatment processes have been described in European Patent Application Publication Nos . 0,553,920 and 0,611,816.
  • Suitable feedstocks for such a hydrotreating process are catalytically cracked gasolines, gas oils, light gas oils, thermally and/or catalytically cracked distillates (such as light cycle oils and cracked cycle oils) and mixtures of two or more of these. Many of these feedstocks normally comprise at least 70% by weight of hydrocarbons boiling between 150 and 450 °C.
  • the carrier comprises a binder in an amount as indicated above.
  • the preferred acidic material in the carrier in case of hydrotreating is an aluminosilicate zeolite, most preferably modified zeolite Y. It has been found that the present catalyst exhibits an excellent hydrotreating activity and is particularly effective in hydrogenating mono-aromatics, even in the presence of substantial amounts of sulphur- and nitrogen-containing compounds. In addition, the present catalyst is also very effective in the hydrogenation of di-aromatics and higher aromatics (tri+ aromatics) .
  • the present invention also relates to a process for preparing the catalysts described above, which process comprises incorporating the catalytically active metals into the refractory oxide carrier, suitably by means of impregnation or ion-exchange techniques, followed by drying and calcining and optionally presulphiding.
  • this process can be carried out by the subsequent steps of :
  • a preferred method of impregnating the carrier is the so-called pore volume impregnation, which involves the treatment of a carrier with a volume of impregnating solution, whereby said volume of impregnating solution is substantially equal to the pore volume of the carrier. In this way, full use is made of the impregnating solution.
  • this impregnation method has been found to be particularly suitable as the resulting catalysts show a particularly good performance.
  • the impregnation step (a) can be carried out using one impregnation solution containing all metal components or can be carried out in two separate impregnation steps, one step for impregnation with platinum and/or palladium and/or iridium and one step for impregnation with manganese and/or rhenium, possibly with an intermediate drying and/or calcining step.
  • Typical manganese compounds are salts thereof which are soluble in water, such as manganese sulphate, manganese nitrate and manganese acetate.
  • Typical rhenium compounds are perrhenic acid, ammonium perrhenate and potassium perrhenate.
  • Typical palladium compounds for use in impregnating solutions are tetrachloropalladium acid (H2 dCl 4 ), palladium nitrate, palladium (II) chloride and its amine complex. The use of H2PdCl4 is preferred.
  • Typical platinum compounds for use in an impregnating solution are hexachloroplatinic acid ( ⁇ tClg) , optionally in the presence of hydrochloric acid, platinum amine hydroxide and the appropriate platinum amine complexes .
  • the catalyst can be presulphided after the final calcination step and prior to contact with the feedstock.
  • Suitable presulphiding methods are known in the art, such as for instance from European Patent Application Publication Nos . 0,181,254; 0,329,499; 0,448,435 and 0,564,317 and International Patent Application Publication Nos. WO 93/02793 and WO 94/25157. Accordingly, in a further embodiment of the present invention, the process for preparing the catalyst comprises the further step of:
  • presulphiding can also take place via in situ pre- sulphidation. This involves contacting the calcined catalyst with a sulphur-containing hydrocarbon feedstock under appropriate conditions, which are normally less severe than the conditions applied during the envisaged operation.
  • the catalyst according to the present invention can be regenerated by methods known in the art .
  • a typical method for recovery of the catalytically active metals from spent catalyst comprises removing the deactivated catalyst from the reactor, washing the catalyst to remove the hydrocarbons, burning off the coke and subsequently recovering the noble metal (s) and the manganese and/or rhenium.
  • the invention is illustrated by the following examples without restricting the invention to these particular embodiments.
  • An acidic carrier consisting of 80% by weight dealuminated zeolite Y (unit cell size of 24.25 A and silica/alumina molar ratio of 80) and 20% by weight of an alumina binder was used.
  • a sample of this carrier was impregnated with an aqueous perrhenic acid (HRe ⁇ 4) solution to reach 20 %wt Re0 2 (corresponding with 17.1 %wt of Re; said weight percentages being based on the weight of the carrier) .
  • the partially prepared catalyst was then dried and calcined for 2 hours at 400 °C, after which impregnation with an aqueous solution of H2PdCl4 took place to reach a PdO content of 5% by weight (corresponding with 4.3% by weight of Pd) .
  • Example 2 A bed consisting of 20 cm 3 of the above PdRe/Y admixed with 80 cm 3 of silicon carbide particles (SiC; diameter 0.21 mm) was placed in a reactor.
  • the PdRe/Y bed thus obtained was presulphided according to the method disclosed in EP-A-0 , 181, 254. This method involved impregnation with di -tertiary nonyl polysulphide diluted in n-heptane, followed by drying for 2 hours at 150 °C under nitrogen at atmospheric pressure.
  • the catalyst was subsequently activated by bringing the reactor on a total pressure of 50 bar with the help of hydrogen at a gas rate of 500 Nl/kg.
  • the temperature was raised from ambient temperature to 250 °C in 2 hours, followed by the introduction of feed and increase of the temperature from 250 to 310 °C at a rate of 10 °C/hr.
  • the temperature of 310 °C was maintained for 100 hours.
  • a feed having the characteristics as indicated in Table I (BP is boiling point, IBP and FBP refer to initial and final boiling point, respectively) was passed over the bed of PdRe/Y.
  • the feed was a blend of 75% by weight of a straight run gasoil and 25% by weight of a light cycle oil.
  • Process conditions included a weight average bed temperature (WABT) of the PdRe/Y bed of 350 °C, a total pressure of 50 bar, a gas rate of 500 Nl/kg and a weight hourly space velocity (WHSV) of 1.0 kg/l.h.
  • WABT weight average bed temperature
  • WHSV weight hourly space velocity
  • the sulphur content and nitrogen content (both in ppmw) , the level of cracking expressed in % by weight of the material formed which has a boiling point below the IBP of the feed (i.e. 150 °C) and contents of mono-, di- and polyaromatics (in mmol/100 grams of product) were determined.
  • the monoaromatics which are found in the product may hence come from three sources: (i) from the unconverted monoaromatics already present in the feed, (ii) from converted diaromatics which were originally present in the feed and (iii) from converted diaromatics which, in return, originate from converted polyaromatics present in the feed.
  • the conversion levels of polyaromatics, diaromatics and monoaromatics were found to be as high as 85.3%, 91.3% and 54.1%, respectively.
  • Example 2 The procedure of Example 2 was repeated except that a PdRe/Y catalyst was used comprising 5 %w PdO (corresponding to 4.3 %w Pd) and 5 %w Re ⁇ 2 (corresponding to 4.3 %w Re) on an acidic carrier consisting of 65 %w modified zeolite Y (unit cell size of 24.32 A and silica/alumina molar ratio of 9.2) and 35 %w silica.
  • a PdRe/Y catalyst comprising 5 %w PdO (corresponding to 4.3 %w Pd) and 5 %w Re ⁇ 2 (corresponding to 4.3 %w Re) on an acidic carrier consisting of 65 %w modified zeolite Y (unit cell size of 24.32 A and silica/alumina molar ratio of 9.2) and 35 %w silica.
  • the feed was a blend of straight run gasoil and light cycle oil having the properties shown in Table III following and the process conditions used were exactly as before except that the feed was contacted with the catalyst at a temperature of 360 °C.
  • the sulphur content and nitrogen content (both in ppmw) , the level of cracking expressed in % by weight of the material formed which has a boiling point below 150 °C and percentage conversions of mono-, di- and triaromatics were all determined.
  • Example 3 The procedure of Example 3 was repeated except that the process was carried out in mild hydrocracking mode (in contrast to the hydrotreating mode of Example 3) by increasing the process temperature to 380 °C. All other process conditions remained the same.
  • the sulphur content and nitrogen content both in ppmw
  • the level of cracking expressed in % by weight of the material formed which has a boiling point below 150 °C
  • the percentage conversions of mono-, di- and triaromatics and the pour point were all determined.

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Catalysts (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Catalyseur comprenant de 0,1 à 15 % en poids d'un métal noble sélectionné dans un ou plusieurs parmi platine, palladium et iridium et de 2 à 40 % en poids soit de manganèse, soit de rhénium sur un support acide, lesdits pourcentages en poids indiquant la quantité de métal en fonction du poids total du support. Utilisation de ce catalyseur dans un procédé consistant à mettre en contact une charge d'hydrocarbure contenant des composés aromatiques avec le catalyseur à température et sous pression élevées en présence d'hydrogène. Procédé servant à préparer ce catalyseur et consistant à incorporer les métaux présentant une activité catalytique dans le support, puis à effectuer un séchage et une calcination.
PCT/EP1997/004013 1996-07-29 1997-07-22 Catalyseur, son utilisation et son procede de preparation WO1998004345A1 (fr)

Priority Applications (7)

Application Number Priority Date Filing Date Title
JP10508477A JP2000515914A (ja) 1996-07-29 1997-07-22 触媒、その使用及び製造方法
BR9710608A BR9710608A (pt) 1996-07-29 1997-07-22 Catalisador uso de um catalisador e processo para sua prepra-Æo
EP97934533A EP0958047A1 (fr) 1996-07-29 1997-07-22 Catalyseur, son utilisation et son procede de preparation
EA199900178A EA199900178A1 (ru) 1996-07-29 1997-07-22 Катализатор, его применение и способ получения
PL97331383A PL331383A1 (en) 1996-07-29 1997-07-22 Catalyst, itsa application and method of obtaining same
AU37709/97A AU725317B2 (en) 1996-07-29 1997-07-22 Catalyst, use thereof and preparation process
NO990411A NO990411L (no) 1996-07-29 1999-01-28 Katalysator, anvendelse derav, og fremgangsmÕte for fremstilling derav

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP96401693.5 1996-07-29
EP96401693 1996-07-29

Publications (1)

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WO1998004345A1 true WO1998004345A1 (fr) 1998-02-05

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EP (1) EP0958047A1 (fr)
JP (1) JP2000515914A (fr)
KR (1) KR20000029529A (fr)
CN (1) CN1275928A (fr)
AU (1) AU725317B2 (fr)
BR (1) BR9710608A (fr)
CA (1) CA2261738A1 (fr)
CZ (1) CZ26599A3 (fr)
EA (1) EA199900178A1 (fr)
ID (1) ID19460A (fr)
NO (1) NO990411L (fr)
PL (1) PL331383A1 (fr)
TR (1) TR199900179T2 (fr)
TW (1) TW464687B (fr)
WO (1) WO1998004345A1 (fr)
ZA (1) ZA976648B (fr)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2812001A1 (fr) * 2000-07-21 2002-01-25 Inst Francais Du Petrole Procede pour l'amelioration du point d'ecoulement de charges paraffiniques avec un catalyseur a base d'un phyllosilicate 2:1 dioctaedrique ponte
WO2011002782A3 (fr) * 2009-07-01 2011-04-21 Chevron U.S.A. Inc. Catalyseur d'hydrotraitement et son procédé de fabrication
CN105642319A (zh) * 2014-12-04 2016-06-08 中国石油化工股份有限公司 一种硫化型铂铼重整催化剂及其制备方法

Families Citing this family (1)

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Publication number Priority date Publication date Assignee Title
KR100419288B1 (ko) * 2001-06-22 2004-02-19 인천정유 주식회사 경질유의 탈방향족화용 촉매의 제조방법

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* Cited by examiner, † Cited by third party
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FR2812001A1 (fr) * 2000-07-21 2002-01-25 Inst Francais Du Petrole Procede pour l'amelioration du point d'ecoulement de charges paraffiniques avec un catalyseur a base d'un phyllosilicate 2:1 dioctaedrique ponte
EP1176188A1 (fr) * 2000-07-21 2002-01-30 Institut Francais Du Petrole Procédé pour l'amelioration du point d'ecoulement de charges paraffiniques
US6736959B2 (en) 2000-07-21 2004-05-18 Institut Francais Du Petrole Process for improving the pour point of feeds containing paraffins using a catalyst based on a bridged dioctahedral 2:1 phyllosilicate
WO2011002782A3 (fr) * 2009-07-01 2011-04-21 Chevron U.S.A. Inc. Catalyseur d'hydrotraitement et son procédé de fabrication
US9187702B2 (en) 2009-07-01 2015-11-17 Chevron U.S.A. Inc. Hydroprocessing catalyst and method of making the same
CN105642319A (zh) * 2014-12-04 2016-06-08 中国石油化工股份有限公司 一种硫化型铂铼重整催化剂及其制备方法

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ID19460A (id) 1998-07-16
AU725317B2 (en) 2000-10-12
EA199900178A1 (ru) 1999-08-26
TW464687B (en) 2001-11-21
KR20000029529A (ko) 2000-05-25
TR199900179T2 (en) 1999-04-21
NO990411D0 (no) 1999-01-28
CN1275928A (zh) 2000-12-06
CZ26599A3 (cs) 1999-12-15
EP0958047A1 (fr) 1999-11-24
PL331383A1 (en) 1999-07-05
ZA976648B (en) 1998-03-03
NO990411L (no) 1999-01-28
AU3770997A (en) 1998-02-20
JP2000515914A (ja) 2000-11-28
BR9710608A (pt) 1999-08-17
CA2261738A1 (fr) 1998-02-05

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