EP0553920A1 - Hydrotreating process - Google Patents

Hydrotreating process Download PDF

Info

Publication number
EP0553920A1
EP0553920A1 EP93200165A EP93200165A EP0553920A1 EP 0553920 A1 EP0553920 A1 EP 0553920A1 EP 93200165 A EP93200165 A EP 93200165A EP 93200165 A EP93200165 A EP 93200165A EP 0553920 A1 EP0553920 A1 EP 0553920A1
Authority
EP
European Patent Office
Prior art keywords
hydrocarbon oil
process according
catalyst bed
liquid
containing gas
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
Application number
EP93200165A
Other languages
German (de)
French (fr)
Other versions
EP0553920B1 (en
Inventor
Swan Tiong Sie
Auke Fimme De Vries
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shell Internationale Research Maatschappij BV
Original Assignee
Shell Internationale Research Maatschappij BV
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=8210385&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0553920(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Shell Internationale Research Maatschappij BV filed Critical Shell Internationale Research Maatschappij BV
Publication of EP0553920A1 publication Critical patent/EP0553920A1/en
Application granted granted Critical
Publication of EP0553920B1 publication Critical patent/EP0553920B1/en
Anticipated expiration legal-status Critical
Revoked legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G65/00Treatment of hydrocarbon oils by two or more hydrotreatment processes only
    • C10G65/02Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only
    • C10G65/04Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural serial stages only including only refining steps
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING 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
    • C10G49/00Treatment 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
    • C10G49/002Apparatus for fixed bed hydrotreatment processes

Definitions

  • the present invention relates to a process for hydrotreating in a single reactor vessel comprising at least an upper and a lower catalyst bed a hydrocarbon oil which is substantially liquid at process conditions and to a reactor vessel suitable for carrying out such process.
  • the present invention relates to a process for hydrotreating in a single reactor vessel comprising at least an upper and a lower catalyst bed, a hydrocarbon oil which is substantially liquid at process conditions, which process comprises:
  • the final hydrotreating step is carried out in the presence of hydrogen which may contain a relatively small amount of hydrogen sulphide, which leads to good hydrotreating results.
  • the present hydrotreating process differs from conventional hydrotreating processes, such as described in US patent specification 4,243,519, in the sequence of the process steps.
  • the final hydrotreating step is carried out in the upper catalyst bed.
  • the final hydrotreating step is carried out in a lower catalyst bed, which is situated further downstream the hydrogen gas flow.
  • the present invention relates furthermore to a reactor vessel suitable for hydrotreating a hydrocarbon oil according to the invention, in which vessel:
  • the process according to the present invention suitably comprises a hydrodesulphurization process in step (iii) followed by a further hydrodesulphurization process in step (i).
  • a hydrodesulphurization process in step (iii) followed by a further hydrodesulphurization process in step (i).
  • Other contaminants, such as nitrogen containing compounds can also to a certain extent be removed in a hydrodesulphurization process.
  • the process suitably involves a hydrodesulphurization process in step (iii) followed by a hydrogenation process in step (i). In that way both the sulphur and the aromatics content of the fresh hydrocarbon oil can be diminished in a commercially attractive way.
  • the hydrocarbon oil subjected to the present process is substantially liquid at process conditions.
  • the liquid phase of the hydrocarbon oil makes that the separation of the hydrotreated hydrocarbon oil from the hydrogen containing gas in step (ii) can be attained in a simple way.
  • this separation is carried out with the help of one or more separating trays consisting of a conventional liquid draw-off tray as used in distillation units.
  • step (iv) can be carried out outside or inside the reactor vessel.
  • the hydrocarbon oil will usually be cooled down and needs heating up before it can be used in step (i). Therefore, separation inside the reactor, preferably with the help of a separating tray as described above, is preferred.
  • the pressure drop over the reactor vessel will generally be between 0.2 and 10 bar, more specifically between 0.5 and 5 bar. It is possible to add hydrogen to the lower catalyst bed. However, in general the hydrogen partial pressure will be higher in the upper catalyst bed than in the lower catalyst bed. The pressure drop will generally make that the hydrogen partial pressure in the upper catalyst bed is between 0.1 and 9 bar, more specifically between 0.4 and 4.5 bar higher than in the lower catalyst bed.
  • clean hydrogen containing gas is meant a gas containing less than 3% by volume of hydrogen sulphide, preferably less than 1% by volume, more preferably less than 0.5 % by volume, most preferably less than 0.1 % by volume.
  • contaminated hydrogen containing gas obtained in step (iv) is cleaned, e.g. by treating it with an amine, and subsequently used in step (i) as clean hydrogen containing gas.
  • a hydrocarbon oil which is substantially liquid at process conditions is understood to comprise a hydrocarbon oil of which a major amount, for example more than 70 % by weight suitably more than 80 % by weight, and preferably more than 95 % by weight, is in the liquid phase.
  • Hydrocarbon oils which can be suitably treated in the process according to the present invention comprise any hydrocarbon which is substantially liquid at process conditions, for example kerosene fractions.
  • a hydrocarbon oil which could be suitably treated in the process would be a gas oil, as the environmental constraints on this oil fraction have become quite strict.
  • a suitable gas oil would be a gas oil substantially, e.g. more than 75% by weight, boiling in the range between 150 and 400 °C.
  • steps (i) and (iii) are suitably carried out at a temperature of between 150 and 450 °C, suitably between 300 and 400 °C, preferably between 325 and 390 °C, more preferably between 340 and 385 °C, and step (i) is suitably carried out at a pressure of between 20 and 85 bar, preferably between 30 and 65 bar, and step (iii) is suitably carried out at a pressure of between 15 and 80 bar, preferably between 25 and 60 bar.
  • a lubricating oil can be hydrotreated, such as a lubricating oil substantially, e.g. more than 95% by weight, boiling in the range between 320 and 600 °C.
  • steps (i) and (iii) are suitably carried out at a temperature of between 300 and 400 °C, preferably between 325 and 390 °C, more preferably between 340 and 385 °C, and a pressure of less than 250 bar, preferably less than 200 bar, more preferably less than 175 bar.
  • the hydrotreating catalyst employed in the process according to the present invention suitably comprises one or more metals from Group 1b, 2a, 4b, 5b, 6b, 7b and 8 of the Periodic Table of the Elements in the Handbook of Chemistry and Physics, 63rd edition, on a solid carrier.
  • the carrier can optionally comprise a zeolite.
  • the hydrotreating process according to the present invention preferably involves in step (i) a hydrogenation process and in step (iii) a hydrodesulphurization process, or in both steps a hydrodesulphurization process.
  • step (i) a hydrogenation catalyst is applied at hydrogenation conditions which include a temperature of between 150 and 350 °C, and in step (iii) a hydrodesulphurization catalyst is applied at hydrodesulphurization conditions.
  • the hydrodesulphurization of step (iii) must in general be carried out such that a sulphur content is attained which is such that the specification on the sulphur tolerance of the hydrogenation catalyst of step (i) is met, as otherwise this hydrogenation catalyst could be poisoned.
  • the hydrocarbon oil obtained in step (iv) contains not more than 15% by volume of sulphur containing compounds, based on volume of sulphur containing compounds present in the fresh hydrocarbon oil, preferably not more than 10%.
  • step (i) in both step (i) and (iii) a hydrodesulphurization catalyst is applied at hydrodesulphurization conditions.
  • the partly hydrotreated hydrocarbon oil obtained in step (iv) suitably contains between 1 and 30% by volume of sulphur containing compounds, based on volume of sulphur containing compounds present in the fresh hydrocarbon oil.
  • the present invention can suitably be carried out in a reactor vessel as shown in Figure 1.
  • the upper catalyst bed can contain either a hydrodesulphurization or a hydrogenation catalyst; the lower catalyst bed contains a hydrodesulphurization catalyst.
  • Clean hydrogen containing gas is fed to the reactor via line 2, while partly hydrotreated hydrocarbon oil is introduced in the upper part of the reactor via line 1.
  • the inlet for gas and the inlet for liquid can be combined. However, it is preferred to have separate inlets.
  • the hydrotreated effluent from the upper catalyst bed is separated from gas with the help of a draw-off tray.
  • the separated hydrotreated hydrocarbon effluent is removed from the reactor via line 3, while used hydrogen containing gas passes the separating tray and reaches the lower catalyst bed. Via line 4 fresh hydrocarbon oil is introduced between the separating tray and the lower catalyst bed.
  • the partly hydrotreated effluent obtained after passing the fresh hydrocarbon oil over the lower catalyst bed, is removed from the reactor via line 5 and separated into partly hydrotreated hydrocarbon oil which is sent to line 1, and contaminated hydrogen containing gas.
  • the contaminated hydrogen containing gas is suitably cleaned by treating it with an amine, so-called scrubbing.
  • the cleaned gas obtained can then, optionally together with make-up hydrogen, be recycled to line 2 and be used again.
  • the process was carried out in a set-up as described in Figure 1.
  • the catalyst present both in the upper and the lower catalyst bed was a hydrodesulphurization catalyst, comprising 3.1% by weight of cobalt and 12.4% by weight of molybdenum, based on total amount of catalyst, on alumina.
  • the catalyst particles were in the shape of 1.2 mm trilobes.
  • a gas oil feedstock of which according to the ASTM distillation curve more than 78% by volume is in the gaseous phase at 383 °C, more than 50% by volume is in the gaseous phase at 345 °C and more than 20% is in the gaseous phase at 300 °C was led to the reactor via line 4.
  • the overall process conditions comprise a temperature of 360 °C and a weight hourly space velocity of 2.0 kg/l.h and a hydrogen to oil ratio of 200 Nl/kg.
  • the hydrogen partial pressure at the outlet of the upper catalyst bed was 24.4 bar, while the hydrogen partial pressure at the outlet of the lower catalyst bed was 23.1 bar. At these process conditions about 7 % by weight of the gas oil feedstock was in the gaseous phase.
  • the sulphur content of the feed, the partly hydrotreated feed and the hydrotreated feed are shown in Table 1, in amount of elemental sulphur on total amount of feed.
  • fresh feedstock as described hereinabove was processed in a set-up similar to the one of Figure 1, at process conditions substantially as described hereinabove. No intermittent hydrogen separation took place between the catalyst beds; no hydrocarbon oil was added or removed between the catalyst beds. The hydrogen partial pressure at the reactor outlet was 23.1 bar. The hydrotreated hydrocarbon oil obtained had a sulphur content of 0.11%wt.

Abstract

A hydrotreating process comprising:
  • (i) further hydrotreating partly hydrotreated hydrocarbon oil in the presence of clean hydrogen containing gas,
  • (ii) separating the effluent of step (i) into hydrotreated hydrocarbon oil and used hydrogen containing gas, which hydrotreated hydrocarbon oil is removed from the process,
  • (iii) hydrotreating fresh hydrocarbon oil in the presence of used hydrogen containing gas obtained in step (ii),
  • (iv) separating the effluent of step (iii) into partly hydrotreated hydrocarbon oil and contaminated hydrogen containing gas, which contaminated hydrogen containing gas is removed from the process, and
  • (v) transporting partly hydrotreated hydrocarbon oil obtained in step (iv) to step (i). Further, the invention relates to a reactor vessel suitable for carrying out such process.

Description

  • The present invention relates to a process for hydrotreating in a single reactor vessel comprising at least an upper and a lower catalyst bed a hydrocarbon oil which is substantially liquid at process conditions and to a reactor vessel suitable for carrying out such process.
  • It is foreseen that the amount of contaminating compounds, such as sulphur and aromatics, allowed to be present in hydrocarbon oils according to environmental legislation, will continuously decrease in the future. Therefore, there is much interest in processes with the help of which the content of such compounds in hydrocarbon oils can be reduced to a low level in a commercially attractive way.
  • In some catalytic desulphurization processes, such as described in e.g. British patent specification 1420248, use is made of two or more fixed-bed catalytic reaction systems, each consisting of one or more reaction vessels. The capital investment needed for such processes utilizing several reaction vessels, is higher than the capital investment needed for the present single reactor vessel process.
  • The present invention relates to a process for hydrotreating in a single reactor vessel comprising at least an upper and a lower catalyst bed, a hydrocarbon oil which is substantially liquid at process conditions, which process comprises:
    • (i) contacting partly hydrotreated hydrocarbon oil obtained in step (iv) described hereinbelow, at elevated temperature and pressure in the upper catalyst bed with a hydrotreating catalyst in the presence of clean hydrogen containing gas,
    • (ii) separating the effluent of step (i) into hydrotreated hydrocarbon oil and used hydrogen containing gas, which hydrotreated hydrocarbon oil is removed from the process,
    • (iii) contacting fresh hydrocarbon oil at elevated temperature and pressure with a hydrotreating catalyst in the lower catalyst bed in the presence of used hydrogen containing gas obtained in step (ii),
    • (iv) separating the effluent of step (iii) into partly hydrotreated hydrocarbon oil and contaminated hydrogen containing gas, which contaminated hydrogen containing gas is removed from the process, and
    • (v) transporting partly hydrotreated hydrocarbon oil obtained in step (iv) to step (i).
  • In the process according to the present invention, the final hydrotreating step is carried out in the presence of hydrogen which may contain a relatively small amount of hydrogen sulphide, which leads to good hydrotreating results.
  • The present hydrotreating process differs from conventional hydrotreating processes, such as described in US patent specification 4,243,519, in the sequence of the process steps. In the process according to the present invention the final hydrotreating step is carried out in the upper catalyst bed. Whereas, on the contrary, in the conventional process, the final hydrotreating step is carried out in a lower catalyst bed, which is situated further downstream the hydrogen gas flow. By operating the final hydrotreating step in the upper catalyst bed, one has the advantage of operating it at the highest hydrogen partial pressure maintained in the vessel, due to the pressure drop over the vessel. A higher hydrogen partial pressure gives better hydrotreating results.
  • Further, the use of a feedstock which is substantially liquid at process conditions makes that the separation of hydrocarbon oil and hydrogen containing gas can be attained without the need to cool down the partly hydrotreated oil, separate gas from liquid and to heat the partly hydrotreated oil up again, which is disadvantageous from an economical point of view.
  • It is now possible to obtain the same good results as in a countercurrent mode of operation without suffering from the inherent disadvantages of countercurrent operation, such as restrictions on the gas and liquid space velocity.
  • The present invention relates furthermore to a reactor vessel suitable for hydrotreating a hydrocarbon oil according to the invention, in which vessel:
    • (a) above the upper zone for retaining a catalyst bed is situated an inlet for gas and an inlet for liquid,
    • (b) between the upper and lower zones for retaining a catalyst bed is situated a separating means for separating liquid and gas,
    • (c) between the upper zone for retaining a catalyst bed and the separating means is situated an outlet for liquid,
    • (d) between the separating means and the lower zone for retaining a catalyst bed is situated an inlet for liquid,
    • (e) below the lower zone for retaining a catalyst bed is present an outlet for gas and an outlet for liquid, or an outlet for liquid and gas,
    to which vessel a means is attached for transporting liquid obtained from the outlet for liquid situated below the lower zone for retaining a catalyst bed to the inlet for liquid situated above the upper zone for retaining a catalyst bed.
  • The process according to the present invention suitably comprises a hydrodesulphurization process in step (iii) followed by a further hydrodesulphurization process in step (i). In this way a very low sulphur level can be attained in a commercially attractive way. Other contaminants, such as nitrogen containing compounds, can also to a certain extent be removed in a hydrodesulphurization process. Further, the process suitably involves a hydrodesulphurization process in step (iii) followed by a hydrogenation process in step (i). In that way both the sulphur and the aromatics content of the fresh hydrocarbon oil can be diminished in a commercially attractive way.
  • The hydrocarbon oil subjected to the present process is substantially liquid at process conditions. The liquid phase of the hydrocarbon oil makes that the separation of the hydrotreated hydrocarbon oil from the hydrogen containing gas in step (ii) can be attained in a simple way. Suitably this separation is carried out with the help of one or more separating trays consisting of a conventional liquid draw-off tray as used in distillation units.
  • The separation of step (iv) can be carried out outside or inside the reactor vessel. In the first case, the hydrocarbon oil will usually be cooled down and needs heating up before it can be used in step (i). Therefore, separation inside the reactor, preferably with the help of a separating tray as described above, is preferred.
  • The pressure drop over the reactor vessel will generally be between 0.2 and 10 bar, more specifically between 0.5 and 5 bar. It is possible to add hydrogen to the lower catalyst bed. However, in general the hydrogen partial pressure will be higher in the upper catalyst bed than in the lower catalyst bed. The pressure drop will generally make that the hydrogen partial pressure in the upper catalyst bed is between 0.1 and 9 bar, more specifically between 0.4 and 4.5 bar higher than in the lower catalyst bed.
  • With the expression "clean hydrogen containing gas" is meant a gas containing less than 3% by volume of hydrogen sulphide, preferably less than 1% by volume, more preferably less than 0.5 % by volume, most preferably less than 0.1 % by volume. Suitably, contaminated hydrogen containing gas obtained in step (iv) is cleaned, e.g. by treating it with an amine, and subsequently used in step (i) as clean hydrogen containing gas.
  • A hydrocarbon oil which is substantially liquid at process conditions, is understood to comprise a hydrocarbon oil of which a major amount, for example more than 70 % by weight suitably more than 80 % by weight, and preferably more than 95 % by weight, is in the liquid phase. Hydrocarbon oils which can be suitably treated in the process according to the present invention, comprise any hydrocarbon which is substantially liquid at process conditions, for example kerosene fractions. A hydrocarbon oil which could be suitably treated in the process would be a gas oil, as the environmental constraints on this oil fraction have become quite strict. A suitable gas oil would be a gas oil substantially, e.g. more than 75% by weight, boiling in the range between 150 and 400 °C.
  • If a gas oil is hydrotreated in the process according to the present invention, steps (i) and (iii) are suitably carried out at a temperature of between 150 and 450 °C, suitably between 300 and 400 °C, preferably between 325 and 390 °C, more preferably between 340 and 385 °C, and step (i) is suitably carried out at a pressure of between 20 and 85 bar, preferably between 30 and 65 bar, and step (iii) is suitably carried out at a pressure of between 15 and 80 bar, preferably between 25 and 60 bar.
  • Further, in the present process suitably a lubricating oil can be hydrotreated, such as a lubricating oil substantially, e.g. more than 95% by weight, boiling in the range between 320 and 600 °C.
  • If a lubricating oil is hydrotreated in the process according to the present invention, steps (i) and (iii) are suitably carried out at a temperature of between 300 and 400 °C, preferably between 325 and 390 °C, more preferably between 340 and 385 °C, and a pressure of less than 250 bar, preferably less than 200 bar, more preferably less than 175 bar.
  • The hydrotreating catalyst employed in the process according to the present invention, suitably comprises one or more metals from Group 1b, 2a, 4b, 5b, 6b, 7b and 8 of the Periodic Table of the Elements in the Handbook of Chemistry and Physics, 63rd edition, on a solid carrier. The carrier can optionally comprise a zeolite.
  • As described above, the hydrotreating process according to the present invention preferably involves in step (i) a hydrogenation process and in step (iii) a hydrodesulphurization process, or in both steps a hydrodesulphurization process.
  • In the first mode, in step (i) a hydrogenation catalyst is applied at hydrogenation conditions which include a temperature of between 150 and 350 °C, and in step (iii) a hydrodesulphurization catalyst is applied at hydrodesulphurization conditions. In such case, the hydrodesulphurization of step (iii) must in general be carried out such that a sulphur content is attained which is such that the specification on the sulphur tolerance of the hydrogenation catalyst of step (i) is met, as otherwise this hydrogenation catalyst could be poisoned. Suitably, the hydrocarbon oil obtained in step (iv) contains not more than 15% by volume of sulphur containing compounds, based on volume of sulphur containing compounds present in the fresh hydrocarbon oil, preferably not more than 10%.
  • In the second mode, in both step (i) and (iii) a hydrodesulphurization catalyst is applied at hydrodesulphurization conditions. In that case, the partly hydrotreated hydrocarbon oil obtained in step (iv) suitably contains between 1 and 30% by volume of sulphur containing compounds, based on volume of sulphur containing compounds present in the fresh hydrocarbon oil.
  • The present invention can suitably be carried out in a reactor vessel as shown in Figure 1.
  • The upper catalyst bed can contain either a hydrodesulphurization or a hydrogenation catalyst; the lower catalyst bed contains a hydrodesulphurization catalyst. Clean hydrogen containing gas is fed to the reactor via line 2, while partly hydrotreated hydrocarbon oil is introduced in the upper part of the reactor via line 1. The inlet for gas and the inlet for liquid can be combined. However, it is preferred to have separate inlets. The hydrotreated effluent from the upper catalyst bed is separated from gas with the help of a draw-off tray. The separated hydrotreated hydrocarbon effluent is removed from the reactor via line 3, while used hydrogen containing gas passes the separating tray and reaches the lower catalyst bed. Via line 4 fresh hydrocarbon oil is introduced between the separating tray and the lower catalyst bed. The partly hydrotreated effluent obtained after passing the fresh hydrocarbon oil over the lower catalyst bed, is removed from the reactor via line 5 and separated into partly hydrotreated hydrocarbon oil which is sent to line 1, and contaminated hydrogen containing gas. The contaminated hydrogen containing gas is suitably cleaned by treating it with an amine, so-called scrubbing. The cleaned gas obtained can then, optionally together with make-up hydrogen, be recycled to line 2 and be used again.
  • The advantages of the present invention will be illustrated by the following example.
  • EXAMPLE
  • The process was carried out in a set-up as described in Figure 1. The catalyst present both in the upper and the lower catalyst bed was a hydrodesulphurization catalyst, comprising 3.1% by weight of cobalt and 12.4% by weight of molybdenum, based on total amount of catalyst, on alumina. The catalyst particles were in the shape of 1.2 mm trilobes.
  • A gas oil feedstock of which according to the ASTM distillation curve more than 78% by volume is in the gaseous phase at 383 °C, more than 50% by volume is in the gaseous phase at 345 °C and more than 20% is in the gaseous phase at 300 °C was led to the reactor via line 4. The overall process conditions comprise a temperature of 360 °C and a weight hourly space velocity of 2.0 kg/l.h and a hydrogen to oil ratio of 200 Nl/kg. The hydrogen partial pressure at the outlet of the upper catalyst bed was 24.4 bar, while the hydrogen partial pressure at the outlet of the lower catalyst bed was 23.1 bar. At these process conditions about 7 % by weight of the gas oil feedstock was in the gaseous phase. The sulphur content of the feed, the partly hydrotreated feed and the hydrotreated feed are shown in Table 1, in amount of elemental sulphur on total amount of feed. Table 1
    feed partly hydrotreated feed hydrotreated feed
    Sulphur content (% by weight) 1.64 0.21 0.06
  • Not according to the invention, fresh feedstock as described hereinabove was processed in a set-up similar to the one of Figure 1, at process conditions substantially as described hereinabove. No intermittent hydrogen separation took place between the catalyst beds; no hydrocarbon oil was added or removed between the catalyst beds. The hydrogen partial pressure at the reactor outlet was 23.1 bar. The hydrotreated hydrocarbon oil obtained had a sulphur content of 0.11%wt.

Claims (15)

  1. Process for hydrotreating in a single reactor vessel comprising at least an upper and a lower catalyst bed, a hydrocarbon oil which is substantially liquid at process conditions, which process comprises:
    (i) contacting partly hydrotreated hydrocarbon oil obtained in step (iv) described hereinbelow, at elevated temperature and pressure in the upper catalyst bed with a hydrotreating catalyst in the presence of clean hydrogen containing gas,
    (ii) separating the effluent of step (i) into hydrotreated hydrocarbon oil and used hydrogen containing gas, which hydrotreated hydrocarbon oil is removed from the process,
    (iii) contacting fresh hydrocarbon oil at elevated temperature and pressure with a hydrotreating catalyst in the lower catalyst bed in the presence of used hydrogen containing gas obtained in step (ii),
    (iv) separating the effluent of step (iii) into partly hydrotreated hydrocarbon oil and contaminated hydrogen containing gas, which contaminated hydrogen containing gas is removed from the process, and
    (v) transporting partly hydrotreated hydrocarbon oil obtained in step (iv) to step (i).
  2. Process according to claim 1, in which contaminated hydrogen containing gas obtained in step (iv) is cleaned and used in step (i).
  3. Process according to claim 2, in which the contaminated hydrogen containing gas is cleaned by treating with an amine.
  4. Process according to any one of claims 1-3, in which the clean hydrogen containing gas contains less than 3% by volume of hydrogen sulphide.
  5. Process according to any one of claims 1-4, in which the hydrocarbon oil is a gas oil substantially boiling in the range between 150 and 400 °C.
  6. Process according to claim 5, in which steps (i) and (iii) are carried out at a temperature of between 325 and 390 °C and step (i) is carried out at a pressure of between 20 and 85 bar, and step (iii) is carried out at a pressure of between 15 and 80 bar.
  7. Process according to any one of claims 1-4, in which the hydrocarbon oil is a lubricating oil substantially boiling in the range between 320 and 600 °C.
  8. Process according to claim 7, in which steps (i) and (iii) are carried out at a temperature of between 325 and 390 °C and a pressure of less than 200 bar.
  9. Process according to any one of claims 1-8, in which the catalyst comprises one or more metals from Group 1b, 2a, 4b, 5b, 6b, 7b and 8 of the Periodic Table of the Elements, on a solid carrier.
  10. Process according to any one of claims 1-9, in which in step (i) a hydrogenation catalyst is applied at hydrogenation conditions, and in step (iii) a hydrodesulphurization catalyst is applied at hydrodesulphurization conditions.
  11. Process according to claim 10, in which the hydrocarbon oil obtained in step (iv) contains not more than 10% by volume of sulphur containing compounds, based on volume of sulphur containing compounds present in the fresh hydrocarbon oil.
  12. Process according to any one of claims 1-9, wherein in step (i) and (iii) a hydrodesulphurization catalyst is applied at hydrodesulphurization conditions.
  13. Process according to claim 12, in which the hydrocarbon oil obtained in step (iv) contains between 1 and 30% by volume of sulphur containing compounds, based on volume of sulphur containing compounds present in the fresh hydrocarbon oil.
  14. Reactor vessel suitable for hydrotreating a hydrocarbon oil according to any one of claims 1-13, in which vessel:
    (a) above the upper zone for retaining a catalyst bed is situated an inlet for gas and an inlet for liquid,
    (b) between the upper and lower zone for retaining a catalyst bed is situated a separating means for separating liquid and gas,
    (c) between the upper zone for retaining a catalyst bed and the separating means is situated an outlet for liquid,
    (d) between the separating means and the lower zone for retaining a catalyst bed is situated an inlet for liquid,
    (e) below the lower zone for retaining a catalyst bed is present an outlet for gas and an outlet for liquid, or an outlet for liquid and gas,
    to which vessel a means is attached for transporting liquid obtained from the outlet for liquid situated below the lower zone for retaining a catalyst bed to the inlet for liquid situated above the upper zone for retaining a catalyst bed.
  15. Hydrocarbons obtained in a process as described in any one of claims 1-13.
EP93200165A 1992-01-24 1993-01-21 Hydrotreating process Revoked EP0553920B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP92200212 1992-01-24
EP92200212 1992-01-24

Publications (2)

Publication Number Publication Date
EP0553920A1 true EP0553920A1 (en) 1993-08-04
EP0553920B1 EP0553920B1 (en) 1996-09-18

Family

ID=8210385

Family Applications (1)

Application Number Title Priority Date Filing Date
EP93200165A Revoked EP0553920B1 (en) 1992-01-24 1993-01-21 Hydrotreating process

Country Status (8)

Country Link
EP (1) EP0553920B1 (en)
JP (1) JP3157323B2 (en)
CA (1) CA2087904C (en)
DE (1) DE69304725T2 (en)
DK (1) DK0553920T3 (en)
ES (1) ES2092742T3 (en)
NO (1) NO306262B1 (en)
SG (1) SG73396A1 (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5705052A (en) * 1996-12-31 1998-01-06 Exxon Research And Engineering Company Multi-stage hydroprocessing in a single reaction vessel
US5720872A (en) * 1996-12-31 1998-02-24 Exxon Research And Engineering Company Multi-stage hydroprocessing with multi-stage stripping in a single stripper vessel
US5968347A (en) * 1994-11-25 1999-10-19 Kvaerner Process Technology Limited Multi-step hydrodesulfurization process
EP1151060A1 (en) * 1998-12-08 2001-11-07 ExxonMobil Research and Engineering Company Production of low sulfur/low aromatics distillates
US6444865B1 (en) 1997-12-01 2002-09-03 Shell Oil Company Process wherein a hydrocarbon feedstock is contacted with a catalyst
US6623622B2 (en) 2000-10-10 2003-09-23 Exxonmobil Research And Engineering Company Two stage diesel fuel hydrotreating and stripping in a single reaction vessel
EP1352946A1 (en) * 2000-11-17 2003-10-15 Jgc Corporation Method of desulfurizing gas oil fraction, desulfurized gas oil, and desulfurizer for gas oil fraction

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101679912B (en) 2007-06-12 2013-08-14 罗迪亚公司 Detergent composition with hydrophilizing soil-release agent and methods for using same
US7524800B2 (en) 2007-06-12 2009-04-28 Rhodia Inc. Mono-, di- and polyol phosphate esters in personal care formulations
CN101679915B (en) 2007-06-12 2013-01-23 罗迪亚公司 Hard surface cleaning composition with hydrophilizing agent and method for cleaning hard surfaces
CA2690744A1 (en) 2007-06-12 2008-12-24 Rhodia, Inc. Mono-, di- and polyol alkoxylate phosphate esters in oral care formulations and methods for using same

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2971900A (en) * 1958-10-17 1961-02-14 Socony Mobil Oil Co Inc Hydrocracking of hydrocarbons
BE755266A (en) * 1969-08-25 1971-02-01 Evans & Son Ltd J APPARATUS FOR SLEEVES OR BODY WORK
US4243519A (en) * 1979-02-14 1981-01-06 Exxon Research & Engineering Co. Hydrorefining process

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE755268A (en) * 1970-08-01 1971-02-25 Texaco Development Corp PRODUCTION OF FUEL FOR ENGINES AND REACTION ENGINES,

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2971900A (en) * 1958-10-17 1961-02-14 Socony Mobil Oil Co Inc Hydrocracking of hydrocarbons
BE755266A (en) * 1969-08-25 1971-02-01 Evans & Son Ltd J APPARATUS FOR SLEEVES OR BODY WORK
US4243519A (en) * 1979-02-14 1981-01-06 Exxon Research & Engineering Co. Hydrorefining process

Cited By (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5968347A (en) * 1994-11-25 1999-10-19 Kvaerner Process Technology Limited Multi-step hydrodesulfurization process
US5720872A (en) * 1996-12-31 1998-02-24 Exxon Research And Engineering Company Multi-stage hydroprocessing with multi-stage stripping in a single stripper vessel
EP0958245A1 (en) * 1996-12-31 1999-11-24 Exxon Research And Engineering Company Multi-stage hydroprocessing in a single reaction vessel
US5705052A (en) * 1996-12-31 1998-01-06 Exxon Research And Engineering Company Multi-stage hydroprocessing in a single reaction vessel
EP0958245B2 (en) 1996-12-31 2012-05-02 ExxonMobil Research and Engineering Company Multi-stage hydroprocessing in a single reaction vessel
EP0958245B1 (en) * 1996-12-31 2004-06-09 ExxonMobil Research and Engineering Company Multi-stage hydroprocessing in a single reaction vessel
US6444865B1 (en) 1997-12-01 2002-09-03 Shell Oil Company Process wherein a hydrocarbon feedstock is contacted with a catalyst
EP1151060A4 (en) * 1998-12-08 2010-08-18 Exxonmobil Res & Eng Co Production of low sulfur/low aromatics distillates
EP1151060A1 (en) * 1998-12-08 2001-11-07 ExxonMobil Research and Engineering Company Production of low sulfur/low aromatics distillates
US6623622B2 (en) 2000-10-10 2003-09-23 Exxonmobil Research And Engineering Company Two stage diesel fuel hydrotreating and stripping in a single reaction vessel
US7276150B2 (en) 2000-11-17 2007-10-02 Jgc Corporation Method of desulfurizing gas oil fraction, desulfurized gas oil, and desulfurizer for gas oil fraction
EP1352946A4 (en) * 2000-11-17 2004-12-01 Jgc Corp Method of desulfurizing gas oil fraction, desulfurized gas oil, and desulfurizer for gas oil fraction
EP2280056A3 (en) * 2000-11-17 2011-02-09 JGC Corporation Apparatus for desulfurizing gas oil fraction
EP1352946A1 (en) * 2000-11-17 2003-10-15 Jgc Corporation Method of desulfurizing gas oil fraction, desulfurized gas oil, and desulfurizer for gas oil fraction

Also Published As

Publication number Publication date
CA2087904C (en) 2004-04-27
DE69304725T2 (en) 1997-03-06
NO306262B1 (en) 1999-10-11
JPH05271668A (en) 1993-10-19
JP3157323B2 (en) 2001-04-16
SG73396A1 (en) 2000-06-20
NO930233L (en) 1993-07-26
NO930233D0 (en) 1993-01-22
EP0553920B1 (en) 1996-09-18
CA2087904A1 (en) 1993-07-25
ES2092742T3 (en) 1996-12-01
DK0553920T3 (en) 1996-10-14
DE69304725D1 (en) 1996-10-24

Similar Documents

Publication Publication Date Title
AU755519B2 (en) Two stage hydroprocessing with vapor-liquid interstage contacting for vapor heteroatom removal
CA1092786A (en) Method for increasing the purity of hydrogen recycle gas
KR100983817B1 (en) Hydrocracking process to maximize diesel with improved aromatic saturation
US6036844A (en) Three stage hydroprocessing including a vapor stage
US6514403B1 (en) Hydrocracking of vacuum gas and other oils using a cocurrent/countercurrent reaction system and a post-treatment reactive distillation system
US6054041A (en) Three stage cocurrent liquid and vapor hydroprocessing
KR20010034022A (en) Hydroprocessing reactor and process having staged reaction zones
EP0553920B1 (en) Hydrotreating process
US6153086A (en) Combination cocurrent and countercurrent staged hydroprocessing with a vapor stage
WO1997038066A1 (en) Process for reverse staging in hydroprocessing reactor systems
US6623622B2 (en) Two stage diesel fuel hydrotreating and stripping in a single reaction vessel
US5985135A (en) Staged upflow and downflow hydroprocessing with noncatalytic removal of upflow stage vapor impurities
AU2002211877A1 (en) Two stage diesel fuel hydrotreating and stripping in a single reaction vessel
EP0611816A1 (en) Hydrotreating process
JP4443052B2 (en) Multi-stage upflow hydrogen treatment with non-contact removal of impurities from the first stage steam effluent
GB2148937A (en) Two-stage petroleum residuum hydroconversion using a countercurrent gas-liquid first stage
KR830000774B1 (en) Hydrocarbon Production Method

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): BE DE DK ES FR GB IT NL SE

17P Request for examination filed

Effective date: 19931231

17Q First examination report despatched

Effective date: 19950802

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): BE DE DK ES FR GB IT NL SE

REG Reference to a national code

Ref country code: DK

Ref legal event code: T3

REF Corresponds to:

Ref document number: 69304725

Country of ref document: DE

Date of ref document: 19961024

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2092742

Country of ref document: ES

Kind code of ref document: T3

ITF It: translation for a ep patent filed

Owner name: ING. C. GREGORJ S.P.A.

ET Fr: translation filed
PLBQ Unpublished change to opponent data

Free format text: ORIGINAL CODE: EPIDOS OPPO

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PLBQ Unpublished change to opponent data

Free format text: ORIGINAL CODE: EPIDOS OPPO

26 Opposition filed

Opponent name: KVAERNER PROCESS TECHNOLOGY LIMITED

Effective date: 19970618

Opponent name: EXXON RESEARCH AND ENGINEERING COMPANY

Effective date: 19970607

PLBF Reply of patent proprietor to notice(s) of opposition

Free format text: ORIGINAL CODE: EPIDOS OBSO

NLR1 Nl: opposition has been filed with the epo

Opponent name: KVAERNER PROCESS TECHNOLOGY LIMITED

Opponent name: EXXON RESEARCH AND ENGINEERING COMPANY

PLBF Reply of patent proprietor to notice(s) of opposition

Free format text: ORIGINAL CODE: EPIDOS OBSO

PLBF Reply of patent proprietor to notice(s) of opposition

Free format text: ORIGINAL CODE: EPIDOS OBSO

RDAH Patent revoked

Free format text: ORIGINAL CODE: EPIDOS REVO

APAC Appeal dossier modified

Free format text: ORIGINAL CODE: EPIDOS NOAPO

APAE Appeal reference modified

Free format text: ORIGINAL CODE: EPIDOS REFNO

APAC Appeal dossier modified

Free format text: ORIGINAL CODE: EPIDOS NOAPO

REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PLBQ Unpublished change to opponent data

Free format text: ORIGINAL CODE: EPIDOS OPPO

PLAB Opposition data, opponent's data or that of the opponent's representative modified

Free format text: ORIGINAL CODE: 0009299OPPO

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20021112

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DK

Payment date: 20021120

Year of fee payment: 11

R26 Opposition filed (corrected)

Opponent name: EXXONMOBIL RESEARCH AND ENGINEERING COMPANY * 1997

Effective date: 19970607

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20021224

Year of fee payment: 11

Ref country code: BE

Payment date: 20021224

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20030120

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20030124

Year of fee payment: 11

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20030131

Year of fee payment: 11

NLR1 Nl: opposition has been filed with the epo

Opponent name: KVAERNER PROCESS TECHNOLOGY LIMITED

Opponent name: EXXONMOBIL RESEARCH AND ENGINEERING COMPANY

APAC Appeal dossier modified

Free format text: ORIGINAL CODE: EPIDOS NOAPO

RDAG Patent revoked

Free format text: ORIGINAL CODE: 0009271

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: PATENT REVOKED

27W Patent revoked

Effective date: 20030404

GBPR Gb: patent revoked under art. 102 of the ep convention designating the uk as contracting state

Free format text: 20030404

REG Reference to a national code

Ref country code: SE

Ref legal event code: ECNC

NLR2 Nl: decision of opposition

Effective date: 20030404

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: SE

Payment date: 20031117

Year of fee payment: 12

APAH Appeal reference modified

Free format text: ORIGINAL CODE: EPIDOSCREFNO