AU2003200318B2 - Upgrading Fischer-Tropsch and petroleum-derived naphthas and distillates - Google Patents
Upgrading Fischer-Tropsch and petroleum-derived naphthas and distillates Download PDFInfo
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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
- 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
- C10G2/00—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon
- C10G2/30—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen
- C10G2/32—Production of liquid hydrocarbon mixtures of undefined composition from oxides of carbon from carbon monoxide with hydrogen with the use of catalysts
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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
- 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
- C10G65/16—Treatment of hydrocarbon oils by two or more hydrotreatment processes only plural parallel stages only including only refining steps
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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
- C10G69/00—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process
- C10G69/02—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process plural serial stages only
- C10G69/08—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one other conversion process plural serial stages only including at least one step of reforming naphtha
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- 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
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36
- B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 - B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
- B01J23/85—Chromium, molybdenum or tungsten
- B01J23/888—Tungsten
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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
- C10G2400/02—Gasoline
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- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
AUSTRALIA
PATENTS ACT 1990 COMPLETE SPECIFICATION NAME OF APPLICANT(S): Chevron U.S.A. Inc.
ADDRESS FOR SERVICE: DAVIES COLLISON CAVE Patent Attorneys 1 Little Collins Street, Melbourne, 3000.
INVENTION TITLE: Upgrading Fischer-Tropsch and petroleum-derived naphthas and distillates The following statement is a full description of this invention, including the best method of performing it known to me/us:- BACKGROUND OF THE INVENTION 1. Field of Invention The present invention is directed to the conversion of remote natural gases into saleable transportation fuels and petroleum products. More specifically, this invention is directed to upgrading by, for example, hydrotreating, hydrocracking and hydrodewaxing Fischer-Tropsch and/or petroleum-derived naphthas and distillates for use in saleable transportation fuels and petroleum products.
2. Description of Related Art The Fischer-Tropsch reaction is a well known reaction, and catalysts and conditions for performing Fischer-Tropsch reactions are well known to those of skill in the art, and are described, for example, in EP 0 921 184A1, the contents of which are hereby incorporated by reference in their entirety. The Fischer-Tropsch process converts synthesis gas into linear hydrocarbons(n-paraffins, linear olefins and minor amounts of fatty acids). Due to the linear nature of such products, once they have been subjected to removal of heteroatoms and isomerization, they are well-suited for use in various transportation fuels and other saleable petroleum products including, but not limited to, jet fuels, diesel fuels and petrochemical feedstocks including, but not limited to, benzene, toluene and xylene.
However, lighter naphtha fractions are generally poorly suited for use in conventional gasolines because their linear nature causes them to exhibit a very low octane rating. Further, although naphtha can be used as a petrochemical feedstock for ethylene production, naphtha has not been found to be suitable for transportation fuels. In addition, even though naphtha may be suitable as a fuel for fuel cell vehicles, because fuel cell vehicles have not yet become widely used, a need still exists for a process to convert naphtha so that it can be used in conventional transportation fuels.
In addition to the need to convert the naphtha fraction of a Fischer-Tropsch process, there is also a need to upgrade hydrotreat, hydrocrack or hydrodewax) heavier boiling distillates from the Fischer-Tropsch process so that they are acceptable for use in transportation fuels and other saleable petroleum products.
More specifically, products of the Fischer-Tropsch process, in finished products, exhibit boiling ranges having unacceptable levels of oxygenates and olefins (alcohols and traces of acids). Also, the content of linear hydrocarbons in such products is so high that the resulting products exhibit unacceptable cold climate properties including, but not limited to, jet freeze point, diesel cloud point, and lube base stock pour point. Traditionally, these products can be upgraded to obtain saleable transportation fuels and lube base stocks by employing various processes including, but not limited to, hydrotreating, hydrocracking, hydrodewaxing, combinations thereof and the like.
Although such processes can upgrade Fischer-Tropsch products suffering from the above-mentioned problems to obtain saleable transportation fuels and other petroleum products, the disadvantage of these processes is that they require hydrogen. That is, in order to perform the above processes, hydrogen must be separately supplied during the application of these processes to successfully upgrade Fischer-Tropsch products. Although hydrogen can be obtained from synthesis gases, hydrogen can only be obtained from synthesis gases by employing expensive separation processes. Expensive separation processes are necessary to ensure that the hydrogen remains separate from carbon oxides that can otherwise poison catalysts used in hydrotreating, hydrocracking and hydrodewaxing processes. In addition, hydrogen can be supplied from a separate facility that reforms natural gas into hydrogen using stream reforming processes.
Unfortunately, the construction and operation of a separate hydrogen production facility is extremely costly. As a result, there is an urgent need for a relatively low-cost source of hydrogen to be used in upgrading processes including, but not limited to, hydrotreating, hydrocracking and hydrodewaxing operations, so that Fischer-Tropsch products can be more inexpensively upgraded to obtain saleable products.
Another problem encountered during upgrading of Fischer-Tropsch distillates is that the stocks created do not contain sulfur but do contain -2- POPRTFMIF2OO3201 IS fpc 203.do-24107/20OS 00 S-3t oxygenates. The least expensive catalysts for hydrotreating, hydrocracking and hydrodewaxing use sulfided Group VI and VIII metals including, but not limited to, nickel, 0 cobalt, molybdenum, tungsten, combinations thereof and the like. Non-sulfided catalysts for hydrotreating, hydrocracking and hydrodewaxing are available but are based on expensive noble metals including, but not limited to, platinum, palladium, combinations Sthereof and the like. Unfortunately, when sulfided catalysts are in the presence of oxygenates and the absence of sulfur, the oxygen in the feedstock replaces sulfur on the catalyst, leading to a decline in the catalyst's performance. Decreases in catalytic performance can appear in various forms including, but not limited to, decreased activity, selectivity and/or stability. To prevent such a decline in performance, manufacturers typically add a sulfur compound to ensure that the catalyst remains adequately sulfided.
Usually, the sulfur compound that is added is a pure chemical such as, for example, a dimethyldisulfide. Unfortunately, pure chemicals are expensive to purchase and require special handling that can create safety concerns and can generate additional costs. As a result, there is a need for a process that maintains sulfided catalysts in their active sulfided state without having to use chemicals.
Finally, there is also a desire for a process for upgrading hydrotreating, hydrocracking or hydrodewaxing) petroleum-derived hydrocarbon products that are produced along with natural gases. Petroleum-derived hydrocarbon products that are produced along with a natural gas can include condensates, naphthas and distillates. These products have chemical compositions that are analogous to compositions of conventional petroleum products, and include a mixture of a variety of hydrocarbons including, but not limited to, linear paraffins, iso-paraffins, cyclo-paraffins, aromatics, mixtures thereof and the like. They also contain sulfur and nitrogen impurities that must be removed to obtain saleable products.
SUMMARY OF INVENTION The process of the present invention seeks to address the above needs. The process of the present invention produces at least one of saleable gasoline components, distillate fuel components and lube base stock components by, for example, hydrotreating, hydrocracking and hydrodewaxing upgrading) Fischer-Tropsch and/or petroleumderived naphthas and distillates.
P:NOPER\EPH\20320031 Spe 203.dc.2407I2008 00 0 cl -4- V) The fuel components produced by embodiments of the present invention have octane values sufficient for use in conventional transportation fuels and petrochemical 00 feedstocks. In addition, during naphtha reformation, the present invention produces hydrogen by-product that can be used in hydrotreating, hydrocracking and hydrodewaxing processes to inexpensively upgrade Fischer-Tropsch products. Thus, the present invention C seeks to inexpensively provide at least a portion of the hydrogen needed for hydrotreatment processes without having to employ expensive separation processes or separate hydrogen production facilities.
Additionally, the present invention can combine Fischer-Tropsch naphthas and distillates with petroleum-derived naphthas and distillates to obtain blended naphthas and distillates having sulphur levels of at least about 1 ppm. Thus, the present invention ensures that sulfided catalysts, used to hydrotreat naphthas and distillates, maintain adequate sulfur levels without having to add sulfur by introducing costly pure chemicals.
Finally, by combining Fischer-Tropsch naphthas and distillates with petroleumderived naphthas and distillates, the present invention can upgrade hydrotreat, hydrocrack or hydrodewax) petroleum hydrocarbon products, including condensates, naphthas and distillates, to obtain saleable gasoline components and petroleum feedstock products.
An aspect of the present invention provides a process for upgrading at least one of a Fischer-Tropsch naphtha and a Fischer-Tropsch distillate to produce at least one of a gasoline component, a distillate fuel component or a lube base stock component, the process comprising: a) mixing a Fischer-Tropsch naphtha and a petroleum-derived naphtha to obtain a blended naphtha having a sulfur level of at least about 1 ppm; b) mixing a Fischer-Tropsch distillate and a petroleum-derived distillate to obtain a blended distillate having a sulfur level of at least about 1 ppm; c) producing a hydrotreated blended naphtha by hydrotreating said blended naphtha to remove oxygenates from said Fischer-Tropsch naphtha and to remove sulfur from said petroleum-derived naphtha; d) reforming said hydrotreated blended naphtha to generate hydrogen byproduct and a gasoline component comprising at least about 10% aromatics; P:OPR\EPH%20320I01 .p 2O3.doc.2407/20 00 V e) hydrotreating said blended distillate generating a hydrotreated blended distillate; and 0 f) upgrading said hydrotreated blended distillate using said hydrogen byproduct to produce at least one of a distillate fuel component and/or a lube base stock component. In embodiments of this aspect hydrotreatment of said blended naphtha and said blended distillate is performed in a single Shydrotreatment reactor. In embodiments hydrotreatment is performed with initial provision of hydrogen. Embodiments of the process further comprise initially adding sulfur to said process so that any catalyst used during hydrotreatment is adequately sulfided.
Another aspect provides a process for upgrading a Fischer-Tropsch naphtha to produce a gasoline component, the process comprising: a) mixing a Fischer-Tropsch naphtha and a petroleum-derived naphtha to obtain a blended naphtha having a sulfur level of at least about I ppm; b) hydrotreating said blended naphtha producing a hydrotreated blended naphtha; c) reforming said hydrotreated blended naphtha producing hydrogen byproduct and a gasoline component having a research octane rating of at least about 80; and d) recirculating said hydrogen by-product to hydrotreat said blended naphtha.
A process according to the present invention for upgrading at least one of a Fischer-Tropsch naphtha and a Fischer-Tropsch distillate, to produce at least one of a gasoline component, a distillate fuel component, or a lube base stock component, can include reforming a Fischer-Tropsch naphtha to produce hydrogen by-product and a gasoline component with a research octane rating of at least about 80. The hydrogen byproduct is then used to upgrade a Fischer-Tropsch distillate to produce distillate fuel component and/or lube base stock blending components.
A process, according to the present invention, for upgrading a Fischer-Tropsch naphtha can include hydrotreating Fischer-Tropsch naphtha to remove oxygenates producing hydrotreated Fischer-Tropsch naphtha. The process can further include P;OPER\EH\2003200318 Isp 203.doc-24/07/2008 00 CI -6lt reforming the hydrotreated Fischer-Tropsch naphtha producing hydrogen by-product and a gasoline component having a research octane rating of at least about 80. Finally, the 00 hydrogen by-product is recirculated to hydrotreat said Fischer-Tropsch naphtha.
Another process, according to the present invention, for upgrading a Fischer-
O
Tropsch naphtha to obtain a gasoline component can include mixing Fischer-Tropsch Cc naphtha with petroleum-derived naphtha to obtain a blended naphtha having a sulfur level 0of at least about 1 ppm. The blended naphtha is hydrotreated to produce hydrotreated blended naphtha. Finally, the hydrotreated blended naphtha is reformed producing hydrogen by-product and a gasoline component having an research octane rating of at least about A process of the present invention for upgrading a Fischer-Tropsch distillate to produce at least one of a distillate fuel and a lube base stock component can include mixing Fischer-Tropsch distillate and petroleum-derived distillate to obtain a blended distillate having a sulfur level of at least about 1 ppm. The blended distillate is hydrotreated producing hydrotreated blended distillate. Finally, the hydrotreated blended distillate is upgraded producing distillate fuel component and/or lube base stock blended components.
Finally, another aspect provides a plant of the present invention for upgrading at least one of a Fischer-Tropsch naphtha and a Fischer-Tropsch distillate to obtain at least one of a gasoline component, a distillate fuel or a lube base feedstock component can include a hydrocarbon source providing a hydrocarbon. A separator separates hydrocarbon gas, hydrocarbon condensate and crude oil from the hydrocarbon. A synthesis gas from the hydrocarbon gas. A Fischer-Tropsch reactor positioned downstream from the synthesis gas generator conducts a Fischer-Tropsch process on the synthesis gas to obtain Fischer- Tropsch naphtha and Fischer-Tropsch distillate. A naphtha hydrotreatment reactor downstream from the Fischer-Tropsch reactor hydrotreats the Fischer-Tropsch naphtha. A naphtha reformer downstream from the hydrotreatment reactor reforms hydrotreated naphtha to obtain hydrogen by-product and a gasoline component including at least about aromatics. A distillate hydrotreatment reactor downstream from the Fischer-Tropsch reactor hydrotreats the Fischer-Tropsch distillate. Finally, a distillate upgrader is P:\OPRTEHI\200J2003 IS pC 203.dom.24/O7/2O8 00 -6A- Sdownstream from the distillate hydrotreatment reactor and relative to the naphtha reformer so that hydrogen by-product from the reformer recirculates to the upgrader so that the o0 upgrader can upgrade hydrotreated distillate to produce distillate fuel and/or a lube base feedstock component. The plant may optionally include a distillation reactor positioned downstream from the separator for distilling the hydrocarbon condensate and the crude oil c to obtain petroleum-derived naphtha and petroleum-derived distillate. In embodiments, the distillation reactor, when present, is positioned relative to the Fischer-Tropsch reactor and the naphtha hydrotreatment reactor so that the Fischer-Tropsch naphtha and the petroleumderived naphtha mix prior to entering the naphtha hydrotreatment reactor to form a blended naphtha having a sulfur level of at least about 1 ppm; and/or the distillation reactor, when present, is positioned relative to the Fischer-Tropsch reactor and the distillate hydrotreatment reactor so that the Fischer-Tropsch distillate and the petroleum-derived distillate mix prior to entering the distillate hydrotreatment reactor to form a blended distillate having a sulfur level of at least about 1 ppm. The hydrotreatment reactors may contain at least one catalyst. The at least one catalyst may comprise at least one of a noble metal and a non-noble metal.
The plant may further comprise a source of sulfur positioned so that sulfur can be initially supplied to ensure that any catalysts present in the naphtha hydrotreatment reactor and/or the distillate hydrotreatment reactor are adequately sulfided. In embodiments, the naphtha hydrotreatment reactor and the distillate hydrotreatment reactor constitute a single hydrotreatment reactor.
BRIEF DESCRIPTION OF THE FIGURES OF THE DRAWING Embodiments of the present invention are described herein, by way of example only, with reference to the following drawings.
Figure 1 is a schematic view of a preferred embodiment of the present invention.
Figure 2 is a schematic view of another preferred embodiment of the present invention.
Figure 3 is a schematic view of another preferred embodiment of the present invention.
PF\PEREFKQ0032031Isp203 doc241/07/200 00 -6Bt DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS Using the present invention, Fischer-Tropsch naphtha, and optionally petroleum- 00 derived naphtha, can be reformed to make aromatics and hydrogen by-product. The resulting aromatics can increase the octane number of the naphtha to permit the naphtha to 5 be used as a conventional gasoline or a blend stock in conventional gasoline. The resulting c aromatics can also be sold as valuable petrochemicals including, but not limited to, benzene, toluene and xylene.
There are two classes of reforming processes: catalytic reforming and AROMAX® reforming. The process of the present invention can employ either or both catalytic reforming or AROMAX® reforming technologies to convert the Fischer-Tropsch naphthas into aromatics. Catalytic reforming, as described, for example, in Catalytic Reforming, by D.M. Little, PennWell Books (1985), is a well-known process. Similarly, AROMAX® reforming is also a well-known process, and is described, for example, in Petroleum Petrochemical International, Volume 12, no. 12, pages 65 to 68, as well as U.S. Patent No.
4,456,527 to Buss et al. The feed to either of these reforming processes should have very low levels ofheteroatoms sulfur, nitrogen, and oxygen). Fischer-Tropsch naphthas generally have very low levels of sulfur and nitrogen, but often have appreciable levels of oxygen in the for of alcohols and traces of acids and other oxygenates. These heteroatoms can be removed by use of a hydrotreater. The preferred hydrotreating catalysts use inexpensive non-noble metals from Groups VI and VIII including, but not limited to, nickel, cobalt, molybdenum, tungsten, combinations thereof and the like. These non-noble metals are active when they are in the sulfided state. To prevent transfer of the sulfur from the sulfided hydrotreating catalysts to the reforming catalysts (which could poison the reforming catalyst), the product is stripped to remove hydrogen sulfide and other light sulfur compounds, and is optionally treated with a sulfur adsorbent.
Examples of the use of adsorbents (guard beds) to protect reforming catalysts are described in U.S. Patents 5,601,698, and 5,322,615 The hydrogen by-product from the reformer is used to upgrade the .distillates by the use of hydrogen consuming processes that include, for example, hydrotreating, hydrocracking, and hydrodewaxing. By using the hydrogen byproduct from the naphtha reformation, the present invention avoids the need for expensive separation processes or separate hydrogen production facilities to supply added hydrogen needed for distillate upgrading.
Although processes of the present invention can produce hydrogen byproduct for use in hydrogen-consumer upgrading processes, at least initially, it may be necessary in processes of the invention to provide hydrogen. In particular, because hydrogen produced in the reformer can be used in other operations, including the hydrotreatment of naphtha and/or distillate, provisions may need to be made to provide hydrogen at startup. There are several solutions to this problem including, but not limited to, providing a separate source of hydrogen, such as from high pressure containers, making the hydrogen from electrolysis units, or providing a source of low-sulfur hydrotreated naphtha for the reformer for startup. In addition, in processes of the invention wherein hydrogen byproduct is not being produced, it is understood that hydrogen is being provided to conduct, for example, hydrotreatment and/or upgrading processes. Moreover, it is also understood that in instances where the amount of hydrogen by-product produced during a process of the present invention is not sufficient to conduct hydrotreatment and/or upgrading processes, additional hydrogen may be added to the process to supplement the hydrogen by-product being consumed by such processes.
In a preferred embodiment, the Fischer-Tropsch naphtha is mixed with a petroleum-derived naphtha to obtain a blended naphtha having a sulfur level above about 1 ppm, preferably above about 10 ppm. This blended naphtha is then hydrotreated over an inexpensive sulfided hydrotreating catalyst to remove oxygenates from the Fischer-Tropsch naphtha and sulfur from the petroleum-derived naphtha. Again, without the presence of some type of sulfur compound in the feedstock, the sulfur in the sulfided hydrotreating catalyst would eventually be removed and the hydrotreating catalyst would suffer a loss in performance.
Likewise, in another preferred embodiment, the Fischer-Tropsch distillate is mixed with a petroleum-derived distillate to increase the sulfur level of the blended distillate to above about 1 ppm, preferably above about 10 ppm. This blended distillate is then hydrotreated over an inexpensive sulfided hydrotreating catalyst to remove oxygenates from the Fischer-Tropsch distillate and sulfur from the petroleum-derived distillate. Without the presence of some type of sulfur compound in the feedstock, the sulfur in the sulfided hydrotreating catalyst would eventually be removed and the hydrotreating catalyst would suffer a loss in performance.
Although the need to maintain sulfided catalysts in a sulfided state while processing oxygen-containing Fischer-Tropsch feedstocks is known in the art, the use of petroleum-derived feedstocks as a source of sulfur is not known. For instance, U.S. Patent 4,080,397 to Mobil describes hydrotreating of 350°F+ Fischer- Tropsch distillates in the presence of added sulfur to prevent oxidation of a sulfided hydrotreating catalyst by oxygenates in the Fischer-Tropsch feed. However, the '397 patent does not describe the source the hydrogen used during hydrotreatment, nor does it describe using petroleum-derived feedstocks as the source of the sulfur compound.
It is also within the scope of this invention that the hydrotreatment of blended streams be done in the same reactor. Thus, a Fischer-Tropsch naphtha and a Fischer-Tropsch distillate can be hydrotreated in one reactor together with a petroleum-derived naphtha, condensate, distillate or combinations thereof, provided that the sulfur content of the blend is greater than about 1 ppm, preferably greater than about 10 ppm.
In addition, while it may be preferable to perform both naphtha reformation and distillate upgrading in a single process, processes, according to the present invention, need not include both naphtha reformation and distillate upgrading processes. That is, it is within the scope of the present invention to have a process wherein naphtha reformation or distillate upgrading are performed separately. In such embodiments it may be necessary to provide hydrogen during start up and/or hydrogen to be used in upgrading processes including, but not limited to, hydrotreating, hydrocracking and hydrodewaxing processes.
In a preferred embodiment wherein naphtha reformation is conducted separately, hydrogen may be supplied initially to be used to hydrotreat the naphtha before reformation. In addition, at least a portion of the hydrogen by-product generated during reformation can be recirculated to hydrotreat naphtha before reformation. The recirculation of hydrogen by-product generated during reformation may substantially limit the amount of hydrogen that needs to be added for hydrotreatment.
Similarly, in a preferred embodiment wherein a distillate is upgraded separately, hydrogen may need to be supplied during both hydrotreatment and upgrading.
A preferred embodiment of the present invention, wherein hydrogen generated during Fischer-Tropsch naphtha reformation is used for distillate upgrading, is depicted in Figure 1. In this embodiment, a methane-containing hydrocarbon gas feed stream 12 is obtained from a methane-containing terrestrial reservoir 11. The hydrocarbon gas feed stream 12 enters a separator 13. The separator 13 separates the hydrocarbon gas feed stream 12 into a heavier condensate stream 15, a crude oil fraction stream 14 and a methane-containing hydrocarbon gas exit stream 16. The hydrocarbon gas exit stream 16 enters a synthesis gas generator 17. A gaseous oxidant stream 18 also enters the synthesis gas generator 17. At least a part of the methane-containing hydrocarbon exit gas 16 is converted by the synthesis gas generator 17 into a synthesis gas stream 19 (a gas mixture containing at least carbon monoxide and hydrogen) by use of the gaseous oxidant stream 18 (air, 02, enriched air, carbon dioxide and combinations thereof). The synthesis gas stream 19 enters a Fischer-Tropsch reactor 20. The Fischer-Tropsch reactor 20 converts the synthesis gas stream 19 into at least a Fischer-Tropsch naphtha stream 21 and a Fischer-Tropsch distillate stream 22. The Fischer-Tropsch naphtha stream 21 enters a naphtha hydrotreatment reactor 23. The Fischer-Tropsch distillate stream 22 enters a distillate hydrotreatment reactor 24. The naphtha hydrotreatment reactor 23 treats the naphtha stream 21 to remove oxygenates to obtain a hydrotreated naphtha stream 25. The distillate hydrotreatment reactor 24 treats the distillate stream 22 to remove oxygenates to obtain a hydrotreated distillate stream 26. The hydrotreated naphtha stream 25 enters a naphtha reformer 27. The hydrotreated distillate stream 26 enters a distillate upgrader 28 wherein the hydrotreated distillate is upgraded by, for example, hydrocracking and/or hydrodewaxing processes. During naphtha reformation a hydrogen by-product stream 29 is generated. The hydrogen by-product stream 29 enters the naphtha hydrotreatment reactor 23, the distillate hydrotreatment reactor 24 and the distillate upgrader 28 providing additional hydrogen for the hydrotreatment processes conducted therein.
Following naphtha reformation, a saleable gasoline component stream containing at least about 10% aromatics, and having a research octane rating of at least about 80, preferably at least about 90, exits the naphtha reformer 27. In addition, a saleable distillate fuel or lube base stock components stream 32 exits the distillate upgrader 28. The catalysts used for hydrotreating the naphtha and distillate, and used to upgrade the hydrotreated distillate either comprise a noble metal including, but not limited to, Pd, Pt, combinations thereof or the like, or a non-noble metal including, but not limited to, Ni, Co, W, Mo, combinations thereof or the like. If used, the non-noble metal catalysts are in a sulfided form, and preferably sulfur is added to the unit either continuously or periodically. The sulfur can be added, for example, in the form of a chemical, such as dimethyldisulfide. If the hydrotreating catalyst is a noble metal (less preferred), it is preferably not sulfided.
Another preferred embodiment of the present invention, wherein hydrogen :,'ated during Fischer-Tropsch naphtha reformation is used for distillate *...ading, is depicted in Figure 2. In this embodiment, a methane-containing :rocarbon feed gas 42 is obtained from a methane-containing terrestrial r :rvoir 41. A heavier condensate stream 45 and/or a crude oil fraction stream 44 are separated from the methane-containing hydrocarbon feed gas 42 in a separator 43. A methane-containing hydrocarbon gas exit stream 46 exits the separator 43 and enters a synthesis gas generator 48. A gaseous oxidant stream 49 also enters the synthesis gas generator 48. A synthesis gas stream 50 exits the in: generator 48 and enters a Fischer-Tropsch reactor 53. The Fischer-Tropsch reactor 53 generates at least a Fischer-Tropsch naphtha stream 54 and a Fischer- Tropsch distillate-containing stream 55. The crude oil stream 44 and the condensate stream 45 enter a distillate reactor 47. At least a petroleum-derived naphtha stream 51 and a petroleum-derived distillate stream 52 exit the distillate reactor 47. The petroleum-derived naphtha stream 51 mixes with the Fischer- Tropsch distillate stream 54 to produce a blended naphtha having more than about 1 ppm sulfur, preferably more than about 10 ppm sulfur. The blended naphtha then enters a naphtha hydrotreatment reactor 56. The petroleum-derived distillate tream 52 mixes with the Fischer-Tropsch distillate stream 55 to produce a blended ,nistillate comprising more than about 1 ppm sulfur, preferably more than about :pij sulfur. The blended distillate enters a distillate hydrotreatment reactor 57.
ihe blended naphtha is hydrotreated to remove oxygenates. A hydrotreated naphtha stream 58 exits the naphtha hydrotreatment reactor 56. The hydrotreated naphtha stream 58 then enters a naphtha reformer 60. The blended distillate is hydrotreated in the distillate hydrotreating reactor 57 to remove oxygenates, and a nydrotreated distillate stream 59 exits the distillate hydrotreatment reactor 57. The hydrotreated distillate stream 59 enters a distillate upgrader 61. During reformation of the blended naphtha in the naphtha reformer 60, a hydrogen byproduct stream 62 is generated. A portion of the hydrogen by-product stream 62 i recirculated in a hydrogen recirculation stream 63 to provide additional hydrogen needed for the hydrotreatment processes being conducted within the naphtha and distillate hydrotreatment reactors 56, 57. In addition, hydrogen from -11- ;':gen by-product stream 62 enters the distillate upgrader 61 to provide :;ional hydrogen for upgrading processes hydrocracking and Sitdewaxing processes) conducted therein for upgrading the blended distillate.
A :aleable gasoline component stream 65, comprising at least about !,-natics, and having a research octane rating of at least about 80, preferably at ieast about 90, exits the naphtha reformer 60 following naphtha reformation.
Finally, a salable distillate fuel or lube base stock component stream 64 exits the distillate upgrader 61.
Another preferred embodiment of the present invention, wherein hydrogen 0o generated during Fischer-Tropsch naphtha reformation is used for distillate upgrading, is depicted in Figure 3. In this embodiment, a methane-containing hydrocarbon feed gas 72 is obtained from a methane-containing terrestrial reservoir 71. A heavier condensate stream 75 and/or crude oil fraction stream 76 are separated from the methane-containing hydrocarbon feed gas 72 in a separator 73. A methane-containing hydrocarbon exit stream gas 74 exits the separator 73 and enters a synthesis gas generator 77. A gaseous oxidant stream 78 also enters the synthesis gas generator 77. A synthesis gas stream 79 exits the synthesis gas generator 77 and enters a Fischer-Tropsch reactor 80. A Pischer-Tropsch product stream 81 exits the Fischer-Tropsch reactor 80. The ::ude oil stream 76 and the condensate stream 75 exit the separator 73 and enter a ;i'illate reactor 89. At least a petroleum-derived naphtha stream 90 and a petroleum-derived distillate stream 91 exit the distillate reactor 89 and mix with the Fischer-Tropsch product stream 81 to obtain a blended product stream, comprising at least about 1 ppm sulfur, preferably at least about 10 ppm sulfur.
The blended product stream enters a hydrotreatment reactor 82, wherein .xygenates are removed from the Fischer-Tropsch distillate and naphtha and sulfur s removed from the petroleum-derived distillate and naphtha. A hydrotreated p:oduct stream 82A exits the hyrotreatment reactor 82 and enters a distillate reactor 83. At least a blended naphtha stream 84 and a blended distillate stream 3( -,it the distillate reactor 83. The blended naphtha stream 84 enters a naphtha -e former 86 wherein the naphtha is reformed generating a hydrogen by-product stream 88 and a salable gasoline product stream 93. The gasoline product stream 93 comprises at least about 10% aromatics and has a research octane rating of at least about 80, preferably at least about 90. The blended distillate stream 85 exits the distillate reactor 83 and enters a distillate upgrader 87. The hydrogen by-product stream 88 exiting the naphtha reformer enters the distillate upgrader 87 providing additional hydrogen needed for upgrading processes hydrocracking and hydrodewaxing processes) conducted therein to upgrade the distillate. In addition, a portion of the hydrogen by-product stream 88 is recirculated in a hydrogen recirculation stream 92 to the hydrotreatment reactor 82 to provide additional hydrogen needed for the hydrotreatment processes conducted therein for the removal of oxygenates and sulfur. Finally, a saleable distillate fuel or lube base stock components stream 94 exits the distillate upgrader 87.
EXAMPLES
The invention will be further illustrated by the following example, which sets forth a particularly advantageous method embodiment. While the Example is provided to illustrate the present invention, it is not intended to limit it.
Example 1 A Fischer-Tropsch naphtha and distillate product are blended to provide a mixture that contains approximately 1 weight oxygen and less than about ppm sulfur. This mixture is hydrocracked over a sulfided nickel tungsten catalyst at 663 0 F, 1.0 LHSV, 77% conversion, 1100 psig, and 10000 SCFB hydrogen recirculation gas rate. After 1500 hours of operation, the product at that time is fractionated and the 300-650 0 F diesel portion is isolated. The sulfur content of the diesel fraction, as determined by the Antek method, is about 3.2 ppm by weight. This same sample is run in duplicate on a Dohrmann analyzer and the resulting sulfur levels are about 2.4 and about 2.6 nanograms per micro liter or about 3 ppm by weight sulfur. Both the Dohrmann and the Antek analyzers use oxidative approaches for the determination of sulfur and are reliable methods. The presence of sulfur in this product is confirmed in subsequent experiments and is believed to be due to displacement of the sulfur from the catalyst with oxygenates in the feedstock. This problem can be avoided by adding a sulfur-containing ",ound to the Fischer-Tropsch feedstock so that the blend has more than about i:m sulfur, preferably more than about 10 ppm sulfur.
While the present invention has been described with reference to specific ,,diments, this application is intended to cover those various changes and S-rutions that may be made by those of ordinary skill in the art without cpci: ,rting from the spirit and scope of the appended claims.
Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or steps.
The reference to any prior art in this specification is not, and should not be taken as, an acknowledgement or any form of suggestion that that prior art forms part of the common general knowledge in Australia.
Claims (24)
1. A process for upgrading at least one of a Fischer-Tropsch naphtha and a Fischer- Tropsch distillate to produce at least one of a gasoline component, a distillate fuel component or a lube base stock component, the process comprising: a) mixing a Fischer-Tropsch naphtha and a petroleum-derived naphtha to obtain a blended naphtha having a sulfur level of at least about 1 ppm; b) mixing a Fischer-Tropsch distillate and a petroleum-derived distillate to obtain a blended distillate having a sulfur level of at least about 1 ppm; c) producing a hydrotreated blended naphtha by hydrotreating said blended naphtha to remove oxygenates from said Fischer-Tropsch naphtha and to remove sulfur from said petroleum-derived naphtha; d) reforming said hydrotreated blended naphtha to generate hydrogen by- product and a gasoline component comprising at least about 10% aromatics; e) hydrotreating said blended distillate generating a hydrotreated blended distillate; and f) upgrading said hydrotreated blended distillate using said hydrogen by- product to produce at least one of a distillate fuel component and/or a lube base stock component.
2. A process for upgrading a Fischer-Tropsch naphtha to produce a gasoline component, the process comprising: a) mixing a Fischer-Tropsch naphtha and a petroleum-derived naphtha to obtain a blended naphtha having a sulfur level of at least about 1 ppm; b) hydrotreating said blended naphtha producing a hydrotreated blended naphtha; c) reforming said hydrotreated blended naphtha producing hydrogen by- product and a gasoline component having a research octane rating of at least about 80; and d) recirculating said hydrogen by-product to hydrotreat said blended naphtha. P:OPER\EFH\2003200318 spe 203,doc-24/07/008 00 -16-
3. The process of claim 1, wherein said gasoline component has a research octane 0rating of at least about
4. The process of claim 2, wherein said gasoline component comprises at least about aromatics. The process of claim 1 or 3, wherein upgrading of said hydrotreated blended distillate is carried out using at least one of a hydrocracking process and a hydrodewaxing process.
6. The process of claim 1 or 3, wherein at least a portion of said hydrogen by-product is recirculated to hydrotreat said blended naphtha and/or said blended distillate.
7. The process of claim 1, 2 or 3, wherein said blended naphtha has a sulfur level of at least about 10 ppm.
8. The process of claim 1 or 3, wherein said blended distillate has a sulfur level of at least about 10 ppm.
9. The process of any one of the preceding claims, wherein said gasoline component has a research octane rating of at least about The process of claim 1, wherein hydrotreatment of said blended naphtha and said blended distillate is performed in a single hydrotreatment reactor.
11. The process of any one of claims 1 to 6 and 9, wherein hydrotreatment is performed using a catalyst comprising at least one of a noble metal and a non-noble metal. P:\OPER\EPH\2003200318 spc 203 doc-24/07/2008 00 O 00 (N-17-
13. The process of claim 11 or 12, wherein said non-noble metal is selected from the group consisting ofNi, Co, W, Mo and combinations thereof.
14. The process of claim 11, 12 or 13, wherein said non-noble metal is sulfided. The process of claim 14, wherein said non-noble metal is sulfided by adding sulfur during said process.
16. The process of claim 15, wherein said sulfur is added by adding a sulfur-containing chemical.
17. The process of claim 16, wherein said sulfur-containing chemical is dimethyldisulfide.
18. The process of any one of claims 11 to 17, wherein said noble metal is not sulfided.
19. The process of claim 1, further comprising initially adding sulfur to said process so that any catalyst used during hydrotreatment is adequately sulfided. The process of any one of claims 1 to 4, and 11 to 18, wherein hydrotreatment is performed with initial provision of hydrogen.
21. The process of claim 1 or 2, further comprising providing additional hydrogen to supplement hydrogen obtained from naphtha reformation.
22. The process of claim 2, wherein immediately prior to hydrotreatment, said blended naphtha comprises about 1 ppm sulfur. P:OPER\EFHU200320031 I pe 203 dor.2410712008 00 g -18-
23. A distillate fuel component produced by the process of any one of claims 1 22.
24. A lube base stock component produced by the process of any one of claims 1, 3, 5, 6, 7, 8 and N 25. A plant for upgrading a least one of a Fischer-Tropsch naphtha and a Fischer- Tropsch distillate to produce at least one of a gasoline component, a distillate fuel or a lube base feedstock component, the plant comprising: a hydrocarbon source for providing a hydrocarbon; a separator for separating hydrocarbon gas, hydrocarbon condensate and crude oil from the hydrocarbon; a synthesis gas generator for generating a synthesis gas from the hydrocarbon gas, the synthesis gas generator positioned downstream from the separator; a Fischer-Tropsch reactor positioned downstream from the synthesis gas generator for conducting a Fischer-Tropsch process on the synthesis gas to obtain Fischer-Tropsch naphtha and Fischer-Tropsch distillate; a naphtha hydrotreatment reactor positioned downstream from the Fischer- Tropsch reactor for hydrotreating the Fischer-Tropsch naphtha produced from the Fischer-Tropsch reactor; a naphtha reformer positioned downsteam from the naphtha hydrotreatment reactor for reforming hydrotreated naphtha produced from the naphtha hydrotreatment reactor to obtain hydrogen by-product and a gasoline component comprising at least about 10% aromatics; a distillate hydrotreatment reactor positioned downstream from the Fischer- Tropsch reactor for hydrotreating the Fischer-Tropsch distillate produced from the Fischer-Tropsch reactor; a distillate upgrader positioned downstream from the distillate hydrotreatment reactor and relative to the naphtha reformer so that hydrogen by-product from the reformer recirculates to the upgrader so that upgrader can upgrade hydrotreated distillate produced from the distillate PKPWR\EPH20032003I8 spc 203 dc.24/07/2008 00 S-19- hydrotreatment reactor to produce a distillate fuel and/or a lube base feedstock component; o0 optionally a distillation reactor positioned downstream from the separator Sfor distilling the hydrocarbon condensate and the crude oil to obtain petroleum-derived naphtha and petroleum-derived distillate.
26. The plant of claim 25, wherein the distillation reactor, when present, is positioned relative to the Fischer-Tropsch reactor and the naphtha hydrotreatment reactor so that the Fischer-Tropsch naphtha and the petroleum-derived naphtha mix prior to entering the naphtha hydrotreatment reactor to form a blended naphtha having a sulfur level of at least about 1 ppm; and/or the distillation reactor, when present, is positioned relative to the Fischer-Tropsch reactor and the distillate hydrotreatment reactor so that the Fischer-Tropsch distillate and the petroleum-derived distillate mix prior to entering the distillate hydrotreatment reactor to form a blended distillate having a sulfur level of at least about 1 ppm.
27. The plant of claim 25 or 26, wherein the hydrotreatment reactors contain at least one catalyst.
28. The plant of claim 27, wherein the at least one catalyst comprises at least one of a noble metal and a non-noble metal.
29. The plant of claim 28, wherein the noble metal and the non-noble metal are as defined in any of claims 11-17. The plant of any one of claims 25 to 29, further comprising a source of sulfur positioned so that sulfur can be initially supplied to ensure that any catalysts present in the naphtha hydrotreatment reactor and/or the distillate hydrotreatment reactor are adequately sulfided. P:OPER\EPH\200320031 spc 203.doc.24/07/20D8 00 0, t 31. The plant of any one of claims 25 to 30, wherein the naphtha hydrotreatment reactor and the distillate hydrotreatment reactor constitute a single hydrotreatment reactor.
32. A process according to claim 1 or 2 or plant according to claim 25 for upgrading at least one Fischer-Tropsch naphtha and a Fischer-Tropsch distillate substantially as Shereinbefore described with reference to the drawings and/or examples.
Applications Claiming Priority (8)
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|---|---|---|---|
| US10/059,224 US7033552B2 (en) | 2002-01-31 | 2002-01-31 | Upgrading Fischer-Tropsch and petroleum-derived naphthas and distillates |
| US10/059,382 US6863802B2 (en) | 2002-01-31 | 2002-01-31 | Upgrading fischer-Tropsch and petroleum-derived naphthas and distillates |
| US10/059,382 | 2002-01-31 | ||
| US10/059,224 | 2002-01-31 | ||
| US10/059,381 US20030141221A1 (en) | 2002-01-31 | 2002-01-31 | Upgrading Fischer-Tropsch and petroleum-derived naphthas and distillates |
| US10/059,383 | 2002-01-31 | ||
| US10/059,383 US20030141220A1 (en) | 2002-01-31 | 2002-01-31 | Upgrading fischer-tropsch and petroleum-derived naphthas and distillates |
| US10/059,381 | 2002-01-31 |
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| BRPI0411711B1 (en) | 2003-06-23 | 2014-06-24 | Shell Int Research | PROCESS FOR PREPARING AN OIL BASIS |
| JP2008525551A (en) * | 2004-12-23 | 2008-07-17 | シエル・インターナシヨネイル・リサーチ・マーチヤツピイ・ベー・ウイ | Method for producing lubricating base oil |
| EP2149594A1 (en) * | 2008-07-28 | 2010-02-03 | Mohammadreza Pircheraghali | Production of gasoline using new method, blending of petroleum material cuts |
| JP5296477B2 (en) * | 2008-09-30 | 2013-09-25 | Jx日鉱日石エネルギー株式会社 | Startup method of naphtha distillate hydrotreating reactor |
| US20150322351A1 (en) * | 2012-12-17 | 2015-11-12 | Shell Oil Company | Integrated gas-to-liquid condensate process |
| WO2014095815A1 (en) * | 2012-12-17 | 2014-06-26 | Shell Internationale Research Maatschappij B.V. | Integrated gas-to-liquid condensate process |
| JP2024010687A (en) * | 2022-07-13 | 2024-01-25 | 三菱重工業株式会社 | Fuel manufacturing equipment and fuel manufacturing method |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001064610A1 (en) * | 2000-02-29 | 2001-09-07 | Chevron U.S.A. Inc. | Synthesis of alkylbenzenes and synlubes from fischer-tropsch products |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3540997A (en) * | 1968-09-27 | 1970-11-17 | Texaco Inc | Production of motor and jet fuels |
| US4041096A (en) * | 1975-09-18 | 1977-08-09 | Mobil Oil Corporation | Method for upgrading C5 plus product of Fischer-Tropsch Synthesis |
| US4080397A (en) * | 1976-07-09 | 1978-03-21 | Mobile Oil Corporation | Method for upgrading synthetic oils boiling above gasoline boiling material |
| US4126644A (en) * | 1976-10-14 | 1978-11-21 | Mobil Oil Corporation | Method of upgrading a fischer-tropsch light oil |
| US4365820A (en) * | 1978-09-12 | 1982-12-28 | Rush Donald L | Trailer connecting running gear |
| US4252736A (en) * | 1979-06-01 | 1981-02-24 | Mobil Oil Corporation | Conversion of synthesis gas to hydrocarbon mixtures utilizing dual reactors |
| US4605680A (en) * | 1981-10-13 | 1986-08-12 | Chevron Research Company | Conversion of synthesis gas to diesel fuel and gasoline |
| FR2602784B1 (en) * | 1986-04-16 | 1988-11-04 | Inst Francais Du Petrole | COMBINED HYDROREFORMING AND HYDROISOMERIZATION PROCESS |
| US4795549A (en) * | 1986-06-16 | 1989-01-03 | Union Carbide Corporation | UHP-Y-containing reforming catalysts and processes |
| US4851109A (en) * | 1987-02-26 | 1989-07-25 | Mobil Oil Corporation | Integrated hydroprocessing scheme for production of premium quality distillates and lubricants |
| DK0583836T4 (en) * | 1992-08-18 | 2002-03-11 | Shell Int Research | Process for the production of hydrocarbon fuels |
| JP3488281B2 (en) * | 1994-05-02 | 2004-01-19 | 日揮株式会社 | Petroleum processing method |
| US5562817A (en) * | 1994-12-20 | 1996-10-08 | Exxon Research And Engineering Company | Reforming using a Pt/Re catalyst |
| US5766274A (en) * | 1997-02-07 | 1998-06-16 | Exxon Research And Engineering Company | Synthetic jet fuel and process for its production |
| JPH10316975A (en) * | 1997-05-16 | 1998-12-02 | Japan Energy Corp | Method for contact reforming of hydrocarbon and method for suppressing coking |
| US5882505A (en) * | 1997-06-03 | 1999-03-16 | Exxon Research And Engineering Company | Conversion of fisher-tropsch waxes to lubricants by countercurrent processing |
| ZA989528B (en) * | 1997-12-03 | 2000-04-19 | Schuemann Sasol S A Pty Ltd | "Production of lubricant base oils". |
| US6075061A (en) * | 1998-06-30 | 2000-06-13 | Exxon Research And Engineering Company | Integrated process for converting natural gas and gas field condensate into high valued liquid products (law713) |
| US6180842B1 (en) * | 1998-08-21 | 2001-01-30 | Exxon Research And Engineering Company | Stability fischer-tropsch diesel fuel and a process for its production |
| SG87095A1 (en) * | 1999-04-02 | 2002-03-19 | Akzo Nobel Nv | Process for effecting ultra-deep hds of hydrocarbon feedstocks |
| FR2799202B1 (en) * | 1999-09-30 | 2002-04-26 | Inst Francais Du Petrole | PROCESS FOR PRODUCING ESSENCES WITH IMPROVED OCTANE INDEX |
| BR0109793A (en) * | 2000-04-03 | 2004-02-10 | Chevron Usa Inc | Integrated process for preparing isools from synthesis gas and distilled fuel composition |
| US6663767B1 (en) * | 2000-05-02 | 2003-12-16 | Exxonmobil Research And Engineering Company | Low sulfur, low emission blends of fischer-tropsch and conventional diesel fuels |
| GB2388611B (en) * | 2001-05-11 | 2004-05-26 | Chevron Usa Inc | Co-hydroprocessing of hydrocarbon synthesis products and crude oil fractions |
| US6833484B2 (en) * | 2001-06-15 | 2004-12-21 | Chevron U.S.A. Inc. | Inhibiting oxidation of a Fischer-Tropsch product using petroleum-derived products |
-
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Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001064610A1 (en) * | 2000-02-29 | 2001-09-07 | Chevron U.S.A. Inc. | Synthesis of alkylbenzenes and synlubes from fischer-tropsch products |
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| BR0215537A (en) | 2004-12-21 |
| JP2005516082A (en) | 2005-06-02 |
| AU2003200318A1 (en) | 2003-08-14 |
| GB2386904A (en) | 2003-10-01 |
| GB0301347D0 (en) | 2003-02-19 |
| GB2386904B (en) | 2005-02-23 |
| WO2003064022A1 (en) | 2003-08-07 |
| JP4748939B2 (en) | 2011-08-17 |
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