• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    A process for the continuous dearomatization of a petroleum fraction into a hydrocarbon fluid with a very low sulfur content and a very low content of aromatic compounds, comprising at least one catalytic hydrogenation step at a temperature of between 80 and 180.degree. pressure between 50 and 160 bar. The catalytic hydrogenation step of said desaromatisation process comprises a plurality of intervertible reactors connected in series.
    公开号:FR3015514A1
    申请号:FR1363388
    申请日:2013-12-23
    公开日:2015-06-26
    发明作者:Xavier Chouan；Patrick Vedrine
    申请人:Total Marketing Services SA；
    IPC主号:
    专利说明:

    [0001] FIELD OF THE INVENTION The invention relates to a process for the continuous dearomatization of a petroleum fraction in a hydrocarbon fluid with a very low sulfur content and a very low content of aromatic compounds, comprising at least a catalytic hydrogenation step at a temperature between 80 and 180 ° C and at a pressure between 50 and 160 bar. In particular, the invention relates to a method of deep dearomatisation of petroleum cutting in which the catalytic hydrogenation step comprises several intervertible reactors connected in series.
    [0002] BACKGROUND OF THE INVENTION Hydrocarbon fluids are widely used as solvents, for example in adhesives, cleaning liquids, explosives, solvents for decorative coatings, paints and printing inks, light oils for applications such as metal mining, metal working or demolding, industrial lubricants and drilling fluids. The hydrocarbon fluids can also be used as diluting oils in adhesives and sealing systems such as silicone mastics, as viscosity-lowering agents in plasticized polyvinylchloride formulations, as solvents in polymeric flocculant formulations, for example in water treatment, mining operations or papermaking and also as thickeners in printing pastes.
    [0003] Hydrocarbon fluids can moreover be used as solvents in a wide range of other applications, for example in chemical reactions. In order to produce these hydrocarbon fluids, the petroleum fractions as feeds are treated on hydrodearomatization units by a catalytic hydrogenation process consisting of several high pressure operated serial reactors. These reactors have one or more catalytic beds. The units are composed of main processing sections which are generally: charge storage, multi-reactor hydrogenation section, distillate separation section and distillation column. R: 35500 35504 TMS 35504--131223-text deposit.docx General scheme of a dearomatization process Charges 3 Hydrogenation reactors The configuration generally implemented for the hydrogenation section is a sequence of several reactors serial. The efficiency of the hydrodearomatization unit by hydrogenation is dependent on several parameters and particularly the level of catalytic activity of the first reactor used as a sulfur trap. This activity decreases over time until it becomes nil after a full period of use. The catalytic activity depends on the amount of sulfur supplied to the catalyst surface by the charges to be treated. The amount of sulfur captured by the catalyst of the first reactor is directly proportional to the sulfur concentration of the petroleum feedstock. Very little sulfur thus arrives at the second and third reactors in series. Sulfur is a poison for the catalyst needed for the dearomatization reaction, and the aromatic compounds must be hydrogenated to obtain high purity products. The catalyst of the first reactor used as a sulfur trap is thereby rapidly saturated by the amount of sulfur added with the feeds to be treated. It is then necessary to change the catalyst of this first reactor. On the other hand, in order to avoid a sulfur overflow on the second reactor, the catalyst of the first reactor will be changed to a maximum saturation of 90% and not of 100% thus causing a decrease in profitability. In contrast, the second and third reactors receiving little sulfur, they will see their replaced catalyst after longer treatment cycles of up to several years. The current configurations of the hydrodearomatization units impose a total shutdown of the whole unit for the catalyst change even if only the reactor 1 is concerned. This complete stop of the units implies a considerable loss of production, the stop being able to last several days. One objective of the application is to provide an improved method of dearomatization for the continuous preparation of hydrocarbon fluids. Another object of the invention is to provide an optimized treatment system of petroleum feeds allowing a reduction of production losses and a flexibility of operability. The aim of the invention is also to allow complete saturation of the hydrodearomatization process hydrogenation catalysts before unloading. SUMMARY OF THE INVENTION The invention relates to a process for the continuous desaromatization of a petroleum fraction in a hydrocarbon fluid with a very low sulfur content and a very low content of aromatic compounds, comprising at least one catalytic hydrogenation step at a temperature of between 80 and 180 ° C and at a pressure between 60 and 160 bar, said hydrogenation step comprises a plurality of intervertible reactors, that is to say, which can be reversed, connected in series. Preferably, the process according to the invention comprises 3 reactors connected in series. The first and second reactors of the process according to the invention can be isolated in turn from other reactors. The process according to the invention makes it possible to change the catalysts of the first and second reactors without prolonged interruption of production. According to one embodiment, the series reactors of the process according to the invention are connected by fixed additional connections making it possible to isolate one of the reactors. According to a second embodiment, the series reactors of the process according to the invention are connected by removable additional connections making it possible to isolate one of the reactors. The series reactors of the process according to the invention comprise catalysts. Said catalysts are changed to 100% saturation.
    [0004] The process according to the invention allows a hydrogenation rate of between 50 and 300 Nm3 / ton of charge. The amount by weight of catalyst in each of the 3 reactors connected in series of the process according to the invention is 0.05-0.5 / 0.10-0.70 / 0.25-0.85, respectively. Preferably, the amount by weight of catalyst in each of the 3 reactors connected in series of the process according to the invention is 0.07-0.25 / 0.15-0.35 / 0.4-0.78 and more preferably 0.10-0.20 / 0.20-0.32 / 0.48-0.70. According to one embodiment, the method according to the invention comprises the steps of: - isolating the first reactor in series, - supplying the second reactor in series by the oil cut and feeding the third reactor in series by the effluent of the second reactor replacing the catalyst of the first reactor, feeding the first reactor with the effluent from the second reactor and supplying the third reactor with the effluent from the first reactor. According to one embodiment, the process according to the invention comprises the steps of: - isolating the second reactor in series, R: 35500 35504 TMS 35504--131223 -document.docx - feeding the first reactor in series by the oil cut and feeding of the third reactor in series by the effluent of the first reactor, - replacement of the catalyst of the second reactor, - supply of the second reactor by the effluent of the first reactor and supply of the third reactor by the effluent of the second reactor . FIGURES FIGS. 1 to 8 are schematic representations of the optimized unit of dearomatization according to the invention.
    [0005] DETAILED DESCRIPTION OF THE INVENTION The process according to the invention relates to an improvement of the operating conditions of the hydrogenation reactors of a desaromatisation unit enabling the production of hydrocarbon fluids. A pre-fractionation step of the petroleum fraction may optionally be carried out before introduction of the cut into the hydrogenation unit. The optionally pre-fractionated petroleum fractions are then hydrogenated. The hydrogen that is used in the hydrogenation unit is typically a high purity hydrogen, for example, whose purity exceeds 99%, but other levels of purity may also be employed. The hydrogenation takes place in one or more reactors in series. The reactors may comprise one or more catalytic beds. Catalytic beds are generally fixed catalytic beds. The process of the present invention preferably comprises two or three reactors, preferably three reactors and is more preferably carried out in three separate reactors. The first reactor involves sulfur scavenging allowing the hydrogenation of essentially all unsaturated compounds and up to about 90% of the aromatic compounds. The flow leaving the first reactor contains essentially no sulfur. In the second stage, that is to say in the second reactor, the hydrogenation of aromatics is continued and up to 99% of the aromatics are thus hydrogenated. The third stage in the third reactor is a finishing stage which makes it possible to obtain aromatic contents of less than 300 ppm, preferably less than 100 ppm and more preferably less than 50 ppm, even in the case of high-point products. boiling. According to the invention, the sequence of reactors is configured so as to allow continuous operation of the unit and thus production without prolonged interruption of hydrocarbon fluids even during the change of the catalysts of the reactors. By prolonged interruption is meant an interruption of the unit of more than several days, preferably R = 35500 + TMS, greater than 2 days. If there is interruption in the process according to the invention, it will be of the order of a few hours and always less than 2 days or even 1 day. The process according to the invention will be described with reference to the accompanying drawings. According to FIG. 1, the hydrogenation unit comprises 3 reactors R1, R2 and R3 connected in series. According to one embodiment of the invention, the improved method comprises 4 additional fixed links (a), (b1), (b2) and (c). During the change of the catalyst of R1, the reactor R2 is directly fed with the feed via the link (a) without passing through the reactor R1. During the change of the catalyst of R1, the reactor R2 then becomes the first reactor and is thus directly fed with the feed via section (a) which no longer passes through the reactor of R1. After the change of the catalyst of R1, the reactor R2 remains the first reactor and the sections (b1) and (b2) connect the effluent of the reactor R2 to the inlet of the reactor R1 which becomes the second reactor. Section (c) makes it possible to connect the effluent from the reactor R1 to the inlet of the reactor R3. (FIG. 3) According to a second embodiment (FIG. 2), the hydrogenation unit according to the invention comprises additional removable connections which also make it possible to maintain the production during the change of the catalyst of the reactor R1. Section (d) thus completely isolates the reactor R1 during the change of its catalyst and thus to ensure increased safety conditions. The reactor R2 will be directly fed with the feed without passing through the reactor R1. The effluent from the reactor R2 will then be directly directed to the reactor inlet R3. Sections (e) and (f) of Figure 4 show the sequence of the hydrogenation reactors after the change of the reactor catalyst R1. The reactor R2 fed with the feed via section (d) remains the first reactor. Section (e) then connects the effluent from reactor R2 to the inlet of reactor R1 which becomes the second reactor. Section (f) makes it possible to connect the effluent from reactor R1 to the inlet of reactor R3.
    [0006] According to a third embodiment of the invention (FIG. 5), the reactor R2 is isolated from the reactors R1 and R3 during the change of its catalyst without interrupting the production. The additional fixed links (a), (b1) and (b2) of FIG. 5 will be closed while the link (c) will be open, thus allowing charge processing via the reactors R1 and then R3 only. The reactor R2 is thus short-circuited for the duration necessary for the change of its catalyst. According to a fourth embodiment of the invention (FIG. 6), the reactor R2 is isolated from the reactors R1 and R3 during the change of its catalyst without interrupting the production by the connection of the additional removable links (g) and (h) such 6. The feedstock to be treated will feed directly to the reactor R1 via section (g) and then the reactor effluent R1 will be directed to the reactor inlet R3 via section (h) so as never to go through the reactor R2. Once the catalyst of the reactor R2 has been renewed and activated, the optimized dearomatization process according to the third and fourth embodiments will be carried out according to FIGS. 7 and 8. by closing the additional fixed links (a), (b1), (b2) and (c) or by virtue of the additional removable connections connected (g), (i) and (j) so that the load to be treated is directed to the reactor R1 then the reactor R2 and finally the reactor R3. The diameter of each additional fixed or removable section will be adapted to the hydrogenation unit and to the forecasting capacities of production. In addition, each section, (a), (b1), (b2) and (c) will include valves to open or close the section as required.
    [0007] The improvement of the process according to the invention thus allows a maximum utilization at 100% saturation of the catalyst of the reactor R1. The yield is thus optimal in contrast to the conventional sequence where the reactor R1 catalyst must be replaced at 90% maximum saturation to avoid overflowing sulfur on the next reactor. The dearomatization process according to the invention allows the use of the reactor R2 as the first reactor during the change of the catalyst of the reactor R1. The reactor R2 will therefore be in direct contact with the sulfur contained in the feeds to be treated for the production of hydrocarbon fluids. The catalyst of the reactor R2 according to the invention will also have to be changed to 100% saturation. Typical hydrogenation catalysts may include the following metals: nickel, platinum, palladium, rhenium, rhodium, nickel tungstate, nickel-molybdenum, molybdenum, cobalt molybdate, nickel molybdate on silica and / or alumina supports, or on zeolites. A preferred catalyst is a Ni-based catalyst on an alumina support whose specific surface area varies between 100 and 200 m 2 / g of catalyst. The typical hydrogenation conditions are as follows: Pressure: 50 to 160 bar, preferably 100 to 150 bar and more preferably 110 to 120 bar. Temperature: 80 to 180 ° C, preferably 120 to 160 ° C and more preferably 130 to 150 ° C. 150 ° C - hourly volume velocity (VVH): 0.2 to 5 h -1, preferably 0.5 to 3 and more preferably 0.8 to 2 - rate of treatment with hydrogen: 50 to 300 Nm 3 / tonne of charge, preferably 80 to 250 and more preferably 100 to 200.
    [0008] No prior hydrodesulphurization of the feed essentially takes place: the sulfur compounds are trapped by the catalyst rather than being released as H2S. Under these conditions, the aromatic content of the final product will remain very low, typically less than 100 ppm, even if its boiling point is high (typically greater than 300 ° C or even greater than 320 ° C). It is possible to use a reactor that has two or three or more catalyst beds. The catalysts may be present in varying or substantially equal amounts in each reactor; for three reactors, the amounts by weight may for example be 0.050.5 / 0.10-0.70 / 0.25-0.85, preferably 0.07-0.25 / 0.15-0. , 35 / 0.4-0.78 and more preferably 0.10-0.20 / 0.20-0.32 / 0.48-0.70. It may be necessary to insert quench boxes in the recycle system to cool effluents from one reactor or catalytic bed to another to control reaction temperatures and thereby the hydrothermal equilibrium of the hydrogenation reaction.
    [0009] In one embodiment, the product obtained and / or the separated gases are at least partially recycled (s) in the feed system stages hydrogenation. This dilution helps to maintain the exothermicity of the reaction within controlled limits, particularly in the first stage. Recycling also allows heat exchange before the reaction and also better control of the temperature.
    [0010] The effluent from the hydrogenation unit contains the hydrogenated product and hydrogen. Flash separators are used to separate the effluents in the gas phase, mainly the residual hydrogen, and in the liquid phase, mainly the hydrogenated hydrocarbons. The process can be carried out using three flash separators, one high pressure, one intermediate pressure and one low pressure very close to atmospheric pressure.
    [0011] The hydrogen gas that is collected at the top of the flash separators can be recycled to the feed system of the hydrogenation unit or at different levels in the hydrogenation units between the reactors. According to the invention, the final product separated is at atmospheric pressure. It then directly feeds the vacuum fractionation unit. Preferably, the fractionation will be at a pressure of between 10 and 50 mbar and more preferably at about 30 mbar. The fractionation can be carried out in such a way that it is possible to simultaneously remove various hydrocarbon fluids from the fractionation column and that their boiling temperature can be predetermined. The hydrogenation reactors, the separators and the fractionation unit can therefore be directly connected without the need to use intermediate tanks, which is usually the case. This integration of hydrogenation and fractionation allows optimized thermal integration combined with a reduction in the number of devices and energy savings. According to the process according to the invention, the petroleum fraction used as filler is a typical refinery type petroleum fraction which may be derived from a hydrocracking unit of the R: 35500 35504 TMS 35504--131223-text deposit .docx distillates and may also include high levels of aromatics such as a conventional ultra-low sulfur diesel, heavy diesel or aviation fuel. The petroleum refinery cut can optionally be hydrocracked to obtain shorter and single molecules by adding hydrogen under high pressure in the presence of a catalyst. Descriptions of hydrocracking processes are provided in Hydrocarbon Processing (November 1996, pages 124-128), in Hydrocracking Science and Technology (1996) and in US 4347124, US 4447315 and WO-A-99/47626. A preferred petroleum cut as a refinery petroleum cutter according to the invention is a hydrocracked gasoil fraction resulting from the vacuum distillation.
    [0012] The optionally hydrocracked refinery oil cut can also be mixed with a hydrocarbon cut resulting from a gas to liquid (GOT) process and / or gaseous condensates and / or a hydrodeoxygenated hydrocarbon cut obtained at from biomass. Ideally, and in accordance with the process according to the invention, the petroleum fraction, whether or not mixed, contains less than 15 ppm of sulfur, preferably less than 8 ppm and more preferably less than 5 ppm (according to EN ISO 20846) and less of 70% by weight of aromatics, preferably less than 50% by weight and more preferably less than 30% by weight (according to the standard IP391 or EN 12916) and has a density of less than 0.830 g / cm 3 (according to EN standard ISO 12185).
    [0013] The fluids produced in accordance with the process of the invention have a boiling range of between 100 and 400 ° C. and have a very low aromatic content generally less than 300 ppm, preferably less than 100 ppm and more preferably less than 50 ppm. . The fluids produced according to the process of the invention also have an extremely low sulfur content, less than 5 ppm, preferably less than 3 ppm and more preferably less than 0.5 ppm, at a level too low to be detectable at conventional analyzers capable of measuring very low levels of sulfur. The fluids produced in accordance with the process of the invention also have: a naphthene content of less than 60% by weight, in particular less than 50% or even less than 40% and / or a polynaphthene content of less than 30% by weight weight, in particular less than 25% or even less than 20% and / or - a paraffin content greater than 40% by weight, in particular greater than 60% or even greater than 70% and / or - an isoparaffin content greater than 20 % by weight, in particular greater than 30% or even greater than 40%. The fluids produced in accordance with the process of the invention possess remarkable properties in terms of aniline point or solvent power, molecular weight, pressure of 10% or more. steam, viscosity, evaporation conditions defined for systems for which drying is important and defined surface tension.
    [0014] The fluids produced according to the process of the invention can be used as drilling liquids, as industrial solvents, in coating fluids, for the extraction of metals, in the mining industry, in explosives, in demoulding formulations concrete, in adhesives, in printing inks, for metal working, as rolling oils, as electro-erosion machining liquids, as anti-rust agents in industrial lubricants, as diluting oils, in sealing or silicone-based polymeric formulations, such as viscosity-lowering in plasticized polyvinyl chloride formulations, in resins, in crop protection phytosanitary formulations, in pharmaceuticals, in paint compositions , in polymers used in the treatment of water, in the manufacture of paper or in printing pastes or as cleaning solvents. EXAMPLE In the remainder of the present description, examples are given by way of illustration of the present invention and are in no way intended to limit its scope. The diagram below shows a comparison between a normal system of series hydrogenation reactors and the optimized system according to the invention during the change of the catalyst of the reactor R1 and the catalyst of the reactor R2. For the purposes of this comparison, it is considered that the 3 reactors of the hydrodearomatization unit have a volume equal to 110 m3 with a catalyst volume for the reactor R1 equal to 25 m3 and equal to 35 m3 for the reactor R2 .
    [0015] According to this scheme, it is found that 221 hours or about 9 days are necessary for the reactor R1 catalyst change operations and 245 hours, or about 10 days for the change of the reactor R2 catalyst. This time is more important for the change of the catalyst of the reactor R1 than for that of the reactor R2 because the volume of the catalyst of R2 is greater.
    [0016] The time required to change the reactor catalyst R1 in an optimized dearomatization unit configuration is the same as that of a normal configuration, about 9 days. However, the optimized configuration of the R1 and R2 reactors of the desaromatisation unit according to the invention makes it possible to continue the production of hydrocarbon fluids during the changes of the catalysts of the reactors R1 and R2 contrary to a normal configuration. On the other hand, the catalyst of the reactors R1 and R2 in the optimized configuration according to the invention are changed to 100% saturation in contrast to a normal configuration with which it is necessary to change the catalyst to 90% saturation to avoid overflowing sulfur to the next reactor. R: 35500 35504 TMS 35504--131223-text deposit.docx t- 4 43 and t P-10 - * C; - ^ r ^ 71 '.54! s. ## EQU1 ##, ## EQU1 ##, ## EQU1 ## S - --Clib- "" "" "" "" "" "'' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' '' - ' .docx
    权利要求:
    Claims (12)
    [0001]
    REVENDICATIONS1. A process for continuously dearomatizing a petroleum fraction into a hydrocarbon fluid with a very low sulfur content and a very low content of aromatic compounds, comprising at least one catalytic hydrogenation step at a temperature of between 80 and 180.degree. pressure between 50 and 160 bars, characterized in that the catalytic hydrogenation stage comprises several intervertible reactors connected in series.
    [0002]
    2. Method according to claim 1 characterized in that the catalytic hydrogenation step comprises three interruptible reactors connected in series each comprising at least one catalyst.
    [0003]
    3. Method according to one of claims 1 or 2 characterized in that the first and second reactors can be isolated in turn.
    [0004]
    4. Method according to one of claims 1, 2 or 3, characterized in that the change of the catalysts of the first and second reactors is done without prolonged interruption of the production of hydrocarbon fluids.
    [0005]
    5. Method according to any one of claims 1 to 4, characterized in that the series reactors are connected by fixed additional links for isolating one of the reactors.
    [0006]
    6. Method according to any one of claims 1 to 4, characterized in that the series reactors are connected by removable additional connections for isolating one of the reactors.
    [0007]
    7. Process according to any one of claims 1 to 6, characterized in that the reactors comprise catalysts, the catalysts of the reactors being changed to 100% saturation.
    [0008]
    8. Method according to any one of claims 1 to 7, characterized in that the hydrogenation rate is between 50 to 300 Nm3 / tonne of petroleum cutting.
    [0009]
    9. Process according to any one of claims 2 to 8, characterized in that the amount by weight of catalyst in each of the reactors is 0.05-0.5 / 0.10-0.70 / 0.25-0. 85. R: 35500 35504 TMS 35504--131223-text deposit.docx
    [0010]
    10. The method of claim 9, characterized in that the amount by weight of catalyst in each of the reactors is 0.07-0.25 / 0.15-0.35 / 0.4-0.78 and more preferably 0.100.20 / 0.20-0.32 / 0.48-0.70.
    [0011]
    11. Method according to one of claims 2 to 10, comprising the steps of: - isolation of the first reactor in series, - supply of the second reactor in series by the oil cut and supply of the third reactor in series by the effluent of the second reactor, - replacement of the catalyst of the first reactor, - supply of the first reactor by the effluent of the second reactor and supply of the third reactor by the effluent of the first reactor.
    [0012]
    12. Method according to one of claims 2 to 10, comprising the steps of: - isolation of the second reactor in series, - supply of the first reactor in series by the oil cut and supply of the third reactor in series by the effluent of the first reactor, - replacement of the catalyst of the second reactor, - supply of the second reactor by the effluent of the first reactor and supply of the third reactor by the effluent of the second reactor. R: 35500 35504 TMS 35504--131223-text deposit.docx
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    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    EP0026508A1|1979-09-26|1981-04-08|Shell Internationale Researchmaatschappij B.V.|Process and apparatus for the demetallization of a hydrocarbon oil|
    US20120283492A1|2009-11-20|2012-11-08|Total Raffinage Marketing|Process for the production of hydrocarbon fluids having a low aromatic content|
    US20130001127A1|2009-11-20|2013-01-03|Total Raffinage Marketing|Process for the production of hydrocarbon fluids having a low aromatic content|
    FR2984915A1|2011-12-22|2013-06-28|IFP Energies Nouvelles|METHOD FOR SELECTIVE HYDROGENATION OF OLEFINIC LOADS WITH PERMUTABLE REACTORS INCLUDING AT LEAST ONE REACTOR SHORT CIRCUITAGE STEP|
    GB834776A|1957-11-26|1960-05-11|Bataafsche Petroleum|A method of preparing a liquid hydrocarbon fuel having a high heat of combustion perunit volume|
    GB1232594A|1967-07-11|1971-05-19|
    JPS4934527B1|1969-04-25|1974-09-14|
    GB1282774A|1969-08-27|1972-07-26|Shell Int Research|A process for the catalytic hydrogenation of hydrocarbon oils or oil fractions and a catalyst therefor|
    GB1218920A|1969-09-26|1971-01-13|Chevron Res|Catalytic production of low pour point lubricating oils|
    US3846278A|1971-09-02|1974-11-05|Lummus Co|Production of jet fuel|
    US3767562A|1971-09-02|1973-10-23|Lummus Co|Production of jet fuel|
    NL153934B|1973-02-02|1977-07-15|Basf Ag|PROCEDURE FOR THE CATALYTIC HYDROGENATION OF AROMATICS, SULFUR AND NITROGEN COMPOUNDS CONTAINING MINERAL OIL FRACTIONS.|
    US4036734A|1973-11-02|1977-07-19|Exxon Research And Engineering Company|Process for manufacturing naphthenic solvents and low aromatics mineral spirits|
    JPS5820657B2|1980-06-24|1983-04-25|Nittetsu Mining Co Ltd|
    US4447315A|1983-04-22|1984-05-08|Uop Inc.|Hydrocracking process|
    US4601814A|1983-05-27|1986-07-22|Total Engineering And Research Company|Method and apparatus for cracking residual oils|
    US4816137A|1983-05-27|1989-03-28|Total Engineering And Research Company|Method for cracking residual oils|
    US4469590A|1983-06-17|1984-09-04|Exxon Research And Engineering Co.|Process for the hydrogenation of aromatic hydrocarbons|
    US4875992A|1987-12-18|1989-10-24|Exxon Research And Engineering Company|Process for the production of high density jet fuel from fused multi-ring aromatics and hydroaromatics|
    US5114562A|1990-08-03|1992-05-19|Uop|Two-stage hydrodesulfurization and hydrogenation process for distillate hydrocarbons|
    US5498810A|1991-11-21|1996-03-12|Uop|Selective isoparaffin synthesis from naphtha|
    FR2714387B1|1993-12-28|1996-02-02|Inst Francais Du Petrole|Process for obtaining a base for fuel for an internal combustion engine by hydrotreatment and extraction and the product obtained.|
    US5612422A|1995-05-04|1997-03-18|The Dow Chemical Company|Process for hydrogenating aromatic polymers|
    FR2734575B1|1995-05-22|1997-08-22|Total Raffinage Distribution|CARBUREACTOR AND PROCESS FOR PREPARING THE SAME|
    FR2757872B1|1996-12-31|1999-06-25|Total Raffinage Distribution|PROCESS FOR HYDROTREATING A HYDROCARBON CHARGE AND DEVICE FOR IMPLEMENTING SAME|
    EP0921179A1|1997-12-05|1999-06-09|Fina Research S.A.|Production of olefins|
    BR9908753B1|1998-03-14|2010-07-13|integrated hydroconversion process.|
    FR2776667B1|1998-03-31|2000-06-16|Total Raffinage Distribution|METHOD AND DEVICE FOR ISOMERIZING HIGH-BENZENE GASOLINE ESSENCES|
    FR2793706B1|1999-05-18|2001-08-03|Total Raffinage Distribution|OXIDE-BASED CATALYTIC SUPPORT OF A METAL FROM GROUP IVB OF THE PERIODIC CLASSIFICATION OF ELEMENTS, ITS PREPARATION AND USES|
    FR2808534B1|2000-05-03|2002-08-02|Total Raffinage Distribution|BIODEGRADABLE LUBRICANT COMPOSITION AND USES THEREOF, ESPECIALLY IN A DRILLING FLUID|
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    CA2416298A1|2000-07-17|2002-01-24|Shell Internationale Research Maatschappij B.V.|Process to prepare water-white lubricant base oil|
    CN1322097C|2000-12-11|2007-06-20|法国石油公司|Method for hydrotreatment of heavy hydrocarbon fraction with switchable reactors and reactors capable of being shorted out|
    EP2439254A3|2002-03-06|2012-06-20|ExxonMobil Chemical Patents Inc.|Improved hydrocarbon fluids|
    EP1342774A1|2002-03-06|2003-09-10|ExxonMobil Chemical Patents Inc.|A process for the production of hydrocarbon fluids|
    FR2850978B1|2003-02-12|2006-08-25|Totalfinaelf France|PROCESS FOR MANUFACTURING HYDROCARBON FLUIDS RICH IN NAPHTHENIC HYDROCARBONS|
    JP2004269685A|2003-03-07|2004-09-30|Nippon Oil Corp|Gas oil composition and its manufacturing method|
    FR2864101B1|2003-12-19|2006-03-17|Total France|CATALYTIC METHOD FOR PURIFYING LIGHT HYDROCARBONS|
    SG158840A1|2005-01-14|2010-02-26|Exxonmobil Chem Patents Inc|Ultra pure fluids|
    JP5105326B2|2007-04-19|2012-12-26|昭和電工株式会社|Hydrogenation method and petrochemical process|
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    法律状态:
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    2016-11-21| PLFP| Fee payment|Year of fee payment: 4 |
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    优先权:
    申请号 | 申请日 | 专利标题
    FR1363388A|FR3015514B1|2013-12-23|2013-12-23|IMPROVED PROCESS FOR DESAROMATIZATION OF PETROLEUM CUTTERS|FR1363388A| FR3015514B1|2013-12-23|2013-12-23|IMPROVED PROCESS FOR DESAROMATIZATION OF PETROLEUM CUTTERS|
    US15/107,360| US10246652B2|2013-12-23|2014-12-15|Process for the dearomatization of petroleum cuts|
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    EP14814825.7A| EP3087160B1|2013-12-23|2014-12-15|Improved method for the removal of aromatics from petroleum fractions|
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    TW103144718A| TW201533230A|2013-12-23|2014-12-22|Improved process for the dearomatization of petroleum cuts|
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