EP0099141B1 - Procédé pour la production de mélanges d'hydrocarbures à faible teneur en asphaltène - Google Patents
Procédé pour la production de mélanges d'hydrocarbures à faible teneur en asphaltène Download PDFInfo
- Publication number
- EP0099141B1 EP0099141B1 EP83200869A EP83200869A EP0099141B1 EP 0099141 B1 EP0099141 B1 EP 0099141B1 EP 83200869 A EP83200869 A EP 83200869A EP 83200869 A EP83200869 A EP 83200869A EP 0099141 B1 EP0099141 B1 EP 0099141B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- deasphalted oil
- feed
- asphaltic bitumen
- asphaltenes
- product
- 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.)
- Expired
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G67/00—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only
- C10G67/02—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only plural serial stages only
- C10G67/04—Treatment of hydrocarbon oils by at least one hydrotreatment process and at least one process for refining in the absence of hydrogen only plural serial stages only including solvent extraction as the refining step in the absence of hydrogen
- C10G67/0454—Solvent desasphalting
- C10G67/0463—The hydrotreatment being a hydrorefining
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10G—CRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
- C10G2300/00—Aspects relating to hydrocarbon processing covered by groups C10G1/00 - C10G99/00
- C10G2300/10—Feedstock materials
- C10G2300/107—Atmospheric residues having a boiling point of at least about 538 °C
Definitions
- the invention relates to a process for the production of deasphalted oils and hydrocarbon oil distillates from asphaltenes-containing hydrocarbon mixtures.
- solvent deasphalting may be used to separate from an atmospheric residue a deasphalted oil which may be subjected to catalytic cracking in the presence or in the absence of hydrogen.
- DA solvent deasphalting
- Another option is to separate an atmospheric residue by vacuum distillation into a vacuum distillate and a vacuum residue, to separate a deasphalted oil from the vacuum residue using DA and to subject both the vacuum distillate and the deasphalted oil to catalytic cracking in the presence or in the absence of hydrogen.
- a drawback to the conventional DA treatment, in which an asphaltenes-containing feed is separated in one step into a deasphalted oil as the desired main product and an asphaltic bitumen as a by-product, is that if a sufficiently high yield of deasphalted oil is to be realised, one must generally accept a deasphalted oil of unsatisfactory quality.
- the quality of the deasphalted oil should be taken to be its suitability to be converted into hydrocarbon oil distillates by catalytic cracking in the presence or in the absence of hydrogen. This suitability becomes better according as the deasphalted oil has, among other things, lower asphaltenes, metal and sulphur contents.
- Deasphalted oil 1 a high-quality deasphalted oil
- deasphalted oil 2 a deasphalted oil of lower quality
- asphaltic bitumen an asphaltic bitumen.
- Deasphalted oil 1 differs from deasphalted oil 2 mainly by its considerably lower asphaltenes, metal and sulphur contents.
- One of the pretreatments investigated was a catalytic hydrotreatment (for the sake of brevity hereinafter referred to as "HT") in which the asphaltenes-containing feed is converted into a product having a reduced asphaltenes content, from which one or more distillate fractions are separated whilst the residue is used as the feed for the two-step DA treatment.
- HT catalytic hydrotreatment
- the yield and quality of the deasphalted oils and the asphaltic bitumen that play a role the yield of light product is of great importance as well.
- the quality of the asphaltic bitumen should be taken to be its suitability to serve as fuel oil component. This suitability is better according to the asphatic bitumen has lower metal and sulphur contents and lower viscosity and density.
- procedure b) is much to be preferred to procedure a).
- the present patent application therefore relates to a process for the production of deasphalted oils and hydrocarbon oil distillates from asphaltenes-containing hydrocarbon mixtures, in which a HT is used to convert an asphaltenes-containing hydrocarbon mixture into a product with a reduced asphaltenes content which is separated by distillation into one or more distillate fractions and a residual fraction and in which two-step DA is used to separate the residual fraction into a deasphalted oil 1 of high quality, a deasphalted oil 2 of lower quality and an asphaltic bitumen.
- the feed used is an asphaltenes-containing hydrocarbon mixture.
- a suitable parameter for the assessment of the asphaltenes content of a hydrocarbon mixture and for the reduction of the asphaltenes content which occurs when a HT is applied to an asphaltenes-containing hydrocarbon mixture is the Ramsbottom Carbon Test value (RCT).
- RCT Ramsbottom Carbon Test value
- the process is preferably applied to hydrocarbon mixtures which substantially boil above 350°C and more than 35%w of which boils above 520°C and which have an RCT of more than 7.5%w. Examples of such hydrocarbon mixtures are residues obtained in the distillation of crude mineral oils and heavy hydrocarbon mixtures obtained from shale and tar sand.
- the process may also be applied to heavy crude mineral oils, to residues obtained in the distillation of products developed in the thermal cracking of hydrocarbon mixtures and to asphaltic bitumen obtained in the solvent deasphalting of asphaltenes-containing hydrocarbon mixtures.
- the process according to the invention is very suitable for application to residues obtained in the vacuum distillation of atmospheric distillation residues of crude mineral oils.
- the process according to the invention is also very suitable for application to residues obtained in the vacuum distillation of atmospheric distillation residues of products developed in the thermal cracking of asphaltenes-containing hydrocarbon mixtures.
- the feed available for the process according to the invention is an atmospheric distillation residue
- the separated vacuum distillate can be subjected to thermal cracking or to catalytic cracking in the presence or in the absence of hydrogen to convert it into light hydrocarbon oil distillates.
- Asphaltenes-containing hydrocarbon mixtures generally contain a considerable proportion of metals, in particular vanadium and nickel. If such hydrocarbon mixtures are subjected to a catalytic treatment, for instance a HT for the reduction of the asphaltenes content, as in the process according to the invention, these metals will deposit on the catalyst used in the HT and thus shorten its life.
- asphaltenes-containing hydrocarbon mixtures with a vanadium+nickel content of more than 50 parts per million by weight (ppmw) should preferably be subjected to demetallization before being contacted with the catalyst used in the HT.
- This demetallization may very suitably be carried out by contacting the asphaltenes-containing hydrocarbon mixture in the presence of hydrogen with a catalyst consisting more than 80%w of silica.
- a catalyst consisting more than 80%w of silica Both catalysts consisting entirely of silica and catalysts containing one or more metals having hydrogenating activity, in particular a combination of nickel and vanadium, present on a carrier support substantially consisting of silica, are suitable for the purpose. If in the process according to the invention a catalytic demetallization in the presence of hydrogen is applied to an asphaltenes-containing feed, this demetallization may be carried out in a separate reactor.
- the two processes may also very suitably be carried out in the same reactor, which will contain a bed of the demetallization catalyst and a bed of the catalyst used in the HT, successively.
- Suitable catalysts for carrying out the HT are those containing at least one metal chosen from the group formed by nickel and cobalt and in addition at least one metal chosen from the group formed by molybdenum and tungsten supported on a carrier, which carrier consists more than 40%w of alumina.
- Very suitable catalysts for use in the HT are those comprising the metal combinations nickel/molybdenum or cobalt/molybdenum on alumina as a carrier.
- the HT is preferably carried out at a temperature of from 300-500°C and in particular of from 350-450°C, a pressure of from 50-300 bar and in particular of from 75-200 bar, a space velocity of from 0.02-10 g.g-'.h-' and in particular of from 0.1-2 g.g -1 .h -1 and a H 2 /feed ratio of from 100-5000 Ni.kg- 1 and in particular of from 500-2000 Ni.kg- 1 .
- the conditions used in a possible catalytic demetallization in the presence of hydrogen the same preference applies as that stated hereinbefore for the HT for the reduction of the asphaltenes content.
- the HT is preferably carried out in such a manner that it yields a product the Cs fraction of which meets the following requirements:
- a product with a reduced asphaltenes content is obtained from which one or more distillate fractions and a heavy fraction are separated.
- the distillate fractions separated from the product may be atmospheric distillates only, but it is preferred to separate a vacuum distillate from the product as well. This vacuum distillate may be converted into light hydrocarbon oil distillates in the manners indicated hereinbefore.
- two-step DA treatment is applied to a distillation residue obtained as one of the products of the HT.
- Suitable solvents for carrying out the DA treatment are waxy hydrocarbons having 3-7 carbon atoms per molecule, such as propane, n-butane isobutane, n-pentane, isopentane and mixtures thereof, such as mixtures of propane and n-butane and mixtures of n-butane and isobutane.
- Suitable solvent/oil weight ratios lie between 7:1 and 1:1.
- the DA treatment is preferably carried out at elevated temperature and pressure.
- the two-step DA treatment may essentially be carried out in two ways.
- the residue from the HT to be treated is subjected to extraction under mild conditions in which the residue is separated into a deasphalted oil 1 and a "light" asphaltic bitumen and subsequently the light asphaltic bitumen is subjected in the second step to a second extraction in which it is separated into a deasphalted oil 2 and the final asphaltic bitumen as a by-product.
- the same solvent can be used in both steps and the degree of extraction is controlled with the aid of the temperature (temperature in the first step higher than in the second step).
- Different solvents may also be used, for instance propane in the first step and n-butane in the second step.
- the residue from the HT to be treated is subjected to extraction under severe conditions in which the residue is separated into a deasphalted oil and the final asphaltic bitumen as a by-product and subsequently the deasphalted oil is separated in the second step into a deasphalted oil 1 and a deasphalted oil 2.
- the mixture of deasphal t ed oil and solvent coming from the extractor need only be fed into a settler in which a higher temperature prevails than that used in the first step.
- each one of these embodiments may be assigned to one of two main classes, depending on whether the asphaltenes-containing feed is subjected to the HT immediately (class I) or whether the asphaltenes-containing feed is first subjected to thermal cracking (for the sake of brevity hereinafter referred to as TC) and the HT is applied to a residual fraction of the thermally cracked product (class II).
- the embodiments belonging to class I may further be arranged according to whether the apparatus in which the process is carried out is confined to a HT zone and a two-step DA zone (class IA) or whether the apparatus in addition to a HT zone and a two-step DA zone also includes a TC zone (class IB), a CC zone (IC) or both a TC zone and a CC zone (class ID), in which the deasphalted oil 2 and/or the asphaltic bitumen separated in the two-step DA zone, are further processed.
- CC as used hereinbefore should be taken to refer to a special type of catalytic, cracking for the preparation of light hydrocarbon oil distillates, in which the feed used is a de- asphalfed oil 2.
- This feed is distinguished from the feed which is normally used in a catalytic cracking process by the fact that the deasphalted oil 2 has, among other things, a much higher RCT and a much higher metal content.
- the object is to obtain as complete as possible a conversion of the asphaltenes-containing feed into deasphalted oil and hydrocarbon oil distillates
- Carrying out the process according to the invention by using a TC treatment and/or a CC treatment yields cracked products from which one or more distillate fractions are separated.
- These distillate fractions may be atmospheric distillates only, but preferably a vacuum distillate should also be separated from the cracked products. This vacuum distillate may be converted into light hydrocarbon oil distillates by the methods mentioned hereinbefore.
- the process according to the invention is carried out in an apparatus which includes a TC zone, whilst the streams which are fed into this TC zone consist of one or more relatively low-asphaltenes streams-such as a deasphalted oil 2-as well as of one or more relatively asphaltenes-rich streams-such as asphaltic bitumen separated in the process and/or the asphaltenes-containing feed which is to be processed with the aid of the process-, it is preferred to use a TC zone which includes two cracking units and to crack the types of feed separately into products from which one or more distillate fractions and a residual fraction are separated.
- a TC zone which includes two cracking units and to crack the types of feed separately into products from which one or more distillate fractions and a residual fraction are separated.
- a heavy fraction of the cracked product coming from the cracking unit in which a relatively low-asphaltenes feed is processed is preferably recirculated to that cracking unit.
- a TC zone which includes two cracking units, then, from the product obtained in the cracking unit in which the relatively asphaltenes-rich feed is cracked, a relatively low-asphaltenes heavy fraction may be separated, if desired, and the latter may be used as a feed component for the cracking unit in which the relatively low-asphaltenes feed is processed.
- a TC zone which includes two cracking units
- the process is carried out in an apparatus consisting of a HT zone composed of a catalytic hydrotreatment unit ⁇ (11), an atmospheric distillation unit (15) and a vacuum distillation unit (16) and a two-step DA zone (12), successively.
- An asphaltenes-containing hydrocarbon mixture (1), together with hydrogen (20), is subjected to a catalytic hydrotreatment.
- the hydrotreated product (21) is separated by atmospheric distillation into a gas fraction (22), an atmospheric distillate (2A) and an atmospheric residue (23).
- the atmospheric residue (23) is separated by vacuum distillation into a vacuum distillate (2B) and a vacuum residue (3).
- the vacuum residue (3) is separated by two-step deasphalting into a deasphalted oil 1 (stream 4), a deasphalted oil 2 (stream 5) and an asphaltic bitumen (6).
- the process is carried out in an apparatus consisting of a HT zone composed of a catalytic hydrotreatment unit (11), an atmospheric distillation unit (15) and a vacuum distillation unit (16), a two-step DA zone (12) and a TC zone composed of a thermal cracking unit (13), a second atmospheric distillation unit (17) and a second vacuum distillation unit (18), successively.
- a HT zone composed of a catalytic hydrotreatment unit (11), an atmospheric distillation unit (15) and a vacuum distillation unit (16), a two-step DA zone (12) and a TC zone composed of a thermal cracking unit (13), a second atmospheric distillation unit (17) and a second vacuum distillation unit (18), successively.
- An asphaltenes-containing hydrocarbon mixture (1) is mixed with a recirculation stream (8) and the mixture (29), together with hydrogen (20), is subjected to a catalyst hydrotreatment.
- the hydrotreated product (21) is separated by atmospheric distillation into a gas fraction (22), an atmospheric distillate (2A) and an atmospheric residue (23).
- the atmospheric residue (23) is separated by vacuum distillation into a vacuum distillate (2B) and a vacuum residue (3).
- the vacuum residue (3) is separated by two-step solvent deasphalting into a deasphalted oil 1 (stream 4), a deasphalted oil 2 (stream 5) and an asphaltic bitumen (6).
- the asphaltic bitumen (6) is divided into two portions (30) and (31). Portion (30) is subjected to thermal cracking.
- the thermally cracked product (24) is separated by atmospheric distillation into a gas fraction (25), an atmospheric distillate (7A) and an atmospheric residue (26).
- the atmospheric residue (26) is separated by vacuum distillation into a vacuum distillate
- the process is carried out in an apparatus consisting of a HT zone composed of a catalytic hydrotreatment unit (11), an atmospheric distillation unit (15) and a vacuum distillation unit (16), a two-step DA zone (12) and a CC zone composed of a catalytic cracking unit (14) and a second atmospheric distillation unit (19), successively.
- An asphaltenes-containing hydrocarbon mixture (1) is mixed with a recirculation stream (10) and the mixture (32), together with hydrogen (20), is subjected to a catalytic hydrotreatment.
- the hydrotreated product (21) is separated by atmospheric distillation into a gas fraction (22), an atmospheric distillate (2A) and an atmospheric residue (23).
- the atmospheric residue (23) is separated by vacuum distillation into a vacuum distillate (2B) and a vacuum residue (3).
- the vacuum residue (3) is separated by two-step solvent deasphalting into a deasphalted oil 1 (stream 4), a deasphalted oil 2 (stream 5) and an asphaltic bitumen (6).
- the deasphalted oil 2 (stream 5) is subjected to catalytic cracking.
- the catalytically cracked product (27) is separated by atmospheric distillation into a gas fraction (28), an atmospheric distillate (9) and an atmospheric residue (10).
- the process is carried out in an apparatus consisting of a HT zone composed of a catalytic hydrotreatment unit (11), an atmospheric distillation unit (15) and a vacuum distillation unit (16), a two-step DA zone (12), a TC zone composed of a thermal cracking unit (13), a second atmospheric distillation unit (17) and a second vacuum distillation unit (18) and a CC zone composed of a catalytic cracking unit (14) and a third atmospheric distillation unit (19), successively.
- An asphaltenes-containing hydrocarbon mixture (1) is mixed with a recirculation stream (34) and the mixture (33), together with hydrogen (20), is subjected to a catalytic hydrotreatment.
- the hydrotreated product (21) is separated by atmospheric distillation into a gas fraction (22), an atmospheric distillate (2A) and an atmospheric residue (23).
- the atmospheric residue (23) is separated by vacuum distillation into a vacuum distillate (2B) and a vacuum residue (3).
- the vacuum residue (3) is separated by two-step solvent deasphalting into a deasphalted oil 1 (stream 4), a deasphalted oil 2 (stream 5) and an asphaltic bitumen (6).
- the asphaltic bitumen (6) is divided into two portions (30) and (31). Portion (30) is subjected to thermal cracking.
- the thermally cracked product (24) is separated by atmospheric distillation into a gas fraction (25), an atmospheric distillate (7A) and an atmospheric residue (26).
- the atmospheric residue (26) is separated by vacuum distillation into a vacuum distillate (7B) and a vacuum residue (8).
- the deasphalted oil 2 (stream 5) is subjected to catalytic cracking.
- the catalytically cracked product (27) is separated by atmospheric distillation into a gas fraction (28), an atmospheric distillate (9) and an atmospheric residue (10).
- Streams (8) and (10) are mixed to form the recirculation stream (34).
- the process is carried out in an apparatus consisting of a TC zone composed of a thermal cracking unit (13), an atmospheric distillation unit (17) and a vacuum distillation unit (18), a HT zone composed of a catalytic hydrotreatment unit (11), a second atmospheric distillation unit (15) and a second vacuum distillation unit (16) and a two-step DA zone (12), successively.
- An asphaltenes-containing hydrocarbon mixture (1) is subjected to thermal cracking.
- the thermally cracked product (24) is separated by atmospheric distillation into a gas fraction (25), an atmospheric distillate (7A) and an atmospheric residue (26).
- the atmospheric residue (26) is separated by vacuum distillation into a vacuum distillate (7B) and a vacuum residue (8).
- the vacuum residue (8), together with hydrogen (20), is subjected to a catalytic hydrotreatment.
- the hydrotreated product (21) is separated by atmospheric distillation into a gas fraction (22), an atmospheric distillate (2A) and an atmospheric residue (23).
- the atmospheric residue (23) is separated by vacuum distillation into a vacuum distillate (2B) and a vacuum residue (3).
- the vacuum residue (3) is separated by two-step solvent deasphalting into a deasphalted oil 1 (stream 4), a deasphalted oil 2 (stream 5) and an asphaltic bitumen (6).
- the present patent application also includes apparatuses for carrying out the embodiments according to the process according to the invention which substantially correspond with those schematically represented in Figures I-VII.
- the starting material was an asphaltenes-containing hydrocarbon mixture obtained as a residue in the vacuum distillation of an atmospheric distillation residue of a crude mineral oil.
- the vacuum residue boiled substantially above 520°C and had an RCT of 18.8%w, an overall vanadium and nickel content of 167 ppmw and a sulphur content of 5.4%w.
- the process was carried out according to the flow diagrams A-E. The following conditions were used in the various zones.
- the catalytic hydrotreatment unit consisted of two reactors, the first of which was filled with a NiN/Si0 2 catalyst containing 0.5 parts by weight (pbw) of nickel and 2.0 pbw of vanadium per 100 pbw of silica and the second of which was filled with a Ni/Mo/AI 2 0 3 catalyst containing 4 pbw of nickel and 12 pbw of molybdenum per 100 pbw of alumina.
- the catalysts were used in a volume ratio 1:4.
- the HT was carried out at a hydrogen pressure at 150 bar, a space velocity (measured over the two reactors) of 0.5 kg of feed per litre of catalyst per hour, a H 2 /feed ratio of 1000 NI per kg and an average temperature of 410°C in the first reactor and 390°C in the second reactor.
- the two-step DA treatment was carried out by contacting the feed to be deasphalted in the first step (in an extractor) with a n-butane/isobutane mixture (weight ratio 65:35) at a temperature of 110°C, a pressure of 40 bar and a solvent/oil weight ratio of 2:1 and, after the asphaltic bitumen has been separated off, separating the deasphalted oil in a second step (in a settler) at a temperature of 140°C and a pressure of 40 bar into a deasphalted oil 1 and a deasphalted oil 2.
- the CC treatment was carried out at a temperature of 510°C, a pressure of 2.2 bar, a space velocity of 2 kg.kg-'.h- 1 and a catalyst renewal rate of 1.0 pbw of catalyst per 1000 pbw of oil and using a zeolite cracking catalyst.
- Example 6 the two-step DA treatment was carried out in substantially the same way as described in the Examples 1-5, with the distinction that the temperature prevailing in the settler described in Example 6 was 144°C.
- asphaltenes-containing hydrocarbon mixture (1) used as starting material was 100 pbw of vacuum residue.
- Table II lists the yields of final products obtained in the experiments described in Examples 1-7.
- Table III lists the properties of the final products obtained in the experiments described in Examples 1-7.
- Example 4 describing experiments in which both a TC treatment and a CC treatment are used, provides a combination of the advantages mentioned for Examples 2 and 3.
- Comparison of Examples 1 and 5 shows that application of a TC treatment to the feed for the HT produces considerably higher yields of hydrocarbon oil distillates.
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Claims (16)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL8202827A NL8202827A (nl) | 1982-07-13 | 1982-07-13 | Werkwijze voor de bereiding van asfaltenenarme koolwaterstofmengsels. |
NL8202827 | 1982-07-13 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0099141A1 EP0099141A1 (fr) | 1984-01-25 |
EP0099141B1 true EP0099141B1 (fr) | 1986-04-23 |
Family
ID=19840023
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP83200869A Expired EP0099141B1 (fr) | 1982-07-13 | 1983-06-14 | Procédé pour la production de mélanges d'hydrocarbures à faible teneur en asphaltène |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP0099141B1 (fr) |
JP (1) | JPS5924790A (fr) |
AU (1) | AU562320B2 (fr) |
CA (1) | CA1198387A (fr) |
DE (1) | DE3363155D1 (fr) |
ES (1) | ES8500315A1 (fr) |
MX (1) | MX162539A (fr) |
NL (1) | NL8202827A (fr) |
ZA (1) | ZA835028B (fr) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1222471A (fr) * | 1985-06-28 | 1987-06-02 | H. John Woods | Methode pour ameliorer le rendement des produits distillables dans le craquage a diluant donneur d'hydrogene |
US5013427A (en) * | 1989-07-18 | 1991-05-07 | Amoco Corportion | Resid hydrotreating with resins |
US10590360B2 (en) | 2015-12-28 | 2020-03-17 | Exxonmobil Research And Engineering Company | Bright stock production from deasphalted oil |
US10647925B2 (en) | 2015-12-28 | 2020-05-12 | Exxonmobil Research And Engineering Company | Fuel components from hydroprocessed deasphalted oils |
US10550341B2 (en) | 2015-12-28 | 2020-02-04 | Exxonmobil Research And Engineering Company | Sequential deasphalting for base stock production |
US10233394B2 (en) * | 2016-04-26 | 2019-03-19 | Saudi Arabian Oil Company | Integrated multi-stage solvent deasphalting and delayed coking process to produce high quality coke |
US10125318B2 (en) | 2016-04-26 | 2018-11-13 | Saudi Arabian Oil Company | Process for producing high quality coke in delayed coker utilizing mixed solvent deasphalting |
US10494579B2 (en) | 2016-04-26 | 2019-12-03 | Exxonmobil Research And Engineering Company | Naphthene-containing distillate stream compositions and uses thereof |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL7510465A (nl) * | 1975-09-05 | 1977-03-08 | Shell Int Research | Werkwijze voor het omzetten van koolwaterstoffen. |
NL7602240A (nl) * | 1976-03-04 | 1977-09-06 | Shell Int Research | Werkwijze voor het omzetten van koolwaterstoffen. |
NL7612960A (nl) * | 1976-11-22 | 1978-05-24 | Shell Int Research | Werkwijze voor het omzetten van koolwater- stoffen. |
NL7702161A (nl) * | 1977-03-01 | 1978-09-05 | Shell Int Research | Werkwijze voor het omzetten van koolwater- stoffen. |
JPS541306A (en) * | 1977-06-07 | 1979-01-08 | Chiyoda Chem Eng & Constr Co Ltd | Hydrogenation of heavy hydrocarbon oil |
GB2031011B (en) * | 1978-10-05 | 1983-01-06 | Chiyoda Chem Eng Construct Co | Processing heavy hydrocarbon oils |
DE3279051D1 (en) * | 1981-06-25 | 1988-10-27 | Shell Int Research | Process for the preparation of a hydrocarbon mixture |
-
1982
- 1982-07-13 NL NL8202827A patent/NL8202827A/nl not_active Application Discontinuation
-
1983
- 1983-06-14 EP EP83200869A patent/EP0099141B1/fr not_active Expired
- 1983-06-14 DE DE8383200869T patent/DE3363155D1/de not_active Expired
- 1983-06-15 CA CA000430430A patent/CA1198387A/fr not_active Expired
- 1983-07-11 ZA ZA835028A patent/ZA835028B/xx unknown
- 1983-07-11 JP JP58124880A patent/JPS5924790A/ja active Pending
- 1983-07-11 AU AU16726/83A patent/AU562320B2/en not_active Ceased
- 1983-07-11 ES ES524008A patent/ES8500315A1/es not_active Expired
- 1983-07-12 MX MX198004A patent/MX162539A/es unknown
Also Published As
Publication number | Publication date |
---|---|
ES524008A0 (es) | 1984-10-01 |
AU562320B2 (en) | 1987-06-04 |
JPS5924790A (ja) | 1984-02-08 |
AU1672683A (en) | 1984-01-19 |
MX162539A (es) | 1991-05-20 |
EP0099141A1 (fr) | 1984-01-25 |
ES8500315A1 (es) | 1984-10-01 |
NL8202827A (nl) | 1984-02-01 |
CA1198387A (fr) | 1985-12-24 |
DE3363155D1 (en) | 1986-05-28 |
ZA835028B (en) | 1984-03-28 |
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