DE971343C - Process for removing vanadium and / or sodium from crude petroleum or petroleum products - Google Patents
Process for removing vanadium and / or sodium from crude petroleum or petroleum productsInfo
- Publication number
- DE971343C DE971343C DEA18212A DEA0018212A DE971343C DE 971343 C DE971343 C DE 971343C DE A18212 A DEA18212 A DE A18212A DE A0018212 A DEA0018212 A DE A0018212A DE 971343 C DE971343 C DE 971343C
- Authority
- DE
- Germany
- Prior art keywords
- petroleum
- sodium
- vanadium
- bauxite
- crude
- 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
Links
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
- C10G45/00—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds
- C10G45/02—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing
- C10G45/04—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used
- C10G45/06—Refining of hydrocarbon oils using hydrogen or hydrogen-generating compounds to eliminate hetero atoms without changing the skeleton of the hydrocarbon involved and without cracking into lower boiling hydrocarbons; Hydrofinishing characterised by the catalyst used containing nickel or cobalt metal, or compounds thereof
-
- 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
Landscapes
- 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)
- Catalysts (AREA)
Description
AUSGEGEBEN AM 15. JANUAR 1959ISSUED JANUARY 15, 1959
A 18212 IVc 123 bA 18212 IVc 123 b
Zusatz zum Patent 970Addition to patent 970
Gegenstand des Hauptpatents ist ein Verfahren zur Entfernung von Natrium und Vanadium aus rohem Erdöl oder Erdölprodukten, wobei das rohe Erdöl oder die Erdölprodukte mit Bauxit in Gegenwart von Wasserstoff unter solchen zwischen 371 und 4270 liegenden Temperaturen, vorzugsweise bei 415°, und solchen zwischen 57 und 71 kg/cm2 liegenden Drücken, vorzugsweise bei 7.1 kg/cm2, behandelt werden, daß Natrium und Vanadium vom Bauxit festgehalten werden.The subject of the main patent is a process for the removal of sodium and vanadium from crude petroleum or petroleum products, wherein the crude petroleum or petroleum products with bauxite in the presence of hydrogen below temperatures between 371 and 427 0 , preferably at 415 °, and between 57 and pressures lying 71 kg / cm 2 , preferably 7.1 kg / cm 2 , are treated so that sodium and vanadium are retained by the bauxite.
Gemäß einer bevorzugten Arbeitsweise werden 714 m3 Wasserstoff je m3 Ausgangsöl verwendet und bei einer Raumströmungsgeschwindigkeit des flüssigen Ausgangsöls von 1 V/V/Std., bezogen auf Bauxit, gearbeitet. In Abwesenheit von Vanadium wird vorzugsweise bei Temperaturen zwischen 343 und 4540, insbesondere bei 415 °, und bei Drücken zwischen 8 bis 15 kg/cm2 gearbeitet.According to a preferred mode of operation, 714 m 3 of hydrogen per m 3 of starting oil are used and the work is carried out at a space flow rate of the liquid starting oil of 1 V / V / hour, based on bauxite. In the absence of vanadium, temperatures between 343 and 454 0 , in particular at 415 °, and pressures between 8 and 15 kg / cm 2 are preferably used.
Es wurde nun gefunden, daß man an Stejle von Bauxit mit einem aus 5 bis 15 Gewichtsprozent Fern-It has now been found that steels of bauxite with a 5 to 15 percent by weight Fern-
oxyd und Aluminiumoxyd bestehenden Kontaktmaterial behandeln kann und das behandelte Öl dabei gegebenenfalls anschließend einer Hydrierungszone zur Entfernung organisch gebundenen Schwefels zuführen kann. Da Katalysatoren aus natürlichem Bauxit entsprechend dem Fundort' des verwendeten Materials in ihrer Aktivität schwanken, ist die Verwendung der erfindungsgemäßen Katalysatoren unter Umständen äußerst wünschenswert. Darüber hinausoxide and aluminum oxide can treat existing contact material and the treated oil in the process if necessary then feed to a hydrogenation zone to remove organically bound sulfur can. Since natural bauxite catalysts are used according to where they were found Materials fluctuate in their activity, the use of the catalysts according to the invention is under Extremely desirable in circumstances. Furthermore
ίο hat sich gezeigt, daß man bei Anwendung geringerer
Raumströmungsgeschwindigkeiten mit den erfindungsgemäßen Katalysatoren das Natrium und Vanadium
häufig besser entfernen kann.
Vorzugsweise arbeitet man beim Verfahren gemäß der Erfindung unter folgenden Bedingungen:It has been shown that the sodium and vanadium can often be removed better when using lower room flow velocities with the catalysts according to the invention.
The process according to the invention is preferably carried out under the following conditions:
Raumströmungsgeschwindigkeit 0,5 ... 2 V/V/Std.Room flow velocity 0.5 ... 2 V / V / hour.
Temperatur 400 ... 430°Temperature 400 ... 430 °
Druck 35 ... 105 atPressure 35 ... 105 at
RückgeführteRepatriated
Wasserstoffmenge 180 ... 1800 m3/m3 Amount of hydrogen 180 ... 1800 m 3 / m 3
Das Verfahren gemäß der Erfindung eignet sich vorzugsweise zur Vorbehandlung von rohem Erdöl oder Erdölprodukten, die zur Entfernung von organisch gebundenem Schwefel katalytisch hydriert werden sollen. So wurde beispielsweise gefunden, daß bei der Hydrofinierung von rohem Erdöl und Erdölrückständen unter Verwendung eines aus Cobalt- und Molybdänoxyden auf einem Aluminiumoxydträger bestehenden Katalysators beachtliche Mengen Vanadium und Natrium von dem Katalysator aufgenommen werden und dadurch die Katalysatoraktivität während des Betriebes ständig abnimmt und bei einer Regeneration in üblicher Weise" nicht voll wiederhergestellt werden kann. Gemäß der Erfindung wird nun in einem kontinuierlichen Verfahren das Vanadium und/oder Natrium enthaltende Erdöl zunächst mit Eisenoxyd auf Aluminiumoxyd behandelt und dann in einer Hydrierungszone von organisch gebundenem Schwefel befreit.The method according to the invention is preferably suitable for the pretreatment of crude petroleum or petroleum products that are catalytically hydrogenated to remove organically bound sulfur should be. For example, it has been found that in the hydrofining of crude petroleum and petroleum residues using one of cobalt and molybdenum oxides on an alumina support existing catalyst, considerable amounts of vanadium and sodium were taken up by the catalyst and as a result the catalyst activity continuously decreases during operation and during regeneration in the usual way "cannot be fully restored. According to the invention, FIG a continuous process the vanadium and / or sodium containing petroleum initially with Treated iron oxide on aluminum oxide and then in a hydrogenation zone of organically bound Sulfur free.
Nachstehend wird die Anwendung des Verfahrens gemäß der Erfindung auf die Behandlung eines Erdölrückstandes gegeben.The application of the method according to the invention to the treatment of a Given petroleum residue.
Entfernung von Natrium und Vanadium aus einem Erdölrückstand, der durch Abtreiben von 47% flüchtiger Stoffe aus einem Kuwaitöl erhalten wurde.Removal of sodium and vanadium from a petroleum residue, which by stripping 47% volatiles obtained from a Kuwait oil.
Betriebsbedingungen:Operating conditions:
Ausgangsöl KuwaitStarting oil Kuwait
53 Volumprozent Rückstand
Raumströmungsgeschwindigkeit .. 1 V/V/Std.53 percent by volume residue
Room flow velocity .. 1 V / V / hour.
Temperatur 416° CTemperature 416 ° C
Druck 70 atPressure 70 at
Rückgeführte Wasserstoffmenge... 720 m3/m3 Amount of recirculated hydrogen ... 720 m 3 / m 3
Flußrichtung aufwärtsDirection of flow upwards
Betriebsdauer 50 StundenOperating time 50 hours
Erzielte Ergebnisse:Results obtained:
Eisenoxyd auf Aluminiumoxyd
(12,8 Gewichtsprozent Fe2O3)Iron oxide on aluminum oxide
(12.8 percent by weight Fe 2 O 3 )
Vanadium, mg/kg...Vanadium, mg / kg ...
Natrium, mg/kg Sodium, mg / kg
Schwefel, Gewichtsprozent Sulfur, weight percent
Spezifisches Gewicht
I5,56/I5,56O specific weight
I5.56 / I5.56 O
Ausgangsöl Starting oil
41,0
39,041.0
39.0
3,89
0,9583.89
0.958
Behandeltes Öl GesamtmengeTotal treated oil
währendwhile
50 Stunden50 hours
erhaltenobtain
21,0
28,021.0
28.0
3,42
0,9433.42
0.943
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB15306/52A GB735520A (en) | 1952-06-18 | 1952-06-18 | Improvements relating to the removal of vanadium and/or sodium from petroleum and hydrocarbons of petroleum origin |
Publications (1)
Publication Number | Publication Date |
---|---|
DE971343C true DE971343C (en) | 1959-01-15 |
Family
ID=10056742
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DEA18212A Expired DE971343C (en) | 1952-06-18 | 1953-06-14 | Process for removing vanadium and / or sodium from crude petroleum or petroleum products |
Country Status (5)
Country | Link |
---|---|
US (1) | US2764525A (en) |
BE (1) | BE520661A (en) |
DE (1) | DE971343C (en) |
FR (1) | FR1082901A (en) |
GB (1) | GB735520A (en) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2914458A (en) * | 1956-05-21 | 1959-11-24 | Phillips Petroleum Co | Metal contaminant removal from catalytic cracking feedstock |
US2951035A (en) * | 1957-09-06 | 1960-08-30 | Sinclair Refining Co | Method for the removal of metal contaminants from petroleum residual stocks |
US2944013A (en) * | 1957-12-09 | 1960-07-05 | Universal Oil Prod Co | Producing metal-free petroleum stocks by hydrogenation |
US3893911A (en) * | 1974-06-24 | 1975-07-08 | Hydrocarbon Research Inc | Demetallization of high metals feedstocks using regenerated catalyst |
US4192736A (en) * | 1978-11-29 | 1980-03-11 | Chevron Research Company | Removal of indigenous metal impurities from an oil with phosphorus oxide-promoted alumina |
US4830736A (en) * | 1986-07-28 | 1989-05-16 | Chevron Research Company | Graded catalyst system for removal of calcium and sodium from a hydrocarbon feedstock |
US4832829A (en) * | 1987-04-27 | 1989-05-23 | Intevep S.A. | Catalyst for the simultaneous hydrodemetallization and hydroconversion of heavy hydrocarbon feedstocks |
EP3078726A1 (en) | 2007-05-03 | 2016-10-12 | Auterra, Inc. | Product containing monomer and polymers of titanyls and methods for making same |
US8764973B2 (en) | 2008-03-26 | 2014-07-01 | Auterra, Inc. | Methods for upgrading of contaminated hydrocarbon streams |
US8894843B2 (en) | 2008-03-26 | 2014-11-25 | Auterra, Inc. | Methods for upgrading of contaminated hydrocarbon streams |
US9061273B2 (en) | 2008-03-26 | 2015-06-23 | Auterra, Inc. | Sulfoxidation catalysts and methods and systems of using same |
US8298404B2 (en) | 2010-09-22 | 2012-10-30 | Auterra, Inc. | Reaction system and products therefrom |
US8241490B2 (en) * | 2008-03-26 | 2012-08-14 | Auterra, Inc. | Methods for upgrading of contaminated hydrocarbon streams |
MX2010010523A (en) * | 2008-03-26 | 2011-11-02 | Auterra Inc | Sulfoxidation catalysts and methods and systems of using same. |
US8197671B2 (en) * | 2008-03-26 | 2012-06-12 | Auterra, Inc. | Methods for upgrading of contaminated hydrocarbon streams |
US9206359B2 (en) | 2008-03-26 | 2015-12-08 | Auterra, Inc. | Methods for upgrading of contaminated hydrocarbon streams |
US9828557B2 (en) | 2010-09-22 | 2017-11-28 | Auterra, Inc. | Reaction system, methods and products therefrom |
WO2016154529A1 (en) | 2015-03-26 | 2016-09-29 | Auterra, Inc. | Adsorbents and methods of use |
US10450516B2 (en) | 2016-03-08 | 2019-10-22 | Auterra, Inc. | Catalytic caustic desulfonylation |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1882000A (en) * | 1925-04-01 | 1932-10-11 | Cross Dev Corp | Process for treating oils |
US2116061A (en) * | 1929-10-26 | 1938-05-03 | Standard Ig Co | Purification of mineral oils, tars, their distillation products, and the like |
US2227089A (en) * | 1938-02-07 | 1940-12-31 | Union Oil Co | Treatment of hydrocarbon oil |
US2383972A (en) * | 1940-06-12 | 1945-09-04 | Standard Oil Dev Co | Recovery of vanadim and nickel from petroleum |
US2411958A (en) * | 1943-11-25 | 1946-12-03 | Du Pont | Method of purifying petroleum products |
US2507523A (en) * | 1946-08-31 | 1950-05-16 | Houdry Process Corp | Conversion of hydrocarbons |
BE517222A (en) * | 1952-01-31 | 1900-01-01 |
-
0
- BE BE520661D patent/BE520661A/xx unknown
-
1952
- 1952-06-18 GB GB15306/52A patent/GB735520A/en not_active Expired
-
1953
- 1953-06-14 DE DEA18212A patent/DE971343C/en not_active Expired
- 1953-06-16 US US362144A patent/US2764525A/en not_active Expired - Lifetime
- 1953-06-16 FR FR1082901D patent/FR1082901A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
BE520661A (en) | |
US2764525A (en) | 1956-09-25 |
GB735520A (en) | 1955-08-24 |
FR1082901A (en) | 1955-01-04 |
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