US2009710A - Method of removing ash-forming components from crude petroleum oil - Google Patents

Method of removing ash-forming components from crude petroleum oil Download PDF

Info

Publication number
US2009710A
US2009710A US472196A US47219630A US2009710A US 2009710 A US2009710 A US 2009710A US 472196 A US472196 A US 472196A US 47219630 A US47219630 A US 47219630A US 2009710 A US2009710 A US 2009710A
Authority
US
United States
Prior art keywords
oil
forming components
acid
removing ash
crude petroleum
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 - Lifetime
Application number
US472196A
Inventor
Ralph T Goodwin
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Standard Oil Development Co
Original Assignee
Standard Oil Development Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Standard Oil Development Co filed Critical Standard Oil Development Co
Priority to US472196A priority Critical patent/US2009710A/en
Application granted granted Critical
Publication of US2009710A publication Critical patent/US2009710A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10GCRACKING HYDROCARBON OILS; PRODUCTION OF LIQUID HYDROCARBON MIXTURES, e.g. BY DESTRUCTIVE HYDROGENATION, OLIGOMERISATION, POLYMERISATION; RECOVERY OF HYDROCARBON OILS FROM OIL-SHALE, OIL-SAND, OR GASES; REFINING MIXTURES MAINLY CONSISTING OF HYDROCARBONS; REFORMING OF NAPHTHA; MINERAL WAXES
    • C10G17/00Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge
    • C10G17/02Refining of hydrocarbon oils in the absence of hydrogen, with acids, acid-forming compounds or acid-containing liquids, e.g. acid sludge with acids or acid-containing liquids, e.g. acid sludge
    • C10G17/04Liquid-liquid treatment forming two immiscible phases
    • C10G17/06Liquid-liquid treatment forming two immiscible phases using acids derived from sulfur or acid sludge thereof

Definitions

  • This invention relates to improvements in removing ash-forming components, such as mineral salts and the like, from oils.
  • the invention is particularly directed to the removal of salt 5 from crude petroleum oil. It is applicable, however, in general to oils which do not form substantial amounts of sediment when treated with dilute mineral acids. Sediment-forming oils are satisfactorily treated by the methods of my Patents Nos. 1,660,294 and 1,660,295 granted February 21, 1928.
  • the salt may be removed by blending the salt containing oil with a cracked petroleum residue, such as is obtained from the operation of pressure stills, cracking coils, and the like. Cracked materials of the type contemplated in this invention are described in the patents mentioned above. In these patents I have described the effect of adding dilute acidic substances to cracked residues and have shown that there is a substantially complete precipitation of carbonaceous sediment from the treated oils.
  • the invention is best carried into effect by mixing the crude oil with for example 25 to 40% by volume of cracking coil tar having an A. P. I. gravity of about '7 to The mixture is then treated with dilute sulphuric acid. Ordinarily a small percentage of acid, to 1% by volume of the oil treated, is suflicient. However, larger proportions of acid may be used without disadvantage.
  • Sulphuric acid is most economical, but other acids having the property of precipitating the sediment may be used, for example, dilute hydrochloric acid, dilute acetic acid, and dilute so-' lutions of salts, such as sodium acid sulfate or aluminum sulfate, which hydrolyze to form acids.
  • Sulphuric acid 30 to 60 B. is suitable. Weaker acids sometimes fail to act completely, and stronger acids may give trouble by the formation of sludge which interferes with the subsequent treatment.
  • the acid used may be diluted treating acid, such as is ordinarily sent to the acid recovery plants operated in connection with refineries. When the oil to be treated contains water, a more concentrated acid may be used so as to allow for dilution when added to the oil. In all cases the use of strong acids in sludge-forming concentration, is avoided.
  • the oil may be treated with the acid at ordinary pressure; sometimes, however, it is advantageous to use pressures above or below atmospheric, depending particularly on the character of the oil and the arrangements for taking care of vapors evolved during the treatment.
  • Heating facilitates the process. It is advantageous to run the cracking coil tar, while hot, into the cold crude oil. In this way the blend is brought to the desired temperature. This is about 200 to 275 F., though considerably higher temperatures, up to 500 or 600 are permissible.
  • the mixture of cracking coil tar and crude oil, heated as above described or in any other suitable way, is treated with the dilute acid. Carbonaceous sediment settles out rapidly, carrying with it the greater part of the salt content of the crude oil and also any mineral matter which may be in the cracking coil tar. This may be naturally occurring mineral matter or may be such as has been added in the form of lime or the like to prevent corrosion of the cracking equipment.
  • the upper layer from which the sediment has been precipitated is substantially free from ashforming components and. is also stabilized with respect to the formation of carbonaceous sediment.
  • any preferred method of mixing the crude oil and the cracking coil tar with each other and with the acid may be adopted.
  • I prefer a continuous treatment such as by the use of mixing columns in which the three streams of material are fed at one end and discharged at the other into a settling tank.
  • the equipment for separating the sediment from the oil may take the form of so-called thickeners, such as are now used in connection with the operation of the methods described in my patents mentioned above.
  • the oil product is not only improved by the removal of ash-forming components, but its viscosity is advantageously lowered.
  • the treated product may be run while hot into the crude stills or the cracking stills. It will be understood that suitable condensers should be provided to collect any low boiling oils which are distilled off during the treatment.
  • Method of removing ash-forming components from a substantially.non-sediment-forming petroleum fuel oil which comprises mixing with the oil about to per cent by volume of cracking coil tar, heating the mixture to between 200 degrees Fahrenheit and 600 degrees Fahrenheit, treating the mixture with about to 1 per cent of sulfuric acid of 30 to degrees Baum, whereby a carbonaceous precipitate is formed carrying with it the ash-forming components of the oil, and separating the precipitated material from the oil.
  • Method of removing ash-forming components from a crude petroleum oil comprising mixing with the oil about 25%-40% by volume of cracking coil tar, heating the mixture and treating the same with about /2%--1% of sulfuric acid of 30-60 Baum, whereby a carbonaceous precipitate is formed carrying with it the ashthe precipitated material from the oil.

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)
  • Treatment Of Sludge (AREA)
  • Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
  • Lubricants (AREA)

Description

Patented July 30, 1935 UNITED STATES METHOD OF REMOVING ASH-FORMING COMPONENTS FROM LEUM OIL CRUDE PETRO- Ralph T. Goodwin, Elizabeth, N. J.,' assignor to Standard Oil Development Company, a corporation of Delaware No Drawing. Application July 31, 1930,
Serial No. 472,196
2 Claims.
This invention relates to improvements in removing ash-forming components, such as mineral salts and the like, from oils. The invention is particularly directed to the removal of salt 5 from crude petroleum oil. It is applicable, however, in general to oils which do not form substantial amounts of sediment when treated with dilute mineral acids. Sediment-forming oils are satisfactorily treated by the methods of my Patents Nos. 1,660,294 and 1,660,295 granted February 21, 1928.
Many oils, particularly crude petroleum oils, contain substantial amounts of mineral salts in substantially permanent suspension. Even after long standing there is little diminution of the salt content.
I have found that the salt may be removed by blending the salt containing oil with a cracked petroleum residue, such as is obtained from the operation of pressure stills, cracking coils, and the like. Cracked materials of the type contemplated in this invention are described in the patents mentioned above. In these patents I have described the effect of adding dilute acidic substances to cracked residues and have shown that there is a substantially complete precipitation of carbonaceous sediment from the treated oils.
I have discovered that the precipitation of this sediment can be used as a means for freeing crude oils or the like from their salt content. The invention is best carried into effect by mixing the crude oil with for example 25 to 40% by volume of cracking coil tar having an A. P. I. gravity of about '7 to The mixture is then treated with dilute sulphuric acid. Ordinarily a small percentage of acid, to 1% by volume of the oil treated, is suflicient. However, larger proportions of acid may be used without disadvantage.
Sulphuric acid is most economical, but other acids having the property of precipitating the sediment may be used, for example, dilute hydrochloric acid, dilute acetic acid, and dilute so-' lutions of salts, such as sodium acid sulfate or aluminum sulfate, which hydrolyze to form acids. Sulphuric acid of 30 to 60 B. is suitable. Weaker acids sometimes fail to act completely, and stronger acids may give trouble by the formation of sludge which interferes with the subsequent treatment. The acid used may be diluted treating acid, such as is ordinarily sent to the acid recovery plants operated in connection with refineries. When the oil to be treated contains water, a more concentrated acid may be used so as to allow for dilution when added to the oil. In all cases the use of strong acids in sludge-forming concentration, is avoided.
The oil may be treated with the acid at ordinary pressure; sometimes, however, it is advantageous to use pressures above or below atmospheric, depending particularly on the character of the oil and the arrangements for taking care of vapors evolved during the treatment.
Heating facilitates the process. It is advantageous to run the cracking coil tar, while hot, into the cold crude oil. In this way the blend is brought to the desired temperature. This is about 200 to 275 F., though considerably higher temperatures, up to 500 or 600 are permissible. The mixture of cracking coil tar and crude oil, heated as above described or in any other suitable way, is treated with the dilute acid. Carbonaceous sediment settles out rapidly, carrying with it the greater part of the salt content of the crude oil and also any mineral matter which may be in the cracking coil tar. This may be naturally occurring mineral matter or may be such as has been added in the form of lime or the like to prevent corrosion of the cracking equipment.
The upper layer from which the sediment has been precipitated is substantially free from ashforming components and. is also stabilized with respect to the formation of carbonaceous sediment.
Any preferred method of mixing the crude oil and the cracking coil tar with each other and with the acid may be adopted. I prefer a continuous treatment such as by the use of mixing columns in which the three streams of material are fed at one end and discharged at the other into a settling tank. The equipment for separating the sediment from the oil may take the form of so-called thickeners, such as are now used in connection with the operation of the methods described in my patents mentioned above.
The oil product is not only improved by the removal of ash-forming components, but its viscosity is advantageously lowered. The treated product may be run while hot into the crude stills or the cracking stills. It will be understood that suitable condensers should be provided to collect any low boiling oils which are distilled off during the treatment.
While, in the foregoing, emphasis has been laid on the treatment of crude oil, it will be understood that the method is applicable to any oil containing ash-forming components, and insufficiently cracked to yield enough sediment on acid treating to throw out ash-forming components. Thus the invention may be applied also to reduced crudes which have been run under non-cracking conditions, to certain fuel oils, and the like.
Various changes and alternative procedures may be adopted within the scope of the appended claims, in which it is my intention to claim all novelty inherent in the invention as broadly as the prior art permits.
I claim: 7
1. Method of removing ash-forming components from a substantially.non-sediment-forming petroleum fuel oil, which comprises mixing with the oil about to per cent by volume of cracking coil tar, heating the mixture to between 200 degrees Fahrenheit and 600 degrees Fahrenheit, treating the mixture with about to 1 per cent of sulfuric acid of 30 to degrees Baum, whereby a carbonaceous precipitate is formed carrying with it the ash-forming components of the oil, and separating the precipitated material from the oil.
2. Method of removing ash-forming components from a crude petroleum oil, comprising mixing with the oil about 25%-40% by volume of cracking coil tar, heating the mixture and treating the same with about /2%--1% of sulfuric acid of 30-60 Baum, whereby a carbonaceous precipitate is formed carrying with it the ashthe precipitated material from the oil.
RALPH T. GOODWIN.
US472196A 1930-07-31 1930-07-31 Method of removing ash-forming components from crude petroleum oil Expired - Lifetime US2009710A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US472196A US2009710A (en) 1930-07-31 1930-07-31 Method of removing ash-forming components from crude petroleum oil

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US472196A US2009710A (en) 1930-07-31 1930-07-31 Method of removing ash-forming components from crude petroleum oil

Publications (1)

Publication Number Publication Date
US2009710A true US2009710A (en) 1935-07-30

Family

ID=23874556

Family Applications (1)

Application Number Title Priority Date Filing Date
US472196A Expired - Lifetime US2009710A (en) 1930-07-31 1930-07-31 Method of removing ash-forming components from crude petroleum oil

Country Status (1)

Country Link
US (1) US2009710A (en)

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2520407A (en) * 1948-11-27 1950-08-29 Sun Oil Co Removal of inorganic matter from petroleum residua
US2545806A (en) * 1950-02-25 1951-03-20 Sun Oil Co Deashing petroleum residua
US2769758A (en) * 1951-03-20 1956-11-06 British Petroleum Co Removal of sodium and vanadium from petroleum hydrocarbons followed by catalytic desulphurisation of said petroleum hydrocarbons
US2793167A (en) * 1954-09-20 1957-05-21 Exxon Research Engineering Co Solvent deasphalting of residual oils with wash oil to remove metal contaminants
US2793168A (en) * 1954-10-15 1957-05-21 Exxon Research Engineering Co Method for solvent deasphalting of residual oil
US2895902A (en) * 1954-04-01 1959-07-21 Exxon Research Engineering Co Removal of metal contaminants from residual oils
US3095368A (en) * 1957-07-31 1963-06-25 Exxon Research Engineering Co Process for removing metallic contaminants from oils
US4425225A (en) 1980-12-31 1984-01-10 Exxon Research And Engineering Co. Reducing metal content of oil feeds
US4537676A (en) * 1980-12-31 1985-08-27 Exxon Research And Engineering Co. Reducing metal content of oil feeds

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2520407A (en) * 1948-11-27 1950-08-29 Sun Oil Co Removal of inorganic matter from petroleum residua
US2545806A (en) * 1950-02-25 1951-03-20 Sun Oil Co Deashing petroleum residua
US2769758A (en) * 1951-03-20 1956-11-06 British Petroleum Co Removal of sodium and vanadium from petroleum hydrocarbons followed by catalytic desulphurisation of said petroleum hydrocarbons
US2895902A (en) * 1954-04-01 1959-07-21 Exxon Research Engineering Co Removal of metal contaminants from residual oils
US2793167A (en) * 1954-09-20 1957-05-21 Exxon Research Engineering Co Solvent deasphalting of residual oils with wash oil to remove metal contaminants
US2793168A (en) * 1954-10-15 1957-05-21 Exxon Research Engineering Co Method for solvent deasphalting of residual oil
US3095368A (en) * 1957-07-31 1963-06-25 Exxon Research Engineering Co Process for removing metallic contaminants from oils
US4425225A (en) 1980-12-31 1984-01-10 Exxon Research And Engineering Co. Reducing metal content of oil feeds
US4537676A (en) * 1980-12-31 1985-08-27 Exxon Research And Engineering Co. Reducing metal content of oil feeds

Similar Documents

Publication Publication Date Title
US2009710A (en) Method of removing ash-forming components from crude petroleum oil
US1801213A (en) Process of refining mineral oils
US2036299A (en) Treatment of petroleum sludges and sludge acids
US2434528A (en) Method for removing ash-forming constituents and sediment from alkaline petroleum residuum
US1660295A (en) Treatment of hydrocarbon residues and product obtained thereby
US1986775A (en) Process of treating hydrocarbon oil containing naphthenic acids
US2058696A (en) Process of stabilizing oils
US1704588A (en) Process of treating petroleum oils
US2520407A (en) Removal of inorganic matter from petroleum residua
US2141297A (en) Process for recovering oil from petroleum acid sludge
US1804451A (en) Process of treating petroleum
US2200534A (en) Low pour point lubricating oil
US1521283A (en) Art of refining oils
US1920248A (en) Process for refining gasoline-containing distillates
US2111920A (en) Sludge separation
US1962182A (en) Treatment of hydrocarbon oils
US1833618A (en) Process of dehydrating and purifying oil
US1413260A (en) Process of distilling crude petroleum and product thereof
US2195833A (en) Treatment of hydrocarbon oils
US2005309A (en) Manufacture of motor fuel from sludge oil
US1745155A (en) Asphalt and road oil and process of producing the same
US1799780A (en) Purification of tar acid-bearing oils
US1631401A (en) Process of making motor fuel
US1708563A (en) Process of imparting fluorescence to oil
US1708602A (en) Process for making a fluorescent product