US2450224A - Method of preparation of barium soap greases - Google Patents

Method of preparation of barium soap greases Download PDF

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Publication number
US2450224A
US2450224A US714640A US71464046A US2450224A US 2450224 A US2450224 A US 2450224A US 714640 A US714640 A US 714640A US 71464046 A US71464046 A US 71464046A US 2450224 A US2450224 A US 2450224A
Authority
US
United States
Prior art keywords
soap
barium
grease
oil
base
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
US714640A
Other languages
English (en)
Inventor
Eric A Bergmann
Harry V Ashburn
George W Eckert
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.)
Texaco Inc
Original Assignee
Texaco Inc
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
Priority to FR956525D priority Critical patent/FR956525A/fr
Application filed by Texaco Inc filed Critical Texaco Inc
Priority to US714640A priority patent/US2450224A/en
Priority to GB30924/47A priority patent/GB651339A/en
Application granted granted Critical
Publication of US2450224A publication Critical patent/US2450224A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M5/00Solid or semi-solid compositions containing as the essential lubricating ingredient mineral lubricating oils or fatty oils and their use
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/125Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10MLUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/10Carboxylix acids; Neutral salts thereof
    • C10M2207/12Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
    • C10M2207/129Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2010/00Metal present as such or in compounds
    • C10N2010/04Groups 2 or 12
    • CCHEMISTRY; METALLURGY
    • C10PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10NINDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2050/00Form in which the lubricant is applied to the material being lubricated
    • C10N2050/10Form in which the lubricant is applied to the material being lubricated semi-solid; greasy

Definitions

  • VGC thenic oil-possessinga VGC of at least ;8'70.
  • barium soap greases have been recog- 5 -It wasalso fourrdthat upon cooling thebarium ".nized as'a'desirable adjunct to the more convensoap base following dehydration:thestructure of tiona'l line oflubricating greases by virtue of their the base -undergoes acomplete- 'phase" change.
  • the concentration of the soap is approximately 50% or greater considerable load is applied to the stirring mechanism and if the stirring mechanism becomes overloaded it may be desirable to incorporate small amounts of the mineral lubricating oil to reduce the load on the stirring mechanism.
  • the addition of the mineral oil at this stage should be controlled so that the concentration of the soap is not reduced to substantially below 40%.
  • any conventional fatty acid material may be used as the acid component of the barium soap, the best yields and quality of grease are obtained by charging fatty acids or mixtures thereof and particularly fatty acids containing at least 16 carbon atoms or predominating amounts of fatty acids of at least 16 carbon atoms.
  • Glycerides such as are contained in the natural fats may be used provided the free glycerin formed on saponification is substantially removed by steam distillation or by prolonged heating in the dehydration stage.
  • the fatty acids found suitable for the preparation of the barium greases include such acids as stearic, palmitic, behenic, oleic, hydroxy stearic, etc.
  • a naphthenic mineral oil possessing a VGC of at least 0.870 is required to effect solvation of the barium soap formed in the saponification stage of the process.
  • This naphthenic mineral oil may be either a distillate or residual lubricating oil of the desired viscosity or may consist of a blend of lubricating oils in which the VGC of the final blend is at least 0.870.
  • the amount of the naphthenic mineral oil charged in the saponification stage is not critical to the invention but for ease of manufacture it is preferable to employ approximately an equal weight of mineral oil based upon the weight of the fatty acids charged. After the saponiflcation further processing and finishing of the grease base may be conducted with any of the conventional lubricating oils, irrespective of the naphthenicity or paraffinicity of the oil.
  • barium soap greases can be prepared neutral or containing free acid or free alkali, as desired, without producing any adverse effect on the stability of the product.
  • Example 310 grams of stearic acid and 372 grams of a naphthenic Pale Oil possessing a S. U. V. at F. of 312 and a VGC of 0.884 were charged to a grease kettle.
  • the stearic acid was melted at 210 F., at which temperature 563 grams of a hot aqueous solution of barium hydroxide (17.6% Ba(OH) 2) were added followed by 50 ml. of water. This mixture was stirred at 210 F. for one-half hour after all the water had evaporated.
  • the temperature was then raised to 310 F. in 25 minutes and held at this temperature for 15 minutes, at which point the grease base was a stiff, taffy-like mass and rather rubbery.
  • a method of preparing a normal barium soap grease composition which comprises saponifying a soap-forming fatty acid with not more than the stoichiometric equivalent of barium hydrate in the presence of a mineral oil possessing a VGC of at least 0.870 to produce a saponification product of normal barium soap, dehydrating the saponification product at temperatures not in excess of the melting point of the soap base, cooling the dehydrated product with continuous stirring to a temperature below the critical transition temperature of the grease base without reducing the concentration of the soap component to substantially below 40%, thereafter adding mineral lubricating oil to obtain the desired consistency and drawing the resulting grease composition.
  • a method of preparing a normal barium soap grease composition which comprises saponifying a fatty acid containing at least 16 carbon, atoms with substantially the stoichiometric quantity of barium hydrate in the presence of a mineral oil possessing a VGC of at least 0.870 to produce a saponification product of normal barium soap, dehydrating the saponification product at temperatures not in excess of the melting point of the soap base, cooling the dehydrated product with continuous stirring to a temperature of approximately 200 F. without reducing the concentration of the soap component to substantially below 40%, thereafter adding mineral lubricating oil to obtain the desired consistency and drawing the resulting grease composition.
  • a method of preparing a normal barium soap grease composition which comprises saponifying a fatty acid containing at least 16 carbon atoms with barium hydrate, in stoichiometric quantities required for the preparation of a normal barium soap, in the presence of a mineral oil possessing a VGC of at least 0.870, dehydrating the saponification product at temperatures not in excess of the melting point of the soap base, cooling the dehydrated product with continuous stirring to a temperature below the critical transition temperature of the normal soap base without reducing the concentration of the normal soap component to substantially less than 40%, thereafter adding mineral lubricating oil to obtain the desired consistency and drawing the finished grease composition.
  • a method of preparing a normal barium soap grease composition which comprises saponifying a fatty acid containing at least 16 carbon atoms with substantially the stoichiometric quantity of barium hydrate in the presence of sufiiicient mineral lubricating oil possessing a VGC of at least 0.870 to effect solvation of the resulting normal barium soap, dehydrating the saponification product at temperatures of approximately 300-320 F., cooling the dehydrated product with continuous stirring to a temperature of approximately 200 F. without reducing the concentration of the soap component to sub s-tantially below 40%, thereafter adding mineral lubricating oil to obtain the desired consistency and drawing the resulting grease composition.
  • a method of preparing a normal barium soap grease composition which comprises saponifying a fatty acid containing at least 16 carbon atoms with not more than the stoichiometric equivalent of barium hydrate in the presence of approximately equal weights, based upon the weight of fatty acid, of a mineral oil possessing a VGC of at least 0.870 to produce an oil solu tion of normal barium soap dehydrating the saponification product at temperatures not in excess of the melting point of the soap base,
  • a method of preparing a normal barium stearate grease composition which comprises saponifying stearic acid with not more than the stoichiornetric equivalent of barium hydrate in the presence of a mineral oil possessing a VGC of at least 0.870 to produce normal barium stearate, dehydrating the saponification product at temperatures not in excess of the melting point of the soap base, cooling the dehydrated product with continuous stirring to a temperature of approximately 200 F. without reducing the concentration of the barium stearate to substantially below 40%, adding mineral lubricating oil to obtain the desired consistency and drawing the resulting grease composition.
  • a method of preparing a normal barium stearate grease composition which comprises saponifying stearic acid with substantially the stoichiometric quantity of barium hydrate in the presence of about an equal quantity based on the stearic acid of a mineral lubricating oil possessing a VGC of at least 0.870 to produce an oil solution of normal barium stearate, dehydrating the sapqnification proctuct at temperatures above 300 F. but not in excess of the melting point of the soap base, cooling the dehydrated product with continuous stirring to a temperature of approximately 200 F. without reducing the concentration of the barium stearate to substantially below thereafter adding mineral lubricating oil to obtain the desired consistency and drawing the resulting grease composition.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
US714640A 1946-12-06 1946-12-06 Method of preparation of barium soap greases Expired - Lifetime US2450224A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
FR956525D FR956525A (en, 2012) 1946-12-06
US714640A US2450224A (en) 1946-12-06 1946-12-06 Method of preparation of barium soap greases
GB30924/47A GB651339A (en) 1946-12-06 1947-11-21 Improvements in or relating to the preparation of normal barium soap grease compositions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US714640A US2450224A (en) 1946-12-06 1946-12-06 Method of preparation of barium soap greases

Publications (1)

Publication Number Publication Date
US2450224A true US2450224A (en) 1948-09-28

Family

ID=24870862

Family Applications (1)

Application Number Title Priority Date Filing Date
US714640A Expired - Lifetime US2450224A (en) 1946-12-06 1946-12-06 Method of preparation of barium soap greases

Country Status (3)

Country Link
US (1) US2450224A (en, 2012)
FR (1) FR956525A (en, 2012)
GB (1) GB651339A (en, 2012)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2504717A (en) * 1947-09-20 1950-04-18 Standard Oil Dev Co Reversible lubricating grease composition
US2607734A (en) * 1950-05-20 1952-08-19 Standard Oil Dev Co Process of manufacturing hydroxy acid greases and product thereof
US2607735A (en) * 1949-03-12 1952-08-19 Standard Oil Dev Co Alkaline earth metal soap greases

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2033148A (en) * 1932-05-17 1936-03-10 Union Oil Co Barium grease
US2070781A (en) * 1935-02-13 1937-02-16 Standard Oil Co Grease
US2154383A (en) * 1936-03-07 1939-04-11 Union Oil Co Barium grease
US2417433A (en) * 1945-04-23 1947-03-18 Union Oil Co Lubricating composition

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2033148A (en) * 1932-05-17 1936-03-10 Union Oil Co Barium grease
US2070781A (en) * 1935-02-13 1937-02-16 Standard Oil Co Grease
US2154383A (en) * 1936-03-07 1939-04-11 Union Oil Co Barium grease
US2417433A (en) * 1945-04-23 1947-03-18 Union Oil Co Lubricating composition

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2504717A (en) * 1947-09-20 1950-04-18 Standard Oil Dev Co Reversible lubricating grease composition
US2607735A (en) * 1949-03-12 1952-08-19 Standard Oil Dev Co Alkaline earth metal soap greases
US2607734A (en) * 1950-05-20 1952-08-19 Standard Oil Dev Co Process of manufacturing hydroxy acid greases and product thereof

Also Published As

Publication number Publication date
GB651339A (en) 1951-03-14
FR956525A (en, 2012) 1950-02-02

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