GB775027A - Improvements in or relating to complex metal salt-soap compounds - Google Patents

Improvements in or relating to complex metal salt-soap compounds

Info

Publication number
GB775027A
GB775027A GB21112/54A GB2111254A GB775027A GB 775027 A GB775027 A GB 775027A GB 21112/54 A GB21112/54 A GB 21112/54A GB 2111254 A GB2111254 A GB 2111254A GB 775027 A GB775027 A GB 775027A
Authority
GB
United Kingdom
Prior art keywords
acids
acid
complex
calcium
oil
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
Application number
GB21112/54A
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.)
ExxonMobil Technology and Engineering Co
Original Assignee
Exxon Research and Engineering Co
Esso Research and Engineering 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 Exxon Research and Engineering Co, Esso Research and Engineering Co filed Critical Exxon Research and Engineering Co
Publication of GB775027A publication Critical patent/GB775027A/en
Priority claimed from US40137A external-priority patent/US3098822A/en
Expired legal-status Critical Current

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    • C10L1/00Liquid carbonaceous fuels
    • C10L1/10Liquid carbonaceous fuels containing additives
    • C10L1/14Organic compounds
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    • C10L1/188Carboxylic acids; metal salts thereof
    • C10L1/1881Carboxylic acids; metal salts thereof carboxylic group attached to an aliphatic carbon atom
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    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
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  • Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
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  • General Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Lubricants (AREA)

Abstract

Greases comprise silicones thickened with a complex of a metal salt of a C12-C30 carboxylic acid and a metal (other than aluminium) salt of an aliphatic carboxylic acid of lower molecular weight than the first, and containing more than 7, preferably 7-45, mols. of the latter salt for each mol. of the first. The C12-C30, preferably C18-C22, acids include saturated and unsaturated fatty acids, e.g. stearic and hydroxy stearic; arachidic, hydrogenated fish oil, tallow, oleic and ricinoleic acids. The lower molecular weight acids include saturated and unsaturated, mono- and poly-carboxylic C1-C6 acids, and hydroxy-acids, e.g. acetic, formic, propionic, acrylic, adipic, and lactic acids. The metals include alkaline earths, particularly Ca, Ba and Mg, heavy metals of Groups 1, 2 and 4, especially Cu, Zn and Pb, either alone or with alkaline earths, and Ni, Co, Cr and Mn. The complexes may be prepared by co-neutralization of the acid mixture in a medium in which the complex is to be used. Heating to 450-550 DEG F. or higher is generally effected to dehydrate and promote complex formation. The acids may be replaced by such derivatives as esters or nitriles under conditions conducive to saponification. Alternatively, the metal salts may be separately preformed and then mixed and heated. The complexes are compounded with silicones to form greases containing 5-30, and detergent or extreme pressure lubricants containing 0.5-20 weight per cent of complex. In examples: (21) silicone fluid is thickened to a grease by mixing with acetic and Hydrofol (hydrogenated fish oil) acids and heating with lime; (22), (23) hydroxystearic acid and di-2-ethyl hexyl sebacate or di - iso - octyl azelate are also incorporated.ALSO:The invention comprises a complex of a metal (other than aluminium) salt of a C12-C30 carboxylic acid and a metal (other than aluminium) salt of an aliphatic carboxylic acid of lower molecular weight than the first, and containing more than 7, preferably 7-45, mols. of the latter salt for each mol. of the first. The C12-330, preferably C18-C22, acids include saturated and unsaturated fatty acids, e.g. stearic and hydroxy stearic, arachidic, hydrogenated fish oil, tallow, oleic, and ricinoleic acids. The lower molecular weight acids include saturated and unsaturated mono- and poly-carboxylic C1-C6 acids and hydroxy-acids, e.g. acetic, formic, propionic, acrylic, adipic, and lactic acids. The metals include alkaline earths, particularly Ca, Ba and Mg, heavy metals of Groups 1, 2, and 4, especially Cu, Zn, and Pb, either alone or with alkaline earths, and Ni, Co, Cr and Mn. The complexes may be prepared by co-neutralization of the acid mixture with, for example, the metal hydroxide or carbonate, if desired in a lubricating oil or other medium in which the complex is to be used. Heating to 450-550 DEG F. or higher is generally effected to dehydrate and promote complex formation. The acids may be replaced by such derivatives as esters or nitriles under conditions conducive to saponification. Alternatively, the metal salts may be separately preformed and then mixed and heated. When the complex is prepared in a liquid medium, it may be isolated by extraction with a solvent, e.g. heptane, isopropanol, acetone or water. The complexes are compounded with mineral or synthetic oils, paints, and residual fuels. The compositions may also include oil-soluble sulphonates equivalent to 25-80 weight per cent of the C12-C30 acid, and less than 5 per cent sulphurized sperm oil. Cobalt complexes are of use as oxo catalysts and paint driers, nickel complexes as hydrogenation catalysts. In examples: (1) greases are prepared by heating mineral oil, Hydrofol acid (hydrogenated fish oil acids), hydrogenated castor oil, and hydrated lime to 130 DEG F., adding various ratios of acetic acid, heating to 500 DEG F., cooling, and homogenizing; (2) the castor oil acid is omitted; (3) mono- and di-hydroxystearic acids are also incorporated to prevent hardening, and phenyl a -naphthylamine added during cooling; (6) and (7) cup greases are prepared by heating a calcium complex salt with a simple soap cup grease; (8) a grease containing equimolar amounts of Hydrofol acid and sulphonic acids as calcium salts is prepared; (9) a mixed sodium-calcium grease is obtained by mixing equal weights of the single metal complex greases; (10) a zinc-calcium grease is prepared by neutralizing the acids with zinc oxide and lime; (11) a softer grade is obtained by cutting back with more mineral oil, and the addition of titania is referred to; (12) greases are compared wherein the calcium acetate is wholly or partly preformed or prepared in situ; (13) the acetate content is part preformed strontium acetate and part calcium acetate made in situ; (14), (15) formic acid or a mixture with acetic is used; (16) lactic acid is the low molecular weight acid; (17) lead acetate is incorporated; (20) a twister ring lubricant comprises a calcium complex concentrate and petrolatum; (21) silicone fluid is thickened to a grease by mixing with acetic and Hydrofol acids and heating with lime; (22), (23) hydroxystearic acid and di-2-ethyl hexyl sebacate or di-iso-octyl azelate are also incorporated; (24) a polyester lubricating oil is used as medium for formation of the calcium complex; (25) calcium sulphonate is included in a calcium complex concentrate used as an additive for heavy duty lubricating oil. Specifications 659,103, 662,650 and 680,438 are referred to.ALSO:The invention comprises a complex of a metal (other than aluminium) salt of a C12-C30 carboxylic acid and a metal (other than aluminium) salt of an aliphatic carboxylic acid of lower molecular weight than the first, and containing more than 7, preferably 7-45, mols of the latter salt for each mol of the first. The C12-C30, preferably C18-C22, acids include saturated and unsaturated fatty acids, e.g. stearic and hydroxy stearic, arachidic, hydrogenated fish oil, tallow, oleic and ricinoleic acids. The lower molecular weight acids include saturated and unsaturated, mono- and polycarboxylic C1-C6 acids, and hydroxy-acids, e.g. acetic, formic, propionic, acrylic, adipic, and lactic acids. The metals include alkaline earths, particularly Ca, Ba and Mg, heavy metals of Groups 1, 2 and 4, especially Cu, Zn and Pb, either alone or with alkaline earths, and Ni, Co, Cr and Mn. The complexes may be prepared by co-neutralization of the acid mixture with, for example, the metal hydroxide or carbonate, if desired in a lubricating oil or other medium in which the complex is to be used. Heating to 450-550 DEG F. or higher is generally effected to dehydrate and promote complex formation. The acids may be replaced by such derivatives as esters or nitriles under conditions conducive to saponification. Alternatively, the metal salts may be separately preformed and then mixed and heated. The complexes may be compounded with mineral or synthetic oils, e.g. esters, complex esters, hydrocarbon polymers, silicones, formals, mercaptals or polyglocol derivatives to form greases containing 5-30, and detergent or extreme pressure lubricants containing 0.5-20 weight per cent of complex; incorporated in metalworking lubricants; added to paints in proportions of 2-4 weight per cent; and to residual fuels, particularly those high in vanadium, as corrosion inhibitors. The compositions may also include oil-soluble sulphonates equivalent to 25-80 weight per cent of the C12-C30 acid, and less than 5 per cent sulphurized sperm oil. Cobalt complexes are of use as paint driers. In examples: (1) greases are prepared by heating mineral oil, Hydrofol acid (hydrogenated fish oil acids), hydrogenated castor oil and hydrated lime to 130 DEG F, adding various ratios of acetic acid, heating to 500 DEG F, cooling, and homogenizing; (2) the castor oil acid is omitted; (3) mono- and di-hydroxystearic acids are also incorporated to prevent hardening, and phenyl -naphthylamine added during cooling; (6) and (7) cup greases are prepared by heating a calcium complex salt with a simple soap cup grease; (8) a grease containing equimolar amounts of Hydrofol acid and sulphonic acids as calcium salts is prepared; (9) a mixed sodium-calcium grease is obtained by mixing equal weights of the single metal complex greases; (10) a zinc-calcium grease is prepared by neutralizing the acids with zinc oxide and lime; (11) a softer grade is obtained by cutting back with more mineral oil, and the addition of titania is referred to; (12) greases are compared wherein the calcium acetate is wholly or partly preformed or prepared in situ; (13) the acetate content is part preformed strontium acetate and part calcium acetate made in situ; (14), (15) formic acid or a mixture with acetic is used; (16) lactic acid is the low molecular weight acid; (17) lead acetate is incorporated; (20) a twister ring lubricant comprises a calcium complex concentrate and petrolatum; (21) silicone fluid is thickened to a grease by mixing with acetic and Hydrofol acids and heating with lime; (22), (23) hyroxystearic acid and di-2-ethyl hexyl sebacate or di-iso-octyl azelate are also incorporated; (24) a polyester lubricating oil is used as medium for formation of the calcium complex; (25) calcium sulphonate is included in a calcium complex concentrate used as an additive for heavy duty lubricating oil; (27) a calcium complex is added to bunker fuel oil containing vanadium; (28) oxidized asphalt is blended with a calcium complex concentrate in preparing a rust preventive. Specifications 659,103, 662,650 and 680,438 are referred to.
GB21112/54A 1953-10-21 1954-07-20 Improvements in or relating to complex metal salt-soap compounds Expired GB775027A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US775027XA 1953-10-21 1953-10-21
US40137A US3098822A (en) 1960-07-01 1960-07-01 Lubricants prepared from iso-oleic acid

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GB775027A true GB775027A (en) 1957-05-15

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Family Applications (2)

Application Number Title Priority Date Filing Date
GB21112/54A Expired GB775027A (en) 1953-10-21 1954-07-20 Improvements in or relating to complex metal salt-soap compounds
GB22996/61A Expired GB995347A (en) 1953-10-21 1961-06-26 Lubricants prepared from alkaline earth metal soaps of iso-oleic acid

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Application Number Title Priority Date Filing Date
GB22996/61A Expired GB995347A (en) 1953-10-21 1961-06-26 Lubricants prepared from alkaline earth metal soaps of iso-oleic acid

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BE (1) BE532545A (en)
DE (2) DE1044328B (en)
FR (1) FR1112207A (en)
GB (2) GB775027A (en)
NL (1) NL96851C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011015337A3 (en) * 2009-08-05 2011-04-21 Skf B.V. A grease composition and methods for manufacturing the grease composition

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL110177C (en) * 1958-03-05
US3077450A (en) * 1960-07-01 1963-02-12 Exxon Research Engineering Co Oil compositions containing soapsalt mixtures
US3098823A (en) * 1960-10-03 1963-07-23 Exxon Research Engineering Co Lubricants containing thickeners prepared from tall oil
DE1955951C2 (en) * 1969-11-06 1983-01-05 Cato Oil and Grease Co., Inc., Oklahoma City, Okla. Grease and method of making a calcium soap complex salt thickened grease
CH631481A5 (en) * 1977-06-02 1982-08-13 Alusuisse SYNTHETIC BEARING LUBRICANT.

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Publication number Priority date Publication date Assignee Title
US2734030A (en) * 1956-02-07 Mixed soap-complex grease compositions
NL75517C (en) * 1949-03-12
US2712527A (en) * 1952-08-26 1955-07-05 Exxon Research Engineering Co Improved lubricating greases containing dihydroxy stearic acid soap
US2844536A (en) * 1954-04-30 1958-07-22 Exxon Research Engineering Co High temperature complex grease manufacturing processes
US2892777A (en) * 1954-06-23 1959-06-30 Exxon Research Engineering Co Process for preparing improved synthetic ester based grease compositions
US2847381A (en) * 1955-12-13 1958-08-12 Pure Oil Co Anhydrous calcium-base grease

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011015337A3 (en) * 2009-08-05 2011-04-21 Skf B.V. A grease composition and methods for manufacturing the grease composition
US9506005B2 (en) 2009-08-05 2016-11-29 Aktoebolaget Skf Grease composition and methods for manufacturing the grease composition

Also Published As

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FR1112207A (en) 1956-03-09
BE532545A (en) 1954-10-30
DE1233079B (en) 1967-01-26
NL96851C (en) 1961-02-15
NL190550B (en) 1960-09-15
GB995347A (en) 1965-06-16
DE1044328B (en) 1958-11-20

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