US2570719A - Foam suppressed lubricant compositions - Google Patents
Foam suppressed lubricant compositions Download PDFInfo
- Publication number
- US2570719A US2570719A US89808A US8980849A US2570719A US 2570719 A US2570719 A US 2570719A US 89808 A US89808 A US 89808A US 8980849 A US8980849 A US 8980849A US 2570719 A US2570719 A US 2570719A
- Authority
- US
- United States
- Prior art keywords
- foam
- oil
- oils
- lubricant compositions
- lubricant
- 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
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- 239000000203 mixture Substances 0.000 title claims description 15
- 239000006260 foam Substances 0.000 title description 19
- 239000000314 lubricant Substances 0.000 title description 12
- 238000005187 foaming Methods 0.000 claims description 9
- 239000003599 detergent Substances 0.000 claims description 7
- 239000000463 material Substances 0.000 claims description 7
- 230000001050 lubricating effect Effects 0.000 claims description 6
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 5
- 239000011707 mineral Substances 0.000 claims description 5
- 239000003921 oil Substances 0.000 description 17
- -1 thio phosphorus acids Chemical class 0.000 description 11
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 125000000217 alkyl group Chemical group 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical class [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 4
- 239000002199 base oil Substances 0.000 description 4
- 238000005461 lubrication Methods 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000007795 chemical reaction product Substances 0.000 description 3
- LIKFHECYJZWXFJ-UHFFFAOYSA-N dimethyldichlorosilane Chemical compound C[Si](C)(Cl)Cl LIKFHECYJZWXFJ-UHFFFAOYSA-N 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 3
- 239000010687 lubricating oil Substances 0.000 description 3
- 150000003141 primary amines Chemical class 0.000 description 3
- FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- NTYJJOPFIAHURM-UHFFFAOYSA-N Histamine Chemical compound NCCC1=CN=CN1 NTYJJOPFIAHURM-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 150000004982 aromatic amines Chemical class 0.000 description 2
- 159000000009 barium salts Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000002000 scavenging effect Effects 0.000 description 2
- 229910000077 silane Inorganic materials 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- YBQZXXMEJHZYMB-UHFFFAOYSA-N 1,2-diphenylhydrazine Chemical compound C=1C=CC=CC=1NNC1=CC=CC=C1 YBQZXXMEJHZYMB-UHFFFAOYSA-N 0.000 description 1
- CDULGHZNHURECF-UHFFFAOYSA-N 2,3-dimethylaniline 2,4-dimethylaniline 2,5-dimethylaniline 2,6-dimethylaniline 3,4-dimethylaniline 3,5-dimethylaniline Chemical group CC1=CC=C(N)C(C)=C1.CC1=CC=C(C)C(N)=C1.CC1=CC(C)=CC(N)=C1.CC1=CC=C(N)C=C1C.CC1=CC=CC(N)=C1C.CC1=CC=CC(C)=C1N CDULGHZNHURECF-UHFFFAOYSA-N 0.000 description 1
- LJKQIQSBHFNMDV-UHFFFAOYSA-N 7-thiabicyclo[4.1.0]hepta-2,4-dien-6-ol Chemical class C1=CC=CC2(O)C1S2 LJKQIQSBHFNMDV-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- OBNDGIHQAIXEAO-UHFFFAOYSA-N [O].[Si] Chemical class [O].[Si] OBNDGIHQAIXEAO-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000003927 aminopyridines Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- RBHJBMIOOPYDBQ-UHFFFAOYSA-N carbon dioxide;propan-2-one Chemical compound O=C=O.CC(C)=O RBHJBMIOOPYDBQ-UHFFFAOYSA-N 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- KZZKOVLJUKWSKX-UHFFFAOYSA-N cyclobutanamine Chemical compound NC1CCC1 KZZKOVLJUKWSKX-UHFFFAOYSA-N 0.000 description 1
- HSOHBWMXECKEKV-UHFFFAOYSA-N cyclooctanamine Chemical compound NC1CCCCCCC1 HSOHBWMXECKEKV-UHFFFAOYSA-N 0.000 description 1
- 239000013530 defoamer Substances 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229960001340 histamine Drugs 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 239000006259 organic additive Substances 0.000 description 1
- 150000002895 organic esters Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 229920005591 polysilicon Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 230000001629 suppression Effects 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- WFLJHDLVVWUGGZ-UHFFFAOYSA-N triacontan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCN WFLJHDLVVWUGGZ-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M171/00—Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
- C10M171/004—Foam inhibited lubricant compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/027—Neutral salts thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/24—Epoxidised acids; Ester derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
- C10M2219/088—Neutral salts
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/087—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Derivatives thereof, e.g. sulfurised phenols
- C10M2219/089—Overbased salts
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/042—Metal salts thereof
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/045—Metal containing thio derivatives
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/10—Phosphatides, e.g. lecithin, cephalin
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/04—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions having a silicon-to-carbon bond, e.g. organo-silanes
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/08—Groups 4 or 14
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
Definitions
- the present invention relates to foam suppressed lubricant compositions, and the like. It relates more particularly to lubricating compositions containing one or more ingredients which tend normally to promote foaming and containing a novel type foam inhibitor.
- foam is distinctly disadvantageous under many circumstances, as, for example, in engine oils for internal combustion engines, particularly the heavy duty type of oils.
- engine oils for internal combustion engines particularly the heavy duty type of oils.
- Many internal combustion engines employ both pressure and splash systems of lubrication,
- the scavenging pump normally has a capacity of several times the volume of the oil returning from the engine, a large amount of air is pumped along with the lubricant and as a result foam tends to build up in the oil reservoir to a point where some oil may be lost through the breather pipe or to a point where the pressure pump delivers foam instead of oil to the various moving parts of the engine with a resultant lack of lubrication.
- oils for gasoline and diesel engines contain dissolved therein from 0.5-5% of various metallo-organic additives, such as metal phenates, phenol sulfides, carboxylates, sulfonates, alcoholates, metal salts of esters of phosphorus and thio phosphorus acids, etc., which as oil soluble detergents act to maintain bearings and the internal surfaces of the engines free of' gummy or varnishlike deposits. Oils containing additives of the above type are especially prone to foam under many conditions.
- the addition to oils of certain non-metallic agents, such as phosphatides, organic esters, fatty compounds; thickeners, etc. also promotes foaming on occasion.
- the present invention is based upon the discovery that the reaction products of alkyl silicon halides with ammonia or with primary amines have excellent properties as foam suppressants in oils, especially mineral base oils, containing detergents or other foam promoters.
- These products which are alkayl amino silanes, may be used in very small quantities, e. g., 0.0001 to 0.01%, for the purpose indicated. Proportions as small as 0.0001% by weight, based on the total lubricant are quite useful. Proportions of -0.00125% to 0.005% are specifically preferred.
- alkyl polysilamines useful for purposes of the present invention may be prepared as follows:
- a lower alkyl silicon halide for example, (CH3)2SiCl2 is reacted with ammonia, or with a primary alkyl or aryl amine to form an amino silane of the following general structure where R is a lower alkyl group, of C1 to C4, R1 is hydrogen or alkyl or aryl, and X is an integer of such value that the polymer has a high molecular weight, e. g., 300 or more, up to several thousand. Where R is methyl or ethyl, as is preferred, the above materials are readily prepared by mere admixture.
- test 1 the sample, maintained at a. temperature of 75 F. is air blown at a constant rate for five minutes, then allowed to set- 31.5 g. of hexadecylamine, discomposition of the lubricant.
- reaction may be conducted at any suitable temperature, for example from F. to about.
- the quantity of foaming suppressor to be used in any given lubricant will vary widely with the Where large amounts of detergents or emulsifiers are present, the quantity of defoamer used should be increased, but in most circumstances a quantity of 0.01% by weight, based on the weight of the total lubricant, will be adequate.
- the NR1 radical may be derived from ammonia gas or from any alkylor aryl primary amine having up to about 30 carbon atoms in the aryl oralkyl group.
- Suitable primary amines are (1) straight chain aliphatic amines such as hexadecylamine,:1,'4- diaminoheptane, triacontylamine, 5-amino octone-2: (2) branched chain aliphatic amines 'such as 3-ethyl,5-methyl hexainine, 4-ethyl,5-
- aromatic amines such as aniline, leucaniline, xylidine, phenylene vigorous agitation in a small quantity of carrier liquid, for example a light' lubricating oil which can be added to the larger mass to obtain a thorough mixing more easily.
- a lubricating composition consisting essentially of a mineral base oil of lubricating grade 1 containing a detergent'and, as a ioaming'suppressor, 0.0001 to 0.01% by weight, based on the total composition, of a material having the general formula: I
- R is a lower alkyl group of 1 to 4 carbon atoms
- R1 is a member of the group consisting of hydrogen, alkyl and aryl
- X is an integer of such value that the polymer has a molecular weight of at least 300.
- composition as in claim 1 wherein the quan-' tity of foaming suppressor is between 0.00125 and 0.005%.
- a mineral base oil composition containing a minor proportion of a foam promoter and 0.0001 to 0.01% by weight, based on the total composition, of a polyamino-silane having a molecular weight of at least .300 of general formula where R is a lower alkyl group of the C1 to 04 range, R1 is selected from the groupconsisting 01' hydrogen, alkyl and aryl.
- composition according to claim 3 wherein the polymer is a primary amine substituted silane polymer.
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Description
Patented Oct. 9, 1951 FOAM SUPPRESSED LUBRICANT COMPOSITIONS Barry W. Rudel, Roselle Park, and Abraham D.
Kirshenbaum, Union, N. J., assignors to Standard Oil Development Company, a corporation of Delaware No Drawing. Application April 26, 1949, Serial No. 89,808
6 Claims. (Cl. 252' 49.6)
The present invention relates to foam suppressed lubricant compositions, and the like. It relates more particularly to lubricating compositions containing one or more ingredients which tend normally to promote foaming and containing a novel type foam inhibitor.
The formation of foam is distinctly disadvantageous under many circumstances, as, for example, in engine oils for internal combustion engines, particularly the heavy duty type of oils. Many internal combustion engines employ both pressure and splash systems of lubrication,
whereas other motors use only one of the systems. In either case the formation of foam on top of the oil during the operation of the motor leads to serious consequences due to lack of lubrication. This is particularly so in pressure lubricating systems employing the so-called dry sump operation where the oil returning from the engine parts is picked up by a scavenging pump and returned to the lubricant reservoir. Since the scavenging pump normally has a capacity of several times the volume of the oil returning from the engine, a large amount of air is pumped along with the lubricant and as a result foam tends to build up in the oil reservoir to a point where some oil may be lost through the breather pipe or to a point where the pressure pump delivers foam instead of oil to the various moving parts of the engine with a resultant lack of lubrication. Many heavy duty lubricating oils for gasoline and diesel engines contain dissolved therein from 0.5-5% of various metallo-organic additives, such as metal phenates, phenol sulfides, carboxylates, sulfonates, alcoholates, metal salts of esters of phosphorus and thio phosphorus acids, etc., which as oil soluble detergents act to maintain bearings and the internal surfaces of the engines free of' gummy or varnishlike deposits. Oils containing additives of the above type are especially prone to foam under many conditions. The addition to oils of certain non-metallic agents, such as phosphatides, organic esters, fatty compounds; thickeners, etc., also promotes foaming on occasion.
In the case of gear lubricants, such as those designed for the lubrication of automobile rear ends and transmissions, when such lubricants show a.marked tendency to form foam during use the foam entraps the lubricant to such an extent that the oil level will fall below the gear train. These oils usually owe their ability to withstand high unit loads to the presence of additives Co a ng sulfur, chlorine or phosphorus or to the presence of lead soaps. Hydraulic and shock absorber oils likewise need protection against foaming.
Various suggestions have been made in the prior artto the effect that certain oxygen-containing materials are useful foam suppressors, especially in oils containing detergents, and the like, which tend to promote foaming. Thus, the patents to Borsoff et al., No. 2,430,857 and No. 2,430,858 suggest the use of alcohols, aldehydes, and the like. Other references, e. g., Larsen and Diamond, Patents Nos. 2,375,007 and 2,406,671, have suggested the use of certain oxygen-silicon compounds for this purpose, these materials being of the type described by Rochow, for example, in his Patent No. 2,258,220. Still other related materials such as cyclo-silicones have been suggested, e. g., in Hersh Patent No. 2,464,231.
The present invention is based upon the discovery that the reaction products of alkyl silicon halides with ammonia or with primary amines have excellent properties as foam suppressants in oils, especially mineral base oils, containing detergents or other foam promoters. These products, which are alkayl amino silanes, may be used in very small quantities, e. g., 0.0001 to 0.01%, for the purpose indicated. Proportions as small as 0.0001% by weight, based on the total lubricant are quite useful. Proportions of -0.00125% to 0.005% are specifically preferred.
In general, alkyl polysilamines useful for purposes of the present invention may be prepared as follows:
A lower alkyl silicon halide, for example, (CH3)2SiCl2 is reacted with ammonia, or with a primary alkyl or aryl amine to form an amino silane of the following general structure where R is a lower alkyl group, of C1 to C4, R1 is hydrogen or alkyl or aryl, and X is an integer of such value that the polymer has a high molecular weight, e. g., 300 or more, up to several thousand. Where R is methyl or ethyl, as is preferred, the above materials are readily prepared by mere admixture.
The invention will be further understood by reference to the following example showing preparation of an amino-silane and its use in varying quantities in oils containing substantial amounts of foam promoting materials of the detergent type.
3 EXAMPLE Method of preparation 14.8 g. of dimethyl silicon dichloride,
was added to 25 cc. of benzene in a 500 cc. Ehrlenmeyer flask. The flask and contents were 1 cooled in a Dry Ice-acetone bath with a calcium chloride drying tube in thestopper to keep water condensate out. solved in 300 cc. of benzene was added to the cold (CH3) 281012. The contents of the flask were then allowed to warm up to room temperature. A reaction took place forming a gel. The benzene and any hydrogen chloride formed were removed by means of a water aspirator and the remaining solid was then air dried. The final product was a white, waxy powder.
Data on foam suppression CRCL-12 foam tests were run on a blend of 2.5 weight per cent of the reaction product of P255 and the barium salt of. tert.-octyl phenol sulfide in a heavy duty mineral base lubricating oil having a viscosity of 50 S. S. U. at 210 F. containing various amounts of the above polyalkyl silamine.
The base oil containing 2.5% by weight of the reaction product of P235 and the barium salt of tert.-octyl phenol sulfide, as above, showed the results set forth in the table.
TABLE Results CR0 L-I2 loam tests For comparative purposes, commercial oxygencontaining polysilicones were also tested and were found unsatisfactory in the third phase of the foaming test.
The details of the foaming test CRC L-12 are as follows: In test 1, the sample, maintained at a. temperature of 75 F. is air blown at a constant rate for five minutes, then allowed to set- 31.5 g. of hexadecylamine, discomposition of the lubricant.
diamine, naphthylamlne, di-phenyl butylamme, di-phenyl hydrazine; (4) alicyclic amines, such as cyclobutylamine, cyclooctylamine, vestrylamine;' (5) heterocyclic amines such as histamine, aminopyridine, and the like. The reaction, being exothermic, may be conducted at any suitable temperature, for example from F. to about.
100 F. or up to 150 F.
The quantity of foaming suppressor to be used in any given lubricant will vary widely with the Where large amounts of detergents or emulsifiers are present, the quantity of defoamer used should be increased, but in most circumstances a quantity of 0.01% by weight, based on the weight of the total lubricant, will be adequate. In order to obtain satisfactory dispersion of the amino silane in the extremely small quantities employed, it is desirable first to disperse it by tie for ten minutes. The volume of foam is measured at the end of both periods and recorded as (A) and (B) respectively. In tests 2 and 3, the identical test is repeated in sequence on a second sample at temperatures of 200 and 75 F.,
' respectively.
While the amino silanes derived from dimethyl silicon dichloride are referred to specifically above, homologs such as diethyl disilicon dichloride are equally useful. I The NR1 radical may be derived from ammonia gas or from any alkylor aryl primary amine having up to about 30 carbon atoms in the aryl oralkyl group.
Suitable primary amines are (1) straight chain aliphatic amines such as hexadecylamine,:1,'4- diaminoheptane, triacontylamine, 5-amino octone-2: (2) branched chain aliphatic amines 'such as 3-ethyl,5-methyl hexainine, 4-ethyl,5-
isopropyl octylamine-3; (3) aromatic amines such as aniline, leucaniline, xylidine, phenylene vigorous agitation in a small quantity of carrier liquid, for example a light' lubricating oil which can be added to the larger mass to obtain a thorough mixing more easily. What is claimed is:
1. A lubricating composition consisting essentially of a mineral base oil of lubricating grade 1 containing a detergent'and, as a ioaming'suppressor, 0.0001 to 0.01% by weight, based on the total composition, of a material having the general formula: I
wherein R is a lower alkyl group of 1 to 4 carbon atoms, R1 is a member of the group consisting of hydrogen, alkyl and aryl, and Xis an integer of such value that the polymer has a molecular weight of at least 300.
2. Composition as in claim 1 wherein the quan-' tity of foaming suppressor is between 0.00125 and 0.005%.
3. A mineral base oil composition containing a minor proportion of a foam promoter and 0.0001 to 0.01% by weight, based on the total composition, of a polyamino-silane having a molecular weight of at least .300 of general formula where R is a lower alkyl group of the C1 to 04 range, R1 is selected from the groupconsisting 01' hydrogen, alkyl and aryl.
4. Composition according to claim 3 wherein the polymer is a primary amine substituted silane polymer.
5. Composition according to claim 1 wherein 7 R1 is an alkyl group.
6. Composition according to claim 1 wherein R1 is a hexadecyl radical.
HARRY w. RUDEL. ABRAHAM D. KIRSHENB UM.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Num er Name Date 2,375,007 Larsen et al. May 1, 1945 2,406,671 Diamond Aug. 2'7, 1946 2,416,504 Trautman et al. Feb. 25, 1947 2,462,635 Haber Feb.;22,'1949 2,464,231 Hersch Mar. 15, 1949
Claims (1)
1. A LUBRICATING COMPOSITION CONSISTING ESSENTIALLY OF A MINERAL BASE OIL OF LUBRICATING GRADE CONTAINING A DETERGENT AND, AS A FOAMING SUPPRESSOR, 0.0001 TO 0.01% BY WEIGHT, BASED ON THE TOTAL COMPOSITION, OF A MATERIAL HAVING THE GENERAL FORMULA:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US89808A US2570719A (en) | 1949-04-26 | 1949-04-26 | Foam suppressed lubricant compositions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US89808A US2570719A (en) | 1949-04-26 | 1949-04-26 | Foam suppressed lubricant compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2570719A true US2570719A (en) | 1951-10-09 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US89808A Expired - Lifetime US2570719A (en) | 1949-04-26 | 1949-04-26 | Foam suppressed lubricant compositions |
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| US (1) | US2570719A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3393218A (en) * | 1964-05-18 | 1968-07-16 | Monsanto Co | Polymeric silazane compounds |
| US3481964A (en) * | 1965-06-15 | 1969-12-02 | Dynamit Nobel Ag | Process for preparing organosilicon nitrogen compounds |
| US4237172A (en) * | 1978-12-04 | 1980-12-02 | Joseph J. Packo | Sealing leaks by polymerization of volatilized aminosilane monomers |
| US4304805A (en) * | 1978-12-04 | 1981-12-08 | Joseph J. Packo | Sealing leaks by polymerization of volatilized aminosilane monomers |
| US20180237724A1 (en) * | 2017-02-22 | 2018-08-23 | Infineum International Limited | Lubricating oil compositions containing pre-ceramic polymers |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2375007A (en) * | 1943-04-15 | 1945-05-01 | Shell Dev | Antifoaming composition |
| US2406671A (en) * | 1944-09-25 | 1946-08-27 | Shell Dev | Cutting oil |
| US2416504A (en) * | 1945-01-03 | 1947-02-25 | Gulf Research Development Co | Prevention of foaming of hydrocarbon oils |
| US2462635A (en) * | 1946-10-22 | 1949-02-22 | Gen Electric | Cyclic polymeric organoaminosilanes |
| US2464231A (en) * | 1945-06-18 | 1949-03-15 | Continental Oil Co | Method for preparing pentamethylene silicone polymers |
-
1949
- 1949-04-26 US US89808A patent/US2570719A/en not_active Expired - Lifetime
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2375007A (en) * | 1943-04-15 | 1945-05-01 | Shell Dev | Antifoaming composition |
| US2406671A (en) * | 1944-09-25 | 1946-08-27 | Shell Dev | Cutting oil |
| US2416504A (en) * | 1945-01-03 | 1947-02-25 | Gulf Research Development Co | Prevention of foaming of hydrocarbon oils |
| US2464231A (en) * | 1945-06-18 | 1949-03-15 | Continental Oil Co | Method for preparing pentamethylene silicone polymers |
| US2462635A (en) * | 1946-10-22 | 1949-02-22 | Gen Electric | Cyclic polymeric organoaminosilanes |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3393218A (en) * | 1964-05-18 | 1968-07-16 | Monsanto Co | Polymeric silazane compounds |
| US3481964A (en) * | 1965-06-15 | 1969-12-02 | Dynamit Nobel Ag | Process for preparing organosilicon nitrogen compounds |
| US4237172A (en) * | 1978-12-04 | 1980-12-02 | Joseph J. Packo | Sealing leaks by polymerization of volatilized aminosilane monomers |
| US4304805A (en) * | 1978-12-04 | 1981-12-08 | Joseph J. Packo | Sealing leaks by polymerization of volatilized aminosilane monomers |
| US20180237724A1 (en) * | 2017-02-22 | 2018-08-23 | Infineum International Limited | Lubricating oil compositions containing pre-ceramic polymers |
| JP2018135518A (en) * | 2017-02-22 | 2018-08-30 | インフィニューム インターナショナル リミテッド | Lubricating oil composition containing pre-ceramic polymers |
| US11352584B2 (en) * | 2017-02-22 | 2022-06-07 | Infineum International Limited | Lubricating oil compositions containing pre-ceramic polymers |
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