USRE34459E - Friction modifier - Google Patents
Friction modifier Download PDFInfo
- Publication number
- USRE34459E USRE34459E US07/916,908 US91690892A USRE34459E US RE34459 E USRE34459 E US RE34459E US 91690892 A US91690892 A US 91690892A US RE34459 E USRE34459 E US RE34459E
- Authority
- US
- United States
- Prior art keywords
- succinimide
- carbon atoms
- weight
- composition according
- 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 - Lifetime
Links
- 239000003607 modifier Substances 0.000 title description 3
- 239000000654 additive Substances 0.000 claims abstract description 30
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 claims abstract description 26
- 239000000203 mixture Substances 0.000 claims abstract description 25
- 230000001603 reducing effect Effects 0.000 claims abstract description 19
- 150000001408 amides Chemical class 0.000 claims abstract description 15
- 230000000996 additive effect Effects 0.000 claims abstract description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 20
- 239000000314 lubricant Substances 0.000 claims description 20
- FATBGEAMYMYZAF-KTKRTIGZSA-N oleamide Chemical compound CCCCCCCC\C=C/CCCCCCCC(N)=O FATBGEAMYMYZAF-KTKRTIGZSA-N 0.000 claims description 10
- 229940113162 oleylamide Drugs 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000003342 alkenyl group Chemical group 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 229960002317 succinimide Drugs 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 5
- 239000010687 lubricating oil Substances 0.000 claims description 5
- HSEMFIZWXHQJAE-UHFFFAOYSA-N hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(N)=O HSEMFIZWXHQJAE-UHFFFAOYSA-N 0.000 claims description 4
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical group CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 claims description 4
- 229920006395 saturated elastomer Polymers 0.000 claims description 4
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 3
- 229930195729 fatty acid Natural products 0.000 claims description 3
- 239000000194 fatty acid Substances 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 2
- 150000004671 saturated fatty acids Chemical class 0.000 claims description 2
- 229940037312 stearamide Drugs 0.000 claims description 2
- 235000021122 unsaturated fatty acids Nutrition 0.000 claims description 2
- 150000004670 unsaturated fatty acids Chemical class 0.000 claims description 2
- TVFZJQVZUYHGCS-UHFFFAOYSA-N 3-hexadecan-2-ylpyrrolidine-2,5-dione Chemical group CCCCCCCCCCCCCCC(C)C1CC(=O)NC1=O TVFZJQVZUYHGCS-UHFFFAOYSA-N 0.000 claims 1
- YJIHKDQDTYEDDY-UHFFFAOYSA-N 3-octadec-6-en-6-ylpyrrolidine-2,5-dione Chemical compound CCCCCCCCCCCC=C(CCCCC)C1CC(=O)NC1=O YJIHKDQDTYEDDY-UHFFFAOYSA-N 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 239000003921 oil Substances 0.000 description 21
- -1 1-propyltridecenyl Chemical group 0.000 description 15
- 239000002480 mineral oil Substances 0.000 description 7
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 6
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 6
- 239000002270 dispersing agent Substances 0.000 description 6
- 150000002148 esters Chemical class 0.000 description 6
- 235000010446 mineral oil Nutrition 0.000 description 6
- 229910052725 zinc Inorganic materials 0.000 description 6
- 239000011701 zinc Substances 0.000 description 6
- 239000004711 α-olefin Substances 0.000 description 6
- 150000002430 hydrocarbons Chemical group 0.000 description 4
- 239000003208 petroleum Substances 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- 150000003871 sulfonates Chemical class 0.000 description 4
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 3
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical class O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- 229920002367 Polyisobutene Polymers 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 150000001342 alkaline earth metals Chemical class 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 229920000768 polyamine Polymers 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- GGQQNYXPYWCUHG-RMTFUQJTSA-N (3e,6e)-deca-3,6-diene Chemical compound CCC\C=C\C\C=C\CC GGQQNYXPYWCUHG-RMTFUQJTSA-N 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- ZHNUHDYFZUAESO-UHFFFAOYSA-N Formamide Chemical compound NC=O ZHNUHDYFZUAESO-UHFFFAOYSA-N 0.000 description 2
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 150000004996 alkyl benzenes Chemical class 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 239000013638 trimer Substances 0.000 description 2
- WJECKFZULSWXPN-UHFFFAOYSA-N 1,2-didodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1CCCCCCCCCCCC WJECKFZULSWXPN-UHFFFAOYSA-N 0.000 description 1
- QKNBJNCOHZTHPH-UHFFFAOYSA-M C(CCCCCCCC)C1=C(C=CC=C1)SP(=S)(OC1=C(C=CC=C1)CCCCCCCCC)[O-].[Zn+] Chemical compound C(CCCCCCCC)C1=C(C=CC=C1)SP(=S)(OC1=C(C=CC=C1)CCCCCCCCC)[O-].[Zn+] QKNBJNCOHZTHPH-UHFFFAOYSA-M 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 239000005069 Extreme pressure additive Substances 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 101100386054 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) CYS3 gene Proteins 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- AOZDHFFNBZAHJF-UHFFFAOYSA-N [3-hexanoyloxy-2,2-bis(hexanoyloxymethyl)propyl] hexanoate Chemical compound CCCCCC(=O)OCC(COC(=O)CCCCC)(COC(=O)CCCCC)COC(=O)CCCCC AOZDHFFNBZAHJF-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- SNCZNSNPXMPCGN-UHFFFAOYSA-N butanediamide Chemical compound NC(=O)CCC(N)=O SNCZNSNPXMPCGN-UHFFFAOYSA-N 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- GHKVUVOPHDYRJC-UHFFFAOYSA-N didodecyl hexanedioate Chemical compound CCCCCCCCCCCCOC(=O)CCCCC(=O)OCCCCCCCCCCCC GHKVUVOPHDYRJC-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- UPCIBFUJJLCOQG-UHFFFAOYSA-L ethyl-[2-[2-[ethyl(dimethyl)azaniumyl]ethyl-methylamino]ethyl]-dimethylazanium;dibromide Chemical compound [Br-].[Br-].CC[N+](C)(C)CCN(C)CC[N+](C)(C)CC UPCIBFUJJLCOQG-UHFFFAOYSA-L 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- 239000003879 lubricant additive Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 235000021281 monounsaturated fatty acids Nutrition 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 229940116351 sebacate Drugs 0.000 description 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 description 1
- 101150035983 str1 gene Proteins 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/16—Amides; Imides
Definitions
- This invention relates to friction modifiers for use in lubricants and lubricant additives.
- Lubricants customarily in use in vehicles driven by internal combustion and other engines include additives designed to reduce engine friction and the fiction between other moving parts.
- One class of such friction reducing additives has been described in European Specification 0020037 in the name of Edwin Cooper Inc.
- the friction reducing additives of this specification comprise a compound having the structure ##STR1## wherein n is an integer from 2 to 4 and wherein Z has the structure R 1 R 2 CH-- wherein .[.R l .]. .Iadd.R 1 .Iaddend.and R 2 are each independently straight or branched chain hydrocarbon groups containing from 1 to 34 carbon atoms such that the total number of carbon atoms in the groups R 1 and R 2 is from 11 to 35.
- the radical Z may be, for example, 1-methylpentadecy, 1-propyltridecenyl, 1-pentyltridecenyl, 1-tridecylpentadecenyl, or 1-tetradecyleicosenyl.
- the above highly preferred additives are made from linear ⁇ -olefins containing from 12 to 36 carbon atoms by isomerizing the ⁇ -olefins to form a mixture of internal olefins and reacting this mixture of internal olefins with maleic acid, anhydride or ester forming an intermediate and reacting the intermediate with ammonia to form amide, imide, or mixtures thereof.
- Additives made from isomerized linear ⁇ -olefins have greatly improved oil solubility compared with additives made with linear ⁇ -olefins.
- Such friction reducing additives are useful in a wide variety of lubricants.
- One class of lubricants in which the above-mentioned friction reducing additives have been used is in lubricating oils for use in wet brake systems.
- Agricultural tractors and similar vehicles, e.g. off-highway vehicles have braking systems which run in the transmission oil of the back axle.
- the oil acts as a heat transfer medium to remove the large amounts of heat generated by braking.
- Such systems are however subject to the problem that the noise generated by braking may have an unacceptably high level.
- there is generally a level of brake pedal pressure above which the noise generated by the braking rapidly rises to an unacceptably high level e.g. over about 100 decibels.
- One function of the friction reducing additives included in the oils used in such braking systems is to maximise the brake pressure which can be used before excessive noise is generated.
- the friction reducing properties of the aforementioned additives may be surprisingly improved by using them in admixture with an oil-soluble saturated or unsaturated acid amide of 1 to 36 preferably 4 to 24 carbon atoms.
- This admixture may be used to enhance the friction reducing properties of lubricants in general, especially in tractor oils. These may be used as lubricants in a wide variety of parts of a tractor e.g. as crankcase lubricant to reduce fuel consumption.
- the admixture finds particular advantage in its use in a wet brake system.
- the present invention accordingly provides a friction reducing additive composition which comprises at least one compound having the structure ##STR2## wherein n and Z are as herein before defined, and, preferably in a ratio of 1:10 to 10:1, at least one oil-soluble acid amide of the formula ##STR3## in which each R, which may be the same or different, is hydrogen or alkyl or alkenyl of 1 to 35 carbon atoms, R 1 and R 2 are each hydrogen or alkyl or alkenyl of 1 to 23 carbon atoms or one of R 1 and .[.R 2 .]. .Iadd.R 2 .Iaddend. is hydrogen and the other is a group RCO-- in which R is as defined above.
- the acid amide is a linear or branched alkyl or alkenyl acid amide of general formula
- R 3 is alkyl or alkenyl of 3 to 23 carbon atoms, or preferably 7 to 21 carbon atoms. More preferably a saturated or unsaturated fatty acid amide of 8 to 20 carbon atoms is used.
- the first type of friction reducing additive is described in European Specification No. 0020037 whose disclosure is incorporated herein by reference.
- the oil-soluble acid amide may be derived from any natural of synthetic acid or mixture of acids although, as indicated above, a fatty acid is preferred.
- the fatty acid should preferably contain at least 8 carbon atoms per molecule, but amides containing more than 20 carbon atoms per molecule are relatively inaccessible and therefore less preferred.
- Amides based on linear saturated or mono-unsaturated fatty acids containing an even number of carbon atoms are easily available and their use is preferred. Specific examples are stearamide, oleylamide, palmitamide, especially oleylamide.
- the combination of friction reducing additives in accordance with the invention may be incorporated directly in a finished lubricant or, more usually, in an additive package including other constituents designed to improve the performance of the lubricant for distribution to manufacturers of the finished oil.
- the package usually contains also 0.5 to 20 wt. percent, preferably 1 to 5 wt. percent of a diluent oil such as a lubricating oil.
- Preferred lubricants in accordance with the invention contain from 0.1% to 2.0% by weight of the long chain succinimide derivative described above and 0.05 to 1% preferably 0.1 to 1% by weight of the long chain fatty acid .[.amide. The.]. .Iadd.amide, the .Iaddend.ratio of the succinimide derivative to the long chain amide being preferably in the range of 5:1 to 1:1 by weight.
- a lubricant composition containing no friction reducing additives was tested in a standard system in which brake pedal pressure is increased until the noise level produced by the brakes begins to rise sharply. If is found in practice that noise level rises only slowly up to a given pedal pressure and then rises steeply. For the oil without friction reducing additives, the pressure above which the noise level began to rise rapidly was only 30 pounds per square inch. If to the same oil is added 1.35% by weight of a succinimide derivative as described above, specifically one in which Z is an alkenyl group containing an average of 22 carbon atoms, the pedal pressure above which noise begins to rise sharply is increased to 70 pounds per square inch.
- a lubricant composition comprising a combination of friction reducing additives also typically comprises one or more, dispersant(s), detergent(s), antioxidant(s) and extreme pressure additives(s). Such additional additives must, of course, be compatible with the friction modifiers mentioned above and with each other.
- the lubricant may also contain as ashless dispersant and an alkaline earth metal salt of a petroleum sulfonic acid or an alkarly sulfonic acid (e.g. alkylbenzene sulfonic acid).
- an alkaline earth metal salt of a petroleum sulfonic acid or an alkarly sulfonic acid e.g. alkylbenzene sulfonic acid.
- the friction-reducing additives can be used in mineral oil or in synthetic oils of a suitable viscosity e.g. viscosity up to about 16 ⁇ 10 -3 m 2 /S (80 SUS) at 100° C. (210° F.).
- a suitable viscosity e.g. viscosity up to about 16 ⁇ 10 -3 m 2 /S (80 SUS) at 100° C. (210° F.).
- Mineral oils include those of suitable viscosity refined from crude oil from all sources including Gulfcoast, midcontienent, Pennsylvania, California, Alaska and the like. Various standard refinery operations can be used in processing the mineral oil.
- Synthetic oil includes both hydrocarbon synthetic oil and synthetic esters.
- Useful synthetic hydrocarbon oils including liquid polymers of ⁇ -olefins having the proper viscosity.
- the hydrogenated liquid oligomers of C 6 -C 12 ⁇ -olefins such as ⁇ -decene trimer.
- alkylbenzenes of proper viscosity can be used, such as didodecylbenzene.
- Useful synthetic esters include the esters of both monocarboxylic acid and polycarboxylic acid as well as monohydroxy alkanols and polyols. Typical examples are didodecyl adipate, trimethylol propane triperlargonate, pentaerythritol tetracaproate, di(2-ethylhexyl)adipate, and dilaurly sebacate.
- Complex esters prepared from mixtures of mono- and dicarboxylic acid and mono- and polyhydroxyl alkanols can also be used.
- Blends of mineral oil with synthetic oil are particularly useful. For example, blends of 5 to 25 weight percent hydrogenerated ⁇ -decene trimer with 75 to 95 weight percent 32 ⁇ 10 -3 m 2 /S(150 SUS 38° C.(100° F.)) mineral oil results in an excellent lubricant. Likewise, blends of about 5 to 25 weight percent di(2-ethylhexyl)adipate with mineral oil of proper viscosity results in a superior lubricating oil. Also blends of synthetic hydrocarbon oil with synthetic esters can be used. Blends of mineral oil with synthetic oil are especially useful when preparing low viscosity oil (e.g. SAE 5W 20) since they permit these low viscosities without contributing excessive volatility.
- low viscosity oil e.g. SAE 5W 20
- the more preferred lubricating oil compositions include zinc dihydrocarbyldithiophosphate (ZDDP) in combination with the present additives.
- ZDDP zinc dihydrocarbyldithiophosphate
- Both zinc dialkydithiophosphates and zinc dialkaryldithiophosphates as well as mixed alkyl-aryl dithiophosphates can be used.
- alkyl-type ZDDP are those in which the hydrocarbyl groups are a mixture of isobutyl and isoamyl alkyl groups.
- Zinc di(nonylphenyl)-dithiophosphate is an example of an aryl-type ZDDP.
- Good results are achieved using sufficient zinc dihydrocarbyldithiophosphate to provide about 0.01 to 0.5 weight percent zinc.
- a preferred concentration supplies about 0.05 to 0.3 weight percent zinc.
- Another additive which may be used in the oil composition is an alkaline earth metal petroleum sulfonate or alkaline earth metal alkaryl aulfonate.
- alkaline earth metal petroleum sulfonate or alkaline earth metal alkaryl aulfonate examples are calcium petroleum sulfonates, magnesium petroleum sulfonates, barium alkarly sufonates, calcium alkaryl sulfonates or magnesium alkarly sulfonates.
- Both the neutral and the overbased sulfonates having base numbers of up to about 400 can be beneficially used. These are used in an amount to provide about 0.05 to 1.5 weight percent alkaline earth metal and more preferably about 0.1 to 1.0 weight percent.
- crankcase oils also contain an ashless dispersant such as a polyolefin succinamide or succinimide of a polyethylene polyamine such as tetraethylenepentamine.
- the polyolefin succinic substituent is preferably a polyisobutene group having a molecular weight of from about 800 to 5,000.
- Such ashless dispersants are more fully described in U.S. Pat. Nos. 3,172,892 and 3,219,666.
- ashles dispersants include the Mannich condensation products of polyolefine substituted phenols, formaldehyde and polyethylene polyamine.
- the polyolefin phenol is a polyisobutylene-substituted phenol in which the polyisobutylene group has a molecular weight of from about 800 to 5,000.
- the preferred polyethylene polyamine is tetracethylene pentamine.
- antioxidants such as alkyl phenols, sulphurised alkyl phenols and alkyl aromatic amines, particularly hindered alkyl phenols.
- Viscosity index improvers, pour point depressants and antifoamants are examples of other additives which may also be present.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Abstract
Description
R.sup.3 --CO--NH.sub.2
Claims (9)
R.sup.3 --CO--NH.sub.2
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US07/916,908 USRE34459E (en) | 1989-03-20 | 1992-07-20 | Friction modifier |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB8906345 | 1989-03-20 | ||
| GB898906345A GB8906345D0 (en) | 1989-03-20 | 1989-03-20 | Friction modifier |
| US07/487,779 US5021176A (en) | 1989-03-20 | 1990-03-05 | Friction modifier |
| US07/916,908 USRE34459E (en) | 1989-03-20 | 1992-07-20 | Friction modifier |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/487,779 Reissue US5021176A (en) | 1989-03-20 | 1990-03-05 | Friction modifier |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| USRE34459E true USRE34459E (en) | 1993-11-30 |
Family
ID=27264374
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/916,908 Expired - Lifetime USRE34459E (en) | 1989-03-20 | 1992-07-20 | Friction modifier |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | USRE34459E (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5767045A (en) * | 1995-12-01 | 1998-06-16 | Ethyl Petroleum Additives Limited | Hydraulic fluids |
| US6165952A (en) | 1999-04-05 | 2000-12-26 | King Industries, Inc. | Ashless rust inhibitor lubricant compositions |
| US6588393B2 (en) | 2000-09-19 | 2003-07-08 | The Lubrizol Corporation | Low-sulfur consumable lubricating oil composition and a method of operating an internal combustion engine using the same |
| US20060264340A1 (en) * | 2005-05-20 | 2006-11-23 | Iyer Ramnath N | Fluid compositions for dual clutch transmissions |
| US20090005275A1 (en) * | 2007-06-28 | 2009-01-01 | Chevron U.S.A. Inc. | Power steering fluid |
| US8557752B2 (en) | 2005-03-23 | 2013-10-15 | Afton Chemical Corporation | Lubricating compositions |
Citations (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3764536A (en) * | 1971-10-14 | 1973-10-09 | Texaco Inc | Overbased calcium salts of alkenylsuccinimide |
| US3894958A (en) * | 1973-11-05 | 1975-07-15 | Texaco Inc | Mixed secondary alkyl amide synthetic lubricant compositions |
| US4048080A (en) * | 1976-06-07 | 1977-09-13 | Texaco Inc. | Lubricating oil composition |
| US4151101A (en) * | 1977-12-23 | 1979-04-24 | Stauffer Chemical Company | Method and composition for controlling foam in non-aqueous fluid systems |
| US4204970A (en) * | 1978-12-07 | 1980-05-27 | Standard Oil Company (Indiana) | Lubricant compositions containing alkylated aromatic amino acid antioxidants |
| US4303535A (en) * | 1980-05-12 | 1981-12-01 | Texaco Inc. | Hydrocarbyl carbamidopropanamide, its method of preparation and lubricating oil composition containing same |
| US4371446A (en) * | 1979-11-15 | 1983-02-01 | Hirotsugu Kinoshita | Lubricant |
| EP0020037B1 (en) * | 1979-05-18 | 1984-08-15 | Edwin Cooper Inc. | Oil-soluble friction-reducing additive, process for the preparation thereof, and lubricating oil or fuel composition containing the additive |
| US4482464A (en) * | 1983-02-14 | 1984-11-13 | Texaco Inc. | Hydrocarbyl-substituted mono- and bis-succinimide having polyamine chain linked hydroxyacyl radicals and mineral oil compositions containing same |
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US5767045A (en) * | 1995-12-01 | 1998-06-16 | Ethyl Petroleum Additives Limited | Hydraulic fluids |
| US6165952A (en) | 1999-04-05 | 2000-12-26 | King Industries, Inc. | Ashless rust inhibitor lubricant compositions |
| US6588393B2 (en) | 2000-09-19 | 2003-07-08 | The Lubrizol Corporation | Low-sulfur consumable lubricating oil composition and a method of operating an internal combustion engine using the same |
| US8557752B2 (en) | 2005-03-23 | 2013-10-15 | Afton Chemical Corporation | Lubricating compositions |
| US20060264340A1 (en) * | 2005-05-20 | 2006-11-23 | Iyer Ramnath N | Fluid compositions for dual clutch transmissions |
| US20090005275A1 (en) * | 2007-06-28 | 2009-01-01 | Chevron U.S.A. Inc. | Power steering fluid |
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