US3418296A - Copolymer concentrate and oil composition - Google Patents
Copolymer concentrate and oil composition Download PDFInfo
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- US3418296A US3418296A US478510A US47851065A US3418296A US 3418296 A US3418296 A US 3418296A US 478510 A US478510 A US 478510A US 47851065 A US47851065 A US 47851065A US 3418296 A US3418296 A US 3418296A
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- oil
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- lubricating
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- 229920001577 copolymer Polymers 0.000 title description 34
- 239000000203 mixture Substances 0.000 title description 17
- 239000012141 concentrate Substances 0.000 title description 8
- 239000010687 lubricating oil Substances 0.000 description 21
- 239000003921 oil Substances 0.000 description 19
- 239000010802 sludge Substances 0.000 description 12
- 125000004432 carbon atom Chemical group C* 0.000 description 10
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 9
- 239000000654 additive Substances 0.000 description 9
- -1 alkyl methacrylates Chemical class 0.000 description 9
- 150000002148 esters Chemical class 0.000 description 8
- 239000003085 diluting agent Substances 0.000 description 7
- 239000002480 mineral oil Substances 0.000 description 7
- 235000010446 mineral oil Nutrition 0.000 description 7
- 239000003599 detergent Substances 0.000 description 6
- 239000002270 dispersing agent Substances 0.000 description 6
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 239000002966 varnish Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 4
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 4
- LNCPIMCVTKXXOY-UHFFFAOYSA-N hexyl 2-methylprop-2-enoate Chemical compound CCCCCCOC(=O)C(C)=C LNCPIMCVTKXXOY-UHFFFAOYSA-N 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- 230000000379 polymerizing effect Effects 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- LGJCFVYMIJLQJO-UHFFFAOYSA-N 1-dodecylperoxydodecane Chemical compound CCCCCCCCCCCCOOCCCCCCCCCCCC LGJCFVYMIJLQJO-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 125000005250 alkyl acrylate group Chemical group 0.000 description 3
- 238000002485 combustion reaction Methods 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 238000010926 purge Methods 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 239000013049 sediment Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- ZMALNMQOXQXZRO-UHFFFAOYSA-N 4-ethenylmorpholin-3-one Chemical compound C=CN1CCOCC1=O ZMALNMQOXQXZRO-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 150000001336 alkenes Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 239000003054 catalyst Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000012298 atmosphere Substances 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
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- 238000006555 catalytic reaction Methods 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000001066 destructive effect Effects 0.000 description 1
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 239000002198 insoluble material Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000012857 radioactive material Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000010689 synthetic lubricating oil Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- JGSUMMPGKPITGK-UHFFFAOYSA-L zinc;n,n-dipentylcarbamodithioate Chemical compound [Zn+2].CCCCCN(C([S-])=S)CCCCC.CCCCCN(C([S-])=S)CCCCC JGSUMMPGKPITGK-UHFFFAOYSA-L 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
- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1812—C12-(meth)acrylate, e.g. lauryl (meth)acrylate
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1818—C13or longer chain (meth)acrylate, e.g. stearyl (meth)acrylate
-
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/064—Di- and triaryl amines
-
- 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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/02—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2217/028—Macromolecular compounds obtained from nitrogen containing monomers by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a nitrogen-containing hetero ring
-
- 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
- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/06—Macromolecular compounds obtained by functionalisation op polymers with a nitrogen containing compound
-
- 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
- C10M2219/06—Thio-acids; Thiocyanates; Derivatives thereof
- C10M2219/062—Thio-acids; Thiocyanates; Derivatives thereof having carbon-to-sulfur double bonds
- C10M2219/066—Thiocarbamic type compounds
- C10M2219/068—Thiocarbamate metal 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
- 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
-
- 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
- C10N2010/04—Groups 2 or 12
-
- 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
- C10N2040/25—Internal-combustion engines
-
- 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
- C10N2040/25—Internal-combustion engines
- C10N2040/251—Alcohol-fuelled engines
-
- 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
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
-
- 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
- C10N2040/25—Internal-combustion engines
- C10N2040/255—Gasoline engines
- C10N2040/28—Rotary engines
Definitions
- This invention relates to copolymers useful in improving lubricating oils and to lubricating oils containing such copolymers.
- Lubricating oils have thus been formulated to improve performance with respect to one of these properties, i.e., improved viscosityindex or better sludge dispersing or detergent action, and in some cases, lubricating oil additives have been prepared which, when blended with a lubricating oil, provide improvement with respect to two of these properties.
- certain high molecular weight polymethacrylic copolymers are useful as both pour-point depressants and Vl-improvers.
- Other copolymers such as those prepared from alkyl methacrylates with N-vinyl-alkyl-oxazolidinone or N-vinylpyrrolidinone are of similar utility.
- No detergent or sludge-dispersant additive for lubricating oils has heretofore been proposed that provides more than a partial answer to the problem of preventing sludge formation and varnish deposition in engines.
- known oil detergents in many cases increase the rate of accumulation of inorganic deposits Within the combustion chambers of engines.
- Another object is to provide a copolymer which, when added to a lubricating oil, greatly improves the dispersant and detergent properties, improves the VI, reduces the pour point, and induces prolonged resistance to sludge and varnish formation.
- lubricating oil is to be interpreted broadly as referring to natural and synthetic lubricating oils. These oils are essentially hydrocarbons which possess lubricating properties regardless of their actual viscosity and include crude or refined petroleums, hydrogenated petroleum oils, or hydrogenatecl cracked petroleum oils, oily high molecular weight hydrocarbons, such as are obtained by the polymerization of olefins or by the condensation of olefins with aromatic hydrocarbons, etc.
- One or more of the above objects are accomplished according to the present invention by copolymerizing at least one alkyl acrylate, or alkyl methacrylate with N- viny1-3-morpholinone (hereinafter designated VM). While a wide latitude is permissible in choosing the acrylic ester and the proportions thereof in the copolymer, it is essential (1) that the copolymer be oil-soluble, (2) that it contain at least one acrylic ester containing an alkyl radical of at least about 12 carbon atoms and (3) that it contain sufiicient VM to improve its sludge-dispersant properties.
- VM N- viny1-3-morpholinone
- the acrylic ester i.e., the alkyl acrylate or methacrylate
- the acrylic ester component consist predominantly of ester or esters wherein the alkyl-radical or radicals contain at least 4, and preferably at least 6 carbon atoms.
- at least about 20 percent, and preferably about 50-80 percent, of the acrylic ester component should contain an alkyl radical of at least 12 carbon atoms.
- the third requirement may be met by the inclusion in the copolymer of only a very small proportion of VM.
- the preferred copolymers contain about 3-30 percent of VM, the optimum usually being about 10-20 percent.
- the acrylic ester component of the copolymer of the invention ordinarily consists of one or more esters having the formula wherein n is an integer from 0 to 1 and R is an alkyl radical containing about 4 to 20 carbon atoms. Best results are obtained when R is a straight-chain primary alkyl radical.
- the acrylic ester component of the copolymer comprises at least one ester wherein R contains 4 to 8 carbon atoms and at least one ester wherein R contains 12-20 carbon atoms.
- the copolymers of the invention are preferably prepared by dissolving one or more of the acrylates or methacrylates and VM in a diluent oil and copolymerizing at elevated temperatures under an oxygen-free atmosphere in the presence of a free-radical-producing compound which acts as a catalyst or initiator. Polymerization may also be induced by irradiation under the influence of high energy fields.
- the latter catalyzation may include the various actinic radiations, including such diverse forms of catalysis as ultraviolet, X-ray and gamma radiations, as well as radiation from radioactive materials and high energy electrons generated from linear accelerators, resonant transformers and the like.
- Elevated temperatures are preferred during the course of the reaction in order to decrease the reaction time.
- the temperature range is about 40 to about 90 C., but temperatures either higher or lower may be employed depending upon the catalyst.
- the diluent oil is preferably a conventional low sulfurcontent oil, such as the parafi'inic hydrocarbon or ester type, which is suitable for addition to lubricating oils.
- the monomers are suitably employed in such proportions that the diluent wherein they are copolymerized will contain, after polymerization, from about 15 percent to about 60 percent, and preferably about 25 percent to 40 percent of copolymer. All percentages specified herein are by weight.
- copolymerization directly in a diluent oil of the type stated is the preferred method, other methods may be employed, as for example, polymerizing the monomers in the lubricating oil in which the copolymer is to be used or in an inert volatile hydrocarbon diluent such as hexane or toluene.
- alternate methods such as these are generally less desirable. For example, when a volatile solvent is employed in place of a diluent oil, it must be removed, e.g., by distillation, after the polymerization, and replaced with oil.
- the oil containing the copolymer may be considered as a concentrate containing the copolymer in the aforesaid amount.
- the concentrate suitably is incorporated into a lubricating oil to the extent that the copolymer will be in an amount in the range of from about 0.1 percent to about 20 percent and preferably from 3 percent to 8 percent of the lubricating oil.
- Example 1 Into a reaction vessel equipped with a means for stirring, purging, and temperature control were placed 200 m1. of white mineral oil (180 SUSSaybolt Universal second), 50 ml. of hexyl methacrylate, 60 ml. of lauryl methacrylate, 60 ml. of stearyl methacrylate, 30 ml. of VM and 1 gram of lauryl peroxide. The mixture was maintained at a temperature in the range of from 60 to 80 C. for 18 hours while under a nitrogen atmosphere. At the end of 18 hours, a concentrate of 50 percent copolymer in white mineral oil was obtained.
- white mineral oil 180 SUSSaybolt Universal second
- 50 ml. of hexyl methacrylate 60 ml. of lauryl methacrylate
- 60 ml. of stearyl methacrylate 60 ml. of stearyl methacrylate
- 30 ml. of VM 1 gram of lauryl per
- Example 2 Into a reaction vessel equipped with a means for stirring, purging, and temperature control were placed 20.8 pounds of 180 SUS white mineral oil, 2.12 pounds of VM, 3.54 pounds of hexyl methacrylate, 5.1 pounds of lauryl methacrylate, 3.4 pounds of stearyl methacrylate, and 95 g. of lauryl peroxide. The mixture was maintained at a temperature of 63 C. for 15 hours while under a nitrogen atmosphere. At the end of 15 hours a concentrate of 40 percent copolymer in white mineral oil was obtained.
- This composition was blended and tested in an engine according to the Co-ordinating Research Council (C.R.C.) FL-2 technique.
- the blend was made by mixing 1.5
- the lubricant containing 2 percent copolymer exhibited excellent improvement with regard to dispersant and detergent properties, VI, pour point, and prolonged resistance to sludge and varnish formation.
- the sludge dispersant characteristic is especially noticeable due to the total sludge rating of 68.4 out of a possible and the varnish rating of 15.0 out of a possible 20.
- the combined sludge and varnish rating of 83.4 is very high.
- Example 3 Into a reaction vessel equipped with a means for stirring, purging, and temperature control were placed 210 g. of white mineral oil, 9 g. of VM, 27 g. of hexyl methacrylate, 33 g. of lauryl methacrylate, 21 g. of stearyl methacrylate, and 1 g. of lauryl peroxide. The mixture was maintained at a temperature of 65 C. for l8 hours while under a nitrogen atmosphere. At the end of 18 hours a concentrate of 30 percent copolymer in white mineral oil was obtained.
- This composition was blended and tested in an engine according to the C.R.C. FL-2 technique.
- the blend was prepared by mixing a suflicient amount of the 30 percent copolymer into SUS solvent refined neutral petroleum oil to produce a 2 percent mixture and in addition, /2 percent of a 50 percent oil blend of zinc diamyl dithiocarbamate, /2 percent of an octylated and styrenated diphenylamine, /2 percent of a zinc dialkyl dithiophosphate, and 0.4 percent of a calcium-organic compound containing combined sulfur, were added as oxidation inhibitors.
- the blend had the following properties and give the following results:
- Example 4 A carbon dispersion test was performed to evaluate the copolymers with regard to their efficiency in improving lubricating oils.
- a paste was prepared by thoroughly blending 20 percent of carbon black into white mineral oil. For the test, 3 g. of this paste were blended with 70 ml. of kerosene containing 1.5 percent of the compound to be tested. The results are given in Table 1 and it is pointed out that the longer the dispersion stands without settling, the better is the additive. Also, in Table 1, there is a column labeled wet. Since moisture accumulates in a crankcase and is destructive with regard to the efliciency of the additive, this column shows the result obtained when 0.3 ml. of water was added to the suspension.
- Example 5 A hexane-insolubles suspension test was performed to further evaluate the polymer with regard to its efliciency in improving lubricating oils.
- hexane-insoluble material was obtained from oil oxidized in a. Doornte type oxidation machine and these insolubles were washed with hexane, dried and dissolved in benzene in an amount sufiicient to form a solution of 2.5 g. per liter.
- An oil-soluble copolymer prepared by polymerizing a mixture of N-vinyl-S-morpholinone and at least one acrylic ester having the formula 6 3.
- An oil-soluble copolymer prepared by polymerizing a mixture consisting essentially of about 10 to 20 percent of N-vinyl-3-morpholinone, 20 to 30 percent of n-hexyl methacrylate, 20 to 50 percent of lauryl methacrylate and 20 to percent of stearyl methacrylate.
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- General Chemical & Material Sciences (AREA)
- Lubricants (AREA)
Description
United States Patent 3,418,296 COPOLYMER 'CONCENTRATE AND OIL COMPOSITION Charles R. Bearden, Lake Jackson, Tex., assignor to The Dow Chemical Company, Midland, Mich., a corporation of Delaware No Drawing. Original application Oct. 25, 1961, Ser. No. 147,489, now Patent No. 3,210,282, dated Oct. 5, 1965. Divided and this application July 1, 1965, Ser. No.
4 Claims. (Cl. 26080.72)
ABSTRACT OF THE DISCLOSURE Novel oil-soluble copolymers of (a) N-vinyl-3-morpholinone and (b) an alkyl acrylate or methacrylate wherein the alkyl radical contains 4-20 carbon atoms, and wherein the proportion of (a) is 3 to 30%, are useful as additives for lubricating oils.
This application is a division of my copending application Ser. No. 147,489 filed Oct. 25, 1961, and now US. 3,210,282.
This invention relates to copolymers useful in improving lubricating oils and to lubricating oils containing such copolymers.
The principal use for lubricating oils is in internal combustion engines, the efficiency of which depends to a large degree upon the quality of the crankcase oils employed. A major problem in the operation of internal combustion engines, which may be broadly classified as spark ignition and diesel types, results from the tendency of conventional crankcase oils to undergo oxidation and other chemical changes that lead to the formation of carbon, resins, and insoluble varnish-like gums which deposit on moving engine parts and separate as sludge that markedly impairs the lubricating properties of the oil. Another source of sludge is the decomposition of the fuel and this source is particularly damaging since the deposits occur on piston surfaces and around piston rings. Sludge formation and gum deposition are most severe in light duty engine operation as exemplified by intermittent use of passenger automobiles and light trucks.
Many materials have been added to lubricating oils to improve them and considerable knowledge of such adjuvants has been gained. Some of the specific additives used to improve the properties of lubricating oils are pour point depressants, the viscosity index improvers (VI improvers), and the sludge dispersants and detergents. Lubricating oils have thus been formulated to improve performance with respect to one of these properties, i.e., improved viscosityindex or better sludge dispersing or detergent action, and in some cases, lubricating oil additives have been prepared which, when blended with a lubricating oil, provide improvement with respect to two of these properties. For example, certain high molecular weight polymethacrylic copolymers are useful as both pour-point depressants and Vl-improvers. Other copolymers, such as those prepared from alkyl methacrylates with N-vinyl-alkyl-oxazolidinone or N-vinylpyrrolidinone are of similar utility. However, among the known lubricating oil additives, there is not one that will improve all the properties of a lubricating oil equally at the same time. No detergent or sludge-dispersant additive for lubricating oils has heretofore been proposed that provides more than a partial answer to the problem of preventing sludge formation and varnish deposition in engines. In fact, known oil detergents in many cases increase the rate of accumulation of inorganic deposits Within the combustion chambers of engines.
3,418,296 Patented Dec. 24, 1968 It is an object of the present invention to provide a copolymer suitable for mixing with lubricating oils.
Another object is to provide a copolymer which, when added to a lubricating oil, greatly improves the dispersant and detergent properties, improves the VI, reduces the pour point, and induces prolonged resistance to sludge and varnish formation. Other objects will appear hereinafter.
It is understood that the term lubricating oil, as used herein, is to be interpreted broadly as referring to natural and synthetic lubricating oils. These oils are essentially hydrocarbons which possess lubricating properties regardless of their actual viscosity and include crude or refined petroleums, hydrogenated petroleum oils, or hydrogenatecl cracked petroleum oils, oily high molecular weight hydrocarbons, such as are obtained by the polymerization of olefins or by the condensation of olefins with aromatic hydrocarbons, etc.
One or more of the above objects are accomplished according to the present invention by copolymerizing at least one alkyl acrylate, or alkyl methacrylate with N- viny1-3-morpholinone (hereinafter designated VM). While a wide latitude is permissible in choosing the acrylic ester and the proportions thereof in the copolymer, it is essential (1) that the copolymer be oil-soluble, (2) that it contain at least one acrylic ester containing an alkyl radical of at least about 12 carbon atoms and (3) that it contain sufiicient VM to improve its sludge-dispersant properties. To meet the first requirement, it is preferred that the acrylic ester (i.e., the alkyl acrylate or methacrylate) component consist predominantly of ester or esters wherein the alkyl-radical or radicals contain at least 4, and preferably at least 6 carbon atoms. To meet the second requirement, at least about 20 percent, and preferably about 50-80 percent, of the acrylic ester component should contain an alkyl radical of at least 12 carbon atoms. Obviously, the first requirement will often inherently be met in fulfilling the second. The third requirement may be met by the inclusion in the copolymer of only a very small proportion of VM. As little as 3 percent usually produces a very evident improvement in the product, though it is generally necessary to use at least 5 percent or even 10 percent, to achieve optimum results. On the other hand, amounts in excess of about 20 percent are usually uneconomical and over about 30 percent produces little, if any, added improvement. Thus, the preferred copolymers contain about 3-30 percent of VM, the optimum usually being about 10-20 percent.
In view of the above considerations, the acrylic ester component of the copolymer of the invention ordinarily consists of one or more esters having the formula wherein n is an integer from 0 to 1 and R is an alkyl radical containing about 4 to 20 carbon atoms. Best results are obtained when R is a straight-chain primary alkyl radical. In a preferred embodiment, the acrylic ester component of the copolymer comprises at least one ester wherein R contains 4 to 8 carbon atoms and at least one ester wherein R contains 12-20 carbon atoms.
The copolymers of the invention are preferably prepared by dissolving one or more of the acrylates or methacrylates and VM in a diluent oil and copolymerizing at elevated temperatures under an oxygen-free atmosphere in the presence of a free-radical-producing compound which acts as a catalyst or initiator. Polymerization may also be induced by irradiation under the influence of high energy fields. The latter catalyzation may include the various actinic radiations, including such diverse forms of catalysis as ultraviolet, X-ray and gamma radiations, as well as radiation from radioactive materials and high energy electrons generated from linear accelerators, resonant transformers and the like.
Elevated temperatures are preferred during the course of the reaction in order to decrease the reaction time. Preferably, the temperature range is about 40 to about 90 C., but temperatures either higher or lower may be employed depending upon the catalyst.
The diluent oil is preferably a conventional low sulfurcontent oil, such as the parafi'inic hydrocarbon or ester type, which is suitable for addition to lubricating oils.
The monomers are suitably employed in such proportions that the diluent wherein they are copolymerized will contain, after polymerization, from about 15 percent to about 60 percent, and preferably about 25 percent to 40 percent of copolymer. All percentages specified herein are by weight. And while copolymerization directly in a diluent oil of the type stated is the preferred method, other methods may be employed, as for example, polymerizing the monomers in the lubricating oil in which the copolymer is to be used or in an inert volatile hydrocarbon diluent such as hexane or toluene. However, alternate methods such as these are generally less desirable. For example, when a volatile solvent is employed in place of a diluent oil, it must be removed, e.g., by distillation, after the polymerization, and replaced with oil.
When the polymerization is brought about in a diluent oil, the oil containing the copolymer may be considered as a concentrate containing the copolymer in the aforesaid amount. The concentrate suitably is incorporated into a lubricating oil to the extent that the copolymer will be in an amount in the range of from about 0.1 percent to about 20 percent and preferably from 3 percent to 8 percent of the lubricating oil.
The following examples illustrate the practice of the present invention.
Example 1 Into a reaction vessel equipped with a means for stirring, purging, and temperature control were placed 200 m1. of white mineral oil (180 SUSSaybolt Universal second), 50 ml. of hexyl methacrylate, 60 ml. of lauryl methacrylate, 60 ml. of stearyl methacrylate, 30 ml. of VM and 1 gram of lauryl peroxide. The mixture was maintained at a temperature in the range of from 60 to 80 C. for 18 hours while under a nitrogen atmosphere. At the end of 18 hours, a concentrate of 50 percent copolymer in white mineral oil was obtained.
Example 2 Into a reaction vessel equipped with a means for stirring, purging, and temperature control were placed 20.8 pounds of 180 SUS white mineral oil, 2.12 pounds of VM, 3.54 pounds of hexyl methacrylate, 5.1 pounds of lauryl methacrylate, 3.4 pounds of stearyl methacrylate, and 95 g. of lauryl peroxide. The mixture was maintained at a temperature of 63 C. for 15 hours while under a nitrogen atmosphere. At the end of 15 hours a concentrate of 40 percent copolymer in white mineral oil was obtained.
This composition was blended and tested in an engine according to the Co-ordinating Research Council (C.R.C.) FL-2 technique. The blend was made by mixing 1.5
.pounds of the above concentrate with 30 pounds of 150 SUS solvent-refined neutral petroleum oil. This produced a petroleum oil containing 2 percent of copolymer. In addition, 0.8 percent of zinc dialkyl dithiophosphate was added as an oxidation inhibitor. The blend had the following properties and give the following results:
As shown by the above results, the lubricant containing 2 percent copolymer exhibited excellent improvement with regard to dispersant and detergent properties, VI, pour point, and prolonged resistance to sludge and varnish formation. The sludge dispersant characteristic is especially noticeable due to the total sludge rating of 68.4 out of a possible and the varnish rating of 15.0 out of a possible 20. The combined sludge and varnish rating of 83.4 is very high.
Example 3 Into a reaction vessel equipped with a means for stirring, purging, and temperature control were placed 210 g. of white mineral oil, 9 g. of VM, 27 g. of hexyl methacrylate, 33 g. of lauryl methacrylate, 21 g. of stearyl methacrylate, and 1 g. of lauryl peroxide. The mixture was maintained at a temperature of 65 C. for l8 hours while under a nitrogen atmosphere. At the end of 18 hours a concentrate of 30 percent copolymer in white mineral oil Was obtained.
This composition was blended and tested in an engine according to the C.R.C. FL-2 technique. The blend was prepared by mixing a suflicient amount of the 30 percent copolymer into SUS solvent refined neutral petroleum oil to produce a 2 percent mixture and in addition, /2 percent of a 50 percent oil blend of zinc diamyl dithiocarbamate, /2 percent of an octylated and styrenated diphenylamine, /2 percent of a zinc dialkyl dithiophosphate, and 0.4 percent of a calcium-organic compound containing combined sulfur, were added as oxidation inhibitors. The blend had the following properties and give the following results:
Example 4 A carbon dispersion test was performed to evaluate the copolymers with regard to their efficiency in improving lubricating oils. A paste was prepared by thoroughly blending 20 percent of carbon black into white mineral oil. For the test, 3 g. of this paste were blended with 70 ml. of kerosene containing 1.5 percent of the compound to be tested. The results are given in Table 1 and it is pointed out that the longer the dispersion stands without settling, the better is the additive. Also, in Table 1, there is a column labeled wet. Since moisture accumulates in a crankcase and is destructive with regard to the efliciency of the additive, this column shows the result obtained when 0.3 ml. of water was added to the suspension.
Example 5 A hexane-insolubles suspension test was performed to further evaluate the polymer with regard to its efliciency in improving lubricating oils. For this test, hexane-insoluble material was obtained from oil oxidized in a. Doornte type oxidation machine and these insolubles were washed with hexane, dried and dissolved in benzene in an amount sufiicient to form a solution of 2.5 g. per liter. In order to test the ability of the additives to suspend sludge, it was necessary to precipitate the oxidized oil insolubles in the presence of the additives. This was accomplished by mixing 20 m1. of the benzene solution with ml. of a kerosene solution containing 1.5 percent copolymer and heating with stirring. Removal of the benzene was effected in 30 to 40 minutes. Vials of this suspension were then observed and the results obtained are shown in Table 2.
TAB LE 2 Product Observation (1) 1.5 percent of eopolymer of Example 1. Clear solution; no sediment. (2) 1.5 percent of barium sulfonate Cloudy solution; sediment.
percent of calcium sullonate Do.
percent 01 a copolymer like No. 5 Heavy sediment.
I claim:
1. An oil-soluble copolymer prepared by polymerizing a mixture of N-vinyl-S-morpholinone and at least one acrylic ester having the formula 6 3. An oil-soluble copolymer prepared by polymerizing a mixture consisting essentially of about 3 to 30 percent of Nvinyl-3-morpholinone and 70-97 percent of a mixture of at least two acrylic esters having the formula wherein n is an integer from 0 to l and R is an alkyl radical containing 4 to 20 carbon atoms, at least one of said esters containing 12 to 20 carbon atoms in the alkyl radical and constituting at least 50 percent of said copolymer, at least one other said ester containing 4 to 8 carbon atoms in the alkyl radical.
4. An oil-soluble copolymer prepared by polymerizing a mixture consisting essentially of about 10 to 20 percent of N-vinyl-3-morpholinone, 20 to 30 percent of n-hexyl methacrylate, 20 to 50 percent of lauryl methacrylate and 20 to percent of stearyl methacrylate.
References Cited UNITED STATES PATENTS 2,987,509 6/ 1961 Burgert 260-88.3 3,163,605 12/1964 Koch ct a1. 252-515 JOSEPH L. SCHOFER, Primary Examiner.
S. M. LEVIN, Assistant Examiner.
US. Cl. X.R.
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US478510A US3418296A (en) | 1961-10-25 | 1965-07-01 | Copolymer concentrate and oil composition |
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US14748961 US3210282A (en) | 1961-10-25 | 1961-10-25 | Copolymer concentrate and oil composition |
US478510A US3418296A (en) | 1961-10-25 | 1965-07-01 | Copolymer concentrate and oil composition |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3892671A (en) * | 1972-08-25 | 1975-07-01 | Exxon Research Engineering Co | Lubricant containing dispersant-pour depressant polymer |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2987509A (en) * | 1957-10-28 | 1961-06-06 | Dow Chemical Co | Nu-vinyl-3-morpholinone compounds |
US3163605A (en) * | 1959-08-12 | 1964-12-29 | Roehm & Haas Gmbh | Lubricating oil additives |
-
1965
- 1965-07-01 US US478510A patent/US3418296A/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2987509A (en) * | 1957-10-28 | 1961-06-06 | Dow Chemical Co | Nu-vinyl-3-morpholinone compounds |
US3163605A (en) * | 1959-08-12 | 1964-12-29 | Roehm & Haas Gmbh | Lubricating oil additives |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3892671A (en) * | 1972-08-25 | 1975-07-01 | Exxon Research Engineering Co | Lubricant containing dispersant-pour depressant polymer |
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