US2330773A - Lubricant - Google Patents
Lubricant Download PDFInfo
- Publication number
- US2330773A US2330773A US410590A US41059041A US2330773A US 2330773 A US2330773 A US 2330773A US 410590 A US410590 A US 410590A US 41059041 A US41059041 A US 41059041A US 2330773 A US2330773 A US 2330773A
- Authority
- US
- United States
- Prior art keywords
- steam
- oil
- lubricant
- tallow
- viscosity
- 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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- 239000000314 lubricant Substances 0.000 title description 27
- 229920000642 polymer Polymers 0.000 description 16
- 239000003921 oil Substances 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000003760 tallow Substances 0.000 description 11
- 239000000839 emulsion Substances 0.000 description 10
- 239000000203 mixture Substances 0.000 description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 239000002480 mineral oil Substances 0.000 description 7
- 235000010446 mineral oil Nutrition 0.000 description 7
- 239000001301 oxygen Substances 0.000 description 7
- 229910052760 oxygen Inorganic materials 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- -1 degras Substances 0.000 description 4
- 239000010688 mineral lubricating oil Substances 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 238000013329 compounding Methods 0.000 description 3
- 239000010727 cylinder oil Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000010685 fatty oil Substances 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 125000005397 methacrylic acid ester group Chemical group 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- QJJDJWUCRAPCOL-UHFFFAOYSA-N 1-ethenoxyoctadecane Chemical compound CCCCCCCCCCCCCCCCCCOC=C QJJDJWUCRAPCOL-UHFFFAOYSA-N 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 125000005396 acrylic acid ester group Chemical group 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 150000001733 carboxylic acid esters Chemical group 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229940052303 ethers for general anesthesia Drugs 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- ZNAOFAIBVOMLPV-UHFFFAOYSA-N hexadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)C(C)=C ZNAOFAIBVOMLPV-UHFFFAOYSA-N 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000001183 hydrocarbyl group Chemical group 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 239000010699 lard oil Substances 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000000346 nonvolatile oil Substances 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 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
- C10M165/00—Lubricating compositions characterised by the additive being a mixture of a macromolecular compound and a compound of unknown or incompletely defined constitution, each of these compounds being essential
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
-
- 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
- C10M2207/40—Fatty vegetable or animal oils
-
- 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
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/404—Fatty vegetable or animal oils obtained from genetically modified species
-
- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/04—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an alcohol or ester thereof; bound to an aldehyde, ketonic, ether, ketal or acetal radical
-
- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/06—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an acyloxy radical of saturated carboxylic or carbonic acid
-
- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/06—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to an acyloxy radical of saturated carboxylic or carbonic acid
- C10M2209/062—Vinyl esters of saturated carboxylic or carbonic acids, e.g. vinyl acetate
-
- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
-
- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/02—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/08—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing monomers having an unsaturated radical bound to a carboxyl radical, e.g. acrylate type
- C10M2209/084—Acrylate; Methacrylate
-
- 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
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
-
- 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
- C10N2040/135—Steam engines or turbines
Definitions
- This invention relates to improved steam cylinder lubricants and methods of preparing same.
- fatty oils and other fatty materials generally not only facilitates emulsification of the lubricant with condensed steam, but also appears to favor formation of emulsions from which the water separates only with great difiiculty and upon long standing.
- One object of the present invention is to provide a lubricant which has great resistance to the washing-oil action of wet steam, in other words, not only a lubricant which has good adhesivity, but has especially good adhesivity under wet steam conditions, so that with the use of this lubricant there will be less scoring of the cylinder walls and less wearing of the moving parts.
- object of this invention i to provide a lubricant which not only has the above-mentioned good lubricating qualities but also shows rapid settling out in the steam emulsion test.
- a third object is to provide a lubricant having the abovedescribed desirable characteristics by the use of a compounding agent which. when subjected to the high temperature frequently used in operating conditions, will decompose without leaving any charred or gummy or other undesirable residue.
- the invention comprises adding to a suitable mineral oil base stock, such as will be described later. a small amount of a. high molecular weight, oxygen-containing polymer which is depolymerizable at high temperature without charring. Small amounts of fatty materials may be. and preferably are, also presentv
- the mineral oil to be used as the base stock is a cylinder oil which may be derived from any of the commonly available crude oils, such as the paraflinic crudes (typified by Pennsylvania crude), naphthenic base crudes. e. g. from California, and mixed base crudes, such as a Mid Continent oil.
- the cylinder oil may be a steamreduced fraction, as from a, Pennsylvania crude,
- the oil is preferably a filtered oil of high quality, and should have a high flash point, low carbon content, good resistance to the development of acidity, and a satisfactorily low pour point.
- the flash point should be at least as high as 500 F. and may range from there on up to 625 R, or higher.
- the viscosity of this mineral oil base stock should be between the approximate limits of 100 and 250 seconds Saybolt at 210 F., with a viscosity index between the approximate limits of 70 and 100.
- the oxygen-containing polymer which is to be incorporated in the above-described base stock. should be of a high molecular weight, e. g., at least 1,000 and may be 50,000, 100,000, or even considerably higher, although it must not be so high in molecular weight as to be insoluble in the mineral oil base stocks referred to.
- these polymers are obtained by polymerizing unsaturated monomeric chemical compounds, such as, esters, eth ers, acids, etc.
- a particularly preferred class of polymers are those produced from esters of acrylic acid and alkyl derivatives thereof, such as methacrylic acid containing a methyl substituent in the alpha position, or other higher alkvl groups. such as, ethyl.
- esters should be derived from monohydric alcohol preferably containing more than 4 carbon atoms, such as amyl, hexyl. hcptyl. octyl, lauryl, cetyl, octadecyl. etc.
- polymers of other vinyl compounds may be used, such as. a stearic acid vinyl ester having a molecular weight of about 5.000. a polymerized vinyl octadecyl ether or polymerized vinyl butyl eth r having a molecular weight of about 3.000 to 10,000 or higher.
- the proportions of ingredients to be used in preparing the steam cylinder lubricants or this invention may, of course, be varied over a very wide range depending upon the particular ingredients used and the operating conditions under which the lubricant is intended to be used, but ordinarily the amount of oxygen-containing polymer should be between the limits of about 0.1 and 2.0%, preferably about 054.0%, and the fatty material, it used. should be about l%. preierably about 23-10% in concentration.
- the steam cylinder lubricant of this invention has good adhesivity to the cylinder walls, valve stems, and other metal parts of the steam cylinder engine and this is especially advantageous under wet steam conditions. It has a high viscosity index (i. e., it shows a relatively low change in viscosity for any particular change in temperature). It results in a relatively lower consumption of lubricant than many lubricants used heretofore.
- the product requires smaller amounts of fatty oil compounding agent than similar products free from such oxygencontalning polymer.
- the steam cylinder lubricant of this invention also has a relatively low steam emulsion number, by which is meant that it permits ready separation of water from the emulsion for re-use in steam boilers or for other purposes and permits re-use of the lubricant.
- the oxygen-containing polymer used is relatively stable at elevated temperatures, and even when exposed to temperatures high enough to cause decomposition, it merely depolymerizes without the formation of any charred or other undesirable residue.
- Acryloid 100 which is the trade name of a product understood to be a polymerized methacrylic acid ester having the general formula capo-coon in which is an aliphatic hydrocarbon group derived from an alcohol having at least 8 carbon atoms and probably 12 or even 16 carbon atoms,
- composition of this invention namely, the composition containing the mineral. oil. acidless tallow, and the acrylate polymer separated completely from the water in the emulsion test in 15 minutes; whereas, a composition identical except lacking the acrylate polymer. and a composition identical except containing a high molecular polyisobutylene, instead of the aorylate polymer, both had only shown a separation of 1'7 cc. of water in 20 minutes.
- a steam cylinder lubricant comprising a major proportion of mineral lubricating oil hav ing a flash point at least as high as 500 F.
- a steam cylinder lubricant comprising at least 80% by weight of a mineral lubricating oil base stock having a flash point of at least 500' F. and a viscosity of 100-250 seconds Saybolt at 210 F., about 0.1 to 2.0% of an oxygen-containing polymer having a molecular weight of at least 1,000, depolymerizable at elevated temperatures without producing charred or other undesirable residue, and about 1-15% by weight of acidless tallow.
- a steam cylinder lubricant comprising a major proportion of mineral lubricating oil having a flash point at least as high as 500 F. and a viscosity of about 100-250 secondsSaybolt at 210" F., about 0.1% to 2.0% of a polymerized acrylic acid ester of a monohydric alcohol containing more than 4 carbon atoms and about 1% to 15% of tallow.
- Lubricant according to claim 5 in which the polymer is a polymerized methacrylic acid ester of a saturated monohydric alcohol having about 5 to 18 carbon atoms.
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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)
Description
a l l Patented Sept. 28, 1943 LUBRICANT John C. Zimmer, Union, and Arnold J. Morway, Clark Township, Union County, N. J., asslgnors to Standard Oil Development Company, a corporation of Delaware No Drawing. Application September 12, 1941 Serial No. 410,590
7 Claims.
This invention relates to improved steam cylinder lubricants and methods of preparing same.
It is well known to those familiar with the compounding of steam cylinder oils and steam plant engineers that the presence of moisture in steam will result in a film of straight mineral oil being rapidly washed 011 from steam engine cylinder walls and other surfaces where steam contacts them. Therefore, to secure proper lubrication under wet steam conditions, such oils have often been compounded with a fatty oil, such as lard oil, degras, or tallow; this helps to prevent lubricant wash-0n", but it does not prevent it completely. Furthermore, the presence of fatty oils and other fatty materials generally not only facilitates emulsification of the lubricant with condensed steam, but also appears to favor formation of emulsions from which the water separates only with great difiiculty and upon long standing.
One object of the present invention is to provide a lubricant which has great resistance to the washing-oil action of wet steam, in other words, not only a lubricant which has good adhesivity, but has especially good adhesivity under wet steam conditions, so that with the use of this lubricant there will be less scoring of the cylinder walls and less wearing of the moving parts. An-
other object of this invention i to provide a lubricant which not only has the above-mentioned good lubricating qualities but also shows rapid settling out in the steam emulsion test. A third object is to provide a lubricant having the abovedescribed desirable characteristics by the use of a compounding agent which. when subjected to the high temperature frequently used in operating conditions, will decompose without leaving any charred or gummy or other undesirable residue.
Broadly. the invention comprises adding to a suitable mineral oil base stock, such as will be described later. a small amount of a. high molecular weight, oxygen-containing polymer which is depolymerizable at high temperature without charring. Small amounts of fatty materials may be. and preferably are, also presentv The mineral oil to be used as the base stock is a cylinder oil which may be derived from any of the commonly available crude oils, such as the paraflinic crudes (typified by Pennsylvania crude), naphthenic base crudes. e. g. from California, and mixed base crudes, such as a Mid Continent oil. The cylinder oil may be a steamreduced fraction, as from a, Pennsylvania crude,
or may be an overhead stock, for example, as produced by distillation under vacuum. The oil is preferably a filtered oil of high quality, and should have a high flash point, low carbon content, good resistance to the development of acidity, and a satisfactorily low pour point. The flash point should be at least as high as 500 F. and may range from there on up to 625 R, or higher. The viscosity of this mineral oil base stock should be between the approximate limits of 100 and 250 seconds Saybolt at 210 F., with a viscosity index between the approximate limits of 70 and 100.
The oxygen-containing polymer which is to be incorporated in the above-described base stock. according to this invention, should be of a high molecular weight, e. g., at least 1,000 and may be 50,000, 100,000, or even considerably higher, although it must not be so high in molecular weight as to be insoluble in the mineral oil base stocks referred to. In general, these polymers are obtained by polymerizing unsaturated monomeric chemical compounds, such as, esters, eth ers, acids, etc. A particularly preferred class of polymers are those produced from esters of acrylic acid and alkyl derivatives thereof, such as methacrylic acid containing a methyl substituent in the alpha position, or other higher alkvl groups. such as, ethyl. propyl, etc., in a similar position: these esters should be derived from monohydric alcohol preferably containing more than 4 carbon atoms, such as amyl, hexyl. hcptyl. octyl, lauryl, cetyl, octadecyl. etc. Such acrylic compounds contain the group CH2==C, and have attached to this latter carbon atom a carboxylic ester group and either a hydrogen or a hydrocarbon group, such as. an alkyl or aryl group.
Although the above polymerized acrylic compounds are preferred, polymers of other vinyl compounds may be used, such as. a stearic acid vinyl ester having a molecular weight of about 5.000. a polymerized vinyl octadecyl ether or polymerized vinyl butyl eth r having a molecular weight of about 3.000 to 10,000 or higher.
In preparing the steam cylinder lubricant of this invention, there is also added some fatty material or so-called "fixed oil," such as tailow, preferablv acidless tallow, or other animal glyceride of the tallow type. Acidless tallow is especially preferred because it gives much better results in combination with the high flash mineral '01] base stock and the oxygen-containing polymer of this invention, than do other fatt mat rials in similar combinations.
The proportions of ingredients to be used in preparing the steam cylinder lubricants or this invention may, of course, be varied over a very wide range depending upon the particular ingredients used and the operating conditions under which the lubricant is intended to be used, but ordinarily the amount of oxygen-containing polymer should be between the limits of about 0.1 and 2.0%, preferably about 054.0%, and the fatty material, it used. should be about l%. preierably about 23-10% in concentration.
The steam cylinder lubricant of this invention has good adhesivity to the cylinder walls, valve stems, and other metal parts of the steam cylinder engine and this is especially advantageous under wet steam conditions. It has a high viscosity index (i. e., it shows a relatively low change in viscosity for any particular change in temperature). It results in a relatively lower consumption of lubricant than many lubricants used heretofore. By reason of the properties of the oxygemcontaining polymer, the product requires smaller amounts of fatty oil compounding agent than similar products free from such oxygencontalning polymer. (In view of the tendency of fatty materials to decompose at high temperature with the production of charred or gummy materials which cause unsatisfactory service, it is desirable to use only the minimum amount of fatty material necessaryl. The steam cylinder lubricant of this invention also has a relatively low steam emulsion number, by which is meant that it permits ready separation of water from the emulsion for re-use in steam boilers or for other purposes and permits re-use of the lubricant. Another important feature of this invention is that the oxygen-containing polymer used is relatively stable at elevated temperatures, and even when exposed to temperatures high enough to cause decomposition, it merely depolymerizes without the formation of any charred or other undesirable residue.
Inspection of the finished steam cylinder lubricant of this invention should show approximately the following characteristics:
The objects and advantages of the invention will be better understood from a consideration oi the following specific examples.
Exmts l 1% of "Acryloid 100," which is the trade name of a product understood to be a polymerized methacrylic acid ester having the general formula capo-coon in which is an aliphatic hydrocarbon group derived from an alcohol having at least 8 carbon atoms and probably 12 or even 16 carbon atoms,
such as a polymerization product of lauryl methacrylate or cetyl methacrylate, dissolved in a concentration of to in light hydrocarbon mineral oil, was dissolved along with 1.5% by weight of acidless taliow in a mineral oil base a stock prepared from a Mid-Continent crude and having the following physical properties.
This composition made a very satlsfactoryl steam cylinder lubricant having the following characteristics:
Gravity, A.P. I 25.2 Viscosity at 100 F. Saybolt sec 2103 Viscosity at 210 F. Saybolt sec 148 Viscosity index 103 Pour, F 20 Flash, "F 505 Fire 580 EXAMPLE 2 Steam emulsion test No. oi cc. water settling out in 20 minutes Blends 7.5% ncidless tailow 91.5% oi A 1.0% poiyisobutylene (about 91.5% oil A All water out in 15 minutes. l.0% acryloid 1 Steam passed into 20 cc. of compounded oil [or 4 to 6 min. or until double oil volume (emulsion). Then the emulsified all set at 200 F. {or 20 minutes.
It is noted from this series of tests that the composition of this invention, namely, the composition containing the mineral. oil. acidless tallow, and the acrylate polymer separated completely from the water in the emulsion test in 15 minutes; whereas, a composition identical except lacking the acrylate polymer. and a composition identical except containing a high molecular polyisobutylene, instead of the aorylate polymer, both had only shown a separation of 1'7 cc. of water in 20 minutes. 1
Exam 3 Steam emulsion test No. of co. water settling out in Blends 20 minutes 7.60% acldless tallow 01.50% oil A All water out in 12 minute". 0 15 lauryl methaerylate l 7. ass to ow. 91. 1 oil A All water out in 15 minutes. 0.35 cetyl methacrylato" 7. tallow 01.50 17 oil A 0.35 oopolymer oi eth l metha- All water out in 10 minutes.
crylate and noc ocylnlpba motbau'ylate.
If desired, various other addition agents'known to the art may also be added to the steam cylin' der lubricants described above: for instance. small amounts of anti-oxidants and dyes.
It is not intended that this invention be limited to the specific examples which have been recited as illustrative of the invention, but. only by the appended claims in which it is intended to claim all novelty inherent in the invention. A
We claim: v 1. A steam cylinder lubricant comprising a major proportion of mineral lubricating oil hav ing a flash point at least as high as 500 F. and
' a viscosity 01 about 100 to 250 seconds Saybolt hesivity to the cylinder walls, valve stems, and
other contacted parts of the steam engine, and having the property of separating rapidly from water in the steam emulsion text, comprising at least 80% of mineral lubircating oil having a flash point of at least 500 F. at a viscosity of about 100-250 seconds Saybolt at 210 F., about 05-10% of polymerized methacrylate ester and about 5 to of acldless tallow.
3. A steam cylinder lubricant comprising at least 80% by weight of a mineral lubricating oil base stock having a flash point of at least 500' F. and a viscosity of 100-250 seconds Saybolt at 210 F., about 0.1 to 2.0% of an oxygen-containing polymer having a molecular weight of at least 1,000, depolymerizable at elevated temperatures without producing charred or other undesirable residue, and about 1-15% by weight of acidless tallow.
4. The process of preparing steam cylinder lubricants which comprises dissolving in a major proportion 01' mineral lubricating oil base stock having a flash point at least as high as 500 F. and a viscosity of about -250 seconds Saybolt at 210 F., about 1-15% by weight of tallow, and at least 0.1% of oxygen-containing polymer having a molecular weight of at least 1,000, depolymerizable at elevated temperatures without leaving charred or other undesirable residue. the amount ofsaid polymer being sufilcient to impart the desired adhesivity to the resulting com-- position and to cause the composition to settle out from water suillcientl rapidly in the steam emulsion test.
5. A steam cylinder lubricant comprising a major proportion of mineral lubricating oil having a flash point at least as high as 500 F. and a viscosity of about 100-250 secondsSaybolt at 210" F., about 0.1% to 2.0% of a polymerized acrylic acid ester of a monohydric alcohol containing more than 4 carbon atoms and about 1% to 15% of tallow.
6. Lubricant according to claim 5 in which the polymer is a polymerized methacrylic acid ester of a saturated monohydric alcohol having about 5 to 18 carbon atoms.
7. Steam cylinder lubricant according to claim 2 in which the polymer is polymerized octal methacrylate.
JOHN C. ZHVJMER. ARNOLD J. MORWAY.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US410590A US2330773A (en) | 1941-09-12 | 1941-09-12 | Lubricant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US410590A US2330773A (en) | 1941-09-12 | 1941-09-12 | Lubricant |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2330773A true US2330773A (en) | 1943-09-28 |
Family
ID=23625385
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US410590A Expired - Lifetime US2330773A (en) | 1941-09-12 | 1941-09-12 | Lubricant |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2330773A (en) |
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2426852A (en) * | 1943-09-15 | 1947-09-02 | Jasco Inc | High temperature lubricant |
| US2435619A (en) * | 1944-01-15 | 1948-02-10 | Standard Oil Dev Co | Lubricant compositions |
| US2441023A (en) * | 1945-01-26 | 1948-05-04 | Shell Dev | Lubricating oil compositions containing polymerized allyl esters of carboxylic acids |
| US2516914A (en) * | 1947-03-21 | 1950-08-01 | Tide Water Associated Oil Comp | Emulsification-inhibited polyacrylate-containing oil compositions |
| US2524563A (en) * | 1946-10-08 | 1950-10-03 | Shell Dev | Lubricant |
| US2706717A (en) * | 1950-08-09 | 1955-04-19 | Basf Ag | Vinyl ether containing hydraulic fluids |
| US2751039A (en) * | 1952-12-23 | 1956-06-19 | California Research Corp | Filters coated with thickened oils |
| US3166508A (en) * | 1963-01-16 | 1965-01-19 | Monsanto Co | Hydrocarbon oils of reduced foaming properties |
| US3265768A (en) * | 1962-11-19 | 1966-08-09 | Monsanto Co | Copolymer mixtures of tetrahydrofurfuryl methacrylate |
| US3496103A (en) * | 1967-05-25 | 1970-02-17 | Us Army | Friction reduction by poly(n-alkyl methacrylates) in solution and dry films |
| US5298177A (en) * | 1991-08-09 | 1994-03-29 | The Lubrizol Corporation | Functional fluid with triglycerides, detergent-inhibitor additives and viscosity modifying additives |
-
1941
- 1941-09-12 US US410590A patent/US2330773A/en not_active Expired - Lifetime
Cited By (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2426852A (en) * | 1943-09-15 | 1947-09-02 | Jasco Inc | High temperature lubricant |
| US2435619A (en) * | 1944-01-15 | 1948-02-10 | Standard Oil Dev Co | Lubricant compositions |
| US2441023A (en) * | 1945-01-26 | 1948-05-04 | Shell Dev | Lubricating oil compositions containing polymerized allyl esters of carboxylic acids |
| US2524563A (en) * | 1946-10-08 | 1950-10-03 | Shell Dev | Lubricant |
| US2516914A (en) * | 1947-03-21 | 1950-08-01 | Tide Water Associated Oil Comp | Emulsification-inhibited polyacrylate-containing oil compositions |
| US2706717A (en) * | 1950-08-09 | 1955-04-19 | Basf Ag | Vinyl ether containing hydraulic fluids |
| US2751039A (en) * | 1952-12-23 | 1956-06-19 | California Research Corp | Filters coated with thickened oils |
| US3265768A (en) * | 1962-11-19 | 1966-08-09 | Monsanto Co | Copolymer mixtures of tetrahydrofurfuryl methacrylate |
| US3166508A (en) * | 1963-01-16 | 1965-01-19 | Monsanto Co | Hydrocarbon oils of reduced foaming properties |
| US3496103A (en) * | 1967-05-25 | 1970-02-17 | Us Army | Friction reduction by poly(n-alkyl methacrylates) in solution and dry films |
| US5298177A (en) * | 1991-08-09 | 1994-03-29 | The Lubrizol Corporation | Functional fluid with triglycerides, detergent-inhibitor additives and viscosity modifying additives |
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