US2816869A - Semi-fluid lubricant - Google Patents
Semi-fluid lubricant Download PDFInfo
- Publication number
- US2816869A US2816869A US587966A US58796656A US2816869A US 2816869 A US2816869 A US 2816869A US 587966 A US587966 A US 587966A US 58796656 A US58796656 A US 58796656A US 2816869 A US2816869 A US 2816869A
- Authority
- US
- United States
- Prior art keywords
- oil
- hydrogenated rosin
- polymerized ethylene
- percent
- 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
Links
- 239000000314 lubricant Substances 0.000 title description 26
- 239000012530 fluid Substances 0.000 title description 6
- 239000000203 mixture Substances 0.000 claims description 52
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 36
- 239000005977 Ethylene Substances 0.000 claims description 35
- 230000001050 lubricating effect Effects 0.000 claims description 12
- 230000009974 thixotropic effect Effects 0.000 claims description 10
- 239000004215 Carbon black (E152) Substances 0.000 claims description 7
- 229930195733 hydrocarbon Natural products 0.000 claims description 7
- 150000002430 hydrocarbons Chemical class 0.000 claims description 7
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 42
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 38
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 38
- 239000003921 oil Substances 0.000 description 34
- 238000003756 stirring Methods 0.000 description 14
- 239000002184 metal Substances 0.000 description 11
- 238000001816 cooling Methods 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000003112 inhibitor Substances 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- BTXXTMOWISPQSJ-UHFFFAOYSA-N 4,4,4-trifluorobutan-2-one Chemical compound CC(=O)CC(F)(F)F BTXXTMOWISPQSJ-UHFFFAOYSA-N 0.000 description 4
- BQACOLQNOUYJCE-FYZZASKESA-N Abietic acid Natural products CC(C)C1=CC2=CC[C@]3(C)[C@](C)(CCC[C@@]3(C)C(=O)O)[C@H]2CC1 BQACOLQNOUYJCE-FYZZASKESA-N 0.000 description 4
- -1 Polyethylenes Polymers 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 230000000996 additive effect Effects 0.000 description 4
- 238000013329 compounding Methods 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- 239000003963 antioxidant agent Substances 0.000 description 3
- 230000003078 antioxidant effect Effects 0.000 description 3
- 235000006708 antioxidants Nutrition 0.000 description 3
- 238000005260 corrosion Methods 0.000 description 3
- 230000007797 corrosion Effects 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000007689 inspection Methods 0.000 description 3
- 238000005461 lubrication Methods 0.000 description 3
- 230000000717 retained effect Effects 0.000 description 3
- 239000004753 textile Substances 0.000 description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 239000002199 base oil Substances 0.000 description 2
- 125000005266 diarylamine group Chemical group 0.000 description 2
- GVPWHKZIJBODOX-UHFFFAOYSA-N dibenzyl disulfide Chemical compound C=1C=CC=CC=1CSSCC1=CC=CC=C1 GVPWHKZIJBODOX-UHFFFAOYSA-N 0.000 description 2
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000001590 oxidative effect Effects 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000002035 prolonged effect Effects 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- PFEFOYRSMXVNEL-UHFFFAOYSA-N 2,4,6-tritert-butylphenol Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 PFEFOYRSMXVNEL-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical compound C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 1
- KEQFTVQCIQJIQW-UHFFFAOYSA-N N-Phenyl-2-naphthylamine Chemical compound C=1C=C2C=CC=CC2=CC=1NC1=CC=CC=C1 KEQFTVQCIQJIQW-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 241000779819 Syncarpia glomulifera Species 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000013556 antirust agent Substances 0.000 description 1
- 239000010951 brass Substances 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 210000005053 lamin Anatomy 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 239000010688 mineral lubricating oil Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 210000003739 neck Anatomy 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 239000001739 pinus spp. Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 238000009987 spinning Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 150000003505 terpenes Chemical class 0.000 description 1
- 235000007586 terpenes Nutrition 0.000 description 1
- 229940036248 turpentine Drugs 0.000 description 1
- 239000002759 woven fabric Substances 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
- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/022—Ethene
-
- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/14—Synthetic waxes, e.g. polythene waxes
-
- 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
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/18—Natural waxes, e.g. ceresin, ozocerite, bees wax, carnauba; Degras
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/20—Rosin acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
- 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
- C10M2215/065—Phenyl-Naphthyl 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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/02—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
- C10M2219/022—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of hydrocarbons, e.g. olefines
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/083—Dibenzyl sulfide
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/086—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing sulfur atoms bound to carbon atoms of six-membered aromatic rings
-
- 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
-
- 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
- C10M2223/041—Triaryl phosphates
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/042—Metal salts thereof
-
- 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
- C10N2040/46—Textile oils
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2070/00—Specific manufacturing methods for lubricant compositions
- C10N2070/02—Concentrating of additives
Definitions
- This invention relates toan improved semi-fluid: lubricant and more particularly to a thixotropic lubricating;
- composition having high adhesive properties in the liquid: state is characterized by
- oils are entirely satisfactory lubricants.
- the lubricant be of such consistency, that it will remain between the working surfaces and not be lost by dripping, leakage or centrifugal force.
- the lubricant be of relatively low viscosity under operating conditions so as to neither; impede the-operation of the mechanism nor increase the power consumption.
- lubricant whichwill stay on the bearing surface is important not only: from. the standpoint of the life of the hearing, but also from the standpoint of the product of the mill. Obviously, lubrication failure of the bearing will result in costlyshuedown of the machinery. Also, leakage of. lubricant onto the productof the mill, whether thread. or Woven fabric, will result in undesirable staining-of the fabric;
- liquid oils can be dispensed from oilcans and aregenerally satisfactory'lubricants, as a general rule they do not have good metal adhesion properties. Greases. have good metal adhesion, properties but are undesirable in that they can notbeappliediby-wick feed or by ordinary oil cans.
- The. soap-thickened lubricants have also. been undesirable in that lubricants having identical properties1 are difiicult to reproduce.
- composition whichwill be sufficiently fluid to apply from anordinary squirt-type oil can and will remainfluid while the bearings on which it is placed are in operationbutwill form a light gel when the bearings are. not inoperation.
- inthe'liquid state can be preparedfrom a high viscosity hydrocarbon. oilbyv compounding therewith smallamountsof each of polymerized ethylene and a hydrogenated rosin, The
- the hydrocarbonv oil employed in the preparation of the thixotropic composition according to this invention can be. either a refined or semi-refined parafiinic-, naph-- thenic-,. or asphalt-base oil, or the oil can be a synthetic oil having a viscosity above about 400 SUS at 100 F. and preferably having a viscosity. of about 400 to. 4000-SUS at 100 F. If desired, ablend of oils of suitable viscosity can be employed instead of a single .oil, by means of which any desiredviscosity within the range of 400to 4000. .SUS. at- 100 F. canbe secured;
- The. amount: of oil employed constitutes from about r0 99 percent by weight of the. total composition. Naturally, the optimum amount: of oil employed in any given instance will. depend, upon the particular oil. employed as well as upon. the characteristics desired in the final composition.
- the polymerized ethylene is a polymerization product of ethylene having a molecularyweight of about 1000 to 40,000 or. more. Polyethylenes'havinga molecular weight within this range, i. e., 19,000, are characterized by. the following approximate characteristics:
- Theamount of polymerized ethylene employed constitutes about 0.2 to about. 5 percent by weight of the total. composition.
- the hydrogenated rosin employed according to the invention is a rosin of at least about 40 percent saturation to and including fully hydrogenated rosin. Rosin, sometimes called colophony, is the residue obtained on distilling turpentine from hard pine resin. Abietic acid, C H O is the chief constituent of rosin and is obtained from. the latter by distillation. Abietic acid is a carboxylic acid containing two double bonds. Hydrogenated rosin is obtained by the addition of hydrogen to the double bonds of abietic acid. The amount of hydrogen added may, be sufficient to saturate the two unsaturated. bonds of abietic acid or it may be any amount to produce substantial partial hydrogenation.
- a particularly useful hydrogenated rosin for the purposes of my, invention is one which has been hydrogenated to about 50 to about 60 percent of capacity and has a melting point of about 168 F.
- the quantity of the hydrogenated rosin employed constitutes from about 0.2 to about 5 percent by weight of the total composition.
- improved, metal adhesion characteristics are obtained when the weight ratio of the hydrogenated rosinto the polymerizedethylene is between. about 1:3 and about 3:1.
- the mixtureof. hydrogenated rosin and polymerized ethylene is added in an amount sufficient to increase the viscosity of the hydrocarbon, oil and to impart thixotropic characteristics thereto.
- Corrosion. inhibitors are particularly desirable in: com: positions used in corrodible alloy, bearings.
- the corrosion inhibitors suitable for. the purpose of the invention are dibenzyl disulfide, alkyl phenyl sulfides,
- the method of forming the polymers is alkyl phosphites, alkaryl phosphites and sulfurized terpenes.
- an oxidation inhibitor such as an alkali insoluble phenol, i. e., 2,6-di-tertiary-butyl-4-methylphenol; 2,4,6-tri-tertiary-butylphenol; etc., and/or a small amount of a diaryl amine.
- diaryl amines which can be used in the composition of the invention may be mentioned diphenylamine, phenyl alpha naphthylamine, phenyl beta naphthylamine, alpha alpha-, alpha beta-, and beta beta-, dinaphth lamines, and the like.
- the amount of the conventional additive agents employed will depend to a large extent upon the conditions to which the composition is subjected, as well as upon the particular additive used. For instance, when the composition is subjected to prolonged use under oxidizing conditions, such as under extreme pressure and temperature, the oxidation inhibitor and extreme pressure agent requirements will be much greater than when relatively mild operating conditions are encountered.
- the amount of the anti-oxidant employed is between about 0.1 and 1.5 percent by weight based upon the weight of the total composition. In any event, the amount of additive employed is sufficient to accomplish the purpose for which it is intended without deleteriously affecting the other desirable characteristics of the composition.
- the hydrogenated rosin is placed in a vessel and then heated until it is liquid. The temperature thus attained is about 200 F.
- the polymerized ethylene is then added with stirring to the melted hydrogenated rosin while continuing to heat to 450 F.
- the mixture is then held at 450 F. for a time sufficient to effect a uniform dispersion. The time required depends upon the size of the batch as well as the efficiency of the dispersing means.
- An oil concentrate of the hydrogenated rosin-polymerized ethylene dispersion is then prepared by adding an amount of oil equivalent to the combined weight of the hydrogenated rosin and polymerized ethylene.
- the metal adhesion test employed in comparing the lubricating compositions is that test ordinarily employed in determining the adhering characteristics of a grease.
- a polished brass or steel disc with a concave surface is mounted on a vertical motor shaft so that the plane of the disc is in a horizontal position.
- the disc is tared.
- One tenth gram of lubricant is placed on the disc.
- the disc plus the lubricant is then reweighed.
- the disc is then attached to. the motor shaft.
- the entire disc is encased in a closed chamber the temperature of which is thermostatically controlled.
- the motor is then run for a period of seven minutes at a selected speed of 200 to 1000 R. P. M. at a selected temperature of to 200 F.
- the disc plus lubricant is reweighed and the lubricant remaining on the disc is calculated as percent lubricant retention.
- a lubricating oil having a viscosity of about 750 SUS at 100 F. was prepared by mixing 68 parts by volume of a Texas oil having a viscosity of about 500 SUS at 100 F. with 32 parts by volume of a Texas oil having a viscosity of about 1900 SUS at 100 F.
- Various amounts of polymerized ethylene and hydrogenated rosin were employed as shown.
- the polymerized ethylene was a solid having a molecular weight of about 19,000.
- the hydrogenated rosin employed was a solid having a melting point of about 168 F.
- the double bonds of the rosin acids had been saturated to an extent of about 50 to 60 percent.
- the blending procedure employed in preparing the compositions was in accordance with the embodiment described hereinabove. In preparing these compositions the rate of cooling from 240 to 120 F. was increased by stirring. Cooling from 120 F. to room temperature was without stirring.
- compositions B, C and D containing from 1 to 2 percent by weight of a mixture of hydrogenated rosin and polymerized ethylene in a 2 to 1, respectively, weight ratio gave remarkably improved metal adhesion characteristics.
- the temperature was maintained constant while varying the speed between 200 and 1000 R. P. M.
- the speed was maintained constant while varying the temperature between 80 and F.
- the compositions of the invention were strikingly superior.
- compositions B, C and E wherein the ratio of hydrogenated rosin to polymerized ethylene is 1:3, 1:2 and 2:1, respectively, gave particularly good retention of the lubricant at temperatures of 80 to 160 F.
- compositions which contain the same proportions of hydrogenated rosin and polymerized ethylene, the only difference being the manner in which cooling is effected.
- Table 3 the compositions were prepared according to the blending procedure described hereinabove. After uniform blends were obtained, compositions A and C were cooled from 240 F. to room temperature without stirring; compositions B and D were cooled from 240 to 120 F. with stirring and then to room temperature without stirring.
- compositions having a ratio of hydrogenated rosin to polymerized ethylene of 2 to 1 are superior in their metal adhesion characteristics to compositions having a ratio of 1 to 1.
- compositions were prepared using a 68-32 blend of 500/3 and 1900/5 Texas oils, equally satisfactory compositions can be obtained by varying the ratio of oils and by using oils of different viscosities. Typical properties of such compositions are as follows:
- composition percent by wt.:
- a lubricating composition consisting essentially of a major proportion of a hydrocarbon oil having a viscosity above about 400 SUS at 100 F. and a minor proportion, sufficient to increase the viscosity of the oil and to impart thixotropic characteristics thereto, of a mixture of hydrogenated rosin of at least about 40 percent saturation and polymerized ethylene having a molecular weight between about 1000 and about 40,000, the weight ratio of hydrogenated rosin to polymerized ethylene being between about 1:3 and about 3:1.
- a thixotropic lubricating composition consisting essentially of a major proportion of a hydrocarbon oil having a viscosity of about 400 to about 4000 SUS at 100 F., about 0.2 to about 5 percent by weight of polymerized ethylene having a molecular weight between about 1000 and about 40,000, and a hydrogenated rosin of at least about 40 percent saturation, the weight ratio of hydrogenated rosin to polymerized ethylene being between about 1:3 and about 3:1.
- a thixotropic lubricating composition consisting essentially of a major proportion of a hydrocarbon oil having a viscosity of about 400 to about 4000 SUS at 100 F., about 0.2 to about 5 percent by weight of polymerized ethylene having a molecular weight between about 1000 and about 40,000, and about 0.2 to about 5 percent by weight of a hydrogenated rosin of at least about 40 percent saturation.
- a thixotropic lubricating composition consisting essentially of a major proportion of a hydrocarbon oil having a viscosity of about 400 to about 4000 SUS at 100 F., about 0.2 to about 5 percent by weight of polymerized ethylene having a molecular weight between about 1000 and about 40,000, and about 0.2 to about 5 percent by weight of a hydrogenated rosin of at least about 40 percent saturation, the weight ratio of hydrogenated rosin to polymerized ethylene being between about 1:3 and about 3:1.
- a thixotropic lubricating composition consisting essentially of a uniform mixture of about to about 99 percent by weight of a mineral lubricating oil having a viscosity of about 400 to about 4000 SUS at 100 F., about 0.2 to about 5 percent by weight of polymerized ethylene having a molecular weight of about 19,000, and about 0.2 to about 5 percent by weight of a hydrogenated rosin saturated to an extent of about 50 to about 60 percent, the weight ratio of hydrogenated rosin to polymerized ethylene being between about 1:3 and about 3:1.
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Description
SEMLFLUID LUBRICANT Paul R. McCarthy, Allison Park, Pa., assiguor to Gulf Research & Development: Company, Pittsburgh, Pa., a corporation of Delaware No Drawing, Appli'cationMay 29,1956, SerialNo. 587,966
Claims; (Cl. 252-57) This invention relates toan improved semi-fluid: lubricant and more particularly to a thixotropic lubricating;
composition having high adhesive properties in the liquid: state.
In certain types of lubrication there are encountered conditions under which neither greasesnor-liquid: oils are entirely satisfactory lubricants. For example, in the lubrication of certain textile machinery such as plain bearings onlooms, top rolls, roll necks andsaddles of drawing, roving and spinning frames, it is desirable that the lubricant be of such consistency, that it will remain between the working surfaces and not be lost by dripping, leakage or centrifugal force. At the same time, his: desirable that the lubricant be of relatively low viscosity under operating conditions so as to neither; impede the-operation of the mechanism nor increase the power consumption.
Employing a textile-machinery. lubricantwhichwill stay on the bearing surface is important not only: from. the standpoint of the life of the hearing, but also from the standpoint of the product of the mill. Obviously, lubrication failure of the bearing will result in costlyshuedown of the machinery. Also, leakage of. lubricant onto the productof the mill, whether thread. or Woven fabric, will result in undesirable staining-of the fabric;
In addition tothe above requirements the, textile machinery lubricant must feedthrough. wickswithout: clogging and must be dispensable from ordinary squirt-type oil cans. While liquid oils can be dispensed from oilcans and aregenerally satisfactory'lubricants, as a general rule they do not have good metal adhesion properties. Greases. have good metal adhesion, properties but are undesirable in that they can notbeappliediby-wick feed or by ordinary oil cans.
Semi-fluid oils of the soap-thickened.typehavexbeen extensively used for lubricating textile machinery. Soapthickened lubricants, however, have certain; shortcomings in that frequently lumps of soapappear which clog the.
wicks. The. soap-thickened lubricants: have also. been undesirable in that lubricants having identical properties1 are difiicult to reproduce. Furthcrmmi Soap-thickened lubricants having suitable adhesive properties, as;a;general: rule, have some unsatisfactory property such, as. being stringy.
It is, therefore, an object achieved by this invention to provide an easily reproducible lubricating. composition whichwill be sufficiently fluid to apply from anordinary squirt-type oil can and will remainfluid while the bearings on which it is placed are in operationbutwill form a light gel when the bearings are. not inoperation.
This and other objectsachieved by this inventionwill become apparent from the following detailed discussion.
I have discovered that a semi-fluid oil having thixotropic.
characteristics and improved metaladhesion. inthe'liquid state can be preparedfrom a high viscosity hydrocarbon. oilbyv compounding therewith smallamountsof each of polymerized ethylene and a hydrogenated rosin, The
1 ited States Patent 2,816,869 Patented Dec. 17, 1957 semi-fluid composition of the invention, since it does not rely. upon soap as a gelling agent, is to be distinguished from greases. insofar as the mode of obtaining a gel consistency is concerned.
The hydrocarbonv oil employed in the preparation of the thixotropic composition according to this invention can be. either a refined or semi-refined parafiinic-, naph-- thenic-,. or asphalt-base oil, or the oil can be a synthetic oil having a viscosity above about 400 SUS at 100 F. and preferably having a viscosity. of about 400 to. 4000-SUS at 100 F. If desired, ablend of oils of suitable viscosity can be employed instead of a single .oil, by means of which any desiredviscosity within the range of 400to 4000. .SUS. at- 100 F. canbe secured; The. amount: of oil employed constitutes from about r0 99 percent by weight of the. total composition. Naturally, the optimum amount: of oil employed in any given instance will. depend, upon the particular oil. employed as well as upon. the characteristics desired in the final composition.
The polymerized ethylene is a polymerization product of ethylene having a molecularyweight of about 1000 to 40,000 or. more. Polyethylenes'havinga molecular weight within this range, i. e., 19,000, are characterized by. the following approximate characteristics:
Softening point, "C 108 Tensile strength, p. s. i 1200 Yield point, p. s. i 1450 These polymerized ethylene compounds are obtained.
by the'thermal or catalytic polymerization of ethylene at high pressure. not a part of the present invention. Theamount of polymerized ethylene employed constitutes about 0.2 to about. 5 percent by weight of the total. composition.
The hydrogenated rosin employed according to the invention is a rosin of at least about 40 percent saturation to and including fully hydrogenated rosin. Rosin, sometimes called colophony, is the residue obtained on distilling turpentine from hard pine resin. Abietic acid, C H O is the chief constituent of rosin and is obtained from. the latter by distillation. Abietic acid is a carboxylic acid containing two double bonds. Hydrogenated rosin is obtained by the addition of hydrogen to the double bonds of abietic acid. The amount of hydrogen added may, be sufficient to saturate the two unsaturated. bonds of abietic acid or it may be any amount to produce substantial partial hydrogenation. A particularly useful hydrogenated rosin for the purposes of my, invention is one which has been hydrogenated to about 50 to about 60 percent of capacity and has a melting point of about 168 F. The quantity of the hydrogenated rosin employed constitutes from about 0.2 to about 5 percent by weight of the total composition. In general, improved, metal adhesion characteristics are obtained when the weight ratio of the hydrogenated rosinto the polymerizedethylene is between. about 1:3 and about 3:1. In any event the mixtureof. hydrogenated rosin and polymerized ethylene is added in an amount sufficient to increase the viscosity of the hydrocarbon, oil and to impart thixotropic characteristics thereto.
In preparing the improved lubricant of my invention I can. also incorporate in the lubricant one or more. of. the so-called addition agents normally added to lubricating. oils for a specific purpose including an anti-oxidant, a corrosion inhibitor, an anti-rust agent, an extreme pressure agent, an anti-foam agent and an oiliness agent. Corrosion. inhibitors are particularly desirable in: com: positions used in corrodible alloy, bearings. Among. the corrosion inhibitors suitable for. the purpose of the invention are dibenzyl disulfide, alkyl phenyl sulfides,
The method of forming the polymers is alkyl phosphites, alkaryl phosphites and sulfurized terpenes. In instances where the lubricant is subjected to prolonged use under oxidizing conditions, I advantageously incorporate in the lubricant a small amount of an oxidation inhibitor such as an alkali insoluble phenol, i. e., 2,6-di-tertiary-butyl-4-methylphenol; 2,4,6-tri-tertiary-butylphenol; etc., and/or a small amount of a diaryl amine. As examples of some of the diaryl amines which can be used in the composition of the invention may be mentioned diphenylamine, phenyl alpha naphthylamine, phenyl beta naphthylamine, alpha alpha-, alpha beta-, and beta beta-, dinaphth lamines, and the like. The amount of the conventional additive agents employed will depend to a large extent upon the conditions to which the composition is subjected, as well as upon the particular additive used. For instance, when the composition is subjected to prolonged use under oxidizing conditions, such as under extreme pressure and temperature, the oxidation inhibitor and extreme pressure agent requirements will be much greater than when relatively mild operating conditions are encountered. Generally, the amount of the anti-oxidant employed is between about 0.1 and 1.5 percent by weight based upon the weight of the total composition. In any event, the amount of additive employed is sufficient to accomplish the purpose for which it is intended without deleteriously affecting the other desirable characteristics of the composition.
In compounding the semi-fiuid lubricant of the invention, various compounding and blending procedures can be used. In accordance with one embodiment, the hydrogenated rosin is placed in a vessel and then heated until it is liquid. The temperature thus attained is about 200 F. The polymerized ethylene is then added with stirring to the melted hydrogenated rosin while continuing to heat to 450 F. The mixture is then held at 450 F. for a time sufficient to effect a uniform dispersion. The time required depends upon the size of the batch as well as the efficiency of the dispersing means. An oil concentrate of the hydrogenated rosin-polymerized ethylene dispersion is then prepared by adding an amount of oil equivalent to the combined weight of the hydrogenated rosin and polymerized ethylene. Heating at 450 F. with stirring is continued until a uniform concentrate is obtained. The concentrate is then added to the base oil having the desired viscosity at 240 F. Stirring is continued to obtain a uniform blend. The mixture is then cooled to room temperature with or without stirring depending upon the viscosity desired in the final product. I have found that cooling Without stirring from 240 F. to room temperature results in a product having a higher viscosity than a similar product which has been cooled from 240 F. to 120 F. with stirring. If a conventional additive such as an anti-oxidant is employed, it can be added to the dispersion of polymerized ethylene and hydrogenated rosin, or it can be added to the oil prior to the preparation of the concentrate. Of course, other compounding means can be employed without deviating from the scope of the invention.
The advantageous properties obtained by incorporating hydrogenated rosin and polymerized ethylene in a 750/45 Texas mineral oil as compared with the oil itself will be illustrated in connection with a metal adhesion test which is indicative of the adhesion characteristics obtainable in commercial application of a lubricant.
The metal adhesion test employed in comparing the lubricating compositions is that test ordinarily employed in determining the adhering characteristics of a grease. In conducting the test, a polished brass or steel disc with a concave surface is mounted on a vertical motor shaft so that the plane of the disc is in a horizontal position. The disc is tared. One tenth gram of lubricant is placed on the disc. The disc plus the lubricant is then reweighed. The disc is then attached to. the motor shaft. The entire disc is encased in a closed chamber the temperature of which is thermostatically controlled. The motor is then run for a period of seven minutes at a selected speed of 200 to 1000 R. P. M. at a selected temperature of to 200 F. At the end of the seven-minute period, the disc plus lubricant is reweighed and the lubricant remaining on the disc is calculated as percent lubricant retention.
In preparing the following compositions, a lubricating oil having a viscosity of about 750 SUS at 100 F. was prepared by mixing 68 parts by volume of a Texas oil having a viscosity of about 500 SUS at 100 F. with 32 parts by volume of a Texas oil having a viscosity of about 1900 SUS at 100 F. Various amounts of polymerized ethylene and hydrogenated rosin were employed as shown. The polymerized ethylene was a solid having a molecular weight of about 19,000. The hydrogenated rosin employed was a solid having a melting point of about 168 F. The double bonds of the rosin acids had been saturated to an extent of about 50 to 60 percent. The blending procedure employed in preparing the compositions was in accordance with the embodiment described hereinabove. In preparing these compositions the rate of cooling from 240 to 120 F. was increased by stirring. Cooling from 120 F. to room temperature was without stirring.
Table 1 A B 0 D Composition. percent by wt.:
750/4.5 Texas oil 98 98. 5 99 Hydrogenated rosin 1.332 1.0 0. 666 Polymerized ethylene 0. 668 0.5 0. 334 Ratio of Hydrogenated rosin to Polymerized ethylene 2:1 2:1 2:1. Inspection:
Viscosity, SUS- at 100 F 753 1, 597 1, 228 1, 153 at 210 F 62 80 4 74. 4 70.3 Adhesion to metal, percent retained (0.1 gm. of lubricant applied to disc rotated for 7 minutes at room temperature)- at 200 R. P. M 100 100 100 100 at 400 R. P. M. 50 100 90 at 600 R. P M 40 80 7O 60 at 800 R. P. M- 30 60 45 35 at1000 R. P. M 40 Adhesion to metal, percent retained (400 R. P. M.)-
at 80 F 63 98 97 85 65 100 45 93 93 88 It can be seen from the data in the above table that compositions B, C and D containing from 1 to 2 percent by weight of a mixture of hydrogenated rosin and polymerized ethylene in a 2 to 1, respectively, weight ratio gave remarkably improved metal adhesion characteristics. In the first series of tests, the temperature was maintained constant while varying the speed between 200 and 1000 R. P. M. In the second series of tests, the speed was maintained constant while varying the temperature between 80 and F. In each series of tests, the compositions of the invention were strikingly superior.
The results of additional tests employing a composition containing two percent by weight of a mixture of hydrogenated rosin and polymerized ethylene in ratios between 1:3 and 3:1 are shown in Table 2. These compositions were prepared by the same procedure used in preparing the compositions reported in Table 1.
The data in Table 2 again show the improved metal adhesion characteristics of compositions within the scope of the invention. It will be noted that compositions B, C and E .wherein the ratio of hydrogenated rosin to polymerized ethylene is 1:3, 1:2 and 2:1, respectively, gave particularly good retention of the lubricant at temperatures of 80 to 160 F.
As disclosed hereinabove, I have found that cooling without stirring from 240 F. to room temperature results in a producthaving a higher viscosity. This point Table 2 A B C D E F Composition, percent by wt.:
750/45 Texas oil 100 98 98 98 98 98 Hydrogenated rosin 0. 48 0.66 1. 1. 34 1. 52 Polymerized ethylene 1. 52 1. 34 1.0 0.66 0. 48 Ratio of Hydrogenated rosin to Polymerized ethylene 1:3 1:2 1 1 2:1 3:1 Inspection:
Viscosity, SUS- at 100 F 753 2, 630 2, 340 1, 118 1, 597 1, 326 at 210 F 62 8 86. 80.2 80. 4 70. 5 Adhesion to metal, percent retained (400 R. P. M.)-
can be illustrated by inspecting the viscosities of lubricating compositions which contain the same proportions of hydrogenated rosin and polymerized ethylene, the only difference being the manner in which cooling is effected. In Table 3, the compositions were prepared according to the blending procedure described hereinabove. After uniform blends were obtained, compositions A and C were cooled from 240 F. to room temperature without stirring; compositions B and D were cooled from 240 to 120 F. with stirring and then to room temperature without stirring.
The above data show that cooling without stirring gives products having higher viscosities than products obtained with increased cooling by stirring. It is also to be noted that compositions having a ratio of hydrogenated rosin to polymerized ethylene of 2 to 1 are superior in their metal adhesion characteristics to compositions having a ratio of 1 to 1.
While the above compositions were prepared using a 68-32 blend of 500/3 and 1900/5 Texas oils, equally satisfactory compositions can be obtained by varying the ratio of oils and by using oils of different viscosities. Typical properties of such compositions are as follows:
Composition, percent by wt.:
100/2 Texas oil 43 20 1900/5 Texas oil-.- 55 78 Hydrogenated rosin 1.332 Polymerized ethylene 0.668 Ratio of hydrogenated rosin to polymerized ethylene 2:1 2: 1 Inspection:
Gravity, API 22. 0 21.1 Viscosity, SUS- at 100 F 728 1, 535
at 210 IL--- 69.0 94.5 Viscosity Index- 74 64 Flash point, 0. 0.: 355 385 Fire point, 0. 0.: 405 445 Pour point, F 5 Color, ASTM Union 4. 75 5. 5 Neutralization Value, ASTM D 97453T Total Acid N o.-- 2.1 2. 1 Ash, percent 0.012
While my invention has been described with reference to various specific examples and'embodiments, it will be understood that the invention is not limited to such examples and embodiments and may be variously practiced within the scope of the claims hereinafter made.
I claim:
1. A lubricating composition consisting essentially of a major proportion of a hydrocarbon oil having a viscosity above about 400 SUS at 100 F. and a minor proportion, sufficient to increase the viscosity of the oil and to impart thixotropic characteristics thereto, of a mixture of hydrogenated rosin of at least about 40 percent saturation and polymerized ethylene having a molecular weight between about 1000 and about 40,000, the weight ratio of hydrogenated rosin to polymerized ethylene being between about 1:3 and about 3:1.
2. A thixotropic lubricating composition consisting essentially of a major proportion of a hydrocarbon oil having a viscosity of about 400 to about 4000 SUS at 100 F., about 0.2 to about 5 percent by weight of polymerized ethylene having a molecular weight between about 1000 and about 40,000, and a hydrogenated rosin of at least about 40 percent saturation, the weight ratio of hydrogenated rosin to polymerized ethylene being between about 1:3 and about 3:1.
3. A thixotropic lubricating composition consisting essentially of a major proportion of a hydrocarbon oil having a viscosity of about 400 to about 4000 SUS at 100 F., about 0.2 to about 5 percent by weight of polymerized ethylene having a molecular weight between about 1000 and about 40,000, and about 0.2 to about 5 percent by weight of a hydrogenated rosin of at least about 40 percent saturation.
4. A thixotropic lubricating composition consisting essentially of a major proportion of a hydrocarbon oil having a viscosity of about 400 to about 4000 SUS at 100 F., about 0.2 to about 5 percent by weight of polymerized ethylene having a molecular weight between about 1000 and about 40,000, and about 0.2 to about 5 percent by weight of a hydrogenated rosin of at least about 40 percent saturation, the weight ratio of hydrogenated rosin to polymerized ethylene being between about 1:3 and about 3:1.
5. A thixotropic lubricating composition consisting essentially of a uniform mixture of about to about 99 percent by weight of a mineral lubricating oil having a viscosity of about 400 to about 4000 SUS at 100 F., about 0.2 to about 5 percent by weight of polymerized ethylene having a molecular weight of about 19,000, and about 0.2 to about 5 percent by weight of a hydrogenated rosin saturated to an extent of about 50 to about 60 percent, the weight ratio of hydrogenated rosin to polymerized ethylene being between about 1:3 and about 3:1.
References Cited in the file of this patent UNITED STATES PATENTS 2,221,953 Read Nov. 19, 1940 2,270,319 Lieber Jan. 20, 1942 2,627,938 Frohmader Feb. 10, 1953 2,628,187 Frohmader Feb. 10, 1953 2,691,647 Field Oct. 12, 1954 2,762,775 Foehr Sept. 11, 1956
Claims (1)
1. A LUBRICATING COMPOSITION CONSISTING ESSENTIALLY OF A MAJOR PROPORTION OF A HYDROCARBON OIL HAVING A VISCOSITY ABOVE ABOUT 400 SUS AT 100*F. AND A MINOR PROPORTION SUFFICIENT TO INCREASE THE VISCOSITY OF THE OIL AND TO IMPART THIXOTROPIC CHARACTERISTICS THERETO, OF A MIXTURE OF HYDROGENATED ROSIN OF AT LEAST ABOUT 40 PERCENT SATURATION AND POLYMERIZED ETHYLENE HAVING A MOLECULAR WEIGHT BETWEEN ABOUT 1000 AND ABOUT 40,000 THE WEIGHT RATIO OF HYDROGENATED RESIN TO POLYMERIZED ETHYLENE BEING BETWEEN ABOUT 1:3 AND ABOUT 3:1.
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US587966A US2816869A (en) | 1956-05-29 | 1956-05-29 | Semi-fluid lubricant |
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US587966A US2816869A (en) | 1956-05-29 | 1956-05-29 | Semi-fluid lubricant |
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Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2221953A (en) * | 1938-02-10 | 1940-11-19 | Standard Oil Dev Co | Lubricating oil composition |
US2270319A (en) * | 1940-07-16 | 1942-01-20 | Standard Oil Dev Co | Lubricant and method of preparing same |
US2628187A (en) * | 1950-05-06 | 1953-02-10 | Res Prod Corp | Medicinal mineral oil vehicle thickened with polyethylene |
US2627938A (en) * | 1948-08-10 | 1953-02-10 | Res Prod Corp | Method of making high viscosity products having petroleum oil base and product of such method |
US2691647A (en) * | 1952-12-06 | 1954-10-12 | Standard Oil Co | Conversion of ethylene and/or propylene to solid polymers in the presence of group 6a metal oxides and alkali metals |
US2762775A (en) * | 1953-09-28 | 1956-09-11 | California Research Corp | Wax and polyethylene for filter adhesives |
-
1956
- 1956-05-29 US US587966A patent/US2816869A/en not_active Expired - Lifetime
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2221953A (en) * | 1938-02-10 | 1940-11-19 | Standard Oil Dev Co | Lubricating oil composition |
US2270319A (en) * | 1940-07-16 | 1942-01-20 | Standard Oil Dev Co | Lubricant and method of preparing same |
US2627938A (en) * | 1948-08-10 | 1953-02-10 | Res Prod Corp | Method of making high viscosity products having petroleum oil base and product of such method |
US2628187A (en) * | 1950-05-06 | 1953-02-10 | Res Prod Corp | Medicinal mineral oil vehicle thickened with polyethylene |
US2691647A (en) * | 1952-12-06 | 1954-10-12 | Standard Oil Co | Conversion of ethylene and/or propylene to solid polymers in the presence of group 6a metal oxides and alkali metals |
US2762775A (en) * | 1953-09-28 | 1956-09-11 | California Research Corp | Wax and polyethylene for filter adhesives |
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