US3929652A - Dual purpose cutting oil - Google Patents
Dual purpose cutting oil Download PDFInfo
- Publication number
- US3929652A US3929652A US523301A US52330174A US3929652A US 3929652 A US3929652 A US 3929652A US 523301 A US523301 A US 523301A US 52330174 A US52330174 A US 52330174A US 3929652 A US3929652 A US 3929652A
- Authority
- US
- United States
- Prior art keywords
- oil
- lubricant
- amount
- weight percent
- thiadiazole
- 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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- 239000010730 cutting oil Substances 0.000 title abstract description 29
- 230000009977 dual effect Effects 0.000 title abstract description 16
- 239000003921 oil Substances 0.000 claims abstract description 49
- 239000000314 lubricant Substances 0.000 claims abstract description 32
- 239000002199 base oil Substances 0.000 claims abstract description 25
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 claims abstract description 14
- -1 Beta -chlorophenethyl Chemical group 0.000 claims abstract description 7
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 7
- 239000002253 acid Substances 0.000 claims description 10
- 239000000203 mixture Substances 0.000 claims description 10
- 239000005077 polysulfide Substances 0.000 claims description 8
- 229920001021 polysulfide Polymers 0.000 claims description 8
- 150000008117 polysulfides Polymers 0.000 claims description 8
- 229910019142 PO4 Inorganic materials 0.000 claims description 6
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 6
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 6
- 125000000068 chlorophenyl group Chemical group 0.000 claims description 6
- 239000010452 phosphate Substances 0.000 claims description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 6
- BIGYLAKFCGVRAN-UHFFFAOYSA-N 1,3,4-thiadiazolidine-2,5-dithione Chemical compound S=C1NNC(=S)S1 BIGYLAKFCGVRAN-UHFFFAOYSA-N 0.000 claims description 5
- 235000018791 Cymbopogon nardus Nutrition 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 5
- 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 claims description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 4
- 239000005977 Ethylene Substances 0.000 claims description 4
- 239000010690 paraffinic oil Substances 0.000 claims description 4
- JJJPTTANZGDADF-UHFFFAOYSA-N thiadiazole-4-thiol Chemical compound SC1=CSN=N1 JJJPTTANZGDADF-UHFFFAOYSA-N 0.000 claims description 4
- 230000017488 activation-induced cell death of T cell Effects 0.000 claims 2
- 241000060340 Citronella Species 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 abstract description 19
- 238000005260 corrosion Methods 0.000 abstract description 13
- 230000007797 corrosion Effects 0.000 abstract description 13
- 229910052802 copper Inorganic materials 0.000 abstract description 12
- 239000010949 copper Substances 0.000 abstract description 12
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract description 11
- 239000003795 chemical substances by application Substances 0.000 abstract description 10
- 239000000654 additive Substances 0.000 description 27
- 230000000996 additive effect Effects 0.000 description 12
- 239000003205 fragrance Substances 0.000 description 8
- 239000005069 Extreme pressure additive Substances 0.000 description 7
- 238000005520 cutting process Methods 0.000 description 7
- 239000002184 metal Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000003595 mist Substances 0.000 description 6
- 238000009472 formulation Methods 0.000 description 5
- 235000019645 odor Nutrition 0.000 description 5
- 230000003647 oxidation Effects 0.000 description 5
- 238000007254 oxidation reaction Methods 0.000 description 5
- 244000166675 Cymbopogon nardus Species 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 4
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 4
- 239000002480 mineral oil Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 description 3
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical group CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 2
- WJQOZHYUIDYNHM-UHFFFAOYSA-N 2-tert-Butylphenol Chemical compound CC(C)(C)C1=CC=CC=C1O WJQOZHYUIDYNHM-UHFFFAOYSA-N 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000011436 cob Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000010721 machine oil Substances 0.000 description 2
- 238000003754 machining Methods 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- AFTBJQDQENGCPC-UHFFFAOYSA-N 2,5-ditert-butyl-4-methylphenol Chemical compound CC1=CC(C(C)(C)C)=C(O)C=C1C(C)(C)C AFTBJQDQENGCPC-UHFFFAOYSA-N 0.000 description 1
- 244000186140 Asperula odorata Species 0.000 description 1
- 235000008526 Galium odoratum Nutrition 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 230000002730 additional effect Effects 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 150000001879 copper Chemical class 0.000 description 1
- 238000012864 cross contamination Methods 0.000 description 1
- PXJJSXABGXMUSU-UHFFFAOYSA-N disulfur dichloride Chemical compound ClSSCl PXJJSXABGXMUSU-UHFFFAOYSA-N 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 125000003106 haloaryl group Chemical group 0.000 description 1
- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 238000005555 metalworking Methods 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 238000002407 reforming Methods 0.000 description 1
- 231100000241 scar Toxicity 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—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
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/08—Aldehydes; Ketones
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/123—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
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- 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
- C10M2207/22—Acids obtained from polymerised unsaturated acids
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- 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
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- 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
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- 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
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- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
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- C—CHEMISTRY; METALLURGY
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- 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
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/102—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon only in the ring
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- C—CHEMISTRY; METALLURGY
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- 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
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/10—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring
- C10M2219/104—Heterocyclic compounds containing sulfur, selenium or tellurium compounds in the ring containing sulfur and carbon with nitrogen or oxygen in the ring
- C10M2219/106—Thiadiazoles
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/042—Metal salts thereof
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/22—Metal working with essential removal of material, e.g. cutting, grinding or drilling
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- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/24—Metal working without essential removal of material, e.g. forming, gorging, drawing, pressing, stamping, rolling or extruding; Punching metal
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/241—Manufacturing joint-less pipes
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- 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
- C10N2040/20—Metal working
- C10N2040/242—Hot working
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- 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
- C10N2040/20—Metal working
- C10N2040/243—Cold working
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- 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
- C10N2040/20—Metal working
- C10N2040/244—Metal working of specific metals
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/244—Metal working of specific metals
- C10N2040/245—Soft metals, e.g. aluminum
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/244—Metal working of specific metals
- C10N2040/246—Iron or steel
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/244—Metal working of specific metals
- C10N2040/247—Stainless steel
Definitions
- ABSTRACT A dual purpose cutting oil is provided which serves as a heavy duty cutting oil and a machine lubricant.
- the oil comprises a base oil, an extreme pressure agent comprising primarily Bis (,B-chlorophenethyl) disulfide and a copper corrosion inhibitor comprising an alkyl derivative of 2,5-di-mercapto 1, 3,4-thiadiazole.
- Metal cutting and grinding have as their objective a progressive removal of metal from the work piece in the form of chips rather than by plastic reforming of the metal.
- metal cutting lubricant In the field of metal cutting, the use of single and multiple point tools is well known and a great deal of metal working lubricant is used in the metal cutting process.
- two types of lubricants are needed: a metal cutting lubricant and a machine oil.
- the cutting oil serves to remove heat generated during machining of the metal and lubricates the cutting tool against the work and chips.
- the machine oil lubricates the machine parts.
- Cutting oils are generally paraffinic or intermediate base mineral oils. These are preferred because such products generally create less fog or smoke than naphthene oil. In severe conditions, which are more normal than not in heavy duty operations, it may be necessary to use an additive package in the cutting oil. These additives will comprise extreme pressure additives,
- the invention is a lubricant which is useful as both a cutting oil and a machine lubricant which comprises a major amount of a base oil and minor amounts of Bis (B-chlorophenethyl) disulfide and minor amounts of an alkyl derivative of 2,5 di-mercapto-l,3,4-thiadiazole.
- the dual purpose oil of our invention is comprised of a base oil and additive package.
- the unique combination of additives in our oil was arrived at after many failures of so called equivalent additives in other combinations.
- each component additive in our oil is used for a purpose for which it is generally known
- the unique feature of our invention is the combination of additives which function collectively to give a single product, all the performance properties hereinafter enumerated without undesirable side effects such as malodor, corrosiveness, or instability. It was found in developing our invention that it was not enough to put together a list of additives wherein each was known in the art to impart a specific property.
- our oil usually more of our oil consists of a base oil which may be paraffinic oil of from about to 170 SUS/100F viscosity and preferably to SUS/100F viscosity. It is also acceptable to use a combination of two or more oils as a base oil wherein one oil may range from about 80 to 120, and preferably from about 85 to 105 SUS/l00F viscosity and the other oil may range from to 220 and preferably from about to SUS/100F viscosity. Paraffinic or intermediate base mineral oils are generally preferred as a base oil in our invention since they generate less fog and smoke than a naphthene oil. However, any suitable base oil may be used.
- the extreme pressure additives useful in our invention are halogenated aryl sulfides. These additives are, particularly, haloaryl polysulfides having one or more halogenated aromatic rings,which if desired can carry side chains containing halogen and/or other substituents.
- the extreme pressure additives are chlorophenyl polysulfides.
- a particularly preferred extreme pressure agent comprises primarily Bis (Ii-chlorophenyl) disulfide which is the reaction product of styrene and sulfur monochloride. This additive is present in amounts ranging from about 0.5 to 10 weight percent and preferably from about 1.0 to 5.0 weight percent of the total oil.
- a copper corrosion inhibitor is needed for the oil of our invention.
- the corrosion inhibitor which is useful for our invention is an alkyl derivative of 2,5di-mercapto-1,3,4-thiadiazole. This copper corrosion inhibitor should be present in amounts ranging from about 0.05 to 5.0 weight percent and preferably from about 0.05 to 0.5 weight percent in the oil of our invention.
- a particularly preferred copper corrosion inhibitor is described in U.S. Pat. Nos. 2,714,125; 2,714,126 and 2,983,716.
- the base oil and the two additives mentioned above will provide an acceptable dual purpose cutting oil, it is preferred that other additives be used to provide additional properties which enhance the desirability of the dual purpose cutting oil. It is particularly preferred that a rust inhibitor be used. It is particularly preferred for our invention that a combination of the extreme pressure agent and a copper corrosion inhibitor above be combined with a rust inhibitor comprising a mixture of alkylmaleic acid, phenol and lauryl acid phosphate. This three component additive system provides a particularly preferred cutting oil.
- the alkylmaleic acid should be present in amounts ranging from about 0.01 to 1.0 weight percent and preferably from about 0.02 and 0.05 weight percent.
- the lauryl acid phosphate should be present in amounts ranging from about 0.001 to 0.01 weight percent and preferably from about 0.002 to 0.005 weight percent.
- the phenol should be present in amounts ranging from trace amounts to about 0.01 weight percent. The percentage of these components is only approximate and may be varied outside of the suggested ranges wihtout departing from the scope of our invention.
- cutting oils have an oxidation inhibitor, an anti-mist additive, and an odorant.
- the oxidation inhibitor may be selected from those known in the art. A great many oxidation inhibitors are available commercially on many are hindered phenols although other types may be acceptable. Several of these might work in the cutting oil and the dual purpose cutting oil of our invention. However, it is preferred that tertiary butyl phenol or 4-methyl-2,5-ditertiary butyl phenol may be used in amounts ranging from about 0.05 to 1.0 weight percent and preferably 0.1 to 0.5 weight percent.
- An anti-mist additive is generally desirable and a few are known in the art. However, it is preferred in the cutting oil of our invention that a copolymer of ethylene and propylene be used.
- a particular preferred copolymer of ethylene and propylene has a molecular weight ranging from about 70,000 to 100,000 and a propylene content of from about 35 to 50 percent. This copolymer is usually used diluted with a paraffinic mineral oil. About 0.1 to 10.0 arid preferably about 0.5 to 5.0 weight percent of an anti-mist additive is desirable.
- the odorant in the oil of our invention may be any of those that are available in the commercial market. Generally, the choice of an odorant is important in that a specific odorant will normally mask only a few types important. In the oil of our invention, it was found that oil of citronella has performed adequately, although other odorants could have been used.
- Table I following gives three formulations of our invention which have acceptable performance properties as listed.
- Table II following, is an illustration of the problems encountered in putting together the formulation of our invention. We found that it was not enough simply to put together an additive package wherein each additive was known in the art to impart a specific property. The additives must be compatible with each other and the base oil, they must compliment each other and function together to give all the properties desired in the intended application.
- Table ll,'following shows a comparison of an oil of our invention (A) and three unsuccessful oils, B, C and D.
- the oils A, B, C and D all contain an additive package of ingredients known in the art to impart qualities which added together should result in a satisfactory dual purpose cutting oil. Yet only A was satisfactory in all respects.
- oil B which contains sulfur and chlorine extreme pressure agents with zinc dialkyl dithiophosphate copper corrosion inhibitor had the desired performance characteristic but developed an unacceptable haziness in storage.
- Oil C contained a non-corrosive extreme pressure additive and did not require a copper corrosion inhibitor. However, the odor of Oil B was considered objectionable to customers and could not be marketed. All attempts to mask the offensive odor failed.
- Oil D was an attempt to develop a suitable product without malodorous or corrosive sulfurized extreme pressure additives. A high extreme pressure level was achieved by using a relatively high concentration of a chlorinated extreme pressure additive. Oil C appeared satisfactory in laboratory tests but gave unsatisfactory maching performance in shop test. Oil A proved satisof odor and thus the selection of an odorant becomes 40 factory in every respect.
- a lubricant comprising polysulfide is present in an amount ranging from 1.0 to
- a lubricant comprising:
- I c. a minor amount of an alkyl derivative of 2,5-dimercapto-l ,3,4-thiadiazole and d. a minor amount of a mixture of alkylmaleic acid,
- a lubricant comprising:
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- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Priority Applications (10)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US523301A US3929652A (en) | 1974-11-13 | 1974-11-13 | Dual purpose cutting oil |
CA235,349A CA1061320A (en) | 1974-11-13 | 1975-09-12 | Dual purpose cutting oil |
GB42119/75A GB1523149A (en) | 1974-11-13 | 1975-10-15 | Dual purpose cutting oil |
SE7512091A SE407074B (sv) | 1974-11-13 | 1975-10-29 | Smorjmedel for anvendning bade som skerolja och maskinsmorjolja |
DE19752549952 DE2549952A1 (de) | 1974-11-13 | 1975-11-07 | Als hochbelastbares schneidoel und als maschinenschmiermittel verwendbare mineralschmieroelformulierung |
FR7534063A FR2291264A1 (fr) | 1974-11-13 | 1975-11-07 | Nouveaux lubrifiants comprenant un polysulfure d'aryle halogene et un derive alkyle de dimercapto-2,5 thiadiazole-1,3,4 |
BR7507394*A BR7507394A (pt) | 1974-11-13 | 1975-11-10 | Lubrificante possuindo uma quantidade principal de oleo de base |
DD189394A DD121336A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1974-11-13 | 1975-11-11 | |
IT29169/75A IT1049057B (it) | 1974-11-13 | 1975-11-11 | Lubrificanti per la lavorazione dei metalli |
AT866475A AT340029B (de) | 1974-11-13 | 1975-11-13 | Als hochbelastbares schneidol und als maschinenschmiermittel verwendbare mineralschmierolformulierung |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US523301A US3929652A (en) | 1974-11-13 | 1974-11-13 | Dual purpose cutting oil |
Publications (1)
Publication Number | Publication Date |
---|---|
US3929652A true US3929652A (en) | 1975-12-30 |
Family
ID=24084441
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US523301A Expired - Lifetime US3929652A (en) | 1974-11-13 | 1974-11-13 | Dual purpose cutting oil |
Country Status (10)
Cited By (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3980573A (en) * | 1975-07-24 | 1976-09-14 | Mobil Oil Corporation | Substituted dimercapto thiadiazoles and lubricant compositions containing same |
US4193882A (en) * | 1973-07-06 | 1980-03-18 | Mobil Oil Corporation | Corrosion inhibited lubricant composition |
US4210544A (en) * | 1976-08-18 | 1980-07-01 | Texaco Inc. | Dual purpose cutting oil composition |
US4216100A (en) * | 1978-08-03 | 1980-08-05 | Texaco Inc. | Pentaerythritol-fatty acid ester lubricant composition |
US4427560A (en) | 1981-12-10 | 1984-01-24 | Union Oil Company Of California | Anti-oxidation and corrosion inhibitors for boron-containing lubricants |
US4490265A (en) * | 1981-12-10 | 1984-12-25 | Union Oil Company Of California | Lubricating compositions |
US4595514A (en) * | 1983-08-23 | 1986-06-17 | Union Oil Company Of California | Boron-containing heterocyclic compound and lubricating compositions containing same |
US4623474A (en) * | 1981-12-10 | 1986-11-18 | Union Oil Company Of California | Oxidation and corrosion inhibitors for boron-containing lubricants |
US4627930A (en) * | 1980-06-12 | 1986-12-09 | Union Oil Company Of California | Boron-containing heterocyclic compounds and lubricating oil containing same |
US4629580A (en) * | 1980-06-12 | 1986-12-16 | Union Oil Company Of California | Boron-containing heterocyclic compounds and lubricating oil containing same |
US4629579A (en) * | 1980-06-12 | 1986-12-16 | Union Oil Company Of California | Boron derivatives |
US4657686A (en) * | 1980-06-12 | 1987-04-14 | Union Oil Company Of California | Lubricating compositions |
US4686056A (en) * | 1980-06-12 | 1987-08-11 | Union Oil Company Of California | Metal-boron derivatives as lubricant additives |
US4724099A (en) * | 1980-06-12 | 1988-02-09 | Union Oil Company Of California | Lubricating compositions |
US4756842A (en) * | 1980-06-12 | 1988-07-12 | Union Oil Company Of California | Lubricating compositions |
US4801729A (en) * | 1980-06-12 | 1989-01-31 | Union Oil Company Of California | Lubricating compositions |
US4846984A (en) * | 1987-09-18 | 1989-07-11 | Mobil Oil Corporation | Lubricant additives derived from aminomercaptothiadiazole and lubricant compositions containing same |
US4892670A (en) * | 1985-01-29 | 1990-01-09 | Union Oil Company Of California | Lubricating compositions |
US5227551A (en) * | 1989-11-19 | 1993-07-13 | Exxon Chemical Patents Inc. | Method of suppressing mist formation from oil-containing functional fluids |
US5318712A (en) * | 1992-10-13 | 1994-06-07 | The Lubrizol Corporation | Lubricants, greases, aqueous fluids and concentrates containing additives derived from dimercaptothiadiazoles |
US5368758A (en) * | 1992-10-13 | 1994-11-29 | The Lubrizol Corporation | Lubricants, greases and aqueous fluids containing additives derived from dimercaptothiadiazoles |
US5874390A (en) * | 1997-12-22 | 1999-02-23 | Cincinnati Milacron Inc. | Aqueous machining fluid and method |
US6204225B1 (en) | 1999-12-13 | 2001-03-20 | Midwest Biologicals, Inc. | Water-dispersible metal working fluid |
US6399548B1 (en) * | 2000-09-22 | 2002-06-04 | Chevron Oronite Company Llc | Functional fluids |
US10647939B2 (en) | 2016-11-18 | 2020-05-12 | International Petroleum Products & Additives Company, Inc. | Thiadiazole components, compositions, and methods |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3459663A (en) * | 1967-04-06 | 1969-08-05 | Sun Oil Co | Aluminum rolling oil |
US3816311A (en) * | 1971-02-19 | 1974-06-11 | Ethyl Corp | Stable phosphate esters |
US3853638A (en) * | 1973-06-25 | 1974-12-10 | Shell Oil Co | Quenching oil composition |
-
1974
- 1974-11-13 US US523301A patent/US3929652A/en not_active Expired - Lifetime
-
1975
- 1975-09-12 CA CA235,349A patent/CA1061320A/en not_active Expired
- 1975-10-15 GB GB42119/75A patent/GB1523149A/en not_active Expired
- 1975-10-29 SE SE7512091A patent/SE407074B/xx unknown
- 1975-11-07 DE DE19752549952 patent/DE2549952A1/de active Pending
- 1975-11-07 FR FR7534063A patent/FR2291264A1/fr not_active Withdrawn
- 1975-11-10 BR BR7507394*A patent/BR7507394A/pt unknown
- 1975-11-11 IT IT29169/75A patent/IT1049057B/it active
- 1975-11-11 DD DD189394A patent/DD121336A5/xx unknown
- 1975-11-13 AT AT866475A patent/AT340029B/de not_active IP Right Cessation
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3459663A (en) * | 1967-04-06 | 1969-08-05 | Sun Oil Co | Aluminum rolling oil |
US3816311A (en) * | 1971-02-19 | 1974-06-11 | Ethyl Corp | Stable phosphate esters |
US3853638A (en) * | 1973-06-25 | 1974-12-10 | Shell Oil Co | Quenching oil composition |
Cited By (27)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4193882A (en) * | 1973-07-06 | 1980-03-18 | Mobil Oil Corporation | Corrosion inhibited lubricant composition |
US3980573A (en) * | 1975-07-24 | 1976-09-14 | Mobil Oil Corporation | Substituted dimercapto thiadiazoles and lubricant compositions containing same |
US4210544A (en) * | 1976-08-18 | 1980-07-01 | Texaco Inc. | Dual purpose cutting oil composition |
US4216100A (en) * | 1978-08-03 | 1980-08-05 | Texaco Inc. | Pentaerythritol-fatty acid ester lubricant composition |
US4801729A (en) * | 1980-06-12 | 1989-01-31 | Union Oil Company Of California | Lubricating compositions |
US4627930A (en) * | 1980-06-12 | 1986-12-09 | Union Oil Company Of California | Boron-containing heterocyclic compounds and lubricating oil containing same |
US4629580A (en) * | 1980-06-12 | 1986-12-16 | Union Oil Company Of California | Boron-containing heterocyclic compounds and lubricating oil containing same |
US4629579A (en) * | 1980-06-12 | 1986-12-16 | Union Oil Company Of California | Boron derivatives |
US4657686A (en) * | 1980-06-12 | 1987-04-14 | Union Oil Company Of California | Lubricating compositions |
US4686056A (en) * | 1980-06-12 | 1987-08-11 | Union Oil Company Of California | Metal-boron derivatives as lubricant additives |
US4724099A (en) * | 1980-06-12 | 1988-02-09 | Union Oil Company Of California | Lubricating compositions |
US4756842A (en) * | 1980-06-12 | 1988-07-12 | Union Oil Company Of California | Lubricating compositions |
US4427560A (en) | 1981-12-10 | 1984-01-24 | Union Oil Company Of California | Anti-oxidation and corrosion inhibitors for boron-containing lubricants |
US4490265A (en) * | 1981-12-10 | 1984-12-25 | Union Oil Company Of California | Lubricating compositions |
US4623474A (en) * | 1981-12-10 | 1986-11-18 | Union Oil Company Of California | Oxidation and corrosion inhibitors for boron-containing lubricants |
US4595514A (en) * | 1983-08-23 | 1986-06-17 | Union Oil Company Of California | Boron-containing heterocyclic compound and lubricating compositions containing same |
US4892670A (en) * | 1985-01-29 | 1990-01-09 | Union Oil Company Of California | Lubricating compositions |
US4846984A (en) * | 1987-09-18 | 1989-07-11 | Mobil Oil Corporation | Lubricant additives derived from aminomercaptothiadiazole and lubricant compositions containing same |
US5227551A (en) * | 1989-11-19 | 1993-07-13 | Exxon Chemical Patents Inc. | Method of suppressing mist formation from oil-containing functional fluids |
US5329055A (en) * | 1991-06-19 | 1994-07-12 | Exxon Chemical Patents Inc. | Method of suppressing mist formation from oil-containing functional fluids |
US5318712A (en) * | 1992-10-13 | 1994-06-07 | The Lubrizol Corporation | Lubricants, greases, aqueous fluids and concentrates containing additives derived from dimercaptothiadiazoles |
US5368758A (en) * | 1992-10-13 | 1994-11-29 | The Lubrizol Corporation | Lubricants, greases and aqueous fluids containing additives derived from dimercaptothiadiazoles |
AU669390B2 (en) * | 1992-10-13 | 1996-06-06 | Lubrizol Corporation, The | Lubricants, greases, and aqueous fluids containing additives derived from dimercaptothiadiazoles |
US5874390A (en) * | 1997-12-22 | 1999-02-23 | Cincinnati Milacron Inc. | Aqueous machining fluid and method |
US6204225B1 (en) | 1999-12-13 | 2001-03-20 | Midwest Biologicals, Inc. | Water-dispersible metal working fluid |
US6399548B1 (en) * | 2000-09-22 | 2002-06-04 | Chevron Oronite Company Llc | Functional fluids |
US10647939B2 (en) | 2016-11-18 | 2020-05-12 | International Petroleum Products & Additives Company, Inc. | Thiadiazole components, compositions, and methods |
Also Published As
Publication number | Publication date |
---|---|
GB1523149A (en) | 1978-08-31 |
CA1061320A (en) | 1979-08-28 |
SE7512091L (sv) | 1976-05-14 |
DE2549952A1 (de) | 1976-05-20 |
AT340029B (de) | 1977-11-25 |
DD121336A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1976-07-20 |
ATA866475A (de) | 1977-03-15 |
FR2291264A1 (fr) | 1976-06-11 |
BR7507394A (pt) | 1976-08-10 |
SE407074B (sv) | 1979-03-12 |
IT1049057B (it) | 1981-01-20 |
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