US2818386A - Soluble cutting oil comprising thickened oil and method of applying the same - Google Patents
Soluble cutting oil comprising thickened oil and method of applying the same Download PDFInfo
- Publication number
- US2818386A US2818386A US398634A US39863453A US2818386A US 2818386 A US2818386 A US 2818386A US 398634 A US398634 A US 398634A US 39863453 A US39863453 A US 39863453A US 2818386 A US2818386 A US 2818386A
- Authority
- US
- United States
- Prior art keywords
- oil
- cutting
- percent
- thickened
- water
- 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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- 239000003921 oil Substances 0.000 title claims description 65
- 238000000034 method Methods 0.000 title claims description 20
- 239000010730 cutting oil Substances 0.000 title description 25
- 238000005520 cutting process Methods 0.000 claims description 45
- 239000000344 soap Substances 0.000 claims description 36
- 239000007788 liquid Substances 0.000 claims description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 22
- 239000003995 emulsifying agent Substances 0.000 claims description 20
- 239000000839 emulsion Substances 0.000 claims description 16
- 229910052751 metal Inorganic materials 0.000 claims description 15
- 239000002184 metal Substances 0.000 claims description 15
- 239000004519 grease Substances 0.000 claims description 11
- 239000010688 mineral lubricating oil Substances 0.000 claims description 7
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 6
- 229930195729 fatty acid Natural products 0.000 claims description 6
- 239000000194 fatty acid Substances 0.000 claims description 6
- 230000006872 improvement Effects 0.000 claims description 6
- 150000004665 fatty acids Chemical class 0.000 claims description 5
- 235000019198 oils Nutrition 0.000 description 62
- 239000000203 mixture Substances 0.000 description 53
- 238000012360 testing method Methods 0.000 description 16
- 239000010687 lubricating oil Substances 0.000 description 14
- 229910000831 Steel Inorganic materials 0.000 description 9
- 150000004671 saturated fatty acids Chemical class 0.000 description 9
- 239000010959 steel Substances 0.000 description 9
- 239000002199 base oil Substances 0.000 description 8
- 239000002562 thickening agent Substances 0.000 description 8
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 6
- 241000158728 Meliaceae Species 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 6
- 239000002480 mineral oil Substances 0.000 description 5
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 239000012530 fluid Substances 0.000 description 4
- 235000010446 mineral oil Nutrition 0.000 description 4
- 235000003441 saturated fatty acids Nutrition 0.000 description 4
- 150000003871 sulfonates Chemical class 0.000 description 4
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 238000005555 metalworking Methods 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- -1 mono- Chemical class 0.000 description 3
- 230000000391 smoking effect Effects 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 238000012937 correction Methods 0.000 description 2
- 239000007822 coupling agent Substances 0.000 description 2
- 239000000295 fuel oil Substances 0.000 description 2
- 238000007689 inspection Methods 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 230000008719 thickening Effects 0.000 description 2
- 238000010792 warming Methods 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- 229910001104 4140 steel Inorganic materials 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 229910000997 High-speed steel Inorganic materials 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 229920001214 Polysorbate 60 Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 229940064004 antiseptic throat preparations Drugs 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 239000003518 caustics Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 229940013317 fish oils Drugs 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000003349 gelling agent Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910000000 metal hydroxide Inorganic materials 0.000 description 1
- 150000004692 metal hydroxides Chemical class 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 238000010979 pH adjustment Methods 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 239000012056 semi-solid material Substances 0.000 description 1
- 239000000779 smoke Substances 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc 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
- C10M173/00—Lubricating compositions containing more than 10% water
-
- 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
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/021—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/022—Hydroxy compounds having hydroxy groups bound to acyclic or cycloaliphatic carbon atoms containing at least two hydroxy 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
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty 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
- 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/404—Fatty vegetable or animal oils obtained from genetically modified species
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/109—Polyethers, i.e. containing di- or higher polyoxyalkylene groups esterified
-
- 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
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
-
- 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
- C10M2219/04—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions containing sulfur-to-oxygen bonds, i.e. sulfones, sulfoxides
- C10M2219/044—Sulfonic acids, Derivatives thereof, e.g. neutral salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/06—Groups 3 or 13
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/08—Groups 4 or 14
-
- 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
- C10N2040/20—Metal working
- C10N2040/22—Metal working with essential removal of material, e.g. cutting, grinding or drilling
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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
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/01—Emulsions, colloids, or micelles
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S29/00—Metal working
- Y10S29/088—Metal working by projecting, squirting or dripping
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T409/00—Gear cutting, milling, or planing
- Y10T409/30—Milling
- Y10T409/303752—Process
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T409/00—Gear cutting, milling, or planing
- Y10T409/30—Milling
- Y10T409/303976—Milling with means to control temperature or lubricate
Definitions
- This; invention relates to cutting liquids employed. in metal working operations and more particularly to soluble cutting oils which are adapted to be directed as a thin, high speed vjet into the angle between the. work and the. cutting edge of the tool.
- a newly developed method of applying cutting oils. is an improvement'over the conventional low pressure, overhead. method of application.
- the new method isidescribed in U. S..Patent 2,653,517' to R. J. S. Pigott.
- a thin, high speed jet of oil is-directed between the work and the cutting surface of thetool.
- a velocity of. the jet such as 225 to 260 feet per second is obtainedby pumping the oil at pressures suchas 300 to 600 pounds per square inch through a small nozzle.
- a soluble cutting oil composition which is particularly adapted to be employed in an emulsion with water in metal working operations in which the cutting liquid is directed at a high velocity between the tool and the work as a thin, high speed jet andwhich comprises an oil-inwater emulsifying agent and a lubricating oil thickened to the consistency of a grease by the addition of a water-insoluble metal soap of a saturated fatty acid.
- Our invention also in general comprises an improvement in the method of working metal in which a thin, high speed jet ofcutting liquid is directed at a high velocity between the tooland the work,.the improvement comprising the use of a. cutting liquid composed of water and a soluble cutting oil of the described composition.
- the lubricating oil base in the compositions of our invention can be a distillate or residual mineral lubricating oilderived from a crude oil of paraflinic, naphthenic or mixed base. It can be a refined or unrefined lubricating oil and can comprise a single stock or any blend which produces a lubricating oil. Suitable oils exist over a wide range of viscosity, for example, from light lubricating oils having a viscosity as low as about 50 SUS at F. to oils having a viscosity as high as about 250 SUS at 210 F.
- the base oil can also be. entirely or in part an oil of non-mineral origin such as, for example, a lubricating oil obtained by Fischer-Tropsch synthesis, by olefin polymerization, etc.
- compositions of our invention contain one or more of certain water-insoluble soaps which are gelling or thickening agents and have the property of forming with mineral oils, gels or mixtures thicker or more viscous than the original oil.
- Soaps which canbe used include the fatty acid soaps of metals such as calcium, aluminum, lead, magnesium, barium, strontium, lithium, etc. Soaps of metals such as zinc are unsuitable because of their inability to form thickened mixtures with oils. Soaps offmetals such as sodium and potassium are. unsuitable because of their. water solubility. It is important that the soaps-be water-insoluble or of low Water solubility so that when the soluble oils of the invention are employed in water emulsions the thickening efifect of the soap on the oil base will not be lost.
- the thickening agents of our compositions are derived from. fatty acids having from about 10 to 24. carbon atoms and predominantly from saturated fatty acids.
- the fatty acids are obtained from animal or vegetable fats or oils which yield a. high. percentage of saturated acids.
- oils andfa'ts include beef and mutton fallow, lard, coconut oil, palm oil, hydrogenated vegetable, ani- Soaps prepared from stocks yielding predominantly unsaturated fatty acids are generally unsuitable because the unsaturated.
- fatty acid soaps are principally soft soaps which do not, perform satisfactorily as. thickening. agents.
- the thickening agent in our compositions can be a.
- water-insoluble soap of a single saturated fatty acid or, as is preferred, a mixture of the soaps such as mixtures derived from natural fats and oils which predominate in saturated fatty acids.
- the oil can, if desired, be thickened by the addition of a grease or other mixture which contains a soup of the indicated, type.
- the particular amount of soap required to thicken properly the base oil will of course be different with different oils, alight oil requiring a greater amount of thickenijng agent than a heavy oil.
- a sufficient amount of the water-insoluble: metal: soap is used to produce a mixture of soap and oil having the consistency at room temper- 3 ature of a semi-fluid grease, the viscosity of the thickened oil being substantially higher than that of the base oil and in any case, if measurable in Saybolt Universal seconds, greater than about 200 SUS at 210 F.
- the thickened oils are not Newtonian liquids and consequently there is no true physical constant of viscosity.
- the apparent viscosity will vary with the rate of shear.
- the most satisfactory method of defining the consistency of such thickened oils is with data obtained by ASTM test D1092-51 which is a standard procedure for measuring, in poises, the apparent viscosity of lubricating grease at room temperature.
- suflicient thicken ing agent is added to thicken the base oil to a consistency corresponding to an apparent viscosity of at least 5.0 poises as measured at 77 F. and at a shear rate of 200 reciprocal seconds by ASTM Dl092-51.
- the maximum limit to which the oil should be thickened it would generally be undesirable to produce a thickened oil having an apparent viscosity greater than about poises at 77 F.
- the amount of water-insoluble soap required to thicken the oil to the proper consistency or apparent viscosity is usually more than about 4 percent by weight of the mixture of oil and soap. As much as about percent by weight soap may be required for some light oils. With very heavy oils amounts somewhat less than 4 percent by weight of soap may suffice.
- the soluble oil of the compositions of our invention is prepared by mixing with the base oil thickened by a waterinsoluble soap, as described above, an emulsifying agent of the oil-in-water type such, for example, as oil-soluble sulfonates, and particularly sodium mahogany sulfonates, obtained in the sulfuric acid treatment of petroleum oils. Either the purified sulfonates or any of the commercial mahogany sulfonates of varying purity can be used.
- oils-in-water emulsifying agents can be used including sulfonated fattty material such as sperm oil, olive oil, cottonseed oil, etc., the stearates and oleates of alkylol amines such as mono-, di-, or triethanolamine and various non-ionic complex esters such as polyoxyethylene sorbitan fatty acid esters.
- the relative amounts of thickened lubricating oil and emulsifying agent in the soluble oil composition will depend upon the ease with which the thickened oil is made emulsifiable and upon the efliciency of the particular emulsifying agent.
- the emulsifying agent will comprise from about 15 to 40 percent by weight of the soluble oil composition including the emulsifying agent, the base oil, and the metal soap thickening agent.
- easily emulsifiable thickened oils as little as 5 percent by weight of the emulsifying agent may suffice, while with difficultly emulsifiable thickened oils it may be necessary that the soluble oil composition comprise as much as weight percent emulsifying agent.
- the soluble oil compositions of our invention can contain minor amounts of materials such as oleic acid or caustic added for the purpose of adjusting the pH of the mixture and affording the maximum stability of the emulsion.
- our compositions may also contain a minor amount of a suitable coupling agent such as diethylene glycol to improve the emulsion stability.
- the soluble oils of our invention may include various agents such as rust inhibitors, extreme pressure agents, antiseptics, etc.
- the lubricating oil base by mixing the oil and preformed soap-typethickening agent in desired quantities and stirring the ingredients while warming to a temperature of, for example, from about to F. until there is obtained a homogeneous mixture of grease consistency having the desired thickness or viscosity.
- the soap can be formed in situ in the lubricating oil. In the latter case, stoichiometrical proportions of a metal hydroxide and a fatty material of the types described are added separately to the oil to form the desired soap within the oil.
- the rate of reaction can be increased if desired by stirring the ingredients at a suitable saponification temperature, for example, 250 to 350 F.
- the selected emulsifying agent is added to the thickened oil, again with stirring While warming until a clear mixture is obtained.
- the maximum emulsifiability of the composition can be obtained by adjusting the pH as by the addition of minor amounts of acid or base until the mixture is easily emulsifiable.
- tions of the invention when the ingredients are incorpo rated in the mixture in adifferent sequence when the ingredients are incorpo rated in the mixture in adifferent sequence.
- the water-insoluble thickening agent and the oil-in-water emulsifying agent can be added simultaneously to the lubricating oil, although in general it is preferred to thicken the oil before the addition of the emulsifying agent in order to insure obtaining'the proper viscosity.
- the cutting composition should contain at least about 5 percent of the soluble oil and usually at compositions above about 20 percent by volume of soluble oil the smoking problem begins to be serious. Therefore, from about 5 to 20 percent by volume of the soluble oil is the preferred range of composition in the emulsion.
- certain operations and with certain soluble oil compositions as little as from 1 to 2 percent emulsions may be employed and in other operations as much as 50 percent by volume emulsions may be employed.
- the base oil for a composition in accordance with our invention was a refined Coastal lubricating oil blend having the following inspection data:
- the mineral lubricating oil was thickened by admixture with calcium soap of tallow to form a composition comprising 94.7 weight percent of the lubricating oil, 4.5 weight percent of the soap, 0.4 weig'ht percent of glycerine and 0.4 weight percent of water.
- the resulting thickened oil was a semi-fluid or semi-solid material having an API gravity of 21.4, a specific gravity (60/60" F.) of 0.925, a pour point of +40 F., a neutralization number of'O.3 and an ash content of 0.4 weight percent.
- the conventional soluble cutting oil comprised 85 parts by weight of a light refined lubricating oil, 14.88 parts by weight of the same commercial sodium mahogany sulfonate mixture employed in the compositions of our invention and 0.12 parts by weight of a rust inhibiting agent (Alkylamine Isoamyl Octyl Orthophosphate).
- the lubricating oil of the conventional soluble oil had the following inspection data:
- the soluble cutting oil of ourinvention described in the example above and the conventional soluble cutting oil were similarly employedas 5 weight percent emulsions in water in the high speed jet method of applying a cutting liquid.
- the cutting compositions were used in lathe tests on A151 4140 mill annealed steel using a high speed steel 6 tool (shape: 1 0 -'1-2" -8--106-6 R). in these tests thecutting compositions were directed in the form ot' a thin jet at a velocity of about 246 feet p'er'second and 0.125 gallon per minute into the angle between the work and the tool.
- the thin jet was obtained by passing the cutting composition through a small orifice (0.0183 inch) --in a nozzle which Was mounted on the carriage of the lathe.
- the cutting compositions were supplied ;to the nozzle at a temperature of about to F. under a pressure of 400 pounds per square inch.
- the depth 'of cut was 0.088 inch and the feed was 0.011 inch per revolution.
- the results of the lathe tests in terms of actual tool life and adjusted tool life are given in the table below.
- a method of adjusing the results is by the calculation of adjusted tool life values such as those presented in the table above. These are obtained as follows: For a particular steel a large number of determinations of the dry tool life of different specimens of the steel are taken and an average value is calculated. For the A181 4140 steel of these tests, at a speed of 140 S. F. M. a dry life value of approximately 1.4 minutes was obtained. This factor which is in effect a machineability rating of the steel, is then used in the following formula to obtain the adjusted tool life for a specimen of this particular steel at any cutting speed.
- cutting liquid compositions of the invention are particularly adapted for application as a thin, high speed jet, as described herein, it should be understood that they are also useful and have important advantages when applied as cutting liquids by other methods, for example, by the conventional overhead method of application.
- the improvement which comprises using as the cutting liquid an emulsion corn prising a major amount of water and a minor amount of an emulsifiable cutting oil comprising from about to 40 percent by weight of an oil-in-water emulsifying agent and from about 60 to 85 percent by weight of a mineral lu- I about 15 to 40 percent by Weight of an oil-soluble sulfonate oil-in-water emulsifying agent and from about 60 to 85 percent by weight of a mineral lubricating oil thickened by the addition of a water-insoluble metal soap of a saturated fatty acid, the amount of said soap being sutdcient to produce a thickened oil of grease consistency having an apparent viscosity at 77 F. greater than about 5 poises at a shear rate of 200 reciprocal seconds.
- the improvement which comprises using as the cutting liquid an emulsion comprising a major amount of water and from about 5 to volume percent of an emulsifiable cutting oil comprising from about 15 to 40 percent by weight of sodium mahogany sulfonate and from about 60 to 85 percent by weight of a thickened mineral oil having the consistency .of a semi-fluid grease and an apparent viscosity at 77 F. greater than about 5 poises at a shear rate of 200 reciprocal seconds, s'aid thickened mineral oil. comprising a mineral lubricating oil having a Saybolt Universal viscosity at 210 F. below about 250 seconds and from about 4 to 40 percent by weight of a thickening agent composed of a water-insoluble metal soap of a fatty material which yields predominantly saturated fatty acids having from about 10 to 24 carbon atoms.
- a soluble cutting oil comprising from about 15 to 40 percent by weight of an oil-in-water emulsifying agent and from about to percent by weight of a mineral lubricating oil thickened by the addition of a water-insoluble metal soap of a saturated fatty acid, the amount of said soap being suflicient to thicken said oil to a grease consistency.
- a soluble cutting oil comprising from about 15 to 40 percent by weight of an oil soluble sulfonate oil-inwater emulsifyingagent and from about 60 to 85 percent by weight of a mineral lubricating oil thickened by the addition of a water-insoluble metal soap of a saturated fatty acid, the amount of said soap being sufficient to "produce a thickened oil of grease consistency having an apparent viscosity at 77 F. greater than about 5 poises at a shear rate of 200 reciprocal seconds.
- a soluble cutting oil comprising from about 15 to j 40 percent by weight of sodium mahogany sulfonate and from about 60 to 85 percent by weight of a thickened mineral oil having the consistency of a semi-fluid grease and an apparent viscosity at 77 F. greater than about 5 poises at 200 reciprocal seconds, said thickened mineral oil comprising a mineral lubricating oil having a Saybolt Universal viscosity at 210 F. below about 250 seconds 7 and from about 4 to 40 percent by weight of a thickening agent composed of a water-insoluble metal soap of a fatty material which yields predominantly saturated fatty acids having from about 10 to 24 carbon atoms.
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- Chemical & Material Sciences (AREA)
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- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
United States Patent No Drawing. Application December 16, 1953 Serial No. 398,634
6 Claims. (Cl. 25233.3)
This; invention relates to cutting liquids employed. in metal working operations and more particularly to soluble cutting oils which are adapted to be directed as a thin, high speed vjet into the angle between the. work and the. cutting edge of the tool.
The application of a cutting oil to, ametal' surface being i worked has conventionally comprised flowing over the metal working tool, either by gravity or under low pressure, a large amount of the oil, the theory being that by floatingthe working surface with the cutting oil the heat evolved in. the operation would bedissipated, the metal chips washed away and the cutting operation lubricated? by the large quantity of oil used. However, in. the cutting operation the. chip which is formed overlies and shields the. cutting edge sothat an-insufficient amount,.if any, of the; cutting oil. flooding the work from overhead finds its way around the chip tothe tool edge. Accordingly, with the conventional overhead stream, little or no, cutting oil reaches the: cutting edge and the tool, is cooled solely by conduction. through, the chip and, through the; tool shank. The ineffective application of cutting liquids by the; conventionalmethod results in one of themajor disadvantages of'dry cutting, namely, the; early breakdown of the. cutting too A newly developed method of applying cutting oils. is an improvement'over the conventional low pressure, overhead. method of application. The new method isidescribed in U. S..Patent 2,653,517' to R. J. S. Pigott. In. the new method a thin, high speed jet of oil is-directed between the work and the cutting surface of thetool. A velocity of. the jet such as 225 to 260 feet per second is obtainedby pumping the oil at pressures suchas 300 to 600 pounds per square inch through a small nozzle. Asa result, it is believed that at least a portion of the oil, possibly as a vapor which thereafter condenses, penetrates the very small clearance between the work and the relief surface of the tool without impinging upon the heel of the tool or otherwise dissipating its energy before reaching its destination. In. his. manner the cu ting. peration is more efiieien ly cooled and lubricated so that the life of. the cutting toolris increased; build-up ofmetal par icles o the cuttin tool is redu ed. or. eliminated, the. surfac of. the fini h d w r is improved. and, other. important advantages are obtained.
While. the newly developed technique of applying the cutting iq id to the work, as. a high. speed jet results inincreasedtool life. even with cutting. liquids. of conventional composition, the conventional. cutting, liquids have not proven to be entirely satisfactory forthe, new technique. A serious problem. encountered in the use of conventional cutting oils in the high speed jet technique has been the formation of large amounts of smoke or vapor during the cutting operation. Conventional soluble cutting oils which reduce the smoking problem are notentirely' satisfactory with respect to the increased tool lifewhich should result-from the use of the high speed jet technique. An object of the present invention is to increase furtherthe advantages obtainable through the highspeed jet method mal or fish oils and the like.
2,818,386 Patented Dec. 31, 1957 2 ofapplying cutting liquids by providing cutting liquids which are particularly adapted for the newly developed method of application.
In accordance with the present invention, we have produced a soluble cutting oil composition which is particularly adapted to be employed in an emulsion with water in metal working operations in which the cutting liquid is directed at a high velocity between the tool and the work as a thin, high speed jet andwhich comprises an oil-inwater emulsifying agent and a lubricating oil thickened to the consistency of a grease by the addition of a water-insoluble metal soap of a saturated fatty acid. Our invention also in general comprises an improvement in the method of working metal in whicha thin, high speed jet ofcutting liquid is directed at a high velocity between the tooland the work,.the improvement comprising the use of a. cutting liquid composed of water and a soluble cutting oil of the described composition.
The lubricating oil base in the compositions of our invention can be a distillate or residual mineral lubricating oilderived from a crude oil of paraflinic, naphthenic or mixed base. It can be a refined or unrefined lubricating oil and can comprise a single stock or any blend which produces a lubricating oil. Suitable oils exist over a wide range of viscosity, for example, from light lubricating oils having a viscosity as low as about 50 SUS at F. to oils having a viscosity as high as about 250 SUS at 210 F. The base oil can also be. entirely or in part an oil of non-mineral origin such as, for example, a lubricating oil obtained by Fischer-Tropsch synthesis, by olefin polymerization, etc.
In addition to a base oil, the compositions of our invention contain one or more of certain water-insoluble soaps which are gelling or thickening agents and have the property of forming with mineral oils, gels or mixtures thicker or more viscous than the original oil. Soaps which canbe used include the fatty acid soaps of metals such as calcium, aluminum, lead, magnesium, barium, strontium, lithium, etc. Soaps of metals such as zinc are unsuitable because of their inability to form thickened mixtures with oils. Soaps offmetals such as sodium and potassium are. unsuitable because of their. water solubility. It is important that the soaps-be water-insoluble or of low Water solubility so that when the soluble oils of the invention are employed in water emulsions the thickening efifect of the soap on the oil base will not be lost.
The thickening agents of our compositions. are derived from. fatty acids having from about 10 to 24. carbon atoms and predominantly from saturated fatty acids. Preferably, the fatty acids are obtained from animal or vegetable fats or oils which yield a. high. percentage of saturated acids. Such oils andfa'ts include beef and mutton fallow, lard, coconut oil, palm oil, hydrogenated vegetable, ani- Soaps prepared from stocks yielding predominantly unsaturated fatty acids are generally unsuitable because the unsaturated. fatty acid soaps are principally soft soaps which do not, perform satisfactorily as. thickening. agents. The thickening agent in our compositions can be a. water-insoluble soap of a single saturated fatty acid, or, as is preferred, a mixture of the soaps such as mixtures derived from natural fats and oils which predominate in saturated fatty acids. Also, the oil can, if desired, be thickened by the addition of a grease or other mixture which contains a soup of the indicated, type.
The particular amount of soap required to thicken properly the base oil will of course be different with different oils, alight oil requiring a greater amount of thickenijng agent than a heavy oil. A sufficient amount of the water-insoluble: metal: soap is used to produce a mixture of soap and oil having the consistency at room temper- 3 ature of a semi-fluid grease, the viscosity of the thickened oil being substantially higher than that of the base oil and in any case, if measurable in Saybolt Universal seconds, greater than about 200 SUS at 210 F. Usually, however, the thickened oils are not Newtonian liquids and consequently there is no true physical constant of viscosity. The apparent viscosity will vary with the rate of shear. The most satisfactory method of defining the consistency of such thickened oils is with data obtained by ASTM test D1092-51 which is a standard procedure for measuring, in poises, the apparent viscosity of lubricating grease at room temperature.
In the compositions of the invention suflicient thicken ing agent is added to thicken the base oil to a consistency corresponding to an apparent viscosity of at least 5.0 poises as measured at 77 F. and at a shear rate of 200 reciprocal seconds by ASTM Dl092-51. As for the maximum limit to which the oil should be thickened, it would generally be undesirable to produce a thickened oil having an apparent viscosity greater than about poises at 77 F.
and 200 reciprocal seconds. (Equivalent to about 10,000 SUS at these conditions.) The amount of water-insoluble soap required to thicken the oil to the proper consistency or apparent viscosity is usually more than about 4 percent by weight of the mixture of oil and soap. As much as about percent by weight soap may be required for some light oils. With very heavy oils amounts somewhat less than 4 percent by weight of soap may suffice.
The soluble oil of the compositions of our invention is prepared by mixing with the base oil thickened by a waterinsoluble soap, as described above, an emulsifying agent of the oil-in-water type such, for example, as oil-soluble sulfonates, and particularly sodium mahogany sulfonates, obtained in the sulfuric acid treatment of petroleum oils. Either the purified sulfonates or any of the commercial mahogany sulfonates of varying purity can be used. Numerous other conventional oil-in-water emulsifying agents can be used including sulfonated fattty material such as sperm oil, olive oil, cottonseed oil, etc., the stearates and oleates of alkylol amines such as mono-, di-, or triethanolamine and various non-ionic complex esters such as polyoxyethylene sorbitan fatty acid esters.
The relative amounts of thickened lubricating oil and emulsifying agent in the soluble oil composition will depend upon the ease with which the thickened oil is made emulsifiable and upon the efliciency of the particular emulsifying agent. Usually the emulsifying agent will comprise from about 15 to 40 percent by weight of the soluble oil composition including the emulsifying agent, the base oil, and the metal soap thickening agent. However, with easily emulsifiable thickened oils as little as 5 percent by weight of the emulsifying agent may suffice, while with difficultly emulsifiable thickened oils it may be necessary that the soluble oil composition comprise as much as weight percent emulsifying agent.
In preparing stable emulsions of oil in water with emulsifying agents of the type indicated, it is often desirable to adjust the pH of the mixture by the addition of acid or basic substances. Therefore, the soluble oil compositions of our invention can contain minor amounts of materials such as oleic acid or caustic added for the purpose of adjusting the pH of the mixture and affording the maximum stability of the emulsion. Our compositions may also contain a minor amount of a suitable coupling agent such as diethylene glycol to improve the emulsion stability.
In addition to the thickened oil, the emulsifying agent, any acid or basic material necessary for pH adjustment, and any desired coupling agent, the soluble oils of our invention may include various agents such as rust inhibitors, extreme pressure agents, antiseptics, etc.
In preparing the soluble oils of our invention, it is preferred first to thicken the lubricating oil base by mixing the oil and preformed soap-typethickening agent in desired quantities and stirring the ingredients while warming to a temperature of, for example, from about to F. until there is obtained a homogeneous mixture of grease consistency having the desired thickness or viscosity. Alternatively, the soap can be formed in situ in the lubricating oil. In the latter case, stoichiometrical proportions of a metal hydroxide and a fatty material of the types described are added separately to the oil to form the desired soap within the oil. The rate of reaction can be increased if desired by stirring the ingredients at a suitable saponification temperature, for example, 250 to 350 F. and at superatmospheric pressure such as 50 to 100 pounds per square inch gauge over a period of an hour or more. Following the addition of soap to thicken the oil to the desired degree, the selected emulsifying agent is added to the thickened oil, again with stirring While warming until a clear mixture is obtained. Finally, the maximum emulsifiability of the composition can be obtained by adjusting the pH as by the addition of minor amounts of acid or base until the mixture is easily emulsifiable.
tions of the invention when the ingredients are incorpo rated in the mixture in adifferent sequence. For example, in forming certain compositions of the invention the water-insoluble thickening agent and the oil-in-water emulsifying agent can be added simultaneously to the lubricating oil, although in general it is preferred to thicken the oil before the addition of the emulsifying agent in order to insure obtaining'the proper viscosity.
The cutting liquid compositions or emulsions of our invention-can vary considerably in the ratio of the-amount of water to the amount of soluble oil depending upon a number of factors such as the emulsifiability of the particular soluble oil composition, the proportion of oil required to lubricate properly the cutting operation, the smoking problem at high oil concentrations, etc. For most cutting operations the cutting composition should contain at least about 5 percent of the soluble oil and usually at compositions above about 20 percent by volume of soluble oil the smoking problem begins to be serious. Therefore, from about 5 to 20 percent by volume of the soluble oil is the preferred range of composition in the emulsion. However, in certain operations and with certain soluble oil compositions as little as from 1 to 2 percent emulsions may be employed and in other operations as much as 50 percent by volume emulsions may be employed.
The following example will illustrate the preparation of a typical composition of our invention.
EXAMPLE The base oil for a composition in accordance with our invention was a refined Coastal lubricating oil blend having the following inspection data:
The mineral lubricating oil was thickened by admixture with calcium soap of tallow to form a composition comprising 94.7 weight percent of the lubricating oil, 4.5 weight percent of the soap, 0.4 weig'ht percent of glycerine and 0.4 weight percent of water. The resulting thickened oil was a semi-fluid or semi-solid material having an API gravity of 21.4, a specific gravity (60/60" F.) of 0.925, a pour point of +40 F., a neutralization number of'O.3 and an ash content of 0.4 weight percent.
- antennae The apparent viscosity data Ifor Qh'e ttliichene'd A deter- :niinedrby ASTM 9.1092 51, wire as follows:
Apparent Viscosity cat-77 F.
Shear Rate, Reciproealseconds J g Approximate vl-"oises Equivalent,
SUS
The thickened 'oil was mixed in a 'ratio=df"7'5'parts by weight with parts by weight of a commercial'emulsifying agent of which the principal active ingredient Was sodium mahogany sul'fonate. This mixture was-"stirred at a temperature of about 120 F. for about "minutes until a clear mixture of soluble cutting oil 'was obtained.
We have employed the soluble'cutt'ingoil dfour invention, described :in .the above example, .in cutting operations'in whichthe soluble suttingoilinan emulsion with water is applied as a thin, high speed j'et between the work and the vcutting edge of .the ito'ol -and the results of these operations demonstrate the superiority of .eur 'cutting oil compositions over conventional soluble .cutting oils.
We have employed a conventional soluble cutting oil in a water emulsion under conditions substantially the same as those in which the cutting liquid of our invention was employed. The conventional soluble cutting oil comprised 85 parts by weight of a light refined lubricating oil, 14.88 parts by weight of the same commercial sodium mahogany sulfonate mixture employed in the compositions of our invention and 0.12 parts by weight of a rust inhibiting agent (Alkylamine Isoamyl Octyl Orthophosphate). The lubricating oil of the conventional soluble oil had the following inspection data:
The soluble cutting oil of ourinvention described in the example above and the conventional soluble cutting oil were similarly employedas 5 weight percent emulsions in water in the high speed jet method of applying a cutting liquid. The cutting compositions were used in lathe tests on A151 4140 mill annealed steel using a high speed steel 6 tool (shape: 1 0 -'1-2" -8--106-6 R). in these tests thecutting compositions were directed in the form ot' a thin jet at a velocity of about 246 feet p'er'second and 0.125 gallon per minute into the angle between the work and the tool. The thin jet was obtained by passing the cutting composition through a small orifice (0.0183 inch) --in a nozzle which Was mounted on the carriage of the lathe. The cutting compositions were supplied ;to the nozzle at a temperature of about to F. under a pressure of 400 pounds per square inch. The depth 'of cut was 0.088 inch and the feed was 0.011 inch per revolution. The results of the lathe tests in terms of actual tool life and adjusted tool life (derived in the manner hereinafter described) are given in the table below.
Results of tool life testsof soluble cutting oils (in '5 vol. percent emulsions with water) Cutting Conventional Tool Life, minutes Composition Cutting of the Composition Invention At 100 SFM: 1
Test N0. 1 292 109 Test; No. 2 129 99 Adjusted Tool Life Average 148. 1 138 At 140 SFM: 1
Test N0. 3 45 18 Test N0. 4 28 14 Test N0. 5 35 Adjusted Tool Life Average 30.2 22
1 SFM=surface feet per minute.
In lathe tests such as those described above, a problem arises in interpreting the tool life results due to unavoidable differences in the machineability of the various steel specimens. Consequently, it is desirable to adjust the test results for the differences in the steel specimens'where possible. A method of adjusing the results is by the calculation of adjusted tool life values such as those presented in the table above. These are obtained as follows: For a particular steel a large number of determinations of the dry tool life of different specimens of the steel are taken and an average value is calculated. For the A181 4140 steel of these tests, at a speed of 140 S. F. M. a dry life value of approximately 1.4 minutes was obtained. This factor which is in effect a machineability rating of the steel, is then used in the following formula to obtain the adjusted tool life for a specimen of this particular steel at any cutting speed.
1.4 X observed tool life Tool life without oil at 1 10 S. F. M.
(All tool life values being in minutes) In each test of a cutting oil a determination is made of dry tool life at 140 S. F. M. for the particular steel specimen being used and of the tool life with the cutting liquid being tested. The adjusted tool life which can then be obtained by the formula furnishes a reliable basis for comparing the efficiency of the various cutting oils by compensating for the machineability of the particular steel specimen. In the table above, the adjusted tool life values are given as the average of adjusted tool life values for the tests made at the same cutting speeds.
The results of the abovedescribed lathe tests show markedly increased tool life for the cutting compositions of our invention as compared with the conventional cutting composition. The superiority is shown in the actual tool life values as well as the adjusted tool life values and at both cutting speeds employed in the tests.
Although the cutting liquid compositions of the invention are particularly adapted for application as a thin, high speed jet, as described herein, it should be understood that they are also useful and have important advantages when applied as cutting liquids by other methods, for example, by the conventional overhead method of application.
Adjusted tool life- Obviously many modifications and variations of the indeparting from the spirit and scope thereof and therefore only such limitations should be imposed as are indicated in the appended claims.
We claim:
1. In a method of working metal in which a thin, high speed jet of cutting liquid is directed at a high velocity between the tool and the work, the improvement which comprises using as the cutting liquid an emulsion corn prising a major amount of water and a minor amount of an emulsifiable cutting oil comprising from about to 40 percent by weight of an oil-in-water emulsifying agent and from about 60 to 85 percent by weight of a mineral lu- I about 15 to 40 percent by Weight of an oil-soluble sulfonate oil-in-water emulsifying agent and from about 60 to 85 percent by weight of a mineral lubricating oil thickened by the addition of a water-insoluble metal soap of a saturated fatty acid, the amount of said soap being sutdcient to produce a thickened oil of grease consistency having an apparent viscosity at 77 F. greater than about 5 poises at a shear rate of 200 reciprocal seconds.
3. In a method of working metal in which a thin, high speed jet of cutting liquid is directed at a high velocity between the tool and the work, the improvement which comprises using as the cutting liquid an emulsion comprising a major amount of water and from about 5 to volume percent of an emulsifiable cutting oil comprising from about 15 to 40 percent by weight of sodium mahogany sulfonate and from about 60 to 85 percent by weight of a thickened mineral oil having the consistency .of a semi-fluid grease and an apparent viscosity at 77 F. greater than about 5 poises at a shear rate of 200 reciprocal seconds, s'aid thickened mineral oil. comprising a mineral lubricating oil having a Saybolt Universal viscosity at 210 F. below about 250 seconds and from about 4 to 40 percent by weight of a thickening agent composed of a water-insoluble metal soap of a fatty material which yields predominantly saturated fatty acids having from about 10 to 24 carbon atoms.
4. A soluble cutting oilcomprising from about 15 to 40 percent by weight of an oil-in-water emulsifying agent and from about to percent by weight of a mineral lubricating oil thickened by the addition of a water-insoluble metal soap of a saturated fatty acid, the amount of said soap being suflicient to thicken said oil to a grease consistency.
5.. A soluble cutting oil comprising from about 15 to 40 percent by weight of an oil soluble sulfonate oil-inwater emulsifyingagent and from about 60 to 85 percent by weight of a mineral lubricating oil thickened by the addition of a water-insoluble metal soap of a saturated fatty acid, the amount of said soap being sufficient to "produce a thickened oil of grease consistency having an apparent viscosity at 77 F. greater than about 5 poises at a shear rate of 200 reciprocal seconds.
6. A soluble cutting oil comprising from about 15 to j 40 percent by weight of sodium mahogany sulfonate and from about 60 to 85 percent by weight of a thickened mineral oil having the consistency of a semi-fluid grease and an apparent viscosity at 77 F. greater than about 5 poises at 200 reciprocal seconds, said thickened mineral oil comprising a mineral lubricating oil having a Saybolt Universal viscosity at 210 F. below about 250 seconds 7 and from about 4 to 40 percent by weight of a thickening agent composed of a water-insoluble metal soap of a fatty material which yields predominantly saturated fatty acids having from about 10 to 24 carbon atoms.
References Cited in the file of this patent UNITED STATES PATENTS 2,001,108 Parker May 14, 1935 2,214,634 Dombrow Sept. 10, 1940 2,653,517 Pigott Sept. 29, 1953 UNITED STATES PATENT OFFICE I CERTIFICATE OF CORRECTION PstentNo. 2,818,386 December 31, 1957 Elliott 5, Francis et en,
It is hereby certified that error appears in the printed specification of the above numbered patent requiring correction and. that the said Letters Patent should read as corrected below.
Column 1, line 25, for "floating" read flooding column '7, line 22, for "comprising" read comprises e Signed and sealed this 18th day of February 1958a (SEAL) Attest: KARL Hg AXLINE ROBERT C. WATSON Commissioner of Patents Attesting Officer
Claims (1)
1.IN A METHOD OF WORKING METAL IN WHICH A THIN, HIGH SPEED JET OF CUTTING LIQUID IS DIRECTED AT A HIGH VELOCITY BETWEEN THE TOOL AND THE WORK, THE IMPROVEMENT WHICH COMPRISES USING AS THE CUTTING LIQUID AN EMULSION COMPRISING A MAJOR AMOUNT OF WATER AND A MINOR AMOUNT OF AN EMULSIFIABLE CUTTING OIL COMPRISING FROM ABOUT 15 TO 40 PERCENT BY WEIGHT OF AN OIL-IN-WATER EMULSIFYING AGENT AND FROM ABOUT 60 TO 85 PERCENT BY WEIGHT OF A MINERAL LUBRICATING OIL THICKENED BY THE ADDITION OF A WATER-INSOLUBLE METAL SOAP OF A STAURATED FATTY ACID, THE AMOUNT OF SAID SOAP BEING SUFFICIENT TO THICKEN SAID OIL TO A GREASE CONSISTENCY.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US398634A US2818386A (en) | 1953-12-16 | 1953-12-16 | Soluble cutting oil comprising thickened oil and method of applying the same |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US398634A US2818386A (en) | 1953-12-16 | 1953-12-16 | Soluble cutting oil comprising thickened oil and method of applying the same |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2818386A true US2818386A (en) | 1957-12-31 |
Family
ID=23576150
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US398634A Expired - Lifetime US2818386A (en) | 1953-12-16 | 1953-12-16 | Soluble cutting oil comprising thickened oil and method of applying the same |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2818386A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2968999A (en) * | 1957-12-31 | 1961-01-24 | Ernest J Breton | Process for cutting metal employing amorphous silica |
| US3640856A (en) * | 1969-01-27 | 1972-02-08 | Chevron Res | Polybutene containing soluble oils |
| US3652415A (en) * | 1969-01-06 | 1972-03-28 | Frank E Bergeron | Lubricating compound |
| US3652414A (en) * | 1969-01-06 | 1972-03-28 | Frank E Bergeron | Anti-seize lubricating compound |
| US3953339A (en) * | 1973-09-14 | 1976-04-27 | Diamond Shamrock Corporation | Coning oil |
| WO1998008921A1 (en) * | 1996-08-28 | 1998-03-05 | Henkel Kommanditgesellschaft Auf Aktien | Use of bismuth compounds in cooling lubricants |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2001108A (en) * | 1931-07-06 | 1935-05-14 | Standard Oil Co California | Stabilized hydrocarbon oil |
| US2214634A (en) * | 1938-05-21 | 1940-09-10 | Nat Oil Prod Co | Cutting oil |
| US2653517A (en) * | 1951-05-29 | 1953-09-29 | Gulf Research Development Co | Method of applying cutting liquids |
-
1953
- 1953-12-16 US US398634A patent/US2818386A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2001108A (en) * | 1931-07-06 | 1935-05-14 | Standard Oil Co California | Stabilized hydrocarbon oil |
| US2214634A (en) * | 1938-05-21 | 1940-09-10 | Nat Oil Prod Co | Cutting oil |
| US2653517A (en) * | 1951-05-29 | 1953-09-29 | Gulf Research Development Co | Method of applying cutting liquids |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2968999A (en) * | 1957-12-31 | 1961-01-24 | Ernest J Breton | Process for cutting metal employing amorphous silica |
| US3652415A (en) * | 1969-01-06 | 1972-03-28 | Frank E Bergeron | Lubricating compound |
| US3652414A (en) * | 1969-01-06 | 1972-03-28 | Frank E Bergeron | Anti-seize lubricating compound |
| US3640856A (en) * | 1969-01-27 | 1972-02-08 | Chevron Res | Polybutene containing soluble oils |
| US3953339A (en) * | 1973-09-14 | 1976-04-27 | Diamond Shamrock Corporation | Coning oil |
| WO1998008921A1 (en) * | 1996-08-28 | 1998-03-05 | Henkel Kommanditgesellschaft Auf Aktien | Use of bismuth compounds in cooling lubricants |
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