US3408297A - Corrosion-resistant soluble oil composition - Google Patents
Corrosion-resistant soluble oil composition Download PDFInfo
- Publication number
- US3408297A US3408297A US530317A US53031766A US3408297A US 3408297 A US3408297 A US 3408297A US 530317 A US530317 A US 530317A US 53031766 A US53031766 A US 53031766A US 3408297 A US3408297 A US 3408297A
- Authority
- US
- United States
- Prior art keywords
- oil
- soluble
- rust
- acids
- oils
- 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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- 239000000203 mixture Substances 0.000 title claims description 23
- 230000007797 corrosion Effects 0.000 title description 7
- 238000005260 corrosion Methods 0.000 title description 7
- 239000003921 oil Substances 0.000 claims description 45
- 239000002253 acid Substances 0.000 claims description 13
- 239000003995 emulsifying agent Substances 0.000 claims description 12
- 150000007513 acids Chemical class 0.000 claims description 10
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Chemical class C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 8
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Chemical class O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 claims description 8
- 150000004985 diamines Chemical class 0.000 claims description 8
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Chemical class OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 claims 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 claims description 6
- 229910052708 sodium Inorganic materials 0.000 claims description 6
- 239000011734 sodium Substances 0.000 claims description 6
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical class CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 4
- 150000003460 sulfonic acids Chemical class 0.000 claims description 4
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Chemical class CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Chemical class CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Chemical class CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 3
- 239000005642 Oleic acid Chemical class 0.000 claims description 3
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Chemical class CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Chemical class CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 3
- 239000002480 mineral oil Substances 0.000 claims description 3
- 235000010446 mineral oil Nutrition 0.000 claims description 3
- 159000000001 potassium salts Chemical class 0.000 claims description 3
- XLYOFNOQVPJJNP-PWCQTSIFSA-N Tritiated water Chemical compound [3H]O[3H] XLYOFNOQVPJJNP-PWCQTSIFSA-N 0.000 claims 1
- 235000019198 oils Nutrition 0.000 description 41
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 24
- -1 amido diamine Chemical class 0.000 description 21
- 125000004432 carbon atom Chemical group C* 0.000 description 15
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical compound OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 239000000654 additive Substances 0.000 description 7
- 125000001931 aliphatic group Chemical group 0.000 description 7
- 239000002585 base Substances 0.000 description 7
- 239000007822 coupling agent Substances 0.000 description 7
- 238000005520 cutting process Methods 0.000 description 7
- 150000002462 imidazolines Chemical class 0.000 description 7
- 239000003112 inhibitor Substances 0.000 description 7
- 230000002401 inhibitory effect Effects 0.000 description 7
- 241000158728 Meliaceae Species 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- MTNDZQHUAFNZQY-UHFFFAOYSA-N imidazoline Chemical compound C1CN=CN1 MTNDZQHUAFNZQY-UHFFFAOYSA-N 0.000 description 6
- 238000000227 grinding Methods 0.000 description 5
- 239000010688 mineral lubricating oil Substances 0.000 description 5
- 238000005507 spraying Methods 0.000 description 5
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
- 229910001018 Cast iron Inorganic materials 0.000 description 4
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 4
- 229910052783 alkali metal Inorganic materials 0.000 description 4
- 150000001340 alkali metals Chemical class 0.000 description 4
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 150000003871 sulfonates Chemical class 0.000 description 4
- 229910000975 Carbon steel Inorganic materials 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 230000000844 anti-bacterial effect Effects 0.000 description 3
- 239000003899 bactericide agent Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000011521 glass Substances 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- 239000010687 lubricating oil Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 125000005608 naphthenic acid group Chemical group 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 229920006395 saturated elastomer Polymers 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- 239000003784 tall oil Substances 0.000 description 3
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 150000001342 alkaline earth metals Chemical class 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 239000002173 cutting fluid Substances 0.000 description 2
- 239000010730 cutting oil Substances 0.000 description 2
- JMGZBMRVDHKMKB-UHFFFAOYSA-L disodium;2-sulfobutanedioate Chemical compound [Na+].[Na+].OS(=O)(=O)C(C([O-])=O)CC([O-])=O JMGZBMRVDHKMKB-UHFFFAOYSA-L 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- 150000002334 glycols Chemical class 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 230000003405 preventing effect Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- 238000010998 test method Methods 0.000 description 2
- RULKYXXCCZZKDZ-UHFFFAOYSA-N 2,3,4,5-tetrachlorophenol Chemical compound OC1=CC(Cl)=C(Cl)C(Cl)=C1Cl RULKYXXCCZZKDZ-UHFFFAOYSA-N 0.000 description 1
- PINLNYXXCCIRAF-UHFFFAOYSA-L C1(=CC=CC=C1)S(=O)(=O)[O-].C=CC.C=CC.[Ca+2].C1(=CC=CC=C1)S(=O)(=O)[O-] Chemical compound C1(=CC=CC=C1)S(=O)(=O)[O-].C=CC.C=CC.[Ca+2].C1(=CC=CC=C1)S(=O)(=O)[O-] PINLNYXXCCIRAF-UHFFFAOYSA-L 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- 241000529895 Stercorarius Species 0.000 description 1
- RAHZWNYVWXNFOC-UHFFFAOYSA-N Sulphur dioxide Chemical compound O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 description 1
- RSWGJHLUYNHPMX-ONCXSQPRSA-N abietic acid Chemical compound C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C(O)=O RSWGJHLUYNHPMX-ONCXSQPRSA-N 0.000 description 1
- 238000010306 acid treatment Methods 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 150000008064 anhydrides Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- MKFUUBCXQNCPIP-UHFFFAOYSA-L calcium;2,3-di(nonyl)naphthalene-1-sulfonate Chemical compound [Ca+2].C1=CC=C2C(S([O-])(=O)=O)=C(CCCCCCCCC)C(CCCCCCCCC)=CC2=C1.C1=CC=C2C(S([O-])(=O)=O)=C(CCCCCCCCC)C(CCCCCCCCC)=CC2=C1 MKFUUBCXQNCPIP-UHFFFAOYSA-L 0.000 description 1
- BCBMWLMZWGMGOM-UHFFFAOYSA-L calcium;2,3-didodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC(S([O-])(=O)=O)=C1CCCCCCCCCCCC.CCCCCCCCCCCCC1=CC=CC(S([O-])(=O)=O)=C1CCCCCCCCCCCC BCBMWLMZWGMGOM-UHFFFAOYSA-L 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical group 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 239000008233 hard water Substances 0.000 description 1
- CVMNKHMWNZSNLW-UHFFFAOYSA-N hexane-1,6-diol;2-(2-hydroxyethoxy)ethanol Chemical compound OCCOCCO.OCCCCCCO CVMNKHMWNZSNLW-UHFFFAOYSA-N 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 150000002646 long chain fatty acid esters Chemical class 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 150000002989 phenols Chemical class 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000010791 quenching Methods 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002195 soluble material Substances 0.000 description 1
- 238000000638 solvent extraction Methods 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 125000003258 trimethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 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
- C10M173/00—Lubricating compositions containing more than 10% water
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
-
- 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
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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
- C10M2207/021—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
-
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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
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
- C10M2207/027—Neutral salts 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
- C10M2207/046—Hydroxy ethers
-
- 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
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- 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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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/16—Naphthenic acids
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/18—Tall oil acids
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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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/20—Rosin acids
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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
- 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
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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
- 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
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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
- 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
- C10M2209/108—Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified
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Definitions
- Soluble oils are used as cutting, spraying and rust preventing oils and generally include, besides the base hydrocarbon oil, a small amount of water, an emulsifying agent and a corrosion or rust inhibitor.
- One important function of cutting fluids is cooling.
- a cutting fluid which inhibits corrosion of both work material and the tool is necessitated.
- Emulsifiable cutting oils which are satisfactory for use with alloy steels frequently lack sufficient rust-inhibiting properties for satisfactory use with cast iron and low carbon steels.
- the fortification of a soluble oil with rust inhibitors is complicated.
- a rust inhibitor must demonstrate a solubility and compatibility with the neat soluble oil. Many of the otherwise acceptable rust inhibiting additives cause the product to gel or to separate upon standing. Furthermore, such additives often require addition in high concentration or have a relativley high degree to toxicity.
- novel soluble oils which contain a mineral lubricating oil as the base or major component, one or more emulsifiers and small amounts of each of the following oil-soluble materials A and B:
- R is an aliphatic hydrocarbon containing at least 6 and preferably 12 to 22 atoms, and R and R are divalent aliphatic hydrocarbon radicals of 2-8 carbon atoms, advantageously 2-4 carbon atoms.
- the members of this class of diamines are cationic and possess a primary and a secondary amine group in addition to the acyl radical attached to the amido nitrogen.
- the acyl radical in the above formula may be straight or branched chain, saturated or unsaturated, and, if desired, may contain nondeleterious substituents.
- the acyl radical is preferably a carboxylic acid residue of a high molecular weight acid, such as oleic, stearic, palmitic, linoleic, ricinoleic, lauric,
- R and R groups may also be substituted but preferably are polymethylene groups.
- Diamine 257 which has the general structure described above, wherein R and R are trimethylene and R is a straight chain unsaturated hydrocarbon radical derived from corn oil and having about 16-18 carbon atoms.
- Diamine 257 is well known in the art, having been described in US. Patent No. 3,024,259 to David D. Sheldahl and Thomas O. Counts, and is characterized by having an acid number of less than 5, an average amine equivalent weight of 210, and one primary and one secondary basic amine group. It has a density of 0.935 at 25 C. and is a viscous liquid or fluid paste.
- I include a component C, as designated below.
- R is an aliphatic hydrocarbon of at least 6, preferably of 10-24 carbon atoms.
- R may be unsaturated, it is preferably saturated, and especially an alkylene radical such as the saturated residue of an olefin polymer.
- the sulfo group be attached to a carbon atom which is beta to the -COOX group.
- X in the formula may be a hydrocarbon group, preferably alkyl of up to about 6 carbon atoms or X may be an alkali metal or ammonium, including organic ammonium, ion.
- the two Xs together may be an alkaline earth metal, or the Xs may be absent to give an anhydride group.
- the R and X groups are such as to provide an oil-soluble sulfo-succinate.
- the preparation of the sulfosuccinate compounds of this invention is described in US. Patent 2,028,091 to Jaegers.
- the R-components are such as to give an agent which is soluble, at least in additive amounts, in the base mineral oil.
- the above-mentioned components can be employed in the following approximate concentrations: about 0.25-5 weight percent of the fatty amido diamine; about 0.25-5 weight percent of the sulfo-succinate; about 0.25-6 weight percent of the substituted imidazoline.
- the exact proportions of the various ingredients of the character described above may vary according to the specific operation in which the soluble oil will be used. Ordinarily, however, the soluble oil will include about 40-95 weight percent mineral lubricating oil base, about 4-20 weight percent of one or more emulsifiers, about 1-5 weight percent of coupling agents, about 1-10 total weight percent of the A, B and C components designated above, and a small amount, for instance, about 1-5 weight percent, of water. Other ingredients, such as bactericides, foam inhibitors, etc., may be present, for example, in amounts of about 1-10 percent by weight.
- the oils used as the base and major component in the emulsifiablc oils of the present invention are mineral lubricating oils,
- the oils used including the petroleum lubricating oils such as refined coastal oils and refined Mid-Continent oils.
- the oils may be refined by acid treatment, solvent extraction, hydrogenation or other procedures.
- various oils of lubricating viscosity can be used in the products of my invention, I prefer to use a substantially anhydrous lubricating oil with a viscosity from about 50-1200 SUS at 100 F., preferably 50150 SUS at 100 F. I have had my best results with an acid-refined coastal oil with a viscosity of about 100 SUS at 100 F.
- I may add a coupling agent.
- the function of such an agent is to couple the aqueous portion of the neat soluble oil to the continuous oil phase to give a clear product and also to couple the neat oil to diluent water added to provide an emulsified soluble oil suitable for use.
- the well-known coupling agents usable in the composition are the aliphatic ether-alcohol compounds containing from about 1-30 carbon atoms, for instance, diethylene glycol; the ether complexes of ethyl Cellosolves, Carbitol, and butyl Cellosolve; the polyether glycols with terminal ether groups; and the polyoxyalkylene glycols, as well as ethylene glycol, propylene glycol, etc.
- One or more of the above coupling agents can be used either alone or in mixtures, and in various amounts. Generally about 0.5-5 percent, preferably about 1-3 weight percent are employed.
- emulsifiers known in the art may be used in the soluble oils of this invention.
- EXAMPLE I 82.35 parts coastal mineral lubricating oil with a viscosity of 100 SUS at 100 F. is charged into a kettle containing 6.0 parts ofsodium mahogany sulfonate (60% sodium mahogany sulfon'ate in lube oil), and the mixture is heated and stirred at a temperature of about l40l50 F. 4.0 parts mixed tall oil and rosin acids and 0.55 part sodium hydroxide dissolved in 2.25 parts water is added followed by 1.2 parts hexylene glycol, 1.0 part of Diamine 257, 1.0 part tetrapropenyl sodium sulfo-succinate and 1.35 parts of tallow imidazoline. The mixture is agitated using an intense mixer for a period of about 30 minutes.
- sulfonates used herein include the salts of synthetic sulfonic acids and petroleum mahogany sulfonic acids; and these may be exemplified by ammonium mahogany sulfonates, calcium dipropylene benzene sulfonate, calcium mahogany petroleum sulfonates, calcium dinonyl naphthalene sulfonate, calcium didodecylbenzene sulfonate, sodium mahogany sulfonates, etc.
- oil-soluble emulsifiers employed may be, for instance, saponified phenols or naphthenic acids, alkali metal, e.g., sodium and potassium, rosin and rosin acid soaps, amine salts of rosin acids, oleates, etc.
- Emulsifiers of the anionic type and the nonionic type may be used, such as, for examples, liquids or solids selected from the group consisting of alkaryl polyoxyalkylene oxyalkanols, and polyoxyethylene derivatives of hexitol anhydride partial long chain fatty acid esters. In general, about 2-10 percent by weight of emulsifier is usually employed.
- Additional optional additives may be used as aforementioned.
- a bactericide I prefer to incorporate tetrachlorophenol; however, various compatible bactericides can be used. Moreover, they can be used either alone or in combination, for instance, in an amount of about 0.5-1 percent by weight. Other agents in small amounts may be present including, for instance, additional corrosion inhibitors.
- compositions of'this invention are frequently dispersed in about 1-20 or more Rust test procedure A
- Freshly out, clean, dry cast iron chips are sifted over an mesh screen to remove fines and dust.
- Approximately 40 grams of the screened 'chips are placed in a clean, dry ml. beaker.
- a 5 percent soluble-oil emulsion (prepared with ppm. CaCO hard water) is poured over the chips.
- the chips are agitated for one minute at 5 minute intervals.
- Five minutes after the third agitation the beaker is covered with a small watch glass and inverted, allowing the emulsion to drain from the chips.
- the inverted beaker, chips and watch glass are placed on clean paper towels.
- the "beaker is drawn to the edge of the watch glass (but retaining the chips inside the beaker) so as to permit continued drainage and the combination is allowed to stand undisturbed for 24 hours.
- the beaker is removed and the chips are observed for the presence of rust,
- Test Result 1 No rust. 3 Heavy rust. a Very heavy rust. 4 Trace rust. Medium rust. Light rust.
- the fatty amido diamine and the imidazoline were effective by themselves, but often caused a separation of the product upon standing, or caused the product to gel.
- the sulfo-succinate was added in combination with the fatty amido diamine and the imidazoline. When all three additives were used in suificient concentrations, excellent corrosion protection was obtained and, moreover, no product separation or gelation occurred.
- the effectiveness of the combination of the fatty amido diamine and substituted imidazoline as low concentrations is also shown by the data. Also, the combination of inhibitors was very effective in oils B, C, D and E, but the amounts of inhibitors had to be varied.
- An emulsifiable oil composition consisting essentially of a mineral oil base as the major component, an emulsifier selected from the group consisting of the sodium and potassium salts of naphthenic acids, oleic acid, rosin acids, tall oil acids and oil-soluble sulfonic acids, about 1-5 weight percent water, about 0.25-5 percent of an oil-soluble fatty amido diamine having the structural formula:
- R is an aliphatic hydrocarbon containing at least 6 carbon atoms, and R and R are divalent aliphatic hydrocarbons of 2-8 carbon atoms, about 0.25-6 weight percent of an oil-soluble, substituted imidazoline having the structural formula:
- R is a monovalent aliphatic hydrocarbon containing at least 6 carbon atoms, said amounts being sufficient to provide rust inhibiting properties, and about earth metal and ammonium salts of sulfo-succinic acid having the structure:
- R is aliphatic hydrocarbon of about 6 to 24 carbon atoms.
- composition of claim 1 wherein the emulsifier is an oil-soluble, aromatic sulfonate.
- composition of claim 1 wherein is added about 0.5-5 percent by weight of a coupling agent.
- An emulsifiable oil composition consisting essentially of a mineral lubricating oil base with a viscosity of about 50-100 SUS at F., about 0.5-3.0 weight percent of a coupling agent, about 2-10 weight percent of an aromatic sulfonate emulsifier, about 0.54 weight percent water, about 0.25-5 percent weight of an oilsoluble fatty amido diamine having the structural formula:
- R is an aliphatic hydrocarbon containing at least 6 carbon atoms, and R and R are divalent aliphatic hydrocarbons of 2-8 carbon atoms, about 0.25-6 weight percent of an oil-soluble, substituted imidazoline having the structural formula:
- R is a monovalent aliphatic hydrocarbon containing at least 6 carbon atoms, and about 0.25-5 percent of an oil-soluble sulfo-succinate selected from the group consisting of alkali metal, alkaline earth metal and 7 I ammonium salts of sulfo-succinic acid having the structure:
- R is aliphatichydrocarbon of about 6 to 24 carbon atoms, said amounts being suificient to provide rustinhibiting properties.
- composition of claim 5 wherein the sulfo-succinate is a sodium salt of sulfo-succinic acid wherein R is tetrapropenyl.
- composition of claim 5 wherein the emulsifier is a mixture of an aromatic sulfonate and a salt selected from the group consisting of the sodium and potassium salts of naphthenic acids, oleic acid, rosin acids and tall DANIEL E. WYMAN, Primary Examiner.
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Description
United States Patent 3,408,297 CORROSION-RESISTANT SOLUBLE OIL COMPOSITION David B. Sheldahl, Griflith, Ind., assiguor to Sinclair Research, Inc., New York, N.Y., a corporation of Delaware No Drawing. Filed Feb. 28, 1966, Ser. No. 530,317 7 Claims. (Cl. 252-335) This invention relates to novel soluble oil compositions having rust-inhibiting properties. More particularly this invention pertains to novel hydrocarbon based emulsifiable oils exhibiting excellent rust-inhibiting properties as a result of the addition of a combination of corrosion inhibiting materials.
Soluble oils are used as cutting, spraying and rust preventing oils and generally include, besides the base hydrocarbon oil, a small amount of water, an emulsifying agent and a corrosion or rust inhibitor. One important function of cutting fluids is cooling. However, due to the increased use of cast iron and low carbon steels, a cutting fluid which inhibits corrosion of both work material and the tool is necessitated. Emulsifiable cutting oils which are satisfactory for use with alloy steels frequently lack sufficient rust-inhibiting properties for satisfactory use with cast iron and low carbon steels. The fortification of a soluble oil with rust inhibitors is complicated. To be an acceptable additive, a rust inhibitor must demonstrate a solubility and compatibility with the neat soluble oil. Many of the otherwise acceptable rust inhibiting additives cause the product to gel or to separate upon standing. Furthermore, such additives often require addition in high concentration or have a relativley high degree to toxicity.
It is an object of this invention to provide a soluble oil for cutting, spraying and grinding which contains a particularly effective combination of materials to inhibit corrosion and rust. Another object of this invention is to provide a soluble oil for cutting, spraying and grinding containing a particularly effective combination of materials that will not cause product separation or gelation, and may be added in economically desirable concentrations. A further object of this invention is to provide a soluble oil for cutting, spraying and grinding having excellent cooling and lubricating properties. It is a still further object of this invention to provide a non-volatile, toxicologically acceptable, soluble oil for cutting, spraying and grinding that can be used with cast iron or low carbon steels.
According to the invention, these desirable objectives are attained by novel soluble oils, which contain a mineral lubricating oil as the base or major component, one or more emulsifiers and small amounts of each of the following oil-soluble materials A and B:
(A) A fatty amido diamine having the structural formula:
wherein R is an aliphatic hydrocarbon containing at least 6 and preferably 12 to 22 atoms, and R and R are divalent aliphatic hydrocarbon radicals of 2-8 carbon atoms, advantageously 2-4 carbon atoms. The members of this class of diamines are cationic and possess a primary and a secondary amine group in addition to the acyl radical attached to the amido nitrogen. The acyl radical in the above formula may be straight or branched chain, saturated or unsaturated, and, if desired, may contain nondeleterious substituents. The acyl radical is preferably a carboxylic acid residue of a high molecular weight acid, such as oleic, stearic, palmitic, linoleic, ricinoleic, lauric,
and like acids. The R and R groups may also be substituted but preferably are polymethylene groups.
A particularly preferred fatty amido diamine is Diamine 257 which has the general structure described above, wherein R and R are trimethylene and R is a straight chain unsaturated hydrocarbon radical derived from corn oil and having about 16-18 carbon atoms. Diamine 257 is well known in the art, having been described in US. Patent No. 3,024,259 to David D. Sheldahl and Thomas O. Counts, and is characterized by having an acid number of less than 5, an average amine equivalent weight of 210, and one primary and one secondary basic amine group. It has a density of 0.935 at 25 C. and is a viscous liquid or fluid paste.
(B) A substituted imidazoline component having the structural formula:
ar H H wherein R is as defined above in connection with component A.
In order to provide preferred compositions which are especially stable, I include a component C, as designated below.
(C) A sulfo-succinate, often having the structural formula:
wherein R is an aliphatic hydrocarbon of at least 6, preferably of 10-24 carbon atoms. Although R may be unsaturated, it is preferably saturated, and especially an alkylene radical such as the saturated residue of an olefin polymer. It is also preferred that the sulfo group be attached to a carbon atom which is beta to the -COOX group. X in the formula may be a hydrocarbon group, preferably alkyl of up to about 6 carbon atoms or X may be an alkali metal or ammonium, including organic ammonium, ion. The two Xs together may be an alkaline earth metal, or the Xs may be absent to give an anhydride group. In any event the R and X groups are such as to provide an oil-soluble sulfo-succinate. The preparation of the sulfosuccinate compounds of this invention is described in US. Patent 2,028,091 to Jaegers.
In each of the components A, B and C, the R-components are such as to give an agent which is soluble, at least in additive amounts, in the base mineral oil.
The above-mentioned components can be employed in the following approximate concentrations: about 0.25-5 weight percent of the fatty amido diamine; about 0.25-5 weight percent of the sulfo-succinate; about 0.25-6 weight percent of the substituted imidazoline.
Since different metal cutting operations are employed in industry, the exact proportions of the various ingredients of the character described above may vary according to the specific operation in which the soluble oil will be used. Ordinarily, however, the soluble oil will include about 40-95 weight percent mineral lubricating oil base, about 4-20 weight percent of one or more emulsifiers, about 1-5 weight percent of coupling agents, about 1-10 total weight percent of the A, B and C components designated above, and a small amount, for instance, about 1-5 weight percent, of water. Other ingredients, such as bactericides, foam inhibitors, etc., may be present, for example, in amounts of about 1-10 percent by weight.
The oils used as the base and major component in the emulsifiablc oils of the present invention are mineral lubricating oils, The oils used including the petroleum lubricating oils such as refined coastal oils and refined Mid-Continent oils. The oils may be refined by acid treatment, solvent extraction, hydrogenation or other procedures. Although various oils of lubricating viscosity can be used in the products of my invention, I prefer to use a substantially anhydrous lubricating oil with a viscosity from about 50-1200 SUS at 100 F., preferably 50150 SUS at 100 F. I have had my best results with an acid-refined coastal oil with a viscosity of about 100 SUS at 100 F.
To improve the emulsifiability of the various components, I may add a coupling agent. The function of such an agent is to couple the aqueous portion of the neat soluble oil to the continuous oil phase to give a clear product and also to couple the neat oil to diluent water added to provide an emulsified soluble oil suitable for use. Among the well-known coupling agents usable in the composition are the aliphatic ether-alcohol compounds containing from about 1-30 carbon atoms, for instance, diethylene glycol; the ether complexes of ethyl Cellosolves, Carbitol, and butyl Cellosolve; the polyether glycols with terminal ether groups; and the polyoxyalkylene glycols, as well as ethylene glycol, propylene glycol, etc. One or more of the above coupling agents can be used either alone or in mixtures, and in various amounts. Generally about 0.5-5 percent, preferably about 1-3 weight percent are employed.
Various emulsifiers known in the art may be used in the soluble oils of this invention. I prefer to use an oil soluble aromatic sulfonate as, for instance, ammonium, alkali and alkaline earth metal aromatic sulfonates. The
. 4 parts of water, depending upon the particular application contemplated. Thus, where the resulting emulsion is to be used as a lubricant for grinding operations, for example, it has been found that about one part of the oil for each 20-80 parts of water, and particularly one part of the oil to 20'or parts of water, producesvery satisfactory results. For use in quenching operations, emulsions formed with one part of soluble oil per 20-40 parts of water have been found to be very advantageous. As a rolling mill oil, emulsions containing one part of the composition for each 5-20 parts of water effect very desirable results.
The following examples will serve to illustrate the present invention but are not to be considered limiting.
EXAMPLE I 82.35 parts coastal mineral lubricating oil with a viscosity of 100 SUS at 100 F. is charged into a kettle containing 6.0 parts ofsodium mahogany sulfonate (60% sodium mahogany sulfon'ate in lube oil), and the mixture is heated and stirred at a temperature of about l40l50 F. 4.0 parts mixed tall oil and rosin acids and 0.55 part sodium hydroxide dissolved in 2.25 parts water is added followed by 1.2 parts hexylene glycol, 1.0 part of Diamine 257, 1.0 part tetrapropenyl sodium sulfo-succinate and 1.35 parts of tallow imidazoline. The mixture is agitated using an intense mixer for a period of about 30 minutes.
. Several soluble oil compositions, listed in Table I were subjected to a rust test, Rust Test Procdure A, to determine their utility as rust-inhibiting cutting oils. Each of the soluble oil compositons is designed for a different metal cutting operation. None of the oils contained any sulfo-succinate substituted imidazoline or fatty amido diamine. The rust test procedure employed is described below:
Cellosoive Diethylene Glycol Hexylene Glycol Rosin Acids Mixed Tall Oil and Rosin Acids Sodium Hydroxide Potassium Hydroxide...
sulfonates used herein include the salts of synthetic sulfonic acids and petroleum mahogany sulfonic acids; and these may be exemplified by ammonium mahogany sulfonates, calcium dipropylene benzene sulfonate, calcium mahogany petroleum sulfonates, calcium dinonyl naphthalene sulfonate, calcium didodecylbenzene sulfonate, sodium mahogany sulfonates, etc. Other oil-soluble emulsifiers employed may be, for instance, saponified phenols or naphthenic acids, alkali metal, e.g., sodium and potassium, rosin and rosin acid soaps, amine salts of rosin acids, oleates, etc. Emulsifiers of the anionic type and the nonionic type may be used, such as, for examples, liquids or solids selected from the group consisting of alkaryl polyoxyalkylene oxyalkanols, and polyoxyethylene derivatives of hexitol anhydride partial long chain fatty acid esters. In general, about 2-10 percent by weight of emulsifier is usually employed.
Additional optional additives may be used as aforementioned. When using a bactericide, I prefer to incorporate tetrachlorophenol; however, various compatible bactericides can be used. Moreover, they can be used either alone or in combination, for instance, in an amount of about 0.5-1 percent by weight. Other agents in small amounts may be present including, for instance, additional corrosion inhibitors.
In use as soluble oil emulsions the compositions of'this invention are frequently dispersed in about 1-20 or more Rust test procedure A Freshly out, clean, dry cast iron chips are sifted over an mesh screen to remove fines and dust. Approximately 40 grams of the screened 'chips are placed in a clean, dry ml. beaker. A 5 percent soluble-oil emulsion (prepared with ppm. CaCO hard water) is poured over the chips. The chips are agitated for one minute at 5 minute intervals. Five minutes after the third agitation, the beaker is covered with a small watch glass and inverted, allowing the emulsion to drain from the chips. The inverted beaker, chips and watch glass are placed on clean paper towels. The "beaker is drawn to the edge of the watch glass (but retaining the chips inside the beaker) so as to permit continued drainage and the combination is allowed to stand undisturbed for 24 hours. The beaker is removed and the chips are observed for the presence of rust,
None of the soluble-oil compositions in Table I that were tested by the above procedure exhibited any rust preventing properties. The chips were badly rusted and fused together.
The same soluble-oil compositions were again given the identical rust test outlined above after addition singly and in combination of various amounts of Diamine 257, tetrapropenyl sodium sulfo-succinate, and
5 tallow imidazoline. The results are reported in Table II as follows:
TABLE II 0.25 to 5 weight percent of a member selected from the group consisting of the oil-soluble alkali metal, alkaline Additive, Parts by Weight Fatty Amldo Diamine Sulfo-Suecinate Substituted Imidazolin Test Result Fatty Amido Diamine Sulio-Succinate Substituted Imidazoline Test Result Fatty Amido Diamine SulIo-Succinate Substituted Imldazoline Test Result Fatty Amide Diamine... Sulio-Sucoiuate substitusteld Imidaz oline.
. l. 1. 0. 1. 35 Test Result Fatty Amldo Diamine.-. 3. 00 2.00 1. 00 Sulfo-Succinate Substituted Imldazoline- 4. 05 2. 70 1. Test Result 1 No rust. 3 Heavy rust. a Very heavy rust. 4 Trace rust. Medium rust. Light rust.
When added to Oil A, the fatty amido diamine and the imidazoline were effective by themselves, but often caused a separation of the product upon standing, or caused the product to gel. To improve the stability of the composition, the sulfo-succinate was added in combination with the fatty amido diamine and the imidazoline. When all three additives were used in suificient concentrations, excellent corrosion protection was obtained and, moreover, no product separation or gelation occurred. The effectiveness of the combination of the fatty amido diamine and substituted imidazoline as low concentrations is also shown by the data. Also, the combination of inhibitors was very effective in oils B, C, D and E, but the amounts of inhibitors had to be varied.
What is claimed:
1. An emulsifiable oil composition consisting essentially of a mineral oil base as the major component, an emulsifier selected from the group consisting of the sodium and potassium salts of naphthenic acids, oleic acid, rosin acids, tall oil acids and oil-soluble sulfonic acids, about 1-5 weight percent water, about 0.25-5 percent of an oil-soluble fatty amido diamine having the structural formula:
0 H H R ll 1% R-1 IR I'HI wherein R is an aliphatic hydrocarbon containing at least 6 carbon atoms, and R and R are divalent aliphatic hydrocarbons of 2-8 carbon atoms, about 0.25-6 weight percent of an oil-soluble, substituted imidazoline having the structural formula:
H N-l-H H E I I wherein R is a monovalent aliphatic hydrocarbon containing at least 6 carbon atoms, said amounts being sufficient to provide rust inhibiting properties, and about earth metal and ammonium salts of sulfo-succinic acid having the structure:
wherein R is aliphatic hydrocarbon of about 6 to 24 carbon atoms.
2. The composition of claim 1 wherein the emulsifier is an oil-soluble, aromatic sulfonate.
3. The composition of claim 1 wherein is added about 0.5-5 percent by weight of a coupling agent.
4. An emulsifiable oil composition consisting essentially of a mineral lubricating oil base with a viscosity of about 50-100 SUS at F., about 0.5-3.0 weight percent of a coupling agent, about 2-10 weight percent of an aromatic sulfonate emulsifier, about 0.54 weight percent water, about 0.25-5 percent weight of an oilsoluble fatty amido diamine having the structural formula:
o R -'-I IRiIIRzI I--H wherein R is an aliphatic hydrocarbon containing at least 6 carbon atoms, and R and R are divalent aliphatic hydrocarbons of 2-8 carbon atoms, about 0.25-6 weight percent of an oil-soluble, substituted imidazoline having the structural formula:
wherein R is a monovalent aliphatic hydrocarbon containing at least 6 carbon atoms, and about 0.25-5 percent of an oil-soluble sulfo-succinate selected from the group consisting of alkali metal, alkaline earth metal and 7 I ammonium salts of sulfo-succinic acid having the structure:
wherein R is aliphatichydrocarbon of about 6 to 24 carbon atoms, said amounts being suificient to provide rustinhibiting properties.
5. The composition of claim 3 in which the coupling agent is an aliphatic ether-alcohol of up to about 30 carbon atoms.
6. The composition of claim 5 wherein the sulfo-succinate is a sodium salt of sulfo-succinic acid wherein R is tetrapropenyl.
7. The composition of claim 5 wherein the emulsifier is a mixture of an aromatic sulfonate and a salt selected from the group consisting of the sodium and potassium salts of naphthenic acids, oleic acid, rosin acids and tall DANIEL E. WYMAN, Primary Examiner.
20 W. H. CANNON, C. F. DEES, Assistant Examiners;
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No. 3,408,297 October 29, 1968 David B. Sheldahl It is certified that error appears in the above identified patent and that said Letters Patent are hereby corrected as shown below:
Column 1, line 34, "to" should read of Column 2 lines 17 to 24, the formula should appear as shown below:
I? //N-CH RC\ N-CH I I H H Column 3, line 5, "including" should read include Column 4, line 30, "procdure" should read procedure Columns 5 and 6, TABLE II, seventh column, last line thereof, "(2)" should read (3) Column 6, line 51 "50-100 SUS at 150 should read 50-150 SUS at 100 F.
Signed and sealed this 17th day of March 1970.
(SEAL) Attest:
EDWARD M.FLETCHER,JR. WILLIAM E. SCHUYLER, JR. Attesting Officer Commissioner of Patents
Claims (1)
1. AN EMULSIFIABLE OIL COMPOSITION CONSISTING ESSENTIALLY OF A MINERAL OIL BASE AS THE MAJOR COMPONENT, AN EMULSIFIER SELECTED FROM THE GROUP CONSISTING OF THE SODIUM AND POTASSIUM SALTS OF NAPHTHENIC ACIDS, OLEIC ACID, ROSIN ACIDS, TALL OIL ACIDS AND OIL-SOLUBLE SULFONIC ACIDS, ABOUT 1-5 WEIGHT PERCENT WATER, ABOUT 0.25-5 PERCENT OF AN OIL-SOLUBLE FATTY AMIDO DIAMINE HAVING THE STRUCTURAL FORMULA:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US530317A US3408297A (en) | 1966-02-28 | 1966-02-28 | Corrosion-resistant soluble oil composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US530317A US3408297A (en) | 1966-02-28 | 1966-02-28 | Corrosion-resistant soluble oil composition |
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| Publication Number | Publication Date |
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| US3408297A true US3408297A (en) | 1968-10-29 |
Family
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| US530317A Expired - Lifetime US3408297A (en) | 1966-02-28 | 1966-02-28 | Corrosion-resistant soluble oil composition |
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Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US3957662A (en) * | 1972-08-08 | 1976-05-18 | Hoffmann-La Roche Inc. | Pharmaceutical lubricants |
| US4375987A (en) * | 1981-11-23 | 1983-03-08 | W. R. Grace & Co. | Additive combination for hydraulic cement compositions |
| US4556496A (en) * | 1984-03-28 | 1985-12-03 | Chevron Research Company | Refrigeration lubricating oil containing dialkyl sulfosuccinate |
| US4869838A (en) * | 1988-08-25 | 1989-09-26 | Exxon Research And Engineering Company | Bis imidazole ethers as metal deactivators |
| US5169545A (en) * | 1991-08-30 | 1992-12-08 | Mobil Oil Corporation | Metal phenate sulfides |
| US5227082A (en) * | 1991-12-23 | 1993-07-13 | Exxon Research And Engineering Company | Lubricating oil having improved rust inhibition and demulsibility |
| WO1995019413A1 (en) * | 1994-01-12 | 1995-07-20 | Unilever N.V. | Lubricant compositions |
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| US2468163A (en) * | 1948-01-10 | 1949-04-26 | Petrolite Corp | Processes for preventing corrosion and corrosion inhibitors |
| US2493483A (en) * | 1948-04-26 | 1950-01-03 | Shell Dev | Marine engine lubricant |
| US2741597A (en) * | 1952-03-08 | 1956-04-10 | Texas Co | Manufacture of alkenyl succinic acid |
| FR1123818A (en) * | 1955-03-19 | 1956-09-28 | Exxon Standard Sa | Anti-rust compositions |
| US2788329A (en) * | 1953-12-02 | 1957-04-09 | American Cyanamid Co | Surface active composition containing a corrosion inhibitor |
| US2887504A (en) * | 1956-09-19 | 1959-05-19 | American Cyanamid Co | Dialkyl esters of sulfodicarboxylic acids |
| US2913410A (en) * | 1955-08-11 | 1959-11-17 | Gulf Oil Corp | Soluble oil |
| US3024259A (en) * | 1957-07-30 | 1962-03-06 | Sinclair Refining Co | Corrosion inhibited composition |
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| US2468163A (en) * | 1948-01-10 | 1949-04-26 | Petrolite Corp | Processes for preventing corrosion and corrosion inhibitors |
| US2493483A (en) * | 1948-04-26 | 1950-01-03 | Shell Dev | Marine engine lubricant |
| US2741597A (en) * | 1952-03-08 | 1956-04-10 | Texas Co | Manufacture of alkenyl succinic acid |
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| US3957662A (en) * | 1972-08-08 | 1976-05-18 | Hoffmann-La Roche Inc. | Pharmaceutical lubricants |
| US4375987A (en) * | 1981-11-23 | 1983-03-08 | W. R. Grace & Co. | Additive combination for hydraulic cement compositions |
| US4556496A (en) * | 1984-03-28 | 1985-12-03 | Chevron Research Company | Refrigeration lubricating oil containing dialkyl sulfosuccinate |
| US4869838A (en) * | 1988-08-25 | 1989-09-26 | Exxon Research And Engineering Company | Bis imidazole ethers as metal deactivators |
| US5169545A (en) * | 1991-08-30 | 1992-12-08 | Mobil Oil Corporation | Metal phenate sulfides |
| US5227082A (en) * | 1991-12-23 | 1993-07-13 | Exxon Research And Engineering Company | Lubricating oil having improved rust inhibition and demulsibility |
| WO1995019413A1 (en) * | 1994-01-12 | 1995-07-20 | Unilever N.V. | Lubricant compositions |
| AU680095B2 (en) * | 1994-01-12 | 1997-07-17 | Unilever N.V. | Lubricant compositions |
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