US2621159A - Metal working lubricant - Google Patents
Metal working lubricant Download PDFInfo
- Publication number
- US2621159A US2621159A US125839A US12583949A US2621159A US 2621159 A US2621159 A US 2621159A US 125839 A US125839 A US 125839A US 12583949 A US12583949 A US 12583949A US 2621159 A US2621159 A US 2621159A
- Authority
- US
- United States
- Prior art keywords
- wax
- lubricant
- metal
- blend
- fatty acids
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000314 lubricant Substances 0.000 title claims description 39
- 238000005555 metalworking Methods 0.000 title claims description 14
- 239000000203 mixture Substances 0.000 claims description 31
- 229930195733 hydrocarbon Natural products 0.000 claims description 11
- 150000002430 hydrocarbons Chemical class 0.000 claims description 11
- 239000000194 fatty acid Substances 0.000 claims description 9
- 239000004215 Carbon black (E152) Substances 0.000 claims description 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 8
- 229930195729 fatty acid Natural products 0.000 claims description 8
- 150000004665 fatty acids Chemical class 0.000 claims description 8
- 229920000642 polymer Polymers 0.000 claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 2
- 239000001993 wax Substances 0.000 description 25
- 229910052751 metal Inorganic materials 0.000 description 21
- 239000002184 metal Substances 0.000 description 21
- 150000001336 alkenes Chemical class 0.000 description 16
- 239000003921 oil Substances 0.000 description 12
- 235000019198 oils Nutrition 0.000 description 12
- 238000005096 rolling process Methods 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 6
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 6
- -1 iron and itsalloys Chemical class 0.000 description 6
- 150000002739 metals Chemical class 0.000 description 6
- 229920001083 polybutene Polymers 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 229920002367 Polyisobutene Polymers 0.000 description 5
- 229920001577 copolymer Polymers 0.000 description 5
- 150000002148 esters Chemical class 0.000 description 5
- 235000019271 petrolatum Nutrition 0.000 description 5
- 238000006116 polymerization reaction Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000004264 Petrolatum Substances 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 239000010408 film Substances 0.000 description 4
- HDINWBRYKNUCEC-UHFFFAOYSA-N methyl 2,2-dichlorooctadecanoate Chemical compound CCCCCCCCCCCCCCCCC(Cl)(Cl)C(=O)OC HDINWBRYKNUCEC-UHFFFAOYSA-N 0.000 description 4
- 229940066842 petrolatum Drugs 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 3
- 235000019482 Palm oil Nutrition 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000002534 ethynyl group Chemical group [H]C#C* 0.000 description 3
- 210000002683 foot Anatomy 0.000 description 3
- 239000002540 palm oil Substances 0.000 description 3
- ADOBXTDBFNCOBN-UHFFFAOYSA-N 1-heptadecene Chemical compound CCCCCCCCCCCCCCCC=C ADOBXTDBFNCOBN-UHFFFAOYSA-N 0.000 description 2
- 241000283153 Cetacea Species 0.000 description 2
- 241001481833 Coryphaena hippurus Species 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- UEXCJVNBTNXOEH-UHFFFAOYSA-N Ethynylbenzene Chemical group C#CC1=CC=CC=C1 UEXCJVNBTNXOEH-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 2
- 240000007817 Olea europaea Species 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 241001125048 Sardina Species 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 239000000356 contaminant Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 235000012343 cottonseed oil Nutrition 0.000 description 2
- HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
- ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
- ILLHQJIJCRNRCJ-UHFFFAOYSA-N dec-1-yne Chemical group CCCCCCCCC#C ILLHQJIJCRNRCJ-UHFFFAOYSA-N 0.000 description 2
- 238000005242 forging Methods 0.000 description 2
- 239000003112 inhibitor Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- CNCMVGXVKBJYNU-UHFFFAOYSA-N methyl oxane-4-carboxylate Chemical compound COC(=O)C1CCOCC1 CNCMVGXVKBJYNU-UHFFFAOYSA-N 0.000 description 2
- 239000012170 montan wax Substances 0.000 description 2
- 230000009972 noncorrosive effect Effects 0.000 description 2
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- PMJHHCWVYXUKFD-UHFFFAOYSA-N piperylene Natural products CC=CC=C PMJHHCWVYXUKFD-UHFFFAOYSA-N 0.000 description 2
- 235000019512 sardine Nutrition 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 238000010186 staining Methods 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- HHXKLDZVQWHLNC-MSUUIHNZSA-N (Z)-9,10-dichlorooctadec-9-enoic acid Chemical compound Cl/C(=C(/CCCCCCCC(=O)O)Cl)/CCCCCCCC HHXKLDZVQWHLNC-MSUUIHNZSA-N 0.000 description 1
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 1
- GKGVPDQNHDBNDR-UHFFFAOYSA-N 2,2-dichlorooctadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(Cl)(Cl)C(O)=O GKGVPDQNHDBNDR-UHFFFAOYSA-N 0.000 description 1
- CFWRDBDJAOHXSH-SECBINFHSA-N 2-azaniumylethyl [(2r)-2,3-diacetyloxypropyl] phosphate Chemical compound CC(=O)OC[C@@H](OC(C)=O)COP(O)(=O)OCCN CFWRDBDJAOHXSH-SECBINFHSA-N 0.000 description 1
- BKOOMYPCSUNDGP-UHFFFAOYSA-N 2-methylbut-2-ene Chemical group CC=C(C)C BKOOMYPCSUNDGP-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
- UZPWKTCMUADILM-UHFFFAOYSA-N 3-methylcyclohexene Chemical compound CC1CCCC=C1 UZPWKTCMUADILM-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 244000226021 Anacardium occidentale Species 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- 240000002791 Brassica napus Species 0.000 description 1
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 1
- 241000273930 Brevoortia tyrannus Species 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 244000146553 Ceiba pentandra Species 0.000 description 1
- 235000003301 Ceiba pentandra Nutrition 0.000 description 1
- 241000251730 Chondrichthyes Species 0.000 description 1
- 241000252203 Clupea harengus Species 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- 241000276457 Gadidae Species 0.000 description 1
- 244000020551 Helianthus annuus Species 0.000 description 1
- 235000003222 Helianthus annuus Nutrition 0.000 description 1
- 241000124008 Mammalia Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 101100166829 Mus musculus Cenpk gene Proteins 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 241000283222 Physeter catodon Species 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 235000004443 Ricinus communis Nutrition 0.000 description 1
- 240000000111 Saccharum officinarum Species 0.000 description 1
- 235000007201 Saccharum officinarum Nutrition 0.000 description 1
- 244000000231 Sesamum indicum Species 0.000 description 1
- 235000003434 Sesamum indicum Nutrition 0.000 description 1
- 241000251778 Squalus acanthias Species 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-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
- 230000002411 adverse Effects 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229910045601 alloy Inorganic materials 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
- 239000012164 animal wax Substances 0.000 description 1
- 238000000137 annealing Methods 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- ZDWGXBPVPXVXMQ-UHFFFAOYSA-N bis(2-ethylhexyl) nonanedioate Chemical compound CCCCC(CC)COC(=O)CCCCCCCC(=O)OCC(CC)CCCC ZDWGXBPVPXVXMQ-UHFFFAOYSA-N 0.000 description 1
- VQLYBLABXAHUDN-UHFFFAOYSA-N bis(4-fluorophenyl)-methyl-(1,2,4-triazol-1-ylmethyl)silane;methyl n-(1h-benzimidazol-2-yl)carbamate Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1.C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 VQLYBLABXAHUDN-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 210000000988 bone and bone Anatomy 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- WFYPICNXBKQZGB-UHFFFAOYSA-N butenyne Chemical group C=CC#C WFYPICNXBKQZGB-UHFFFAOYSA-N 0.000 description 1
- ULRRMYHDWKTYFI-UHFFFAOYSA-N butyl 2,2-dichlorooctadecanoate Chemical compound ClC(C(=O)OCCCC)(CCCCCCCCCCCCCCCC)Cl ULRRMYHDWKTYFI-UHFFFAOYSA-N 0.000 description 1
- 239000010495 camellia oil Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 239000004203 carnauba wax Substances 0.000 description 1
- 235000013869 carnauba wax Nutrition 0.000 description 1
- 235000020226 cashew nut Nutrition 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000007334 copolymerization reaction Methods 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 230000006324 decarbonylation Effects 0.000 description 1
- 238000006606 decarbonylation reaction Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000005695 dehalogenation reaction Methods 0.000 description 1
- 230000018044 dehydration Effects 0.000 description 1
- 238000006297 dehydration reaction Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- UKFTXGSXCYEAKH-UHFFFAOYSA-N dicyanomercury 1,3,5,7-tetrazatricyclo[3.3.1.13,7]decane Chemical group N#C[Hg]C#N.N#C[Hg]C#N.C1N2CN3CN1CN(C2)C3 UKFTXGSXCYEAKH-UHFFFAOYSA-N 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- ZQPPMHVWECSIRJ-MDZDMXLPSA-N elaidic acid Chemical compound CCCCCCCC\C=C\CCCCCCCC(O)=O ZQPPMHVWECSIRJ-MDZDMXLPSA-N 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 235000019197 fats Nutrition 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 238000001640 fractional crystallisation Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 235000019514 herring Nutrition 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000005984 hydrogenation reaction Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000012182 japan wax Substances 0.000 description 1
- 239000000787 lecithin Substances 0.000 description 1
- 229940067606 lecithin Drugs 0.000 description 1
- 235000010445 lecithin Nutrition 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000010687 lubricating oil Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- RGKRENMOPWOQSN-OTZFSBHDSA-N methyl (Z,12R)-9,10-dichloro-12-hydroxyoctadec-9-enoate Chemical compound Cl/C(=C(/CCCCCCCC(=O)OC)Cl)/C[C@H](O)CCCCCC RGKRENMOPWOQSN-OTZFSBHDSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- NKBWPOSQERPBFI-UHFFFAOYSA-N octadecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCCCC NKBWPOSQERPBFI-UHFFFAOYSA-N 0.000 description 1
- 229940055577 oleyl alcohol Drugs 0.000 description 1
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
- 238000013021 overheating Methods 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 235000019809 paraffin wax Nutrition 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 235000020030 perry Nutrition 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920005606 polypropylene copolymer Polymers 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- MWWATHDPGQKSAR-UHFFFAOYSA-N propyne Chemical compound CC#C MWWATHDPGQKSAR-UHFFFAOYSA-N 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- 229940119224 salmon oil Drugs 0.000 description 1
- 239000010686 shark liver oil Substances 0.000 description 1
- 239000012177 spermaceti Substances 0.000 description 1
- 229940084106 spermaceti Drugs 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229920003051 synthetic elastomer Polymers 0.000 description 1
- 239000005061 synthetic rubber Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000012178 vegetable wax Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 210000002268 wool Anatomy 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
- C10M3/00—Liquid compositions essentially based on lubricating components other than mineral lubricating oils or fatty oils and their use as lubricants; Use as lubricants of single liquid substances
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/022—Ethene
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/026—Butene
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
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- C10M2219/024—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of esters, e.g. fats
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- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
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- C10N2040/245—Soft metals, e.g. aluminum
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- C10N2040/246—Iron or steel
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- C10N2040/247—Stainless steel
Definitions
- Thisinvention relates to novel'lubricants and methods of :making themJ'More particularly; this --inventionpertains to metal working or'rmetalfabrication lubricants" for' use in rolling, drawing,
- lubricantamust act primarily 1 as a coolant and i l as a lubricant.
- a metal-working lubricant such as a rolling lubricant having outstanding properties can be prepared by forming a blend of a waxy hydrocarbon, substantially non-aromatic and a polymeric olefin, waxy hydrocarbon comprising at least 80% and preferably 85 to 95% of the blend, said blend having admixed therein as a primary ingredient from about 3% to about and preferably from about 3% to 6 of a halo-organic compound such as halo waxes, halo-fatty acids and esters thereof and the like.
- Waxy materials can be recovered from residuum lube oil fractions, and these wax fractions can be split still further into special wax cuts having desired characteristics by use of selective solvents. This is based on a difi'erence in solubility of different waxy fractions in a given solvent.
- the aromatic constituents can be removed by successively cooling the mixture down to between about 40 F. and 76 F. so as to remove the aromatics which remain substantially soluble in the solvent as the temperature is lowered, while the straight-chain waxes and isoparafiins become substantially insoluble in the solvent.
- the straight-chain Waxes can be separated from the isoparaffins by extraction and fractional crystallization.
- waxy hydrocarbons may be admixed with synthetic waxes produced by polymerization of olefins under pressure or by dehydrating long-chain fatty alcohols such as octadecyl alcohol and the like.
- Admixed with nonaromatic waxy hydrocarbon may be minor amounts of Waxy materials obtained from nonhydrocarbon services such as marine or animal waxes, vegetable waxes and the like, and specifically may be illustrated by spermaceti, Japan wax, carnauba wax, montan wax, sugar cane wax. cotton wax, etc., and the mixture oxidized.
- the other constituent of the base blend is a polymeric unsaturated hydrocarbon and may be monoand/or polyolefinic and/or acetylenic hydrocarbons, which may, if desired, have attached polar groups, said polymeric materials being of rather high molecular weight such as above 300 and preferably above 1,500 and may even be within the limits of 5,000 or 10,000 or even higher, such as 100,000 or 500,000, etc.
- olefinic products may be obtained from various sources and by various means.
- olefins may be obtained by hydrogenation of parafiins, such as by the cracking of paraffin waxes, or by the dehalogenation of alkyl halides and the like.
- olefinic starting materials for the production of such polymers individual olefins or mixtures of olefins and non-olefinic hydrocarbons may be used.
- Starting materials may Y be butylenes, amylenes, refinery gases containing normally gaseous olefins and cracked distillates or other relatively low-boiling hydrocarbon mixtures containing normally liquid olefins, and mixtures of normally liquid olefins containing dissolved therein normally gaseous olefins.
- Polymers resulting from the treatment of monoolefins preferably iso-monoolefins such as isobutylene and isoamylene and/or copolymers obtained by the polymerization of hydrocarbon mixtures such as isoolefins and normal olefins may be used.
- the polymerization of these olefins and their mixtures may be obtained by use of suitable catalysts such as Friedel-Crafts type and the like.
- olefinic and/or acetylinic hydrocarbons which may be obtained from any source and utilized in forming the desired sulfurized products of this invention are ethylene, propylene, butene-l, butene-2, isobutylene, the amylele, hexene-l, 4-methyl-pentene-1, 4,4-dimethylpentene-l, 4-methyl-pentene-2, octene-l, decene-l, cetene-l, styrene, cyclohexene, 3-methylcyclohexene, 1,4-diphenyl, butene-2, butadiene 1,3, pentadiene-1,3, pentadiene-L4, hexadiene- 1,5, hexadiene-1,4, pentadecene-8, heptadecene, hexadecene-l, tridecene-7, nonadecene-lO, 3,9- dieth
- Copolymers of olefins and non-aromatic hydrocarbons may also be used.
- the olefins which may be used to form the copolymers of this type include isobutylene, 2-methylbutene-1,2, ethylbutene-l, secondary and tertiary amylenes, hexylenes and the like.
- the non-aromatic hydrocarbons may include butadiene, isoprene, cyclopentadiene, 2,3-dimethylbutadiene-1,3, pentadiene-1,3, hexadiene-2,4, the substituted di- -olefins such as diisobutenyl; the acetylenes such as acetylene, vinyl acetylene and the like.
- the copolymerization is preferably carried out in the presence of a Friedel-Crafts type catalyst and in the presence of a suitable diluent such as liquified ethylene, propane and the like.
- the catalysts which may be employed during the polymerization reaction may be any Friedel- Crafts catalyst such as are listed by Galloway in Chemical Review 17, 327 (1925).
- the polymerization may be carried out at low temperatures such as below zero degrees centigrade, or at elevated temperatures such as above 50 C. and C. and higher.
- compositions of this invention are:
- Polyisobutylene polymer (mol. wt. 1,5005,000) Polyethylene polymer (mol. wt. LOGO-10,000) Polybutenes (mol. Wt. 5,000-6,000)
- wax o'lcflns, halogenated fatty acids having at least 8 and preferably 12 to 24. carbon. atoms in the molecule, esters of said fatty acids-and the like.
- the halo radical or radicals maybe: chlo' rine, bromine, fluorine, and/01s iodine.
- Agents which. are specifically preferred arechlorinated parafiin wax, chlorinated cracked wax, chlorinated foots oil, olefin of Clo-C24,.
- chlorinated synthetic rubber chloro-bromo-parafiin wax, dichlorostearic acid, dichloro-oleic acid, methyl dichloro-stearate, butyl dichloro-stearate, polybromostearic acid, methyl polybromostearic acid, methyl dichloro-ricinoleate, chlorinated.
- waxy esters e. g., beeswax, montan wax, and the like.
- Highly desirable metal-working lubricants such as rolling and drawing lubricants can be prepared by using formulations within the following range Material Amount Base blend; Berce nt v l. Waxy-hydrocarbon t 804) 1 2. Polymeric material mol. wt. 30050D,000 and p 97 89 prefrably'l,500-5,000 20-5" PrimaryAdditive:
- Halo-organic compound e. g,',. chlorinated paraflin' wax or methyldichloro-st'earate', etc. 2-l0" Secondary or optional Additives:
- compositions. of this invention are:
- composition C Per cent Dichlorostearic acid Polyisobutylene (mol. wt. -l,50010,000) 5 Residue petrolatum Balance Composition E Per cent Methyl dichlorostearate 3 Sulfurized sperm oil 1 Polyisobutylene 5 Soft wax obtained from residue petrolatum (M. P. 40 C.) Balance Composition F Per cent Chlorinated parafiin wax Polybutene (mol. wt. 8,000-10,000) 5-10 Residue petrolatum Balance Table I below further illustrates compositions of this invention:
- Composition 10%; olei'c; acid+ 3% chlorinatedparaflin wax-i in p'a'rafiim wax;
- composition Z 1% tricresyl phosphate in mineralloilz In conjunction with compositions of this in.-
- compositions such as:
- codfish porpoise body and jaw oils codliver salmon oil dogfish sardine and sardine liver oils dolphin body seal oil dolphin fish shark and shark liver oils herring sperm whale body and head oils 1apfish whale 011, etc. menhaden B. Natural-occurring fatty acids of high molecular weights:
- ricinoleie ricinelaidic stearate di-2-ethyl hexyl-azelate, n-decyl hydrogen phthalite or succinate, octadecyl stearate.
- Esters of inorganic acids e. g., phosphatidic materials such as cephalin and lecithin.
- Rolling lubricants of this invention are well adapted as rust inhibitors after the rolled sheet has been worked.
- the roll lubricant of this invention may be applied to the rolls of a sheet metal rolling mill by any suitable means such as spraying. dripping, or the like. It may be applied to the sheet metal prior to or during rolling.
- compositions of this invention may be used as drawing lubricants, forging and die lubricants and in various other processes where drawing m z-an10 of mammal used and can be e ranges 75 and working of metals requires lubrication.
- a metal-working lubricant consisting essentially of a base blend of a soft residue wax and an olefinic hydrocarbon polymer having a molecular weight above 300, said soft residue wax constituting at least 80% of the blend and the polymer constituting essentially the remainder of said blend, and having incorporated in said base blend from 2% to 10% based on the total lubricant, of a halogenated extreme pressure compound selected from the group consisting of halogenated wave, halogenated high molecular weight fatty acids, and hologenated esters of said fatty acids.
- a metal-working lubricant consisting essentially of the following components in the specified proportions:
- a metal-working lubricant consisting essentially of the following components in the specified n proportions:
- a metal working lubricant consisting essentially of the following components in the specified proportions:
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Description
Patented Dec. 9, 1952 {UNITED STATES PATENT Calif., 'assignorsto Shell. Development Com- 'pany,-. San Francisco, Calif; a 1 corporation of Delaware NoDrawing. *ApplicationNovember 5,1949, Serial No. 125,839
Thisinvention relates to novel'lubricants and methods of :making themJ'More particularly; this --inventionpertains to metal working or'rmetalfabrication lubricants" for' use in rolling, drawing,
p drawing; rod and tube i'drawing, :forging of metals and th like.
' Problems '1 encountered :in lubricating. metals under: conditions of the .usesl referred to in the previous paragraph are particularly complex because of the. various factors encountered, such as high temperature, excess pressure, emulsificatiompresence of foreign bodies or contaminants, work speeds and the like. To eifectively lubricate under these adverse :conditions, the
lubricantamust act" primarily 1 as a coolant and i l as a lubricant.
In the afield of rolling lubricants'palm oil has been considered to be .most- 'efiicient and 1 suitable for .use' in connection 'with the heavier: metals such as iron and itsalloys, steels. "However, palm ers,='which'igreatlyincreases operating cost. .Also,
it hasna tendency to stain some metalsuriaces which on annealing mars the surface andexerts a detrimental efiect when such *metalsz are to be subsequently tinned/coated and the like. :In addition, metal surfaces which become too heavily: coated: with palm oil-cause excessive slippage of the. rolls thereby decreasing. rolling: efiiciency. :Palm oil is not always'readilyiavailable;
hence acheap andefiective substitute 'for'it is greatly .desired.
To meet the requirements demanded of: ajgood metal-fabricating lubricant, such: as a roll lubricant, it must. have as: essential properties film strength. ability to. reduce friction, "ability :to wet metals in presence= of *waterpability to pro duce a good lustreon metalisurfacerworkedyease of re- 40 metal -:and non-staining and ric-emulsifying properties, i.- e.,'-separating from water and contaminants, including fines.
7 .FILM' STRENGTH When lubricated metal surfaces areforced to slide past each'other under high pressures, there is a tendency for surface asperitiesto penetrate the lubricant film and the penetrating metal to adhere to the opposingmetal surface; this permits the transfer of metal from one surface to another. This phenomenon, known in metalworking operation as pick-up of the worked metal by the die or roll, may become very pronounced at elevated temperatures. Although high temperatures may be a result of high friction and may lead to pick-up," it is generally agreed that the ability of a lubricant to prevent adhesion of metal surfaces is a property distinct from and notnecessarily related to ability" of the :12 lubricant to reduce friction between sliding-stir faces which do I not adhere. iFor -this" reasong the ability eta-lubricant to form surfacefilmsltvhich prevent actual KmetaPto-metaI" contact I and: ad-
5 :hesion is veryl essential.
- REDUCTION OFFRLICTION 'iRoll lubricants must :pos's'ess the-'- ability to reduce friction'between the rolls and theiworksheet p in .order to "reduce; power consumption, increase reduction per-pass: andzgive 'a lower limit toethe metal thickness,; prevent, overheating 'andiminimize the force which must be appliedrto the rolls. -Thegproperty of a lubricant'to reduce friction is 15 referred to 'looselywas oiliness and dependsiupon oil has serious drawbacks, particularly in some :applicationain' that it isdifiicult to'remove from metal surfaces thereby requirin the use of cleanthe sheer strengthiof the .film formed on ametal surface and to the rheological behavior of thin films of oilwhen" subjected to-highpre'ssures.
WETABILITY' AND ADHESION Sincerolllubricantsare usually used-in icon- -junction with water as. acoolant, theymust possessthe property of displacing water from metal surfaces and resistthe 4 washing action. ofwlarge quantities of water applied-t0 the rolls-andwofl; sheet. Often washing water :is applie'd in the form of a high pressure stream so that the ability of the lubricant to adhere-tometal-surfaces issof paramount importance.
LUSTRE Theappearance ofthe. surface of rolled-stock referred to in practice as lustreis markedly influenced by the character of the rolllubricant.
3? To accomplish this, lubricants'used for thisjpurpose should prevent microscopic tears on the worked metal surface.
EASE 'OF *R'EMOVALA'NDNON-STAIN1NG CORROSION RESISTANT Efficient roll lubricants in' addition to fb'ein'g able to withstand high temperature and pressure must be non-corrosive during the rollirigprocess and preferably actas a corrosion inhibitor after no the rolling processfparticularly in"cases"where 3 the rolled metal is stored for'long intervals before being further worked.
It is an object of this invention to provide an improved metal-rolling lubricant. It is another object of this invention to provide a lubricant for metal working which is stable and non-corrosive. Still another object of this invention is to provide a tacky metal-working lubricant havin the property of resisting water displacement from metal surfaces. Furthermore, it is an object to provide a metal-working lubricant which is non-staining and which can be easily removed from lubricated surfaces. A more specific object is to provide an improved lubricant for use in the working of aluminum, stainless steel and other metals and alloys.
It has now been discovered that a metal-working lubricant such as a rolling lubricant having outstanding properties can be prepared by forming a blend of a waxy hydrocarbon, substantially non-aromatic and a polymeric olefin, waxy hydrocarbon comprising at least 80% and preferably 85 to 95% of the blend, said blend having admixed therein as a primary ingredient from about 3% to about and preferably from about 3% to 6 of a halo-organic compound such as halo waxes, halo-fatty acids and esters thereof and the like.
Waxy materials can be recovered from residuum lube oil fractions, and these wax fractions can be split still further into special wax cuts having desired characteristics by use of selective solvents. This is based on a difi'erence in solubility of different waxy fractions in a given solvent. Thus, when using a methylethyl ketone type solvent, the aromatic constituents can be removed by successively cooling the mixture down to between about 40 F. and 76 F. so as to remove the aromatics which remain substantially soluble in the solvent as the temperature is lowered, while the straight-chain waxes and isoparafiins become substantially insoluble in the solvent. The straight-chain Waxes can be separated from the isoparaffins by extraction and fractional crystallization.
The above type of waxy hydrocarbons may be admixed with synthetic waxes produced by polymerization of olefins under pressure or by dehydrating long-chain fatty alcohols such as octadecyl alcohol and the like. Admixed with nonaromatic waxy hydrocarbon may be minor amounts of Waxy materials obtained from nonhydrocarbon services such as marine or animal waxes, vegetable waxes and the like, and specifically may be illustrated by spermaceti, Japan wax, carnauba wax, montan wax, sugar cane wax. cotton wax, etc., and the mixture oxidized.
The other constituent of the base blend is a polymeric unsaturated hydrocarbon and may be monoand/or polyolefinic and/or acetylenic hydrocarbons, which may, if desired, have attached polar groups, said polymeric materials being of rather high molecular weight such as above 300 and preferably above 1,500 and may even be within the limits of 5,000 or 10,000 or even higher, such as 100,000 or 500,000, etc.
These olefinic products may be obtained from various sources and by various means. Thus, olefins may be obtained by hydrogenation of parafiins, such as by the cracking of paraffin waxes, or by the dehalogenation of alkyl halides and the like. Also, as olefinic starting materials for the production of such polymers, individual olefins or mixtures of olefins and non-olefinic hydrocarbons may be used. Starting materials may Y be butylenes, amylenes, refinery gases containing normally gaseous olefins and cracked distillates or other relatively low-boiling hydrocarbon mixtures containing normally liquid olefins, and mixtures of normally liquid olefins containing dissolved therein normally gaseous olefins. Polymers resulting from the treatment of monoolefins preferably iso-monoolefins such as isobutylene and isoamylene and/or copolymers obtained by the polymerization of hydrocarbon mixtures such as isoolefins and normal olefins may be used. The polymerization of these olefins and their mixtures may be obtained by use of suitable catalysts such as Friedel-Crafts type and the like.
Examples of olefinic and/or acetylinic hydrocarbons which may be obtained from any source and utilized in forming the desired sulfurized products of this invention are ethylene, propylene, butene-l, butene-2, isobutylene, the amylele, hexene-l, 4-methyl-pentene-1, 4,4-dimethylpentene-l, 4-methyl-pentene-2, octene-l, decene-l, cetene-l, styrene, cyclohexene, 3-methylcyclohexene, 1,4-diphenyl, butene-2, butadiene 1,3, pentadiene-1,3, pentadiene-L4, hexadiene- 1,5, hexadiene-1,4, pentadecene-8, heptadecene, hexadecene-l, tridecene-7, nonadecene-lO, 3,9- diethyltridecene-6, dodecene-l, triacontene-14, pentatriacontene-l'l, olefins, obtained by decarbonylation of oleyl alcohol or such unsaturated alcohols as are obtained by carboxyl reduction of sperm alcohol, olefins obtained by dehydration of high molecular weight saturated alcohols, etc., acetylene, propyne, butyne-l, pentyne-Z, hexyne- 1, cetyne-l, octyl acetylene, phenyl acetylene, etc, and their homologues and analogues.
Copolymers of olefins and non-aromatic hydrocarbons may also be used. The olefins which may be used to form the copolymers of this type include isobutylene, 2-methylbutene-1,2, ethylbutene-l, secondary and tertiary amylenes, hexylenes and the like. The non-aromatic hydrocarbons may include butadiene, isoprene, cyclopentadiene, 2,3-dimethylbutadiene-1,3, pentadiene-1,3, hexadiene-2,4, the substituted di- -olefins such as diisobutenyl; the acetylenes such as acetylene, vinyl acetylene and the like.
The copolymerization is preferably carried out in the presence of a Friedel-Crafts type catalyst and in the presence of a suitable diluent such as liquified ethylene, propane and the like.
- The catalysts which may be employed during the polymerization reaction may be any Friedel- Crafts catalyst such as are listed by Galloway in Chemical Review 17, 327 (1925). The polymerization may be carried out at low temperatures such as below zero degrees centigrade, or at elevated temperatures such as above 50 C. and C. and higher.
Among the most preferred polymeric materials suitable for use in compositions of this invention are:
Polyisobutylene polymer (mol. wt. 1,5005,000) Polyethylene polymer (mol. wt. LOGO-10,000) Polybutenes (mol. Wt. 5,000-6,000)
Copolymer of isobutylene and ethylene (mol. wt.
Copolymer of propylene and wt. EGO-10,000)
Copolymer of butadiene and wt. l5,000-20,000)
isobutylene (mol.
isobutylene (mol.
wax: o'lcflns, halogenated fatty acids having at least 8 and preferably 12 to 24. carbon. atoms in the molecule, esters of said fatty acids-and the like. The halo radical or radicals maybe: chlo' rine, bromine, fluorine, and/01s iodine. Agents which. are specifically preferred arechlorinated parafiin wax, chlorinated cracked wax, chlorinated foots oil, olefin of Clo-C24,. chlorinated synthetic rubber, chloro-bromo-parafiin wax, dichlorostearic acid, dichloro-oleic acid, methyl dichloro-stearate, butyl dichloro-stearate, polybromostearic acid, methyl polybromostearic acid, methyl dichloro-ricinoleate, chlorinated. waxy esters, e. g., beeswax, montan wax, and the like.
Highly desirable metal-working lubricants such as rolling and drawing lubricants can be prepared by using formulations within the following range Material Amount Base blend; Berce nt v l. Waxy-hydrocarbon t 804) 1 2. Polymeric material mol. wt. 30050D,000 and p 97 89 prefrably'l,500-5,000 20-5" PrimaryAdditive:
3. Halo-organic compound, e. g,',. chlorinated paraflin' wax or methyldichloro-st'earate', etc. 2-l0" Secondary or optional Additives:
4; Amines,.sul.fonates, etc (H.
Specific compositions. of this invention: are:
C (imposition .4
Per. cent Methyl. dichlorostearate .u 3 Polybutene' (mol.. wt. 8,000-l0,000)f I0;
Soft Wax residue (M. P. 39"'-4=0'- C.) Balance:
Composition C Per cent Dichlorostearic acid Polyisobutylene (mol. wt. -l,50010,000) 5 Residue petrolatum Balance Composition E Per cent Methyl dichlorostearate 3 Sulfurized sperm oil 1 Polyisobutylene 5 Soft wax obtained from residue petrolatum (M. P. 40 C.) Balance Composition F Per cent Chlorinated parafiin wax Polybutene (mol. wt. 8,000-10,000) 5-10 Residue petrolatum Balance Table I below further illustrates compositions of this invention:
Table I petrolatum residual wax 2: :r z (b) polymeric materialpolyethylene Z polybutene a: :r
30C. C C:
Composition D' p D 1 D p otir bsinoirnz 5 .10 2042 .69 .045- GompcsitionF .65: 1.0411 -67 .1140 GompositionX 2.1 .16 Composition Y" 1.5 .101 GompositioIlZZL c E 2.2 2.25.
D=S C3l'fdialneter;. mm; =Coefi. of friction, average of values at 30, 40, 50 and 60scconds'a =seizure v Compsitlon2X=10%polybutanem residuepetrolatunr.
4 Composition =10%; olei'c; acid+ 3% chlorinatedparaflin wax-i in p'a'rafiim wax;
Composition Z=1% tricresyl phosphate in mineralloilz In conjunction with compositions of this in.-
-' vention, minor amounts, generally less than- 1%,
of other additives can be added, if desired, in order to fortify the compositions, such as:
A. High molecular weight; fatty acids derived.
7 4 from-animal, vegetable, marine oils,-.e. g-.,
1. Animal o'il:
tallow neats foot lard wool fat bone horse foot oils, etc.. 2.- Vegetable oils:
castor corn cashew" cottonseed" peanut kapok. cocoanut rapeseed ioiobaseed ravison olive sesame; olive kernel sunflower palm oil teaseed oils;.'et'c'.v palm kernel oils 3. Marine oils:
codfish porpoise body and jaw oils codliver salmon oil dogfish sardine and sardine liver oils dolphin body seal oil dolphin fish shark and shark liver oils herring sperm whale body and head oils 1apfish whale 011, etc. menhaden B. Natural-occurring fatty acids of high molecular weights:
1. Saturated:
capric stearic undecylic arachidic lauric lignoceric myristic cerotic palmitic montanic acids, etc. 2 Unsaturated A oleic linolenic linoleic brassidic erucic elaidic acids, etc. 3. Substituted fatty acids:
ricinoleie ricinelaidic stearate, di-2-ethyl hexyl-azelate, n-decyl hydrogen phthalite or succinate, octadecyl stearate.
2. Esters of inorganic acids, e. g., phosphatidic materials such as cephalin and lecithin.
D. Sulfur-containing materials, e. g.,
sulfurized sperm oil sulfurized cottonseed oil sulfurized fatty acids as listed under part B Rolling lubricants of this invention are well adapted as rust inhibitors after the rolled sheet has been worked.
The roll lubricant of this invention may be applied to the rolls of a sheet metal rolling mill by any suitable means such as spraying. dripping, or the like. It may be applied to the sheet metal prior to or during rolling.
In addition to being an excellent roll lubricant, compositions of this invention may be used as drawing lubricants, forging and die lubricants and in various other processes where drawing m z-an10 of mammal used and can be e ranges 75 and working of metals requires lubrication.
disclosed in column 5.
It is to be understood that while the features of the invention have been described and illustrated in connection with certain specific examples, the invention, however, is not to be limited thereto or otherwise restricted except by the prior art and the scope of the appended claims.
The invention claimed is:
1. A metal-working lubricant consisting essentially of a base blend of a soft residue wax and an olefinic hydrocarbon polymer having a molecular weight above 300, said soft residue wax constituting at least 80% of the blend and the polymer constituting essentially the remainder of said blend, and having incorporated in said base blend from 2% to 10% based on the total lubricant, of a halogenated extreme pressure compound selected from the group consisting of halogenated wave, halogenated high molecular weight fatty acids, and hologenated esters of said fatty acids.
2. A metal-working lubricant consisting essentially of the following components in the specified proportions:
Per cent Methyl dichlorostearate 3 25 Polybutene (mol. wt. 8,000-10,000) 10 Solt wax residue (M. P. 3940 C.) Balance 3. A metal-working lubricant consisting essentially of the following components in the specified n proportions:
Per cent Chlorinated paraflin wax (40% C1.) 3 Polybutene (mol. wt. 8,000-10,000) 5-10 Soft residue wax Balance 4. A metal-working lubricant consisting essen tially of the following components in the specifled proportions:
Per cent Methyl dichlorostearic acid 3 Oleic acid l Polyisobutylene 5 Soft residue wax Balance 5. A metal working lubricant consisting essentially of the following components in the specified proportions:
I Per cent Methyl dichlorostearate' 3 Sulfurized sperm oil 1 Polyisobutylene 5 Soft residue wax Balance GEORGE L. PERRY. SAMUEL K. TALLEY.
REFERENCES CITED The following references are of record in the OTHER REFERENCES Lubrication as Affected by Physical Properties of Lubricants, Williams, January 1935, Industrial and Engineering Chemistry, vol. 27, No. 1, PD. 64 and 65.
Claims (1)
1. A METAL-WORKING LUBRICANT CONSISTING ESSENTIALLY OF A BASE BLEND OF A SOFT RESIDUE WAX AND AN OLEFINIC HYDROCARBON POLYMER HAVING A MOLECULAR WEIGHT ABOVE 300, AND SOFT RESIDUE WAX CONSTITUTING AT LEAST 80% OF THE BLEND AND THE POLYMER CONSTITUTING ESSENTIALLY THE REMAINDER OF SAID BLEND, AND HAVING INCORPORATED IN SAID BASE BLEND FROM 2% TO 10% BASED ON THE TOTAL LUBRICANT, OF A HALOGENATED EXTREME PRESSURE COMPOUND SELECTED FROM THE GROUP CONSISTING OF HALOGENATED WAVE, HALOGENATED HIGH MOLECULAR WEIGHT FATTY ACIDS, AND HOLOGENATED ESTERS OF SAID FATTY ACIDS.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US125839A US2621159A (en) | 1949-11-05 | 1949-11-05 | Metal working lubricant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US125839A US2621159A (en) | 1949-11-05 | 1949-11-05 | Metal working lubricant |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2621159A true US2621159A (en) | 1952-12-09 |
Family
ID=22421656
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US125839A Expired - Lifetime US2621159A (en) | 1949-11-05 | 1949-11-05 | Metal working lubricant |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2621159A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3167511A (en) * | 1961-04-13 | 1965-01-26 | Socony Mobil Oil Co Inc | Metal working lubricant |
| US3340194A (en) * | 1962-09-11 | 1967-09-05 | Sun Oil Co | Metal working lubricant |
| US4256594A (en) * | 1979-05-04 | 1981-03-17 | The Lubrizol Corporation | Hot melt metal working lubricants containing phosphorus-containing compositions |
| US4358509A (en) * | 1979-05-04 | 1982-11-09 | The Lubrizol Corporation | Novel metal working additive compositions, lubricants containing them and metal workpieces coated with same |
| FR2530655A1 (en) * | 1982-07-26 | 1984-01-27 | Sp K Tekh | Lubricant for the working of metals by cold deformation. |
| US4659493A (en) * | 1983-10-03 | 1987-04-21 | Kali-Chemie Aktiengesellschaft | Process for producing novel products by hydrogen fluoride with esters of fatty acids |
| US4687587A (en) * | 1985-01-29 | 1987-08-18 | Alcan International Limited | Metal forming lubricant |
| US4968323A (en) * | 1987-11-02 | 1990-11-06 | Mobil Oil Corporation | Metalworking fluid composition |
| US20040132587A1 (en) * | 2003-01-07 | 2004-07-08 | Siegling America, Llc | Treadmill belt |
| US20040132586A1 (en) * | 2003-01-07 | 2004-07-08 | Siegling America, Llc | Treadmill belt |
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| US1041484A (en) * | 1912-01-31 | 1912-10-15 | Hayden A Kern | Composition to facilitate the tapping of aluminum or the like. |
| US1944941A (en) * | 1932-06-11 | 1934-01-30 | Continental Oil Co | Lubricating oil |
| US1948194A (en) * | 1931-11-17 | 1934-02-20 | Ironsides Company | Metal-forming lubricants |
| US2126128A (en) * | 1934-05-17 | 1938-08-09 | Harley A Montgomery | Lubricant and method of lubricating metal during forming operations |
| US2256603A (en) * | 1941-09-23 | Processing with nonstainingcom | ||
| US2316925A (en) * | 1939-08-19 | 1943-04-20 | Pure Oil Co | Halogenated aliphatic lubricant additive |
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| US2256603A (en) * | 1941-09-23 | Processing with nonstainingcom | ||
| US1041484A (en) * | 1912-01-31 | 1912-10-15 | Hayden A Kern | Composition to facilitate the tapping of aluminum or the like. |
| US1948194A (en) * | 1931-11-17 | 1934-02-20 | Ironsides Company | Metal-forming lubricants |
| US1944941A (en) * | 1932-06-11 | 1934-01-30 | Continental Oil Co | Lubricating oil |
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Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3167511A (en) * | 1961-04-13 | 1965-01-26 | Socony Mobil Oil Co Inc | Metal working lubricant |
| US3340194A (en) * | 1962-09-11 | 1967-09-05 | Sun Oil Co | Metal working lubricant |
| US4256594A (en) * | 1979-05-04 | 1981-03-17 | The Lubrizol Corporation | Hot melt metal working lubricants containing phosphorus-containing compositions |
| US4358509A (en) * | 1979-05-04 | 1982-11-09 | The Lubrizol Corporation | Novel metal working additive compositions, lubricants containing them and metal workpieces coated with same |
| FR2530655A1 (en) * | 1982-07-26 | 1984-01-27 | Sp K Tekh | Lubricant for the working of metals by cold deformation. |
| US4659493A (en) * | 1983-10-03 | 1987-04-21 | Kali-Chemie Aktiengesellschaft | Process for producing novel products by hydrogen fluoride with esters of fatty acids |
| US4687587A (en) * | 1985-01-29 | 1987-08-18 | Alcan International Limited | Metal forming lubricant |
| US4968323A (en) * | 1987-11-02 | 1990-11-06 | Mobil Oil Corporation | Metalworking fluid composition |
| US20040132587A1 (en) * | 2003-01-07 | 2004-07-08 | Siegling America, Llc | Treadmill belt |
| US20040132586A1 (en) * | 2003-01-07 | 2004-07-08 | Siegling America, Llc | Treadmill belt |
| US7549938B2 (en) | 2003-01-07 | 2009-06-23 | Forbo Financial Services Ag | Treadmill belt |
| US20090258744A1 (en) * | 2003-01-07 | 2009-10-15 | Forbo Siegling, Llc | Belt |
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