US3794595A - Working of non-ferrous metals - Google Patents
Working of non-ferrous metals Download PDFInfo
- Publication number
- US3794595A US3794595A US00251308A US3794595DA US3794595A US 3794595 A US3794595 A US 3794595A US 00251308 A US00251308 A US 00251308A US 3794595D A US3794595D A US 3794595DA US 3794595 A US3794595 A US 3794595A
- Authority
- US
- United States
- Prior art keywords
- lubricant
- working
- debris
- nonylphenol
- phenolic compound
- 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
- 229910052751 metal Inorganic materials 0.000 title abstract description 27
- 239000002184 metal Substances 0.000 title abstract description 27
- -1 ferrous metals Chemical class 0.000 title description 16
- 239000000314 lubricant Substances 0.000 abstract description 33
- 150000002989 phenols Chemical class 0.000 abstract description 21
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical class OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 abstract description 5
- TUJKJAMUKRIRHC-UHFFFAOYSA-N hydroxyl Chemical class [OH] TUJKJAMUKRIRHC-UHFFFAOYSA-N 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 description 15
- 238000000034 method Methods 0.000 description 15
- 239000000203 mixture Substances 0.000 description 14
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 12
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 11
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 7
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 7
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 7
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 7
- 239000005642 Oleic acid Substances 0.000 description 7
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 7
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 7
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- 230000003247 decreasing effect Effects 0.000 description 6
- 235000014113 dietary fatty acids Nutrition 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 239000000194 fatty acid Substances 0.000 description 6
- 229930195729 fatty acid Natural products 0.000 description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 6
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 description 5
- 229910045601 alloy Inorganic materials 0.000 description 5
- 239000000956 alloy Substances 0.000 description 5
- 150000004665 fatty acids Chemical class 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229910052726 zirconium Inorganic materials 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 4
- 229910001093 Zr alloy Inorganic materials 0.000 description 4
- 239000000460 chlorine Substances 0.000 description 4
- 230000001050 lubricating effect Effects 0.000 description 4
- 238000005461 lubrication Methods 0.000 description 4
- 239000002480 mineral oil Substances 0.000 description 4
- 235000010446 mineral oil Nutrition 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 239000000344 soap Substances 0.000 description 4
- 229910052719 titanium Inorganic materials 0.000 description 4
- 239000010936 titanium Substances 0.000 description 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 125000000623 heterocyclic group Chemical group 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- GJYCVCVHRSWLNY-UHFFFAOYSA-N 2-butylphenol Chemical compound CCCCC1=CC=CC=C1O GJYCVCVHRSWLNY-UHFFFAOYSA-N 0.000 description 2
- CYEJMVLDXAUOPN-UHFFFAOYSA-N 2-dodecylphenol Chemical compound CCCCCCCCCCCCC1=CC=CC=C1O CYEJMVLDXAUOPN-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- IXQGCWUGDFDQMF-UHFFFAOYSA-N o-Hydroxyethylbenzene Natural products CCC1=CC=CC=C1O IXQGCWUGDFDQMF-UHFFFAOYSA-N 0.000 description 2
- 229940114930 potassium stearate Drugs 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 125000001424 substituent group Chemical group 0.000 description 2
- KHWQFISNNNRGLV-UHFFFAOYSA-N 2,4,6-tributylphenol Chemical compound CCCCC1=CC(CCCC)=C(O)C(CCCC)=C1 KHWQFISNNNRGLV-UHFFFAOYSA-N 0.000 description 1
- KOHSRHXKURUXCP-UHFFFAOYSA-N 2,4,6-triethylphenol Chemical compound CCC1=CC(CC)=C(O)C(CC)=C1 KOHSRHXKURUXCP-UHFFFAOYSA-N 0.000 description 1
- BPRYUXCVCCNUFE-UHFFFAOYSA-N 2,4,6-trimethylphenol Chemical compound CC1=CC(C)=C(O)C(C)=C1 BPRYUXCVCCNUFE-UHFFFAOYSA-N 0.000 description 1
- KPZBEZVZFBDKCG-UHFFFAOYSA-N 2,4-dibutylphenol Chemical compound CCCCC1=CC=C(O)C(CCCC)=C1 KPZBEZVZFBDKCG-UHFFFAOYSA-N 0.000 description 1
- DNNOMBLBBPCGSW-UHFFFAOYSA-N 2,5-dipentylphenol Chemical compound CCCCCC1=CC=C(CCCCC)C(O)=C1 DNNOMBLBBPCGSW-UHFFFAOYSA-N 0.000 description 1
- LZFZQYNTEZSWCP-UHFFFAOYSA-N 2,6-dibutyl-4-methylphenol Chemical compound CCCCC1=CC(C)=CC(CCCC)=C1O LZFZQYNTEZSWCP-UHFFFAOYSA-N 0.000 description 1
- OJFDKJIDBSKDRV-UHFFFAOYSA-N 2,6-dimethyl-4-nonylphenol Chemical compound CCCCCCCCCC1=CC(C)=C(O)C(C)=C1 OJFDKJIDBSKDRV-UHFFFAOYSA-N 0.000 description 1
- CELSEOKAEJGADX-UHFFFAOYSA-N 2,6-dimethyl-4-octylphenol Chemical compound CCCCCCCCC1=CC(C)=C(O)C(C)=C1 CELSEOKAEJGADX-UHFFFAOYSA-N 0.000 description 1
- MYOXWOWYELCAJM-UHFFFAOYSA-N 2,6-dioctylphenol Chemical compound CCCCCCCCC1=CC=CC(CCCCCCCC)=C1O MYOXWOWYELCAJM-UHFFFAOYSA-N 0.000 description 1
- UIXRDRQSWYSVNK-UHFFFAOYSA-N 2-butyl-4,6-dimethylphenol Chemical compound CCCCC1=CC(C)=CC(C)=C1O UIXRDRQSWYSVNK-UHFFFAOYSA-N 0.000 description 1
- FDIPWBUDOCPIMH-UHFFFAOYSA-N 2-decylphenol Chemical compound CCCCCCCCCCC1=CC=CC=C1O FDIPWBUDOCPIMH-UHFFFAOYSA-N 0.000 description 1
- FIWYWGLEPWBBQU-UHFFFAOYSA-N 2-heptylphenol Chemical compound CCCCCCCC1=CC=CC=C1O FIWYWGLEPWBBQU-UHFFFAOYSA-N 0.000 description 1
- HMWIHOZPGQRZLR-UHFFFAOYSA-N 2-hexadecylphenol Chemical compound CCCCCCCCCCCCCCCCC1=CC=CC=C1O HMWIHOZPGQRZLR-UHFFFAOYSA-N 0.000 description 1
- ABMULKFGWTYIIK-UHFFFAOYSA-N 2-hexylphenol Chemical compound CCCCCCC1=CC=CC=C1O ABMULKFGWTYIIK-UHFFFAOYSA-N 0.000 description 1
- QEMHBAGGYKJNSS-UHFFFAOYSA-N 2-icosylphenol Chemical compound CCCCCCCCCCCCCCCCCCCCC1=CC=CC=C1O QEMHBAGGYKJNSS-UHFFFAOYSA-N 0.000 description 1
- UNEWUWSOXCISIP-UHFFFAOYSA-N 2-methyl-6-nonylphenol Chemical compound CCCCCCCCCC1=CC=CC(C)=C1O UNEWUWSOXCISIP-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- MQORMNICGUXRRV-UHFFFAOYSA-N 2-nonadecylphenol Chemical compound CCCCCCCCCCCCCCCCCCCC1=CC=CC=C1O MQORMNICGUXRRV-UHFFFAOYSA-N 0.000 description 1
- WCRKLZYTQVZTMM-UHFFFAOYSA-N 2-octadecylphenol Chemical compound CCCCCCCCCCCCCCCCCCC1=CC=CC=C1O WCRKLZYTQVZTMM-UHFFFAOYSA-N 0.000 description 1
- RGDDVTHQUAQTIE-UHFFFAOYSA-N 2-pentadecylphenol Chemical compound CCCCCCCCCCCCCCCC1=CC=CC=C1O RGDDVTHQUAQTIE-UHFFFAOYSA-N 0.000 description 1
- MEEKGULDSDXFCN-UHFFFAOYSA-N 2-pentylphenol Chemical compound CCCCCC1=CC=CC=C1O MEEKGULDSDXFCN-UHFFFAOYSA-N 0.000 description 1
- LCHYEKKJCUJAKN-UHFFFAOYSA-N 2-propylphenol Chemical compound CCCC1=CC=CC=C1O LCHYEKKJCUJAKN-UHFFFAOYSA-N 0.000 description 1
- JOONSONEBWTBLT-UHFFFAOYSA-N 2-tetradecylphenol Chemical compound CCCCCCCCCCCCCCC1=CC=CC=C1O JOONSONEBWTBLT-UHFFFAOYSA-N 0.000 description 1
- RGVIYLQXUDJMCP-UHFFFAOYSA-N 2-tridecylphenol Chemical compound CCCCCCCCCCCCCC1=CC=CC=C1O RGVIYLQXUDJMCP-UHFFFAOYSA-N 0.000 description 1
- UVNKQUXHHOZJLS-UHFFFAOYSA-N 2-undecylphenol Chemical compound CCCCCCCCCCCC1=CC=CC=C1O UVNKQUXHHOZJLS-UHFFFAOYSA-N 0.000 description 1
- DHURZBNESRVDPJ-UHFFFAOYSA-N 4-heptadecylphenol Chemical compound CCCCCCCCCCCCCCCCCC1=CC=C(O)C=C1 DHURZBNESRVDPJ-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 229910001369 Brass Inorganic materials 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 229910000906 Bronze Inorganic materials 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 230000000573 anti-seizure effect Effects 0.000 description 1
- 239000010951 brass Substances 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
- 239000010974 bronze Substances 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 125000005265 dialkylamine group Chemical group 0.000 description 1
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 239000004519 grease Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 229910001959 inorganic nitrate Inorganic materials 0.000 description 1
- 229910052816 inorganic phosphate Inorganic materials 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
- 235000020130 leben Nutrition 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 229940082615 organic nitrates used in cardiac disease Drugs 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 238000010079 rubber tapping Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- KBMBVTRWEAAZEY-UHFFFAOYSA-N trisulfane Chemical compound SSS KBMBVTRWEAAZEY-UHFFFAOYSA-N 0.000 description 1
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
Classifications
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16N—LUBRICATING
- F16N15/00—Lubrication with substances other than oil or grease; Lubrication characterised by the use of particular lubricants in particular apparatus or conditions
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/08—Inorganic acids or 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
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/08—Inorganic acids or salts thereof
- C10M2201/081—Inorganic acids or salts thereof containing halogen
-
- 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
- C10M2201/08—Inorganic acids or salts thereof
- C10M2201/082—Inorganic acids or salts thereof containing nitrogen
-
- 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
- C10M2201/08—Inorganic acids or salts thereof
- C10M2201/084—Inorganic acids or salts thereof containing sulfur, selenium or tellurium
-
- 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
- C10M2201/085—Phosphorus oxides, acids or salts
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/02—Hydroxy compounds
- C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
-
- 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
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
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Definitions
- a lubricant is needed to serve as an antiwear and antiseize agent, as Well as a coolant.
- the requirements for a satisfactory lubricant in the working of ferrous metals are not as severe as in the case of non-ferrous metals. Accordingly, the prior art is replete with numerous lubricants for use with ferrous metals and these lubricants include oil, fat, grease, soaps, detergents, emulsions, etc. However, these lubricants generally are not satisfactory for use in the working of nonferrous metals and particularly zirconium, titanium and alloys thereof.
- lubrication of non-ferrous metals is accomplished by utilizing a lubricant comprising a phenolic compound in which the hydroxyl is attached directly to the phenol nucleus.
- the phenolic compound is an alkyl phenol in which the alkyl group contains from 1 to 24 and still more particularly from 5 to 12 carbon atoms.
- the phenolic compound may be utilized alone or in admixture with other suitable lubricating ingredients.
- the lubricant set forth in the present invention is particularly advantageous for use in the working of nonferrous metals, it is understood that the lubricant also may be utilized to advantage in the working of ferrous metals.
- the working of the metal may take various forms including drawing, rolling, extruding, cutting, drilling, broaching, tapping, threading, etc.
- the lubricant set forth herein is of especial advantage for use in tube'reducing or similar operations.
- the lubricant In addition to serving as an antiwear and anti-seizure agent, the lubricant must survive the chemical and thermal environment at the interface to avoid formation of wear debris which is difiicult to remove from the finished article.
- the lubricant also must avoid corrosion of the metal, staining and must not excessively alter the surface structure of the metal. This latter requirement is particularly important in the case of zirconium and titanium because of the desirability to prevent formation of the open grain surface.
- the lubricant for use in the present invention is phenol but preferably is an alkyl phenol in which the alkyl group contains from 1 to 24 and preferably from 5 to 12 carbon atoms.
- Illustrative examples in this embodiment of the preferred alkyl phenols comprise pentylphenol, hexylphenol, heptylphenol, octylphenol, nonylphenol, decylphenol, undecylphenol, dodecylphenol, with the alkyl group being in the ortho, meta or preferably in the para position, or mixture thereof.
- alkyl phenols included in this embodiment comprise methylphenol, ethylphenol, propylphenol, butylphenol, tridecylphenol, tetradecylphenol, pentadecylphenol, hexadecylphenol, heptadecylphenol, octadecylphenol, nonadecylphenol, eicosylphenol, again with the alkyl group being in the ortho, meta or preferably in the para position.
- the alkyl group may be of primary, secondary or tertiary configuration.
- the phenolic compound contains two or more alkyl groups of from 1 to 20 carbon atoms each.
- the alkyl groups are of the same chain length and in another embodiment the alkyl groups are of different chain length. With two alkyl groups, these may be in the positions 2,3-, 2,4-, 2,5-, 2,6-, 3,4- or 3,5-positions. With three alkyl groups, the alkyl groups may be in the positions 2,3,4-, 2,3,5, 2,3,6-, 2,4,5-, 2,4,6- or 3,4,5-positions.
- phenolic compounds in these embodiments include 2,4-dibutylphenol, 2,5-diamylphenol, 2,6-dioctylphenol, Z-methyl 4 octylphenol, 2-methyl-6-nonylphenol, 2,4,6-trimethylphenol, 2, 4,6-triethylphenol, 2,4,6-tributylphenol, 2,6-dimethyl-4- octylphenol, 2,6-dimethyl-4-nonylphenol, 2-butyl-4,6-dimethylphenol, 2,6-dibutyl-4-methylphenol, etc.
- alkyl groups may be of primary, secondary and/or tertiary configuration and that a mixture of the monoand/or polyalkyl phenols may be used.
- the phenolic compound may contain other substituents attached to the phenolic ring. These substituents may contain halogen, sulfur, oxygen, etc. Of the halogen substituents, chlorine is preferred, the other halogens being bromine, iodine and/or fluorine.
- the sulfur may be in the form of mercapto, thioether, heterocyclic sulfur, etc.
- the nitrogen may be in the form of amine, alkylamine or dialkylamine in which the alkyl contains from 1 to about 10 carbon atoms each, heterocyclic nitrogen, etc.
- the other oxygen may be as hydroxyl, ether, carbonyl, heterocyclic oxygen, etc. It is understood that these variously substituted phenolic compounds are not necessarily equivalent.
- the phenolic compound set forth herein may be used in admixture with other lubricating ingredients and may be in the form of a solution or emulsion.
- the other ingredient comprises a fatty acid and particularly oleic acid.
- fatty acids include decylenic, dodecylenic, palmitoleic, ricinoleic, petroselinic, vaccenic, linoleic, linolenic, eleostearic, licanic, parinaric, gadoleic, cetoleic, selacholeic, etc., as illustrative of unsaturated fatty acids and butyric, isovaleric, caproic, caprylic, capric, lauric,
- the lubricating composition may contain mineral oil, sulfonated oil, alcohols, ethers, fatty acid esters, alkanolamine soaps of fatty acids, alkali metal soaps of fatty acids, salts, organic nitrates, inorganic nitrates, organic phosphates, inorganic phosphates, various water based lubricants, etc.
- the composition may be utilized as an emulsion, either with or without water.
- these additional ingredients will be selected from those described in the prior art.
- the phenolic compound may be used in these compositions in the range of from about 1% to about 99% and preferably from about to about 80% by weight of the final composition, exclusive of water or solvent utilized in the final composition.
- the lubricant of the present invention is utilized in conventional manner, which will depend on the particular procedure employed in the working of the metal. In any event, the lubricant must be applied in a manner that it will be present at the points of contact of the metals in moving relationship to each other. Also, the amount of lubricant will be suificient to accomplish effective lubrication, which amount also will depend upon the particular working procedure employed.
- phenolic compound having the hydroxyl directly attached to the phenol nucleus.
- the phenolic compound may be used alone or in admixture with other ingredients as described hereinbefore.
- a total of about 2 g. of lubricant is utilized. About 1.8 g. of lubricant is applied to the disc and about 0.2 g. of lubricant is applied to the pin.
- the equipment is enclosed in a housing which is heated for varying the temperature of the run which, in these evaluations, can be within the range of from 72 to 212 F.
- the speed is fixed at 6 r.p.m.
- an original load of 100 g. is increased in units of 100 g. at intervals of 1.67 minutes to a maximum load of 1300 g.
- a strain gage circuit is used as sensing element in converting the frictional effects into equivalent electrical responses, which then are recorded on a continuous chart recorder. The coeflicient of friction is determined for each time interval.
- the diameter of the wear spot on the pin is measured. The pin and disc are visually inspected immediately after the test to determine the amount of debris.
- the following table reports runs made using nonylphenol as the lubricant and a run using a mixture of 90% nonylphenol and 10% oleic acid. For comparative purposes, the table also reports the results of a run using oleic acid alone as the lubricant. These runs were made at a temperature of 212 F.
- EXAMPLE II The lubricant used in this example is octylphenol, which was evaluated in the same manner as described in Example I.
- the coefiicient of friction decreased from 0.125 to 0.111 after 202 minutes and a load of 1300 g.
- the wear area was 0.181 mm. and the debris was light to moderate.
- EXAMPLE III The lubricant used in this example is dodecylphenol and the evaluation was made in the same manner as described in Example I.
- the coefiicient decreased from 0.150 to 0.095 after 202 minutes and a load of 1300 g.
- the debris again was light to moderate and the wear area was 0.138 mm.
- EXAMPLE IV An additional evaluation was made in the same manner as described in Example I but using a mixture of 90% nonylphenol and 10% stearic acid. The coetficient of friction decreased from 0.084 to 0.067 during the run of 202 minutes. The amount of debris was light and the wear area was 0.196 mm.
- EXAMPLE V Another evaluation was made in the same manner as above but using an emulsion of 30% by weight of octylphenol, 10% by weight of potassium stearate and 60% by weight of water as the lubricant. The coefiicient of friction decreased from 0.134 to 0.053. The amount of debris was light and the wear area was 0.138 mmf
- EXAMPLE VI Another evaluation was made using a mixture of 90% by weight nonylphenol and 10% by weight of Neustrene 060 (a refined hydrogenated tallow glyceride) as the lubricant in the same manner as described in the previous examples. The coefficient of friction decreased from 0.117 to 0.095. The amount of debris was light and the wear area was 0.138 mmfi. In contrast, another run using only the Neustrene 0.60 as the lubricant formed more debris which is described as being moderate.
- EXAMPLE VII An evaluation was made in the same manner as hereinbefore described using a mixture of 50% nonylphenol and 50% by weight of mineral oil.
- the mineral oil is available commercially as Sentry 20 and is a solvent extracted neutral oil having a viscosity, SUS, of 205 at 100 F.
- the coefficient of friction in this run decreased from 0.134 to 0.089 after 202 minutes and a final load of 1300 g.
- the debris was light and the wear area was 0.166 mm?. In another run using only the mineral oil, the amount of debris was described as heavy.
- EXAMPLE VHI As hereinbefore set forth, it is an essential feature of the present invention that the hydroxyl group is attached directly to the phenol nucleus. This criticality is demonstrated in a run in which oxyethylated nonlyphenol containing 9-10 oxyethylene groups was used as the lubricant. This oxyethylated nonylphenol is available commercially as Triton X-lOO. When used as a lubricant and evaluated in the same manner as described in the previous examples, considerable debris was formed and the wear area was 0.273 mm.
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- Engineering & Computer Science (AREA)
- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Lubricants (AREA)
- Metal Extraction Processes (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US25130872A | 1972-05-08 | 1972-05-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3794595A true US3794595A (en) | 1974-02-26 |
Family
ID=22951380
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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US00251308A Expired - Lifetime US3794595A (en) | 1972-05-08 | 1972-05-08 | Working of non-ferrous metals |
Country Status (7)
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5108634A (en) * | 1988-01-29 | 1992-04-28 | Idemitsu Kosan Company Limited | Lubricating oil composition comprising a specified base oil and an alkyl substituted phenol |
CN111014326A (zh) * | 2019-12-25 | 2020-04-17 | 南京派诺金属表面处理技术有限公司 | 一种用于钢帘线的拉丝粉及其制备方法 |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS54142483U (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1978-03-28 | 1979-10-03 |
-
1972
- 1972-05-08 US US00251308A patent/US3794595A/en not_active Expired - Lifetime
-
1973
- 1973-04-11 IT IT49378/73A patent/IT980167B/it active
- 1973-04-28 DE DE2321657A patent/DE2321657C3/de not_active Expired
- 1973-05-07 GB GB2163873A patent/GB1425487A/en not_active Expired
- 1973-05-07 SE SE7306387A patent/SE394895B/xx unknown
- 1973-05-08 JP JP48050397A patent/JPS5212865B2/ja not_active Expired
- 1973-05-08 FR FR7316461A patent/FR2184326A5/fr not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5108634A (en) * | 1988-01-29 | 1992-04-28 | Idemitsu Kosan Company Limited | Lubricating oil composition comprising a specified base oil and an alkyl substituted phenol |
CN111014326A (zh) * | 2019-12-25 | 2020-04-17 | 南京派诺金属表面处理技术有限公司 | 一种用于钢帘线的拉丝粉及其制备方法 |
Also Published As
Publication number | Publication date |
---|---|
SE394895B (sv) | 1977-07-18 |
JPS4947759A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1974-05-09 |
IT980167B (it) | 1974-09-30 |
FR2184326A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1973-12-21 |
DE2321657A1 (de) | 1973-11-22 |
JPS5212865B2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1977-04-09 |
GB1425487A (en) | 1976-02-18 |
DE2321657B2 (de) | 1978-01-26 |
DE2321657C3 (de) | 1978-10-05 |
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AS | Assignment |
Owner name: IKKO WOLVERINE INC., A CORP. OF DE, STATELESS Free format text: ASSIGNOR ASSIGNS THE ENTIRE INTEREST, SUBJECT TO LICENSE RECITED;ASSIGNOR:UOP INC., A CORP. OF DE;REEL/FRAME:003914/0724 Effective date: 19810522 Owner name: IKKO WOLVERINE INC., A CORP. OF DE Free format text: ASSIGNOR ASSIGNS THE ENTIRE INTEREST, SUBJECT TO LICENSE RECITED.;ASSIGNOR:UOP INC., A CORP. OF DE;REEL/FRAME:003914/0724 Effective date: 19810522 |