US20040072702A1 - Method for cold rolling metals using an aqueous lubricant comprising at least a carboxylic acid, a phosphate ester and a wax - Google Patents
Method for cold rolling metals using an aqueous lubricant comprising at least a carboxylic acid, a phosphate ester and a wax Download PDFInfo
- Publication number
- US20040072702A1 US20040072702A1 US10/467,151 US46715103A US2004072702A1 US 20040072702 A1 US20040072702 A1 US 20040072702A1 US 46715103 A US46715103 A US 46715103A US 2004072702 A1 US2004072702 A1 US 2004072702A1
- Authority
- US
- United States
- Prior art keywords
- radicals
- carbon atoms
- lubricant
- mixture
- phosphate ester
- 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.)
- Abandoned
Links
- 239000000314 lubricant Substances 0.000 title claims abstract description 41
- 229910052751 metal Inorganic materials 0.000 title claims abstract description 38
- 239000002184 metal Substances 0.000 title claims abstract description 38
- 238000000034 method Methods 0.000 title claims abstract description 31
- -1 phosphate ester Chemical class 0.000 title claims abstract description 26
- 229910019142 PO4 Inorganic materials 0.000 title claims abstract description 19
- 239000010452 phosphate Substances 0.000 title claims abstract description 18
- 238000005097 cold rolling Methods 0.000 title claims abstract description 16
- 150000002739 metals Chemical class 0.000 title claims abstract description 12
- 150000001732 carboxylic acid derivatives Chemical class 0.000 title claims abstract 4
- 239000000203 mixture Substances 0.000 claims abstract description 37
- 239000002253 acid Substances 0.000 claims abstract description 27
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 20
- 239000004215 Carbon black (E152) Substances 0.000 claims abstract description 8
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 8
- 229910052500 inorganic mineral Inorganic materials 0.000 claims abstract description 8
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 8
- 239000011707 mineral Substances 0.000 claims abstract description 7
- 238000002844 melting Methods 0.000 claims abstract description 6
- 230000008018 melting Effects 0.000 claims abstract description 6
- 239000002245 particle Substances 0.000 claims abstract description 6
- 239000001993 wax Substances 0.000 claims description 26
- 150000001875 compounds Chemical class 0.000 claims description 10
- 125000000524 functional group Chemical group 0.000 claims description 8
- 150000007530 organic bases Chemical class 0.000 claims description 7
- 150000007513 acids Chemical class 0.000 claims description 5
- 150000001408 amides Chemical group 0.000 claims description 5
- 150000002148 esters Chemical class 0.000 claims description 5
- 229910001220 stainless steel Inorganic materials 0.000 claims description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 4
- 239000007864 aqueous solution Substances 0.000 claims description 4
- 229910052802 copper Inorganic materials 0.000 claims description 4
- 239000010949 copper Substances 0.000 claims description 4
- 150000002500 ions Chemical class 0.000 claims description 4
- 239000011203 carbon fibre reinforced carbon Substances 0.000 claims description 3
- 150000001768 cations Chemical class 0.000 claims description 3
- 239000012074 organic phase Substances 0.000 claims description 3
- 239000010935 stainless steel Substances 0.000 claims description 3
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical class [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 claims description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 2
- 229910001369 Brass Inorganic materials 0.000 claims description 2
- 229910000906 Bronze Inorganic materials 0.000 claims description 2
- 229910000831 Steel Inorganic materials 0.000 claims description 2
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 150000001340 alkali metals Chemical class 0.000 claims description 2
- 229910045601 alloy Inorganic materials 0.000 claims description 2
- 239000000956 alloy Substances 0.000 claims description 2
- 235000011114 ammonium hydroxide Nutrition 0.000 claims description 2
- 239000010951 brass Substances 0.000 claims description 2
- 239000010974 bronze Substances 0.000 claims description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 2
- 239000010941 cobalt Substances 0.000 claims description 2
- 229910017052 cobalt Inorganic materials 0.000 claims description 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 claims description 2
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 claims description 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
- 229910052759 nickel Inorganic materials 0.000 claims description 2
- 239000012188 paraffin wax Substances 0.000 claims description 2
- 235000019809 paraffin wax Nutrition 0.000 claims description 2
- 235000019271 petrolatum Nutrition 0.000 claims description 2
- 229920000768 polyamine Polymers 0.000 claims description 2
- 150000003141 primary amines Chemical class 0.000 claims description 2
- 150000003335 secondary amines Chemical class 0.000 claims description 2
- 239000010959 steel Substances 0.000 claims description 2
- 150000003512 tertiary amines Chemical class 0.000 claims description 2
- 239000011135 tin Substances 0.000 claims description 2
- 229910052718 tin Inorganic materials 0.000 claims description 2
- 229910052725 zinc Inorganic materials 0.000 claims description 2
- 239000011701 zinc Substances 0.000 claims description 2
- 150000007514 bases Chemical class 0.000 claims 1
- 125000005702 oxyalkylene group Chemical group 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 abstract description 12
- 230000001747 exhibiting effect Effects 0.000 abstract 1
- 235000021317 phosphate Nutrition 0.000 description 13
- 239000005069 Extreme pressure additive Substances 0.000 description 10
- 239000006185 dispersion Substances 0.000 description 9
- 238000005096 rolling process Methods 0.000 description 9
- 239000000654 additive Substances 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 235000019198 oils Nutrition 0.000 description 8
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 6
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 6
- 239000007787 solid Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 239000002736 nonionic surfactant Substances 0.000 description 4
- 239000011593 sulfur Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- 150000001412 amines Chemical class 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 239000012736 aqueous medium Substances 0.000 description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 2
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical group C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 150000004671 saturated fatty acids Chemical class 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-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
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-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
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 235000021357 Behenic acid Nutrition 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 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
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 235000021353 Lignoceric acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 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
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 1
- MUBKMWFYVHYZAI-UHFFFAOYSA-N [Al].[Cu].[Zn] Chemical compound [Al].[Cu].[Zn] MUBKMWFYVHYZAI-UHFFFAOYSA-N 0.000 description 1
- 150000001242 acetic acid derivatives Chemical class 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 1
- 235000020661 alpha-linolenic acid Nutrition 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
- LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 1
- 238000000149 argon plasma sintering Methods 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000003139 buffering effect Effects 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 125000005587 carbonate group Chemical group 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000006482 condensation reaction Methods 0.000 description 1
- 230000001934 delay Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical class CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 150000004675 formic acid derivatives Chemical class 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 229910052738 indium Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 235000020778 linoleic acid Nutrition 0.000 description 1
- OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
- 229960004488 linolenic acid Drugs 0.000 description 1
- KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 1
- 125000005645 linoleyl group Chemical group 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 229910001510 metal chloride Inorganic materials 0.000 description 1
- 229910001463 metal phosphate Inorganic materials 0.000 description 1
- 229910052976 metal sulfide Inorganic materials 0.000 description 1
- 239000000693 micelle Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 125000001117 oleyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])/C([H])=C([H])\C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 235000003441 saturated fatty acids Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- QZZGJDVWLFXDLK-UHFFFAOYSA-N tetracosanoic acid Chemical class CCCCCCCCCCCCCCCCCCCCCCCC(O)=O QZZGJDVWLFXDLK-UHFFFAOYSA-N 0.000 description 1
- 238000004627 transmission electron microscopy Methods 0.000 description 1
- 238000011282 treatment Methods 0.000 description 1
- 150000003626 triacylglycerols Chemical class 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C10M171/00—Lubricating compositions characterised by purely physical criteria, e.g. containing as base-material, thickener or additive, ingredients which are characterised exclusively by their numerically specified physical properties, i.e. containing ingredients which are physically well-defined but for which the chemical nature is either unspecified or only very vaguely indicated
- C10M171/06—Particles of special shape or size
-
- 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
- C10M173/02—Lubricating compositions containing more than 10% water not containing mineral or fatty oils
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/04—Elements
- C10M2201/041—Carbon; Graphite; Carbon black
-
- 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
- C10M2201/06—Metal compounds
- C10M2201/062—Oxides; Hydroxides; Carbonates or bicarbonates
-
- 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
- C10M2201/18—Ammonia
-
- 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
- C10M2205/14—Synthetic waxes, e.g. polythene waxes
-
- 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
- C10M2205/16—Paraffin waxes; Petrolatum, e.g. slack wax
-
- 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
- C10M2205/18—Natural waxes, e.g. ceresin, ozocerite, bees wax, carnauba; Degras
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/122—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms monocarboxylic
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/121—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms
- C10M2207/123—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of seven or less carbon atoms polycarboxylic
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—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
- C10M2207/126—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 monocarboxylic
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—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
- C10M2207/127—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 polycarboxylic
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
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- 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
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/041—Triaryl phosphates
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/02—Groups 1 or 11
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/04—Groups 2 or 12
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/12—Groups 6 or 16
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/14—Group 7
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2010/00—Metal present as such or in compounds
- C10N2010/16—Groups 8, 9, or 10
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
- C10N2020/055—Particles related characteristics
- C10N2020/06—Particles of special shape or size
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/243—Cold working
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/244—Metal working of specific metals
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/244—Metal working of specific metals
- C10N2040/245—Soft metals, e.g. aluminum
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/244—Metal working of specific metals
- C10N2040/246—Iron or steel
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/244—Metal working of specific metals
- C10N2040/247—Stainless steel
Definitions
- the subject of the present invention is a cold rolling process for metals using an aqueous lubricant comprising a mixture based on at least one carboxylic acid, on at least one phosphate ester and including at least one wax.
- lubricants such as for example whole oils and aqueous lubricants.
- the other additives used are based on sulfur (sulfur-containing esters, sulfur-containing oils) or based on phosphorus (phosphate esters) or mixtures thereof. They result in the formation of a metal sulfide or a metal phosphate.
- the object of the present invention is to propose a cold rolling process for metals that does not have the drawbacks of the usual processes.
- the process according to the invention makes it possible to work under very severe conditions, representative of high-productivity conditions, while still maintaining the surface finish (coloration, brightness) of the deformed metal.
- a cold rolling process for metals using an aqueous lubricant comprising (1) at least one mixture based on at least one acid chosen from saturated or unsaturated, monocarboxylic or polycarboxylic acids containing 5 to 40 carbon atoms; on at least one acid phosphate ester of formula (RO) x —P( ⁇ O) (OH) x′ , in which formula R is an optionally polyalkoxylated hydrocarbon radical, x and x′ being equal to 1 or 2, provided that the sum of x and x′ is equal to 3; the carboxylic acid and/or the acid phosphate ester being optionally neutralized by an organic or mineral base; and (2) at least one natural or synthetic wax having a melting point not less than 50° C. and having a mean particle size ranging between 0.5-10 ⁇ m.
- formula R is an optionally polyalkoxylated hydrocarbon radical, x and x′ being equal to 1 or 2, provided that the sum of x and x′ is equal to 3
- the size measurements are carried out either by laser diffraction or by light scattering. There is no difficulty for those skilled in the art to choose one of these two methods depending on the size of the objects.
- conventional lubricant is understood to mean either a whole oil containing one or more extreme-pressure additives, or an aqueous lubricant also containing one or more extreme-pressure additives. It should be noted that conventional extreme-pressure additives are compounds containing phosphorus (such as for example phosphates) or sulfur (such as especially sulfonates).
- an aqueous lubricant according to the invention allows the productivity of cold rolling operations to be significantly improved.
- this lubricant it is possible to increase the thickness reduction ratio of the rolled metal by at least 15%, more particularly by at least 20% and highly advantageously by at least 30%, compared with the maximum reduction ratio achievable by a rolling mill using a conventional lubricant, whether a whole oil containing one or more extreme-pressure additives or an aqueous lubricant containing one or more extreme-pressure additives.
- the aqueous lubricant comprises at least one mixture based on at least one acid chosen from saturated or unsaturated, monocarboxylic or polycarboxylic acids containing 5 to 40 carbon atoms; on at least one acid phosphate ester of formula (RO) x —P( ⁇ O) (OH) x′ , in which formula R is an optionally polyalkoxylated hydrocarbon radical, x and x′ being equal to 1 or 2, provided that the sum of x and x′ is equal to 3, the carboxylic acid and/or the acid phosphate ester being optionally neutralized by an organic or mineral base.
- formula R is an optionally polyalkoxylated hydrocarbon radical, x and x′ being equal to 1 or 2, provided that the sum of x and x′ is equal to 3, the carboxylic acid and/or the acid phosphate ester being optionally neutralized by an organic or mineral base.
- the mixture (1) may be an aqueous solution or an aqueous dispersion.
- the term “dispersion” denotes a dispersion of vesicles, droplets or micelles in an aqueous medium.
- the carboxylic acid used possesses one or more carboxylic functional groups and at least one radical containing 5 to 40 carbon atoms, said radical being a linear or branched, alkyl or alkenyl radical having one or more ethylenically unsaturated groups (carbon-carbon double bonds) and optionally being substituted with one or more hydroxyl radicals.
- the acid possesses one or more carboxylic functional groups and a radical containing 7 to 30 carbon atoms, optionally substituted with one or more hydroxyl radicals and optionally having one or more ethylenically unsaturated groups.
- said acid possesses one carboxylic functional group or two.
- this second functional group may or may not be at the end of the chain.
- the carboxylic acid is a saturated or unsaturated fatty acid, more particularly comprising a single carboxylic functional group, or a mixture of several fatty acids.
- saturated fatty acids mention may be made of caproic, caprylic, capric, lauric, myristic, stearic, isostearic, palmitic, behenic and lignoceric acids.
- unsaturated fatty acids examples include the unsaturated fatty acids having a single ethylenically unsaturated group, such as linderic, myristoleic, palmitoleic, oleic and erucic acids; unsaturated fatty acids having two ethylenically unsaturated groups, such as linoleic acid; unsaturated fatty acids having three ethylenically unsaturated groups, such as linolenic acid; and unsaturated fatty acids carrying a hydroxyl group, such as ricinoleic acid, as well as mixtures thereof.
- unsaturated fatty acids having a single ethylenically unsaturated group such as linderic, myristoleic, palmitoleic, oleic and erucic acids
- unsaturated fatty acids having two ethylenically unsaturated groups such as linoleic acid
- R is a hydrocarbon radical containing 1 to 30 carbon atoms, said radical being a saturated or unsaturated, aliphatic or cycloaliphatic radical or an aromatic radical.
- the radicals R which are identical or different, are linear or branched radicals containing 8 to 26 carbon atoms, these being alkyl radicals or alkenyl radicals carrying one or more ethylenically unsaturated groups.
- radicals R which may or may not be identical, may be aromatic radicals carrying alkyl, arylalkyl or alkylaryl substituents, these radicals containing 6 to 30 carbon atoms.
- aromatic radicals carrying alkyl, arylalkyl or alkylaryl substituents, these radicals containing 6 to 30 carbon atoms.
- the OA groups which may or may not be identical, correspond to an oxyethylene, oxypropylene or oxybutylene radical, or mixtures thereof.
- said group corresponds to an oxyethylene and/or oxypropylene radical.
- this is preferably between 0 and 80.
- the acid phosphate ester forming part of the composition of the mixture (1) may be formed from a combination of several of them.
- carboxylic acid and/or the acid phosphate ester may be in a form neutralized by a mineral or organic base.
- bases used are preferably water-soluble.
- water-soluble bases is understood to mean compounds soluble in an aqueous medium, at 20° C., with a concentration of from 3 to 7% by weight.
- the bases employed are organic bases but are more particularly chosen from primary, secondary or tertiary amines or polyamines comprising at least one linear, branched or cyclic hydrocarbon radical having 1 to 40 carbon atoms, said radical being optionally substituted with one or more hydroxyl radicals and/or one or more alkoxylated groups.
- the said alkoxylated groups are preferably ethoxylated units.
- the number of alkoxylated units, if present, is less than or equal to 100.
- the amines when the amines have at least two amine functional groups, said functional groups are separated in pairs by a number of carbon atoms ranging between 2 and 5.
- Suitable amines mention may be made of monoethanolamine, diethanolamine, ethylenediamine, aminoethylethanolamine and aminomethylpropanolamine.
- Polyalkoxylated fatty amines may also be used as organic base, such as for example those sold by Rhodia Chimie under the name RHODAMEEN® CS20.
- At least the carboxylic acid is neutralized by an organic base, the amount of the latter being such that the total number of moles of amine functional groups is at least equal to the total number of moles of carboxylic acid functional groups, and preferably at least twice as large.
- the mixture (1) may optionally furthermore include at least one nonionic surfactant.
- the use of this type of compound may be desired when the mixture (1) is in the form of a dispersion.
- polyalkoxylated alkylphenols in particular those in which the alkyl substituent is a C 6 -C 12 one;
- polyalkoxylated mono-, di- or tri-(alkylaryl)phenol preferably chosen from those in which the alkyl substituent is a C 1 -C 6 one;
- polyalkoxylated aliphatics more particularly C 8 -C 22 alcohols
- polyalkoxylated units if present, of these nonionic surfactants usually varies from 2 to 100. It should be noted that the term “polyalkoxylated units” is understood to mean ethoxylated units, propoxylated units or mixtures thereof.
- the amount of surfactant usually varies, if it is present, between 1 and 30% by total weight of the mixture (1).
- the contents of carboxylic acid, of acid phosphate ester, optionally of base, preferably an organic base, and optionally of nonionic surfactant are such that the solids content of the aqueous medium is at least 10% by weight. More precisely, the solids content is between 10 and 70% by weight. Preferably, the solids content varies between 10 and 40% by weight.
- the pH of the mixture (1) ranges between 7 and 9. This pH range may inter alia be achieved by the addition of a buffer agent to said mixture.
- said mixture (1) is combined with at least one metal in the form of a multivalent ion. More particularly, said metal may be in the form of a divalent ion or a trivalent ion. Likewise, it would not be excluded to use several metals, in identical or different oxidation states.
- said metal is chosen from columns IIA, VIII, IB, IIB and VIB, with the exception of cobalt and nickel.
- the metals are chosen from calcium, magnesium, copper, zinc, iron, aluminum and chromium, by themselves or as mixtures.
- the mixture (1) associated with the metal is more precisely in the form of a dispersion comprising lamellar crystallites having a length ranging between 0.1 and 100 ⁇ m, a width ranging between 0.5 and 30 ⁇ m and a thickness ranging between 5 and 200 nm.
- These crystallites comprise a stack of organic phases (O) and of aqueous solutions (A) in the sequence O/[A/O]n, n being an integer different from 0 and such that a stack has a thickness of 5 to 200 nm. More particularly, n is between 1 and 20.
- the size of the crystallites their length is advantageously between 0.5 and 20 ⁇ m.
- the width of the lamellar crystallites is more particularly between 0.5 and 10 ⁇ m.
- the thickness of the lamellar crystallites is preferably between 10 and 100 nm.
- the abovementioned dimensions of the lamellar crystallites correspond to average values. In other words, there is a distribution in the sizes of the lamellar crystallites, the average of which lies within the above ranges.
- the measurements of the dimensions of the lamellar crystallites are carried out using transmission electron microscopy on a specimen vitrified cryogenically (Cryo-Met—see O. Aguerre-Chariol, M. Deruelle, T.
- the crystallites are advantageously used in the presence of at least one nonionic surfactant.
- the crystallites may be obtained by bringing a solution or dispersion containing the acid phosphate ester and the optionally neutralized carboxylic acid into contact with the metal in ionic and/or metallic form.
- this may equally well be in its metallic form or in the form of a multivalent cation.
- Said cation may itself be in the form of a solid, a solution or a dispersion.
- the metal is used in the form of a solution, preferably an aqueous solution
- a solution preferably an aqueous solution
- salts of mineral acids such as halides, with chlorides for example, or nitrates
- salts or organic acids such as, among others, formates and acetates.
- metal in an oxide, hydroxide or carbonate form, or the metal itself.
- the contacting is carried out in the presence of at least one compound having the effect of buffering the pH. More particularly, one or more compounds are chosen such that the pH of the medium is between 7 and 9.
- the contacting takes place with stirring.
- the metal in the chosen form is introduced into the mixture (1), the carboxylic acid preferably being neutralized by an organic base.
- the operation advantageously takes place at a temperature below 100° C. and preferably at a temperature ranging between 20 and 60° C.
- the aqueous lubricant used in the cold rolling process according to the invention furthermore includes at least one natural or synthetic wax, having a melting point not less than 50° C. and having a mean particle size ranging between 0.5-10 ⁇ m.
- the wax or waxes are dispersed within the mixture (1) in a homogeneous and stable manner.
- these waxes are chosen from natural waxes of the type consisting of paraffin waxes or synthetic waxes having ester and/or amide functional groups.
- the waxes used are those having amide functional groups.
- Said waxes may be obtained, for example, by a condensation reaction, and more particularly by a reaction of an ester or acid functional group with an amine functional group.
- these waxes have a degree of polymerization of at most 10 and advantageously at most 3.
- the aforementioned waxes correspond to the following formula: R′—CO-A-(CR′′ 2 ) n′′ A-CO′R′, in which formula the radicals R′, which may or may not be identical, represent an aliphatic radical containing 5 to 22 carbon atoms, said radical being saturated or having one or more conjugated or nonconjugated carbon-carbon double bonds; the radicals R′′, which may or may not be identical, represent a hydrogen atom or an alkyl radical containing 1 to 4 carbon atoms; n represents an integer between 2 and 12; and the radicals A, which may or may not be identical, represent —O— or —NH—. It should be noted that the radicals A are preferably of the same type.
- the melting point of the waxes is not less than 80° C.
- the wax content in the aqueous lubricant during its use is between 0.05 and 10% by weight of the lubricant, preferably between 0.05 and 5% by weight of the lubricant.
- the wax may be introduced into the mixture either by incorporating the wax particles, the size of which lies within the abovementioned range, into said mixture. It is also possible to introduce the wax by adding the latter in molten form to the mixture, and to precipitate it in the mixture, the operation advantageously taking place by carrying out a grinding operation so as to obtain the appropriate size of particles.
- the aqueous lubricants according to the invention may also include additives that are conventional in this field, such as preservatives, anticorrosion agents, antifoams and stabilizers.
- the metals on which such treatments may be carried out are especially, and mainly, steels, stainless steels, aluminum, copper, zinc, tin, copper-based alloys (bronze, brass), etc.
- the present invention is most particularly applicable to the cold rolling of stainless steel.
- the rolled metal was coiled stainless steel, 10 mm in width and about 0.4 mm in thickness.
- the applied force on the rolls varied from 200 metric tonnes/m to 1200 metric tonnes/m, so as to obtain a sheet reduction ratio varying from 20 to 55%.
- the lubricant according to the invention made it possible to obtain, for a linear speed of the rolls of 5 m/s, reduction ratios of at least 55% without having reached the clamping limit of the rolling mill.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Lubricants (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US11/866,850 US7776799B2 (en) | 2001-02-05 | 2007-10-03 | Cold rolling process for metals using an aqueous lubricant comprising at least one carboxylic acid, one phosphate ester and one wax |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR01/01566 | 2001-02-05 | ||
| FR0101566A FR2820431B1 (fr) | 2001-02-06 | 2001-02-06 | Procede de deformation de metaux mettant en oeuvre un lubrifiant aqueux additive permettant d'augmenter la productivite |
| PCT/FR2002/000436 WO2002062931A1 (fr) | 2001-02-05 | 2002-02-05 | Procede de laminage a froid de metaux utilisant un lubrifiant aqueux comprenant au moins un acide carboxylique, un ester phosphate et une cire |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/866,850 Continuation US7776799B2 (en) | 2001-02-05 | 2007-10-03 | Cold rolling process for metals using an aqueous lubricant comprising at least one carboxylic acid, one phosphate ester and one wax |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US20040072702A1 true US20040072702A1 (en) | 2004-04-15 |
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Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US10/467,151 Abandoned US20040072702A1 (en) | 2001-02-05 | 2002-02-05 | Method for cold rolling metals using an aqueous lubricant comprising at least a carboxylic acid, a phosphate ester and a wax |
| US11/866,850 Expired - Fee Related US7776799B2 (en) | 2001-02-05 | 2007-10-03 | Cold rolling process for metals using an aqueous lubricant comprising at least one carboxylic acid, one phosphate ester and one wax |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US11/866,850 Expired - Fee Related US7776799B2 (en) | 2001-02-05 | 2007-10-03 | Cold rolling process for metals using an aqueous lubricant comprising at least one carboxylic acid, one phosphate ester and one wax |
Country Status (12)
| Country | Link |
|---|---|
| US (2) | US20040072702A1 (fr) |
| EP (1) | EP1358305A1 (fr) |
| JP (1) | JP4017523B2 (fr) |
| KR (1) | KR100512088B1 (fr) |
| CN (1) | CN1272416C (fr) |
| AU (1) | AU2002235983B2 (fr) |
| BR (1) | BR0206983A (fr) |
| CA (1) | CA2437601C (fr) |
| FR (1) | FR2820431B1 (fr) |
| MX (1) | MXPA03006878A (fr) |
| RU (1) | RU2265645C2 (fr) |
| WO (1) | WO2002062931A1 (fr) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2913355A1 (fr) * | 2007-03-08 | 2008-09-12 | Michelin Soc Tech | Procece de trefilage humide de fils d'acier destines au renforcement de bandages pneumatiques |
| FR2913356A1 (fr) * | 2007-03-08 | 2008-09-12 | Rhodia Recherches & Tech | Lubrification par des dispersions dans des procedes de deformation des metaux |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010129953A1 (fr) * | 2009-05-08 | 2010-11-11 | Quaker Chemical Corporation | Lubrifiant à solution aqueuse pour laminage à froid de l'acier |
| CA2835019C (fr) * | 2011-05-06 | 2018-04-10 | Chemetall Gmbh | Fluide de travail de metal sans cov sans amine |
| JP5890152B2 (ja) * | 2011-11-17 | 2016-03-22 | 出光興産株式会社 | 水溶性金属加工油剤、金属加工液、及び金属加工方法 |
| KR102075213B1 (ko) * | 2017-12-21 | 2020-02-07 | 주식회사 포스코 | 열연강판 냉각용 조성물 및 이를 이용한 열연 강판의 냉각 방법 |
| EP4006184A4 (fr) | 2019-07-31 | 2022-08-31 | JFE Steel Corporation | Tôle d'acier électromagnétique non orienté et procédé pour sa fabrication |
| CN113462448A (zh) * | 2021-06-08 | 2021-10-01 | 青岛华瑞泰格工贸有限公司 | 一种可生物降解的低发烟型金属挤压攻丝油 |
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| US3966619A (en) * | 1974-11-04 | 1976-06-29 | Alcan Research And Development Limited | Lubricants for cold working of aluminium |
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| FR2130981A5 (fr) * | 1971-03-29 | 1972-11-10 | Rhone Poulenc Sa | |
| US4362634A (en) * | 1980-03-19 | 1982-12-07 | Stauffer Chemical Company | Metal working lubricant and lubricant emulsion |
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- 2002-02-05 KR KR10-2003-7010311A patent/KR100512088B1/ko not_active Expired - Fee Related
- 2002-02-05 EP EP02702454A patent/EP1358305A1/fr not_active Withdrawn
- 2002-02-05 JP JP2002563269A patent/JP4017523B2/ja not_active Expired - Lifetime
- 2002-02-05 AU AU2002235983A patent/AU2002235983B2/en not_active Ceased
- 2002-02-05 BR BR0206983-0A patent/BR0206983A/pt not_active Application Discontinuation
- 2002-02-05 CA CA2437601A patent/CA2437601C/fr not_active Expired - Fee Related
- 2002-02-05 CN CNB028054113A patent/CN1272416C/zh not_active Expired - Fee Related
- 2002-02-05 WO PCT/FR2002/000436 patent/WO2002062931A1/fr not_active Ceased
- 2002-02-05 MX MXPA03006878A patent/MXPA03006878A/es active IP Right Grant
- 2002-02-05 RU RU2003127020/04A patent/RU2265645C2/ru not_active IP Right Cessation
- 2002-02-05 US US10/467,151 patent/US20040072702A1/en not_active Abandoned
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- 2007-10-03 US US11/866,850 patent/US7776799B2/en not_active Expired - Fee Related
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2913355A1 (fr) * | 2007-03-08 | 2008-09-12 | Michelin Soc Tech | Procece de trefilage humide de fils d'acier destines au renforcement de bandages pneumatiques |
| FR2913356A1 (fr) * | 2007-03-08 | 2008-09-12 | Rhodia Recherches & Tech | Lubrification par des dispersions dans des procedes de deformation des metaux |
| WO2008110493A1 (fr) * | 2007-03-08 | 2008-09-18 | Rhodia Operations | Lubrification par des dispersions dans des procédés de déformation des métaux |
| WO2008113481A1 (fr) * | 2007-03-08 | 2008-09-25 | Societe De Technologie Michelin | Procede de trefilage humide de fils d'acier destines au renforcement de bandages pneumatiques |
| US20100170624A1 (en) * | 2007-03-08 | 2010-07-08 | Societe De Technologie Michelin | Method for the Wet Drawing of Steel Cables for Reinforcing Tires |
| US8555689B2 (en) * | 2007-03-08 | 2013-10-15 | Michelin Recherche Et Technique S.A. | Method for the wet drawing of steel cables for reinforcing tires |
Also Published As
| Publication number | Publication date |
|---|---|
| KR20030082584A (ko) | 2003-10-22 |
| KR100512088B1 (ko) | 2005-09-02 |
| RU2003127020A (ru) | 2005-02-27 |
| US7776799B2 (en) | 2010-08-17 |
| CA2437601A1 (fr) | 2002-08-15 |
| AU2002235983B9 (en) | 2002-08-19 |
| FR2820431A1 (fr) | 2002-08-09 |
| FR2820431B1 (fr) | 2007-04-27 |
| EP1358305A1 (fr) | 2003-11-05 |
| CN1494584A (zh) | 2004-05-05 |
| US20080028812A1 (en) | 2008-02-07 |
| AU2002235983B2 (en) | 2004-10-14 |
| RU2265645C2 (ru) | 2005-12-10 |
| CA2437601C (fr) | 2011-01-11 |
| CN1272416C (zh) | 2006-08-30 |
| BR0206983A (pt) | 2004-02-10 |
| JP4017523B2 (ja) | 2007-12-05 |
| MXPA03006878A (es) | 2005-04-11 |
| WO2002062931A1 (fr) | 2002-08-15 |
| JP2004527598A (ja) | 2004-09-09 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| AS | Assignment |
Owner name: CHIMIE, RHODIA, FRANCE Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNORS:RAISON, DOMINIQUE;LE HELLOCO, JEAN-GUY;REEL/FRAME:014695/0064 Effective date: 20030916 |
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| STCB | Information on status: application discontinuation |
Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION |