CA1115684A - Metal working emulsion - Google Patents
Metal working emulsionInfo
- Publication number
- CA1115684A CA1115684A CA322,726A CA322726A CA1115684A CA 1115684 A CA1115684 A CA 1115684A CA 322726 A CA322726 A CA 322726A CA 1115684 A CA1115684 A CA 1115684A
- Authority
- CA
- Canada
- Prior art keywords
- weight
- metal working
- parts
- oil
- emulsion according
- 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
Links
- 239000000839 emulsion Substances 0.000 title claims abstract description 82
- 238000005555 metalworking Methods 0.000 title claims abstract description 48
- 239000003921 oil Substances 0.000 claims abstract description 64
- 235000014113 dietary fatty acids Nutrition 0.000 claims abstract description 51
- 229930195729 fatty acid Natural products 0.000 claims abstract description 51
- 239000000194 fatty acid Substances 0.000 claims abstract description 51
- 150000004665 fatty acids Chemical class 0.000 claims abstract description 49
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 32
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims abstract description 22
- 239000000344 soap Substances 0.000 claims abstract description 20
- 150000001412 amines Chemical class 0.000 claims abstract description 14
- 239000003513 alkali Substances 0.000 claims abstract description 11
- 235000019198 oils Nutrition 0.000 claims description 63
- LDVVTQMJQSCDMK-UHFFFAOYSA-N 1,3-dihydroxypropan-2-yl formate Chemical compound OCC(CO)OC=O LDVVTQMJQSCDMK-UHFFFAOYSA-N 0.000 claims description 25
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 13
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 13
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 13
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 13
- 239000005642 Oleic acid Substances 0.000 claims description 13
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 13
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 13
- 235000019484 Rapeseed oil Nutrition 0.000 claims description 11
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical group OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 10
- 238000002844 melting Methods 0.000 claims description 7
- 230000008018 melting Effects 0.000 claims description 7
- DPUOLQHDNGRHBS-UHFFFAOYSA-N Brassidinsaeure Natural products CCCCCCCCC=CCCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-UHFFFAOYSA-N 0.000 claims description 5
- URXZXNYJPAJJOQ-UHFFFAOYSA-N Erucic acid Natural products CCCCCCC=CCCCCCCCCCCCC(O)=O URXZXNYJPAJJOQ-UHFFFAOYSA-N 0.000 claims description 5
- 239000000654 additive Substances 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- DPUOLQHDNGRHBS-KTKRTIGZSA-N erucic acid Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(O)=O DPUOLQHDNGRHBS-KTKRTIGZSA-N 0.000 claims description 5
- 239000010685 fatty oil Substances 0.000 claims description 5
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 3
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 3
- 239000008158 vegetable oil Substances 0.000 claims description 3
- RZRNAYUHWVFMIP-KTKRTIGZSA-N 1-oleoylglycerol Chemical group CCCCCCCC\C=C/CCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-KTKRTIGZSA-N 0.000 claims description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 2
- 235000019483 Peanut oil Nutrition 0.000 claims description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical group CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 claims description 2
- 235000019197 fats Nutrition 0.000 claims description 2
- RZRNAYUHWVFMIP-UHFFFAOYSA-N monoelaidin Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(O)CO RZRNAYUHWVFMIP-UHFFFAOYSA-N 0.000 claims description 2
- 239000004006 olive oil Substances 0.000 claims description 2
- 235000008390 olive oil Nutrition 0.000 claims description 2
- 239000000312 peanut oil Substances 0.000 claims description 2
- 239000011591 potassium Substances 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 3
- 235000019737 Animal fat Nutrition 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 230000032050 esterification Effects 0.000 claims 1
- 238000005886 esterification reaction Methods 0.000 claims 1
- 235000019869 fractionated palm oil Nutrition 0.000 claims 1
- 229940096992 potassium oleate Drugs 0.000 claims 1
- MLICVSDCCDDWMD-KVVVOXFISA-M potassium;(z)-octadec-9-enoate Chemical compound [K+].CCCCCCCC\C=C/CCCCCCCC([O-])=O MLICVSDCCDDWMD-KVVVOXFISA-M 0.000 claims 1
- 230000001050 lubricating effect Effects 0.000 abstract description 11
- 238000005520 cutting process Methods 0.000 abstract description 8
- 238000003754 machining Methods 0.000 abstract description 6
- 238000001816 cooling Methods 0.000 abstract description 5
- -1 fatty acid monoglycerides Chemical class 0.000 abstract description 3
- 230000001804 emulsifying effect Effects 0.000 abstract description 2
- 238000005096 rolling process Methods 0.000 abstract description 2
- 239000002173 cutting fluid Substances 0.000 description 11
- 239000002480 mineral oil Substances 0.000 description 11
- 239000008367 deionised water Substances 0.000 description 9
- 235000010446 mineral oil Nutrition 0.000 description 8
- 238000009736 wetting Methods 0.000 description 8
- 239000012141 concentrate Substances 0.000 description 7
- 235000008504 concentrate Nutrition 0.000 description 7
- 240000002791 Brassica napus Species 0.000 description 6
- 235000004977 Brassica sinapistrum Nutrition 0.000 description 6
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 6
- 238000005553 drilling Methods 0.000 description 5
- 238000010079 rubber tapping Methods 0.000 description 5
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 5
- 230000000694 effects Effects 0.000 description 4
- 230000007613 environmental effect Effects 0.000 description 4
- 238000000227 grinding Methods 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000779 smoke Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000005069 Extreme pressure additive Substances 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- SEQDDYPDSLOBDC-UHFFFAOYSA-N Temazepam Chemical compound N=1C(O)C(=O)N(C)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1 SEQDDYPDSLOBDC-UHFFFAOYSA-N 0.000 description 3
- 239000003963 antioxidant agent Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- 239000003595 mist Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000002699 waste material Substances 0.000 description 3
- UOFRJXGVFHUJER-UHFFFAOYSA-N 2-[bis(2-hydroxyethyl)amino]ethanol;hydrate Chemical compound [OH-].OCC[NH+](CCO)CCO UOFRJXGVFHUJER-UHFFFAOYSA-N 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- 201000004624 Dermatitis Diseases 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 206010020751 Hypersensitivity Diseases 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 206010028980 Neoplasm Diseases 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 229910001315 Tool steel Inorganic materials 0.000 description 2
- 239000010775 animal oil Substances 0.000 description 2
- 230000003078 antioxidant effect Effects 0.000 description 2
- 208000010668 atopic eczema Diseases 0.000 description 2
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 2
- 201000011510 cancer Diseases 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- 239000006185 dispersion Substances 0.000 description 2
- 239000003995 emulsifying agent Substances 0.000 description 2
- 238000000265 homogenisation Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 2
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000002994 raw material Substances 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000008399 tap water Substances 0.000 description 2
- 235000020679 tap water Nutrition 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910001018 Cast iron Inorganic materials 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 235000021314 Palmitic acid Nutrition 0.000 description 1
- 238000012356 Product development Methods 0.000 description 1
- 206010040880 Skin irritation Diseases 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 238000013019 agitation Methods 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
- TXVHTIQJNYSSKO-UHFFFAOYSA-N benzo[e]pyrene Chemical class C1=CC=C2C3=CC=CC=C3C3=CC=CC4=CC=C1C2=C34 TXVHTIQJNYSSKO-UHFFFAOYSA-N 0.000 description 1
- CZBZUDVBLSSABA-UHFFFAOYSA-N butylated hydroxyanisole Chemical compound COC1=CC=C(O)C(C(C)(C)C)=C1.COC1=CC=C(O)C=C1C(C)(C)C CZBZUDVBLSSABA-UHFFFAOYSA-N 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 230000000711 cancerogenic effect Effects 0.000 description 1
- 231100000315 carcinogenic Toxicity 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 238000005238 degreasing Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000003925 fat Substances 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000005189 flocculation Methods 0.000 description 1
- 230000016615 flocculation Effects 0.000 description 1
- 235000021588 free fatty acids Nutrition 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000007794 irritation Effects 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
- 239000000314 lubricant Substances 0.000 description 1
- 238000005461 lubrication Methods 0.000 description 1
- 231100000516 lung damage Toxicity 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- 235000014593 oils and fats Nutrition 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 229940114930 potassium stearate Drugs 0.000 description 1
- ANBFRLKBEIFNQU-UHFFFAOYSA-M potassium;octadecanoate Chemical compound [K+].CCCCCCCCCCCCCCCCCC([O-])=O ANBFRLKBEIFNQU-UHFFFAOYSA-M 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000010865 sewage Substances 0.000 description 1
- 230000036556 skin irritation Effects 0.000 description 1
- 231100000475 skin irritation Toxicity 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000020354 squash Nutrition 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000007514 turning Methods 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M173/00—Lubricating compositions containing more than 10% water
-
- C—CHEMISTRY; METALLURGY
- 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
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/125—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of eight up to twenty-nine carbon atoms, i.e. fatty acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/10—Carboxylix acids; Neutral salts thereof
- C10M2207/12—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2207/129—Carboxylix acids; Neutral salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having hydrocarbon chains of thirty or more carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/281—Esters of (cyclo)aliphatic monocarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/282—Esters of (cyclo)aliphatic oolycarboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/28—Esters
- C10M2207/283—Esters of polyhydroxy compounds
-
- 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
- C10M2207/28—Esters
- C10M2207/286—Esters of polymerised unsaturated acids
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/40—Fatty vegetable or animal oils
- C10M2207/404—Fatty vegetable or animal oils obtained from genetically modified species
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/04—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions containing carbon, hydrogen, halogen, and oxygen
- C10M2211/044—Acids; Salts or esters 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
- C10M2211/00—Organic non-macromolecular compounds containing halogen as ingredients in lubricant compositions
- C10M2211/06—Perfluorinated compounds
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
- C10M2215/042—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms containing hydroxy groups; Alkoxylated derivatives thereof
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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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/24—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions having hydrocarbon substituents containing thirty or more carbon atoms, e.g. nitrogen derivatives of substituted succinic acid
- C10M2215/26—Amines
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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
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/02—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds
- C10M2219/024—Sulfur-containing compounds obtained by sulfurisation with sulfur or sulfur-containing compounds of esters, e.g. fats
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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
- C10N2040/22—Metal working with essential removal of material, e.g. cutting, grinding or drilling
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/24—Metal working without essential removal of material, e.g. forming, gorging, drawing, pressing, stamping, rolling or extruding; Punching metal
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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
- C10N2040/241—Manufacturing joint-less pipes
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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
- C10N2040/242—Hot 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
- C10N2040/243—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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- 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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- 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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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
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- C10N2040/247—Stainless steel
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- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/01—Emulsions, colloids, or micelles
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Abstract
METAL WORKING EMULSION
ABSTRACT OF THE DISCLOSURE
Metal working emulsion of the oil-in-water type, with good stability and unlimited dilutability, intended for use at deforming metal working, mainly machining by detachment of cuttings, but also suitable for deepdrawing and rolling. The emulsion is based on triglyceride oils and components of these. The emulsifying system consists of fatty acid monoglycerides and alkali soaps of fatty acids.
The cooling and lubricating properties are further increased by the addition of fatty acids and an alkanolamine or fatty amine.
ABSTRACT OF THE DISCLOSURE
Metal working emulsion of the oil-in-water type, with good stability and unlimited dilutability, intended for use at deforming metal working, mainly machining by detachment of cuttings, but also suitable for deepdrawing and rolling. The emulsion is based on triglyceride oils and components of these. The emulsifying system consists of fatty acid monoglycerides and alkali soaps of fatty acids.
The cooling and lubricating properties are further increased by the addition of fatty acids and an alkanolamine or fatty amine.
Description
This invention relates to an emulsion with lubricating and cooling abilities, intended for use at deforming metal working, mainly machining by detachment of cuttings, but also suitable for deepdrawing an~ rolling.
In machining by detachment of cuttings like drilling, turning, milling, tapping and grinding, cutting fluids based on mineral oil products are usually used, mainly because of the relative cheapness of the mineral oils. In most cases, they consist of water emulsions, and to meet the requirements of the metal working industryl a long list of additives are used, e.g. EP-additives to improve lubrication (EP = Extreme Pressure).
In recent years increased attention to working environments and industrial safety has created the need for a new type of metal working fluid. Unsatisfactory working environments and accompanying medical complaints are common problems with the products used in the metal working industry today. The mineral oil-based products produce oil smoke and oil mist at the working premises, as well as fouling in and around the machines. The mineral oil and the additives used can cause irritation of the skin, eczema and allergic reactions. Risk of cancer is present on prolonged skin exposure, and risk of lung damage is present on inhalation of the oil smoke and the oil mist. Lately there have been several reports on the presence of carcinogenic substances in cutting lllS68~
fluids. Mineral oils contain polyaromatic hydrocarbons, e.g. benzopyrenes. Because of the high temperatures in the cutting zone, it is also probable that polyaromatic compounds are formed when the products are used.
Environmental control legislation imposes heavy requirements on the metal working industry's handling of waste water. The technology of purifying spent emulsions and degreasing baths has grown complicated, because product development has resulted in the use of more and more additives and more stable emulsifier systems. Consequently the treatment of spent cutting fluids, mainly emulsions, has become very troublesome and expensive.
Smaller companies have to use specialized waste disposal services and only the largest companies have their own emulsion breaking plants, which however don't always function satisfactorily.
The breaking of the emulsions results in a water phase, which has to be treated further in conventional sewage treatment plants, and an oil containing sludge, which has to be disposed of, or at the best is usable as a fuel. A reuse of the oil is not an alternative. Consequently the industry is very much in need of a new type of cutting fluid, and the requirements on such a fluid are extensive:
- to have minimal detrimental effect on man and the environment, - to form very little oil smoke and oil mist, - facilitate an easy waste treatment without disposal problems, - to be uncomplicated in composition and with few additives, and - to be resistant to attack by micro-organisms.
Fatty oils, i.e., vegetable oils and animal oils and fats, are by function suitable raw materials for lubricants, and have earlier been used extensively before the cheaper mineral oils came to completely dominate the market. Contrary to mineral Gils, fatty oils are renewable, proenvironmental and can be completely broken down biologically.
For metal cutting or grinding, it is generally advantageous to use a cutting fluid in the form of a water-containing emulsion of the oil-in-water type, through which an improved cooling effect is achieved at the same time as the lubricating effect of the oil part is retained.
Also, from an economic point of view, a water emulsion is considerably more favorable.
These emulsions can be prepared in ready-to-use concentrations, but from transportation and handling aspects it is more suitable to first prepare a concentrate, which later can be diluted with water by the user - the metal working industry.
The requirements for such a concentrated emulsion are that the stability should be very good, that it should be easily and unlimitedly dilutable with water, and that it should be stable as an emulsion even when diluted. To be able to manufacture such an emulsion, one has to use special emulsifiers (surface active agents).
Strong synthetic surfactants may be used, but because of the health and environmental problems, referred to above, these should be avoided.
The object of this invention is to prepare a metal working emulsion, of the oil-in-water type, based on triglyceride oils, which is adequately stable, which can be unlimitedly diluted, and which at the same time has sufficiently good and lubricating properties, compared to those products used today, without having their undesirable environmental and health aspects.
We have found that, surprisingly, starting from triglyceride oils, one can prepare an emulsion which fulfills the requirements of stability and dilutability with aid of an emulsifying system comprising fatty acid monoglycerides and alkali soaps of fatty acids. By using only "natural" and completely harmless components the requirements of the product from environmental aspects are fulfilled.
To bring the lubricating and cooling properties of the emulsion to the level of the mineral oil based products, however, additional components are required.
We have found that the use of an organic amine, such as an alkanolamine, e.g.
triethanolamine, or a fatty amine, considerably increases the wetting properties of the emulsion and, thereby, its cooling effect. It has further been shown, that the addition of free fatty acid to the glyceride oil increases its lubricating properties. In fact, the amine and the fatty acid are believed to be present in the emulsion mainly as their salts, i.e. as soaps.
The present invention is thus a metal working emulsion consisting essentially of an oil phase dispersed in a continuous water phase wherein the oil phase comprises:
0.5 - 50 parts by weight of triglyceride oil, 0.1 - 10 parts by weight of fatty acid monoglyceride, 0.05 - 10 parts by weight of a fatty acid, and 0.05 - 10 parts by weight of an alkanolamine or a fatty amine;
and the water phase comprises:
0.05 - 3 parts by weight of an alkali soap of fatty acids, and 45 - 98 parts by weight of water.
The larger amounts of fatty components are used when preparing the emulsion concentrates, which, as mentioned earlier are usually prepared at the manufacturer's plant, and the lower amounts are used when preparing the ready-to-use emulsions.
When preparing the oil phase the fatty acid monoglyceride the fatty acid and the amine are dissolved in the triglyceride oil at a temperature of 40 - 70C. The wa~er phase is prepared by dissolving the alkali soap at a temperature of 20 - 70C, preferably at 20 - 40C.
The oil phase is slowly mixed into the water phase, while stirring, at a temperature of 20 _ 50C.
For the preparation of the ready-to-use emulsions it is thereafter enough with just powerful agitation to obtain a stable emulsion, while for the preparation of the emulsion concentrate, homogenization of the product is usually required. The homogenization is preferably carried out at a temperature of 40 - 60C in a conventional homogenizer.
The triglyceride oil may be animal or vegetable oil, or oil mixture, which has a solidifying point low enough to allow a convenient handling of the emulsion in the concentrated as well as the ready-to-use form, but which at the l~S~84 same time is mainly free from fatty acids like linolenic acid to avoid oxidation and polymerization difficulties. The oil should therefore be preferably liquid at room temperature, and have an oleic acid content of at least 40%.
Especially suitable oils, from a functional point of view, are olive oil, peanut oil and lobra oil (rapeseed oil with a low content of erucic acid).
Also the lowest melting fractions of fractionated fats, like e.g. "palm olein", have been found excellent for this purpose.
The fatty acid monoglyceride should be of the so called "soft product" type, i.e. have a melting point below 60C. The best product is pure oleic acid monoglYceride, (mono-oleoglycerol), but also other commercial products can be used, a~
1~ ~r~Je/n~(r~
Dimodan ~, a molecular distilled monoglyceride manufactured by Grindstedvaerket, Denmark, from edible, refined lard, with an approximate fatty acid composition of 30% palmitic acid, 18% stearic acid and 40% oleic acid.
It is also possible to use the so called technical monoglYcerides, manufactured through glycerolysis (glycerolesterification) of e.g. lobra oil. Such products, with a content of 40-60%
monoglycerides, are easy to manufacture without complicated equipment. and therefore of interest.
Of course, if such products are used, the ratio between triglyceride oil to glycerolysis product must be adjusted so that the content of ~ ~S~34 monoglyceride in the emulsion is correct. The oil soluble monoglyceride is used, primarily because of its surface active properties, as the lipophilic component of the emulsion system.
The surface activity also imparts a wetting effect, through which the lubricating effect of the oil increases.
The fatty acid is preferably oleic acid.
The requirements on this component are the same as on the oil and the monoglyceride: to be liquid at room temperature, that is to have a titer lower than 25C, and not to contain substantial quantities of more unsaturated homologues.
The fatty acid has shown to increase the lubricating effect substantially. The presence of fatty acid prevents the formation of odor at more severe machining operations, which is believed partly to result from the fatty acid's improvement of the lubricating effect and partly to be connected with the formation of soaps of amine and fatty acid.
As alkanolamine, an amine with 2-4 carbon atoms in the alkanol-part is preferred. Especially suitable is triethanolamine, which as well as having good wetting and rust-preventing properties, also has the advantage of being dermatologically harmless, which is also evident in its wide use in cosmetic preparations.
The amine can also be based on fatty raw materials, whereby the same good wetting and rust-preventing properties can be achieved. Suitably a fatty amine with 8 to 18 carbon atoms in the carbon chain can be used; especially suitable is dodecylamine.
The fatty acid soap is suitably a sodium- or potassium salt of a fatty acid with 12-22 carbon atoms, usually 16 or 18 carbon atoms (palmitic- or steraic acid). Potassium stearate gives slightly better results than does sodium stearate, but if stearic soaps are to be used, de-ionized water must be used to prevent flocculation of calcium and magnesium soaps. When using oleic acid soaps (sodium or potassium) this problem is fully avoided, although when manufacturing the concentrate it is advisable to use de-ionized water.
In metal working operations with very heavy contact pressure, the lubricating properties of the metal working emulsion can, if needed, be further increased by adding a slightly chlorinated and/or sulfurized triglyceride oil. These components are well compatible with the metal working emulsion according to the invention. Preferably 20-40% of the triglyceride oil is replaced by such components at extremely heavy operations.
To prevent problems with oxidation and polymerization an antioxidant can possibly be added. Suitable antioxidants are butyl hydroxyanisole, BHA, and butyl hydroxytoluene, BHT.
C, _g_ Advantageously e.g. Eastman Kokak's products Tenox (a trade mark)
In machining by detachment of cuttings like drilling, turning, milling, tapping and grinding, cutting fluids based on mineral oil products are usually used, mainly because of the relative cheapness of the mineral oils. In most cases, they consist of water emulsions, and to meet the requirements of the metal working industryl a long list of additives are used, e.g. EP-additives to improve lubrication (EP = Extreme Pressure).
In recent years increased attention to working environments and industrial safety has created the need for a new type of metal working fluid. Unsatisfactory working environments and accompanying medical complaints are common problems with the products used in the metal working industry today. The mineral oil-based products produce oil smoke and oil mist at the working premises, as well as fouling in and around the machines. The mineral oil and the additives used can cause irritation of the skin, eczema and allergic reactions. Risk of cancer is present on prolonged skin exposure, and risk of lung damage is present on inhalation of the oil smoke and the oil mist. Lately there have been several reports on the presence of carcinogenic substances in cutting lllS68~
fluids. Mineral oils contain polyaromatic hydrocarbons, e.g. benzopyrenes. Because of the high temperatures in the cutting zone, it is also probable that polyaromatic compounds are formed when the products are used.
Environmental control legislation imposes heavy requirements on the metal working industry's handling of waste water. The technology of purifying spent emulsions and degreasing baths has grown complicated, because product development has resulted in the use of more and more additives and more stable emulsifier systems. Consequently the treatment of spent cutting fluids, mainly emulsions, has become very troublesome and expensive.
Smaller companies have to use specialized waste disposal services and only the largest companies have their own emulsion breaking plants, which however don't always function satisfactorily.
The breaking of the emulsions results in a water phase, which has to be treated further in conventional sewage treatment plants, and an oil containing sludge, which has to be disposed of, or at the best is usable as a fuel. A reuse of the oil is not an alternative. Consequently the industry is very much in need of a new type of cutting fluid, and the requirements on such a fluid are extensive:
- to have minimal detrimental effect on man and the environment, - to form very little oil smoke and oil mist, - facilitate an easy waste treatment without disposal problems, - to be uncomplicated in composition and with few additives, and - to be resistant to attack by micro-organisms.
Fatty oils, i.e., vegetable oils and animal oils and fats, are by function suitable raw materials for lubricants, and have earlier been used extensively before the cheaper mineral oils came to completely dominate the market. Contrary to mineral Gils, fatty oils are renewable, proenvironmental and can be completely broken down biologically.
For metal cutting or grinding, it is generally advantageous to use a cutting fluid in the form of a water-containing emulsion of the oil-in-water type, through which an improved cooling effect is achieved at the same time as the lubricating effect of the oil part is retained.
Also, from an economic point of view, a water emulsion is considerably more favorable.
These emulsions can be prepared in ready-to-use concentrations, but from transportation and handling aspects it is more suitable to first prepare a concentrate, which later can be diluted with water by the user - the metal working industry.
The requirements for such a concentrated emulsion are that the stability should be very good, that it should be easily and unlimitedly dilutable with water, and that it should be stable as an emulsion even when diluted. To be able to manufacture such an emulsion, one has to use special emulsifiers (surface active agents).
Strong synthetic surfactants may be used, but because of the health and environmental problems, referred to above, these should be avoided.
The object of this invention is to prepare a metal working emulsion, of the oil-in-water type, based on triglyceride oils, which is adequately stable, which can be unlimitedly diluted, and which at the same time has sufficiently good and lubricating properties, compared to those products used today, without having their undesirable environmental and health aspects.
We have found that, surprisingly, starting from triglyceride oils, one can prepare an emulsion which fulfills the requirements of stability and dilutability with aid of an emulsifying system comprising fatty acid monoglycerides and alkali soaps of fatty acids. By using only "natural" and completely harmless components the requirements of the product from environmental aspects are fulfilled.
To bring the lubricating and cooling properties of the emulsion to the level of the mineral oil based products, however, additional components are required.
We have found that the use of an organic amine, such as an alkanolamine, e.g.
triethanolamine, or a fatty amine, considerably increases the wetting properties of the emulsion and, thereby, its cooling effect. It has further been shown, that the addition of free fatty acid to the glyceride oil increases its lubricating properties. In fact, the amine and the fatty acid are believed to be present in the emulsion mainly as their salts, i.e. as soaps.
The present invention is thus a metal working emulsion consisting essentially of an oil phase dispersed in a continuous water phase wherein the oil phase comprises:
0.5 - 50 parts by weight of triglyceride oil, 0.1 - 10 parts by weight of fatty acid monoglyceride, 0.05 - 10 parts by weight of a fatty acid, and 0.05 - 10 parts by weight of an alkanolamine or a fatty amine;
and the water phase comprises:
0.05 - 3 parts by weight of an alkali soap of fatty acids, and 45 - 98 parts by weight of water.
The larger amounts of fatty components are used when preparing the emulsion concentrates, which, as mentioned earlier are usually prepared at the manufacturer's plant, and the lower amounts are used when preparing the ready-to-use emulsions.
When preparing the oil phase the fatty acid monoglyceride the fatty acid and the amine are dissolved in the triglyceride oil at a temperature of 40 - 70C. The wa~er phase is prepared by dissolving the alkali soap at a temperature of 20 - 70C, preferably at 20 - 40C.
The oil phase is slowly mixed into the water phase, while stirring, at a temperature of 20 _ 50C.
For the preparation of the ready-to-use emulsions it is thereafter enough with just powerful agitation to obtain a stable emulsion, while for the preparation of the emulsion concentrate, homogenization of the product is usually required. The homogenization is preferably carried out at a temperature of 40 - 60C in a conventional homogenizer.
The triglyceride oil may be animal or vegetable oil, or oil mixture, which has a solidifying point low enough to allow a convenient handling of the emulsion in the concentrated as well as the ready-to-use form, but which at the l~S~84 same time is mainly free from fatty acids like linolenic acid to avoid oxidation and polymerization difficulties. The oil should therefore be preferably liquid at room temperature, and have an oleic acid content of at least 40%.
Especially suitable oils, from a functional point of view, are olive oil, peanut oil and lobra oil (rapeseed oil with a low content of erucic acid).
Also the lowest melting fractions of fractionated fats, like e.g. "palm olein", have been found excellent for this purpose.
The fatty acid monoglyceride should be of the so called "soft product" type, i.e. have a melting point below 60C. The best product is pure oleic acid monoglYceride, (mono-oleoglycerol), but also other commercial products can be used, a~
1~ ~r~Je/n~(r~
Dimodan ~, a molecular distilled monoglyceride manufactured by Grindstedvaerket, Denmark, from edible, refined lard, with an approximate fatty acid composition of 30% palmitic acid, 18% stearic acid and 40% oleic acid.
It is also possible to use the so called technical monoglYcerides, manufactured through glycerolysis (glycerolesterification) of e.g. lobra oil. Such products, with a content of 40-60%
monoglycerides, are easy to manufacture without complicated equipment. and therefore of interest.
Of course, if such products are used, the ratio between triglyceride oil to glycerolysis product must be adjusted so that the content of ~ ~S~34 monoglyceride in the emulsion is correct. The oil soluble monoglyceride is used, primarily because of its surface active properties, as the lipophilic component of the emulsion system.
The surface activity also imparts a wetting effect, through which the lubricating effect of the oil increases.
The fatty acid is preferably oleic acid.
The requirements on this component are the same as on the oil and the monoglyceride: to be liquid at room temperature, that is to have a titer lower than 25C, and not to contain substantial quantities of more unsaturated homologues.
The fatty acid has shown to increase the lubricating effect substantially. The presence of fatty acid prevents the formation of odor at more severe machining operations, which is believed partly to result from the fatty acid's improvement of the lubricating effect and partly to be connected with the formation of soaps of amine and fatty acid.
As alkanolamine, an amine with 2-4 carbon atoms in the alkanol-part is preferred. Especially suitable is triethanolamine, which as well as having good wetting and rust-preventing properties, also has the advantage of being dermatologically harmless, which is also evident in its wide use in cosmetic preparations.
The amine can also be based on fatty raw materials, whereby the same good wetting and rust-preventing properties can be achieved. Suitably a fatty amine with 8 to 18 carbon atoms in the carbon chain can be used; especially suitable is dodecylamine.
The fatty acid soap is suitably a sodium- or potassium salt of a fatty acid with 12-22 carbon atoms, usually 16 or 18 carbon atoms (palmitic- or steraic acid). Potassium stearate gives slightly better results than does sodium stearate, but if stearic soaps are to be used, de-ionized water must be used to prevent flocculation of calcium and magnesium soaps. When using oleic acid soaps (sodium or potassium) this problem is fully avoided, although when manufacturing the concentrate it is advisable to use de-ionized water.
In metal working operations with very heavy contact pressure, the lubricating properties of the metal working emulsion can, if needed, be further increased by adding a slightly chlorinated and/or sulfurized triglyceride oil. These components are well compatible with the metal working emulsion according to the invention. Preferably 20-40% of the triglyceride oil is replaced by such components at extremely heavy operations.
To prevent problems with oxidation and polymerization an antioxidant can possibly be added. Suitable antioxidants are butyl hydroxyanisole, BHA, and butyl hydroxytoluene, BHT.
C, _g_ Advantageously e.g. Eastman Kokak's products Tenox (a trade mark)
2 or Tenox 6 (a trade mark) can be used. These agents are suitably added in an amount o~ 0.1-1.0 percent by weight to the concentrated emulsion.
Under the unfavorable conditions encountered in the workshop environment, attack by micro-organisms can easily take place. If these micro-organisms are allowed to develop uncontrolled for a sufficiently long time, an unpleasant odor may develop. Also, the corrosion inhibiting properties of the emulsion may decrease through the formation of acid degradiation products in the same way as takes place when using traditional mineral oil based products. This is avoided by adding a bacteria controlling agent to the metal working emulsion. A formaldehyde releasing agent can be used e.g.
~rotan BK, (a trade mark) which is manufactured by Schulke Mayr GmbH.
Thus, the product manufactured according to the invention offered from the user's point of view a long list of advantages:
The product is completely based on fatty oils or components of these. These oils are renewable, proenvironmental and bio-degradable.
The occurrance of skin irritation, eczema and allergic reactions can considerably be reduced, and the risk of cancer can be removed.
Because of the higher molecular weight of the triglyceride oils, and the considerably lower vapor pressure in connection therewith, no ,~, --1 0--~ .~
l~lS~
troublesome oil smoke will be formed. Generally this means a considerably cleaner working environment.
Products based on fatty oils present no difficulty from the standpoint of waste treatment.
By using known proper separation techniques the fatty phase can easily be separated, and the remaining water doesn't require any special cleaning before discharge. The fatty phase can 10easily be separated by hydrolysis with known techniques, and the recovered fatty acids can be reused.
The invention is further illustrated by the following examples:
Example 1. Preparation of a metal working emulsion in concentrated form.
Oil phase: 34.7 parts by weight of palm olein 4.9 parts by weight of monoglyceride Dimodan S
202.7 parts by weight of rapeseed fatty acids 2.7 parts by weight of triethanolamine Water phase: 1.1 parts by weight of sodium oleate 5~0 parts by weight of de-ionized water The palm olein was a low melting fraction of palm oil. The content of oleic acid in the palm 30 olein was 50%.
The components of the oil phase were mixed at 60-70C. The soap was dissolved in water 8~
at 25C, after which the oil phase was added slowly and while stirring to the water phase. The dispersion so obtained was thereafter homogenized at 50C in a homogenizer of conventional type.
The emulsion concentrate could be diluted easily and unlimitedly with water of various hardness (0-12dH). Both the emulsion concentrate and the diluted emulsions were stable during storage, i.e., the oil not having a tendency to separate.
The product was tested in a dilution 1:10 in a multiple-spindle drilling machine in production, where the working operation was tapping in aluminum. After 1 month of working the function of the emulsion was unchanged, and completely comparable with the function of a conventional mineral oil based emulsion.
Example 2. A metal working emulsion was prepared for testing in a heavy loaded numerically controlled automatic lathe. Many iron-metals, e.g. cast iron and hardened tool-steel were worked by tools with a cutting edge of hard metal. The metal working emulsion was prepared as follows:
Oil phase: 27.9 parts by weight of rapeseed oil 11.7 parts by weight of technical monoglyceride from rapeseed oil 2.7 parts by weight of rapeseed fatty acids 2.7 parts by weight of triethanolamine illS6~34 0.4 parts by weight of an antioxidant, Tenox 6 Water phase: 1.1 parts by weight of sodium oleate 55.0 parts by weight of de-ionized water The rapeseed oil was of the low erucic acid type with an oleic acid content of 52%. The technical monoglyceride had a content of 40~ actual monoglyceride. The components in the oil phase were mixed at a temperature of 40-50C. Thereafter the oil phase was added slowly, while stirring, to the water phase. The dispersion obtained was homogenized at 50C in a conventional homogenizer equipment.
The emulsion concentrate obtained in this way was diluted 1:15 in tap water and tested in an automatic lathe. After 3 months of running the function of the metal working emulsion was unchanged. The worked parts showed no tendencies of corrosion. The metal working emulsion caused no drying coatings; on the contrary, the machine surfaces were very easy to keep clean.
Example 3. This example is intended to illustrate the improved lubricating effect imparted to the emulsion by the fatty acid.
Two metal working emulsions in ready-to-use concentration were prepared for testing in a cylinder-grinding machine. The metal working emulsions were prepared from the following components:
1~5684 Sample A Parts by Weight Oil Phase:
rapeseed oil 2.00 technical monoglyceride from rapeseed oil0.78 triethanolamine 0.18 Water Phase:
sodium stearate 0.10 de-ionized water 97 Sample B Parts by Weight Oil Phase:
rapeseed oil 1.80 technical monoglyceride from rapeseed oil0.78 rapeseed fatty acid0.20 triethanolamine 0.18 Water Phase:
sodium stearate 0.10 de-ionized water 97 The rapeseed oil was of the low erucic acid type with an oleic acid content of 60%. The technical monoglyceride had a content of 40% actual monoglyceride.
The components in the oil phase were mixed at 40-50C, and the sodium stearate was dissolved in the water phase at 60-70C.
Thereafter the oil phase was added slowly to the water phase while stirring intensively, whereby a stable emulsion was obtained.
The metal working emulsions prepared in this way were tested in a cylinder-grinding machine by working hardened tool-steel. It was found that regarding the surface fineness of the material, as well as the relative wear of the abrasive wheel, sample B (with fatty acid addition) gave better results than sample A (without fatty acid addition). On the average, the surface fineness was 10% better and the relative wear of the abrasive wheel 30~ lower with sample B than with sample A. The results were completely comparable with those obtained when using conventional mineral oil based emulsions without EP-additives.
Example 4. This example is intended to illustrate the improved wetting function obtained by adding triethanolamine to the emulsion.
Two emulsion samples were prepared according to the same process as in Example 3:
Sample A Parts by Weight Oil Phase:
rapeseed oil 3.50 monoglyceride of oleic acid 1.00 triethanolamine 0.50 Water Phase:
sodium stearate 0.10 de-ionized water 95 Sample B Parts by Weight Oil Phase:
rapeseed oil 4.00 monoglyceride of oleic acid 1.00 Water Phase:
sodium stearate 0.10 de-ionized water 95 The rapeseed oil was of the low erucic acid type with an oleic acid content of 60%.
Measurements were made of the wetting capacity of these emulsions on steel surfaces. It was hereby found that emulsion sample B (without triethanolamine) gave a wetting angle of 40-45, and emulsion sample A (with triethanolamine) gave a wetting angle of 15-20. This latter result was even somewhat better than what is obtained with 10conventional mineral oil based emulsions.
Example 5. A metal working emulsion was prepared according to Example 1 with the following ingredients.:
Oil phase:34.3 parts by weight of palm olein 4.8 parts by weight of monoglyceride Dimodan S
2.7 parts of weight of rapeseed fatty acids 5.4 parts by weight of triethanolamine Water phase: 1.1 parts by weight of sodium oleate 55.0 parts by weight of de-ionized water The metal working emulsion was tested for a longer period of time in a numerically controlled machine tool for drilling and tapping. In the machine toughened steel was worked with high speed tools.
Under the unfavorable conditions encountered in the workshop environment, attack by micro-organisms can easily take place. If these micro-organisms are allowed to develop uncontrolled for a sufficiently long time, an unpleasant odor may develop. Also, the corrosion inhibiting properties of the emulsion may decrease through the formation of acid degradiation products in the same way as takes place when using traditional mineral oil based products. This is avoided by adding a bacteria controlling agent to the metal working emulsion. A formaldehyde releasing agent can be used e.g.
~rotan BK, (a trade mark) which is manufactured by Schulke Mayr GmbH.
Thus, the product manufactured according to the invention offered from the user's point of view a long list of advantages:
The product is completely based on fatty oils or components of these. These oils are renewable, proenvironmental and bio-degradable.
The occurrance of skin irritation, eczema and allergic reactions can considerably be reduced, and the risk of cancer can be removed.
Because of the higher molecular weight of the triglyceride oils, and the considerably lower vapor pressure in connection therewith, no ,~, --1 0--~ .~
l~lS~
troublesome oil smoke will be formed. Generally this means a considerably cleaner working environment.
Products based on fatty oils present no difficulty from the standpoint of waste treatment.
By using known proper separation techniques the fatty phase can easily be separated, and the remaining water doesn't require any special cleaning before discharge. The fatty phase can 10easily be separated by hydrolysis with known techniques, and the recovered fatty acids can be reused.
The invention is further illustrated by the following examples:
Example 1. Preparation of a metal working emulsion in concentrated form.
Oil phase: 34.7 parts by weight of palm olein 4.9 parts by weight of monoglyceride Dimodan S
202.7 parts by weight of rapeseed fatty acids 2.7 parts by weight of triethanolamine Water phase: 1.1 parts by weight of sodium oleate 5~0 parts by weight of de-ionized water The palm olein was a low melting fraction of palm oil. The content of oleic acid in the palm 30 olein was 50%.
The components of the oil phase were mixed at 60-70C. The soap was dissolved in water 8~
at 25C, after which the oil phase was added slowly and while stirring to the water phase. The dispersion so obtained was thereafter homogenized at 50C in a homogenizer of conventional type.
The emulsion concentrate could be diluted easily and unlimitedly with water of various hardness (0-12dH). Both the emulsion concentrate and the diluted emulsions were stable during storage, i.e., the oil not having a tendency to separate.
The product was tested in a dilution 1:10 in a multiple-spindle drilling machine in production, where the working operation was tapping in aluminum. After 1 month of working the function of the emulsion was unchanged, and completely comparable with the function of a conventional mineral oil based emulsion.
Example 2. A metal working emulsion was prepared for testing in a heavy loaded numerically controlled automatic lathe. Many iron-metals, e.g. cast iron and hardened tool-steel were worked by tools with a cutting edge of hard metal. The metal working emulsion was prepared as follows:
Oil phase: 27.9 parts by weight of rapeseed oil 11.7 parts by weight of technical monoglyceride from rapeseed oil 2.7 parts by weight of rapeseed fatty acids 2.7 parts by weight of triethanolamine illS6~34 0.4 parts by weight of an antioxidant, Tenox 6 Water phase: 1.1 parts by weight of sodium oleate 55.0 parts by weight of de-ionized water The rapeseed oil was of the low erucic acid type with an oleic acid content of 52%. The technical monoglyceride had a content of 40~ actual monoglyceride. The components in the oil phase were mixed at a temperature of 40-50C. Thereafter the oil phase was added slowly, while stirring, to the water phase. The dispersion obtained was homogenized at 50C in a conventional homogenizer equipment.
The emulsion concentrate obtained in this way was diluted 1:15 in tap water and tested in an automatic lathe. After 3 months of running the function of the metal working emulsion was unchanged. The worked parts showed no tendencies of corrosion. The metal working emulsion caused no drying coatings; on the contrary, the machine surfaces were very easy to keep clean.
Example 3. This example is intended to illustrate the improved lubricating effect imparted to the emulsion by the fatty acid.
Two metal working emulsions in ready-to-use concentration were prepared for testing in a cylinder-grinding machine. The metal working emulsions were prepared from the following components:
1~5684 Sample A Parts by Weight Oil Phase:
rapeseed oil 2.00 technical monoglyceride from rapeseed oil0.78 triethanolamine 0.18 Water Phase:
sodium stearate 0.10 de-ionized water 97 Sample B Parts by Weight Oil Phase:
rapeseed oil 1.80 technical monoglyceride from rapeseed oil0.78 rapeseed fatty acid0.20 triethanolamine 0.18 Water Phase:
sodium stearate 0.10 de-ionized water 97 The rapeseed oil was of the low erucic acid type with an oleic acid content of 60%. The technical monoglyceride had a content of 40% actual monoglyceride.
The components in the oil phase were mixed at 40-50C, and the sodium stearate was dissolved in the water phase at 60-70C.
Thereafter the oil phase was added slowly to the water phase while stirring intensively, whereby a stable emulsion was obtained.
The metal working emulsions prepared in this way were tested in a cylinder-grinding machine by working hardened tool-steel. It was found that regarding the surface fineness of the material, as well as the relative wear of the abrasive wheel, sample B (with fatty acid addition) gave better results than sample A (without fatty acid addition). On the average, the surface fineness was 10% better and the relative wear of the abrasive wheel 30~ lower with sample B than with sample A. The results were completely comparable with those obtained when using conventional mineral oil based emulsions without EP-additives.
Example 4. This example is intended to illustrate the improved wetting function obtained by adding triethanolamine to the emulsion.
Two emulsion samples were prepared according to the same process as in Example 3:
Sample A Parts by Weight Oil Phase:
rapeseed oil 3.50 monoglyceride of oleic acid 1.00 triethanolamine 0.50 Water Phase:
sodium stearate 0.10 de-ionized water 95 Sample B Parts by Weight Oil Phase:
rapeseed oil 4.00 monoglyceride of oleic acid 1.00 Water Phase:
sodium stearate 0.10 de-ionized water 95 The rapeseed oil was of the low erucic acid type with an oleic acid content of 60%.
Measurements were made of the wetting capacity of these emulsions on steel surfaces. It was hereby found that emulsion sample B (without triethanolamine) gave a wetting angle of 40-45, and emulsion sample A (with triethanolamine) gave a wetting angle of 15-20. This latter result was even somewhat better than what is obtained with 10conventional mineral oil based emulsions.
Example 5. A metal working emulsion was prepared according to Example 1 with the following ingredients.:
Oil phase:34.3 parts by weight of palm olein 4.8 parts by weight of monoglyceride Dimodan S
2.7 parts of weight of rapeseed fatty acids 5.4 parts by weight of triethanolamine Water phase: 1.1 parts by weight of sodium oleate 55.0 parts by weight of de-ionized water The metal working emulsion was tested for a longer period of time in a numerically controlled machine tool for drilling and tapping. In the machine toughened steel was worked with high speed tools.
3~The machining results were compared to those obtained when a conventional cutting fluid of s~
the emulsion type with EP-additives was used. The conventional cutting fluid was especially intended for heavy machining like drilling, tapping, thread cutting and deep drawing in different iron materials. Both cutting fluids were used in the same dilution, about 15 times, with ordinary tap water.
The surface smoothness of the worked parts was equal for the conventional cutting fluid and for the cutting fluid according to this invention. The lifetime of the tools for the drilling operation was equally good. For the tapping operation the lifetime with the cutting fluid according to this invention was even somewhat better than with the conventional cutting fluid.
the emulsion type with EP-additives was used. The conventional cutting fluid was especially intended for heavy machining like drilling, tapping, thread cutting and deep drawing in different iron materials. Both cutting fluids were used in the same dilution, about 15 times, with ordinary tap water.
The surface smoothness of the worked parts was equal for the conventional cutting fluid and for the cutting fluid according to this invention. The lifetime of the tools for the drilling operation was equally good. For the tapping operation the lifetime with the cutting fluid according to this invention was even somewhat better than with the conventional cutting fluid.
Claims (21)
PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS FOLLOWS:
1. A metal working emulsion with good stability and unlimited dilutability for deforming metalworking, comprising an oil phase which is dispersed in a continuous water phase;
the oil phase comprising 0.5 - 50 parts by weight of triglyceride oil, 0.1 - 10 parts by weight of fatty acid monoglyceride, 0.05 - 10 parts by weight of fatty acid, and 0.05 - 10 parts by weight of alkanolamine or fatty amine;
and the water phase comprising 0.05 - 3 parts by weight of alkali soaps of fatty acids, and 45 - 98 parts by weight of water.
the oil phase comprising 0.5 - 50 parts by weight of triglyceride oil, 0.1 - 10 parts by weight of fatty acid monoglyceride, 0.05 - 10 parts by weight of fatty acid, and 0.05 - 10 parts by weight of alkanolamine or fatty amine;
and the water phase comprising 0.05 - 3 parts by weight of alkali soaps of fatty acids, and 45 - 98 parts by weight of water.
2. A metal working emulsion according to claim l in concentrated form, wherein the oil phase comprises 15 - 50 parts by weight of triglyceride oil, 2 - 10 parts by weight of fatty acid monoglyceride, 1 - 10 parts by weight of fatty acid, and 1 - 10 parts by weight of alkanolamine or fatty amine;
and the water phase comprises 0.05 - 3 parts by weight of alkali soaps of fatty acids, and 45 - 60 parts by weight of water.
and the water phase comprises 0.05 - 3 parts by weight of alkali soaps of fatty acids, and 45 - 60 parts by weight of water.
3. A metal working emulsion according to claim 1 in a ready-to-use form, wherein the oil phase comprises 0.5 - 10 parts by weight of triglyceride oil, 0.1 - 2 parts by weight of fatty acid monoglyceride, 0.05 - 2 parts by weight of fatty acid, and 0.05 - 1 parts by weight of alkanolamine or fatty amine;
and the water phase comprises 0.05 - 0.5 parts by weight of alkali soaps of fatty acids, and 90 - 98 parts by weight of water.
and the water phase comprises 0.05 - 0.5 parts by weight of alkali soaps of fatty acids, and 90 - 98 parts by weight of water.
4. A metal working emulsion according to claim 1, wherein the triglyceride oil is a fatty oil, liquid at room temperature and having an oleic acid content of at least 45% by weight.
5. A metal working emulsion according to claim 4 wherein the triglyceride oil is chosen from the group of olive oil, peanut oil and rapeseed oil of the low erucic acid type.
6. A metal working emulsion according to claim 4 wherein the triglyceride oil is the lowest melting fraction of a fractionated fat.
7. A metal working emulsion according to claim 1, wherein the fatty acids in the fatty acid monoglyceride are fatty acids with 16 to 18 carbon atoms, at least 40% by weight being oleic acid.
8. A metal working emulsion according to claim 7, wherein the fatty acid monoglyceride is oleic acid monoglyceride.
9. A metal working emulsion according to claim 1, wherein the fatty acid monoglyceride is a technical grade fatty acid monoglyceride obtained through esterification of a triglyceride oil with glycerol.
10. A metal working emulsion according to claim 1, wherein the fatty acid has a titer lower than 25°C.
11. A metal working emulsion according to claim 10, wherein the fatty acid is oleic acid.
12. A metal working emulsion according to claim 1, wherein the alkanolamine is triethanolamine.
13. A metal working emulsion according to claim 1 wherein the fatty amine is dodecyl amine.
14. A metal working emulsion according to claim 1, wherein the alkali soaps of the fatty acids are sodium soaps of fatty acids with a titer below 25°C.
15. A metal working emulsion according to claim 1, wherein the alkali soaps of the fatty acids are potassium soaps of fatty acids with a titer below 25°C.
16. A metal working emulsion according to claim 1 wherein the alkali soaps of the fatty acids are sodium oleate.
17. A metal working emulsion according to claim 1 wherein the alkali soaps of the fatty acids are potassium oleate.
18. A metal working emulsion according to claim 1, wherein 20-40% by weight of the triglyceride oil is replaced by a high pressure additive consisting of a slightly chlorinated or sulfurized triglyceride oil.
19. A metal working emulsion according to claim 4 wherein the triglyceride oil is the lowest melting fraction of a fractionated palm oil.
20. A metal working emulsion according to claim 4 wherein the triglyceride oil is the lowest melting fraction of a hydrogenated and fractionated vegetable oil.
21. A metal working emulsion according to claim 4 wherein the triglyceride oil is the lowest melting fraction of a fractionated animal fat.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| SE7802533A SE415107B (en) | 1978-03-07 | 1978-03-07 | METAL WORKING EMULSION CONTAINING TRIGLYCERID OIL |
| SE7802533-5 | 1978-03-07 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1115684A true CA1115684A (en) | 1982-01-05 |
Family
ID=20334200
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA322,726A Expired CA1115684A (en) | 1978-03-07 | 1979-03-05 | Metal working emulsion |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | USRE31242E (en) |
| AT (1) | AT365630B (en) |
| BE (1) | BE874665A (en) |
| CA (1) | CA1115684A (en) |
| CH (1) | CH639687A5 (en) |
| CS (1) | CS212712B2 (en) |
| DD (1) | DD142204A5 (en) |
| DE (1) | DE2907863C2 (en) |
| DK (1) | DK93079A (en) |
| ES (1) | ES478364A1 (en) |
| FI (1) | FI62680C (en) |
| FR (1) | FR2419317A1 (en) |
| GB (1) | GB2016516B (en) |
| IT (1) | IT1113413B (en) |
| LU (1) | LU80993A1 (en) |
| NL (1) | NL7901522A (en) |
| NO (1) | NO145622C (en) |
| PL (1) | PL117140B1 (en) |
| PT (1) | PT69306A (en) |
| SE (1) | SE415107B (en) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4378235A (en) * | 1981-10-05 | 1983-03-29 | Nalco Chemical Company | Scrubbing media for removing volatile organic material from paint spray booths |
| US5391310A (en) * | 1993-11-23 | 1995-02-21 | Cincinnati Milacron Inc. | Sulfurized aqueous machining fluid composition |
| US6204225B1 (en) * | 1999-12-13 | 2001-03-20 | Midwest Biologicals, Inc. | Water-dispersible metal working fluid |
| DE10349808A1 (en) * | 2003-10-24 | 2005-05-25 | Cognis Deutschland Gmbh & Co. Kg | Emulsifiers for drilling fluid |
| US7595288B2 (en) * | 2004-02-06 | 2009-09-29 | Henkel Kommanditgesellschaft Auf Aktien | Antimicrobial metal working fluids |
| US8168575B2 (en) * | 2006-05-05 | 2012-05-01 | Angus Chemical Company | Metalworking fluids comprising neutralized fatty acids |
| EP2029694A4 (en) * | 2006-06-20 | 2009-09-23 | Mi Llc | POLYMERIC MATERIALS HIGHLY RAMIFIED AS COATING OF ALLOYING AGENTS |
| FR2971515B1 (en) * | 2011-02-14 | 2013-02-22 | Michel Martin | OIL FOR MECHANICAL SAW CHAIN. |
| ES2525892B2 (en) * | 2013-06-25 | 2015-06-30 | Universidad De Huelva | Biodegradable fats and procedure for obtaining them from residual oleins |
| PL3393530T3 (en) | 2015-12-23 | 2022-12-05 | Henkel Ag & Co. Kgaa | Metal working fluid |
Family Cites Families (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE545763C (en) * | 1929-03-10 | 1932-03-05 | Goldschmidt Ag Th | Process for the production of emulsions |
| US2238478A (en) * | 1939-03-04 | 1941-04-15 | Hercules Powder Co Ltd | Lubricant and process for making the same |
| US2258552A (en) * | 1939-03-06 | 1941-10-07 | Elmer F Harris | Cold rolling solution |
| US2896486A (en) * | 1952-08-28 | 1959-07-28 | Wallace Mcclung Donnelly | Process of cold rolling steel sheets |
| US2948681A (en) * | 1955-10-25 | 1960-08-09 | Standard Oil Co | Wire-drawing lubricating composition |
| DE1240208B (en) * | 1961-09-29 | 1967-05-11 | Gustav Niemann Dr Ing | Running-in agent for roller and sliding pairs |
| US3205172A (en) * | 1961-12-22 | 1965-09-07 | Eastman Kodak Co | Universal machining fluid |
| DE1644871B2 (en) * | 1964-05-08 | 1973-03-08 | Dynamit Nobel Ag, 5210 Troisdorf | LUBRICANT |
| US3311557A (en) * | 1964-11-30 | 1967-03-28 | Shell Oil Co | Lubricant for rolling metals |
| US3278430A (en) * | 1965-03-29 | 1966-10-11 | Skotch Products Corp | Aqueous base lubricant and like material |
| FR1492213A (en) * | 1966-07-01 | 1967-08-18 | Henry W Peabody Ind Ltd | Cold rolling process |
| US3492815A (en) * | 1967-03-10 | 1970-02-03 | Thiokol Chemical Corp | Means for forming radial slots in solid propellant grains |
| GB1383198A (en) * | 1971-02-16 | 1975-02-05 | Shell Int Research | Hot rolling of metals |
| FR2157700B1 (en) * | 1971-10-26 | 1975-07-18 | Shell Berre Raffinage | |
| US3835052A (en) * | 1971-11-15 | 1974-09-10 | Kaiser Aluminium Chem Corp | Emulsion for hot rolling aluminum products |
| DE2318086A1 (en) * | 1973-04-11 | 1974-10-31 | Hoechst Ag | FREEZE-THAW STABLE POLYMERLATICES AS ADDITIVES TO Aqueous COOLING LUBRICANTS |
| CH586280A5 (en) * | 1973-05-29 | 1977-03-31 | Nussbaum Eugen | |
| DE2442844C3 (en) * | 1974-09-06 | 1979-08-02 | Zahnradfabrik Friedrichshafen Ag, 7990 Friedrichshafen | Corrosion-inhibiting aqueous solution for machined workpieces made of metals and plastics |
| DE2519905C3 (en) * | 1975-05-03 | 1979-06-21 | Rasselstein Ag, 5450 Neuwied | Process for the production of deep-drawn and / or ironed cans from tinplate |
-
1978
- 1978-03-07 SE SE7802533A patent/SE415107B/en not_active IP Right Cessation
-
1979
- 1979-02-26 NL NL7901522A patent/NL7901522A/en not_active Application Discontinuation
- 1979-02-27 FR FR7904947A patent/FR2419317A1/en active Granted
- 1979-02-27 IT IT20594/79A patent/IT1113413B/en active
- 1979-03-01 DE DE2907863A patent/DE2907863C2/en not_active Expired
- 1979-03-05 PT PT69306A patent/PT69306A/en unknown
- 1979-03-05 LU LU80993A patent/LU80993A1/en unknown
- 1979-03-05 CA CA322,726A patent/CA1115684A/en not_active Expired
- 1979-03-05 FI FI790735A patent/FI62680C/en not_active IP Right Cessation
- 1979-03-06 DK DK93079A patent/DK93079A/en not_active Application Discontinuation
- 1979-03-06 NO NO790748A patent/NO145622C/en unknown
- 1979-03-06 AT AT0168279A patent/AT365630B/en not_active IP Right Cessation
- 1979-03-06 ES ES478364A patent/ES478364A1/en not_active Expired
- 1979-03-06 DD DD79211404A patent/DD142204A5/en unknown
- 1979-03-06 PL PL1979213922A patent/PL117140B1/en unknown
- 1979-03-07 GB GB7908077A patent/GB2016516B/en not_active Expired
- 1979-03-07 CS CS791538A patent/CS212712B2/en unknown
- 1979-03-07 BE BE0/193878A patent/BE874665A/en not_active IP Right Cessation
- 1979-03-07 CH CH221979A patent/CH639687A5/en not_active IP Right Cessation
-
1981
- 1981-07-20 US US06/285,295 patent/USRE31242E/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| FI62680B (en) | 1982-10-29 |
| USRE31242E (en) | 1983-05-17 |
| PT69306A (en) | 1979-04-01 |
| NO790748L (en) | 1979-09-10 |
| FR2419317A1 (en) | 1979-10-05 |
| ES478364A1 (en) | 1980-01-01 |
| IT1113413B (en) | 1986-01-20 |
| SE415107B (en) | 1980-09-08 |
| PL213922A1 (en) | 1979-11-05 |
| GB2016516A (en) | 1979-09-26 |
| AT365630B (en) | 1982-02-10 |
| IT7920594A0 (en) | 1979-02-27 |
| LU80993A1 (en) | 1979-06-18 |
| FI62680C (en) | 1983-02-10 |
| DE2907863A1 (en) | 1979-09-13 |
| SE7802533L (en) | 1979-09-08 |
| DD142204A5 (en) | 1980-06-11 |
| NL7901522A (en) | 1979-09-11 |
| BE874665A (en) | 1979-07-02 |
| FI790735A7 (en) | 1979-09-08 |
| DK93079A (en) | 1979-09-08 |
| NO145622C (en) | 1982-04-28 |
| CH639687A5 (en) | 1983-11-30 |
| CS212712B2 (en) | 1982-03-26 |
| NO145622B (en) | 1982-01-18 |
| GB2016516B (en) | 1982-08-18 |
| FR2419317B1 (en) | 1984-03-09 |
| ATA168279A (en) | 1981-06-15 |
| PL117140B1 (en) | 1981-07-31 |
| DE2907863C2 (en) | 1982-10-28 |
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