NO140677B - Hydraulisk vaeskeblanding, spesielt for anvendelse i luftfartoeyer - Google Patents
Hydraulisk vaeskeblanding, spesielt for anvendelse i luftfartoeyer Download PDFInfo
- Publication number
- NO140677B NO140677B NO750422A NO750422A NO140677B NO 140677 B NO140677 B NO 140677B NO 750422 A NO750422 A NO 750422A NO 750422 A NO750422 A NO 750422A NO 140677 B NO140677 B NO 140677B
- Authority
- NO
- Norway
- Prior art keywords
- acid
- weight
- phosphates
- phenyl
- alkyl
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 26
- 239000007788 liquid Substances 0.000 title description 16
- 239000002994 raw material Substances 0.000 claims description 25
- 239000012530 fluid Substances 0.000 claims description 20
- 239000000654 additive Substances 0.000 claims description 9
- 230000000996 additive effect Effects 0.000 claims description 9
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 5
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 3
- 150000007942 carboxylates Chemical class 0.000 claims description 2
- -1 cycloalkyl carboxylate Chemical class 0.000 description 21
- 229910019142 PO4 Inorganic materials 0.000 description 18
- 235000021317 phosphate Nutrition 0.000 description 18
- 239000002253 acid Substances 0.000 description 13
- 125000000217 alkyl group Chemical group 0.000 description 13
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 10
- XQVWYOYUZDUNRW-UHFFFAOYSA-N N-Phenyl-1-naphthylamine Chemical class C=1C=CC2=CC=CC=C2C=1NC1=CC=CC=C1 XQVWYOYUZDUNRW-UHFFFAOYSA-N 0.000 description 9
- 125000003118 aryl group Chemical group 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 239000004593 Epoxy Substances 0.000 description 7
- 239000000463 material Substances 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- 125000003107 substituted aryl group Chemical group 0.000 description 7
- 125000002947 alkylene group Chemical group 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 6
- 229910052739 hydrogen Inorganic materials 0.000 description 6
- 239000001257 hydrogen Substances 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 6
- 239000010452 phosphate Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000003112 inhibitor Substances 0.000 description 5
- 239000002480 mineral oil Substances 0.000 description 5
- 229920000728 polyester Polymers 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 125000000547 substituted alkyl group Chemical group 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 4
- 229910052760 oxygen Inorganic materials 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 239000002562 thickening agent Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 3
- 239000012964 benzotriazole Substances 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 125000000853 cresyl group Chemical group C1(=CC=C(C=C1)C)* 0.000 description 3
- 150000001991 dicarboxylic acids Chemical class 0.000 description 3
- 235000019441 ethanol Nutrition 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical class CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 3
- LAIUFBWHERIJIH-UHFFFAOYSA-N 3-Methylheptane Chemical compound CCCCC(C)CC LAIUFBWHERIJIH-UHFFFAOYSA-N 0.000 description 2
- YXALYBMHAYZKAP-UHFFFAOYSA-N 7-oxabicyclo[4.1.0]heptan-4-ylmethyl 7-oxabicyclo[4.1.0]heptane-4-carboxylate Chemical compound C1CC2OC2CC1C(=O)OCC1CC2OC2CC1 YXALYBMHAYZKAP-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 125000004423 acyloxy group Chemical group 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical compound C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 230000032050 esterification Effects 0.000 description 2
- 238000005886 esterification reaction Methods 0.000 description 2
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N malic acid Chemical compound OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 2
- 235000010446 mineral oil Nutrition 0.000 description 2
- 238000006384 oligomerization reaction Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 150000003014 phosphoric acid esters Chemical class 0.000 description 2
- GUEIZVNYDFNHJU-UHFFFAOYSA-N quinizarin Chemical compound O=C1C2=CC=CC=C2C(=O)C2=C1C(O)=CC=C2O GUEIZVNYDFNHJU-UHFFFAOYSA-N 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- KOWVWXQNQNCRRS-UHFFFAOYSA-N tris(2,4-dimethylphenyl) phosphate Chemical compound CC1=CC(C)=CC=C1OP(=O)(OC=1C(=CC(C)=CC=1)C)OC1=CC=C(C)C=C1C KOWVWXQNQNCRRS-UHFFFAOYSA-N 0.000 description 2
- 125000005023 xylyl group Chemical group 0.000 description 2
- UUBPRIUBEQJUQL-UHFFFAOYSA-N (1-methylcyclohexyl)methanol Chemical compound OCC1(C)CCCCC1 UUBPRIUBEQJUQL-UHFFFAOYSA-N 0.000 description 1
- WENIXZFPXMQPQQ-UHFFFAOYSA-N 2,2-dimethylheptan-1-ol Chemical compound CCCCCC(C)(C)CO WENIXZFPXMQPQQ-UHFFFAOYSA-N 0.000 description 1
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical group CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 description 1
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 description 1
- LIAWCKFOFPPVGF-UHFFFAOYSA-N 2-ethyladamantane Chemical compound C1C(C2)CC3CC1C(CC)C2C3 LIAWCKFOFPPVGF-UHFFFAOYSA-N 0.000 description 1
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
- MGGQLCDQMPVBKC-UHFFFAOYSA-N 4-propylnonan-4-yl dihydrogen phosphate Chemical class CCCCCC(CCC)(CCC)OP(=O)(O)O MGGQLCDQMPVBKC-UHFFFAOYSA-N 0.000 description 1
- GMMHKHNCJNRQGK-UHFFFAOYSA-N 4-propylundecan-4-yl dihydrogen phosphate Chemical class CCCCCCCC(CCC)(CCC)OP(=O)(O)O GMMHKHNCJNRQGK-UHFFFAOYSA-N 0.000 description 1
- 229910000851 Alloy steel Inorganic materials 0.000 description 1
- 229910000906 Bronze Inorganic materials 0.000 description 1
- KCLJHKVTILZQIS-UHFFFAOYSA-N C(CCCCCCCC)C1=C(C=CC=C1)CC(CCCC)CC Chemical compound C(CCCCCCCC)C1=C(C=CC=C1)CC(CCCC)CC KCLJHKVTILZQIS-UHFFFAOYSA-N 0.000 description 1
- 239000004129 EU approved improving agent Substances 0.000 description 1
- UUGLJVMIFJNVFH-UHFFFAOYSA-N Hexyl benzoate Chemical compound CCCCCCOC(=O)C1=CC=CC=C1 UUGLJVMIFJNVFH-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- NIYNIOYNNFXGFN-UHFFFAOYSA-N [4-(hydroxymethyl)cyclohexyl]methanol;7-oxabicyclo[4.1.0]heptane-4-carboxylic acid Chemical compound OCC1CCC(CO)CC1.C1C(C(=O)O)CCC2OC21.C1C(C(=O)O)CCC2OC21 NIYNIOYNNFXGFN-UHFFFAOYSA-N 0.000 description 1
- 239000000370 acceptor Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 239000001361 adipic acid Substances 0.000 description 1
- 235000011037 adipic acid Nutrition 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 239000004411 aluminium Substances 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
- 239000003963 antioxidant agent Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 239000004305 biphenyl Substances 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 239000010974 bronze Substances 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000003245 coal Substances 0.000 description 1
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 1
- MMOHDYOWOWFVFY-UHFFFAOYSA-N dihexyl propyl phosphate Chemical class CCCCCCOP(=O)(OCCC)OCCCCCC MMOHDYOWOWFVFY-UHFFFAOYSA-N 0.000 description 1
- 238000006471 dimerization reaction Methods 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- KWKXNDCHNDYVRT-UHFFFAOYSA-N dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229910001651 emery Inorganic materials 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 239000011344 liquid material Substances 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- 239000006078 metal deactivator Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical compound OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 description 1
- 229940117969 neopentyl glycol Drugs 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001490 poly(butyl methacrylate) polymer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920005567 polycyclic polymer Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 150000008442 polyphenolic compounds Chemical class 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- JZALLXAUNPOCEU-UHFFFAOYSA-N tetradecylbenzene Chemical compound CCCCCCCCCCCCCCC1=CC=CC=C1 JZALLXAUNPOCEU-UHFFFAOYSA-N 0.000 description 1
- 238000005979 thermal decomposition reaction Methods 0.000 description 1
- SFENPMLASUEABX-UHFFFAOYSA-N trihexyl phosphate Chemical class CCCCCCOP(=O)(OCCCCCC)OCCCCCC SFENPMLASUEABX-UHFFFAOYSA-N 0.000 description 1
- QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
- WVPGXJOLGGFBCR-UHFFFAOYSA-N trioctyl phosphate Chemical class CCCCCCCCOP(=O)(OCCCCCCCC)OCCCCCCCC WVPGXJOLGGFBCR-UHFFFAOYSA-N 0.000 description 1
- RXPQRKFMDQNODS-UHFFFAOYSA-N tripropyl phosphate Chemical class CCCOP(=O)(OCCC)OCCC RXPQRKFMDQNODS-UHFFFAOYSA-N 0.000 description 1
- 239000004711 α-olefin 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
- C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
- C10M169/04—Mixtures of base-materials and additives
- C10M169/044—Mixtures of base-materials and additives the additives being a mixture of non-macromolecular and macromolecular 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
- C10M105/00—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound
- C10M105/74—Lubricating compositions characterised by the base-material being a non-macromolecular organic compound containing phosphorus
-
- 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
- C10M125/00—Lubricating compositions characterised by the additive being an inorganic material
- C10M125/14—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
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/16—Ethers
- C10M129/18—Epoxides
-
- 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
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/24—Aldehydes; Ketones
-
- 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
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/26—Carboxylic acids; Salts thereof
- C10M129/28—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms
- C10M129/38—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms
- C10M129/42—Carboxylic acids; Salts thereof having carboxyl groups bound to acyclic or cycloaliphatic carbon atoms having 8 or more carbon atoms polycarboxylic
-
- 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
- C10M129/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen
- C10M129/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing oxygen having a carbon chain of less than 30 atoms
- C10M129/66—Epoxidised acids or esters
-
- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/04—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M133/12—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to a carbon atom of a six-membered aromatic ring
-
- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/38—Heterocyclic nitrogen compounds
- C10M133/44—Five-membered ring containing nitrogen and carbon only
-
- 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
- C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
- C10M141/06—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic nitrogen-containing compound
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- Inorganic Chemistry (AREA)
- Lubricants (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
- Fluid-Pressure Circuits (AREA)
Description
Det er kjent en rekke væsker som er tenkt brukt for overføring av kraft i forskjellige hydrauliske systemer inklusive noen væsker som er tenkt brukt i de hydrauliske systemer i luftfar-tøyer. De hydrauliske kraftsystemer i luftfartøyer og visse industri-elle systemer for drift av forskjellige mekanismer stiller strenge krav til den hydrauliske væske som anvendes. Ikke bare må den hydrauliske væske tilfredsstille strenge funksjonelle og anvendelses-krav, men i tillegg må en slik væske være tilstrekkelig ubrennbar til å tilfredsstille krav om brannresistens. I visse tilfeller må denne væskes viskositetskarakteristika være slik at den kan anvendes over et vidt temperaturområde, det vil si at den må ha adekvat viskositet ved høye temperaturer, lav viskositet ved lave temperaturer, og dens viskositet må forandre seg lite med temperaturen.
Dens hellepunkt må være lavt. Dens flyktighet må være lav ved for-høyede brukstemperaturer, det vil si at selektiv fordampning eller flyktiggjørelse av enhver viktig komponent må ikke finne sted ved høye brukstemperaturer. Den må være i besittelse av tilstrekkelig smøreevne og mekanisk stabilitet til at den kan brukes i hydrauliske systemer i luftfartøyer, hvor det settes særlig strenge krav til den anvendte væske. Den må være kjemisk stabil slik at den motstår slike kjemiske reaksjoner som oksydasjon, varmenedbrytning osv.,
slik at den vil holde seg stabil under bruksbetingelser mot tap av ønskede karakteristika som skyldes store og plutselige forandringer med hensyn til trykk, temperatur, høye strekkstyrker og kontakt med forskjellige metaller som for eksempel kan være aluminium, bronse, visse stållegeringer, kadmium, magnesium og liknende. Den må heller ikke skade eller svelle tetningsringer og pakninger i det industri-elle eller luftfartøyhydrauliske system. Den må ikke ha ugunstig innflytelse på materialene som systemet er konstruert av, og hvis det blir en lekkasje, må den ikke ha ugunstig innvirkning på de forskjellige deler av hydrauliske system som den tilfeldigvis kommer i
kontakt med.
Det er foreslått forskjellige hydrauliske væskeblandinger. Disse kan som funksjonelle væsker, også kalt basisråstoffmaterialer, f.eks. inneholde estere og amider av en fosforsyre, mineralolje og syntetiske hydrokarbonoljer, monoestere, dikarboksylsyreestere og estere av flerverdige forbindelser.
Fosfatestere som er blitt tilsatt egnede'"hellepunkts-nedsettende midler, viskositetsindeksforbedrende midler, rust-inhibitorer, korrosjonsinhibitorer osv., er blant de beste som hittil er foreslått, og disse er i utstrakt grad blitt brukt som hydrauliske væsker i luftfartøyer.
Disse væsker kan imidlertid oppvise uønsket syreopp-
bygning under bruk. Hvis denne syreoppbygning blir for sterk,
vil basisråstoffmaterialene bli brutt ned og tape sine fysikalske egenskaper med hensyn til viskositet og liknende. Syren kan også angripe metalldelene i det hydrauliske system som eksponeres for væskene. I den hensikt å bekjempe dette syreangrep tilsettes korrosjonsinhibitorer til de funksjonelle væskeblandinger.
Det er oppdaget at det kan tilveiebringes forbedret syrestabilitet i et funksjonelt væskemateriale når det i væsken er til stede en bestemt additiv-kombinasjon som omfatter et epoksycykloalkylkarboksylat.
Oppfinnelsen tilveiebringer følgelig en hydraulisk væskeblanding hvis karakteristiske trekk er at additiv-kombinasjonen foruten epoksycykloalkylkarboksylat inneholder fenyl-ct-naftylamin, og vektforholdet mellom disse er i området 1:10 til 10:1.
Tilsetning av additiv-kombinasjonen gir uventede synergi-stiske resultater med hensyn til forbedret syrestabilitet og visko-sitetsstabilitet hos den funksjonelle væske, uten å oppvise noen skadelige karakteristika så som oppbygning av slam, metallkorrosjon o. 1.
De epoksycykloalkylkarboksylat-forbindelser som inngår i produktet i henhold til oppfinnelsen er eksemplifisert ved følgende
strukturformel:
R er et alkylradikal med 1-12 karbonatomer, R2 er , hydrogen eller et alkylradikal med 1-9 karbonatomer, og n og m er 3-8.
Foretrukne epoksyforbindelser er 3,4-epoksycykloalkyl-karboksylatene. Representative for denne klasse er 3,4-epoksy-cykloheksylmetyl, 3,4-epoksycykloheksankarboksylat som er spesielt foretrukket og har følgende formel:
De fenylnaftylaminer som anvendes, kan være illustrert ved følgende formel:
hvor R', R<11> og R'<*>' kan være like eller forskjellige og er medlemmer av gruppen som består av hydrogen, alkyl, aryl, ;alkaryl og aralkyl med 1-16 karbonatomer. ;Spesielt foretrukne medlemmer av denne gruppe er fenyl-a-naftylamin, oktylert fenyl-a-naftylamin (fenyl-a-naftylamin alkylert med diisobutylen i et 1:1 - 3:1 molforhold), dioktyl-fenyl-a-naftylamin, trioktylfenyl-a-naftylamin o.l. ;Konsentrasjonen av cykloalkylepoksyd og fenylnaftylamin ;i den funksjonelle væske justeres alt etter det spesielle system og de funksjonelle væskeblandinger som i henhold til oppfinnelsen inneholder tilstrekkelige mengder av cykloalkylepoksyd og fenylnaftylamin til å inhibere syreoppbygning. Det har således vist seg at konsentrasjonen av cykloalkylepoksyd og fenylnaftylamin som er nødvendig for å inhibere og regulere syreoppbygningen i et basisråstoffmateriale, varierer med basisråstoffmaterialet eller ;blandinger av basisråstoffmaterialer. Siden epoksyforbindelsen og fenyl-a-naftylaminet innarbeides i væsken i mengder som er tilstrekkelige til å inhibere syreoppbygning, og etter som væskeegen-skapene kan endres ved innarbeidelse av et fremmed element, har det generelt vist seg at et foretrukket totalt nivå med hensyn til additiv-kombinasjonen er fra 0,10 til 5,0 vekt% regnet på hele væsken, mens 10,0 vekt% additivkonsentrasjon er satt som øvre grense. Vektforholdet mellom epoksyforbindelse og fenyl-a-naftylamin kan variere fra 1:10 til 10:1, og mest foretrukket er 1:1. ;Den hydrauliske væskeblanding i henhold til oppfinnelsen kan bygges opp på enhver måte som er kjent for fagmannen på området for innarbeidelse av et additiv i et basisråstoffmateriale. Således kan epoksyforbindelsen og fenyl-a-naftylaminet tilsettes i hvilken som helst rekkefølge, eller samlet, til basisråstoffmaterialet under omrøring til det oppnås en homogen væskeblanding. ;Basisråstoffmaterialer som er egnet for anvendelse i hydrauliske væskeblandinger i henhold til oppfinnelsen, kan være estere og amider av en fosforsyre som kan være representert ved strukturformelen: hvor Y er utvalgt fra gruppen som består av oksygen, svovel og ;Y, er utvalgt fra gruppen som består av oksygen, svovel og og Y2 er utvalgt fra gruppen som består av oksygen, svovel og ;R, R^, <R>2, <R>3, R^ og R,, er hver utvalgt fra gruppen som består av alkyl, aryl, substituert aryl og substituert alkyl med 1-30 karbonatomer, hvor R, R1} R2, R3, R4 og R5 hver kan være identiske eller forskjellige med hensyn til hvilken som helst av de andre radikaler, og a, b og c er hele tall med verdien 0 eller 1 og summen av a+b+c er fra 1 til 3. ;Typiske eksempler på substituerte alkylradikaler ;er halogenalkylradikalene som kan være representert ved struktur- ;formelen: ;;hvor Hal betyr halogen, m er mindre eller lik 2n+^ og n kan ha hvilken som helst verdi fra 0 til 18, og R& og R? kan være hydrogen, halogen eller alkyl. De halogenerte alkylradikaler kan være primære, sekundære eller tertiære. ;Typiske eksempler på aryl- og substituerte aryl-radikaler er fenyl, kresyl, xylyl, halogenert fenyl, kresyl og xylyl hvor det tilgjengelige hydrogen på aryl eller substituert aryl er delvis eller helt erstattet med halogen, o-, m- og p-trifluormetyl-fenyl, 0-, m- og p-2,2,2-trifluoretylfenyl, 0-, m- og p-3,3,3-tri-fluorpropylfenyl og o-, m- og p-4,4,4-trifluorbutylfenyl. ;Dikarboksylsyreestere som er egnet som basisrå-stof fmaterialer , er representert ved strukturformelen: ;hvor <R>2Q og R22 hver er utvalgt fra gruppen som består av alkyl, substituert alkyl, aryl og substituert aryl og R2^ er et toverdig radikal som er utvalgt fra gruppen som består av alkylen og substituert alkylen og er fremstilt ved forestring av dikarboksylsyrer som adipinsyre, azelainsyre, suberinsyre, sebacinsyre, hydroksyrav-syre, fumarsyre, maleinsyre, etc, med slike alkoholer som butyl-alkohol, heksylalkohol, 2-etylheksylalkohol, dodecylalkohol, 2,2-dimetylheptanol, 1-metylcykloheksylmetanol, etc. ;Typiske eksempler på alkyl, aryl, substituert alkyl og substituert aryl er gitt ovenfor. ;Polyestere som er egnet som basisråstoffmaterialer, er representert ved strukturformelen: ;hvor R-, er utvalgt fra gruppen som består av hydrogen og alkyl, ;<R>24 og R25 er hver utvalgt fra gruppen som består av alkyl, ;substituert alkyl, aryl og substituert aryl, a er et helt tall med verdi 0 eller 1, Z er et helt tall med verdi 1 eller 2, og når Z er 1, er R2^ utvalgt fra gruppen som består av hydrogen, ;alkyl, acyloksy og substituert acyloksy, og når Z er 2* er R26
oksygen og fremstilt ved forestring av slike polyalkoholer som pentaerytritol, dipentaerytritol, trimetylolpropan, trimetyloletan og neopentylglykol med slike syrer som propion-, smør-, isosmør-, n-valerian-, kapron-, n-heptyl-, kapryl-, 2-etylheksan, 2,2-di-metylheptan- og p elargonsyre. Typiske eksempler på alkyl, substituert alkyl, aryl og substituert aryl er gitt ovenfor.
Andre estere som også er egnet som basisråstoffmaterialer, er monoesterne.
Hydrokarbonoljer inklusive mineraloljer som stammer
fra petroleumkilder, og syntetiske hydrokarbonoljer er egnede basis-råstof fmaterialer . De fysikalske karakteristika for funksjonelle væsker som stammer fra en mineralolje, er utvalgt på basis av kravene til væskesystemene, og derfor innbefatter denne oppfinnelse som basisråstoffmaterialer mineraloljer som har et vidt område av viskositeter og flyktigheter så som mineraloljer på naftenbasis, paraffinbasis eller blandet basis.
De syntetiske hydrokarbonoljer inkluderer, men er ikke begrenset til, slike oljer som stammer fra oligomerisering av olefiner så som polybutener og oljer som stammer fra høye a-olefiner med 8-20 karbonatomer ved syrekatalysert dimerisering og ved oligomerisering under anvendelse av trialuminiumalkylforbindelser som katalysatorer.
Også innbefattet innenfor oppfinnelsens ramme er blandinger av to eller flere av de ovenfor beskrevne basisråstoffmaterialer som kan anvendes som basisråstoffmaterialer.
De hydrauliske væskeblandinger i henhold til
oppfinnelsen kan også inneholde farvestoffer, hellepunktnedsettende midler, skumhindrende midler, viskositetsindeksforbedrende midler, for eksempel polyalkylakrylater, polyalkyl-metakrylater, polycykliske polymerer, polyuretaner, polyalkylen-
oksyder og polyestere, smøremidler, vann o.l.
Også inkludert innenfor oppfinnelsens ramme er det
at basisråstoffmaterialene som er omtalt ovenfor, kan anvendes enkelt-vis eller som en væskeblanding som inneholder to eller flere basis-råstof fmaterialer i varierende mengdeforhdd. Basisråstoffmaterialene kan også inneholde andre væsker som, i tillegg til de funksjonelle væsker, inkluderer ønskede væsker som stammer fra kullprodukter, syntetiske produkter og syntetiske oljer, for eksempel alkylen-polymerer ( for eksempel polymerer av propylen, butylen, etc, og blandinger derav), polymerer av alkylenoksydtype (for eksempel propylenoksydpolymerer), samt derivater, inklusive alkylenoksyd-polymerer som er fremstilt ved polymerisering av alkylenoksyd i nærvær av vann eller alkohol, for eksempel etylalkohol, alkyl-
benzener, (for eksempel monoalkylbenzen slik som dodecylbenzen, tetradecylbenzen etc.) og dialkylbenzen (for eksempel n-nonyl-2-etylheksylbenzen); og polyfenoler (for eksempel bifenyl- og terfenylforbindelser) .
I den foretrukne form av oppfinnelsen vil cykloalkyl-epoksydet og fenylnaftylaminet være kombinert med et fosfat-
holdig basisråstoffmateriale. Basisråstoffmaterialet vil primært bestå av trialkylfosfater som er til stede i mengder fra 50 til 95 vekti og fortrinnsvis fra 60 til 90 vekti. Trialkylfos-
fåtene som gir optimale resultater, er slike hvor hver av alkylgruppene inneholder fra 1 til 20 karbonatomer, fortrinnsvis fra 3
til 12 karbonatomer og mer fortrinnsvis fra 4 til 9 karbonatomer. Alkylgruppene er fortrinnsvis av rettkjedet konfigurasjon. Et enkelt
trialkylfosfat kan inneholde alkylgrupper i alle tre stillinger eller kan ha en blanding av forskjellige alkylgrupper. Blandinger av forskjellige trialkylfosfater kan anvendes. Egnede typer av trialkylfosfater som kan anvendes som basisråstoffmateriale-blanding, inkluderer tripropylfosfater, tributylfosfater, triheksyl-fosfater, trioktylfosfater, dipropyloktylfosfater, dibutyloktyl-fosfater, dipropylheksylfosfate , diheksyloktylfosfate, diheksyl-propylfosfat og propylbutyloktylfosfat.
Trialkylfosfåtene kan være kombinert med triarylfosfater. Foretrukne triarylfosfater er kresyldifenylfosfat, trikrecylfosfat, trixylenylfosfat, tert.butylfenylfenylfosfater, etylfenyldikresylfosfat eller isopropylfenyldifenylfosfat, fenyl-bis(4-a-metylbenzylfenyl)fosfat. Det foretrekkes ved utførelse av oppfinnelsen å anvende et basisråstoffmateriale som primært inneholder trixylenylfosfat. Triarylfosfåtene funksjonerer som fortykningsmiddel for trialkylfosfåtene. Således kan mengden av triarylfosfat variere mellom ca. 0 og ca. 35 vekti. Det foretrukne område av triarylfosfåtene vil være fra ca. 5 til ca. 30 vekti av blandingen.
Konvensjonelle polymere fortykningsmidler eller viskositetsindeksforbedrende midler kan blandes med blandingen av trialkyl- og triarylfosfatmateriale for oppnåelse av den ønskede viskositet. Typiske fortykningsmidler som anvendes, kan være polyakrylater, polymetakrylater, polyetylenoksyder, polypropylen-oksyder, polyestere og liknende.
Fortrinnsvis anvendes en polyester som er basert på azelainsyre og en diol i området 0,3 til 20 vekti som viskositets-indeksf orbedrende middel.
Korrosjonsinhibitorer, for eksempel benzotriazol, kinizarin eller liknende i en mengde som varierer mellom 0,001 og 0,5 vekti, kan tilsettes til blandingen og blandes grundig med denne. Et farvestoff i et konsentrasjonsområde mellom 5 og 20 ppm kan tilsettes til blandingen og blandes med denne på en konvensjonell måte. Effektive mengder av et silikon-skumhindrende middel kan også inn-blandes i blandingen, og dette er vanligvis mest effektivt i en mengde som varierer mellom 5 og 50 ppm. De funksjonelle væsker i henhold til oppfinnelsen kan inneholde opp til ca. 1 vekti vann.
Det foretrekkes imidlertid å opprettholde vann-nivåer under 0,6 vekti og mest fortrinnsvis under 0,3 vekti.
Det har vist seg at når epoksycyklo-alkylkarboksylatet og fenyl-a-naftylaminet blandes i de riktige mengdeforhold med det ovenfor angitte foretrukne basisråstoffmateriale, får man hydrauliske væskeblandinger hvis egenskaper er de kjente kommersielle væsker overlegne.
Oppfinnelsen kan bedre forstås ved hjelp av det følgende eksempel. Alle deler og prosenter angir vekt, med mindre annet er angitt.
Eksempel.
Det ble fremstilt prøver av basisråstoffmateriale, be-stående av tilnærmet 68% tributylfosfat, 19% blandede aryl-fosfater med en viskositet på ca. 150 SUS, 12% av et polybutyl-metakrylat-viskositetsindeksforbedrende middel, 0,5% vann, 0,02% benzotriazolmetalldeaktivator og en alkylravsyre-rust-inhibitor som var tilsatt 1 vekt% 3,4-epoksycykloheksylmetyl-3,4-epoksycykloheksankarboksylat og 1 vekt% av følgende anti-oksydasjonsmidler:
Disse tester viser at fenyl-a-naftylamin stabiliserer produktet i størst utstrekning i nærvær av det cykloalkylepoksyd som er omtalt ovenfor.
I en rekke liknende oksydasjonstester som ble utført
på en blanding som besto av ca. 79 vekt% tributylfosfat, 10 vekt% blandede kresyl- og xylenylfosfater, 9 vekt% av et poly-esterfortykningsmiddel, "Plastolein" 9789 fra Emery Industries,
1 vekt% fenyl-a-naftylamin og 0,0 2 vekt% benzotriazol, samt ca. 0,25 vekt% vann, ble følgende resultater oppnådd med forskjellige epoksysyreakseptorer i en 1,0 vekt% konsentrasjon:
Disse resultater viser i tilknytning til resultatene ved begynnelsen av eksemplet at fenyl-a-naftylamin og 3,4-epoksycykloheksylmetyl-3,4-epoksycykloheksankarboksylat danner en enestående synergistisk additivkombinasjon for stabilisering av fosfatestere.
Claims (1)
- Hydraulisk væskeblanding, spesielt for anvendelse i luftfartøyer, omfattende en blanding av et basisråstoffmateriale som i alt vesentlig består av en eller flere estere av en fosforsyre og 0,1-10 vekt%, regnet på hele blandingen, av en additivkombinasjon omfattende et epoksycykloalkylkarboksylat, karakteritser<t> ved at additivkombinasjonen også inneholder fenyl-a-naftylamin, idet vektforholdet mellom epoksycykloalkylkarboksylat og fenyl-a-naftylamin er fra 1:10 til 10:1.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US05/441,697 US3941708A (en) | 1974-02-11 | 1974-02-11 | Hydraulic fluid antioxidant system |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO750422L NO750422L (no) | 1975-08-12 |
| NO140677B true NO140677B (no) | 1979-07-09 |
| NO140677C NO140677C (no) | 1979-10-17 |
Family
ID=23753934
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO750422A NO140677C (no) | 1974-02-11 | 1975-02-10 | Hydraulisk vaeskeblanding, spesielt for anvendelse i luftfartoeyer |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US3941708A (no) |
| JP (1) | JPS6038440B2 (no) |
| BE (1) | BE825339A (no) |
| CA (1) | CA1048011A (no) |
| CH (1) | CH616957A5 (no) |
| DE (1) | DE2505116C2 (no) |
| DK (1) | DK144380C (no) |
| FR (1) | FR2260616B1 (no) |
| GB (1) | GB1506197A (no) |
| IL (1) | IL46500A (no) |
| IN (1) | IN142709B (no) |
| IT (1) | IT1029650B (no) |
| NL (1) | NL7501425A (no) |
| NO (1) | NO140677C (no) |
| SE (1) | SE410006B (no) |
| SU (1) | SU652900A3 (no) |
| ZA (1) | ZA75841B (no) |
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| US4252662A (en) * | 1974-02-11 | 1981-02-24 | Stauffer Chemical Company | Functional fluids containing ammonium salts of phosphorus acids |
| US4461713A (en) * | 1983-04-01 | 1984-07-24 | Stauffer Chemical Company | Acid-resistant phosphate ester functional fluids |
| US4645615A (en) * | 1986-02-27 | 1987-02-24 | Fmc Corporation | Fire-resistant hydraulic fluid |
| JP3038062B2 (ja) * | 1991-10-15 | 2000-05-08 | 旭電化工業株式会社 | 冷凍機用潤滑剤 |
| USRE37101E1 (en) | 1992-06-11 | 2001-03-20 | Solutia Inc. | Stabilized phosphate ester-based functional fluid compositions |
| ATE371714T1 (de) | 1998-10-23 | 2007-09-15 | Exxonmobil Res & Eng Co | Verwendung von phosphatesterhaltigen basisölen als flugzeughydraulikflüssigkeit |
| WO2000024848A1 (en) * | 1998-10-23 | 2000-05-04 | Exxonmobil Research And Engineering Company | Phosphate ester base stocks and aircraft hydraulic fluids comprising the same |
| AU5960501A (en) * | 2000-05-09 | 2001-11-20 | Solutia Inc | Functional fluid compositions containing epoxide acid scavengers |
| AU2002212954A1 (en) | 2000-08-04 | 2002-02-18 | Exxonmobil Research And Engineering Company | Method for lubricating high pressure hydraulic system using phosphate ester hydraulic fluid |
| US6717005B2 (en) | 2002-05-13 | 2004-04-06 | Akzo Nobel N.V. | Epoxy-stabilized polyphosphate compositions |
| US7470381B2 (en) * | 2003-07-25 | 2008-12-30 | Rohmax Additives Gmbh | Functional fluid and the use thereof |
| US7910529B2 (en) * | 2004-11-03 | 2011-03-22 | Solutia, Inc. | Functional fluid compositions |
| MX349932B (es) | 2010-10-01 | 2017-08-21 | Tyco Fire Products Lp | Espumas para extincion de fuego acuosas con bajo contenido de fluor. |
| MX2015006082A (es) * | 2012-11-16 | 2015-08-12 | Basf Se | Composiciones de lubricante que comprenden compuestos epoxido para mejorar la compatibilidad del sello de fluoropolimero. |
| WO2014153140A1 (en) | 2013-03-14 | 2014-09-25 | Tyco Fire & Security Gmbh | Trimethylglycine as a freeze suppressant in fire fighting foams |
| EP2969055B1 (en) | 2013-03-15 | 2020-05-06 | Tyco Fire Products LP | Perfluoroalkyl composition with reduced chain length |
| EP3126015B1 (en) | 2014-04-02 | 2020-08-19 | Tyco Fire Products LP | Fire extinguishing compositions |
| EP3256224B1 (en) | 2015-02-13 | 2020-09-09 | Tyco Fire Products LP | Use of an indicator as a marker in foam concentrates |
| EP3429700B1 (en) | 2016-03-18 | 2020-12-23 | Tyco Fire Products LP | Organosiloxane compounds as active ingredients in fluorine free fire suppression foams |
| ES2888124T3 (es) | 2016-03-18 | 2021-12-30 | Tyco Fire Products Lp | Compuestos de poliorganosiloxano como componentes activos en espumas de supresión de incendios libres de flúor |
| EP3490683A1 (en) | 2016-07-29 | 2019-06-05 | Tyco Fire Products LP | Firefighting foam compositions containing deep eutectic solvents |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB734644A (en) * | 1953-07-17 | 1955-08-03 | Shell Refining & Marketing Co | Compositions suitable for use as hydraulic fluids |
| US3019191A (en) * | 1954-09-28 | 1962-01-30 | California Research Corp | Stabilized hydraulic fluid composition |
| US2930758A (en) * | 1956-09-28 | 1960-03-29 | Texaco Inc | Ester-base lubricant containing anti-oxidant mixtures |
| US2982734A (en) * | 1957-06-14 | 1961-05-02 | Shell Oil Co | Power transmission mineral oil base fluid |
| BE596160A (no) * | 1959-10-20 | |||
| BE700905A (no) * | 1966-07-05 | 1968-01-04 | ||
| GB1153546A (en) * | 1966-08-30 | 1969-05-29 | Chevron Res | Hydraulic Fluids |
| US3637507A (en) * | 1968-02-12 | 1972-01-25 | Stauffer Chemical Co | Aircraft hydraulic fluid and method of controlling acid buildup therein with acid acceptor |
| US3574117A (en) * | 1968-05-21 | 1971-04-06 | Chevron Res | Hydraulic fluid containing alkyl 1,2,3,4,7,7 - hexachlorobicyclo-(2.2.1)-hept-2-ene-5-carboxylate base |
| BE792993A (fr) * | 1971-12-20 | 1973-06-19 | Monsanto Co | Compositions de fluides fonctionnels contenant des stabilisantsepoxyde |
-
1974
- 1974-02-11 US US05/441,697 patent/US3941708A/en not_active Expired - Lifetime
-
1975
- 1975-01-23 IL IL46500A patent/IL46500A/en unknown
- 1975-01-29 IN IN180/CAL/75A patent/IN142709B/en unknown
- 1975-01-31 JP JP50013312A patent/JPS6038440B2/ja not_active Expired
- 1975-02-05 DK DK39175A patent/DK144380C/da active
- 1975-02-06 NL NL7501425A patent/NL7501425A/xx not_active Application Discontinuation
- 1975-02-07 BE BE7000608A patent/BE825339A/xx not_active IP Right Cessation
- 1975-02-07 IT IT48061/75A patent/IT1029650B/it active
- 1975-02-07 DE DE2505116A patent/DE2505116C2/de not_active Expired
- 1975-02-10 NO NO750422A patent/NO140677C/no unknown
- 1975-02-10 FR FR7504032A patent/FR2260616B1/fr not_active Expired
- 1975-02-10 ZA ZA00750841A patent/ZA75841B/xx unknown
- 1975-02-10 CA CA219,715A patent/CA1048011A/en not_active Expired
- 1975-02-10 SU SU752106084A patent/SU652900A3/ru active
- 1975-02-10 SE SE7501452A patent/SE410006B/xx not_active IP Right Cessation
- 1975-02-11 GB GB5753/75A patent/GB1506197A/en not_active Expired
- 1975-02-11 CH CH159675A patent/CH616957A5/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| SE410006B (sv) | 1979-09-17 |
| DE2505116C2 (de) | 1985-06-20 |
| FR2260616B1 (no) | 1982-04-23 |
| SE7501452L (no) | 1975-08-12 |
| SU652900A3 (ru) | 1979-03-15 |
| DK144380C (da) | 1982-08-02 |
| US3941708A (en) | 1976-03-02 |
| IT1029650B (it) | 1979-03-20 |
| IN142709B (no) | 1977-08-20 |
| CH616957A5 (no) | 1980-04-30 |
| JPS50115181A (no) | 1975-09-09 |
| NL7501425A (nl) | 1975-08-13 |
| DE2505116A1 (de) | 1975-08-14 |
| ZA75841B (en) | 1976-01-28 |
| NO750422L (no) | 1975-08-12 |
| AU7759875A (en) | 1976-07-29 |
| NO140677C (no) | 1979-10-17 |
| GB1506197A (en) | 1978-04-05 |
| DK144380B (da) | 1982-03-01 |
| CA1048011A (en) | 1979-02-06 |
| IL46500A (en) | 1977-06-30 |
| DK39175A (no) | 1975-10-06 |
| BE825339A (nl) | 1975-08-07 |
| JPS6038440B2 (ja) | 1985-08-31 |
| IL46500A0 (en) | 1975-04-25 |
| FR2260616A1 (no) | 1975-09-05 |
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