EP0326975B1 - Lubricant for traction drive with continuously variable transmission - Google Patents
Lubricant for traction drive with continuously variable transmission Download PDFInfo
- Publication number
- EP0326975B1 EP0326975B1 EP89101495A EP89101495A EP0326975B1 EP 0326975 B1 EP0326975 B1 EP 0326975B1 EP 89101495 A EP89101495 A EP 89101495A EP 89101495 A EP89101495 A EP 89101495A EP 0326975 B1 EP0326975 B1 EP 0326975B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- lubricant
- lubricant according
- weight
- amine
- aliphatic
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000000314 lubricant Substances 0.000 title claims abstract description 37
- 230000005540 biological transmission Effects 0.000 title claims abstract description 22
- RVZJVYCTFGOEHX-UHFFFAOYSA-N phosphetane Chemical class C1CPC1 RVZJVYCTFGOEHX-UHFFFAOYSA-N 0.000 claims description 10
- 125000001931 aliphatic group Chemical group 0.000 claims description 9
- 239000000203 mixture Substances 0.000 claims description 8
- 229920002367 Polyisobutene Polymers 0.000 claims description 6
- 239000000654 additive Substances 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 229930195733 hydrocarbon Natural products 0.000 claims description 5
- 150000003141 primary amines Chemical class 0.000 claims description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 4
- 150000003335 secondary amines Chemical class 0.000 claims description 4
- 150000003512 tertiary amines Chemical class 0.000 claims description 4
- 230000000996 additive effect Effects 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 239000012530 fluid Substances 0.000 claims description 3
- 150000002430 hydrocarbons Chemical class 0.000 claims description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 3
- 150000007530 organic bases Chemical class 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 2
- 239000002518 antifoaming agent Substances 0.000 claims description 2
- 238000005260 corrosion Methods 0.000 claims description 2
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 2
- 229920006395 saturated elastomer Polymers 0.000 claims description 2
- 239000011593 sulfur Substances 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 230000009347 mechanical transmission Effects 0.000 claims 1
- -1 hydrocarbon radicals Chemical class 0.000 description 43
- 238000012360 testing method Methods 0.000 description 11
- 150000001412 amines Chemical class 0.000 description 10
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- 125000000217 alkyl group Chemical group 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 239000001257 hydrogen Substances 0.000 description 4
- 125000001477 organic nitrogen group Chemical group 0.000 description 4
- JLTDJTHDQAWBAV-UHFFFAOYSA-N phenyldimethylamine Natural products CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 description 4
- 239000004215 Carbon black (E152) Substances 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
- 239000007983 Tris buffer Substances 0.000 description 3
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- 229910052757 nitrogen Inorganic materials 0.000 description 3
- AXWLKJWVMMAXBD-UHFFFAOYSA-N 1-butylpiperidine Chemical compound CCCCN1CCCCC1 AXWLKJWVMMAXBD-UHFFFAOYSA-N 0.000 description 2
- PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 2
- HWWYDZCSSYKIAD-UHFFFAOYSA-N 3,5-dimethylpyridine Chemical compound CC1=CN=CC(C)=C1 HWWYDZCSSYKIAD-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- SVYKKECYCPFKGB-UHFFFAOYSA-N N,N-dimethylcyclohexylamine Chemical compound CN(C)C1CCCCC1 SVYKKECYCPFKGB-UHFFFAOYSA-N 0.000 description 2
- YJLYANLCNIKXMG-UHFFFAOYSA-N N-Methyldioctylamine Chemical compound CCCCCCCCN(C)CCCCCCCC YJLYANLCNIKXMG-UHFFFAOYSA-N 0.000 description 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 238000004140 cleaning Methods 0.000 description 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 230000001050 lubricating effect Effects 0.000 description 2
- 239000010687 lubricating oil Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- YWFWDNVOPHGWMX-UHFFFAOYSA-N n,n-dimethyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)C YWFWDNVOPHGWMX-UHFFFAOYSA-N 0.000 description 2
- NHLUVTZJQOJKCC-UHFFFAOYSA-N n,n-dimethylhexadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCN(C)C NHLUVTZJQOJKCC-UHFFFAOYSA-N 0.000 description 2
- XTAZYLNFDRKIHJ-UHFFFAOYSA-N n,n-dioctyloctan-1-amine Chemical compound CCCCCCCCN(CCCCCCCC)CCCCCCCC XTAZYLNFDRKIHJ-UHFFFAOYSA-N 0.000 description 2
- SNKUXFQNFUTEJL-UHFFFAOYSA-N n-butyl-n-methyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)CCCC SNKUXFQNFUTEJL-UHFFFAOYSA-N 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- BZUFRDUAJRZTDW-UHFFFAOYSA-N 1,3-thiaphosphetane Chemical class C1PCS1 BZUFRDUAJRZTDW-UHFFFAOYSA-N 0.000 description 1
- ONQBOTKLCMXPOF-UHFFFAOYSA-N 1-ethylpyrrolidine Chemical compound CCN1CCCC1 ONQBOTKLCMXPOF-UHFFFAOYSA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- ANFXTILBDGTSEG-UHFFFAOYSA-N 1-methyl-4,5-dihydroimidazole Chemical compound CN1CCN=C1 ANFXTILBDGTSEG-UHFFFAOYSA-N 0.000 description 1
- QIJIUJYANDSEKG-UHFFFAOYSA-N 2,4,4-trimethylpentan-2-amine Chemical compound CC(C)(C)CC(C)(C)N QIJIUJYANDSEKG-UHFFFAOYSA-N 0.000 description 1
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 description 1
- 125000004974 2-butenyl group Chemical group C(C=CC)* 0.000 description 1
- 125000006040 2-hexenyl group Chemical group 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- DZNCHORQQWFQFG-UHFFFAOYSA-N 3-hydroxy-1,3$l^{5}-thiaphosphetane 3-oxide Chemical compound OP1(=O)CSC1 DZNCHORQQWFQFG-UHFFFAOYSA-N 0.000 description 1
- AAIUWVOMXTVLRG-UHFFFAOYSA-N 8,8-dimethylnonan-1-amine Chemical compound CC(C)(C)CCCCCCCN AAIUWVOMXTVLRG-UHFFFAOYSA-N 0.000 description 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 1
- 0 CN([C@@]1*C1)P Chemical compound CN([C@@]1*C1)P 0.000 description 1
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- XTUVJUMINZSXGF-UHFFFAOYSA-N N-methylcyclohexylamine Chemical compound CNC1CCCCC1 XTUVJUMINZSXGF-UHFFFAOYSA-N 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- PLZVEHJLHYMBBY-UHFFFAOYSA-N Tetradecylamine Chemical compound CCCCCCCCCCCCCCN PLZVEHJLHYMBBY-UHFFFAOYSA-N 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 230000032683 aging Effects 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000002837 carbocyclic group Chemical group 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 125000004855 decalinyl group Chemical group C1(CCCC2CCCCC12)* 0.000 description 1
- 125000002704 decyl 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])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- XXBDWLFCJWSEKW-UHFFFAOYSA-N dimethylbenzylamine Chemical compound CN(C)CC1=CC=CC=C1 XXBDWLFCJWSEKW-UHFFFAOYSA-N 0.000 description 1
- VFFDVELHRCMPLY-UHFFFAOYSA-N dimethyldodecyl amine Natural products CC(C)CCCCCCCCCCCN VFFDVELHRCMPLY-UHFFFAOYSA-N 0.000 description 1
- 125000003438 dodecyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical class CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 238000007046 ethoxylation reaction Methods 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 229910052745 lead Inorganic materials 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- YWWNNLPSZSEZNZ-UHFFFAOYSA-N n,n-dimethyldecan-1-amine Chemical compound CCCCCCCCCCN(C)C YWWNNLPSZSEZNZ-UHFFFAOYSA-N 0.000 description 1
- WCVHUIPWSPEOIG-UHFFFAOYSA-N n,n-dimethylheptadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCN(C)C WCVHUIPWSPEOIG-UHFFFAOYSA-N 0.000 description 1
- AMAADDMFZSZCNT-UHFFFAOYSA-N n,n-dimethylnonan-1-amine Chemical compound CCCCCCCCCN(C)C AMAADDMFZSZCNT-UHFFFAOYSA-N 0.000 description 1
- ZUHZZVMEUAUWHY-UHFFFAOYSA-N n,n-dimethylpropan-1-amine Chemical compound CCCN(C)C ZUHZZVMEUAUWHY-UHFFFAOYSA-N 0.000 description 1
- KKXPLPXCGLIJCT-UHFFFAOYSA-N n-(2-phenylethyl)dodecan-1-amine Chemical compound CCCCCCCCCCCCNCCC1=CC=CC=C1 KKXPLPXCGLIJCT-UHFFFAOYSA-N 0.000 description 1
- RPAQCQVPCFVWMN-UHFFFAOYSA-N n-decyl-n-methylaniline Chemical compound CCCCCCCCCCN(C)C1=CC=CC=C1 RPAQCQVPCFVWMN-UHFFFAOYSA-N 0.000 description 1
- LCIULXVEXKRTGU-UHFFFAOYSA-N n-decyl-n-propan-2-yldecan-1-amine Chemical compound CCCCCCCCCCN(C(C)C)CCCCCCCCCC LCIULXVEXKRTGU-UHFFFAOYSA-N 0.000 description 1
- UWHRNIXHZAWBMF-UHFFFAOYSA-N n-dodecyl-n-methyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)CCCCCCCCCCCC UWHRNIXHZAWBMF-UHFFFAOYSA-N 0.000 description 1
- MJCJUDJQDGGKOX-UHFFFAOYSA-N n-dodecyldodecan-1-amine Chemical compound CCCCCCCCCCCCNCCCCCCCCCCCC MJCJUDJQDGGKOX-UHFFFAOYSA-N 0.000 description 1
- HFSDOIOMGCNPIB-UHFFFAOYSA-N n-methyl-2-octan-3-yldodecan-1-amine Chemical compound CCCCCCCCCCC(CNC)C(CC)CCCCC HFSDOIOMGCNPIB-UHFFFAOYSA-N 0.000 description 1
- CQFRPHDWUIZNOK-UHFFFAOYSA-N n-methyl-n-octyldecan-1-amine Chemical compound CCCCCCCCCCN(C)CCCCCCCC CQFRPHDWUIZNOK-UHFFFAOYSA-N 0.000 description 1
- KKJDTCBLJTWINH-UHFFFAOYSA-N n-methyl-n-phenylnaphthalen-1-amine Chemical compound C=1C=CC2=CC=CC=C2C=1N(C)C1=CC=CC=C1 KKJDTCBLJTWINH-UHFFFAOYSA-N 0.000 description 1
- OMEMQVZNTDHENJ-UHFFFAOYSA-N n-methyldodecan-1-amine Chemical compound CCCCCCCCCCCCNC OMEMQVZNTDHENJ-UHFFFAOYSA-N 0.000 description 1
- SZEGKVHRCLBFKJ-UHFFFAOYSA-N n-methyloctadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCCNC SZEGKVHRCLBFKJ-UHFFFAOYSA-N 0.000 description 1
- SEGJNMCIMOLEDM-UHFFFAOYSA-N n-methyloctan-1-amine Chemical compound CCCCCCCCNC SEGJNMCIMOLEDM-UHFFFAOYSA-N 0.000 description 1
- GCULWAWIZUGXTO-UHFFFAOYSA-N n-octylaniline Chemical compound CCCCCCCCNC1=CC=CC=C1 GCULWAWIZUGXTO-UHFFFAOYSA-N 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- IOQPZZOEVPZRBK-UHFFFAOYSA-N octan-1-amine Chemical compound CCCCCCCCN IOQPZZOEVPZRBK-UHFFFAOYSA-N 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- ZNSWGHZWUUFFKV-UHFFFAOYSA-N piperidine;pyridine Chemical compound C1CCNCC1.C1=CC=NC=C1 ZNSWGHZWUUFFKV-UHFFFAOYSA-N 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- SWZDQOUHBYYPJD-UHFFFAOYSA-N tridodecylamine Chemical compound CCCCCCCCCCCCN(CCCCCCCCCCCC)CCCCCCCCCCCC SWZDQOUHBYYPJD-UHFFFAOYSA-N 0.000 description 1
- 229940086542 triethylamine Drugs 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- 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
-
- 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
- C10M101/00—Lubricating compositions characterised by the base-material being a mineral or fatty oil
- C10M101/02—Petroleum fractions
-
- 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
- C10M107/00—Lubricating compositions characterised by the base-material being a macromolecular compound
- C10M107/02—Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation
- C10M107/08—Hydrocarbon polymers; Hydrocarbon polymers modified by oxidation containing butene
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M137/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
- C10M137/12—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having a phosphorus-to-carbon bond
-
- 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
- C10M137/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus
- C10M137/12—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having a phosphorus-to-carbon bond
- C10M137/14—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having a phosphorus-to-carbon bond containing sulfur
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/02—Well-defined aliphatic 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/02—Well-defined aliphatic compounds
- C10M2203/022—Well-defined aliphatic compounds saturated
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/02—Well-defined aliphatic compounds
- C10M2203/024—Well-defined aliphatic compounds unsaturated
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/04—Well-defined cycloaliphatic 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/102—Aliphatic fractions
- C10M2203/1025—Aliphatic fractions used as base material
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/104—Aromatic fractions
- C10M2203/1045—Aromatic fractions used as base material
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/106—Naphthenic fractions
- C10M2203/1065—Naphthenic fractions used as base material
-
- 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
- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
- C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
- C10M2203/108—Residual fractions, e.g. bright stocks
- C10M2203/1085—Residual fractions, e.g. bright stocks used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/026—Butene
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
- C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
- C10M2205/026—Butene
- C10M2205/0265—Butene used as base material
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/06—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/06—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
- C10M2223/061—Metal salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/06—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
- C10M2223/063—Ammonium or amine salts
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/06—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds
- C10M2223/065—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having phosphorus-to-carbon bonds containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2020/00—Specified physical or chemical properties or characteristics, i.e. function, of component of lubricating compositions
- C10N2020/01—Physico-chemical properties
-
- 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
- C10N2040/02—Bearings
Definitions
- the present invention relates to a lubricant for transmissions with continuously variable power transmission. It is particularly suitable for pull chain transmissions.
- a well-known push chain transmission is, for example, the CVT transmission with Van Doorne push link belt. (Drive technology 26, (1987) No. 8, page 47-52).
- the lubricant is of great importance for pull and push chain gearboxes. It should not only have a good lubricating effect in order to keep the wear on the chains low, but it must also have a certain coefficient of friction in order to enable the power transmission. The coefficient of friction must be higher than with conventional lubricating oils, but not as high as with so-called traction fluids.
- DE-OS 3127970 discloses a lubricant which consists of a hydrocarbon oil which contains 19-30 hydrocarbon atoms and 3 six-membered carbocyclic rings.
- DE-A-3321773 describes a lubricant which contains decalin rings connected by carbon bridges.
- DE-A-3337503 discloses a lubricant from the same applicant which also contains hydrogenated condensed aromatics.
- Phosphetane derivatives as an additive to conventional lubricants are disclosed in DE-A-2715529.
- the naphthenic component is a highly refined or fully hydrated product. Such products are available on the market. Of course, they can also be produced by refining in our own plants.
- polyisobutene component can be found on the market available product.
- the naphthenic component is contained in the lubricant in a concentration of 10 to 80% by weight, preferably 15 to 50% by weight.
- the polyisobutene component is present in the lubricant in a concentration of 10 to 80% by weight, preferably 40 to 70% by weight.
- any mono- or divalent organic nitrogen base can be used as the base for salt formation with the 1,3-thiaphosphetanes.
- oil-soluble nitrogen bases are suitable for use in lubricants, and in particular those with a total C number of 6-40 C atoms.
- Monovalent compounds are preferably used as the oil-soluble organic nitrogen bases, and in particular primary, secondary or tertiary amines of the formula R5 R6NR7, where R5 and R6 independently of one another are hydrogen or an aliphatic or aromatic radical, and R7 is an aliphatic or aromatic radical.
- R5, R6 and R7 are an aliphatic radical, it may be branched or straight-chain alkyl which may be interrupted with O and / or S, such as methyl, ethyl, n-propyl, isopropyl, t-butyl, amyl, hexyl, 1-methylpentyl , t-octyl, 2-ethyl-hexyl, n-decyl, 2-ethyl-decyl, n-tetradecyl, n-octadecyl, n-eicosyl, 2,7,8-trimethyl-decyl, 4-isobutyl-2,5 -dimethyl-heptyl, octacosoyl, dotriacontyl, hexatriacontyl or tetracontyl.
- O and / or S such as methyl, ethyl, n-propyl
- R5, R6 and R7 can also be an aliphatic radical which may be interrupted with O or S, branched or straight-chain alkenyl such as allyl, vinyl, 2-butenyl, 2-hexenyl, 2-dodecenyl or 2-hexatriacontenyl.
- the total C number of the radicals R5, R6 and R7 should be 6 to 40.
- the amino group can optionally also be ethoxylated, the degree of ethoxylation having to be matched to the desired oil solubility of the product.
- R5, R6 and R7 represent an aromatic radical, this is a phenyl group which is optionally substituted by alkyl groups each having 1 to 12 carbon atoms, such as methyl, ethyl, propyl, butyl, hexyl, oxyl, decyl or dodecyl.
- organic nitrogen bases of the formula R5 R6NR7 to be used are those in which R5 and R6 independently of one another are hydrogen or an aliphatic radical, and R7 is a phenyl group which is optionally substituted by alkyl groups.
- primary organic nitrogen bases of the formula H2NR8 are particularly preferably used, in which R8 is optionally interrupted by O or S, branched or straight-chain alkyl or alkenyl each having 6 to 40, and in particular each having 8 to 24, carbon atoms.
- mixtures of different nitrogen bases are often used, e.g. Primene 81-R (mixture of primary C12-C15 t-alkylamines, from Rohm and Haas, USA).
- the salts which have a uniform nitrogen component are equally suitable.
- amines examples include: Methylamine, ethylamine, propylamine, butylamine, t-butylamine, hexylamine, octylamine, (2-ethylhexyl) amine, t-octylamine, decylamine, t-dodecylamine, tetradecylamine, octadecylamine, phenylamine, benzylamine, (nonylphenyl) amine, cyclohexylamine, pyridine Piperidine, dimethylamine, methyloctylamine, didodecylamine, methyloctadecylamine, methylcyclohexylamine, phenyloctylamine, trimethylamine, dimethylcyclohexylamine, methyloctyldecylamine, (octoxyethyl) amine, (octylthio
- Examples of phosphetane compounds according to the invention are: Dodecylammonium salt of 3-hydroxy-3-oxo-1,3-thiaphosphetane Di-n-butylammonium salt of 3-mercapto-3-thio-1,3-thiaphosphetane Tri-n-octylammonium salt of 3-hydroxy-3-oxo-1,3-thiaphosphetane (2,6-di-tert-butyl-phenyl) ammonium salt of 3-mercapto-3-oxo-1,3-oxaphosphetane (2,6-diethyl-phenyl) -diethylammonium salt of 3-hydroxy-3-oxo-1,3-thiaphosphetane Tri-n-nonyl ammonium salt of 3-hydroxy-3-oxo-1,3-oxaphosphetane Di- (2-ethyl-hexyl) ammoni
- a specific one or several of the mentioned phophetane derivatives can be used.
- the lubricant according to the invention has been carefully tested in numerous tests both in the CVT transmission test bench and in the vehicle.
- test gear was filled with approx. 5 L test oil before each start of the test.
- Each start-up cycle lasted almost 1 minute, corresponding to a distance of 1 km.
- Tests were carried out with distances of 12,000, 24,000 and 38,000 km.
- the start-up cycle was chosen so that the chain and tapered pulleys were subjected to the highest possible load through constant adjustment, standstill adjustment and correspondingly high sliding components.
- the clutch was started at medium engine speed and medium engine torque and quickly accelerated to a driving speed of approx. 120 km / h. Then the brakes were applied fully and the converter ratio was reset to the starting gear at the same time.
- the evaluation criteria for the quality of the lubricant used were the closure on the weighing pressure pieces used, the formation of gray spots on the conical disks and the coefficient of friction.
- a typical lubricant formulation contained the following components: namely viscosity improvers such as, for example, polymethacrylates, anti-foaming agents, anti-corrosion agents and antioxidants, for example of the phenol and / or amine type.
- viscosity improvers such as, for example, polymethacrylates, anti-foaming agents, anti-corrosion agents and antioxidants, for example of the phenol and / or amine type.
- wear protection additives e.g. phosphorus and / or sulfur based.
- the results show that the lubricant according to the invention has excellent shear stability.
- the neutralization number and saponification number also show that oil aging can also be regarded as very low.
- composition of the lubricant was varied within the limits specified, with numerous phosphetane derivatives being added in the disclosed amount ranges, which were prepared according to DE-A-2715529 and the literature cited therein. Similar good test results were obtained.
Landscapes
- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Lubricants (AREA)
- General Details Of Gearings (AREA)
- Friction Gearing (AREA)
- Gears, Cams (AREA)
Abstract
Description
Die vorliegende Erfindung betrifft ein Schmiermittel für Getriebe mit stufenloser Kraftübertragung. Es ist besonders geeignet für Zugkettengetriebe.The present invention relates to a lubricant for transmissions with continuously variable power transmission. It is particularly suitable for pull chain transmissions.
Es ist dem Fachmann bekannt, daß Getriebe mit stufenloser Kraftübertragung (CVT-Getriebe, Continuously Variable Transmission) an Bedeutung gewinnen, da Kraftfahrzeuge mit solchen Getrieben einen sehr guten Wirkungsgrad, geringe Geräuschentwicklung und geringen Kraftstoffverbrauch besitzen. Wie bei konventionellen automatischen Getrieben erübrigt sich das Schalten.It is known to the person skilled in the art that transmissions with continuously variable transmission (CVT transmission, Continuously Variable Transmission) are gaining importance, since motor vehicles with such transmissions have very good efficiency, low noise and low fuel consumption. As with conventional automatic transmissions, shifting is not necessary.
Man unterscheidet zwischen Schubkettengetrieben und Zugkettengetrieben.A distinction is made between push chain drives and pull chain drives.
Ein bekanntes Schubkettengetriebe ist beispielsweise das CVT-Getriebe mit Van-Doorne-Schubgliederband. (Antriebstechnik 26, (1987) Nr. 8, Seite 47-52).A well-known push chain transmission is, for example, the CVT transmission with Van Doorne push link belt. (Drive technology 26, (1987) No. 8, page 47-52).
Für Zug- und Schubkettengetriebe ist das Schmiermittel von sehr großer Bedeutung. Es soll nicht nur gute Schmierwirkung besitzen, um den Verschleiß an den Ketten gering zu halten, sondern es muß zusätzlich eine bestimmte Reibungszahl besitzen, um die Kraftübertragung zu ermöglichen. Die Reibungszahl muß höher als bei konventionellen Schmierölen sein, jedoch nicht so hoch wie bei sog. Traktionfluids.The lubricant is of great importance for pull and push chain gearboxes. It should not only have a good lubricating effect in order to keep the wear on the chains low, but it must also have a certain coefficient of friction in order to enable the power transmission. The coefficient of friction must be higher than with conventional lubricating oils, but not as high as with so-called traction fluids.
Bei letzerem ist eine möglichst hohe Reibungszahl erwünscht, da die Aufgabenstellung, gleichzeitig Kettenglieder zu schmieren, entfällt. Es laufen vielmehr Scheiben oder Rollen aufeinander, deren "Schlupf" so klein wie möglich sein soll. Ist die Umdrehungsgeschwindigkeit eines Körpers V1 und die des anderen V2, so ist der Schlupfwert als
Schmiermittel für Zugkettengetriebe sind in der Literatur bereits beschrieben.Lubricants for pull chain transmissions have already been described in the literature.
So offenbart DE-OS 3127970 ein Schmiermittel das aus einem Kohlenwasserstofföl besteht, das 19-30 Kohlenwasserstoffatome enthält sowie 3 sechsgliedrige carbocyclische Ringe.For example, DE-OS 3127970 discloses a lubricant which consists of a hydrocarbon oil which contains 19-30 hydrocarbon atoms and 3 six-membered carbocyclic rings.
In DE-A-3321773 ist ein Schmiermittel beschrieben, das durch Kohlenstoffbrücken verbundene Dekalinringe enthält.DE-A-3321773 describes a lubricant which contains decalin rings connected by carbon bridges.
IN DE-A-3337503 ist von der gleichen Anmelderin ein Schmiermittel offenbart, das ebenfalls hydrierte kondensierte Aromaten enthält.DE-A-3337503 discloses a lubricant from the same applicant which also contains hydrogenated condensed aromatics.
Phosphetanderivate als Zusatz zu üblichen Schmiermitteln sind in DE-A-2715529 offenbart.Phosphetane derivatives as an additive to conventional lubricants are disclosed in DE-A-2715529.
Die Anmelderin hat nunmehr überraschend gefunden, daß ein für Getriebe mit stufenloser Kraftübertragung insbesondere Zugkettengetriebe hervorragend geeignetes Schmiermittel dadurch gekennzeichnet ist, daß es 10 bis 80 Gew.-% naphthenische Kohlenwasserstoffe enthält, 80 bis 10 Gew.-% Polyisobuten mit einem Polymerisationsgrad von Mol Gew. 200 bis 10.000, bevorzugt Mol Gew. 300 bis 6000 und ein Additiv aus wenigstens einem Phosphetanderivat der allgemeinen Formel
- X₁, X₂ und X₃
- unabhängig voneinander O oder S bedeuten
- n
- falls X₁ O ist, 1 und falls X₁ S ist, 1-2 bedeutet,
- Z
- eine ein- oder mehrwertige stickstoffhaltige öllösliche organische Base ist,
- m
- 1-2 ist und
- p
- 1-2 bedeutet.
The applicant has now surprisingly found that a lubricant which is excellently suitable for transmissions with continuously variable power transmission, in particular pull chain transmissions, is characterized in that it contains 10 to 80% by weight of naphthenic hydrocarbons, 80 to 10% by weight of polyisobutene with a degree of polymerization of mol% 200 to 10,000, preferably moles by weight, 300 to 6000 and an additive of at least one phosphetane derivative of the general formula
- X₁, X₂ and X₃
- independently represent O or S.
- n
- if X₁ is O, 1 and if X₁ is S, means 1-2,
- Z
- is a mono- or polyvalent nitrogen-containing oil-soluble organic base,
- m
- Is 1-2 and
- p
- 1-2 means.
Bevorzugt bedeutet
- X₁
- S
- n
- 1-2
- X₂ und X₃
- O und
- Z
- ein primäres, sekundäres oder tertiäres Amin der Formel N R₅ R₆ R₇, worin R₅ und R₆ unabhängig voneinander Wasserstoff oder einen aliphatischen oder aromatischen Rest und R₇ einen aliphatischen oder aromatischen Rest bedeuten.
Preferably means
- X₁
- S
- n
- 1-2
- X₂ and X₃
- O and
- Z
- a primary, secondary or tertiary amine of the formula N R₅ R₆ R₇, wherein R₅ and R₆ independently of one another are hydrogen or an aliphatic or aromatic radical and R₇ is an aliphatic or aromatic radical.
Besonders bevorzugt bedeutet
- X₁
- S
- n
- 1
- X₂ und X₃
- O und
- Z
- ein primäres Amin der Formel H₂ N R₈, worin R₈ einen aliphatischen Rest bedeutet und
- m
- = 1
Means particularly preferred
- X₁
- S
- n
- 1
- X₂ and X₃
- O and
- Z
- a primary amine of the formula H₂ N R₈, wherein R₈ is an aliphatic radical and
- m
- = 1
Bei der naphthenischen Komponente handelt es sich um ein hoch ausraffiniertes bzw. durchhydriertes Produkt. Solche Produkte sind auf dem Markt erhältlich. Sie können natürlich auch durch Raffination in eigenen Anlagen erzeugt werden.The naphthenic component is a highly refined or fully hydrated product. Such products are available on the market. Of course, they can also be produced by refining in our own plants.
Ebenso kann die Polyisobuten-Komponente ein auf dem Markt erhältliches Produkt sein.Likewise, the polyisobutene component can be found on the market available product.
Die naphthenische Komponente ist in dem Schmiermittel in einer Konzentration von 10 bis 80 Gew.-%, bevorzugt von 15 bis 50 Gew.-% enthalten.The naphthenic component is contained in the lubricant in a concentration of 10 to 80% by weight, preferably 15 to 50% by weight.
Die Polyisobuten-Komponente ist in einer Konzentration von 10 bis 80 Gew.-% im Schmiermittel enthalten, bevorzugt von 40 bis 70 Gew.-%.The polyisobutene component is present in the lubricant in a concentration of 10 to 80% by weight, preferably 40 to 70% by weight.
Die Gruppen am viergliedrigen Ring R₁, R₂, R₃ und R₄ des Phosphetanderivats können gleich oder unterschiedlich sein. Sie sind bevorzugt H, können jedoch auch C₁-C₄-Kohlenwasserstoffreste sein, die verzweigt, ringförmig und geradkettig sein können, wobei
- X₁, X₂ und X₃
- unabhängig voneinander O oder S bedeuten
- n
- falls X₁ O ist, 1 und falls X₁ S ist, 1-6 bedeutet,
- Z
- eine ein- oder mehrwertige stickstoffhaltige öllösliche organische Base ist,
- m
- 1-2 ist und
- p
- 1-2 bedeutet.
The groups on the four-membered ring R₁, R₂, R₃ and R₄ of the phosphetane derivative can be the same or different. They are preferably H, but can also be C₁-C₄ hydrocarbon radicals, which can be branched, ring-shaped and straight-chain, wherein
- X₁, X₂ and X₃
- independently represent O or S.
- n
- if X₁ is O, 1 and if X₁ is S, means 1-6,
- Z
- is a mono- or polyvalent nitrogen-containing oil-soluble organic base,
- m
- Is 1-2 and
- p
- 1-2 means.
Bevorzugt bedeutet
- X₁
- S
- n
- 1-2
- X₂ und X₃
- O und
- Z
- ein primäres, sekundäres oder tertiäres Amin der Formel N R₅ R₆ R₇, worin R₅ und R₆ unabhängig voneinander Wasserstoff oder einen aliphatischen oder aromatischen Rest und R₇ einen aliphatischen oder aromatischen Rest bedeuten.
Preferably means
- X₁
- S
- n
- 1-2
- X₂ and X₃
- O and
- Z
- a primary, secondary or tertiary amine of the formula N R₅ R₆ R₇, wherein R₅ and R₆ independently of one another are hydrogen or an aliphatic or aromatic radical and R₇ is an aliphatic or aromatic radical.
Besonders bevorzugt bedeuten
- X₁
- S
- n
- 1
- X₂ und X₃
- O und
- Z
- ein primäres Amin der Formel H₂ N R₃ ist, worin R₃ einen aliphatischen Rest bedeutet und
- m
- = 1
Mean particularly preferred
- X₁
- S
- n
- 1
- X₂ and X₃
- O and
- Z
- is a primary amine of the formula H₂N R₃, wherein R₃ is an aliphatic radical and
- m
- = 1
Als Base für die Salzbildung mit den 1,3-Thiaphosphetanen kann grundsätzlich jede ein- oder zweiwertige organische Stickstoffbase verwendet werden. Aus praktischen Gründen eignen sich für die Anwendung in Schmiermitteln nur öllösliche Stickstoffbasen und insbesondere solche mit einer Gesamt-C-Zahl von 6-40 C-Atomen.In principle, any mono- or divalent organic nitrogen base can be used as the base for salt formation with the 1,3-thiaphosphetanes. For practical reasons, only oil-soluble nitrogen bases are suitable for use in lubricants, and in particular those with a total C number of 6-40 C atoms.
Bevorzugt werden als öllösliche organische Stickstoffbasen einwertige Verbindungen eingesetzt, und insbesondere primäre, sekundäre oder tertiäre Amine der Formel R₅ R₆NR₇, worin R₅ und R₆ unabhängig voneinander Wasserstoff oder einen aliphatischen oder aromatischen Rest, und R₇ einen aliphatischen oder aromatischen Rest bedeuten.Monovalent compounds are preferably used as the oil-soluble organic nitrogen bases, and in particular primary, secondary or tertiary amines of the formula R₅ R₆NR₇, where R₅ and R₆ independently of one another are hydrogen or an aliphatic or aromatic radical, and R₇ is an aliphatic or aromatic radical.
Bedeuten R₅, R₆ und R₇ einen aliphatischen Rest, so kann es sich dabei um gegebenenfalls mit O und/oder S unterbrochenes verzweigtes oder geradkettiges Alkyl wie Methyl, Aethyl, n-Propyl, Isopropyl, t-Butyl, Amyl, Hexyl, 1-Methylpentyl, t-Octyl, 2-Aethyl-hexyl, n-Decyl, 2-Aethyl-decyl, n-Tetradecyl, n-Octadecyl, n-Eicosyl, 2,7,8-Trimethyl-decyl, 4-Isobutyl-2,5-dimethyl-heptyl, Octacosoyl, Dotriacontyl, Hexatriacontyl oder Tetracontyl handeln. R₅, R₆ und R₇ können jedoch als aliphatischer Rest auch gegebenenfalls mit O oder S unterbrochenes, verzweigtes oder geradkettiges Alkenyl wie Allyl, Vinyl, 2-Butenyl, 2-Hexenyl, 2-Dodecenyl oder 2-Hexatriacontenyl sein. Die Gesamt C-Zahl der Reste R₅, R₆ und R₇ soll dabei 6 bis 40 betragen.If R₅, R₆ and R₇ are an aliphatic radical, it may be branched or straight-chain alkyl which may be interrupted with O and / or S, such as methyl, ethyl, n-propyl, isopropyl, t-butyl, amyl, hexyl, 1-methylpentyl , t-octyl, 2-ethyl-hexyl, n-decyl, 2-ethyl-decyl, n-tetradecyl, n-octadecyl, n-eicosyl, 2,7,8-trimethyl-decyl, 4-isobutyl-2,5 -dimethyl-heptyl, octacosoyl, dotriacontyl, hexatriacontyl or tetracontyl. However, R₅, R₆ and R₇ can also be an aliphatic radical which may be interrupted with O or S, branched or straight-chain alkenyl such as allyl, vinyl, 2-butenyl, 2-hexenyl, 2-dodecenyl or 2-hexatriacontenyl. The total C number of the radicals R₅, R₆ and R₇ should be 6 to 40.
Die Aminogruppe kann gegebenenfalls auch äthoxyliert sein, wobei der Aethoxylierungsgrad auf die angestrebte Öllöslichkeit des Produktes abgestimmt werden muß.The amino group can optionally also be ethoxylated, the degree of ethoxylation having to be matched to the desired oil solubility of the product.
Bedeuten R₅, R₆ und R₇ einen aromatischen Rest, so handelt es sich dabei um eine gegebenenfalls durch Alkylgruppen mit je 1 bis 12 C-Atomen wie Methyl, Aethyl, Propyl, Butyl, Hexyl, Oxtyl, Decyl oder Dodecyl substituierte Phenylgruppe.If R₅, R₆ and R₇ represent an aromatic radical, this is a phenyl group which is optionally substituted by alkyl groups each having 1 to 12 carbon atoms, such as methyl, ethyl, propyl, butyl, hexyl, oxyl, decyl or dodecyl.
Unter den zu verwendenden organischen Stickstoffbasen der Formel R₅ R₆NR₇ sind solche zu nennen, in den R₅ und R₆ unabhängig voneinander Wasserstoff oder einen aliphatischen Rest bedeuten, und R₇ eine gegebenenfalls durch Alkylgruppen substituierte Phenylgruppe bedeutet.Among the organic nitrogen bases of the formula R₅ R₆NR₇ to be used are those in which R₅ and R₆ independently of one another are hydrogen or an aliphatic radical, and R₇ is a phenyl group which is optionally substituted by alkyl groups.
Besonders bevorzugt werden jedoch primäre organische Stickstoffbasen der Formel H₂NR₈ eingesetzt, worin R₈ gegebenenfalls durch O oder S unterbrochenes, verzweigtes oder geradkettiges Alkyl oder Alkenyl mit je 6 bis 40, und insbesondere mit je 8 bis 24 C-Atomen bedeutet.However, primary organic nitrogen bases of the formula H₂NR₈ are particularly preferably used, in which R₈ is optionally interrupted by O or S, branched or straight-chain alkyl or alkenyl each having 6 to 40, and in particular each having 8 to 24, carbon atoms.
In der Praxis werden oft Gemische von verschiedenen Stickstoffbasen eingesetzt, wie z.B. Primene 81-R (Gemisch primärer C₁₂-C₁₅ t-Alkylamine, von Rohm und Haas, USA). Ebensogut eignen sich jedoch auch die Salze welche eine einheitliche Stickstoffkomponente besitzen.In practice, mixtures of different nitrogen bases are often used, e.g. Primene 81-R (mixture of primary C₁₂-C₁₅ t-alkylamines, from Rohm and Haas, USA). However, the salts which have a uniform nitrogen component are equally suitable.
Beispiele für solche Amine sind:
Methylamin, Aethylamin, Propylamin, Butylamin, t-Butylamin, Hexylamin, Octylamin, (2-Aethylhexyl)amin, t-Octylamin, Decylamin, t-Dodecylamin, Tetradecylamin, Octadecylamin, Phenylamin, Benzylamin, (Nonylphenyl)amin, Cyclohexylamin, Pyridin, Piperidin, Dimethylamin, Methyloctylamin, Didodecylamin, Methyloctadecylamin, Methylcyclohexylamin, Phenyloctylamin, Trimethylamin, Dimethylcyclohexylamin, Methyloctyldecylamin, (Octoxyäthyl)amin, (Octylthioäthyl)amin, (t-Dodecylthioäthyl)-amin, Dodecyl-dimethylamin, Hexadecyl-dimethylamin, Decyldimethyl-amin, Didodecylmethyl-amin, Methyl-butyl-dodecyl-amin, Dimethyl-propylamin, Trioctyl-amin, Dioctyl-methylamin, Dodecylbenzyl-methyl-amin, Nonylphenyl-dimethylamin, Phenyl-dodecyl-methyl-amin, Phenyl-dimethyl-amin, Phenyl-dimethyl-amin, Allyl-dibutyl-amin, Methyl-dodecyl-amin, Heptadecyl-dimethyl-amin, Dioctyl-methyl-amin, Methyl-α-naphthyl-phenyl-amin, Cyclohexyl-dimethyl-amin, Nonyl-dimethyl-amin, Tris(n-tridecyl)amin, Tris(n-dodecyl)-amin, Tris(isooctyl)amin, Methylbutylhexadecyl-amin, Tri-äthyl-amin, 3,5-Dimethyl-pyridin, 2-(Aethylhexyl)-methyl-dodecyl-amin, (Methyläthyl)-didecyl-amin, Methyl-butyl-dodecyl-amin, Dimethyl-dodecyl-amin, Hexadecyl-dimethyl-amin, Tris(i-dodecyl)-amin, Dimethyl-benzyl-amin, Dimethyl-(tert.-octylphenyl)-amin, (N-Methyl)-1-imidazolin (N-Methyl)-1-pyrrazolin, Oxazolin, Chinolin, Pyrrolidin, N-Aethyl-pyrrolidin, N-Methyl-piperidin, N-Butyl-piperidin, N-Butyl-piperidin, Thiazol, N-Methyl-phenothiamin.Examples of such amines are:
Methylamine, ethylamine, propylamine, butylamine, t-butylamine, hexylamine, octylamine, (2-ethylhexyl) amine, t-octylamine, decylamine, t-dodecylamine, tetradecylamine, octadecylamine, phenylamine, benzylamine, (nonylphenyl) amine, cyclohexylamine, pyridine Piperidine, dimethylamine, methyloctylamine, didodecylamine, methyloctadecylamine, methylcyclohexylamine, phenyloctylamine, trimethylamine, dimethylcyclohexylamine, methyloctyldecylamine, (octoxyethyl) amine, (octylthioethyl) amine, (t-dodecylthioethyl) amine Dodecyldimethylamine, hexadecyldimethylamine, decyldimethylamine, didodecylmethylamine, methylbutyldodecylamine, dimethylpropylamine, trioctylamine, dioctylmethylamine, dodecylbenzylmethylamine, nonylphenyldimethylamine, phenyl methyl-amine, phenyl-dimethyl-amine, phenyl-dimethyl-amine, allyl-dibutyl-amine, methyl-dodecyl-amine, heptadecyl-dimethyl-amine, dioctyl-methyl-amine, methyl-α-naphthyl-phenyl-amine, Cyclohexyl-dimethyl-amine, nonyl-dimethyl-amine, tris (n-tridecyl) amine, tris (n-dodecyl) amine, tris (isooctyl) amine, methylbutylhexadecyl amine, tri-ethyl amine, 3,5-dimethyl -pyridine, 2- (ethylhexyl) -methyl-dodecyl-amine, (methylethyl) -didecyl-amine, methyl-butyl-dodecyl-amine, dimethyl-dodecyl-amine, hexadecyl-dimethyl-amine, tris (i-dodecyl) - amine, dimethylbenzylamine, dimethyl- (tert-octylphenyl) amine, (N-methyl) -1-imidazoline (N-methyl) -1-pyrrazoline, oxazoline, quinoline, pyrrolidine, N-ethyl-pyrrolidine, N-methyl-piperidine, N-butyl-piperidine, N-butyl-piperidine, thiazole, N-methyl-phenothia min.
Beispiele von erfindungsgemäßen Phosphetan ― Verbindungen sind:
Dodecylammoniumsalz des 3-Hydroxy-3-oxo-1,3-thiaphosphetans
Di-n-butylammoniumsalz des 3-Mercapto-3-thio-1,3-thiaphosphetans
Tri-n-octylammoniumsalz des 3-Hydroxy-3-oxo-1,3-thiaphosphetans
(2,6-di-tert.-butyl-phenyl)-ammoniumsalz des 3-Mercapto-3-oxo-1,3-oxaphosphetans
(2,6-Diäthyl-phenyl)-diäthylammoniumsalz des 3-Hydroxy-3-oxo-1,3-thiaphosphetans
Tri-n-nonyl-ammoniumsalz des 3-Hydroxy-3-oxo-1,3-oxaphosphetans
Di-(2-äthyl-hexyl)-ammoniumsalz des 3-Hydroxy-3-oxo-1,3-thiaphosphetans.Examples of phosphetane compounds according to the invention are:
Dodecylammonium salt of 3-hydroxy-3-oxo-1,3-thiaphosphetane
Di-n-butylammonium salt of 3-mercapto-3-thio-1,3-thiaphosphetane
Tri-n-octylammonium salt of 3-hydroxy-3-oxo-1,3-thiaphosphetane
(2,6-di-tert-butyl-phenyl) ammonium salt of 3-mercapto-3-oxo-1,3-oxaphosphetane
(2,6-diethyl-phenyl) -diethylammonium salt of 3-hydroxy-3-oxo-1,3-thiaphosphetane
Tri-n-nonyl ammonium salt of 3-hydroxy-3-oxo-1,3-oxaphosphetane
Di- (2-ethyl-hexyl) ammonium salt of 3-hydroxy-3-oxo-1,3-thiaphosphetane.
Es kann ein bestimmtes oder es können mehrere der genannten Phophetanderivate eingesetzt werden.A specific one or several of the mentioned phophetane derivatives can be used.
Die Untersuchungen der Anmelderin haben überraschend ergeben, daß der Verschleiß an den Ketten durch die erfindungsgemäßen Phosphetanderivate sehr stark herabgesetzt wird, so daß ein Schmiermittel erhalten wird, das sowohl die erwünschte Reibungszahl als auch einen geringen Kettenverschleiß ergibt.The investigations by the applicant have surprisingly shown that the wear on the chains is reduced very greatly by the phosphetane derivatives according to the invention, so that a lubricant is obtained which gives both the desired coefficient of friction and low chain wear.
Das erfindungsgemäße Schmiermittel wurde sowohl im CVT-Getriebeprüfstand als auch im Fahrzeug in zahlreichen Tests sorgfältig geprüft.The lubricant according to the invention has been carefully tested in numerous tests both in the CVT transmission test bench and in the vehicle.
Das Versuchsgetriebe wurde vor jedem Versuchsbeginn mit ca. 5 L Versuchsöl gefüllt.The test gear was filled with approx. 5 L test oil before each start of the test.
Zwischen den Versuchen erfolgte eine gründliche Reinigung und anschließendes Spülen mit ca. 1,5 L des neuen Versuchs-Schmieröls.Between the tests, thorough cleaning followed by rinsing with approx. 1.5 L of the new test lubricating oil.
Nach jeweils 3000 KWh (entsprechend 12.000 km Prüflauf) wurden zur Untersuchung 50 ml Schmiermittel entnommen und dieselbe Menge Frischöl nachgefüllt.After every 3000 KWh (corresponding to 12,000 km test run), 50 ml of lubricant were removed for testing and the same amount of fresh oil was added.
Jeder Anfahrzyklus dauerte knapp 1 Minute, entsprechend etwa einer Fahrstrecke von 1 km.Each start-up cycle lasted almost 1 minute, corresponding to a distance of 1 km.
Es wurden Versuche mit Fahrstrecken von 12.000, 24.000 und 38.000 km durchgeführt.Tests were carried out with distances of 12,000, 24,000 and 38,000 km.
Der Anfahrzyklus wurde so gewählt, daß Kette und Kegelscheiben der höchstmöglichen Belastung durch ständige Verstellung, Stillstandsverstellung und dementsprechend hohe Gleitanteile ausgesetzt waren.The start-up cycle was chosen so that the chain and tapered pulleys were subjected to the highest possible load through constant adjustment, standstill adjustment and correspondingly high sliding components.
Übertragen auf ein Fahrzeug wurde bei springender Kupplung bei mittlerer Motordrehzahl und mittlerem Motorennennmoment angefahren und schnell auf eine Fahrgeschwindigkeit von ca. 120 km/h beschleunigt. Dann erfolgte eine Vollbremsung bei gleichzeitiger Rückverstellung der Wandlerübersetzung in den Anfahrgang.Transferred to a vehicle, the clutch was started at medium engine speed and medium engine torque and quickly accelerated to a driving speed of approx. 120 km / h. Then the brakes were applied fully and the converter ratio was reset to the starting gear at the same time.
Bewertungskriterien für die Qualität des eingesetzten Schmierstoffs war der Verschließ an den eingesetzten Wiegedruckstükken, die Bildung von Graufleckigkeit auf den Kegelscheiben und die Reibungszahl.The evaluation criteria for the quality of the lubricant used were the closure on the weighing pressure pieces used, the formation of gray spots on the conical disks and the coefficient of friction.
Eine typische Schmiermittel-Rezeptur enthielt folgende Komponenten:
nämlich Viskositätsverbesserer wie z.B. Polymethacrylate, Antischaummittel, Korrosionsschutzmittel und Antioxidantien z.B. des Phenol- und/oder Amintyps.A typical lubricant formulation contained the following components:
namely viscosity improvers such as, for example, polymethacrylates, anti-foaming agents, anti-corrosion agents and antioxidants, for example of the phenol and / or amine type.
Außerdem ist es vorteilhaft Verschleißschutzadditive z.B. auf Phosphor- und/oder Schwefelbasis einzusetzen.It is also advantageous to use wear protection additives e.g. phosphorus and / or sulfur based.
Als Additive können auf dem Markt erhältliche, jedoch auch sonstige Produkte eingesetzt werden.However, other products available on the market can also be used as additives.
Als Phosphetan wurde
eingesetzt.When was phosphetane
used.
Folgende Ergebnisse wurden erhalten:
Die Tabelle zeigt, daß bei optimaler Reibungszahl eine überraschende Verschleißverminderung im Falle des erfindungsgemäßen Musters III eintritt.
Ohne Zusatz des Phosphetans ergibt das der Formulierung des Musters III entsprechende Muster IV jedoch weder eine brauchbare Verschleißzahl noch eine brauchbare Reinbungszahl.The table shows that with an optimal coefficient of friction there is a surprising reduction in wear in the case of the pattern III according to the invention.
Without the addition of the phosphetane, however, the pattern IV corresponding to the formulation of pattern III neither gives a usable wear number nor a usable cleaning number.
Es wurden 3 Proben mit Kilometerleistungen von
- a,
- 13.000 km
- b,
- 25.000 km
und
- c,
- 38.000 km
untersucht.
- a,
- 13,000 km
- b,
- 25,000 km
and
- c,
- 38,000 km
examined.
Aus den Ergebnissen geht hervor, daß das erfindungsgemäße Schmiermittel eine ausgezeichnete Scherstabilität besitzt. Aus Neutralisationszahl und Verseifungszahl geht ferner hervor, daß auch die Ölalterung als sehr gering anzusehen ist.
Aus Tabelle 3 geht bei den Proben a-c hervor, daß aufgrund der sehr geringen Gehalte an Cu und Fe und der vernachlässigbaren Zunahmen dieser Metalle, die Additivierung einen hervorragenden Verschleißschutz gewährleistet. Ölwechselintervalle können demgemäß ohne weiteres auf über 40.000 km verlängert werden.From Table 3 it can be seen for samples ac that the very low levels of Cu and Fe and the negligible increases in these metals, the additives ensure excellent wear protection. Oil change intervals can therefore be easily extended to over 40,000 km.
Zusätzlich wurden die Gehalte an Pb, Si, Mn, Mo, Ca, Zn, Ni, Al, Cr, B, P, Mg, Ba und Sn geprüft.In addition, the levels of Pb, Si, Mn, Mo, Ca, Zn, Ni, Al, Cr, B, P, Mg, Ba and Sn were checked.
Bei diesen Elementen wurden gegenüber dem Rückstellmuster (Originalprobe) keine Änderungen festgestellt.No changes were found in these elements compared to the reserve sample (original sample).
Die Zusammensetzung des Schmiermittels wurde in den Ansprüchen angegebenen Grenzen variiert, wobei zahlreiche Phosphetanderivate in den offenbarten Mengenbereichen zugesetzt wurden, die nach DE-A-2715529 und der dort zitierten Literatur hergestellt wurden. Es wurden hierbei ähnlich gute Testergebnisse erhalten.The composition of the lubricant was varied within the limits specified, with numerous phosphetane derivatives being added in the disclosed amount ranges, which were prepared according to DE-A-2715529 and the literature cited therein. Similar good test results were obtained.
Nur einige der untersuchten Schmiermittel-Mischungen sind in Tabelle 4 zusammengefaßt.
Claims (13)
preferably
particularly preferable
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT89101495T ATE65795T1 (en) | 1988-02-05 | 1989-01-28 | LUBRICANT FOR CONTINUOUSLY VARIABLE TRANSMISSION. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE3803399 | 1988-02-05 | ||
DE3803399 | 1988-02-05 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0326975A1 EP0326975A1 (en) | 1989-08-09 |
EP0326975B1 true EP0326975B1 (en) | 1991-07-31 |
Family
ID=6346664
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP89101495A Expired - Lifetime EP0326975B1 (en) | 1988-02-05 | 1989-01-28 | Lubricant for traction drive with continuously variable transmission |
Country Status (7)
Country | Link |
---|---|
US (1) | US4950414A (en) |
EP (1) | EP0326975B1 (en) |
JP (1) | JPH02196895A (en) |
AT (1) | ATE65795T1 (en) |
DE (1) | DE58900194D1 (en) |
ES (1) | ES2010973B3 (en) |
GR (2) | GR890300198T1 (en) |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2657088B1 (en) * | 1990-01-15 | 1994-04-15 | Bp France | HYDRO-SYNTHETIC LUBRICATING OIL. |
JP4456708B2 (en) * | 1999-12-28 | 2010-04-28 | 出光興産株式会社 | Lubricating oil composition containing cyclic organophosphorus compound |
IL141094A0 (en) * | 2001-01-25 | 2002-02-10 | Ran Siman Tov | Continuous variable transmission |
WO2004026998A1 (en) * | 2002-09-18 | 2004-04-01 | Idemitsu Kosan Co., Ltd. | Traction drive fluid compositions |
JP4910266B2 (en) * | 2004-03-01 | 2012-04-04 | 栗田工業株式会社 | Nitrification method and treatment method of ammonia-containing nitrogen water |
US7367913B2 (en) | 2005-02-11 | 2008-05-06 | Team Industries, Inc. | Wet brake system for vehicles |
US7754664B2 (en) * | 2006-09-19 | 2010-07-13 | Ut-Battelle, Llc | Lubricants or lubricant additives composed of ionic liquids containing ammonium cations |
US20140171348A1 (en) | 2012-12-14 | 2014-06-19 | Exxonmobil Research And Engineering Company | Ionic liquids as lubricating oil base stocks, cobase stocks and multifunctional functional fluids |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2117323C3 (en) * | 1971-04-08 | 1978-08-31 | Robert Bosch Gmbh, 7000 Stuttgart | Temperature switch |
JPS4844301A (en) * | 1972-02-18 | 1973-06-26 | ||
ZA738714B (en) * | 1973-10-01 | 1975-06-25 | Lubrizol Corp | Lubricant compositions |
CH620905A5 (en) * | 1976-04-12 | 1980-12-31 | Ciba Geigy Ag | |
US4670173A (en) * | 1985-12-19 | 1987-06-02 | The Lubrizol Corporation | Oil-soluble reaction products of an acylated reaction product, a polyamine, and mono-functional acid |
-
1989
- 1989-01-28 ES ES89101495T patent/ES2010973B3/en not_active Expired - Lifetime
- 1989-01-28 EP EP89101495A patent/EP0326975B1/en not_active Expired - Lifetime
- 1989-01-28 AT AT89101495T patent/ATE65795T1/en not_active IP Right Cessation
- 1989-01-28 DE DE8989101495T patent/DE58900194D1/en not_active Expired - Lifetime
- 1989-01-31 US US07/304,778 patent/US4950414A/en not_active Expired - Lifetime
- 1989-02-03 JP JP1024126A patent/JPH02196895A/en active Granted
-
1990
- 1990-10-31 GR GR89300198T patent/GR890300198T1/en unknown
-
1991
- 1991-10-16 GR GR91401546T patent/GR3002900T3/en unknown
Also Published As
Publication number | Publication date |
---|---|
DE58900194D1 (en) | 1991-09-05 |
ES2010973B3 (en) | 1992-03-16 |
ES2010973A4 (en) | 1989-12-16 |
ATE65795T1 (en) | 1991-08-15 |
JPH0588918B2 (en) | 1993-12-24 |
US4950414A (en) | 1990-08-21 |
GR3002900T3 (en) | 1993-01-25 |
JPH02196895A (en) | 1990-08-03 |
GR890300198T1 (en) | 1990-10-31 |
EP0326975A1 (en) | 1989-08-09 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE2530230C3 (en) | Extreme pressure lubricating oil and process for its manufacture | |
DE69413636T2 (en) | Friction modifying compositions and their use | |
DE2745909C2 (en) | ||
DE69525968T2 (en) | ENGINE OIL WITH IMPROVED PROPERTIES TO SAVE FUEL | |
DE69533096T2 (en) | Ashless lubricant | |
DE69730568T2 (en) | Viscosity index improvers for phosphate ester based hydraulic fluids | |
DE2258966C2 (en) | Lubricating oil mixture | |
DE69411563T2 (en) | LUBRICATING OIL COMPOSITION | |
DE3687106T2 (en) | LUBRICANT COMPOSITION FOR POWER TRANSFER. | |
DE2530378A1 (en) | LUBRICATING OIL COMPOSITIONS | |
DE1644925B2 (en) | Use of organic compounds as a liquid component of traction gears | |
DE1063312B (en) | lubricant | |
DE69719114T2 (en) | Lubricating oil composition for automatic transmissions | |
EP0326975B1 (en) | Lubricant for traction drive with continuously variable transmission | |
DE3687214T2 (en) | Lubricant composition for power transmission. | |
DE2422609A1 (en) | LUBRICATING OIL FORMULATION | |
DE69327453T2 (en) | USE OF INORGANIC PHOSPHORIC COMPOUNDS AS A FRICTION IMPROVER IN LUBRICANT COMPOSITIONS FOR LIQUID CLUTCHES OR LIQUID BRAKES | |
DE3876432T2 (en) | HYDRAULIC LIQUIDS. | |
DE1594432C3 (en) | Lubricating oil | |
EP0184043B1 (en) | Lubricant additive | |
DE69321758T2 (en) | Boron-containing additive for lubricating oils and processes to prepare the additive mentioned | |
DE69006163T2 (en) | Silicone grease composition. | |
DE3001000C2 (en) | ||
DE3750468T2 (en) | POWER TRANSFER METHOD. | |
DE2155828A1 (en) | Lubricating oil formulation |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 19890131 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH DE ES FR GB GR IT LI LU NL SE |
|
ITCL | It: translation for ep claims filed |
Representative=s name: SOCIETA' ITALIANA BREVETTI S.P.A. |
|
TCNL | Nl: translation of patent claims filed | ||
EL | Fr: translation of claims filed | ||
17Q | First examination report despatched |
Effective date: 19900813 |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: MINERALOELWERKE WENZEL UND WEIDMANN ZWEIGNIEDERLAS |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE CH DE ES FR GB GR IT LI LU NL SE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 19910731 |
|
REF | Corresponds to: |
Ref document number: 65795 Country of ref document: AT Date of ref document: 19910815 Kind code of ref document: T |
|
REF | Corresponds to: |
Ref document number: 58900194 Country of ref document: DE Date of ref document: 19910905 |
|
ITF | It: translation for a ep patent filed | ||
ET | Fr: translation filed | ||
GBT | Gb: translation of ep patent filed (gb section 77(6)(a)/1977) | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: SE Payment date: 19911216 Year of fee payment: 4 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2010973 Country of ref document: ES Kind code of ref document: B3 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
REG | Reference to a national code |
Ref country code: GR Ref legal event code: FG4A Free format text: 3002900 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: AT Payment date: 19921214 Year of fee payment: 5 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: LU Payment date: 19921215 Year of fee payment: 5 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: CH Payment date: 19930111 Year of fee payment: 5 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 19930113 Year of fee payment: 5 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 19930114 Year of fee payment: 5 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Effective date: 19930129 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: NL Payment date: 19930131 Year of fee payment: 5 |
|
EPTA | Lu: last paid annual fee | ||
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19940128 Ref country code: AT Effective date: 19940128 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19940129 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Effective date: 19940131 Ref country code: CH Effective date: 19940131 Ref country code: BE Effective date: 19940131 |
|
BERE | Be: lapsed |
Owner name: MINERALOLWERKE WENZEL UND WEIDMANN ZWEIGNIEDERLAS Effective date: 19940131 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Effective date: 19940801 |
|
NLV4 | Nl: lapsed or anulled due to non-payment of the annual fee | ||
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
REG | Reference to a national code |
Ref country code: GR Ref legal event code: MM2A Free format text: 3002900 |
|
EUG | Se: european patent has lapsed |
Ref document number: 89101495.3 Effective date: 19930810 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 19970128 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: 728V |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 19980119 Year of fee payment: 10 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 19980320 Year of fee payment: 10 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 19980505 Year of fee payment: 10 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: TP |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: 732E Ref country code: GB Ref legal event code: 728Y |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19990128 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 19990405 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 19990128 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19990930 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 19991103 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED. Effective date: 20050128 |