CH615217A5 - Hydraulic fluid - Google Patents

Hydraulic fluid Download PDF

Info

Publication number: CH615217A5
Authority: CH; Switzerland
Prior art keywords: phosphate; liquid according; hydraulic liquid; ammonium; alkyl
Prior art date: 1974-02-11

Application number

CH159875A

Other languages

German (de)

English (en)

Inventor

Theodore Alan Marolewski

Fred Jaffe

Original Assignee

Stauffer Chemical Co

Priority date (The priority date 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 date listed.)

1974-02-11

Filing date

1975-02-11

Publication date

1980-01-15

1975-02-11 Application filed by Stauffer Chemical Co filed Critical Stauffer Chemical Co

1980-01-15 Publication of CH615217A5 publication Critical patent/CH615217A5/de

Links

239000012530 fluid Substances 0.000 title claims description 36
-1 monocarboxylic acid esters Chemical class 0.000 claims description 106
239000007788 liquid Substances 0.000 claims description 92
229910019142 PO4 Inorganic materials 0.000 claims description 41
235000021317 phosphate Nutrition 0.000 claims description 41
239000000203 mixture Substances 0.000 claims description 37
239000010452 phosphate Substances 0.000 claims description 26
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 25
125000000217 alkyl group Chemical group 0.000 claims description 25
150000003863 ammonium salts Chemical class 0.000 claims description 17
125000003118 aryl group Chemical group 0.000 claims description 17
239000002253 acid Substances 0.000 claims description 16
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 14
150000002148 esters Chemical class 0.000 claims description 13
150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 13
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 11
125000004432 carbon atom Chemical group C* 0.000 claims description 11
239000003921 oil Substances 0.000 claims description 11
229910052760 oxygen Inorganic materials 0.000 claims description 11
239000001301 oxygen Substances 0.000 claims description 11
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 10
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 9
125000003545 alkoxy group Chemical group 0.000 claims description 9
125000003710 aryl alkyl group Chemical group 0.000 claims description 9
229910052739 hydrogen Inorganic materials 0.000 claims description 9
239000001257 hydrogen Substances 0.000 claims description 9
239000002480 mineral oil Substances 0.000 claims description 9
125000000547 substituted alkyl group Chemical group 0.000 claims description 9
229910052717 sulfur Chemical group 0.000 claims description 9
239000011593 sulfur Chemical group 0.000 claims description 9
239000004215 Carbon black (E152) Substances 0.000 claims description 8
125000002877 alkyl aryl group Chemical group 0.000 claims description 8
229930195733 hydrocarbon Natural products 0.000 claims description 8
150000002430 hydrocarbons Chemical class 0.000 claims description 8
229910052605 nesosilicate Inorganic materials 0.000 claims description 8
150000004762 orthosilicates Chemical class 0.000 claims description 8
229910052698 phosphorus Inorganic materials 0.000 claims description 8
239000011574 phosphorus Substances 0.000 claims description 8
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 7
235000010290 biphenyl Nutrition 0.000 claims description 6
239000002562 thickening agent Substances 0.000 claims description 6
150000001408 amides Chemical class 0.000 claims description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
229920013636 polyphenyl ether polymer Polymers 0.000 claims description 5
229920001296 polysiloxane Polymers 0.000 claims description 5
239000002518 antifoaming agent Substances 0.000 claims description 4
150000004074 biphenyls Chemical class 0.000 claims description 4
235000010446 mineral oil Nutrition 0.000 claims description 4
150000001298 alcohols Chemical class 0.000 claims description 3
239000003963 antioxidant agent Substances 0.000 claims description 3
150000003568 thioethers Chemical class 0.000 claims description 3
125000005248 alkyl aryloxy group Chemical group 0.000 claims description 2
125000004414 alkyl thio group Chemical group 0.000 claims description 2
125000005110 aryl thio group Chemical group 0.000 claims description 2
125000004104 aryloxy group Chemical group 0.000 claims description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 2
229920001281 polyalkylene Polymers 0.000 claims description 2
229920006389 polyphenyl polymer Polymers 0.000 claims description 2
150000005846 sugar alcohols Polymers 0.000 claims description 2
230000003078 antioxidant effect Effects 0.000 claims 1
150000001990 dicarboxylic acid derivatives Chemical class 0.000 claims 1
125000004435 hydrogen atom Chemical class [H]* 0.000 claims 1
230000003628 erosive effect Effects 0.000 description 16
235000011007 phosphoric acid Nutrition 0.000 description 13
239000000460 chlorine Substances 0.000 description 9
JRJIWSUAKOQLGW-UHFFFAOYSA-M diphenyl phosphate;dodecyl(trimethyl)azanium Chemical compound CCCCCCCCCCCC[N+](C)(C)C.C=1C=CC=CC=1OP(=O)([O-])OC1=CC=CC=C1 JRJIWSUAKOQLGW-UHFFFAOYSA-M 0.000 description 9
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 8
229910052801 chlorine Inorganic materials 0.000 description 8
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
238000012360 testing method Methods 0.000 description 8
150000003254 radicals Chemical class 0.000 description 7
239000000654 additive Substances 0.000 description 6
230000000996 additive effect Effects 0.000 description 6
229910052751 metal Inorganic materials 0.000 description 6
239000002184 metal Substances 0.000 description 6
239000002904 solvent Substances 0.000 description 6
150000007513 acids Chemical class 0.000 description 5
125000002947 alkylene group Chemical group 0.000 description 5
VICYBMUVWHJEFT-UHFFFAOYSA-N dodecyltrimethylammonium ion Chemical compound CCCCCCCCCCCC[N+](C)(C)C VICYBMUVWHJEFT-UHFFFAOYSA-N 0.000 description 5
239000011737 fluorine Substances 0.000 description 5
229910052731 fluorine Inorganic materials 0.000 description 5
238000009472 formulation Methods 0.000 description 5
150000002431 hydrogen Chemical class 0.000 description 5
150000003016 phosphoric acids Chemical class 0.000 description 5
229920000728 polyester Polymers 0.000 description 5
229920000642 polymer Polymers 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 description 4
238000006243 chemical reaction Methods 0.000 description 4
239000000356 contaminant Substances 0.000 description 4
238000011109 contamination Methods 0.000 description 4
ASMQGLCHMVWBQR-UHFFFAOYSA-M diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(=O)([O-])OC1=CC=CC=C1 ASMQGLCHMVWBQR-UHFFFAOYSA-M 0.000 description 4
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 4
238000002474 experimental method Methods 0.000 description 4
229910052736 halogen Inorganic materials 0.000 description 4
150000002367 halogens Chemical group 0.000 description 4
239000000314 lubricant Substances 0.000 description 4
BDJRBEYXGGNYIS-UHFFFAOYSA-N nonanedioic acid Chemical compound OC(=O)CCCCCCCC(O)=O BDJRBEYXGGNYIS-UHFFFAOYSA-N 0.000 description 4
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
150000001412 amines Chemical class 0.000 description 3
150000005840 aryl radicals Chemical class 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
230000008859 change Effects 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
MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 3
150000001991 dicarboxylic acids Chemical class 0.000 description 3
239000000975 dye Substances 0.000 description 3
235000019441 ethanol Nutrition 0.000 description 3
238000001914 filtration Methods 0.000 description 3
239000000463 material Substances 0.000 description 3
238000000034 method Methods 0.000 description 3
CAAULPUQFIIOTL-UHFFFAOYSA-N methyl dihydrogen phosphate Chemical compound COP(O)(O)=O CAAULPUQFIIOTL-UHFFFAOYSA-N 0.000 description 3
230000003647 oxidation Effects 0.000 description 3
238000007254 oxidation reaction Methods 0.000 description 3
FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Inorganic materials [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 3
239000000126 substance Substances 0.000 description 3
125000006276 2-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C(*)C([H])=C1[H] 0.000 description 2
125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 description 2
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
125000006275 3-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C([H])C(*)=C1[H] 0.000 description 2
125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
239000004254 Ammonium phosphate Substances 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
241000251730 Chondrichthyes Species 0.000 description 2
KKUKTXOBAWVSHC-UHFFFAOYSA-N Dimethylphosphate Chemical compound COP(O)(=O)OC KKUKTXOBAWVSHC-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
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
229910000831 Steel Inorganic materials 0.000 description 2
239000000370 acceptor Substances 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
229910052782 aluminium Inorganic materials 0.000 description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
229910000148 ammonium phosphate Inorganic materials 0.000 description 2
235000019289 ammonium phosphates Nutrition 0.000 description 2
150000001555 benzenes Chemical class 0.000 description 2
QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 description 2
239000012964 benzotriazole Substances 0.000 description 2
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
YOUGRGFIHBUKRS-UHFFFAOYSA-N benzyl(trimethyl)azanium Chemical compound C[N+](C)(C)CC1=CC=CC=C1 YOUGRGFIHBUKRS-UHFFFAOYSA-N 0.000 description 2
230000033228 biological regulation Effects 0.000 description 2
239000004305 biphenyl Substances 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
VQRZNCVKGHWIHL-UHFFFAOYSA-N butyl-dodecyl-dimethylazanium Chemical compound CCCCCCCCCCCC[N+](C)(C)CCCC VQRZNCVKGHWIHL-UHFFFAOYSA-N 0.000 description 2
229910052799 carbon Inorganic materials 0.000 description 2
229910052798 chalcogen Inorganic materials 0.000 description 2
150000001787 chalcogens Chemical class 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
HTDKEJXHILZNPP-UHFFFAOYSA-N dioctyl hydrogen phosphate Chemical compound CCCCCCCCOP(O)(=O)OCCCCCCCC HTDKEJXHILZNPP-UHFFFAOYSA-N 0.000 description 2
USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical class C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 description 2
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 2
JRBPAEWTRLWTQC-UHFFFAOYSA-O dodecylazanium Chemical compound CCCCCCCCCCCC[NH3+] JRBPAEWTRLWTQC-UHFFFAOYSA-O 0.000 description 2
ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 2
FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 2
238000010348 incorporation Methods 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-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
FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 2
WWZKQHOCKIZLMA-UHFFFAOYSA-N octanoic acid Chemical compound CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 2
239000003208 petroleum Substances 0.000 description 2
CMPQUABWPXYYSH-UHFFFAOYSA-N phenyl phosphate Chemical compound OP(O)(=O)OC1=CC=CC=C1 CMPQUABWPXYYSH-UHFFFAOYSA-N 0.000 description 2
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 2
150000003014 phosphoric acid esters Chemical class 0.000 description 2
125000001453 quaternary ammonium group Chemical group 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
CXMXRPHRNRROMY-UHFFFAOYSA-N sebacic acid Chemical compound OC(=O)CCCCCCCCC(O)=O CXMXRPHRNRROMY-UHFFFAOYSA-N 0.000 description 2
229910052710 silicon Inorganic materials 0.000 description 2
239000010703 silicon Substances 0.000 description 2
239000011734 sodium Substances 0.000 description 2
239000011780 sodium chloride Substances 0.000 description 2
239000000243 solution Substances 0.000 description 2
238000013112 stability test Methods 0.000 description 2
239000010959 steel Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
TYFQFVWCELRYAO-UHFFFAOYSA-N suberic acid Chemical compound OC(=O)CCCCCCC(O)=O TYFQFVWCELRYAO-UHFFFAOYSA-N 0.000 description 2
125000003107 substituted aryl group Chemical group 0.000 description 2
150000001911 terphenyls Chemical class 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
STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 2
150000005691 triesters Chemical class 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
OAGSJMRKTNUIFI-UHFFFAOYSA-N (2-tert-butylphenyl) phenyl hydrogen phosphate Chemical compound CC(C)(C)C1=CC=CC=C1OP(O)(=O)OC1=CC=CC=C1 OAGSJMRKTNUIFI-UHFFFAOYSA-N 0.000 description 1
UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
PWZSCBSKFVJMJH-UHFFFAOYSA-N 1,1-diethylpyrrolidin-1-ium Chemical compound CC[N+]1(CC)CCCC1 PWZSCBSKFVJMJH-UHFFFAOYSA-N 0.000 description 1
VLUJYLLZTZWVLO-UHFFFAOYSA-N 1,3,5-trimethylpyridin-1-ium Chemical compound CC1=CC(C)=C[N+](C)=C1 VLUJYLLZTZWVLO-UHFFFAOYSA-N 0.000 description 1
OXHNLMTVIGZXSG-UHFFFAOYSA-N 1-Methylpyrrole Chemical compound CN1C=CC=C1 OXHNLMTVIGZXSG-UHFFFAOYSA-N 0.000 description 1
UVCPHBWNKAXVPC-UHFFFAOYSA-N 1-butyl-1-methylpiperidin-1-ium Chemical compound CCCC[N+]1(C)CCCCC1 UVCPHBWNKAXVPC-UHFFFAOYSA-N 0.000 description 1
AZWDISHHPONIAX-UHFFFAOYSA-N 1-butylquinolin-1-ium Chemical compound C1=CC=C2[N+](CCCC)=CC=CC2=C1 AZWDISHHPONIAX-UHFFFAOYSA-N 0.000 description 1
125000006219 1-ethylpentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
FHZKIKVDRZVWKN-UHFFFAOYSA-N 1-hexyl-1-methylpiperidin-1-ium Chemical compound CCCCCC[N+]1(C)CCCCC1 FHZKIKVDRZVWKN-UHFFFAOYSA-N 0.000 description 1
RGCAQUUSBHVLJD-UHFFFAOYSA-N 1-phenoxy-4-(4-phenoxyphenyl)benzene Chemical group C=1C=C(C=2C=CC(OC=3C=CC=CC=3)=CC=2)C=CC=1OC1=CC=CC=C1 RGCAQUUSBHVLJD-UHFFFAOYSA-N 0.000 description 1
OUHKUIFYPILFLR-UHFFFAOYSA-N 10-phenyldecyl dihydrogen phosphate Chemical compound OP(O)(=O)OCCCCCCCCCCC1=CC=CC=C1 OUHKUIFYPILFLR-UHFFFAOYSA-N 0.000 description 1
UQJDVLPHTXQTRP-UHFFFAOYSA-N 2,2-bis(heptanoyloxymethyl)butyl heptanoate Chemical compound CCCCCCC(=O)OCC(CC)(COC(=O)CCCCCC)COC(=O)CCCCCC UQJDVLPHTXQTRP-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
MALIONKMKPITBV-UHFFFAOYSA-N 2-(3-chloro-4-hydroxyphenyl)-n-[2-(4-sulfamoylphenyl)ethyl]acetamide Chemical compound C1=CC(S(=O)(=O)N)=CC=C1CCNC(=O)CC1=CC=C(O)C(Cl)=C1 MALIONKMKPITBV-UHFFFAOYSA-N 0.000 description 1
YEVQZPWSVWZAOB-UHFFFAOYSA-N 2-(bromomethyl)-1-iodo-4-(trifluoromethyl)benzene Chemical compound FC(F)(F)C1=CC=C(I)C(CBr)=C1 YEVQZPWSVWZAOB-UHFFFAOYSA-N 0.000 description 1
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 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
125000005916 2-methylpentyl group Chemical group 0.000 description 1
125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 1
NJGWLKSNYBXRST-UHFFFAOYSA-N 3-methyl-1,3-oxazol-3-ium Chemical compound C[N+]=1C=COC=1 NJGWLKSNYBXRST-UHFFFAOYSA-N 0.000 description 1
BSNYRHXXCHPRMD-UHFFFAOYSA-N 3-propan-2-yl-1,3-thiazol-3-ium Chemical compound CC(C)[N+]=1C=CSC=1 BSNYRHXXCHPRMD-UHFFFAOYSA-N 0.000 description 1
125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 1
125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 1
GMMHKHNCJNRQGK-UHFFFAOYSA-N 4-propylundecan-4-yl dihydrogen phosphate Chemical compound CCCCCCCC(CCC)(CCC)OP(=O)(O)O GMMHKHNCJNRQGK-UHFFFAOYSA-N 0.000 description 1
BWDBEAQIHAEVLV-UHFFFAOYSA-N 6-methylheptan-1-ol Chemical compound CC(C)CCCCCO BWDBEAQIHAEVLV-UHFFFAOYSA-N 0.000 description 1
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 1
VVZBFOKBSDGVGZ-UHFFFAOYSA-N BENZALKONIUM Chemical compound CCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 VVZBFOKBSDGVGZ-UHFFFAOYSA-N 0.000 description 1
229920002799 BoPET Polymers 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
XDWOXEILGBUSMX-UHFFFAOYSA-N C1(=CC=CC=C1)OP(=O)(OC1=CC=CC=C1)[O-].C(CCC)[NH+](CCCC)CCCC Chemical compound C1(=CC=CC=C1)OP(=O)(OC1=CC=CC=C1)[O-].C(CCC)[NH+](CCCC)CCCC XDWOXEILGBUSMX-UHFFFAOYSA-N 0.000 description 1
ZMJZPHOKNFRFCA-UHFFFAOYSA-N CP(OC)([O-])=O.CC1=C(C(=C(C=C1)[NH2+]C(C)(C)CC(C)(C)C)C)C Chemical compound CP(OC)([O-])=O.CC1=C(C(=C(C=C1)[NH2+]C(C)(C)CC(C)(C)C)C)C ZMJZPHOKNFRFCA-UHFFFAOYSA-N 0.000 description 1
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QJGNGYJQLYUZMF-UHFFFAOYSA-M butyl(tridodecyl)azanium;dibutyl phosphate Chemical compound CCCCOP([O-])(=O)OCCCC.CCCCCCCCCCCC[N+](CCCC)(CCCCCCCCCCCC)CCCCCCCCCCCC QJGNGYJQLYUZMF-UHFFFAOYSA-M 0.000 description 1
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238000000354 decomposition reaction Methods 0.000 description 1
QRDHBZVZOGZIPS-UHFFFAOYSA-M decyl(trimethyl)azanium;dimethyl phosphate Chemical compound COP([O-])(=O)OC.CCCCCCCCCC[N+](C)(C)C QRDHBZVZOGZIPS-UHFFFAOYSA-M 0.000 description 1
KGDSLVFPNUHHEZ-UHFFFAOYSA-N decyl-dimethyl-phenylazanium Chemical compound CCCCCCCCCC[N+](C)(C)C1=CC=CC=C1 KGDSLVFPNUHHEZ-UHFFFAOYSA-N 0.000 description 1
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HDFFVHSMHLDSLO-UHFFFAOYSA-M dibenzyl phosphate Chemical compound C=1C=CC=CC=1COP(=O)([O-])OCC1=CC=CC=C1 HDFFVHSMHLDSLO-UHFFFAOYSA-M 0.000 description 1
RYWWDVQVRVCYQQ-UHFFFAOYSA-M dibenzyl phosphate;dodecyl(trimethyl)azanium Chemical compound CCCCCCCCCCCC[N+](C)(C)C.C=1C=CC=CC=1COP(=O)([O-])OCC1=CC=CC=C1 RYWWDVQVRVCYQQ-UHFFFAOYSA-M 0.000 description 1
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IQBXMBQJJDZLEG-UHFFFAOYSA-M diethyl phosphate;ethyl-hexadecyl-dimethylazanium Chemical compound CCOP([O-])(=O)OCC.CCCCCCCCCCCCCCCC[N+](C)(C)CC IQBXMBQJJDZLEG-UHFFFAOYSA-M 0.000 description 1
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KMDITUZJIRZAEN-UHFFFAOYSA-M dimethyl phosphate;dodecyl(trimethyl)azanium Chemical compound COP([O-])(=O)OC.CCCCCCCCCCCC[N+](C)(C)C KMDITUZJIRZAEN-UHFFFAOYSA-M 0.000 description 1
NIVBFZHDQNWHDN-UHFFFAOYSA-M dimethyl phosphate;hexadecyl(trimethyl)azanium Chemical compound COP([O-])(=O)OC.CCCCCCCCCCCCCCCC[N+](C)(C)C NIVBFZHDQNWHDN-UHFFFAOYSA-M 0.000 description 1
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150000002009 diols Chemical class 0.000 description 1
SMEYBPJSNSKWNY-UHFFFAOYSA-M diphenyl phosphate heptadecyl(trimethyl)azanium Chemical compound P(=O)(OC1=CC=CC=C1)(OC1=CC=CC=C1)[O-].C(CCCCCCCCCCCCCCCC)[N+](C)(C)C SMEYBPJSNSKWNY-UHFFFAOYSA-M 0.000 description 1
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AYRZIFCHYUSKJR-UHFFFAOYSA-N diphenyl phosphate;methylazanium Chemical compound [NH3+]C.C=1C=CC=CC=1OP(=O)([O-])OC1=CC=CC=C1 AYRZIFCHYUSKJR-UHFFFAOYSA-N 0.000 description 1
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CAGAVJNNBVXWHV-UHFFFAOYSA-M diphenyl phosphate;trimethyl(tridecyl)azanium Chemical compound CCCCCCCCCCCCC[N+](C)(C)C.C=1C=CC=CC=1OP(=O)([O-])OC1=CC=CC=C1 CAGAVJNNBVXWHV-UHFFFAOYSA-M 0.000 description 1
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239000001530 fumaric acid Substances 0.000 description 1
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239000011521 glass Substances 0.000 description 1
125000001188 haloalkyl group Chemical group 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
PYGSKMBEVAICCR-UHFFFAOYSA-N hexa-1,5-diene Chemical group C=CCCC=C PYGSKMBEVAICCR-UHFFFAOYSA-N 0.000 description 1
DBBBNPFIGLYHFN-UHFFFAOYSA-N hexadec-1-enyl(trimethyl)azanium Chemical compound CCCCCCCCCCCCCCC=C[N+](C)(C)C DBBBNPFIGLYHFN-UHFFFAOYSA-N 0.000 description 1
JFPQEFOUPGQVJO-UHFFFAOYSA-M hexadec-1-enyl(trimethyl)azanium;methyl phenyl phosphate Chemical compound COP([O-])(=O)OC1=CC=CC=C1.CCCCCCCCCCCCCCC=C[N+](C)(C)C JFPQEFOUPGQVJO-UHFFFAOYSA-M 0.000 description 1
XZZMUWLTXGGDIG-UHFFFAOYSA-M hexadecyl(methoxy)phosphinate tetramethylazanium Chemical compound C(CCCCCCCCCCCCCCC)P(OC)([O-])=O.C[N+](C)(C)C XZZMUWLTXGGDIG-UHFFFAOYSA-M 0.000 description 1
JDPSFRXPDJVJMV-UHFFFAOYSA-N hexadecylphosphonic acid Chemical compound CCCCCCCCCCCCCCCCP(O)(O)=O JDPSFRXPDJVJMV-UHFFFAOYSA-N 0.000 description 1
LIQQCWRJOJCVDF-UHFFFAOYSA-N hexyl dipropyl phosphate Chemical compound CCCCCCOP(=O)(OCCC)OCCC LIQQCWRJOJCVDF-UHFFFAOYSA-N 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
ZSSIYIZVIFNDRJ-UHFFFAOYSA-N hydroxy-phenoxy-phenylsulfanyl-sulfanylidene-lambda5-phosphane Chemical compound C=1C=CC=CC=1SP(=S)(O)OC1=CC=CC=C1 ZSSIYIZVIFNDRJ-UHFFFAOYSA-N 0.000 description 1
239000012535 impurity Substances 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
125000003717 m-cresyl group Chemical group [H]C1=C([H])C(O*)=C([H])C(=C1[H])C([H])([H])[H] 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
238000005259 measurement Methods 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
239000007769 metal material Substances 0.000 description 1
DWHMMGGJCLDORC-UHFFFAOYSA-N methoxy(methyl)phosphinic acid Chemical compound COP(C)(O)=O DWHMMGGJCLDORC-UHFFFAOYSA-N 0.000 description 1
RCYGJPUVEBRNJN-UHFFFAOYSA-M methoxy(octyl)phosphinate tetramethylazanium Chemical compound C(CCCCCCC)P(OC)([O-])=O.C[N+](C)(C)C RCYGJPUVEBRNJN-UHFFFAOYSA-M 0.000 description 1
JZLMFLOCXAPMTK-UHFFFAOYSA-N methoxy(octyl)phosphinic acid Chemical compound CCCCCCCCP(O)(=O)OC JZLMFLOCXAPMTK-UHFFFAOYSA-N 0.000 description 1
XGGRTYNQGDQBHO-UHFFFAOYSA-M methoxy-(2-methoxy-2-oxoethyl)phosphinate tetramethylazanium Chemical compound C[N+](C)(C)C.COC(=O)CP([O-])(=O)OC XGGRTYNQGDQBHO-UHFFFAOYSA-M 0.000 description 1
BXVTXRIOHHFSQZ-UHFFFAOYSA-N methyl phenyl hydrogen phosphate Chemical compound COP(O)(=O)OC1=CC=CC=C1 BXVTXRIOHHFSQZ-UHFFFAOYSA-N 0.000 description 1
CUVNYGRZKFAAOQ-UHFFFAOYSA-N methyl-tri(tridecyl)azanium Chemical compound CCCCCCCCCCCCC[N+](C)(CCCCCCCCCCCCC)CCCCCCCCCCCCC CUVNYGRZKFAAOQ-UHFFFAOYSA-N 0.000 description 1
YACKEPLHDIMKIO-UHFFFAOYSA-N methylphosphonic acid Chemical compound CP(O)(O)=O YACKEPLHDIMKIO-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
NYUYKRKWPLUHNX-UHFFFAOYSA-N n,n-dimethyldodec-1-en-1-amine Chemical compound CCCCCCCCCCC=CN(C)C NYUYKRKWPLUHNX-UHFFFAOYSA-N 0.000 description 1
SNKUXFQNFUTEJL-UHFFFAOYSA-N n-butyl-n-methyldodecan-1-amine Chemical compound CCCCCCCCCCCCN(C)CCCC SNKUXFQNFUTEJL-UHFFFAOYSA-N 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
238000006386 neutralization reaction Methods 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000000486 o-cresyl group Chemical group [H]C1=C([H])C(O*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
229960002446 octanoic acid Drugs 0.000 description 1
YAFOVCNAQTZDQB-UHFFFAOYSA-N octyl diphenyl phosphate Chemical compound C=1C=CC=CC=1OP(=O)(OCCCCCCCC)OC1=CC=CC=C1 YAFOVCNAQTZDQB-UHFFFAOYSA-N 0.000 description 1
238000006384 oligomerization reaction Methods 0.000 description 1
230000003606 oligomerizing effect Effects 0.000 description 1
KDYDROJHRSCHEF-UHFFFAOYSA-M oxido-phenoxy-phenylsulfanyl-sulfanylidene-$l^{5}-phosphane;trimethyl(octadecyl)azanium Chemical compound C=1C=CC=CC=1SP(=S)([O-])OC1=CC=CC=C1.CCCCCCCCCCCCCCCCCC[N+](C)(C)C KDYDROJHRSCHEF-UHFFFAOYSA-M 0.000 description 1
125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
125000000552 p-cresyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1O*)C([H])([H])[H] 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
229920000233 poly(alkylene oxides) Polymers 0.000 description 1
229920000058 polyacrylate 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
239000004926 polymethyl methacrylate Substances 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
239000001103 potassium chloride Substances 0.000 description 1
235000011164 potassium chloride Nutrition 0.000 description 1
238000001556 precipitation Methods 0.000 description 1
230000002265 prevention Effects 0.000 description 1
230000008569 process Effects 0.000 description 1
MIWQHLIBMIMIRX-UHFFFAOYSA-N propan-2-ylbenzene Chemical compound C[C](C)C1=CC=CC=C1 MIWQHLIBMIMIRX-UHFFFAOYSA-N 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
150000003242 quaternary ammonium salts Chemical class 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
238000011160 research Methods 0.000 description 1
230000004044 response Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
JZALLXAUNPOCEU-UHFFFAOYSA-N tetradecylbenzene Chemical compound CCCCCCCCCCCCCCC1=CC=CC=C1 JZALLXAUNPOCEU-UHFFFAOYSA-N 0.000 description 1
MQHSFMJHURNQIE-UHFFFAOYSA-N tetrakis(2-ethylhexyl) silicate Chemical class CCCCC(CC)CO[Si](OCC(CC)CCCC)(OCC(CC)CCCC)OCC(CC)CCCC MQHSFMJHURNQIE-UHFFFAOYSA-N 0.000 description 1
QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
OZLXDDRBXFHZNO-UHFFFAOYSA-N tetraoctyl silicate Chemical compound CCCCCCCCO[Si](OCCCCCCCC)(OCCCCCCCC)OCCCCCCCC OZLXDDRBXFHZNO-UHFFFAOYSA-N 0.000 description 1
239000010936 titanium Substances 0.000 description 1
229910052719 titanium Inorganic materials 0.000 description 1
125000003944 tolyl group Chemical group 0.000 description 1
238000012546 transfer Methods 0.000 description 1
RQPWVAXZWDTDPH-UHFFFAOYSA-N tridodecyl(methyl)azanium Chemical compound CCCCCCCCCCCC[N+](C)(CCCCCCCCCCCC)CCCCCCCCCCCC RQPWVAXZWDTDPH-UHFFFAOYSA-N 0.000 description 1
SEACXNRNJAXIBM-UHFFFAOYSA-N triethyl(methyl)azanium Chemical compound CC[N+](C)(CC)CC SEACXNRNJAXIBM-UHFFFAOYSA-N 0.000 description 1
ZVFDPYZBJGKPII-UHFFFAOYSA-N trimethyl(nonyl)azanium Chemical compound CCCCCCCCC[N+](C)(C)C ZVFDPYZBJGKPII-UHFFFAOYSA-N 0.000 description 1
CUHTWKRYGOJCEX-UHFFFAOYSA-N trimethyl(tridecyl)azanium Chemical compound CCCCCCCCCCCCC[N+](C)(C)C CUHTWKRYGOJCEX-UHFFFAOYSA-N 0.000 description 1
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
QXJQHYBHAIHNGG-UHFFFAOYSA-N trimethylolethane Chemical compound OCC(C)(CO)CO QXJQHYBHAIHNGG-UHFFFAOYSA-N 0.000 description 1
ZNEOHLHCKGUAEB-UHFFFAOYSA-N trimethylphenylammonium Chemical compound C[N+](C)(C)C1=CC=CC=C1 ZNEOHLHCKGUAEB-UHFFFAOYSA-N 0.000 description 1
XTAZYLNFDRKIHJ-UHFFFAOYSA-O trioctylazanium Chemical compound CCCCCCCC[NH+](CCCCCCCC)CCCCCCCC XTAZYLNFDRKIHJ-UHFFFAOYSA-O 0.000 description 1
RXPQRKFMDQNODS-UHFFFAOYSA-N tripropyl phosphate Chemical compound CCCOP(=O)(OCCC)OCCC RXPQRKFMDQNODS-UHFFFAOYSA-N 0.000 description 1
LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
LZABKCXEHHOOHI-UHFFFAOYSA-N tris(2-ethylbutyl) tris(2-ethylbutoxy)silyl silicate Chemical compound CCC(CC)CO[Si](OCC(CC)CC)(OCC(CC)CC)O[Si](OCC(CC)CC)(OCC(CC)CC)OCC(CC)CC LZABKCXEHHOOHI-UHFFFAOYSA-N 0.000 description 1
IRAUUSOWFPPUNG-UHFFFAOYSA-N tris(2-ethylhexyl) tris(2-ethylhexoxy)silyl silicate Chemical compound CCCCC(CC)CO[Si](OCC(CC)CCCC)(OCC(CC)CCCC)O[Si](OCC(CC)CCCC)(OCC(CC)CCCC)OCC(CC)CCCC IRAUUSOWFPPUNG-UHFFFAOYSA-N 0.000 description 1
230000004580 weight loss Effects 0.000 description 1

Classifications

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- C10M137/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing phosphorus having no phosphorus-to-carbon bond
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- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
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- 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
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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
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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
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- C10M2229/046—Siloxanes with specific structure containing silicon-oxygen-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
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- C10M2229/04—Siloxanes with specific structure
- C10M2229/047—Siloxanes with specific structure containing alkylene oxide groups
- 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
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- C10M2229/04—Siloxanes with specific structure
- C10M2229/048—Siloxanes with specific structure containing carboxyl groups
- 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
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- C10M2229/04—Siloxanes with specific structure
- C10M2229/05—Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
- 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
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- C10M2229/04—Siloxanes with specific structure
- C10M2229/05—Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon
- C10M2229/051—Siloxanes with specific structure containing atoms other than silicon, hydrogen, oxygen or carbon containing halogen
- 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
- C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
- C10N2030/08—Resistance to extreme temperature
- 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
- 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
- C10N2040/08—Hydraulic fluids, e.g. brake-fluids
- 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
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- C10N2040/12—Gas-turbines
- 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
- C10N2040/12—Gas-turbines
- C10N2040/13—Aircraft turbines
- 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
- C10N2040/135—Steam engines or turbines
- 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
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- C10N2040/14—Electric or magnetic purposes
- C10N2040/16—Dielectric; Insulating oil or insulators
- 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
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- C10N2040/17—Electric or magnetic purposes for electric contacts
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
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- C10N2040/30—Refrigerators lubricants or compressors lubricants
- 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
- C10N2040/32—Wires, ropes or cables lubricants
- 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
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- C10N2040/34—Lubricating-sealants
- 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
- C10N2040/36—Release agents or mold release agents
- 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
- C10N2040/38—Conveyors or chain belts
- 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
- C10N2040/40—Generators or electric motors in oil or gas winning field
- 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
- C10N2040/42—Flashing oils or marking oils
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- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/44—Super vacuum or supercritical use
- 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
- C10N2040/50—Medical uses
- 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
- C10N2050/00—Form in which the lubricant is applied to the material being lubricated
- C10N2050/10—Semi-solids; greasy

Landscapes

Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Organic Chemistry (AREA)
Lubricants (AREA)
Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)
Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
Other Liquid Machine Or Engine Such As Wave Power Use (AREA)
Preventing Corrosion Or Incrustation Of Metals (AREA)
Catalysts (AREA)

CH159875A 1974-02-11 1975-02-11 Hydraulic fluid CH615217A5 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US44169874A	1974-02-11	1974-02-11

Publications (1)

Publication Number	Publication Date
CH615217A5 true CH615217A5 (en)	1980-01-15

Family

ID=23753936

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH159875A CH615217A5 (en)	1974-02-11	1975-02-11	Hydraulic fluid

Country Status (17)

Country	Link
JP (1)	JPS50115183A (no)
AR (1)	AR208190A1 (no)
BE (1)	BE825342A (no)
CA (1)	CA1070291A (no)
CH (1)	CH615217A5 (no)
DE (1)	DE2505189A1 (no)
DK (1)	DK38975A (no)
FR (1)	FR2260617B1 (no)
GB (1)	GB1506196A (no)
IL (1)	IL46483A (no)
IN (1)	IN142832B (no)
IT (1)	IT1029652B (no)
NL (1)	NL7501552A (no)
NO (1)	NO141016C (no)
SE (1)	SE7501453L (no)
SU (1)	SU679151A3 (no)
ZA (1)	ZA75843B (no)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
FR2309628A1 (fr) *	1975-01-09	1976-11-26	Cetehor	Procede d'amelioration des proprietes lubrifiantes des fluides polysiloxanes par addition de polysiloxanes oxydes polaires
IT1159851B (it) *	1978-06-20	1987-03-04	Cselt Centro Studi Lab Telecom	Perfezionamenti ai sistemi di trasmissione a divisione di lunghezza d'onda
DE3010669C2 (de) *	1980-03-20	1986-02-20	Mobil Oil Ag In Deutschland, 2000 Hamburg	Schwer entflammbare Flüssigkeit
JPS61108767A (ja) *	1984-10-31	1986-05-27	竹本油脂株式会社	合成繊維用帯電防止剤
US5336847A (en) *	1991-05-09	1994-08-09	Fuji Electric Co., Ltd.	Stationary induction apparatus containing uninflammable insulating liquid
JP3139905B2 (ja) *	1993-12-29	2001-03-05	ニチアス株式会社	オイル塗布ローラのオイル保持筒
DE59813902D1 (de)	1997-09-18	2007-03-29	Ciba Sc Holding Ag	Schmierstoffzusammensetzungen mit Thiophosphorsäureestern und Dithiophosphorsäureestern
JP2014118531A (ja) *	2012-12-19	2014-06-30	Tosoh Corp	４級アンモニウム塩を含有するブロック剤解離触媒及びその用途

1975
- 1975-01-01 AR AR257606A patent/AR208190A1/es active
- 1975-01-21 IL IL46483A patent/IL46483A/en unknown
- 1975-01-22 IN IN134/CAL/75A patent/IN142832B/en unknown
- 1975-01-31 JP JP50013314A patent/JPS50115183A/ja active Pending
- 1975-02-05 DK DK38975*#A patent/DK38975A/da unknown
- 1975-02-07 DE DE19752505189 patent/DE2505189A1/de active Pending
- 1975-02-07 IT IT48062/75A patent/IT1029652B/it active
- 1975-02-07 BE BE7000611A patent/BE825342A/xx unknown
- 1975-02-07 CA CA218,751A patent/CA1070291A/en not_active Expired
- 1975-02-10 FR FR7504033A patent/FR2260617B1/fr not_active Expired
- 1975-02-10 NL NL7501552A patent/NL7501552A/xx unknown
- 1975-02-10 NO NO750423A patent/NO141016C/no unknown
- 1975-02-10 SE SE7501453A patent/SE7501453L/xx unknown
- 1975-02-10 ZA ZA00750843A patent/ZA75843B/xx unknown
- 1975-02-11 CH CH159875A patent/CH615217A5/de not_active IP Right Cessation
- 1975-02-11 GB GB5752/75A patent/GB1506196A/en not_active Expired
- 1975-02-11 SU SU752108223A patent/SU679151A3/ru active

Also Published As

Publication number	Publication date
CA1070291A (en)	1980-01-22
NO141016C (no)	1979-12-27
SU679151A3 (ru)	1979-08-05
DE2505189A1 (de)	1975-08-14
FR2260617A1 (no)	1975-09-05
NO141016B (no)	1979-09-17
GB1506196A (en)	1978-04-05
IL46483A (en)	1977-11-30
SE7501453L (no)	1975-08-12
IN142832B (no)	1977-08-27
AR208190A1 (es)	1976-12-09
JPS50115183A (no)	1975-09-09
NL7501552A (nl)	1975-08-13
IT1029652B (it)	1979-03-20
FR2260617B1 (no)	1978-12-08
NO750423L (no)	1975-08-12
IL46483A0 (en)	1975-04-25
DK38975A (no)	1975-10-06
AU7758075A (en)	1976-07-29
BE825342A (nl)	1975-08-07
ZA75843B (en)	1976-01-28

Legal Events

Date	Code	Title	Description
1981-10-30	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
DE69915232T2 (de)	2005-04-14	Schmiermittelzusammensetzungen
DE2262185C3 (de)	1981-10-15	Funktionelle Flüssigkeiten und deren Verwendung
DE2505116C2 (de)	1985-06-20	Hydraulische Flüssigkeit
DE1906293C3 (de)	1979-06-07	Hydraulische Flüssigkeit für Flugzeuge
DE1644930C3 (de)	1979-07-19	Schmiermittel
DE2505115A1 (de)	1975-08-14	Hydraulische fluessigkeit
CH615217A5 (en)	1980-01-15	Hydraulic fluid
DE2131926A1 (de)	1972-01-05	Hydraulik-Fluessigkeiten mit einem Gehalt an quaternaeren Phosphoniumsalzen
DE944625C (de)	1956-06-21	Schmieroel
DE2850244A1 (de)	1980-05-29	Additiv fuer die metallbearbeitung
DE1914555A1 (de)	1970-02-19	Fluessige Zubereitung und deren Verwendung als funktionelle Fluessigkeiten
DE1794078A1 (de)	1971-11-18	Als Basis fuer hydraulische Fluessigkeiten geeignete Zusammensetzung
DE69017749T2 (de)	1995-07-06	Silikonflüssigkeiten für Visco-Kupplungen.
DE1644922B2 (de)	1974-01-31	Wärme-, Kraftübertragungs- und Schmiermittel
DE2512890C3 (de)	1982-03-11	Funktionelle Flüssigkeiten und Verwendung dieser Flüssigkeiten
DE2357199A1 (de)	1974-08-01	Schmiermittel
DE1957955C3 (de)	1975-09-04	Halbflüssige synthetische Schmiermittel
DE929207C (de)	1955-06-20	Schmiermittel, insbesondere hydraulische Fluessigkeit
EP1171552A1 (de)	2002-01-16	Hydraulische flüssigkeiten, enthaltend cyclische carbonsäurederivate
DE2512891A1 (de)	1975-10-09	Epoxydstabilisatoren-enthaltende funktionelle fluessigkeiten
DE1644931B2 (de)	1981-07-09	Schmiermittel in Form von Schmierölen und Schmierfetten
DE2430954B2 (de)	1976-12-09	Fuer hydraulische und daempf-zwecke geeignete fluessige wasserfreie organosiliciumzubereitung
US3374291A (en)	1968-03-19	Trithiophosphites of mercapto acid esters
DE1644919C3 (de)	1976-05-06	Flüssige Mischungen
US2511731A (en)	1950-06-13	Extreme pressure lubricants