DE2827741A1 - Funktionelle fluide - Google Patents
Funktionelle fluideInfo
- Publication number
- DE2827741A1 DE2827741A1 DE19782827741 DE2827741A DE2827741A1 DE 2827741 A1 DE2827741 A1 DE 2827741A1 DE 19782827741 DE19782827741 DE 19782827741 DE 2827741 A DE2827741 A DE 2827741A DE 2827741 A1 DE2827741 A1 DE 2827741A1
- Authority
- DE
- Germany
- Prior art keywords
- radical
- general formula
- carbon atoms
- group
- alkyl
- 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.)
- Ceased
Links
- -1 alicyclic radical Chemical class 0.000 claims description 66
- 239000012530 fluid Substances 0.000 claims description 61
- 125000004432 carbon atom Chemical group C* 0.000 claims description 44
- 150000003254 radicals Chemical class 0.000 claims description 43
- 150000001875 compounds Chemical class 0.000 claims description 22
- 239000003921 oil Substances 0.000 claims description 16
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 15
- 229930195733 hydrocarbon Natural products 0.000 claims description 9
- 150000002430 hydrocarbons Chemical class 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
- SLRMQYXOBQWXCR-UHFFFAOYSA-N 2154-56-5 Chemical compound [CH2]C1=CC=CC=C1 SLRMQYXOBQWXCR-UHFFFAOYSA-N 0.000 claims description 7
- 150000001412 amines Chemical class 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 229910000077 silane Inorganic materials 0.000 claims description 5
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- 238000001816 cooling Methods 0.000 claims description 4
- 239000002480 mineral oil Substances 0.000 claims description 4
- 235000010446 mineral oil Nutrition 0.000 claims description 3
- 150000004756 silanes Chemical class 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 125000003118 aryl group Chemical group 0.000 claims 5
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N ethyl Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 claims 2
- 229910003849 O-Si Inorganic materials 0.000 claims 1
- 229910003872 O—Si Inorganic materials 0.000 claims 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- 150000003335 secondary amines Chemical class 0.000 claims 1
- 150000003512 tertiary amines Chemical class 0.000 claims 1
- ORGHESHFQPYLAO-UHFFFAOYSA-N vinyl radical Chemical compound C=[CH] ORGHESHFQPYLAO-UHFFFAOYSA-N 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 150000005840 aryl radicals Chemical class 0.000 description 5
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 230000004888 barrier function Effects 0.000 description 3
- 229920001971 elastomer Polymers 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 238000009833 condensation Methods 0.000 description 2
- 230000005494 condensation Effects 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 description 2
- 229920000768 polyamine Polymers 0.000 description 2
- 150000003141 primary amines Chemical class 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical compound O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 2
- COBPKKZHLDDMTB-UHFFFAOYSA-N 2-[2-(2-butoxyethoxy)ethoxy]ethanol Chemical group CCCCOCCOCCOCCO COBPKKZHLDDMTB-UHFFFAOYSA-N 0.000 description 1
- RREANTFLPGEWEN-MBLPBCRHSA-N 7-[4-[[(3z)-3-[4-amino-5-[(3,4,5-trimethoxyphenyl)methyl]pyrimidin-2-yl]imino-5-fluoro-2-oxoindol-1-yl]methyl]piperazin-1-yl]-1-cyclopropyl-6-fluoro-4-oxoquinoline-3-carboxylic acid Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(\N=C/3C4=CC(F)=CC=C4N(CN4CCN(CC4)C=4C(=CC=5C(=O)C(C(O)=O)=CN(C=5C=4)C4CC4)F)C\3=O)=NC=2)N)=C1 RREANTFLPGEWEN-MBLPBCRHSA-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
- 239000005046 Chlorosilane Substances 0.000 description 1
- 101150065749 Churc1 gene Proteins 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical compound CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920000459 Nitrile rubber Polymers 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920002367 Polyisobutene Polymers 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000002199 base oil Substances 0.000 description 1
- 150000001555 benzenes Chemical class 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- KOPOQZFJUQMUML-UHFFFAOYSA-N chlorosilane Chemical class Cl[SiH3] KOPOQZFJUQMUML-UHFFFAOYSA-N 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 230000002950 deficient Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
- 150000002440 hydroxy compounds Chemical class 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 229960002317 succinimide Drugs 0.000 description 1
- 230000002522 swelling effect Effects 0.000 description 1
- 208000024891 symptom Diseases 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
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/04—Esters of silicic acids
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- C10M139/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing atoms of elements not provided for in groups C10M127/00 - C10M137/00
- C10M139/04—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing atoms of elements not provided for in groups C10M127/00 - C10M137/00 having a silicon-to-carbon bond, e.g. silanes
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- C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
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- C10M2203/104—Aromatic fractions
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/04—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to acyclic or cycloaliphatic carbon atoms
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- 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
-
- 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
- C10N2040/44—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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Lubricants (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB26670/77A GB1595701A (en) | 1977-06-24 | 1977-06-24 | Fluids suitable for use as hydraulic fluids electrical oils heat transfer fluids and refrigerant oils |
Publications (1)
Publication Number | Publication Date |
---|---|
DE2827741A1 true DE2827741A1 (de) | 1979-01-18 |
Family
ID=10247328
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19782827741 Ceased DE2827741A1 (de) | 1977-06-24 | 1978-06-23 | Funktionelle fluide |
Country Status (10)
Country | Link |
---|---|
JP (1) | JPS6051517B2 (sv) |
AU (1) | AU524142B2 (sv) |
BE (1) | BE868422A (sv) |
CA (1) | CA1103652A (sv) |
DE (1) | DE2827741A1 (sv) |
FR (1) | FR2395308A1 (sv) |
GB (1) | GB1595701A (sv) |
IT (1) | IT1097273B (sv) |
SE (1) | SE425608B (sv) |
ZA (1) | ZA783614B (sv) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5770196A (en) * | 1980-10-22 | 1982-04-30 | Toray Silicone Co Ltd | Hydraulic oil |
US4332957A (en) * | 1980-12-22 | 1982-06-01 | National Distillers & Chemical Corp. | Phenoxyalkoxy silanes |
DE4213321A1 (de) * | 1992-04-23 | 1993-10-28 | Bayer Ag | Thermostabilisierung von aromatischen Polycarbonaten |
JP5057630B2 (ja) * | 2003-02-18 | 2012-10-24 | 昭和シェル石油株式会社 | 工業用潤滑油組成物 |
JP7153323B2 (ja) * | 2018-10-19 | 2022-10-14 | 国立研究開発法人産業技術総合研究所 | 合成潤滑油 |
CN111039973B (zh) * | 2019-12-30 | 2023-04-07 | 江苏奥克化学有限公司 | 有机硅改性的烯醇化合物及其制备方法 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU390096A1 (ru) * | 1971-08-30 | 1973-07-11 | Способ получения замещенных эфиров ортокремниевой кислоты | |
DE2513476A1 (de) * | 1974-03-27 | 1975-10-02 | Castrol Ltd | Hydraulische fluessigkeitszubereitungen |
DE2652719A1 (de) * | 1975-11-21 | 1977-05-26 | Castrol Ltd | Silanderivate und sie enthaltende hydraulikfluessigkeiten |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2129281A (en) * | 1936-03-23 | 1938-09-06 | Continental Oil Co | Lubricating oils |
FR1343967A (fr) * | 1961-12-29 | 1963-11-22 | Monsanto Chemicals | Perfectionnements aux fluides fonctionnels |
CA975347A (en) * | 1970-09-25 | 1975-09-30 | David A. Csejka | Alkyl (polyalkoxy) silanes as components in hydraulic fluids |
US3814691A (en) * | 1970-09-25 | 1974-06-04 | Olin Corp | Alkyl(polyalkoxy)silanes as components in hydraulic fluids |
US4075115A (en) * | 1972-09-18 | 1978-02-21 | General Electric Company | Silicone fluid useful as a brake fluid |
US3816313A (en) * | 1972-11-17 | 1974-06-11 | Exxon Research Engineering Co | Lubricant providing improved fatigue life |
GB1480738A (en) * | 1973-09-25 | 1977-07-20 | Castrol Ltd | Hydraulic fluids |
US3994948A (en) * | 1973-09-25 | 1976-11-30 | Castrol Limited | Hydraulic fluids |
US4016088A (en) * | 1973-09-25 | 1977-04-05 | Castrol Limited | Hydraulic fluids |
JPS5061124A (sv) * | 1973-09-28 | 1975-05-26 | ||
US4141851A (en) * | 1975-11-21 | 1979-02-27 | Castrol Limited | Silane derivatives |
-
1977
- 1977-06-24 GB GB26670/77A patent/GB1595701A/en not_active Expired
-
1978
- 1978-06-22 SE SE7807146A patent/SE425608B/sv not_active IP Right Cessation
- 1978-06-23 ZA ZA783614A patent/ZA783614B/xx unknown
- 1978-06-23 AU AU37416/78A patent/AU524142B2/en not_active Expired
- 1978-06-23 FR FR7818833A patent/FR2395308A1/fr active Granted
- 1978-06-23 DE DE19782827741 patent/DE2827741A1/de not_active Ceased
- 1978-06-23 BE BE188821A patent/BE868422A/xx not_active IP Right Cessation
- 1978-06-23 JP JP53076927A patent/JPS6051517B2/ja not_active Expired
- 1978-06-23 IT IT24927/78A patent/IT1097273B/it active
- 1978-06-23 CA CA306,086A patent/CA1103652A/en not_active Expired
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SU390096A1 (ru) * | 1971-08-30 | 1973-07-11 | Способ получения замещенных эфиров ортокремниевой кислоты | |
DE2513476A1 (de) * | 1974-03-27 | 1975-10-02 | Castrol Ltd | Hydraulische fluessigkeitszubereitungen |
DE2652719A1 (de) * | 1975-11-21 | 1977-05-26 | Castrol Ltd | Silanderivate und sie enthaltende hydraulikfluessigkeiten |
Also Published As
Publication number | Publication date |
---|---|
IT1097273B (it) | 1985-08-31 |
AU3741678A (en) | 1980-01-03 |
GB1595701A (en) | 1981-08-19 |
CA1103652A (en) | 1981-06-23 |
FR2395308A1 (fr) | 1979-01-19 |
SE425608B (sv) | 1982-10-18 |
IT7824927A0 (it) | 1978-06-23 |
SE7807146L (sv) | 1978-12-25 |
BE868422A (fr) | 1978-10-16 |
JPS5417386A (en) | 1979-02-08 |
JPS6051517B2 (ja) | 1985-11-14 |
ZA783614B (en) | 1980-03-26 |
FR2395308B1 (sv) | 1984-12-28 |
AU524142B2 (en) | 1982-09-02 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
8110 | Request for examination paragraph 44 | ||
8128 | New person/name/address of the agent |
Representative=s name: SCHWABE, H., DIPL.-ING. SANDMAIR, K., DIPL.-CHEM. |
|
8131 | Rejection |