CH618731A5 - - Google Patents

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Publication number: CH618731A5
Authority: CH; Switzerland
Prior art keywords: group; groups; ester; radicals; formula
Prior art date: 1974-07-12

Application number

CH911175A

Other languages

German (de)

English (en)

Inventor

Herbert Frank Askew

Colin John Harrington

Terry John Patrick Bridgwater

Original Assignee

Castrol Ltd

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.)

1974-07-12

Filing date

1975-07-11

Publication date

1980-08-15

1975-07-11 Application filed by Castrol Ltd filed Critical Castrol Ltd

1980-08-15 Publication of CH618731A5 publication Critical patent/CH618731A5/de

Links

239000000203 mixture Substances 0.000 claims description 38
150000002148 esters Chemical class 0.000 claims description 37
239000002253 acid Substances 0.000 claims description 25
ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 22
229910052796 boron Inorganic materials 0.000 claims description 22
125000000217 alkyl group Chemical group 0.000 claims description 20
150000001412 amines Chemical class 0.000 claims description 17
150000002905 orthoesters Chemical class 0.000 claims description 17
125000004432 carbon atom Chemical group C* 0.000 claims description 16
239000003921 oil Substances 0.000 claims description 14
235000010338 boric acid Nutrition 0.000 claims description 10
239000002480 mineral oil Substances 0.000 claims description 9
235000010446 mineral oil Nutrition 0.000 claims description 9
125000003710 aryl alkyl group Chemical group 0.000 claims description 8
125000003118 aryl group Chemical group 0.000 claims description 8
125000002947 alkylene group Chemical group 0.000 claims description 7
125000002877 alkyl aryl group Chemical group 0.000 claims description 6
KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 6
239000004327 boric acid Substances 0.000 claims description 6
239000012530 fluid Substances 0.000 claims description 6
239000000314 lubricant Substances 0.000 claims description 6
125000002723 alicyclic group Chemical group 0.000 claims description 4
125000005619 boric acid group Chemical class 0.000 claims description 4
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
230000007062 hydrolysis Effects 0.000 claims description 4
238000006460 hydrolysis reaction Methods 0.000 claims description 4
239000010687 lubricating oil Substances 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 3
150000001875 compounds Chemical class 0.000 claims description 3
230000008021 deposition Effects 0.000 claims description 3
125000005702 oxyalkylene group Chemical group 0.000 claims description 3
229910052698 phosphorus Inorganic materials 0.000 claims description 3
239000011574 phosphorus Substances 0.000 claims description 3
239000004215 Carbon black (E152) Substances 0.000 claims description 2
239000005977 Ethylene Substances 0.000 claims description 2
PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims description 2
125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
229930195733 hydrocarbon Natural products 0.000 claims description 2
150000002430 hydrocarbons Chemical class 0.000 claims description 2
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 2
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 2
150000001733 carboxylic acid esters Chemical class 0.000 claims 1
KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims 1
239000007788 liquid Substances 0.000 description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
-1 glycol ethers Chemical class 0.000 description 10
239000007983 Tris buffer Substances 0.000 description 8
BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 7
QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical compound COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 description 5
239000002199 base oil Substances 0.000 description 4
LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 4
JBNCQQVJICVAHS-UHFFFAOYSA-N 1-[di(tridecoxy)methoxy]tridecane Chemical compound CCCCCCCCCCCCCOC(OCCCCCCCCCCCCC)OCCCCCCCCCCCCC JBNCQQVJICVAHS-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
239000003708 ampul Substances 0.000 description 3
229910052799 carbon Inorganic materials 0.000 description 3
238000001816 cooling Methods 0.000 description 3
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
229920001971 elastomer Polymers 0.000 description 3
229920000768 polyamine Polymers 0.000 description 3
229920001451 polypropylene glycol Polymers 0.000 description 3
150000003141 primary amines Chemical class 0.000 description 3
AAIUWVOMXTVLRG-UHFFFAOYSA-N 8,8-dimethylnonan-1-amine Chemical compound CC(C)(C)CCCCCCCN AAIUWVOMXTVLRG-UHFFFAOYSA-N 0.000 description 2
229920000459 Nitrile rubber Polymers 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
150000007513 acids Chemical class 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
238000009833 condensation Methods 0.000 description 2
230000005494 condensation Effects 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
239000011521 glass Substances 0.000 description 2
238000010438 heat treatment Methods 0.000 description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 2
238000000034 method Methods 0.000 description 2
235000011007 phosphoric acid Nutrition 0.000 description 2
229920001296 polysiloxane Polymers 0.000 description 2
KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 2
HSECWXDHHAMHQA-UHFFFAOYSA-N 2-(2-methoxypropoxy)propan-1-ol;2-[2-(2-methoxypropoxy)propoxy]propan-1-ol Chemical compound COC(C)COC(C)CO.COC(C)COC(C)COC(C)CO HSECWXDHHAMHQA-UHFFFAOYSA-N 0.000 description 1
COBPKKZHLDDMTB-UHFFFAOYSA-N 2-[2-(2-butoxyethoxy)ethoxy]ethanol Chemical compound CCCCOCCOCCOCCO COBPKKZHLDDMTB-UHFFFAOYSA-N 0.000 description 1
LCZVSXRMYJUNFX-UHFFFAOYSA-N 2-[2-(2-hydroxypropoxy)propoxy]propan-1-ol Chemical compound CC(O)COC(C)COC(C)CO LCZVSXRMYJUNFX-UHFFFAOYSA-N 0.000 description 1
POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-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
229910019142 PO4 Inorganic materials 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
150000001555 benzenes Chemical class 0.000 description 1
238000009835 boiling Methods 0.000 description 1
150000001642 boronic acid derivatives Chemical class 0.000 description 1
125000003262 carboxylic acid ester group Chemical class [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 description 1
238000001035 drying Methods 0.000 description 1
125000004185 ester group Chemical group 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 description 1
239000003350 kerosene Substances 0.000 description 1
150000002763 monocarboxylic acids Chemical class 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
150000003016 phosphoric acids Chemical class 0.000 description 1
229920001281 polyalkylene Polymers 0.000 description 1
PDEDQSAFHNADLV-UHFFFAOYSA-M potassium;disodium;dinitrate;nitrite Chemical compound [Na+].[Na+].[K+].[O-]N=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O PDEDQSAFHNADLV-UHFFFAOYSA-M 0.000 description 1
238000000926 separation method Methods 0.000 description 1
239000000243 solution Substances 0.000 description 1
230000008961 swelling Effects 0.000 description 1
ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
VDIBRAAMAUQZOL-UHFFFAOYSA-N tritridecyl borate Chemical compound CCCCCCCCCCCCCOB(OCCCCCCCCCCCCC)OCCCCCCCCCCCCC VDIBRAAMAUQZOL-UHFFFAOYSA-N 0.000 description 1

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- C10M1/00—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants
- C10M1/08—Liquid compositions essentially based on mineral lubricating oils or fatty oils; Their use as lubricants with additives
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
- C10M2207/04—Ethers; Acetals; Ortho-esters; Ortho-carbonates
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- C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
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- C10M2207/283—Esters of polyhydroxy compounds
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- C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
- C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/104—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing two carbon atoms only
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- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
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- C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
- C10M2209/107—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of two or more specified different alkylene oxides covered by groups C10M2209/104 - C10M2209/106
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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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- C10M2215/02—Amines, e.g. polyalkylene polyamines; Quaternary amines
- C10M2215/06—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings
- C10M2215/062—Amines, e.g. polyalkylene polyamines; Quaternary amines having amino groups bound to carbon atoms of six-membered aromatic rings containing hydroxy groups bound to the aromatic ring
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- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
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- C10M2217/00—Organic macromolecular compounds containing nitrogen as ingredients in lubricant compositions
- C10M2217/04—Macromolecular compounds from nitrogen-containing monomers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
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- C10M2223/04—Phosphate esters
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- C10M2223/00—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions
- C10M2223/02—Organic non-macromolecular compounds containing phosphorus as ingredients in lubricant compositions having no phosphorus-to-carbon bonds
- C10M2223/04—Phosphate esters
- C10M2223/042—Metal salts thereof
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- C10M2227/00—Organic non-macromolecular compounds containing atoms of elements not provided for in groups C10M2203/00, C10M2207/00, C10M2211/00, C10M2215/00, C10M2219/00 or C10M2223/00 as ingredients in lubricant compositions
- C10M2227/06—Organic compounds derived from inorganic acids or metal salts
- C10M2227/061—Esters derived from boron
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- C10M2227/06—Organic compounds derived from inorganic acids or metal salts
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- C10M2227/062—Cyclic esters
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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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- C10M2229/02—Unspecified siloxanes; Silicones
- 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
- C10M2229/00—Organic macromolecular compounds containing atoms of elements not provided for in groups C10M2205/00, C10M2209/00, C10M2213/00, C10M2217/00, C10M2221/00 or C10M2225/00 as ingredients in lubricant compositions
- 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
- 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

Landscapes

Chemical & Material Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Engineering & Computer Science (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Lubricants (AREA)

CH911175A 1974-07-12 1975-07-11 CH618731A5 (sv)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
GB31036/74A GB1513881A (en)	1974-07-12	1974-07-12	Hydraulic fluids
GB1311375		1975-03-27

Publications (1)

Publication Number	Publication Date
CH618731A5 true CH618731A5 (sv)	1980-08-15

Family

ID=26249558

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH911175A CH618731A5 (sv)	1974-07-12	1975-07-11

Country Status (17)

Country	Link
US (1)	US4450087A (sv)
JP (1)	JPS6227119B2 (sv)
AR (1)	AR207155A1 (sv)
BE (1)	BE831317A (sv)
BR (1)	BR7504420A (sv)
CA (1)	CA1052368A (sv)
CH (1)	CH618731A5 (sv)
DE (1)	DE2531086A1 (sv)
DK (1)	DK152846C (sv)
FR (1)	FR2277883A1 (sv)
GB (1)	GB1513881A (sv)
IE (1)	IE41422B1 (sv)
IT (1)	IT1039236B (sv)
NL (1)	NL7508329A (sv)
NO (1)	NO142479C (sv)
SE (1)	SE417612B (sv)
ZA (1)	ZA754458B (sv)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1568684A (en) *	1976-01-28	1980-06-04	Castrol Ltd	Hydraulic fluids
JPS5661496A (en) *	1979-10-23	1981-05-26	Asahi Denka Kogyo Kk	Hydraulic fluid composition
JPS60176555A (ja) *	1984-02-23	1985-09-10	Ueno Seiyaku Kk	中華麺の保存方法
US4594378A (en) *	1985-03-25	1986-06-10	The Lubrizol Corporation	Polymeric compositions, oil compositions containing said polymeric compositions, transmission fluids and hydraulic fluids
EP0216909B1 (en) *	1985-04-08	1990-02-28	The Lubrizol Corporation	Lubricating oils comprising boron- and sulfur-containing compositions, and their method of preparation
SE513181C2 (sv) *	1997-12-19	2000-07-24	Akzo Nobel Nv	En ortoesterbaserad tensid, dess tillverkning och användning
JP2001055441A (ja)	1999-06-11	2001-02-27	Toyota Motor Corp	イオン導電性分子、イオン導電体及びイオン導電体の製造方法
WO2002062930A2 (en) *	2001-02-07	2002-08-15	The Lubrizol Corporation	Boron containing lubricating oil composition containing a low level of sulfur and phosphorus
JP3761502B2 (ja) *	2002-08-05	2006-03-29	成勝佐藤	プラスチック成形用機能性薬剤、その用途および使用方法
JP4456817B2 (ja) *	2003-02-03	2010-04-28	本田技研工業株式会社	水溶性金属加工用潤滑剤
US20110167841A1 (en) *	2004-06-04	2011-07-14	Brasscorp Limited	Compositions and methods for injection of sealants and/or drying agents into air conditioning and refrigeration systems
JP5414537B2 (ja)	2007-01-30	2014-02-12	ザルブリゾルコーポレイション	改善されたトランスミッション流体のための分散剤の組み合わせ
KR102158921B1 (ko)	2015-11-11	2020-09-22	에프톤 케미칼 코포레이션	보록신 기반 씰 혼용성 제제

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3125528A (en) *		1964-03-17		Method of lubricating automotive
US2996451A (en) *	1956-04-19	1961-08-15	Ethyl Corp	Liquid hydrocarbon compositions
US3080412A (en) *	1959-03-31	1963-03-05	Dow Chemical Co	Borate esters of glycol monoethers
US3200074A (en) *	1963-05-20	1965-08-10	Texaco Inc	Lubricating compositions containing borate ester-amine complexes
US3637794A (en) *	1967-04-13	1972-01-25	Olin Mathieson	Borate esters prepared by successive reactions of boric acid with glycol monoethers and polyols
NL147779C (sv) *	1969-12-16
US3903006A (en) *	1969-12-16	1975-09-02	Castrol Ltd	Synthetic esters
GB1341901A (en) *	1971-01-21	1973-12-25	Burmah Oil Trading Ltd	Hydraulic fluids

1974
- 1974-07-12 GB GB31036/74A patent/GB1513881A/en not_active Expired
1975
- 1975-01-01 AR ARGB259556A patent/AR207155A1/es active
- 1975-07-11 SE SE7507982A patent/SE417612B/sv not_active IP Right Cessation
- 1975-07-11 BR BR7504420*A patent/BR7504420A/pt unknown
- 1975-07-11 IE IE1549/75A patent/IE41422B1/en unknown
- 1975-07-11 FR FR7521884A patent/FR2277883A1/fr active Granted
- 1975-07-11 JP JP50085738A patent/JPS6227119B2/ja not_active Expired
- 1975-07-11 NO NO752498A patent/NO142479C/no unknown
- 1975-07-11 CH CH911175A patent/CH618731A5/de not_active IP Right Cessation
- 1975-07-11 NL NL7508329A patent/NL7508329A/xx not_active Application Discontinuation
- 1975-07-11 BE BE158255A patent/BE831317A/xx not_active IP Right Cessation
- 1975-07-11 DK DK315575A patent/DK152846C/da not_active IP Right Cessation
- 1975-07-11 DE DE19752531086 patent/DE2531086A1/de active Granted
- 1975-07-11 IT IT25345/75A patent/IT1039236B/it active
- 1975-07-11 CA CA231,285A patent/CA1052368A/en not_active Expired
- 1975-07-11 ZA ZA754458A patent/ZA754458B/xx unknown
1983
- 1983-03-18 US US06/476,561 patent/US4450087A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
DK152846B (da)	1988-05-24
IT1039236B (it)	1979-12-10
US4450087A (en)	1984-05-22
FR2277883A1 (fr)	1976-02-06
NO142479B (no)	1980-05-19
NO142479C (no)	1980-08-27
IE41422B1 (en)	1980-01-02
DE2531086A1 (de)	1976-01-22
GB1513881A (en)	1978-06-14
IE41422L (en)	1976-01-12
NL7508329A (nl)	1976-01-14
ZA754458B (en)	1977-02-23
AU8298675A (en)	1977-01-13
AR207155A1 (es)	1976-09-15
DE2531086C2 (sv)	1992-08-13
JPS5134882A (sv)	1976-03-24
SE417612B (sv)	1981-03-30
DK315575A (da)	1976-01-13
BR7504420A (pt)	1976-07-06
NO752498L (sv)	1976-01-13
SE7507982L (sv)	1976-01-13
BE831317A (fr)	1975-11-03
CA1052368A (en)	1979-04-10
DK152846C (da)	1988-10-24
FR2277883B1 (sv)	1982-03-19
JPS6227119B2 (sv)	1987-06-12

Publication	Publication Date	Title
CH618731A5 (sv)	1980-08-15
DE68901901T2 (de)	1992-12-17	Oelloesliche phosphorhaltige verschleissschutzadditive fuer schmieroele.
DE1771597C3 (de)	1978-10-19	Schmier- und Trennmittel für Giasformen
EP0028789B1 (de)	1983-08-31	Hydraulische Flüssigkeit mit verbesserten Eigenschaften
DE907207C (de)	1954-03-22	Schaumverhindernde Mittel
DE2107095C3 (de)	1982-03-25	Funktionelle Flüsskigkeiten und ihre Verwendung
DE2057196A1 (de)	1971-06-09	Verbesserte Schmiermittelmassen
DE2457097C3 (de)	1983-12-22	Hydraulische Flüssigkeit
DE1148682B (de)	1963-05-16	Emulgierbares Schmiermittelkonzentrat und Schmiermittel fuer die Glasverformung
DE1594393B2 (sv)	1974-08-01
DE1946432A1 (de)	1970-05-06	Methylalkylsilikon-Schmierfettzusammensetzung und Verfahren zu seiner Herstellung
DE3138835A1 (de)	1983-04-14	Verfahren zur herstellung von gegebenenfalls polymeren organosilanestern mit polyolen
DE1594530B2 (de)	1974-09-19	Hydraulische Flüssigkeiten
DE2532228C3 (de)	1986-07-31	Hydraulische Flüssigkeiten
EP0380782B1 (de)	1993-06-09	Flüssige Enthalogenierungsmittel
DE2046368B2 (de)	1981-07-09	Zusatz für Schmiermittelmischungen
EP0013925B1 (de)	1983-01-19	Bremsflüssigkeit für Motorfahrzeuge
DE2202732C3 (de)	1984-02-23	Hydraulische Flüssigkeiten
DE2062034A1 (sv)	1971-07-01
EP0011730B1 (de)	1982-10-06	Bremsflüssigkeiten mit konservierender Wirkung mit einem Gehalt an Ölsäure
AT204670B (de)	1959-08-10	Kraftstoff-Schmiermittel-Gemisch und Schmierölmischung
DE853487C (de)	1952-10-23	Hydraulische Fluessigkeiten
DE2437936A1 (de)	1976-02-19	Ortho-borsaeureester und deren verwendung als bestandteil von bremsfluessigkeiten
DD296284A5 (de)	1991-11-28	Verfahren zur herstellung borhaltiger polymerer
DE2948849C2 (sv)	1988-06-30

Legal Events

Date	Code	Title	Description
1995-03-31	PL	Patent ceased
2024-10-31	PL	Patent ceased