SE502764C2 - Användning av en alkoxilerad alkanolamin tillsammans med en alkoxilerad alkohol som friktionsreducerande medel - Google Patents

Användning av en alkoxilerad alkanolamin tillsammans med en alkoxilerad alkohol som friktionsreducerande medel

Info

Publication number: SE502764C2
Authority: SE; Sweden
Prior art keywords: alkoxylated; use according; alkanolamide; carbon atoms; water
Prior art date: 1995-01-19

Application number

SE9500159A

Other languages

English (en)

Swedish (sv)

Other versions

SE9500159D0 (sv

SE9500159L (sv

Inventor

Martin Hellsten

Ian Harwigsson

Original Assignee

Akzo Nobel Nv

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.)

1995-01-19

Filing date

1995-01-19

Publication date

1996-01-08

1995-01-19 Application filed by Akzo Nobel Nv filed Critical Akzo Nobel Nv

1995-01-19 Priority to SE9500159A priority Critical patent/SE502764C2/sv

1995-01-19 Publication of SE9500159D0 publication Critical patent/SE9500159D0/xx

1996-01-08 Publication of SE9500159L publication Critical patent/SE9500159L/

1996-01-08 Publication of SE502764C2 publication Critical patent/SE502764C2/sv

1996-01-09 Priority to EP96900586A priority patent/EP0804516B1/de

1996-01-09 Priority to US08/875,186 priority patent/US5979479A/en

1996-01-09 Priority to DE69600479T priority patent/DE69600479T2/de

1996-01-09 Priority to CA002206985A priority patent/CA2206985C/en

1996-01-09 Priority to PCT/EP1996/000155 priority patent/WO1996022341A1/en

1996-01-09 Priority to ES96900586T priority patent/ES2120282T3/es

1996-01-09 Priority to JP8522032A priority patent/JPH11500764A/ja

Links

LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title claims abstract description 23
239000003638 chemical reducing agent Substances 0.000 title 1
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 13
125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 13
239000000203 mixture Substances 0.000 claims abstract description 12
125000005529 alkyleneoxy group Chemical group 0.000 claims abstract description 9
239000007787 solid Substances 0.000 claims abstract 2
-1 ethyleneoxy groups Chemical group 0.000 claims description 5
229920006395 saturated elastomer Polymers 0.000 claims description 5
238000002425 crystallisation Methods 0.000 claims description 2
230000008025 crystallization Effects 0.000 claims description 2
229930195734 saturated hydrocarbon Natural products 0.000 claims description 2
229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 2
239000012530 fluid Substances 0.000 claims 2
239000002826 coolant Substances 0.000 claims 1
239000007788 liquid Substances 0.000 abstract description 4
125000004429 atom Chemical group 0.000 abstract 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 27
239000004094 surface-active agent Substances 0.000 description 10
239000000243 solution Substances 0.000 description 9
238000012360 testing method Methods 0.000 description 9
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 6
235000014113 dietary fatty acids Nutrition 0.000 description 6
230000000694 effects Effects 0.000 description 6
229930195729 fatty acid Natural products 0.000 description 6
239000000194 fatty acid Substances 0.000 description 6
239000000047 product Substances 0.000 description 6
150000004665 fatty acids Chemical class 0.000 description 5
230000001603 reducing effect Effects 0.000 description 5
POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 4
239000008233 hard water Substances 0.000 description 4
239000012085 test solution Substances 0.000 description 4
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 3
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 3
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 3
239000005642 Oleic acid Substances 0.000 description 3
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 3
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
150000001298 alcohols Chemical class 0.000 description 3
125000002947 alkylene group Chemical group 0.000 description 3
238000005260 corrosion Methods 0.000 description 3
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 3
238000000034 method Methods 0.000 description 3
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 3
150000003512 tertiary amines Chemical class 0.000 description 3
244000188595 Brassica sinapistrum Species 0.000 description 2
235000004977 Brassica sinapistrum Nutrition 0.000 description 2
239000005639 Lauric acid Substances 0.000 description 2
235000021355 Stearic acid Nutrition 0.000 description 2
239000000654 additive Substances 0.000 description 2
125000000217 alkyl group Chemical group 0.000 description 2
DTOSIQBPPRVQHS-PDBXOOCHSA-N alpha-linolenic acid Chemical compound CC\C=C/C\C=C/C\C=C/CCCCCCCC(O)=O DTOSIQBPPRVQHS-PDBXOOCHSA-N 0.000 description 2
235000020661 alpha-linolenic acid Nutrition 0.000 description 2
239000007864 aqueous solution Substances 0.000 description 2
150000001735 carboxylic acids Chemical class 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
238000001816 cooling Methods 0.000 description 2
230000007797 corrosion Effects 0.000 description 2
230000008021 deposition Effects 0.000 description 2
239000003792 electrolyte Substances 0.000 description 2
238000007046 ethoxylation reaction Methods 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
231100000086 high toxicity Toxicity 0.000 description 2
230000002209 hydrophobic effect Effects 0.000 description 2
239000003112 inhibitor Substances 0.000 description 2
229960004488 linolenic acid Drugs 0.000 description 2
KQQKGWQCNNTQJW-UHFFFAOYSA-N linolenic acid Natural products CC=CCCC=CCC=CCCCCCCCC(O)=O KQQKGWQCNNTQJW-UHFFFAOYSA-N 0.000 description 2
238000005259 measurement Methods 0.000 description 2
QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 2
238000005086 pumping Methods 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
239000008117 stearic acid Substances 0.000 description 2
238000003756 stirring Methods 0.000 description 2
GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 1
RXYPXQSKLGGKOL-UHFFFAOYSA-N 1,4-dimethylpiperazine Chemical compound CN1CCN(C)CC1 RXYPXQSKLGGKOL-UHFFFAOYSA-N 0.000 description 1
NFDXQGNDWIPXQL-UHFFFAOYSA-N 1-cyclooctyldiazocane Chemical compound C1CCCCCCC1N1NCCCCCC1 NFDXQGNDWIPXQL-UHFFFAOYSA-N 0.000 description 1
OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical class CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
OYHQOLUKZRVURQ-HZJYTTRNSA-N Linoleic acid Chemical compound CCCCC\C=C/C\C=C/CCCCCCCC(O)=O OYHQOLUKZRVURQ-HZJYTTRNSA-N 0.000 description 1
KWYHDKDOAIKMQN-UHFFFAOYSA-N N,N,N',N'-tetramethylethylenediamine Chemical compound CN(C)CCN(C)C KWYHDKDOAIKMQN-UHFFFAOYSA-N 0.000 description 1
235000021314 Palmitic acid Nutrition 0.000 description 1
239000004809 Teflon Substances 0.000 description 1
229920006362 Teflon® Polymers 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
125000005211 alkyl trimethyl ammonium group Chemical group 0.000 description 1
230000002862 amidating effect Effects 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
238000007098 aminolysis reaction Methods 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
239000007798 antifreeze agent Substances 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000000498 cooling water Substances 0.000 description 1
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
239000012973 diazabicyclooctane Substances 0.000 description 1
239000012971 dimethylpiperazine Substances 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000012467 final product Substances 0.000 description 1
239000013505 freshwater Substances 0.000 description 1
239000011521 glass Substances 0.000 description 1
239000003673 groundwater Substances 0.000 description 1
238000007037 hydroformylation reaction Methods 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
239000011630 iodine Substances 0.000 description 1
235000020778 linoleic acid Nutrition 0.000 description 1
OYHQOLUKZRVURQ-IXWMQOLASA-N linoleic acid Natural products CCCCC\C=C/C\C=C\CCCCCCCC(O)=O OYHQOLUKZRVURQ-IXWMQOLASA-N 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
239000000693 micelle Substances 0.000 description 1
UQKAOOAFEFCDGT-UHFFFAOYSA-N n,n-dimethyloctan-1-amine Chemical compound CCCCCCCCN(C)C UQKAOOAFEFCDGT-UHFFFAOYSA-N 0.000 description 1
WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
229940055577 oleyl alcohol Drugs 0.000 description 1
XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
238000010992 reflux Methods 0.000 description 1
YGSDEFSMJLZEOE-UHFFFAOYSA-M salicylate Chemical compound OC1=CC=CC=C1C([O-])=O YGSDEFSMJLZEOE-UHFFFAOYSA-M 0.000 description 1
229960001860 salicylate Drugs 0.000 description 1
235000010344 sodium nitrate Nutrition 0.000 description 1
235000010288 sodium nitrite Nutrition 0.000 description 1
239000002904 solvent Substances 0.000 description 1
230000000087 stabilizing effect Effects 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
238000012546 transfer Methods 0.000 description 1
IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 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
- C10M173/00—Lubricating compositions containing more than 10% water
- C10M173/02—Lubricating compositions containing more than 10% water not containing mineral or fatty oils
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- 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
- 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
- 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
- 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
- C10M2209/108—Polyethers, i.e. containing di- or higher polyoxyalkylene groups etherified
- 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
- C10M2215/00—Organic non-macromolecular compounds containing nitrogen as ingredients in lubricant Compositions
- C10M2215/08—Amides [having hydrocarbon substituents containing less than thirty carbon atoms]
- C10M2215/082—Amides [having hydrocarbon substituents containing less than thirty carbon atoms] containing hydroxyl groups; Alkoxylated derivatives
- 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
- C10N2030/06—Oiliness; Film-strength; Anti-wear; Resistance to extreme pressure
- 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
- C10N2060/00—Chemical after-treatment of the constituents of the lubricating composition
- C10N2060/06—Chemical after-treatment of the constituents of the lubricating composition by epoxydes or oxyalkylation reactions
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T137/00—Fluid handling
- Y10T137/0318—Processes
- Y10T137/0391—Affecting flow by the addition of material or energy

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Materials Engineering (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Oil, Petroleum & Natural Gas (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Lubricants (AREA)
Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
Aftertreatments Of Artificial And Natural Stones (AREA)

SE9500159A 1995-01-19 1995-01-19 Användning av en alkoxilerad alkanolamin tillsammans med en alkoxilerad alkohol som friktionsreducerande medel SE502764C2 (sv)

Priority Applications (8)

Application Number	Priority Date	Filing Date	Title
SE9500159A SE502764C2 (sv)	1995-01-19	1995-01-19	Användning av en alkoxilerad alkanolamin tillsammans med en alkoxilerad alkohol som friktionsreducerande medel
EP96900586A EP0804516B1 (de)	1995-01-19	1996-01-09	Verwendung von alkoxyalkanolamid neben alkoxyalalkohol als reibungsreduzierend mittel
US08/875,186 US5979479A (en)	1995-01-19	1996-01-09	Use of alkoxylated alkanolamide together with alkoxylated alcohol as a friction-reducing agent
DE69600479T DE69600479T2 (de)	1995-01-19	1996-01-09	Verwendung von alkoxyalkanolamid neben alkoxyalalkohol als reibungsreduzierend mittel
CA002206985A CA2206985C (en)	1995-01-19	1996-01-09	Use of alkoxylated alkanolamide together with alkoxylated alcohol as a friction-reducing agent
PCT/EP1996/000155 WO1996022341A1 (en)	1995-01-19	1996-01-09	Use of alkoxylated alkanolamide together with alkoxylated alcohol as a friction-reducing agent
ES96900586T ES2120282T3 (es)	1995-01-19	1996-01-09	Uso de alcanolamida alcoxilada junto con alcohol alcoxilado como agente reductor de la friccion.
JP8522032A JPH11500764A (ja)	1995-01-19	1996-01-09	アルコキシル化アルコールと併用したアルコキシル化アルカノールアミドの摩擦低減剤としての使用

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
SE9500159A SE502764C2 (sv)	1995-01-19	1995-01-19	Användning av en alkoxilerad alkanolamin tillsammans med en alkoxilerad alkohol som friktionsreducerande medel

Publications (3)

Publication Number	Publication Date
SE9500159D0 SE9500159D0 (sv)	1995-01-19
SE9500159L SE9500159L (sv)	1996-01-08
SE502764C2 true SE502764C2 (sv)	1996-01-08

Family

ID=20396864

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SE9500159A SE502764C2 (sv)	1995-01-19	1995-01-19	Användning av en alkoxilerad alkanolamin tillsammans med en alkoxilerad alkohol som friktionsreducerande medel

Country Status (8)

Country	Link
US (1)	US5979479A (de)
EP (1)	EP0804516B1 (de)
JP (1)	JPH11500764A (de)
CA (1)	CA2206985C (de)
DE (1)	DE69600479T2 (de)
ES (1)	ES2120282T3 (de)
SE (1)	SE502764C2 (de)
WO (1)	WO1996022341A1 (de)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5760199A (en) *	1995-07-13	1998-06-02	Akzo Nobel Nv	Polysaccharide acid amide comprising fatty alkyl group in amide
US6821952B1 (en)	1995-07-20	2004-11-23	Perkinelmer Las, Inc.	Fluorescent vasoactive intestinal peptide (VIP)
KR100455839B1 (ko)	1999-11-26	2004-11-06	제이에프이 엔지니어링 가부시키가이샤	수화물계 축열재 및 그 제조방법, 수화물계 축열재를 이용한 축열장치, 그리고 수화물계 냉열수송매체
US6468956B1 (en) *	2000-05-24	2002-10-22	Huish Detergents, Inc.	Composition containing α-sulfofatty acid ester and hydrotrope and methods of making and using the same
WO2003102474A1 (en) *	2002-05-31	2003-12-11	Jfe Engineering Corporation	Hydrate slurry manufacturing device
US8119585B2 (en) *	2005-11-30	2012-02-21	Huntsman International Llc	Liquid nonionic surfactants for emulsion polymerization and other applications
ES2551739T3 (es) *	2008-07-11	2015-11-23	Basf Se	Composición y método para mejorar el ahorro de combustible de motores de combustión interna con combustible de hidrocarburos
JP7009213B2 (ja) *	2014-10-31	2022-02-10	ビーエーエスエフソシエタス・ヨーロピア	潤滑剤組成物中のアルコキシル化アミド、エステル、および摩耗防止剤

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3961639A (en) *	1973-09-10	1976-06-08	The Curators Of The University Of Missouri	Methods and compositions for reducing the frictional resistance to flow of aqueous liquids
US4379063A (en) *	1981-02-20	1983-04-05	Cincinnati Milacron Inc.	Novel functional fluid
US4427562A (en) *	1982-05-06	1984-01-24	Mobil Oil Corporation	Friction reducers for lubricants and fuels
DD281435A5 (de) *	1984-12-27	1990-08-08	Guben Chemiefaserwerk	Wasserarme praeparation fuer polymerfaeden
DD281434A5 (de) *	1984-12-27	1990-08-08	Guben Chemiefaserwerk	Wasserarme praeparation fuer polymerfaeden
SE467826B (sv) *	1991-01-31	1992-09-21	Berol Nobel Ab	Anvaendning av alkoxilerad alkanolamid som friktionsreducerande medel
DE69422081T2 (de) *	1993-04-19	2000-07-20	Reckitt & Colman Inc., Wayne	Allzweckreinigungsmittelzusammensetzung

1995
- 1995-01-19 SE SE9500159A patent/SE502764C2/sv not_active IP Right Cessation
1996
- 1996-01-09 WO PCT/EP1996/000155 patent/WO1996022341A1/en not_active Ceased
- 1996-01-09 JP JP8522032A patent/JPH11500764A/ja not_active Ceased
- 1996-01-09 US US08/875,186 patent/US5979479A/en not_active Expired - Lifetime
- 1996-01-09 CA CA002206985A patent/CA2206985C/en not_active Expired - Fee Related
- 1996-01-09 ES ES96900586T patent/ES2120282T3/es not_active Expired - Lifetime
- 1996-01-09 EP EP96900586A patent/EP0804516B1/de not_active Expired - Lifetime
- 1996-01-09 DE DE69600479T patent/DE69600479T2/de not_active Expired - Lifetime

Also Published As

Publication number	Publication date
DE69600479D1 (de)	1998-09-03
WO1996022341A1 (en)	1996-07-25
SE9500159D0 (sv)	1995-01-19
CA2206985A1 (en)	1996-07-25
JPH11500764A (ja)	1999-01-19
SE9500159L (sv)	1996-01-08
EP0804516B1 (de)	1998-07-29
EP0804516A1 (de)	1997-11-05
US5979479A (en)	1999-11-09
ES2120282T3 (es)	1998-10-16
CA2206985C (en)	2006-01-03
DE69600479T2 (de)	1998-12-24

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