EP0823494A1 - Lactobionsäureamide enthaltende Korrosionschutzmittel und Korrosions-Inhibitoren - Google Patents
Lactobionsäureamide enthaltende Korrosionschutzmittel und Korrosions-Inhibitoren Download PDFInfo
- Publication number
- EP0823494A1 EP0823494A1 EP97113202A EP97113202A EP0823494A1 EP 0823494 A1 EP0823494 A1 EP 0823494A1 EP 97113202 A EP97113202 A EP 97113202A EP 97113202 A EP97113202 A EP 97113202A EP 0823494 A1 EP0823494 A1 EP 0823494A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- lactobionic acid
- corrosion
- carbon atoms
- agents
- chain length
- 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.)
- Granted
Links
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
- 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
- C10M133/00—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen
- C10M133/02—Lubricating compositions characterised by the additive being an organic non-macromolecular compound containing nitrogen having a carbon chain of less than 30 atoms
- C10M133/16—Amides; Imides
-
- C—CHEMISTRY; METALLURGY
- C23—COATING METALLIC MATERIAL; COATING MATERIAL WITH METALLIC MATERIAL; CHEMICAL SURFACE TREATMENT; DIFFUSION TREATMENT OF METALLIC MATERIAL; COATING BY VACUUM EVAPORATION, BY SPUTTERING, BY ION IMPLANTATION OR BY CHEMICAL VAPOUR DEPOSITION, IN GENERAL; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL
- C23F—NON-MECHANICAL REMOVAL OF METALLIC MATERIAL FROM SURFACE; INHIBITING CORROSION OF METALLIC MATERIAL OR INCRUSTATION IN GENERAL; MULTI-STEP PROCESSES FOR SURFACE TREATMENT OF METALLIC MATERIAL INVOLVING AT LEAST ONE PROCESS PROVIDED FOR IN CLASS C23 AND AT LEAST ONE PROCESS COVERED BY SUBCLASS C21D OR C22F OR CLASS C25
- C23F11/00—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent
- C23F11/08—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids
- C23F11/10—Inhibiting corrosion of metallic material by applying inhibitors to the surface in danger of corrosion or adding them to the corrosive agent in other liquids using organic inhibitors
- C23F11/14—Nitrogen-containing compounds
- C23F11/145—Amides; N-substituted amides
-
- 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
- C10M2201/00—Inorganic compounds or elements as ingredients in lubricant compositions
- C10M2201/02—Water
-
- 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
-
- 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
- C10M2215/082—Amides containing hydroxyl groups; Alkoxylated derivatives
-
- 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
- C10M2215/086—Imides
-
- 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
- C10M2215/12—Partial amides of polycarboxylic acids
-
- 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
- C10M2215/12—Partial amides of polycarboxylic acids
- C10M2215/122—Phtalamic acid
-
- 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
- C10M2215/28—Amides; Imides
-
- 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
- C10N2040/20—Metal working
-
- 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
- C10N2040/20—Metal working
- C10N2040/22—Metal working with essential removal of material, e.g. cutting, grinding or drilling
-
- 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
- C10N2050/01—Emulsions, colloids, or micelles
Definitions
- the invention relates to anti-corrosion agents and corrosion inhibitors, which lactobionic acid N-alkylamides and / or Lactobionic acid alkylamine amides and / or di-lactobionic acid alkyl diamides contain.
- B. Cutting, grinding or drilling become anti-corrosion agents used to protect the machined metal objects from rusting to protect.
- Many of the usual anti-corrosion agents contain sulfur-containing compounds such.
- B. petroleum sulfonates or alkylarylsulfonic acids or nitrogenous ones Connections such as B. secondary one or alkanolamines.
- Sulfur-containing corrosion protection agents have the disadvantage that their active ingredients are slightly sulfur-reducing Microorganisms are modified or broken down.
- amine-containing Corrosion protection agents which are secondary in particular contain one, there is a possibility that they are hazardous to health Nitrosamines are released, which are have previously formed through uncontrolled chemical reactions. So there is still a need for new anti-corrosion agents, which these disadvantages of the prior art Technology does not have.
- the present invention is therefore based on the object new anti-corrosion agents and anti-corrosion agents To provide agents.
- lactobionic acid N-alkylamides whose saturated or unsaturated bound via the amide function Alkyl group a chain length of more than 18, preferably Have 19-30 carbon atoms
- lactobionic acid alkylaminamides, their saturated or unsaturated bound via the amide function Alkyl group has a chain length of 8 to 30 carbon atoms have, and Di-Lactobionklarealkyldiamide, whose about the amide function bonded saturated or unsaturated alkyl group have a chain length of 8 to 30 carbon atoms, have a corrosion-inhibiting effect.
- the invention thus relates to anticorrosive agents or corrosion inhibitors that the compounds mentioned their mixtures contain and the use of the compounds mentioned or mixtures thereof as anti-corrosion agents and / or as an additive in metalworking agents for treatment of metals.
- the treatment of the metals can be done by dipping, Coating, spraying with the agents according to the invention.
- the anti-corrosion agents contain or inhibitors lactobionic acid N-alkylamides, which by the implementation of lactobionic acid or reactive Lactobionic acid derivatives, preferably lactobionic acid lactone, with a primary fatty amine mixture.
- Primary fatty amines are used in the context of the present invention denotes primary amines, which one of the aliphatic radical a fatty acid equivalent aliphatic residue with more than 18 carbon atoms, especially 19 to 30 carbon atoms contain.
- Fettamines can e.g. B. technically obtained from fatty acids by first converting them to their nitriles which are subsequently reduced to amines.
- fatty amine mixtures are made from rapeseed oil or castor oil or a technical fatty acid mixture with a carbon chain length of more than 18 carbon atoms, used.
- lactobionic acid alkylaminamides and / or di-lactobionic acid alkyl diamides by the implementation of lactobionic acid or reactive Lactobionic acid derivatives, preferably lactobionic acid lactone, with an ⁇ , ⁇ -primary diamine or an ⁇ , ⁇ -primary diamine mixture were used.
- ⁇ , ⁇ primary diamines within the scope of the invention, ⁇ , ⁇ primary fatty diamines denotes the aliphatic residue of a fatty acid with 8 contain up to 30 carbon atoms.
- These fat diamonds can e.g. B. technically obtained from fatty acids in known Way to be implemented to the corresponding diamines.
- Prefers are fatty diamines or their mixtures that are made from natural occurring or technical fatty acid mixtures obtained were used. The proportion of unsaturated fatty diamines fluctuates between approx. 5 and 85% by weight.
- the corrosion protection agent according to the invention preferably contains the lactobionic acid N-alkylamides and / or the lactobionic acid alkylaminamides and / or the di-lactobionic acid alkyl diamides in the form of an aqueous solution.
- the aqueous solutions can be used alone or in a mixture with other compounds used as an anti-corrosion agent or inhibitor will.
- the content of lactobionic acid derivatives, based on the aqueous solution can be the usual for anti-corrosion agents Concentration range, expediently in the concentration range from 0.01 to 20% by weight, e.g. B. in the concentration range from 0.5 to 10% by weight.
- the anti-corrosion agents or inhibitors, the lactobionic acid N-alkylamides and / or lactobionic acid alkylaminamides and / or dilactobionic acid alkyl diamides in an aqueous solution may contain completely clear solutions or, in particular in the presence of other compounds, finely divided emulsions be transparent, opaque or milky.
- lactobionic acid derivatives used can also be used for corrosion protection agents usual connections, e.g. B. petroleum sulfonates, Mineral oils or other additives are mixed and used Treatment of metals can be used.
- the lactobionic acid derivatives used according to the invention show emulsifying and corrosion-inhibiting effects in mineral oil-containing, aqueous metalworking agents.
- Another The invention therefore relates to their use in particular water-containing metalworking agents. Under metal working tools are all common for metalworking Liquids, especially cooling lubricants, drilling, Cutting and grinding oils, rust removal, paint stripping and passivation agents Understood. It is therefore possible to use metalworking emulsions to produce which contain a high level of water, without rusting.
- the corrosion protection used is characterized by good corrosion protection Lactobionic acid derivatives thanks to excellent skin tolerance and high biodegradability.
- lactobionic acid derivatives The corrosion-inhibiting effect of lactobionic acid derivatives was by means of the chips / filter paper method according to the DIN 51360, part 2, determined.
- the anti-corrosion properties were determined in accordance with the DIN standard 51360, part 2.
- Gray cast iron chips (material DIN 1691-GG30 of about 5 mm x 5 mm in size) were washed with petroleum ether, sieved through a wire sieve and dried at about 105 ° C. in a drying cabinet. After drying, it was avoided to touch the chips by hand.
- a round filter made of filter paper (diameter 40 mm) was placed in a Petri dish and evenly sprinkled with 2 g ( ⁇ 0.1 g) of the dried chips. The chips were then uniformly wetted with 2 ml of the solution to be examined using a full pipette. The lid of the Petri dish was put on and the Petri dish was left to stand for 2 hours at room temperature.
- the chips were removed from the round filter, the round filter rinsed under running water, swirled in acetone for about 5 seconds and dried at room temperature.
- the degree of corrosion of the corrosion marks on the round filter was determined by visual inspection.
- the degree of corrosion determined for the anticorrosive agents according to the invention is given in the table below.
- a test was only carried out with pure tap water without any additional additives. The corrosion protection effect for a 3% aqueous solution of lactobiontetracosanamide, lactobion-12-aminododecanamide and di-lactobiondodecane-1,12-diamide was determined in each case with tap water.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Lubricants (AREA)
Abstract
Description
In eine Petri-Schale wurde ein Rundfilter aus Filtrierpapier (Durchmesser 40 mm) gelegt und mit 2 g (± 0,1 g) der getrockneten Späne gleichmäßig bestreut. Anschließend wurden die Späne mit 2 ml der zu untersuchenden Lösung mittels einer Vollpipette gleichmäßig benetzt. Es wurde der Deckel der Petri-Schale aufgelegt und die Petri-Schale für 2 Stunden bei Raumtemperatur stehengelassen. Dann wurden die Späne vom Rundfilter entfernt, das Rundfilter unter fließendem Wasser abgespült, in Aceton etwa für 5 Sekunden geschwenkt und bei Raumtemperatur getrocknet. Sofort anschließend an das Reinigen und Trocknen des Rundfilters wurde der Korrosionsgrad der Korrosionsabzeichnungen auf dem Rundfilter durch Sichtprüfung festgestellt. In der nachfolgenden Tabelle wird der ermittelte Korrosionsgrad für die erfindungsgemäßen Korrosionsschutzmittel angegeben. Zur besseren Beurteilung wurde ein Versuch nur mit reinem Leitungswasser ohne weiteren Zusatz durchgeführt. Es wurde jeweils die Korrosionsschutzwirkung für eine mit Leitungswasser angesetzte 3%ige wäßrige Lösung von Lactobiontetracosanamid, Lactobion-12-aminododecanamid und Di-Lactobiondodecan-1,12-diamid ermittelt.
Korrosionsgrad | |
Wasser | starke Korrosion (Korrosionsgrad IV) |
Lactobiontetracosanamid (3 Gew.-% in H2O) | keine Korrosion (Korrosionsgrad 0) |
Lactobion-12-aminododecanamid (3 Gew.-% in H2O) | Spuren von Korrosion (Korrosionsgrad 0-I) |
Di-Lactobiondodecan-1,12-diamid (3 Gew.-% in H2O) | keine Korrosion (Korrosionsgrad 0) |
Claims (6)
- Korrosionsschutzmittel oder Korrosionsinhibitor, enthaltend Lactobionsäure-N-alkylamide mit über die Amidfunktion gebundenen gesättigten oder teilweise ungesättigten Alkylresten mit einer Kettenlänge von mehr als 18 Kohlenstoffatomen und/oder Lactobionsäurealkylaminamide mit über die Amidfunktion gebundenen gesättigten oder teilweise ungesättigen Alkylresten mit einer Kettenlänge von 8 bis 30 Kohlenstoffatomen und/oder Di-Lactobionsäurealkyldiamide mit über die Amidfunktion gebundenen gesättigten oder teilweise ungesättigten Alkylresten mit einer Kettenlänge von 8 bis 30 Kohlenstoffatomen.
- Korrosionschutzmittel nach Anspruch 1, dadurch gekennzeichnet, daß es Lactobionsäure-N-alkylamide und/oder Lactobionsäurealkylaminamide und/oder Di-Lactobionsäurealkyldiamide in einer Menge von 0,01 bis 20 Gew.-%, vorzugsweise 0,5 bis 10 Gew.-%, enthält.
- Verwendung eines Korrosionsschutzmittels oder Korrosionsinhibitors gemäß Anspruch 1 und 2 als Additiv in Metallbearbeitungsmitteln.
- Verwendung von Lactobionsäure-N-alkylamiden mit über die Amidfunktion gebundenen gesättigten oder teilweise ungesättigten Alkylresten mit einer Kettenlänge von mehr als 18, vorzugsweise 19 bis 30 Kohlenstoffatomen und/oder Lactobionsäurealkylaminamide und /oder Di-Lactobionsäurealkyldiamide in Korrosionsschutzmitteln und/oder Metallbearbeitungsmitteln.
- Verfahren zur Metallbehandlung unter Verwendung von Lactobionsäure-N-alkylamiden als Korrosionsschutzmittel und/oder als Additiv in Metallbearbeitungsmitteln, wobei die Metalle mit einer Mischung die Lactobionsäure-N-alkylamide mit über die Amidfunktion gebundenen gesättigten oder teilweise ungesättigten Alkylresten mit einer Kettenlänge von mehr als 18 Kohlenstoffatomen und/oder Lactobionsäurealkylaminamide mit über die Amidfunktion gebundenen gesättigten oder teilweise ungesättigten Alkylresten mit einer Kettenlänge von 8 bis 30 Kohlenstoffatomen und/oder Di-Lactobionsäurealkyldiamide mit über die Amidfunktion gebundenen gesättigten oder teilweise ungesättigten Alkylresten mit einer Kettenlänge von 8 bis 30 Kohlenstoffatomen enthält oder daraus besteht, behandelt werden.
- Verfahren zur Behandlung der Metalle nach Anspruch 1, wobei die Metalle mit einer Mischung die Lactobionsäure-N-alkylamide und/oder Lactobionsäurealkylaminamide und/oder Di-Lactobionsäurealkyldiamide in einer Menge von 0,01 bis 20 Gew.-%, vorzugsweise 0,5 bis 10 Gew.-%, enthält, behandelt werden.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19631959 | 1996-08-08 | ||
DE19631959A DE19631959A1 (de) | 1996-08-08 | 1996-08-08 | Lactobionsäureamide enthaltende Korrosionsschutzmittel und Korrosions-Inhibitoren |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0823494A1 true EP0823494A1 (de) | 1998-02-11 |
EP0823494B1 EP0823494B1 (de) | 1999-12-29 |
Family
ID=7802080
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP97113202A Expired - Lifetime EP0823494B1 (de) | 1996-08-08 | 1997-07-31 | Lactobionsäureamide enthaltende Korrosionschutzmittel und Korrosions-Inhibitoren |
Country Status (4)
Country | Link |
---|---|
US (1) | US5795851A (de) |
EP (1) | EP0823494B1 (de) |
AT (1) | ATE188263T1 (de) |
DE (2) | DE19631959A1 (de) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6846788B2 (en) | 2001-06-07 | 2005-01-25 | Ecolab Inc. | Methods for removing silver-oxide |
US8136236B2 (en) * | 2009-09-15 | 2012-03-20 | John Mezzalingua Associates, Inc. | Method for manufacturing a coaxial cable |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2752334A (en) * | 1952-03-01 | 1956-06-26 | Nat Dairy Res Lab Inc | Nu-substituted lactobionamides |
EP0541467A2 (de) * | 1991-11-05 | 1993-05-12 | Stepan Europe | Alkyldiamide mit zwei Zucker-Gruppen als amphiphilische Verbindungen |
EP0550278A1 (de) * | 1991-12-31 | 1993-07-07 | Unilever Plc | Nichtionische Glykolipidtenside enthaltende Waschmittelzusammensetzungen |
EP0550106A1 (de) * | 1991-12-31 | 1993-07-07 | Unilever N.V. | Verfahren zur Herstellung von N-substituierten Aldonamiden |
EP0569869A1 (de) * | 1992-05-11 | 1993-11-18 | Solvay Deutschland GmbH | Lactobionsäureamidzusammensetzungen und deren Verwendung |
US5401839A (en) * | 1993-03-23 | 1995-03-28 | Lever Brothers Company, Division Of Conopco, Inc. | Process of preparing N-substituted aldonamides having improved color and color stability |
EP0688781A1 (de) * | 1994-06-17 | 1995-12-27 | Kodak Limited | Nichtionische oberflächenaktive Verbindungen |
EP0726335A1 (de) * | 1995-02-13 | 1996-08-14 | Solvay Deutschland GmbH | Lactobionsäureamid enthaltende Korrosionsschutzmittel |
EP0748813A1 (de) * | 1995-06-15 | 1996-12-18 | Akzo Nobel N.V. | Verfahren zur Herstellung von N-substituiertem Aldonamid |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5336765A (en) * | 1991-12-31 | 1994-08-09 | Lever Brothers Company, Division Of Conopco, Inc. | Process of preparing N-substituted aldobionamides |
GB9424444D0 (en) * | 1994-12-02 | 1995-01-18 | Unilever Plc | Detergent compositions |
-
1996
- 1996-08-08 DE DE19631959A patent/DE19631959A1/de not_active Withdrawn
-
1997
- 1997-07-31 AT AT97113202T patent/ATE188263T1/de not_active IP Right Cessation
- 1997-07-31 DE DE59700922T patent/DE59700922D1/de not_active Expired - Fee Related
- 1997-07-31 EP EP97113202A patent/EP0823494B1/de not_active Expired - Lifetime
- 1997-08-08 US US08/908,809 patent/US5795851A/en not_active Expired - Fee Related
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2752334A (en) * | 1952-03-01 | 1956-06-26 | Nat Dairy Res Lab Inc | Nu-substituted lactobionamides |
EP0541467A2 (de) * | 1991-11-05 | 1993-05-12 | Stepan Europe | Alkyldiamide mit zwei Zucker-Gruppen als amphiphilische Verbindungen |
EP0550278A1 (de) * | 1991-12-31 | 1993-07-07 | Unilever Plc | Nichtionische Glykolipidtenside enthaltende Waschmittelzusammensetzungen |
EP0550106A1 (de) * | 1991-12-31 | 1993-07-07 | Unilever N.V. | Verfahren zur Herstellung von N-substituierten Aldonamiden |
EP0569869A1 (de) * | 1992-05-11 | 1993-11-18 | Solvay Deutschland GmbH | Lactobionsäureamidzusammensetzungen und deren Verwendung |
US5401839A (en) * | 1993-03-23 | 1995-03-28 | Lever Brothers Company, Division Of Conopco, Inc. | Process of preparing N-substituted aldonamides having improved color and color stability |
EP0688781A1 (de) * | 1994-06-17 | 1995-12-27 | Kodak Limited | Nichtionische oberflächenaktive Verbindungen |
EP0726335A1 (de) * | 1995-02-13 | 1996-08-14 | Solvay Deutschland GmbH | Lactobionsäureamid enthaltende Korrosionsschutzmittel |
EP0748813A1 (de) * | 1995-06-15 | 1996-12-18 | Akzo Nobel N.V. | Verfahren zur Herstellung von N-substituiertem Aldonamid |
Also Published As
Publication number | Publication date |
---|---|
ATE188263T1 (de) | 2000-01-15 |
US5795851A (en) | 1998-08-18 |
DE59700922D1 (de) | 2000-02-03 |
EP0823494B1 (de) | 1999-12-29 |
DE19631959A1 (de) | 1998-02-12 |
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