EP0561842A1 - Teppichreinigungsmittel. - Google Patents
Teppichreinigungsmittel.Info
- Publication number
- EP0561842A1 EP0561842A1 EP91920831A EP91920831A EP0561842A1 EP 0561842 A1 EP0561842 A1 EP 0561842A1 EP 91920831 A EP91920831 A EP 91920831A EP 91920831 A EP91920831 A EP 91920831A EP 0561842 A1 EP0561842 A1 EP 0561842A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- weight
- cleaning
- oleic acid
- textile
- solution
- 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
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0026—Low foaming or foam regulating compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/28—Sulfonation products derived from fatty acids or their derivatives, e.g. esters, amides
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0031—Carpet, upholstery, fur or leather cleansers
Definitions
- the invention relates to a low foaming Teppiehreim 'restriction means and a method for the purification of large-area textile surfaces under Ver ⁇ application of such an agent.
- powdered products are often used, which are sprinkled on the carpets and suctioned off after a mechanical treatment.
- a more intensive cleaning is carried out with aqueous cleaning liquors which are applied to the carpets and are removed from the carpets together with the dirt after a certain exposure time, if appropriate using mechanics.
- a cleaning solution is first sprayed onto the carpets and worked into the carpets with the aid of brushes or similar mechanisms before the carpets are suctioned off again from the cleaning solution or the foam which is caused by the mechanics has arisen, are freed, and a liquid extraction process in which the cleaning agent solution is sprayed onto the carpet via a pressure nozzle in order to be sucked off the carpet immediately afterwards by a suction nozzle located a few centimeters behind the pressure nozzle bar.
- Such devices which have recently been offered for carpet cleaning in the household, essentially consist of a storage container which contains a generally aqueous surfactant solution through a hose is sprayed onto the textile surface to be cleaned via a nozzle and penetrates more or less deeply into the material to be cleaned.
- the cleaning effect can be increased by a brush attached to the end of the hose near the nozzle.
- a suction device which conveys the used cleaning agent solution into a dirty water tank. So that the sucked-in dirty water does not overflow, there is a float contact in the dirty water tank which switches off the pumps for spraying the cleaning agent solution and sucking in the dirty water when the tank is full, so that the dirty water tank can be emptied.
- the task was therefore to develop a low-foaming cleaning agent for carpet cleaning, which is particularly suitable for use in spray extraction cleaning devices.
- the invention therefore also relates to carpet cleaning agents which contain the salts mentioned together with other active cleaning agents.
- the carpet cleaning agents according to the invention are essentially aqueous concentrates which can be used as such or after dilution with water for textile cleaning. They are characterized by good cleaning performance with extremely low foaming even under high mechanical stress.
- Another object of the invention is a process for cleaning large-area textiles, in particular carpets, with the aid of aqueous solutions containing surfactants, in which the textile is impregnated with such a solution and, if appropriate, mechanically treated, and the solution is then immediately suctioned off is largely removed from the textile and the textile is dried if desired, the process being characterized in that a cleaning solution is used which has been prepared by diluting a carpet cleaning agent which contains an alkali metal or ammonium salt of sulfonated oleic acid as the surfactant component.
- the expression “immediately after” results from the distance between the pressure and suction nozzles, which is normally about 1 cm to 15 cm, and the speed, normally 0.5 cm per second to 50 cm per second, with which the nozzle strips are moved over the textile to be cleaned, and means a period of generally less than 2 seconds, in particular less than 1 second.
- the oleic acid derivatives used according to the invention as the surfactant component are neutralized sulfonation products. These are known, for example, from British Patent GB 1278421 and German Laid-Open Specification 3926 344. As described there, they can be reacted with oleic acid or technical mixtures which contain them, as are obtainable from renewable raw materials, in particular beef tallow, sunflower oil, rapeseed oil or olive oil, with gaseous sulfur trioxide and subsequent hydrolysis and neutralization with aqueous bases, in particular solutions of alkali or ammonium hydroxides.
- the mixtures obtained from alkenylsulfonic acid-carboxylic acid salts and hydroxyalkylsulfonic acid-carboxylic acid salts can, depending on the origin of the technical oleic acid starting material, comprise more or less large proportions of salts of saturated fatty acids and sulfates. Formation products of other unsaturated fatty acids which generally do not impair the advantageous action of the sulfonated oleic acid in the cleaning agents according to the invention.
- Such sulfonated oleic acid salts are preferably present in the carpet cleaning agents according to the invention in amounts of 10% by weight to 80% by weight, in particular 15% by weight to 50% by weight.
- the agents according to the invention can contain other surfactants which are low in foams as far as possible and which are primarily nonionic and, preferably, anionic surfactants, even if in individual cases ⁇ set of other types of surfactants may be appropriate.
- Suitable anionic surfactants are in particular those of the sulfate or sulfonate type, but other types such as soaps, long-chain N-acyl sarcosinates, salts of fatty acid cyanamides or salts of ether carboxylic acids, such as those obtained from long-chain alkyl or alkylphenyl polyglycol ethers and chloroacetic acid, can also be used ⁇ are used.
- the anionic surfactants are preferably used in the form of the sodium salts.
- Particularly suitable surfactants of the sulfate type are the sulfuric acid monoesters of long-chain primary alcohols of natural and synthetic origin with 10 to 20 C atoms, that is to say of fatty alcohols, such as, for example, coconut fatty alcohols, tallow fatty alcohols, oleyl alcohol, or the C ⁇ o to C20-0xoa - OK _- o _ e ⁇ and those of secondary alcohols of these chain lengths.
- fatty alcohols such as, for example, coconut fatty alcohols, tallow fatty alcohols, oleyl alcohol, or the C ⁇ o to C20-0xoa - OK _- o _ e ⁇ and those of secondary alcohols of these chain lengths.
- the sulfation products of the reaction products of C4 to C12 alcohols alkoxylated with 1 to 12 moles of ethylene oxide with 1,2-epoxyalkanes as are obtainable, for example, by the process described in German Offenlegungsschrift DE 3723354
- the sulfuric acid monoesters of the aliphatic primary or secondary alcohols alkoxylated with 1 to 6 mol of ethylene oxide come into consideration.
- Usable surfactants of the sulfonate type are the alkanesulfonates which can be obtained from C12- to Cig-alkanes by sulfochlorination or sulfoxidation and subsequent hydrolysis or neutralization, and also the olefin sulfonates as obtained from long-chain monoolefins with an end or internal double bond by sulfonation with gaseous sulfur trioxide and subsequent alkaline or acidic hydrolysis of the sulfonation products.
- Suitable nonionic surfactants for the process according to the invention are, in particular, addition products of 1 to 30, preferably 3 to 15, moles of ethylene oxide with 1 mole of a compound having 10 to 20 carbon atoms from the group of alcohols, alkylphenols, carboxylic acids and carboxamides.
- the addition products of ethylene oxide and / or propylene oxide onto long-chain primary or secondary alcohols, such as, for example, fatty alcohols or oxo alcohols, are particularly important.
- the well-known high-foaming oligoglycosides of the alcohols mentioned are also suitable.
- Such additional surfactants can be present in the agents according to the invention preferably in amounts not exceeding 40% by weight, in particular from 5% by weight to 20% by weight.
- the carpet cleaning agents according to the invention contain water as the preferred solvent, water-miscible organic solvents can be present in minor amounts. These include, in particular, alcohols with 1 to 4 carbon atoms, glycols with 2 to 4 carbon atoms and the di- and triglycols which can be derived from them and the corresponding glycol ethers.
- Such solvents are, for example, methanol, ethanol, propanol, isopropanol, tert-butanol, ethylene glycol, propylene glycol, butylene glycol, diethylene glycol, triethylene glycol, dipropylene glycol, diethylene glycol monomethyl ether, diethylene glycol monoethyl ether, diethylene glycol monopropyl ether and ethylene glycol butobutylene ether.
- Such solvents are preferably contained in the agents according to the invention not more than 10% by weight, in particular from 1% by weight to 7% by weight.
- the agent according to the invention can contain further auxiliaries customary in carpet cleaning agents. Preservatives, re-soiling agents, inorganic salts, antistatic substances, dye and perfume are particularly mentioned.
- auxiliaries especially those which are present in the cleaning agent in large quantities, preference is given to those which lead to solid residues after drying on the carpet.
- the auxiliaries which are intended to reduce the re-soiling of the carpet are primarily water-soluble or water-dispersible polymers which, after drying, do not lead to films, but instead lead to brittle residues.
- Corresponding polymers of acrylic acid and / or methacrylic acid or their copolymers with other ethylenically unsaturated monomers, for example styrene, are preferably used.
- Such substances which prevent re-soiling are contained in the agents according to the invention in amounts of between 2 and 30% by weight, in particular between 5% by weight and 20% by weight.
- Quaternary ammonium compounds which absorb material onto the textile are usually used as active ingredients which are intended to provide the carpet with an antistatic finish.
- Inorganic salts can also have an antistatic effect on the carpet.
- the content of such antistatic agents in the cleaning agents according to the invention is preferably not more than 1% by weight, in particular from 0.01% by weight to 0.5% by weight.
- the heavy metal complexing agents which can be used in the agents according to the invention are primarily aminopolycarboxylic acids and polyphosphonic acids or their salts, for example nitrilotriacetic acid and hydroxyethane diphosphonic acid.
- Such complexing agents are contained in the cleaning agents according to the invention preferably in amounts not exceeding 10% by weight, in particular from 0.5% by weight to 2% by weight.
- Preservative, dye and perfume are preferably in the carpet cleaning agents according to the invention in amounts of not more than 3% by weight, in particular from 0.01% to 1% by weight and particularly preferably from 0.1% by weight. % to 0.5 wt .-% contain.
- the production of the concentrates according to the invention has no difficulty. It can be done by simply mixing the components, which can be present as such or in the form of aqueous solutions.
- a ready-to-use cleaning solution can easily be prepared by diluting the cleaning agents according to the invention with water. Due to the low foam development and the low stability of the foam, when using the agent according to the invention, higher application concentrations can be used in the cleaning process than in the previous processes, so that even heavily soiled textiles can be cleaned in a single operation.
- a characteristic feature of the method according to the invention is the composition of the cleaning solution used, which is obtained by diluting the carpet cleaning agent concentrate according to the invention with water.
- the pH of the ready-to-use solution is preferably between 4 and 12, in particular between 6 and 8.
- the method according to the invention preferably uses a spray extraction device described above. After the detergent solution has been removed, the carpet is dried. This can be done by leaving it alone in the air, which can mean drying times of up to 2 days. However, it is also possible to accelerate drying by using air blowers or heat radiators.
- the new cleaning process has its particular advantages when cleaning carpets on site, since permanently installed carpets are not accessible to the cleaning processes for movable textiles.
- the method according to the invention has the same advantages in the case of other textiles which are not readily accessible to a conventional washing process, such as wall coverings and upholstered furniture. When used on movable carpets, it also offers advantages over the washing processes which are very complex in the case of textiles of this type because of its ease of implementation.
- the method according to the invention is characterized not only by a good result in surface cleaning, but also by a low tendency towards re-soiling of the cleaned textile. Pretreatment of the textiles to be cleaned is normally not necessary.
- the process is suitable for carpets made of synthetic fibers, such as polyamide, as well as for relatively sensitive textiles made of natural fibers, such as wool. Examples
- Example 1 Preparation of the disodium salt of sulfonated oleic acid
- the disodium salt of sulfonated oleic acid used for the preparation of the cleaning agents according to the invention was obtained by sulfonating a technical oleic acid from beef tallow (composition: 70.7% by weight oleic acid, 11-8% by weight linoleic acid, the rest other C12 to C20 ⁇ Fatty acids; acid number 200.4, iodine number 98.3) with sulfur trioxide and subsequent neutralization and hydrolysis.
- the sulfonation was carried out in a tubular glass falling film reactor (length 110 cm, inner diameter 6 m) surrounded by a heating or cooling jacket, which was provided at the head with a feed device for oleic acid and a gas inlet tube.
- the oleic acid was applied at a constant rate of 550 g per hour.
- Gaseous sulfur trioxide (produced by heating oleum) was diluted with nitrogen to a concentration of 5 vol.% Sulfur trioxide and introduced into the reactor at a rate such that the molar ratio of olefinic double bonds present in the technical oleic acid (calculated from the iodine number) to sulfur trioxide was 1: 0.9.
- the reaction temperature was kept at 50 ° C. with the aid of a water circuit through the reactor jacket. After leaving the reactor, the reaction mixture was collected in a glass vessel which contained 25% by weight aqueous sodium hydroxide solution and heated to 90 ° C. at a pH of 8 to 9 for 2 hours.
- the desired disodium salt (Tl) was obtained in a concentration of 60% by weight in water.
- the cleaning agents according to the invention characterized in Table 1 below by their composition were prepared by simply mixing the constituents. , g -
- Table 1 Composition of the agents according to the invention [% by weight]
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Catching Or Destruction (AREA)
- Air-Conditioning For Vehicles (AREA)
- Photoreceptors In Electrophotography (AREA)
Description
Claims
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4039348 | 1990-12-10 | ||
| DE4039348A DE4039348A1 (de) | 1990-12-10 | 1990-12-10 | Teppichreinigungsmittel |
| PCT/EP1991/002274 WO1992010558A1 (de) | 1990-12-10 | 1991-12-02 | Teppichreinigungsmittel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP0561842A1 true EP0561842A1 (de) | 1993-09-29 |
| EP0561842B1 EP0561842B1 (de) | 1996-10-23 |
Family
ID=6419967
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP91920831A Expired - Lifetime EP0561842B1 (de) | 1990-12-10 | 1991-12-02 | Teppichreinigungsmittel |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US5429684A (de) |
| EP (1) | EP0561842B1 (de) |
| JP (1) | JPH06503371A (de) |
| AT (1) | ATE144549T1 (de) |
| CA (1) | CA2098197A1 (de) |
| DE (2) | DE4039348A1 (de) |
| DK (1) | DK0561842T3 (de) |
| ES (1) | ES2094829T3 (de) |
| FI (1) | FI932601A0 (de) |
| GR (1) | GR3021680T3 (de) |
| NO (1) | NO302374B1 (de) |
| WO (1) | WO1992010558A1 (de) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB9221185D0 (en) * | 1992-10-08 | 1992-11-25 | Sweeney Mark W | Cleaning composition |
| WO1997004069A1 (en) * | 1995-07-18 | 1997-02-06 | Unilever N.V. | Concentrated aqueous degreasing cleanser |
| US6852487B1 (en) | 1996-02-09 | 2005-02-08 | Cornell Research Foundation, Inc. | Detection of nucleic acid sequence differences using the ligase detection reaction with addressable arrays |
| EP2332958B1 (de) * | 1996-02-09 | 2016-04-20 | Cornell Research Foundation, Inc. | Detektion von Unterschieden in der Sequenz von Nukleinsäuren mittels der Ligasedetektionsreaktion und adressierbaren Arrays |
| US5780421A (en) * | 1996-03-05 | 1998-07-14 | Henkel Corporation | Sulfated/sulfonated surfactants |
| US5837665A (en) * | 1996-05-02 | 1998-11-17 | Young; Robert | Spot cleaner for carpets |
| EP1736554B1 (de) | 1996-05-29 | 2013-10-09 | Cornell Research Foundation, Inc. | Bestimmung von Unterschieden in der Nukleinsäuresequenz mittels einer Kombination von Ligasebestimmung und Polymerasekettenreaktion |
| FR2756197B1 (fr) | 1996-11-25 | 1999-01-08 | Inst Francais Du Petrole | Composition et son utilisation pour convertir un gaz contenant de l'hydrogene sulfure et de l'anhydride sulfureux en soufre |
| US5955413A (en) * | 1997-10-24 | 1999-09-21 | 3M Innovative Properties Company | Carpet cleaning and reapplication system based on methacrylic acid polymer, sequestrant, and anionic surfactant |
| DE19751859A1 (de) | 1997-11-22 | 1999-07-29 | Henkel Ecolab Gmbh & Co Ohg | Mittel zum Reinigen von harten Oberflächen |
| AU3303300A (en) | 1999-03-18 | 2000-10-04 | Mark Gary Mullane | Cleaning formulation |
| US6326344B1 (en) | 2000-01-27 | 2001-12-04 | Ecolab Inc. | Carpet spot removal composition |
| EP1303639A2 (de) | 2000-04-14 | 2003-04-23 | Cornell Research Foundation, Inc. | DESIGNMETHODE FüR EINEN ADRESSIERBARER ARRAY ZUR DETEKTION VON NUCLEINSäURE SEQUENZUNTERSCHIEDEN UNTER VERWENDUNG EINER LIGASE DETEKTIONSREAKTION |
| EP1184449A1 (de) * | 2000-09-04 | 2002-03-06 | The Procter & Gamble Company | Teppichreinigungsmittel enthaltend ein absorbierendes quellbares Material |
| GB0109754D0 (en) * | 2001-04-20 | 2001-06-13 | Quest Int | Floor treatment compositions |
| US7135449B2 (en) * | 2004-02-20 | 2006-11-14 | Milliken & Company | Composition for removal of odors and contaminants from textiles and method |
| US7998920B2 (en) * | 2008-01-22 | 2011-08-16 | Stepan Company | Sulfonated estolide compositions containing magnesium sulfate and processes employing them |
| US7666828B2 (en) | 2008-01-22 | 2010-02-23 | Stepan Company | Sulfonated estolides and other derivatives of fatty acids, methods of making them, and compositions and processes employing them |
| US7879790B2 (en) * | 2008-01-22 | 2011-02-01 | Stepan Company | Mixed salts of sulfonated estolides and other derivatives of fatty acids, and methods of making them |
| EP2271616B1 (de) * | 2008-03-28 | 2020-11-11 | Ecolab USA Inc. | Sulfoperoxycarbonsäuren, deren herstellung und anwendungsverfahren als bleichmittel und antimikrobielle mittel |
| US8119588B2 (en) * | 2009-01-21 | 2012-02-21 | Stepan Company | Hard surface cleaner compositions of sulfonated estolides and other derivatives of fatty acids and uses thereof |
| US8058223B2 (en) * | 2009-01-21 | 2011-11-15 | Stepan Company | Automatic or machine dishwashing compositions of sulfonated estolides and other derivatives of fatty acids and uses thereof |
| US7884064B2 (en) * | 2009-01-21 | 2011-02-08 | Stepan Company | Light duty liquid detergent compositions of sulfonated estolides and other derivatives of fatty acids |
| US8124577B2 (en) * | 2009-01-21 | 2012-02-28 | Stepan Company | Personal care compositions of sulfonated estolides and other derivatives of fatty acids and uses thereof |
| JP5965801B2 (ja) * | 2012-09-26 | 2016-08-10 | ライオン株式会社 | 洗浄剤、食品製造機器洗浄用又は食器洗浄用の洗浄剤及び洗浄方法 |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2634238A (en) * | 1953-04-07 | Calcium hypochlorite detergent | ||
| US1433887A (en) * | 1922-06-17 | 1922-10-31 | S S Stafford Inc | Cleansing and polishing preparation |
| US3567364A (en) * | 1967-01-03 | 1971-03-02 | Robert A James | Treatment of fabrics,skins and furs |
| US3497456A (en) * | 1967-02-23 | 1970-02-24 | Millmaster Onyx Corp | Cleaning composition |
| CA817377A (en) * | 1967-03-20 | 1969-07-08 | W.R. Grace And Co. | Foamed detergent composition |
| GB1278421A (en) * | 1969-06-27 | 1972-06-21 | Lankro Chem Ltd | The sulphonation of unsaturated carboxylic acids |
| BE759066A (fr) * | 1969-11-17 | 1971-05-17 | Atlantic Richfield Co | Compositions de shampooings |
| US3716488A (en) * | 1970-09-04 | 1973-02-13 | Stevens & Co Inc J P | Textile fabric cleaning compositions |
| US3723323A (en) * | 1971-04-22 | 1973-03-27 | Johnson & Son Inc S C | Fabric treating shampoo compositions |
| US4294729A (en) * | 1979-12-17 | 1981-10-13 | International Business Machines Corporation | Composition containing alcohol and use thereof for epoxy removal |
| CH646044A5 (de) * | 1983-01-26 | 1984-11-15 | Gottfried Gremminger | Flaechen-reinigungsgeraet. |
| DE3723354A1 (de) * | 1987-07-15 | 1989-01-26 | Henkel Kgaa | Sulfatierte hydroxy-mischether, verfahren zu ihrer herstellung und ihre verwendung |
| US5073298A (en) * | 1988-07-20 | 1991-12-17 | Dow Corning Corporation | Antimicrobial antifoam compositions and methods |
| DE3900699A1 (de) * | 1989-01-12 | 1990-07-19 | Henkel Kgaa | Verwendung von monocarbonsaeurepolyoxyalkylester-sulfonaten als schaumarme netzmittel in waessrigen alkalischen behandlungsmitteln fuer textile flaechengebilde |
| DE3926344A1 (de) * | 1989-08-09 | 1991-02-28 | Henkel Kgaa | Verfahren zur herstellung von hellfarbigen oelsaeuresulfonaten |
| DE4007755A1 (de) * | 1990-03-12 | 1991-09-19 | Henkel Kgaa | Schaeumende tensidzubereitungen |
-
1990
- 1990-12-10 DE DE4039348A patent/DE4039348A1/de not_active Withdrawn
-
1991
- 1991-12-02 CA CA002098197A patent/CA2098197A1/en not_active Abandoned
- 1991-12-02 AT AT91920831T patent/ATE144549T1/de not_active IP Right Cessation
- 1991-12-02 WO PCT/EP1991/002274 patent/WO1992010558A1/de not_active Ceased
- 1991-12-02 US US08/074,849 patent/US5429684A/en not_active Expired - Fee Related
- 1991-12-02 ES ES91920831T patent/ES2094829T3/es not_active Expired - Lifetime
- 1991-12-02 EP EP91920831A patent/EP0561842B1/de not_active Expired - Lifetime
- 1991-12-02 JP JP3518691A patent/JPH06503371A/ja active Pending
- 1991-12-02 FI FI932601A patent/FI932601A0/fi not_active Application Discontinuation
- 1991-12-02 DK DK91920831.4T patent/DK0561842T3/da active
- 1991-12-02 DE DE59108308T patent/DE59108308D1/de not_active Expired - Fee Related
-
1993
- 1993-05-06 NO NO931661A patent/NO302374B1/no unknown
-
1996
- 1996-11-15 GR GR960403054T patent/GR3021680T3/el unknown
Non-Patent Citations (1)
| Title |
|---|
| See references of WO9210558A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0561842B1 (de) | 1996-10-23 |
| JPH06503371A (ja) | 1994-04-14 |
| DE4039348A1 (de) | 1992-06-11 |
| NO931661D0 (no) | 1993-05-06 |
| GR3021680T3 (en) | 1997-02-28 |
| DK0561842T3 (da) | 1997-03-24 |
| NO302374B1 (no) | 1998-02-23 |
| US5429684A (en) | 1995-07-04 |
| ES2094829T3 (es) | 1997-02-01 |
| FI932601L (fi) | 1993-06-07 |
| NO931661L (no) | 1993-05-06 |
| WO1992010558A1 (de) | 1992-06-25 |
| FI932601A7 (fi) | 1993-06-07 |
| DE59108308D1 (de) | 1996-11-28 |
| FI932601A0 (fi) | 1993-06-07 |
| CA2098197A1 (en) | 1992-06-10 |
| ATE144549T1 (de) | 1996-11-15 |
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