EP0572453A1 - Melange d'au moins deux alcools alcoxyles et son utilisation comme additif tensio-actif antimousse dans des produits de nettoyage par des procedes de nettoyage en machine. - Google Patents

Melange d'au moins deux alcools alcoxyles et son utilisation comme additif tensio-actif antimousse dans des produits de nettoyage par des procedes de nettoyage en machine.

Info

Publication number
EP0572453A1
EP0572453A1 EP92904485A EP92904485A EP0572453A1 EP 0572453 A1 EP0572453 A1 EP 0572453A1 EP 92904485 A EP92904485 A EP 92904485A EP 92904485 A EP92904485 A EP 92904485A EP 0572453 A1 EP0572453 A1 EP 0572453A1
Authority
EP
European Patent Office
Prior art keywords
mixture
alkoxylated alcohols
foam
alkoxylated
cleaning
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
Application number
EP92904485A
Other languages
German (de)
English (en)
Other versions
EP0572453B1 (fr
Inventor
Dieter Stoeckigt
Richard Baur
Horst Trapp
Johannes Perner
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
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.)
Filing date
Publication date
Application filed by BASF SE filed Critical BASF SE
Publication of EP0572453A1 publication Critical patent/EP0572453A1/fr
Application granted granted Critical
Publication of EP0572453B1 publication Critical patent/EP0572453B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/0005Other compounding ingredients characterised by their effect
    • C11D3/0026Low foaming or foam regulating compositions
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/722Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
    • C11D1/66Non-ionic compounds
    • C11D1/825Mixtures of compounds all of which are non-ionic
    • C11D1/8255Mixtures of compounds all of which are non-ionic containing a combination of compounds differently alcoxylised or with differently alkylated chains

Definitions

  • the present invention relates to a mixture of at least two alkoxylated alcohols of the general formula I.
  • x denotes a number between 1 and 12 and y denotes a number between 1 and 15,
  • an alkoxylated alcohol carries a straight-chain or branched C ⁇ -Ci ⁇ -alkyl group as the radical R and another carries a straight-chain or branched C ⁇ o-C2o-alkyl group as the radical R, but the two radicals R are in the average number of carbon atoms must distinguish at least 0.5, and both alkoxylated alcohols are present in a ratio of 10:90 to 90:10.
  • the invention also relates to the use of this mixture as a foam-suppressing surfactant additive in cleaning agents for machine-operated cleaning processes. Furthermore, the invention relates to detergents containing such mixtures of alkoxylated alcohols I.
  • wetting agents such as ethylene and / or propylene oxide adducts with alcohols, phenols or amines may be mentioned, for example.
  • EP-A 161 537 (2) relates to the use of non-ionic surfactants which are end group-capped with methyl, ethyl or allyl radicals and which can be obtained by stepwise alkoxylation of C 8 -C 22 -alkanols with at least two different alkylene oxides, as low-foam, foam-suppressing and Biodegradable surfactants in industrial cleaning processes.
  • EP-B 019 173 (3) relates to the use of Cg-C s-alkanols first reacted with propylene oxide and then with ethylene oxide as low-foaming and biodegradable surfactant additives in dishwashing detergents for dishwashers.
  • surfactants of the type mentioned and mixtures thereof also prove to be in need of improvement when used in cleaning agents for mechanically running cleaning processes, in particular the foam-damping behavior and the dispersibility in water are not yet optimal.
  • the present invention was therefore based on the object of remedying the deficiencies described in the prior art. We have found that this object is achieved by the mixture of at least two alkoxylated alcohols I defined at the outset and its use as a foam-suppressing surfactant additive in cleaning agents for machine-operated cleaning processes.
  • Examples of straight-chain or branched C ⁇ -Ci ⁇ - or C ⁇ o-C2 ⁇ ⁇ alkyl radicals for R are: n-octyl, 2-ethylhexyl, n-nonyl, iso-nonyl, n-decyl, iso-decyl, n-undecyl, n -Dodecyl, n-tridecyl, iso-tridecyl, n-tetradecyl, n-pentadecyl, n-hexadecyl, n-heptadecyl, n-octadecyl and n-eicosyl.
  • the radicals R are preferably straight-chain or only branched to a small extent, i.e. they contain a maximum of 3 methyl or ethyl side chains.
  • R is a residue of naturally occurring fatty alcohols or preferably of synthetically produced oxo or Ziegler alcohols.
  • alcohols which can be used well after the oxo synthesis are Cg / Cu, C 12 C I-C13 C15 and Cis / Ci ⁇ -alkanol mixtures.
  • Examples of readily usable alcohols produced by the Ziegler synthesis are ⁇ / C ⁇ o, C ⁇ o / C! 2-, C12 C1 -, C 12 / C ⁇ 6 - and C ⁇ 6 / C 2 o-alkanol mixtures.
  • alkanols used in the synthesis of the compounds I generally represent statistical homologues and isomer mixtures, it is expedient to speak of an average number of carbon atoms. This average value usually represents the maximum frequency.
  • Alkanols prepared in a manner known per se. These methods are known to the person skilled in the art and require no further explanation.
  • the degree of ethoxylation x is 1 to 12, preferably 2 to 5, in particular 3 to 4; the degree of propoxylation is 1 to 15, preferably 2 to 6, in particular 4 to 6.
  • the degrees of alkoxylation x and y generally also represent average values.
  • a mixture of at least two, preferably two or three, in particular two, alkoxylated alcohols I is used, two radicals R having to differ by at least 0.5 in the average number of carbon atoms, and the corresponding two alkoxylated alcohols in the ratio of 10:90 to 90:10, preferably 25:75 to 75:25.
  • a difference in the average number of C atoms of the two radicals R of at least 1, in particular a difference of 1 to 2, is particularly favorable.
  • Mechanical cleaning processes are mainly found in the metal industry, in the food industry, e.g. the beverage, canning, sugar industry or milk, meat and fat processing industry, in the catering trade and also in the household.
  • metal objects often have to be removed after their manufacture or processing soiling and residues, which originate from drawing and rolling greases or organic corrosion protection agents. All surfaces of containers and tools that come into contact with food during production and processing, as well as during transport, must be cleaned from food residues and other contaminants at certain intervals.
  • a typical example of an industrially carried out machine cleaning process from the beverage industry is the washing of used bottles which, for example, contained beer, milk, soft drinks or mineral water.
  • a rinse aid commonly used here contains nonionic surfactants, hydrotropes (solubilizers) such as isopropanol, ethanol and / or cumene sulfonate, water and, if appropriate, organic or inorganic acids and auxiliaries such as colorants and preservatives.
  • the present invention also relates to a process for the preparation of cleaning agents for machine-running cleaning processes, in particular rinse aids for machine dishwashing, which is characterized in that a mixture of at least two alkoxylated alcohols I is added to these agents as a foam-suppressing surfactant additive.
  • the present invention furthermore relates to cleaning agents for machine-operated cleaning processes which contain a mixture of at least two alkoxylated alcohols I as a foam-suppressing surfactant additive in an amount of 0.1 to 40% by weight, preferably 0.5 to 20% by weight. , based on the total amount of the formulation.
  • the present invention furthermore relates to rinse aids for machine dishwashing, which comprise a mixture of at least two alkoxylated alcohols I as foam-suppressing surfactant additive in an amount of 0.5 to 30% by weight, preferably 1 to 15% by weight. %, based on the total amount of the formulation.
  • rinse aid formulations for machine dishwashing in the household were produced.
  • the following table shows the compositions of these formulations.
  • the cloud point was determined in accordance with DIN 53 917. From practical studies, it is known that falling cloud points, equivalent to an increase in hydrophobicity, result in improvements in the foaming behavior, but on the other hand reduce the dispersibility, which leads to an uneven distribution of the rinse aid in the washing liquor and thus to a deterioration ⁇ the behavior of the drainage (spots, stripes and streaks) leads. At cloud points ⁇ 40 ° C., instability, ie phase separation, of the rinse aid formulation is also observed.
  • the foam damping behavior is checked in the dishwasher by the so-called "egg test". In this case, the number of revolutions of a spray arm is determined by magnetic induction measurement in a commercially available domestic dishwasher with the aid of a counter.
  • Foam formation which occurs particularly in the presence of proteins (protein), reduces the number of revolutions of the spray arm. Because of the reduced recoil force, the number of revolutions therefore represents a measure of the suitability of surfactants in cleaning devices with high mechanics.
  • the test time is 12 minutes, the average number of revolutions per minute being calculated from the total number of revolutions.
  • the washing process is started at room temperature, after about 10 minutes the temperature of the rinsing water is 60 ° C.
  • the rinse aid formulation is injected into a glass tube through which tap water at 90 ° C. flows through a membrane pump. At the end of the glass tube, the dispersion produced in this way is sprayed through a second nozzle into a beaker. With a running time of about 3.5 minutes, about 30 ml of rinse aid formulation are metered into a water stream of 2 liters of water at 90 ° C. The dispersion is visually assessed and graded in the glass tube and beaker, based on the following grading scheme:
  • Grade 3 moderate dispersion in the glass tube, moderately dispersed in the beaker (fine droplets of approx. 1 mm)
  • Grade 4 good dispersion in the tube, fine dispersion in a beaker (droplets ⁇ 0.5 mm)
  • compositions Composition, cloud point, dishwasher speed and dispersibility of rinse aid formulations
  • Surfactant A C ⁇ 3 / Ci5-oxo alcohol + 11 mol ethylene oxide + 2 mol butylene oxide according to (1)
  • Surfactant B Cg / Cn-oxo alcohol + 7 mol ethylene oxide + 1 mol butylene oxide + methyl end group lock according to (2)
  • Surfactant C Ci 3 / C15 oxo alcohol + 4 mol propylene oxide + 2 mol ethylene oxide according to (3)
  • Example 5 shows that when using the surfactant additives to be used according to the invention (Examples 5 and 6), rinse aid formulations are obtained which combine excellent foam-damping behavior with excellent dispersibility, despite a sometimes very low cloud point (Example 5). Frequently, the lowering of the cloud point by adding a hydrophobic surfactant leads to an improvement in foam damping, but at the same time to a loss of the dispersing properties. The cloud point is usually raised again by the addition of solubilizers and thus the dispersibility is improved.
  • Example 5 shows that by adding the specified mixtures of compounds I to solubilizers to raise the cloud point completely or at least partially.
  • Comparative Examples 2, 3, 4 and 7 show how the addition of or mixture of known agents from the prior art improves foam damping somewhat, but the dispersibility is impaired by lowering the cloud point.

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)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Un mélange contenant au moins deux alcools alcoxylés et répondant à la formule (I), dans laquelle x vaut un chiffre entre 1 et 12 et y vaut un chiffre entre 1 et 15. Un des alcools alcoxylés porte en tant que reste R un groupe alkyle C8-C18 à chaîne droite ou ramifiée, alors que l'autre alcool alcoxylé porte en tant que reste R un groupe alkyle C10-C20 à chaîne droite ou ramifiée, les deux restes R devant présenter un nombre moyen d'atomes de carbone qui diffère d'au moins 0,5. Le rapport entre les deux alcools alcoxylés est compris entre 10 : 90 et 90 : 10. Ce mélange est utile comme additif tensio-actif antimousse dans des produits de nettoyage destinés à des procédés de lavage en machine.
EP92904485A 1991-02-22 1992-02-11 Methode pour la preparation d'un melange de deux alcools alcoxyles et son utilisation comme additif tensio-actif anti-mousse dans des produits de nettoyage pour des procedes de nettoyage en machine Expired - Lifetime EP0572453B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE4105602A DE4105602A1 (de) 1991-02-22 1991-02-22 Verwendung einer mischung aus mindestens zwei alkoxylierten alkoholen als schaumdaempfender tensidzusatz in reinigungsmitteln fuer maschinell ablaufende reinigungsprozesse
DE4105602 1991-02-22
PCT/EP1992/000289 WO1992014808A1 (fr) 1991-02-22 1992-02-11 Melange d'au moins deux alcools alcoxyles et son utilisation comme additif tensio-actif antimousse dans des produits de nettoyage par des procedes de nettoyage en machine

Publications (2)

Publication Number Publication Date
EP0572453A1 true EP0572453A1 (fr) 1993-12-08
EP0572453B1 EP0572453B1 (fr) 1995-08-30

Family

ID=6425681

Family Applications (1)

Application Number Title Priority Date Filing Date
EP92904485A Expired - Lifetime EP0572453B1 (fr) 1991-02-22 1992-02-11 Methode pour la preparation d'un melange de deux alcools alcoxyles et son utilisation comme additif tensio-actif anti-mousse dans des produits de nettoyage pour des procedes de nettoyage en machine

Country Status (8)

Country Link
US (1) US5536884A (fr)
EP (1) EP0572453B1 (fr)
JP (1) JPH06505044A (fr)
AT (1) ATE127150T1 (fr)
CA (1) CA2104468A1 (fr)
DE (2) DE4105602A1 (fr)
DK (1) DK0572453T3 (fr)
WO (1) WO1992014808A1 (fr)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022234523A1 (fr) * 2021-05-05 2022-11-10 Sabic Global Technologies B.V. Procédé pour l'éthoxylation d'un mélange d'alcool gras à chaîne droite et d'alcool gras à chaîne ramifiée dans une réaction en une seule étape

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4236506A1 (de) * 1992-10-29 1994-05-05 Henkel Kgaa Verfahren zur Herstellung wäßriger Lösungen anionischer Tenside mit verbesserter Kältestabilität
US6506340B1 (en) 1993-06-01 2003-01-14 Cobe Cardiovascular, Inc. Antifoaming device and method for extracorporeal blood processing
DE4426889A1 (de) * 1994-07-29 1996-02-01 Hoechst Ag Mischungen von Alkoxylaten als schaumdämpfendes Mittel und deren Verwendung
JP2983884B2 (ja) * 1995-05-19 1999-11-29 日本ペイント株式会社 アルカリ脱脂洗浄方法
AU709865B2 (en) * 1995-07-17 1999-09-09 Henkel Corporation The use of alkoxylated alcohols to control foaming of alkyl polyglycosides in cleaning compositions
US6106633A (en) * 1996-04-09 2000-08-22 Diversey Lever, Inc. Method of preventing damage to bottle labels and composition thereof
WO1997038079A1 (fr) * 1996-04-09 1997-10-16 Unilever N.V. Solution servant a laver une bouteille sans provoquer d'attaque chimique
DE19621843A1 (de) * 1996-05-30 1997-12-04 Basf Ag Blockförmige iso-Tridecanolalkoxylate als schaumarme oder schaumdämpfende Tenside
US6133218A (en) * 1997-07-29 2000-10-17 Basf Corporation Aqueous based solvent free cleaner compositions containing two nonionic surfactants
US6534550B1 (en) * 2000-03-29 2003-03-18 Gerald C. Walterick, Jr. Foam control composition and method for controlling foam in aqueous systems
ATE493374T1 (de) 2002-04-26 2011-01-15 Basf Se Alkoxylatgemische und diese enthaltende waschmittel
CA2671752A1 (fr) * 2006-12-14 2008-06-19 Basf Se Emulsifiants non ioniques pour l'emulsification spontanee d'emulsions concentrees
CN101578130A (zh) * 2007-01-11 2009-11-11 陶氏环球技术公司 烷氧基化物混合物表面活性剂
BRPI0917973A2 (pt) 2008-08-11 2015-11-17 Basf Se processo para o pós-tratamento de materiais têxteis tingidos e/ ou impressos.
CN101530759B (zh) * 2009-03-11 2011-02-09 南京四新科技应用研究所有限公司 一种分散高级脂肪醇混合物的方法
JP5402789B2 (ja) * 2010-03-31 2014-01-29 ダイキン工業株式会社 フルオロポリマー水性分散液
EP2963100B1 (fr) * 2014-07-04 2018-09-19 Kolb Distribution Ltd. Compositions aqueuses de rinçage
CN107073482A (zh) 2014-09-18 2017-08-18 阿克苏诺贝尔化学品国际有限公司 支化醇及其烷氧基化物作为二级捕集剂的用途
US10017714B2 (en) 2015-05-19 2018-07-10 Ecolab Usa Inc. Efficient surfactant system on plastic and all types of ware
PL3636691T3 (pl) 2015-10-07 2021-09-27 Elementis Specialties, Inc. Środek zwilżający i przeciwpieniący
CN106434098A (zh) * 2016-09-30 2017-02-22 泸州国御机械设备有限公司 摊凉机自动清洗装置
DE102016225904A1 (de) * 2016-12-21 2018-06-21 Henkel Ag & Co. Kgaa Klarspülformulierung
EP3575335A1 (fr) * 2018-05-30 2019-12-04 Hexion GmbH Procédé de fabrication d'un produit alcoxylé
CA3107070A1 (fr) 2018-07-25 2020-01-30 Ecolab Usa Inc. Formulation d'adjuvant de rincage pour le nettoyage de pieces automobiles

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2918047A1 (de) * 1979-05-04 1980-12-11 Huels Chemische Werke Ag Biologisch abbaubare und schwachschaeumende tenside, verfahren zu ihrer herstellung und ihre verwendung in reinigungsmitteln
DE2918826A1 (de) * 1979-05-10 1980-11-27 Basf Ag Verwendung von alkoxylierten alkoholen als biologisch abbaubare, schaumarme tenside in wasch- und reinigungsmitteln
DE3005515A1 (de) * 1980-02-14 1981-08-20 Basf Ag, 6700 Ludwigshafen Verwendung von butoxylierten ethylenoxidaddukten an hoehere alkohole als schaumarme tenside in spuel- und reinigungsmitteln
DE3418523A1 (de) * 1984-05-18 1985-11-21 Basf Ag, 6700 Ludwigshafen Endgruppenverschlossene fettalkoholalkoxylate fuer industrielle reinigungsprozesse, insbesondere fuer die flaschenwaesche und fuer die metallreinigung
ATE68519T1 (de) * 1986-07-24 1991-11-15 Henkel Kgaa Schaumarme und/oder schaumdaempfende tensidgemische und ihre verwendung.
DE3818062A1 (de) * 1988-05-27 1989-12-07 Henkel Kgaa Schaumdrueckende alkylpolyglykolether fuer reinigungsmittel (i)
JPH08147497A (ja) * 1994-11-25 1996-06-07 Canon Inc 画像処理方法及びその装置

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO9214808A1 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022234523A1 (fr) * 2021-05-05 2022-11-10 Sabic Global Technologies B.V. Procédé pour l'éthoxylation d'un mélange d'alcool gras à chaîne droite et d'alcool gras à chaîne ramifiée dans une réaction en une seule étape

Also Published As

Publication number Publication date
WO1992014808A1 (fr) 1992-09-03
CA2104468A1 (fr) 1992-08-23
US5536884A (en) 1996-07-16
EP0572453B1 (fr) 1995-08-30
DE4105602A1 (de) 1992-08-27
DK0572453T3 (da) 1995-09-18
JPH06505044A (ja) 1994-06-09
DE59203477D1 (de) 1995-10-05
ATE127150T1 (de) 1995-09-15

Similar Documents

Publication Publication Date Title
EP0572453A1 (fr) Melange d'au moins deux alcools alcoxyles et son utilisation comme additif tensio-actif antimousse dans des produits de nettoyage par des procedes de nettoyage en machine.
EP0019173B1 (fr) Utilisation d'alcools alcoxylés comme tensioactifs biodégradables et peu moussants dans des agents de lavage pour vaisseller pour des lave-vaisselles
EP0254208B1 (fr) Mélanges d'agents tensio-actifs peu moussants et/ou anti-mousse et leur utilisation
EP0034275B1 (fr) Produits d'addition d'oxyde d'éthylène butoxylés à des alcools supérieurs comme tensides pauvres en mousse dans détergents de rinçage et de nettoyage
EP0197434B1 (fr) Produits de rinçage pour le lavage mécanique de la vaisselle
EP0161537A2 (fr) Alcoxylates d'alcool gras ayant des groupes terminaux pour les procédés industriels de nettoyage spécialement pour le lavage de bouteilles et pour le nettoyage du métal
AT394861B (de) Fluessiges biologisch abbaubares tensid und waschmittelzusammensetzung
DE1617239B2 (de) Wenig schäumende Spülmittel für automatische Geschirrspülmaschinen
EP0343503A1 (fr) Ethers de polyglycol supprimant la mousse pour des produits de nettoyage
EP0906150B1 (fr) Iso-tridecanolalcoxylates sequences utilises comme tensioactifs peu moussants ou antimousse
DE3317337C2 (fr)
DE3431156A1 (de) Polyoxyalkylierte alkohole und zusammensetzung auf deren basis
DE3928600A1 (de) Schaumdaempfende mehrstoffgemische mit tensidcharakter fuer die maschinelle geschirr- und flaschenreinigung
DE2449354C3 (fr)
DE2153460A1 (de) Geschirrspuelmittel
DE4426889A1 (de) Mischungen von Alkoxylaten als schaumdämpfendes Mittel und deren Verwendung
US4172044A (en) Process and concentrates for clear-rinsing in mechanical dishwashing
DE3614825A1 (de) Verwendung von alkylaminopolyglykolethern als schaumdrueckende zusaetze in schaumarmen reinigungsmitteln
DE2149251C3 (de) Geschirrspulmittel
DE2351387C3 (de) Geschirrspulmittelszusammensetzungen
DE1519545A1 (de) Oberflaechenaktives Mittel
WO1997005223A1 (fr) Melange tensioactif aqueux
DE2855778A1 (de) Fluessiges reinigungsmittel
DE2715351B2 (de) Flüssige, maschinell anwendbare Geschirrspülmittelkonzentrate
EP0095136B1 (fr) Produits de rinçage à utiliser pour le lavage machinal de la vaisselle

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 19930816

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU NL SE

17Q First examination report despatched

Effective date: 19940615

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE CH DE DK ES FR GB GR IT LI LU NL SE

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 19950830

Ref country code: ES

Free format text: THE PATENT HAS BEEN ANNULLED BY A DECISION OF A NATIONAL AUTHORITY

Effective date: 19950830

Ref country code: BE

Effective date: 19950830

REF Corresponds to:

Ref document number: 127150

Country of ref document: AT

Date of ref document: 19950915

Kind code of ref document: T

REG Reference to a national code

Ref country code: DK

Ref legal event code: T3

REF Corresponds to:

Ref document number: 59203477

Country of ref document: DE

Date of ref document: 19951005

GBT Gb: translation of ep patent filed (gb section 77(6)(a)/1977)

Effective date: 19950908

ITF It: translation for a ep patent filed

Owner name: ING. C. GREGORJ S.P.A.

ET Fr: translation filed
PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AT

Effective date: 19960211

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 19960229

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
REG Reference to a national code

Ref country code: GB

Ref legal event code: IF02

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DK

Payment date: 20020125

Year of fee payment: 11

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DK

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20030228

REG Reference to a national code

Ref country code: DK

Ref legal event code: EBP

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: NL

Payment date: 20110224

Year of fee payment: 20

Ref country code: IT

Payment date: 20110222

Year of fee payment: 20

Ref country code: FR

Payment date: 20110314

Year of fee payment: 20

Ref country code: SE

Payment date: 20110223

Year of fee payment: 20

Ref country code: CH

Payment date: 20110225

Year of fee payment: 20

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20110228

Year of fee payment: 20

Ref country code: DE

Payment date: 20110427

Year of fee payment: 20

REG Reference to a national code

Ref country code: DE

Ref legal event code: R071

Ref document number: 59203477

Country of ref document: DE

REG Reference to a national code

Ref country code: DE

Ref legal event code: R071

Ref document number: 59203477

Country of ref document: DE

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

REG Reference to a national code

Ref country code: NL

Ref legal event code: V4

Effective date: 20120211

REG Reference to a national code

Ref country code: GB

Ref legal event code: PE20

Expiry date: 20120210

REG Reference to a national code

Ref country code: SE

Ref legal event code: EUG

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20120212

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF EXPIRATION OF PROTECTION

Effective date: 20120210