EP0728180B1 - Additiv für die glasflaschenreinigung und seine verwendung zur verringerung der glaskorrosion - Google Patents

Additiv für die glasflaschenreinigung und seine verwendung zur verringerung der glaskorrosion Download PDF

Info

Publication number
EP0728180B1
EP0728180B1 EP94931560A EP94931560A EP0728180B1 EP 0728180 B1 EP0728180 B1 EP 0728180B1 EP 94931560 A EP94931560 A EP 94931560A EP 94931560 A EP94931560 A EP 94931560A EP 0728180 B1 EP0728180 B1 EP 0728180B1
Authority
EP
European Patent Office
Prior art keywords
acid
additive
acids
group
weight
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.)
Expired - Lifetime
Application number
EP94931560A
Other languages
German (de)
English (en)
French (fr)
Other versions
EP0728180A1 (de
Inventor
Harald Kluschanzoff
Karl-Heinz Schröder
Thomas Wershofen
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.)
Ecolab GmbH and Co oHG
Original Assignee
Henkel Ecolab GmbH and Co KG
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=6502420&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0728180(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Henkel Ecolab GmbH and Co KG filed Critical Henkel Ecolab GmbH and Co KG
Publication of EP0728180A1 publication Critical patent/EP0728180A1/de
Application granted granted Critical
Publication of EP0728180B1 publication Critical patent/EP0728180B1/de
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
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/22Organic compounds
    • C11D7/26Organic compounds containing oxygen
    • C11D7/265Carboxylic acids or salts thereof
    • 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
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/02Inorganic compounds
    • C11D7/04Water-soluble compounds
    • C11D7/08Acids
    • 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
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/22Organic compounds
    • C11D7/32Organic compounds containing nitrogen
    • C11D7/3245Aminoacids
    • 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
    • C11D7/00Compositions of detergents based essentially on non-surface-active compounds
    • C11D7/22Organic compounds
    • C11D7/36Organic compounds containing phosphorus

Definitions

  • the invention relates to a new additive for aqueous alkaline cleaning solutions for machine bottle cleaning systems for glass bottles, especially for beverage bottles.
  • the additive has the task of the alkaline bottle cleaning usually occurs glass corrosion to reduce. Further aspects of the invention relate to the use of the Additives in aqueous cleaning solutions for machine cleaning of Glass bottles.
  • bottles are cleaned thoroughly.
  • Bottle cleaning machines of the bottling plants are used for this Usually strongly alkaline.
  • the alkali metal hydroxide content is usually in the range 0.5 to 5, in particular 1 to 3% by weight.
  • suitable products and processes achieve the desired cleaning effect.
  • An unwanted one The effect of bottle cleaning is glass corrosion. Underneath it is understood that the surface of the glass bottles is chemically attacked becomes what leads to surface roughness. A sequela is common difficult cleaning of the rough surface and the risk of growth of microorganisms in cracks and holes in the surface. From the It is known from practice and from laboratory tests that the corrosiveness of those containing sodium hydroxide Cleaner solutions due to an increased proportion of sodium carbonate increases.
  • the object of the invention is therefore to an active ingredient combination for aqueous alkaline cleaning solutions to provide for the mechanical cleaning of glass bottles, which, in addition to cleaning-enhancing properties, reduce the Glass corrosion contributes.
  • the object of the invention is this Formulate active ingredient combination in the form of a concentrate that as Additive can be added to the aqueous alkaline cleaning solution on site can.
  • Aliphatic hydroxymono-, hydroxydi- or hydroxytricarboxylic acids with 3 up to 6 carbon atoms and 1 to 5 hydroxyl groups are more technical as components Cleaner known. It is also known to use cleaning solutions containing mineral diphosphonic acids of the general formula (I) given below, aminomethylenephosphonic acids of the general formula (II) or phosphonocarboxylic acids to add the general formula (III). It is assumed that the acids or their anions complexing properties in particular compared to the hardening ions of water. The above Phosphonic and phosphonocarboxylic acids also show so-called hardness-stabilizing (scale-inhibiting) properties.
  • DE-C-23 25 829 describes a sequestering agent for 2- and 3-valent cations in the form of a mixture of 1-hydroxyethane-1,1-diphosphonic acid, Aminotrimethylene phosphonic acid and 2-phosphonobutane 1,2,4-tricarboxylic acid or their water-soluble salts.
  • This font contains detailed information about which geminal diphosphonic acids, aminomethylene phosphonic acids and phosphonocarboxylic acids as a sequestering agent combination can be chosen.
  • Phosphonic acid types are also in the sense as phosphonic acid components of the present invention.
  • W092 / 08824 discloses an aqueous alkaline cleaner for aluminum a pH between 10 and 12, which is an alkaline builder component, Aminoalkyl or hydroxyalkyldiphosphonic acids, surfactants and complexing agents for aluminum contains.
  • complexing agents for aluminum among others Gluconate and tartate indicated.
  • German Patent application DE-A-42 32 612 is the use of a combination from a phosphonic acid, an oxidizing agent and at least one short-chain organic carboxylic acid, selected from among others tartaric acid and citric acid, in acidic aqueous solutions that have a pH in the range have from 0 to 3 for the removal of magnetite deposits in water-bearing Systems known.
  • the concentrates also contain a combination of different ones Phosphonic acids represented by the general formulas given below I, II and III are writable, and partly gluconic acid. It is the total phosphonic acid content is greater than the gluconic acid content.
  • Known high wetting capacity preferably for cleaning plastic surfaces be used.
  • constituents essential to the invention they contain monoamino or diaminomono or dicarboxylic acids or their Amides in combination with longer chain carboxylic acids and non-ionic Surfactants.
  • Optional components in these cleaners can be: hydroxypolycarboxylic acids such as tartaric acid and citric acid, geminal diphosphonic acids such as 1-hydroxyethane-1,1-diphosphonic acid, aminophosphonic acids and phosphonopolycarboxylic acids.
  • these cleaners can be used as builder substances Contain alkali metal hydroxides.
  • the additive preferably contains 10 to 20% by weight, based on the free Acid, one or more of the carboxylic acids of group a) or their water-soluble Salts and 2 to 6% by weight, based on the free acid, one or more of the phosphonic acids of group b) or their water-soluble salts and 74 to 88 % By weight of water or an aqueous solution of further auxiliaries.
  • the acids which can be used according to the invention are in the application solution in the form of their anions, regardless of whether the additive is them contains as free acids or as water-soluble salts. If you put the carboxylic acids of group a) and / or the phosphonic acids of group b) as water-soluble Salts, the alkali metal or ammonium salts are special suitable, preferably sodium salts are used.
  • the term "Water-soluble” is to be understood to mean that the salts in the aqueous Phase of the additive in the concentration ranges mentioned above, based on the free acids, are soluble.
  • Hydroxyacetic acids of group a) include, in particular, hydroxyacetic acid, Lactic acid, gluconic acid, tartronic acid, malic acid, tartaric acid and citric acid into consideration.
  • amino carboxylic acids are according to the invention of group a).
  • the naturally occurring alpha amino acids or Amino acid derivatives are usually those with the amino group Carbon atom chiral and are in the L-form.
  • the chiral L-amino acids for the technical purpose according to the invention offer no particular advantage, they are considered natural or nature-identical Active ingredients are preferably used.
  • amino acids in the form of their racemates or in optically active form for example use find: glycine, alanine, valine, leucine, isoleucine, beta-alanine, gamma-aminobutyric acid, epsilon aminocaproic acid, glutamine, glutamic acid, Aspartic acid, aminomalonic acid, aminoadipic acid and 2-amino-2-methylpentanedioic acid.
  • the amino acids can also carry hydroxyl groups. Examples include serine and threonine.
  • the additive is 2 to 4, preferably 3 different carboxylic acids and especially hydroxycarboxylic acids from the group a) contains, the combination of gluconic acid, lactic acid and citric acid leads to particularly positive results. It is cheap if the additive is gluconic acid, lactic acid and citric acid or their water-soluble salts in a weight ratio of 1: (0.5 to 1.5): (0.5 to 1.5), preferably in a weight ratio of 1: (0.7 to 1.0): (0.8 to 1.2) contains.
  • the additive or phosphonic acids whose water-soluble salts contain the general formula (I) and / or (III), preferably at least one phosphonic acid of the formulas (I) and (III), in particular 1-hydroxyethane-1,1-diphosphonic acid and 2-phosphonobutane-1,2,4-tricarboxylic acid, be used.
  • a preferred additive is characterized in that it is a phosphonic acid or their water-soluble salts of the general formulas (I) and (III) in a weight ratio of 1:10 to 10: 1, preferably 1: 1 to 10: 1, in particular 6: 1 to 9: 1 contains.
  • an aqueous solution c) is preferably one Defoamer solution used, it being recommended in the context of the invention is that the defoamer has a proportion based on the total additive from 1 to 25, preferably 10 to 20 and in particular 13 to 18% by weight matters.
  • the defoamer can be selected empirically depending on the type of contamination of the glass bottles. Those polyglycol ethers which are recommended in EP-B-124 815 as foam-suppressing additives in low-foam cleaning agents have proven successful. Accordingly, the defoamer is preferably selected from the group of polyethylene glycol ethers of the general formula (IV) R 4 -O- (CH 2 -CH 2 -O) n -R 5 in which R 4 is a straight-chain or branched alkyl or alkenyl radical with 8 to 18 C atoms, n is a number from 7 to 12, preferably from 8 to 10, and R 5 is an alkyl radical with 4 to 8 C atoms, in particular with 4 C atoms mean.
  • R 4 is a straight-chain or branched alkyl or alkenyl radical with 8 to 18 C atoms
  • n is a number from 7 to 12, preferably from 8 to 10
  • R 5 is an alkyl radical with 4
  • nonionic surfactants can be based on ethoxylation and / or propoxylation products of fatty alcohols or fatty amines.
  • a Particularly suitable product group from ethoxylated fatty amines is in the DE-A-36 03 579 cited above.
  • the ones described there Fatty amine ethoxylates are also used as additives to increase cleaning performance the additives of the invention are suitable.
  • surface-active auxiliaries reaction products of fatty amines with 10 to 18 carbon atoms with 8 to 16 mol ethylene oxide into consideration. It is favorable if that or the nonionic surfactants in the aqueous solution c) in a are present in such an amount that they relate to the total additive Make up proportion of 1 to 6, preferably from 2 to 4 wt .-%.
  • the polyether chain obtained by alkoxylation of the defoaming and of the surface-active auxiliaries can be conventional or so-called there is a "narrow" homolog distribution.
  • the ready-to-use Cleaning solution or the concentrated additive for this analytical contains easily determinable lead substances.
  • a soluble iodide, especially potassium iodide comes in Consider its content in the bath solution by iodometric titration can be easily determined.
  • the additive contains such a lead substance in a concentration that is in the diluted bath solution can be easily determined, but not too application or wastewater problems.
  • the invention Contain additive 0.1 to 0.5 wt .-% potassium iodide.
  • the invention relates to the use of the additive in an aqueous cleaning solution containing alkali metal hydroxide mechanical cleaning of glass bottles.
  • the use is characterized by that the cleaning solution has an active ingredient content of is adjustable in that the additive described above in such amounts to the cleaning solution that the content of the cleaning solution of carboxylic acids of group a) 100 to 1,000 mg / l, preferably 200 up to 800 mg / l, in particular 300 to 600 mg / l and of phosphonic acids Group b) is 50 to 400 mg / l, preferably 75 to 200 mg / l.
  • the NaOH content of the cleaning solution is in the technically usual range of 0.5 to 5% by weight, preferably 1 to 3% by weight.
  • the use according to the invention can advantageously be carried out in this way be that the additive described above, which is an active ingredient concentrate represents, in the appropriate dosage of alkali metal hydroxide-containing Adds cleaning solution.
  • the use according to the invention can of course also be done in that the individual Active substances in the above-mentioned concentration range of the cleaning solution separately admits. From the comparison of the concentrations of the Active substances of groups a) and b) in the finished cleaning solution and in Additive can be made by diluting the additive accordingly resulting concentrations of other excipients nonionic surfactants, defoamers and easily calculate lead substances.
  • the use is further characterized in that the bottles with the cleaning solution at temperatures between 40 and 90 ° C, preferably between 55 and 85 ° C for a period of 1 to 30 minutes, preferably 3 to 20 minutes in contact.
  • the invention is illustrated by the examples shown below.
  • test solutions included (except Cf. 1) 2 wt .-% sodium carbonate to the conditions in technical Approximately simulate baths. In practice, the sodium carbonate content of cleaning solutions fluctuate greatly. All test solutions included 2.5% by weight of NaOH, the components listed in Table 1 and water ad 100%. Comparative solution 1 was free of carbonate.
  • Table 1 shows the test results.
  • Additive concentrates were prepared in the form of aqueous solutions for addition to aqueous alkaline cleaning solutions for machine bottle cleaning by introducing the required amount of water and dissolving the other components therein with stirring at room temperature.
  • a to K have the same meaning as in Table 1, L means potassium iodide.
  • the active substance and auxiliary substance contents in the additive are stated in% by weight; the difference to 100% by weight is water.

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)
  • Health & Medical Sciences (AREA)
  • Emergency Medicine (AREA)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)
  • Surface Treatment Of Glass (AREA)
EP94931560A 1993-11-12 1994-11-03 Additiv für die glasflaschenreinigung und seine verwendung zur verringerung der glaskorrosion Expired - Lifetime EP0728180B1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DE4338626A DE4338626A1 (de) 1993-11-12 1993-11-12 Additiv für die Glasflaschenreinigung und seine Verwendung zur Verringerung der Glaskorrosion
DE4338626 1993-11-12
PCT/EP1994/003618 WO1995013350A1 (de) 1993-11-12 1994-11-03 Additiv für die glasflaschenreinigung und seine verwendung zur verringerung der glaskorrosion

Publications (2)

Publication Number Publication Date
EP0728180A1 EP0728180A1 (de) 1996-08-28
EP0728180B1 true EP0728180B1 (de) 1998-08-26

Family

ID=6502420

Family Applications (1)

Application Number Title Priority Date Filing Date
EP94931560A Expired - Lifetime EP0728180B1 (de) 1993-11-12 1994-11-03 Additiv für die glasflaschenreinigung und seine verwendung zur verringerung der glaskorrosion

Country Status (7)

Country Link
EP (1) EP0728180B1 (da)
AT (1) ATE170213T1 (da)
CA (1) CA2176336A1 (da)
DE (2) DE4338626A1 (da)
DK (1) DK0728180T3 (da)
PL (1) PL314308A1 (da)
WO (1) WO1995013350A1 (da)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19945169C2 (de) * 1999-09-21 2001-09-20 Tensid Chemie G Maier Gmbh Verfahren zum Kaschieren von Oberflächenanteilen und/oder-zerklüftungen von Flaschen aus Glas sowie entsprechende Verwendung einer nichtionischen Tensidlösung
US6395693B1 (en) 1999-09-27 2002-05-28 Cabot Microelectronics Corporation Cleaning solution for semiconductor surfaces following chemical-mechanical polishing
EP1292661A1 (en) * 2000-05-31 2003-03-19 Unilever Plc Rinse aid compositions
DE10049657C2 (de) * 2000-10-07 2003-02-27 Henkel Kgaa Maschinelles Geschirreinigungsverfahren und maschinelle Geschirrspülmittel mit verbessertem Korrosionsschutz
US6835702B2 (en) 2000-11-07 2004-12-28 Ecolab Inc. Compositions and methods for mitigating corrosion of applied color designs
TWI362415B (en) * 2003-10-27 2012-04-21 Wako Pure Chem Ind Ltd Novel detergent and method for cleaning
DE102009025411B4 (de) 2009-06-16 2011-05-19 Innovent E.V. Technologieentwicklung Verwendung von Zinkstaubpartikeln oder Partikelstaub, der Zink oder eine Zinkverbindung enthält, als Korrosionsschutzmittel für Glas
EP3540033B1 (en) 2010-11-11 2023-08-23 Ecolab USA Inc. Process for cleaning and label removal for bottles
HUE055958T2 (hu) * 2014-03-24 2022-01-28 Chemische Fabrik Dr Weigert Gmbh & Co Kg Tisztítószer és eljárás edények tisztítására
BE1021365B1 (fr) * 2014-09-01 2015-11-06 Sopura S.A. Additif de lavage

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3519353A1 (de) * 1985-05-30 1986-12-04 Henkel KGaA, 4000 Düsseldorf Schmelzblockfoermige, alkalihydroxidhaltige mittel fuer das maschinelle reinigen von geschirr und verfahren zu ihrer herstellung
DE3603579A1 (de) * 1986-02-06 1987-08-13 Henkel Kgaa Verwendung ethoxylierter fettamine als loesungsvermittler
EP0476212A1 (en) * 1990-09-17 1992-03-25 The Procter & Gamble Company Liquid detergent compositions
JP2869834B2 (ja) * 1992-07-17 1999-03-10 大三工業株式会社 ガラスの白化防止方法
DE4232612A1 (de) * 1992-09-29 1994-03-31 Henkel Kgaa Entfernung von Magnetitbelägen in wasserführenden Systemen

Also Published As

Publication number Publication date
PL314308A1 (en) 1996-09-02
DE4338626A1 (de) 1995-05-18
DE59406789D1 (de) 1998-10-01
WO1995013350A1 (de) 1995-05-18
EP0728180A1 (de) 1996-08-28
CA2176336A1 (en) 1995-05-18
ATE170213T1 (de) 1998-09-15
DK0728180T3 (da) 1999-06-28

Similar Documents

Publication Publication Date Title
EP0254208B1 (de) Schaumarme und/oder schaumdämpfende Tensidgemische und ihre Verwendung
EP0710274B1 (de) Reinigungsmittel mit hohem benetzungsvermögen
EP0231886B1 (de) Verwendung ethoxylierter Fettamine als Lösungsvermittler
EP0303928B1 (de) Schaumdrückende Zusätze in schaumarmen Reinigungsmitteln
EP0986631B1 (de) Schaumarmes reinigungsmittel
DE3048642A1 (de) "tensidgemisch zur reinigung harter oberlaechen"
EP0104434A2 (de) Flüssiges, von anorganischen Gerüstsalzen im wesentlichen freies Wasch- und Reinigungsmittel
EP0946697B1 (de) Mischungen von alkoxylaten mit schaumdämpfender und desinfizierender wirkung und deren verwendung in reinigungsmitteln
EP0728180B1 (de) Additiv für die glasflaschenreinigung und seine verwendung zur verringerung der glaskorrosion
DE60210786T2 (de) Reinigungszusammensetzung und verfahren zu ihrer verwendung
DE4001595A1 (de) Demulgierende, pulverfoermige oder fluessige reinigungsmittel und deren verwendung
DE69838116T2 (de) Verfahren zur Behandlung einer Substratoberfläche und Behandlungsmittel hierfür
EP0325909A2 (de) Verwendung endgruppen-verschlossener Fettalkoholethoxylate für schaumarme Reinigungsmittel
DE69728303T2 (de) Reinigungsmittel
EP0806472A1 (de) Verfahren und Kit zum Reinigen von Geschirr
DE69921394T2 (de) Flüssige Reinigungsmittel
DE60215321T2 (de) Verfahren zum entfernen von haftendem organischem material
EP1239935B1 (de) Entschäumerzubereitung und deren verwendung
DE2015022B2 (de) Mittel zum Stabilisieren der Wasserhärte, insbesondere in Reinigungslösungen
DE3642218A1 (de) Enzymhaltiges fluessiges wasch- und reinigungsmittel
DE3818014A1 (de) Schaumdrueckende alkylpolyglykolether fuer reinigungsmittel (ii)
AT259733B (de) Alkal isches Reinigungsmittel
EP0971019B1 (de) Verfahren zur Reinigung von Geschirr
EP0658187B1 (de) Flüssige alkalische reinigungsmittel mit einem gehalt an sulfoölsauren disalzen und deren verwendung
WO1993006200A1 (de) Fettalkoholpolyalkylenglykole mit eingeengter homologenverteilung in schaumarmen tauchreinigern

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: 19960503

AK Designated contracting states

Kind code of ref document: A1

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

17Q First examination report despatched

Effective date: 19970619

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

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 IE IT LI NL SE

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

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRE;WARNING: LAPSES OF ITALIAN PATENTS WITH EFFECTIVE DATE BEFORE 2007 MAY HAVE OCCURRED AT ANY TIME BEFORE 2007. THE CORRECT EFFECTIVE DATE MAY BE DIFFERENT FROM THE ONE RECORDED.SCRIBED TIME-LIMIT

Effective date: 19980826

Ref country code: GR

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

Effective date: 19980826

Ref country code: GB

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: 19980826

Ref country code: FR

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: 19980826

Ref country code: ES

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

Effective date: 19980826

REF Corresponds to:

Ref document number: 170213

Country of ref document: AT

Date of ref document: 19980915

Kind code of ref document: T

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REF Corresponds to:

Ref document number: 59406789

Country of ref document: DE

Date of ref document: 19981001

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

Free format text: GERMAN

EN Fr: translation not filed
GBV Gb: ep patent (uk) treated as always having been void in accordance with gb section 77(7)/1977 [no translation filed]

Effective date: 19980826

REG Reference to a national code

Ref country code: DK

Ref legal event code: T3

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

Ref country code: AT

Payment date: 20051004

Year of fee payment: 12

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

Ref country code: DK

Payment date: 20051005

Year of fee payment: 12

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

Ref country code: IE

Payment date: 20051026

Year of fee payment: 12

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

Ref country code: SE

Payment date: 20051107

Year of fee payment: 12

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

Ref country code: BE

Payment date: 20051207

Year of fee payment: 12

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

Ref country code: CH

Payment date: 20051216

Year of fee payment: 12

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

Ref country code: IE

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

Effective date: 20061103

Ref country code: AT

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

Effective date: 20061103

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

Ref country code: SE

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

Effective date: 20061104

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

Ref country code: LI

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

Effective date: 20061130

Ref country code: DK

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

Effective date: 20061130

Ref country code: CH

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

Effective date: 20061130

Ref country code: BE

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

Effective date: 20061130

REG Reference to a national code

Ref country code: DK

Ref legal event code: EBP

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

EUG Se: european patent has lapsed
REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

BERE Be: lapsed

Owner name: *HENKEL-ECOLAB G.M.B.H. & CO. OHG

Effective date: 20061130

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

Ref country code: DE

Payment date: 20131030

Year of fee payment: 20

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

Ref country code: NL

Payment date: 20131109

Year of fee payment: 20

REG Reference to a national code

Ref country code: DE

Ref legal event code: R082

Ref document number: 59406789

Country of ref document: DE

Representative=s name: GODEMEYER BLUM LENZE PATENTANWAELTE, PARTNERSC, DE

Ref country code: DE

Ref legal event code: R082

Ref document number: 59406789

Country of ref document: DE

Representative=s name: GODEMEYER BLUM LENZE PARTNERSCHAFT, PATENTANWA, DE

REG Reference to a national code

Ref country code: DE

Ref legal event code: R071

Ref document number: 59406789

Country of ref document: DE

REG Reference to a national code

Ref country code: DE

Ref legal event code: R071

Ref document number: 59406789

Country of ref document: DE

REG Reference to a national code

Ref country code: NL

Ref legal event code: V4

Effective date: 20141103