EP0844301A2 - Méthode pour enlever les moisissures des bouteilles en plastiques et additif anti-moisissure - Google Patents

Méthode pour enlever les moisissures des bouteilles en plastiques et additif anti-moisissure Download PDF

Info

Publication number
EP0844301A2
EP0844301A2 EP97203528A EP97203528A EP0844301A2 EP 0844301 A2 EP0844301 A2 EP 0844301A2 EP 97203528 A EP97203528 A EP 97203528A EP 97203528 A EP97203528 A EP 97203528A EP 0844301 A2 EP0844301 A2 EP 0844301A2
Authority
EP
European Patent Office
Prior art keywords
surfactant
sodium
bottles
ppm
group
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
EP97203528A
Other languages
German (de)
English (en)
Other versions
EP0844301A3 (fr
EP0844301B1 (fr
Inventor
Carol A. Rouillard
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.)
Diversey Inc
Original Assignee
Unilever PLC
Unilever NV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Unilever PLC, Unilever NV filed Critical Unilever PLC
Publication of EP0844301A2 publication Critical patent/EP0844301A2/fr
Publication of EP0844301A3 publication Critical patent/EP0844301A3/fr
Application granted granted Critical
Publication of EP0844301B1 publication Critical patent/EP0844301B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

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
    • C11D3/16Organic compounds
    • C11D3/36Organic compounds containing phosphorus
    • 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
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/06Phosphates, including polyphosphates
    • 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
    • C11D2111/00Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
    • C11D2111/10Objects to be cleaned
    • C11D2111/14Hard surfaces
    • C11D2111/18Glass; Plastics

Definitions

  • bottles such as soft drink bottles are repeatedly cleaned and reused.
  • the used bottles are passed through a bottle-washing apparatus which cleans the bottle, permitting it to be refilled and reused.
  • Both plastic and glass bottles are subject to reuse.
  • Mold tightly adheres to the surface of bottles, both plastic and glass, and is relatively difficult to remove. Mold can be removed from glass bottles by simply operating at temperatures above 60°C, which is typically done. But with plastic containers, this is not possible. At temperatures higher than 60°C, most plastic containers will shrink. Further, higher temperatures and higher alkalinity promote stress cracking which is unsightly and eventually can cause the bottle to leak or break open. Certain surfactants also promote stress cracking. Other harsh chemicals such as bleaches will remove mold. But these would corrode the equipment and therefore are unacceptable. EDTA is currently used to enhance mold removal. However, this is not always totally effective.
  • the present invention is premised upon the realization that an alkaline wash solution which includes an effective amount of a complex phosphate, in combination with a suitable surfactant, either nonionic or anionic, will effectively remove mold from plastic surfaces at temperatures less than 60°C. This, in turn, permits the removal of mold from the plastic surface without destruction of the plastic container.
  • a suitable surfactant either nonionic or anionic
  • the present invention is premised on the realization that the removal of mold is enhanced by the further addition of an effective amount of a phosphonate which is also useful in the cleaning of the bottle.
  • the bottle-washing solution will also include a chelating agent such as sodium gluconate, sodium glucoheptonate, or sodium boroheptonate.
  • gluconates are considered to be less effective at milder alkalinities, it provides a significant improvement in mold removal in this system.
  • These combined components provide an extremely effective bottle-washing solution which outperforms currently-used bottle washing formulations in the removal of mold from plastic surfaces.
  • the formulation of the present invention even with the added surfactant, does not further promote stress cracking relative to commercially available formulations. Although formulated primarily for plastic containers, this formulation will also assist in removal of mold from glass containers as well.
  • the Figure is a graph showing the test results of Example 2 demonstrating mold removal from bottles in a commercial bottle washing apparatus.
  • the present invention is a method and solution for cleaning reusable plastic bottles and is particularly directed at mold removal.
  • the reusable plastic bottles cleaned according to the present invention can be formed from many different plastics.
  • Most reusable plastic bottles are currently formed from polyesters such as polyethylene terephthalate, polybutylene terephthalate, polyethylene naphthalate, and polycarbonate.
  • any reusable plastic bottle which can be subjected to an alkaline wash is suitable for use in the present invention.
  • bottle washing apparatuses generally include three or four sections.
  • the bottles are introduced into the machine and supported throughout the washing process by individual holders or pockets.
  • Bottles are initially directed to a prerinse section which is designed to remove large particles and labels.
  • water and residuals from the cleaning process are directed at the bottles as they are introduced into the machine.
  • the bottles are conveyed to a cleaning or soaking section where they are soaked in a caustic solution at an elevated temperature, generally no higher than 60°C for plastic bottles such as PET bottles. After 7 to about 30 minutes (generally 9-11 minutes) in the soaking section the bottles are taken to a warm rinse and then to a final potable water rinse. The final rinse is then reused for the subsequent initial prerinse.
  • the cleaning or soaking solution is a caustic solution.
  • this contains 0.5 to 5.0%, and preferably 1.0 to 3.0%, sodium hydroxide for PET containers. This acts to clean the bottles and dissolve metals such as metal foils of the label and the closure rings.
  • This caustic solution also, in combination with temperature and contact time, renders the bottles commercially sterile. However, at caustic concentrations greater than 3% stress cracking of the plastic bottles is excessive.
  • the soaking solution will include an additive to enhance mold removal.
  • the mold-removing additive is a combination of complex phosphates, surfactants, and preferably chelating agents, particularly gluconates and related agents, as well as threshold water conditioners such as the phosphonates.
  • the additive itself is formed in a concentrated stable aqueous solution or a premixed powder which is formulated with the above components in a proportion to provide for effective use concentration of all the components when added.
  • the soaking solution in the bottle washing apparatus i.e., at use concentration, should have 1000 to 2500 ppm of the complex phosphates.
  • Complex phosphates include the common polyphosphates. Particular phosphates which can be employed include sodium tripolyphosphate, potassium tripolyphosphate, sodium potassium tripolyphosphate, tetrapotassium pyrophosphate, and tetrasodium pyrophosphate, as well as others.
  • the wash solution must include an effective amount of a surfactant, either an anionic surfactant, a nonionic surfactant, an amphoteric surfactant, or a mixture thereof. It is important that the surfactants be selected so that they do not promote stress cracking of the plastic bottles.
  • the most effective nonionic surfactants are the polyalkoxylated fatty alcohols and the polyethoxylated straight chain alcohols. These are also preferred since they contribute to foam control.
  • alkoxylated alcohol surfactants include Makon NF 12, Plurafac LF 221, Plurafac LF 223, Plurafac LF 431, Polytergent SLF18, and Triton DF12, a modified polyethoxylated alcohol.
  • suitable nonionics include alkyl polyglycosides such as Triton BG10, Triton CGIO, and EO -PO block copolymers such as Industrol N-3.
  • Suitable anionics include sodium C 14 - C 16 alpha olefin sulfonates such as Bioterge AS-40, alkyl aryl sulfonates, carboxylated alcohols such as Polytergent CSI, alkali metal salts of phosphate esters such as Triton H66, alkali metal alkanoates such as Monatrope 1250, fatty alcohol polyglycol ether carboxylic acids such as Akypo LF 4, dioctylsulfosuccinate such as Monawet MO70, modified ethoxylates such as Mona NF 10 and Triton DF 20, and alkali metal xylene sulfonates such as Eltesol PX93.
  • alkali metal salts of phosphate esters such as Triton H66
  • alkali metal alkanoates such as Monatrope 1250
  • fatty alcohol polyglycol ether carboxylic acids such as Akypo LF 4, diocty
  • Suitable amphoterics include alkyl and alkyl alkoxy iminodiproprionates such as lauryl iminodiproprionate and isodecyloxypropyl iminodipropionate sold under the trademark Alkali surfactant.
  • ppm surfactant Generally 200-1000 ppm surfactant will be used in the soaking solution. The upper limit is determined by economics. Concentrations greater than 1000 ppm provide little added benefit. A blend of surfactants may be preferred to reduce stress cracking and improve efficiency.
  • the formulation optionally includes 500-1000 ppm of an organic phosphonate.
  • organophosphonates include aminotrimethylene phosphonic acid, 1-hydroxyethylene (1,1 diphosphonic acid), hexamethylenediaminetetramethylene phosphonic acid, diethylenetriaminepentamethylene phosphonic acid, and phosphonobutanetricarboxylic acid. These assist not only in mold removal, but also carry over to the rinse section of the bottle washer to provide threshold water conditioning in that section, reducing scale.
  • the present invention can also include one or more chelating agents.
  • Suitable chelating agents are the gluconates and comparable compositions. Particular chelating agents include sodium gluconate or gluconic acid, sodium glucoheptonate, and sodium boroheptonate. These should be present in the wash solution at a concentration of from 500 ppm to 2000 ppm.
  • the concentrated formulation can be stated in terms of a ratio of parts by weight actives.
  • the mold removing composition of the present invention will generally include from 10 to 25 parts by weight of the complex phosphate, 2 to 10 parts by weight of the surfactant, and optionally but preferably 5 to 10 parts by weight of the phosphonate, and 5 to 20 parts by weight of the chelating agent, which is preferably sodium gluconate.
  • Said surfactant is desirably either an anionic surfactant selected from alkylaryl sulfonates, C 14 -C 16 alpha olefin sulfonates and alkyl sulfosuccinates, or a nonionic surfactant selected from polyalkoxylated fatty alcohols and polyethoxylated straight chain alcohols. Most preferred surfactant for use in said composition is iminodipropionate. If said composition is formulated as a liquid, it will also include an amount of caustic liquid to maintain an alkaline pH. The balance of the product would then be water. Generally, it is desirable to have as high an actives content as possible. With the present formulation, an actives content of 40% to 50% can be achieved.
  • Table 1 shows three different liquid formulations of the present invention. With liquid formulations, each of the individual components is simply combined with water. The order of addition is not significant. These are blended until a stable solution is formed.
  • Raw Materials Formula 1 Formula 2 Formula 3 Soft Water 50.87 51.07 53.24 Sodium Gluconate 7.0 7.0 7.0 Dequest 2000 3.0 3.0 3.0 Caustic Liquid 50% 2.0 2.0 2.0 KTPP Liquid 50 27.13 27.13 27.13 Plurafac LF221 (Nonionic 95%) 1.0 (0.95) 0.32 (0.30) Plurafac LF223 (Nonionic 98%) 1.0 (0.98) 0.31 (0.30) Triton BG 10 (Nonionic 70%) Akypo LF4 (Anionic 90%) 2.0 (1.8) 2.0 (1.8) 2.0 (1.8) Eltesol PX93 7.0 6.8 5.0
  • An amount of the concentrated composition is added to the soaking solution to provide an acceptable level of actives in the soaking solution.
  • the use concentration will be 0.5 to 1.5% with 1.25% preferred.
  • test results indicate that the sodium tripolyphosphate, in combination with the nonionic surfactant, is particularly effective at removing mold, and that the Formula 3 is a significant improvement over the combination of sodium tripolyphosphate and nonionic surfactant by itself. Further, test results indicated that the addition of Formula 3, in spite of the use of the surfactant, promoted less stress cracking than other commercial additives. Thus, the present invention provides better mold removal and promotes less stress cracking than commercially available products.
  • Exemplary dry formulations which are useful in assisting mold removal are listed below, as well as an indication of mold removal efficacy in laboratory studies: POWDERS Material: Weight Percent STPP, granular 45.00 SKTP, granular 63.00 Sodium gluconate 25.00 25.00 Dequest 2016D 6.00 6.00 Makon NF 12 6.00 Soda Ash 15.00 Poly Tergent SLF-18 6.00 Poly Tergent CS-1 3.00 Mold Removal 90-100% 100% W/w additives 0.4% 0.4% NaOH 2.80% 1.50%

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)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)
  • Separation, Recovery Or Treatment Of Waste Materials Containing Plastics (AREA)
  • Moulds For Moulding Plastics Or The Like (AREA)
  • Containers Having Bodies Formed In One Piece (AREA)
EP97203528A 1996-11-26 1997-11-12 Méthode pour enlever les moisissures des bouteilles en plastiques et additif anti-moisissure Expired - Lifetime EP0844301B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US75603496A 1996-11-26 1996-11-26
US756034 1996-11-26

Publications (3)

Publication Number Publication Date
EP0844301A2 true EP0844301A2 (fr) 1998-05-27
EP0844301A3 EP0844301A3 (fr) 1999-03-03
EP0844301B1 EP0844301B1 (fr) 2003-03-26

Family

ID=25041755

Family Applications (1)

Application Number Title Priority Date Filing Date
EP97203528A Expired - Lifetime EP0844301B1 (fr) 1996-11-26 1997-11-12 Méthode pour enlever les moisissures des bouteilles en plastiques et additif anti-moisissure

Country Status (5)

Country Link
EP (1) EP0844301B1 (fr)
CA (1) CA2221470C (fr)
DE (1) DE69720143T2 (fr)
DK (1) DK0844301T3 (fr)
ES (1) ES2196256T3 (fr)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6362149B1 (en) 2000-08-03 2002-03-26 Ecolab Inc. Plastics compatible detergent composition and method of cleaning plastics comprising reverse polyoxyalkylene block co-polymer
WO2002038715A2 (fr) * 2000-11-07 2002-05-16 Ecolab Inc. Compositions et procedes d'attenuation de la corrosion de motifs en couleur appliques
WO2004027001A1 (fr) * 2002-09-18 2004-04-01 Ecolab Inc. Additif destine a etre utilise dans des compositions de lavage de bouteilles
US6835702B2 (en) 2000-11-07 2004-12-28 Ecolab Inc. Compositions and methods for mitigating corrosion of applied color designs
WO2006052578A2 (fr) * 2004-11-03 2006-05-18 Johnsondiversey, Inc. Procede de nettoyage de recipients recycles
DE102007022110A1 (de) 2007-05-11 2008-11-13 Edmund Bromm Verfahren zum Beseitigen und Abtöten von Schimmel
US11028344B2 (en) 2016-08-16 2021-06-08 Diversey, Inc. Composition for aesthetic improvement of food and beverage containers and methods thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3669893A (en) * 1968-07-22 1972-06-13 Monsanto Co Inhibiting agents, washing compositions and solutions containing the same, and processes for using the same

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61118499A (ja) * 1984-11-14 1986-06-05 株式会社 ネオス スプレ−洗浄用洗浄剤
JPH07116474B2 (ja) * 1993-06-11 1995-12-13 ティーポール株式会社 高濃度アルカリ液体洗浄剤組成物及びその製造方法

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3669893A (en) * 1968-07-22 1972-06-13 Monsanto Co Inhibiting agents, washing compositions and solutions containing the same, and processes for using the same

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
DATABASE WPI Section Ch, Week 8629 Derwent Publications Ltd., London, GB; Class A97, AN 86-186120 XP002005616 & JP 61 118499 A (NEOS KK), 5 June 1986 *
DATABASE WPI Section Ch, Week 9510 Derwent Publications Ltd., London, GB; Class D25, AN 95-070581 XP002037099 & JP 06 346099 A (TEEPOL KK) , 20 December 1994 *

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6362149B1 (en) 2000-08-03 2002-03-26 Ecolab Inc. Plastics compatible detergent composition and method of cleaning plastics comprising reverse polyoxyalkylene block co-polymer
US6838422B2 (en) 2000-08-03 2005-01-04 Ecolab Inc. Plastics compatible detergent composition and method of cleaning plastics
WO2002038715A2 (fr) * 2000-11-07 2002-05-16 Ecolab Inc. Compositions et procedes d'attenuation de la corrosion de motifs en couleur appliques
WO2002038715A3 (fr) * 2000-11-07 2002-11-07 Ecolab Inc Compositions et procedes d'attenuation de la corrosion de motifs en couleur appliques
US6835702B2 (en) 2000-11-07 2004-12-28 Ecolab Inc. Compositions and methods for mitigating corrosion of applied color designs
WO2004027001A1 (fr) * 2002-09-18 2004-04-01 Ecolab Inc. Additif destine a etre utilise dans des compositions de lavage de bouteilles
US7148188B2 (en) 2002-09-18 2006-12-12 Ecolab Inc. Bottlewash additive comprising an alkyl diphenylene oxide disulfonate
WO2006052578A2 (fr) * 2004-11-03 2006-05-18 Johnsondiversey, Inc. Procede de nettoyage de recipients recycles
WO2006052578A3 (fr) * 2004-11-03 2006-08-10 Johnson Diversey Inc Procede de nettoyage de recipients recycles
AU2005305095B2 (en) * 2004-11-03 2011-07-14 Diversey, Inc. Method of cleaning containers for recycling
DE102007022110A1 (de) 2007-05-11 2008-11-13 Edmund Bromm Verfahren zum Beseitigen und Abtöten von Schimmel
US11028344B2 (en) 2016-08-16 2021-06-08 Diversey, Inc. Composition for aesthetic improvement of food and beverage containers and methods thereof

Also Published As

Publication number Publication date
CA2221470A1 (fr) 1998-05-26
CA2221470C (fr) 2008-08-12
ES2196256T3 (es) 2003-12-16
EP0844301A3 (fr) 1999-03-03
DE69720143T2 (de) 2003-09-11
EP0844301B1 (fr) 2003-03-26
DE69720143D1 (de) 2003-04-30
DK0844301T3 (da) 2003-07-21

Similar Documents

Publication Publication Date Title
AU728702B2 (en) Anti-etch bottle washing solution
AU702565B2 (en) Improved proteolytic enzyme cleaner
US4081395A (en) Alkaline detergent compositions
US11629312B2 (en) Solvent application in bottle wash using amidine based formulas
CN103849498A (zh) 清洗添加剂及使用该清洗添加剂的清洗方法
US2976248A (en) Bottle washing composition and method
EP1148955B1 (fr) Procede de nettoyage de bouteilles consignees
EP0844301B1 (fr) Méthode pour enlever les moisissures des bouteilles en plastiques et additif anti-moisissure
US6106633A (en) Method of preventing damage to bottle labels and composition thereof
US6554005B1 (en) Cleaning method for polyethylene terephthalate containers
WO2004027001A1 (fr) Additif destine a etre utilise dans des compositions de lavage de bouteilles
US6247478B1 (en) Cleaning method for polyethylene terephthalate containers
JP4163754B2 (ja) ポリエチレンテレフタレート容器の洗浄方法
AU716488B2 (en) Cleaning formulation, additive for a cleaning formulation and process for cleaning bottles using such
AU1848295A (en) Improved performance cast detergent
CA2197314C (fr) Nettoyant ameliore a base d'enzyme proteolytique
CA2246339A1 (fr) Procede permettant de nettoyer des bouteilles pour boissons
RU1778172C (ru) Моюща композици дл очистки твердой поверхности
GB1575094A (en) Detergent compositions
PL188662B1 (pl) Sposób czyszczenia pojemników z politereftalanu etylenu i alkaliczny roztwór myjący do czyszczenia pojemników z politereftalanu etylenu
MXPA96006427A (en) Molded detergent with better performance
MXPA99004582A (en) Cleaning method for polyethylene terephtalate containers
CZ624690A3 (en) agent for degreasing, cleaning and sanitation of objects made of metal, glass or ceramic
WO2008138392A1 (fr) Nettoyage de polycarbonate
NZ335914A (en) Cleaning method for polyethylene terephthalate containers using an alkaline wash solution

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

AK Designated contracting states

Kind code of ref document: A2

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

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

PUAL Search report despatched

Free format text: ORIGINAL CODE: 0009013

AK Designated contracting states

Kind code of ref document: A3

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

AX Request for extension of the european patent

Free format text: AL;LT;LV;MK;RO;SI

17P Request for examination filed

Effective date: 19990218

AKX Designation fees paid

Free format text: CH DE DK ES FR GB IT LI NL SE

17Q First examination report despatched

Effective date: 20020404

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

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: UNILEVER PLC

Owner name: UNILEVER N.V.

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: JOHNSONDIVERSEY, INC.

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

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

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

REF Corresponds to:

Ref document number: 69720143

Country of ref document: DE

Date of ref document: 20030430

Kind code of ref document: P

REG Reference to a national code

Ref country code: SE

Ref legal event code: TRGR

REG Reference to a national code

Ref country code: DK

Ref legal event code: T3

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2196256

Country of ref document: ES

Kind code of ref document: T3

ET Fr: translation filed
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

Effective date: 20031230

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

Ref country code: DK

Payment date: 20051129

Year of fee payment: 9

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: 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: PFA

Owner name: JOHNSONDIVERSEY, INC.

Free format text: JOHNSONDIVERSEY, INC.#8310 16TH STREET#STURTEVANT, WISCONSIN 53177-0902 (US) -TRANSFER TO- JOHNSONDIVERSEY, INC.#8310 16TH STREET#STURTEVANT, WISCONSIN 53177-0902 (US)

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

Ref country code: NL

Payment date: 20081124

Year of fee payment: 12

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

Ref country code: ES

Payment date: 20081126

Year of fee payment: 12

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

Ref country code: IT

Payment date: 20081126

Year of fee payment: 12

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

Ref country code: FR

Payment date: 20081117

Year of fee payment: 12

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

Ref country code: GB

Payment date: 20081128

Year of fee payment: 12

REG Reference to a national code

Ref country code: NL

Ref legal event code: V1

Effective date: 20100601

REG Reference to a national code

Ref country code: CH

Ref legal event code: PFA

Owner name: DIVERSEY, INC.

Free format text: JOHNSONDIVERSEY, INC.#8310 16TH STREET#STURTEVANT, WISCONSIN 53177-0902 (US) -TRANSFER TO- DIVERSEY, INC.#8310 16TH STREET - M/S 509#STURTEVANT, WI 53177-0902 (US)

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20091112

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20100730

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

Ref country code: NL

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

Effective date: 20100601

Ref country code: FR

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

Effective date: 20091130

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 NON-PAYMENT OF DUE FEES

Effective date: 20091112

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

Ref country code: DE

Payment date: 20101126

Year of fee payment: 14

Ref country code: CH

Payment date: 20101124

Year of fee payment: 14

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 NON-PAYMENT OF DUE FEES

Effective date: 20091112

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

Ref country code: SE

Payment date: 20101126

Year of fee payment: 14

REG Reference to a national code

Ref country code: ES

Ref legal event code: FD2A

Effective date: 20110401

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

Ref country code: ES

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

Effective date: 20110321

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

Ref country code: ES

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

Effective date: 20091113

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

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: LI

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

Effective date: 20111130

Ref country code: CH

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

Effective date: 20111130

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 69720143

Country of ref document: DE

Effective date: 20120601

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: 20111113

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 NON-PAYMENT OF DUE FEES

Effective date: 20120601