EP0427577B1 - Suspension aqueuse de zéolite comprenant une résine silicone - Google Patents

Suspension aqueuse de zéolite comprenant une résine silicone Download PDF

Info

Publication number
EP0427577B1
EP0427577B1 EP90402760A EP90402760A EP0427577B1 EP 0427577 B1 EP0427577 B1 EP 0427577B1 EP 90402760 A EP90402760 A EP 90402760A EP 90402760 A EP90402760 A EP 90402760A EP 0427577 B1 EP0427577 B1 EP 0427577B1
Authority
EP
European Patent Office
Prior art keywords
suspension
stabilizer
weight
suspension according
chosen
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
EP90402760A
Other languages
German (de)
English (en)
French (fr)
Other versions
EP0427577A1 (fr
Inventor
Philippe Jost
Marc Malassis
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.)
Rhodia Chimie SAS
Original Assignee
Rhone Poulenc Chimie SA
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 Rhone Poulenc Chimie SA filed Critical Rhone Poulenc Chimie SA
Publication of EP0427577A1 publication Critical patent/EP0427577A1/fr
Application granted granted Critical
Publication of EP0427577B1 publication Critical patent/EP0427577B1/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
    • 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
    • C11D3/37Polymers
    • C11D3/3703Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C11D3/373Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
    • 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
    • C11D3/12Water-insoluble compounds
    • C11D3/124Silicon containing, e.g. silica, silex, quartz or glass beads
    • C11D3/1246Silicates, e.g. diatomaceous earth
    • C11D3/128Aluminium silicates, e.g. zeolites
    • C11D3/1286Stabilised aqueous aluminosilicate suspensions

Definitions

  • the present invention relates to aqueous zeolite suspensions.
  • aqueous suspensions of zeolites present many industrial handling difficulties due to their very particular rheological behavior.
  • suspensions have a dilating behavior. Their viscosity is very high. They are therefore difficult to pump, which makes their use, for example their introduction into possibly sprayable detergent mixtures, difficult or even impossible. In addition, these suspensions tend to sediment or gel, which makes them difficult to transport or store. So there is a real problem there.
  • the main object of the invention is therefore a system for obtaining aqueous suspensions of low viscosity zeolite, in particular pumpable.
  • Another object of the invention is a system which also makes it possible to obtain a stable aqueous suspension.
  • the aqueous zeolite suspension also comprises at least one stabilizer.
  • silicone resins has the effect of considerably lowering the viscosity of the zeolite suspensions. It also makes it possible to obtain manipulable suspensions with a higher dry extract, for example of at least 55%. Finally, it has been observed that the resins do not influence the exchange capacity of the zeolites.
  • the zeolites used in the context of the present invention include crystalline, amorphous and mixed crystalline-amorphous, natural or synthetic zeolites.
  • finely divided zeolites are used having an average diameter of primary particles of between 0.1 and 10 ⁇ m and, advantageously, between 0.5 and 5 ⁇ m, as well as a theoretical cation exchange power greater than 100 mg of CaCO3 / g of anhydrous product and preferably greater than 200 mg.
  • Use is also more particularly made of zeolites of type A, X or Y and in particular 4A and 13X.
  • zeolites obtained by the processes described in the French patent applications in the name of the Applicant No. 2,376,074, 2,384,716, 2,392,932, 2,528,722.
  • the last reference cited refers in particular to zeolites having a speed constant, related to the surface of the zeolites per liter of solution greater than 0.15 s ⁇ 1.lm ⁇ , preferably greater than 0.25 and advantageously between 0.4 and 4 s ⁇ 1.lm ⁇ .
  • These zeolites have particularly interesting qualities in the use in detergency.
  • Application FR-A-2 392 932 in particular mentions zeolites obtained by a process consisting in injecting a sodium silicate solution in the axis of a venturi while a sodium aluminate solution is injected coaxially at the same venturi with recycling of the mixture obtained.
  • the suspensions can have a variable zeolite concentration depending on the application. This concentration is between 40 and 51% by weight.
  • the pH of the suspensions is also a function of their use. In the detergency application, this pH expressed at 1% by weight of dry zeolite is approximately 11.
  • a silicone resin having the definition given above is used in suspensions of the type described above.
  • silicone resins are branched organopolysiloxane polymers which are well known and commercially available.
  • radicals R of the units constituting these resins are preferably alkyl radicals having 1 to 6 carbon atoms inclusive.
  • alkyl radicals R of the methyl, ethyl, isopropyl, tert-butyl and n-hexyl radicals.
  • These resins are preferably hydroxylated and in this case have a weight content of hydroxyl group of between 0.1 and 10%.
  • resins examples include MQ resins, MDQ resins, TD resins and MDT resins.
  • Resins having a molecular mass of less than 25,000 can be used more particularly.
  • the resins can be used in the solid state or in the form of aqueous emulsions or of emulsions or solution in an organic solvent.
  • the amounts used are between 0.01 and 2% by weight of the composition, more particularly between 0.05 and 0.3% by weight of solid products, relative to the final suspension.
  • suspensions which are stable that is to say which do not settle or little.
  • these suspensions can be transported or stored without difficulty.
  • the suspensions comprise, in addition to the siliconate, a stabilizer.
  • magnesium is preferably used.
  • the cation can, moreover, be provided in the form of a halide, in particular a chloride, more particularly uses magnesium chloride, for example magnesium chloride hexahydrate.
  • the amount of cation used generally varies between 0.002 and 0.5% relative to the weight of the final suspension.
  • stabilizers which can be used according to the invention, mention may be made of natural polysaccharides of animal origin such as chitosame and chitin; of plant origin such as carragenanes, alginates, gum arabic, guar, carob, tara, cassia, konjak mannan, and finally those of bacterial or biogum origin.
  • animal origin such as chitosame and chitin
  • plant origin such as carragenanes, alginates, gum arabic, guar, carob, tara, cassia, konjak mannan, and finally those of bacterial or biogum origin.
  • Biogums are polysaccharides of high molecular weight, generally greater than a million, obtained by fermentation of a carbohydrate under the action of a microorganism.
  • biogum which can be used in the suspension which is the subject of the present invention there may be mentioned more particularly, xanthan gum, that is to say that obtained by fermentation under the action of bacteria or fungi belonging to the genus Xanthomonas such as Xanthomonas begoniae , Xanthomonas campestris , Xanthomonas carotae , Xanthomonas hederae , Xanthomonas incanae, Xanthomonas malvacearum, Xanthomonas papavericola , Xanthomonas phaseoli , Xanthomonas pisi , Xanthomonas vasculorum, Xanthomonas vesicatoria , Xanthomonas .
  • Xanthan gum that is to say that obtained by fermentation under the action of bacteria or fungi belonging to the genus Xanthomonas such as X
  • Xanthan gums are commonly found commercially.
  • gellan gum obtained from Pseudomonas Elodea, Rhamsan and Welan gums obtained from Alcaligenes.
  • cellulose and starch or their derivatives. Mention may be made, for example, of carboxymethylcellulose, methylcellulose, ethylcellulose, hydroxymethylcellulose, cyanoethylated starch, carboxymethylated starch.
  • polysaccharides are used in solid form, in powder, or in aqueous solution. They are generally used in an amount which varies between 0.001 and 2%, and more particularly from 0.01 and 0.5% by weight relative to the final suspension.
  • carboxylic acids and their salts and in particular acetic, formic, oxalic, malic, citric and tartaric acids.
  • alkaline salts such as NaHCO3, NaCl, Na2CO3, Na2SO4 and sodium pyrophosphate or tripolyphosphate.
  • water-soluble polymers of acrylic acid crosslinked with a sucrose polyallylether for example in a proportion of approximately 1% and having an average of approximately 5.8 allyl groups for each molecule of sucrose. , polymers with a molecular weight greater than 1,000,000.
  • Polymers of this type can be found in the CARBOPOL® series, for example CARBOPOL® 934, 940 and 941.
  • the amounts used as a percentage by weight relative to the final suspension vary between 0.001 and 2%.
  • aqueous suspensions based on zeolite according to the invention are prepared by chaining the following steps: the desired amount of silicone resin, and optionally at least one stabilizer, is introduced into an aqueous zeolite suspension, and mixing is carried out.
  • the pH of the suspensions can be adjusted to the desired value in a known manner by the addition of any suitable neutralizing agent.
  • Suspensions comprising zeolites and stabilized by the systems which have just been described can be used in numerous applications.
  • They can be used in the form of suspensions based essentially on zeolites and the stabilizing additives mentioned above. In this case they can enter into the preparation of detergent compositions. They can be used in any field other than detergency for which zeolites are used, for example in stationery.
  • the present invention also relates to detergent compositions, in particular for liquid detergents, comprising, in addition to the suspensions based on zeolite and stabilizers of the invention, all the other additives known in detergency such as bleaching agents, foam control agents, anti-redeposition agents, perfumes, dyes, enzymes.
  • the dry extract of the aqueous zeolite suspension is given in percentage by weight in% of anhydrous zeolite determined by a measurement of loss on ignition at 850 ° C. for one hour.
  • the pH indicated is given for an aqueous dispersion containing 1% of dry zeolite and it is measured using a high alkalite pH electrode.
  • the RHEOMAT® 30 equipped with the centered measurement system B is used as rheometer.
  • the measurement consists in performing a cycle in speed gradient (ascent plus descent).
  • the range of speed gradient explored is between 0.0215 and 157.9 s ⁇ 1, which corresponds to rotational speeds of the mobile from 0.0476 to 350 revolutions per minute.
  • the viscosities reported in the examples correspond to measurements obtained during the descent in speed gradient.
  • the sedimentation is determined by introducing the zeolite suspension into graduated cylinders of 50 or 100 cc. The volumes of supernatant and decantate are measured every five days. The test pieces are left at room temperature (20 ° C) or placed in a thermostatically controlled enclosure.
  • a resin is used in which R is methyl. This resin is used here in the solid state. It is marketed by the applicant under the reference RHODORSIL® 865 A in the form of an emulsion.
  • Test 1 is carried out with 0.17% by weight of resin relative to the suspension and 1% by weight of oxalic acid.
  • Test 2 is made for comparison on the same suspension brought to the same pH with oxalic acid alone in the same quantity; the suspension of test 2 is stable but it is found to be viscous.
  • Test 3 is carried out for comparison on a suspension containing 49.7% of zeolite but not containing either resin or oxalic acid; it is found that the suspension of test 3 is not stable.
  • Test 1 2 comparison 3 comparison Anhydrous zeolite% weight suspension 49.3 49.3 49.7 pH 10.87 10.86 11.57 Viscosity (in mPa.s) at 5s ⁇ 1 4030 7130 5920 Sedimentation Supernatant% volume 5 days 3 3.5 10 days 8 6 15 days Decantate % volume 5 days ⁇ 1 60 10 days ⁇ 1 90 15 days

Landscapes

  • Chemical & Material Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Silicates, Zeolites, And Molecular Sieves (AREA)
  • Detergent Compositions (AREA)
  • Silicon Polymers (AREA)
  • Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
  • Fluid-Damping Devices (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
EP90402760A 1989-10-09 1990-10-05 Suspension aqueuse de zéolite comprenant une résine silicone Expired - Lifetime EP0427577B1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR8913137 1989-10-09
FR8913137A FR2652818B1 (fr) 1989-10-09 1989-10-09 Suspension de zeolite comprenant une resine silicone.

Publications (2)

Publication Number Publication Date
EP0427577A1 EP0427577A1 (fr) 1991-05-15
EP0427577B1 true EP0427577B1 (fr) 1996-03-27

Family

ID=9386193

Family Applications (1)

Application Number Title Priority Date Filing Date
EP90402760A Expired - Lifetime EP0427577B1 (fr) 1989-10-09 1990-10-05 Suspension aqueuse de zéolite comprenant une résine silicone

Country Status (14)

Country Link
US (1) US5064562A (no)
EP (1) EP0427577B1 (no)
JP (1) JPH03207797A (no)
KR (1) KR910008122A (no)
AT (1) ATE136054T1 (no)
BR (1) BR9005012A (no)
CA (1) CA2027013A1 (no)
DE (1) DE69026198D1 (no)
FI (1) FI904946A0 (no)
FR (1) FR2652818B1 (no)
IE (1) IE903594A1 (no)
NO (1) NO177189C (no)
PT (1) PT95532A (no)
YU (1) YU47378B (no)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2652819B1 (fr) * 1989-10-09 1994-01-07 Rhone Poulenc Chimie Suspension de zeolite comprenant un siliconate.
IT1250437B (it) * 1991-07-01 1995-04-07 Paolo Colombo Sospensioni acquose stabili e facilmente pompabili di zeolite
GB9315671D0 (en) * 1993-07-29 1993-09-15 Dow Corning Sa Foam control agents and their use
JP4889096B2 (ja) * 2006-02-09 2012-02-29 株式会社 資生堂 抗菌性ゼオライト及びこれを含有する皮膚外用剤
US20150258150A1 (en) * 2014-03-14 2015-09-17 Osprey Biotechnics, Inc. Bacillus amyloliquefaciens strain

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2702855A (en) * 1946-02-01 1955-02-22 Bess Leon Differentiating circuits
US3769222A (en) * 1971-02-09 1973-10-30 Colgate Palmolive Co Free flowing nonionic surfactants
DE2854484A1 (de) * 1978-12-16 1980-06-26 Bayer Ag Stabile waessrige zeolith-suspensionen
US4402867A (en) * 1981-12-22 1983-09-06 Mobil Oil Corporation Silica-modified zeolite catalysts
DE3208598A1 (de) * 1982-03-10 1983-09-22 Degussa Ag, 6000 Frankfurt Verfahren zur herstellung von mit organosilanen oberflaechenmodifizierten zeolithen
FR2523950B1 (fr) * 1982-03-23 1985-11-22 Mizusawa Industrial Chem Procede de preparation d'une suspension de zeolite dont la stabilite statique et la stabilite dynamique sont excellentes
US4545919A (en) * 1982-08-31 1985-10-08 Ciba-Geigy Corporation Detergent composition for washing off dyeings obtained with fibre-reactive dyes and washing process comprising the use thereof
GB8401875D0 (en) * 1984-01-25 1984-02-29 Procter & Gamble Liquid detergent compositions
DE3408040A1 (de) * 1984-03-05 1985-09-12 Henkel KGaA, 4000 Düsseldorf Stabilisierte, waessrige zeolith-suspension
FR2568790B1 (fr) * 1984-08-10 1990-01-12 Rhone Poulenc Chim Base Procede d'obtention d'une suspension aqueuse stable et pompable de zeolite et suspension ainsi obtenue
US4639321A (en) * 1985-01-22 1987-01-27 The Procter And Gamble Company Liquid detergent compositions containing organo-functional polysiloxanes
JPS61256915A (ja) * 1985-05-10 1986-11-14 Showa Koki Kk ゼオライトスラリ−
DE3536934A1 (de) * 1985-10-17 1987-04-23 Bayer Ag Elektroviskose fluessigkeiten
JPS62153116A (ja) * 1985-12-24 1987-07-08 Showa Koki Kk 水性ゼオライトスラリ−
JPS62167216A (ja) * 1986-01-17 1987-07-23 Lion Corp 水性ゼオライト懸濁液
US4673516A (en) * 1986-09-02 1987-06-16 Integral Corporation Aqueous hydrogel lubricant
DE3805624A1 (de) * 1988-02-24 1989-08-31 Degussa Pulverfoermiger waschmittelentschaeumer

Also Published As

Publication number Publication date
YU188690A (sh) 1993-10-20
CA2027013A1 (fr) 1991-04-10
JPH03207797A (ja) 1991-09-11
FR2652818A1 (fr) 1991-04-12
NO904360L (no) 1991-04-10
US5064562A (en) 1991-11-12
IE903594A1 (en) 1991-05-08
KR910008122A (ko) 1991-05-30
DE69026198D1 (de) 1996-05-02
EP0427577A1 (fr) 1991-05-15
FR2652818B1 (fr) 1994-04-01
PT95532A (pt) 1991-08-14
NO904360D0 (no) 1990-10-08
NO177189C (no) 1995-08-02
NO177189B (no) 1995-04-24
BR9005012A (pt) 1991-09-10
FI904946A0 (fi) 1990-10-08
ATE136054T1 (de) 1996-04-15
YU47378B (sh) 1995-01-31

Similar Documents

Publication Publication Date Title
EP0233110B2 (fr) Utilisation d'un sel pour influencer l'écoulement de compositions épaissies
CA1330612C (fr) Granules de biopolymere a dispersabilite et dissolution rapides
EP0654482B1 (fr) Compositions à base de polymères cationiques et de gomme xanthane anionique
EP1192215A1 (fr) Dispersion de microfibrilles et/ou de microcristaux, notamment de cellulose, dans un solvant organique
FR2688222A1 (fr) Composes polymeres de l'acide glucuronique, procede de preparation et utilisation notamment en tant que moyens gelifiants, epaississants, hydratants, stabilisants, chelatants ou floculants.
FR2531093A1 (fr) Suspensions concentrees pompables de polymeres hydrosolubles
EP0001192A1 (fr) Compositions gélifiantes à base de galactomannanes et de xanthane désacétylé et procédé d'obtention
EP0079836B1 (fr) Compositions à base de gommes hydrosolubles, leur préparation et leur utilisation
CN1227598A (zh) 含黄原胶的酸性清洁剂组合物
EP0422998B1 (fr) Suspension aqueuse de zéolite comprenant un siliconate
EP0427577B1 (fr) Suspension aqueuse de zéolite comprenant une résine silicone
CN1334822A (zh) 制备低粘性水溶性的纤维素醚的方法
FR2759376A1 (fr) Procede pour obtenir des microfibrilles de cellulose cationiques ou leurs derives solubles, ainsi que celluloses obtenues par ce procede
CA2073622C (fr) Composition derivant d'un succinoglycane, son procede de preparation et ses applications
EP0071547B1 (fr) Dispersions aqueuses de compositions organopolysiloxaniques antimousses
FR2639645A1 (fr) Solutions liquides concentrees de polysaccharides
FR2652820A1 (fr) Suspensions stables de zeolites comprenant un succinoglycane.
FR2540879A1 (fr) Suspensions concentrees de polymeres hydrosolubles
FR2760757A1 (fr) Procede de depolymerisation d'alginate et fragments d'alginate ainsi obtenus
EP0699433A2 (fr) Composition cosmétique ou pharmaceutique contenant des dérivés du chitosane
FR2805267A1 (fr) Biopolymere dispersable et a hydratation rapide
JPH0273898A (ja) 液状クレンザー
FR2863270A1 (fr) Polysaccharides, leur procede de preparation et leur utilisation

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: A1

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

17P Request for examination filed

Effective date: 19910718

17Q First examination report despatched

Effective date: 19950329

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 IT LI LU 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 PRESCRIBED TIME-LIMIT;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.

Effective date: 19960327

Ref country code: ES

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

Effective date: 19960327

Ref country code: AT

Effective date: 19960327

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: 19960327

Ref country code: DK

Effective date: 19960327

Ref country code: NL

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: 19960327

Ref country code: GB

Effective date: 19960327

REF Corresponds to:

Ref document number: 136054

Country of ref document: AT

Date of ref document: 19960415

Kind code of ref document: T

REF Corresponds to:

Ref document number: 69026198

Country of ref document: DE

Date of ref document: 19960502

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

Ref country code: SE

Effective date: 19960627

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

Ref country code: DE

Effective date: 19960628

NLV1 Nl: lapsed or annulled due to failure to fulfill the requirements of art. 29p and 29m of the patents act
GBV Gb: ep patent (uk) treated as always having been void in accordance with gb section 77(7)/1977 [no translation filed]

Effective date: 19960327

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

Ref country code: CH

Effective date: 19961031

Ref country code: LU

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

Effective date: 19961031

Ref country code: LI

Effective date: 19961031

Ref country code: BE

Effective date: 19961031

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
BERE Be: lapsed

Owner name: RHONE-POULENC CHIMIE

Effective date: 19961031

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

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

Ref country code: FR

Effective date: 19970630

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST