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EP0331370A2 - Composition détergente - Google Patents

Composition détergente Download PDF

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Publication number
EP0331370A2
EP0331370A2 EP19890301851 EP89301851A EP0331370A2 EP 0331370 A2 EP0331370 A2 EP 0331370A2 EP 19890301851 EP19890301851 EP 19890301851 EP 89301851 A EP89301851 A EP 89301851A EP 0331370 A2 EP0331370 A2 EP 0331370A2
Authority
EP
European Patent Office
Prior art keywords
composition
present
liquid
zeolite
detergent
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
EP19890301851
Other languages
German (de)
English (en)
Other versions
EP0331370A3 (en
EP0331370B2 (fr
EP0331370B1 (fr
Inventor
Jakob Van Dijk
Hidde Frankena
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.)
Unilever PLC
Original Assignee
Unilever PLC
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
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10632461&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP0331370(A2) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Unilever PLC filed Critical Unilever PLC
Publication of EP0331370A2 publication Critical patent/EP0331370A2/fr
Publication of EP0331370A3 publication Critical patent/EP0331370A3/en
Application granted granted Critical
Publication of EP0331370B1 publication Critical patent/EP0331370B1/fr
Publication of EP0331370B2 publication Critical patent/EP0331370B2/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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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
    • C11D3/02Inorganic compounds ; Elemental compounds
    • C11D3/04Water-soluble compounds
    • C11D3/08Silicates
    • 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

Definitions

  • the present invention relates to detergent compositions.
  • it relates to liquid machine dishwashing detergent compositions suitable for use in cleansing food soils from cooking utensils, dishes, glasses and similar ware.
  • the present invention relates to a stable, pourable, aqueous system comprising at least partially undissolved builder salts and a dissolved alkali silicate, the composition being essentially free of conventional structuring agents.
  • the system is characterised by its thixotropic nature.
  • Detergents for use in domestic machine dishwashers are generally available in powdered or granular forms.
  • solid compositions exhibit a number of disadvantages for the producer and user.
  • the compositions cannot generally be spray-dried, and thus separate manufacturing facilities to those generally used for powdered detergents must be built.
  • the powders often incorporate large lumps caused by caking during storage at high humidity. This can cause difficulties in dispersion. Powdered forms of the product are often very dusty, which can affect dispensing as well as causing irritation.
  • liquid detergents must meet certain requirements. Firstly, the liquid must be a uniform mixture of ingredients in order to deliver the optimum combination of active components to the wash with each dose.
  • active components we mean those components which actually take part in the cleaning, rather than those acting as fillers. In many formulations described in the art, this requires that the liquid be shaken before each use in order to re-mix the different components.
  • a preferred product should be stable against physical separation and segregation of the active components during storage.
  • Particulate solids for example detergency builders, should remain suspended in liquid detergents.
  • some kind of structuring system is necessary. In aqueous detergent liquids this may be achieved either by "external structuring", ie adding an additional component such as a polymer or clay, or using the interaction of the water in the liquid and the detergent actives themselves, to form an "internal structure" to support the solids (eg secondary alkane sulphonates and phosphonates).
  • external structuring ie adding an additional component such as a polymer or clay, or using the interaction of the water in the liquid and the detergent actives themselves, to form an "internal structure" to support the solids (eg secondary alkane sulphonates and phosphonates).
  • microscopic investigation indicates that some type of suspending network is formed.
  • the phrase 'structuring agent' as used herein is taken to mean any component, e.g. clay, polymer or biocellulosic, which at suitable amounts within a liquid imparts a structure to said liquid, usually by network formation.
  • the use of such agents, particularly clay, in lower amounts is not to be taken as being excluded from compositions. Such low amounts may act as builders or rinse aids.
  • the critical amount of the component in question may only be determined by reference to experiments or the prior art.
  • the detergent For use with machine dishwashers, the detergent must be compatible with the dishwashing equipment presently available.
  • Home dishwashing machines use a detergent cup which has been designed to house powdered or granular solid detergent and deliver it to a specific wash cycle.
  • the cups are usually held vertically on the dishwasher door and are not designed to contain low viscosity liquids. Consequently, liquids for use as machine dishwashing detergents must possess sufficient viscosity to be effectively retained in the cup and avoid leakage into the machine during cycles which precede the wash. Excessive leakage will lead to under-dosing in the wash cycle and may affect cleaning performance. However, they must not be so viscous that they cannot be washed out of the dispensing cup at the appropriate time.
  • GB 1 527 706 discloses a slurry structured by the addition of synthetic polymers. However, it is thought that the low yield point in liquids containing, eg polyacrylate as the only structuring agent, causes poor cup retention.
  • GB 2 140 450 discloses liquids structured with clay. The clay lowers the amount of active component which can be delivered in each dose. Furthermore, the presence of insoluble clay minerals can negatively affect glass spotting and filming performance.
  • the use of biopolymers or cellulosics within a liquid detergent base has also been proposed to provide thickened systems, eg US 4 226 736 and US 4 260 528.
  • GB 2 185 037 has disclosed the use of long-chain fatty acids to provide a thickening effect.
  • the systems described in the prior art are all, in principle, structured by the use of external, network-forming structurants and, in general, these liquids possess a shear thinning character, ie they exhibit a high viscosity at low shear rate and a low viscosity at high shear rate. Furthermore, and this illustrates the thixotropic nature of the liquids, the viscosity of these liquids is time-dependent after distortion has taken place.
  • the present invention makes use of different principles to obtain pourable and stable liquid systems.
  • the present invention does not involve the use of a network-forming structurant. Due to the absence of such a structurant, which in the current state of the art is judged to be essential for keeping the solid particles well suspended, the present invention involves liquid systems (dispersions) which are Newtonian (eg not shear thinning) over a broad range of shear rate values: 1-100 sec ⁇ 1.
  • compositions of the present invention the solids are present as individual particles and not as flocculates.
  • Addition of an electrolyte may broaden the range in which the desired rheological behaviour is observed.
  • the deflocculation effect can be illustrated by the following observation: the addition of 40% zeolite 4A to a 20% sodium disilicate (ratio 3.6) solution results in the formation of a viscous, shear thinning unusable paste outside the scope of the invention. Adjusting the silicate ratio with NaOH or KOH the viscosity will drop considerably and a thin, pourable, pseudo-Newtonian system is obtained by deflocculation of the particles.
  • a stable, viscous, liquid detergent composition comprising:
  • the ratio of the alkali-metal silicate is between 0.5 and 3.0, preferably between 0.5 and 2.2 and more preferably between 0.6 and 1.9.
  • the preferred rheological behaviour is identified by the Thixotropic Index (TI) which has to be between 0.5 and 2.5.
  • the Thixotropic Index is herein defined as the ratio of the apparent LVT Brookfield viscosity of a sample after 3 minutes at room temperature using a No 4 spindle at (a) 3 rpm and (b) 30 rpm.
  • compositions according to the present invention may be used in formulating detergent liquid cleaning products. These may be formulated in a very wide range of specific forms, according to the intended use. They may be formulated as cleaners for hard surfaces (with or without abrasive) or as agents for ware washing (cleaning of dishes, cutlery etc) either by hand or mechanical means, as well as in the form of specialised cleaning products, such as for cleaning surgical apparatus or artificial dentures.
  • Products formulated for ware washing, in particular for use in machine dishwashers, constitute a preferred form of the present invention.
  • composition according to the present invention has improved rheology and stability in comparison to compositions of the prior art and can deliver a high and uniform dosage of active ingredients to the machine wash cycle.
  • the detergent builder material may preferably be a non-phosphate builder salt.
  • Such builders include water-soluble inorganic carbonate and bicarbonate.
  • Water-soluble organic builders which may be used include polyacetates, carboxylates, polycarboxylates and polyhydroxy sulphonates, at least a proportion of the salt remaining undissolved.
  • Particularly preferred as builders are zeolite and amorphous silica/alumina builders.
  • Aluminosilicates of the zeolite type may be prepared as described in US 2 882 243 (Union Carbide) or of the amorphous type as described in EP 0 097 512 (Unilever).
  • the aluminosilicate is preferably of the formula 0.8-1.5 Na2O; Al2O3; 1.7 - 3.0 SiO2; 2 - 6 H2O.
  • Examples of other suitable builders are NTA, EDTA, CMOS and DPA.
  • the builder may constitute from 5-60%, most preferably from 20-40%.
  • the second essential component of the present invention is a silicate material.
  • disilicates are particularly preferred, although metasilicates may also be included.
  • the alkali-metal silicates which are used serve as anti-corrosion agents, protecting metal and china surfaces against harshly alkaline environments present during a dishwashing cycle.
  • the silicate-based material may constitute from 3-40%, most preferably from 5-20%.
  • the present invention comprises compositions which do not necessarily contain any detergent surfactants.
  • the compositions may be used for the delivery of caustic agents to the wash liquor during mechanical dishwashing operations.
  • one or more detergent surfactant agents may be selected from one or more of nonionic, anionic, cationic, zwitterionc and amphoteric agents.
  • Such agents are commercially available and will be well known by those skilled in the art; for instance, they are fully described in the literature, such as in "Surface Active Agents and Detergents", Volumes I and II by Schwarz, Perry and Berch.
  • any detergent active material comprises one or more nonionic agents, for example the condensation products of alcohols having from 8-16 carbon atoms, and alkyl phenols with alkylene oxides including ethylene oxide, propylene oxide, butylene oxide and mixtures thereof.
  • the alcohols are linear, having from 12-15 carbon atoms, and are condensed with 2-10 mols of ethylene oxide.
  • Most preferred are those compounds which are generally regarded as "low-foaming", especially those where the alkylene oxide chain is terminated by a moiety other than hydrogen.
  • compositions according to the present invention may be prepared by admixture of the various components.
  • An alkali-metal hypochlorite may be present in the formula as an agent for removing tea, coffee and other food stains from cups, dishes, flatware, etc.
  • the bleach source may be present in the mixture at from 0.1-10 wt %, with the most preferred range being from 0.1-2 wt % (percentages as active chlorine).
  • Electrolytes such as NaCl, NaI, Na2SO4 may be included in the composition at from 0.1 to 10 wt %.
  • Defoamers may be included in the composition. These defoamers may be of the general type of slightly soluble alkyl carboxylates, alkyl phosphates, hydrophobic silicas, silicone defoamers, or many others. In addition to being an effective defoamer, the species should be stable to hypochlorite.
  • the defoamer may optionally be present in the composition at from 0-5 wt %, more preferably from 0.1-1 wt %, and most preferably from 0.1-0.5 wt %.
  • the products according to the present invention exhibit a high degree of stability at room temperature, in comparison to other systems. Unlike known liquids, the products produced in accordance with the present invention do not require shaking in order to redisperse the ingredients. Furthermore, compositions formulated in accordance with the present invention exhibit a higher density (1.7-1.8) than comparable products of the prior art. This is particularly important when considering transportation. A more concentrated liquid benefits from lower packing and transport costs. Also, a unit dose will deliver more active ingredients per unit dose than products produced in accordance with the art.
  • Liquid systems according to the present invention are not susceptible to setting after storage. Even after prolonged storage the product does not solidify and no setting has been observed. The inference is that the product can be dosed without shaking or squeezing the bottle which is required for the current liquids with an external structurant. Dealing with bottles of 1.5-2.5 kg this benefits the convenience aspect of the product.
  • compositions of the present invention provide a liquid system which is very convenient for consumers whilst being also perfectly suitable for an automatic dosing application.
  • the automatic dosing principle can be used for domestic as well as industrial dishwashing machines.
  • compositions according to the present invention are pourable from rest without need for shear thinning. Dispenser behaviour is strongly determined by the rheological properties of the liquid. In the prior art, Newtonian liquids are not considered to be suitable. Some of the liquids according to the present invention have been tested to measure dispenser cup leakage in a number of commercially-­available dispenser types. It was found that the degree of dispenser cup leakage was acceptable if the liquid had a viscosity of at least 2000 mPAS.
  • dishwashing compositions formulated according to the present invention show less tendency to cause spot formation on glass than other conventionally structured (eg by polymers or clays) liquid detergent systems. This is particularly noticeable after a number of wash cycles.
  • a further possible use of the system of the invention arises when considering systems incorporating zeolite as the builder.
  • Zeolite slurrys of the prior art are known to be unstable.
  • the liquids of the present invention provide a stable zeolite slurry which does not separate on standing.
  • the slurry can be spray dried as a basis for formulating powders for, e.g. fabric or ware washing.
  • the composition With the addition of KOH to lower the silicate ratio, the composition exhibits pseudo-Newtonian behaviour. When no KOH is added, the liquid is shear thinning.
  • the stability of liquid compositions according to the present invention was measured as the percentage of separation at 1, 2, 3 and 4 weeks after storage at 20°C.
  • Zeolite Disilicate KOH t (weeks) 1 2 3 4 % Separation 13 20 10 3 6 13 12 36 20 10 0 1 1 1 46 20 10 0 1 1 1 50 20 10 0 0 0 0 32 20 5 1 2 2 2 48 20 5 1 1 1 1
  • the build-up of spots over 4 washes is measured as the number of spots on a glass tumbler: 0 1 1-5 2 6-10 3 11-20 4 >20 5
  • composition wt% Zeolite 4A 42 Sokalan Polymer (20% slurry) 5 Disilicate (ratio 2.0) 20 K OH (85% soln) 5 HOCl (as Cl2) 1 Water to 100
  • composition was found not to have separated over a period of weeks and was suitable for cleaning dishes in a machine dishwasher.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (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)
EP89301851A 1988-02-26 1989-02-24 Procédé de fabrication d'une composition détergente Expired - Lifetime EP0331370B2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB888804590A GB8804590D0 (en) 1988-02-26 1988-02-26 Detergent compositions
GB8804590 1988-02-26

Publications (4)

Publication Number Publication Date
EP0331370A2 true EP0331370A2 (fr) 1989-09-06
EP0331370A3 EP0331370A3 (en) 1990-07-25
EP0331370B1 EP0331370B1 (fr) 1994-10-05
EP0331370B2 EP0331370B2 (fr) 1999-06-09

Family

ID=10632461

Family Applications (1)

Application Number Title Priority Date Filing Date
EP89301851A Expired - Lifetime EP0331370B2 (fr) 1988-02-26 1989-02-24 Procédé de fabrication d'une composition détergente

Country Status (9)

Country Link
EP (1) EP0331370B2 (fr)
JP (1) JPH07799B2 (fr)
AU (1) AU615517B2 (fr)
BR (1) BR8900868A (fr)
CA (1) CA1312521C (fr)
DE (1) DE68918612T3 (fr)
ES (1) ES2063812T5 (fr)
GB (1) GB8804590D0 (fr)
ZA (1) ZA891459B (fr)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994004655A1 (fr) * 1992-08-19 1994-03-03 Colgate-Palmolive Company Detergent pour lave-vaisselle automatique
WO1994004647A1 (fr) * 1992-08-19 1994-03-03 Colgate-Palmolive Company Silicates structures et leur utilisation dans des lave-vaisselle automatiques
WO1994004646A1 (fr) * 1992-08-19 1994-03-03 Colgate-Palmolive Company Composition detergente
TR28439A (tr) * 1993-08-18 1996-06-24 Colgate Palmolive Co Yapilandirilmis silikatlar ve otomatik bulasik makinelerinde kullanimlari.
US6001791A (en) * 1995-07-19 1999-12-14 Henkel Kommanditgesellschaft Auf Aktien Paste-form washing-up agent and its manufacture
EP2199386A1 (fr) 1993-10-08 2010-06-23 Novozymes A/S Variants d'amylase

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6443965B2 (ja) * 2014-07-31 2018-12-26 花王株式会社 液体漂白剤組成物
JP6655388B2 (ja) * 2015-12-28 2020-02-26 ライオン株式会社 食器洗い機用洗浄剤及びその製造方法、並びにスクイズ容器入り洗浄剤製品

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT330930B (de) * 1973-04-13 1976-07-26 Henkel & Cie Gmbh Verfahren zur herstellung von festen, schuttfahigen wasch- oder reinigungsmitteln mit einem gehalt an calcium bindenden substanzen
JPS5464504A (en) * 1977-11-01 1979-05-24 Nippon Chem Ind Co Ltd:The Zeolite slurry for detergents
JPS5464531A (en) * 1977-11-02 1979-05-24 Nippon Zeon Co Ltd Water-dilutable coating composition
EP0079646B1 (fr) * 1981-11-16 1986-05-21 Unilever N.V. Composition détergente liquide
MX167884B (es) * 1983-12-22 1993-04-20 Albright & Wilson Composicion detergente liquida
GB8334250D0 (en) * 1983-12-22 1984-02-01 Albright & Wilson Liquid detergent compositions

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994004655A1 (fr) * 1992-08-19 1994-03-03 Colgate-Palmolive Company Detergent pour lave-vaisselle automatique
WO1994004647A1 (fr) * 1992-08-19 1994-03-03 Colgate-Palmolive Company Silicates structures et leur utilisation dans des lave-vaisselle automatiques
WO1994004646A1 (fr) * 1992-08-19 1994-03-03 Colgate-Palmolive Company Composition detergente
TR27483A (tr) * 1992-08-19 1995-06-07 Colgate Palmolive Co En azindan bir hidroksil grubuna sahip olan bir organik bilesigi ihtiva eden otomatik bulasik yikama deterjani.
TR28432A (tr) * 1992-08-19 1996-06-24 Colgate Palmolive Co Alkali metal silikat ve siklikazot ihtiva eden bilesik iceren temizleme bilesimi.
TR28439A (tr) * 1993-08-18 1996-06-24 Colgate Palmolive Co Yapilandirilmis silikatlar ve otomatik bulasik makinelerinde kullanimlari.
EP2199386A1 (fr) 1993-10-08 2010-06-23 Novozymes A/S Variants d'amylase
US6001791A (en) * 1995-07-19 1999-12-14 Henkel Kommanditgesellschaft Auf Aktien Paste-form washing-up agent and its manufacture

Also Published As

Publication number Publication date
JPH01261500A (ja) 1989-10-18
EP0331370A3 (en) 1990-07-25
ES2063812T5 (es) 1999-08-16
AU615517B2 (en) 1991-10-03
DE68918612T3 (de) 1999-08-19
BR8900868A (pt) 1989-10-17
CA1312521C (fr) 1993-01-12
DE68918612T2 (de) 1995-02-09
EP0331370B2 (fr) 1999-06-09
DE68918612D1 (de) 1994-11-10
JPH07799B2 (ja) 1995-01-11
AU3029989A (en) 1989-08-31
EP0331370B1 (fr) 1994-10-05
ZA891459B (en) 1990-10-31
ES2063812T3 (es) 1995-01-16
GB8804590D0 (en) 1988-03-30

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