Classifications

• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
  • C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
  • C11D17/0013—Liquid compositions with insoluble particles in suspension
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
  • C11D17/0008—Detergent materials or soaps characterised by their shape or physical properties aqueous liquid non soap compositions
  • C11D17/003—Colloidal solutions, e.g. gels; Thixotropic solutions or pastes
• • C—CHEMISTRY; METALLURGY
  • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
  • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
  • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
  • C11D3/02—Inorganic compounds ; Elemental compounds
  • C11D3/04—Water-soluble compounds
  • C11D3/06—Phosphates, including polyphosphates

Definitions

• This invention relates to fluid compositions, particularly detergent compositions, comprising a continuous and one or more discontinuous phases, the fluid stably containing small bubbles of gas.
• One aspect of the invention relates to compositions in which gas bubbles of a particular size range remain dispersed. Applicants have not only discovered the gas bubble component of compositions, but have also discovered how control and refinement of incorporation of these bubbles into compositions imparts a surprising stability against phase separation.
• a further aspect of the invention is a process for stabilising compositions by the incorporation of gas bubbles. Most particularly, the invention relates to compositions which comprise solid particles of a very small size (less than 5 microns) and a process for stabilising compositions by incorporation of gas bubbles therein.
• compositions with a continuous and one or more discontinuous phases can be rendered quite stable against separation into different phases, a phenomenon known as syneresis, by incorporating bubbles of gas having diameters of from 3 to 150 microns, with the average diameter being from 3 to 45 microns.
• the resulting "aerated" composition is greatly more stable against separation over longer storage times and high temperatures then the non-aerated composition.
• This stability is an important characteristic: stable compositions not only provide a generally identical mix of components from one dose to the next, they also avoid the appearance of unattractive separation layers.
• compositions of the present invention comprise a continuous and one or more discontinuous phases together with from about 1% up to about 20% by volume of gas in bubbles having diameters of 3 to 150 microns. A surfactant must also be present.
• the bubbles are present throughout the continuous phase of the composition, which also has one or more non-gaseous discontinuous phases dispersed throughout.
• the continuous phase of the invention is generally liquid, although ingredients in the continuous or one of the discontinuous phases may impart a high viscosity or thixotropy to the composition, making the total composition a gel, paste or soft solid.
• the compositions coming within the invention cover a wide range of materials. They may comprise a liquid continuous phase with a liquid or solid discontinuous phase and may be aqueous or non-aqueous. They are generally useful as detergent cleaning compositions, such as mechanical dishwashing, hard surface or fabric washing compositions. These particular types of compositions only illustrate and do not limit the scope of the compositions within the invention.
• the frothing agent added to water selectively controls the wettability of the minerals.
• An air bubble usually does not adhere to a clean mineral surface.
• the mineral acquires a hydrophobic coating and an air bubble may attach quite readily.
• the greater the affinity between the hydrophobic mineral surface and the bubble the larger the area of surface area contact between the bubble and mineral will be, and the smaller the contact angle between the two is.
• GB 2 140 451 (Lion Corp) describes a liquid detergent composition which contains a polishing agent and has non-skin roughness.
• the composition has alkyl polyethoxylene sulphate and amine oxide as surfactants; clay as thickening and stabiliser; an insoluble scouring powder of average particle size 1 to 150 microns; and 2.5% to 8.5% by volume of gas bubbles having 0.1 to 0.7 millimetre average diameter. Substantially all the bubbles are smaller than 1.5 millimetres in size. If the amount of amine oxide exceeds 5% by weight, the dispersion stability is lost.
• GB 1 304 080 (Colgate) permits bubbles of 0.1-4 millimetres in size in dentifrice compositions.
• Bubbles have also been incorporated into liquid detergent compositions.
• GB 2 140 451 (Lion) and JP 60/076598 (Lion) incorporate gas bubbles of 0.1-0.7 millimetre and 50-700 microns diameter respectively into their liquid detergents.
• liquid detergent composition comprising:
• compositions of the invention incorporate bubbles, but within the following limits: 1% to 20% by volume of gas is present as bubbles which range in size from 3 to 150 microns, and have an average size of 3 to 45 microns.
• compositions having a continuous and one or more discontinuous phases, and incorporating a surface active agent When gas is present within these limits in compositions having a continuous and one or more discontinuous phases, and incorporating a surface active agent, it is found that the gas imparts a surprising stability against phase separation to the compositions.
• the stability of these aerated compositions is believed to be due not to any structured liquid effect, eg lamellar phase structures, but rather to the interaction of the gas bubbles with the one or more discontinuous phases.
• the bubbles appear to co-operate with only the one or more discontinuous phase materials.
• the bubbles appear to reduce the density of the one or more discontinuous phase materials to a value close to the density of the continuous phase.
• the stability of the compositions is believed to result from this substantial equalisation of the density of the continuous with the one or more discontinuous phases.
• the one or more discontinuous phases of compositions of the invention have a density which is greater than that of the continuous phase. If there are multiple discontinuous phases in a composition, that composition may still benefit from aeration if the average density of all the discontinuous phases is substantially greater than the density of the continuous phase.
• compositions of the invention resist separation, not only over long storage periods at ambient temperature, but also over long times at elevated temperatures (37°C). Surprisingly, the gas bubbles remain in the composition during exposure to these elevated temperatures and do not dissolve, coalesce into larger bubbles or rise to the surface of the composition to any significant degree.
• the size of gas bubbles incorporated into compositions of the invention has been found important.
• the bubbles are effective to stabilise the compositions when they range in size from 3 to 150 microns. Bubbles of less than about 3 microns are found to have a tendency to dissolve in the continuous phase, while those larger than about 150 microns usually rise to the uppermost surface of the composition and/or coalesce with other bubbles. It is found that if a majority of the bubbles either dissolve in, or rise to the surface of the continuous medium, they no longer impart a stabilising effect.
• the optimal average bubble diameter is 3 to 45 microns: bubbles of this size tend not to dissolve or rise out of the composition.
• compositions of the invention may be made under large-scale industrial conditions, fine control of bubble sizes will not always be practicable. It is expected the aeration processes to be used (discussed below) will generate a range of non-uniform bubble sizes only partly within the range of 3 to 45 microns. Bubbles outside this range are not expected to decrease stability in the compositions if at least 70% of the bubbles are within the 3 to 45 microns range, preferably if 85% of the bubbles are within that range and, most preferably, if 90% or more fall within 3 to 45 microns.
• bubble sizes may be obtained either a wide or narrow range of bubble sizes.
• a wide distribution of non-uniform bubble sizes over the 3 to 45 micron range is acceptable.
• it is also acceptable to have a narrower cut of bubble sizes such as 10 to 40 microns to reduce or avoid bubble dissolution or rising.
• an even narrower range of 15 to 30 microns is acceptable as this range is believed to cover the size of bubbles least likely to dissolve or coalesce with other bubbles.
• the gas bubbles be evenly dispersed through the compositions of the invention. So as to avoid such variations, with local syneresis as a possible result, the gas bubbles should be distributed evenly through the entire composition.
• Suitable gases for incorporation in the composition are those which do not damage or interact with the composition's components.
• gases include the noble gases as well as nitrogen, oxygen, air, and carbon dioxide.
• aerosol propellants which are halogenated hydrocarbons may be used, providing that they are not too soluble in the phases of the composition.
• an important aspect of the invention is the realisation that gas bubbles incorporated into a liquid continuous phase appear to lower the density of the solid discontinuous phase suspended therein to a value roughly equal to that of the liquid continuous phase.
• the composition achieves stability when D* discon is set equal to the density of the liquid continuous phase (D cont ).
• D cont the density of the liquid continuous phase
• This volume may in turn be converted to a weight percentage, if desired, of the final stabilised composition by multiplying the volume of gas by the density of that particular gas.
• compositions of the invention may have from 1 to 20% by volume of gas incorporated therein to achieve stability.
• gas for compositions described below, it has been observed that from 3 to 15%, or 8% to 10% gas by volume may stabilise the composition.
• the gas may be added in such an excessive amount, which does not stabilise the composition, it is important to determine the amount of gas needed to bring the density of continuous and discontinuous phases into proximity. To do so requires knowledge of the density of the different phases.
• the density of the continuous and discontinuous phases may be calculated or measured before being mixed together.
• the calculated or experimental value for the continuous or discontinuous phase density may be used to determine the amount of gas to be incorporated. Depending on the process of incorporating gas into the compositions, one may have to run a series of plant trials to determine the time required to aerate the composition to a sufficient but not an excessive degree.
• the continuous phase may be aqueous or non-aqueous.
• non-aqueous fluids are described in GB 2 194 546 (Colgate) and include nonionic materials.
• a surfactant should be present. Only very low levels are required. For example, in a detergent composition only 0.0001 wt % may be necessary. A suitable range for incorporation is from 0.001 wt % to 0.5 wt %, preferably 0.05 to 0.4 wt %.
• anionic surfactants may be used in the cleaning compositions of the invention, including anionic, nonionic, zwitterionic and amphoteric.
• the anionic surfactants include soaps, alkyl benzene sulphonates, primary alkyl sulphates, secondary alcohol sulphates, linear ethoxy sulphates and alpha-olefin sulphonates.
• the alkyl chains in these anionics may suitably be from 8 to 22 carbons long.
• the anionics suitably have from 1 to 8 ethylene oxide groups.
• the nonionic surfactants may suitably be alkoxylated fatty alcohols or fatty amides, the alkyl groups having from 6 to 20 carbons and the alkoxyl groups having from 2 to 4 carbons. There may be from 1 to 10 alkoxyl groups per molecule.
• Other suitable nonionics include block copolymers such as Pluronics and Tergitols. Zwitterionic surfactants may be present as well. When amine oxides are used as surfactants, they should be present at over 5% by weight.
• the discontinuous phase may preferably be an alkali-metal condensed phosphate present in the composition as a water hardness sequestering agent or builder.
• Tripolyphosphate is the preferred sequestrant although pyrophosphate, hexametaphosphate, or other condensed phosphates may be used.
• the sequestrant may be present in the formula from about 5% to 40%, with 15% to 25% by weight being more preferred.
• Use of the sequestrant, such as sodium tripolyphosphate in excess of its solubility limit within the formula requires that the solid be present as particles suspended in the composition. The presence of solids will affect the viscosity of the liquid.
• inorganic builders which may be used are sodium and potassium salts of polyphosphate, orthophosphate, carbonate, bicarbonate, sesquicarbonate and borate.
• Other detergent builders can also be used in the present invention. They are generally sodium and potassium salts of the following: citrates, nitrilotriacetates, phytates, polyphosphates, oxydisuccinates, oxydiacetates, carboxymethyloxy succinates, tetracarboxylates, starch and oxydised heteropolymeric polysaccharides.
• Sodium citrate is an especially preferred builder.
• Water-insoluble aluminosilicate ion-exchange materials may be used as alternative builders. These are crystalline or amorphous materials of general formula (Cat 2/n O) x .Al2O3(SiO2) y .ZH2O wherein Cat is a cation having a valency n that is exchangeable with calcium (eg Na+ or A+); x is a number from 0.7 to 1.5; y is a number from 1.3-4; and Z is such that the bound water content is from 1% to 28% by weight.
• Cat is a cation having a valency n that is exchangeable with calcium (eg Na+ or A+); x is a number from 0.7 to 1.5; y is a number from 1.3-4; and Z is such that the bound water content is from 1% to 28% by weight.
• Cat is a cation having a valency n that is exchangeable with calcium (eg Na+ or A+); x is a number from
• Suitable adjuncts to the cleaning or detergent compositions include enzymes, bleach and softeners.
• the pH of the present compositions will generally be in the slightly alkaline range.
• enzyme When enzyme is present the pH is preferably from 5 to 9.
• chlorine bleaches When chlorine bleaches are present, it is preferable to keep the pH in the 8 to 13 range in order to preserve chlorine activity.
• One cleaning composition that could be further improved by aeration is a thixotropic liquid machine dishwashing composition described in our co-pending European patent application 0 316 152.
• the dishwashing composition must be a uniform mixture of ingredients to deliver the optimum combination of active components with each dose. Consequently, the aeration of the present invention would be very useful in contributing to the stability of the composition of our copending EP 0 316 152.
• the dishwashing composition has high viscosity when at rest but undergoes a viscosity decrease under the influence of applied shear.
• the preferred compositions have a reversible decrease in viscosity with time after removal of the shear. Agitation of the liquid in its container, such as shaking or squeezing, supplies sufficient shear strain to initiate shear-thinning behaviour and increased liquid flow. The liquid should quickly regain its structure after pouring. These liquid characteristics are termed "thixotropy".
• the thixotropic dishwashing composition is aqueous and comprises 25-30 wt % of an alkali-metal builder and 25-30 wt % of an alkali-metal silicate, a stabiliser system stabilising 0.05-5% by weight of an alkyl phosphate, phosphonate, sulphate or sulphonate with from 10% to 15% gas present as bubbles ranging in size from 3 to 45 microns.
• the composition further comprises a detergent active.
• the continuous phase of the formulation comprises the water and metal silicate, while the non-gaseous discontinuous phase comprises solid particles of the builder material. (Usually under 5% of the builder dissolves in the aqueous phase.) Any detergent actives are believed to associate with the solid builder particles.
• the liquid dishwashing compositions may also preferably incorporate a bleach, eg. a hypochlorite, which may be present in the continuous phase at 0.5 to 5 wt %.
• a bleach eg. a hypochlorite
• the system is stable when these bleaches are included in comparison to some systems of the prior art, wherein the presence of hypochlorite destroys system stability.
• the dishwashing composition has improved rheology and stability and can deliver a high and uniform dosage of active ingredients to the machine wash cycle.
• the system has good stability against physical separation upon storage, providing a more uniform product. Poor physical stability can lead to development of a stratified liquid through separation of a fluid layer and a solids layer. This requires remixing by the end user through vigorous shaking of the container.
• the structuring system may also be adjusted to develop optimum fluid rheology in terms of low shear rate attributes, giving physical stability, cup retention and moderate shear rate flow behaviour during dispensing into the wash cycle.
• the product according to the present invention may be a thixotropic machine dishwashing detergent in the form of a slurry-like paste.
• the product possesses a viscosity of between 5-50 Pas at 0.9s ⁇ 1 and a viscosity between 500-5000mPas at 20s ⁇ 1 (Haake RV2 at 20°C, MV2 rotor).
• the stabilising alkyl derivatives may be long chain alkyl, ie C10-C22, sulphates, sulphonates, phosphates, phosphites, or phosphonates.
• Preferred are phosphorous based compounds, which also assist in foam dispersion.
• the higher alkyl phosphates and phosphonic acids are also preferred due to their tendency to reduce corrosion of metals and erosion of vitreous enamel surfaces.
• sulphates or sulphonates are to be used, such as alkyl benzene sulphonates, it is preferred to additionally use a phosphate or phosphonate.
• compositions in which very small particles of a solid are dispersed through the continuous phase which may be stabilised by the incorporation of gas bubbles.
• Substantially all of the solid particles are less than 5 microns in size.
• Preferably, at least 90% of the particles are smaller than 4 microns and, even more preferably, at least 75% of the particles are smaller than 2 microns.
• Up to about 5% of the particles may be larger than 5 microns.
• the smallest particles may be under 1 micron in size; however, no exact minimum particle size is determinable due to the difficulty of measuring particle sizes of 1 micron or less.
• the gas bubbles are believed to contribute to stabilisation of the composition, possibly by interaction with the solid particles (which may form a network) in a manner resembling the bubble-particle interaction in the flotation technology.
• the particles here may be coated with active, as the active is not seen to appear in the liquid active phase. Such a hydrophobic particle would, presumably, be able to form a large area of contact with a gas bubble.
• the applicants offer this possibility as an aid to understanding the invention which, however, in no way limits the scope of the invention.
• the analogy to flotation technology is not deemed to be an exact one because the purpose of flotation technology is to separate materials whereas any bubble-particle interaction here acts to maintain the composition in a stable form.
• the bubbles in flotation technology are very mobile, whereas it is desired that the bubbles in the compositions of the invention do not rise to the surface.
• the particles present in the thixotropic, aqueous liquid cleaning composition may be comprised of sodium tripolyphosphate hexahydrate crystals.
• STP when added, is usually an anhydrous product having a size range of nearly 1 cm, the crystals of STP hexahydrate in the compositions are very small.
• Part of the STP hexahydrate of the compositions may be replaced by other materials, eg other phosphate and/or builder salts including zeolites, or water-insoluble clays. It is preferred, however, that at least 30% of the particles less than 5 microns in size which contribute to stability be STP hexahydrate.
• the recrystallisation of STP to a network of very small STP 6aq particles is solely responsible for the high viscosity and shear thinning behaviour of the liquid. It is preferred that the composition should have a viscosity of 15-30 PaS at 0.9 s ⁇ 1 and 2-6 PaS at 20s ⁇ 1 as measured at RTP on a Haake viscometer.
• alkali-metal carbonate may be used as an alkaline buffering agent and may be present from 0 to 30 wt%, or more preferably from 2 to 10 wt%.
• alkali-metal metasilicates or alkali-metal silicates with a molar ratio of SiO2/Na2O and/or K2O of from 2.0 to 3.25 may be used as alkaline sources and as anti-corrosion agents to protect metal and china surfaces against the harshly alkaline environments present in the wash.
• the silicate may be used in the form of an aqueous liquor or a solid and may be present in the formula from 0.1 to 40 wt% or 0.1 to 30 wt%, more preferably from 10 to 25 wt%.
• An alkali-metal hydroxide may be used as an alkaline source and as a means to boost the pH of the liquid detergent concentrate to stabilise the hypochlorite.
• Sodium or potassium hydroxide in the form of an aqueous liquor or as a solid may be used in the formula at from 0.1 to 9 wt%, preferably from 0.5 to 7 wt%.
• Polymers may be added to the system to provide a further building effect. These polymers constitute part of the continuous phase.
• the polymer used should be of a synthetic type and be water-soluble. Examples of applicable polymers are polyacrylic acid and its alkali-metal salts, polymethacrylic acid and its alkali-metal salts, and copolymers of these with alkyl acrylates and alkyl methacrylates, copolymers of these with maleic anhydrides, polyacrylamide and partially hydrolysed polyacrylamide, polyacrylonitrile and its partially hydrolysed forms, polymethacrylonitrile and its partially hydrolysed forms, polystyrenesulphonic acid and its alkali-metal salts, polymaleic anhydride and its alkali-metal salts, poly n-vinyl lactams (poly-vinyl pyrrolidone, poly(N-vinyl caprolactam, etc), and polymers of N-substituted acrylamides or mixtures thereof
• polymers have a weight average molecular weight of from 1,000 to 15,000,000 with a molecular weight of from 10,000 to 400,000 preferred, and 100,000 to 250,000 most preferred. These polymers may be used in the acid or the neutralised form.
• the polymers should be of a hypochlorite-stable type with polyacrylate and polymethacrylate being most preferred.
• the polymer should be of a purity such that it contains a minimum of unsaturated monomers, chemically reactive initiators, terminators, or surfactants present which will hasten the rate of hypochlorite decomposition.
• the polymer may be present in the formula from 0.05 to 10 wt%, preferably 0.1-0.5 wt%.
• Clays such as hectorites and montmorillonites may be included in the compositions of the invention. These constitute a second, separate discontinuous phase from the sequestrant particles. They assist in reduction of spot formation on glassware, and may be present at from 0.3 to 20 wt%. Particularly preferred is the addition of laponite clay at 0.5-2 wt%. An increase in solids level implies a need for lower levels of stabiliser to achieve stability.
• Clay may also be incorporated in such amounts so as to provide a thickening effect (see Colgate's GB 2 164 350).
• the product has been shown to possess a high degree of stability at room temperature, whilst also demonstrating a suitably low viscosity to assist dispensing.
• the pH of the composition may range from 10-14, preferably 10.5-12.5. It also demonstrates an improved washing performance in comparison to other thickened machine dishwashing systems.
• the liquid detergent composition of the invention may be adapted for use in fabric washing and may further contain any of the adjuncts normally used in fabric washing detergent compositions, eg sequestering agents such as ethylene diamine tetraacetate; alkali silicates for adjusting the pH; soil suspending and anti-redeposition agents such as sodium carboxymethylcellulose, polyvinylpyrrolidone etc; fluorescent agents; perfumes, germicides and colourants.
• adjuncts normally used in fabric washing detergent compositions, eg sequestering agents such as ethylene diamine tetraacetate; alkali silicates for adjusting the pH; soil suspending and anti-redeposition agents such as sodium carboxymethylcellulose, polyvinylpyrrolidone etc; fluorescent agents; perfumes, germicides and colourants.
• lather depressors such as silicones; and enzymes, particularly proteolytic and amylolytic enzymes; and peroxygen or chlorine bleaches, such as sodium perborate and potassium dichlorocyanurate, including bleach activators, such as N,N,N′,N′-tetraacetyl ethylene diamine, may be necessary to formulate a complete heavy duty detergent composition suitable for use in washing machine operations.
• compositions comprising 20-30 wt % of an alkaline metal phosphate, 20-30 wt % of an alkaline metal silicate, 0.1 to 0.5 wt % of a detergent active and water, said compositions further comprising 7 to 11 vol % of air of a particle size as hereinbefore defined according to the invention.
• the dishwashing composition has a viscosity at 0.9s ⁇ 1 of 20-30 PaS and at 20s ⁇ 1 of 2-3 PaS.
• said composition has a density of 1.4 to 1.5 g/cm3.
• a further aspect of the present invention is the process for stabilising the composition with a liquid continuous and one or more discontinuous phases.
• the process comprises aerating the composition with a gas up to 1 to 20% by volume, the gas being present in bubbles size 3-150 microns with average diameter of 3-45 microns.
• the aeration may be performed during mixing of the composition or afterwards. Depending on the identity and viscosity of the final composition, it may be preferred to aerate during composition mixing. Thus, the difficulty of aerating a viscous liquid and the corrosion of equipment from aerating a highly alkaline composition may be avoided.
• aeration should not start until after addition of the STP or other builder.
• the builder is the major part of the discontinuous phase, the composition becomes increasingly viscous as more builder is added.
• aeration should be stopped after about 50% of the builder is added, the composition being too viscous to aerate by means of mixing equipment beyond that point.
• aeration When aeration is performed during mixing the components, it is usually performed by agitation of the composition components. This agitation may be part of blending the components, as by rotating a mixer blade at a speed which entrains air.
• Suitable devices for aerating the composition include mixing tanks with a stirring blade, turbines, or impellers. The mixing tank may have a closed or open top.
• other mixers such as a cavity transfer mixer described in International Patent Application WO 83/03222 (Rubber and Plastics Research Association) may be used to aerate.
• agitation by these means alone it is found that the size of air bubbles entrained covers quite a large range, from less than 1 micron to over 1 centimetre.
• composition or composition components may be circulated through a circulation loop.
• a circulation loop breaks down all bubbles to a size less than 150 microns.
• aeration by agitation and passage through a circulation loop is preferred, as it requires less time and puts more of the entrained air into the desired bubble size.
• agitation may be the simplest process of aerating
• agitation does have drawbacks.
• One major drawback is the difficulty of incorporating a uniform amount of air into a series of compositions.
• the composition may be mixed without agitation, then charged while under pressure with gas. If the gas added to the composition is dispersed through one or more orifices of diameter 1-150 microns, the size of bubbles dispersed through the composition should also be about 1-150 microns.
• the advantage of this means of aerating is that more exact amounts of gas may be added to the composition under the more controlled conditions. The result is greater reproducibility of the amount of air added from batch to batch.
• the compositions may be aerated to an excess level, ie to a point where the density of the one or more discontinuous phases is less than 85% of the density of the continuous phase.
• This aeration to excess may be performed either by agitation or addition of gas under pressure.
• a controled de-aeration takes place by subjecting the composition to a lowered air pressure (eg, lower than 0.2 atmospheres). This lowered pressure will remove some of the gas in the composition.
• a lowered air pressure eg, lower than 0.2 atmospheres
• a thixotropic machine dishwashing composition was prepared according to the following formulation: Ingredient Wt % Sodium Tripolyphosphate 24.5 Sodum Disilicate 23.0 Na OH 2.0 Av Cl2 1.2 Stearyl Phosphate 0.2 Sodium Alkyl Sulphonate 0.2 Water to 100.0
• a premix of water, NaOH, SAS and stearyl phosphate was prepared at 75° and held in a side tank.
• a main paddle mixing tank was mixed, at ambient temperature, water (10%), disilicate (48% of a 50% solution), Na OH (4% of a 50% soluton), hypochlorite (8% of a 15% solution).
• the premix solution was added at 35°C and the mixing tip speed increased from 1.5ms ⁇ 1 to 3ms ⁇ 1.
• the temperature was raised to 50°C and the STP (Thermphos NW ex Hoechst) added.
• the mixing speed was raised to 4ms ⁇ 1.
• compositions according to the present invention formulated as machine dishwashing liquids, spot, film and cleaning tests were carried out using the above prepared composition.
• the liquid was used in a Miele G560 machine on a 65°C programme.
• a standard set of dishware, soiled with a standard evaluation soil was cleaned ten times, using tap water of 8° German hardness, without using a water softener or a rinse aid. Dosage was 2g/l.
• a basic detergent composition was formulated according to the procedure of Example 1: Wt % Sodium Tripolyphosphate 24.5 Disilicate (2.0) 23.0 Na OH 2.0 Av Cl2 1.0 Water to 100.0 with the addition of various actives. Density and phase separation was measured. Actives A 2 3 SAS - 0.1 - PAS - - 0.1 Stearyl Phosphate - 0.1 0.1 Density (g/cm3) 1.547 1.453 1.447 pH 13.8 13.8 13.8 Separation (vol%) - 3 weeks 37°C 5 1 0 RT 1 0 0 3°C 0 0 0 0
• Comparative Example A could not be made with a lower density.

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• 1988
  • 1988-07-01 GB GB888815669A patent/GB8815669D0/en active Pending
• 1989
  • 1989-06-28 AU AU37083/89A patent/AU624154B2/en not_active Ceased
  • 1989-06-29 ES ES89306599T patent/ES2063131T5/es not_active Expired - Lifetime
  • 1989-06-29 DE DE68913833T patent/DE68913833T3/de not_active Expired - Fee Related
  • 1989-06-29 CA CA000604394A patent/CA1324744C/en not_active Expired - Fee Related
  • 1989-06-29 EP EP89306599A patent/EP0349314B2/de not_active Expired - Lifetime
  • 1989-06-30 BR BR898903259A patent/BR8903259A/pt not_active IP Right Cessation
  • 1989-06-30 ZA ZA895004A patent/ZA895004B/xx unknown
  • 1989-06-30 JP JP1169721A patent/JPH0280499A/ja active Pending

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