EP0316152A1 - Use of alkyl phosphates for the stabilisation of thixotropic compositions - Google Patents
Use of alkyl phosphates for the stabilisation of thixotropic compositions Download PDFInfo
- Publication number
- EP0316152A1 EP0316152A1 EP19880310546 EP88310546A EP0316152A1 EP 0316152 A1 EP0316152 A1 EP 0316152A1 EP 19880310546 EP19880310546 EP 19880310546 EP 88310546 A EP88310546 A EP 88310546A EP 0316152 A1 EP0316152 A1 EP 0316152A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- alkali
- metal
- composition
- builder
- sulphate
- 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
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 37
- -1 alkyl phosphates Chemical class 0.000 title claims abstract description 19
- 229910019142 PO4 Inorganic materials 0.000 title claims abstract description 13
- 230000009974 thixotropic effect Effects 0.000 title claims abstract description 10
- 235000021317 phosphate Nutrition 0.000 title description 8
- 230000006641 stabilisation Effects 0.000 title 1
- 239000007788 liquid Substances 0.000 claims abstract description 34
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 11
- 239000010452 phosphate Substances 0.000 claims abstract description 8
- 229910052910 alkali metal silicate Inorganic materials 0.000 claims abstract description 7
- 150000001340 alkali metals Chemical class 0.000 claims abstract description 7
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 claims abstract description 7
- 229910021653 sulphate ion Inorganic materials 0.000 claims abstract description 7
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims abstract description 6
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 claims abstract description 6
- 238000004140 cleaning Methods 0.000 claims abstract description 6
- 239000003599 detergent Substances 0.000 claims description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 239000004927 clay Substances 0.000 claims description 7
- 239000003381 stabilizer Substances 0.000 claims description 7
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 claims description 5
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 5
- 239000007844 bleaching agent Substances 0.000 claims description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 4
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 claims description 4
- 239000000460 chlorine Substances 0.000 claims description 4
- 229910052801 chlorine Inorganic materials 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 4
- 229910000288 alkali metal carbonate Inorganic materials 0.000 claims description 2
- 150000008041 alkali metal carbonates Chemical class 0.000 claims description 2
- 230000008719 thickening Effects 0.000 claims description 2
- 239000011149 active material Substances 0.000 claims 2
- 229910000318 alkali metal phosphate Inorganic materials 0.000 claims 1
- 238000003860 storage Methods 0.000 abstract description 3
- 238000005191 phase separation Methods 0.000 abstract 1
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 description 22
- 238000004851 dishwashing Methods 0.000 description 13
- 229920000642 polymer Polymers 0.000 description 10
- 238000000926 separation method Methods 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 5
- 235000019832 sodium triphosphate Nutrition 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000000518 rheometry Methods 0.000 description 4
- 239000003352 sequestering agent Substances 0.000 description 4
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 229920001222 biopolymer Polymers 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 230000014759 maintenance of location Effects 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 2
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
- JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 description 1
- 229920002845 Poly(methacrylic acid) Polymers 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 125000005250 alkyl acrylate group Chemical group 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000006172 buffering agent Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 1
- 235000011180 diphosphates Nutrition 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 230000003628 erosive effect Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 229940005740 hexametaphosphate Drugs 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229940094522 laponite Drugs 0.000 description 1
- XCOBTUNSZUJCDH-UHFFFAOYSA-B lithium magnesium sodium silicate Chemical compound [Li+].[Li+].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Na+].[Na+].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].[Mg+2].O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3.O1[Si](O2)([O-])O[Si]3([O-])O[Si]1([O-])O[Si]2([O-])O3 XCOBTUNSZUJCDH-UHFFFAOYSA-B 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical class O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 229920000141 poly(maleic anhydride) Polymers 0.000 description 1
- 229920003214 poly(methacrylonitrile) Polymers 0.000 description 1
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 229920002239 polyacrylonitrile Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000013042 solid detergent Substances 0.000 description 1
- 230000003019 stabilising effect Effects 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000000037 vitreous enamel Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000010457 zeolite Substances 0.000 description 1
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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/395—Bleaching agents
- C11D3/3956—Liquid compositions
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/34—Derivatives of acids of phosphorus
- C11D1/342—Phosphonates; Phosphinates or phosphonites
-
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/34—Derivatives of acids of phosphorus
- C11D1/345—Phosphates or phosphites
Definitions
- the present invention relates to machine dishwashing liquid detergent compositions suitable for use in cleansing food soils from cooking utensils, dishes and glasses. More particularly, the present invention relates to an aqueous thixotropic structured system comprising an alkaline source and builder salts.
- liquid forms of detergent for machine dishwashing offers several advantages over powdered or granular forms. These advantages include greater ease of handling in dispensing and dosing, the elimination of lump formation, "caking" and dust, and improved solubility.
- liquid detergents must meet certain requirements. Firstly, the liquid detergent must be a uniform mixture of ingredients to deliver the optimum combination of active components to the wash with each dose. In most current formulations, this requires that the liquid be shaken before each use to remix the components. A preferred product should be stable against physical separation and segregation of its active components. High viscosity at low shear rate contributes to physical stability of the liquid and protects against separation of the active components.
- Physical stability can be achieved through the use of suspending or viscosifying systems to enhance the liquid rheological properties. These agents must maintain viscosity at low shear rate under the high ionic strength conditions present in a well-built liquid detergent, and must be chemically compatible with the other components of the formula, especially the chlorine bleach used to assist stain removal.
- the liquid dishwashing 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 not designed to contain low viscosity liquids. Consequently, liquids for use as machine dishwashing detergents must possess high 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.
- thixotropic liquid detergent composition suitable for use in a machine dishwasher which is structured by interaction between the components, giving a positive effect on the rheology of the components, without the need to include a conventional thickening agent. This effect is shown in viscosity increases and in yield point enhancement.
- 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 at levels used for structuring 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. Since most biopolymers react readily with hypochlorite, these systems are unstable and exhibit a gradual loss in viscosity if hypochlorite is present.
- Micellar structured liquids are known in other areas, eg in thickened bleach systems (GB 1 466 560), usually containing over 90 wt% hypochlorite solution and no builder. Systems thickened by synergistic action with urea (eg GB 1 579 668) are also known.
- GB 2 185 037 describes aqueous, thixotropic machine dishwashing detergents which are structured by fatty mono- or polycarboxylic acid.
- an aqueous, thixotropic liquid cleaning composition comprising an alkali-metal builder and an alkali metal silicate and a stabiliser comprising from 0.05 to 5% by weight of an alkyl phosphate, phosphonate, sulphate or sulphonate, said composition optionally comprising a detergent active.
- the present invention is based upon the discovery that the alkyl derivatives named may be used as liquid stabilisers.
- Alkyl phosphates have previously been described for use in machine dishwashing compositions as foam depressors, but we do not believe that their use as liquid stabilisers has previously been described. Structuring occurs independently of the presence of active detergent.
- compositions according to the present invention may also preferably incorporate a bleach, eg. a hypochlorite.
- 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.
- composition according to the present invention has improved rheology and stability and can deliver a high and uniform dosage of active ingredients to the machine wash cycle.
- An improvement of the structuring also results in easier dispensing from the product container to the dispenser and from the dispenser to the machine wash at the appropriate time.
- the system of the present invention 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 of the invention 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 is a thixotropic machine dishwashing detergent in the form of a slurry-like paste.
- the product possesses a yield point of between 5-50 Pa and a viscosity between 500-5000mPas at 20 ⁇ 1s (Haake RV2 at 20°C, MV2 rotor).
- the stabilisers according to the present invention are long chain alkyl, ie C10-C22, sulphates, sulphonates, phosphates, phosphites or phosphonates.
- Preferred are phosphorous based compounds. Particularly preferred are compounds selected from those listed in Table 1 below, or mixtures thereof:
- ALF-5 (Lancro Chemicals Limited).
- 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.
- An alkali-metal condensed phosphate may be present in the formula 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 should be present in the formula from 0.1 to 35 wt% with 15 to 30 wt% 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 fine particles which are suspended by the structuring system. The presence of solids will affect the viscosity of the liquid and may modify the range of the structurants needed to deliver the proper rheology. Zeolites may also be used as builders.
- An 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 1.0 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 30 wt%, more preferably from 2 to 20 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 25 wt%, preferably from 0.5 to 15 wt%.
- Polymers may be added to the system to provide a further building effect.
- 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 mortmorillonites may be included in the compositions of the invention. These assist in reduction of spot formation on glassware, and may be present at from 0.5 to 20 wt%. It has also been found that the presence of the structuring agents characterising the present invention assists in the production of low-viscosity, stable, clay-structured products described in the art without the need to incorporate known structuring agents, such as polymers, actives, etc. Particularly preferred is the addition of laponite clay at 0.5-2 wt%. An increase in solds level implies a need for lower levels of stabiliser to achieve stability.
- the system may incorporate a bleach generating system, such as a hypochlorite, at from 0.5 to 5 wt% active chlrine.
- Actives may optionally be included within the system. Preferred are nonionic actives. However, low levels of anionic actives such as secondary alkyl sulphates may be included.
- the product according to the invention may be prepared by initial formulation of a premix comprising the stabilising component and water, the addition of this premix to a silicate and alkali-metal hydroxide mixture, and the subsequent addition of builder and hypochlorite.
- the process is preferably carried out at above 40°C.
- the product according to the invention 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 12-13.5. It also demonstrates an improved washing performance in comparison to other thickened machine dishwashing systems.
- a basic machine dishwashing liquid system was formulated, and viscosity and stability investigated at different levels of ALF-5 addition.
- Base system STP 20.0 Na-disilicate 19.0 Na-carbonate 6.0 Na-OH 2.5 Hypochlorite (Av.Cl2) 1.0 Water to 100.0 ALF-5 Viscosity (20 sec ⁇ 1) Separation (%) (wt%) (mPas) 1 week 37°C RT 8 week 37°C RT 0 993 1 1 6 5 0.16 1300 0 0 0 0 0.50 990 0 0 0 0 1.00 1273 0 0 0 0 0 0
- compositions were prepared and found to be stable for 8 weeks at RT and 37°C: wt% STP (anhydrous) 20 25 Na Disilicate 19 16 Na Carbonate 6 2 Na OH 2.5 2.5 Ti O2 0.2 - SAS - 0.2 HOCl (as Av.Cl2) 1.0 1.0 ALF-5 0.16 0.16 Water to 100
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- 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)
- Detergent Compositions (AREA)
Abstract
Description
- The present invention relates to machine dishwashing liquid detergent compositions suitable for use in cleansing food soils from cooking utensils, dishes and glasses. More particularly, the present invention relates to an aqueous thixotropic structured system comprising an alkaline source and builder salts.
- The use of liquid forms of detergent for machine dishwashing offers several advantages over powdered or granular forms. These advantages include greater ease of handling in dispensing and dosing, the elimination of lump formation, "caking" and dust, and improved solubility.
- However, liquid detergents must meet certain requirements. Firstly, the liquid detergent must be a uniform mixture of ingredients to deliver the optimum combination of active components to the wash with each dose. In most current formulations, this requires that the liquid be shaken before each use to remix the components. A preferred product should be stable against physical separation and segregation of its active components. High viscosity at low shear rate contributes to physical stability of the liquid and protects against separation of the active components.
- Physical stability can be achieved through the use of suspending or viscosifying systems to enhance the liquid rheological properties. These agents must maintain viscosity at low shear rate under the high ionic strength conditions present in a well-built liquid detergent, and must be chemically compatible with the other components of the formula, especially the chlorine bleach used to assist stain removal.
- The liquid dishwashing 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 not designed to contain low viscosity liquids. Consequently, liquids for use as machine dishwashing detergents must possess high 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.
- Although high viscosity is desirable under storage conditions or while the material is in the detergent cup, the liquid must readily and conveniently dispense from its container. Therefore, a liquid that undergoes a viscosity decrease under the influence of applied shear such that the decrease is reversible with time after the removal of shear is preferable for this application. This behaviour is termed "shear-thinning" and is desirable for liquid dishwashing detergents. Agitation of the liquid in the container, such as squeezing or shaking, will supply sufficient shear strain to initiate shear-thinning behaviour and increased liquid flow. Optimum flow properties would allow for easily pourable fluids which maintain sufficient viscosity at higher shear rates to prevent or minimise excessive spillage. The liquid should quickly regain its structure after dispensing. This liquid characteristic is termed "thixotropy".
- There is now disclosed a thixotropic liquid detergent composition suitable for use in a machine dishwasher which is structured by interaction between the components, giving a positive effect on the rheology of the components, without the need to include a conventional thickening agent. This effect is shown in viscosity increases and in yield point enhancement.
- The prior art has disclosed a number of systems for thickening of machine dishwashing compositions. 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 at levels used for structuring 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. Since most biopolymers react readily with hypochlorite, these systems are unstable and exhibit a gradual loss in viscosity if hypochlorite is present.
- Micellar structured liquids are known in other areas, eg in thickened bleach systems (GB 1 466 560), usually containing over 90 wt% hypochlorite solution and no builder. Systems thickened by synergistic action with urea (eg GB 1 579 668) are also known. GB 2 185 037 describes aqueous, thixotropic machine dishwashing detergents which are structured by fatty mono- or polycarboxylic acid.
- According to the present invention there is provided an aqueous, thixotropic liquid cleaning composition comprising an alkali-metal builder and an alkali metal silicate and a stabiliser comprising from 0.05 to 5% by weight of an alkyl phosphate, phosphonate, sulphate or sulphonate, said composition optionally comprising a detergent active.
- The present invention is based upon the discovery that the alkyl derivatives named may be used as liquid stabilisers. Alkyl phosphates have previously been described for use in machine dishwashing compositions as foam depressors, but we do not believe that their use as liquid stabilisers has previously been described. Structuring occurs independently of the presence of active detergent.
- The compositions according to the present invention may also preferably incorporate 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 composition according to the present invention has improved rheology and stability and can deliver a high and uniform dosage of active ingredients to the machine wash cycle. An improvement of the structuring also results in easier dispensing from the product container to the dispenser and from the dispenser to the machine wash at the appropriate time.
- The system of the present invention 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 of the invention 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 is a thixotropic machine dishwashing detergent in the form of a slurry-like paste. The product possesses a yield point of between 5-50 Pa and a viscosity between 500-5000mPas at 20⁻¹s (Haake RV2 at 20°C, MV2 rotor).
-
- Most preferred is the mixture of C₁₆/C₁₈ alkyl dihydrogen phosphate and dialkyl hydrogen phosphate, referred to hereafter as ALF-5 (Lancro Chemicals Limited).
- 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.
- If sulphates or sulphonates are to be used, such as alkyl benzene sulphonates, it is preferred to additionally use a phosphate or phosphonate.
- An alkali-metal condensed phosphate may be present in the formula 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 should be present in the formula from 0.1 to 35 wt% with 15 to 30 wt% 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 fine particles which are suspended by the structuring system. The presence of solids will affect the viscosity of the liquid and may modify the range of the structurants needed to deliver the proper rheology. Zeolites may also be used as builders.
- The sources of alkalinity are used in combination in the more preferred embodiments of this invention. An 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%.
- Pure alkali-metal metasilicates or alkali-metal silicates with a molar ratio of SiO₂/Na₂O and/or K₂O of from 1.0 to 3.25 (or mixtures of 2 or more metasilicate and/or silicates) 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 30 wt%, more preferably from 2 to 20 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 25 wt%, preferably from 0.5 to 15 wt%.
- Polymers may be added to the system to provide a further building effect. 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. These 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 mortmorillonites may be included in the compositions of the invention. These assist in reduction of spot formation on glassware, and may be present at from 0.5 to 20 wt%. It has also been found that the presence of the structuring agents characterising the present invention assists in the production of low-viscosity, stable, clay-structured products described in the art without the need to incorporate known structuring agents, such as polymers, actives, etc. Particularly preferred is the addition of laponite clay at 0.5-2 wt%. An increase in solds level implies a need for lower levels of stabiliser to achieve stability.
- The system may incorporate a bleach generating system, such as a hypochlorite, at from 0.5 to 5 wt% active chlrine. Actives may optionally be included within the system. Preferred are nonionic actives. However, low levels of anionic actives such as secondary alkyl sulphates may be included.
- Conventional additives such as colourants and perfumes may be present in the composition in amounts not exceeding 5 wt%. Other foam depressors may be included.
- The product according to the invention may be prepared by initial formulation of a premix comprising the stabilising component and water, the addition of this premix to a silicate and alkali-metal hydroxide mixture, and the subsequent addition of builder and hypochlorite. The process is preferably carried out at above 40°C.
- The product according to the invention 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 12-13.5. It also demonstrates an improved washing performance in comparison to other thickened machine dishwashing systems.
- The invention will now be further illustrated by means of the following non-limiting Examples.
- A basic machine dishwashing liquid system was formulated, and viscosity and stability investigated at different levels of ALF-5 addition.
wt% Base system: STP 20.0 Na-disilicate 19.0 Na-carbonate 6.0 Na-OH 2.5 Hypochlorite (Av.Cl₂) 1.0 Water to 100.0 ALF-5 Viscosity (20 sec⁻¹) Separation (%) (wt%) (mPas) 1 week 37°C RT 8 week 37°C RT 0 993 1 1 6 5 0.16 1300 0 0 0 0 0.50 990 0 0 0 0 1.00 1273 0 0 0 0 - The incorporation of different levels of ALF-5 into a clay-structured system was carried out in order to examine any increased stability.
wt% Base system: STP (anhydrous) 20.5 Na-disilicate 11.0 Na-carbonate 6.0 Na-OH 1.2 Hypochlorite (Av.Cl₂) 1.0 Clay 2.0 Water to 100.0 ALF-5 Viscosity (20 sec⁻¹) Separation (%) (wt%) (mPas) 4 week 37°C RT 12 week 37°C RT 0 1645 12 6 17 15 0.1 1805 3 5 7 6 0.5 2375 3 0 7 3 At a clay level of 3.5 wt%, after 8 weeks: 37°C RT 0 1715 6 11 0.16 1835 0 0 - The following compositions were prepared and found to be stable for 8 weeks at RT and 37°C:
wt% STP (anhydrous) 20 25 Na Disilicate 19 16 Na Carbonate 6 2 Na OH 2.5 2.5 Ti O₂ 0.2 - SAS - 0.2 HOCl (as Av.Cl₂) 1.0 1.0 ALF-5 0.16 0.16 Water to 100
Claims (8)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8726308 | 1987-11-10 | ||
GB878726308A GB8726308D0 (en) | 1987-11-10 | 1987-11-10 | Machine dishwashing composition |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0316152A1 true EP0316152A1 (en) | 1989-05-17 |
EP0316152B1 EP0316152B1 (en) | 1993-05-12 |
Family
ID=10626729
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP88310546A Expired - Lifetime EP0316152B1 (en) | 1987-11-10 | 1988-11-09 | Use of alkyl phosphates for the stabilisation of thixotropic compositions |
Country Status (9)
Country | Link |
---|---|
EP (1) | EP0316152B1 (en) |
JP (1) | JPH0757879B2 (en) |
AU (1) | AU616218B2 (en) |
BR (1) | BR8807287A (en) |
DE (1) | DE3880967T2 (en) |
ES (1) | ES2054827T3 (en) |
GB (1) | GB8726308D0 (en) |
WO (1) | WO1989004359A1 (en) |
ZA (1) | ZA888398B (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1994010272A1 (en) * | 1992-11-03 | 1994-05-11 | The Procter & Gamble Company | Cleaning with short-chain surfactants |
WO1999003958A1 (en) * | 1997-07-17 | 1999-01-28 | Henkel Kommanditgesellschaft Auf Aktien | Use of electrolyte mixtures as sequestering agents |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4794920B2 (en) * | 2005-06-21 | 2011-10-19 | 花王株式会社 | Aqueous liquid detergent composition |
JP5138188B2 (en) * | 2006-07-21 | 2013-02-06 | 株式会社Adeka | Cleaning composition |
US20080108537A1 (en) * | 2006-11-03 | 2008-05-08 | Rees Wayne M | Corrosion inhibitor system for mildly acidic to ph neutral halogen bleach-containing cleaning compositions |
Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2193871A1 (en) * | 1972-07-25 | 1974-02-22 | Colgate Palmolive Co | |
FR2330763A1 (en) * | 1975-11-07 | 1977-06-03 | Unilever Nv | CLEANING COMPOSITION IN PARTICULAR FOR DISHWASHING |
FR2520004A1 (en) * | 1982-01-18 | 1983-07-22 | Colgate Palmolive Co | THIXOTROPIC PROPER GEL TYPE GEL COMPOSITIONS FOR AUTOMATIC DISHWASHING MACHINES |
US4431559A (en) * | 1981-10-06 | 1984-02-14 | Texize, Division Of Mortonthiokol | Dishwashing composition and method |
GB2140450A (en) * | 1983-05-24 | 1984-11-28 | Colgate Palmolive Co | Thixotropic automatic dishwasher composition with chlorine bleach |
EP0142197A2 (en) * | 1983-11-04 | 1985-05-22 | The Procter & Gamble Company | Hypochlorite bleach containing surfactant and organic antifoamant |
GB2163448A (en) * | 1984-08-13 | 1986-02-26 | Colgate Palmolive Co | Detergent for automatic dishwasher |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ZA83272B (en) * | 1982-01-18 | 1984-08-29 | Colgate Palmolive Co | Gell-type automatic dishwasher compositions having thixotropic properties |
GR862954B (en) * | 1986-01-07 | 1987-05-08 | Colgate Palmolive Co | Thixotropic aqueous suspensions |
DE3863131D1 (en) * | 1987-06-12 | 1991-07-11 | Unilever Nv | LIQUID DETERGENT COMPOSITION FOR DISHWASHER. |
NZ226708A (en) * | 1987-10-28 | 1990-09-26 | Colgate Palmolive Co | Thixotropic dishwshing composition with silica and polycrylic acid polymer/salt |
-
1987
- 1987-11-10 GB GB878726308A patent/GB8726308D0/en active Pending
-
1988
- 1988-11-09 ES ES88310546T patent/ES2054827T3/en not_active Expired - Lifetime
- 1988-11-09 DE DE8888310546T patent/DE3880967T2/en not_active Expired - Fee Related
- 1988-11-09 BR BR888807287A patent/BR8807287A/en not_active Application Discontinuation
- 1988-11-09 WO PCT/GB1988/000967 patent/WO1989004359A1/en unknown
- 1988-11-09 EP EP88310546A patent/EP0316152B1/en not_active Expired - Lifetime
- 1988-11-09 JP JP63508853A patent/JPH0757879B2/en not_active Expired - Lifetime
- 1988-11-09 ZA ZA888398A patent/ZA888398B/en unknown
- 1988-11-10 AU AU24988/88A patent/AU616218B2/en not_active Ceased
Patent Citations (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2193871A1 (en) * | 1972-07-25 | 1974-02-22 | Colgate Palmolive Co | |
FR2330763A1 (en) * | 1975-11-07 | 1977-06-03 | Unilever Nv | CLEANING COMPOSITION IN PARTICULAR FOR DISHWASHING |
US4431559A (en) * | 1981-10-06 | 1984-02-14 | Texize, Division Of Mortonthiokol | Dishwashing composition and method |
FR2520004A1 (en) * | 1982-01-18 | 1983-07-22 | Colgate Palmolive Co | THIXOTROPIC PROPER GEL TYPE GEL COMPOSITIONS FOR AUTOMATIC DISHWASHING MACHINES |
GB2140450A (en) * | 1983-05-24 | 1984-11-28 | Colgate Palmolive Co | Thixotropic automatic dishwasher composition with chlorine bleach |
EP0142197A2 (en) * | 1983-11-04 | 1985-05-22 | The Procter & Gamble Company | Hypochlorite bleach containing surfactant and organic antifoamant |
GB2163448A (en) * | 1984-08-13 | 1986-02-26 | Colgate Palmolive Co | Detergent for automatic dishwasher |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
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WO1994010272A1 (en) * | 1992-11-03 | 1994-05-11 | The Procter & Gamble Company | Cleaning with short-chain surfactants |
TR28396A (en) * | 1992-11-03 | 1996-05-30 | Procter & Gamble | Cleaning with short chain surfactants. |
US6180583B1 (en) | 1992-11-03 | 2001-01-30 | The Procter & Gamble Company | Cleaning compositions containing short-chain surfactants |
WO1999003958A1 (en) * | 1997-07-17 | 1999-01-28 | Henkel Kommanditgesellschaft Auf Aktien | Use of electrolyte mixtures as sequestering agents |
Also Published As
Publication number | Publication date |
---|---|
JPH0757879B2 (en) | 1995-06-21 |
AU2498888A (en) | 1989-05-11 |
AU616218B2 (en) | 1991-10-24 |
BR8807287A (en) | 1990-03-27 |
DE3880967D1 (en) | 1993-06-17 |
GB8726308D0 (en) | 1987-12-16 |
EP0316152B1 (en) | 1993-05-12 |
WO1989004359A1 (en) | 1989-05-18 |
ES2054827T3 (en) | 1994-08-16 |
DE3880967T2 (en) | 1993-08-26 |
JPH02502025A (en) | 1990-07-05 |
ZA888398B (en) | 1990-07-25 |
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