AU692718B2 - Pigmented rheopectic cleaning compositions with thixotropic properties - Google Patents
Pigmented rheopectic cleaning compositions with thixotropic propertiesInfo
- Publication number
- AU692718B2 AU692718B2 AU65431/96A AU6543196A AU692718B2 AU 692718 B2 AU692718 B2 AU 692718B2 AU 65431/96 A AU65431/96 A AU 65431/96A AU 6543196 A AU6543196 A AU 6543196A AU 692718 B2 AU692718 B2 AU 692718B2
- Authority
- AU
- Australia
- Prior art keywords
- hypochlorite
- sodium
- alkali metal
- weight
- oxide
- 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.)
- Ceased
Links
- 239000000203 mixture Substances 0.000 title claims description 68
- 238000004140 cleaning Methods 0.000 title description 7
- 230000009974 thixotropic effect Effects 0.000 title description 5
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Chemical compound Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 claims description 58
- 229910052783 alkali metal Inorganic materials 0.000 claims description 31
- -1 alkali metal hypochlorite Chemical class 0.000 claims description 25
- 239000004927 clay Substances 0.000 claims description 22
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical group [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 18
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 18
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical group [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 claims description 16
- 235000013799 ultramarine blue Nutrition 0.000 claims description 16
- 239000000049 pigment Substances 0.000 claims description 15
- 150000001340 alkali metals Chemical class 0.000 claims description 12
- 125000000217 alkyl group Chemical group 0.000 claims description 11
- 239000011780 sodium chloride Substances 0.000 claims description 9
- 239000000440 bentonite Substances 0.000 claims description 8
- 229910000278 bentonite Inorganic materials 0.000 claims description 8
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 8
- 239000005708 Sodium hypochlorite Substances 0.000 claims description 7
- SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical group [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 claims description 7
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical group [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 claims description 7
- HFQQZARZPUDIFP-UHFFFAOYSA-M sodium;2-dodecylbenzenesulfonate Chemical group [Na+].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O HFQQZARZPUDIFP-UHFFFAOYSA-M 0.000 claims description 7
- 239000003381 stabilizer Substances 0.000 claims description 7
- 150000003512 tertiary amines Chemical class 0.000 claims description 7
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group 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 claims description 6
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical group [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 6
- 150000001412 amines Chemical class 0.000 claims description 6
- 229910052744 lithium Inorganic materials 0.000 claims description 6
- 229910052700 potassium Chemical group 0.000 claims description 6
- 239000011591 potassium Chemical group 0.000 claims description 6
- 229940071089 sarcosinate Drugs 0.000 claims description 6
- 108700004121 sarkosyl Proteins 0.000 claims description 6
- 229910052708 sodium Inorganic materials 0.000 claims description 6
- 239000011734 sodium Chemical group 0.000 claims description 6
- 229940045885 sodium lauroyl sarcosinate Drugs 0.000 claims 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 description 5
- SYELZBGXAIXKHU-UHFFFAOYSA-N dodecyldimethylamine N-oxide Chemical group CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 claims description 5
- ONHFWHCMZAJCFB-UHFFFAOYSA-N myristamine oxide Chemical compound CCCCCCCCCCCCCC[N+](C)(C)[O-] ONHFWHCMZAJCFB-UHFFFAOYSA-N 0.000 claims description 5
- 239000001023 inorganic pigment Substances 0.000 claims description 4
- ZUFONQSOSYEWCN-UHFFFAOYSA-M sodium;2-(methylamino)acetate Chemical compound [Na+].CNCC([O-])=O ZUFONQSOSYEWCN-UHFFFAOYSA-M 0.000 claims description 4
- 150000004996 alkyl benzenes Chemical class 0.000 claims description 3
- 239000001055 blue pigment Substances 0.000 claims description 3
- 239000000725 suspension Substances 0.000 description 8
- 239000007844 bleaching agent Substances 0.000 description 7
- 239000004094 surface-active agent Substances 0.000 description 7
- 239000012530 fluid Substances 0.000 description 6
- 230000015556 catabolic process Effects 0.000 description 5
- 238000006731 degradation reaction Methods 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 230000008719 thickening Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 238000013019 agitation Methods 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000002562 thickening agent Substances 0.000 description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 230000002411 adverse Effects 0.000 description 2
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 2
- 239000011575 calcium Substances 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- CRHLEZORXKQUEI-UHFFFAOYSA-N dialuminum;cobalt(2+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Al+3].[Al+3].[Co+2].[Co+2] CRHLEZORXKQUEI-UHFFFAOYSA-N 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000003205 fragrance Substances 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 239000000693 micelle Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000000518 rheometry Methods 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- 239000000344 soap Substances 0.000 description 2
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 101100459438 Caenorhabditis elegans nac-1 gene Proteins 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- 238000005282 brightening Methods 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000001032 cobalt pigment Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 239000000645 desinfectant Substances 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical class [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 229910052909 inorganic silicate Inorganic materials 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 239000012860 organic pigment Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 238000005185 salting out Methods 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000004408 titanium dioxide 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
- C11D1/66—Non-ionic compounds
- C11D1/83—Mixtures of non-ionic with anionic compounds
-
- 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
- C11D3/12—Water-insoluble compounds
- C11D3/124—Silicon containing, e.g. silica, silex, quartz or glass beads
- C11D3/1246—Silicates, e.g. diatomaceous earth
- C11D3/1253—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite
- C11D3/1266—Layer silicates, e.g. talcum, kaolin, clay, bentonite, smectite, montmorillonite, hectorite or attapulgite in 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/40—Dyes ; Pigments
-
- 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
- C11D3/40—Dyes ; Pigments
- C11D3/42—Brightening agents ; Blueing agents
-
- 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
- C11D1/04—Carboxylic acids or salts thereof
- C11D1/10—Amino carboxylic acids; Imino carboxylic acids; Fatty acid condensates thereof
-
- 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
- C11D1/66—Non-ionic compounds
- C11D1/75—Amino oxides
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Detergent Compositions (AREA)
- Biological Depolymerization Polymers (AREA)
Description
PIGMENTED RHEOPECTIC CLEANING COMPOSITIONS
WITH THIXOTROPIC PROPERTIES
Field ofthe Invention This invention relates to thickened liquid bleach-containing compositions useful for hard surface cleaning, and particular to such compositions which include bleach-stable pigments.
Background ofthe Invention Thickened bleach compositions possess a number of advantages over unthickened bleach compositions. The more viscous, thickened solutions adhere to vertical and inclined surfaces for a longer period of time as compared or disinfectant activity ofthe thickened compositions is more effective on the intended areas. To provide a thickened hypochlorite composition having an acceptable shelf-life, the rate of decomposition of alkali metal hypochlorite as well as the phase behaviour ofthe composition must be considered. As is known, alkali metal hypochlorite degradation may be illustrated by the following equation:
NaOC 1 < — > NaC 1 + XΛ O2
Many conventional thickening agents accelerate the degradation ofthe hypochlorite and thus are problematic for use in hypochlorite compositions. Also, the inclusion of conventional thickening agents and surfactants is difficult because the resulting hypochlorite composition has a tendency to separate into two or more phases, particularly at elevated temperatures. Many thickening agents are themselves unstable in the presence of an alkali metal hypochlorite. Thus,
achieving sufficient viscosity in hypochlorite compositions by conventional agents and additives in addition to providing a hypochlorite composition having acceptable stability is difficult.
It is also desirable, for commercial and aesthetic reasons, to provide thickened bleach-containing cleaner compositions which have distinctive coloration. The realm of bleach stable colourants is fairly small due to the tendency of organic dyes to degrade in the presence of strong oxidizers.
U.S. Patent No. 4,474,677 (Foxlee) suggests the use of certain halogenated copper phthalocyanine pigments for aqueous alkali metal hypochlorite compositions. While this class of pigments is considered to be bleach-stable, slow degradation ofthe pigment molecule releases copper which catalyzes the degradation of hypochlorite. U.S. Patent No. 4,271,030 (Brierley) describes a suspension of ultramarine blue using calcium soap floes. Use of calcium soap floes is not desirable due to the high concentration required, 50% by volume ofthe composition, or from a cleaning standpoint due to a tendency to precipitate onto hard surfaces. U.S. Patent No. 4,952,333 (Cramer) describes a bleaching and brightening composition using polymers to suspend ultramarine blue in an emulsified polymer matrix. This composition however would not be an effective hard surface cleaner due to its low detergency. U.S. Patent No. 4,917,814 (Maclntyre) describes the use of cobalt aluminate to colour thickened hypochlorite solutions. Cobalt pigments were found to be superior to ultramarine blue for suspension properties. While this is not disputed, it should be pointed out that, under higher temperature conditions than employed in Maclntyre, surfactant thickened compositions will lose viscosity and allow sedimentation ofthe pigment. Consumer products require stability when exposed to these higher temperatures during distribution and storage.
Summary ofthe Invention This invention provides thickened hypochlorite compositions with enhanced rheological properties which are capable of stably suspending inorganic pigments. The thickening system is a blend of surfactants and clay that is rheopectic at low shear rates, which helps to stably suspend the pigment, but thixotropic at higher shear rates, which allows the product to dispense easily from a container to aid in the cleaning of hard surfaces. By definition, rheopexy and thixotropy are opposite flow properties. Having both properties present in a single fluid is quite advantageous. Non-limiting examples of inorganic colourants that can be utilized, include ultramarine blue, cobalt aluminate blue, titanium dioxide and calcium carbonate. This invention focuses on the use of ultramarine blue which is preferred due to its consumer appeal, low toxicity, and colour intensity compared to other pigments. The composition behaves as a highly structured liquid and exhibits some unique and unexpected flow properties. This occurs despite the low solids content, less than 10%, ofthe formula as compared to other structured liquids, some of which are known in the category of liquid laundry detergents. This characteristic helps to solve the problem of pigment sedimentation while still maintaining thin fluid flow properties which help to achieve good surface coverage for products such as liquid toilet bowl cleaners. The composition also has good phase-stability and hypochlorite-stability.
The compositions of this invention comprise:
(a) an alkali metal hypochlorite, preferably sodium hypochlorite,
(b) bentonite clay, (c) a tertiary amine oxide having one long-chain alkyl group of from 10 to 16 carbon atoms and two lower alkyl groups,
(d) an alkali metal salt, preferably sodium chloride,
(e) a pH stabilizer to provide a pH of 11 or higher,
(f) an alkali metal C i o - C 16 alkyl sarcosinate,
(g) a Cio - Cj4 straight chain alkylbenzene sulphonate, and (h) an inorganic pigment, preferably ultramarine blue. The desired rheological properties and phase stability described above are achieved through the careful blending of clay, surfactants and electrolytes. In particular, the molar ratio ofthe tertiary amine oxide (c) to the alkylbenzene sulphonate (g) should range from about 5:1 to about 11:1. Useful non-pigmented compositions analogous to the compositions of this invention can be prepared without the pigment (h).
The viscosity ofthe composition can range from about 200 cps to about 1000 cps. The preferred range is from about 300 - 500 cps.
Brief Description ofthe Drawings Figures 1 and 2 are graphs showing the rheological properties of a preferred embodiment of this invention.
Figures 3 and 4 are graphs showing certain rheological properties of a formulation according to this insertion (Figure 3) and comparable properties of a similar composition without the clay (Figure 4).
Detailed Disclosure
The inventive composition is a hypochlorite stable, single phase, thickened hypochlorite bleach composition capable of adhering to vertical or inclined surfaces longer than thinner compositions. The composition is an effective agent for stain and soil removal as well as disinfection. The high level of hypochlorite stability and single solution phase behaviour ofthe composition enables the composition to have an acceptable shelf life. The compositions include also an
organic pigment in suspension. In these pigmented compositions, the colour stability, particularly where the pigment is ultramarine blue, is uniquely advantageous.
Preferably the alkali metal ofthe alkali metal hypochlorite is selected from lithium, potassium or sodium. For purposes of cost and availability, sodium hypochlorite is currently preferred. The alkali metal hypochlorite may have other by-products ofthe manufacturing process present without adversely affecting the composition. The amount of alkali metal hypochlorite employed is within the range of about 0.5 weight % to about 10 weight %, preferably from 1.0 weight % to 5.0 weight %, and more preferably from 1.5 weight % to 3.0 weight %.
Bentonite clay is a colloidal hydrated aluminum silicate clay found in North America. It consists principally of montmorillonite (Al2θ3»4Siθ2»H2θ) and usually also contains some magnesium, iron and calcium carbonate. Bentonite clay is preferred for use in the compositions of this invention, but other clays of similar structure and/or properties may be used. The amount of Bentonite clay in the composition should range from about 0.15 weight % to about 1.5 weight %, preferably from 0.25 weight % to 1.0 weight %. The tertiary amine oxide is ofthe formula:
R2
, I
R1— N— O
I
R3
wherein R1 is an alkyl group containing from about 10 to about 16 carbon atoms and each of R2 and R3 is a lower alkyl group containing from 1 to 3 carbon atoms.
R1, R2 and R3 may be a straight or branched chain; R1 may contain an odd or an even number of carbon atoms. Amine oxides of mixed chain length may be used, which may contain a predominance of one or more chain lengths. Preferably, the tertiary amine oxide is selected from myristyldimethylamine oxide, lauryldimethylamine oxide, and mixtures thereof. Most preferably employed is myristyldimethylamine oxide. The amount ofthe tertiary amine oxide employed is preferably in the range from about 0.5 weight % to about 2.5 weight %, more preferably from 0.9 weight % to 1.8 weight %, and most preferably from 1.0 weight % to 1.5 weight %. The alkali metal salt may be selected from any number of water-soluble alkali metal salts and mixtures thereof, with the alkali metal preferably being lithium, potassium, or sodium, and the anion ion preferably being a halide (such as chloride, fluoride, bromide and iodide). More preferably the alkali metal salt is selected from the group consisting of sodium chloride, lithium chloride, potassium chloride, and mixtures thereof. For purposes of cost and availability, the alkali metal salt most preferred is sodium chloride and may be used in varying amounts to reduce hypochlorite degradation, limited only by the avoidance of a "salting out" ofthe solution (where the surfactants become insoluble in water). When sodium chloride is used, the preferred amount is in the range of about 0.25 weight % to about 2.0 weight %, preferably from 0.5 weight % to 1.5 weight %.
An alkali metal hydroxide is the preferred pH stabilizer included in the composition, although any pH stabilizer may be employed as long as the stability and viscosity ofthe composition are not adversely affected. Other pH stabilizers which may be used, for example, include carbonate buffers. The alkali metal of the preferred hydroxide may be lithium, potassium, or sodium. Sodium hydroxide and potassium hydroxide are particularly useful pH stabilizers due to cost and availability, with sodium hydroxide most preferred. The alkali metal hydroxide is
included in the composition in an effective amount to adjust the composition to a pH level of at least about 11, more preferably from 12 to 13.5, and most preferably within the range from 12 to 13.
The alkali metal alkyl sarcosinate may be represented by the formula: CH3
R4 - C - N - CH2COO- M+
II o wherein R4 is a branched or straight chain C10-C16 alkyl group and M is an alkali metal cation (such as lithium, potassium or sodium). Sodium lauroyl sarcosinate is most preferred. The amount of alkali metal alkyl sarcosinate that may be used preferably ranges from about 0.10 weight % to about 0.75 weight %, more preferably 0.12 weight % to 0.60 weight %, and most preferably from 0.15 weight % to 0.30 weight %.
The alkali metal C 10 to C 14 straight chain alkylbenzene sulphonate is preferably defined wherein the alkali metal is potassium, lithium, or sodium. Most preferably employed is sodium dodecylbenzene sulphonate. Preferably the amount of sulphonate used is within the range of from about 0.08 weight % to about 0.8 weight %, more preferably from 0.1 weight % to 0.5 weight %, and most preferably from 0.15 weight % to 0.4 weight %.
In these pigmented compositions, the preferred pigment is ultramarine blue which is an inorganic silicate. Although this material is inert to hypochlorite oxidation and does not catalyze decomposition of hypochlorite, it is insoluble and requires suspension in the hypochlorite solution. Such suspension cannot be achieved merely by dispensing particles of ultramarine blue in hypochlorite solution, because the pigment has a density of 2.35 and settles out even when it is of very fine particle size. The thickening system employed in the composition of this invention provides excellent suspension for ultramarine blue pigment particles.
The amount of ultramarine blue in the composition of this invention ranges from about 0.01 weight % to about 0.50 weight %, preferably about 0.05 weight %. The molar ratio ofthe tertiary amine oxide to alkali metal alkylbenzene sulphonate should fall within the range of from about 5:1 to about 11 : 1. Preferably, the molar ratio is from 6:1 to 10:1, and more preferably from 7:1 to 9:1.
The composition offers improved viscosity for alkali metal hypochlorite bleaches while at the same time providing a commercially acceptable pigmented composition with excellent colour stability. Although not wishing to be bound to any particular theory, it is believed that the primary interaction is between the clay and the amine oxide components ofthe formula. In the preferred embodiment of the example set forth below, the combination ofthe clay, sodium chloride, and the sodium hydroxide in solution causes the clay platelets to align in an edge-to-face structure. Some ofthe amine oxide acts to stabilize the structure through both ionic and steric interaction. Sulphonate and sarcosinate surfactants combine with the remaining amine oxide to form organic structures or micelles which boost viscosity. It is further theorized that these micelles interact with the clay structure to develop the unique rheology ofthe composition.
This invention provides a commercially advantageous coloured thickening system which exhibits thixotropic properties for easy dispensing, particularly from a spray container. Cleaning products employing this thickening system have a sufficiently high level of quiescent viscosity to keep the inorganic pigment particles in suspension.
The invention will be better understood by reference to the following examples which are included for the purpose of illustration, and are not be be construed as limitations.
Example 1 A blue-pigmented hand surface cleaner was prepared which had the following ingredients, all percentages being by weight.
Ingredient bentonite clay (Gelwhite H) 1.00% ultramarine blue 0.05% sodium chloride 1.00% sodium hydroxide 2.50% myristyldimethylamine oxide 5.60% sodium hypochlorite 2.50% sodium dodecylbenzene sulphonate 0.72% sodium lauroyl sarcosinate 1.00% fragrance 0.065% deionized water q.s. to 100%
The cleaner composition was prepared by dispensing in the main vessel (1) Gelwhite H, a montmorillomite clay (Southern Clay Products) in water, using a homogenizer until the clay is fully hydrated, and adding the Ultramarine blue with further agitation. In a separate vessel (2), sodium chloride and a 25% solution of sodium hydroxide were dissolved in water. The contents of vessel (2) were added to vessel (1) with high agitation. The remaining ingredients were added, with agitation, in the following order: Ammonyx MO, a 30% solution of myristyldimethylamine oxide, Stepan Company; fragrance; a 16.67% solution of sodium hypochlorite bleach; Biosoft D-40, a 40% solution of sodium dodecylbenzene sulphonate, Stepan Company; and Hamposyl L-30, a 30% solution of sodium lauroyl sarcosinate, W.R. Grace & Company.
Figure 1 shows the rheology profile of this preferred embodiment. It summarizes the shear stress as a function of time at four shear rates. The formula appears to be rheopectic at both 1 and 10 sec"1, under conditions of constant shear. The thixotropic character is evident at 50 sec-1. Figure 2 captures the stress growth behaviour at the inception of flow at the first shear rate, 1 sec-1. Testing was conducted with the Rheometrics Scientific RFSII rheometer, 50 mm parallel plate, 0.9 mm spacing, 316SS tooling, 25C, 0.002 - 10 gr-cm force rebalance.
An analogous formula without the clay and pigment components exhibits dramatically different rheological properties. See Figures 3 and 4. In the examination of plots of G', a measure ofthe elastic strength of a viscoelastic fluid, and G", a measure ofthe mechanical energy dissipated during the deformation of structured fluid, the formula with clay behaves as a highly structured fluid with significant strain dependence. The analogous formula behaves as a predominantly viscous fluid with no significant strain dependence. This difference indicates a significant interaction between the clay component and the surfactants present in the formulation.
Examples 2-5 Following the procedure ofExample 1, the following additional compositions were prepared:
Comparative Example A cleaning composition containing ultramarine blue pigment, but without bentonite clay was prepared, and the pigment-settling characteristics were compared with the composition ofExample 1. The comparative composition was prepared using the method ofExample 1. The two compositions were maintained in a quiescent state for a period of six weeks at 40°C. The following table shows the ingredients ofthe compositions and the relevant rheological data.
TABLE
These data show that, in contrast to the excellent suspension characteristics of Example 1, in the Comparative Example, which contains only half the amount of pigment, settles out within three weeks.
Claims
1. A thickened pigmented aqueous hypochlorite composition comprising, on a weight basis:
(a) from 0.5%) to 10% of an alkali metal hypochlorite;
(b) from 0.25% to 1 % of bentonite clay;
(c) from 0.5% to 2.5%) of a tertiary amine oxide ofthe formula
R2
I
Rl— N— O
I
R3 wherein Rl is an alkyl of from 10 to 16 carbon atoms, and each of R2 and R3 is alkyl of from 1 to 3 carbon atoms;
(d) from 0.25% to 2.0% of an alkali metal salt;
(e) a pH stabilizer in sufficient amount to provide a pH of 11 or higher;
(f) from 0.10%) to 0.75% of an alkali metal sarcosinate ofthe formula
CH3 R4 . c - N - CH2COO" M+
II o
wherein R4 is a straight chain alkyl of from 10 to 16 carbon atoms and M is lithium, sodium or potassium;
(g) from 0.08 to 0.80%) of an alkali metal alkylbenzene sulphonate in which the alkyl group is straight chained and has from 10 to 14 carbon atoms; and
(h) from 0.01%) to 0.5%) of an inorganic pigment wherein the molar ratio of (c) to (g) ranges from 5 : 1 to 11 : 1.
2. A hypochlorite composition according to claim 1 in which (h) the pigment is ultramarine blue.
3. A hypochlorite composition according to claim 2 in which: (a) the alkali metal hypochlorite is sodium hypochlorite,
(c) the amine oxide is lauryldimethylamine oxide, myristyldimethylamine oxide or mixtures thereof,
(d) the alkali metal salt is sodium chloride,
(e) the pH stabilizer is sodium hydroxide in sufficient amount to provide a pH of from 12 to 13.5,
(f) the sarcosinate is sodium lauroyl sarcosinate,
(g) the alkali metal alkylbenzene sulphonate is sodium dodecylbenzene sulphonate.
4. A hypochlorite composition according to claim 3 in which (c) the amine oxide is lauryldimethylamine oxide.
5. A hypochlorite composition according to claim 4 which comprises, by weight
(a) from 1% to 5% sodium hypochlorite,
(b) from 0.25% to 1 % bentonite clay,
(c) from 0.9% to 1.8%) lauryldimethylamine oxide,
(d) from 0.5% to 1.5% sodium chloride,
(f) from 0.12% to 0.60%) sodium lauroyl sarcosinate,
(g) from 0.10% to 0.50%) sodium dodecylbenzene sulphonate, and (h) about 0.05% ultramarine blue pigment, wherein the molar ratio of (c) to (g) is from 6:1 to 10: 1.
6. A hypochlorite composition according to claim 5 which comprises, by weight
(a) from 1.5% to 3.0%> sodium hypochlorite,
(c) from 1.0%) to 1.5% lauryldimethylamine oxide,
(f) from 0.15% to 0.30%) sodium lauroyl sarcosinate, and
(g) from 0.15% to 0.40%) sodium dodecylbenzene sulphonate, wherein the molar ratio of (c) to (g) ranges from 7:1 to 9:1.
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9516372A GB2304113B (en) | 1995-08-10 | 1995-08-10 | Hard surface cleaner |
| GB9516372 | 1995-08-10 | ||
| US08/619,864 US5688435A (en) | 1995-08-10 | 1996-03-18 | Pigmented rheopectic cleaning compositions with thixotropic properties |
| US619864 | 1996-03-18 | ||
| PCT/US1996/011409 WO1997006233A1 (en) | 1995-08-10 | 1996-07-08 | Pigmented rheopectic cleaning compositions with thixotropic properties |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU6543196A AU6543196A (en) | 1997-03-05 |
| AU692718B2 true AU692718B2 (en) | 1998-06-11 |
Family
ID=26307551
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU65431/96A Ceased AU692718B2 (en) | 1995-08-10 | 1996-07-08 | Pigmented rheopectic cleaning compositions with thixotropic properties |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP0859826A4 (en) |
| CN (1) | CN1102649C (en) |
| AU (1) | AU692718B2 (en) |
| BR (1) | BR9609898A (en) |
| CA (1) | CA2228674C (en) |
| IN (1) | IN189237B (en) |
| MX (1) | MX9801081A (en) |
| NZ (1) | NZ313386A (en) |
| WO (1) | WO1997006233A1 (en) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE19722809A1 (en) * | 1997-05-30 | 1998-12-03 | Henkel Kgaa | cleaning supplies |
| GB9727517D0 (en) * | 1997-12-31 | 1998-02-25 | Jeyes Group Plc | Liquid bleach composition |
| DE19821695A1 (en) * | 1998-05-14 | 1999-11-25 | Henkel Kgaa | Stable coloring of solid or liquid machine dishwashing agents |
| WO2000055291A1 (en) * | 1999-03-17 | 2000-09-21 | R.T. Vanderbilt Company, Inc. | Stabilizer for bleach-containing cleaners |
| EP1416038B1 (en) * | 2002-10-29 | 2007-01-03 | Unilever Plc | Thickened liquid bleaching compositions |
| US20040254085A1 (en) * | 2003-05-19 | 2004-12-16 | Johnsondiversey, Inc. | [high caustic contact cleaner] |
| DE102005058642B3 (en) * | 2005-12-07 | 2007-07-26 | Henkel Kgaa | Increasing the stability of liquid hypochlorite-containing detergents and cleaners |
| DE102005062008B3 (en) | 2005-12-22 | 2007-08-30 | Henkel Kgaa | Odor reduction of hypochlorite-containing agents |
| DE102005063177A1 (en) | 2005-12-30 | 2007-07-05 | Henkel Kgaa | Use of diethylene-penta-methylene phosphonic acid for the stabilization of optical brightener in aqueous liquid detergent containing alkali hypochlorite |
| DE102006003336A1 (en) * | 2006-01-23 | 2007-07-26 | Henkel Kgaa | Sprayable all-purpose cleaner |
| EP1911832A1 (en) * | 2006-10-13 | 2008-04-16 | Unilever N.V. | Bleaching composition |
| US20090197790A1 (en) * | 2008-02-05 | 2009-08-06 | Amcol International Corporation | Drip resistant cleaning compositions |
| CA3065556C (en) * | 2017-06-08 | 2022-11-08 | The Procter & Gamble Company | Non-homogeneous compositions |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4789495A (en) * | 1987-05-18 | 1988-12-06 | The Drackett Company | Hypochlorite compositions containing a tertiary alcohol |
| US5089162A (en) * | 1989-05-08 | 1992-02-18 | Lever Brothers Company, Division Of Conopco, Inc. | Cleaning compositions with bleach-stable colorant |
| US5549842A (en) * | 1993-12-29 | 1996-08-27 | Reckitt & Colman Inc. | Thickened alkali metal hypochlorite composition |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2849225A1 (en) * | 1977-11-18 | 1979-05-23 | Unilever Nv | POURABLE, LIQUID BLEACHING AGENTS |
| US4552680A (en) * | 1983-11-04 | 1985-11-12 | The Procter & Gamble Company | Hypochlorite bleach containing surfactant and organic antifoamant |
| US4623476A (en) * | 1984-03-30 | 1986-11-18 | The Procter & Gamble Company | Stable suspension of pigments in aqueous hypochlorite bleach compositions |
| US4714562A (en) * | 1987-03-06 | 1987-12-22 | The Procter & Gamble Company | Automatic dishwasher detergent composition |
| JP2594404B2 (en) * | 1992-12-22 | 1997-03-26 | 花王株式会社 | Liquid bleach composition |
-
1996
- 1996-07-08 BR BR9609898A patent/BR9609898A/en not_active Application Discontinuation
- 1996-07-08 CA CA002228674A patent/CA2228674C/en not_active Expired - Fee Related
- 1996-07-08 AU AU65431/96A patent/AU692718B2/en not_active Ceased
- 1996-07-08 MX MX9801081A patent/MX9801081A/en not_active IP Right Cessation
- 1996-07-08 EP EP96925280A patent/EP0859826A4/en not_active Withdrawn
- 1996-07-08 NZ NZ313386A patent/NZ313386A/en unknown
- 1996-07-08 WO PCT/US1996/011409 patent/WO1997006233A1/en not_active Ceased
- 1996-07-08 CN CN96196185A patent/CN1102649C/en not_active Expired - Fee Related
- 1996-08-09 IN IN1429CA1996 patent/IN189237B/en unknown
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4789495A (en) * | 1987-05-18 | 1988-12-06 | The Drackett Company | Hypochlorite compositions containing a tertiary alcohol |
| US5089162A (en) * | 1989-05-08 | 1992-02-18 | Lever Brothers Company, Division Of Conopco, Inc. | Cleaning compositions with bleach-stable colorant |
| US5549842A (en) * | 1993-12-29 | 1996-08-27 | Reckitt & Colman Inc. | Thickened alkali metal hypochlorite composition |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0859826A4 (en) | 1999-11-24 |
| CN1192775A (en) | 1998-09-09 |
| AU6543196A (en) | 1997-03-05 |
| BR9609898A (en) | 1999-05-25 |
| CA2228674A1 (en) | 1997-02-20 |
| EP0859826A1 (en) | 1998-08-26 |
| CA2228674C (en) | 2000-10-10 |
| NZ313386A (en) | 1998-07-28 |
| IN189237B (en) | 2003-01-11 |
| CN1102649C (en) | 2003-03-05 |
| WO1997006233A1 (en) | 1997-02-20 |
| MX9801081A (en) | 1998-04-30 |
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Legal Events
| Date | Code | Title | Description |
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| PC | Assignment registered |
Owner name: RECKITT BENCKISER INC. Free format text: FORMER OWNER WAS: RECKITT AND COLMAN INC. |
|
| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |