MXPA98001081A - Reproductive cleaning compositions pigmented with tixotropi properties - Google Patents
Reproductive cleaning compositions pigmented with tixotropi propertiesInfo
- Publication number
- MXPA98001081A MXPA98001081A MXPA/A/1998/001081A MX9801081A MXPA98001081A MX PA98001081 A MXPA98001081 A MX PA98001081A MX 9801081 A MX9801081 A MX 9801081A MX PA98001081 A MXPA98001081 A MX PA98001081A
- Authority
- MX
- Mexico
- Prior art keywords
- sodium
- hypochlorite
- alkali metal
- composition
- oxide
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 69
- 238000004140 cleaning Methods 0.000 title abstract description 10
- 230000001850 reproductive Effects 0.000 title 1
- WQYVRQLZKVEZGA-UHFFFAOYSA-N hypochlorite Inorganic materials Cl[O-] WQYVRQLZKVEZGA-UHFFFAOYSA-N 0.000 claims abstract description 60
- 229910052783 alkali metal Inorganic materials 0.000 claims abstract description 31
- -1 alkali metal hypochlorite Chemical class 0.000 claims abstract description 25
- 239000004927 clay Substances 0.000 claims abstract description 23
- 229910052570 clay Inorganic materials 0.000 claims abstract description 23
- 239000011780 sodium chloride Substances 0.000 claims abstract description 18
- 235000013799 ultramarine blue Nutrition 0.000 claims abstract description 13
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 12
- 239000003381 stabilizer Substances 0.000 claims abstract description 9
- HWKQNAWCHQMZHK-UHFFFAOYSA-N Trolnitrate Chemical compound [O-][N+](=O)OCCN(CCO[N+]([O-])=O)CCO[N+]([O-])=O HWKQNAWCHQMZHK-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000000440 bentonite Substances 0.000 claims abstract description 8
- 229910000278 bentonite Inorganic materials 0.000 claims abstract description 8
- 239000001023 inorganic pigment Substances 0.000 claims abstract description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M sodium chloride Chemical group [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims description 20
- 239000000049 pigment Substances 0.000 claims description 17
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Chemical group [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 15
- 239000004615 ingredient Substances 0.000 claims description 10
- 150000001340 alkali metals Chemical class 0.000 claims description 9
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 8
- SUKJFIGYRHOWBL-UHFFFAOYSA-N Sodium hypochlorite Chemical group [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 claims description 7
- 239000005708 Sodium hypochlorite Substances 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
- 150000003512 tertiary amines Chemical class 0.000 claims description 7
- 150000001412 amines Chemical class 0.000 claims description 6
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical group [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 claims description 6
- WHXSMMKQMYFTQS-UHFFFAOYSA-N lithium Chemical group [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 claims description 6
- 229910052744 lithium Inorganic materials 0.000 claims description 6
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 6
- 229910052700 potassium Inorganic materials 0.000 claims description 6
- 239000011591 potassium Chemical group 0.000 claims description 6
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical group [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 claims description 6
- 229910052708 sodium Chemical group 0.000 claims description 6
- 239000011734 sodium Chemical group 0.000 claims description 6
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 claims description 6
- 229940045885 sodium lauroyl sarcosinate Drugs 0.000 claims description 6
- SYELZBGXAIXKHU-UHFFFAOYSA-N Lauryldimethylamine oxide Chemical group CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 claims description 5
- 229940071089 sarcosinate Drugs 0.000 claims description 5
- ONHFWHCMZAJCFB-UHFFFAOYSA-N Myristamine oxide Chemical compound CCCCCCCCCCCCCC[N+](C)(C)[O-] ONHFWHCMZAJCFB-UHFFFAOYSA-N 0.000 claims description 4
- FSYKKLYZXJSNPZ-UHFFFAOYSA-M sarcosinate Chemical compound CNCC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-M 0.000 claims description 4
- KWKXNDCHNDYVRT-UHFFFAOYSA-N Dodecylbenzene Chemical compound CCCCCCCCCCCCC1=CC=CC=C1 KWKXNDCHNDYVRT-UHFFFAOYSA-N 0.000 claims description 3
- 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 3
- 239000000126 substance Substances 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims 2
- 239000002184 metal Substances 0.000 claims 2
- 229940048098 Sodium Sarcosinate Drugs 0.000 claims 1
- 239000001055 blue pigment Substances 0.000 claims 1
- 150000003839 salts Chemical class 0.000 claims 1
- ZUFONQSOSYEWCN-UHFFFAOYSA-M sodium;2-(methylamino)acetate Chemical compound [Na+].CNCC([O-])=O ZUFONQSOSYEWCN-UHFFFAOYSA-M 0.000 claims 1
- GHNRTXCRBJQVGN-UHFFFAOYSA-N 4-dodecan-6-ylbenzenesulfonic acid Chemical compound CCCCCCC(CCCCC)C1=CC=C(S(O)(=O)=O)C=C1 GHNRTXCRBJQVGN-UHFFFAOYSA-N 0.000 abstract description 4
- 239000007844 bleaching agent Substances 0.000 abstract description 3
- 239000000725 suspension Substances 0.000 description 7
- 239000012530 fluid Substances 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- 230000015556 catabolic process Effects 0.000 description 5
- 230000004059 degradation Effects 0.000 description 5
- 238000006731 degradation reaction Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 238000004061 bleaching Methods 0.000 description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 239000002245 particle Substances 0.000 description 4
- IRERQBUNZFJFGC-UHFFFAOYSA-L Azure blue Chemical compound [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 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000005520 cutting process Methods 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 230000003993 interaction Effects 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 229960003563 Calcium Carbonate Drugs 0.000 description 2
- CJZGTCYPCWQAJB-UHFFFAOYSA-L Calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M Lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-L Sulphite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 2
- 150000008044 alkali metal hydroxides Chemical class 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
- 230000000249 desinfective Effects 0.000 description 2
- 239000003599 detergent Substances 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
- 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 2
- KARVSHNNUWMXFO-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane;hydrate Chemical compound O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Al]O[Al]=O KARVSHNNUWMXFO-UHFFFAOYSA-N 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000693 micelle Substances 0.000 description 2
- 229910052901 montmorillonite Inorganic materials 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 238000004062 sedimentation Methods 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- PNEYBMLMFCGWSK-UHFFFAOYSA-N AI2O3 Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 210000001772 Blood Platelets Anatomy 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate dianion Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- VVOLVFOSOPJKED-UHFFFAOYSA-N Copper phthalocyanine Chemical class [Cu].N=1C2=NC(C3=CC=CC=C33)=NC3=NC(C3=CC=CC=C33)=NC3=NC(C3=CC=CC=C33)=NC3=NC=1C1=CC=CC=C12 VVOLVFOSOPJKED-UHFFFAOYSA-N 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L Magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- UIIMBOGNXHQVGW-UHFFFAOYSA-M buffer Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000001032 cobalt pigment Substances 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 230000000875 corresponding Effects 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 238000011033 desalting Methods 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- XGZRAKBCYZIBKP-UHFFFAOYSA-L disodium;dihydroxide Chemical compound [OH-].[OH-].[Na+].[Na+] XGZRAKBCYZIBKP-UHFFFAOYSA-L 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- RAQDACVRFCEPDA-UHFFFAOYSA-L ferrous carbonate Chemical compound [Fe+2].[O-]C([O-])=O RAQDACVRFCEPDA-UHFFFAOYSA-L 0.000 description 1
- KRHYYFGTRYWZRS-UHFFFAOYSA-M fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxyl anion Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 1
- HCQWRNRRURULEY-UHFFFAOYSA-L lithium;potassium;dichloride Chemical compound [Li+].[Cl-].[Cl-].[K+] HCQWRNRRURULEY-UHFFFAOYSA-L 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 238000003754 machining Methods 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
- 238000000034 method Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 230000001590 oxidative Effects 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N oxo-oxoalumanyloxy-[oxo(oxoalumanyloxy)silyl]oxysilane;dihydrate Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- BPQQTUXANYXVAA-UHFFFAOYSA-N silicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
Abstract
A hard surface cleaning composition containing pigmented bleach comprises an alkali metal hypochlorite, bentonite clay, mono- (long chain alkyl) -tertiary amine, an alkali metal salt, a pH stabilizer to achieve a pH of 11. or greater, an alkali metal alkyl arcosinate, an alkylbenzenesulfonate and an inorganic pigment which is preferably ultramarine blue. The cleaning composition has excellent color stability as well as phase stability and hypochloride stability
Description
REPEPTIC CLEANING COMPOSITIONS PIGMENTED WITH THIXOTROPIC PROPERTIES
FIELD DB THE INVENTION This invention relates to compositions containing a thickened bleach liquid useful for the cleaning of rough surfaces and, in particular, to those compositions that include stable pigments in the presence of bleaches.
BACKGROUND OF THE INVENTION Thickened bleaching compositions offer a number of advantages over non-thickened bleaching compositions. The more viscous and thicker solutions adhere to vertical and inclined surfaces for a longer period, and the disinfectant activity of the thick compositions is more effective in the chosen areas. In order to provide a thickened hypochlorite composition having an acceptable shelf life, the decomposition rate of the alkali metal hypochlorite and the phase behavior of the composition must be taken into account. As is known, the degradation of alkali metal hypochlorite can be illustrated by the following equation: P1087 / 98MX NaOCI NaCl +% 02
Many conventional thickening agents accelerate the degradation of hypochlorite and, consequently, its use in hypochlorite compositions is problematic because the resulting hypochlorite composition tends to separate into two or more phases, especially under high temperature conditions. Many of the thickening agents are unstable in the presence of alkali metal hypochlorite. Therefore, it is not easy to achieve sufficient viscosity in hypochlorite compositions using conventional agents and additives and to provide, in addition, a hypochlorite composition with adequate stability. It is also desirable, for aesthetic and commercial reasons, to provide cleaning compositions containing thickened whiteners that exhibit a coloration that distinguishes them. The scope of stable dyes in the presence of bleaches is quite small due to the tendency of organic dyes to degrade against strong oxidants. U.S. Patent No. 4,474,677 (Foxlee) suggests using certain halogenated cupric phthalocyanine pigments with aqueous alkali metal hypochlorite compositions. While this class of pigments is
P1087 / 98MX considered stable in the presence of bleaches, the slow degradation of the pigment molecule releases copper that catalyzes the degradation of hypochlorite. U.S. Patent No. 4,271,030 (Brierley) discloses a suspension of ultramarine blue using calcium soap flakes. The use of calcium soap in flakes is not convenient due to the high concentration required, 50% by volume of the composition or, in terms of cleaning, because it tends to precipitate on rough surfaces. U.S. Patent No. 4,952,333 (Cramer) discloses a bleaching composition that revives colors and uses polymers to suspend ultramarine blue pigment in an emulsified polymer matrix. This composition, however, is not a good cleaner for rough surfaces due to its low detergent capacity. U.S. Patent No. 4,917,814 (MacIntyre) describes the use of cobalt aluminate with thickened and colored hypochlorite solutions. Cobalt pigments have better suspension properties than ultramarine blue. It should be noted, unless proven otherwise, that under conditions of higher temperatures than those used by MacIntyre, the thickened surfactant compositions lose viscosity and allow the pigment to settle. Consumer products must be stable when exposed to
P1087 / 98MX such temperatures during the storage and distribution period.
SUMMARY INVENTION This invention provides thickened hypochlorite compositions with improved rheological properties capable of stably suspending inorganic pigments. The thickening system consists of a reopéctica mixture of surfactant ingredients and clays at low speed of bearing and thixotropic effort at high speed of cutting effort, which allows the product to be easily dispensed from a container to proceed with the cleaning of rough surfaces. By definition, reopexy and thixotropy are opposite flow properties. The presence of both properties in the same fluid is particularly advantageous. An unlimited number of examples of inorganic dyes can be used, including ultramarine blue, cobalt aluminate blue, titanium dioxide and calcium carbonate. This invention concentrates on the use of ultramarine blue, a preferred pigment for its acceptance among consumers, low toxicity and color intensity in comparison with other pigments. The compositions behave as highly structured liquids and exhibit flow properties
P1087 / 98MX unique and unexpected. This occurs despite the low solids content, less than 10%, of the formula compared to other structured liquids, many of them known in the category of liquid detergents for laundry. This feature helps solve the problem of pigment sedimentation without losing the properties of thin-film fluid flow that allows products such as toilet cleaners to achieve greater surface coverage. The composition shows good phase stability and is stable in the presence of hypochlorite. The compositions of the invention comprise: a) an alkali metal hypochlorite, preferably sodium hypochlorite, b) bentonite clay, c) a tertiary amine oxide having a long chain alkyl group composed of 10 to 16 carbon atoms and two lower alkyl groups, d) an alkali metal salt, preferably sodium chloride, e) a pH stabilizer to reach a pH of 11 or higher, f) an alkali metal Cis-Cis alkyl sarcosinate, g) an alkylbenzene sulfonate C10 -C16 linear chain and
P1087 / 98MX h) an inorganic pigment, preferably ultramarine blue. The desired rheological properties and the phase stability described above are achieved by carefully mixing the clay, the surfactants and the electrolytes. In particular, the molar ratio between the tertiary amine oxide (c) and the alkylbenzene sulfonate (g) should be between 5: 1 and 11: 1. Compositions without useful pigments analogous to the compositions of this invention can be prepared without the pigment (h). The viscosity of the composition can vary between 200 cps and 1000 cps. The preferred range is 300 to 500 cps.
BRIEF DESCRIPTION OF THE 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 the present invention (Figure 3) and comparable properties of a similar composition without clay (Figure 4).
P1087 / 98MX DESCRIPTION OF THE INVENTION The composition of the invention is a bleaching composition of hypochlorite thickened in a single phase, stable in the presence of hypochlorite capable of adhering to vertical or inclined surfaces for longer periods than the diluent compositions. The composition is an effective agent for disinfecting and removing stains. The high level of stability in the presence of hypochlorite and the phase behavior of the single solution allow the shelf life of the composition to be acceptable. The compositions further include an organic pigment in suspension. In these pigmented compositions, the stability of the color, especially when dealing with ultramarine blue, is singularly advantageous. The alkali metal of the alkali metal hypochlorite is preferably selected from lithium, potassium or sodium. In terms of costs and availability, sodium hypochlorite is currently preferred. The alkali metal hypochlorite may have other products derived from the manufacturing process without adversely affecting the composition. The amount of alkali metal hypochlorite used ranges from 0.5 to 10% by weight, preferably between 1.0 and 5.0% by weight and more preferably between 1.5 and 3.0% by weight.
P1087 / 98MX weight. Bentonite clay is a colloidal hydrated aluminum silicate clay found in North America. This clay is mainly composed of montmorillonite (AI2O3 • 4SÍO2 -H 0) and, in general, contains a little magnesium, iron and calcium carbonate. While in the present invention it is preferred to use bentonite clay, other clays of structure and / or similar properties can also be used. The amount of bentonite clay present in the composition should range between 0.15 and 1.5% by weight, preferably between 0.25% and 1.0% by weight. The tertiary amine oxide has the following formula:
where R is an alkyl group containing from 10 to 16 carbon atoms and each R 2 and R 3 is a lower alkyl group containing from 1 to 3 carbon atoms. R, R and R3 may be straight or branched chain; R may contain an even or odd number of carbon atoms. Amine oxides of different chain length can be used,
P1087 / 98MX where one or more lengths may predominate. Preferably, the tertiary amine oxide is selected from a group consisting of myristyldimethylamine oxide, lauryldimethylamine oxide or mixtures of said substances. Miristyldimethylamine oxide is more preferably used. The amount of tertiary amine oxide used is between 0.5 and 2.5% by weight, more preferably between 0.9 and 1.8% by weight and more preferably still between 1.0 and 1.5% by weight. The alkali metal salt can be selected from the alkali metal salts soluble in water and their mixtures; as the alkali metal, lithium, potassium or sodium is preferred, and as an anion ion, a halide (such as, for example, chloride, fluoride, bromide and iodide). More preferably, the alkali metal salt is selected from a group consisting of sodium chloride, lithium chloride, potassium chloride and mixtures of these substances. The most preferred alkali metal salt in terms of costs and availability is sodium chloride which can be used in different quantities in order to reduce the degradation of hypochlorite, with the only limitation of avoiding the "desalting" of the solution, in which case the surfactants become insoluble in water). If sodium chloride is used, the preferred amount is found
P1087 / 98MX comprised between 0.25 and 2.0% by weight, more preferably between 0.5 and 1.5% by weight. While any pH stabilizer can be used as long as it does not affect the stability and viscosity of the composition, it is preferred to include an alkali metal hydroxide in the composition as a pH stabilizer. Other pH stabilizers can be used, for example, those that include carbonate buffers. The alkali metal of the preferred hydroxide may be lithium, potassium or sodium. Sodium hydroxide and potassium hydroxide are especially useful as pH stabilizers because of their cost and availability, with sodium hydroxide being most preferred. The alkali metal hydroxide is incorporated into the composition in an amount effective to bring the pH of the composition to a level of at least 11, more preferably from 12 to 13.5 and more preferably from 12 to 13. The alkali metal alkyl sarcosinate can be represent by the following formula:
CH3 R4 - C - N - CH2COO M +
P1087 / 98MX where R4 is a straight or branched chain C? Or C Ci6 alkyl group and M is an alkali metal cation (such as, for example, lithium, potassium or sodium). Sodium lauroyl sarcosinate is most preferably used. The amount of alkali metal alkyl sarcosinate that can be used ranges from 0.10 to 0.75% by weight, more preferably from 0.12 to 0.60% by weight and more preferably even from 0.15 to 0.30% by weight. The straight chain alkylbenzene sulphonate of 10 to 14 carbon-alkali metal atoms preferably contain potassium, lithium or sodium as the alkali metal. Sodium dodecylbenzenesulfonate is most preferably used. Preferably the amount of sulfonate used is between 0.08 and 0.8% by weight, more preferably between 0.1 and 0.5% by weight and more preferably still between 0.15 and 0.4% by weight. In these pigmented compositions, the preferred pigment is ultramarine blue which is an organic silicate. Although this material is inert to the oxidation of hypochlorite and does not catalyze the decomposition of hypochlorite, it is insoluble and must be suspended in the hypochlorite solution. Said suspension can not be achieved by distributing particles of ultramarine blue in hypochlorite solution because the pigment has a density of 2.35 and sediments even when the size of the
P1087 / 98MX particles are very fine. The thickening system used in the composition of the present invention provides excellent suspension conditions for ultramarine blue pigment particles. The amount of ultramarine blue in the composition of the invention ranges from 0.01 to 0.50% by weight, preferably 0.05%. The molar ratio between the tertiary amine oxide and the alkali metal alkylbenzene sulfonate should be between 5: 1 and 11: 1; preferably between 6: 1 and 10: 1 and more preferably between 7: 1 and 9: 1. The composition offers higher viscosity for alkali metal hypochlorite bleaches while providing a commercially acceptable pigmented composition with excellent color stability. While not intended to support any particular theory, it is believed that the primary interaction occurs between the components corresponding to the clay and the amine oxide of the formula. In the preferred embodiment of the example presented below, as a consequence of the combination of clay, sodium chloride and sodium hydroxide solution the clay platelets are aligned according to a chant-face structure. Part of the amine oxide acts as a stabilizer of the structure by ionic or steric interaction. The ingredients
P1087 / 98MX sulfonate and sarcosinate surfactants combine with the rest of the amine oxide to form organic structures or micelles that increase viscosity. The theory further indicates that the micelles interact with the structure of the clay to give the composition unique rheological properties. The present invention provides a commercially advantageous colored thickening system having thixotropic properties that allow the product to be dispensed easily, especially if an atomizer container is used. The cleaning products employing this thickening system have a degree of quiescent viscosity sufficient to keep the inorganic pigment particles in suspension. The invention will be better understood if reference is made to the following examples which are included for illustrative purposes and should not be construed restrictively.
Example 1 A blue manual surface cleaner containing the following ingredients was prepared, all percentages correspond to percentages by weight.
P1087 / 98MX 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 dodecylbenzenesulfonate 0.72% sodium lauroyl sarcosinate 1.00% fragrance 0.065% deionized water csplOO%
To prepare the composition of the cleaner was placed in the main container (1) Gelwhite H, montmorillonite clay (Southern Clay Products) in water and a homogenizer was used until the clay was completely dehydrated. Ultramarine blue was added and the composition was stirred. In a separate vessel (2), sodium chloride and a 25% sodium hydroxide solution were dissolved in water. While stirring the container the remaining ingredients were added in the following order: Ammonyx MO, a solution of myristyldimethylamine oxide, Stepan Company; a 16.67% sodium hypochlorite bleach solution; Biosoft D-40, a solution of sodium dodecylbenzenesulfonate, Stepan
P1087 / 98MX Company; and Hamposyl L-30, a solution of sodium lauroyl sarcosinate, W. R. Grace & Company Figure 1 shows the rheological profile of this preferred embodiment. It summarizes the cutting effort as a function of time in four speeds of cutting effort. The formula presents reopécticas properties so much to 1 as to 10 seg ~ in constant conditions of effort of cut. The thixotropic character is evident at 50 sec. "Figure 2 captures the increase in tension at the start of the flow at the first shear rate, and the tests were performed with a Rheometrics Scientific OFSII rheometer., 50 mm parallel plate, 0.9 mm spacing, machining 316SS, 25C, force balance adjustment of 0.002-10 g / cm. An analogous formula that does not include clay or pigments shows radically different rheological properties. See Figures 3 and 4. If one examines the path of G ', a measurement of the elastic resistance of a viscoelastic fluid, and G ", a measurement of the mechanical energy dissipated during the deformation of a structured fluid, it will be seen that the formula that presents clay behaves like a highly structured fluid with a significant dependence on effort.The analogous formula behaves like a predominantly viscous fluid with
P1087 / 98MX a little significant dependence on effort. This difference denotes a significant interaction between the clay component and the surfactant ingredients present in the formula.
The 2-s compounds The following additional compositions were prepared according to the procedure described in Example 1:
P1087 / 98MX
Comparative Example A cleaning composition containing ultramarine blue pigment but not containing clay was prepared. The sedimentation characteristics of the pigment were compared with the composition of Example 1. The comparative composition was prepared according to the method applied in Example 1. The two compositions were kept in a quiescent state for a period of 6 weeks at 40 ° C. The following table shows the ingredients of the compositions and the relevant rheological data.
P1087 / 98MX TABLE
These data indicate that, unlike the excellent suspension characteristics of Example 1, in the Comparative Example containing only half the pigment, it sediments within three weeks.
P1087 / 98MX
Claims (6)
1. P1087 / 98MX
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9516372A GB2304113B (en) | 1995-08-10 | 1995-08-10 | Hard surface cleaner |
GB9516372.1 | 1995-08-10 | ||
US08619864 | 1996-03-18 | ||
US08/619,864 US5688435A (en) | 1995-08-10 | 1996-03-18 | Pigmented rheopectic cleaning compositions with thixotropic properties |
PCT/US1996/011409 WO1997006233A1 (en) | 1995-08-10 | 1996-07-08 | Pigmented rheopectic cleaning compositions with thixotropic properties |
Publications (2)
Publication Number | Publication Date |
---|---|
MXPA98001081A true MXPA98001081A (en) | 1998-04-01 |
MX9801081A MX9801081A (en) | 1998-04-30 |
Family
ID=26307551
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
MX9801081A MX9801081A (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 |
EP3645691A1 (en) * | 2017-06-08 | 2020-05-06 | The Procter and Gamble Company | Non-homogeneous compositions |
Family Cites Families (8)
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 |
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 |
JP2594404B2 (en) * | 1992-12-22 | 1997-03-26 | 花王株式会社 | Liquid bleach composition |
ES2160152T3 (en) * | 1993-12-29 | 2001-11-01 | Reckitt Benckiser Inc | ALKALINE METAL HIPOCLORITE HIPOCLORITE COMPOSITIONS. |
-
1996
- 1996-07-08 CA CA002228674A patent/CA2228674C/en not_active Expired - Fee Related
- 1996-07-08 BR BR9609898A patent/BR9609898A/en not_active Application Discontinuation
- 1996-07-08 WO PCT/US1996/011409 patent/WO1997006233A1/en not_active Application Discontinuation
- 1996-07-08 NZ NZ313386A patent/NZ313386A/en unknown
- 1996-07-08 MX MX9801081A patent/MX9801081A/en not_active IP Right Cessation
- 1996-07-08 AU AU65431/96A patent/AU692718B2/en not_active Ceased
- 1996-07-08 CN CN96196185A patent/CN1102649C/en not_active Expired - Fee Related
- 1996-07-08 EP EP96925280A patent/EP0859826A4/en not_active Withdrawn
- 1996-08-09 IN IN1429CA1996 patent/IN189237B/en unknown
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