AU2006350750A1 - Foaming hard surface cleaner - Google Patents
Foaming hard surface cleaner Download PDFInfo
- Publication number
- AU2006350750A1 AU2006350750A1 AU2006350750A AU2006350750A AU2006350750A1 AU 2006350750 A1 AU2006350750 A1 AU 2006350750A1 AU 2006350750 A AU2006350750 A AU 2006350750A AU 2006350750 A AU2006350750 A AU 2006350750A AU 2006350750 A1 AU2006350750 A1 AU 2006350750A1
- Authority
- AU
- Australia
- Prior art keywords
- composition
- foamable composition
- horizontal line
- foamable
- run down
- 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
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
- 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
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/02—Anionic compounds
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/14—Sulfonic acids or sulfuric acid esters; Salts thereof derived from aliphatic hydrocarbons or mono-alcohols
- C11D1/146—Sulfuric acid esters
-
- 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
- C11D1/12—Sulfonic acids or sulfuric acid esters; Salts thereof
- C11D1/29—Sulfates of polyoxyalkylene ethers
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
- C11D17/04—Detergent materials or soaps characterised by their shape or physical properties combined with or containing other objects
- C11D17/041—Compositions releasably affixed on a substrate or incorporated into a dispensing means
-
- 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
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/0094—High foaming 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
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2003—Alcohols; Phenols
- C11D3/2006—Monohydric alcohols
- C11D3/201—Monohydric alcohols linear
-
- 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
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2068—Ethers
-
- 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)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Detergent Compositions (AREA)
Description
WO 2008/060303 PCT/US2006/061047 TITLE OF THE INVENTION FOAMING HARD SURFACE CLEANER BACKGROUND OF THE INVENTION [00011 Hard surface cleaners are usually mostly water that include cleaning materials, fragrance, and color. Hard Surface cleaners are usually sprayed onto a surface and then wiped to clean the surface. Because hard surface cleaners are mostly water, they will drip when applied to vertical surfaces because of gravity. [0002] This requires a person to quickly wipe the surface before the hard surface cleaner drips down the surface to be cleaned. The dripping of the hard surface cleaner does not allow for a longer residence time of the hard surface cleaner on the surface to effect more cleaning. It would be desirable to have a hard surface cleaner that could remain in place when applied to a surface. BRIEF SUMMARY OF INVENTION [00031 A foamable composition comprising: a) at least one anionic surfactant chosen from a salt of an alkyl sulfate and a salt of an alkyl ether sulfate in an amount of about 0.01 to about 1% by weight of the composition; b) at least one glycol ether in an amount of about 0.1 to about 1.5% by weight of the composition; c) at least one alcohol in an amount of about 2 to about 6% by weight of the composition; and d) water. [00041 A foamable composition comprising: a) at least one anionic surfactant chosen from a salt of an alkyl sulfate and a salt of an alkyl ether sulfate; b) at least one glycol ether; and c) at least one alcohol; and d) water, WO 2008/060303 PCT/US2006/061047 wherein the composition has a run down time of greater than about 15 seconds, wherein the run down time is measured by providing a vertical glass surface, which is perpendicular to the earth's surface, with a first horizontal line that is 10 cm above a second horizontal line and both are parallel to the earth's surface, applying the composition to the vertical glass surface at the first horizontal line from a distance of 20 cm perpendicular to the surface, and measuring the time for the composition to run down from the first horizontal line to the second horizontal line. DETAILED DESCRIPTION OF INVENTION [00051 As used throughout, ranges are used as a shorthand for describing each and every value that is within the range. Any value within the range can be selected as the terminus of the range. [00061 All references to amounts in this specification are by active weight of the material in the total composition. The active weight of a material is the actual amount of the material not including other materials, such as water, in the form in which it is supplied. [0007] As used throughout, the counter ion for the salt of a surfactant can be a metal ion, an ammonium ion, or an amine. Metal cations that can be used include, but are not limited to, alkali metal ions and alkaline earth ions. In some embodiments, the metal cation ion can be lithium, sodium, potassium, magnesium, or calcium. In some embodiments, the amine is triethanolamine. [00081 The foaming composition includes at least one anionic surfactant chosen from a salt of an alkyl sulfate surfactant and a salt of an alkyl ether sulfate surfactant. In one embodiment, the surfactant is present in the composition in an amount of about 0.1 to about 1% by weight. [00091 In one embodiment, the surfactant comprises a triethanolamine alkyl sulfate. In one embodiment, the alkyl is a C10 to C14 alkyl. In another embodiment the surfactant comprises a triethanolamine lauryl sulfate. In one embodiment, the triethanolamine alkyl sulfate is present-in an amount of about 0.1 to about 0.3% by 2 WO 2008/060303 PCT/US2006/061047 weight, and in another embodiment in an amount of about 0.18 to about 0.22% by weight. [00101 In another embodiment, the surfactant comprises the salt of an alkyl ether sulfate. In one embodiment, the alkyl is a C1O to C14. In one embodiment the surfactant is a sodium lauryl ether sulfate. In one embodiment, there is an average of about 1 to about 10 moles of ethylene oxide per mole. In another embodiment, there is an average of about 2 to about 3 moles of ethylene oxide per mole. In one embodiment, the sodium lauryl ether sulfate is present in an amount of about 0.05 to about 0.2% by weight, and in another embodiment at 0.06 to about 0.08% by weight. [00111 In addition to the anionic surfactant, the foaming composition can include an amine oxide surfactant. Amine oxide semi-polar nonionic surfactants can comprise compounds and mixtures of compounds having the formula: R2 Ri(C 2
H
4 0)n NvO R3 wherein RI is an alkyl, 2-hydroxyalkyl, 3-hydroxyalkyl, or 3-alkoxy-2-hydroxypropyl radical in which the alkyl and alkoxy, respectively, contain from 8 to 18 carbon atoms, R2 and R 3 are each methyl, ethyl, propyl, isopropyl, 2-hydroxyethyl, 2-hydroxypropyl, or 3-hydroxypropyl, and n is from 0 to 10. Particularly preferred are amine oxides of the formula: R, I ~
R
1 -N 3m-O R 3 wherein R 1 is a C 12
-
16 alkyl and R 2 and R 3 are methyl or ethyl. Examples of the above ethylene oxide condensates, amides, and amine oxides are described in U.S. Pat. No. 4,316,824. In one embodiment the amine oxides comprise alkyl amine oxides and/or cocoamidopropyl amine oxide. In one embodiment, the ratio of anionic surfactant to amine oxide surfactant is about 3:1 to about 4:1. 3 WO 2008/060303 PCT/US2006/061047 [00121 The composition additionally includes at least one glycol ether. In one embodiment, the amount of glycol ether is about 0.1 to about 1.5% by weight. Examples of glycol ethers include, but are not limited to, propylene glycol n-butyl ether, propylene glycol n-propyl ether, ethylene glycol n-hexal ether, ethylene glycol n-butyl ether, dipropylene glycol methyl ether, and combinations thereof. In one embodiment, the composition includes propylene glycol n-butyl ether in an amount up to about 1.5% by weight, and in another embodiment at about 1.25% by weight. [00131 The foaming composition includes at least one alcohol. Any alcohol can be used in the composition. In one embodiment, the alcohol comprises a C 1
-C
6 alkyl alcohol. In one embodiment, the alcohol is chosen from methanol, ethanol, n-propanol, isopropanol, n-butyl alcohol, sec-butyl alcohol, isobutyl alcohol, tert-butyl alcohol, 1- 2 or 3- pentanol, neopentyl alcohol, and/or hexanol. In certain embodiments, the alcohol is present in the composition in an amount of about 2 to about 6% by weight, about 3 to about 5% by weight, about 3 to about 4.5% by weight, or in another embodiment, the amount is about 4% by weight. [00141 In one embodiment, the at least one alcohol comprises ethanol. In another embodiment, ethanol is present in the composition in an amount of about 2 to about 6% by weight, about 3 to about 5% by weight, about 3 to about 4.5% by weight, or in another embodiment, the amount is about 4% by weight. In another embodiment, the alcohol comprises ethanol and isopropanol. In another embodiment, isopropanol is present in an amount of 0 to about 1.5% by weight, and in another embodiment the isopropanol is present at about 1% by weight. [00151 The composition can optionally include at least one dispersant. The dispersant can be present in any amount that provides a dispersant effect. In one embodiment, the dispersant is present in an amount of about 0.01 to about 1 % by weight. In one embodiment, the dispersant is a maleic acid/olefin copolymer. In one embodiment, a dispersant of this type is a maleic acid/ diisobutylene copolymer available from Rohm and Haas under the trade name ACUSOLTm 460NK. 4 WO 2008/060303 PCT/US2006/061047 [00161 The composition can additionally include any fragrance or perfume. In one embodiment, the perfume is present in an amount of about 0.03 to about 0.08% by weight. The composition can additionally include any dye or coloring agent. Additionally the composition can contain any pH agent, a biocide/ antibacterial agent, or any other material for a desired effect. Also, ammonium hydroxide and/or vinegar can be included, and in one embodiment they can be included up to about 0.2% by weight. In one embodiment, citric acid can be used to adjust the pH of the composition. [0017] Water can be included in the composition in any amount to make the sum of the amount of materials in the composition total 100 weight percent. [00181 The composition when applied as a foam to a vertical glass surface will have a run down time of greater than about 15 seconds. In other embodiments, the run down time is greater than about 18 seconds, greater than about 20 seconds, greater than about 23 seconds, or about 15 to about 30 seconds. Run down time is measured by applying the foamed composition to a vertical glass surface, which is perpendicular to the earth's surface, at a first horizontal line marked on the surface from a distance of 20 cm perpendicular to the surface using a foaming dispenser. A second horizontal line is marked 10 cm below the first horizontal line on the glass surface. Run down time is the time that it takes the composition to run down from the first line to the second line. Both the first and second horizontal lines are parallel to the earth's surface. [0019] In one embodiment, the foam is generated by a foaming dispenser that mixes air with the composition when it is dispensed. In this embodiment, the composition does not contain any propellants that would eject the composition from the container or cause the composition to foam. Any foaming dispenser can be used with the composition. In one embodiment, the dispenser is available from MeadWestvaco Calmar GmbH under the product name TS 800 Top Gun Trigger Sprayer. [00201 The composition can be used as a cleaner on all surfaces. In one embodiment, the surface is a horizontal surface, which is parallel to the earth's surface. In one embodiment, the surface is a non-horizontal surfaces, such as those that are angled at greater than 0 to 900 to the earth's surface. In another embodiment, the 5 WO 2008/060303 PCT/US2006/061047 composition can be used as a cleaner on a vertical surface, which is perpendicular to the earth's surface. In one embodiment, the composition is a glass cleaner. [00211 The composition can be used in a method for removing soil from a surface comprising applying the composition to the surface and removing the composition. Removing includes, but is not limited to, wiping, squeegeeing, rinsing, and mopping. The surface can be, horizontal, non-horizontal, or vertical. [0022] The invention is further described in the following examples. The examples are merely illustrative and do not in any way limit the scope of the invention as described and claimed. EXAMPLE 1 [0023] The following table illustrates a prophetic example that can be made by mixing the ingredients. Material % by weight Triethanolamine lauryl sulfate 0.18-0.22 Propylene glycol n-butyl ether 0.1-1.5 Ethanol 3-4.5 Minors 0.1-0.3 Demineralized water Q.S. EXAMPLE 2 [00241 The following table illustrates a prophetic example that can be made by mixing the ingredients. Material % by weight Triethanolamine lauryl sulfate 0.18-0.22 Propylene glycol n-butyl ether 0.1-1.5 Ethanol 3-4.5 ACUSOL 460 NK 0.4 Minors 0.1-0.3 Demineralized water Q.S. 6- WO 2008/060303 PCT/US2006/061047 EXAMPLE 3 [00251 The following composition according to the invention was prepared by mixing the ingredients. The composition was added to a container with a foaming dispenser. Material % by weight Triethanolamine lauryl sulfate 0.2 Propylene glycol n-butyl ether 1.25 Ethanol 4 26 0 BE Ammonium Hydroxide 0.44 Demineralized water Q.S. [00261 The composition was compared against AJAXTM Triple Action Glass Cleaner, which is commercially available in Europe in a conventional glass cleaner spray bottle, in the run down test described above. A positioning device was used to position each container so that they sprayed at the same point on the vertical glass surface. Several runs were conducted, and the results are shown in the table below. Time is in seconds. Inventive Comparative 23 6 29 7 25 7 29 10 23 9 23 6 23 6 19 8 20 9 22 7 Average 23.6 7.5 [00271 It can be seen from the table that the foamable composition according to the invention was able to stay in place for a longer time as compared to a conventional glass cleaner. 7
Claims (24)
1. A foamable composition comprising: a) at least one anionic surfactant chosen from a salt of an alkyl sulfate and a salt of an alkyl ether sulfate in an amount of about 0.01 to about 1% by weight of the composition; b) at least one glycol ether in an amount of about 0.1 to about 1.5% by weight of the composition; c) at least one alcohol in an amount of about 2 to about 6% by weight of the composition; and d) water.
2. The foamable composition of claim 1, wherein the anionic surfactant comprises a triethanolamine alkyl sulfate.
3. The foamable composition of claim 1, wherein the anionic surfactant is triethanolamine lauryl sulfate.
4. -The foamable composition of claim 1, wherein the anionic surfactant is the salt of an alkyl ether sulfate.
5. The foamable composition of claim 1, wherein the anionic surfactant is sodium lauryl ether sulfate.
6. The foamable composition of claim 1, wherein the glycol ether is propylene glycol n-butyl ether.
7. The foamable composition of claim 1, wherein the alcohol comprises a ClC6 alkyl alcohol.
8. The foamable composition of claim 1, wherein the alcohol is ethanol.
9. The foamable composition of claim 1, wherein the alcohol comprises ethanol and isopropanol. 8 WO 2008/060303 PCT/US2006/061047
10. The foamable composition of claim 1 further comprising an amine oxide surfactant.
11. The foamable composition of claim 10, wherein the amine oxide is present in the foamable composition in a ratio of anionic surfactant to amine oxide surfactant is about 3:1 to about 4:1.
12. The foamable composition of claim 1 further comprising a dispersant.
13. The foamable composition of claim 12, wherein the dispersant comprises a copolymer of maleic acid and an olefin.
14. The foamable composition of claim 1, wherein the anionic surfactant comprises triethanolamine lauryl sulfate, the glycol ether comprises propylene glycol n butyl ether, and the alcohol comprises ethanol.
15. The foamable composition of claim 1 further comprising a material chosen from a pH agent, a fragrance, a perfume, a coloring agent, a dye, a biocide/ antibacterial agent, ammonium hydroxide, and vinegar.
16. The foamable composition of claim 1, wherein the composition has a run down time of greater than about 15 seconds, wherein the run down time is measured by providing a vertical glass surface with a first horizontal line that is 10 cm above a second horizontal line, applying the composition to the vertical glass surface at the first horizontal line from a distance of 20 cm perpendicular to the surface, and measuring the time for the composition to run down from the first horizontal line to the second horizontal line.
17. The foamable composition of claim 16, wherein the run down time is greater than about 20 seconds.
18. An article comprising a container with a dispenser that foams a composition that is dispensed through the dispenser and the foamable composition of claim 1 disposed in the container. 9 WO 2008/060303 PCT/US2006/061047
19. A foamable composition comprising: a) at least one anionic surfactant chosen from a salt of an alkyl sulfate and a salt of an alkyl ether sulfate; b) at least one glycol ether; c) at least one alcohol; and d) water, wherein the composition has a run down time of greater than about 15 seconds, wherein the run down time is measured by providing a vertical glass surface, which is perpendicular to the earth's surface, with a first horizontal line that is 10 cm above a second horizontal line and both are parallel to the earth's surface, applying the composition to the vertical glass surface at the first horizontal line from a distance of 20 cm perpendicular to the surface, and measuring the time for the composition to run down from the first horizontal line to the second horizontal line.
20. The foamable composition of claim 19, wherein the run down time is greater than about 20 seconds.
21. A method for removing soil from a surface comprising applying the composition of claim 1 to the surface and removing the composition.
22. The method of claim 21, wherein the surface is a vertical surface.
23. A method for removing soil from a surface comprising applying the composition of claim 19 to the surface and removing the composition.
24. The method of claim 23, wherein the surface is a vertical surface. 10
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/US2006/061047 WO2008060303A1 (en) | 2006-11-17 | 2006-11-17 | Foaming hard surface cleaner |
Publications (2)
Publication Number | Publication Date |
---|---|
AU2006350750A1 true AU2006350750A1 (en) | 2008-05-22 |
AU2006350750B2 AU2006350750B2 (en) | 2011-05-12 |
Family
ID=38255536
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2006350750A Ceased AU2006350750B2 (en) | 2006-11-17 | 2006-11-17 | Foaming hard surface cleaner |
Country Status (14)
Country | Link |
---|---|
EP (1) | EP2097501B1 (en) |
CN (1) | CN101563442B (en) |
AU (1) | AU2006350750B2 (en) |
CA (1) | CA2669329C (en) |
CR (1) | CR10800A (en) |
DK (1) | DK2097501T3 (en) |
EC (1) | ECSP099329A (en) |
ES (1) | ES2388617T3 (en) |
MX (1) | MX2009005155A (en) |
NO (1) | NO20092326L (en) |
NZ (1) | NZ576960A (en) |
PL (1) | PL2097501T3 (en) |
PT (1) | PT2097501E (en) |
WO (1) | WO2008060303A1 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2683235B1 (en) * | 2011-03-08 | 2014-12-31 | Sca Hygiene Products AB | Low alcohol antimicrobial cleansing composition |
WO2019115297A1 (en) * | 2017-12-12 | 2019-06-20 | Unilever N.V. | Foamable cleaning composition |
CN111718804A (en) * | 2020-07-24 | 2020-09-29 | 上海绿瑞生物科技有限公司 | Foam type cleaning agent composition and application thereof |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3463735A (en) * | 1967-10-18 | 1969-08-26 | Drackett Co | Glass cleaning composition |
US4606842A (en) * | 1982-03-05 | 1986-08-19 | Drackett Company | Cleaning composition for glass and similar hard surfaces |
ZA925727B (en) * | 1991-08-09 | 1993-03-10 | Bristol Myers Squibb Co | Glass cleaning composition. |
AU8457898A (en) * | 1997-08-13 | 1999-03-08 | Procter & Gamble Company, The | Glass cleaner compositions having good surface lubricity and alkaline buffer |
GB2339789A (en) * | 1998-07-16 | 2000-02-09 | Reckitt & Colman Inc | Aqueous cleaning and surface treatment compositions |
US7666826B2 (en) * | 2002-11-27 | 2010-02-23 | Ecolab Inc. | Foam dispenser for use in foaming cleaning composition |
US20050026796A1 (en) * | 2003-07-30 | 2005-02-03 | Colgate-Palmolive Company | Foam glass cleaning composition |
DE102005044513A1 (en) * | 2005-09-16 | 2007-03-22 | Henkel Kgaa | Cleaning agent for hard surfaces |
-
2006
- 2006-11-17 PT PT06839936T patent/PT2097501E/en unknown
- 2006-11-17 WO PCT/US2006/061047 patent/WO2008060303A1/en active Application Filing
- 2006-11-17 ES ES06839936T patent/ES2388617T3/en active Active
- 2006-11-17 CN CN2006800563931A patent/CN101563442B/en not_active Expired - Fee Related
- 2006-11-17 PL PL06839936T patent/PL2097501T3/en unknown
- 2006-11-17 NZ NZ576960A patent/NZ576960A/en not_active IP Right Cessation
- 2006-11-17 CA CA2669329A patent/CA2669329C/en not_active Expired - Fee Related
- 2006-11-17 DK DK06839936.9T patent/DK2097501T3/en active
- 2006-11-17 AU AU2006350750A patent/AU2006350750B2/en not_active Ceased
- 2006-11-17 EP EP06839936A patent/EP2097501B1/en not_active Not-in-force
- 2006-11-17 MX MX2009005155A patent/MX2009005155A/en active IP Right Grant
-
2009
- 2009-05-14 EC EC2009009329A patent/ECSP099329A/en unknown
- 2009-05-15 CR CR10800A patent/CR10800A/en unknown
- 2009-06-16 NO NO20092326A patent/NO20092326L/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
ES2388617T3 (en) | 2012-10-17 |
EP2097501A1 (en) | 2009-09-09 |
CA2669329C (en) | 2013-10-01 |
CN101563442B (en) | 2013-06-19 |
PT2097501E (en) | 2012-09-10 |
MX2009005155A (en) | 2009-05-25 |
EP2097501B1 (en) | 2012-06-06 |
WO2008060303A1 (en) | 2008-05-22 |
CR10800A (en) | 2009-09-03 |
NZ576960A (en) | 2011-11-25 |
PL2097501T3 (en) | 2012-10-31 |
AU2006350750B2 (en) | 2011-05-12 |
CA2669329A1 (en) | 2008-05-22 |
CN101563442A (en) | 2009-10-21 |
DK2097501T3 (en) | 2012-09-17 |
NO20092326L (en) | 2009-08-04 |
ECSP099329A (en) | 2009-06-30 |
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MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |