EP2702130A1 - Hard surface treatment composition - Google Patents
Hard surface treatment compositionInfo
- Publication number
- EP2702130A1 EP2702130A1 EP12713139.9A EP12713139A EP2702130A1 EP 2702130 A1 EP2702130 A1 EP 2702130A1 EP 12713139 A EP12713139 A EP 12713139A EP 2702130 A1 EP2702130 A1 EP 2702130A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- solution
- pac
- composition
- minutes
- transmittance
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 53
- 238000004381 surface treatment Methods 0.000 title claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 42
- 239000000758 substrate Substances 0.000 claims abstract description 38
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims abstract description 16
- 229920000642 polymer Polymers 0.000 claims abstract description 16
- 238000000034 method Methods 0.000 claims abstract description 7
- 239000002253 acid Substances 0.000 claims abstract description 4
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 93
- 229920002125 SokalanĀ® Polymers 0.000 claims description 50
- 239000004584 polyacrylic acid Substances 0.000 claims description 29
- 239000007788 liquid Substances 0.000 claims description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
- 239000007921 spray Substances 0.000 claims description 11
- 239000002904 solvent Substances 0.000 claims description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical group OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- 150000007524 organic acids Chemical class 0.000 claims description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 4
- 238000004140 cleaning Methods 0.000 claims description 4
- 239000004744 fabric Substances 0.000 claims description 2
- 230000008021 deposition Effects 0.000 abstract description 5
- 230000000694 effects Effects 0.000 abstract description 5
- 238000009877 rendering Methods 0.000 abstract description 4
- 238000009833 condensation Methods 0.000 abstract description 3
- 229920005646 polycarboxylate Polymers 0.000 abstract description 3
- 239000000243 solution Substances 0.000 description 93
- 239000011521 glass Substances 0.000 description 70
- 238000002834 transmittance Methods 0.000 description 37
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 36
- 229960004106 citric acid Drugs 0.000 description 30
- 239000011550 stock solution Substances 0.000 description 29
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonium chloride Substances [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 19
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical compound [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 19
- 235000011114 ammonium hydroxide Nutrition 0.000 description 19
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 16
- 229910000069 nitrogen hydride Inorganic materials 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 6
- -1 aluminium hydroxychloride Chemical compound 0.000 description 5
- KQTIIICEAUMSDG-UHFFFAOYSA-N tricarballylic acid Chemical compound OC(=O)CC(C(O)=O)CC(O)=O KQTIIICEAUMSDG-UHFFFAOYSA-N 0.000 description 5
- 230000008901 benefit Effects 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 229920000058 polyacrylate Polymers 0.000 description 4
- 229910052782 aluminium Inorganic materials 0.000 description 3
- 239000004411 aluminium Substances 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- JGDITNMASUZKPW-UHFFFAOYSA-K aluminium trichloride hexahydrate Chemical compound O.O.O.O.O.O.Cl[Al](Cl)Cl JGDITNMASUZKPW-UHFFFAOYSA-K 0.000 description 3
- 229940009861 aluminum chloride hexahydrate Drugs 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 2
- QMKYBPDZANOJGF-UHFFFAOYSA-N benzene-1,3,5-tricarboxylic acid Chemical compound OC(=O)C1=CC(C(O)=O)=CC(C(O)=O)=C1 QMKYBPDZANOJGF-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- 239000001124 (E)-prop-1-ene-1,2,3-tricarboxylic acid Substances 0.000 description 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
- 101100365548 Caenorhabditis elegans set-14 gene Proteins 0.000 description 1
- 101100477392 Caenorhabditis elegans set-17 gene Proteins 0.000 description 1
- 101100042371 Caenorhabditis elegans set-3 gene Proteins 0.000 description 1
- 101100421296 Caenorhabditis elegans set-6 gene Proteins 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- YASYEJJMZJALEJ-UHFFFAOYSA-N Citric acid monohydrate Chemical compound O.OC(=O)CC(O)(C(O)=O)CC(O)=O YASYEJJMZJALEJ-UHFFFAOYSA-N 0.000 description 1
- ODBLHEXUDAPZAU-ZAFYKAAXSA-N D-threo-isocitric acid Chemical compound OC(=O)[C@H](O)[C@@H](C(O)=O)CC(O)=O ODBLHEXUDAPZAU-ZAFYKAAXSA-N 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 102100029768 Histone-lysine N-methyltransferase SETD1A Human genes 0.000 description 1
- 102100027704 Histone-lysine N-methyltransferase SETD7 Human genes 0.000 description 1
- 101000865038 Homo sapiens Histone-lysine N-methyltransferase SETD1A Proteins 0.000 description 1
- 101000650682 Homo sapiens Histone-lysine N-methyltransferase SETD7 Proteins 0.000 description 1
- ODBLHEXUDAPZAU-FONMRSAGSA-N Isocitric acid Natural products OC(=O)[C@@H](O)[C@H](C(O)=O)CC(O)=O ODBLHEXUDAPZAU-FONMRSAGSA-N 0.000 description 1
- 101100533306 Mus musculus Setx gene Proteins 0.000 description 1
- 229930182556 Polyacetal Natural products 0.000 description 1
- 101150104646 SET4 gene Proteins 0.000 description 1
- 101150117538 Set2 gene Proteins 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 229940091181 aconitic acid Drugs 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- GTZCVFVGUGFEME-IWQZZHSRSA-N cis-aconitic acid Chemical compound OC(=O)C\C(C(O)=O)=C\C(O)=O GTZCVFVGUGFEME-IWQZZHSRSA-N 0.000 description 1
- 229960002303 citric acid monohydrate Drugs 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000005661 hydrophobic surface Effects 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000003446 ligand Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000012046 mixed solvent Substances 0.000 description 1
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 235000009048 phenolic acids Nutrition 0.000 description 1
- 150000007965 phenolic acids Chemical class 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920000867 polyelectrolyte Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- 229920006324 polyoxymethylene Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- ODBLHEXUDAPZAU-UHFFFAOYSA-N threo-D-isocitric acid Natural products OC(=O)C(O)C(C(O)=O)CC(O)=O ODBLHEXUDAPZAU-UHFFFAOYSA-N 0.000 description 1
- GTZCVFVGUGFEME-UHFFFAOYSA-N trans-aconitic acid Natural products OC(=O)CC(C(O)=O)=CC(O)=O GTZCVFVGUGFEME-UHFFFAOYSA-N 0.000 description 1
- 150000003628 tricarboxylic acids Chemical class 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
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3746—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/3757—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions
- C11D3/3765—(Co)polymerised carboxylic acids, -anhydrides, -esters in solid and liquid compositions 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/02—Inorganic compounds
- C11D7/04—Water-soluble compounds
- C11D7/06—Hydroxides
-
- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/02—Inorganic compounds
- C11D7/04—Water-soluble compounds
- C11D7/10—Salts
-
- 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/26—Organic compounds containing oxygen
- C11D7/265—Carboxylic acids or salts 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
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/50—Solvents
- C11D7/5004—Organic solvents
Definitions
- the present invention relates to a composition and a method for treating substrates, in particular hard surfaces, to make the substrate hydrophilic; and for imparting anti- fogging / anti-condensation properties onto said surface.
- US2008/0274930 discloses ware washing compositions comprising surfactant, an alkalinity source, and corrosion inhibitor; and mentions the use of aluminium III salts, and polymers. Similarly tooth treatment compositions are known.
- US5844019 discloses a tooth cleaning composition comprising carboxylic acid, quaternary ammonium salts and aluminium III salts.
- the object of the present invention is to provide a composition for rendering a surface less susceptible for vapour deposition. It is another object to provide for a composition for rendering a surface hydrophilic.
- composition comprising poly aluminium chloride, a
- polycarboxylate polymer and a weak acid when applied to a surface, renders said surface super hydrophilic, thus causing the repellence of small water droplets to provide and anti-fogging effect.
- the present invention provides a surface treatment composition
- a surface treatment composition comprising 0.05 - 5% of poly aluminium chloride, 0.05 - 5% of a carboxylic polymer, 0.01 - 5% of a weak organic acid, and aqueous liquid; wherein the pH of the composition is between 7 and 9.5; and wherein the PAC : carboxylic polymer is at least 2:5.
- the invention provides a process for treating a substrate (e.g. fabrics, hard surfaces) comprising the steps of treating the substrate with a composition according to the invention, and leaving the substrate to dry.
- a substrate e.g. fabrics, hard surfaces
- the invention provides a bottled cleaning composition comprising the compositions according to the invention.
- glass surface is meant any surface having a vitreous or vitrified surface, including but not limited to glass and vitreous tiles.
- the invention relates to a composition for treating a surface comprising poly aluminium chloride, poly acrylic acid polymer, a weak organic acid and water; and wherein the pH of the composition is between 7 and 9.5, and wherein the PAC to polymer ratio is at least 2:5.
- Poly aluminium chloride is a known polyelectrolyte.
- the aluminium content is typically 12-20%.
- PAC may have small amount of impurities including traces of S0 4 2" , C0 3 2"; N0 3 ā , Br ā , HC0 3 ā , and HS0 4 " ; but such impurities are typically present in a concentration of less than 2%, more preferably less than 1 %, still more preferably less than 0.5% or even less than 0.1 % by weight of the PAC.
- the PAC is present in the composition in a concentration of between 0.05 - 5% by weight, preferably not more than 4%, more preferably not more than 3%, still more preferably not more than 2.5%, or even less than 2%.
- Carboxylic polymer preferably not more than 4%, more preferably not more than 3%, still more preferably not more than 2.5%, or even less than 2%.
- Preferred carboxylic polymers are polyacrylates, polymaleates, polyacetates, polyhydroxyacrylates, polyacrylate/polymaleate and polyacrylate/ polymethacrylate copolymers, aminopolycarboxylates and polyacetal carboxylates.
- Poly(acrylic acid) or PAA is the most preferred polymer.
- the monomer of poly(acrylic acid) is acrylic acid. In a water solution at neutral pH, many of the side chains of PAA will lose their protons and acquire a negative charge.
- PAA is thus understood to be a polymer of repeating units of -[CH2-CH(COOH)] n -.
- the polymer is present in the composition in a concentration of between 0.05 - 5% by weight, preferably not more than 4%, more preferably not more than 3%, still more preferably not more than 2.5%, or even less than 2%.
- the PAC : polymer ratio is at least 2:5. Preferably between 2:5 and 20:1 , more preferably between 1 :1 and 10: 1.
- Preferred organic acids are organic acids selected from, such as di- and tri-carboxylic acids containing ā -hydroxyl groups, and phenolic acids with ortho-hydroxyls should be considered.
- Tricarboxylic chelating ligands include but are not limited to citric acid are isocitric acid, aconitic acid, propane-1 ,2,3-tricarboxylic acid (tricarballylic acid, carballylic acid), trimesic acid. Other examples include gluconic, tartaric, EDTA or their derivatives. Citric acid is the most preferred.
- the acid is present in the composition in a concentration of between 0.01 - 5% by weight, preferably the concentration is at least 0.05%, but preferably not more than 4%, more preferably not more than 3%, still more preferably not more than 2.5%, or even less than 2%.
- Optional ingredients are present in the composition in a concentration of between 0.01 - 5% by weight, preferably the concentration is at least 0.05%, but preferably not more than 4%, more preferably not more than 3%, still more preferably not more than 2.5%, or even less than 2%.
- composition is preferably an aqueous liquid.
- aqueous liquid is a solvent and water mixture
- the solvents are preferably lower alcohols, more preferably methanol, ethanol and/or isopropanol. Although the presence of solvent is somewhat detrimental to the desired hydrophilicity, the benefit is that the surface dries faster.
- the solvent is typically present in the aqueous liquid in a concentration of between 1 and 20%, more preferably between 2 and 10%, more preferably between 3 and 8% by weight of the liquid.
- the invention provides a process for treating a substrate, comprising the steps in sequence of applying the composition according to the invention to a hard surface and leaving the surface to dry.
- the surface is preferably not rinsed between these steps.
- the surface may be wiped after application of the composition and then be left to dry.
- the surface is found to be more hydrophilic after treatment, and thereby less susceptible to deposition of fog or frost.
- composition may be packaged in the form of any commercially available liquid composition, typically in the form of a bottle containing the liquid.
- the composition is preferably applied using a trigger spray applicator.
- a trigger spray application enables fast and easy use for the consumer and additionally it brings a suitable amount of air into the composition, which aides in the foam formation.
- the compositions of the invention may be stored in and dispensed by any suitable means, but spray applicators are particularly preferred. Pump dispensers (whether spray or non-spray pumps) are also possible.
- the present invention provides a container for a liquid hard surface cleaner, the container comprising a reservoir containing the hard surface cleaning composition of the invention, and spray dispenser for dispensing the composition in the form of a spray.
- the spray dispenser is preferably a trigger spray but may be any mechanical means for ejecting the liquid in spray or aerosol form.
- Stock solutions were prepared by mixing 0.5 g/L polyacrylic acid 0.5 g/L PAC in water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 8.5 using ammonia solution or NaOH solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped till dry. Application to surfaces:
- the treated glass slides were kept in the freezer at -15 C for 10 minutes. The slides were then exposed to hot steam at 100 C for 5 seconds. The fog generated on the glass slides was then analyzed instantly by measuring the transmittance in the visible light in a spectrophotometer (PERKIN Elmer Lambda 900), between 400-700nm. Higher transmittance of a treated glass slide is a measure of less fog generation.
- a spectrophotometer PERKIN Elmer Lambda 900
- the treated glass slides were kept in the freezer at -15 C for 10 minutes. The slides were then exposed to room temperature (25 C) for 5 seconds. Then analyzed instantly by measuring the transmittance in the visible light in a spectrophotometer (PERKIN Elmer Lambda 900), between 400-700nm. Higher transmittance of a treated glass slide is a measure of less frost generation.
- Example 1 effect of variation in the ratio of the ingredients PAC and PAA
- Set1 Stock solutions were prepared by mixing 2.5 g/L polyacrylic acid 0.5 g/L PAC in water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 8.5 using ammonia solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped till dry.
- Set3 Stock solutions were prepared by mixing 0.5 g/L polyacrylic acid 0.5 g/L PAC in water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 8.5 using ammonia solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped till dry.
- Set4 Stock solutions were prepared by mixing 1 g/L polyacrylic acid 2.5 g/L PAC in water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 8.5 using ammonia solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped till dry.
- a blank (a) is included for comparison; the blank being a clean, untreated glass slide.
- the glass slides were kept in the freezer at -15 C for 10 minutes.
- the slides were then exposed to hot steam at 100 C for 5 seconds.
- the fog generated on the glass slides was then analyzed instantly by measuring the transmittance in the visible light in a spectrophotometer (PERKIN Elmer Lambda 900), between 400-700nm. Higher transmittance of a treated glass slide is a measure of less fog generation.
- PAA 450 K 77 77 77 1 PAC PAA 450 K (1 : 5) 72 73 73
- Set8 Stock solutions were prepared by mixing 0.5 g/L polyacrylic acid 0.5 g/L PAC in water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 8.5 using ammonia solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped dry.
- Set f Stock solutions were prepared by mixing 0.05 g/L polyacrylic acid 0.05 g/L PAC in water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 8.5 using ammonia solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped dry. A blank (d) is included for comparison; the blank being a clean, untreated glass slide.
- the glass slides were kept in the freezer at -15 C for 10 minutes. The slides were then exposed to hot steam at 100 C for 5 seconds. The fog generated on the glass slides was then analyzed instantly by measuring the transmittance in the visible light in a spectrophotometer (PERKIN Elmer Lambda 900), between 400-700nm. Higher transmittance of a treated glass slide is a measure of less fog generation.
- a spectrophotometer PERKIN Elmer Lambda 900
- the transmittance data in the table below show the transparency of the slide. The higher the transmittance, the better the transparency, the lower the transmittance, the more fogging.
- Set9 Stock solutions were prepared by mixing 0.5 g/L polyacrylic acid 0.5 g/L PAC in water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 8.5 using ammonia solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped till dry.
- Set10 Stock solutions were prepared by mixing 0.5 g/L polyacrylic acid 0.5 g/L PAC in 5% ethanol and 95% water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 8.5 using ammonia solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped till dry.
- Set11 Stock solutions were prepared by mixing 0.5 g/L polyacrylic acid 0.5 g/L PAC n 20% ethanol and 80% water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 8.5 using ammonia solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped till dry.
- a blank (g) is included for comparison; the blank being a clean, untreated glass slide.
- the glass slides were kept in the freezer at -15 C for 10 minutes.
- the slides were then exposed to hot steam at 100 C for 5 seconds.
- the fog generated on the glass slides was then analyzed instantly by measuring the transmittance in the visible light in a spectrophotometer (PERKIN Elmer Lambda 900), between 400-700nm. Higher transmittance of a treated glass slide is a measure of less fog generation.
- the transmittance data in the table below show the transparency of the slide. The higher the transmittance, the better the transparency, the lower the transmittance, the more fogging.
- compositions according to the invention are compared to compositions missing at least one of the required ingredients.
- Set12 Stock solutions were prepared by mixing 0.5 g/L polyacrylic acid 0.5 g/L PAC in water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 8.5 using ammonia solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped till dry.
- Set13 Stock solutions were prepared by mixing 0.5 g/L polyacrylic acid 0.5 g/L PAC in 5% ethanol and 95% water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 8.5 using NaOH solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped till dry.
- Set H-O Control sets with the absence of one of the ingredients or experimental conditions
- the treated glass slides were kept in the freezer at -15 C for 10 minutes. The slides were then exposed to hot steam at 100 C for 5 seconds. The fog generated on the glass slides was then analyzed instantly by measuring the transmittance in the visible light in a spectrophotometer (PERKIN Elmer Lambda 900), between 400-700nm. Higher transmittance of a treated glass slide is a measure of less fog generation.
- a spectrophotometer PERKIN Elmer Lambda 900
- compositions are summarised in the table below.
- the transmittance is higher when ammonia is used compared to NaOH, thought to be caused by some absorbance of green light by the NaOH near the longer wavelengths.
- Set14 Stock solutions were prepared by mixing 0.5 g/L polyacrylic acid 0.5 g/L PAC in water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 6 using NaOH solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped till dry.
- Set15 Stock solutions were prepared by mixing 0.5 g/L polyacrylic acid 0.5 g/L PAC in water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 7 using NaOH solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped till dry.
- Sets P-S In sets Q to S, stock solutions were prepared by mixing 0.5 g/L polyacrylic acid 0.5 g/L PAC in water. To it 0.5 g/L citric acid solution was added. The solution pH was made acidic to 2,4,5 using HCI solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped till dry. Set P is untreated.
- the treated glass slides were kept in the freezer at -15 C for 10 minutes. The slides were then exposed to hot steam at 100 C for 5 seconds. The fog generated on the glass slides was then analyzed instantly by measuring the transmittance in the visible light in a spectrophotometer (PERKIN Elmer Lambda 900), between 400-700nm.
- a spectrophotometer PERKIN Elmer Lambda 900
- Set17 Stock solutions were prepared by mixing 0.5 g/L polyacrylic acid 0.5 g/L PAC in water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 8.5 using ammonia solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped till dry.
- the glass slides were kept in the freezer at -15 C for 10 minutes. The slides were then exposed to room temperature (25 C) for 5 seconds. Then analyzed instantly by measuring the transmittance in the visible light in a spectrophotometer (PERKIN Elmer Lambda 900), between 400-700nm. Higher transmittance of a treated glass slide is a measure of less frost generation.
- T is a blank included for comparison; the blank being a clean, untreated glass slide wavelength (nm)
- SetV Stock solutions were prepared by mixing 0.5 g/L polyacrylic acid 0.5 g/L aluminum chloride hexahydrate in water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 8.5 using ammonia solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped till dry.
- SetX Stock solutions were prepared by mixing 0.5 g/L polyacrylic acid 0.5 g/L aluminum chloride hexahydrate in water. To it 0.5 g/L citric acid solution was added. The solution pH was made alkaline to 8.5 using NaOH solution. 0.5 ml of the solution was applied on the glass substrate, left for 2 minutes and then wiped till dry. U and W are blank included for comparison; the blank being a clean, untreated glass slide.
- the treated glass slides were kept in the freezer at -15 C for 10 minutes. The slides were then exposed to hot steam at 100 C for 5 seconds. The fog generated on the glass slides was then analyzed instantly by measuring the transmittance in the visible light in a spectrophotometer (PERKIN Elmer Lambda 900), between 400-700nm.
- a spectrophotometer PERKIN Elmer Lambda 900
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Inorganic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- Detergent Compositions (AREA)
- Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Paints Or Removers (AREA)
Abstract
Description
Claims
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PL12713139T PL2702130T3 (en) | 2011-04-25 | 2012-04-04 | Hard surface treatment composition |
| EP12713139.9A EP2702130B1 (en) | 2011-04-25 | 2012-04-04 | Hard surface treatment composition |
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN1294MU2011 | 2011-04-25 | ||
| EP11170341 | 2011-06-17 | ||
| PCT/EP2012/056182 WO2012146473A1 (en) | 2011-04-25 | 2012-04-04 | Hard surface treatment composition |
| EP12713139.9A EP2702130B1 (en) | 2011-04-25 | 2012-04-04 | Hard surface treatment composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP2702130A1 true EP2702130A1 (en) | 2014-03-05 |
| EP2702130B1 EP2702130B1 (en) | 2015-01-21 |
Family
ID=45937363
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP12713139.9A Not-in-force EP2702130B1 (en) | 2011-04-25 | 2012-04-04 | Hard surface treatment composition |
Country Status (9)
| Country | Link |
|---|---|
| EP (1) | EP2702130B1 (en) |
| CN (1) | CN103502417B (en) |
| AR (1) | AR086478A1 (en) |
| BR (1) | BR112013026942A2 (en) |
| EA (1) | EA024377B1 (en) |
| ES (1) | ES2535378T3 (en) |
| PL (1) | PL2702130T3 (en) |
| WO (1) | WO2012146473A1 (en) |
| ZA (1) | ZA201307828B (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107917569B (en) * | 2017-11-21 | 2020-06-09 | å京空é“ęŗēµē ē©¶ę | Method for preventing dewing and water drop infiltration on surface of electric connector in refrigeration assembly |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3494739B2 (en) | 1995-02-13 | 2004-02-09 | ę Ŗå¼ä¼ē¤¾ćøć¼ć·ć¼ | Tooth surface treatment agent for dental glass ionomer cement |
| DE19948859A1 (en) * | 1999-10-08 | 2001-11-08 | Henkel Kgaa | Thixotropic aqueous detergent |
| US7048806B2 (en) * | 2003-12-16 | 2006-05-23 | The Clorox Company | Cleaning substrates having low soil redeposition |
| JP5563444B2 (en) | 2007-05-04 | 2014-07-30 | ćØć³ć©ć ć¤ć³ć³ć¼ćć¬ć¤ćć£ć | Method using water-soluble magnesium compound as cleaning agent |
| US8088723B2 (en) * | 2008-10-30 | 2012-01-03 | The Clorox Company | Polyaluminum compositions |
| BRPI0922236A2 (en) * | 2008-12-16 | 2019-10-01 | Unilever Nv | method, solid composition of a substrate treatment, and its use |
-
2012
- 2012-04-04 ES ES12713139.9T patent/ES2535378T3/en active Active
- 2012-04-04 BR BR112013026942A patent/BR112013026942A2/en not_active IP Right Cessation
- 2012-04-04 WO PCT/EP2012/056182 patent/WO2012146473A1/en not_active Ceased
- 2012-04-04 PL PL12713139T patent/PL2702130T3/en unknown
- 2012-04-04 CN CN201280019870.2A patent/CN103502417B/en not_active Expired - Fee Related
- 2012-04-04 EP EP12713139.9A patent/EP2702130B1/en not_active Not-in-force
- 2012-04-04 EA EA201301191A patent/EA024377B1/en not_active IP Right Cessation
- 2012-04-23 AR ARP120101386A patent/AR086478A1/en unknown
-
2013
- 2013-10-21 ZA ZA2013/07828A patent/ZA201307828B/en unknown
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2012146473A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CN103502417B (en) | 2015-10-21 |
| CN103502417A (en) | 2014-01-08 |
| PL2702130T3 (en) | 2015-06-30 |
| ES2535378T3 (en) | 2015-05-08 |
| EA201301191A1 (en) | 2014-03-31 |
| EA024377B1 (en) | 2016-09-30 |
| BR112013026942A2 (en) | 2017-01-10 |
| EP2702130B1 (en) | 2015-01-21 |
| ZA201307828B (en) | 2015-01-28 |
| AR086478A1 (en) | 2013-12-18 |
| WO2012146473A1 (en) | 2012-11-01 |
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