CA2022561C - Floor degreaser concentrate - Google Patents
Floor degreaser concentrateInfo
- Publication number
- CA2022561C CA2022561C CA 2022561 CA2022561A CA2022561C CA 2022561 C CA2022561 C CA 2022561C CA 2022561 CA2022561 CA 2022561 CA 2022561 A CA2022561 A CA 2022561A CA 2022561 C CA2022561 C CA 2022561C
- Authority
- CA
- Canada
- Prior art keywords
- acid
- cleaning
- concentrate
- compositions
- nonionic
- 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.)
- Expired - Lifetime
Links
- 239000012141 concentrate Substances 0.000 title claims abstract description 23
- 239000013527 degreasing agent Substances 0.000 title 1
- 239000000203 mixture Substances 0.000 claims abstract description 72
- 238000004140 cleaning Methods 0.000 claims abstract description 25
- 239000002736 nonionic surfactant Substances 0.000 claims abstract description 14
- 239000003945 anionic surfactant Substances 0.000 claims abstract description 12
- 239000004094 surface-active agent Substances 0.000 claims abstract description 10
- 150000007522 mineralic acids Chemical class 0.000 claims abstract description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 25
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 18
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 13
- -1 poly(alkyleneoxy) Polymers 0.000 claims description 12
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical class OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 10
- 150000007524 organic acids Chemical class 0.000 claims description 10
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- 150000002191 fatty alcohols Chemical class 0.000 claims description 4
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 3
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical group CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 claims description 2
- 239000002202 Polyethylene glycol Substances 0.000 claims description 2
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 claims description 2
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- 239000002253 acid Substances 0.000 description 20
- 125000000217 alkyl group Chemical group 0.000 description 8
- 229910052708 sodium Inorganic materials 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 5
- 125000000129 anionic group Chemical group 0.000 description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 238000010790 dilution Methods 0.000 description 4
- 239000012895 dilution Substances 0.000 description 4
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 4
- 239000004711 α-olefin Substances 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- 230000002378 acidificating effect Effects 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 150000004665 fatty acids Chemical class 0.000 description 3
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical compound OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000005228 aryl sulfonate group Chemical group 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 150000001735 carboxylic acids Chemical class 0.000 description 2
- 235000015165 citric acid Nutrition 0.000 description 2
- 235000012208 gluconic acid Nutrition 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 2
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical compound OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-UHFFFAOYSA-N 0.000 description 1
- HRPQWSOMACYCRG-UHFFFAOYSA-N 3-dodecylbenzenesulfonic acid Chemical compound CCCCCCCCCCCCC1=CC=CC(S(O)(=O)=O)=C1 HRPQWSOMACYCRG-UHFFFAOYSA-N 0.000 description 1
- RNMDNPCBIKJCQP-UHFFFAOYSA-N 5-nonyl-7-oxabicyclo[4.1.0]hepta-1,3,5-trien-2-ol Chemical compound C(CCCCCCCC)C1=C2C(=C(C=C1)O)O2 RNMDNPCBIKJCQP-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 101150013573 INVE gene Proteins 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 150000004703 alkoxides Chemical class 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- OGBUMNBNEWYMNJ-UHFFFAOYSA-N batilol Chemical class CCCCCCCCCCCCCCCCCCOCC(O)CO OGBUMNBNEWYMNJ-UHFFFAOYSA-N 0.000 description 1
- OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical compound [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 description 1
- 235000019846 buffering salt Nutrition 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid group Chemical class C(CC(O)(C(=O)O)CC(=O)O)(=O)O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 1
- 229940096386 coconut alcohol Drugs 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical class CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000013410 fast food Nutrition 0.000 description 1
- 239000008394 flocculating agent Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 229910021485 fumed silica Inorganic materials 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000011086 high cleaning Methods 0.000 description 1
- GPRLSGONYQIRFK-UHFFFAOYSA-N hydron Chemical compound [H+] GPRLSGONYQIRFK-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229940045996 isethionic acid Drugs 0.000 description 1
- 235000015250 liver sausages Nutrition 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- UTTVXKGNTWZECK-UHFFFAOYSA-N n,n-dimethyloctadecan-1-amine oxide Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)[O-] UTTVXKGNTWZECK-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 108700004121 sarkosyl Proteins 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 1
- 229940045885 sodium lauroyl sarcosinate Drugs 0.000 description 1
- 229940048109 sodium methyl cocoyl taurate Drugs 0.000 description 1
- FVEFRICMTUKAML-UHFFFAOYSA-M sodium tetradecyl sulfate Chemical compound [Na+].CCCCC(CC)CCC(CC(C)C)OS([O-])(=O)=O FVEFRICMTUKAML-UHFFFAOYSA-M 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 150000008054 sulfonate salts Chemical class 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 101150076562 virB gene Proteins 0.000 description 1
Landscapes
- Detergent Compositions (AREA)
Abstract
Phase stable, aqueous cleaning concentrates containing an inorganic acid together with an organic carboxylic acid which has a pKa value of from 1.0 to 5 and a nonionic or anionic surfactant, or mixtures of such surfactants are described.
Description
Docket: 18237 FIELD OF INVENTION
This invE:ntion concerns acidic cleaning compositions which are particularly useful in cleaning tile floors. More specifically, the invention concerns concentrated compositions, i.e., compositions to which water or other solvent is added prior to use.
HACRGROUND OF THE INVENTION
Cleaning compositions containing a strong mineral acid such as hydrochloric acid are known.
U.S. Patent 3,793,221 to Otrhalek describes a concentrate composition comprising 15-40% of aqueous HC1; 1-6% of an organic acid selected from oxalic, tartaric and citric acids;
7-23% nonionic surfactant; and 76-24% water. The sum of the amounts of surfactant is from 10-30% by weight of the composition, and the nonionic surfactant is about 75-90% by weight of the total surfactants. For use, the concentrate of this patent is diluted with from 1 - 5 parts water.
U.S. Patent 4,032, 466 also to Otrhalek discloses acid cleaning concentrat~ss similar to the compositions of the X221 patent but also coni~aining 1-12% of a flocculating agent. The water content varie:~ from 75-12%.
U.S. Patent 4,749,508 to Cockrell, Jr, et al discloses an acidic floor cleanser in ready to use concentrate form comprising 1-6% of an acid having a pKa value greater than 2.8 at 25°C; typically, citric, tartaric, malic, acetic, glycolic or gluconic acids. Additionally, the compositions contain 0.1-15%
~ 25 61 of an acid such as sulfuric, phosphoric, hydrochloric, or nitric acid with a pKa value of less than 2.5 at 25°C together with sufficient buffering salt to provide a composition having a pH of 1-6. The composition may also contain a surfactant, fumed silica or other selected :ingredients.
Schmidt pat al in U.S. Patent 3,443,492 discloses a process for cleaning evaporation tubes with a mixture of an organic acid and a mineral acid. The former is utilized in an amount of from 20-X40% by weight of the total acid in the composition.
U.S. PatE~nt 3,218,260 to Lewandowski discloses a cleaning composition comprising an acid in combination with an anionic surfactant which is an ethoxylated hydrophobic base, the agent containing at: least 10 moles of ethylene oxide per mole of the base. The compositions of the patent are said to be characterized by good clarity in water.
U.S. Pate:nt 4,409,525 to Dodge discloses an etchant comprising a strong' acid, a weak organic acid, and a water miscible solvent. A characteristic of the compositions of this invention is that they contain a minimum amount of water, i.e.
less than 30% by weight.
Martucci, in U.S. Patent 4,675,120 discloses compositions containing controlled amounts of hydrogen ion, the availability of which is maintained by combining strong and weak acid pairs.
W
,_ I
20225fi1 Aqueous glass cleaning compositions are disclosed in U.S. Patent 4,477,364 to have a pH of less than 1 and contain 1-13%, HF together with 85-99% mineral hydrocarboxylic or dicarboxylic acid.
Commercial, floor cleaning products are also known.
One such composition is SURE TRAC'~ sold by the ~rackett Company.
The composition is an aqueous mixture containing an anionic and a nonionic surfactant together with hydrochloric and glycolic acids, and is typically used after dilution with water.
Compositions such as SURE TRAC are excellent floor degreasers and are Especially useful for quarry tile and concrete floors often providsad in large food dispensing operations such as fast food restaurants. Although the ready-to-use aspect of such products is advantageous, they suffer the disadvantage that they contain large amounts of water. The high proportions of water adds to the cost of shipping and warehousing. Concentrates, on the other hand, although less expensive than ready-to-use compositions are often times not satisfactory because of a tendency to phase ou.t on storage or when subjected to temperature stress. Moreover, the manufacture and bulk storage of the concentrate and before its final packaging for customer use is difficult in view of the tendency of the concentrate to separate on standing. In many instances once separation has~occurred, it is difficult if not impossible to reconstitute and reobtain the properties of the original composition, especially viscosity.
Accordingly, it is an object of this invention to provide floor cleaning concentrates which do not suffer the disadvantages of the high water content compositions and have good storage stability, even under temperature stress.
This invE:ntion concerns acidic cleaning compositions which are particularly useful in cleaning tile floors. More specifically, the invention concerns concentrated compositions, i.e., compositions to which water or other solvent is added prior to use.
HACRGROUND OF THE INVENTION
Cleaning compositions containing a strong mineral acid such as hydrochloric acid are known.
U.S. Patent 3,793,221 to Otrhalek describes a concentrate composition comprising 15-40% of aqueous HC1; 1-6% of an organic acid selected from oxalic, tartaric and citric acids;
7-23% nonionic surfactant; and 76-24% water. The sum of the amounts of surfactant is from 10-30% by weight of the composition, and the nonionic surfactant is about 75-90% by weight of the total surfactants. For use, the concentrate of this patent is diluted with from 1 - 5 parts water.
U.S. Patent 4,032, 466 also to Otrhalek discloses acid cleaning concentrat~ss similar to the compositions of the X221 patent but also coni~aining 1-12% of a flocculating agent. The water content varie:~ from 75-12%.
U.S. Patent 4,749,508 to Cockrell, Jr, et al discloses an acidic floor cleanser in ready to use concentrate form comprising 1-6% of an acid having a pKa value greater than 2.8 at 25°C; typically, citric, tartaric, malic, acetic, glycolic or gluconic acids. Additionally, the compositions contain 0.1-15%
~ 25 61 of an acid such as sulfuric, phosphoric, hydrochloric, or nitric acid with a pKa value of less than 2.5 at 25°C together with sufficient buffering salt to provide a composition having a pH of 1-6. The composition may also contain a surfactant, fumed silica or other selected :ingredients.
Schmidt pat al in U.S. Patent 3,443,492 discloses a process for cleaning evaporation tubes with a mixture of an organic acid and a mineral acid. The former is utilized in an amount of from 20-X40% by weight of the total acid in the composition.
U.S. PatE~nt 3,218,260 to Lewandowski discloses a cleaning composition comprising an acid in combination with an anionic surfactant which is an ethoxylated hydrophobic base, the agent containing at: least 10 moles of ethylene oxide per mole of the base. The compositions of the patent are said to be characterized by good clarity in water.
U.S. Pate:nt 4,409,525 to Dodge discloses an etchant comprising a strong' acid, a weak organic acid, and a water miscible solvent. A characteristic of the compositions of this invention is that they contain a minimum amount of water, i.e.
less than 30% by weight.
Martucci, in U.S. Patent 4,675,120 discloses compositions containing controlled amounts of hydrogen ion, the availability of which is maintained by combining strong and weak acid pairs.
W
,_ I
20225fi1 Aqueous glass cleaning compositions are disclosed in U.S. Patent 4,477,364 to have a pH of less than 1 and contain 1-13%, HF together with 85-99% mineral hydrocarboxylic or dicarboxylic acid.
Commercial, floor cleaning products are also known.
One such composition is SURE TRAC'~ sold by the ~rackett Company.
The composition is an aqueous mixture containing an anionic and a nonionic surfactant together with hydrochloric and glycolic acids, and is typically used after dilution with water.
Compositions such as SURE TRAC are excellent floor degreasers and are Especially useful for quarry tile and concrete floors often providsad in large food dispensing operations such as fast food restaurants. Although the ready-to-use aspect of such products is advantageous, they suffer the disadvantage that they contain large amounts of water. The high proportions of water adds to the cost of shipping and warehousing. Concentrates, on the other hand, although less expensive than ready-to-use compositions are often times not satisfactory because of a tendency to phase ou.t on storage or when subjected to temperature stress. Moreover, the manufacture and bulk storage of the concentrate and before its final packaging for customer use is difficult in view of the tendency of the concentrate to separate on standing. In many instances once separation has~occurred, it is difficult if not impossible to reconstitute and reobtain the properties of the original composition, especially viscosity.
Accordingly, it is an object of this invention to provide floor cleaning concentrates which do not suffer the disadvantages of the high water content compositions and have good storage stability, even under temperature stress.
~ ~ ~
-.\ ~a\
20 2~~1 SUMMARY OF THE INVENTION
The cleaning compositions of this invention are concentrated aqueous compositions which will not separate into phases on storage even when subjected to temperature abuse. They comprise aqueous concentrates of water, a mineral acid, an organic acid and at least one anionic or nonionic surfactant.
They may be employed directly or in admixture with additional water.
More specifically, the invention provides a phase stable aqueous cleaning concentrate which does not separate into two or more phases when stored for 28 days at 125° F, the concentrate consisting essentially of, by weight based on the total weight, about 54~ water, about 2~ of an inorganic acid selected from the group consisting of hydrochloric and phosphoric acid, about 11~ of an organic acid having a pKa value of from 1 to 5, and about 32~ of surfactants as a mixture of nonionic and anionic surfactants at weight ratio of 0.5:1 to 2.1:1.
Unless otherwise noted, all concentrations, including HC1, are on an anhydrous weight percent active basis.
The presently preferred inorganic acid is hydrochloric acid because it is easy to use and readily available at a reasonable cost.
Carboxylic: acids, especially hydroxy carboxylic acids may be employed. The presently preferred organic acid is glycolic acid because it is easy to work with and readily compatible with the other components of the composition.
~~~~~~1 Typically useful carboxylic acids are those acids with pKa values of above about 1.0 to 5, preferably from 2.5 to 4. These include, for example:, malic, glycolic, hydroxybenzoic, acetic, tartaric, gamma hydroxylbutyric, citric and gluconic acids.
Anionic and nonionic surfactants that are compatible with the highly acidic environment present in the compositions of the invention are suitable and are present, after dilution of the concentrate with water in an effective cleaning amount. In the concentrate composition of the present invention, the surfactant is present in an amount of from about 12 to about 40% by weight, preferably from about 24 to about 36%. A blend of an anionic and a nonionic is particularly suitable, especially in a weight ratio of nonionic to anionic of from about 0.89:1 to about 1.3:1, most preferably from about 1.0:1 to about 1.1:1.
Broadly, tlhe anionic surfactants are water-soluble alkyl or alkylaryl c~~mpounds, the alkyl having from about 8 to about 22 carbons, in~~luding a sulfate or sulfonate substituent group that has been base-neutralized, typically to provide an alkali metal, e.g., aodium or potassium, or an ammonium cation, including, for example: (1) alkyl and alkylaryl sulfates and sulfonates having preferably 8 to 18 carbons in the alkyl group, which may be straight: or branched chain, e.g., sodium lauryl sulfate and sodium dodecylbenzene sulfonate: (2) alphaolefin aryl sulfonates preferabl~r having from about 10 to 18 carbons in the olefin, e.g., sodium X14-16 olefin sulfonate, which is a mixture of long-chain sulfonate salts prepared by sulfonation of X14-16 alpha-olefins and chiefly comprising sodium alkene sulfonates and sodium hydroxyalkane sulfonates: (3) sulfated and sulfonated monoglycerides, especially those derived from coconut oil fatty acids: (4) sulfate enters of ethoxylated fatty alchols having 1-t a ~- ~0~2~~'1 mols ethylene oxide, e.g., sodium polyoxyethylene (7 mol EO) lauryl ether sulfate, and of ethoxylated alkyl phenols having 10 mole ethylene oxide and 8 to 12 carbons in the alkyl, e.g., ammonium poloxyethylene (4 mol EO) nonyl phenol ether sulfate:
(5) base-neutralized esters of fatty acids and isethionic acid, e.g., sodium lauroy,l isethionate: (6) fatty acid amides of a methyl tauride, e.g., sodium methyl cocoyl taurate: (7) -acetoxy- or acetam.ido-alkane sulfonates, and (8) sarcosinates having from 8 to 22 carbons, e.g., sodium lauroyl sarcosinate.
The nonionics include (1) fatty alcohol alkoxylates, especially ethoxylal:es, wherein the alkyl group has from 8 to 22, preferably 12 to 18,, carbons, and typically 6 to 15 mol alkoxide per molecule, e.g., coconut alcohol condensed with about nine mols ethylene oxide;' (2) fatty acid alkoxylates having from about 6 to about 15 mols alkoxylate, especially the ethoxylate: (3) alkylphenoxy alkoxyl.ates, especially the ethoxylates, containing 6 to 12 carbons, preferably octyl or nonyl, in the alkyl, and hav ing about 5 to 25, ~~referably 5 to 15 mols alkylene oxide per molecule, e.g., nonl~l phenol ethoxylated with about 9.5 mols ethylene oxide(Igep~~l~ CO-630); (4) condensates of ethylene oxide with a hydrophobic vase formed by condensation of propylene oxide with propylene glycol, e.g., nonionic surfactants of the Pluronice series manufactured by BASF Wyandotte, (5) condensates of ethylene oxide with an amine or amide: (6) fatty amine oxides, e.g., stearyl dimethyl amine oxide, and (7) alkylolamides.
As used in the two preceding paragraphs, water solubility shall mean that the amount of surfactant or blend of surfactants used are completely miscible in the compositions of the present invention, at the water concentration present therein.
"~s 6 Preferred avionics are the alkyl and alkylaryl sulfates and the alpha-olefin aryl sulfonates, which may be included in the form of the free acid while preferred nonionics are the fatty alcohol ethoxylates having 6 to 15 cools of ethylene oxide per molecule.
A number of specific anionic surfactants are available and can be employed in the practice of this invention. The presently preferred member of the class is dodecylbenzene sulfonic acid which is available as CALSOFT'n" LAS-99 from Pilot Chemical. Other usE:ful anionic surfactants include sodium alpha olefin sulfonates and sodium lauryl sulfate.
The presently preferred nonionic surfactant is nonylphenoxypoly (et:hyleneoxy) ethanol having an average of 9 cools of ethylene ox~.de per molecule. It is sold by G.A.F.
Corporation, Chemical Product Division as IGEPAL (CO-630). Other nonionic surfactant:. useful in the invention include TRITON1'M X-100 which is octylpheno~:ypolyethoxy ethanol containing 9 cools of ethylene oxide per molecule, sold by Union Carbide, and TERGITOL'~
15-S-7, 15-S-9 or 1~~-S-12. These are polyethylene glycol ethers of a mixture of synthetic C11-C15 fatty alcohols containing, respectively 7, 9 and 12 cools of ethylene oxides. These products are also available from Union Carbide.
The principal and most characteristic property of the compositions of this invention is that they do not tend to phase out on storage even when subjected to temperature abuse such as an alternate freeze-thaw cycle. Preferably, the products of this invention do not separate into two or more phases when stored for three months at room temperature and one month at 125°F/51.7oC.
x.
~42~~1 In addition, the product should preferably pass through at least one freeze-thaw cyc7.e without separation. When measured by these criteria, the products of this invention are stable.
Dilute ac~;~eous compositions such as SURE TRAC
containing relatively large amounts of water are phase stable and do not separate on standing. The stability of the products is commercially acceptable even at elevated and reduced temperatures.
It would f~e expected that this phase stability would be lost as the relative: amount of water in the compositions is decreased and the relative amounts of the active components increased. This, indeed, is what is observed with most compositions of this nature. Surprisingly, however, the concentrated compositions of this invention have been discovered to manifest a phase stable concentration zone between phase unstable zones which are either more or less concentrated in non-aqueous components. Stability is defined as a composition that resists separation into two or more phases for a period of not less than about one month at 100°F.
This unexpected phenomenon is illustrated in the following Table 1.
_ g _ ~~ ~ ~ 1 ~ ~~~2~~,~ p Component % By Wt. % By Wt. % By Wt.
Blend 1 Blend 2 Blend 3 Dodecylbenzene sulfonic acid 12 16 20 Nonyl phenol ethoxylate- 9 cools 12 16 20 ethylene oxide Glycolic acidl 8.4 11.2 14 Hydrochloric acid2 1.54 2.05 2.56 Water 66.06 54.75 43.44 l: 70% glycolic acid calculated as anhydrous acid 2: 20o Baume (about 32%) hydrochloric acid calculated as anhydrous acid When tested for stability by the procedures described above, it was obser~red that Blends 1 and 3 were unstable, whereas Blend 2 was stable. It will be noted that in Hlend 1 the amounts of active components are less than in Blend 2, and that in Blend 3 the % by weight o1' active components is higher than in Blend 2.
Blend 2 remains stable even when subjected to 125°F for 28 days or to freeze-thaw.
In special situations where high cleaning power is required, the concentrated compositions of this invention can be employed directly, i.e. as a ready-to-use composition.
- g -~ ~D ~2~1 ,.
In most in:atances, however, the selected compositon will be diluted with wat~ar prior to use or as used. For example, the composition may be mixed with water at any desired ratio, e.g. at a concentrate: water ratio of from about 1:250 to about 1:4, preferably from about 1:125 to 1:24. Alternatively, the concentrate can be ~uixed with water utilizing any of a variety of special spray devicEa such as a Gilmore'~ sprayer which may be attached to a hose t:o siphon the concentrate from a closed holding vessel. ThE~ dilution rate may be selected based on the cleaning need.
The actual use of the compositions, with or without dilution, is conventional, i.e. the composition is applied to the surface to be cleaned. The surface is scoured to the extent necessary and then rinsed.
The viscosity of the concentrates of this invention is from about 50 to 20a cps, preferably from 100 to 150 cps. This high viscosity is a special advantage when the compositions are employed in the ready-to-use mode. The reason is that the viscous compositions do not tend to run so that the active components remain in contact with the surface to be cleaned.
The mineral and organic acid components of the composition of the invention assist in the cleansing operation by functioning as mild etchants. By so doing, they increase the surface area of the surface to be cleaned, e.g. the tiles, thereby increasing their non-skid properties. Glycolic acid also has some chelating ability which contributes to the cleaning activity.
j,~~< ~ .~' ,~, a ~~ ~~~1 The amount of inorganic acid in the compositions is from about 0.4 to 2.25, preferably 1.5 to 2.0, calculated as active acid on an anhydrous basis. The amount of organic carboxylic acid is from about ti to 20, preferably 9 to 13 on the same basis.
The compositions of this invention are preferably prepared by forming an aqueous solution of the surfactant and thereafter adding in sequence the selected organic acid followed by the inorganic acid, e.g., glycolic acid followed by hydrochloric acid. This order of addition reduces the likelihood of phasing during manufacture. The acids should be added with thorough mixing to l:orm homogeneous compositions.
In this di:oclosure and in the claims, the amounts of all components are calculated as weight percent based on the total weight of the compo:~ition.
The following examples are given by way of illustration only and are not to be considered limitations of this invention, many apparent variations of which are possible without departing from the spirit or ~~cope thereof.
~ ~0 ~~ ~ ' EXAMPLES 1 to 24 The :following cleaning concentrates are illustrative of the compositions of the present invention. In the examples, the g:Lycolic acid is 70% and the hydrochloric acid is a 20° Baume. HCl <:omposition.
Example Water I(~EPAL GLYCOLIC CALSOFT HYDROCHLORIC
CO-630 Acid,70% LAS-99 ACID 32%
1 48.1 7_6.0 16.0 14.0 5.9 2 50.6 7.6.0 14.0 14.0 5.4 3 52.1 7.6.0 14.0 12.0 5.9 4 43.6 7.6.0 18.0 16.0 6.4 44.6 7.8.0 16.0 16.0 5.4 6 44.6 7.6.0 18.0 16.0 5.4 7 45.6 7.6.0 18.0 14.0 6.4
-.\ ~a\
20 2~~1 SUMMARY OF THE INVENTION
The cleaning compositions of this invention are concentrated aqueous compositions which will not separate into phases on storage even when subjected to temperature abuse. They comprise aqueous concentrates of water, a mineral acid, an organic acid and at least one anionic or nonionic surfactant.
They may be employed directly or in admixture with additional water.
More specifically, the invention provides a phase stable aqueous cleaning concentrate which does not separate into two or more phases when stored for 28 days at 125° F, the concentrate consisting essentially of, by weight based on the total weight, about 54~ water, about 2~ of an inorganic acid selected from the group consisting of hydrochloric and phosphoric acid, about 11~ of an organic acid having a pKa value of from 1 to 5, and about 32~ of surfactants as a mixture of nonionic and anionic surfactants at weight ratio of 0.5:1 to 2.1:1.
Unless otherwise noted, all concentrations, including HC1, are on an anhydrous weight percent active basis.
The presently preferred inorganic acid is hydrochloric acid because it is easy to use and readily available at a reasonable cost.
Carboxylic: acids, especially hydroxy carboxylic acids may be employed. The presently preferred organic acid is glycolic acid because it is easy to work with and readily compatible with the other components of the composition.
~~~~~~1 Typically useful carboxylic acids are those acids with pKa values of above about 1.0 to 5, preferably from 2.5 to 4. These include, for example:, malic, glycolic, hydroxybenzoic, acetic, tartaric, gamma hydroxylbutyric, citric and gluconic acids.
Anionic and nonionic surfactants that are compatible with the highly acidic environment present in the compositions of the invention are suitable and are present, after dilution of the concentrate with water in an effective cleaning amount. In the concentrate composition of the present invention, the surfactant is present in an amount of from about 12 to about 40% by weight, preferably from about 24 to about 36%. A blend of an anionic and a nonionic is particularly suitable, especially in a weight ratio of nonionic to anionic of from about 0.89:1 to about 1.3:1, most preferably from about 1.0:1 to about 1.1:1.
Broadly, tlhe anionic surfactants are water-soluble alkyl or alkylaryl c~~mpounds, the alkyl having from about 8 to about 22 carbons, in~~luding a sulfate or sulfonate substituent group that has been base-neutralized, typically to provide an alkali metal, e.g., aodium or potassium, or an ammonium cation, including, for example: (1) alkyl and alkylaryl sulfates and sulfonates having preferably 8 to 18 carbons in the alkyl group, which may be straight: or branched chain, e.g., sodium lauryl sulfate and sodium dodecylbenzene sulfonate: (2) alphaolefin aryl sulfonates preferabl~r having from about 10 to 18 carbons in the olefin, e.g., sodium X14-16 olefin sulfonate, which is a mixture of long-chain sulfonate salts prepared by sulfonation of X14-16 alpha-olefins and chiefly comprising sodium alkene sulfonates and sodium hydroxyalkane sulfonates: (3) sulfated and sulfonated monoglycerides, especially those derived from coconut oil fatty acids: (4) sulfate enters of ethoxylated fatty alchols having 1-t a ~- ~0~2~~'1 mols ethylene oxide, e.g., sodium polyoxyethylene (7 mol EO) lauryl ether sulfate, and of ethoxylated alkyl phenols having 10 mole ethylene oxide and 8 to 12 carbons in the alkyl, e.g., ammonium poloxyethylene (4 mol EO) nonyl phenol ether sulfate:
(5) base-neutralized esters of fatty acids and isethionic acid, e.g., sodium lauroy,l isethionate: (6) fatty acid amides of a methyl tauride, e.g., sodium methyl cocoyl taurate: (7) -acetoxy- or acetam.ido-alkane sulfonates, and (8) sarcosinates having from 8 to 22 carbons, e.g., sodium lauroyl sarcosinate.
The nonionics include (1) fatty alcohol alkoxylates, especially ethoxylal:es, wherein the alkyl group has from 8 to 22, preferably 12 to 18,, carbons, and typically 6 to 15 mol alkoxide per molecule, e.g., coconut alcohol condensed with about nine mols ethylene oxide;' (2) fatty acid alkoxylates having from about 6 to about 15 mols alkoxylate, especially the ethoxylate: (3) alkylphenoxy alkoxyl.ates, especially the ethoxylates, containing 6 to 12 carbons, preferably octyl or nonyl, in the alkyl, and hav ing about 5 to 25, ~~referably 5 to 15 mols alkylene oxide per molecule, e.g., nonl~l phenol ethoxylated with about 9.5 mols ethylene oxide(Igep~~l~ CO-630); (4) condensates of ethylene oxide with a hydrophobic vase formed by condensation of propylene oxide with propylene glycol, e.g., nonionic surfactants of the Pluronice series manufactured by BASF Wyandotte, (5) condensates of ethylene oxide with an amine or amide: (6) fatty amine oxides, e.g., stearyl dimethyl amine oxide, and (7) alkylolamides.
As used in the two preceding paragraphs, water solubility shall mean that the amount of surfactant or blend of surfactants used are completely miscible in the compositions of the present invention, at the water concentration present therein.
"~s 6 Preferred avionics are the alkyl and alkylaryl sulfates and the alpha-olefin aryl sulfonates, which may be included in the form of the free acid while preferred nonionics are the fatty alcohol ethoxylates having 6 to 15 cools of ethylene oxide per molecule.
A number of specific anionic surfactants are available and can be employed in the practice of this invention. The presently preferred member of the class is dodecylbenzene sulfonic acid which is available as CALSOFT'n" LAS-99 from Pilot Chemical. Other usE:ful anionic surfactants include sodium alpha olefin sulfonates and sodium lauryl sulfate.
The presently preferred nonionic surfactant is nonylphenoxypoly (et:hyleneoxy) ethanol having an average of 9 cools of ethylene ox~.de per molecule. It is sold by G.A.F.
Corporation, Chemical Product Division as IGEPAL (CO-630). Other nonionic surfactant:. useful in the invention include TRITON1'M X-100 which is octylpheno~:ypolyethoxy ethanol containing 9 cools of ethylene oxide per molecule, sold by Union Carbide, and TERGITOL'~
15-S-7, 15-S-9 or 1~~-S-12. These are polyethylene glycol ethers of a mixture of synthetic C11-C15 fatty alcohols containing, respectively 7, 9 and 12 cools of ethylene oxides. These products are also available from Union Carbide.
The principal and most characteristic property of the compositions of this invention is that they do not tend to phase out on storage even when subjected to temperature abuse such as an alternate freeze-thaw cycle. Preferably, the products of this invention do not separate into two or more phases when stored for three months at room temperature and one month at 125°F/51.7oC.
x.
~42~~1 In addition, the product should preferably pass through at least one freeze-thaw cyc7.e without separation. When measured by these criteria, the products of this invention are stable.
Dilute ac~;~eous compositions such as SURE TRAC
containing relatively large amounts of water are phase stable and do not separate on standing. The stability of the products is commercially acceptable even at elevated and reduced temperatures.
It would f~e expected that this phase stability would be lost as the relative: amount of water in the compositions is decreased and the relative amounts of the active components increased. This, indeed, is what is observed with most compositions of this nature. Surprisingly, however, the concentrated compositions of this invention have been discovered to manifest a phase stable concentration zone between phase unstable zones which are either more or less concentrated in non-aqueous components. Stability is defined as a composition that resists separation into two or more phases for a period of not less than about one month at 100°F.
This unexpected phenomenon is illustrated in the following Table 1.
_ g _ ~~ ~ ~ 1 ~ ~~~2~~,~ p Component % By Wt. % By Wt. % By Wt.
Blend 1 Blend 2 Blend 3 Dodecylbenzene sulfonic acid 12 16 20 Nonyl phenol ethoxylate- 9 cools 12 16 20 ethylene oxide Glycolic acidl 8.4 11.2 14 Hydrochloric acid2 1.54 2.05 2.56 Water 66.06 54.75 43.44 l: 70% glycolic acid calculated as anhydrous acid 2: 20o Baume (about 32%) hydrochloric acid calculated as anhydrous acid When tested for stability by the procedures described above, it was obser~red that Blends 1 and 3 were unstable, whereas Blend 2 was stable. It will be noted that in Hlend 1 the amounts of active components are less than in Blend 2, and that in Blend 3 the % by weight o1' active components is higher than in Blend 2.
Blend 2 remains stable even when subjected to 125°F for 28 days or to freeze-thaw.
In special situations where high cleaning power is required, the concentrated compositions of this invention can be employed directly, i.e. as a ready-to-use composition.
- g -~ ~D ~2~1 ,.
In most in:atances, however, the selected compositon will be diluted with wat~ar prior to use or as used. For example, the composition may be mixed with water at any desired ratio, e.g. at a concentrate: water ratio of from about 1:250 to about 1:4, preferably from about 1:125 to 1:24. Alternatively, the concentrate can be ~uixed with water utilizing any of a variety of special spray devicEa such as a Gilmore'~ sprayer which may be attached to a hose t:o siphon the concentrate from a closed holding vessel. ThE~ dilution rate may be selected based on the cleaning need.
The actual use of the compositions, with or without dilution, is conventional, i.e. the composition is applied to the surface to be cleaned. The surface is scoured to the extent necessary and then rinsed.
The viscosity of the concentrates of this invention is from about 50 to 20a cps, preferably from 100 to 150 cps. This high viscosity is a special advantage when the compositions are employed in the ready-to-use mode. The reason is that the viscous compositions do not tend to run so that the active components remain in contact with the surface to be cleaned.
The mineral and organic acid components of the composition of the invention assist in the cleansing operation by functioning as mild etchants. By so doing, they increase the surface area of the surface to be cleaned, e.g. the tiles, thereby increasing their non-skid properties. Glycolic acid also has some chelating ability which contributes to the cleaning activity.
j,~~< ~ .~' ,~, a ~~ ~~~1 The amount of inorganic acid in the compositions is from about 0.4 to 2.25, preferably 1.5 to 2.0, calculated as active acid on an anhydrous basis. The amount of organic carboxylic acid is from about ti to 20, preferably 9 to 13 on the same basis.
The compositions of this invention are preferably prepared by forming an aqueous solution of the surfactant and thereafter adding in sequence the selected organic acid followed by the inorganic acid, e.g., glycolic acid followed by hydrochloric acid. This order of addition reduces the likelihood of phasing during manufacture. The acids should be added with thorough mixing to l:orm homogeneous compositions.
In this di:oclosure and in the claims, the amounts of all components are calculated as weight percent based on the total weight of the compo:~ition.
The following examples are given by way of illustration only and are not to be considered limitations of this invention, many apparent variations of which are possible without departing from the spirit or ~~cope thereof.
~ ~0 ~~ ~ ' EXAMPLES 1 to 24 The :following cleaning concentrates are illustrative of the compositions of the present invention. In the examples, the g:Lycolic acid is 70% and the hydrochloric acid is a 20° Baume. HCl <:omposition.
Example Water I(~EPAL GLYCOLIC CALSOFT HYDROCHLORIC
CO-630 Acid,70% LAS-99 ACID 32%
1 48.1 7_6.0 16.0 14.0 5.9 2 50.6 7.6.0 14.0 14.0 5.4 3 52.1 7.6.0 14.0 12.0 5.9 4 43.6 7.6.0 18.0 16.0 6.4 44.6 7.8.0 16.0 16.0 5.4 6 44.6 7.6.0 18.0 16.0 5.4 7 45.6 7.6.0 18.0 14.0 6.4
Claims (9)
1. A phase stable aqueous cleaning concentrate which does not separate into two or more phases when stored for 28 days at 125° F, the concentrate consisting essentially of, by weight based on the total weight, about 54% water, about 2%
of an inorganic acid selected from the group consisting of hydrochloric and phosphoric acid, about 11% of an organic acid having a pKa value of from 1 to 5, and about 32% of surfactants as a mixture of nonionic and anionic surfactants at weight ratio of 0.5:1 to 2.1:1, the weight of said inorganic acids being on an anhydrous basis.
of an inorganic acid selected from the group consisting of hydrochloric and phosphoric acid, about 11% of an organic acid having a pKa value of from 1 to 5, and about 32% of surfactants as a mixture of nonionic and anionic surfactants at weight ratio of 0.5:1 to 2.1:1, the weight of said inorganic acids being on an anhydrous basis.
2. The cleaning concentrate of claim 1 containing the mixture of nonionic and anionic surfactants in a weight ratio of 0.89:1 to 1.3:1.
3. The cleaning concentrate of claim 1 containing a mixture of nonionic and anionic surfactants at a weight ratio of 1.0:1 to 1.1:1.
4. The cleaning composition of claim 1, 2 or 3 containing hydrochloric acid.
5. The cleaning composition of claim 1, 2 or 3 containing phosphoric acid.
6. The cleaning composition of claim 1, 2 or 3 containing hydrochloric and glycolic acids.
7. The cleaning composition of claim 1, 2 or 4 wherein the anionic surfactant is dodecylbenzene sulfonic acid.
8. The cleaning composition of claim 1, 2 or 3 wherein the nonionic surfactant is an alkylphenoxyl poly(alkyleneoxy) ethanol of from about 9 to 12 mols of ethylene oxide per molecule, or a polyethylene glycol ether of a C11-C15 fatty alcohol having 7 to 12 mols of ethylene oxide per molecule.
9. The cleaning compositions of claim 1, 2 or 3 wherein the pKa value of the organic acid is from 2.5 to 4.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US41476289A | 1989-09-29 | 1989-09-29 | |
| US414,762 | 1989-09-29 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2022561A1 CA2022561A1 (en) | 1991-03-30 |
| CA2022561C true CA2022561C (en) | 1999-12-21 |
Family
ID=23642849
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA 2022561 Expired - Lifetime CA2022561C (en) | 1989-09-29 | 1990-08-02 | Floor degreaser concentrate |
Country Status (1)
| Country | Link |
|---|---|
| CA (1) | CA2022561C (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107057875A (en) * | 2017-04-12 | 2017-08-18 | 佛山市德可为装饰材料有限公司 | Cleaning agent for cleaning ceramic tile back side attachment |
-
1990
- 1990-08-02 CA CA 2022561 patent/CA2022561C/en not_active Expired - Lifetime
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN107057875A (en) * | 2017-04-12 | 2017-08-18 | 佛山市德可为装饰材料有限公司 | Cleaning agent for cleaning ceramic tile back side attachment |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2022561A1 (en) | 1991-03-30 |
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