US3846172A - One step method for removing waterinsoluble coatings applied to a substrate - Google Patents
One step method for removing waterinsoluble coatings applied to a substrate Download PDFInfo
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- US3846172A US3846172A US00350401A US35040173A US3846172A US 3846172 A US3846172 A US 3846172A US 00350401 A US00350401 A US 00350401A US 35040173 A US35040173 A US 35040173A US 3846172 A US3846172 A US 3846172A
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- United States
- Prior art keywords
- substrate
- water
- coating
- solution
- paint
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Links
- 239000000758 substrate Substances 0.000 title claims abstract description 64
- 238000000576 coating method Methods 0.000 title claims abstract description 62
- 238000000034 method Methods 0.000 title claims abstract description 55
- 239000011248 coating agent Substances 0.000 claims abstract description 56
- 239000007864 aqueous solution Substances 0.000 claims abstract description 45
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 43
- 239000000243 solution Substances 0.000 claims abstract description 41
- 239000000463 material Substances 0.000 claims abstract description 37
- 230000004888 barrier function Effects 0.000 claims abstract description 32
- 238000001035 drying Methods 0.000 claims abstract description 19
- 230000009471 action Effects 0.000 claims abstract description 16
- 239000002195 soluble material Substances 0.000 claims abstract description 10
- 238000009825 accumulation Methods 0.000 claims abstract description 7
- 238000000151 deposition Methods 0.000 claims abstract description 6
- 230000000694 effects Effects 0.000 claims abstract description 6
- 230000001464 adherent effect Effects 0.000 claims abstract description 4
- 239000003973 paint Substances 0.000 description 46
- 239000003599 detergent Substances 0.000 description 30
- 239000010408 film Substances 0.000 description 24
- 239000007921 spray Substances 0.000 description 20
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 18
- 239000004115 Sodium Silicate Substances 0.000 description 17
- 229910052911 sodium silicate Inorganic materials 0.000 description 17
- 150000001875 compounds Chemical class 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 229910052783 alkali metal Inorganic materials 0.000 description 10
- BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 9
- -1 alkali metal hypophosphates Chemical class 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- 235000011180 diphosphates Nutrition 0.000 description 8
- 125000005341 metaphosphate group Chemical group 0.000 description 8
- 239000012047 saturated solution Substances 0.000 description 8
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical group [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 8
- TVZISJTYELEYPI-UHFFFAOYSA-N hypodiphosphoric acid Chemical class OP(O)(=O)P(O)(O)=O TVZISJTYELEYPI-UHFFFAOYSA-N 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 7
- 235000019832 sodium triphosphate Nutrition 0.000 description 7
- 244000215068 Acacia senegal Species 0.000 description 6
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 6
- 229920000084 Gum arabic Polymers 0.000 description 6
- 239000000205 acacia gum Substances 0.000 description 6
- 235000010489 acacia gum Nutrition 0.000 description 6
- XPPKVPWEQAFLFU-UHFFFAOYSA-J diphosphate(4-) Chemical compound [O-]P([O-])(=O)OP([O-])([O-])=O XPPKVPWEQAFLFU-UHFFFAOYSA-J 0.000 description 6
- 239000008103 glucose Substances 0.000 description 6
- 229940005740 hexametaphosphate Drugs 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- UNXRWKVEANCORM-UHFFFAOYSA-I triphosphate(5-) Chemical compound [O-]P([O-])(=O)OP([O-])(=O)OP([O-])([O-])=O UNXRWKVEANCORM-UHFFFAOYSA-I 0.000 description 6
- 241000416162 Astragalus gummifer Species 0.000 description 5
- 108010082495 Dietary Plant Proteins Proteins 0.000 description 5
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 5
- 229930006000 Sucrose Natural products 0.000 description 5
- 229920001615 Tragacanth Polymers 0.000 description 5
- 239000005018 casein Substances 0.000 description 5
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 5
- 235000021240 caseins Nutrition 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 5
- 150000003839 salts Chemical class 0.000 description 5
- 239000005720 sucrose Substances 0.000 description 5
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 4
- FEWJPZIEWOKRBE-JCYAYHJZSA-L L-tartrate(2-) Chemical compound [O-]C(=O)[C@H](O)[C@@H](O)C([O-])=O FEWJPZIEWOKRBE-JCYAYHJZSA-L 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 4
- 238000013019 agitation Methods 0.000 description 4
- 229940001468 citrate Drugs 0.000 description 4
- 238000004140 cleaning Methods 0.000 description 4
- 229940001447 lactate Drugs 0.000 description 4
- 230000008569 process Effects 0.000 description 4
- 229940095064 tartrate Drugs 0.000 description 4
- 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 3
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 229920000847 nonoxynol Polymers 0.000 description 3
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 3
- 229920001451 polypropylene glycol Polymers 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 150000001449 anionic compounds Chemical class 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 150000001767 cationic compounds Chemical class 0.000 description 2
- 239000013530 defoamer Substances 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 229910017053 inorganic salt Inorganic materials 0.000 description 2
- 150000008040 ionic compounds Chemical class 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000010422 painting Methods 0.000 description 2
- 150000004760 silicates Chemical class 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- CDOUZKKFHVEKRI-UHFFFAOYSA-N 3-bromo-n-[(prop-2-enoylamino)methyl]propanamide Chemical compound BrCCC(=O)NCNC(=O)C=C CDOUZKKFHVEKRI-UHFFFAOYSA-N 0.000 description 1
- CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical compound C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241001397173 Kali <angiosperm> Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 150000001860 citric acid derivatives Chemical class 0.000 description 1
- 210000003298 dental enamel Anatomy 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- MOTZDAYCYVMXPC-UHFFFAOYSA-N dodecyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOS(O)(=O)=O MOTZDAYCYVMXPC-UHFFFAOYSA-N 0.000 description 1
- 229940043264 dodecyl sulfate Drugs 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000002320 enamel (paints) Substances 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 150000003893 lactate salts Chemical class 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- OFPXSFXSNFPTHF-UHFFFAOYSA-N oxaprozin Chemical compound O1C(CCC(=O)O)=NC(C=2C=CC=CC=2)=C1C1=CC=CC=C1 OFPXSFXSNFPTHF-UHFFFAOYSA-N 0.000 description 1
- 229960002739 oxaprozin Drugs 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 238000004886 process control Methods 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 235000018102 proteins Nutrition 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000001509 sodium citrate Substances 0.000 description 1
- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical group [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 239000001540 sodium lactate Substances 0.000 description 1
- 229940005581 sodium lactate Drugs 0.000 description 1
- 235000011088 sodium lactate Nutrition 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 229910000162 sodium phosphate Inorganic materials 0.000 description 1
- JUAHWAGHDQJOLT-UHFFFAOYSA-M sodium;propane-2-sulfonate Chemical compound [Na+].CC(C)S([O-])(=O)=O JUAHWAGHDQJOLT-UHFFFAOYSA-M 0.000 description 1
- 238000009494 specialized coating Methods 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 150000003892 tartrate salts Chemical class 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 235000011178 triphosphate Nutrition 0.000 description 1
- 239000001226 triphosphate Substances 0.000 description 1
- 125000002264 triphosphate group Chemical class [H]OP(=O)(O[H])OP(=O)(O[H])OP(=O)(O[H])O* 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/32—Processes for applying liquids or other fluent materials using means for protecting parts of a surface not to be coated, e.g. using stencils, resists
- B05D1/322—Removable films used as masks
- B05D1/327—Masking layer made of washable film
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/008—Temporary coatings
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D9/00—Chemical paint or ink removers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/32—Processes for applying liquids or other fluent materials using means for protecting parts of a surface not to be coated, e.g. using stencils, resists
Abstract
1. A METHOD FOR REMOVING A WATER INSOLUBLE COATING FROM A SUBSTRATE TO WHICH THE COATING IS NORMALLY ADHERENT WHICH COMPRISES: 8A) DEPOSITING ON SAID SURFACE A BARRIER COATING OF A WATER SOLUBLE MATERIAL; (B) EFFECTING THE ACCUMULATION ON SAID BARRIER COATING OF SAID WATER-INSOLUBLE COATING; (C) EFFECTING THE REMOVAL OF SAID WATER-SOLUBLE COATING BY SUBJECTING SAID COATED SUBSTRATE TO THE ACTION OF AN AQUEOUS SOLUTION CONTAINING A WATER SOLUTION BARRIER COATING MATERIAL WHICH SOLUTION, UPON SUBSEQUENT DRYING, REDEPOSITS SAID WATER SOLUBLE BARRIER COATING ON SAID SUBSTRATE, THE TEMPERATURE OF SAID SOLUTION BEING IN THE RANGE OF ABOUT 170*-205*F. AND THE PERIOD OF TIME OF SUBJECTING SAID SUBSTRATE TO SAID ACTION BEING A TIME SUFFICIENT FOR THE TEMPERATURE OF SAID SUBSTRATE TO APPROACH THAT OF SAID SOLUTION; AND (D) DRYING SAID SUBSTRATE TO EFFECT SAID REDEPOSITION.
Description
United States Patent 3,846,172 ONE STEP METHOD FOR REMOVING WATER- INSOLUBLE COATINGS APPLIED TO A SUB- STRATE Charles G. Fossati, 1175 Grayton, Grosse Pointe Park, Mich. 48224 No Drawing. Continuation-impart of abandoned application Ser. No. 228,380, Feb. 22, 1972. This application Apr. 12, 1973, Ser. No. 350,401
Int. Cl. B08b 7/00 US. Cl. 134-4 37 Claims ABSTRACT OF THE DISCLOSURE Water-insoluble coatings, such as paint and the like, are effectively removed from spray masks and other substrates by applying to the surface of the substrate an aqueous solution of a film-forming material; drying the solution to form a film; and after subsequent use, when paint or the like has accumulated on the coated mask, immersing the substrate in a heated bath of the same aqueous solution, thereby removing the paint therefrom and concurrently redepositing the film onto the surface of the substrate.
Relationship to Other Patent Applications This application is a continuation-in-part of my prior application Ser. No. 228,380 filed Feb. 22, 1972, and now abandoned.
BACKGROUND OF THE INVENTION I. Field of the Invention The present invention pertains primarily to decorative coating operations. More particularly, the present invention concerns the use of spray masks and similar substrates and the removal of paint therefrom and even more particularly to certain compositions and methods used in such operations.
II. Description of the Prior Art In the decorative painting art, a paint spray mask having accurately formed openings is positioned adjacent the workpiece which is to be painted. The openings in the mask define the areas of the workpiece surface which are to be painted. Paint is applied to the workpiece surface by use of a spray gun or the like, and after a number of workpieces have been painted, producing an accumulation of paint on the paint spray mask, the latter must be cleaned.
A number of methods have been developed to remove the paint from such paint spray masks. The most common method employed is to spray the painted masks with a solvent, such as a chlorinated hydrocarbon, a ketone or an aromatic hydrocarbon. While the use of such solvents is eifective, such use is characterized by several disadvantages. The more volatile solvents represent a fire hazard, while others are toxic. Further, such solvents not only represent a high initial investment, but they tend to increase cleaning costs as solvents must be constantly replenished because of evaporation losses. It has also been extremely difficult to dispose of solvent paint cleaning residues since they may not be disposed of through septic fields or sanitary sewers. Disposing of such residues thus represents an additional expense in the use of such solvent systems.
To avoid solvent-type systems, it has been suggested that a Wax or similar emulsion be applied to the paint spray mask. The emulsion is sprayed on the mask and allowed to dry and solidify on the mask surface. The accumulation of paint over this surface can then be removed by immersing the mask in hot or boiling water,
whereby the wax converts from a solid to a liquid and floats off carrying the paint with it. Although such a system has been efiective in eliminating the use of solvents, it also has some notable disadvantages. For example, it requires a specialized coating on the mask surface, thus adding an extra operation to the cleaning process. Further, the wax tends to create a fairly heavy film which may interfere with fine painting details in use, and thus the kind of mask on which such a wax system can be utilized is limited. More particularly, wax systems applied by spray have a tendency to emit wax particles into the atmosphere, resulting in the deposit of wax particles on production parts, which eventually must be rejected as paint will not adhere Where the wax particles have been deposited.
Even later methods designed to cope with this problem entail the use of an aqueous gel as a coating for the mask prior to application of paint, the gel then being removable with steam or hot water. However, this method is also disadvantageous in three respects. First, the process controls required to form a gel of sutficient utility are too precise for efficient commercialization. Secondly, the use of steam or hot water to remove the gel creates not only an unnecessary step in the process but a waste disposal problem as well. Thirdly, application by spray causes the same problem as wax does, i.e. particles get into atmosphere and their deposit on parts in production causes rejects.
SUMMARY OF THE INVENTION The present invention provides a method for removing a water-insoluble coating such as a paint or the like, from a substrate, such as a spray mask or other device, fixture, or structure. The method comprises applying an aqueous solution of certain film-forming materials to the substrate; drying the aqueous solution to form a barrier film, or coating, on the surface of the substrate; and then, after accumulating paint on the substrate, subjecting the painted substrate to the action of the same aqueous solution. It is a feature of the invention that as the foregoing steps are carried out cyclically, accumulated paint is, in each cycle, substantially completely removed from the substrate and concurrently the substrate is wetted with a solution which, upon subsequent drying, redeposits the barrier coating on the substrate to facilitate the removal of a subsequent accumulation of paint.
For a more complete understanding of the present invention, reference is made to the following detailed description and examples thereof.
DESCRIPTION OF THE PREFERRED EMBODIMENTS In accordance with the present invention, a method for removing a water-insoluble coating, such as a paint or the like, from the surface of a substrate, such as a spray mask or other substrate, generally comprises:
(a) depositing on the substrate a barrier coating of a water-soluble material;
(b) effecting the accumulation on said barrier coating of said water-insoluble coating;
(c) effecting the removal of said water-insoluble coating by subjecting the coated substrate to the action of an aqueous solution, which upon subsequent drying, redeposits said water-soluble barrier coating on said substrate, the temperature of the solution being in the range of about 212 F.; and
(d) drying said substrate to effect said redeposition.
The expression, subjected to the action of the aqueous solution is used herein to mean (a) that the coated substrate is immersed in the solution while the latter is agitated, (b) the solution is sprayed against the substrate, or the like in a manner which causes the solution to redissolve the barrier coating and mechanically strip off the paint coating.
It will be appreciated by those skilled in the art that the present process defines a distinct improvement in that it is possible by the invention to concurrently strip the waterinsoluble coating from the substrate and rewet the substrate with a solution which, upon drying, redeposits the initial barrier film. Thus, in essence, a one-shot process for protecting substrates from water-insoluble coatings is provided herein. Further, the solution of the film-forming material can be readily filtered, decanted, or otherwise treated to remove the insoluble coating from the system. In this manner the aqueous solution can be reused almost indefinitely with very little waste.
The term barrier coating or barrier film, as used herein, means a coating which is impervious to paint, resistant to penetration by paint, prevents effective contact of paint with a substrate, or the like in a manner such that the normally adherent paint does not adhere to the substrate at all, or weakly so.
The aqueous solution contemplated for use in the practice of the present invention can consist of a film forming material as the sole solute but it is preferred that an aqueous solution comprise a film forming material and a detergent.
The film-forming materials which are most advantageously employed in the practice of the present invention are, for the most part, water-soluble salts or certain water-soluble, naturally occurring materials. The most valuable of the salts are the alkali metal hypophosphates, hexametaphosphates, metaphosphates, orthophosphates, pyrophosphates, triphosphates, silicates, citrates, tartrates and lactates. The most valuable of the naturally occurring materials are casein, sucrose, glucose, gum arabic, gum tragacanth, vegetable proteins and the like, as well as mixtures thereof. The term alkali metal includes sodium, potassium, and ammonium.
In the practice of the present invention the preferred film-forming material is an alkali metal silicate; e.g. sodium silicate. Sodium silicate, as presently commercially available, does not have a fixed chemical formula and is defined in terms of SiO content and Na O content. Although all commercially available forms thereof (e.g., metasilicate, orthosilicate, disilicate, Water glass) will work in the practice of the present invention, it is preferred that the sodium silicate have a minimum SiO to Na O ratio of about 2:1, and a ratio preferably within a range of from about 2: 1 to 4: 1.
The inclusion of detergents, or cleansers, although not essential to the successful practice of the present invention, renders the invention more valuable and practicable. These compounds have been found to assist in the invention in a number of ways. First, they reduce the surface tension of the water, thereby effecting a uniform deposition of the film-forming material. Second, they emulsify the paint, thereby avoiding the redeposition thereof. Further, some inorganic salt detergents act as water conditioners and some tend to improve the barrier film formed on the substrate.
Representative of useful inorganic detergents are, for example, the alkali metal hydroxides, carbonates, silicates, hypophosphates, hexametaphosphates, metaphosphates, orthophosphates, pyrophosphates, tripolyphosphates, and mixtures thereof.
Representative of the useful organic detergents are the anionic, cationic, and non-ionic detergents, for example; lauryl sulfate, sodium isopropyl sulfonate, dioctyl sodium sulfonate, diamyl sodium sulfonate, quaternary ammonium salts, ethoxylated polyoxypropylene glycol, ethoxylated alkyl phenols and the like. (See, for example, McCutcheons: Detergents and Emulsifiers, 1971 Edition and the surfactants disclosed in US. Pat. Nos. 2,674,619 and 2,677,700 by way of example).
In the practice of the present invention, the preferred detergent is sodium orthophosphate.
The concentration of the film forming material can be any concentration which is effective in forming a barrier film, that is, it can be that of a saturated solution or any lesser concentration which provides an adequate thickness of film. Generally, however, I prefer to prepare and store a solution wherein the film forming material is at a concentration of about 150% by weight and use the solution either at that concentration or, in some cases, in more diluted form. Where the degree of solubility permits, I particularly prefer to prepare and store the solution with a concentration of film forming material at about 15-30% by weight and use the solution at that concentration or diluted up to as much as three times its volume with water (that is, a final preferred concentration of film forming material in the range of 330% by weight).
It will be apparent that the concentration of a saturated solution of a film forming material varies considerably from one material to another. Similarly the concentration of a saturated solution of any one such material may be considerably different at ambient temperatures as compared to 200 F. for example. Therefore, a mixture may be prepared at 75 F., for example, which comprises a saturated solution of a film forming salt and a proportion of the undissolved solid salt, the latter going into solution at or below the temperature at which the solution is used.
The detergents vary widely in their most effective concentrations but generally may be used, if at all, in a concentration up to about 25% by weight. However, any lowering of the surface tension is desirable and therefore relatively minor proportions of detergent can be used with advantage. Where the detergent is an inorganic salt, it is used preferably in the range of 15-25% by weight. Where the cleansing agent is an organic detergent, it is most often used in relatively lower percentages, that is, a fraction of one percent up to about 10% by weight. Matters such as excessive foaming on the one hand, and the attainment of a desired emulsification of paint particles on the other hand tend to dictate the proportion of a particular organic detergent. Where necessary defoamers may be used.
Some materials; for example, sodium silicate and sodium phosphate, are both film forming materials and detergents.
As indicated the ratio of film forming material to detergent can vary widely. It is preferred however, to use a ratio of film forming material to inorganic detergent in the range of 3:1 to 0.5 :1 or even better in the range of 2:1 to 1:1.
In carrying out the method of the invention, the clean, unused substrate is first subjected to the action of the film forming solution preferably at a temperature ranging from to 212 IE, or, better, at a temperature ranging from about to 205 F., by any suitable method such as spray application, immersion or the like. After the diluted aqueous solution has wetted the spray mask, the water is evaporated to thereby deposit a film thereon. Water evaporation can be accomplished by any suitable drying means; such as forced heat, maintaining the substrate at an elevated temperature sufficient to evaporate the water upon exposure to ambient or room temperatures, or simply with ambient temperatures air from a compressed air source directed from an air nozzle at the substrate.
After the film is formed, the spray mask is ready for use. When following use, sufficient amounts of paint have accumulated on the surface of the mask to necessitate the cleaning thereof, the mask is preferably immersed in a heated bath of the aqueous solution, maintained under agitation, and at a temperature ranging from about 110 to 212 F., preferably a temperature ranging from about 170 to 205 F., to remove substantially 100% of the paint and to concurrently reapply an aqueous solution of film-forming material to the spray mask.
In a preferred mode of practicing the invention, the spray mask is immersed in the diluted aqueous solution maintained at the hereinbefore defined temperature for a period of time sufficient to permit the paint mask to reach a temperature approaching that of the aqueous solution, generally in a period of time ranging from about seconds to 3 minutes, usually from about 1 to 1 /2 minutes. After the mask is removed from the heated solution, the solution is then allowed to dry thereon. This may be achieved solely through the emission of heat from the spray inask and is usually completed in about seconds to 1 minute. The mask is then ready for reuse.
The time of immersion can be important also to the removal of paint in that paint is more easily removed if 10 it has dried; that is, expelled solvent, polymerized, or the like depending on the type of paint used and its mechanism of drying. Subjecting the paint layer to the action of the aqueous solution at a temperature of 170205 F., for at least one minute assists in such drying and the 15 more complete removal of paint.
It will be apparent to those skilled in the art that if the diluted solution used for application of the film-forming material is maintained under agitation, then this same solution can be used for removal of the paint and reappli- 2,0
cation of the solution. Thus, the present invention provides, in its preferred embodiment, and as it is carried out cyclically, for the removal of water-insoluble coatings from a substrate, with the concurrent application thereon of the aqueous solution which, upon subsequent drying,
redeposits a protective coating of a water-soluble, filmforming material.
For a more complete understanding of the present invention, following are specific, non-limiting, examples thereof. In the examples, all parts are by weight, absent indications to the contrary.
Example I Into a heated tank maintained at 195 F., equipped with agitation means, and containing a diluted aqueous solution of a film-forming material was immersed a spray mask for about 1 minute. The mask, which was then at a temperature of about 195 F., was removed from the tank and the aqueous solution was allowed to dry in an open atmosphere, leaving a uniform thin film thereon.
The mask was then sprayed with a commercially purchased enamel paint until it was substantially completely coated with the paint.
Thereafter, the spray mask was reimmersed in the heated tank, under agitation, for a period of about 3 minutes, during which time the paint was removed therefrom and a new aqueous solution of film-forming material was deposited thereon. The mask was then dried, repainted and reimmersed in the aqueous solution cyclically.
The aqueous film-forming solutions employed were as follows:
A Ingredient: Parts Sodium silicate (SiO :Na O=2.87:l) 7.56 Sodium orthophosphate 4.9 Ethoxylated nonylphenol (65% ethylene oxide) 0.25 Water 87.29
100.0 B Ingredient: Parts Glucose 6.25 Sodium citrate 6.25 Water 87.5
100.0 C Ingredient: Parts Soya protein 4.4 Ethoxyplated polyoxypropylene glycol (80% ethylene oxide 6.25 Water 89.35
6 D Ingredient: Parts Sodium silicate '(SiO :Na 'O-=2.87:1) 7.5 Water 92.5
100.0 E Ingredient: Parts Gum arabic 6.25 Sodium carbonate 5.0 Ethoxylated polyoxypropylene glycol ethylene oxide) 0.25 Water 88.5
F Ingredient: Parts Sodium lactate 5.25 Dioctyl sodium sulfosuccinate 5.5 Ethoxylated nonylphenol (65% ethylene oxide) 0.25 Water 89.0
Composition E exhibited more foaming than was desirable and, therefore, 0.12% of a commercially available defoamer was added.
The following table shows the efficiency in paint removal exhibited by each of the above solutions by visual observation:
Percent paint removal Film First Second Film-forming solution properties application application Example II Ingredient: Parts Sodium silicate (SiO :Na =3.22:l) 9.17 Sodium orthophosphate 7.08 Ethoxylated nonylphenol (65 ethylene oxide) 0.24 Water 83.46
A commercially available defoamer (0.05%) was used to reduce the foaming.
The foregoing examples were repeated using a wide variety of film-forming materials, a wide variety of detergents, a wide variety of percentages of chemicals, and various temperatures up to the boiling point of the aqueous solution. In this manner the various preferred chemicals and preferred operating conditions, as set forth above, were determined.
The term water-insoluble coating includes those formed from paints wherein water is used as a reducer, or diluent, with an organic solvent; those formed from paints wherein water is used as a vehicle for an emulsion,
7 or latex; and the like, as well as the more traditional water-free paints, lacquers, enamels, and the like.
I claim:
1. A method for removing a water insoluble coating from a substrate to which the coating is normally adherent which comprises:
(a) depositing on said substrate a barrier coating of a water soluble material;
(b) efiecting the accumulation on said barrier coating of said water-insoluble coating;
(c) effecting the removal of said water-insoluble coating by subjecting said coated substrate to the action of an aqueous solution containing a water soluble barrier coating material which solution, upon subsequent drying, redeposits said water soluble barrier coating on said substrate, the temperature of said solution being in the range of about 170205 F. and the period of time of subjecting said substrate to said action being a time sufiicient for the temperature of said substrate to approach that of said solution; and
(d) drying said substrate to effect said redeposition.
2. The method of claim 1 wherein the initial deposition of said barrier coating is made by subjecting the substrate to the action of said aqueous solution.
3. The method of claim 1 wherein said coated substrate is subjected to the action of said aqueous solution by immersing said coated substrate in an agitated bath'of said solution.
4. The method of claim 1 wherein said barrier coating comprises a compound selected from the group of water soluble, film-forming materials consisting of casein; sucrose; glucose; gum arabic; gum tragacanth; vegetable protein; an alkali metal orthophosphate, hypophosphate, hexametaphosphate, metaphosphate, pyrophosphate, tripolyphosphate, silicate, citrate, tartrate, or lactate; and mixtures thereof.
5. The method of claim 4 wherein said barrier coating comprises sodium silicate.
6. The method of claim 1 wherein said aqueous solution comprises a compound selected from the group of water soluble, film-forming materials consisting of casein; sucrose; glucose; gum arabic; gum tragacanth; vegetable protein; an alkali metal orthophosphate, hypophosphate, hexametaphosphate, metaphosphate, pyrophosphate, tripolyphosphate, silicate, citrate, tartrate, or lactate; and mixtures thereof; said compound being at a concentration sufiicient, upon said drying, to deposit said barrier coating on said substrate.
7. The method of claim 8 wherein said aqueous solution comprises between about one percent by weight and a saturated solution of said compound.
8. The method of claim 6 wherein said aqueous solution comprises about 3-30 percent by weight of said compound.
9. The method of claim 1 wherein said aqueous solution comprises a detergent in a concentration sufiicient to effect the lowering of the surface tension of said solution.
10. The method of claim 9 wherein said detergent is selected from the group consisting of an organic anionic compound; an organic cationic compound; an organic non-ionic compound; an alkali metal orthophosphate, hypophosphate, hexametaphosphate, metaphosphate, pyrophosphate, tripolyphosphate, or silicate; and mixtures thereof.
11. The method of claim 9 wherein said material is an alkali metal silicate and said detergent is an alkali metal orthophosphate.
12. The method of claim 11 wherein said silicate is sodium silicate and said orthophosphate is sodium orthophosphate.
13. The method of claim 12 wherein said sodium silicate has a SiO :Na ratio in the range of 2:1 to 4:1 and the proportion of said sodium silicate to said sodium orthophosphate is in the range of about 3 :1 to 0.5: 1.
14. The method of claim 9 wherein said detergent is an 8 alkali metal salt detergent in a finite concentration up to about 25 percent.
15. The method of claim 1 wherein said aqueous solution comprises between about one percent by weight and a saturated solution of said water soluble material.
16. The method of claim 1 wherein said aqueous solution comprises about 3-30 percent by weight of said water soluble material.
17. The method of claim 1 wherein said aqueous solution comprises said water soluble material and an inorganic detergent in a ratio by weight in the range of 3:1 to 0.5:1.
18. The method of claim 17 wherein said ratio is in the range of 2:1 to 1:1.
19. The method of claim 1 wherein said aqueous solution comprises sodium silicate wherein the ratio siO tNa O is in the range of 2:1 to 4:1.
20. In the method (a) wherein a substrate is coated with a barrier coating to facilitate removal of a water insoluble paint coating to be coated thereon;
(b) wherein said barrier coating is then coated with said water-insoluble paint coating;
(c) wherein said coatings are subsequently removed;
and
(d) wherein said steps are repeated cyclically:
the improvement which comprises carrying out the step of removing said coatings by subjecting said coated substrate to the action of an aqueous solution containing a water soluble barrier coating material which solution, upon subsequent drying, deposits a water soluble barrier coating on said substrate, the temperature of said solution being in the range of about 205 F. and the period of time of subjecting said substrate to said action being a time sufiicient for the temperature of said substrate to approach that of said solution.
21. The method of claim 20 wherein said coated substrate is subjected to the action of said aqueous solution by immersing said coating substrate in an agitated bath of said solution.
22. The method of claim 20 wherein said barrier coating comprises a compound selected from the group of water soluble, film-forming materials consisting of casein; sucrose; glucose, gum arabic, gum tragacanth; vegetable protein; an alkali metal orthophosphate, hypophosphate, hexametaphosphate, metaphosphate, pyrophosphate, tripolyphosphate, silicate, citrate, tartrate, or lactate; and mixtures thereof.
23. The method of claim 22 wherein said barrier coating is sodium silicate.
24. The method of claim 20 wherein said aqueous solution comprises a compound selected from the group of water soluble, film-forming materials consisting of casein; sucrose; glucose; gum arabic; gum tragacanth; vegetable protein; an alkali metal orthophosphate, hypophosphate, hexametaphosphate, metaphosphate, pyrophosphate, tripolyphosphate, silicate, citrate, tartrate, or lactate; and mixtures thereof; said compound being at a concentration suflicient, upon said drying, to deposit said barrier coating on said substrate.
25. The method of claim 24 wherein said aqueous solution comprises between about one percent by weight and a saturated solution of said compound.
26. The method of claim 24 wherein said aqueous solution comprises about 3-30 percent by weight of said compound.
27. The method of claim 20 wherein said aqueous solution comprises a detergent in a concentration sufiicient to effect the lowering of the surface tension of said solution.
28. The method of claim 27 wherein said detergent is selected from the group consisting of an organic anionic compound; an organic cationic compound; an organic noll'ionic compound; ll a kali. metal orthophosphate,
hypophosphate, hexametaphosphate, metaphosphate, pyrophosphate, tripolyphosphate, or silicate; and mixtures thereof.
29. The method of claim 27 wherein said material is an alkali metal silicate and said detergent is an alkali metal orthophosphate.
30. The method of claim 29 wherein said silicate is sodium silicate and said orthophosphate is sodium orthophosphate.
31. The method of claim 30 wherein said sodium silicate has a SiO :Na O ratio in the range of 2:1 to 4:1 and the proportion of said sodium silicate to said sodium orthophosphate is in the range of about 3 :1 to 0.5: l.
32. The method of claim 27 wherein said detergent is an alkali rnetal salt detergent in a finite concentration up to about 25 percent.
33. The method of claim 20 wherein said aqueous solution comprises between about one percent by weight and a saturated solution of said water soluble material.
34. The method of claim 20 wherein said aqueous solution comprises about 3-30 percent by weight of said water soluble material.
35. The method of claim 20 wherein said aqueous solution comprises said water soluble material and an inor- :ganic detergent in a ratio by weight in the range of 3:1 to 0.5 :1.
36. The method of claim 35 wherein said ratio is in the range of 2:1 to 1:1.
37. The method of claim 20 wherein said aqueous solution comprises sodium silicate wherein the ratio SiO :Na O is in the range of 2:1 to 4:1.
References Cited UNITED STATES PATENTS 3,531,311 9/1970 Prior 1062 X 2,992,186 7/1961 Hellsten 252-435 3,455,737 7/1969 Seibert 134-29 X 2,991,188 7/1961 Wing et a1. 134-4 X S. LEON BASHORE, Primary Examiner M. S. ALVO, Assistant Examiner US. Cl. X.R.
UNITED STATES PATENT OFFICE QERTIFICATE 0F CORRECTION Patent No. 846,172 Dated 11-5-74 Inventor(s) Charles G. FOssatl It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Column 7, line 49, delete "8" and insert --6-.
Signed and Scaled this sixteenth D ay 0F September 1975 [SEAL] Arrest:
RUTH C. MASON C. MARSHALL DANN Arresting Officer Commissioner oj'Parents and Trademarks
Claims (1)
1. A METHOD FOR REMOVING A WATER INSOLUBLE COATING FROM A SUBSTRATE TO WHICH THE COATING IS NORMALLY ADHERENT WHICH COMPRISES: 8A) DEPOSITING ON SAID SURFACE A BARRIER COATING OF A WATER SOLUBLE MATERIAL; (B) EFFECTING THE ACCUMULATION ON SAID BARRIER COATING OF SAID WATER-INSOLUBLE COATING; (C) EFFECTING THE REMOVAL OF SAID WATER-SOLUBLE COATING BY SUBJECTING SAID COATED SUBSTRATE TO THE ACTION OF AN AQUEOUS SOLUTION CONTAINING A WATER SOLUTION BARRIER COATING MATERIAL WHICH SOLUTION, UPON SUBSEQUENT DRYING, REDEPOSITS SAID WATER SOLUBLE BARRIER COATING ON SAID SUBSTRATE, THE TEMPERATURE OF SAID SOLUTION BEING IN THE RANGE OF ABOUT 170*-205*F. AND THE PERIOD OF TIME OF SUBJECTING SAID SUBSTRATE TO SAID ACTION BEING A TIME SUFFICIENT FOR THE TEMPERATURE OF SAID SUBSTRATE TO APPROACH THAT OF SAID SOLUTION; AND (D) DRYING SAID SUBSTRATE TO EFFECT SAID REDEPOSITION.
Priority Applications (12)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US00350401A US3846172A (en) | 1972-02-22 | 1973-04-12 | One step method for removing waterinsoluble coatings applied to a substrate |
CA190,994A CA1012853A (en) | 1973-04-12 | 1974-01-25 | Composition and method for removing water-insoluble coatings applied to a substrate |
GB625174A GB1457577A (en) | 1973-04-12 | 1974-02-12 | Composition and method for removing water-insoluble coat9ngs applied to a substrate |
SE7401828A SE404026B (en) | 1973-04-12 | 1974-02-12 | PROCEDURE FOR REMOVING WATER-UNOLUTE COATINGS FROM SUBSTRATE SURFACES |
NL7402985A NL7402985A (en) | 1973-04-12 | 1974-03-05 | |
BE142211A BE812557A (en) | 1973-04-12 | 1974-03-20 | PROCESS FOR REMOVING WATER INSOLUBLE COATINGS APPLIED TO A SUBSTRATE |
LU69670A LU69670A1 (en) | 1973-04-12 | 1974-03-20 | |
IT484374A IT1013656B (en) | 1973-04-12 | 1974-03-20 | METHOD AND COMPOUND TO KEEP CLEAN FROM WATER INSOLUBLE PAINTS AND COATINGS IN GENERAL AND PARTICULARLY THE SPRAYING MASKS FOR THE PERFORMANCE OF DECORATIVE WORKS |
FR7409576A FR2225221B1 (en) | 1973-04-12 | 1974-03-20 | |
JP3315274A JPS5026841A (en) | 1973-04-12 | 1974-03-26 | |
DE19742415976 DE2415976C3 (en) | 1973-04-12 | 1974-04-02 | Process for the removal of a water-insoluble adhesive protective layer from a substrate and for the renewed formation of a protective layer |
ES425157A ES425157A1 (en) | 1973-04-12 | 1974-04-09 | Composition and method for removing water-insoluble coat9ngs applied to a substrate |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US22838072A | 1972-02-22 | 1972-02-22 | |
US00350401A US3846172A (en) | 1972-02-22 | 1973-04-12 | One step method for removing waterinsoluble coatings applied to a substrate |
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US3846172A true US3846172A (en) | 1974-11-05 |
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US00350401A Expired - Lifetime US3846172A (en) | 1972-02-22 | 1973-04-12 | One step method for removing waterinsoluble coatings applied to a substrate |
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Cited By (15)
Publication number | Priority date | Publication date | Assignee | Title |
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DE2728464A1 (en) * | 1976-06-30 | 1978-01-05 | Nordtend Ab | PROCEDURES FOR THE PROTECTION AND CLEANING OF SURFACES SUBJECT TO CONTAMINATION WITH HYDROPHOBIC, IN PARTICULAR OILY SUBSTANCES |
US4200671A (en) * | 1978-05-05 | 1980-04-29 | The Dow Chemical Company | Method for removing paint from a substrate |
US4548967A (en) * | 1984-04-19 | 1985-10-22 | Nalco Chemical Company | Masking agent for paint spray booths |
EP0302813A2 (en) * | 1987-05-11 | 1989-02-08 | Helmuth Schmoock | Sheet having a metallized surface with a window, method and apparatus for its manufacture |
US4844833A (en) * | 1986-01-28 | 1989-07-04 | Kaken Kogyo, Co., Ltd. | Paint peeling composition and paint peeling method |
US4867900A (en) * | 1987-03-05 | 1989-09-19 | Kaken Kogyo, Co., Ltd. | Paint peeling composition |
US4877691A (en) * | 1985-11-27 | 1989-10-31 | Kay Chemical Company | Soil release agent and method to facilitate the cleaning of ovens used for cooking |
US5017303A (en) * | 1986-01-28 | 1991-05-21 | Kaken Tech Co., Ltd. | Paint peeling composition and paint peeling method |
EP0431239A1 (en) * | 1989-11-17 | 1991-06-12 | Patrick W. Marsek | Liquid spray method |
US5201946A (en) * | 1989-11-17 | 1993-04-13 | Marsek Patrick W | Liquid spray mask and method |
US5320682A (en) * | 1992-08-07 | 1994-06-14 | Chrysler Corporation | Method for cleaning paint residue from walls of a paint booth |
US5389138A (en) * | 1993-03-31 | 1995-02-14 | Kay Chemical Company | Oven pretreatment and cleaning composition containing silicone |
US5415923A (en) * | 1991-03-28 | 1995-05-16 | International Paper Company | Paint masking material comprising a fibrous base coated on one surface with a paint-permeable coating and coated on the other surface with a paint-impervious coating |
US5798325A (en) * | 1997-01-24 | 1998-08-25 | Henkel Corporation | Composition and process for barrier coating and/or cleaning paint masks |
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Cited By (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE2728464A1 (en) * | 1976-06-30 | 1978-01-05 | Nordtend Ab | PROCEDURES FOR THE PROTECTION AND CLEANING OF SURFACES SUBJECT TO CONTAMINATION WITH HYDROPHOBIC, IN PARTICULAR OILY SUBSTANCES |
US4200671A (en) * | 1978-05-05 | 1980-04-29 | The Dow Chemical Company | Method for removing paint from a substrate |
US4548967A (en) * | 1984-04-19 | 1985-10-22 | Nalco Chemical Company | Masking agent for paint spray booths |
US4877691A (en) * | 1985-11-27 | 1989-10-31 | Kay Chemical Company | Soil release agent and method to facilitate the cleaning of ovens used for cooking |
US4844833A (en) * | 1986-01-28 | 1989-07-04 | Kaken Kogyo, Co., Ltd. | Paint peeling composition and paint peeling method |
US5017303A (en) * | 1986-01-28 | 1991-05-21 | Kaken Tech Co., Ltd. | Paint peeling composition and paint peeling method |
US4867900A (en) * | 1987-03-05 | 1989-09-19 | Kaken Kogyo, Co., Ltd. | Paint peeling composition |
EP0302813A2 (en) * | 1987-05-11 | 1989-02-08 | Helmuth Schmoock | Sheet having a metallized surface with a window, method and apparatus for its manufacture |
EP0302813A3 (en) * | 1987-05-11 | 1990-02-28 | Helmuth Schmoock | Sheet having a metallized surface with a window, method and apparatus for its manufacture |
US5104711A (en) * | 1989-11-17 | 1992-04-14 | Marsek Patrick W | Liquid spray masking system and method |
EP0431239A1 (en) * | 1989-11-17 | 1991-06-12 | Patrick W. Marsek | Liquid spray method |
US5201946A (en) * | 1989-11-17 | 1993-04-13 | Marsek Patrick W | Liquid spray mask and method |
US5415923A (en) * | 1991-03-28 | 1995-05-16 | International Paper Company | Paint masking material comprising a fibrous base coated on one surface with a paint-permeable coating and coated on the other surface with a paint-impervious coating |
US5320682A (en) * | 1992-08-07 | 1994-06-14 | Chrysler Corporation | Method for cleaning paint residue from walls of a paint booth |
US5389138A (en) * | 1993-03-31 | 1995-02-14 | Kay Chemical Company | Oven pretreatment and cleaning composition containing silicone |
US5480493A (en) * | 1993-03-31 | 1996-01-02 | Kay Chemical Company | Method for cleaning a oven surface with a composition containing silicone |
US5662998A (en) * | 1993-03-31 | 1997-09-02 | Kay Chemical Company | Oven pretreatment and cleaning film containing silicone |
US5798325A (en) * | 1997-01-24 | 1998-08-25 | Henkel Corporation | Composition and process for barrier coating and/or cleaning paint masks |
CN104152044A (en) * | 2014-07-30 | 2014-11-19 | 郑州佰沃生物质材料有限公司 | Peanut protein coating and preparation method thereof |
CN104152044B (en) * | 2014-07-30 | 2016-04-20 | 郑州佰沃生物质材料有限公司 | A kind of Semen arachidis hypogaeae protein coating and preparation method thereof |
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