CA2378886A1 - Paint stripper compositions - Google Patents

Paint stripper compositions Download PDF

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Publication number
CA2378886A1
CA2378886A1 CA002378886A CA2378886A CA2378886A1 CA 2378886 A1 CA2378886 A1 CA 2378886A1 CA 002378886 A CA002378886 A CA 002378886A CA 2378886 A CA2378886 A CA 2378886A CA 2378886 A1 CA2378886 A1 CA 2378886A1
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composition
weight
foregoing
combination
aromatic
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CA002378886A
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French (fr)
Inventor
Sergio Vitomir
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FREEWORLD COATINGS GLOBAL Pty Ltd
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Individual
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    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D9/00Chemical paint or ink removers

Abstract

The present invention is directed to a paint stripping composition comprisin g (a) from about 0.5 to about 50 % by weight of an aromatic alcohol, such as benzyl alcohol; (b) from about 0.5 to about 20 % by weight of malic acid; an d (c) from about 15 to about 60 % by weight of water. The pH of the compositio n broadly ranges from about 2 to about 3. The stripping composition of the present invention is free of chlorinated solvents, environmentally safe, and user-friendly. It is non-corrosive or only slightly corrosive to substrates, non-flammable, non-toxic, low odor, and fully biodegradable. A method of preparing the paint stripping composition is also provided.

Description

PAINT STRIPPER COMPOSITIONS
Field of the Invention This invention relates to paint stripper compositions containing malic acid and methods of preparing the same.
Background of the Invention For decades, strong acids and halocarbon solvent-based compositions were employed in stripping various protective coatings from metal and other substrates.
Increased awareness of the detrimental impact of such paint strippers on health and environment, in recent years, resulted in government legislative bodies all over the world restricting and/or prohibiting the use of these materials. Furthermore, these paint strippers often damaged the substrates to which they were applied.
Wilkins et al., U.S. Patent No. 5,215,675 provides an aqueous stripping composition based on a soluble ester such as ethyl lactate and a peroxide such as hydrogen peroxide.
Distaso, U.S. Patent No. 5,405,548 and U.S. Patent No. 5,542,986 describe the use of methylbenzyl formate or benzyl formate and formic acid in an aque-ous-based system for stripping various protective coatings.
However, these prior art compositions suffer from several disadvantages, namely, low solvency (low efficacy), high cost, corrosiveness, narrow range of stability, and extremely strong, unpleasant, and irntating odor.
Summary of the Invention The present invention is directed to a paint stripper composition comprising (a) from about 5 to about 50% by weight of aromatic alcohol; (b) from about 0. S to about 20% by weight of malic acid; and (c) from about 1 S to about 60%
by weight of water. The pH of the composition broadly ranges from about 2 to about 3.
The paint stripper composition of the present invention is free of chlorinated solvents, environmentally safe and user-friendly. It is also non-corrosive or only slightly corrosive to substrates, non-flammable, non-toxic, low odor, and fully biodegradable.
Another embodiment of the invention is a method of preparing the composition comprising dispersing (i) a polar phase containing (a) from about 0.5 to about 20 parts by weight of malic acid and (b) from about 1 S to about 60 parts by weight of deionized or distilled water into (ii) a non-polar phase containing from about 5 to about 50 parts by weight of aromatic alcohol.
Yet another embodiment of the invention is a method for removing paint or a coating from a substrate comprising applying a paint or coating removing effective amount of the paint stripper composition of the present invention.
Detailed Description of the Invention The paint stripper composition of the present invention comprises (a) from about S to about 50% by weight of (i) an aromatic alcohol having the formula X
Z
where X, Y, and Z are all hydrogen or two hydrogens and a methyl, (ii) an aromatic alcohol having the formula O-R-OH
where R is ethylene, propylene, or isopropylene, or (iii) a mixture thereof;
(b) from about 0.5 to about 20% by weight of malic acid; and (c) from about 1 S to about 60%
by weight of water based upon 100% weight of total composition. The composition preferably comprises (a) from about 25 to about 35% by weight of aromatic alcohol; (b) from about 0.5 to about 5% by weight of malic acid; and (c) from about 20 to about 50% by weight of water. More preferably, the composition comprises from about 0.5 to about 3% by weight of malic acid.
The composition typically has a pH of from about 2 to about 3.
Suitable aromatic alcohols include, but are not limited to, benzyl alcohol, phenoxy propanol, phenoxy ethanol, and any combination of any of the foregoing.
Preferably, the aromatic alcohol is benzyl alcohol.
The malic acid of the composition initiates removal of paint or a coating on a substrate. In particular, compositions of the present invention have been found to be very effective at removing antifouling paint from various substrates, including, but not limited to, polyester and metallic substrates. Malic acid is also non-corrosive to metallic substrates.
Additionally, malic acid is a good fluxing agent. Hence, the paint stripper composition ofthe present invention spreads verywell on solid surfaces, which improves the efficacy of stripping by reducing the waiting time for the paint to start lifting.
The presence of deionized water in the composition enhances the overall stripping effectiveness of the composition. When the protective coating on a substrate to which the composition is applied is polar, e.g., polyurethanes, the presence of a solvent with a high dielectric constant such as water (s=80.2@20°C) has a positive effect in separating charged areas, thus allowing other solvents in the composition to soften the coating.
The water preferably contains no more than about 1 % by weight of dissolved inorganic salts and preferably less than about 200 ppm. Distilled or deionized water having an electrical conductivity less than about 400 mho/cm is particularly preferred. Failure to follow the above specified water parameters may result in decomposition of peroxides in the composition, which may retard the stripping performance of the composition.
The composition may also include an aromatic ether having the formula R'-CHz-O-CHZ-Rz where R' and RZ are hydrogen and phenyl or both phenyl. A
preferred S aromatic ether is benzyl ether. The composition preferably includes from about 1 to about 30% by weight of aromatic ether based upon 100% weight of total composition.
The weight ratio of aromatic alcohol to aromatic ether is preferably from about 3:1 to about 1:1 and more preferably about 2.5:1.
An aromatic hydrocarbon cosolvent may be included in the composition.
The aromatic hydrocarbon cosolvent may be a mixture of one or more aromatic hydrocarbon solvents. The aromatic hydrocarbon cosolvent improves the stability of the composition thereby increasing the shelf life of the composition. It also improves the rheological properties ofthe composition and the speed ofpenetration ofthe composition into paints and coatings. Furthermore, the aromatic hydrocarbon solvent reduces the surface tension and evaporation rate of the composition. Preferably, the aromatic hydrocarbon solvent has a flash point above about 150°F and more preferably above about 190°F. Naphthalene depleted aromatic hydrocarbons are preferable since naphthalene has a noxious odor and is hazardous. Suitable aromatic hydrocarbon cosolvents, include, but are not limited to, Aromatic 200ND available from Exxon Chemicals of Houston, TX; Solvesso 200 available from Esso Corporation of Toronto, Canada; metaphenoxy benzyl alcohol; and any combination of any of the foregoing. The composition typically comprises from about 0.5 to about 40% by weight and more preferably from about 1 to about 30% by weight of aromatic hydrocarbon cosolvent based upon 100% weight of total composition. The weight ratio of water to aromatic hydrocarbon cosolvent is typically from about 30:1 to about 1.5:1 and preferably from about 20:1 to about 1.7:1.
The composition may include a second hydroxycarboxylic acid having the empirical formula C"Hm(COOH)XOHy where n, x, and y are independently integers greater than 1 and m is equal to 2n+2-(x+y), A preferred hydroxycarboxylic acid is glycolic acid.

S
The inventor has discovered that the combination of malic acid and glycolic acid in a paint stripper composition of the present invention greatly enhances removal of antifouling paint from a substrate. Preferably the composition contains from about 0.5 to about 10% by weight and more preferably from about 0.5 to about 3.5% by weight of the second hydroxycarboxylic acid based upon 100% weight of total composition.
A peroxide generating agent may also be included in the composition.
Preferably, the peroxide generating agent is hydrogen peroxide, magnesium peroxide, or any combination of any of the foregoing. On most metal surfaces, including aluminum and its alloys, a decomposition reaction of hydrogen peroxide takes place, generating an intermediate nascent oxygen which associates instantaneously, producing gaseous oxygen and water. The oxygen accelerates the stripping process by initiating the lifting of the softened protective coating and allowing new quantities of the paint stripping composi-tion to penetrate the metal-coating interface.
The composition typically comprises from about 0.5 to about 30% by weight and preferably from about 0.5 to about 10% by weight of peroxide generating agent based upon 100% weight of total composition. Paint stripper compositions of the present invention which contain hydrogen peroxide preferably have a pH less than about 3. At a pH above 3, the hydrogen peroxide begins to decompose. The malic acid in the composition stabilizes the composition and prevents the hydrogen peroxide from decomposing. The malic acid also lowers the pH of the composition, which further stabilizes the hydrogen peroxide.
The composition may include other adjuvants such as coupling agents, stabilizers, chelating agents, corrosion inhibitors, rheologymodifying agents, evaporation retardants, solubilizer-emulsifiers, and any combination of any of the foregoing.
Suitable coupling agents include, but are not limited to, alkylene glycols, dimethylsulfoxide (DMSO), and any combination of any of the foregoing. A
preferred coupling agent is propylene glycol. The composition typically comprises from about 0.5 to about 5% by weight of coupling agent based upon 100% weight of total composition.

Suitable stabilizers include, but are not limited to, acetanilide. The composition typically comprises from about 0.01 to about 3% by weight of stabilizer based upon 100% weight of total composition.
Suitable chelating agents include, but are not limited to, phosphonic acids, such as bis(hexamethylene)triamino penta(methylene phosphonic) acid and phosphoric acid; citric acid; ethylenediaminetetraacetic acid (EDTA); and any combination of any of the foregoing. The composition typically comprises from about 0.5 to about 4% by weight of chelating agent based upon 100% weight of total composition.
Suitable corrosion inhibitors include, but are not limited to, benzotriazoles, such as 2-mercaptobenzothiazole, toluoltriazole, benzotriazole, 2(3H) benzothiazolethione; borates; and any combination of any of the foregoing. The composition typically comprises from about 0.3 to about 3% by weight of corrosion inhibitor based upon 100% weight of total composition.
Suitable rheology modifying agents include, but are not limited to, hydroxypropyl cellulose, hydroxypropyl methyl cellulose, hydroxyethyl cellulose, fumed silica, precipitated silica, castor oil, and any combination of any of the foregoing. A
preferred rheology modifying agent is hydroxypropyl cellulose. The composition typically comprises from about 0.1 to about 3% by weight of rheology modifying agent based upon 100% weight of total composition.
Suitable evaporation retardants include, but are not limited to, silicone fluid, a water-based wax emulsion, paraffin oil, paraffin wax, and any combination of any of the foregoing. A preferred evaporation retardant is paraffin wax. The composition typically comprises from about 0.1 to about 3 % by weight of evaporation retardant based upon 100% weight of total composition.
Suitable solubilizer-emulsifiers include, but are not limited to, fluorinated alkyl esters; polyethoxylated sorbitan ester, such as polyethoxylated sorbitan monolaurate, polyethoxylated sorbitan monopalmitate, polyethoxylated sorbitan monostearate, polyethoxylated sorbitan tristearate, and polyethoxylated sorbitan monooleate; trioleate polysorbates; and any combination of any of the foregoing. A

preferred solubilizer-emulsifier is polyethoxylated sorbitan monooleate. The composition typically comprises from about 0.1 to about 5% by weight of solubilizer-emulsifier based upon 100% weight of total composition.
Other adjuvants as known to those skilled in the art may also be included in the composition.
The paint stripper compositions of the present invention is prepared by admixing, (i) a polar phase comprising malic acid and deionized or distilled water with (ii) a non-polar phase comprising aromatic alcohol.
The polar phase is prepared by admixing, with continuous mixing, from about 0.5 to about 20 parts by weight of malic acid and from about 15 to about 60 parts by weight of deionized or distilled water. Preferably, from about 0.5 to about 40 parts by weight of aromatic hydrocarbon cosolvent, from about 0. S to about 10 parts by weight of a peroxide generating agent, and from about 0.5 to about 10 parts by weight of the aforementioned second hydroxycarboxylic acid are added to the polar phase. A
coupling agent, emulsifier/solubilizer, stabilizer, and chelating agent may also be added to the polar phase.
Though hydrogen peroxide is commercially available at concentrations up to 70% by weight, the use of 30-35% concentration is preferred. Such concentrations can be achieved by diluting the higher concentration grades of hydrogen peroxide with deion-ized water.
An aromatic ether, evaporation retardant, corrosion inhibitor, and rheology modifying agent may be added to the non-polar phase. Typically, the non-polar phase comprises from about 10 to about 80 parts by weight and preferably from about 10 to about 50 parts by weight of the paint stripper composition based upon 100 parts by weight of total composition.
The compositions of the present invention are useful in removing and stripping paints, such as oil-based paints, and various other protective coatings, such as epoxies, polysulfides, urethanes, polyurethanes, vinyl esters, alkyds, and acrylics. A paint or coating removing and/or stripping effective amount of the composition is applied to the substrate. When the composition is applied as a paste, the composition is typically applied with a thickness equal to that of the coating to be removed. The stripper composition may need to be applied one or more times to remove one or more coatings from a substrate.
S Examples of suitable substrates include, but are not limited to, metallic substrates, such as steel, aluminum, and their alloys; polyester substrates, such as gelcoated substrates; and composites, such as Kevlar~ available from E.I. du Pont de Nemours and Company of Wilmington, DE.
Methods of applying the stripper include, but are not limited to, spraying, soaking, immersing, brushing, and the like.
Description of the Preferred Embodiments The following examples illustrate the invention without limitation. All parts and percentages are given by weight unless otherwise indicated.
Examples 1-6 and Comparative Examples 1A and 1B
The paint stripper compositions of Examples 1-6 and Comparative Examples 1A and 1B in Table 1 were prepared as follows. All amounts in Table 1 are given in parts by weight. Paraffin wax, benzotriazole, and hydroxypropyl cellulose were added to benzyl alcohol with continuous mixing to form a non-polar mixture. A
polar mixture was prepared by admixing malic acid, deionized water, propylene glycol, sorbitan monooleate, an aromatic hydrocarbon cosolvent (Solvesso 200TM), hydrogen peroxide, and glycolic acid. The non-polar mixture was dispersed for about 2 to about 3 hours into the polar mixture to form the paint stripper composition. The paint stripper compositions were stored for 7 days before being tested.

Table 1 Ingredient Examples Comparativ a Examples Benzyl Alcohol 35.0 35.0 35.0 35.0 35.0 35.0 35.0 35.0 Solvesso 200TM' 3.80 3.80 3.80 3.80 3.80 3.80 3.80 3.80 Malic Acid 1.00 3.00 3.00 3.00 5.00 10.0 Glycolic Acid 0.50 3.00 0.50 5.00 3.00 Hydrogen Peroxide 0.50 0.50 0.50 0.50 5.00 10.0 Polysorbate Ester 5.00 5.00 5.00 5.00 5.00 5.00 5.00 5.00 Hydroxypropyl 0.25 0.25 0.25 0.25 0.25 0.25 0.25 0.25 Cellulose Propylene Glycol 5.00 5.00 5.00 5.00 5.00 5.00 5.00 5.00 Paraffin Wax 0.20 0.20 0.20 0.20 0.20 0.20 0.20 0.20 Deionized Water Balance to ' - Solvesso 200TM is available from Esso Corporation of Toronto, Canada.
8 aluminum alloy 2024-T3 test panels (4" x 5") were primed with MIL-P-85582B (Product No. 44-GN24) Water Borne and topcoated with MIL-C-85285BC
(Product No. 03-W-127A) colour 17925, available from Deft Inc. of Irvine, CA.
Each paint stripper composition was tested as follows. A thin film of the composition was coated onto the test panel at room temperature (1 S-20 ° C). The effec-tiveness of the composition was evaluated as a percent of removed coating as a function of time. The results are shown in Table 2 below.

Table 2 Paint Stripper Percentage of Percentage Time of Composition Topcoat RemovedPrimer Removed Example 1 100 100 5 hours S Example 2 100 100 4 hours, 1 S

minutes Example 3 100 100 3 hours, 45 minutes Example 4 100 100 3 hours, 50 minutes Example S 100 100 4 hours Example 6 80 50 24 hours 10 Comparative 20 0 24 hours Example 1A

Comparative 80 10 24 hours Example 1B

Example 7 The paint stripper composition in Table 3 below was prepared by the method described in Examples 1-6.

Table 3 Ingredient % Weight Benzyl Alcohol 35.00 Solvesso 200T"' z 5.60 Paraffin Wax 0.30 Polyethoxylated Sorbitan Monooleate0.50 Glycolic Acid 3.00 Hydroxypropyl Cellulose 0.50 Hydrogen Peroxide 0.50 Propylene Glycol 1.50 Malic Acid 1.20 Water S 1.90 Total 100.00 z - Solvesso 200TM is available from Esso Corporation of Toronto, Canada.
Example 8 The paint stripper composition in Table 4 below was prepared by the method described in Examples 1-6.

Table 4 Ingredient % Weight Benzyl Alcohol 35.00 Solvesso 2OOTM 3 6.60 Paraffin Wax 0.30 Polyethoxylated Sorbitan Monooleate0.50 Hydroxypropyl Cellulose 0.37 Hydrogen Peroxide 4.00 Propylene Glycol 1.50 Malic Acid 1.00 Water 50.73 Total 100.00 3 - Solvesso 200TM is available from Esso Corporation of Toronto, Canada.

Example 9 The paint stripper composition in Table 5 below was prepared by the method described in Examples 1-6.
Table S
Ingredient % Weight Benzyl Alcohol 35.00 Solvesso 200T"'' 4 6.60 Paraffin Wax 0.30 Polyethoxylated Sorbitan Monooleate0.50 Hydroxypropyl Cellulose 0.50 Propylene Glycol 1.50 Malic Acid 1.20 Water 54.40 Total 100.00 4 - Solvesso 200TM is available from Esso Corporation of Toronto, Canada.
All patents, applications, articles, publications, and test methods mentioned above are hereby incorporated by reference.
Many variations of the present invention will suggest themselves to those skilled in the art in light of the above detailed description. Such obvious variations are within the full intended scope of the appended claims.

Claims (24)

What is claimed is:
1. An aqueous paint stripper composition comprising:
(a) from about 5 to about 50% by weight of (i) an aromatic alcohol having the formula wherein X, Y, and Z are all hydrogen or two hydrogens and a methyl, (ii) an aromatic alcohol having the formula wherein R is ethylene, propylene, or isopropylene, or (iii) a mixture thereof;
(b) from about 0.5 to about 20% by weight of malic acid; and (c) from about 15 to about 60% by weight of water.
2. The composition of claim 1, wherein said composition has a pH
of from about 2 to about 3.
3. The composition of claim 1, wherein said aromatic alcohol is benzyl alcohol.
4. The composition of claim 1, wherein said composition comprises from about 5 to about 50% by weight of said aromatic alcohol.
5. The composition of claim 1, further comprising an aromatic ether having the formula R1-CH2-O-CH2-R1 where R1 and R2 are hydrogen and phenyl or both phenyl.
6. The composition of claim 1, further comprising an aromatic hydrocarbon cosolvent.
7. The composition of claim 1, wherein said aromatic hydrocarbon cosolvent is a naphthalene depleted aromatic hydrocarbon cosolvent.
8. The composition of claim 1, wherein said aromatic hydrocarbon cosolvent has a flash point above about 150° F.
9. The composition of claim 1, wherein the weight ratio of water to aromatic hydrocarbon cosolvent is from about 30:1 to about 1.5:1.
10. The composition of claim 1, wherein said composition further comprises a second hydroxycarboxylic acid having the formula C n H m(COOH)x OH
y wherein n, x, and y are independently integers greater than 1 and m is equal to 2n+2-(x+y).
11. The composition of claim 10, wherein said second hydroxycarboxylic acid is glycolic acid.
12. The composition of claim 1, wherein said composition further comprises a peroxide generating agent.
13. The composition of claim 12, wherein said peroxide generating agent is selected from the group consisting of hydrogen peroxide, magnesium peroxide, and any combination of any of the foregoing.
14. The composition of claim 1, wherein said composition further comprises a coupling agent, stabilizer, chelating agent, corrosion inhibitor, rheology modifying agent, evaporation retardant, solubilizer-emulsifier, and any combination of any of the foregoing.
15. The composition of claim 14, wherein said coupling agent is selected from the group consisting of alkylene glycols, dimethylsulfoxide, and any combination of any of the foregoing.
16. The composition of claim 14, wherein said chelating agent is selected from the group consisting of phosphonic acids, citric acid.
ethylenediaminetetraacetic acid, and any combination of any of the foregoing.
17. The composition of claim 14, wherein said corrosion inhibitor is selected from the group consisting of benzotriazoles, borates, and any combination of any of the foregoing.
18. The composition of claim 14, wherein said rheology modifying agent is selected from the group consisting of hydroxypropyl cellulose, hydroxypropyl methyl cellulose, hydroxyethyl cellulose, fumed silica, precipitated silica, castor oil, and any combination of any of the foregoing.
19. The composition of claim 14, wherein said evaporation retardant is selected from the group consisting of silicone fluid, water-based wax emulsion, paraffin oil, paraffin wax, and any combination of any of the foregoing.
20. The composition of claim 14, wherein said solubilizer-emulsifier is a polyethoxylated sorbitan ester, trioleate polysorbate, or a fluorinated alkyl ester.
21. A process for preparing a paint stripper composition, said process comprising dispersing (i) a polar phase containing from about 0.5 to about 20 parts by weight of malic acid and from about 15 to about 60 parts by weight of deionized or distilled water into (ii) a non-polar phase containing from about 5 to about 50 parts by weight of benzyl alcohol to form said paint stripper composition.
22. The process of claim 21, wherein said polar phase further comprises from about 0.5 to about 40 parts by weight of aromatic hydrocarbon cosolvent.
23. The process of claim 21, wherein said polar phase further comprises from about 0.5 to about 30 parts of hydrogen peroxide.
24. A method for removing paint or a coating from a substrate comprising applying a paint or coating removing effective amount of the aqueous paint stripper composition of claim 1.
CA002378886A 1999-07-19 2000-07-12 Paint stripper compositions Abandoned CA2378886A1 (en)

Applications Claiming Priority (3)

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US09/356,437 1999-07-19
US09/356,437 US6200940B1 (en) 1999-07-19 1999-07-19 Paint stripper compositions
PCT/IB2000/000945 WO2001005898A1 (en) 1999-07-19 2000-07-12 Paint stripper compositions

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AU (1) AU5559100A (en)
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WO (1) WO2001005898A1 (en)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6200940B1 (en) * 1999-07-19 2001-03-13 Napier International Technologies, Inc. Paint stripper compositions
US6887837B2 (en) * 2001-01-04 2005-05-03 Henkel Kommandirgesellschaft Auf Aktien Water-based paint-removing solution
US7179774B2 (en) * 2002-06-19 2007-02-20 Henkel Kommanditgesellschaft Auf Aktien Flushing solutions for coatings removal
US7482316B2 (en) * 2001-01-04 2009-01-27 Henkel Kommanditgesellschaft Auf Aktien Water-based flushing solution for paints and other coatings
CA2470021A1 (en) * 2001-12-14 2003-06-26 Aero-Chem, Llc Cyclic ether based paint remover
DE10161844A1 (en) * 2001-12-15 2003-06-26 Henkel Kgaa Aqueous alkaline paint stripper
US7091163B2 (en) * 2002-06-25 2006-08-15 Henkel Kommanditgesellschaft Auf Aktien Flushing solutions for coatings removal
DE10236512A1 (en) * 2002-08-09 2004-02-19 Scheidel Gmbh & Co. Kg paint stripper
US7179775B2 (en) * 2002-09-11 2007-02-20 Henkel Kommanditgesellschaft Auf Aktien Coating removal compositions
US7052556B1 (en) * 2003-03-10 2006-05-30 Montie-Targosz Enterprises, Llc Process for removal of paint from plastic substrates
CA2591547A1 (en) * 2003-12-16 2006-06-30 Peter J. Hurley Heavy metal-remediating paint stripper
US7462587B2 (en) * 2004-04-29 2008-12-09 General Chemical Corp Composition for removing a film from a substrate, a method of removing a film from a substrate, and a method of making the composition
US7674760B2 (en) * 2005-10-18 2010-03-09 Ecolab Inc. Floor stripper/cleaner containing organic acid-base pair
AU2008252561A1 (en) * 2007-04-30 2008-11-27 Peel Away Limited Paint remover
CA2697249C (en) * 2007-08-15 2016-10-04 Virox Technologies Inc. Antimicrobial compositions
US20090131296A1 (en) * 2007-11-21 2009-05-21 Ecolab Inc. Floor Stripper For Chemically-Resistant Crosslinked Floor Finishes
BRPI1008022A2 (en) 2009-02-09 2016-03-15 Advanced Biocatalystics Corp composition, and method for removing residues from organic foods or oil
WO2014032166A1 (en) * 2012-08-29 2014-03-06 Protocol Environmental Solutions, Inc. Antifouling paint remover
WO2014041010A1 (en) * 2012-09-11 2014-03-20 Akzo Nobel Chemicals International B.V. Stabilization of paint stripper formulations
US9090851B2 (en) 2013-03-13 2015-07-28 Hydrite Chemical Co. Oil extraction method and composition for use in the method
US9816050B2 (en) 2014-10-27 2017-11-14 Dean Blankenburg Oil extraction method and composition for use in the method
DE102015116486B4 (en) 2015-09-29 2020-04-23 ESC GmbH Ingenieursgesellschaft für Oberflächen-Reinigungstechnik Process for stripping light alloy wheels from motor vehicles
JP7218286B2 (en) * 2017-03-28 2023-02-06 株式会社ネオス Coating stripping composition and coating stripping method
US11827812B2 (en) 2017-06-20 2023-11-28 W.M. Barr & Company, Inc. Paint remover composition and method of making
US11708502B2 (en) 2017-06-20 2023-07-25 W.M. Barr & Company, Inc. Paint remover composition and method of making
US10450535B2 (en) 2017-10-18 2019-10-22 Virox Technologies Inc. Shelf-stable hydrogen peroxide antimicrobial compositions
US20190330481A1 (en) * 2018-04-27 2019-10-31 W.M. Barr & Company, Inc. Paint remover having reduced flammability
US10891136B1 (en) 2018-05-22 2021-01-12 Marvell Asia Pte, Ltd. Data transmission between memory and on chip memory of inference engine for machine learning via a single data gathering instruction
WO2020045361A1 (en) * 2018-08-30 2020-03-05 株式会社ネオス Coating film removing composition and method for removing coating film
JP7264087B2 (en) * 2020-02-28 2023-04-25 日信化学工業株式会社 Coating stripping agent and stripping method using the coating stripping agent
JP2021134319A (en) * 2020-02-28 2021-09-13 日信化学工業株式会社 Coated film-peeling agent and peeling method using coated film-peeling agent

Family Cites Families (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3355385A (en) 1965-06-18 1967-11-28 Pennsalt Chemical Corp Process for removing organic coatings
US4120810A (en) 1974-10-07 1978-10-17 Palmer David A Paint remover with improved safety characteristics
US3979219A (en) 1975-03-06 1976-09-07 Fremont Industries, Inc. Wood finish remover
US4269724A (en) 1980-02-13 1981-05-26 Hodson James V Composition for paint stripper
US4683157A (en) 1982-11-15 1987-07-28 Mosser Mark F Thixotropic coating compositions and methods
US4732695A (en) 1987-02-02 1988-03-22 Texo Corporation Paint stripper compositions having reduced toxicity
US4812255A (en) 1987-03-04 1989-03-14 Gaf Corporation Paint removing compositions
US5015410A (en) 1990-02-20 1991-05-14 Arco Chemical Technology, Inc. Paint stripper compositions containing N-methyl-2-pyrrolidone, aliphatic hydrocarbons, and aromatic hydrocarbons
AU640069B2 (en) 1991-01-30 1993-08-12 Atofina Chemicals, Inc. Paint strippers
US5405548A (en) 1991-01-30 1995-04-11 Elf Atochem North America Inc. Methylbenzyl formate paint strippers
US5106525A (en) 1991-04-12 1992-04-21 Arco Chemical Technology, L.P. Paint stripper compositions containing gamma-butyrolactone
US5391234A (en) * 1991-08-05 1995-02-21 Henkel Corporation Cleaning or stripping composition and method
US5319055A (en) 1991-10-18 1994-06-07 Rohm And Haas Company Non-aqueous thickening agents
US5215675A (en) 1992-03-16 1993-06-01 Isp Investments Inc. Aqueous stripping composition containing peroxide and water soluble ester
US5387363A (en) 1992-06-02 1995-02-07 Elf Atochem North America, Inc. Water in oil emulsions
US5454985A (en) 1992-11-06 1995-10-03 Gage Products Company Paint stripping composition
JP2906201B2 (en) 1992-12-09 1999-06-14 花王株式会社 Hair cosmetics
US5425893A (en) 1993-04-14 1995-06-20 Stevens; Edwin Photoreactive paint stripping compositions and methods
EP0723568B1 (en) 1993-10-15 1999-05-26 Minnesota Mining And Manufacturing Company Improved paint stripper
US5411678A (en) 1994-02-07 1995-05-02 Mcgean-Rohco, Inc. Paint stripper
US5569410A (en) 1994-11-17 1996-10-29 Elf Atochem North America, Inc. Ammonium bicarbonate/ammonium carbamate activated benzyl alcohol paint stripper
JP2911792B2 (en) * 1995-09-29 1999-06-23 東京応化工業株式会社 Stripper composition for resist
US6221823B1 (en) * 1995-10-25 2001-04-24 Reckitt Benckiser Inc. Germicidal, acidic hard surface cleaning compositions
JP3236220B2 (en) * 1995-11-13 2001-12-10 東京応化工業株式会社 Stripper composition for resist
FR2756835B1 (en) 1996-12-06 1999-03-26 Atochem Elf Sa AQUEOUS COMPOSITIONS FOR THE SCRAPING OF HIGH-CROSS-LINKING PAINTS AND PRIMERS
US5728666A (en) * 1996-12-19 1998-03-17 Napier International Technologies, Inc. Water-based alcohol hydroxycarboxylic peroxide compositions and their preparation
SG73541A1 (en) 1997-09-23 2000-06-20 Rohco Inc Mcgean Paint stripper compositions
US5977042A (en) * 1998-10-01 1999-11-02 S. C. Johnson Commercial Markets, Inc. Concentrated stripper composition and method
US5928435A (en) * 1998-11-11 1999-07-27 Enthone-Omi, Inc. Method for removing organic coatings from substrates using carboxylic acids, organic solvents, and corrosion inhibitors
US6200940B1 (en) * 1999-07-19 2001-03-13 Napier International Technologies, Inc. Paint stripper compositions

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US6200940B1 (en) 2001-03-13
JP2003505528A (en) 2003-02-12

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