WO2001005898A1 - Paint stripper compositions - Google Patents

Paint stripper compositions Download PDF

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Publication number
WO2001005898A1
WO2001005898A1 PCT/IB2000/000945 IB0000945W WO0105898A1 WO 2001005898 A1 WO2001005898 A1 WO 2001005898A1 IB 0000945 W IB0000945 W IB 0000945W WO 0105898 A1 WO0105898 A1 WO 0105898A1
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Prior art keywords
composition
weight
foregoing
combination
aromatic
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PCT/IB2000/000945
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French (fr)
Inventor
Sergio Vitomir
Original Assignee
Napier Environmental Technologies Inc.
Priority date (The priority date 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 date listed.)
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Publication date
Application filed by Napier Environmental Technologies Inc. filed Critical Napier Environmental Technologies Inc.
Priority to AU55591/00A priority Critical patent/AU5559100A/en
Priority to JP2001511119A priority patent/JP2003505528A/en
Priority to CA002378886A priority patent/CA2378886A1/en
Publication of WO2001005898A1 publication Critical patent/WO2001005898A1/en

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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

Definitions

  • This invention relates to paint stripper compositions containing malic acid and methods of preparing the same.
  • 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.
  • 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 aqueous-based system for stripping various protective coatings.
  • the present invention is directed to a paint stripper composition
  • a paint stripper composition comprising (a) from about 5 to about 50% by weight of aromatic alcohol; (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.
  • 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 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 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.
  • the paint stripper composition of the present invention comprises (a) from about 5 to about 50% by weight of (i) an aromatic alcohol having the formula
  • 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 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.
  • the aromatic alcohol is benzyl alcohol.
  • compositions of the present invention initiates removal of paint or a coating on a substrate.
  • 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.
  • the paint stripper composition of the present invention spreads very well 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.
  • the protective coating on a substrate to which the composition is applied is polar, e.g. , polyurethanes
  • 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'-CH 2 -O-CH 2 -R 2 where R 1 and R 2 are hydrogen and phenyl or both phenyl.
  • a preferred 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 of the composition and the speed of penetration of the composition into paints and coatings.
  • the aromatic hydrocarbon solvent reduces the surface tension and evaporation rate of the composition.
  • 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 n H m (COOH) x OH y 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.
  • 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.
  • 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.
  • the peroxide generating agent is hydrogen peroxide, magnesium peroxide, or any combination of any of the foregoing.
  • the peroxide generating agent is hydrogen peroxide, magnesium peroxide, or any combination of any of the foregoing.
  • 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 composition 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, rheo logy modifying 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 solubihzer-emulsifier is polyethoxylated sorbitan monooleate.
  • the composition typically comprises from about 0.1 to about 5% by weight of solubihzer-emulsifier based upon 100% weight of total 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.
  • from about 0.5 to about 40 parts by weight of aromatic hydrocarbon cosolvent, from about 0.5 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.
  • 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.
  • 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.
  • 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.
  • 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.
  • Examples 1A and IB 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
  • Each paint stripper composition was tested as follows. A thin film of the composition was coated onto the test panel at room temperature (15-20° C). The effectiveness 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
  • Example 7 The paint stripper composition in Table 3 below was prepared by the method described in Examples 1-6.
  • 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.
  • Example 9 The paint stripper composition in Table 5 below was prepared by the method described in Examples 1-6.
  • Solvesso 200TM is available from Esso Corporation of Toronto, Canada.

Abstract

The present invention is directed to a paint stripping composition comprising (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; and (c) from about 15 to about 60 % by weight of water. The pH of the composition 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 aqueous-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 irritating 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 0.5 to about 20% by weight of malic acid; and (c) from about 15 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 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 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 5 to about 50% by weight of (i) an aromatic alcohol having the formula
Figure imgf000003_0001
where X, Y, and Z are all hydrogen or two hydrogens and a methyl, (ii) an aromatic alcohol having the formula
Figure imgf000003_0002
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 15 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 of the present invention spreads very well 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 (ε=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'-CH2-O-CH2-R2 where R1 and R2 are hydrogen and phenyl or both phenyl. A preferred 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 of the composition and the speed of penetration of the 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 CnHm(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. 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 composition 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, rheo logy modifying 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 solubihzer-emulsifier is polyethoxylated sorbitan monooleate. The composition typically comprises from about 0.1 to about 5% by weight of solubihzer-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 0.5 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. 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 IB
The paint stopper compositions of Examples 1-6 and Comparative
Examples 1A and IB 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 200™), 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
Figure imgf000010_0001
- Solvesso 200™ 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 (15-20° C). The effectiveness 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
Figure imgf000011_0001
Example 7 The paint stripper composition in Table 3 below was prepared by the method described in Examples 1-6.
Table 3
Figure imgf000012_0001
Solvesso 200™ 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
Figure imgf000013_0001
- Solvesso 200™ 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 5
Figure imgf000014_0001
Solvesso 200™ 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

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
Figure imgf000015_0001
wherein X, Y, and Z are all hydrogen or two hydrogens and a methyl,
(ii) an aromatic alcohol having the formula
Figure imgf000015_0002
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, wherein said composition has a pH of from about 2 to about 3.
2. The composition of claim 1 , wherein said aromatic alcohol is benzyl alcohol.
3. The composition of claim 1, wherein said composition comprises from about 5 to about 50% by weight of said aromatic alcohol.
4. The composition of claim 1 , further comprising an aromatic ether having the formula R'-CH2-O-CH2-R2 where R1 and R2 are hydrogen and phenyl or both phenyl.
5. The composition of claim 1, further comprising an aromatic hydrocarbon cosolvent.
6. The composition of claim 1, wherein said aromatic hydrocarbon cosolvent is a naphthalene depleted aromatic hydrocarbon cosolvent.
7. The composition of claim 1, wherein said aromatic hydrocarbon cosolvent has a flash point above about 150° F.
8. 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.
9. The composition of claim 1, wherein said composition further comprises a second hydroxycarboxylic acid having the formula CnHm(COOH)xOHy wherein n, x, and y are independently integers greater than 1 and m is equal to 2n+2- (x+y).
10. The composition of claim 9, wherein said second hydroxycarboxylic acid is glycolic acid.
11. The composition of claim 1 , wherein said composition further comprises a peroxide generating agent.
12. The composition of claim 11, wherein said peroxide generating agent is selected from the group consisting of hydrogen peroxide, magnesium peroxide, and any combination of any of the foregoing.
13. The composition of claim 1, wherein said composition further comprises a coupling agent, stabilizer, chelating agent, cooosion inhibitor, rheology modifying agent, evaporation retardant, solubihzer-emulsifier, and any combination of any of the foregoing.
14. The composition of claim 13, wherein said coupling agent is selected from the group consisting of alkylene glycols, dimethylsulfoxide, and any combination of any of the foregoing.
15. The composition of claim 13, 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.
16. The composition of claim 13, wherein said cooosion inhibitor is selected from the group consisting of benzotriazoles, borates, and any combination of any of the foregoing.
17. The composition of claim 13, 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.
18. The composition of claim 13 , 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.
19. The composition of claim 13, wherein said solubihzer-emulsifier is a polyethoxylated sorbitan ester, trioleate polysorbate, or a fluorinated alkyl ester.
20. 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.
21. The process of claim 20, wherein said polar phase further comprises from about 0.5 to about 40 parts by weight of aromatic hydrocarbon cosolvent.
22. The process of claim 20, wherein said polar phase further comprises from about 0.5 to about 30 parts of hydrogen peroxide.
23. 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.
PCT/IB2000/000945 1999-07-19 2000-07-12 Paint stripper compositions WO2001005898A1 (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1388575A1 (en) * 2002-08-09 2004-02-11 Scheidel GmbH & Co. KG Stripping composition
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

Families Citing this family (28)

* 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
AU2002360594A1 (en) * 2001-12-14 2003-06-30 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
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
EP1702050A4 (en) * 2003-12-16 2007-04-04 Solucorp Ind Ltd 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
WO2008142562A1 (en) * 2007-04-30 2008-11-27 Michael Brailsford Paint remover
EP2182811A4 (en) * 2007-08-15 2012-11-28 Virox Technologies Inc Antimicrobial compositions
US20090131296A1 (en) * 2007-11-21 2009-05-21 Ecolab Inc. Floor Stripper For Chemically-Resistant Crosslinked Floor Finishes
CA2753361A1 (en) 2009-02-09 2010-08-12 Advanced Biocatalytics Corporation Cleaning compositions and methods for burnt-on food and oil residues
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
SG11201907982TA (en) * 2017-03-28 2019-09-27 Neos Co Ltd Coating film stripping composition and method for stripping coating film
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
JP6953617B2 (en) * 2018-08-30 2021-10-27 株式会社ネオス Coating film peeling composition and coating film peeling method
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

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0497130A2 (en) * 1991-01-30 1992-08-05 Elf Atochem North America, Inc. Paint strippers
US5215675A (en) * 1992-03-16 1993-06-01 Isp Investments Inc. Aqueous stripping composition containing peroxide and water soluble ester
US5405548A (en) * 1991-01-30 1995-04-11 Elf Atochem North America Inc. Methylbenzyl formate paint strippers
EP0846735A1 (en) * 1996-12-06 1998-06-10 Elf Atochem S.A. Aqueous paint stripper for removing coatings and highly crosslinked primers
EP0903381A2 (en) * 1997-09-23 1999-03-24 McGean-Rohco Inc. Paint stripper compositions

Family Cites Families (25)

* 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
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
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
JPH09503812A (en) 1993-10-15 1997-04-15 ミネソタ マイニング アンド マニュファクチャリング カンパニー Improved paint remover
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
US5728666A (en) * 1996-12-19 1998-03-17 Napier International Technologies, Inc. Water-based alcohol hydroxycarboxylic peroxide compositions and their preparation
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

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0497130A2 (en) * 1991-01-30 1992-08-05 Elf Atochem North America, Inc. Paint strippers
US5405548A (en) * 1991-01-30 1995-04-11 Elf Atochem North America Inc. Methylbenzyl formate paint strippers
US5215675A (en) * 1992-03-16 1993-06-01 Isp Investments Inc. Aqueous stripping composition containing peroxide and water soluble ester
EP0846735A1 (en) * 1996-12-06 1998-06-10 Elf Atochem S.A. Aqueous paint stripper for removing coatings and highly crosslinked primers
EP0903381A2 (en) * 1997-09-23 1999-03-24 McGean-Rohco Inc. Paint stripper compositions

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1388575A1 (en) * 2002-08-09 2004-02-11 Scheidel GmbH & Co. KG Stripping composition
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

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US6465405B1 (en) 2002-10-15

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