US2705207A - Method for removing paint and varnish - Google Patents

Method for removing paint and varnish Download PDF

Info

Publication number
US2705207A
US2705207A US426943A US42694354A US2705207A US 2705207 A US2705207 A US 2705207A US 426943 A US426943 A US 426943A US 42694354 A US42694354 A US 42694354A US 2705207 A US2705207 A US 2705207A
Authority
US
United States
Prior art keywords
film
varnish
paint
alcohol
softened
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US426943A
Inventor
Ralph E Stevens
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Individual
Original Assignee
Individual
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.)
Filing date
Publication date
Application filed by Individual filed Critical Individual
Priority to US426943A priority Critical patent/US2705207A/en
Application granted granted Critical
Publication of US2705207A publication Critical patent/US2705207A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C09D9/005Chemical paint or ink removers containing organic solvents

Definitions

  • This invention relates, as indicated, to a process for paint or varnish removal, and more specifically to a method for preparing furniture or the like for refinishing.
  • Another object is to provide an improved method for removing dried paint, varnish, enamel, etc. films in which the chemical agents used are less irritating to the refinishers.
  • Still another object is to provide an improved method for paint, varnish, etc. removal which yields more complete removal of the old film from intricate design or mill work necessitating little or no further preparation before refinishing.
  • Another object of this invention is to provide an improved method for paint, varnish and lacquer removal in which the old film is removed as substantially larger continuous sheets than heretofore.
  • this invention comprises the provision of an improved method for removal of dried organic films from a substrate which comprises coating said film with a composition comprising a major amount of a liquid halogen-containing alkane of no more than 2 carbon atoms and having a boilin'gpoint less than about 100 C. and a minor amount of a cellulose derivative, and after the dried film has softened, overcoating the softened film with a composition comprising in admixture a normally liquid hydrocarbon, an alcohol and an ester of an aliphatic carboxylic acid and an alcohol, which ester contains from 3 to 5 carbon atoms, and then stripping the resulting soft film from the substrate.
  • the swelling agent which loosens the film from the substrate and permits ready removal of the entire mass from the substrate.
  • halogens may be present as the swelling agents for the initial treating fluid.
  • Such normally liquid halogen-containing methanes or ethanes are usually present in non-flammable paint and varnish removers.
  • a second essential ingredient of the first treating liquid is a film-forming material which while preferably, although not necessarily, soluble in the composition, is or becomes a surface coating acting as a blotter for the halogen compound-varnish solvate.
  • a very satisfactory class of such film formers includes the water-insoluble gums, e. g., cellulose ethers and esters of both organic and inorganic acids.
  • cellulose ethers and esters of both organic and inorganic acids e. g., cellulose ethers and esters of both organic and inorganic acids.
  • theweight ratio of the halogen compound to the cellulose film-forming com- To improve the solubility of the cellulose derivative in the system, a small amount of alcohol, e. g., methyl, ethyl, iso-propyl alcohol, or mixed alcohols may be used.
  • the composition may also contain an HCl acceptor to improve shelf stability of the composition. Alkylene oxides may be used for this purpose. Such additional ingredients enhance the practical utility of the basic two component paint and varnish remover.
  • the second treating liquid is usually applied after the first has had at least a minimum of 30 seconds to work on the old film. it may, however, be applied with a longer or shorter lapse of time.
  • the purpose of the second liquid is two-fold. It contains a powerful solvent, e. g., acetone, dioxane, or an acetate ester of methyl, ethyl, propyl, butyl, or amyl alcohols such ascommonly employed in lacquer solvents. It also contains a material which is a solvent for the lacquer solvent agent, but which is in itself a poor solvent for cellulose derivatives. These are usually aliphatic hydrocarbons of petroleum origin or aromatic hydrocarbons, or a blend of both.
  • aliphatic hydrocarbons useful herein are any of the normally liquid aliphatic hydrocarbons boiling below about 400 F., e. g., petroleum fractions such as kerosene, gas oil, gasolene, mineral spirits, petroleum ether, etc., or the refined materials such as hexane, heptane, cyclohexane, octane, decane, etc. It apparently makes no difference whether the aliphatic hydrocarbon is saturated or unsaturated.
  • the aromatic hydrocarbons useful herein include benzene, toluene and xylene.
  • hydrocarbon portion of the second composition usually amounts to from 50% to 75% by weight, and may be a single hydrocarbon or a mixture of members selected from the three classes of hydrocarbons mentioned above.
  • An essential component of the second treating solution is an aliphatic alcohol, e. g., methyl, ethyl, or iso-propyl alcohol or a mixture thereof. From 4% to 10% by weight of the second solution is alcohol.
  • Solution B may be admixed with a normally gaseous propellant material, e. g., a' fluorochloro methane, such as FzCClz, etc., and applied from an aerosol can as a fine spray.
  • a normally gaseous propellant material e. g., a' fluorochloro methane, such as FzCClz, etc.
  • the method of removing a dried organic film from a substrate comprising coating said film with a paint and varnish remover comprising a major amount of a normally liquid halogen-containing alkene of no more than 2 carbon atoms and having a boiling point less than about 100 C., and a minor amount of a cellulose derivative, after the old film has softened, overcoating the softened film with a second composition comprising in admixture a normally liquid hydrocarbon, an alcohol, and an ester of an aliphatic carboxylic acid and an alcohol, which ester contains from 3 to 5 carbon atoms, and then stripping the resulting softened and loosened old film from the substrate.
  • the second composition comprises in admixture a mixture of normally liquid hydrocarbons,an aliphatic alcohol, and an ester of acetic acid and a low molecular weight alcohol of no more than 3 carbon atoms.
  • the normally liquid hydrocarbon is a mixture of an aliphatic hydrocarbon, an aromatic hydrocarbon and a terpene hydrocarbon.

Description

United States Patent Ofiiice 2,705,207 Patented Mar. 29, 1955 METHOD FOR REMOVING PAINT AND VARNISH Ralph E. Stevens, Toledo, Ohio N Drawing. Application April 30, 1954, Serial No. 426,943
9 Claims. (Cl. 134-26) This invention relates, as indicated, to a process for paint or varnish removal, and more specifically to a method for preparing furniture or the like for refinishing.
Prior practice in surface refinishing has evolved from the earlier mechanical techniques of sanding, scraping, and burning to the current practice of employing solvents. While much of the hard labor is now avoided with such solvents, this has been achieved at the expense of neatness. Solvent removal methods do reduce the time required over the earlier methods. However, the chemicals used frequently burn and dry out the skin of the worker. The soft gummy residue that is produced quickly clogs tools used to remove it, e. g., steel wool, spatulas, etc. If the surface from which the old dried film is being removed is certain types of mill work or filigree, it is very difficult to clean the surface.
It is a principal object of this invention, therefore, to provide an improved method for removing paint, lacquer, and varnish films from a substrate.
Another object is to provide an improved method for removing dried paint, varnish, enamel, etc. films in which the chemical agents used are less irritating to the refinishers.
Still another object is to provide an improved method for paint, varnish, etc. removal which yields more complete removal of the old film from intricate design or mill work necessitating little or no further preparation before refinishing.
Another object of this invention is to provide an improved method for paint, varnish and lacquer removal in which the old film is removed as substantially larger continuous sheets than heretofore.
Other objects of this invention appear as the description proceeds.
To the accomplishment of the foregoing and related ends, said invention, then, consists of the means hereinafter fully described and particularly pointed out in the appended claims, the following description setting forth in detail certain illustrative embodiments of the invention, such disclosed means constituting, however, but a few of the various forms in which the principle of this invention may be employed.
Broadly stated, this invention comprises the provision of an improved method for removal of dried organic films from a substrate which comprises coating said film with a composition comprising a major amount of a liquid halogen-containing alkane of no more than 2 carbon atoms and having a boilin'gpoint less than about 100 C. and a minor amount of a cellulose derivative, and after the dried film has softened, overcoating the softened film with a composition comprising in admixture a normally liquid hydrocarbon, an alcohol and an ester of an aliphatic carboxylic acid and an alcohol, which ester contains from 3 to 5 carbon atoms, and then stripping the resulting soft film from the substrate.
Thus this invention contemplates the sequential treatment of a hardened paint, varnish or lacquer film with two liquid compositions, the first of which is a combination of a swelling agent and a film-forming material, and the second of which contains non-solvent diluents and low boiling solvents for both the old film and the new film. The solvent action is believed to be such as to cause partial intermingling of the new and the old films for adhesion of one to the other but on evaporation from the mass leaves behind a film system which is insoluble in the remaining solvents and diluents. The film also entraps pound is from about 5:1 to about 25:1.
the swelling agent which loosens the film from the substrate and permits ready removal of the entire mass from the substrate.
As above indicated, a principal ingredient of the remover system is a normally liquid halogen-containing alkane of no more than two carbon atoms having a boiling point of less than about C. There are relatively few materials which are thus included among which may be mentioned methylene chloride, ethylene chloride, methylene bromide, ethylidene dichloride, 2,2-difluorol,2-dibromoethane, 2,2-difluoro-1,l-dichloroethane, 2,2- difluoro-l-iodoethane, carbon tetrachloride. Chloroform will Work, but for obvious reasons its use is not recommended. Thus, any halogen, i. e., chlorine, bromine, iodine, or fluorine, and combination of halogens may be present as the swelling agents for the initial treating fluid. Such normally liquid halogen-containing methanes or ethanes are usually present in non-flammable paint and varnish removers.
A second essential ingredient of the first treating liquid is a film-forming material which while preferably, although not necessarily, soluble in the composition, is or becomes a surface coating acting as a blotter for the halogen compound-varnish solvate. A very satisfactory class of such film formers includes the water-insoluble gums, e. g., cellulose ethers and esters of both organic and inorganic acids. Thus, nitrocellulose, cellulose acetate, cellulose acetate-butyrate, cellulose propionate, cellulose acetate-propionate, and other such aliphatic carboxylic acid esters of cellulose; ethoxy cellulose, benzyl cellulose, etc.
In the paint and varnish remover, theweight ratio of the halogen compound to the cellulose film-forming com- To improve the solubility of the cellulose derivative in the system, a small amount of alcohol, e. g., methyl, ethyl, iso-propyl alcohol, or mixed alcohols may be used. The composition may also contain an HCl acceptor to improve shelf stability of the composition. Alkylene oxides may be used for this purpose. Such additional ingredients enhance the practical utility of the basic two component paint and varnish remover.
The second treating liquid is usually applied after the first has had at least a minimum of 30 seconds to work on the old film. it may, however, be applied with a longer or shorter lapse of time. The purpose of the second liquid is two-fold. It contains a powerful solvent, e. g., acetone, dioxane, or an acetate ester of methyl, ethyl, propyl, butyl, or amyl alcohols such ascommonly employed in lacquer solvents. It also contains a material which is a solvent for the lacquer solvent agent, but which is in itself a poor solvent for cellulose derivatives. These are usually aliphatic hydrocarbons of petroleum origin or aromatic hydrocarbons, or a blend of both. Examples of aliphatic hydrocarbons useful hereinare any of the normally liquid aliphatic hydrocarbons boiling below about 400 F., e. g., petroleum fractions such as kerosene, gas oil, gasolene, mineral spirits, petroleum ether, etc., or the refined materials such as hexane, heptane, cyclohexane, octane, decane, etc. It apparently makes no difference whether the aliphatic hydrocarbon is saturated or unsaturated. The aromatic hydrocarbons useful herein include benzene, toluene and xylene.
It is frequently desirable to include in the hydrocarbon portion of the second composition a terpene hydrocarbon such as turpentine, alpha pinene, beta pinene, limonene, dipentene, or the like. The hydrocarbon portion of the second treating liquid usually amounts to from 50% to 75% by weight, and may be a single hydrocarbon or a mixture of members selected from the three classes of hydrocarbons mentioned above.
An essential component of the second treating solution is an aliphatic alcohol, e. g., methyl, ethyl, or iso-propyl alcohol or a mixture thereof. From 4% to 10% by weight of the second solution is alcohol.
It is convenient at this point to give examples of solutions A and B which may be used in carrying out the procedure constituting my invention, it being understood 0 that such examples are formulated in accordance with the broader teachings above as illustrative of the mode of compounding such materials, but not limiting the scope of the invention to such compositions. Those skilled in the art will readily comprehend the formulation of other solutions after an understanding of those herein exemplified.
Example 1 Solution A: Parts Methylene chloride (CHzClz) 92 Ethoxy cellulose (45%48% std.) 8 Ethyl alcohol 7 Solution B: Parts Toluene 25 Mineral spirits 50 Ethyl acetate 25 Ethyl alcohol l Example 11 Solution A: Parts Ethylene chloride (C2H4Cl2) 85 Cellulose acetate-butyrate 7 Solution B: Parts Xylol Turpentine 5 Mineral spiri 45 Acetone Ethyl alcohol 10 Butyl cellosolve (mono butyl ether of ethylene glycol) Example 111 Solution A: Parts Carbon tetrachloride 50 Methylene chloride 35 Cellulose nitrate 9 Solution B: Parts Benzene Turpentine 10 Hexane 65 Butyl acetate 15 Methyl alcohol 10 Example IV Solution A: Parts Methylene chloride 96 Cellulose acetate 5 Ethyl alcohol 6 Parafiin w x 2 Propylene oxide .5 Solution B: Parts Turpentine 1 Ethyl alcohol 2 Toluene 3.5 Mineral spirits 7 Ethyl acetate 3.5
The manner of application of these solutions is not critical. They may be sprayed, brushed, rolled or wiped.
on the surface. Since the surface after exposure to solution A is quite sticky and wet, brush or spray application of Solution B is preferred. For example, Solution B may be admixed with a normally gaseous propellant material, e. g., a' fluorochloro methane, such as FzCClz, etc., and applied from an aerosol can as a fine spray.
A procedure in accordance with this invention involves application of a paint and varnish remover such as exemplified above as Solution A. The remover is allowed to act on the old paint or varnish film until it begins to soften. Usually from a few seconds to several minutes are required. Then Solution B is applied directly to the partially softened old film by spray or brush, for example. After a short time of a few minutes, the old paint or varnish film can be removed almost as an intact stripable film which is not sticky or gummy. Tools remain unclogg'ed. In many cases, the film may be picked up with the fingers and stripped off. Removal is much easier and complicated designs and mill work are readily freed of old finish. Little or no preparation of the bare surface is required prior to refinishing in many cases. Considerable labor is therefore saved.
Other modes of applying the principle of this invention may be employed instead of those specifically set forth above, changes being made as regards the details herein disclosed, provided the elements set forth in any of the following claims, or the equivalent of such be employed.
It is, therefore, particularly pointed out and distinctly claimed as the invention:
1. The method of removing a dried organic film from a substrate comprising coating said film with a paint and varnish remover comprising a major amount of a normally liquid halogen-containing alkene of no more than 2 carbon atoms and having a boiling point less than about 100 C., and a minor amount of a cellulose derivative, after the old film has softened, overcoating the softened film with a second composition comprising in admixture a normally liquid hydrocarbon, an alcohol, and an ester of an aliphatic carboxylic acid and an alcohol, which ester contains from 3 to 5 carbon atoms, and then stripping the resulting softened and loosened old film from the substrate.
2. The method 'of claim 1 in which the paint and varnish remover comprises a major amount of methylene chloride and a minor amount of a cellulose ester of an aliphatic carboxylic acid.
3. The method of claim 1 in which the paint and varnish remover comprises a major amount of methylene chloride and a minor amount of cellulose acetate.
4. The method of claim 1 in which the paint and varnish remover has the following composition:
Parts Methylene chloride 50-100 Cellulose acetate 3-7 Ethyl alcohol 4-8 Propylene oxide 0.5
5. The method of claim 1 in which the second composition comprises in admixture a mixture of normally liquid hydrocarbons,an aliphatic alcohol, and an ester of acetic acid and a low molecular weight alcohol of no more than 3 carbon atoms.
6. The method of claim 1 in which the normally liquid hydrocarbon is a mixture of an aliphatic hydrocarbon and an aromatic hydrocarbon.
7. The method of claim 1 in which the normally liquid hydrocarbon is a mixture of an aliphatic hydrocarbon, an aromatic hydrocarbon and a terpene hydrocarbon.
8. The method of claim 1 in which the second composition has the following formulation:
5O Parts Turpentine 1 Ethyl alcohol 2 Toluene 3.5 Mineral spirits 7 Ethyl acetate 3.5
9. The method of removing a dried organic film from a substrate comprising coating said film with a paint and varnish remover having the following formulation:
after the old film has softened, overcoating the softened film with a second composition having the following formulation:
Parts Turpentine 1 Ethyl alcohol 2 Toluene 3.5 Mineral spirits 7 Ethyl acetate 3.5
and thenstripping the resulting softened and loosened old film from the substrate.
No references cited.

Claims (1)

1. THE METHOD OF REMOVING A DRIED ORGANIC FILM FORM A SUBSTRATE COMPRISING COATING SAID FILM WITH A PAINT AND VARNISH REMOVER COMPRISING A MAJOR AMOUNT OF A NORMALLY LIQUID HALOGEN-CONTAINING ALKENE OF NO MORE THAN 2 CARBON ATOMS AND HAVING A BOILING POINT LESS THAN ABOUT 100* C., AND A MINOR AMOUNT OF A CELLULOSE DERIVATIVE, AFTER THE OLD FILM HAS SOFTENED, OVERCOATING THE SOFTENED FILM WITH A SECOND COMPOSITION COMPRISING IN ADMIXTURE A NORMALLY LIQUID HYDROCARBON, AN ALCOHOL, AND AN ESTER OF AN ALIPHATIC CARBOXYLIC ACID AND AN ALCOHOL, WHICH ESTER CONTAINS FROM 3 TO 5 CARBON ATOMS, AND THEN STRIPPING THE RESULTING SOFTENED AND LOOSENED OLD FILM FROM THE SUBSTRATE.
US426943A 1954-04-30 1954-04-30 Method for removing paint and varnish Expired - Lifetime US2705207A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US426943A US2705207A (en) 1954-04-30 1954-04-30 Method for removing paint and varnish

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US426943A US2705207A (en) 1954-04-30 1954-04-30 Method for removing paint and varnish

Publications (1)

Publication Number Publication Date
US2705207A true US2705207A (en) 1955-03-29

Family

ID=23692828

Family Applications (1)

Application Number Title Priority Date Filing Date
US426943A Expired - Lifetime US2705207A (en) 1954-04-30 1954-04-30 Method for removing paint and varnish

Country Status (1)

Country Link
US (1) US2705207A (en)

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3360472A (en) * 1963-10-03 1967-12-26 Colgate Palmolive Co Paint remover composition
US3468814A (en) * 1966-02-21 1969-09-23 Allied Chem Self-propelled aerosol composition and method of using same to coat plates useful in thin-layer chromatography
US3538007A (en) * 1967-12-04 1970-11-03 Grace W R & Co Paint stripper for aluminum and magnesium surfaces
US3920472A (en) * 1974-11-29 1975-11-18 Us Navy Decal removal method
US3983047A (en) * 1974-11-29 1976-09-28 The United States Of America As Represented By The Secretary Of The Navy Decal removal composition
US4285827A (en) * 1978-08-24 1981-08-25 R.J. Hamer Limited Emulsified film forming polymer and methylene chloride/water paint stripper
US4309300A (en) * 1979-05-04 1982-01-05 Mcdonnell Douglas Corporation Cleaning solvent and method of cleaning a metal surface
WO1991000893A2 (en) * 1989-06-30 1991-01-24 Stevens Sciences Corp. Paint stripper and varnish remover compositions and related methods
US5124062A (en) * 1989-06-30 1992-06-23 Stevens Sciences Corp. Paint stripper and varnish remover compositions, methods for making these compositions and methods for removing paint and other polymeric coatings from flexible and inflexible surfaces
US5167853A (en) * 1989-06-30 1992-12-01 Stevens Sciences, Corp. Paint stripper and varnish remover compositions containing organoclay rheological additives, methods for making these compositions and methods for removing paint and other polymeric coatings from flexible and inflexible surfaces
US5334256A (en) * 1993-06-02 1994-08-02 Howe Charles R Paint stripping composition
US5425893A (en) * 1993-04-14 1995-06-20 Stevens; Edwin Photoreactive paint stripping compositions and methods
US5454878A (en) * 1994-02-17 1995-10-03 Lockheed Idaho Technologies Company Method for removing hydrocarbon contaminants from solid materials
US5691289A (en) * 1994-11-17 1997-11-25 Kay Chemical Company Cleaning compositions and methods of using the same
US7052556B1 (en) 2003-03-10 2006-05-30 Montie-Targosz Enterprises, Llc Process for removal of paint from plastic substrates
EP1748061A1 (en) * 2004-04-20 2007-01-31 Tokai Corporation Liquid fuel for burning utensil

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
None *

Cited By (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3360472A (en) * 1963-10-03 1967-12-26 Colgate Palmolive Co Paint remover composition
US3468814A (en) * 1966-02-21 1969-09-23 Allied Chem Self-propelled aerosol composition and method of using same to coat plates useful in thin-layer chromatography
US3538007A (en) * 1967-12-04 1970-11-03 Grace W R & Co Paint stripper for aluminum and magnesium surfaces
US3920472A (en) * 1974-11-29 1975-11-18 Us Navy Decal removal method
US3983047A (en) * 1974-11-29 1976-09-28 The United States Of America As Represented By The Secretary Of The Navy Decal removal composition
US4285827A (en) * 1978-08-24 1981-08-25 R.J. Hamer Limited Emulsified film forming polymer and methylene chloride/water paint stripper
US4309300A (en) * 1979-05-04 1982-01-05 Mcdonnell Douglas Corporation Cleaning solvent and method of cleaning a metal surface
WO1991000893A2 (en) * 1989-06-30 1991-01-24 Stevens Sciences Corp. Paint stripper and varnish remover compositions and related methods
WO1991000893A3 (en) * 1989-06-30 1991-02-21 Stevens Sciences Corp Paint stripper and varnish remover compositions and related methods
US5098591A (en) * 1989-06-30 1992-03-24 Stevens Sciences Corp. Paint stripper and varnish remover compositions containing organoclay rheological additives, methods for making these compositions and methods for removing paint and other polymeric coatings from flexible and inflexible surfaces
US5124062A (en) * 1989-06-30 1992-06-23 Stevens Sciences Corp. Paint stripper and varnish remover compositions, methods for making these compositions and methods for removing paint and other polymeric coatings from flexible and inflexible surfaces
US5167853A (en) * 1989-06-30 1992-12-01 Stevens Sciences, Corp. Paint stripper and varnish remover compositions containing organoclay rheological additives, methods for making these compositions and methods for removing paint and other polymeric coatings from flexible and inflexible surfaces
US5597788A (en) * 1993-04-14 1997-01-28 Stevens; Edwin Paint stripping compositions and methods
US5425893A (en) * 1993-04-14 1995-06-20 Stevens; Edwin Photoreactive paint stripping compositions and methods
US5427710A (en) * 1993-04-14 1995-06-27 Stevens; Edwin Paint stripping compositions and methods
US5334256A (en) * 1993-06-02 1994-08-02 Howe Charles R Paint stripping composition
US5454878A (en) * 1994-02-17 1995-10-03 Lockheed Idaho Technologies Company Method for removing hydrocarbon contaminants from solid materials
US5691289A (en) * 1994-11-17 1997-11-25 Kay Chemical Company Cleaning compositions and methods of using the same
US6071867A (en) * 1994-11-17 2000-06-06 Kay Chemical Company Cleaning compositions and methods of using the same
US7052556B1 (en) 2003-03-10 2006-05-30 Montie-Targosz Enterprises, Llc Process for removal of paint from plastic substrates
US7258750B1 (en) 2003-03-10 2007-08-21 Montie-Targosz Llc Process for removal of paint from plastic substrates
US7416612B1 (en) 2003-03-10 2008-08-26 Paul Montie Process for removal of paint from plastic substrates
US7744701B1 (en) 2003-03-10 2010-06-29 Montie-Targosz Llc Process for removal of paint from plastic substrates
US7879155B1 (en) 2003-03-10 2011-02-01 Montie-Targosz Enterprises, Llc Process for removal of paint from plastic substrates
EP1748061A1 (en) * 2004-04-20 2007-01-31 Tokai Corporation Liquid fuel for burning utensil
US20070266619A1 (en) * 2004-04-20 2007-11-22 Masato Seki Liquid Fuel for Burning Utensil
EP1748061A4 (en) * 2004-04-20 2010-05-26 Tokai Corp Liquid fuel for burning utensil

Similar Documents

Publication Publication Date Title
US2705207A (en) Method for removing paint and varnish
US4749510A (en) Paint stripping composition and method of making and using the same
US5124062A (en) Paint stripper and varnish remover compositions, methods for making these compositions and methods for removing paint and other polymeric coatings from flexible and inflexible surfaces
US6096699A (en) Environmentally friendly solvent
EP0483285B1 (en) Paint stripper and varnish remover compositions and related methods
US5035829A (en) Paint removing compositions
CA2382600C (en) Environmentally friendly solvent
CA2063739C (en) Method of activating n-methyl-e-pyrrolidone (nmp) and/or gamma-butyrolactone (blo) varnish and paint remover solvents
WO1988006640A1 (en) Paint removing compositions
US5049300A (en) Method of activating acidified NMP to provide an effective paint remover composition
US2495729A (en) Method of removing coatings from surfaces
US5413729A (en) Composition containing lactone and ester for removing coatings
US5049314A (en) Paint stripping composition consisting essentially of NMP and ethyl-3-ethoxy propionate
US5332526A (en) Multi-purpose paint and varnish stripper
US5167853A (en) Paint stripper and varnish remover compositions containing organoclay rheological additives, methods for making these compositions and methods for removing paint and other polymeric coatings from flexible and inflexible surfaces
JPH10502947A (en) Paint release aid composition
US3094491A (en) Wax-free paint remover
US5691290A (en) Cleaning composition
US5154848A (en) Method of activating N-methyl-2-pyrrolidone (NMP) with ethyl 3-ethoxypropionate (EEP) to provide improved varnish and paint remover solvents
EP0065381A2 (en) Stripping agents
US5217640A (en) Method of activating α-butyrolactone (BLO) with ethyl 3-ethoxypropionate (EEP) to provide improved varnish and paint remover solvents
US1974744A (en) Finish remover composition
US2495728A (en) Composition for removing paint and varnish from coated surfaces
US1918224A (en) Paint and varnish remover
US2346622A (en) Remover for paint, varnish, and the like