US1143111A - Paint and varnish remover. - Google Patents
Paint and varnish remover. Download PDFInfo
- Publication number
- US1143111A US1143111A US387273A US1907387273A US1143111A US 1143111 A US1143111 A US 1143111A US 387273 A US387273 A US 387273A US 1907387273 A US1907387273 A US 1907387273A US 1143111 A US1143111 A US 1143111A
- Authority
- US
- United States
- Prior art keywords
- paint
- parts
- remover
- methyl
- varnish
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
- 239000003973 paint Substances 0.000 title description 6
- 239000002966 varnish Substances 0.000 title description 6
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 15
- 239000002904 solvent Substances 0.000 description 10
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 5
- 239000002253 acid Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 239000012185 ceresin wax Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 229940032007 methylethyl ketone Drugs 0.000 description 2
- 239000000049 pigment Substances 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- AOPDRZXCEAKHHW-UHFFFAOYSA-N 1-pentoxypentane Chemical class CCCCCOCCCCC AOPDRZXCEAKHHW-UHFFFAOYSA-N 0.000 description 1
- HCFAJYNVAYBARA-UHFFFAOYSA-N 4-heptanone Chemical compound CCCC(=O)CCC HCFAJYNVAYBARA-UHFFFAOYSA-N 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 1
- 241000276489 Merlangius merlangus Species 0.000 description 1
- 239000000020 Nitrocellulose Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229910000004 White lead Inorganic materials 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- -1 compound ethers Chemical class 0.000 description 1
- 239000011928 denatured alcohol Substances 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- MJEMIOXXNCZZFK-UHFFFAOYSA-N ethylone Chemical compound CCNC(C)C(=O)C1=CC=C2OCOC2=C1 MJEMIOXXNCZZFK-UHFFFAOYSA-N 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 239000005002 finish coating Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000011121 hardwood Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- PGMYKACGEOXYJE-UHFFFAOYSA-N pentyl acetate Chemical class CCCCCOC(C)=O PGMYKACGEOXYJE-UHFFFAOYSA-N 0.000 description 1
- PJGSXYOJTGTZAV-UHFFFAOYSA-N pinacolone Chemical compound CC(=O)C(C)(C)C PJGSXYOJTGTZAV-UHFFFAOYSA-N 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 239000002641 tar oil Substances 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/72—Ethers of polyoxyalkylene glycols
Definitions
- My invention -relates to paint and varnish removers of an acid character and especially to those containing a vola-tileinstead of a non-volatile acid so that when the coating ofpaint or varnish hasbeen removed any acid remaining on the treated surface may quickly evaporate and leave the same in a i'it condition for the application of a new finish coating.
- My invention is designed to'provide an especially efficient remover for coatings containing readily decomposable paint pigments, such as the carbonates, among which white lead is the most noteworthy example.
- paint pigments such as the carbonates
- My remover is applied to such coatings the pigments are immediately attacked by the acid and rapidly disintegrated under the influence of the chemical action.
- this action vis especially eEective owing to the simultaneous mechanical disintegration of the paint or varnish coating due to the evolution and escape of carbon dioxid.
- The'evolution of gas also increases the eiliciency of the neutral volatile solvents present to amarked degree ash the latter are subjected to a continual agitation thereby, resulting in submitting the surface imder treatment to all parts of the,
- butyric acid For the purposes of this invention I prefer to use butyric acid.
- rinated hydrocarbons such as carbon tetrachlorid and chlorbenzol
- the simple ethers such as methyl, ethyl and amyl ethers, and compound ethers such as methyl, ethyl and amyl acetates
- carbon disulid Ethyl alcohol or one or more substances having similar solvent properties may also be added, such as methyl, amyl and denatured alcohols; the ketones, as acetone, methyl acetone, which as is Well known contains methyl alcohol, acetone and other ketonic solvents, methyl ethyl ketone, acetone oil, butyrone ztmd pinacolin; and lightoil of hard wood ar.
- An illustrative remover of this kind adapted for application in a thin layer to the surface being treated is: methyl acetone, 30 parts; benzol, 25y parts; butyric acid, 4 parts, and ceresin wax, 1 part.
- a remover of this character might be used with advantage: denatured alcohol, Ll0 parts; methyl-ethyl ketone, 25 parts; butyric acid, 6 parts, and ceresin wax, i part.
- rlhe -stiifeningmaterial may be omitted altogether from this composition ifV desired.
- vsolvents from the preceding lists such as suitable proportions of one or more chlorinated solvent salcoho1s, ethers, esters, ketones or tar oils mentioned, might, of
- the finish remover comprising approximately ketonic and alcoholic solvents 4 6.- ⁇ Thefinish remover consisting substanstantially of methyl acetone thirty parts,
- the finish remover comprising large proportions of composite volatile finish softening material, a few per cent. at least of butyric acid and incorporated thickening z5 material.
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
Description
par
sirio.
CARIJETON ELLIS, F LARCHMONT, NTEW YORlK, ASSIGNOR T0 GHADELOID CHEMICL COMPANY, 0F NEW YORK, Y., A CORPORATION OF WESlIl VIRGINIA.
spei'fmation of Letters Patent.
PAINT AND VARNISH Patted June 15, 1915..
No Drawing. Original application led February 26, 1902, Serial No. 359,509.. Divided and this application filed August 6, `190'?.
ToV all 'whom/ it may concern Be it known that I, CARLETON ELL'Is, a
I citizen of the United States, and a resident of Larchmont, Westchester county, State of New York, have invented a new and useful Improvement in Paint and Varnish Rel movers, of which the' following is a specification, this being a divisional application based on the disclosure of my application Serial No. 359,509, filed February 26,1907, which discloses and claims. the invention more broadly than this case which is limited to removers comprising butyric acid in connection with various other components.
My invention -relates to paint and varnish removers of an acid character and especially to those containing a vola-tileinstead of a non-volatile acid so that when the coating ofpaint or varnish hasbeen removed any acid remaining on the treated surface may quickly evaporate and leave the same in a i'it condition for the application of a new finish coating.
My invention is designed to'provide an especially efficient remover for coatings containing readily decomposable paint pigments, such as the carbonates, among which white lead is the most noteworthy example. When my remover is applied to such coatings the pigments are immediately attacked by the acid and rapidly disintegrated under the influence of the chemical action. In the `case of carbonates this actionvis especially eEective owing to the simultaneous mechanical disintegration of the paint or varnish coating due to the evolution and escape of carbon dioxid. The'evolution of gas also increases the eiliciency of the neutral volatile solvents present to amarked degree ash the latter are subjected to a continual agitation thereby, resulting in submitting the surface imder treatment to all parts of the,
body of solvents alike. 4,
For the purposes of this invention I prefer to use butyric acid. By the term butyric I wish it to be understood that I mean either normal butyric or isobutyric acid or a mixture of the two. This may be mixed with benzol or one 'or more substances allied' thereto inV their solvent properties such-as the 4benzol homologues,including. toluol, xylol and cumene; the petroleumhydrocarbons, such as benzin and kerosene; the chlo- Serial N o. 387,273.
rinated hydrocarbons, such as carbon tetrachlorid and chlorbenzol; the simple ethers such as methyl, ethyl and amyl ethers, and compound ethers such as methyl, ethyl and amyl acetates; and carbon disulid. Ethyl alcohol or one or more substances having similar solvent properties may also be added, such as methyl, amyl and denatured alcohols; the ketones, as acetone, methyl acetone, which as is Well known contains methyl alcohol, acetone and other ketonic solvents, methyl ethyl ketone, acetone oil, butyrone ztmd pinacolin; and lightoil of hard wood ar. kind to this mixture to retard the evaporation of the solvents, although I do not con- Sider this essential. Among such substances that are useful in this. connection may be mentioned wood flour, starch, Whiting, infusorial earth, the soaps, -the waxes and nitrocellulose. These thickners when added are incorporated during agitation so as t0 secure as homogeneous a mixture as possible.
more of the solvents are rst incorporated in the solvents. which dissolve them most readily.
An illustrative remover of this kind adapted for application in a thin layer to the surface being treated is: methyl acetone, 30 parts; benzol, 25y parts; butyric acid, 4 parts, and ceresin wax, 1 part.
For dipping or tank work a remover of this character might be used with advantage: denatured alcohol, Ll0 parts; methyl-ethyl ketone, 25 parts; butyric acid, 6 parts, and ceresin wax, i part.
rlhe -stiifeningmaterial may be omitted altogether from this composition ifV desired.
Other vsolvents from the preceding lists, such as suitable proportions of one or more chlorinated solvent salcoho1s, ethers, esters, ketones or tar oils mentioned, might, of
course, be added to or substituted in the above compositions. In some of these mixtures reaction probably takes place between I preferably add a thickener of some p yThose thickeners which are soluble in one or methyl acetonethirty parts, benzol twentyve parts, butyric acid four parts and ceresin wax one part.
2. The finish remover comprising approximately ketonic and alcoholic solvents 4 6.- `Thefinish remover consisting substanstantially of methyl acetone thirty parts,
benzol twenty-five parts, butyric acid four 20 parts and incorporated sti'ening material.
7. The finish remover comprising large proportions of composite volatile finish softening material, a few per cent. at least of butyric acid and incorporated thickening z5 material.
In testimony whereof I have hereunto signed my name in the presence of two Witnesses.
oAnLEToN ELLIS.
Witnesses:
SAMUEL R. BELL, HARRY W.. BROWN.j
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US387273A US1143111A (en) | 1907-02-26 | 1907-08-06 | Paint and varnish remover. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US35950907A US1147849A (en) | 1907-02-26 | 1907-02-26 | Paint or varnish remover. |
| US387273A US1143111A (en) | 1907-02-26 | 1907-08-06 | Paint and varnish remover. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1143111A true US1143111A (en) | 1915-06-15 |
Family
ID=3211203
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US387273A Expired - Lifetime US1143111A (en) | 1907-02-26 | 1907-08-06 | Paint and varnish remover. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1143111A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2630409A (en) * | 1949-10-06 | 1953-03-03 | Du Pont | Paint and varnish remover |
| US3635836A (en) * | 1969-11-10 | 1972-01-18 | Gen Mills Inc | Thickened compositions and the process of preparing same |
| US4517025A (en) * | 1982-05-17 | 1985-05-14 | Amchem Products, Inc. | Method for removing sealant contamination |
-
1907
- 1907-08-06 US US387273A patent/US1143111A/en not_active Expired - Lifetime
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2630409A (en) * | 1949-10-06 | 1953-03-03 | Du Pont | Paint and varnish remover |
| US3635836A (en) * | 1969-11-10 | 1972-01-18 | Gen Mills Inc | Thickened compositions and the process of preparing same |
| US4517025A (en) * | 1982-05-17 | 1985-05-14 | Amchem Products, Inc. | Method for removing sealant contamination |
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