US1118642A - Finish-remover. - Google Patents
Finish-remover. Download PDFInfo
- Publication number
- US1118642A US1118642A US68777012A US1912687770A US1118642A US 1118642 A US1118642 A US 1118642A US 68777012 A US68777012 A US 68777012A US 1912687770 A US1912687770 A US 1912687770A US 1118642 A US1118642 A US 1118642A
- Authority
- US
- United States
- Prior art keywords
- parts
- finish
- camphor
- remover
- solvent
- Prior art date
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- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 42
- 239000000463 material Substances 0.000 description 33
- 239000002904 solvent Substances 0.000 description 33
- 229930008380 camphor Natural products 0.000 description 23
- DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 22
- 241000723346 Cinnamomum camphora Species 0.000 description 18
- 229960000846 camphor Drugs 0.000 description 17
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 16
- 229920002160 Celluloid Polymers 0.000 description 11
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 10
- 239000007788 liquid Substances 0.000 description 10
- 150000001875 compounds Chemical class 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 239000001993 wax Substances 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 235000007586 terpenes Nutrition 0.000 description 5
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 150000003505 terpenes Chemical class 0.000 description 4
- LSPHULWDVZXLIL-UHFFFAOYSA-N (+/-)-Camphoric acid Chemical compound CC1(C)C(C(O)=O)CCC1(C)C(O)=O LSPHULWDVZXLIL-UHFFFAOYSA-N 0.000 description 3
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 3
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 3
- 241000779819 Syncarpia glomulifera Species 0.000 description 3
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000001739 pinus spp. Substances 0.000 description 3
- 229940036248 turpentine Drugs 0.000 description 3
- DTGKSKDOIYIVQL-WEDXCCLWSA-N (+)-borneol Chemical compound C1C[C@@]2(C)[C@@H](O)C[C@@H]1C2(C)C DTGKSKDOIYIVQL-WEDXCCLWSA-N 0.000 description 2
- REPVLJRCJUVQFA-UHFFFAOYSA-N (-)-isopinocampheol Natural products C1C(O)C(C)C2C(C)(C)C1C2 REPVLJRCJUVQFA-UHFFFAOYSA-N 0.000 description 2
- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 2
- CKDOCTFBFTVPSN-UHFFFAOYSA-N borneol Natural products C1CC2(C)C(C)CC1C2(C)C CKDOCTFBFTVPSN-UHFFFAOYSA-N 0.000 description 2
- 229940116229 borneol Drugs 0.000 description 2
- 230000003197 catalytic effect Effects 0.000 description 2
- DTGKSKDOIYIVQL-UHFFFAOYSA-N dl-isoborneol Natural products C1CC2(C)C(O)CC1C2(C)C DTGKSKDOIYIVQL-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000012184 mineral wax Substances 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- DNNLEMIRRGUGOZ-UHFFFAOYSA-N oxygen(2-);thorium(4+) Chemical compound [O-2].[O-2].[Th+4] DNNLEMIRRGUGOZ-UHFFFAOYSA-N 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 1
- DEWLEGDTCGBNGU-UHFFFAOYSA-N 1,3-dichloropropan-2-ol Chemical compound ClCC(O)CCl DEWLEGDTCGBNGU-UHFFFAOYSA-N 0.000 description 1
- IBSQPLPBRSHTTG-UHFFFAOYSA-N 1-chloro-2-methylbenzene Chemical compound CC1=CC=CC=C1Cl IBSQPLPBRSHTTG-UHFFFAOYSA-N 0.000 description 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N Alumina Chemical compound [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- YZCKVEUIGOORGS-UHFFFAOYSA-N Hydrogen atom Chemical compound [H] YZCKVEUIGOORGS-UHFFFAOYSA-N 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 241000276489 Merlangius merlangus Species 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-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
- 150000007513 acids Chemical class 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 235000013871 bee wax Nutrition 0.000 description 1
- 239000012166 beeswax Substances 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- -1 camphor terpenes Chemical class 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 229910052763 palladium Inorganic materials 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- LKTOWUZQHJSGAK-UHFFFAOYSA-N phenol;4,7,7-trimethylbicyclo[2.2.1]heptan-3-one Chemical compound OC1=CC=CC=C1.C1CC2(C)C(=O)CC1C2(C)C LKTOWUZQHJSGAK-UHFFFAOYSA-N 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 239000010665 pine oil Substances 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000002966 varnish 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/2093—Esters; Carbonates
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D9/00—Chemical paint or ink removers
- C09D9/005—Chemical paint or ink removers containing organic solvents
Definitions
- This invention relates especially to finish removers comprising phenol camphor or similar compounds, together with incorporated volatile organic solvent material and waxy or other suitable stifi'ening material if desired.
- Various solid camphor terpenes have the peculiar property of combining with phenols in definite proportions so as to form compounds which have distinctive properties Widely different. from the com-.
- camphorate solvents may be first formed and then incorporated with other remover ingredients or may be conveniently formed by bringing the components together in solution with the other remover ingredients.
- camphoric terpenes seem to combine most readily in equimolecular proportions, although not only a camphorate but a bicamphorate can be formed with carbolic acid or with other phenols, such, for instance, as cresylic acid.
- These compounds are heavy liquids having .a very general and desirable solvent action on many paint or varnish gums, resins or binders so as to be desirable components for finish removers. It is also desirable to incorporate a suitable small proportion of such practically non-volatile material in removers to prevent any possibility of the drying out of finish on which waxy removershave actedto soften or,loosen the same.
- the main remover solvents may comprise loosening. finish solvent material, that is solvents of a generally alcoholic character or action in removers, such as methyl, ethyl,
- propyl, butyl, benzyl and other strict alcopenetrating finish solvent material may also e be used, that is solvent material of a gen erally benzolic character or action 1n remqw'g.- ers, such as benzol and its homologues,
- toluol, xylol and their commercial forms such as commercial toluol, solvent naphtha;
- d ethers such as: bet'anaphthol ether, benzyl.
- Suitable heavy solvents such as may be used to minimize any tendency to drying out of the remover may comprise epichlorhydrin, dichlorhydrin or chlorinated lycerole or ethyl or methyl phenates.
- thyl phenate and methyl phenate and the corresponding cresylates are also desirable solvents which may be conveniently produced in various ways, the combination of the components being facilitated by suitable catalytic material such as aluminum oxid, thorium oxid or the like at a temperature of 350 to 400" C. or so, the thorium oxid having especially desirable catalytic action in this connection and promoting the formation of these particular compounds when the components are brought together in this way.
- Su1table stilfening material may be used in such removers preferably comprising suitable Waxy evaporation-retarding material, such-as parafiin, ceresin or other mineral wax, although beeswax and other waxy bodies may be used and also other stifiening material, such as cellulose esters, nitrocellulose, which may be used in the form of scrap celluloid which usually contains nitrocellulose and suflicient incorporated camphor to combine with phenol and form the camphorated solvents referred to.
- suitable Waxy evaporation-retarding material such-as parafiin, ceresin or other mineral wax, although beeswax and other waxy bodies may be used and also other stifiening material, such as cellulose esters, nitrocellulose, which may be used in the form of scrap celluloid which usually contains nitrocellulose and suflicient incorporated camphor to combine with phenol and form the camphorated solvents referred to.
- llnert stidening material may also be incorporated if desired, such for example as wood flour, starch, infusorial earth, whiting and the like, it being of course understood that the soluble thickeners are preferably methyl acetate, 20 parts of benzol, 10 parts of benzyl alcoholp l parts of laurel camphor, 10 parts of scra would-contain nitrocell ose, and about 4 parts of camphor,'6 artsof carbolic acid and 2 parts of parafin.
- Another illustrative remover may comprise 20 parts 'of acetone, 20 parts of methyl acetone,30 parts of benzol, '15 parts of ordinarycamphor, 10
- compositions may comprise 30 parts of acetone, 25 parts of benzol, 30 parts of laurehor Borneol' camphor and 20 parts of carbolicior, cresylicacid and 3 to 5parts of parafiin
- I illustrative composition suitable for general purposes may ⁇ comprise 20 parts of chlo rinated methyl acetoneor. of-tetrachlorethian'e, 20 parts or acetone, V 2 parts of laurel camphor, 2 parts of celluloid scrap, 4 parts of carbolic acid and to 3 parts of parafiin-"Another generally useful composition may comprise 30 parts of methyl alcohol, 30 parts of acetone,
- tive composition may comprise 4:0 parts of acetone 20 parts of benzol, 3Q of'camphor, a parts at earholic acid and a parts including first; dissolved in the more energetic solvents therefor with a slight increase of temperacelluloid which,
- the finish remover comprising ap proximately 20 parts of methyl alcohol, 10
- the finish remover comprising approximately 30 parts of alcohol, 25 parts of acetone, 20 parts of methyl acetate, 20 parts of benzol, 4: parts of camphor, 10 parts of celluloid scrap containing camphor, 6 parts of phenol combined with suchca'mphor to form a liquid finish solvent compound and mineral Wax.
- finish remover comprising ap- V proximately 90 parts of volatile organic finish solvent material comprising an alcohol, l parts of camphor, 10 parts of celluloid comprising camphor, phenol combined therewith and incorporated wax,
- finish remover consisting in greater proportion of loosening finish solvent material comprising a ketone, aromatic penetrating solvent material, celluloid containing camphor, phenol combined therewith and incorporated waxy material.
- the finish remover consisting in greater part of volatile finish solvent material','including ketonic finish solvent material, cel luloid containing 'camphor, carbolic acid 7.
- remover comprising liquid finish solvent material, solid camphoric terpene material capableof combining with phenol mdl: car- .bolic acid combined therewith.
- solid camphoric terpene material capable of forming a liquid finish solvent by combina-.
- finish remover oonsistin in greater part of volatile organic finish so vent dissolving or softening finish material comprising solid camphoric ternene material and phenolic material combined therewith.
- liquid solvent suitable for use in dissolving or softening finish material comprising therewith.
- the finish remover comprising vola tile organic finish solvent material, 'pyroxyhn, camphor, phenol combined therewith and incorporated Wax.
- finish remover consisting in camphor and carbolic acid combined greater part of -volatilecomposite finish solvent material including benzol and we tone, celluloid containing camphor, phenol and incorporated wax.
- the substantially non-aqueous finish remover consisting in greater part of volatile organic finish solvent material andcomprising a liquid finish solvent cam horic compound formed by combining a soli camphoric terpene material with carbolicacid.
- the substantially non-aqueous finish remover consisting in greater part of volatile organic finish solvent material and comprising a liquid finish solvent cam horic compound formed by combining a soli camphoric terpenematerial with carbolic acid, and incorporated wax.
- the finish remover consisting in greater proportion of volatile composite organic finishsolvent material comprising acetone and a miscible aromatic solvent, celluloid containing camphor and incorporatedcatholic acid and wax material.
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- Chemical & Material Sciences (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Emergency Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Materials Engineering (AREA)
- Detergent Compositions (AREA)
- Paints Or Removers (AREA)
Description
mam.
iiNiTE s'rATEs PATENT QFFICE.
CARLETON' ELLIS, 0F MONTCLATR, NEW JERSEY, ASSIGNOR TO OHADE'LOID CHEMICAL COMPANY, OF NEW YORK, N. Y., A CORPORATION OF WEST VIRGINIA.
'FINISH-REMOVER.
No Drawing.
To all whom it may concern Be it known that I, CARLETON ELLIS, a citizen pf the United States, and resident of Montclair, county of Essex, and State of New Jersey, have made a certain new and useful Invention Relating to Finish-Removers, of which the following is a specification.
This invention relates especially to finish removers comprising phenol camphor or similar compounds, together with incorporated volatile organic solvent material and waxy or other suitable stifi'ening material if desired. Various solid camphor terpenes have the peculiar property of combining with phenols in definite proportions so as to form compounds which have distinctive properties Widely different. from the com-.
ponents used. Ordinary laurel camphor, Borneol camphor and the turpentine camphors or their derivatives may be combined in this way with carbolic or cresylic acids. For instance, pure crystallized carbolic acid vwhich melts at 43C. when combined with laurel camphor which melts at 175 C. forms a liquid solvent. melting much below zero.
Such combinations may be effected when the I -stance, these camphorate solvents may be first formed and then incorporated with other remover ingredients or may be conveniently formed by bringing the components together in solution with the other remover ingredients. These camphoric terpenes seem to combine most readily in equimolecular proportions, although not only a camphorate but a bicamphorate can be formed with carbolic acid or with other phenols, such, for instance, as cresylic acid. These compounds are heavy liquids having .a very general and desirable solvent action on many paint or varnish gums, resins or binders so as to be desirable components for finish removers. It is also desirable to incorporate a suitable small proportion of such practically non-volatile material in removers to prevent any possibility of the drying out of finish on which waxy removershave actedto soften or,loosen the same.
Specification of Letters Patent. Patented Nov 24, 1914, Application filed April 1, 1912. Serial No. 687,770.
In this way even under extreme service conditions it is practically impossible for the wax or treated finish to form an undesirably hard coating even if allowed to stand for unusually long periods.
The main remover solvents may comprise loosening. finish solvent material, that is solvents of a generally alcoholic character or action in removers, such as methyl, ethyl,
propyl, butyl, benzyl and other strict alcopenetrating finish solvent material may also e be used, that is solvent material of a gen erally benzolic character or action 1n remqw'g.- ers, such as benzol and its homologues,
toluol, xylol and their commercial forms, such as commercial toluol, solvent naphtha;
and the somewhat analogouspetrolemnnydrocarbons, such as naphtha and benzin and the chlorinated derivatives, such as' chlorbenzol, chlortoluol and other chlorinated solvents, such as carbon-tetrachlorid, tetrachlorethane and the like, and also turpentine, wood turpentine and various esters an .pentine, pine oil and so forth,;by nascent hydrogen as by agitation of the solvent with sodium, potassium or the like or by other treatment with hydrogen in the presence of active metallic material, such as platinum,
d ethers, such as: bet'anaphthol ether, benzyl.
palladium and so forth. Suitable heavy solvents, such as may be used to minimize any tendency to drying out of the remover may comprise epichlorhydrin, dichlorhydrin or chlorinated lycerole or ethyl or methyl phenates. thyl phenate and methyl phenate and the corresponding cresylates are also desirable solvents which may be conveniently produced in various ways, the combination of the components being facilitated by suitable catalytic material such as aluminum oxid, thorium oxid or the like at a temperature of 350 to 400" C. or so, the thorium oxid having especially desirable catalytic action in this connection and promoting the formation of these particular compounds when the components are brought together in this way.
Su1table stilfening material may be used in such removers preferably comprising suitable Waxy evaporation-retarding material, such-as parafiin, ceresin or other mineral wax, although beeswax and other waxy bodies may be used and also other stifiening material, such as cellulose esters, nitrocellulose, which may be used in the form of scrap celluloid which usually contains nitrocellulose and suflicient incorporated camphor to combine with phenol and form the camphorated solvents referred to. llnert stidening material may also be incorporated if desired, such for example as wood flour, starch, infusorial earth, whiting and the like, it being of course understood that the soluble thickeners are preferably methyl acetate, 20 parts of benzol, 10 parts of benzyl alcoholp l parts of laurel camphor, 10 parts of scra would-contain nitrocell ose, and about 4 parts of camphor,'6 artsof carbolic acid and 2 parts of parafin. Another illustrative remover may comprise 20 parts 'of acetone, 20 parts of methyl acetone,30 parts of benzol, '15 parts of ordinarycamphor, 10
.parts of carbolic acid and 5 parts of parafin;
Another illustrative composition may comprise 30 parts of acetone, 25 parts of benzol, 30 parts of laurehor Borneol' camphor and 20 parts of carbolicior, cresylicacid and 3 to 5parts of parafiin I illustrative composition suitable for general purposes may {comprise 20 parts of chlo rinated methyl acetoneor. of-tetrachlorethian'e, 20 parts or acetone, V 2 parts of laurel camphor, 2 parts of celluloid scrap, 4 parts of carbolic acid and to 3 parts of parafiin-"Another generally useful composition may comprise 30 parts of methyl alcohol, 30 parts of acetone,
benzol, 10 partsnf celluloid'fscrap, 4 partsof carbolic or cresylic acid and 1 part of Another illustraparafin or ceresin' vvax. tive composition may comprise 4:0 parts of acetone 20 parts of benzol, 3Q of'camphor, a parts at earholic acid and a parts including first; dissolved in the more energetic solvents therefor with a slight increase of temperacelluloid which,
or ceresmwax. Another 35 arts or benzol,"
40 parts or;
of parafiin. Another illustrative composihol,-20 parts of laurel camphor, 5 parts of scrap celluloid, 2 parts of parts of carbolic acid.-
Having described this invention in connection with a number of illustrative ingredients, formulas, proportions and procparaflin and 15 esses, to the details of which disclosure the invention is not of course to be limited, what is claimed as new is:
1. The finish remover comprising ap proximately 20 parts of methyl alcohol, 10
parts of benzyl alcohol, 2-5 parts of acetone,-
20 parts of methyl acetate, 20 parts of henzol, 4 parts of laurel camphor, 10 parts of celluloid containing about 4 parts of camphor. 6 parts of carbplic acid and 2 parts of 2. The finish remover comprising approximately 30 parts of alcohol, 25 parts of acetone, 20 parts of methyl acetate, 20 parts of benzol, 4: parts of camphor, 10 parts of celluloid scrap containing camphor, 6 parts of phenol combined with suchca'mphor to form a liquid finish solvent compound and mineral Wax.
3. The finish remover comprising ap- V proximately 90 parts of volatile organic finish solvent material comprising an alcohol, l parts of camphor, 10 parts of celluloid comprising camphor, phenol combined therewith and incorporated wax,
4. The finish remover consisting in greater proportion of loosening finish solvent material comprising a ketone, aromatic penetrating solvent material, celluloid containing camphor, phenol combined therewith and incorporated waxy material.
5. The finish remover consisting in greater part of volatile finish solvent material','including ketonic finish solvent material, cel luloid containing 'camphor, carbolic acid 7. The. substantially non-aqueous finish.
remover comprising liquid finish solvent material, solid camphoric terpene material capableof combining with phenol mdl: car- .bolic acid combined therewith.
8. The finish removercomprising larger part liquid organic finish solvent material. solid camphoric terpene material capable of forming a liquid finish solvent by combina-.
tion with carbolic acid and phenol combined therewith.
a The remover consisting in greater combined therewith and incorporated waxy I '115 part of volatile organic finishsolVent. ma-
terial comprising a finish solvent ketone, solid cam horicterpene material and phenol, combined therewith to form a liquid finish .solvent compound.
10. The finish remover oonsistin in greater part of volatile organic finish so vent dissolving or softening finish material comprising solid camphoric ternene material and phenolic material combined therewith.
13. The liquid solvent suitable for use in dissolving or softening finish material comprising therewith.
'14. The finish remover comprising vola tile organic finish solvent material, 'pyroxyhn, camphor, phenol combined therewith and incorporated Wax.
15. The finish remover consisting in camphor and carbolic acid combined greater part of -volatilecomposite finish solvent material including benzol and we tone, celluloid containing camphor, phenol and incorporated wax.
16. The substantially non-aqueous finish remover consisting in greater part of volatile organic finish solvent material andcomprising a liquid finish solvent cam horic compound formed by combining a soli camphoric terpene material with carbolicacid.
17. The substantially non-aqueous finish remover consisting in greater part of volatile organic finish solvent material and comprising a liquid finish solvent cam horic compound formed by combining a soli camphoric terpenematerial with carbolic acid, and incorporated wax. a
18. The finish remover consisting in greater proportion of volatile composite organic finishsolvent material comprising acetone and a miscible aromatic solvent, celluloid containing camphor and incorporatedcatholic acid and wax material.
. 0 LETON ELLIS. Witnesses:
HARRY L. Duncan,
Jnssm B; KAY.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US68777012A US1118642A (en) | 1912-04-01 | 1912-04-01 | Finish-remover. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US68777012A US1118642A (en) | 1912-04-01 | 1912-04-01 | Finish-remover. |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US1118642A true US1118642A (en) | 1914-11-24 |
Family
ID=3186815
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US68777012A Expired - Lifetime US1118642A (en) | 1912-04-01 | 1912-04-01 | Finish-remover. |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US1118642A (en) |
-
1912
- 1912-04-01 US US68777012A patent/US1118642A/en not_active Expired - Lifetime
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