US2292541A - Acceleration of the seasoning speed of surface coverings - Google Patents
Acceleration of the seasoning speed of surface coverings Download PDFInfo
- Publication number
- US2292541A US2292541A US331811A US33181140A US2292541A US 2292541 A US2292541 A US 2292541A US 331811 A US331811 A US 331811A US 33181140 A US33181140 A US 33181140A US 2292541 A US2292541 A US 2292541A
- Authority
- US
- United States
- Prior art keywords
- oil
- siccative
- acceleration
- seasoning
- binders
- 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
- 235000011194 food seasoning agent Nutrition 0.000 title description 7
- 230000001133 acceleration Effects 0.000 title description 3
- 239000003921 oil Substances 0.000 description 23
- 235000019198 oils Nutrition 0.000 description 22
- 239000000203 mixture Substances 0.000 description 19
- 239000011230 binding agent Substances 0.000 description 15
- 238000001035 drying Methods 0.000 description 9
- 238000000034 method Methods 0.000 description 7
- 229920005989 resin Polymers 0.000 description 7
- 239000011347 resin Substances 0.000 description 7
- VZXTWGWHSMCWGA-UHFFFAOYSA-N 1,3,5-triazine-2,4-diamine Chemical compound NC1=NC=NC(N)=N1 VZXTWGWHSMCWGA-UHFFFAOYSA-N 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 229920000180 alkyd Polymers 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 241000276489 Merlangius merlangus Species 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 description 2
- 238000003490 calendering Methods 0.000 description 2
- 239000007795 chemical reaction product Substances 0.000 description 2
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 235000011087 fumaric acid Nutrition 0.000 description 2
- 238000001879 gelation Methods 0.000 description 2
- 239000000944 linseed oil Substances 0.000 description 2
- 235000021388 linseed oil Nutrition 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 150000003505 terpenes Chemical class 0.000 description 2
- 235000007586 terpenes Nutrition 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- GRWFGVWFFZKLTI-UHFFFAOYSA-N α-pinene Chemical compound CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 2
- GRWFGVWFFZKLTI-IUCAKERBSA-N 1S,5S-(-)-alpha-Pinene Natural products CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 241000016649 Copaifera officinalis Species 0.000 description 1
- XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 239000004868 Kauri gum Substances 0.000 description 1
- 235000004347 Perilla Nutrition 0.000 description 1
- 244000124853 Perilla frutescens Species 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- 229910000004 White lead Inorganic materials 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 1
- 238000005452 bending Methods 0.000 description 1
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 150000002238 fumaric acids Chemical class 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 description 1
- 239000011133 lead Substances 0.000 description 1
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 1
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 1
- 229940107698 malachite green Drugs 0.000 description 1
- 150000002689 maleic acids Chemical class 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- GEMHFKXPOCTAIP-UHFFFAOYSA-N n,n-dimethyl-n'-phenylcarbamimidoyl chloride Chemical compound CN(C)C(Cl)=NC1=CC=CC=C1 GEMHFKXPOCTAIP-UHFFFAOYSA-N 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 150000007519 polyprotic acids Polymers 0.000 description 1
- 229960003351 prussian blue Drugs 0.000 description 1
- 239000013225 prussian blue Substances 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 235000020238 sunflower seed Nutrition 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical class OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- 239000002383 tung oil Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
Classifications
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06N—WALL, FLOOR, OR LIKE COVERING MATERIALS, e.g. LINOLEUM, OILCLOTH, ARTIFICIAL LEATHER, ROOFING FELT, CONSISTING OF A FIBROUS WEB COATED WITH A LAYER OF MACROMOLECULAR MATERIAL; FLEXIBLE SHEET MATERIAL NOT OTHERWISE PROVIDED FOR
- D06N3/00—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof
- D06N3/007—Artificial leather, oilcloth or other material obtained by covering fibrous webs with macromolecular material, e.g. resins, rubber or derivatives thereof characterised by mechanical or physical treatments
- D06N3/0079—Suction, vacuum treatment
-
- 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
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/08—Polyesters modified with higher fatty oils or their acids, or with natural resins or resin acids
Definitions
- This invention relates to the acceleration of the compositions such as floor covering compositions containing siccative binders.
- An object of this invention is to provide accelerators for surface covering compositions containing siccative binders which will cause such compositions to cure more rapidly.
- drier e. g. 0.1% cobalt naphthenate
- the compacted mass which is delivered from the mixer may be disintegrated, as by a set of scratch rolls which comprises a plurality of rolls having intermeshing teeth projectingfrom their surfaces.
- the resulting material is sheeted on calender rolls or optionally it may be further .rate of curing or seasoning of surface covering mixed and disintegrated and then calendered.”
- the material may be calendered on to burlap or other fibrous backing if desired.
- the sheeted material is placed in a. stoving. oven through which a current of heated air from about 70 C. to about 90 C. is circulated until the material is completely seasoned, i. e., until the sheet acquires the necessary degree of hardness. Higher or lower temperatures may be used if desirable.
- the hardness may be measured by any of the methods generally employed in the manufacture of linoleum. See the Federal Stock Catalogue (U. S. Government Printing Ofiice), section 4,
- the time required for seasoning a 2 mm. sheet of the above composition is about 4 to 5 days.
- the resulting seasoned floor or surface covering has about the same strength, flexibility and color as compositions not containing the accelerator; ties may be changed by many other accelerators sufliciently and in such a way that the materials One or more of these propersiccative oil as used herein other gums produced therewith are unsatisfactory.
- the seasoning speed of a 2 mm. sheet of the same mixture which does not contain the formoguanamine is about 18 to 20 days.
- the siccative binder utilized in the above example is an alkyd resin which has siccative properties, i. e., a reaction product of fumaric acid with a non-conjugated terpene (alpha pinene) and triethylene glycol, modified with linseed oil fatty acids.
- Other similar resins may be used which are drying oil-modified reaction products of maleic or fumaric acids with a terpene and a polyhydric alcohol.
- Other alkyd resins which are modified with drying oils may be used such as the phthalic-glyceride resins, the glycolrmaleic resins, and mixed resins such as the phthalicfumaric-glycol-glyceride resins.
- the seasoning temperature may be varied appropriately and, of course, the time required may be diiferent. About the same proportional accelerating effect is obtained when various siccative binders are employed.
- binders which may be used are those which are derived from the drying oils and may be made in any convenient well-known manner, such as the method described in British Patent 305,656, or the binders may comprise any of the various alkyd resins having siccative properties.
- linseed oil is preferable for economic reasons, but other siccative oils may oil, tung oil, soya-bean oil, perilla oil, ,oiticica oil,.
- Scheiber oil,sunflower-seed. oil, etc. is intended to include not only the so-called drying oils but also the so-called semi-drying oils. Furthermore, it is possible to use mixtures of siccative oils with other fatty oils of the non-drying type.
- so-called scrim-oil or shed oil either alone or fluxed with rosin or or resins and/or mixed with a proportion of the so-called mechanical oil. Either of these types of oils may be used singly if desired.
- siccative oil binders In the preparation of the siccative oil binders is customary to use rosin in admixture with the oil although other substances of the same type may be used, e. g., Kauri gum, Congo gum, ester and/or the whiting and e. g., about 0.005-1%.
- pigments which may be used the following are included: lithopone, barytes, zinc oxide, titanium oxide, chromates, red lead, white lead, malachite green, chrome green, chrome yellow, Prussian blue, etc. Similarly dyes and lakes may be used if desirable.
- driers in the preparation of the binders.
- the drier is usually added to the binder during the oxidation process and if desirable additional drier may be added when the binder, fillers, etc., are mixed together.
- Suitable driers include the oil-soluble salts such as the naphthenates, resinates and linoleates of cobalt, lead, manganese, zinc and chromium. Only a small proportion of these driers' based on the siccative oil content is generally sumcient,
- seasoning as applied to linoleum compositions indicates the process of curing by heating or equivalent treatment to polymerize oxidize the composition to a stage wherein the floor covering is sufficiently hard and resistant to abrasion to be suitable for its intended purpose and yet is still suiiiciently flexible to permit the usual bending and rolling required of llineigemn.
- matrix is similarly iron oxide
- formoguanamine is generally suflicient, e. g., (Ll-5% of the siccative composition but obviously' smaller or larger proportions may be used it desirable. In some instances, the alkali resistance may be improved somewhat by the use of formoguanamine.
- My accelerator is preferably added mixing of the binder with the fillers, though it may be added before or during the oxidation of the-binder. If my acceleratoris added before or during the oxidation, it may inhibit somewhat the gelation of the siccative binder. It is to be noted, however, that after gelation, my accelerator speeds up the curing of the siccative composition.
- a surface covering composition including a-siccative material selected from the group consisting of drying oils and drying oil modified polyhvdric alcohol-polybasic acid resins, the step which comprises adding to such a composition formoguanamine.
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Textile Engineering (AREA)
- Paints Or Removers (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
Patented Aug. 11, 1942 ACCELERATION OF THE SEASONING SPEED OF SURFACE COVERINGS Donald G. Patterson, Stamford, Conn., assignor to American Cyanamid Company, New York,
v N. Y., a corporation of Maine No Drawing. Application April 26, 1940,
' Serial No. 331,811
1 Claim. This invention relates to the acceleration of the compositions such as floor covering compositions containing siccative binders.
- An object of this invention is to provide accelerators for surface covering compositions containing siccative binders which will cause such compositions to cure more rapidly.
This and other objects are attained by incorporating in a siccative composition which is to be used in a floor covering composition or other surface covering composition formoguanamine.
The following example is given by way of illustration and not in limitation.
' Example Parts by weight siccative bi r 30 Wood flour 30 Whiting 20 Lithopone 20 Formoguanamine 0.1
These substances with or without a small proportion of drier, e. g., 0.1% cobalt naphthenate, are mixed together, e. g., in an internal mixer. The compacted mass which is delivered from the mixer may be disintegrated, as by a set of scratch rolls which comprises a plurality of rolls having intermeshing teeth projectingfrom their surfaces. The resulting material is sheeted on calender rolls or optionally it may be further .rate of curing or seasoning of surface covering mixed and disintegrated and then calendered."
The material may be calendered on to burlap or other fibrous backing if desired. The sheeted material is placed in a. stoving. oven through which a current of heated air from about 70 C. to about 90 C. is circulated until the material is completely seasoned, i. e., until the sheet acquires the necessary degree of hardness. Higher or lower temperatures may be used if desirable.
The hardness may be measured by any of the methods generally employed in the manufacture of linoleum. See the Federal Stock Catalogue (U. S. Government Printing Ofiice), section 4,
part 5, pages ILL-L351 et seq. and pages LLL-L-36l et seq., for the method employed herein. The time required for seasoning a 2 mm. sheet of the above composition is about 4 to 5 days. The resulting seasoned floor or surface covering has about the same strength, flexibility and color as compositions not containing the accelerator; ties may be changed by many other accelerators sufliciently and in such a way that the materials One or more of these propersiccative oil as used herein other gums produced therewith are unsatisfactory. The seasoning speed of a 2 mm. sheet of the same mixture which does not contain the formoguanamine is about 18 to 20 days.
The siccative binder utilized in the above example is an alkyd resin which has siccative properties, i. e., a reaction product of fumaric acid with a non-conjugated terpene (alpha pinene) and triethylene glycol, modified with linseed oil fatty acids. Other similar resins may be used which are drying oil-modified reaction products of maleic or fumaric acids with a terpene and a polyhydric alcohol. Other alkyd resins which are modified with drying oils may be used such as the phthalic-glyceride resins, the glycolrmaleic resins, and mixed resins such as the phthalicfumaric-glycol-glyceride resins. With other types of binders, the seasoning temperature may be varied appropriately and, of course, the time required may be diiferent. About the same proportional accelerating effect is obtained when various siccative binders are employed.
Other binders which may be used are those which are derived from the drying oils and may be made in any convenient well-known manner, such as the method described in British Patent 305,656, or the binders may comprise any of the various alkyd resins having siccative properties. For drying oil binders, linseed oil is preferable for economic reasons, but other siccative oils may oil, tung oil, soya-bean oil, perilla oil, ,oiticica oil,.
Scheiber oil,sunflower-seed. oil, etc. The. term is intended to include not only the so-called drying oils but also the so-called semi-drying oils. Furthermore, it is possible to use mixtures of siccative oils with other fatty oils of the non-drying type.
It may be preferable in the manufacture of linoleum tomake use of so-called scrim-oil or shed oil either alone or fluxed with rosin or or resins and/or mixed with a proportion of the so-called mechanical oil. Either of these types of oils may be used singly if desired.
In the preparation of the siccative oil binders is customary to use rosin in admixture with the oil although other substances of the same type may be used, e. g., Kauri gum, Congo gum, ester and/or the whiting and e. g., about 0.005-1%.
- and/or glass, etc. Among the pigments which may be used the following are included: lithopone, barytes, zinc oxide, titanium oxide, chromates, red lead, white lead, malachite green, chrome green, chrome yellow, Prussian blue, etc. Similarly dyes and lakes may be used if desirable.
It is generally preferable to use driers in the preparation of the binders. The drier is usually added to the binder during the oxidation process and if desirable additional drier may be added when the binder, fillers, etc., are mixed together. Suitable driers include the oil-soluble salts such as the naphthenates, resinates and linoleates of cobalt, lead, manganese, zinc and chromium. Only a small proportion of these driers' based on the siccative oil content is generally sumcient,
although larger proportions may be used as expedient. Obviously. various mixtures of driers may be used.
The term "seasoning as applied to linoleum compositions indicates the process of curing by heating or equivalent treatment to polymerize oxidize the composition to a stage wherein the floor covering is sufficiently hard and resistant to abrasion to be suitable for its intended purpose and yet is still suiiiciently flexible to permit the usual bending and rolling required of llineigemn. The term "maturing" is similarly iron oxide,
' I have found that only a small proportion of formoguanamine is generally suflicient, e. g., (Ll-5% of the siccative composition but obviously' smaller or larger proportions may be used it desirable. In some instances, the alkali resistance may be improved somewhat by the use of formoguanamine.
My accelerator is preferably added mixing of the binder with the fillers, though it may be added before or during the oxidation of the-binder. If my acceleratoris added before or during the oxidation, it may inhibit somewhat the gelation of the siccative binder. It is to be noted, however, that after gelation, my accelerator speeds up the curing of the siccative composition.
Obviously many modifications in the processes and compositions described above may be made without departing from the spirit and scope of the invention as defined in the appended claim.
I claim:
In a process of curing a surface covering composition including a-siccative material selected from the group consisting of drying oils and drying oil modified polyhvdric alcohol-polybasic acid resins, the step which comprises adding to such a composition formoguanamine.
during the nomm G. rims.
etc., aiv
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US331811A US2292541A (en) | 1940-04-26 | 1940-04-26 | Acceleration of the seasoning speed of surface coverings |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US331811A US2292541A (en) | 1940-04-26 | 1940-04-26 | Acceleration of the seasoning speed of surface coverings |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2292541A true US2292541A (en) | 1942-08-11 |
Family
ID=23295473
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US331811A Expired - Lifetime US2292541A (en) | 1940-04-26 | 1940-04-26 | Acceleration of the seasoning speed of surface coverings |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2292541A (en) |
-
1940
- 1940-04-26 US US331811A patent/US2292541A/en not_active Expired - Lifetime
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