US3149994A - Surface texturing system and materials therefor - Google Patents
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- US3149994A US3149994A US727538A US72753858A US3149994A US 3149994 A US3149994 A US 3149994A US 727538 A US727538 A US 727538A US 72753858 A US72753858 A US 72753858A US 3149994 A US3149994 A US 3149994A
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- 239000000463 material Substances 0.000 title description 7
- 239000000203 mixture Substances 0.000 claims description 36
- 238000000034 method Methods 0.000 claims description 21
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 13
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims description 13
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 13
- 239000008199 coating composition Substances 0.000 claims description 6
- 239000004615 ingredient Substances 0.000 claims description 5
- 239000002904 solvent Substances 0.000 description 40
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 21
- 229920005989 resin Polymers 0.000 description 20
- 239000011347 resin Substances 0.000 description 20
- 239000002798 polar solvent Substances 0.000 description 15
- 229920001296 polysiloxane Polymers 0.000 description 15
- -1 diacetone alcohols Chemical class 0.000 description 13
- 239000007787 solid Substances 0.000 description 12
- 239000007921 spray Substances 0.000 description 9
- 229920000180 alkyd Polymers 0.000 description 7
- 238000000576 coating method Methods 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- 238000000151 deposition Methods 0.000 description 6
- 238000001704 evaporation Methods 0.000 description 6
- 150000002576 ketones Chemical class 0.000 description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 6
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 230000008020 evaporation Effects 0.000 description 5
- 239000010985 leather Substances 0.000 description 5
- 229920002545 silicone oil Polymers 0.000 description 5
- 239000008096 xylene Substances 0.000 description 5
- POAOYUHQDCAZBD-UHFFFAOYSA-N 2-butoxyethanol Chemical compound CCCCOCCO POAOYUHQDCAZBD-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 4
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 4
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 4
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 4
- 229940043265 methyl isobutyl ketone Drugs 0.000 description 4
- 229920002037 poly(vinyl butyral) polymer Polymers 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000004593 Epoxy Substances 0.000 description 3
- 239000004965 Silica aerogel Substances 0.000 description 3
- 229920001807 Urea-formaldehyde Polymers 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 229920006158 high molecular weight polymer Polymers 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 229920002050 silicone resin Polymers 0.000 description 3
- SVONRAPFKPVNKG-UHFFFAOYSA-N 2-ethoxyethyl acetate Chemical compound CCOCCOC(C)=O SVONRAPFKPVNKG-UHFFFAOYSA-N 0.000 description 2
- 229920000877 Melamine resin Polymers 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- 229920001944 Plastisol Polymers 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- LZBCVRCTAYKYHR-UHFFFAOYSA-N acetic acid;chloroethene Chemical compound ClC=C.CC(O)=O LZBCVRCTAYKYHR-UHFFFAOYSA-N 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 210000003298 dental enamel Anatomy 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 239000004922 lacquer Substances 0.000 description 2
- 239000006233 lamp black Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229940032007 methylethyl ketone Drugs 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 239000003921 oil Substances 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 239000004999 plastisol Substances 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 239000012260 resinous material Substances 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000004408 titanium dioxide Substances 0.000 description 2
- 239000002966 varnish Substances 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- XFNGYPLLARFULH-UHFFFAOYSA-N 1,2,4-oxadiazetidin-3-one Chemical compound O=C1NON1 XFNGYPLLARFULH-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 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 1
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 1
- 239000001856 Ethyl cellulose Substances 0.000 description 1
- ZZSNKZQZMQGXPY-UHFFFAOYSA-N Ethyl cellulose Chemical compound CCOCC1OC(OC)C(OCC)C(OCC)C1OC1C(O)C(O)C(OC)C(CO)O1 ZZSNKZQZMQGXPY-UHFFFAOYSA-N 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 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 1
- 241000272534 Struthio camelus Species 0.000 description 1
- DHXVGJBLRPWPCS-UHFFFAOYSA-N Tetrahydropyran Chemical compound C1CCOCC1 DHXVGJBLRPWPCS-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 229920006222 acrylic ester polymer Polymers 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- GZCGUPFRVQAUEE-SLPGGIOYSA-N aldehydo-D-glucose Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C=O GZCGUPFRVQAUEE-SLPGGIOYSA-N 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 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
- 239000006229 carbon black Substances 0.000 description 1
- 229920002301 cellulose acetate Polymers 0.000 description 1
- 229920006217 cellulose acetate butyrate Polymers 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
- PQPVPZTVJLXQAS-UHFFFAOYSA-N hydroxy-methyl-phenylsilicon Chemical class C[Si](O)C1=CC=CC=C1 PQPVPZTVJLXQAS-UHFFFAOYSA-N 0.000 description 1
- 239000005453 ketone based solvent Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- ODGAOXROABLFNM-UHFFFAOYSA-N polynoxylin Chemical compound O=C.NC(N)=O ODGAOXROABLFNM-UHFFFAOYSA-N 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920006215 polyvinyl ketone Polymers 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 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 1
- 230000003245 working effect Effects 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B44—DECORATIVE ARTS
- B44F—SPECIAL DESIGNS OR PICTURES
- B44F9/00—Designs imitating natural patterns
- B44F9/12—Designs imitating natural patterns of leather
-
- 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
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S428/00—Stock material or miscellaneous articles
- Y10S428/904—Artificial leather
Definitions
- the present invention is intended and adapted to overcome the disadvantages inherent in the prior art and to provide a method whereby a leather-like finish is provided which can hardly be distinguished from natural leather.
- the method of the present invention is primarily a two-step method.
- a ground coat consisting essentially of a resin or plastic material, a solvent, and such other usual ingredients of a ground coat which are ordinarily employed. It is permitted to dry partially but only to such an extent as to accommodate the top or pattern coat.
- the second step of the operation is the laying down of the pattern coat which consists essentially of a resinous or plastic material having cobwebbing characteristics.
- Such a coat may contain in addition to the resinous material and the solvent, the other usual ingredients such as modifying agents, pigments and the like.
- An essential. feature of the pattern coating composition is that it contains a silicone in quite small amounts. Usually the minimum is .0l% of the liquid coating composition, and the maximum may be the limit of compatibility thereof with the other constituents of the composition.
- polar solvents are usually the low molecular weight ketones, esters and alcohols, such substances being readily volatile under the usual conditions of application. It has been found that mixtures of polar solvents are preferable to the use of a single polar solvent. Such solvents are classified as fast, medium and slow, based upon the rate of evaporation thereof at temperatures ordinarily encountered in producing coatings.
- the polar solvents have a high degree of penetrating power into the ground coat and they effect a lowering of the surface tension. This is best obtained by the use of ketones as a part of the mixture of polar solvents.
- the pattern coat is sprayed onto the ground coat so that the resinous material is projected in the form of threads and forms a pattern or design on the ground coat.
- the solvent in the pattern coat lowers the viscosity of the ground coat at those areas Where it strikes.
- the silicone having a high degree of surface activity lowers the surface tension of the ground coat solution so that the threads sink into and are fixed as the solvent evaporates. The slower the evaporation of the solvent, the greater the penetration, but the mixture of solvents of different rapidity gives the best results as it enables the operator to determine the amount of penetration which he desires and thus controls the operation as designed.
- the silicone oils are preferred and it has been found that a wide range of .viscosities are adapted for the purpose.
- the silicone resins are less effective and require a considerable addition, say, about 5% or more, which renders the use thereof expensive. From the technical standpoint the silicone used must have a great deal of surface activity.
- the ground coat is of a usual composition and may embody the various known resins and solvents although it is preferred for the present invention to have polar solvents present therein. After the ground coat is applied, it is allowed to set for a short time until it is wet to the touch but not tacky or sticky. A practical test to determine the correct degree of dryness thereof is to touch it with the finger and if some of the composition remains on the finger, the condition is satisfactory. Another test is that when the pattern coat is applied it should sink into the surface of the ground coat. The presence of the slow solvent retards evaporation and permits the sinking of the surface coat. The speed of drying of the ground coat is affected by various conditions such as the temperathe tip or orifice, the distance of the spray gun from the of the solvents. The user will readily determine from the conditions, the time element in applying the pattern coating after the ground coat is applied.
- the character of the pattern coat is affected by other factors such as the setting of the spray gun, variations in the amount of the pattern coat being deposited, the ratio of air to composition, the size of the nozzle and needle, the adjustment of the tip or orifice, the distance of the spray gun from the object and similar factors. After a few trials, the ordinary operator will be enabled to correctly conduct the spray operation.
- compositions have been described as containing resins and solvents, modifying agents are usually incorporated in both the ground and pattern coats.
- Resins may be added to the pattern coat to alter the characteristics of the webbing resins and such additions should or may not be compatible with the basic composition.
- Pigments, dyes and sheen modifiers as known in the art may be introduced. If the pattern composition has a relatively high viscosity, the deposited patterns are relatively large with deep valleys, and vice versa. The patterns are affected by the spray gun settings.
- Styrenated alkyds, rosin modified alkyds, nitrocellulose lacquers and polyamide-catalyzed epoxies being air dry materials, lend themselves to the vast field of wood as well as metal coatings.
- the epoxy again is the recommended ground coat base because of its superior toughness and durability as well as its superior leather-like araaooa texture when topcoated properly.
- a primer or sealer is suggested to seal the pores of the wood before applying the pattern coat.
- the epon-urea resin vehicle is preferred as the base for the ground coat; first, because it seems to work best since it contains polar solvents; and second, because when topcoated and cured, it will provide a tough, adherent and abrasion and chemical resistant finish.
- Example 1 The following is a compositionhaving a low molecular weight polymer and a fast solvent. The total solids content thereof is about 40.4%.
- Dimethyl polysiloxane (4-30 cs. at 100 F.) 0.4
- Example 2 This composition illustrates the use of a low molecular weight polymer and a slow solvent. The total solids content thereof is about 45.4%.
- Example 3 The following illustrates the use of a high molecular weight polymer and a fast solvent in which the total solids content is about 9.1%.
- the composition contains a high molecular weight polymer and a medium fast solvent having a total solids content of 12.2%.
- Methyl-isobutyl ketone 87.8 Dimethyl polysiloxane (4-30 cs. at 100 F.) 0.2
- Example 5 The composition contains a high molecular weight polymer and a slow solvent, the composition having a total solids content of about 16.9%.
- Example 6 The following composition has a total solids content of about 32.2%.
- Example 7 The following composition has a total solids content of about 25.2%.
- Example 8 Dimethyl polysiloxane cs. at 100 F.) 0.2
- Example 8 The following composition has a total solids content of about 30.2%.
- Example 9 The following composition has a total solids content of about 63.5%.
- Example 10 V The following composition has a total solids content of about 31.0%.
- Example 11 The following is the composition of a commercially acceptable pattern coat providing a brown leather finish:
- the formulations include silicates which are introduced to lower the gloss. Pigments are included in order to obtain the desired color and a ketone resin is provided to improve adhesion. Fast, medium and slow solvents are included to provide good working properties.
- the atomizing air pressure is usually 25 lbs. and in Example 12 it is usually about 50 lbs.
- silicone oil which is generally dimethyl polysiloxane.
- the viscosities thereof may vary widely and depending upon the viscosity will depend the exact amount thereof to be used. Generally those silicone oils having a viscosity of about 0.65 to about 1,000,000 centistokes are preferred. Other oils of this character are also usable, as for example the phenyl methyl siloxane compounds. Silicone resins are suitable under special conditions but are considered to be inferior to the silicone oils. While it is preferred to use the minimum amounts of silicone oils, the maximum thereof is limited only by the factors of compatibility or cost.
- polar solvents such as ketones improves the leather-like effects although they are not absolutely necessary.
- Such less polar solvents as toluene may be used with good results.
- the use of a mixture of slow, medium and fast evaporating polar solvents (ketones, ethers, esters, alcohols is recommended), so that a heavy coat will not sag and yet will remain wet long enough to enable the pattern coat to leave an impression.
- the fast solvents may include aromatic hydrocarbons such as toluene, or aliphatic hydrocarbons such as naphtha. If a large object is to be coated, an increased proportion of a slow solvent, such as butyl Cellosolve, should be incorporated in the ground coat. Likewise in the summer, when the temperature reaches 90 or 100 F, more diacetone alcohol or butyl Cellosolve should replace some of the methyl isobutyl ketone to prevent the ground coat from drying too fast. In cold temperature, the reverse procedure should be followed. The same principle applies to the pattern coat as well. Below is a partial list of solvents and their evaporation rates that may be used in both the ground and the pattern coats:
- varnish or lacquer resins include drying and non-drying alkyd resins, urea-formaldehyde, melamineformaldehyde, vinyl chloride-acetate, polyacrylic ester, epoxy, nitrified ester, polyester, phenol-formaldehyde varnish, nitrocellulose, ethyl cellulose, cellulose acetate, cellulose acetate-butyrate, chlorinated rubber, vinyl toluene, japan, polyamide, latex, silicone resin, polyvinyl butyral, styrenated alkyd, plastisol and organosol.
- Example 13 Epon resin l8 Urea-formaldehyde resin 9 Rutile titanium dioxide l9 Silica aerogel 1 Ethyl acetate and Cellosolve acetate 25 Butyl alcohol 6 Toluene and xylene 22
- Example 14 Melamine-formaldehyde resin Short drying soya alkyd resin 55 Silica aerogel 2 Butyl Cellosolve and naphtha 15.3 Yellow and red iron oxide l6 Lampblack and titanium dioxide 1.7
- Example 15 Maleic modified vinyl-chloride acetate l5 Cyclohexanone 25 Methyl isobutyl ketone 15 Xylene 3 0 Titanium dioxide 14.7 Lampblack 0.3
- the ground coat is sprayed at 50 lbs. of air pressure to a dry film thickness of 1 to 3 mils, depending on the type of vehicle and on whether it is to be air dried or baked. For example, to spray a baking epoxy-urea type of ground coat at a film thickness greater than 1.5 dry mils would be running the risk of producing a blistered film.
- the pattern coat is sprayed over the ground coat at any time up to seconds later, using approximately 25 lbs. of atomizing air pressure, and standing 1.5 to 2 feet from the object being coated. After a flash-dry period of five to 10 minutes, the coating is baked at about 325 F. for 15 minutes.
- the baking schedule will depend on the type of ground coat as well as the users oven facilities. Air-dry ground coats have been successfully formulated. In unusual cases, where large objects are to be sprayed, the air-set time between the ground coat and the pattern coat may be extended to five or six minutes by reducing both coats 10 to 20% with an extra slow solvent such as butyl Cellosolve.
- the sprayer can control the pattern desired, whether fine or heavy, by narrowing or widening the fan, and by increasing or decreasing the amount of pattern coat coming from spray gun.
- the formulator by increasing the proportion of fast solvents can produce a finer pattern and, conversely, by increasing the amount of slow solvents will produce a coarse pattern.
- the shorter the time between the ground coat and the pattern coat e.g., 10 to 15 seconds, the more the pattern coat will spread out over the ground coat. A long air-set time will minimize the spreading tendency.
- the preferable appearance is a matter of personal taste.
- a method of making a film having a leather-like finish which comprises depositing a ground coat containing a resin and a solvent, permitting said solvent to evaporate for a sufiicient time to leave said ground coat wet enough to enable a pattern coat to become impressed therein, then at said time depositing on said ground coat a pattern coat comprising a resin which is compatible with methyl polysiloxane, a solvent, and a methyl polysiloxane in the amount of at least about .01% of said pattern composition up to the limit of compatibility thereof.
- a method of making a film having a leather-like finish which comprises depositing a ground coat containing a resin and a solvent, permitting said solvent to evaporate for a sufficient time to leave said ground coat wet enough to enable a pattern coat to become impressed therein, then at said time depositing on said ground coat Z t. a pattern coat containing a resin which is compatible with methyl polysiloxane, a solvent, and a methyl polysiloxane in the amount of at least about 01% of said pattern composition up to the limit of compatibility thereof, then air diying said deposit.
- a method of making a film having a leather-like finish which comprises depositing a ground coat containing a resin and a solvent, permitting said solvent to evaporate for a sufficient time to leave said ground coat Wet enough 'to enable a pattern coat to become impressed therein, then at said time depositing on said ground coat a pattern coat containing a resin Which is compatible with methyl polysiloxane, a solvent, and a methyl polysiloxane in the amount of at least about 01% of said pattern composition up to the limit of compatibility thereof, then air drying said deposit for several minutes, and finally baking said deposit.
- a process for producing a decorative finish on a surface to be coated which comprises the steps of 1) applying a resinous film-forming composition to said surface and thereafter, before said composition sets (2) applying a coating composition containing as an essential V ingredient from 0.01% to 1% by weight of dimethyl polysiloxane.
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- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Treatment And Processing Of Natural Fur Or Leather (AREA)
- Paints Or Removers (AREA)
Description
p 22, 1964 J. 5. CONGLETON ETAL 3,149,994
SURFACE TEXTURING sysmu AND MATERIALS THEREFOR Filed April 10, 1958 .Spray Ground Coaf Air 8e! 0 to 6 Min.
Max/mum Spray Pattern 000/ With Dimef/ry/ Si/oxane Air Dry or Bake INVENTOR JOHN S. CONGLETON AR THUR S. SIMON BY EW+ BW ATTORNEY United States Patent 3,149,994 SURFACE TEXTURING SYSTEM AND MATERIALS THEREFOR John S. Congleton, Kinneion, and Arthur S. Simon, Belleville, N.J., assignors to Maas 8: Wallstein Co., Newark,
NJ a corporation of New Jersey Filed Apr. 10, 1958, Ser. No. 727,538 14 Claims. (Cl. 117--45) The present application is directed to liquid coating compositions and more particularly to an improved method whereby certain decorative effects resembling natural leathers are obtained.
There have been prior attempts to produce coatings on various bases, which would have a texture resembling leather. In one such process, it was necessary to first lay down a film with a primer composition, which was baked, after which it was sprayed with a plastisol or organosol enamel. Thereafter the enamel was sprayed with a solvent in order to give the desired texture, and then the assembly was baked. Such a product had only a faint resemblance to leather; the film was too thick and the cost thereof was relatively high. The appearance was that of a small stipple and could be produced only in a monocolor.
The present invention is intended and adapted to overcome the disadvantages inherent in the prior art and to provide a method whereby a leather-like finish is provided which can hardly be distinguished from natural leather.
It is also among the objects of the present invention to provide a method which permits great flexibility in the conditions of operation so that as a result, at the will of the operator, a variety of types of leather can be simulated.
It is further among the objects of the present invention to provide a method which is rapid, effective, inexpensive, which can be conducted by even relatively unskilled workers and which enables the use of the ordinary equipment used in making coating films.
The method of the present invention is primarily a two-step method. In the first step there is provided a ground coat consisting essentially of a resin or plastic material, a solvent, and such other usual ingredients of a ground coat which are ordinarily employed. It is permitted to dry partially but only to such an extent as to accommodate the top or pattern coat. The second step of the operation is the laying down of the pattern coat which consists essentially of a resinous or plastic material having cobwebbing characteristics. Such a coat may contain in addition to the resinous material and the solvent, the other usual ingredients such as modifying agents, pigments and the like.
An essential. feature of the pattern coating composition is that it contains a silicone in quite small amounts. Usually the minimum is .0l% of the liquid coating composition, and the maximum may be the limit of compatibility thereof with the other constituents of the composition.
Another feature of the invention is the use of polar solvents in conjunction with the siiicones. Such polar solvents are usually the low molecular weight ketones, esters and alcohols, such substances being readily volatile under the usual conditions of application. It has been found that mixtures of polar solvents are preferable to the use of a single polar solvent. Such solvents are classified as fast, medium and slow, based upon the rate of evaporation thereof at temperatures ordinarily encountered in producing coatings.
It is considered that the use of the silicones together with polar solvents provides a synergistic action whereby the improved results of the invention are obtained. The polar solvents have a high degree of penetrating power into the ground coat and they effect a lowering of the surface tension. This is best obtained by the use of ketones as a part of the mixture of polar solvents. The pattern coat is sprayed onto the ground coat so that the resinous material is projected in the form of threads and forms a pattern or design on the ground coat. The solvent in the pattern coat lowers the viscosity of the ground coat at those areas Where it strikes. The silicone having a high degree of surface activity lowers the surface tension of the ground coat solution so that the threads sink into and are fixed as the solvent evaporates. The slower the evaporation of the solvent, the greater the penetration, but the mixture of solvents of different rapidity gives the best results as it enables the operator to determine the amount of penetration which he desires and thus controls the operation as designed.
The silicone oils are preferred and it has been found that a wide range of .viscosities are adapted for the purpose. The silicone resins are less effective and require a considerable addition, say, about 5% or more, which renders the use thereof expensive. From the technical standpoint the silicone used must have a great deal of surface activity.
The ground coat is of a usual composition and may embody the various known resins and solvents although it is preferred for the present invention to have polar solvents present therein. After the ground coat is applied, it is allowed to set for a short time until it is wet to the touch but not tacky or sticky. A practical test to determine the correct degree of dryness thereof is to touch it with the finger and if some of the composition remains on the finger, the condition is satisfactory. Another test is that when the pattern coat is applied it should sink into the surface of the ground coat. The presence of the slow solvent retards evaporation and permits the sinking of the surface coat. The speed of drying of the ground coat is affected by various conditions such as the temperathe tip or orifice, the distance of the spray gun from the of the solvents. The user will readily determine from the conditions, the time element in applying the pattern coating after the ground coat is applied.
The faster the solvent in the ground coat, the shorter is the time for the application of the pattern coat. Ordinarily the time would vary from about 10 seconds up to two minutes interval but under some conditions, the interval may be up to five or sixminutes. The character of the pattern coat is affected by other factors such as the setting of the spray gun, variations in the amount of the pattern coat being deposited, the ratio of air to composition, the size of the nozzle and needle, the adjustment of the tip or orifice, the distance of the spray gun from the object and similar factors. After a few trials, the ordinary operator will be enabled to correctly conduct the spray operation.
While the above compositions have been described as containing resins and solvents, modifying agents are usually incorporated in both the ground and pattern coats. Resins may be added to the pattern coat to alter the characteristics of the webbing resins and such additions should or may not be compatible with the basic composition. Pigments, dyes and sheen modifiers as known in the art may be introduced. If the pattern composition has a relatively high viscosity, the deposited patterns are relatively large with deep valleys, and vice versa. The patterns are affected by the spray gun settings.
Styrenated alkyds, rosin modified alkyds, nitrocellulose lacquers and polyamide-catalyzed epoxies, being air dry materials, lend themselves to the vast field of wood as well as metal coatings. The epoxy again is the recommended ground coat base because of its superior toughness and durability as well as its superior leather-like araaooa texture when topcoated properly. A primer or sealer is suggested to seal the pores of the wood before applying the pattern coat. The epon-urea resin vehicle is preferred as the base for the ground coat; first, because it seems to work best since it contains polar solvents; and second, because when topcoated and cured, it will provide a tough, adherent and abrasion and chemical resistant finish.
In the accompanying drawing, the single figure is a self-explanatory flow sheet of the process involved in practicing the present invention.
The following examples are illustrative of the various "formulations using various types of polymers with varying amounts of solids and solvents having various rates of evaporation. From these examples, it will be noted that the slower the solvent, the higher will the solids content and/ or the viscosity have to be in order to produce the desired cobwebbing effect. These are basic formulations and are not to be considered as the best for commercial use since they are intended to illustrate the extremes in solvents and polymers. In these examples, the proportions of the constituents are given by weight.
Example 1 The following is a compositionhaving a low molecular weight polymer and a fast solvent. The total solids content thereof is about 40.4%.
Styrenated phthalic-glycerine-maleic alkyd 80.0
Methyl-ethyl ketone 19.6
Dimethyl polysiloxane (4-30 cs. at 100 F.) 0.4 Example 2 This composition illustrates the use of a low molecular weight polymer and a slow solvent. The total solids content thereof is about 45.4%.
Styrenated rosin-phthalic glyceride alkyd r 90.0 High flash naphtha 9.6 Dimethyl polysiloxane (4-30 cs. at 100) 0.4
Example 3 The following illustrates the use of a high molecular weight polymer and a fast solvent in which the total solids content is about 9.1%.
The composition contains a high molecular weight polymer anda medium fast solvent having a total solids content of 12.2%.
Polyvinyl butyral resin 12.0
Methyl-isobutyl ketone 87.8 Dimethyl polysiloxane (4-30 cs. at 100 F.) 0.2
Example 5 The composition contains a high molecular weight polymer and a slow solvent, the composition having a total solids content of about 16.9%.
Polyvinyl butyral resin 16.7 Isophorone 83.1 Dimethyl polysiloxane (430 cs. at 100 F.) 0.2
The following examples show the use of still other webbing resins or compositions used in the pattern coat whereby a cobwebbing effect is obtained.
Example 6 The following composition has a total solids content of about 32.2%.
Acrylic ester polymer 80.0 Toluene 19.8
Dimethyl polysiloxane '(100 cs. at 100 F.) 0.2
4 Example 7 The following composition has a total solids content of about 25.2%.
Chlorinated rubber (20 'centipoises) 25.0
Xylene 68.4
Solvent naphtha 6.4
Dimethyl polysiloxane cs. at 100 F.) 0.2 Example 8 The following composition has a total solids content of about 30.2%.
Hydroxylated vinyl chloride-acetate copolymer 30.0 Acetone 69.8 Dimethyl polysiloxane (100 cs. at 100 F.) 0.2
Example 9 The following composition has a total solids content of about 63.5%.
Epichlorohydrin-bisphenol (epoxy) resin 62.5
Acetone 36.5
Dimethyl polysiloxane (100 cs. at 100 F.) 1.0
Example 10 V The following composition has a total solids content of about 31.0%.
Polystyrene 79.2 Toluene 20.6 Dimethyl polysiloxane (100 cs. at 100 F.) 0.2
The following examples illustrate the wide variety of complete pattern coatings containing not only the basic materials but other constituents normal to the coating compositions.
Example 11 The following is the composition of a commercially acceptable pattern coat providing a brown leather finish:
to give a leather-like finish resembling pigskin or ostrich skin.
Polyvinyl butyral and ketone resins 14.780
Red iron oxide and carbon black 3.355 Silica aerogel 0.440 Ethyl. butyl and diacetone alcohols 28.260 Ethyl Cellosolve Q 10.000 Methyl ethyl and methyl isobutyl ketones 17.330 Toluene and xylene 25.780 Citric acid 0.005 Dimethyl polysiloxane (200 cs. at 25 C.) 0.050
In Examples 11 and 12, the formulations include silicates which are introduced to lower the gloss. Pigments are included in order to obtain the desired color and a ketone resin is provided to improve adhesion. Fast, medium and slow solvents are included to provide good working properties. In Example 11 the atomizing air pressure is usually 25 lbs. and in Example 12 it is usually about 50 lbs.
The important and essential ingredient of all of the above compositions of Examples 1 to 12 is a silicone oil which is generally dimethyl polysiloxane. The viscosities thereof may vary widely and depending upon the viscosity will depend the exact amount thereof to be used. Generally those silicone oils having a viscosity of about 0.65 to about 1,000,000 centistokes are preferred. Other oils of this character are also usable, as for example the phenyl methyl siloxane compounds. Silicone resins are suitable under special conditions but are considered to be inferior to the silicone oils. While it is preferred to use the minimum amounts of silicone oils, the maximum thereof is limited only by the factors of compatibility or cost.
The use of polar solvents such as ketones improves the leather-like effects although they are not absolutely necessary. Such less polar solvents as toluene may be used with good results. To obtain optimum results, it is highly desirable to include medium and slow ketone solvents in the ground coat as well as the pattern coat.
The use of a mixture of slow, medium and fast evaporating polar solvents (ketones, ethers, esters, alcohols is recommended), so that a heavy coat will not sag and yet will remain wet long enough to enable the pattern coat to leave an impression. The fast solvents may include aromatic hydrocarbons such as toluene, or aliphatic hydrocarbons such as naphtha. If a large object is to be coated, an increased proportion of a slow solvent, such as butyl Cellosolve, should be incorporated in the ground coat. Likewise in the summer, when the temperature reaches 90 or 100 F, more diacetone alcohol or butyl Cellosolve should replace some of the methyl isobutyl ketone to prevent the ground coat from drying too fast. In cold temperature, the reverse procedure should be followed. The same principle applies to the pattern coat as well. Below is a partial list of solvents and their evaporation rates that may be used in both the ground and the pattern coats:
Extra slow: Isophorone, butyl Cellosolve, and cyclohexanol.
Slow: Diacetone alcohol, Cellosolve acetate, and cyclohexanone.
Medium: Butanol, xylene, butyl acetate, VM & P naphtha,
and methyl isobutyl ketone.
Fast: Toluene, methyl ethyl ketone, and ethyl acetate.
In the ground coat practically the entire field of varnish or lacquer resins may be used. They include drying and non-drying alkyd resins, urea-formaldehyde, melamineformaldehyde, vinyl chloride-acetate, polyacrylic ester, epoxy, nitrified ester, polyester, phenol-formaldehyde varnish, nitrocellulose, ethyl cellulose, cellulose acetate, cellulose acetate-butyrate, chlorinated rubber, vinyl toluene, japan, polyamide, latex, silicone resin, polyvinyl butyral, styrenated alkyd, plastisol and organosol.
The following examples illustrate a few of the very great number of ground coats which might be used.
Example 13 Epon resin l8 Urea-formaldehyde resin 9 Rutile titanium dioxide l9 Silica aerogel 1 Ethyl acetate and Cellosolve acetate 25 Butyl alcohol 6 Toluene and xylene 22 Example 14 Melamine-formaldehyde resin Short drying soya alkyd resin 55 Silica aerogel 2 Butyl Cellosolve and naphtha 15.3 Yellow and red iron oxide l6 Lampblack and titanium dioxide 1.7
Example 15 Maleic modified vinyl-chloride acetate l5 Cyclohexanone 25 Methyl isobutyl ketone 15 Xylene 3 0 Titanium dioxide 14.7 Lampblack 0.3
It is possible to achieve a multi-colored etfect if the user so desires. Normally, the ground coat is sprayed at 50 lbs. of air pressure to a dry film thickness of 1 to 3 mils, depending on the type of vehicle and on whether it is to be air dried or baked. For example, to spray a baking epoxy-urea type of ground coat at a film thickness greater than 1.5 dry mils would be running the risk of producing a blistered film. The pattern coat is sprayed over the ground coat at any time up to seconds later, using approximately 25 lbs. of atomizing air pressure, and standing 1.5 to 2 feet from the object being coated. After a flash-dry period of five to 10 minutes, the coating is baked at about 325 F. for 15 minutes. The baking schedule will depend on the type of ground coat as well as the users oven facilities. Air-dry ground coats have been successfully formulated. In unusual cases, where large objects are to be sprayed, the air-set time between the ground coat and the pattern coat may be extended to five or six minutes by reducing both coats 10 to 20% with an extra slow solvent such as butyl Cellosolve.
The sprayer can control the pattern desired, whether fine or heavy, by narrowing or widening the fan, and by increasing or decreasing the amount of pattern coat coming from spray gun. The formulator, by increasing the proportion of fast solvents can produce a finer pattern and, conversely, by increasing the amount of slow solvents will produce a coarse pattern. Also, the shorter the time between the ground coat and the pattern coat, e.g., 10 to 15 seconds, the more the pattern coat will spread out over the ground coat. A long air-set time will minimize the spreading tendency. The preferable appearance is a matter of personal taste.
We claim:
1. A method of making a film having a leather-like finish which comprises depositing a ground coat containing a resin and a solvent, permitting said solvent to evaporate for a sufiicient time to leave said ground coat wet enough to enable a pattern coat to become impressed therein, then at said time depositing on said ground coat a pattern coat comprising a resin which is compatible with methyl polysiloxane, a solvent, and a methyl polysiloxane in the amount of at least about .01% of said pattern composition up to the limit of compatibility thereof.
2. A method according to claim 1 in which said pattern coat solvent is at least in part a polar solvent.
3. A method according to claim 1 in which said ground coat solvent is at least in par a polar solvent.
4. A method according to claim 2 in which a mixture of polar solvent of differing volatility is provided.
5. A method according to claim 1 in which said polysiloxane is taken from the class consisting of 'dimethyland phenyl-methyl-polysiloxane.
6. A method according to claim 1 in which said pattern composition contains cobwebbing resins.
7. A method according to claim 1 in which said polysiloxane is in the form of an oil.
8. A method according to claim 1 in which said polysiloxane is in the form of a resin.
9. A method according to claim 1 in which said polysiloxane has a viscosity of about 0.65 to 1,000,000 centistokes at 25 C.
10. A method according to claim 1 in which said pattern coat is applied after about 10 to 120 seconds.
11. A method according to claim 1 in which at least one of said coats is deposited by spraying.
12. A method of making a film having a leather-like finish which comprises depositing a ground coat containing a resin and a solvent, permitting said solvent to evaporate for a sufficient time to leave said ground coat wet enough to enable a pattern coat to become impressed therein, then at said time depositing on said ground coat Z t. a pattern coat containing a resin which is compatible with methyl polysiloxane, a solvent, and a methyl polysiloxane in the amount of at least about 01% of said pattern composition up to the limit of compatibility thereof, then air diying said deposit.
13. A method of making a film having a leather-like finish which comprises depositing a ground coat containing a resin and a solvent, permitting said solvent to evaporate for a sufficient time to leave said ground coat Wet enough 'to enable a pattern coat to become impressed therein, then at said time depositing on said ground coat a pattern coat containing a resin Which is compatible with methyl polysiloxane, a solvent, and a methyl polysiloxane in the amount of at least about 01% of said pattern composition up to the limit of compatibility thereof, then air drying said deposit for several minutes, and finally baking said deposit.
14. A process for producing a decorative finish on a surface to be coated Which comprises the steps of 1) applying a resinous film-forming composition to said surface and thereafter, before said composition sets (2) applying a coating composition containing as an essential V ingredient from 0.01% to 1% by weight of dimethyl polysiloxane.
References Cited in the file of this patent UNITED STATES PATENTS OTHER REFERENCES Burrell: Organic Finishing, December 1955, pp. 15-20.
UNITED STATES PATENT OFFICE CERTIFICATE OF CORRECTION Patent No, 3, 149,994 September 22 1964 John So Congleton et 31,
It is hereby certified that error appears in the above numbered patent requiring correction and that the said Letters Patent should read as corrected below.
In the grant lines 2 and 12 and in the heading to the printed specification line 5 for "Maas 81 Wallstein each occurrence read Maas 81 Waldstein Signed and sealed this 30th day of March 1965,
(SEAL) Allest:
ERNEST W. SWIDER EDWARD J. BRENNER Attesting Officer Commissioner of Patents
Claims (1)
14. A PROCESS FOR PRODUCING A DECORATIVE FINISH ON A SURFACE TO BE COATED WHICH COMPRISES THE STEPS OF (1) APPLYING A RESINOUS FILM-FORMING COMPOSITION TO SAID SURFACE AND THEREAFTER, BEFORE SAID COMPOSITION SETS (2) APPLYING A COATING COMPOSITION CONTAINING AS AN ESSENTIAL INGREDIENT FROM 0.01% TO 1% BY WEIGHT OF DIMETHYL POLYSILOXANE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US727538A US3149994A (en) | 1958-04-10 | 1958-04-10 | Surface texturing system and materials therefor |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US727538A US3149994A (en) | 1958-04-10 | 1958-04-10 | Surface texturing system and materials therefor |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3149994A true US3149994A (en) | 1964-09-22 |
Family
ID=24923062
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US727538A Expired - Lifetime US3149994A (en) | 1958-04-10 | 1958-04-10 | Surface texturing system and materials therefor |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3149994A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3355312A (en) * | 1963-11-27 | 1967-11-28 | Eastman Kodak Co | Multicolor coating process and coated article |
| US3549407A (en) * | 1968-02-29 | 1970-12-22 | Du Pont | Process for applying a textured decorative coating to a metal substrate and article thereof |
| US3723171A (en) * | 1969-09-15 | 1973-03-27 | O Fuchs | Process for the manufacture of pvf shaped articles |
| US4029831A (en) * | 1975-06-19 | 1977-06-14 | Masonite Corporation | Method of making a multi-gloss panel |
| EP0060907A1 (en) * | 1981-03-21 | 1982-09-29 | Burlington Industries, Inc. | Drapery fabric foam backing |
| US4362774A (en) * | 1979-12-27 | 1982-12-07 | Burlington Industries, Inc. | Drapery fabric foam backing |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2523065A (en) * | 1947-12-29 | 1950-09-19 | Gen Electric | Pigmented coating compositions containing liquid alkyl polysiloxane |
| US2643240A (en) * | 1950-04-13 | 1953-06-23 | Union Carbide & Carbon Corp | Polysiloxane antifoam agents |
| US2724704A (en) * | 1955-11-22 | Alkyd-silicone coaung | ||
| US3063866A (en) * | 1960-12-02 | 1962-11-13 | Gen Mills Inc | Method of forming bismuth whiskers |
-
1958
- 1958-04-10 US US727538A patent/US3149994A/en not_active Expired - Lifetime
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2724704A (en) * | 1955-11-22 | Alkyd-silicone coaung | ||
| US2523065A (en) * | 1947-12-29 | 1950-09-19 | Gen Electric | Pigmented coating compositions containing liquid alkyl polysiloxane |
| US2643240A (en) * | 1950-04-13 | 1953-06-23 | Union Carbide & Carbon Corp | Polysiloxane antifoam agents |
| US3063866A (en) * | 1960-12-02 | 1962-11-13 | Gen Mills Inc | Method of forming bismuth whiskers |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3355312A (en) * | 1963-11-27 | 1967-11-28 | Eastman Kodak Co | Multicolor coating process and coated article |
| US3549407A (en) * | 1968-02-29 | 1970-12-22 | Du Pont | Process for applying a textured decorative coating to a metal substrate and article thereof |
| US3723171A (en) * | 1969-09-15 | 1973-03-27 | O Fuchs | Process for the manufacture of pvf shaped articles |
| US4029831A (en) * | 1975-06-19 | 1977-06-14 | Masonite Corporation | Method of making a multi-gloss panel |
| US4362774A (en) * | 1979-12-27 | 1982-12-07 | Burlington Industries, Inc. | Drapery fabric foam backing |
| EP0060907A1 (en) * | 1981-03-21 | 1982-09-29 | Burlington Industries, Inc. | Drapery fabric foam backing |
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