US2747997A - Decoration of cellulosic, metal and vitreous surfaces - Google Patents
Decoration of cellulosic, metal and vitreous surfaces Download PDFInfo
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- US2747997A US2747997A US312478A US31247852A US2747997A US 2747997 A US2747997 A US 2747997A US 312478 A US312478 A US 312478A US 31247852 A US31247852 A US 31247852A US 2747997 A US2747997 A US 2747997A
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- fluorescent
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- 229910052751 metal Inorganic materials 0.000 title description 6
- 239000002184 metal Substances 0.000 title description 6
- 238000005034 decoration Methods 0.000 title description 4
- 239000000203 mixture Substances 0.000 description 24
- 229920000642 polymer Polymers 0.000 description 20
- 238000000034 method Methods 0.000 description 14
- 239000000049 pigment Substances 0.000 description 11
- XLLIQLLCWZCATF-UHFFFAOYSA-N ethylene glycol monomethyl ether acetate Natural products COCCOC(C)=O XLLIQLLCWZCATF-UHFFFAOYSA-N 0.000 description 10
- 239000011521 glass Substances 0.000 description 9
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 8
- 239000004372 Polyvinyl alcohol Substances 0.000 description 8
- 238000000576 coating method Methods 0.000 description 8
- 229920002451 polyvinyl alcohol Polymers 0.000 description 8
- 229920002554 vinyl polymer Polymers 0.000 description 8
- 239000011248 coating agent Substances 0.000 description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 229940114081 cinnamate Drugs 0.000 description 6
- WBYWAXJHAXSJNI-UHFFFAOYSA-N cinnamic acid group Chemical class C(C=CC1=CC=CC=C1)(=O)O WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 4
- 239000003960 organic solvent Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- -1 albumen Substances 0.000 description 3
- LHMRXAIRPKSGDE-UHFFFAOYSA-N benzo[a]anthracene-7,12-dione Chemical compound C1=CC2=CC=CC=C2C2=C1C(=O)C1=CC=CC=C1C2=O LHMRXAIRPKSGDE-UHFFFAOYSA-N 0.000 description 3
- 235000013985 cinnamic acid Nutrition 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- WOGITNXCNOTRLK-VOTSOKGWSA-N (e)-3-phenylprop-2-enoyl chloride Chemical compound ClC(=O)\C=C\C1=CC=CC=C1 WOGITNXCNOTRLK-VOTSOKGWSA-N 0.000 description 2
- IAHOUQOWMXVMEH-UHFFFAOYSA-N 2,4,6-trinitroaniline Chemical compound NC1=C([N+]([O-])=O)C=C([N+]([O-])=O)C=C1[N+]([O-])=O IAHOUQOWMXVMEH-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- 108010010803 Gelatin Proteins 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000005083 Zinc sulfide Substances 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 150000003934 aromatic aldehydes Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229930016911 cinnamic acid Natural products 0.000 description 2
- ZOIVSVWBENBHNT-UHFFFAOYSA-N dizinc;silicate Chemical compound [Zn+2].[Zn+2].[O-][Si]([O-])([O-])[O-] ZOIVSVWBENBHNT-UHFFFAOYSA-N 0.000 description 2
- 229920000159 gelatin Polymers 0.000 description 2
- 239000008273 gelatin Substances 0.000 description 2
- 235000019322 gelatine Nutrition 0.000 description 2
- 235000011852 gelatine desserts Nutrition 0.000 description 2
- 239000003292 glue Substances 0.000 description 2
- 229920006395 saturated elastomer Polymers 0.000 description 2
- 229920003002 synthetic resin Polymers 0.000 description 2
- 239000000057 synthetic resin Substances 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 2
- 229910000165 zinc phosphate Inorganic materials 0.000 description 2
- 229910052984 zinc sulfide Inorganic materials 0.000 description 2
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 2
- WWXMVRYHLZMQIG-SNAWJCMRSA-N 3-nitrocinnamic acid Chemical compound OC(=O)\C=C\C1=CC=CC([N+]([O-])=O)=C1 WWXMVRYHLZMQIG-SNAWJCMRSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- WBYWAXJHAXSJNI-SREVYHEPSA-N Cinnamic acid Chemical compound OC(=O)\C=C/C1=CC=CC=C1 WBYWAXJHAXSJNI-SREVYHEPSA-N 0.000 description 1
- 238000005727 Friedel-Crafts reaction Methods 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- 206010034960 Photophobia Diseases 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 238000005882 aldol condensation reaction Methods 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000008425 anthrones Chemical class 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000001055 blue pigment Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002361 compost Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- PBZROIMXDZTJDF-UHFFFAOYSA-N hepta-1,6-dien-4-one Chemical compound C=CCC(=O)CC=C PBZROIMXDZTJDF-UHFFFAOYSA-N 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
- 150000002576 ketones Chemical class 0.000 description 1
- 229910052981 lead sulfide Inorganic materials 0.000 description 1
- 229940056932 lead sulfide Drugs 0.000 description 1
- 208000013469 light sensitivity Diseases 0.000 description 1
- QFVDKARCPMTZCS-UHFFFAOYSA-N methylrosaniline Chemical compound C1=CC(N(C)C)=CC=C1C(O)(C=1C=CC(=CC=1)N(C)C)C1=CC=C(N(C)C)C=C1 QFVDKARCPMTZCS-UHFFFAOYSA-N 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 229960003351 prussian blue Drugs 0.000 description 1
- 239000013225 prussian blue Substances 0.000 description 1
- 150000004053 quinones Chemical class 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- XNGYKPINNDWGGF-UHFFFAOYSA-L silver oxalate Chemical compound [Ag+].[Ag+].[O-]C(=O)C([O-])=O XNGYKPINNDWGGF-UHFFFAOYSA-L 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 229940044603 styrene Drugs 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- FUSUHKVFWTUUBE-UHFFFAOYSA-N vinyl methyl ketone Natural products CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 1
- 230000004304 visual acuity Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 description 1
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J9/00—Apparatus or processes specially adapted for the manufacture, installation, removal, maintenance of electric discharge tubes, discharge lamps, or parts thereof; Recovery of material from discharge tubes or lamps
- H01J9/20—Manufacture of screens on or from which an image or pattern is formed, picked up, converted or stored; Applying coatings to the vessel
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03F—PHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
- G03F7/00—Photomechanical, e.g. photolithographic, production of textured or patterned surfaces, e.g. printing surfaces; Materials therefor, e.g. comprising photoresists; Apparatus specially adapted therefor
- G03F7/0005—Production of optical devices or components in so far as characterised by the lithographic processes or materials used therefor
- G03F7/0007—Filters, e.g. additive colour filters; Components for display devices
-
- 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
- Y10S430/00—Radiation imagery chemistry: process, composition, or product thereof
- Y10S430/1053—Imaging affecting physical property or radiation sensitive material, or producing nonplanar or printing surface - process, composition, or product: radiation sensitive composition or product or process of making binder containing
- Y10S430/1055—Radiation sensitive composition or product or process of making
- Y10S430/106—Binder containing
- Y10S430/109—Polyester
Definitions
- dichroma'te'd glue compositions require high intensity and duration of exposure to light to obtain the best results and such compositions are notoriously unstable.
- a process involving the use of a dichrornate sensitized mixture of gelatin and a synthetic resin is disclosed in U. S. Patent 2,472,128. This process is characterized by producing direct positive images by exposure of the composition to light followed by removal of the exposed regions from the supportcarrying the sensitive layer. In spite of the advantages of the process difficulty of reproducibility in the process and low resolving power have limited the usefulness of the process.
- pigmented compositions containing certain polymers which are inherently lightsensitive and which can be sensitized to increase their speed, are especially efficacious for decorative purposes such as those set forth in detail in the following examples.
- the pigmented compositions of the invention contain in addition to pigments, synthetic polymers having combined polymeric units containing groups of structurein which R is an aryl group as above mentioned.
- Particularly efficacious polymers under the above general formulas are the polyvinyl alcohol esters of cinnamic acids such as cinnamic acid and m-nitrocinnamic acid.
- R is an aryl group' as above.
- The" polymers are preferably made by reacting polyvinyl alcohol with cinnamoyl halides as described in the Minsk U. S. patent application Serial No. 207,052 filed January 20, 1952.
- the polymer obtained by substantially fully ester-ifyil'rg. polyvinyl alcohol with cinnamoyl chloride and containing about mole percent or combined vinyl cinnamat'e groups is particularly useful in our invention.
- useful polymers having groups of the formula immediately above in which R is an alkyl group are obtained by reacting polyvinyl alcohol with the desired saturated aliphatic acid halide such as crotonyl chloride to obtain an ester of polyvinyl alcohol.
- Useful pol mers having structures falling under the two first-mentioned general formulas above are polymers such as those obtained by reacting polymers containing ac'etyl groups with aromatic aldehydes as disclosed in the Unruh et a l.
- a typical polymer of this type is that obtained by ace'tylatirig polystyrene and condensing the acetyl groups of the resultant polymer with ben'z'aldehyde, am: saldehyde, etc.
- the pigmented compositions preferably but not necessarily contain a light-sensitizing agent such as nitro compounds, triphenylmethane dyes, anthrones, quinones, or ketones such as disclosed in the Minsk et al. U. S. patent application Serial No. 148,684 filed March 9, 1950, now U. S. Patent 2,610,120, granted September 9, 1952, and- Serial Nos. 207,048-51 filed January 20,- 1951,- now U. S. Patents 2,690,966, 2,670,285, 2,670,286, and 2,670,287 respectively, e. g. picramide, 1,2-benzanthraquinone, crystal violet carbinol base, or 4,4'- tetramethyldiarrlinodiphenylketone.
- a light-sensitizing agent such as nitro compounds, triphenylmethane dyes, anthrones, quinones, or ketones
- the pigment components of the composition will vary according to the requirements of the particular process under consideration as will be seen from consideration of the examples following, illustrating various uses for the pigmented polymeric composition.
- thepigment used has a color contrasting with the background of the product on which the decoration is to be formed.
- the general procedure of decorating the various surfaces is also illustrated in the examples following and includes coating-and drying the light-sensitive compost tion on the desired surface, exposing the coatings preferably under a design to render the coating insoluble in organic solvents only in the region of exposure, followed by removal of the unexposed portion of the coating with an organic solvent leaving a pigmented design on the surface.
- designs of the pigmented polymeric compositions applied to a surface by hand or through stencils can be insolubilized by exposure to light and the solvent treating step is therefore not required to obtain an insoluble design on the given surface.
- Example 1 This example illustrates the preparation of pigmented images on a glass support particularly in a process of making a fluorescent screen of use in television systems.
- Three fluorescent pigmented dopes were prepared by milling 20 grams of three difierent inorganic fluorescent pigments into 100 cc. of a dope containing 20% of polyvinyl cinnamate (polyvinyl alcohol substantially 100% esterified with cinnarnoyl chloride) in ethylene glycol monomethyl ether acetate. The dopes were each sensitized with 4,4-tetramethyldiaminodiphenyl ketone.
- the first dope containing zinc phosphate as the fluorescent pigment which fluoresces red when excited, was sprayed on to a glass surface, dried and exposed to a screen having light transmitting apertures such as a perforate plate or half-tone screen, for minutes at 3 feet from a 35-ampere MacBeth white flame carbon are, developed in a tank containing a solvent mixture of xylene and ethylene glycol monomethyl ether acetate (4:1), dried and swabbed with a cotton tuft saturated with isopropyl alcohol to remove excess pigment.
- the process is partic ularly adapted to forming such fluorescent images which are fired to burn off the polymer and sinter the phosphors onto surfaces of vacuum tubes or other elements of use in the transmission and reception of color television broadcasts.
- polyvinyl cinnamate burns away more quickly and completely than gelatin or polyvinyl alcohol media.
- our process may be used to form a multiplicity of fluorescent pigmented images on supports such as glass.
- Stage A shows the sensitive element including a glass support carrying a sensitive layer of a mixture of the light-sensitive polymer such as polyvinyl cinnamate and fluorescent pigment, being exposed to light under a screen 13 having light-transmitting apertures 14 such as a perforated metal plate.
- the exposing rays impinge on area 12; of layer 11 and thereby render the polymer in the layer in that area insoluble in organic solvents.
- Example 2 This example illustrates the preparation of pigmented images on cellulosic surfaces.
- Ultramarine Blue pigment (3.75 gms.) was milled into 100 cc. of a 7.5% solution of polyvinyl cinnamate in ethylene glycol monomethyl ether acetate and the lightsensitivityof the composition was increased by the addition of picramide. The composition was then coated on to a paper support, exposed for 1 minute at 4 feet from a Eli-ampere white flame arc, and developed with methyl ethyl ketone to remove the pigmented composition from the unexposed regions and excess pigment was removed by swabbing with a cotton swab saturated with isopropyl alcohol. The result was to obtain a blue image on the paper surface.
- Example 3 This example illustrates a method for the preparation of a pigmented image on a metal support particularly suitable for template use.
- the resulting dope was coated on to a clean aluminum sheet and after drying was exposed for 1 /2 minutes at 4 feet from a 35-ampere white flame arc. The exposed coating was then developed as described in the above examples to obtain a blue pigmented image on the aluminum sheet.
- Example 5 This example illustrates the application of our invention to the preparation of metal images on vitreous surfaces for use in electrical work.
- a composition for use in forming a fluorescent image on a surface comprising a mixture of a member of the class consisting of zinc phosphate, zinc sulfide and zinc orthosilicate and a light-sensitive substantially fully esterified cinnamic acid ester of polyvinyl alcohol.
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
May 29, 1956 J. G. SMiTH ET AL 2,747,997
DECORATION OF CELLULOSIC. METAL AND VITREOUS SURFACES Filed Oct. 1, 1952 LIGHT EXPOSURE zozozoxg 305.1507
LIGHT SENSITIVE POLYMER- FLUORESCENT P/GMENT SUPPORT (GLASS) JAMES 6 SMITH EARL SUNOEEN INVENTORS M i I United States Patent signors to Eastman Kodak Company, Rochester, N. Y., a corporation of New Jerse Application October 1, 1952', Serial No. 312,478
1 claim. (Gl. 95 -7 This invention relates to photographic processes for the formation or" images on various surfaces by means of pigmented light-sensitive polymeric compositions.
In various manufacturing processes it is desirable from time to time to form a pigmented design on selected areas of a product which design is securely bonded to the product. For example, in the production of patterns and templates it is customary to form a design of a product on a thin metal or other support to serve as a guide in preparing the final product. Photographic methods are especially suitable for such work particularly since much hand work is dispensed with. In the past, various light-sensitive compositions have been employed for the decoration of surfaces such as pigmented glue, albumen, and syntheticresin compositions. In general, such compositions have been found to be lacking partly due to their inherently low light-sensitivity, poor stabili ty, etc. For example, dichroma'te'd glue compositions require high intensity and duration of exposure to light to obtain the best results and such compositions are notoriously unstable. A process involving the use of a dichrornate sensitized mixture of gelatin and a synthetic resin is disclosed in U. S. Patent 2,472,128. This process is characterized by producing direct positive images by exposure of the composition to light followed by removal of the exposed regions from the supportcarrying the sensitive layer. In spite of the advantages of the process difficulty of reproducibility in the process and low resolving power have limited the usefulness of the process.
We have discovered that pigmented compositions containing certain polymers which are inherently lightsensitive and which can be sensitized to increase their speed, are especially efficacious for decorative purposes such as those set forth in detail in the following examples.
The figures of the accompanying. drawings illustrate our invention and show in greatly enlarged cross-sectional view the appearance of a typical light-sensitive element at various stages in the production of a design on a vitreous surface.
The pigmented compositions of the invention contain in addition to pigments, synthetic polymers having combined polymeric units containing groups of structurein which R is an aryl group as above mentioned.
Particularly efficacious polymers under the above general formulas are the polyvinyl alcohol esters of cinnamic acids such as cinnamic acid and m-nitrocinnamic acid.
ice
These polymers contain combined polmeric units of structure.
in which R is an aryl group' as above. The" polymers are preferably made by reacting polyvinyl alcohol with cinnamoyl halides as described in the Minsk U. S. patent application Serial No. 207,052 filed January 20, 1952. For example, the polymer obtained by substantially fully ester-ifyil'rg. polyvinyl alcohol with cinnamoyl chloride and containing about mole percent or combined vinyl cinnamat'e groups is particularly useful in our invention. Similarly useful polymers having groups of the formula immediately above in which R is an alkyl group are obtained by reacting polyvinyl alcohol with the desired saturated aliphatic acid halide such as crotonyl chloride to obtain an ester of polyvinyl alcohol.
Useful pol mers having structures falling under the two first-mentioned general formulas above are polymers such as those obtained by reacting polymers containing ac'etyl groups with aromatic aldehydes as disclosed in the Unruh et a l. U. S. patent applicatio Serial Nos. 246,- 515, 2465 16, and 246,517 filed September 1 3, 1951,- now U. S. Patents 2,716,102, 2,716,097, and 2,706,725 respectively. A typical polymer of this type is that obtained by ace'tylatirig polystyrene and condensing the acetyl groups of the resultant polymer with ben'z'aldehyde, am: saldehyde, etc. in a Claisen-Schmidt reaction to obtain a vinyl Benzalaeetophenene polymer having pdlyi'iieri units of structure Similarly, vinylmethylketone polymers condensed with aromatic aldehydes to obtain polymers having the units (CH2'-CH-)n' OCH=CHR are very useful in our invention.
Other polymers contemplated for use in the lightsensitive pigmented compositions are those disclosed in the Allen et al. U. S. Patent 2,566,302 granted September 4, 1951. These resins are made by cinnamoylating sty rene polymers with, for example, cinnamoyl chloride in a Friedel-Crafts reaction.
In addition to containing the polymeric constituents above mentioned the pigmented compositions preferably but not necessarily contain a light-sensitizing agent such as nitro compounds, triphenylmethane dyes, anthrones, quinones, or ketones such as disclosed in the Minsk et al. U. S. patent application Serial No. 148,684 filed March 9, 1950, now U. S. Patent 2,610,120, granted September 9, 1952, and- Serial Nos. 207,048-51 filed January 20,- 1951,- now U. S. Patents 2,690,966, 2,670,285, 2,670,286, and 2,670,287 respectively, e. g. picramide, 1,2-benzanthraquinone, crystal violet carbinol base, or 4,4'- tetramethyldiarrlinodiphenylketone.
The pigment components of the composition will vary according to the requirements of the particular process under consideration as will be seen from consideration of the examples following, illustrating various uses for the pigmented polymeric composition. In general, thepigment used has a color contrasting with the background of the product on which the decoration is to be formed.
The general procedure of decorating the various surfaces is also illustrated in the examples following and includes coating-and drying the light-sensitive compost tion on the desired surface, exposing the coatings preferably under a design to render the coating insoluble in organic solvents only in the region of exposure, followed by removal of the unexposed portion of the coating with an organic solvent leaving a pigmented design on the surface. Of course, designs of the pigmented polymeric compositions applied to a surface by hand or through stencils can be insolubilized by exposure to light and the solvent treating step is therefore not required to obtain an insoluble design on the given surface.
The following examples illustrate our invention.
Example 1 This example illustrates the preparation of pigmented images on a glass support particularly in a process of making a fluorescent screen of use in television systems.
Three fluorescent pigmented dopes were prepared by milling 20 grams of three difierent inorganic fluorescent pigments into 100 cc. of a dope containing 20% of polyvinyl cinnamate (polyvinyl alcohol substantially 100% esterified with cinnarnoyl chloride) in ethylene glycol monomethyl ether acetate. The dopes were each sensitized with 4,4-tetramethyldiaminodiphenyl ketone. The first dope containing zinc phosphate as the fluorescent pigment which fluoresces red when excited, was sprayed on to a glass surface, dried and exposed to a screen having light transmitting apertures such as a perforate plate or half-tone screen, for minutes at 3 feet from a 35-ampere MacBeth white flame carbon are, developed in a tank containing a solvent mixture of xylene and ethylene glycol monomethyl ether acetate (4:1), dried and swabbed with a cotton tuft saturated with isopropyl alcohol to remove excess pigment.
The second dope containing zinc sulfide which fluoresces blue when excited, was sprayed over the first image, dried and the resultant coating exposed through the same apertured screen at a difi'erent angle in order to insolubilize the coating in a different region of the glass surface. Following this the element was developed with solvent and cleaned to remove excess pigment as mentioned above. The third dope containing zinc orthosilicate which fluoresces green when excited, was sprayed over the first two images on the glass surface and exposed through the same screen at a new angle after which the soluble region of the coating was removed as above described leaving three adjacent polymeric images each consisting of a fluorescent pigment and insoluble polymer occupying different areas of the glass surface. As is apparent, the process is partic ularly adapted to forming such fluorescent images which are fired to burn off the polymer and sinter the phosphors onto surfaces of vacuum tubes or other elements of use in the transmission and reception of color television broadcasts. It has been found that, e. g., polyvinyl cinnamate burns away more quickly and completely than gelatin or polyvinyl alcohol media. Except in those cases where it may be desirable to produce only one pigmented polymeric image having fluorescent properties on a given support, our process may be used to form a multiplicity of fluorescent pigmented images on supports such as glass.
The procedure just described for forming fluorescent pigmented polymeric images on a support is illustrated in part in the accompanying drawings wherein Stage A shows the sensitive element including a glass support carrying a sensitive layer of a mixture of the light-sensitive polymer such as polyvinyl cinnamate and fluorescent pigment, being exposed to light under a screen 13 having light-transmitting apertures 14 such as a perforated metal plate. As shown, the exposing rays impinge on area 12; of layer 11 and thereby render the polymer in the layer in that area insoluble in organic solvents. When the element is treated with organic solvents in which the unexposed areas of layer 11 are soluble the result is to remove those areas from the glass support leaving a relief image 15 containing insoluble polymer and fluorescent pigment on the support as shown in Stage B. As mentioned in this example the element of Stage B can then be re-coated Example 2 This example illustrates the preparation of pigmented images on cellulosic surfaces.
Ultramarine Blue pigment (3.75 gms.) was milled into 100 cc. of a 7.5% solution of polyvinyl cinnamate in ethylene glycol monomethyl ether acetate and the lightsensitivityof the composition was increased by the addition of picramide. The composition was then coated on to a paper support, exposed for 1 minute at 4 feet from a Eli-ampere white flame arc, and developed with methyl ethyl ketone to remove the pigmented composition from the unexposed regions and excess pigment was removed by swabbing with a cotton swab saturated with isopropyl alcohol. The result was to obtain a blue image on the paper surface.
Example 3 Example 4 This example illustrates a method for the preparation of a pigmented image on a metal support particularly suitable for template use.
A 1,2-benzanthraquinone sensitized 7.5% polyvinyl cinnamate dope in a mixture of toluene and ethylene glycol monomethyl ether acetate (5:3) was pigmented with 5 grams of Prussian blue pigment per 100 cc. of solution. The resulting dope was coated on to a clean aluminum sheet and after drying was exposed for 1 /2 minutes at 4 feet from a 35-ampere white flame arc. The exposed coating was then developed as described in the above examples to obtain a blue pigmented image on the aluminum sheet.
Example 5 This example illustrates the application of our invention to the preparation of metal images on vitreous surfaces for use in electrical work.
7 /2 grams of silver oxalate and 5 grams of lead sulfide were pigmented into cc. of a 1,2-benzanthraquinone sensitized 7.5% polyvinyl cinnamate dope in a mixture of ethylene glycol monomethyl ether acetate and toluene (3:5). This composition was then sprayed on to a porcelain disk and after drying exposed for 1 /2 minutes at 18 inches from a 35-ampere white flame carbon arc, the coating developed with solvent as in the previous examples and dried. Thereafter the disk was fired until a metal image was obtained, a temperature of 1150" F. being suitable for this purpose.
What we claim is:
A composition for use in forming a fluorescent image on a surface, comprising a mixture of a member of the class consisting of zinc phosphate, zinc sulfide and zinc orthosilicate and a light-sensitive substantially fully esterified cinnamic acid ester of polyvinyl alcohol.
References Cited in the file of this patent UNITED STATES PATENTS 6 Reppe et a1 May 31, 1938 Ellis Mar. 26, 1940 Staehle June 7, 1949 Minsk et a1. Sept. 9, 1952 FOREIGN PATENTS Great Britain June 2, 1921 Great Britain Oct. 30, 1942
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| Application Number | Priority Date | Filing Date | Title |
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| US312478A US2747997A (en) | 1952-10-01 | 1952-10-01 | Decoration of cellulosic, metal and vitreous surfaces |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US312478A US2747997A (en) | 1952-10-01 | 1952-10-01 | Decoration of cellulosic, metal and vitreous surfaces |
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| Publication Number | Publication Date |
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| US2747997A true US2747997A (en) | 1956-05-29 |
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| US312478A Expired - Lifetime US2747997A (en) | 1952-10-01 | 1952-10-01 | Decoration of cellulosic, metal and vitreous surfaces |
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Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2872316A (en) * | 1955-06-20 | 1959-02-03 | Sylvania Electric Prod | Method of producing patterns |
| US2897089A (en) * | 1956-03-14 | 1959-07-28 | Gen Electric | Method of printing color phosphor patterns |
| US2929708A (en) * | 1954-10-26 | 1960-03-22 | Gen Aniline & Film Corp | Phosphor screens for color television and method of preparing the same while using diazotype materials |
| US2989398A (en) * | 1955-11-01 | 1961-06-20 | Philco Corp | Method of manufacturing electrical apparatus |
| US3005708A (en) * | 1957-05-29 | 1961-10-24 | Westinghouse Electric Corp | Method of making a screen member |
| US3047422A (en) * | 1956-01-09 | 1962-07-31 | Miehle Goss Dexter Inc | Coating material and method of drying same |
| US3080232A (en) * | 1957-11-29 | 1963-03-05 | Sanders Associates Inc | Method for photographically producing electrical conductor patterns inside a hollow object |
| US3097096A (en) * | 1955-01-19 | 1963-07-09 | Oster Gerald | Photopolymerization with the formation of relief images |
| US3131060A (en) * | 1959-02-26 | 1964-04-28 | Gevaert Photo Prod Nv | Electrophotographic material |
| US3181172A (en) * | 1962-12-26 | 1965-04-27 | Ampex | Storage media |
| US3198634A (en) * | 1956-06-25 | 1965-08-03 | Philco Corp | Method of depositing particulate solid material on selected portions of a substrate |
| US3205202A (en) * | 1955-08-10 | 1965-09-07 | Bayer Ag | Process for improving the brightness of synthetic polymers and products resulting therefrom |
| US3226233A (en) * | 1960-06-13 | 1965-12-28 | Miehle Goss Dexter Inc | Photosensitive compositions containing leucocyanides of triphenylmethane dyes |
| US3269838A (en) * | 1963-03-18 | 1966-08-30 | Rca Corp | Method of making luminescent screens for cathode ray tubes |
| US3271321A (en) * | 1959-06-24 | 1966-09-06 | Basf Ag | Resins homogeneously brightened with bis-styrylbenzenes |
| US3909930A (en) * | 1972-05-23 | 1975-10-07 | Motorola Inc | Method for fabricating a liquid crystal display device |
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|---|---|---|---|---|
| GB163903A (en) * | 1920-05-07 | 1921-06-02 | Leonard Angelo Levy | Improvements in x-ray plates and the like |
| US1574357A (en) * | 1922-03-08 | 1926-02-23 | Wadsworth Watch Case Co | Photographic media and process |
| US1965710A (en) * | 1931-01-21 | 1934-07-10 | Eastman Kodak Co | Photomechanical resist |
| US2118864A (en) * | 1932-03-05 | 1938-05-31 | Ig Farbenindustrie Ag | Polymerization products from vinyl esters |
| US2063348A (en) * | 1936-03-10 | 1936-12-08 | Eastman Kodak Co | Method of making a colored photographic image |
| US2195362A (en) * | 1936-05-21 | 1940-03-26 | Ellis Foster Co | Glycol-maleic acid resin and process of making same |
| GB548953A (en) * | 1941-04-28 | 1942-10-30 | Adrian Cornwell Clyne | Improvements in or relating to the production of photographic light-sensitive layers or sheets |
| US2472128A (en) * | 1947-05-03 | 1949-06-07 | Eastman Kodak Co | Coloring ceramic objects |
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Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2929708A (en) * | 1954-10-26 | 1960-03-22 | Gen Aniline & Film Corp | Phosphor screens for color television and method of preparing the same while using diazotype materials |
| US3097096A (en) * | 1955-01-19 | 1963-07-09 | Oster Gerald | Photopolymerization with the formation of relief images |
| US2872316A (en) * | 1955-06-20 | 1959-02-03 | Sylvania Electric Prod | Method of producing patterns |
| US3205202A (en) * | 1955-08-10 | 1965-09-07 | Bayer Ag | Process for improving the brightness of synthetic polymers and products resulting therefrom |
| US2989398A (en) * | 1955-11-01 | 1961-06-20 | Philco Corp | Method of manufacturing electrical apparatus |
| US3047422A (en) * | 1956-01-09 | 1962-07-31 | Miehle Goss Dexter Inc | Coating material and method of drying same |
| US2897089A (en) * | 1956-03-14 | 1959-07-28 | Gen Electric | Method of printing color phosphor patterns |
| US3198634A (en) * | 1956-06-25 | 1965-08-03 | Philco Corp | Method of depositing particulate solid material on selected portions of a substrate |
| US3005708A (en) * | 1957-05-29 | 1961-10-24 | Westinghouse Electric Corp | Method of making a screen member |
| US3080232A (en) * | 1957-11-29 | 1963-03-05 | Sanders Associates Inc | Method for photographically producing electrical conductor patterns inside a hollow object |
| US3131060A (en) * | 1959-02-26 | 1964-04-28 | Gevaert Photo Prod Nv | Electrophotographic material |
| US3271321A (en) * | 1959-06-24 | 1966-09-06 | Basf Ag | Resins homogeneously brightened with bis-styrylbenzenes |
| US3226233A (en) * | 1960-06-13 | 1965-12-28 | Miehle Goss Dexter Inc | Photosensitive compositions containing leucocyanides of triphenylmethane dyes |
| US3181172A (en) * | 1962-12-26 | 1965-04-27 | Ampex | Storage media |
| US3269838A (en) * | 1963-03-18 | 1966-08-30 | Rca Corp | Method of making luminescent screens for cathode ray tubes |
| US3909930A (en) * | 1972-05-23 | 1975-10-07 | Motorola Inc | Method for fabricating a liquid crystal display device |
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