US3776754A - Production of luminescent screens - Google Patents
Production of luminescent screens Download PDFInfo
- Publication number
- US3776754A US3776754A US00165319A US3776754DA US3776754A US 3776754 A US3776754 A US 3776754A US 00165319 A US00165319 A US 00165319A US 3776754D A US3776754D A US 3776754DA US 3776754 A US3776754 A US 3776754A
- Authority
- US
- United States
- Prior art keywords
- phosphor
- maleic anhydride
- binder
- coating
- vinyl ether
- 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
- 238000004519 manufacturing process Methods 0.000 title abstract description 24
- 239000011230 binding agent Substances 0.000 claims abstract description 41
- 238000000034 method Methods 0.000 claims abstract description 40
- 239000000463 material Substances 0.000 claims abstract description 36
- 230000008569 process Effects 0.000 claims abstract description 20
- -1 alkyl vinyl ether Chemical compound 0.000 claims description 16
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 14
- 229920001577 copolymer Polymers 0.000 claims description 12
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 125000004432 carbon atom Chemical group C* 0.000 claims description 3
- 239000004094 surface-active agent Substances 0.000 claims description 2
- 230000005855 radiation Effects 0.000 abstract description 19
- 150000001875 compounds Chemical class 0.000 abstract description 8
- 230000006872 improvement Effects 0.000 abstract description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract description 3
- 230000009471 action Effects 0.000 abstract description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 35
- 238000000576 coating method Methods 0.000 description 28
- 239000011248 coating agent Substances 0.000 description 26
- 239000000203 mixture Substances 0.000 description 20
- 230000000694 effects Effects 0.000 description 11
- 238000010894 electron beam technology Methods 0.000 description 11
- 238000012545 processing Methods 0.000 description 10
- 239000011651 chromium Substances 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
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- 238000002360 preparation method Methods 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 5
- 239000002184 metal Substances 0.000 description 5
- 239000011368 organic material Substances 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- 230000035945 sensitivity Effects 0.000 description 5
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 4
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 4
- 206010034960 Photophobia Diseases 0.000 description 4
- 239000012736 aqueous medium Substances 0.000 description 4
- 229910052804 chromium Inorganic materials 0.000 description 4
- 239000000084 colloidal system Substances 0.000 description 4
- 239000003086 colorant Substances 0.000 description 4
- 208000013469 light sensitivity Diseases 0.000 description 4
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 4
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 4
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 4
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 3
- 239000004372 Polyvinyl alcohol Substances 0.000 description 3
- WGLPBDUCMAPZCE-UHFFFAOYSA-N Trioxochromium Chemical compound O=[Cr](=O)=O WGLPBDUCMAPZCE-UHFFFAOYSA-N 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 239000003054 catalyst Substances 0.000 description 3
- 238000004132 cross linking Methods 0.000 description 3
- 238000011161 development Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 229920002451 polyvinyl alcohol Polymers 0.000 description 3
- 230000001235 sensitizing effect Effects 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 230000003595 spectral effect Effects 0.000 description 3
- GXZPMXGRNUXGHN-UHFFFAOYSA-N 1-ethenoxy-2-methoxyethane Chemical compound COCCOC=C GXZPMXGRNUXGHN-UHFFFAOYSA-N 0.000 description 2
- OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- FNVVDDWYPIWYQN-UHFFFAOYSA-N 3-ethenylfuran-2,5-dione Chemical compound C=CC1=CC(=O)OC1=O FNVVDDWYPIWYQN-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
- 108010010803 Gelatin Proteins 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 2
- 239000004698 Polyethylene Substances 0.000 description 2
- 239000004743 Polypropylene Substances 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical compound C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 2
- 238000005269 aluminizing Methods 0.000 description 2
- JOSWYUNQBRPBDN-UHFFFAOYSA-P ammonium dichromate Chemical compound [NH4+].[NH4+].[O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O JOSWYUNQBRPBDN-UHFFFAOYSA-P 0.000 description 2
- 238000007630 basic procedure Methods 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- ZCDOYSPFYFSLEW-UHFFFAOYSA-N chromate(2-) Chemical class [O-][Cr]([O-])(=O)=O ZCDOYSPFYFSLEW-UHFFFAOYSA-N 0.000 description 2
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 2
- 239000000470 constituent Substances 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- 230000008021 deposition Effects 0.000 description 2
- SOCTUWSJJQCPFX-UHFFFAOYSA-N dichromate(2-) Chemical class [O-][Cr](=O)(=O)O[Cr]([O-])(=O)=O SOCTUWSJJQCPFX-UHFFFAOYSA-N 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000005670 electromagnetic radiation Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 description 2
- UPBDXRPQPOWRKR-UHFFFAOYSA-N furan-2,5-dione;methoxyethene Chemical compound COC=C.O=C1OC(=O)C=C1 UPBDXRPQPOWRKR-UHFFFAOYSA-N 0.000 description 2
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-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
- 238000010348 incorporation Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N n,n'-methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 2
- 230000007935 neutral effect Effects 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 229920002432 poly(vinyl methyl ether) polymer Polymers 0.000 description 2
- 229920000573 polyethylene Polymers 0.000 description 2
- 229920001155 polypropylene Polymers 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 239000002002 slurry Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 238000009987 spinning Methods 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 238000005507 spraying Methods 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 239000011837 N,N-methylenebisacrylamide Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 235000005811 Viola adunca Nutrition 0.000 description 1
- 240000009038 Viola odorata Species 0.000 description 1
- 235000013487 Viola odorata Nutrition 0.000 description 1
- 235000002254 Viola papilionacea Nutrition 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- ABXXWVKOBZHNNF-UHFFFAOYSA-N chromium(3+);dioxido(dioxo)chromium Chemical compound [Cr+3].[Cr+3].[O-][Cr]([O-])(=O)=O.[O-][Cr]([O-])(=O)=O.[O-][Cr]([O-])(=O)=O ABXXWVKOBZHNNF-UHFFFAOYSA-N 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000006735 deficit Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 238000009795 derivation Methods 0.000 description 1
- QDOXWKRWXJOMAK-UHFFFAOYSA-N dichromium trioxide Chemical compound O=[Cr]O[Cr]=O QDOXWKRWXJOMAK-UHFFFAOYSA-N 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- YYXLGGIKSIZHSF-UHFFFAOYSA-N ethene;furan-2,5-dione Chemical compound C=C.O=C1OC(=O)C=C1 YYXLGGIKSIZHSF-UHFFFAOYSA-N 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- WOLATMHLPFJRGC-UHFFFAOYSA-N furan-2,5-dione;styrene Chemical compound O=C1OC(=O)C=C1.C=CC1=CC=CC=C1 WOLATMHLPFJRGC-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000000383 hazardous chemical Substances 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 238000005286 illumination Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000008676 import Effects 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 238000003780 insertion Methods 0.000 description 1
- 230000037431 insertion Effects 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 238000012332 laboratory investigation Methods 0.000 description 1
- 238000007644 letterpress printing Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 239000002609 medium Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000003504 photosensitizing agent Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 238000007639 printing Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 230000000135 prohibitive effect Effects 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- 238000012827 research and development Methods 0.000 description 1
- 239000012260 resinous material Substances 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 238000007650 screen-printing Methods 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
Classifications
-
- 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
- G03F7/004—Photosensitive materials
- G03F7/04—Chromates
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01J—ELECTRIC DISCHARGE TUBES OR DISCHARGE LAMPS
- H01J29/00—Details of cathode-ray tubes or of electron-beam tubes of the types covered by group H01J31/00
- H01J29/02—Electrodes; Screens; Mounting, supporting, spacing or insulating thereof
- H01J29/10—Screens on or from which an image or pattern is formed, picked up, converted or stored
- H01J29/18—Luminescent screens
- H01J29/22—Luminescent screens characterised by the binder or adhesive for securing the luminescent material to its support, e.g. vessel
- H01J29/225—Luminescent screens characterised by the binder or adhesive for securing the luminescent material to its support, e.g. vessel photosensitive adhesive
-
- 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
- H01J9/22—Applying luminescent coatings
- H01J9/227—Applying luminescent coatings with luminescent material discontinuously arranged, e.g. in dots or lines
- H01J9/2275—Applying luminescent coatings with luminescent material discontinuously arranged, e.g. in dots or lines including the exposition of a substance responsive to a particular radiation
-
- 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
- Y10S430/143—Electron beam
Definitions
- the present invention relates in general to the manufacture of color television picture tubes and in particular to the provision of improved compositions and processing for such purposes.
- phosphor glass screens of the type commonly employed in the fabrication of color television picture tubes comprise a plate provided with finely discrete patterns of three different phosphors each of which is capable of emitting radiation of a different primary color, i.e., red, green and blue.
- tubes of this nature are constructed in such fashion that a thin perforated metal mask is mounted parallel to the screen and a short distance away from the screen toward the gun end of the tube, such metal mask being provided with a concatenation of holes.
- Each of the holes provided in the metal mask corresponds to each of the primary colors, i.e., is positioned to illuminate a trio of red, green and blue emitting phosphor dots comprising a single unit of the aggregate phosphor do't pattern carried by the luminescent screen.
- three electron guns are mounted symmetrically about the axis of the tube. Each of the gun, mask and dotted screen elements are positioned in such manner that the electron beam from each gun is directed through the holes in the mask so as to strike phosphor dots of one primary color only.
- color television picture tube manufacturing based upon photographic reproduction methods has met with a fairly impressive measure of commercial success.
- a photosensitive organic carrier or binder which, in the presence of a suitable catalyst material, undergoes a change in solubility characteristics as a direct result of actinic exposure.
- Such carriers or binders are often referred to in the art as colloid carriers, the quoted term connoting resinous materials of synthetic derivation or natural origin, with typical representatives including polyvinyl alcohol, gelatin and the like.
- the requisite level of light-sensitivity is ordinarily imparted to the binder component by the incorporation of a suitable sensitizing agent such as potassium or ammonium dichromate.
- the binder material thus sensitized is thereafter applied to the inside surface of the television picture tube viewing panel by any one of several conventional coating techniques, e.g., flowing, spraying, whirling, etc. Any excess coating material can thereafter be readily removed by draining or spinning in a whirl coater until a uniform and even surface is obtained. It will be understood that the selection of a particular coating technique maywell obviate any necessity for the use of auxiliary expedients whereby to obtain an even coating; thus, in the case of spray coating, the removal of excess light-sensitive binder may be easily accomplished by merely controlling the quantity of coating deposited by the spray applicator whereas uniformity of coating application may be controlled by judicious selection of the spray pattern.
- any one of several conventional coating techniques e.g., flowing, spraying, whirling, etc.
- Any excess coating material can thereafter be readily removed by draining or spinning in a whirl coater until a uniform and even surface is obtained.
- a uniform screen of dry powered luminescent phosphor e.g., green phosphor of the i type commonly use d,'is sprayed "or otherwise deposited upon the tacky, radiation energy-sensitive layer.
- the phosphor-containing coating is then dried by conventional means and thereupon exposed to a radiant en- .ergy source through a conventional shadow mask.
- latent-image dot pattern thus laid down represents the illumination locus or excitation area for one of the three primary colors, i.e., red, green or blue corresponding to one of the three cathode emitters of the tricolor tube.
- the final step involved in the formation of the phosphor pattern comprises the development operation wherein the entire surface of the panel is subjected to a wash-out operation, i.e., washed with a developing fluid such as deionized water, this treatment serving to remove the unhardened or non-exposed areas'of the coating while permitting the exposed or hardened areas to remain intact.
- a wash-out operation i.e., washed with a developing fluid such as deionized water
- the dot patterns corresponding to the remaining primary color aspects in this case the blue and red additive primary color aspects, conform in arrangement, i.e., distribution, pattern, etc., to the blue and red cathode emitters respectively of the tricolor tube.
- one such ramification involves as an essential expedient the actinic exposure of the radiation-sensitive coating prior to drying, i.e., while such coating remains in a tacky condition.
- a uniform screen of dry powdered phosphor is sprayed or otherwise deposited upon the coating surface.
- the terminal point in the processing would comprise the development operation wherein the exposed and sprayed surface is treated with deionized water or other suitable solution whereby to effect physical removal of the unexposed, unhardened coating areas.
- the entire sequence of operations would then be repeated for each of the remaining primary color aspects in the manner hereinbefore described.
- the phosphor is provided in the form of a preliminary slurry or dispersion with the binder material, admixing being effected according to conventional techniques, the filmforming composition being thereafter applied to the inside surface of the picture tube panel by flowing or whirling. Following removal of excess coating by drain-' ing or spinning the coated layer thus obtained is exposed and developed in the manner previously delineated, the involved sequence of operation being repeated for each of the primary color aspects.
- the processing subsequent to the laying down of the tricolor phosphor pattern and incidental to the obtention of a final color television picture tube unit is for the most part involving, for example, the usual steps of lacquering, aluminizing, inserting the shadow mask, sealing both sections of the tube to form an integral unit and finally, evacuating and baking at a temperature sufficient to burn away the binder.
- binder compositions sensitive to radiation of corpuscular nature e.g., electron beam
- the corpuscular radiation serves to provide the requisite quantity of energy necessary to effect insolubilization of the binder component, e.g., by crosslinking of organic polymeric constituents, polymerization of monomeric constituents, etc.
- the polymeric binder materials thus far provided in the art exhibit an appreciable sensitivity to the radiant emissions of the phosphor particles, the blue phosphor being particularly offensive in this regard since its locus of emissions emanates from the violet-blue portion of the spectrum.
- the foregoing thus precludes the use of the blue-emitting phosphor in the binder composition prior to electronbeam exposure since the light emitted by the blue phosphor upon electron beam excitation would cause non-purposive and inadvertent exposure effects, the latter, in all probability, resulting in undesired growth in dot dimension. Continued exposure would of course aggravate this tendency.
- binder compositions possessed of appreciable lightsensitivity imposes the burdensome restriction that electron beam exposure be carried out in the absence of phosphor, the latter being applied in a separate operation subsequent to'expo'sure. Processing is of course encumbered while the economic consequences involved may well be prohibitive.
- a primary object of the present invention resides in the provision of compositions and processing uniquely and beneficially adapted for use in connection with the manufacture of luminescent tricolor screens for color television picture tubes wherein the foregoing and related disadvantages are eliminated or at least mitigated to a substantial extent.
- Another object of the present invention resides in the provision of a process for the preparation of color television tubes wherein problems associated with residual metal contamination are eliminated.
- Yet another object of the present invention resides in the provision of a process for the preparation of color television tubes capable or providing sharp dot patterns of excellent brightness.
- a further object of the present invention resides in the provision of a process for the preparation of luminescent screens for color television tubes comprising polymeric resists and wherein any necessity for the utilization of organic solvent media in developing the resist image is completely obviated.
- a still further object of the present invention resides in the provision of a process for color television tube manufacture capable of expeditious implementation and wherein any necessity for post-exposure incorporation of phosphor into the binder'composition is completely obviated.
- the organic binder material be light-insensitive.
- the term "light-insensitivity is to be accorded the following significance.
- the polymerization, crosslinking etc. of many ethylenically unsaturated organic materials may be effected by exposure to certain types of electromagnetic radiation and especially ultra-violet radiation. Since many of such organic materials exhibit appreciable sensitivity to such spectral radiation the use of catalysts or other promotors to augment the reaction is completely unnecessary.
- the insolubilization of organic polymeric resist materials is often carried out by the utilization of electromagnetic radiation emanating from the violet-blue region of the spectrum as the activating influence. In fact, the hardening reaction may occur merely upon standing ofsuch materials for relatively short periods of time.
- Ethylenically unsaturated compounds of this type prove unsuitable for use in the preparation of luminescent screens for color television tubes in view of their sensitivity to the radiation emitted by the blue phosphor upon electron beam excitation, i.e., the blue-violet radiation emitted during the exposure interval is capable of initiating polymerization, cross-linking etc. If ethylenic compounds of this type are to be used it becomes necessary to omit the blue phosphor until exposure is completed.
- the binder compounds contemplated by the present'invention remain unaffected 'by the radiation emissions of eachof the red, green and blue phosphor particles which occur during exposure.
- the blue phosphor may be present in the binder composition during the exposure step, thereby avoiding the multi-step procedure which would otherwise be necessary.
- Maleic anhydride polymers preferred for use comprise those containing from about 10 percent to about 65 percent on a mole basis of maleic anhydride units with the remainder comprising, for example, alkyl vinyl ether units, the alkyl moiety containing from one to about carbon atoms, e.g., methyl, isobutyl, dodeeyl, hexadecyl, oetadecyl, .etc.; ethylene; propylene; styrene; etc.
- Polymers of this general type are commercially available from the General Aniline and Film Corporation under the trademark designation GAN- TREZ,” GANTREZ AN l49,” which comprises a copolymer of maleic anhydride and methyl vinyl ether having a specific viscosity of 2.0 measured at 25C as a one percent solution in methyl ethyl ketone.
- Polymeric materials of this type can be readily deposited in the form of a uniform continuous layer according to conventional technique whereby to provide a coated layer having the required stability and resistance to viscosity changes upon standing.
- the coating operation may be facilitated by the employment of the polymeric material in specific viscosities ranging from about .05 to about 5.0 as measured in one percent solutions in methyl ethyl ketone at 25C.
- Optimum coating solution viscosities within the foregoing range can be readily determined in a particular circumstance by routine laboratory investigation.
- the light-insensitive binder materials of the present invention may be utilized in the following manner.
- the electron beam-sensitive polymer, monomer or mixture thereof is first dissolved in aqueous media.
- the phosphor particles are thereupon dispersed in the aqueous medium.
- the thickness value selected is not a particularly critical factor in the practiceof the present invention and thus may be selected from those values customarily employed in the art for such purposes. In general, thinner coatings are preferred in order to achieve the requisite degree of insolubilization.
- the coating thickness selected should be conducive to the provision of a structurally stable coating whereby to permit the selective removal of non-insolubilized areas following exposure without deleteriously affecting the exposed areas, e.g., undercutting.
- the coating be excessively thin, inadvertent removal of exposed areas may result with consequent impairment of phosphor pattern reproduction.
- the solution viscosity value selected will be influenced to a great extent by the coating method employed, i.e., flowing, whirling, etc. After allowing the layer thus deposited to dry, the shadow mask is positioned in the panel face. The picture tube.
- the tube assembly is thereupon evacuated.
- the shadow mask is then swept by an electron beam emanating from the appropriate electron gun, i.e., that gun whose corpuscular emissions correspond to the particular color emitting phosphor pattern being laid down. Exposure is effected for a period of time sufficient to impart the requisite insolubilization to those areas subjected to the electron beam. Upon completion of the exposure, air is admitted to the system and the shadow mask retrieved.
- the shadow mask containing the latent image dot pattern in the form of insolubilized areas is treated with aqueous media whereby to effect removal of non-exposed areas, the latter corresponding to non-insolubilized portions.
- the foregoing sequence of operations is thereafter repeated for each of the remaining two primary colors whereby to form a complete tricolor phosphor dot pattern.
- the process of the present invention makes possible the attainment of a most precise position relation between the electron gun, the shadow mask and the phosphor dot for each of the three colors.
- the phosphor dot reproduction obtained is of distinctly superior quality, i.e., extremely sharp, bright and totally free of metal contamination. This, of course, results in enhanced brilliance of emission upon electronic excitation of the phosphor.
- overexposure to the electron beam does not result in exaggerated growth in the dot dimension; this result obtains since the scattered light emissions emanatingfrom the phosphor particles dispersed throughout the binder material are innocuous as regards imparting hardening effects to the binder material.
- water-soluble as used in the context of the present invention is intended to encompass those ethylenically unsaturated materials which exhibit a sufficient degree of water-solubility, dispersibility or sensitivity to permit their expeditious coating in an aqueous system.
- ethylenically unsaturated compound in the form of an aqueous dispersion, suspension, emulsion, etc. in order to facilitate the attainment of an optimum coating.
- suitable suspending agents, emulsifying agents and dispersants well known in the art for such purposes.
- a'process for the preparation of luminescent screens for color television tubes the improvement which consists essentially of the sequential steps of exposing to corpuscular radiation a surface coated with a corpuscular radiation sensitive composition consisting essentially of a water soluble organic binder layer insolubilizable by corpuscular radiation containing inorganic phosphor particles uniformly dispersed therein, said organic binder material being unaffected by radiation emissions produced by said inorganic phosphor particles during said exposure, said exposure being sufficient to effect insolubilization of said binder material in the radiation-struck areas and thereafter treating said binder composition with water whereby to remove only unexposed non-insolubilized portions, and wherein said organic binder material comprises a member selected from the group consisting of polyvinyl pyrrolidone, polyethylene, polypropylene, polystyrene, polyvinyl methyl ether, poly (methoxy ethyl) vinyl ether, vinyl methyl ether/maleic anhydride copolymer, ethylene
- said organic binder material comprises a copolymer of maleic anhydride and an alkyl vinyl ether wherein said alkyl moiety contains from one to about 20 carbon atoms and has a specific viscosity ranging from about .05 to about 5.0 measured at 25C as a one percent solution in methyl ethyl ketone.
- maleic anhydride/methyl vinyl ether copolymer contains from about 10 percent to about percent on a mole basis of maleic anhydride and has a specific viscosity of 2.0 measured at 25 as a one percent solution in methyl ethyl ketones.
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Abstract
Process for the production of luminescent screens for color television tubes, the improvement comprising the use of lightinsensitive ethylenically unsaturated vinyl compounds as the binder material, said compounds being capable of undergoing a hardening action when subjected to corpuscular radiation.
Description
United States Patent 1 1 1111 3,776,754 Levinos Dec. 4, 1973 [541 PRODUCTION OF LUMINESCENT 3,003,873 10 1961 Zworykin 117 33.s CM NS 3,527,652 9/1970 Ozaki et al.. 96/36.1 2,727,828 12/1955 Law 117/33.5 CM Inventor: Steven Levmos, C NJ. 3,630,868 12/1971 Marans 117/93.31
3,62 12 1971 [73] Ass'gnem GAF comramn New York 3,273, 63?) 9/1966 1 1 77 9 313 [22] Filed; July 22, 1971 3,247,012 4/1966 Burlant 117/93.31
[21] Appl. No.: 165,319
Primary Examiner--Wi1liam D. Martin kehftcd Application Data Assistant ExaminerJohn H. Newsome [63] Continuatlon of Ser. No. 679,617, Nov. 1, 1967, Attorney walter C Kehm and Samson B Leavm at abandoned.
a1. [52] 11.8. C1. 117/33.5 CM, 96/1 E, 96/36.l, 117/93.3l, 117/161 UA, 117/161 UB, 117/161UC,1l7/161UE,117/161UF,
117/161 UN, 117/161 UZ [57] ABSTRACT [51] 'f Bm 1/ Cosf 3/00 H011 29/22 Process for the production of luminescent screens for [58] Fleld of Search 117/93.31, 33.5 CM, color television tubes the improvement comprising 117/161 16] 161 161 UB5 the use of light-insensitive ethylenically unsaturated l E vinyl compounds as the binder material, said compounds being capable of undergoing a hardening ac- [56] References cued tion when subjected to corpuscular radiation.
UNITED STATES PATENTS 2,897,089 7/1959 Ahlburg et a1 117/33.5 CM 5 Claims, N0 Drawings PRODUCTION OF LUMINESCENT SCREENS This application is a streamlined continuation of prior co-pending application Ser. No. 679,617, filed Nov. 1, 1967, and now abandoned.
The present invention relates in general to the manufacture of color television picture tubes and in particular to the provision of improved compositions and processing for such purposes. I
As is well known, phosphor glass screens of the type commonly employed in the fabrication of color television picture tubes comprise a plate provided with finely discrete patterns of three different phosphors each of which is capable of emitting radiation of a different primary color, i.e., red, green and blue. In general, tubes of this nature are constructed in such fashion that a thin perforated metal mask is mounted parallel to the screen and a short distance away from the screen toward the gun end of the tube, such metal mask being provided with a concatenation of holes. Each of the holes provided in the metal mask corresponds to each of the primary colors, i.e., is positioned to illuminate a trio of red, green and blue emitting phosphor dots comprising a single unit of the aggregate phosphor do't pattern carried by the luminescent screen. In addition, three electron guns are mounted symmetrically about the axis of the tube. Each of the gun, mask and dotted screen elements are positioned in such manner that the electron beam from each gun is directed through the holes in the mask so as to strike phosphor dots of one primary color only.
Methods for the production of color television picture tubes of the aperture mask type are legion being extensively described in the prior art both patent and otherwise. For purposes of general classification, such methods are acknowledged to fall within one of three categories, namely, those based upon photographic reproduction techniques and silk screen printing respectively as well as numerous other processes currently considered to be of lesser commercial importance, e.g., letterpressprinting, electrostatic printing, methods involving the settling of phosphors through masks, etc.
Although the methodology thus-far promulgated in regard to color television tube manufacture is found in the vast majority of instances toprovide satisfactory re sults, certain limitations which inhei'e in the very nature of such processing have nevertheless been confronted which tend to circumscribe severely the tube manufactures scope of operation with respect to for example, selection of the materials essential to the implementation of such methods, the processing conditions necessary for optimum performance, etc. For example, it has been ascertained that thesilk screen process is limited, for efficacious practice, to those applications wherein the plate employed as the support for the phosphor screen pattern is absolutely flat or planar. Consequently, processes of this type are sustantially inapplicable as such in those instances involving the use of a plate element of arcuate or otherwise irregular configuration. The gravity of this particular limitation becomes acutely evident when it is realized that much of the industrial endeavor relating to the manufacture of color television tubes is specifically concerned with the fabrication of non-planar picture tube surfaces and particularly when the latter is of relatively large size. Color television picture tube technology has established to a reasonable certainity that picture tubes of arcuate as distinguished from planar configuration provide a much more highly efficient and practical tube structure. However, prior industrial efforts to extend the applicability of the silk-screen picture tube manufacturing process for the production of curved television tube surfaces have for the most part met with but marginal success. Invariably, 'resort to complex if not highly expensive ramifications, modifications, etc. of the basic technique is made necessary in order to implement such processing with any degree of efficacy.
In contradistinction, color television picture tube manufacturing based upon photographic reproduction methods has met with a fairly impressive measure of commercial success. In general, such methods are implemented by the utilization of a photosensitive organic carrier or binder which, in the presence of a suitable catalyst material, undergoes a change in solubility characteristics as a direct result of actinic exposure. Such carriers or binders are often referred to in the art as colloid carriers, the quoted term connoting resinous materials of synthetic derivation or natural origin, with typical representatives including polyvinyl alcohol, gelatin and the like. The requisite level of light-sensitivity is ordinarily imparted to the binder component by the incorporation of a suitable sensitizing agent such as potassium or ammonium dichromate. The binder material thus sensitized is thereafter applied to the inside surface of the television picture tube viewing panel by any one of several conventional coating techniques, e.g., flowing, spraying, whirling, etc. Any excess coating material can thereafter be readily removed by draining or spinning in a whirl coater until a uniform and even surface is obtained. It will be understood that the selection of a particular coating technique maywell obviate any necessity for the use of auxiliary expedients whereby to obtain an even coating; thus, in the case of spray coating, the removal of excess light-sensitive binder may be easily accomplished by merely controlling the quantity of coating deposited by the spray applicator whereas uniformity of coating application may be controlled by judicious selection of the spray pattern. Upon completion 'of the coating operation and prior to drying of the coating thus deposited, i.e., while such coating remains in a moist or tacky state, a uniform screen of dry powered luminescent phosphor, e.g., green phosphor of the i type commonly use d,'is sprayed "or otherwise deposited upon the tacky, radiation energy-sensitive layer. The phosphor-containing coating is then dried by conventional means and thereupon exposed to a radiant en- .ergy source through a conventional shadow mask. The
latent-image dot pattern thus laid down represents the illumination locus or excitation area for one of the three primary colors, i.e., red, green or blue corresponding to one of the three cathode emitters of the tricolor tube. The final step involved in the formation of the phosphor pattern comprises the development operation wherein the entire surface of the panel is subjected to a wash-out operation, i.e., washed with a developing fluid such as deionized water, this treatment serving to remove the unhardened or non-exposed areas'of the coating while permitting the exposed or hardened areas to remain intact. The aforedescribed chronology of operations is then repeated in its entirety for each of the remaining primary color aspects. In this manner there is obtained a complete tricolor pattern. As will be recognized, the dot patterns corresponding to the remaining primary color aspects, in this case the blue and red additive primary color aspects, conform in arrangement, i.e., distribution, pattern, etc., to the blue and red cathode emitters respectively of the tricolor tube. I
It will be appreciated of course that a number of ramifications to the aforedescribed basic procedure are exploited on a commercial scale. For example, one such ramification involves as an essential expedient the actinic exposure of the radiation-sensitive coating prior to drying, i.e., while such coating remains in a tacky condition. Upon completion of the exposure, a uniform screen of dry powdered phosphor is sprayed or otherwise deposited upon the coating surface. Again, the terminal point in the processing would comprise the development operation wherein the exposed and sprayed surface is treated with deionized water or other suitable solution whereby to effect physical removal of the unexposed, unhardened coating areas. The entire sequence of operations would then be repeated for each of the remaining primary color aspects in the manner hereinbefore described.
A still further ramification to the aforedescribed basic procedure and one currently enjoying relatively wide-spread commercial exploitation, involves as a signal feature, the utilization of the phosphor material in the form of a mixture, e.g., slurry or dispersion in the binder material. According to such method, the phosphor is provided in the form of a preliminary slurry or dispersion with the binder material, admixing being effected according to conventional techniques, the filmforming composition being thereafter applied to the inside surface of the picture tube panel by flowing or whirling. Following removal of excess coating by drain-' ing or spinning the coated layer thus obtained is exposed and developed in the manner previously delineated, the involved sequence of operation being repeated for each of the primary color aspects.
The processing subsequent to the laying down of the tricolor phosphor pattern and incidental to the obtention of a final color television picture tube unit is for the most part involving, for example, the usual steps of lacquering, aluminizing, inserting the shadow mask, sealing both sections of the tube to form an integral unit and finally, evacuating and baking at a temperature sufficient to burn away the binder.
Despite the fact that color television picture tube manufacturing operations of the aforedescribed type have met with a significant measure ofcommercial success, certain disadvantages and shortcomings have nevertheless been encountered in practice which tend to detract significantly from their commercial feasibility V and desirability. Perhaps the most serious objection relates to the nature of the sensitizing material employed for purposes of imparting the requisite spectral response to the composition. To a great extent, commercial operations, as presently embodied, rely almost invariably upon the use of alkali metal dichromate sensitizing agents in combination with polyvinyl alcohol resin binders for use in the manufacture ofluminescent screens for color television tubes. However, prior attempts to produce luminescent screens possessed of optimum luminosity, brilliance, etc. have, practically without exception been vitiated due to the fact that residual chromium, in significant quantities, remains in the light-hardened areas of the coating. Unless removed at some phase of screen manufacture, e.g., development, wash-out, etc., such fugitive chromium remains present in the form of an oxide the latter resulting in a serious loss of brilliance of the phosphor material on electronic excitation. Such a situation is of course of critical import since it directly affects the viewing quality of the picture tube. The deleterious effects thus resulting are further aggravated by the fact that the point-to-point density distribution of the fugitive chromium may vary significantly with the concomitant result that not only is picture contrast seriously impaired, but more importantly, the capacity of the luminescent screen to accurately reflect the color component values directly attributable to electronic excitation is seriously reduced. Without intending to be bound by any theory, the following hypotheses have nevertheless been postulated in explanation of the foregoing situation. Eder, in an article published many years ago relating to quantitative studies of brichromated gelatin, concluded that bichromates in the presence of oxidizable organic matter tend to undergo decomposition according to a series of relatively complicated reactions resulting in the formation of neutral chromates as well as a chromic chromate, m CrO .n Cr O wherein m and n represent numerical coefficients, the latter compound further decomposing into chromic acid and green chromium oxide as a result of subsequent washing. The neutral chromate and chromic acid are, according to theoretical exposition, carried away by the water employed during the wash-out step. The chromium oxide, however, combines with the carrier or binder resulting in the formation of an insoluble complex, the reactions hypothesized therefor being the following:
light CrzO7- CrOr m CrOg-n Cr O;
colloid removed by washing e CrO; CnOa hardened colloid colloid According to further evidence gathered by Popovitski, the product was identified as 4 Cr O 3 CrO which was presumed'to result according to the following reactions:
Regardless of the reaction mechanism actually responsible for the presence of fugitive chromium, there is ample evidence to indicate that approximately 19 percent of the total dichromate salt sensitizer employed in the initial charge remains in the cross-linked polyvinyl alcohol in the form of the insoluble chromic oxide. In addition, it has been estimated that almost 22 percent of the dichromate salt sensitizer remains behind as the insoluble chromic oxide in those instances wherein ammonium dichromate is employed as the photosensitizer. The use of light-sensitive catalysts presents the further disadvantage that a considerable cost increment results since such materials are invariably quite expenswe.
Thus, in an effort to circumvent theor foregoing problems, the use of binder compositions sensitive to radiation of corpuscular nature, e.g., electron beam, has been suggested for use in color television tube manufacture. The corpuscular radiation serves to provide the requisite quantity of energy necessary to effect insolubilization of the binder component, e.g., by crosslinking of organic polymeric constituents, polymerization of monomeric constituents, etc. Methods of this type although ameliorating somewhat the problems attendant upon the use of photosensitive binder composi tions nevertheless pose rather serious problems to the processor, such problems finding their genesis in the inherent light-sensitivity of the resin component.
The practical significance of the foregoing will be made readily manifest in the following description. In those methods of color television tube manufacture wherein the red, green and blue phosphors are initially provided in the binder composition to be subjected to electron beam exposure, it is of course imperative that the radiant emissions of each of the phosphors be inconsequential, i.e., that the composition be insensitive to the light emitted by such phosphors. This is essential in order to assure that the totality of hardening action is attributable solely to the direct effects of the exposure beam. Any departure from such condition would involve as an unavoidable. consequence the insolubilization of binder in non-image areas and/or excessive hardening due to overexposure. Thus, it has been determined that the polymeric binder materials thus far provided in the art exhibit an appreciable sensitivity to the radiant emissions of the phosphor particles, the blue phosphor being particularly offensive in this regard since its locus of emissions emanates from the violet-blue portion of the spectrum. The foregoing thus precludes the use of the blue-emitting phosphor in the binder composition prior to electronbeam exposure since the light emitted by the blue phosphor upon electron beam excitation would cause non-purposive and inadvertent exposure effects, the latter, in all probability, resulting in undesired growth in dot dimension. Continued exposure would of course aggravate this tendency. Thus, as a practical necessity, the use of binder compositions possessed of appreciable lightsensitivity imposes the burdensome restriction that electron beam exposure be carried out in the absence of phosphor, the latter being applied in a separate operation subsequent to'expo'sure. Processing is of course encumbered while the economic consequences involved may well be prohibitive.
A further disadvantage characterizing the methods heretofore providedin the art inheres in the nature of the resist-forming material. Thus, the ethylenically unsaturated compounds heretofore proposed for such use are adapted for solvent removal techniques wherein the solvent comprises an organic material. This, of course,
poses a significant disadvantage since such'solvent materials are invariably costly, difficult to handle, store,
etc. and very often present considerable health hazards to personnel. Consequently, processing is correspondingly burdened in view of the special precautions which must necessarily be excercised with regard to the use of organic solvent media.
In an effort to overcome or otherwise alleviate the foregoing and related disadvantages, considerable industrial activity has centered around the research and development of more effective methods, materials, etc. for the production of luminescent screens for color television picture tubes. Although much in the way of meritorious achievement has characterized the efforts thus far expended in this regard, the problems surrounding the obtention of luminescent screens having I 6 the desired degree of brilliance, luminosity, etc. continue to challenge tube-manufacturing technology.
In accordance with the discovery forming the basis of the present invention, it has been ascertained that the use of a relatively delimited class of ethylenically unsaturated organic material having predetermined spectral sensitivity characteristics and capable of undergoing insolubilization when subjected to corpuscular radiation makes possible optimum realization of the manifold advantages inherent in resist forming techniques based upon the use of corpuscular radiation when applied to color television tube manufacture, while eliminating the problems associated with spurious hardening effects typifying the procedures heretofore provided in the art.
Thus, a primary object of the present invention resides in the provision of compositions and processing uniquely and beneficially adapted for use in connection with the manufacture of luminescent tricolor screens for color television picture tubes wherein the foregoing and related disadvantages are eliminated or at least mitigated to a substantial extent.
Another object of the present invention resides in the provision of a process for the preparation of color television tubes wherein problems associated with residual metal contamination are eliminated.
Yet another object of the present invention resides in the provision of a process for the preparation of color television tubes capable or providing sharp dot patterns of excellent brightness.
A further object of the present invention resides in the provision of a process for the preparation of luminescent screens for color television tubes comprising polymeric resists and wherein any necessity for the utilization of organic solvent media in developing the resist image is completely obviated.
A still further object of the present invention resides in the provision of a process for color television tube manufacture capable of expeditious implementation and wherein any necessity for post-exposure incorporation of phosphor into the binder'composition is completely obviated.
Further objects and advantages of the present invention will become apparent hereinafter as the description proceeds. I
' The attainment of the foregoing and related objects is made possible in accordance with the present invention which in its broaded aspects includes the provision of a process for the preparation of luminescent screens for color television tubes which comprises exposing to corpuscular radiation a light-insensitive composition comprising a light-insensitive organic binder layer containing inorganic phosphor particles uniformly dispersed therein, said exposure being sufficient to effect insolubilization of said binder material in the radiationstruck areas and thereafter treating said binder composition with aqueous media whereby to remove noninsolubilized portions, and wherein said organic binder material comprises a member selected from the group consisting of (l) polymers, (2) monomers, and (3) mixtures of l) and (2) of water-soluble ethylenically unsaturated vinyl compounds containing at least one grouping of the formula As specific examples of binder materials falling within the ambit of the foregoing definition there may be mentioned in particular and without necessary limitation polyvinyl pyrrolidone, polyethylene, polypropylene, polystyrene, polyvinyl acetate, polyvinyl methyl ether, poly(methoxyethyl) vinyl ether; eopolymers including vinyl methyl ether/maleic anhydride, ethylene/- maleic anhydride, isobutyl vinyl ether/maleic anhydride, styrene/maleic anhydride, vinyl pyrrolidone/- maleic anhydride, poly(methoxyethyl) vinyl ether/- maleic anhydride, polyvinyl pyrrolidone/allyl amine; monomers including acrylamide, N,N'-methylenebisacrylamide, acrylic acid, methyl methacrylate, divinyl benzene, vinyl stearate, and the like.
It is critically important to the realization of the improvements described herein that the organic binder material be light-insensitive.
Within the context of the present invention, the term "light-insensitivity is to be accorded the following significance. As is well known, the polymerization, crosslinking etc. of many ethylenically unsaturated organic materials may be effected by exposure to certain types of electromagnetic radiation and especially ultra-violet radiation. Since many of such organic materials exhibit appreciable sensitivity to such spectral radiation the use of catalysts or other promotors to augment the reaction is completely unnecessary. Thus, the insolubilization of organic polymeric resist materials is often carried out by the utilization of electromagnetic radiation emanating from the violet-blue region of the spectrum as the activating influence. In fact, the hardening reaction may occur merely upon standing ofsuch materials for relatively short periods of time. Ethylenically unsaturated compounds of this type prove unsuitable for use in the preparation of luminescent screens for color television tubes in view of their sensitivity to the radiation emitted by the blue phosphor upon electron beam excitation, i.e., the blue-violet radiation emitted during the exposure interval is capable of initiating polymerization, cross-linking etc. If ethylenic compounds of this type are to be used it becomes necessary to omit the blue phosphor until exposure is completed.
in contradistinction to ethylenic materials of the aforedescribed type, the binder compounds contemplated by the present'invention remain unaffected 'by the radiation emissions of eachof the red, green and blue phosphor particles which occur during exposure. Thus, the blue phosphor may be present in the binder composition during the exposure step, thereby avoiding the multi-step procedure which would otherwise be necessary.
Particularly beneficial results are obtained in accordance with the present invention with the use of, for example, polymers of maleic anhydride, e.g., homopolymers, eopolymers with an alkyl vinyl ether, etc.
Maleic anhydride polymers preferred for use comprise those containing from about 10 percent to about 65 percent on a mole basis of maleic anhydride units with the remainder comprising, for example, alkyl vinyl ether units, the alkyl moiety containing from one to about carbon atoms, e.g., methyl, isobutyl, dodeeyl, hexadecyl, oetadecyl, .etc.; ethylene; propylene; styrene; etc. Polymers of this general type are commercially available from the General Aniline and Film Corporation under the trademark designation GAN- TREZ," GANTREZ AN l49," which comprises a copolymer of maleic anhydride and methyl vinyl ether having a specific viscosity of 2.0 measured at 25C as a one percent solution in methyl ethyl ketone.
Polymeric materials of this type can be readily deposited in the form of a uniform continuous layer according to conventional technique whereby to provide a coated layer having the required stability and resistance to viscosity changes upon standing. In general, it is found that the coating operation may be facilitated by the employment of the polymeric material in specific viscosities ranging from about .05 to about 5.0 as measured in one percent solutions in methyl ethyl ketone at 25C. Optimum coating solution viscosities within the foregoing range can be readily determined in a particular circumstance by routine laboratory investigation.
The light-insensitive binder materials of the present invention may be utilized in the following manner. The electron beam-sensitive polymer, monomer or mixture thereof is first dissolved in aqueous media. The phosphor particles are thereupon dispersed in the aqueous medium. At this point, it is usually desirable to effect any necessary viscosity adjustment in the solution, such adjustments being consonant with expeditious deposition of the medium in the form ofa continuous and uniform coating of the desired thickness. The thickness value selected is not a particularly critical factor in the practiceof the present invention and thus may be selected from those values customarily employed in the art for such purposes. In general, thinner coatings are preferred in order to achieve the requisite degree of insolubilization. However, the coating thickness selected should be conducive to the provision of a structurally stable coating whereby to permit the selective removal of non-insolubilized areas following exposure without deleteriously affecting the exposed areas, e.g., undercutting. Thus, should the coating be excessively thin, inadvertent removal of exposed areas may result with consequent impairment of phosphor pattern reproduction. It will also be appreciated that the solution viscosity value selected will be influenced to a great extent by the coating method employed, i.e., flowing, whirling, etc. After allowing the layer thus deposited to dry, the shadow mask is positioned in the panel face. The picture tube. face and that portion of the tube housing the electron guns are accurately positioned against each other employing a gasket of suitable material along the area of contact. The tube assembly is thereupon evacuated. The shadow mask is then swept by an electron beam emanating from the appropriate electron gun, i.e., that gun whose corpuscular emissions correspond to the particular color emitting phosphor pattern being laid down. Exposure is effected for a period of time sufficient to impart the requisite insolubilization to those areas subjected to the electron beam. Upon completion of the exposure, air is admitted to the system and the shadow mask retrieved. Thereupon, the shadow mask containing the latent image dot pattern in the form of insolubilized areas is treated with aqueous media whereby to effect removal of non-exposed areas, the latter corresponding to non-insolubilized portions. The foregoing sequence of operations is thereafter repeated for each of the remaining two primary colors whereby to form a complete tricolor phosphor dot pattern.
Thereafter, the usual steps of lacquering, aluminizing, shadow mask insertion, tube section sealing whereby to form an integral unit, baking and evacuating to burn away the binder, may thereafter be resorted to for purposes of providing the final product.
As the foregoing explanation makes clear, the process of the present invention makes possible the attainment of a most precise position relation between the electron gun, the shadow mask and the phosphor dot for each of the three colors. The phosphor dot reproduction obtained is of distinctly superior quality, i.e., extremely sharp, bright and totally free of metal contamination. This, of course, results in enhanced brilliance of emission upon electronic excitation of the phosphor. Moreover, and in contradistinction to processing involving the use of photosensitive binders, overexposure to the electron beam does not result in exaggerated growth in the dot dimension; this result obtains since the scattered light emissions emanatingfrom the phosphor particles dispersed throughout the binder material are innocuous as regards imparting hardening effects to the binder material.
The term water-soluble as used in the context of the present invention is intended to encompass those ethylenically unsaturated materials which exhibit a sufficient degree of water-solubility, dispersibility or sensitivity to permit their expeditious coating in an aqueous system. Thus, it is recognized that particular circumstances dictate the feasibility of providing the ethylenically unsaturated compound in the form of an aqueous dispersion, suspension, emulsion, etc. in order to facilitate the attainment of an optimum coating. This can be readily achieved by the use of suitable suspending agents, emulsifying agents and dispersants well known in the art for such purposes. Regardless of the nature of the system employed for effecting deposition of the ethylenic material in the form of a uniform coating, it will be understood that it remains a critical imperative that such organic material be devoid of light-sensitivity as explained hereinbefore.
The present invention has been described with respect to certain preferred embodiments thereof and there will become obvious to persons skilled in the art variations, modifications and equivalents which are understood as coming within the scope of the present invention.
I claim:
I. In a'process for the preparation of luminescent screens for color television tubes, the improvement which consists essentially of the sequential steps of exposing to corpuscular radiation a surface coated with a corpuscular radiation sensitive composition consisting essentially of a water soluble organic binder layer insolubilizable by corpuscular radiation containing inorganic phosphor particles uniformly dispersed therein, said organic binder material being unaffected by radiation emissions produced by said inorganic phosphor particles during said exposure, said exposure being sufficient to effect insolubilization of said binder material in the radiation-struck areas and thereafter treating said binder composition with water whereby to remove only unexposed non-insolubilized portions, and wherein said organic binder material comprises a member selected from the group consisting of polyvinyl pyrrolidone, polyethylene, polypropylene, polystyrene, polyvinyl methyl ether, poly (methoxy ethyl) vinyl ether, vinyl methyl ether/maleic anhydride copolymer, ethylene/maleic anhydride copolymer, isobutyl vinyl ether/maleic anhydride copolymer, styrene/maleic anhydride copolymer, vinyl pyrrolidone/maleic anhydride copolymer, poly (methoxy ethyl) vinyl ether/maleic anhydride copolymer, polyvinyl pyrrolidone/allyl amine copolymer, acrylamide, N, N- methylenebisacrylamide, acrylic acid, methyl methylacrylate, divinyl benzene, vinyl stearate, and mixtures thereof.
2. A process according to claim 1 wherein said organic binder material comprises a copolymer of maleic anhydride and an alkyl vinyl ether wherein said alkyl moiety contains from one to about 20 carbon atoms and has a specific viscosity ranging from about .05 to about 5.0 measured at 25C as a one percent solution in methyl ethyl ketone.
3. A process according to claim 2 wherein said alkyl vinyl ether comprises methyl vinyl ether.
4. A process according to claim 2 wherein said maleic anhydride/methyl vinyl ether copolymer contains from about 10 percent to about percent on a mole basis of maleic anhydride and has a specific viscosity of 2.0 measured at 25 as a one percent solution in methyl ethyl ketones.
5. A process according to claim 1 wherein said water contains a surface active agent.
Claims (4)
- 2. A process according to claim 1 wherein said organic binder material comprises a copolymer of maleic anhydride and an alkyl vinyl ether wherein said alkyl moiety contains from one to about 20 carbon atoms and has a specific viscosity ranging from about .05 to about 5.0 measured at 25*C as a one percent solution in methyl ethyl ketone.
- 3. A process according to claim 2 wherein said alkyl vinyl ether comprises methyl vinyl ether.
- 4. A process according to claim 2 wherein said maleic anhydride/methyl vinyl ether copolymer contains from about 10 percent to about 65 percent on a mole basis of maleic anhydride and has a specific viscosity of 2.0 measured at 25* as a one percent solution in methyl ethyl ketones.
- 5. A process according to claim 1 wherein said water contains a surface active agent.
Applications Claiming Priority (1)
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US16531971A | 1971-07-22 | 1971-07-22 |
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US3776754A true US3776754A (en) | 1973-12-04 |
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US00165319A Expired - Lifetime US3776754A (en) | 1971-07-22 | 1971-07-22 | Production of luminescent screens |
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Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4139657A (en) * | 1976-05-10 | 1979-02-13 | Hitachi, Ltd. | Process for producing color television picture tube |
US4188449A (en) * | 1977-08-04 | 1980-02-12 | Eastman Kodak Company | Phosphorescent screens |
US4243698A (en) * | 1978-08-12 | 1981-01-06 | Licentia Patent-Verwaltungs-G.M.B.H. | Method for producing a pigment coating |
US4475032A (en) * | 1981-06-12 | 1984-10-02 | U.S. Philips Corporation | Plasma spraying of conversion screens |
US5411806A (en) * | 1994-10-07 | 1995-05-02 | Minnesota Mining And Manufacturing Company | Method for the manufacture of a phosphor screen and resulting article |
US5569485A (en) * | 1994-10-07 | 1996-10-29 | Minnesota Mining And Manufacturing Company | Method for the manufacture of a radiographic intensifying screen with antistat |
US6692660B2 (en) | 2001-04-26 | 2004-02-17 | Nanogram Corporation | High luminescence phosphor particles and related particle compositions |
US20050118411A1 (en) * | 2001-08-17 | 2005-06-02 | Nanogram Corporation | Optical materials and optical devices |
EP1607996A2 (en) * | 2004-06-17 | 2005-12-21 | Samsung SDI Co., Ltd. | Method of manufacturing phosphor layer structure |
US20060132020A1 (en) * | 1997-10-31 | 2006-06-22 | Nanogram Corporation | Phosphors |
US7507382B2 (en) | 1999-03-10 | 2009-03-24 | Nanogram Corporation | Multiple reactant nozzles for a flowing reactor |
-
1971
- 1971-07-22 US US00165319A patent/US3776754A/en not_active Expired - Lifetime
Cited By (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4139657A (en) * | 1976-05-10 | 1979-02-13 | Hitachi, Ltd. | Process for producing color television picture tube |
US4188449A (en) * | 1977-08-04 | 1980-02-12 | Eastman Kodak Company | Phosphorescent screens |
US4243698A (en) * | 1978-08-12 | 1981-01-06 | Licentia Patent-Verwaltungs-G.M.B.H. | Method for producing a pigment coating |
US4475032A (en) * | 1981-06-12 | 1984-10-02 | U.S. Philips Corporation | Plasma spraying of conversion screens |
US5411806A (en) * | 1994-10-07 | 1995-05-02 | Minnesota Mining And Manufacturing Company | Method for the manufacture of a phosphor screen and resulting article |
US5569485A (en) * | 1994-10-07 | 1996-10-29 | Minnesota Mining And Manufacturing Company | Method for the manufacture of a radiographic intensifying screen with antistat |
US6027810A (en) * | 1994-10-07 | 2000-02-22 | Minnesota Mining & Manufacturing | Radiographic intensifying screen with antistat |
US20060132020A1 (en) * | 1997-10-31 | 2006-06-22 | Nanogram Corporation | Phosphors |
US7132783B1 (en) | 1997-10-31 | 2006-11-07 | Nanogram Corporation | Phosphor particles having specific distribution of average diameters |
US7507382B2 (en) | 1999-03-10 | 2009-03-24 | Nanogram Corporation | Multiple reactant nozzles for a flowing reactor |
US7101520B2 (en) | 2001-04-26 | 2006-09-05 | Nanogram Corporation | High luminescence phosphor particles and methods for producing the particles |
US6692660B2 (en) | 2001-04-26 | 2004-02-17 | Nanogram Corporation | High luminescence phosphor particles and related particle compositions |
US20050118411A1 (en) * | 2001-08-17 | 2005-06-02 | Nanogram Corporation | Optical materials and optical devices |
US7306845B2 (en) | 2001-08-17 | 2007-12-11 | Neophotonics Corporation | Optical materials and optical devices |
US7776406B2 (en) | 2001-08-17 | 2010-08-17 | Neophotonics Corporation | Optical materials and optical devices |
US20050281941A1 (en) * | 2004-06-17 | 2005-12-22 | Jung-Na Heo | Method of manufacturing phosphor layer structure |
EP1607996A2 (en) * | 2004-06-17 | 2005-12-21 | Samsung SDI Co., Ltd. | Method of manufacturing phosphor layer structure |
EP1607996A3 (en) * | 2004-06-17 | 2007-04-25 | Samsung SDI Co., Ltd. | Method of manufacturing phosphor layer structure |
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