US3642477A - Imaging method - Google Patents
Imaging method Download PDFInfo
- Publication number
- US3642477A US3642477A US819067A US3642477DA US3642477A US 3642477 A US3642477 A US 3642477A US 819067 A US819067 A US 819067A US 3642477D A US3642477D A US 3642477DA US 3642477 A US3642477 A US 3642477A
- Authority
- US
- United States
- Prior art keywords
- light
- master
- direct positive
- opaque
- white
- 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
- 238000003384 imaging method Methods 0.000 title description 4
- 239000000463 material Substances 0.000 claims abstract description 59
- 238000000034 method Methods 0.000 claims description 24
- 239000000203 mixture Substances 0.000 claims description 18
- 239000000049 pigment Substances 0.000 claims description 18
- 239000011248 coating agent Substances 0.000 claims description 15
- 238000000576 coating method Methods 0.000 claims description 15
- 239000006185 dispersion Substances 0.000 claims description 6
- 239000011230 binding agent Substances 0.000 claims description 2
- 239000011159 matrix material Substances 0.000 claims description 2
- 239000002952 polymeric resin Substances 0.000 claims description 2
- 229920003002 synthetic resin Polymers 0.000 claims description 2
- 238000011161 development Methods 0.000 abstract description 12
- 230000005540 biological transmission Effects 0.000 abstract description 8
- 239000000839 emulsion Substances 0.000 description 14
- 230000018109 developmental process Effects 0.000 description 11
- 239000004332 silver Substances 0.000 description 10
- 229910052709 silver Inorganic materials 0.000 description 10
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 8
- 238000001228 spectrum Methods 0.000 description 7
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 229910052724 xenon Inorganic materials 0.000 description 6
- FHNFHKCVQCLJFQ-UHFFFAOYSA-N xenon atom Chemical compound [Xe] FHNFHKCVQCLJFQ-UHFFFAOYSA-N 0.000 description 6
- 238000012822 chemical development Methods 0.000 description 5
- 239000000975 dye Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 239000000853 adhesive Substances 0.000 description 4
- 230000001070 adhesive effect Effects 0.000 description 4
- 229920000180 alkyd Polymers 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 229910000019 calcium carbonate Inorganic materials 0.000 description 4
- -1 silver halide Chemical class 0.000 description 4
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000002131 composite material Substances 0.000 description 3
- 230000035945 sensitivity Effects 0.000 description 3
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 2
- 239000000020 Nitrocellulose Substances 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
- 238000001914 filtration Methods 0.000 description 2
- MOUPNEIJQCETIW-UHFFFAOYSA-N lead chromate Chemical compound [Pb+2].[O-][Cr]([O-])(=O)=O MOUPNEIJQCETIW-UHFFFAOYSA-N 0.000 description 2
- 229920001220 nitrocellulos Polymers 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000139 polyethylene terephthalate Polymers 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- 239000001052 yellow pigment Substances 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 229940090898 Desensitizer Drugs 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
- 230000002238 attenuated effect Effects 0.000 description 1
- 239000003638 chemical reducing agent Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 238000007730 finishing process Methods 0.000 description 1
- 230000006870 function Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000004615 ingredient Substances 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
- 208000013469 light sensitivity Diseases 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000001053 orange pigment Substances 0.000 description 1
- ZDCHZHDOCCIZIY-UHFFFAOYSA-N phthalic acid;propane-1,2,3-triol Chemical class OCC(O)CO.OC(=O)C1=CC=CC=C1C(O)=O ZDCHZHDOCCIZIY-UHFFFAOYSA-N 0.000 description 1
- 229920006267 polyester film Polymers 0.000 description 1
- 229960003351 prussian blue Drugs 0.000 description 1
- 239000013225 prussian blue Substances 0.000 description 1
- 230000008929 regeneration Effects 0.000 description 1
- 238000011069 regeneration method Methods 0.000 description 1
- 231100000812 repeated exposure Toxicity 0.000 description 1
- OARRHUQTFTUEOS-UHFFFAOYSA-N safranin Chemical compound [Cl-].C=12C=C(N)C(C)=CC2=NC2=CC(C)=C(N)C=C2[N+]=1C1=CC=CC=C1 OARRHUQTFTUEOS-UHFFFAOYSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Images
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
- G03F1/00—Originals for photomechanical production of textured or patterned surfaces, e.g., masks, photo-masks, reticles; Mask blanks or pellicles therefor; Containers specially adapted therefor; Preparation thereof
- G03F1/54—Absorbers, e.g. of opaque materials
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/485—Direct positive emulsions
- G03C1/48515—Direct positive emulsions prefogged
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/08—Photoprinting; Processes and means for preventing photoprinting
Definitions
- ABSTRACT [21 1 Appl- 819,067 images are vformed on direct positive photographic material in a single white-light exposure through the use of a master sheet 52] u.s.c
- Herschel Effect might be. considered to be somewhat of a misnomer with respect to modern. direct positive photographic materials since the prefogging of the photographic material was achieved by- Herschel (1839) by means of an overall light exposure, whereas presentcommercially available direct positive photographic papers are prefogged and presensitized chemically through the use of reducing agents and dyes such as the Pinakryptol dyes. Regardless of the process employed to createthe fogging nuclei, however, the'behavior of the resultingdirect positive photographic material remains such as to become defogged or rendered incapable of image-forming development upon exposure to longer wave length light, as in the yellow and red ranges of the white-light spectrum.
- scribe coat which generally comprises a transparent base having a heavily-pigmented, readily-removable opaque coating.
- Some such pigmented scribe materials are described in US. Pat. No. 2,999,016.
- Original drawings on such material are accomplished through the removal of portions of the opaque scribe coat to create a negative of the topographic or other land feature layout. Symbolic indicia and lettering are normally prepared separately in positive form on a transparent overlay sheet which is later combined in the photocomposition process with the negative master of the topographic layout.
- the reversal characteristics of direct positive materials are particularly well adapted to the employment of such comparative .positive and negative photocomposition layouts and overlays.
- the most practical method of composing an archival plate required the steps of exposing a directpositive sheet through the positiveindicia overlay to a relatively long-wave yellow .light thereby creating,” by reversal, a latent image of the opaque indicia in the directpositive sheet.
- this initially exposed direct positive sheet was again exposed through the negative scribed master to a relatively short durationwhite-light exposure which creates a new silver-center latent image in the defogged areas of the direct positive sheet.
- Subsequent chemical development of the direct positive sheet results in apositive image of both the indicia and the topographic features.
- An object of the present invention is to provide a method of photocomposition employing direct positive photographic materials and whichv comprises a single light-exposure step thereby obviating excessive make ready time, and precise overlay registration.
- the method of the present invention employs as the medium for preparation of the original exposure master a material which has the selective light transmissive properties of a Herschel light filter. That is, the medium on which the topographic or. other features are carried transmits in its nonimage areas only the longer wave lengths of light, as in the yellow and red spectrum bands. Direct positive photographic material exposed to light from a carbon arc or xenon lamp source through such a master medium will be effectively reversed or defogged.
- Symbolic indicia and lettering may be readily applied to the surface of the master medium by means of ink drawing or transfer lettering and form opaque indicia elements which are desired to be reproduced in the final composite master plate.
- the resulting exposure master is placed upon a sheet of direct positive photographic material and the combination exposed to a white light source for a time sufficient to defog" the direct positive material in areas lying immediately beneath the light filter composition layer and the direct positive material is then subjected to chemical development.
- the resulting silver image on the developed direct positive material is located in areas corresponding to the opaque indicia and the transparent features of the original master.
- An original exposure master ltl is made up of a transparent base sheet 12 of polyester film,,glass or the like hearing on-its surface a coating of a selective light filter composition l4.
- the light filter layer' is preferably of a pigmented, scribable composition or a peelable film including appropriate dyes or colored pigments to render the composition transmissive of light wave lengths in the Herschel range," that is, in the spectrum band of wave lengths substantially longer than the peak wave length sensitivity of the direct positive photographic material to be employed.
- Open areas 16 represent portions of the filter layer 14 which are removed as by scribing or peeling and represent an original line drawing of topographic features and the like. Removal of the filter layer material from areas 16 creates in the master medium 10 open window areas which are substantially wholly transmissive of white light through the transparent base 12.
- opaque symbolic indicia or lettering 18 Upon the filter layer 14 and in appropriate relation to the basic scribed topographic features in the master are located opaque symbolic indicia or lettering 18 to complete the original exposure master.
- the symbolic indicia may be applied in India ink or adhesive transfer lettering, or may be photographically created on the filter layer or in a transparent overlay which is combined with the original drawing of the topographic features in the filter master medium prior to light exposure.
- a sheet of direct positive photographic material 20 is shown disposed in underlying relationship to the original master 10. While the composite of master l and direct positive material 20 will normally be that of a contiguous association, these sheets are shown in the drawing as being separated to some degree for clarity in representation.
- the master and the copy sheet may be in face-to-back or face-to-face relation depending upon the form in which the master is prepared. In some instances a face-to-face combination is preferred in order to obtain clearer images.
- the direct positive material 20 is made up of a base 22 which may be opaque or transparent and a prefogged photographic silver halide emulsion 24.
- the direct positive material 20 may be any of the many commercially available direct positive photographic products. Such a material is Keuffel & Esser Co.
- Autopositive Film (43rd Edition Cat. No. 392843) which includes in the photosensitive layer a desensitizer such as a Pinakryptol or Safranine dye in a silver halide emulsion fogged with chemically-induced silver development centers or nuclei.
- a desensitizer such as a Pinakryptol or Safranine dye in a silver halide emulsion fogged with chemically-induced silver development centers or nuclei.
- the direct positive material 20 shown in the drawing is depicted as having undergone various changes in the emulsion layer as a result of the light exposure according to the present invention. Only area 26 of the emulsion layer is in the original prefogged developable state characteristic of direct positive photographic material, the remaining areas having been changed to some extent by incident radiation as will be later described.
- the combination of direct positive material 20 and the original master is exposed to white light from a source generally represented at 30.
- This light source may be any type ofsource normally used in the graphic arts, for example: a carbon are or xenon lamp, and will have substantial radiation throughout the visible light bands.
- White light from source 30 is shown as rays 32 which are completely absorbed by opaque indicia 18 and completely transmitted by open areas 16 in the master 10, passing through the transparent base 12 in substantially unattenuated form to incidence upon the emulsion 24 of the direct positive material 20.
- White light rays 32 which are incident upon the filter layer of master 10 are attenuated in such a manner that light rays 34 of preselected wave lengths are transmitted to emulsion 24 of the direct positive material 20.
- the wave length band of rays 34 is determined by the filtering dyes and/or pigments in filter layer 14 so as to have the appropriate Herschel effect upon the original direct positive emulsion 24.
- the final step in the process of the present invention is the chemical development of the exposed photographic material 20. Development is carried out in common commercially available chemical developing solutions and results in a finished print 40 having silver images 42 of substantially equal density corresponding to the transparent line features and opaque indicia in the original master 10. As in common photographic finishing processes, the developed print 40 may be chemically fixed, washed and dried to obtain a master of archival keeping quality.
- a dispersion of the following composition was ball-milled to coatable consistency and coated to a dry thickness of 0.6 mil on a 5.0 mil sheet of biaxially oriented polyethylene terepthalate film (in this and following examples all ingredient amounts are in parts by weight unless otherwise specified):
- Alkyd resin oil modified glycerol phthalate
- Calcium carbonate pigment 35
- A20 orange pigment (Cl pigment orange 25) 5.0 Red Lake pigment (Cl pigment red 53) 15
- Solvent toluol, xylene, and/or ethyl I25 acetate
- the resulting scribe coat master medium was greater than about 70 percent transmissive of light in the spectrum bands above 6,200 A. and transmitted substantially no light in the spectrum bands below 5,600 A.
- Topographic map features were scribed in the resulting material, thereby forming a master of transparent lines in a background of the red scribe coat.
- the transparent areas of the scribe lines transmitted substantially all light in the spectrum bands between about 4,000 A. and 7,000 A. from a white light source.
- EXAMPLE 2 A sheet of commercially available direct positive film (Keuffel & Esser Company Catalogue No. 39-2843) was placed in underlying contact with the master prepared according to example 1. The combination was exposed for three minutes at a distance of 0.5 m. to the light of a 3,500 watt xenon lamp. After exposure, areas of the direct positive film coating corresponding to the transparent scribed lines of the original were visible as a printout image.
- the exposed direct positive material was developed for 10 seconds in a commercially available direct positive emulsion developer solution, usually a high-contrast hydroquinone developer, and resulted in the development of dense black images corresponding to the transparent lines and the opaque ink lettering of the original described in example l.
- the print was fixed in ordinary hypo solution and washed and dried according to common procedures to provide a permanent solution.
- EXAMPLE 3 A dispersion of the following composition was ball-milled to a coatable consistency and was coated and dried to a thickness Nitrocellulose 5.0 Alkyd resin 35 Calcium carbonate pigment ll Prussian blue pigment 9.0 (CI pigment blue 27) Chrome yellow pigment 4.0 (CI pigment yellow 34) Solvent 200 On the resulting dried coating was applied a ball-mill dispersion of the following composition to a dry thickness of about 0.6 mils:
- a master original was prepared from this material by scribing away portions of the coating in the image of topographic features followed by the application to the surface of the scribe coat material of black opaque adhesive transfer lettering denoting symbolic indicia.
- the resulting master was substantially wholly transparent in the scribed line areas to light between about 4,000 A. and 7,000 A, and was substantially opaque to light in that range in the lettered areas.
- the resulting master was used to expose a sheet of direct positive photographic material as in example 2, the direct positive material having a peak sensitivity between about 4,600 and 4,800 A,
- the combination of the master and the direct positive material was exposed to a xenon lamp as in example 2 for a period of about 3.5 minutes and was developed, fixed and washed according to common photographic procedures to obtain a permanent image of dense black corresponding to the scribed lines and the opaque lettering ofthe master original.
- EXAMPLE 4 A scribed original was prepared as in example 1 employing a scribe coat medium of the following composition:
- Nitrocellulose 5 Alkyd resin Calcium carbonate pigment Chrome yellow pigment 6.5 (Cl pigment yellow 34) Solvent 200 The scribe coat exhibited greater than about 35 percent transmission above 5,800 A. and substantially no light transmission below wavelengths of about 5,200 A.
- Black opaque adhesive transfer lettering and India ink were employed to form opaque indicia on the scribe master of the original.
- the scribed and opaque indicia areas transmitted, respectively, substantially all and substantially no light between about 4,000 A. and 7,000 A.
- the resulting master was employed to expose a sheet of commercially available direct positive material as in example 2, the exposure being for about 3 minutes to the xenon lamp. Subsequent development, fixing, washing and drying provided a permanent black image corresponding to the scribed lines and opaque lettering of the original.
- a peelable coat master medium was prepared by coating a balLmill dispersion of the following composition on a sheet of biaxially oriented polyethylene terepthalate film to a dry thickness of about 0.6 mils:
- the coated composition was dried to effect removal of solvents and resulted in a film which was self-sustaining and peelable from the polyester base sheet.
- a master original common methods were employed to remove desired portions of the peelable coating and thereby form line and open window images in the material. For example, desired open window areas were circumscribed with a cutting blade instrument and the coating within the defined area peeled away from the transparent polyester base. In the background areas the resulting master exhibited light transmission of greater than about 25 percent above 6,300 A. and substantially no transmission of light below about 5,800 A. The open window areas of the master transmitted substantially all light between about 4,000 A. and 7,000 A. The master was completed by the application of opaque adhesive transfer lettering through which substantially no visible light was transmitted and the master was employed to expose direct positive photographic material as in example 2.
- the direct positive material was developed, fixed, washed and dried to provide a black image in areas corresponding to the open window and opaque lettered areas of the original.
- a method of imaging direct positive photographic material having fogging nuclei consisting essentially of:
- a master bearing features to be reproduced as images on said material said master consisting essentially 1. a layer of light-filter composition selectively transmissive only of light of wave lengths substantially greater than the peak light sensitivity of said direct positive material,
- said coating comprises a film-forming composition of a polymeric resin and a colored pigment.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
Abstract
Description
Claims (5)
- 2. at least one of said features in the form of a light-opaque area substantially wholly nontransmissive of white light, and
- 2. The method according to claim 1 wherein the light-filter layer of said master comprises a transparent support and a readily removable coating thereon of a composition of said selective light-transmissivity.
- 3. The method according to claim 2 wherein said coating comprises a dispersion of colored pigment in a resinous binder matrix.
- 3. at least one of said features in the form of an open aRea in said light-filter layer, said open area being substantially wholly white-light transmissive, b. positioning said master in overlaying relation upon said direct positive material; and c. exposing the resulting overlay combination, from the master side, to white light for a time sufficient to destroy the fogging nuclei is said direct positive material in areas underlying solely said light-filter composition layer; and d. chemically developing the exposed photographic material.
- 4. The method according to claim 2 wherein said coating comprises a film-forming composition of a polymeric resin and a colored pigment.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US81906769A | 1969-04-24 | 1969-04-24 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3642477A true US3642477A (en) | 1972-02-15 |
Family
ID=25227125
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US819067A Expired - Lifetime US3642477A (en) | 1969-04-24 | 1969-04-24 | Imaging method |
Country Status (2)
Country | Link |
---|---|
US (1) | US3642477A (en) |
CA (1) | CA920865A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3945827A (en) * | 1974-08-02 | 1976-03-23 | Barry David Brown | Methods of making printed circuit boards utilizing an image transparency mode with Herschel-effect film |
US4028104A (en) * | 1975-04-21 | 1977-06-07 | Hughes Aircraft Company | Infrared hologram recording method |
US4264551A (en) * | 1978-08-25 | 1981-04-28 | Matsushita Electrical Industrial Co., Ltd. | Recorded disk reproducing system |
WO1981001886A1 (en) * | 1979-12-31 | 1981-07-09 | Ncr Co | Method and apparatus for fabricating a translucent graded density medium |
US4619889A (en) * | 1983-01-24 | 1986-10-28 | Fuji Photo Film Co., Ltd. | Image forming method |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2912325A (en) * | 1954-02-12 | 1959-11-10 | Eastman Kodak Co | Light-sensitive film prescreened by herschel exposure |
US2999016A (en) * | 1955-03-24 | 1961-09-05 | Keuffel & Esser Co | Drawing material |
US3124458A (en) * | 1961-03-10 | 1964-03-10 | Direct positive photographic materials | |
US3178997A (en) * | 1961-05-02 | 1965-04-20 | Technicolor Corp | Image-processing system |
US3526507A (en) * | 1965-04-28 | 1970-09-01 | Keuffel & Esser Co | Autopositive reproduction material |
-
1969
- 1969-04-24 US US819067A patent/US3642477A/en not_active Expired - Lifetime
-
1970
- 1970-03-31 CA CA078671A patent/CA920865A/en not_active Expired
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2912325A (en) * | 1954-02-12 | 1959-11-10 | Eastman Kodak Co | Light-sensitive film prescreened by herschel exposure |
US2999016A (en) * | 1955-03-24 | 1961-09-05 | Keuffel & Esser Co | Drawing material |
US3124458A (en) * | 1961-03-10 | 1964-03-10 | Direct positive photographic materials | |
US3178997A (en) * | 1961-05-02 | 1965-04-20 | Technicolor Corp | Image-processing system |
US3526507A (en) * | 1965-04-28 | 1970-09-01 | Keuffel & Esser Co | Autopositive reproduction material |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3945827A (en) * | 1974-08-02 | 1976-03-23 | Barry David Brown | Methods of making printed circuit boards utilizing an image transparency mode with Herschel-effect film |
US4028104A (en) * | 1975-04-21 | 1977-06-07 | Hughes Aircraft Company | Infrared hologram recording method |
US4264551A (en) * | 1978-08-25 | 1981-04-28 | Matsushita Electrical Industrial Co., Ltd. | Recorded disk reproducing system |
WO1981001886A1 (en) * | 1979-12-31 | 1981-07-09 | Ncr Co | Method and apparatus for fabricating a translucent graded density medium |
US4284715A (en) * | 1979-12-31 | 1981-08-18 | Ncr Corporation | Method and apparatus for fabricating a translucent graded density membrane |
US4619889A (en) * | 1983-01-24 | 1986-10-28 | Fuji Photo Film Co., Ltd. | Image forming method |
Also Published As
Publication number | Publication date |
---|---|
CA920865A (en) | 1973-02-13 |
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Legal Events
Date | Code | Title | Description |
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AS | Assignment |
Owner name: CHEMICAL BANK, A BANKING INSTITUTION OF, NEW YORK Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808 Effective date: 19820323 Owner name: BANK OF CALIFORNIA N.A. THE; A NATIONAL BANKING AS Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808 Effective date: 19820323 Owner name: CONTINENTAL ILLINOIS NATIONAL BANK & TRUST CO., OF Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808 Effective date: 19820323 Owner name: CHEMICAL BANK, A BANKING INSTITUTION OF NY. Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808 Effective date: 19820323 Owner name: CHASE MANHATTAN BANK, N.A. THE; A NATIONAL BANKING Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808 Effective date: 19820323 Owner name: SECURITY NATIONAL BANK, A NATIONAL BANKING ASSOCIA Free format text: SECURITY INTEREST;ASSIGNOR:KEUFFEL & ESSER COMPANY A.N.J. CORP;REEL/FRAME:003969/0808 Effective date: 19820323 |