US3156564A - Production of photographic images making use of the intensity-reversal effect - Google Patents

Production of photographic images making use of the intensity-reversal effect Download PDF

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Publication number
US3156564A
US3156564A US797056A US79705659A US3156564A US 3156564 A US3156564 A US 3156564A US 797056 A US797056 A US 797056A US 79705659 A US79705659 A US 79705659A US 3156564 A US3156564 A US 3156564A
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exposure
intensity
layer
emulsion
image
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US797056A
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Wartburg Rene Von
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    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03FPHOTOMECHANICAL PRODUCTION OF TEXTURED OR PATTERNED SURFACES, e.g. FOR PRINTING, FOR PROCESSING OF SEMICONDUCTOR DEVICES; MATERIALS THEREFOR; ORIGINALS THEREFOR; APPARATUS SPECIALLY ADAPTED THEREFOR
    • G03F5/00Screening processes; Screens therefor
    • G03F5/24Screening processes; Screens therefor by multiple exposure, e.g. combined processes for line photo and screen
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/485Direct positive emulsions
    • G03C1/48592Positive image obtained by various effects other than photohole bleaching or internal image desensitisation, e.g. Sabatier, Clayden effect
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S430/00Radiation imagery chemistry: process, composition, or product thereof
    • Y10S430/141Direct positive material

Definitions

  • the invention relates to the production of screened and non-screened direct positive images and to the production of compensated or tonevalue corrected cop'es from negatives having a large image density range.
  • these processes are carried out by means of special silver halide emulsions which contain silver iodide and are subjected to a physical ripening in the presence of at least one inhibitor andwhich are not subjected to chemical ripening.
  • the intensity reversal effect consists in that, with a layer subjected to brief initial exposure with a high light intensity, the latent image completely or partially loses its capacity for chemical development when the layer is after-exposed for a long period with low light intensity. It is clear from the aforesaid literature references that the intensity reversal ei ect occurs in more or less pronounced form with different (high sensitive and low sensitive) layers and can be used for practical purposes. However, the works reference to above do not disclose the special layer and exposure conditions which lead to a reproducible intensity-reversal effect and which can be used. in practice.
  • direct positive images with improved photographic properties are produced while making use of the intensity-reversal effect by means of a silver halide emulsion containing silve iodide, preferably silver iodo bromide emulsion, which is subjected to physical or Ostwald ripening in the presence of at least one photographic .inhibitor'or stabilizer and which has not received a chemical ripening.
  • silve iodide preferably silver iodo bromide emulsion
  • the silversalt of'said emulsion preferably consists of I 3,156,564 Patented Nov. 10, 1964 0.1-50 mol percent of silver iodide and 99.9-50 percent of silver bromide, whereby amounts of 0.1-12 mol percent of silver iodide have proved to be especially advantageous.
  • the silver bromide of said emulsion may be partially re placed by silver chloride.
  • the physical ripening of the emulsion is preferably performed in the presence of a surplus of water-soluble bromides, especially potassium bromide, whereby a surplus of 5-400, especially 5-200, mol percent of bromides over the theoretical amount has proved to be especially advantageous. It is furthermore possible to use besides silver salts small amounts of other heavy metal salts such as, for instance, thallium salts, in the preparation of the present emulsions.
  • inhibitors there come into question the well-known substances which are used in the photographic art as ripening retarders in the production of silver halide emulsions, as stabilizers for increasing the stability of silver halide emulsion layers, or as anti-fogging additives to silver halide developers.
  • Preferred inhibitors are the 1,3, 4-triazaindolizines, especially the 7-hydroxy-1,3,4-triazaindolizines, as they are, for instance, disclosed in United States Patents Nos. 2,444,605; 2,444,606 and 2,449,225.
  • the 7-hydroxy-1,3,4-triazaindolizines which are substituted in the 6-position by a halogen atom especially by chlorine or bromine.
  • inhibitors are, for instance, benzotriazole (lH-benzotriazole or 1,2,3-benzotriazole), methylbenzotriazole, o-nitrobenzotriazole, histidene, ethylbenzoxazole, N-ethylpyrrole and 2,3-dimethylquinoxmine (2,3-dimethyl-l,4-benzodiazine).
  • the inhibitors are generally applied in amounts of about 0.01-1 g. per 100 g. of silver.
  • the precipitation of the silver salt is carried out at 40- (1., with gelatin or another suitable film-forming agent used as a protective colloid.
  • the precipitation of the silver salt is carried out in the presence of a molar surplus of a water-soluble bromide, especially potassium bromide, in order to achieve a physical ripening of the precipitated silver salts. It is furthermore possible to carry out the precipitation in the presence of ammonia.
  • the emulsions are Washed with Water, whereby the emulsions are adjusted to a volume conductivity of about 900-1600 international reciprocal ohmcentimeters.
  • the inhibitor which is present in the emulsion is washed out at least partially.
  • the emulsion is not subjected to chemical ripening (chemical ripening isusually applied in the production of highly sensitive silver halide emulsions by subjecting the washed emulsions to a heattreatment in the presence of chemical sensitizers). It has proved advantageous to add to the present washed emulsions water-soluble bromides, as, for instance, potassium bromide, in amounts of 1-4 g. per liter of emulsion.
  • the photographic layer produced from these emulsions in well-known manner either on a paper, a film or a glass support, should have a high silver content as, for instance, 2-50 g. preferably 10-50 g. of silver per square meter.
  • a layer of the said type shows a pronounced intensityreversal effect. if such a layer is subjected to a diffused initial exposure with a burning period of 10* sec.
  • printing refers to contact printing and also to enlargement or reduction by optical image formation.
  • Example 1 An emulsion having the following specification is prepared by use of the following four solutions:
  • an electronic flash-lamp For the brief initial exposure of the layer produced from said emulsion, an electronic flash-lamp is employed.
  • the intensity of the initial exposure depends on the desired density of the final image and on the sensitivity of the direct duplicate material.
  • the initial exposure can be obtained with a single electronic flash exposure or by a relatively large number of electronc flash exposures of lower intensity.
  • a photographic film having a silver halide layer with a thickness of 20 microns there may be obtained a maximum density of 4 after development of the exposed layer with an ordinary silver halide developer.
  • the layer thus initially exposed can now be exposed in contact with the printing original or in a camera, the exposure advantageously being effected through a mirror in order to obtain an image which is not laterally reversed.
  • the slow exposure which is in principle to be at least 100 times longer than the initial exposure, is so chosen that subsequently an image of the desired density distribution is formed. For instance, exposures which are 10 to 10 and preferably 10 to 10 times longer than the initial exposure. If the exposure is made in the camera, an original is, for instance, exposed with 4 carbon-arc lamps a distance of 1 meter, said lamps being arranged an angle of about 45. If the aperture or diaphragm stop of the camera is adjusted to f/ 11 (U.S. No. 8), the exposure time amounts to 10 to 20 seconds.
  • the layer is then developed with a conventional developer, whereupon it is fixed in the usual way with an acid fixing bath, and thereafter rinsed and dried. The result is a direct duplicate of the original.
  • Example 2 An emulsion is prepared as described in Example 1 and this emulsion is subjected in liquid form in a layer of thickness of for example 0.1 mm. either to a single brief initial exposure of high light intensity or to several brief initial exposures of lower intensity, if desired by allowing the emulsion to flow between two light-pervious plates suitably spaced apart during the exposure to light. Thereafter, the initially exposed emulsion is cast on to the final layer support. After drying, the slow exposure for forming the image is carried out as indicated in Example 1. Conventional photographic processing then provides a direct duplicate of the original.
  • Example 3 An emulsion is prepared as described in Example 1 and this is cast in a layer of thickness of for example 0.2 mm. on to a support, for example a conveyor belt. After the layer has solidified, this is subjected either to a single brief initial exposure with light of high intensity or to several brief initial exposures with light of lower intensity. Thereafter, the layer is again melted and cast on to the final layer support. After drying, the slow exposure for forming the image is carried out as indicated in Example 1. Usual photographic development also provides a direct duplicate of the original in this case.
  • the intensityreversal effect may also be used for the production of screened duplicates from continuous tone originals.
  • the usual procedure is for the original to be processed to give a screened exposure or print by using a screen in a camera or in contact.
  • This process presupposes the use of a screen or raster. Consequently the practice has frequently been adopted of using special prescreened photographic materials for the exposure or print. Such materials have a different light-sensitivity at different areas, this sensitivity showing a continuous increase and decrease according to the screen spacing.
  • a screened or lined image is formed after the normal processing thereof, the tone values of this image being opposite to those of the original.
  • a screened direct duplicate of the original is produced.
  • the procedure followed according to the invention is that a screen is first of all printed by brief exposure with light of high intensity on to a photographic material of steep intensity and showing a pronounced intensity-reversal effect, and thereafter the original to be screened is printed thereon by relatively long exposure with light of weak intensity, whereafter the material is developed in the usual way and thus a screened direct duplicate of the original is obtained.
  • the intensity-reversal effect can be used for the production of direct duplicates by the first brief exposure to light being so diffused over the entire layer that without subsequent exposure, the maximum density of the layer could be developed.
  • the subsequent slow exposure is thereafter carried out to form an image.
  • a duplicate of the exposed original is obtained.
  • the process is modified, in that the brief initial exposure is not diffused, but is made through a raster or screen.
  • a screen it is either possible to use a half-tone screen in contact with the layer or a lined screen at a suitable spacing from the layer.
  • the exposure is so chosen that also at the areas at which the layer receives the smallest light quantities, the layer would be completely blackened by an immediate development.
  • the layer has experienced a varying initial exposure, according to the scale of the screen it also has a positive sensitivity distributed in the manner of a screen. If the positive density curve of the type of layer employed is sufficiently strong, a screen duplicate of the original is consequently formed when an original is exposed and thereafter developed. For carrying through this process there are advantageously used the emulsions disclosed hereinbefore.
  • Example 4 A layer having a strong intensity-reversal effect and a steep gradation of the slow exposure, of for example 7: 10, is briefly exposed to light behind a contact screen by means of an electronic flash lamp, i.e., for a period of maximum duration of 10- sec. with high intensity light.
  • the exposure to light takes place for example at a distance of 60 cm. with a light having a discharge energy of 50 watt-seconds. Instead of using this single exposure, it is also possible to make several brief exposures with light of lower intensity.
  • the layer thus prepared is used in a reproduction camera.
  • an exposure time of 20 seconds is necessary'for the slow exposure which takes at least 100 times longer than the flash exposure, this exposure being made with illumination from a low light intensity using four are lamps, each of 30 amperes at a distance of 1 meter, and a diaphragm stop of f/ 22, in order to obtain a correctly screened duplicate of the original after development has taken place in the usual way.
  • the layer used for performing this process may be produced from the emulsion disclosed in Example 1.
  • the process of the present invention may also be used for the production of compensated copies from negatives which have a large image density range, whereby especially ad disadvantageous results are obtained with the speical emulsions disclosed hereinbefore.
  • compensated prints from negatives (or positives) having a large image density range can be produced more easily by means of a silver halide emulsion layer having pronounced intensity-reversal effect susceptibility, whereby printing .is carried through in such a way that withthe short time exposure an image of the negative is sharply or distinctlyformed and withthe longtime exposure an image of the negative is blurred or indistinctly formed.
  • two contrasting photographic processes are combined, one process being an image-forming process in which an image of the negative is sharply formed, and the other being a compensating or desensitizing process in which an image of the negative is indistinctly formed. After the exposure, the layers are developed in the usual way.
  • the silver halide emulsion layer is exposed to the image to be reproduced in focus with said image when exposing said layer with the high intensity light and the layer is exposed to said image slightly out of focus with said image with the low intensity light, and at the same magnification as the first mentioned exposure.
  • the high intensity exposure can be carried out first of all as the image-formingoperation, this being followed by the low intensity exposure for the compensating operation. However, it is also possible to operate in the reverse sequence.
  • Example 5 on to the paper and the synthesizing brief exposure is made.
  • a flash energy 1,000 watt-seconds.
  • the paper is covered with a sheet of opal glass.
  • a second slow degradating exposure is now carried out.
  • the necessary lack of sharpness or blurring is produced by the opal glass.
  • an exposure time of for example seconds is necessary under the conditions described above.
  • the photographic material is thereafter developed and fixed in the usual way. The result is the desired compensated print.
  • Example 6 A compensated print such as that of Example 2 can also be obtained with the same arrangement and by using the same type of layer if the sequence of the two exposures is reversed.
  • the layer is image-wise desensitized.
  • the synthesizing brief and sharp exposure is then carried out by means of an electronic flash.
  • the procedure for the enlargement is the same, except that the sequence of the exposures is reversed and the previous slow exposure is now for example extended to 30 minutes.
  • the improvement according to which the emulsion used is one which has been subjected to a grain size ripening while containing an anti-fogging agent, and has not been subjected to a chemical ripening.
  • the anti-fogging agent is selected from the class consisting of hemetriazole, methylbenzotriazole, 6-nitrobenzothiazole, histidine, ethylbenzoxazole, n-ethylpyrrole and 2,3-dimethylquinoxaline.

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  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • General Physics & Mathematics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Silver Salt Photography Or Processing Solution Therefor (AREA)
US797056A 1958-03-11 1959-03-04 Production of photographic images making use of the intensity-reversal effect Expired - Lifetime US3156564A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CH5698458A CH367706A (de) 1958-03-11 1958-03-11 Verfahren zur photographischen Herstellung von Direkt-Duplikaten

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US (1) US3156564A (de)
BE (1) BE576568A (de)
CH (1) CH367706A (de)
DE (1) DE1172953B (de)
FR (1) FR1221305A (de)
GB (1) GB882690A (de)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3519426A (en) * 1966-12-27 1970-07-07 Eastman Kodak Co Preparation of silver halide emulsions having high covering power
US3661592A (en) * 1969-11-06 1972-05-09 Agfa Gevaert Nv Photographic fine grain silver halide materials
US4140531A (en) * 1975-09-10 1979-02-20 Minnesota Mining And Manufacturing Company Light-handleable photographic materials
US4232116A (en) * 1979-01-31 1980-11-04 Minnesota Mining And Manufacturing Company Light-handleable photographic materials
US4610958A (en) * 1983-12-07 1986-09-09 Konishiroku Photo Industry Co., Ltd. Process of preparing a silver halide emulsion
US4683192A (en) * 1984-04-19 1987-07-28 Fuji Photo Film Co., Ltd. Silver halide photographic emulsions and process for producing them

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2401051A (en) * 1939-09-26 1946-05-28 Photo Positive Corp Photographic emulsions and methods
US2444605A (en) * 1945-12-15 1948-07-06 Gen Aniline & Film Corp Stabilizers for photographic emulsions
US2691586A (en) * 1952-06-04 1954-10-12 Eastman Kodak Co Photographic light-sensitive material for making halftones
US2708626A (en) * 1952-06-04 1955-05-17 Eastman Kodak Co Photographic processes using prescreened material
US2912328A (en) * 1954-04-09 1959-11-10 Eastman Kodak Co Direct positive prescreened photographic material
US2912326A (en) * 1954-04-09 1959-11-10 Eastman Kodak Co Direct positive prescreened photographic material
US3000739A (en) * 1957-04-02 1961-09-19 Du Pont Process for preparing silver halide emulsions

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2444867A (en) * 1945-07-26 1948-07-06 Eastman Kodak Co Photographic masking using the clayden effect
BE543288A (de) * 1954-12-10

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2401051A (en) * 1939-09-26 1946-05-28 Photo Positive Corp Photographic emulsions and methods
US2444605A (en) * 1945-12-15 1948-07-06 Gen Aniline & Film Corp Stabilizers for photographic emulsions
US2691586A (en) * 1952-06-04 1954-10-12 Eastman Kodak Co Photographic light-sensitive material for making halftones
US2691585A (en) * 1952-06-04 1954-10-12 Eastman Kodak Co Prescreened posterizing photographic film
US2708626A (en) * 1952-06-04 1955-05-17 Eastman Kodak Co Photographic processes using prescreened material
US2912328A (en) * 1954-04-09 1959-11-10 Eastman Kodak Co Direct positive prescreened photographic material
US2912326A (en) * 1954-04-09 1959-11-10 Eastman Kodak Co Direct positive prescreened photographic material
US3000739A (en) * 1957-04-02 1961-09-19 Du Pont Process for preparing silver halide emulsions

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3519426A (en) * 1966-12-27 1970-07-07 Eastman Kodak Co Preparation of silver halide emulsions having high covering power
US3661592A (en) * 1969-11-06 1972-05-09 Agfa Gevaert Nv Photographic fine grain silver halide materials
US4140531A (en) * 1975-09-10 1979-02-20 Minnesota Mining And Manufacturing Company Light-handleable photographic materials
US4232116A (en) * 1979-01-31 1980-11-04 Minnesota Mining And Manufacturing Company Light-handleable photographic materials
US4610958A (en) * 1983-12-07 1986-09-09 Konishiroku Photo Industry Co., Ltd. Process of preparing a silver halide emulsion
US4683192A (en) * 1984-04-19 1987-07-28 Fuji Photo Film Co., Ltd. Silver halide photographic emulsions and process for producing them

Also Published As

Publication number Publication date
DE1172953B (de) 1964-06-25
FR1221305A (fr) 1960-06-01
GB882690A (en) 1961-11-15
BE576568A (de)
CH367706A (de) 1963-02-28

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