US3837886A - Process for producing photographic materials - Google Patents

Process for producing photographic materials Download PDF

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Publication number
US3837886A
US3837886A US00142815A US14281571A US3837886A US 3837886 A US3837886 A US 3837886A US 00142815 A US00142815 A US 00142815A US 14281571 A US14281571 A US 14281571A US 3837886 A US3837886 A US 3837886A
Authority
US
United States
Prior art keywords
film
polystyrene film
electrodeless discharge
polystyrene
discharge treatment
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
Application number
US00142815A
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English (en)
Inventor
S Tatsuta
W Ueno
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fujifilm Holdings Corp
Original Assignee
Fuji Photo Film Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Fuji Photo Film Co Ltd filed Critical Fuji Photo Film Co Ltd
Application granted granted Critical
Publication of US3837886A publication Critical patent/US3837886A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Classifications

    • 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
    • G03C1/76Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/795Photosensitive materials characterised by the base or auxiliary layers the base being of macromolecular substances
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29CSHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
    • B29C59/00Surface shaping of articles, e.g. embossing; Apparatus therefor
    • B29C59/14Surface shaping of articles, e.g. embossing; Apparatus therefor by plasma treatment
    • 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
    • G03C1/76Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/91Photosensitive materials characterised by the base or auxiliary layers characterised by subbing layers or subbing means
    • G03C1/915Photosensitive materials characterised by the base or auxiliary layers characterised by subbing layers or subbing means using mechanical or physical means therefor, e.g. corona
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B29WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
    • B29KINDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
    • B29K2025/00Use of polymers of vinyl-aromatic compounds or derivatives thereof as moulding material

Definitions

  • baryta paper consisting of paper made from pulp and a coating composed of a kneaded mixture of fine powders of barium sulfate, a small amount of a binder, such as gelatin, and water has been used as a support for a photographic material, such as photographic paper or diffusion transfer process photographic paper.
  • a photographic material such as photographic paper or diffusion transfer process photographic paper.
  • Such support exhibits certain defects, such as shrinkage or expansion with humidity changes, and especially shrinkage after development, prolonged drying time after development, and low resistance to water.
  • a process for producing a photographic material which comprises contacting a biaxially drawn, surfaceroughened polystyrene film with an active gas generated by a high frequency electrodeless discharge under reduced pressure or in a stream of helium or oxygen under reduced pressure, and thereafter coating an emulsion or suspension containing gelatin as a binder on the polystyrene film so treated.
  • the emulsion or suspension containing gelatin as a binder used in the invention is meant an aqueous emulsion or suspension of gelatin prepared by adding silver halides, such as silver chloride, silver bromide, silver chlorobromide or silver iodobromide, photosensitive diazo compounds or a substance which becomes the nucleus of development of an image-receiving material used in the silver halide diffusion transfer photography, with or without other ingredients.
  • silver halides such as silver chloride, silver bromide, silver chlorobromide or silver iodobromide, photosensitive diazo compounds or a substance which becomes the nucleus of development of an image-receiving material used in the silver halide diffusion transfer photography, with or without other ingredients.
  • the biaxially drawn, surface-roughened polystyrene film used in the present invention is obtained by biaxially drawing a film of a polystyrene resin in a conventional manner and subjecting the drawn film to various surface-roughening treatments.
  • the biaxial drawing may be effected simultaneously or in two stages.
  • the roughening of the surface of the drawn polystyrene film is effected, for example, by contacting the drawn film with an organic solvent which dissolves or swells the polystyrene resin, such as tetrahydrofuran, methyl acetate, ethyl acetate, acetone, methyl ethyl ketone, methyl isobutyl ketone, methyl chloride, ethylene chloride, cyclohexane, benzene, and dimethylformamide either alone or in admixture, and then contacting the treated film with water or with an organic solvent, such as methanol or ethanol, which does not dissolve the polystyrene resin and is miscible with the organic solvent used in the aforementioned swelling treatment.
  • an organic solvent such as methanol or ethanol
  • the contacting of the film with the solvent is accomplished specifically by immersing the film in the organic solvent, coating the organic solvent on the film by means of a roller coater or brush, or spraying the organic solvent onto the film bymeans of a sprayer.
  • the surface-toughening may also be effected by mechanically rubbing the surface of the film; or incorporating a blowing agent which will evolve a gas by heat into the film in advance thus rendering the entire film cloudy white; or forming a mixture of polystyrene and another material into a film, and then dissolving out the other material selectively from the film. Any of these surfaceroughening methods will be applicable to the process of the present invention.
  • the polystyrene resin may contain white pigments, such as titanium dioxide, barium sulfate, calcium sulfate, barium carbonate, lithopone, alumina white, calcium carbonate, silica white, laolin, white lead, barite powder, flowers of zinc, talc, aluminum hydroxide and limestone.
  • white pigments such as titanium dioxide, barium sulfate, calcium sulfate, barium carbonate, lithopone, alumina white, calcium carbonate, silica white, laolin, white lead, barite powder, flowers of zinc, talc, aluminum hydroxide and limestone.
  • colored pigments may also be incorporated in the polystyrene resin.
  • yellow pigments such as chrome yellow and cadmium yellow, various red, orange or blue pigments and mixtures thereof. All of these are well known to those skilled in the art. Whitening or opacification of the film by such methods enables a photographic material produced from this resin to provide an effective picture.
  • the polystyrene resin is exceptionally superior in water resistance, dimensional stability, and rigidity.
  • Films of polystyrene which have been subjected to the aforementioned treatment have excellent whiteness and translucence, and thus are suitable as supports for photographic materials.
  • such films are hydrophobic and chemically inert, and therefore, a difficulty arises in that when a hydrophilic, gelatincontaining emulsion is coated on the surface of the film, the coated film does not adhere firmly to the polystyrene support.
  • the polystyrene film whose surface has been roughened by the methods described is contacted with the active atoms or molecules of a gas generated by a high frequency electrodeless discharge under reduced pressure or in a stream of an inert gas or oxygen under reduced pressure.
  • the high frequency electrodeless discharge in the present invention is performed by placing the film to be treated in a discharge tube, maintaining the tube under a vacuum of 0.1 mm Hg or less, inducing discharge at a frequency of 13.56 MHz, and maintaining this state; or after the initiation of discharge, introducing oxygen or helium at a flow rate of I00 cc/min. or less, and continuing the discharge.
  • This type of discharge is well known as shown by U.S. Pat. No.
  • a transparent polystyrene film which has not been subjected to such surface-roughened treatment will have a reduced angle of contact of 5 to 30 when subjected to the aforementioned electrodeless discharge, and it will be seen that its surface has been rendered hydrophilic to some extent.
  • the cohesion and destruction strength at this time fully meets the bond strength required between the surface of a support of a photographic material and a coating such as a photographic emulsion layer or an image-receiving layer.
  • the bond strength between the support and the coating of the gelatincontaining emulsion obtained above is not reduced even after a long lapse of time.
  • the atmosphere in which the electrodeless discharge treatment of the present invention is performed does not affect the adhesion between the film support and the coating whether it is air under reduced pressure, a stream of an inert gas, or a stream of oxygen.
  • the bond strength between a surface-roughened, biaxially drawn polystyrene film support and a coating of a gelatin-containing emulsion or suspension becomes larger than the cohesion and destruction strength of the support itself merely by exposing the film for several seconds to an atmosphere of active gas generated by excitation due to the electrodeless discharge. Satisfactory results are thus obtained.
  • Adhesion Test in Dry Condition A sample is prepared by coating an emulsion containing gelatin as a binder on a support of polystyrene film. A 0.14 mm thick cellulose triacetate film is adhered to the coated surface of the sample using an epoxy resin adhesive. This sample is then left to stand for one day at 23C. and a relative humidity of percent. Thereafter, the sample is cut into a rectangular shape having a width of 1 cm and a length of 15 cm. The cellulose triacetate film is peeled off at a pulling rate of 7.38 cm/min. The peel strength is measured by means of a strain gauge. Where the Examples state that the adhesion is good," it means that the sample has a peel strength of 8 g/mm or more which is a bond strength sufficient for use as a photographic material.
  • EXAMPLE 1 A O. 1 mm thick biaxially drawn polystyrene film support was immersed for 3 seconds in a solvent consisting of 7 parts of ethyl acetate and 1 part of ethanol, and then for 30 seconds in methanol to render the film whitely translucent. The film whose surface had thus been roughened when subjected to a discharge treatment in a stream of helium using a high frequency electrodeless discharge device (LTA type low temperature asher apparatus made by Tracerlab, U.S.A.). For comparison, a transparent polystyrene film whose surface had not been roughened in any way was subjected to the discharge treatment under the same conditions.
  • a high frequency electrodeless discharge device LTA type low temperature asher apparatus made by Tracerlab, U.S.A.
  • EXAMPLE 2 Pressure 10 mmHg Flow rate of oxygen 10 cc/min. Output 50 W Frequency 13.56 MHz Discharge treatment time 10. 30 and 60 seconds An aqueous gelatin solution of the following formulation was coated on the treated film as an undercoat.
  • Formalin (20% aqueous solution 4 cc.
  • a silver halide photographic emulsion of the same formulation as set forth in Example 1 was coated on top of the undercoat.
  • Each of the resulting photographic materials exhibited good bond strength of 3.5 g/mm or more in a wet condition and 20 g/mm or more in a dry condition.
  • the adhesion obtained between the film and the coatings was extremely good.
  • EXAMPLE 3 A 0.2 mm thick biaxially drawn polystyrene film was immersed in a solvent consisting of 1 part of acetone and 1 part of methyl ethyl ketone for 3 seconds, and then in methanol for 30 seconds to form a white translucent polystyrene film having a microporous surface layer (surface-roughened). The surface-roughened film was subjected to the high frequency electrodeless discharge treatment under the same conditions as set forth in Example 2. Thereafter, a coating solution for forming an image-receiving layer in the silver salt diffusion transfer process was coated on the polystyrene film so treated.
  • the coating solution had the following formulation:
  • said organic solvent is a member selected from the group consisting of tetrahydrofuran, methyl acetate, ethyl acetate. acetone, methyl ethyl ketone, methyl isobutyl ketone, methyl chloride, ethylene chloride, cyclohexane. benzene and dimethylformamide and mixtures of same.
  • said white pigment is a member selected from the group consisting of titanium dioxide, barium sulfate, calcium sulfate, barium carbonate. lithopone, alumina white, calcium carbonate, silica white, laolin. white lead, barite powder, flowers of zinc, talc, aluminum hydroxide and lime-

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  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • General Physics & Mathematics (AREA)
  • Spectroscopy & Molecular Physics (AREA)
  • Plasma & Fusion (AREA)
  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
  • Treatments Of Macromolecular Shaped Articles (AREA)
  • Laminated Bodies (AREA)
US00142815A 1970-05-15 1971-05-12 Process for producing photographic materials Expired - Lifetime US3837886A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP45041358A JPS4932135B1 (enrdf_load_stackoverflow) 1970-05-15 1970-05-15

Publications (1)

Publication Number Publication Date
US3837886A true US3837886A (en) 1974-09-24

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Family Applications (1)

Application Number Title Priority Date Filing Date
US00142815A Expired - Lifetime US3837886A (en) 1970-05-15 1971-05-12 Process for producing photographic materials

Country Status (7)

Country Link
US (1) US3837886A (enrdf_load_stackoverflow)
JP (1) JPS4932135B1 (enrdf_load_stackoverflow)
CA (1) CA971128A (enrdf_load_stackoverflow)
DE (1) DE2123785A1 (enrdf_load_stackoverflow)
FR (1) FR2091561A5 (enrdf_load_stackoverflow)
GB (1) GB1315244A (enrdf_load_stackoverflow)
NL (1) NL7106652A (enrdf_load_stackoverflow)

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3976817A (en) * 1971-08-25 1976-08-24 Fuji Photo Film Co., Ltd. Method of preparing diffusion transfer image-receiving materials
US4009037A (en) * 1973-02-01 1977-02-22 Imperial Chemical Industries Limited Coated synthetic film materials
US4113918A (en) * 1972-03-03 1978-09-12 Konishiroku Photo Industry Co., Ltd. Undercoat-applied plastic films
US5425980A (en) * 1994-02-22 1995-06-20 Eastman Kodak Company Use of glow discharge treatment to promote adhesion of aqueous coats to substrate
EP0699954A2 (en) 1994-09-01 1996-03-06 Eastman Kodak Company Near atmospheric pressure treatment of polymers using helium discharges
US5618659A (en) * 1995-03-01 1997-04-08 Eastman Kodak Company Photographic element containing a nitrogen glow-discharge treated polyester substrate
EP0790525A2 (en) 1996-02-13 1997-08-20 Eastman Kodak Company Atmospheric pressure glow discharge treatment of polymeric supports to promote adhesion for photographic applications
US5718995A (en) * 1996-06-12 1998-02-17 Eastman Kodak Company Composite support for an imaging element, and imaging element comprising such composite support
US5726001A (en) * 1996-06-12 1998-03-10 Eastman Kodak Company Composite support for imaging elements comprising an electrically-conductive layer and polyurethane adhesion promoting layer on an energetic surface-treated polymeric film
US5789145A (en) * 1996-07-23 1998-08-04 Eastman Kodak Company Atmospheric pressure glow discharge treatment of base material for photographic applications
US20140348586A1 (en) * 2009-12-31 2014-11-27 Heatwurx, Inc. System and method for controlling an asphalt repair apparatus
US9416499B2 (en) 2009-12-31 2016-08-16 Heatwurx, Inc. System and method for sensing and managing pothole location and pothole characteristics

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS564900B2 (enrdf_load_stackoverflow) * 1973-03-01 1981-02-02
EP0208618A3 (en) * 1985-07-09 1987-06-24 Shin-Etsu Chemical Co., Ltd. A mesh and printing screen for screen printing and a method for the preparation thereof
EP0220121A3 (en) * 1985-10-14 1987-07-01 Shin-Etsu Chemical Co., Ltd. A method for the preparation of a screen mesh for screen printing
CN112852295B (zh) * 2021-02-26 2022-05-06 几何智慧城市科技(广州)有限公司 液晶显示屏易洁净涂层剂的制备方法、储存方法及其应用

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3697305A (en) * 1969-12-08 1972-10-10 Fuji Photo Film Co Ltd Method for producing a photographic element

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3697305A (en) * 1969-12-08 1972-10-10 Fuji Photo Film Co Ltd Method for producing a photographic element

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3976817A (en) * 1971-08-25 1976-08-24 Fuji Photo Film Co., Ltd. Method of preparing diffusion transfer image-receiving materials
US4113918A (en) * 1972-03-03 1978-09-12 Konishiroku Photo Industry Co., Ltd. Undercoat-applied plastic films
US4009037A (en) * 1973-02-01 1977-02-22 Imperial Chemical Industries Limited Coated synthetic film materials
US5576164A (en) * 1994-02-22 1996-11-19 Eastman Kodak Company Photographic element having a polyester substrate with an oxygen modified surface region
US5425980A (en) * 1994-02-22 1995-06-20 Eastman Kodak Company Use of glow discharge treatment to promote adhesion of aqueous coats to substrate
US5538841A (en) * 1994-02-22 1996-07-23 Eastman Kodak Company Use of glow discharge treatment to promote adhesion of aqueous coatings to substrate
US5582921A (en) * 1994-02-22 1996-12-10 Eastman Kodak Company Use of glow discharge treatment to promote adhesion of aqueous coatings to substrate
EP0699954A2 (en) 1994-09-01 1996-03-06 Eastman Kodak Company Near atmospheric pressure treatment of polymers using helium discharges
US5558843A (en) * 1994-09-01 1996-09-24 Eastman Kodak Company Near atmospheric pressure treatment of polymers using helium discharges
US5767469A (en) * 1994-09-01 1998-06-16 Eastman Kodak Company Near atmospheric pressure treatment of polymers using helium discharges
US5618659A (en) * 1995-03-01 1997-04-08 Eastman Kodak Company Photographic element containing a nitrogen glow-discharge treated polyester substrate
EP0790525A2 (en) 1996-02-13 1997-08-20 Eastman Kodak Company Atmospheric pressure glow discharge treatment of polymeric supports to promote adhesion for photographic applications
US5714308A (en) * 1996-02-13 1998-02-03 Eastman Kodak Company Atmospheric pressure glow discharge treatment of polymeric supports to promote adhesion for photographic applications
US5718995A (en) * 1996-06-12 1998-02-17 Eastman Kodak Company Composite support for an imaging element, and imaging element comprising such composite support
US5726001A (en) * 1996-06-12 1998-03-10 Eastman Kodak Company Composite support for imaging elements comprising an electrically-conductive layer and polyurethane adhesion promoting layer on an energetic surface-treated polymeric film
US5789145A (en) * 1996-07-23 1998-08-04 Eastman Kodak Company Atmospheric pressure glow discharge treatment of base material for photographic applications
US20140348586A1 (en) * 2009-12-31 2014-11-27 Heatwurx, Inc. System and method for controlling an asphalt repair apparatus
US9022686B2 (en) * 2009-12-31 2015-05-05 Heatwurx, Inc. System and method for controlling an asphalt repair apparatus
US9416499B2 (en) 2009-12-31 2016-08-16 Heatwurx, Inc. System and method for sensing and managing pothole location and pothole characteristics

Also Published As

Publication number Publication date
FR2091561A5 (enrdf_load_stackoverflow) 1972-01-14
DE2123785A1 (de) 1971-11-18
JPS4932135B1 (enrdf_load_stackoverflow) 1974-08-28
NL7106652A (enrdf_load_stackoverflow) 1971-11-17
GB1315244A (en) 1973-05-02
CA971128A (en) 1975-07-15

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