US2844465A - Photographic process - Google Patents

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US2844465A
US2844465A US416965A US41696554A US2844465A US 2844465 A US2844465 A US 2844465A US 416965 A US416965 A US 416965A US 41696554 A US41696554 A US 41696554A US 2844465 A US2844465 A US 2844465A
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activator
image
paper
print
sensitized
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US416965A
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Chalkley Lyman
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    • 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
    • G03C1/72Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705
    • G03C1/73Photosensitive compositions not covered by the groups G03C1/005 - G03C1/705 containing organic compounds
    • G03C1/732Leuco dyes

Definitions

  • This invention relates to a photographic process, and more particularly to one in which the image is completely' developed by action of light, and is then fixed by' the evaporation of' a volatile component of the photosensitive material.
  • An object of the invention is to provide a photographic process which produces finished prints without chemical manipulation.
  • the process is extremely simple; It is very flexible in that images may be obtained in a variety of colors on paper, cloth and film. Dimensional stability of paper prints is good.
  • Other advantages will appear from the following description.
  • j i The. process employs a photosensitive system comprising at least two components both of which are necessary for the photochemical reaction, and one of which is volatile, that is has a boiling point at a pressure of 760 mm. of mercury of less than 325 C.
  • the process consists in printing'out a fully formed image upon a suitably sensitized paper, cloth, or other material, and fixing the image by evaporation of the volatile component.
  • Co-pending application Serial No; 194,017, now'Patent Number 2,676,887, issued April 27, 1954, of which the present application is a continuation-in-part discloses a photosensitive system consisting of'a basic dye cyanide and an organic photoactivator, which may be volatile. Many of the photosensitive materials described in the co-pending application may be usedin the presently described process.
  • suitable hydrophobic dye cyanides are the cyanides of crystal violet, malachite green, rosaniline, pararosaniline, brilliant green, and similar dyes.
  • cyanides which contain hydrophilic groups, such as quaternary ammonium, and sulfonic acid, should not be .employed to sensitize the materials used in the present process. Thus paper sensitized with the cyanide of methyl green, which would contain a quaternary ammonium group, would not be suitable.
  • Any photoactivator may be employed if it is sulficiently volatile.
  • suitable activators are, acetonitrile, valeronitrile, 'capronitrile, aniline, monomethylaniline, phenylmethyl carbinol, benzyl alcohol, beta-.phenylethyl alcohol, veratrole, ethylene glycol diethyl ether, tetraethylene glycol dimethyl ether.
  • previously known activators such as ethyl alcohol and acetic acid, may be used. However, for practical speed in fixing the image, the relatively non-volatile activators are less desirable.
  • ethyl and butylphosphates are satisfactory activators for materials used in the present process, but the ortho and meta cresyl phosphates, while excellent activators, are less suitable because of their low volatility.
  • the activator used in the present process should preferably boil below 325 C. at a pressure of 760 mm. of mercury. 1
  • Commercial products suitable for printing frame glasses are Vitaglass, Corex D, Corex A, Coming glass N'o..7-9 IO, fuzed quartz etc. Ordinary photographic film is quite suitable for the: master copy support, as are most of the commercially available tracing cloths.
  • Printing is carried out until: the image has the desired depth of color.
  • the image. from. a negative master copy is a positive-
  • The, image. is fully formed in printingv and no. operation of chemical development is employed.
  • Fixing is carried. out'in darkness or light free from the ultraviolet radiation to. which the materials are sensitive, and. consists in evaporation of the. activator.
  • Method. 1. is always applicable and requires normallyonly an. hour or two with paper prints when the activator has a boiling point of-up to- 210 C.
  • Method 2 also is always. applicable and is faster than 1.
  • Methods 3 and- 4 are still faster, but the temperatures employed.
  • Fixing is complete when the activator has. been re moved. Adequacy of fixing can be determined by a brief test exposure of 'a portion of the print to ultraviolet radiation. When no color develops on such exposure fixing is adequate. However, removal of the:
  • activator can: often be judged. by odor or appearance of the print. Of course only volatile activators should be present in the photosensitive material. If a non-volatile activator is present as an impurity in the volatile activator, paper, film, or other materials employed, fixing will not be complete.
  • Example 1 ing on it a stream of air heated to 100 until the odor of the resorcinol dimethyl ether has disappeared, and an exposure of a portion of the print to direct sunlight for 1 minute produces no appreciable image.
  • Example 2 Water leaf paper is sensitized by dipping in a A of 1% solution of pararosaniline cyanide in acetonitrile, and the excess solution removed by blotting with a fresh 3 piece of paper.
  • the sensitized paper is printed immediately by sunlight in a frame equipped with a Vitaglass glass.
  • a silver photographic negative on safety film is used as the master copy.
  • Between the negative and the sensitized paper is placed a film .of thin. clear colorless cellophane to protect the negative from possible damage by diffusion of the acetonitrile.
  • Behind the sensitized paper is placed a sheet of thin aluminum foil to prevent evaporation of acetonitrile during printing. When the image has been printed to suflicient depth, the print is fixed by hanging in free air at room temperature for about ten minutes.
  • Example 3 Paper sensitized and printed as in Example 2 is fixed by heating to 100 for 1 minute in a constant tempera ture oven.
  • Printing is by the radiation from a quartz mercury lamp until the green image is suificiently strong.
  • the print is fixed by exposure for 1 minute to a stream of air heated to. 100 C.
  • Example 5 The images formed on the sensitized water leaf papers tend to run, i. e. to difiuse laterally in the paper, and thus to give a soft focus eifect to the print even when the negative is sharp. For some purposes this eflfect is desirable, but not for the reproduction of fine lines or print. Sharper images are obtained by the use of sized papers.
  • a rosin sized paper is sensitized by brushing with a fresh /2 of 1% solution of crystal violet cyanide in benzyl alcohol.
  • Printing is carried out immediately after sensitization be hind an India ink drawing on tracing cloth, and the image is fixed by exposure of the print for a few minutes to a stream of air heated to 100 C.
  • Example 6 Starch sized paper is sensitized by brushing with a solution of crystal violet cyanide saturated at 16 C. in phenylmethyl carbinol. The paper is printed behind a 6!. master copy printed in black ink on Winston Extra Thin tracing paper. The print is fixed by blowing a stream of air on it at room temperature.
  • a photographic process comprising the steps of printing out an image by ultraviolet radiation upon material sensitized with a hydrophobic amino triphenylmethane dye cyanide activated by an organic activator boiling below 325 C. at a pressure of 760 mm. of mercury selected from the group consisting of veratrole, resorcinol dimethyl ether, an ethylene glycol ether, a phosphoric acid ester of a monohydroxy compound, an aromatic amine containing a hydrogen atom on the nitrogen atom, a nitrile in which the cyano group is attached to a carbon atom which also holds a hydrogen atom, an aromatic carbinol and a lower aliphatic alcohol and fixing the image by blowing a stream of air over the print until the activator is completely removed.
  • a photographic process comprising the steps of printing out an image by ultraviolet radiation upon material sensitized with a hydrophobic amino triphenylmethane dye cyanide activated by an organic activator boiling below 325 C. at a pressure of 760 mm. of mercury selected from the group consisting of veratrole, resorcinol dimethyl ether, an ethylene glycol ether, a phosphoric acid ester of a monohydroxy compound, an aromatic amine containing a hydrogen atom on the nitrogen atom, a nitrile in which the cyano group is attached to a carbon atom which also holds a hydrogen atom, an aromatic carbinol, and a lower aliphatic alcohol; and fixing the image by heating the print above the boiling point of said activator until the activator is completely evaporated.
  • a hydrophobic amino triphenylmethane dye cyanide activated by an organic activator boiling below 325 C. at a pressure of 760 mm. of mercury selected from the group consisting of veratrole,

Description

United States Patent 2,844,465 PHOTOGRAPI-IIC PROCESS. Lyman Chalkley, Prince. Georges County, Md.
N0 Drawing. Application March 17,1954 Serial No. 416,965-
Claims. (Cl. 96-48) This invention relates to a photographic process, and more particularly to one in which the image is completely' developed by action of light, and is then fixed by' the evaporation of' a volatile component of the photosensitive material.
An object of the invention is to provide a photographic process which produces finished prints without chemical manipulation. The process is extremely simple; It is very flexible in that images may be obtained in a variety of colors on paper, cloth and film. Dimensional stability of paper prints is good. Other advantages will appear from the following description. j i The. process employs a photosensitive system comprising at least two components both of which are necessary for the photochemical reaction, and one of which is volatile, that is has a boiling point at a pressure of 760 mm. of mercury of less than 325 C. The process consists in printing'out a fully formed image upon a suitably sensitized paper, cloth, or other material, and fixing the image by evaporation of the volatile component.
Co-pending application Serial No; 194,017, now'Patent Number 2,676,887, issued April 27, 1954, of which the present application is a continuation-in-part discloses a photosensitive system consisting of'a basic dye cyanide and an organic photoactivator, which may be volatile. Many of the photosensitive materials described in the co-pending application may be usedin the presently described process.
For the present process materials sensitized; with hydrophobic dye cyanides are satisfactory. Examples; of
' suitable hydrophobic dye cyanides are the cyanides of crystal violet, malachite green, rosaniline, pararosaniline, brilliant green, and similar dyes. On the other hand, cyanides which contain hydrophilic groups, such as quaternary ammonium, and sulfonic acid, should not be .employed to sensitize the materials used in the present process. Thus paper sensitized with the cyanide of methyl green, which would contain a quaternary ammonium group, would not be suitable.
Any photoactivator may be employed if it is sulficiently volatile. Examples of suitable activators are, acetonitrile, valeronitrile, 'capronitrile, aniline, monomethylaniline, phenylmethyl carbinol, benzyl alcohol, beta-.phenylethyl alcohol, veratrole, ethylene glycol diethyl ether, tetraethylene glycol dimethyl ether. In addition to activators disclosed in the co-pending application, previously known activators, such as ethyl alcohol and acetic acid, may be used. However, for practical speed in fixing the image, the relatively non-volatile activators are less desirable. Thus ethyl and butylphosphates are satisfactory activators for materials used in the present process, but the ortho and meta cresyl phosphates, while excellent activators, are less suitable because of their low volatility. The activator used in the present process should preferably boil below 325 C. at a pressure of 760 mm. of mercury. 1
ICC
Because the activated dye cyanides are sensitive only to ultraviolet radiation, printing should be carried out by direct sunlight, an ultraviolet cored. carbon arc, a quartz mercury lamp. sunlamp, or, other source ofv radiations shorter than 3300 A. U. Any printing frame glass that may be used, and the film, tracing cloth, paper or. other support for the master copy, from which the print is made, should transmit some radiation shorter than 3300 A. U. Commercial products suitable for printing frame glasses are Vitaglass, Corex D, Corex A, Coming glass N'o..7-9 IO, fuzed quartz etc. Ordinary photographic film is quite suitable for the: master copy support, as are most of the commercially available tracing cloths.
Printing is carried out until: the image has the desired depth of color. The image. from. a negative master copy is a positive- The, image. is fully formed in printingv and no. operation of chemical development is employed.
Fixing; is carried. out'in darkness or light free from the ultraviolet radiation to. which the materials are sensitive, and. consists in evaporation of the. activator. A, variety of methods maybe employed, such'as:
(1) Hanging-the print at room temperature in free.
Method. 1. is always applicable and requires normallyonly an. hour or two with paper prints when the activator has a boiling point of-up to- 210 C. Method 2 also is always. applicable and is faster than 1. Methods 3 and- 4 are still faster, but the temperatures employed.
should be adapted to the material being fixed. Generallyit is desirable to use temperatures that are not higher than a about C. to avoid heat induced decompositions.
Even 100 C. may at times be too high a temperature. because, for example; a film containing a low boiling activator might be blistered by the vapor formed rapidly and trapped in. the. film.
Fixing is complete when the activator has. been re moved. Adequacy of fixing can be determined by a brief test exposure of 'a portion of the print to ultraviolet radiation. When no color develops on such exposure fixing is adequate. However, removal of the:
activator can: often be judged. by odor or appearance of the print. Of course only volatile activators should be present in the photosensitive material. If a non-volatile activator is present as an impurity in the volatile activator, paper, film, or other materials employed, fixing will not be complete.
The following examples will illustrate the process more clearly.
Example 1 ing on it a stream of air heated to 100 until the odor of the resorcinol dimethyl ether has disappeared, and an exposure of a portion of the print to direct sunlight for 1 minute produces no appreciable image.
Example 2 Water leaf paper is sensitized by dipping in a A of 1% solution of pararosaniline cyanide in acetonitrile, and the excess solution removed by blotting with a fresh 3 piece of paper. The sensitized paper is printed immediately by sunlight in a frame equipped with a Vitaglass glass. A silver photographic negative on safety film is used as the master copy. Between the negative and the sensitized paper is placed a film .of thin. clear colorless cellophane to protect the negative from possible damage by diffusion of the acetonitrile. Behind the sensitized paper is placed a sheet of thin aluminum foil to prevent evaporation of acetonitrile during printing. When the image has been printed to suflicient depth, the print is fixed by hanging in free air at room temperature for about ten minutes.
Example 3 Paper sensitized and printed as in Example 2 is fixed by heating to 100 for 1 minute in a constant tempera ture oven.
Example 4 stencil in a printing frame equipped with a Coming 7910 glass and a sheet of aluminum foil behind the paper to prevent evaporation of the alcohol. Printing is by the radiation from a quartz mercury lamp until the green image is suificiently strong. The print is fixed by exposure for 1 minute to a stream of air heated to. 100 C.
Example 5 The images formed on the sensitized water leaf papers tend to run, i. e. to difiuse laterally in the paper, and thus to give a soft focus eifect to the print even when the negative is sharp. For some purposes this eflfect is desirable, but not for the reproduction of fine lines or print. Sharper images are obtained by the use of sized papers. A rosin sized paper is sensitized by brushing with a fresh /2 of 1% solution of crystal violet cyanide in benzyl alcohol. (At low temperatures the dye cyanide may crystallize from old solutions of this concentration.) Printing is carried out immediately after sensitization be hind an India ink drawing on tracing cloth, and the image is fixed by exposure of the print for a few minutes to a stream of air heated to 100 C.
Example 6 Starch sized paper is sensitized by brushing with a solution of crystal violet cyanide saturated at 16 C. in phenylmethyl carbinol. The paper is printed behind a 6!. master copy printed in black ink on Winston Extra Thin tracing paper. The print is fixed by blowing a stream of air on it at room temperature.
I claim:
1. A photographic process comprising the steps of printing out an image by ultraviolet radiation upon material sensitized with a hydrophobic amino triphenylmethane dye cyanide activated by an organic activator boiling below 325 C. at a pressure of 760 mm. of mercury selected from the group consisting of veratrole, resorcinol dimethyl ether, an ethylene glycol ether, a phosphoric acid ester of a monohydroxy compound, an aromatic amine containing a hydrogen atom on the nitrogen atom, a nitrile in which the cyano group is attached to a carbon atom which also holds a hydrogen atom, an aromatic carbinol and a lower aliphatic alcohol and fixing the image by blowing a stream of air over the print until the activator is completely removed.
2. The process of claim 1 in which the air is heated.
3. The process of claim 1 in which the activator boils below C. and is evaporated by blowing a stream of air over the print at a temperature above the boiling point of said activator but not in excess of about 100 C.
4. A photographic process comprising the steps of printing out an image by ultraviolet radiation upon material sensitized with a hydrophobic amino triphenylmethane dye cyanide activated by an organic activator boiling below 325 C. at a pressure of 760 mm. of mercury selected from the group consisting of veratrole, resorcinol dimethyl ether, an ethylene glycol ether, a phosphoric acid ester of a monohydroxy compound, an aromatic amine containing a hydrogen atom on the nitrogen atom, a nitrile in which the cyano group is attached to a carbon atom which also holds a hydrogen atom, an aromatic carbinol, and a lower aliphatic alcohol; and fixing the image by heating the print above the boiling point of said activator until the activator is completely evaporated.
5. The process of claim 4 in which the activator boils below 100 C. and the print is heated above the boiling point of said activator but not in excess of 100 C.'
References Cited in the file of this patent UNITED STATES PATENTS 2,308,058 Crowley Ian. 12, 1943 2,324,060 Boughton July 13, 1943 2,346,090 Staehle Apr. 4, 1944 2,441,561 Chalkley May 18, 1948 2,676,887 Chalkley Apr. 27, 1954

Claims (1)

1. A PHOTOGRAPHIC PROCESS COMPRISING THE STEPS OF PRINTING OUT AN IMAGE BY ULTRAVIOLET RADIATION UPON MATERIAL SENSITIZED WITH A HYDROPHOBIC AMINO TRIPHENYLMETHANE DYE CYANIDE ACTIVATED BY AN ORGANIC ACTIVATOR BOILING BELOW 325*C. AT A PRESSURE 760 MM. OF MERCURY SELECTED FROM THE GROUP CONSISTING OF VERATROLE, RESORCINOL DIMETHYL ETHER, AN ETHYLENE GLYCOL ETHER, A PHOSPHORIC ACID ESTER OF A MONOHYDROXY COMPOUND, AND AROMATIC AMINE CONTAINING A HYDROGEN ATOM ON THE NITROGEN ATOM, A NITRILE IN WHICH THE CYANO GROUP IS ATTACHED TO A CARBON ATOM WHICH ALSO HOLDS A HYDROGEN ATOM, AN AROMATIC CARBINOL AND A LOWER ALIPHATIC ALCOHOL AND FIXING THE IMAGE BY BLOWING A STREAM OF AIR OVER THE PRINT UNTIL THE ACTIVATOR IS COMPLETELY REMOVED.
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Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3072481A (en) * 1957-09-17 1963-01-08 Ncr Co Light sensitive element and process for recording images thereon
US3113024A (en) * 1962-05-15 1963-12-03 Horizons Inc Photosensitive composition containing leuco dye and method for producing visible images using said composition
US3116675A (en) * 1959-06-08 1964-01-07 Thompson Ramo Wooldridge Inc Distinct and accurate symbol displays on photo products
US3121012A (en) * 1960-02-08 1964-02-11 Miehle Goss Dexter Inc Light sensitive triphenylmethane leucocyanide compositions
US3140947A (en) * 1961-01-25 1964-07-14 Ncr Co Graphic data copy sheet and method of using it
US3282693A (en) * 1960-02-05 1966-11-01 Eastman Kodak Co Photographic printout methods and materials utilizing organic azide compounds and coupler compounds therefor
FR2487526A1 (en) * 1980-07-25 1982-01-29 Bicron Corp RADIOCHROMIC LIQUID SOLUTION FOR MEASURING RADIATION DOSES RECEIVED BY A PERSON
US4466941A (en) * 1982-02-11 1984-08-21 Evreka, Inc. Photosensitive compositions and products
US4731323A (en) * 1982-02-11 1988-03-15 Evreka, Inc. Methods of measurement and detection employing photosensitive compositions and products

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2308058A (en) * 1940-10-03 1943-01-12 Huey Co Developer for diazo prints
US2324060A (en) * 1940-10-09 1943-07-13 Eastman Kodak Co Photographic copying paper
US2346090A (en) * 1942-08-19 1944-04-04 Eastman Kodak Co Photographic bleach-out layer
US2441561A (en) * 1943-07-23 1948-05-18 Chalkley Lyman Photochemical preparation of stable dyes
US2676887A (en) * 1950-11-03 1954-04-27 Chalkley Lyman Photochemical process and product

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2308058A (en) * 1940-10-03 1943-01-12 Huey Co Developer for diazo prints
US2324060A (en) * 1940-10-09 1943-07-13 Eastman Kodak Co Photographic copying paper
US2346090A (en) * 1942-08-19 1944-04-04 Eastman Kodak Co Photographic bleach-out layer
US2441561A (en) * 1943-07-23 1948-05-18 Chalkley Lyman Photochemical preparation of stable dyes
US2676887A (en) * 1950-11-03 1954-04-27 Chalkley Lyman Photochemical process and product

Cited By (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3072481A (en) * 1957-09-17 1963-01-08 Ncr Co Light sensitive element and process for recording images thereon
US3090687A (en) * 1957-11-06 1963-05-21 Ncr Co Photo-chemical printing
US3116675A (en) * 1959-06-08 1964-01-07 Thompson Ramo Wooldridge Inc Distinct and accurate symbol displays on photo products
US3282693A (en) * 1960-02-05 1966-11-01 Eastman Kodak Co Photographic printout methods and materials utilizing organic azide compounds and coupler compounds therefor
US3121012A (en) * 1960-02-08 1964-02-11 Miehle Goss Dexter Inc Light sensitive triphenylmethane leucocyanide compositions
US3140947A (en) * 1961-01-25 1964-07-14 Ncr Co Graphic data copy sheet and method of using it
US3113024A (en) * 1962-05-15 1963-12-03 Horizons Inc Photosensitive composition containing leuco dye and method for producing visible images using said composition
FR2487526A1 (en) * 1980-07-25 1982-01-29 Bicron Corp RADIOCHROMIC LIQUID SOLUTION FOR MEASURING RADIATION DOSES RECEIVED BY A PERSON
WO1982000527A1 (en) * 1980-07-25 1982-02-18 Corp Bicron Radiochromic liquid solution
US4466941A (en) * 1982-02-11 1984-08-21 Evreka, Inc. Photosensitive compositions and products
US4731323A (en) * 1982-02-11 1988-03-15 Evreka, Inc. Methods of measurement and detection employing photosensitive compositions and products

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