US3529962A - Process of washing and protecting photographic silver images - Google Patents
Process of washing and protecting photographic silver images Download PDFInfo
- Publication number
- US3529962A US3529962A US487597A US3529962DA US3529962A US 3529962 A US3529962 A US 3529962A US 487597 A US487597 A US 487597A US 3529962D A US3529962D A US 3529962DA US 3529962 A US3529962 A US 3529962A
- Authority
- US
- United States
- Prior art keywords
- composition
- image
- silver
- polyvinyl alcohol
- water
- 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
Classifications
-
- 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
- G03C11/00—Auxiliary processes in photography
- G03C11/08—Varnishing, e.g. application of protective layers on finished photographic prints
Definitions
- This invention relates to a composition of matter comprising a novel mixture of materials, and more particularly to the washing and protecting of a photographic silver image by applying to at least one of its faces in a layer a composition containing water for dissolving residual water-soluble processing reagents from the image and a novel mixture of materials for producing a protective coating on the image when the composition is dried.
- Objects of the present invention are: to provide a process for increasing the stability of a photographic silver image with a novel composition comprising water for washing the image when the composition is applied and a solution of such materials for forming a coating upon the image when the composition is dried; to provide, as a novel product, a protected photographic image produced by such a process; to provide, for use in a process of the foregoing type, a composition comprising a carboxylic acid substituted partial acetal of polyvinyl alcohol; and to provide, for use in a process of the foregoing type, a composition comprising a polymer of the name group and a salt of a heavy metal which forms an insoluble sulfide.
- the invention accordingly comprises the process involving the several steps and the relation and order of one or more of such steps with respect to each of the others, and the composition and product possessing the features, properties and the relation of elements which are exemplified in the following detailed disclosure and the scope of the application of which will be indicated in the appended claims.
- the process of the present invention is particularly useful for washing and protecting thin photographic silver images prepared in accordance with well known diffusion transfer processes, for example, as described in US. Pat. No. 2,719,791, issued to Edwin H. Land on Oct. 4, 1935.
- An extremely thin, photographic silver image of the foregoing type ordinarily retains traces of the photographic reagents with which it has been processed, and the continued presence of which may adversely affect its stability.
- silver may be oxidized by sulfur from the residue of sodium thiosulfate which has been employed as a solvent.
- the silver may be oxidized by numerous oxidizing agents present in the atmosphere.
- the image may comprise traces of silver ion in equilibrium with the "ice metallic silver; where the image is subjected to materials which form insoluble silver residues, such as sulfides, they react with the silver ion, causing more metallic silver to shift to the ionic state, ultimately detroying the silver image entirely. Furthermore, traces of unoxidized developer, if oxidized by atmospheric oxygen, may discolor the highlights of the image.
- compositions of matter contemplated by the present invention generally comprise mixtures of compatible components which together possess properties not possessed by the components themselves.
- these components include an aromatic 0r aliphatic carboxylic acid substituted partial acetal of polyvinyl alcohol and preferably, a salt of a heavy metal which forms an insoluble sulfide and a volatile alkaline material, such as ammonia.
- the polymeric material functions primarily to impart to the composition the following unusual combination: substantial impermeability to elemental sulfur and hydrogen sulfide, for example from sulfur-containing materials with which the composition may come into contact; image stability throughout Wide temperature and humidity ranges; resistance to generalized oxidation of silver; resistance to the effects of prolonged solar radiation; optical clarity; and non-tackiness.
- the heavy metal salt in conjunction with the polymeric material functions primarily to impart to the composition excellent resistance to penetration by sulfides, for example, from the atmosphere, abrasion resistance, and, further, contributes to the nontackiness of the composition.
- a preferred composition for this purpose comprises a solution prepared from: (1) a salt of a heavy metal which forms an insoluble sulfide; (2) water; (3) a water-miscible organic solvent; (4) a volatile alkaline material and (5) a polymer composed of the recurring unit having the formula:
- polymers composed of the recurring unit of:
- the polymeric materials of this invention may be prepared by reacting a low molecular weight polyvinyl alcohol, preferably one which is completely hydrolyzed, with a compound having the formula RCHO, where R has the same meaning as is given above, in the presence of an acid catalyst.
- the polymers may be prepared by reacting polyvinyl alcohol with an ester having the formula:
- oonom-o 0 O-R o O-R where m is an integer from 14, inclusive, and each R is an alkyl radical, or the corresponding acetals of the above esters, and subsequently hydrolyzing the ester group to the corresponding acid.
- m is an integer from 14, inclusive
- each R is an alkyl radical, or the corresponding acetals of the above esters, and subsequently hydrolyzing the ester group to the corresponding acid.
- a total of 28% to 42% of the hydroxyl groups on the polyvinyl alcohol chain are substituted with the acid function groups. It has been found that if the substitution is as low as 20%, the resulting composition may be undesirably viscous. The substitution can theoretically be as high as about 90% but there are substantially no advantages to be gained thereby.
- the composition contain a salt of a heavy metal which forms an insoluble sulfide in a concentration sufficient to provide the coating formed on the face of the image when the composition is dried with the quantity of salt which is large relative to the quantity of the silver in the image. Consequently, atmospheric contaminants, e.g., sulfides which penetrate the coating react with the heavy metal salt in preference to the silver ion of the image as discussed above.
- concentration of the heavy metal salt ranges approximately from 1% to 15%.
- the heavy metal salt preferably alkali soluble, may contain a heavy metal cation such as zirconium or zinc, and an anion such as acetate, sulfate, nitrate and formate; heavy metal salts which are pale in appearance and which react to form pale sulfides are preferred.
- the salts of zinc in particular are preferred because they and their sulfides are white.
- the quantity of salt although large relative to the quantit of silver in the image, should be so small that the salt and its sulfide do not appreciably affect the appearance of the image.
- the composition contains zinc oxide as the salt of a heavy metal and ammonia as the alkaline material. It has been found that when ammonia and zinc oxide are used in conjunction with the polymeric materials described herein, a particularly non-tacky, hard coating is formed. It is believed that the zinc oxide and ammonia react to form a zinc ammonium complex which complex, in turn, enters a state of equilibrium with zinc hydroxide and ammonia. When the composition is applied as a coating to photographic images, ammonia evaporates, generating additional zinc hydroxide. As zinc hydroxide is formed, however, it reacts with the available carboxylic acid groups on the polymer chain in such a way as to cross-link the materials.
- the organic solvent examples of which are low molecular weight alcohols such as methanol, ethanol and isopropanol, dioxane and low molecular weight ketones such as acetone and methylethyl ketone, and the base, preferably weak, an example of which is ammonia, cooperate to cause the polymer, which is ordinarily insoluble in water alone, to dissolve.
- the water-miscible, organic solvent functions addditionally to impart to the solution an overall, quick-drying character.
- ammonia is the alkaline material of choice
- other commercially available amines also provide satisfactory coating ingredients, the purpose of such materials being to dissolve the acidic polymeric material and to impart to the final composition a pH of at least about 8, and preferably, about 9 or higher.
- alkaline print-coating compositions is further described and claimed in copending application Ser. No. 487,578 filed concurrently herewith.
- the preferred material for this purpose is a hydantoin formaldehyde condensation polymer, such as that described in US. Pat. No. 2,874,045, issued Feb. 17, 1959 to Edwin H. Land, for Process of Washing and Protecting Photographic Silver Images.
- Phthalaldehydic acid partial acetal of polyvinyl alcohol polymer composed of the recurring unit 88 grams (2 moles) of low viscosity, low molecular weight polyvinyl alcohol having less than 1% acetate were dissolved in 500 cc. of water and cooled. 150 grams (1 mole) of hthalaldehydic acid were added with stirring and the mixture was heated at 50 C. under nitrogen. 1 cc. of concentrated sulfuric acid was added. The polymer separated as a soft, rubbery mass. After four hours, the liquid was decanted and the product washed in hot water. It was further purified by precipitation from ethanol water (containing 1 gram of potassium acetate) into water, washed in water and dried. The final product was predominantly the phthalaldehydic acid partial acetal of polyvinyl alcohol, with a small amount of the corresponding phthalide; the composition was confirmed by infrared analysis.
- EXAMPLE 2 4-formyl butyric acid partial acetal of polyvinyl alcohol polymer composed of the recurring unit 4.4 grams (0.1 mole) of polyvinyl alcohol were added to a mixture of 14.4 grams of ethyl-4-formyl butyrate and 40 ml. of glacial acetic acid. 0.5 gram of p-toluene sulfonic acid was added and the mixture stirred at 60 C. for about 18 hours. The polymer, ethyl-4-forrnyl butyrate partial acetal of polyvinyl alcohol, was isolated by precipitation into ether and purified by reprecipitation from methanol into ether and dried under vacuum at 45 C.
- the thus-prepared polymer was hydrolyzed by dissolving it in 50 ml. of dioxane and adding 50 ml. of 5% aqueous sodium hydroxide. The mixture was heated on a steam cone for about one hour, after which dilute (5%) hydrochloric acid was added slowly until all the polymer had precipitated. The resulting pH was 6. The polymer was washed in water and precipitated from methanol into water and dried at 40 C. under vacuum. 3 grams of dry polymer were recovered.
- EXAMPLE 3 3-formyl propionic acid partial acetal of polyvinyl alcohol polymer composed of the recurring unit 4.4 grams (0.1 mole) of polyvinyl alcohol were added to a mixture of 13.0 grams of ethyl-3-formyl propionate and 40 ml. of glacial acetic acid. 0.5 gram of p-toluene sulfonic acid was added and the mixture stirred at 60 C. for about 18 hours. The resulting polymer, ethyl-3- formyl propionate partial acetal of polyvinyl alcohol, was isolated by precipitation into ether and purified by reprecipitation from methanol into ether and dried under vacuum at 45 C.
- This polymer was hydrolyzed by dissolving it in 50 ml. of dioxane and adding 50 ml. of 5% aqueous sodium hydroxide. The mixture was heated on a steam cone for about one hour and dilute (5%) hydrochloric acid was added slowly until all the polymer had precipitated and the pH was 6. The polymer was washed in water and precipitated from methanol into water and dried at 40 C. under vacuum. 3.5 grams of dry polymer were recovered.
- the preferred coating composition may be prepared by dissolving the polymeric materials in the water, organic solvent and base at a temperature ranging from room temperature to about 40 C. under a reflux condenser to prevent evaporation. Thereafter, the heavy metal salt is added.
- a preferred composition comprises the foregoing ingredients in the following proportions:
- EXAMPLE 4 A composition for washing and protecting photographic silver images was prepared by combining and blending the following materials to provide a uniform solution:
- the final pH was about 9.
- EXAMPLE 5 A composition was washing and protecting photographic silver images was prepared by combining and blending the following materials to provide a uniform solution:
- the final pH was about 9.
- Silver transfer images were prepared by exposing photosensitive silver halide elements to a step-wedge, and developing the latent images formed thereby by spreading between the exposed photosensitive elements and superposed image-receiving elements a processing composition containing a viscous aqueous solution of a silver halide developing agent, a silver halide solvent, and an alkali.
- the respective elements were maintained in superposed relation for a predetermined period, during which time the exposed silver halide was reduced to silver in the photosensitive elements.
- the unreduced silver halide formed a water-soluble complex silver salt which diffused through the layer of composition to the image-receiving elements where, upon being reduced to silver, it formed a silver print.
- the photosensitive elements, together with the layer of composition were stripped from the image-receptive elements.
- the photographic silver images so prepared were swabbed by means of an aborbent applicator with the solutions of Example 4 or 5.
- the photographic prints so treated dried rapidly under ordinary atmospheric conditions, after which they were subjected to the following tests:
- the composition of the present invention is applied to a photographic silver image to be washed and protected by means of an absorbent applicator composed, for example, of flannel, cotton batting, or cellulose sponge charged with the composition.
- an absorbent applicator composed, for example, of flannel, cotton batting, or cellulose sponge charged with the composition.
- the preferred composition referred to above after being swabbed by means of such an absorbent applicator onto a thin photographic silver image of the above-described type, rapidly dries under ordinary atmospheric conditions to form a coating having excellent protective properties for the image.
- R is selected from the group consisting of 5 coon and (CH COOH, and m is an integer from 1-4, inclusive, said composition has a pH of at least 8; and drying said layer to form a protective coating on said print.
- polymer is a phthalaldehydic acid substituted partial acetal of polyvinyl alcohol having a total of 28 to 42% of the hydroxy groups on the polyvinyl alcohol chain substituted with the acid-substituted acetal groups.
- a composition comprising a solution prepared from a film-forming polymer of a carboxylic acid partial acetal of polyvinyl alcohol composed of the recurring unit having the formula:
- carboxylic acid partial acetal of polyvinyl alcohol is a phthalaldehydic acid partial acetal of polyvinyl alcohol having a total of 28% to 42% of the hydroxy group on the polyvinyl alcohol chain substituted with acid function.
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- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US48759665A | 1965-09-15 | 1965-09-15 | |
US48759765A | 1965-09-15 | 1965-09-15 | |
US48757865A | 1965-09-15 | 1965-09-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3529962A true US3529962A (en) | 1970-09-22 |
Family
ID=27413766
Family Applications (3)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US487597A Expired - Lifetime US3529962A (en) | 1965-09-15 | 1965-09-15 | Process of washing and protecting photographic silver images |
US487596A Expired - Lifetime US3533790A (en) | 1965-09-15 | 1965-09-15 | Method for washing and protecting photographic silver images |
US487578A Expired - Lifetime US3533789A (en) | 1965-09-15 | 1965-09-15 | Process of washing and protecting a diffusion transfer photographic silver print |
Family Applications After (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US487596A Expired - Lifetime US3533790A (en) | 1965-09-15 | 1965-09-15 | Method for washing and protecting photographic silver images |
US487578A Expired - Lifetime US3533789A (en) | 1965-09-15 | 1965-09-15 | Process of washing and protecting a diffusion transfer photographic silver print |
Country Status (5)
Country | Link |
---|---|
US (3) | US3529962A (enrdf_load_html_response) |
BE (1) | BE686815A (enrdf_load_html_response) |
DE (1) | DE1572008C3 (enrdf_load_html_response) |
GB (2) | GB1164642A (enrdf_load_html_response) |
NL (1) | NL6612967A (enrdf_load_html_response) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3864129A (en) * | 1972-01-24 | 1975-02-04 | Du Pont | Photographic activating bath |
Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2830900A (en) * | 1956-10-04 | 1958-04-15 | Polaroid Corp | Process of washing and protecting photographic silver images, and photographic products thereof |
US2874045A (en) * | 1954-02-26 | 1959-02-17 | Polaroid Corp | Process of washing and protecting photographic silver images |
US2956877A (en) * | 1956-10-04 | 1960-10-18 | Polaroid Corp | Process of washing and protecting photographic silver images, and photographic products thereof |
US2979477A (en) * | 1958-05-08 | 1961-04-11 | Polaroid Corp | Composition comprising a vinylpyridine polymer and a hydantoin formaldehyde condensation polymer |
US3174858A (en) * | 1959-09-24 | 1965-03-23 | Gevaert Photo Prod Nv | Process for obtaining multiple photographic positive images by diffusiontransfer |
US3325283A (en) * | 1964-01-16 | 1967-06-13 | Polaroid Corp | Photographic diffusion transfer products and processes employing image receiving elements containing a layer of polyvinyl pyrrolidone and polyvinyl hydrogen phthalate |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB496049A (en) * | 1937-04-19 | 1938-11-21 | Ig Farbenindustrie Ag | Improved manufacture of light-sensitive photographic preparations |
US2759825A (en) * | 1948-02-12 | 1956-08-21 | Polaroid Corp | Photographic image transfer process |
BE530033A (enrdf_load_html_response) * | 1953-07-01 | |||
US2855298A (en) * | 1954-02-24 | 1958-10-07 | Polaroid Corp | Methods for washing and protecting photographic silver images |
US2794740A (en) * | 1954-02-24 | 1957-06-04 | Polaroid Corp | Methods for washing and protecting photographic silver images |
-
1965
- 1965-09-15 US US487597A patent/US3529962A/en not_active Expired - Lifetime
- 1965-09-15 US US487596A patent/US3533790A/en not_active Expired - Lifetime
- 1965-09-15 US US487578A patent/US3533789A/en not_active Expired - Lifetime
-
1966
- 1966-09-13 BE BE686815D patent/BE686815A/xx not_active IP Right Cessation
- 1966-09-13 GB GB05582/69A patent/GB1164642A/en not_active Expired
- 1966-09-13 GB GB40898/66A patent/GB1164641A/en not_active Expired
- 1966-09-14 NL NL6612967A patent/NL6612967A/xx unknown
- 1966-09-15 DE DE1572008A patent/DE1572008C3/de not_active Expired
Patent Citations (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2874045A (en) * | 1954-02-26 | 1959-02-17 | Polaroid Corp | Process of washing and protecting photographic silver images |
US2830900A (en) * | 1956-10-04 | 1958-04-15 | Polaroid Corp | Process of washing and protecting photographic silver images, and photographic products thereof |
US2956877A (en) * | 1956-10-04 | 1960-10-18 | Polaroid Corp | Process of washing and protecting photographic silver images, and photographic products thereof |
US2979477A (en) * | 1958-05-08 | 1961-04-11 | Polaroid Corp | Composition comprising a vinylpyridine polymer and a hydantoin formaldehyde condensation polymer |
US3174858A (en) * | 1959-09-24 | 1965-03-23 | Gevaert Photo Prod Nv | Process for obtaining multiple photographic positive images by diffusiontransfer |
US3325283A (en) * | 1964-01-16 | 1967-06-13 | Polaroid Corp | Photographic diffusion transfer products and processes employing image receiving elements containing a layer of polyvinyl pyrrolidone and polyvinyl hydrogen phthalate |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3864129A (en) * | 1972-01-24 | 1975-02-04 | Du Pont | Photographic activating bath |
Also Published As
Publication number | Publication date |
---|---|
GB1164642A (en) | 1969-09-17 |
DE1572008B2 (de) | 1978-12-14 |
US3533790A (en) | 1970-10-13 |
GB1164641A (en) | 1969-09-17 |
BE686815A (enrdf_load_html_response) | 1967-03-13 |
NL6612967A (enrdf_load_html_response) | 1967-03-16 |
DE1572008A1 (de) | 1970-02-19 |
US3533789A (en) | 1970-10-13 |
DE1572008C3 (de) | 1979-08-23 |
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