US3549379A - Copying materials - Google Patents
Copying materials Download PDFInfo
- Publication number
- US3549379A US3549379A US619013A US3549379DA US3549379A US 3549379 A US3549379 A US 3549379A US 619013 A US619013 A US 619013A US 3549379D A US3549379D A US 3549379DA US 3549379 A US3549379 A US 3549379A
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- United States
- Prior art keywords
- light
- silver
- composition
- image
- silver salt
- 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
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- 239000000463 material Substances 0.000 title description 7
- 239000000203 mixture Substances 0.000 description 23
- -1 halide ion Chemical class 0.000 description 15
- 229910052709 silver Inorganic materials 0.000 description 14
- 239000004332 silver Substances 0.000 description 14
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 14
- 229920002451 polyvinyl alcohol Polymers 0.000 description 10
- 238000000576 coating method Methods 0.000 description 9
- 239000006185 dispersion Substances 0.000 description 9
- 238000010438 heat treatment Methods 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 8
- SQGYOTSLMSWVJD-UHFFFAOYSA-N silver(1+) nitrate Chemical compound [Ag+].[O-]N(=O)=O SQGYOTSLMSWVJD-UHFFFAOYSA-N 0.000 description 8
- 239000004372 Polyvinyl alcohol Substances 0.000 description 7
- 239000007864 aqueous solution Substances 0.000 description 7
- 229920002689 polyvinyl acetate Polymers 0.000 description 7
- 239000011118 polyvinyl acetate Substances 0.000 description 7
- 239000002244 precipitate Substances 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 6
- IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 6
- 238000003756 stirring Methods 0.000 description 5
- 150000001504 aryl thiols Chemical class 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 229910001961 silver nitrate Inorganic materials 0.000 description 4
- RBWNDBNSJFCLBZ-UHFFFAOYSA-N 7-methyl-5,6,7,8-tetrahydro-3h-[1]benzothiolo[2,3-d]pyrimidine-4-thione Chemical compound N1=CNC(=S)C2=C1SC1=C2CCC(C)C1 RBWNDBNSJFCLBZ-UHFFFAOYSA-N 0.000 description 3
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 3
- OCJMOWCFGYPILO-UHFFFAOYSA-O NC(C=CC=C1)=C1[S+]=S(O)(O)=O Chemical compound NC(C=CC=C1)=C1[S+]=S(O)(O)=O OCJMOWCFGYPILO-UHFFFAOYSA-O 0.000 description 3
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- DZVCFNFOPIZQKX-LTHRDKTGSA-M merocyanine Chemical compound [Na+].O=C1N(CCCC)C(=O)N(CCCC)C(=O)C1=C\C=C\C=C/1N(CCCS([O-])(=O)=O)C2=CC=CC=C2O\1 DZVCFNFOPIZQKX-LTHRDKTGSA-M 0.000 description 3
- 230000003595 spectral effect Effects 0.000 description 3
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 3
- 229910052721 tungsten Inorganic materials 0.000 description 3
- 239000010937 tungsten Substances 0.000 description 3
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 238000000354 decomposition reaction Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000001747 exhibiting effect Effects 0.000 description 2
- 150000004820 halides Chemical class 0.000 description 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- ANRHNWWPFJCPAZ-UHFFFAOYSA-M thionine Chemical compound [Cl-].C1=CC(N)=CC2=[S+]C3=CC(N)=CC=C3N=C21 ANRHNWWPFJCPAZ-UHFFFAOYSA-M 0.000 description 2
- 238000005406 washing Methods 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 206010034960 Photophobia Diseases 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 125000003545 alkoxy group Chemical group 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 238000000498 ball milling Methods 0.000 description 1
- 229910052793 cadmium Inorganic materials 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 208000013469 light sensitivity Diseases 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000002985 plastic film Substances 0.000 description 1
- 229920006255 plastic film Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 150000003378 silver Chemical class 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 1
- 239000003232 water-soluble binding agent Substances 0.000 description 1
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
- G03C5/00—Photographic processes or agents therefor; Regeneration of such processing agents
- G03C5/26—Processes using silver-salt-containing photosensitive materials or agents therefor
- G03C5/262—Processes using silver-salt-containing photosensitive materials or agents therefor using materials covered by groups G03C1/42 and G03C1/43
-
- 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
- G03C1/494—Silver salt compositions other than silver halide emulsions; Photothermographic systems ; Thermographic systems using noble metal compounds
- G03C1/498—Photothermographic systems, e.g. dry silver
Definitions
- This invention is concerned with improvement in or relating to copying materials. More especially the invention relates to a light sensitive composition which can be coated onto a suitable backing sheet and used in the production of permanent copies of originals.
- a light sensitive composition in accordance with the invention which comprises a silver halide and a silver salt of an aryl thiol (a silver mercaptide) containing an excess of silver ions in the form of an inorganic oxyacid silver salt.
- Such a light sensitive composition makes use of the known light sensitivity of silver halides but does not have the disadvantage of requiring long and numerous development steps other than a simple heating.
- the silver salts used in the compositions in accordance with the invention are decomposed by heat and this decomposition is catalyzed by the silver halide where this has been exposed to light. It appears that the composition is sensitized to light of short wavelength by the silver halide and a latent image is formed in this silver halide by the action of light.
- the heating decomposes the silver salt of the aryl thiol and the decomposition is catalyzed imagewise by the silver halide so as to give a brownishblack image.
- the unexposed regions are almost insensitive to light and so the image formed is largely fixed.
- the silver salt of the aryl thiol containing an excess of silver ions combined with an inorganic oxyacid is preferably prepared by reacting an aryl thiosulphuric acid having the general formula:
- Ar represents a benzene or naphthalene nucleus
- R represents an -NH NHR', NR'R", --OH, OR', SH or SR group, where R and R", which may be the same or different, each represent an alkyl group, a substituted alkyl group, an aralkyl group or an aryl group, or R' and R together form a ring, and R either represents a hydrogen atom or a substituent such as an alkyl or alkoxy group or a halogen atom; with a soluble silver salt such as silver nitrate or silver perchlorate.
- This silver salt should preferably be in excess to an extent of about 1.5 moles of soluble silver salt per mole of aryl thiosulphuric acid.
- compositions prepared as described above are made light sensitive by forming in the composition some silver halide. This can be accomplished, for example, by dispersing the composition in an aqueous medium containing a. water soluble binder, such for example as, polyvinyl alcohol, polyvinyl alcohol/acetate copolymer or polyvinyl pyrrolidone, and adding a water soluble halide, eg a potassium or cadmium halide.
- a water soluble binder such for example as, polyvinyl alcohol, polyvinyl alcohol/acetate copolymer or polyvinyl pyrrolidone
- a water soluble halide eg a potassium or cadmium halide.
- These light sensitive compositions are particularly sensitive to ultra violet and blue light but the sensitivity can be extended to longer wavelengths by the addition of spectral sensitizers such for example as the cyanine and merocyanine types of dye.
- the light sensitive compositions can be used in the form of a coating on a backing sheet of, for example, paper or plastic film.
- EXAMPLE 1 S-Z-aminophenyl thiosulfuric acid (0.66 gram mole) was dissolved in 3 litres of distilled water at C. 700 ml. of an aqueous silver nitrate solution containing 1 gram mole of silver nitrate was then run into the stirred solution of the acid during a period of eight minutes. The yellow precipitate formed was allowed to stand for twelve hours. filtered, washed with water and dried.
- the coating so prepared was exposed through a negative held in contact with it to tungsten light for 10 meter candle seconds and was subsequently developed by holding in contact with a heated smooth-surfaced copper cylinder at C. for ten seconds. A black-brown image of the negative on a substantially light insensitive pale yellow background was thereby produced.
- EXAMPLE 2 10 g. of the silver salt prepared as in Example 1 was ball milled for sixteen hours with 100 ml. of a 5% aqueous solution of polyvinyl alcohol/ acetate copolymer. The resultant dispersion was stirred and 7 ml. of a 0.42 M
- the coating so prepared was exposed through a negative to meter candle seconds of tungsten light followed by development at 175 C. A brown-black positive image was formed on a substantially light insensitive pale yellow background.
- EXAMPLE 4 10 g. of the yellow precipitate prepared as in Example 1 were ball milled for 16 hours with 100 ml. of a 5% aqueous solution of a polyvinyl alcohol/acetate copolymer (Gelvatol 40/20). The resunltant dispersion was stirred and 20 ml. of 0.42 M aqueous potassium chloride solution were added. After continued stirring for 45 minutes, the dispersion was coated onto paper base and dried. Exposure of the coating through a negative to tungsten light for 10 metre candle seconds followed by development at 175 C. for 10 seconds gave a brown-black positive image on a pale yellow background.
- a polyvinyl alcohol/acetate copolymer Gelvatol 40/20
- EXAMPLE 5 2.5 g. of the yellow precipitate prepared as in Example 1 were ball milled for 16 hours with ml. of a 5% aqueous solution of polyvinyl alcohol/ acetate copolymer (Gelvatol /20). The resultant dispersion was stirred and 2.5 ml. of a 0.42 M aqueous potassium bromide solution were added, followed by 4 ml. of a 0.001 molar aqueous solution of the following merocyanine dye:
- the light sensitive compositions and coatings, prepared in accordance with the invention yield an image which is largely fixed by the simple step of heating the coating after it has been exposed to a light image; such time consuming steps as wet development, wet fixing, washing and drying are not required.
- a light-sensitive composition formed by a process comprising mixing together aqueous solutions of S-2- aminophenylthiosulfuric acid and of soluble silver salt to form a silver-containing heat-decomposable precipitate, and treating said precipitate with halide ion.
- composition of claim 1 wherein the molar ratio of said S-2-aminophenylthiosulfuric acid and said soluble silver salt is between 111.5 and 1:3.
- composition of claim 1 wherein the precipitate is treated in aqueous suspension by addition of a Watersoluble halide.
- composition of claim 1 wherein said soluble silver salt is silver nitrate or silver perchlorate.
- Sheet material capable of exhibiting a stable visible image on exposure to a light-image followed by heating, said sheet material comprising a backing having over one surface thereof the dried residue of a coating of the composition of claim 1 in which is included a binder.
- Sheet material capable of exhibiting a stable visible image on exposure to a light-image followed by heating, said sheet material comprising a backing having over one surface thereof the dried residue of a coating of the composition of claim 5 in which is included a binder.
- a method of producing a visible image comprising exposing a sheet material as defined in claim 7 to a light image having radiant energy within the range including visible and ultraviolet light and heating the exposed sheet to a temperature and for a time sufficient to develop a corresponding visible image.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Non-Silver Salt Photosensitive Materials And Non-Silver Salt Photography (AREA)
Description
United States Patent Office 3,549,379 Patented Dec. 22, 1970 US. Cl. 96-1141 9 Claims ABSTRACT OF THE DISCLOSURE A heat-decomposable reaction product of an aryl thiol and a water-soluble silver salt of an inorganic oxyacid is made light-sensitive by treatment with halide ion and when then exposed to light is decomposable at a reduced temperature to give a visible change.
This invention is concerned with improvement in or relating to copying materials. More especially the invention relates to a light sensitive composition which can be coated onto a suitable backing sheet and used in the production of permanent copies of originals.
Conventional light sensitive compositions which include silver halides have the disadvantage that when they are used to make permanent copies of an original they require the time consuming and inconvenient steps of Wet development, wet fixing, washing and then drying. Many attempts have been made to obtain a light sensitive composition which after exposure to a light image gives a permanent copy with only one simple processing step, such as heating, but no completely successful composition has been prepared.
These difficulties are overcome to a large extent by a light sensitive composition in accordance with the invention which comprises a silver halide and a silver salt of an aryl thiol (a silver mercaptide) containing an excess of silver ions in the form of an inorganic oxyacid silver salt.
Such a light sensitive composition makes use of the known light sensitivity of silver halides but does not have the disadvantage of requiring long and numerous development steps other than a simple heating.
The silver salts used in the compositions in accordance with the invention are decomposed by heat and this decomposition is catalyzed by the silver halide where this has been exposed to light. It appears that the composition is sensitized to light of short wavelength by the silver halide and a latent image is formed in this silver halide by the action of light. The heating decomposes the silver salt of the aryl thiol and the decomposition is catalyzed imagewise by the silver halide so as to give a brownishblack image. After the heat treatment causing development in the light-struck regions to produce a negative image, the unexposed regions are almost insensitive to light and so the image formed is largely fixed.
The silver salt of the aryl thiol containing an excess of silver ions combined with an inorganic oxyacid is preferably prepared by reacting an aryl thiosulphuric acid having the general formula:
S SOaH any wherein Ar represents a benzene or naphthalene nucleus, and in which R represents an -NH NHR', NR'R", --OH, OR', SH or SR group, where R and R", which may be the same or different, each represent an alkyl group, a substituted alkyl group, an aralkyl group or an aryl group, or R' and R together form a ring, and R either represents a hydrogen atom or a substituent such as an alkyl or alkoxy group or a halogen atom; with a soluble silver salt such as silver nitrate or silver perchlorate. This silver salt should preferably be in excess to an extent of about 1.5 moles of soluble silver salt per mole of aryl thiosulphuric acid.
We believe that in such a composition the excess silver ions combined with an inorganic oxyacid are derived from a reaction such as that exemplified by the following equation:
Si.S 03H S A m BAgNOs H O Compositions prepared as described above are made light sensitive by forming in the composition some silver halide. This can be accomplished, for example, by dispersing the composition in an aqueous medium containing a. water soluble binder, such for example as, polyvinyl alcohol, polyvinyl alcohol/acetate copolymer or polyvinyl pyrrolidone, and adding a water soluble halide, eg a potassium or cadmium halide.
These light sensitive compositions are particularly sensitive to ultra violet and blue light but the sensitivity can be extended to longer wavelengths by the addition of spectral sensitizers such for example as the cyanine and merocyanine types of dye.
The light sensitive compositions can be used in the form of a coating on a backing sheet of, for example, paper or plastic film.
The invention will now be described with reference to the following examples.
EXAMPLE 1 S-Z-aminophenyl thiosulfuric acid (0.66 gram mole) was dissolved in 3 litres of distilled water at C. 700 ml. of an aqueous silver nitrate solution containing 1 gram mole of silver nitrate was then run into the stirred solution of the acid during a period of eight minutes. The yellow precipitate formed was allowed to stand for twelve hours. filtered, washed with water and dried.
10 g. of the above silver salt was ball milled for sixteen hours with ml. of a 5% aqueous solution of Gelvatol 40/20 a water-soluble polyvinyl alcohol/acetate copolymer formed by partial hydrolysis of polyvinyl acetate, containing 37-42% residual unhydrolyzed ester, having a viscosity, as a 4% solution in water, of 2-3 centipoise, and having an approximate weight average molecular weight of 3000. The resultant dispersion was stirred and 20 ml. of a 0.42 molar aqueous potassium bromide solution was added to'make the composition light sensitive. After continued stirring for one hour the dispersion was coated onto a paper base and air dried. Suitable coating weights were found to be within the range of approximately 5 to 100 mg. of silver per square decimeter.
The coating so prepared was exposed through a negative held in contact with it to tungsten light for 10 meter candle seconds and was subsequently developed by holding in contact with a heated smooth-surfaced copper cylinder at C. for ten seconds. A black-brown image of the negative on a substantially light insensitive pale yellow background was thereby produced.
EXAMPLE 2 10 g. of the silver salt prepared as in Example 1 was ball milled for sixteen hours with 100 ml. of a 5% aqueous solution of polyvinyl alcohol/ acetate copolymer. The resultant dispersion was stirred and 7 ml. of a 0.42 M
+ AgzSO; BHNOs EXAMPLE 3 To a stirred solution of 3.1 .g. of S-2-aminophenyl thiosulphuric acid in 100 ml. of water was added a solution of 6.2 g. of silver perchlorate in 20 ml. of water. After stirring for three minutes, the yellow precipitate so formed was filtered off, well washed with water and dried at 50 C.
10 g. of the silver salt prepared by the above procedure was dispersed in 100 ml. of a 5% aqueous solution of water-soluble polyvinyl alcohol/acetate copolymer by ball milling for 16 hours. The resultant dispersion was sensitized to light by the addition of 20 ml. of 0.42 M aqueous potassium bromide solution. After stirring for one hour the dispersion was coated onto paper base and dried.
The coating so prepared Was exposed through a negative to meter candle seconds of tungsten light followed by development at 175 C. A brown-black positive image was formed on a substantially light insensitive pale yellow background.
EXAMPLE 4 10 g. of the yellow precipitate prepared as in Example 1 were ball milled for 16 hours with 100 ml. of a 5% aqueous solution of a polyvinyl alcohol/acetate copolymer (Gelvatol 40/20). The resunltant dispersion was stirred and 20 ml. of 0.42 M aqueous potassium chloride solution were added. After continued stirring for 45 minutes, the dispersion was coated onto paper base and dried. Exposure of the coating through a negative to tungsten light for 10 metre candle seconds followed by development at 175 C. for 10 seconds gave a brown-black positive image on a pale yellow background.
EXAMPLE 5 2.5 g. of the yellow precipitate prepared as in Example 1 were ball milled for 16 hours with ml. of a 5% aqueous solution of polyvinyl alcohol/ acetate copolymer (Gelvatol /20). The resultant dispersion was stirred and 2.5 ml. of a 0.42 M aqueous potassium bromide solution were added, followed by 4 ml. of a 0.001 molar aqueous solution of the following merocyanine dye:
v After stirring for 5 minutes the dispersion was coated onto paper base and dried.
Exposure of such a sheet to white light behind a nega- 4 tive and a series of narrow cut spectral filters followed by 'development at C. for 10 seconds showed an extended photographic response into the green region of the spectrum.
It will be apparent from the above examples that the light sensitive compositions and coatings, prepared in accordance with the invention, yield an image which is largely fixed by the simple step of heating the coating after it has been exposed to a light image; such time consuming steps as wet development, wet fixing, washing and drying are not required.
What we claim is: I
1. A light-sensitive composition formed by a process comprising mixing together aqueous solutions of S-2- aminophenylthiosulfuric acid and of soluble silver salt to form a silver-containing heat-decomposable precipitate, and treating said precipitate with halide ion.
2. Composition of claim 1 wherein the molar ratio of said S-2-aminophenylthiosulfuric acid and said soluble silver salt is between 111.5 and 1:3.
3. Composition of claim 1 wherein the precipitate is treated in aqueous suspension by addition of a Watersoluble halide.
4. Composition of claim 1 wherein said soluble silver salt is silver nitrate or silver perchlorate.
5. Composition of claim 1 wherein is included a cyanine or merocyanine spectral sensitizer dye.
6. Sheet material capable of exhibiting a stable visible image on exposure to a light-image followed by heating, said sheet material comprising a backing having over one surface thereof the dried residue of a coating of the composition of claim 1 in which is included a binder.
7. Sheet material capable of exhibiting a stable visible image on exposure to a light-image followed by heating, said sheet material comprising a backing having over one surface thereof the dried residue of a coating of the composition of claim 5 in which is included a binder.
8. Method of producing a visible image comprising exposing a sheet materialas defined in claim 6 to a lightimage having a radiant energy within the range including visible and ultraviolet light and heating the exposed sheet to a temperature and for a time sufficient to develop a corresponding visible image.
9. A method of producing a visible image comprising exposing a sheet material as defined in claim 7 to a light image having radiant energy within the range including visible and ultraviolet light and heating the exposed sheet to a temperature and for a time sufficient to develop a corresponding visible image.
References Cited UNITED STATES PATENTS 3,155,507 11/1964 Blake 9694 3,206,309 9/1965 Haist 9694 3,384,485 5/1968 Blake 96-94 NORMAN G. TORCHIN, Primary Examiner M. KELLEY, Assistant Examiner US. Cl. X.R. 961 14.6
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9020/66A GB1178800A (en) | 1966-03-01 | 1966-03-01 | Improvements in or relating to Copying Materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3549379A true US3549379A (en) | 1970-12-22 |
Family
ID=9863826
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US619013A Expired - Lifetime US3549379A (en) | 1966-03-01 | 1967-02-27 | Copying materials |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US3549379A (en) |
| GB (1) | GB1178800A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3719495A (en) * | 1969-10-03 | 1973-03-06 | Minnesota Mining & Mfg | Use of merocyanine compounds in photothermosensitive systems |
| US4105451A (en) * | 1976-12-22 | 1978-08-08 | Eastman Kodak Company | Photothermographic material, composition and process |
| US4161408A (en) * | 1977-06-06 | 1979-07-17 | Minnesota Mining And Manufacturing Company | Method for the preparation of a photothermographic system |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3751249A (en) * | 1971-03-15 | 1973-08-07 | Eastman Kodak Co | Photothermic silver halide element containing a bis-beta-naphthol reducing agent and a 1, 3-dihydroxy-benzene reducing agent |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3155507A (en) * | 1961-12-08 | 1964-11-03 | Du Pont | Photographic processes |
| US3206309A (en) * | 1962-12-03 | 1965-09-14 | Eastman Kodak Co | Light-sensitive silver compounds and photographic methods |
-
1966
- 1966-03-01 GB GB9020/66A patent/GB1178800A/en not_active Expired
-
1967
- 1967-02-27 US US619013A patent/US3549379A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3155507A (en) * | 1961-12-08 | 1964-11-03 | Du Pont | Photographic processes |
| US3384485A (en) * | 1961-12-08 | 1968-05-21 | Du Pont | Silver halide emulsions photosolubilized with optical sensitizing dyes and silver mercaptides |
| US3206309A (en) * | 1962-12-03 | 1965-09-14 | Eastman Kodak Co | Light-sensitive silver compounds and photographic methods |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3719495A (en) * | 1969-10-03 | 1973-03-06 | Minnesota Mining & Mfg | Use of merocyanine compounds in photothermosensitive systems |
| US4105451A (en) * | 1976-12-22 | 1978-08-08 | Eastman Kodak Company | Photothermographic material, composition and process |
| US4161408A (en) * | 1977-06-06 | 1979-07-17 | Minnesota Mining And Manufacturing Company | Method for the preparation of a photothermographic system |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1178800A (en) | 1970-01-21 |
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