US3736139A - Heat and light stabilization of photosensitive elements containing poly-halogenated hydrocarbons,n-vinylcarbazoles and difurfurylidene pentaerythritols - Google Patents
Heat and light stabilization of photosensitive elements containing poly-halogenated hydrocarbons,n-vinylcarbazoles and difurfurylidene pentaerythritols Download PDFInfo
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- US3736139A US3736139A US00213536A US3736139DA US3736139A US 3736139 A US3736139 A US 3736139A US 00213536 A US00213536 A US 00213536A US 3736139D A US3736139D A US 3736139DA US 3736139 A US3736139 A US 3736139A
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- difurfurylidene
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- photosensitive elements
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/32—Phosphorus-containing compounds
Definitions
- the present invention relates to a new image forming process which shows a positive response and by which stable black images are produced.
- the present invention provides a positive photographic system treated by a dry treatment which is not subject to the faults of the prior art.
- the basic components of the photosensitive element are: (a) polyhalogenated hydrocarbon; (b) N-vinylcarbazole and (c) difurfiurylidene pentaerythritol.
- This photosensitive element is prepared by dispersing these components as discrete globules in a water soluble binder and applying the dispersion onto a suitable support.
- hydroquinone or resorcinol derivatives may be used in order to improve shelf-life, and sensitizers such as ferrocene and anthraquinone derivatives may be added.
- Positive images can be obtained by treating the photosensitive element having such composition by three steps: (1) image-wise exposure; (2) heating; and (3) blanket exposure.
- image-wise exposure For example, when the sensitive element is exposed to light for 5 seconds through a positive at a distance of 30 cm. from a 250 w. high pressure mercury arc lamp, heated at C. for 10 seconds and exposed again to light for 10 seconds by a mercury arc lamp, positive images having a black color on a yellow background are obtained.
- the light strength needed varies with kinds of light wavelengths and cannot clearly be defined.
- the lightsensitive material of the present invention largely depends on the light strength and does not form color unless the light strength is higher, even though the exposure time is prolonged.
- the critical intensity (Ic) is determined on the lightstrength needed to show the density of Fog +0.1 when exposed for a certain period of time, e.g., 25 seconds, by varying the light wave lengths and the light-strength as shown in the attached figure. Ic is a minimum lightstrength and varies somewhat with the wave lengths employed.
- 1c ranges from 0.1)(10 erg/cm. sec to 1 10 erg/ cm. sec and is 'sufiicient so long as it is more than the above range, for example, at least 10 erg/cm. sec is necessary on the light of the wave length having the highest sensitivity.
- the strength of the first and second exposure is within the above range.
- the short heating time is desirable, although the heating temperature is high.
- the resulting images hardly change even though left in a light room.
- the light room is used for investigating the change of the photo-sensitive element after treatment by the scattered light from the sun in a room.
- Such a positive response is obtained when difurfurylidene pentaerythritol is used together with a water soluble binder.
- This invention provides a black image obtained by positive working, which is a simplified dry process using heat and light.
- the polyhalogenated hydrocarbon is selected from the group of the compounds which produce free radicals or IOIlS upon exposure to light of a suitable wavelength.
- polyhalogenated hydrocarbon examples include carbon tetrabromide (CBr hexachloroethane (C Cl and iodoform (CHI
- CBr hexachloroethane C Cl and iodoform
- CHI carbon tetrabromide
- water soluble substances such as gelatin, polyvinyl alcohol, casein, starch, hydroxyethyl cellulose, carboxymethyl cellulose, polyvinyl pyrrodidone and polyethyleneglycol.
- the molecular weight for the binder is thousands to hundred thousands, preferably 20,000 to 100,000.
- composition of the mandatory materials are as follows:
- the ratio of the N-vinylcarbazole/polyhalogenated hydrocarbon is 50/ l to 1/5, preferably /1 to 1/5.
- the ratio of the N vinylcarbazole/difurfurylidene pentaerythritol is 100/1 to 1/10, preferably /1 to 1/2.
- the ratio of the binder/light-sensitive material is 1/100 to 20/1, preferably l/10 to 5/1.
- Example 1 An acetone solution of 5 g. of N-vinylcarbazole was added to 50 ml. of a 16% aqueous gelatin solution. The mixture was stirred at 70 C. for 2 minutes with a homomixer to finely disperse the N-vinylcarbazole in the gelatin. After adding 4 g. of carbon tetrabromide and a dichloroethane solution of 0.5 g. difurfurylidene pentraerythritol, the mixture was similarly dispersed. The amount of acetone 5 ml., and the amount of dichloroethane is 5 ml. The resulting dispersion was applied to baryta paper to provide a photosensitive element after drying.
- a black image on a light yellow background was obtained by exposing this photosensitive element to light for 10 seconds through a positive at a distance of 30 cm. from a 250 w. super high pressure mercury arc lamp, heating at 100 C. for 10 seconds and exposing further for 10 seconds by a mercury arc lamp.
- a black image on a yellow background could be obtained by leaving the element in a light room and omitting the last exposure by the mercury arc lamp. The resulting images hardly changed in a light room.
- the photosensitive element was treated by the method described in US. Patent 3,476,562, 1.9-, a, bla k i ag 91 a ye low ba g und cou d be 4 obtained by exposing for 10 seconds through a photographic positive at a distance of 35 cm. from a 300 w. incandescent electric lamp. But the yellow background changed into brown color in a light room, which meant the fixing had not been carried out completely.
- Example 2 G N-vinylcarbazole 5 Carbon tetrabromide 4 Difurfurylidene pentaerythritol 0.5 p-Bis(Z-tetrahydropyranyloxy) benzene 0.25
- a photosensitive element was produced by dispersing the abovementioned components in an aqueous gelatin solution by the same procedure as in Example 1.
- Example 3 A photosensitive element was produced substituting polyvinyl alcohol for the gelatin in Example 2. By carrying out the same exposing and heating treatments as in Example 2, a black image on a light yellow background was obtained.
- Example 4 The same result as in Example 1 was obtained when iodoform was used instead of carbon tetrabromide in Example 1.
- Example 5 G N-vinylcarbazole 5 Carbon tetrabromide 2 Hexachloroethane l Difurfurylidene pentaerythritol 0.5
- a stable positive image which hardly changed in a light room was obtained by treating a photosensitive element prepared by dispersing the abovementioned components in an aqueous solution of polyvinyl alcohol and thereafter heating and exposing as in Example 1.
- the most important commercial embodiments are as follows. Duplicating by micro-film image or slide-film image. Duplication can be carried out on both of a positive and negative image, and generally on the positive image.
- the binders are gelatin, polyvinyl alcohol, gum arabic, polyvinylpyrrolidone, etc.
- the globule size is 0.1 to 30 preferably 0.5 to 10;.
- an image forming process by dry treatment which comprises imagewise exposing a photosensitive element comprising a support having thereon a polyhalogenated hydrocarbon and N-vinylcarbazole dispersed as discrete globules in a water-soluble binder to ultraviolet rays or visible rays and heating, the improvement comprising said photosensitive element containing difurfury'lidene pentaerythritol and the improvement further comprising exposing uniformly said imagewise exposed element to ultraviolet rays or visible rays after the heating thereof, by which a black positive image is obtained; said polyhalogenated hydrocarbon having the following general formula;
- R is a hydrogen atom, X, COOR' or R is H, CH or C H X is Cl, Br or I; and m and n are an integer of 2 or 3.
- water soluble binder is selected from the group consisting of casein, starch, hydroxyethyl cellulose,
Abstract
PHOTOSENSITIVE ELEMENTS COMPRISING A POLYHALOGENATED HYDROCARBON, N-VINYLCARBAZOLE AND DIFURFURYLIDENE PENTAERYTHRITOL DISPERSED IN A WATER SOLUBLE BINDER, AND, IF DESIRED, A STABILIZER AND A SENSITIZER.
Description
y 1973 HIROSHI YAMASHITA ET AL 3,
" HEAT AND LIGHT STABILIZATION OF PHOTOSENSITIVE ELEMENTS CONTAINING POLYHALOGENATED HYDROCARBONS,
N-VINYLCARBAZOLES AND DIFURFURYLIDENE PENTAERYTHRITOLS Filed Dec. 29, 1971 FIG. EXPOSURE TIME 25 SEC.
DENSITY (D) United States Patent fice Patented May 29, 1973 U.S. Cl. 9648 R 6 Claims ABSTRACT OF THE DISCLOSURE Photosen'sitive elements comprising a polyhalogenated hydrocarbon, N-vinylcarbazole and difurfurylidene pentaerythritol dispersed in a water soluble binder, and, if desired, a stabilizer and a sensitizer.
BACKGROUND OF THE INVENTION Field of the invention The present invention relates to a new image forming process which shows a positive response and by which stable black images are produced.
Description of the prior art Hitherto, though many photosensitive elements comprising an organic amine and a polyhalogenated compound have been known, most of them are negativeworking photosensitive elements. Examples of positiveworking photosensitive elements are as follows. In U.S. Patent 3,042,519 there is disclosed a photosensitive element which comprises a polyhalogenated hydrocarbon and a N-vinyl compound dispersed in a parafiin Wax which shows a positive response when it is subjected to imagewise exposure by light of 2200-2600 A. and then subjected to blanket exposure by light of 3500-4500 A. In this case, it is necessary to use ultraviolet rays of ultrashort wavelengths such as (2200-2600 A.), and consequently there is a disadvantage on practical use because the photographic film absorbs such ultraviolet rays.
In U.S. Patents 3,102,027 and 3,104,973, there is described a process which utilizes the phenomena that a system comprising a merocyanine or a cyanine dye and a halogenated hydrocarbon fades upon exposure to light. This process involves problems at fixing.
In German Patent No. 1,265,578, positive metal images are obtained by exposing a system comprising a combination of metallocene-halogenated hydrocarbon to light and then treating with a noble metal solution. This process has the disadvantage that it requires a wet treatment.
In Japanese Pat. Pub. No. Sho 44-l7'022, positive copies are obtained by treating with a dye solution, but this is also by a wet treatment.
In U.S. Patent 3,476,562 it is disclosed that positive images or negative images can be obtained using a combination of N-vinylcarbazole and carbon tetrabromide. The positive images are obtained by exposing to light for 2 seconds through a positive by means of a 300 W slide projector, exposing to near ultraviolet rays for 15 seconds and heating at C. for 10 seconds. Though this is a skillful system which utilizes the phenomenon that N-vinylcarbazole causes a polymerization reaction in addition to a color forming reaction, complete fixing cannot be carried out because of the color forming reaction between the resulting polymer and the remaining carbon tetrabromide. Further, the images lack light fastness.
SUMMARY OF THE INVENTION The present invention provides a positive photographic system treated by a dry treatment which is not subject to the faults of the prior art. The basic components of the photosensitive element are: (a) polyhalogenated hydrocarbon; (b) N-vinylcarbazole and (c) difurfiurylidene pentaerythritol.
This photosensitive element is prepared by dispersing these components as discrete globules in a water soluble binder and applying the dispersion onto a suitable support.
Additionally, hydroquinone or resorcinol derivatives may be used in order to improve shelf-life, and sensitizers such as ferrocene and anthraquinone derivatives may be added.
Positive images can be obtained by treating the photosensitive element having such composition by three steps: (1) image-wise exposure; (2) heating; and (3) blanket exposure. For example, when the sensitive element is exposed to light for 5 seconds through a positive at a distance of 30 cm. from a 250 w. high pressure mercury arc lamp, heated at C. for 10 seconds and exposed again to light for 10 seconds by a mercury arc lamp, positive images having a black color on a yellow background are obtained.
The light strength needed varies with kinds of light wavelengths and cannot clearly be defined. The lightsensitive material of the present invention largely depends on the light strength and does not form color unless the light strength is higher, even though the exposure time is prolonged.
The critical intensity (Ic) is determined on the lightstrength needed to show the density of Fog +0.1 when exposed for a certain period of time, e.g., 25 seconds, by varying the light wave lengths and the light-strength as shown in the attached figure. Ic is a minimum lightstrength and varies somewhat with the wave lengths employed.
1c ranges from 0.1)(10 erg/cm. sec to 1 10 erg/ cm. sec and is 'sufiicient so long as it is more than the above range, for example, at least 10 erg/cm. sec is necessary on the light of the wave length having the highest sensitivity. The strength of the first and second exposure is Within the above range.
The short heating time is desirable, although the heating temperature is high.
The above range is included within the conditions as described in U.S.P. 3,476,562 (7090 C.; 10 seconds; 176-176 C. (375 F.); 107 C., 5 seconds; 107 C., 2-5 seconds). It is used for fixing heating in the present 3 invention, while it is used for developing heating in U.S.P. 3,476,562, as is clear from the description on column 8, lines 23 to 27, which during such heating or column 9, lines .13 to 14, by heating development exposure.
The resulting images hardly change even though left in a light room. The light room is used for investigating the change of the photo-sensitive element after treatment by the scattered light from the sun in a room. Such a positive response is obtained when difurfurylidene pentaerythritol is used together with a water soluble binder.
This invention provides a black image obtained by positive working, which is a simplified dry process using heat and light.
DETAILED DESCRIPTION OF THE INVENTION As the polyhalogenated hydrocarbon, there are compounds represented by the following formula:
wherein The polyhalogenated hydrocarbon is selected from the group of the compounds which produce free radicals or IOIlS upon exposure to light of a suitable wavelength.
Additional examples of the polyhalogenated hydrocarbon are carbon tetrabromide (CBr hexachloroethane (C Cl and iodoform (CHI As the binder, there are water soluble substances such as gelatin, polyvinyl alcohol, casein, starch, hydroxyethyl cellulose, carboxymethyl cellulose, polyvinyl pyrrodidone and polyethyleneglycol. The molecular weight for the binder is thousands to hundred thousands, preferably 20,000 to 100,000.
The composition of the mandatory materials are as follows:
The ratio of the N-vinylcarbazole/polyhalogenated hydrocarbon is 50/ l to 1/5, preferably /1 to 1/5.
The ratio of the N vinylcarbazole/difurfurylidene pentaerythritol is 100/1 to 1/10, preferably /1 to 1/2.
The ratio of the binder/light-sensitive material is 1/100 to 20/1, preferably l/10 to 5/1.
The following examples are oifered to explain the present invention in great detail. The treatment of the photosensitive element, exposure and heating were carried out under a photographic red safety lamp.
Example 1 An acetone solution of 5 g. of N-vinylcarbazole was added to 50 ml. of a 16% aqueous gelatin solution. The mixture was stirred at 70 C. for 2 minutes with a homomixer to finely disperse the N-vinylcarbazole in the gelatin. After adding 4 g. of carbon tetrabromide and a dichloroethane solution of 0.5 g. difurfurylidene pentraerythritol, the mixture was similarly dispersed. The amount of acetone 5 ml., and the amount of dichloroethane is 5 ml. The resulting dispersion was applied to baryta paper to provide a photosensitive element after drying.
A black image on a light yellow background was obtained by exposing this photosensitive element to light for 10 seconds through a positive at a distance of 30 cm. from a 250 w. super high pressure mercury arc lamp, heating at 100 C. for 10 seconds and exposing further for 10 seconds by a mercury arc lamp. Similarly, a black image on a yellow background could be obtained by leaving the element in a light room and omitting the last exposure by the mercury arc lamp. The resulting images hardly changed in a light room.
On the other hand, the photosensitive element was treated by the method described in US. Patent 3,476,562, 1.9-, a, bla k i ag 91 a ye low ba g und cou d be 4 obtained by exposing for 10 seconds through a photographic positive at a distance of 35 cm. from a 300 w. incandescent electric lamp. But the yellow background changed into brown color in a light room, which meant the fixing had not been carried out completely.
Example 2 G. N-vinylcarbazole 5 Carbon tetrabromide 4 Difurfurylidene pentaerythritol 0.5 p-Bis(Z-tetrahydropyranyloxy) benzene 0.25
A photosensitive element was produced by dispersing the abovementioned components in an aqueous gelatin solution by the same procedure as in Example 1.
When the sensitive element was exposed to light for 10 seconds through a photographic positive at a distance of 30 cm. from a 250 w. mercury arc lamp, heated at 80 C. for one minute and then exposed further for 10 seconds by a mercury lamp, a black image which was identical to that of the original was produced on a light yelow background. This image hardly changed in a light room.
Example 3 A photosensitive element was produced substituting polyvinyl alcohol for the gelatin in Example 2. By carrying out the same exposing and heating treatments as in Example 2, a black image on a light yellow background was obtained.
Example 4 The same result as in Example 1 was obtained when iodoform was used instead of carbon tetrabromide in Example 1.
Example 5 G. N-vinylcarbazole 5 Carbon tetrabromide 2 Hexachloroethane l Difurfurylidene pentaerythritol 0.5
A stable positive image which hardly changed in a light room was obtained by treating a photosensitive element prepared by dispersing the abovementioned components in an aqueous solution of polyvinyl alcohol and thereafter heating and exposing as in Example 1.
The most important commercial embodiments are as follows. Duplicating by micro-film image or slide-film image. Duplication can be carried out on both of a positive and negative image, and generally on the positive image. The binders are gelatin, polyvinyl alcohol, gum arabic, polyvinylpyrrolidone, etc. The globule size is 0.1 to 30 preferably 0.5 to 10;.
While the invention has been particularly shown and described with reference to preferred embodiments thereof, it will be understood by those skilled in the art that various changes in form and details may be made therein without departing from the spirit and scope of the invention.
What is claimed is:
1. In an image forming process by dry treatment which comprises imagewise exposing a photosensitive element comprising a support having thereon a polyhalogenated hydrocarbon and N-vinylcarbazole dispersed as discrete globules in a water-soluble binder to ultraviolet rays or visible rays and heating, the improvement comprising said photosensitive element containing difurfury'lidene pentaerythritol and the improvement further comprising exposing uniformly said imagewise exposed element to ultraviolet rays or visible rays after the heating thereof, by which a black positive image is obtained; said polyhalogenated hydrocarbon having the following general formula;
wherein R is a hydrogen atom, X, COOR' or R is H, CH or C H X is Cl, Br or I; and m and n are an integer of 2 or 3.
2. An image forming process as claimed in claim 1 wherein said water soluble binder is selected from the group consisting of casein, starch, hydroxyethyl cellulose,
carboxymethyl cellulose, polyethylene glycol, gelatin, 10
polyvinyl alcohol, gum arabic, and polyvinylpyrrolidone. 3. An image forming process as claimed in claim 1 wherein said weight ratio of the N-vinylcarbazole to polyhalogenated hydrocarbon is 50/1 to 1/5.
4. An image forming process as claimed in claim 1 wherein said weight ratio of the N-vinylcarbazole/difurfurylidene pentaerythritol is 100/1 to 1/10.
5 ture range, and 0.5 sec. to 10 min. of time range.
References Cited UNITED STATES PATENTS 3,394,395 7/1968 Mattor et al. 969O R 3,544,322 12/1970 Yamada 96-48 R 3,697,276 10/1972 Lewis et a1. 96-48 HD NORMAN G. TORCHIN, Primary Examiner 15 W. H. LOUIE, JR. Assistant Examiner US. Cl. X.R. 96-48 HD, 90 R
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP45121450A JPS4920979B1 (en) | 1970-12-29 | 1970-12-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3736139A true US3736139A (en) | 1973-05-29 |
Family
ID=14811421
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US00213536A Expired - Lifetime US3736139A (en) | 1970-12-29 | 1971-12-29 | Heat and light stabilization of photosensitive elements containing poly-halogenated hydrocarbons,n-vinylcarbazoles and difurfurylidene pentaerythritols |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3736139A (en) |
| JP (1) | JPS4920979B1 (en) |
| DE (1) | DE2165374A1 (en) |
| FR (1) | FR2120988A5 (en) |
| GB (1) | GB1358107A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4077805A (en) * | 1974-10-25 | 1978-03-07 | Shirow Asakawa | Light-sensitive composition containing antioxidant |
| US4399209A (en) * | 1981-11-12 | 1983-08-16 | The Mead Corporation | Transfer imaging system |
| US4416966A (en) * | 1982-08-25 | 1983-11-22 | The Mead Corporation | Capsular imaging system comprising decolorizing agent |
| US4440846A (en) * | 1981-11-12 | 1984-04-03 | Mead Corporation | Photocopy sheet employing encapsulated radiation sensitive composition and imaging process |
| US4482624A (en) * | 1983-02-15 | 1984-11-13 | The Mead Corporation | Photosensitive material employing encapsulated radiation sensitive composition and process for improving sensitivity by sequestering oxygen |
| US4508807A (en) * | 1983-07-11 | 1985-04-02 | Mead Corporation | Photosensitive material employing encapsulated radiation sensitive composition and a transparentizable image-receiving layer |
| US4535050A (en) * | 1983-07-18 | 1985-08-13 | The Mead Corporation | Peeling development of photosensitive materials employing microencapsulated radiation sensitive compositions |
| US4562137A (en) * | 1982-12-30 | 1985-12-31 | The Mead Corporation | Photosensitive material employing encapsulated radiation sensitive composition |
| US4822714A (en) * | 1981-11-12 | 1989-04-18 | The Mead Corporation | Transfer imaging system |
| US4903991A (en) * | 1983-07-18 | 1990-02-27 | The Mead Corporation | Document security system |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5315153A (en) * | 1976-07-27 | 1978-02-10 | Canon Inc | Hologram |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1093724A (en) * | 1964-03-12 | 1967-12-06 | Warren S D Co | Photographic mediums based on furfurylidens |
-
1970
- 1970-12-29 JP JP45121450A patent/JPS4920979B1/ja active Pending
-
1971
- 1971-12-28 FR FR7147048A patent/FR2120988A5/fr not_active Expired
- 1971-12-29 US US00213536A patent/US3736139A/en not_active Expired - Lifetime
- 1971-12-29 GB GB6056171A patent/GB1358107A/en not_active Expired
- 1971-12-29 DE DE19712165374 patent/DE2165374A1/en active Pending
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4077805A (en) * | 1974-10-25 | 1978-03-07 | Shirow Asakawa | Light-sensitive composition containing antioxidant |
| US4399209A (en) * | 1981-11-12 | 1983-08-16 | The Mead Corporation | Transfer imaging system |
| US4440846A (en) * | 1981-11-12 | 1984-04-03 | Mead Corporation | Photocopy sheet employing encapsulated radiation sensitive composition and imaging process |
| US4822714A (en) * | 1981-11-12 | 1989-04-18 | The Mead Corporation | Transfer imaging system |
| US4416966A (en) * | 1982-08-25 | 1983-11-22 | The Mead Corporation | Capsular imaging system comprising decolorizing agent |
| US4562137A (en) * | 1982-12-30 | 1985-12-31 | The Mead Corporation | Photosensitive material employing encapsulated radiation sensitive composition |
| US4482624A (en) * | 1983-02-15 | 1984-11-13 | The Mead Corporation | Photosensitive material employing encapsulated radiation sensitive composition and process for improving sensitivity by sequestering oxygen |
| US4508807A (en) * | 1983-07-11 | 1985-04-02 | Mead Corporation | Photosensitive material employing encapsulated radiation sensitive composition and a transparentizable image-receiving layer |
| US4535050A (en) * | 1983-07-18 | 1985-08-13 | The Mead Corporation | Peeling development of photosensitive materials employing microencapsulated radiation sensitive compositions |
| US4903991A (en) * | 1983-07-18 | 1990-02-27 | The Mead Corporation | Document security system |
Also Published As
| Publication number | Publication date |
|---|---|
| FR2120988A5 (en) | 1972-08-18 |
| GB1358107A (en) | 1974-06-26 |
| DE2165374A1 (en) | 1972-07-13 |
| JPS4920979B1 (en) | 1974-05-29 |
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