US2685512A - Photographic element containing arylidene derivative of fluorene - Google Patents
Photographic element containing arylidene derivative of fluorene Download PDFInfo
- Publication number
- US2685512A US2685512A US317865A US31786552A US2685512A US 2685512 A US2685512 A US 2685512A US 317865 A US317865 A US 317865A US 31786552 A US31786552 A US 31786552A US 2685512 A US2685512 A US 2685512A
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- Prior art keywords
- photographic element
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- ultraviolet
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- -1 arylidene derivative of fluorene Chemical class 0.000 title claims description 8
- 150000001875 compounds Chemical class 0.000 claims description 22
- 239000000839 emulsion Substances 0.000 claims description 10
- 229910052709 silver Inorganic materials 0.000 claims description 5
- 239000004332 silver Substances 0.000 claims description 5
- 230000005855 radiation Effects 0.000 description 13
- 239000000463 material Substances 0.000 description 12
- 108010010803 Gelatin Proteins 0.000 description 5
- 238000005562 fading Methods 0.000 description 5
- 229920000159 gelatin Polymers 0.000 description 5
- 239000008273 gelatin Substances 0.000 description 5
- 235000019322 gelatine Nutrition 0.000 description 5
- 235000011852 gelatine desserts Nutrition 0.000 description 5
- 230000009931 harmful effect Effects 0.000 description 5
- 125000003118 aryl group Chemical group 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229910052799 carbon Inorganic materials 0.000 description 2
- 229920002678 cellulose Polymers 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 125000006276 2-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C(*)C([H])=C1[H] 0.000 description 1
- 125000006275 3-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C([H])C(*)=C1[H] 0.000 description 1
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 description 1
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 1
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 1
- CYHBKEFSAGTGJG-UHFFFAOYSA-N 9-[(2-methoxyphenyl)methylidene]fluorene Chemical compound COC1=C(C=C2C3=CC=CC=C3C=3C=CC=CC23)C=CC=C1 CYHBKEFSAGTGJG-UHFFFAOYSA-N 0.000 description 1
- RMQMLYMBZGDKBY-UHFFFAOYSA-N 9-benzylidenefluorene Chemical compound C12=CC=CC=C2C2=CC=CC=C2C1=CC1=CC=CC=C1 RMQMLYMBZGDKBY-UHFFFAOYSA-N 0.000 description 1
- 241000518994 Conta Species 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- YSMRWXYRXBRSND-UHFFFAOYSA-N TOTP Chemical compound CC1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C)OC1=CC=CC=C1C YSMRWXYRXBRSND-UHFFFAOYSA-N 0.000 description 1
- 239000006096 absorbing agent Substances 0.000 description 1
- 150000001241 acetals Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004646 arylidenes Chemical class 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 238000003287 bathing Methods 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 239000012043 crude product Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000007888 film coating Substances 0.000 description 1
- 238000009501 film coating Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000001429 visible spectrum Methods 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
- 238000004383 yellowing Methods 0.000 description 1
Images
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
- G03C1/00—Photosensitive materials
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/815—Photosensitive materials characterised by the base or auxiliary layers characterised by means for filtering or absorbing ultraviolet light, e.g. optical bleaching
- G03C1/8155—Organic compounds therefor
Definitions
- This invention relates to new photographic elements protected against the harmful effects of ultraviolet radiation.
- R. represents an aryl group, such as phenyl, o, m, and p-tolyl, 0-, m, and p-chlorophenyl, o, m, and p-bromophenyl, o-, m, and p-methoxyphenyl, o-, m, and p-sulfophenyl, o-, m, and p-carboxyphenyl, etc.
- aryl group such as phenyl, o, m, and p-tolyl, 0-, m, and p-chlorophenyl, o, m, and p-bromophenyl, o-, m, and p-methoxyphenyl, o-, m, and p-sulfophenyl, o-, m, and p-carboxyphenyl, etc.
- FIG. 1 illustrates schematically a cross-sectional view of a sensitive photographic element having an ultraviolet filter layer containing one of the compounds repre-
- These ultraviolet absorbing compounds can be incorporated in the photographic element in a variety of ways, depending on the ultimate use of the photographic element and the degree of pro" tection desired.
- the ultraviolet absorbing compound can be dissolved or dispersed in a solvent medium together with a colloidal binder, such as gelatin, cellulose esters (e. g. cellulose acetate, etc.), synthetic resins (e. g. polyvinyl acetals, hydrolyzed polyvinyl acetate, etc.), etc., and the resulting mixture coated over the lightsensitive layer of the photographic element.
- a colloidal binder such as gelatin, cellulose esters (e. g. cellulose acetate, etc.), synthetic resins (e. g. polyvinyl acetals, hydrolyzed polyvinyl acetate, etc.), etc.
- the ultraviolet filter layer need not be an outer layer, but this layer can be placed over one of the layers subject to the harmful effects of ultraviolet radiation.
- the ultraviolet filter layer can be placed between the blue and green sensitive layers.
- the ultraviolet filter layer can be placed between the green and the red sensitiv layers.
- the material useful in absorbing the ultraviolet radiation can be incorporated directly in the light-sensitive emulsion instead of. or in addition to, being present in another layer. The amount of ultraviolet absorbing compound used can be varied, depending upon the effect desired and the use to which the material is to be put.
- the support of the photographic element can be transparent, such as a cellulose ester support, for the support can be opaque, such as a paper support.
- Other supports, such as glass, metal, etc., can be employed, if desired.
- Example 1 2.0 g. (0.087 g. atom) of sodium were dissolved in 190 cc. of absolute ethanol. To this solution were added 10.0 g. (0.060 mole.) of fluorene (92% purity) and 6.0 g. (-0.57 mole) .of vbenzaldehyde.
- Example 1 The following example briefly describes the manner of using the compound obtained in Example 1 in a photographic element.
- Example 2 The compound obtained in Example 1 above dissolved in tricresyl phosphate in a 1:3 ra io, and this solution was mixed with a gelatin dispersion which was coated :on film. A separate ccating on paper was also made, After one weeks exposure on an east window, the coatings showed neither fading nor print-out. A square of the film coating was placed over a paper coatcontaining a standard magenta coupler, and this was exposed in a similar manner to ulta violet radiation. No fading nor print-out was observed in the magenta layer.
- ether compounds selected from those represented by the above general formula can be employed.
- the following are typical compounds which can be employed in my invention.
- FIG. 1 illustrates schematically a cross-sectional view of a photographic element containing a layer having incorporated therein S-benzal'fiuorene, which is representative of the ultraviolet absorbing agents which can be employed in my invention.
- a support H] of any suitable material such as cellulose acetate or paper, having thereon a sensitive emulsion layer H-is coated with a filter layer 12 having incorporated therein ll-benzalfiuorene, or some other ultraviolet absorbing compound selected from those represented by the above general formula.
- the drawing is merely representativ of other structures which can be employed in my invention, and that the element can have other layers, not shown, such as additional light-sensitive layers, subbing layers, antihalation layers, etc.
- the ultraviolet absorbing compound contains a solubiiizing group, such as carboxyl ,.hydroxy1, 'sulfo, etc.
- the compound can be incorporated into the photographic element by bathing the photographic element in an aqueous solution of the ultraviolet absorbing compound.
- the ultraviolet absorbing compound is concentrated mostly in the outside gelatin overcoat, although it is also present in the remaining layers containing gelatin.
- the ultraviolet absorbing compound can be incorporated in the photographic element during the preparation thereof, or the ultraviolet absorbing compound can be incorporated in the finished and processed element in those cases where the element has an opaque support, such as paper, in which case, the ultraviolet absorbing compound functions primarily as a stabilizer for the images subject to fading upon exposure to ultraviolet radiation. Such would be the case where the photorap'hic element isa multilayer material.
- a photographic element having thereon a photographic silver halide emulsion layer and in one of the layers of said element a compound selected from those represented by the following general formula:
- a photographic element comprising a support, at least one photographic gelatino-silver halide emulsion layer, and coated over said photographic gelatino-silver halide emulsion layer a gelatin layer containing a compound selected from those represented by the following general formula:
- R is an aryl group
- R represents an aryl group
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Silver Salt Photography Or Processing Solution Therefor (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
3, 1954 G w SAWDEY I 2,685,512
PHOTOGRAPHIC ELEMENT CONTAINING ARYLIDENE DERIVATIVE OF FLUORENE Filed Oct. 31. 1952 FILTER LAYER CONTA/Nl/VG "BENZALFLUORENE EMULS/OIV \SUPPORT Georgew'Sallldey IN V EN TOR. M 2
ATTIYG-AGIZ' Patented Aug. 3, 1954 PHOTOGRAPHIC ELEMENT CONTAINING ARYLIDENE DERIVATIVE RENE OF FLUO- George W. Sawdey, Rochester, N. Y., assignor to Eastman Kodak Company, Rochester, N. Y., a corporation of New Jersey Application October 31, 1952, Serial No. 317,865
5 Claims.
This invention relates to new photographic elements protected against the harmful effects of ultraviolet radiation.
It is known that certain materials, such as cellulosic films and photographic layers, are adversely effected by ultraviolet radiation when such materials are exposed to daylight. In the case of photographic layers, the ultraviolet radiation sometimes causes undesired exposure of the layer, or layers, since photographic silver halide emulsions are sensitive to blue, violet and ultraviolet regions of the spectrum, in addition to any other sensitivity which may be given them, and in the exposur of such material, it is frequently desirable to prevent the action of ultraviolet light on the sensitive emulsion. This is especially true in the case of photographic materials designed for use in color photography where the film has been sensitized to the longer Wavelength regions where it is desirable to record only the rays of the visible spectrum.
Color photographs on multilayer photographic material, particularly where the dye images are formed in sensitive emulsion layers by color development, are susceptible to fading and dis coloration by the action of ultraviolet radiation to which the photographs are subjected during viewing. It is also known that the residual couplers contained in the emulsion layers after formation of the picture images in certain proc- I esses, are attacked by ultraviolet radiation and form a stain which is undesirable in the finished photograph. The action of ultraviolet radiation on finished color photographs is particularly noticeable in positive prints on paper or other opaque supports, since this type of print is frequently viewed in daylight where there is a high content of ultraviolet radiation. This dye fading and yellowing appears to be caused primarily by those wavelengths of light which lie close to the visual region of the spectrum, i. e. 360-400 millimicrons. I have now found that certain ultraviolet absorbing compounds can be used to overcome the afore-mentioned diificulties, without attending harmful action by the ultraviolet absorbing compound itself.
It is, therefore, an object of my invention to provide new photographic elements protected against the harmful effects of ultraviolet radiation. A further object is to provide photographic ell) ' sented by the above general formula.
color materials which have been protected against the harmful effects of ultraviolet radiation. Other objects will become apparent from a consideration of the following description.
The ultraviolet absorbing compounds which I propose to employ in my invention are advantageously represented by the following general formula:
wherein R. represents an aryl group, such as phenyl, o, m, and p-tolyl, 0-, m, and p-chlorophenyl, o, m, and p-bromophenyl, o-, m, and p-methoxyphenyl, o-, m, and p-sulfophenyl, o-, m, and p-carboxyphenyl, etc.
Th accompanying drawing illustrates schematically a cross-sectional view of a sensitive photographic element having an ultraviolet filter layer containing one of the compounds repre- These ultraviolet absorbing compounds can be incorporated in the photographic element in a variety of ways, depending on the ultimate use of the photographic element and the degree of pro" tection desired. Advantageously, the ultraviolet absorbing compound can be dissolved or dispersed in a solvent medium together with a colloidal binder, such as gelatin, cellulose esters (e. g. cellulose acetate, etc.), synthetic resins (e. g. polyvinyl acetals, hydrolyzed polyvinyl acetate, etc.), etc., and the resulting mixture coated over the lightsensitive layer of the photographic element. Where the photographic element is a material intended for use in color photography, the ultraviolet filter layer need not be an outer layer, but this layer can be placed over one of the layers subject to the harmful effects of ultraviolet radiation. For example, in a multilayer material comprising three differentially sensitized layers, the red sensitive layer being adjacent to the support, the green sensitive layer being superposed on the red sensitive layer, and the blue sensitive layer being outermost with respect to the other light-sensitive layers, the ultraviolet filter layer can be placed between the blue and green sensitive layers. Alternatively, the ultraviolet filter layer can be placed between the green and the red sensitiv layers. If desired, the material useful in absorbing the ultraviolet radiation can be incorporated directly in the light-sensitive emulsion instead of. or in addition to, being present in another layer. The amount of ultraviolet absorbing compound used can be varied, depending upon the effect desired and the use to which the material is to be put.
The support of the photographic element can be transparent, such as a cellulose ester support, for the support can be opaque, such as a paper support. Other supports, such as glass, metal, etc., can be employed, if desired.
The following example will serve to illustrate the manner whereby the compounds represented by the above general formula can be prepared.
Example 1 2.0 g. (0.087 g. atom) of sodium were dissolved in 190 cc. of absolute ethanol. To this solution were added 10.0 g. (0.060 mole.) of fluorene (92% purity) and 6.0 g. (-0.57 mole) .of vbenzaldehyde.
The reaction mixture was allowed to stand for two days, at the end of which time the solution was evaporated to crystallization. The crude product was twice recrystallized from ethanol. There was thus obtained a cream-white crystalline powder having a melting point of 74-? 5 C., in a yield of approximately 65% of the theoretical quantity. Analysis of the product gave the following results:
Calculated for Gaul-I14: Carbon, 84.4%; hydrogen, 5.6%. Found: Carbon, 84.0%; hydrogen, 5.6%.
The above method is similar to that described by Thiele in Beric'hte, vol. 33, pages 852-3.
The following example briefly describes the manner of using the compound obtained in Example 1 in a photographic element.
Example .2
The compound obtained in Example 1 above dissolved in tricresyl phosphate in a 1:3 ra io, and this solution was mixed with a gelatin dispersion which was coated :on film. A separate ccating on paper was also made, After one weeks exposure on an east window, the coatings showed neither fading nor print-out. A square of the film coating was placed over a paper coatcontaining a standard magenta coupler, and this was exposed in a similar manner to ulta violet radiation. No fading nor print-out was observed in the magenta layer.
In a manner similar to that described above, ether compounds selected from those represented by the above general formula can be employed. The following are typical compounds which can be employed in my invention.
9-p-chlorobenzalflu'orene CHJ 9-o-methoxybenzalfluorene The accompanying drawing illustrates schematically a cross-sectional view of a photographic element containing a layer having incorporated therein S-benzal'fiuorene, which is representative of the ultraviolet absorbing agents which can be employed in my invention. As shown in the single figure of the drawing, a support H] of any suitable material, such as cellulose acetate or paper, having thereon a sensitive emulsion layer H-is coated with a filter layer 12 having incorporated therein ll-benzalfiuorene, or some other ultraviolet absorbing compound selected from those represented by the above general formula. t will be understood that the drawing is merely representativ of other structures which can be employed in my invention, and that the element can have other layers, not shown, such as additional light-sensitive layers, subbing layers, antihalation layers, etc.
In those cases where the ultraviolet absorbing compound contains a solubiiizing group, such as carboxyl ,.hydroxy1, 'sulfo, etc., the compound can be incorporated into the photographic element by bathing the photographic element in an aqueous solution of the ultraviolet absorbing compound. When treating the photographic element in this manner, the ultraviolet absorbing compound is concentrated mostly in the outside gelatin overcoat, although it is also present in the remaining layers containing gelatin. The ultraviolet absorbing compound can be incorporated in the photographic element during the preparation thereof, or the ultraviolet absorbing compound can be incorporated in the finished and processed element in those cases where the element has an opaque support, such as paper, in which case, the ultraviolet absorbing compound functions primarily as a stabilizer for the images subject to fading upon exposure to ultraviolet radiation. Such would be the case where the photorap'hic element isa multilayer material.
What I claim as my invention .and desire secured by Letters Patent of the United States is:
1. A photographic element having thereon a photographic silver halide emulsion layer and in one of the layers of said element a compound selected from those represented by the following general formula:
:=O'H'R selected from those represented by the following general formula:
i=OH-R Q wherein R represents an aryl group.
3. A photographic element comprising a support, at least one photographic gelatino-silver halide emulsion layer, and coated over said photographic gelatino-silver halide emulsion layer a gelatin layer containing a compound selected from those represented by the following general formula:
wherein R is an aryl group.
wherein R represents an aryl group.
No references cited.
Claims (1)
1. A PHOTOGRAPHIC ELEMENT HAVING THEREON A PHOTOGRAPHIC SILVER HALIDE EMULSION LAYER AND IN ONE OF THE LAYERS OF SAID ELEMENT A COMPOUND SELECTED FROM THOSE REPRESENTED BY THE FOLLOWING GENERAL FORMULA:
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BE523920D BE523920A (en) | 1952-10-31 | ||
| US317865A US2685512A (en) | 1952-10-31 | 1952-10-31 | Photographic element containing arylidene derivative of fluorene |
| GB30107/53A GB735417A (en) | 1952-10-31 | 1953-10-30 | Photographic materials containing ultraviolet radiation absorbing compounds |
| FR1094899D FR1094899A (en) | 1952-10-31 | 1953-10-30 | Method of protection against ultraviolet light and its applications, in particular in photography |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US317865A US2685512A (en) | 1952-10-31 | 1952-10-31 | Photographic element containing arylidene derivative of fluorene |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2685512A true US2685512A (en) | 1954-08-03 |
Family
ID=23235587
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US317865A Expired - Lifetime US2685512A (en) | 1952-10-31 | 1952-10-31 | Photographic element containing arylidene derivative of fluorene |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US2685512A (en) |
| BE (1) | BE523920A (en) |
| FR (1) | FR1094899A (en) |
| GB (1) | GB735417A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2784087A (en) * | 1954-09-20 | 1957-03-05 | Eastman Kodak Co | Photographic light sensitive elements containing ultra-violet filters |
| US2984568A (en) * | 1956-11-26 | 1961-05-16 | Gevaert Photo Prod Nv | Photographic antihalation and protective layer comprising a nitrated styrene-maleic acid copolymer |
| WO2013103139A1 (en) | 2012-01-06 | 2013-07-11 | コニカミノルタアドバンストレイヤー株式会社 | Film mirror, film mirror manufacturing method, film mirror for photovoltaic power generation, and reflection device for photovoltaic power generation |
-
0
- BE BE523920D patent/BE523920A/xx unknown
-
1952
- 1952-10-31 US US317865A patent/US2685512A/en not_active Expired - Lifetime
-
1953
- 1953-10-30 FR FR1094899D patent/FR1094899A/en not_active Expired
- 1953-10-30 GB GB30107/53A patent/GB735417A/en not_active Expired
Non-Patent Citations (1)
| Title |
|---|
| None * |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2784087A (en) * | 1954-09-20 | 1957-03-05 | Eastman Kodak Co | Photographic light sensitive elements containing ultra-violet filters |
| US2984568A (en) * | 1956-11-26 | 1961-05-16 | Gevaert Photo Prod Nv | Photographic antihalation and protective layer comprising a nitrated styrene-maleic acid copolymer |
| WO2013103139A1 (en) | 2012-01-06 | 2013-07-11 | コニカミノルタアドバンストレイヤー株式会社 | Film mirror, film mirror manufacturing method, film mirror for photovoltaic power generation, and reflection device for photovoltaic power generation |
Also Published As
| Publication number | Publication date |
|---|---|
| GB735417A (en) | 1955-08-17 |
| BE523920A (en) | |
| FR1094899A (en) | 1955-05-25 |
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