US3393073A - High contrast photographic emulsions - Google Patents
High contrast photographic emulsions Download PDFInfo
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- US3393073A US3393073A US448887A US44888765A US3393073A US 3393073 A US3393073 A US 3393073A US 448887 A US448887 A US 448887A US 44888765 A US44888765 A US 44888765A US 3393073 A US3393073 A US 3393073A
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- 239000000839 emulsion Substances 0.000 title claims description 67
- -1 SILVER HALIDE Chemical class 0.000 claims description 43
- 229910052709 silver Inorganic materials 0.000 claims description 39
- 239000004332 silver Substances 0.000 claims description 39
- 229920000642 polymer Polymers 0.000 claims description 37
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 28
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 20
- 239000002244 precipitate Substances 0.000 claims description 14
- SJOOOZPMQAWAOP-UHFFFAOYSA-N [Ag].BrCl Chemical compound [Ag].BrCl SJOOOZPMQAWAOP-UHFFFAOYSA-N 0.000 claims description 10
- 230000001376 precipitating effect Effects 0.000 claims description 7
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 6
- 229920003169 water-soluble polymer Polymers 0.000 claims description 3
- 230000007547 defect Effects 0.000 description 15
- 206010027146 Melanoderma Diseases 0.000 description 11
- 238000000034 method Methods 0.000 description 11
- 108010010803 Gelatin Proteins 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 229920000159 gelatin Polymers 0.000 description 9
- 239000008273 gelatin Substances 0.000 description 9
- 235000019322 gelatine Nutrition 0.000 description 9
- 235000011852 gelatine desserts Nutrition 0.000 description 9
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 7
- 229910021607 Silver chloride Inorganic materials 0.000 description 6
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 6
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 5
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 5
- 235000002906 tartaric acid Nutrition 0.000 description 5
- 239000011975 tartaric acid Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 4
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 4
- 239000002253 acid Substances 0.000 description 4
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000000576 coating method Methods 0.000 description 3
- 208000015181 infectious disease Diseases 0.000 description 3
- 230000002458 infectious effect Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000004848 polyfunctional curative Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 102100036601 Aggrecan core protein Human genes 0.000 description 2
- 101000999998 Homo sapiens Aggrecan core protein Proteins 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 229920002301 cellulose acetate Polymers 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 2
- 229920000728 polyester Polymers 0.000 description 2
- 229920000193 polymethacrylate Polymers 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- OJVAMHKKJGICOG-UHFFFAOYSA-N 2,5-hexanedione Chemical compound CC(=O)CCC(C)=O OJVAMHKKJGICOG-UHFFFAOYSA-N 0.000 description 1
- JKFYKCYQEWQPTM-UHFFFAOYSA-N 2-azaniumyl-2-(4-fluorophenyl)acetate Chemical compound OC(=O)C(N)C1=CC=C(F)C=C1 JKFYKCYQEWQPTM-UHFFFAOYSA-N 0.000 description 1
- 239000004342 Benzoyl peroxide Substances 0.000 description 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
- 206010073306 Exposure to radiation Diseases 0.000 description 1
- 241001082241 Lythrum hyssopifolia Species 0.000 description 1
- 229920002319 Poly(methyl acrylate) Polymers 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229910021612 Silver iodide Inorganic materials 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical group OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 235000019400 benzoyl peroxide Nutrition 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229920003064 carboxyethyl cellulose Polymers 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 229920001577 copolymer Chemical group 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- RLSSMJSEOOYNOY-UHFFFAOYSA-N m-cresol Chemical compound CC1=CC=CC(O)=C1 RLSSMJSEOOYNOY-UHFFFAOYSA-N 0.000 description 1
- 229940100630 metacresol Drugs 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 239000002685 polymerization catalyst Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- KUKFKAPJCRZILJ-UHFFFAOYSA-N prop-2-enenitrile;prop-2-enoic acid Chemical compound C=CC#N.OC(=O)C=C KUKFKAPJCRZILJ-UHFFFAOYSA-N 0.000 description 1
- ADZWSOLPGZMUMY-UHFFFAOYSA-M silver bromide Chemical compound [Ag]Br ADZWSOLPGZMUMY-UHFFFAOYSA-M 0.000 description 1
- 229940045105 silver iodide Drugs 0.000 description 1
- 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 1
- 239000000126 substance Substances 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical class OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 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
- G03C1/00—Photosensitive materials
- G03C1/005—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
- G03C1/04—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with macromolecular additives; with layer-forming substances
Definitions
- This invention relates to photography, and more particularlyjto high contrast gelatin silver halide emulsions and to a" method for the preparation of halftone patterns.
- Oine'object of our' invention is to provide high contrast photographic silver halide emulsions which have a reduced tendency to exhibit the black spots defect upon development.
- Another object of our invention is to provide a method for the preparation of halftone patterns which results'in 'a substantial reduction of the black spot defect.
- Other object of our invention will appearherein.
- a high contrast'silver halide emulsion containing a high proportion of silver chloride, and a polymer selected from the group consisting of poly(N-allcanolacrylamide); poly(N- alkanol methacrylamide); and polymershaving the following forrnula; l h
- our invention provides a method'for the preparation of halftone patterns by exposing a dried, thin photographic silver halide emulsion layer one photographic support to a halftone image and develfoping the resulting exposed silver halide image layer to a high contrast
- the methodof our invention featuring the improvement which comprises employing a high contrast photographic silver halide emulsion layer which contains a high percentage'of silver chloride, and ajpoly'mer selected from the group consisting of poly(N-alkanolacrylamide); poly(N-alkanolmethacrylamide); and, polymers having the following formula:
- poly(N-alkanolacrylamide) may be prepared by initially forming N-hydroxyalkylacrylamide (or methacryla-mide) in accordance with the method described in U.S. Patent 2,593,888, and these monomers may be polymerized to highly water soluble polymers using a conventional polymerization catalyst such as benzoyl peroxide.
- these polymers may be prepared by reacting poly(methacrylate) or poly(methylmethacrylate) with an alkano'lamine. This method of preparing the polymers employed in the invention is described below:
- the polyamide which we employ in our invention is advantageously prepared from tartaric acid and ethylenediamine. A convenient method for the preparation of this polymer is described below.
- PREPARATION OF POLYMER Polymerization of the prepolymer was carried out by dissolving 60 grams of the prepolymer in 600 cc. of metacresol. The mixture was mechanically stirred and heated. Polymerization began at about C. and the temperature was maintained between 170 C. and C. until all the polymer had dissolved. The polymer was precipitated from solution by pouring in a large volume of a methanol solution. The precipitate was washed by decantation in alcohol, drained, dissolved in water and reprecipitated with methyl alcohol, drained and washed with acetone to facilitate drying. The polymer is hygroscopic and preferably is obtained in an atmosphere of low relative humidity. The degree of polymerization was about 25 and the molecular weight about 5,000.
- Example I The ethylenediamine-tartatic acid polymer obtained above was added to a spectrally sensitized high contrast silver chlorobromide gelatin emulsion at a concentration of 25 grams of the polymer per mole of silver halide.
- the high contrast silver chlorobromide emulsion was prepared by the method describe-d in U.S. Patent 2,756,148 and contained 65 mole percent chloride and 35 mole percent bromide.
- Samples of the emulsion containing the polymer as well as samples which did not contain the polymer were coated on both cellulose acetate and polyester supports. The emulsion were coated at a coverage of 478 mg. of silver per square foot and 473 mg. of gelatin per square foot. Samples of each coating were exposed on an Eastman 1B sensitometer and processed for various times in Kodak Kodalith Developer. The results obtained are shown in Table 1 below.
- the polymers useful in our invention are water soluble and include the polymer of tartaric acid and ethylenediamine, poly(N-alkanolacrylamides) and poly(N-alkanolmethacrylamides).
- the alkanol group in such polymers preferably contains from 1-4 carbon atoms, and advantageously is an N-fi-alkanol group.
- These polymers are most useful in emulsions at concentrations of from 10 30 grams of polymer per mole of silver salt.
- the effectiveness of the emulsions of our invention containing the defined polymer is increased with respect to avoidance of the black spot defect by lowering the pH of the emulsion to about 3.5.
- Any suitable acid inorganic or organic may be employed which does not interfere with the photographic TABLE 1 Rel. Speed at Various Development Times Dot Quality at Various Development Times Black in Minutes in Minutes Spot Su pport Rating at 1. 75 2. 25 2. 75 3. 25 1. 75 2. 25 2. 75 3. 25 2.25 Mm.
- Example II The emulsion described in Example I was coated onto a conventional film support, and exposed to a step Wedge through a magneta contact screen. The method of using such contact screens is described in How to Use the Kodak Magenta Contact Screen, Kodak pamphlet No. Q-21, 1956. The exposed coatings were developed for 2.25 minutes in Kodalith Developer. The occurrence of the black spot defect was rated, this time on a scale from 0 to 7. Again, the gradations from 0 to 7 are equal and the most pronounced black spot defect is indicated by 7 whereas the lower the number the greater the reduction indicated in the black spot defect. The emulsion, together with the polymers of the invention and various other related polymers were tested at normal and lowered pH with the results shown in Table 2.
- the polymers which we employ in the invention may be added to the emulsion in any convenient manner and at any stage of the preparation of the emulsion with the one provision that the polymers employed must be added to an emulsion which is substantially free of gelatin hardener.
- a gelatin hardener may be incorporated in the emulsion after the addition of the polymers employed in the invention.
- the high contrast emulsions employed in our invention include those which contain from to 100% silver chloride.
- the emulsions employed in our invention contain from 70 to 92% silver chloride, from 8 to 30 mole percent silver bromide and up to 5 mole percent silver iodide (it being understood that these emulsions always contain at least 60 mole percent silver chloride).
- Sensi- Control iil e (5 g Polylgcrylamide (24 g.)
- PEA refers to poly(N-/3-ethan0lacrylamide)
- PTAEDA refers to the polymer of tartaric acid and ethylenediamine
- ACAN refers to copoly- (acrylic acid-acrylonitrile) as described in US. Patent 2,968,558.
- the use of the polymers of the invention substantially reduce the occurrence of the black spot defect.
- the black spot defect is further reduced when emulsions containing the polymers employed in the invention contain sufiicient sulfuric acid to reduce the pH thereof.
- the table further shows that polymers closely related to those employed in the invention such as carboxyethylcellulose, polyacrylamide, polyvinylpyrrolidone and copoly(acrylic acidacrylonitrile) fail to provide any substantial reduction in the occurrence of the black spot defect.
- the silver chlorobromide is precipitated at a higher temperature (50 C. to C.) than normally is used.
- the emulsions of our invention are preferably gelatin silver halide emulsions
- any other suitable colloid binder suitable for dispersing light-sensitive silver halide
- Typical useful colloid binders include all those described in US. Patent 3,039,873, col. 13, lines 37-71.
- half-tone as used in the foregoing description and in the following claims means not only dot patterns but also the well known line patterns. That is, line screens can also be employed according to the present invention to provide the unusual effects illustrated.
- the emulsions of our invention may contain any of the sensitizers, both chemical and optical, speed increasing compounds, gelatin plasticizers, gelatin hardeners and coating aids described in US. Patent 3,039,873, cols. 9-12, and the emulsions may be coated on any suitable support, including cellulose ester, polyester, polycarbonate, polyethylene coated paper, polyolefin, and the like.
- a high contrast silver halide emulsion selected from the group consisting of silver halide emulsions containing 60 to 100 mole percent chloride, to 40 mole percent bromide and 0 to mole percent iodide, and silver halide emulsions containing from 40 to 90 mole percent chloride and from 10 to 60 mole percent bromide prepared by first precipitating a relatively chloride rich silver halide precipitate and converting the precipitate to a bromide enriched silver chlorobromide emulsion by the addition of bromide ions, said emulsion having incorporated therein, in a quantity suflicient to effectively reduce black spots, a water-soluble polymer selected from the group consisting of poly(N-alkanolacrylamide); poly(N-alkanolmethacrylamide); and the polymers having the following structural formula:
- a photographic element comprising a high contrast photographic silver halide emulsion selected from the group consisting of silver halide emulsions containing 60 to 100 mole percent chloride, 0 to 40 mole percent bromide and 0 to 5 mole percent iodide, and silver halide emulsions containing from 40 to 90 mole percent chloride and from 10 to 60 mole percent bromide prepared by first precipitating a relatively chloride rich silver halide precipitate and converting the precipitate to a bromide enriched silver chlorobromide emulsion by the addition of bromide ions, said emulsion having incorporated therein, in a quantity suificient to effective reduce black spots, a polymer selected from the group consisting of poly (N-alkanolacrylamide) poly(N-alkanolmethacrylamide) and, polymers having the following formula:
- a photographic element comprising a high contrast silver halide emulsion selected from the group consisting of silver halide emulsions containing 60 to 100 mole percent chloride, 0 to 40 mole percent bromide and 0 to 5 mole percent iodide, and silver halide emulsions containing from 40 to 90 mole percent chloride and from 10 to mole percent bromide prepared by first precipitating a relatively chloride rich silver halide precipitate and converting the precipitate to a bromide enriched silver chlorobromide emulsion by the addition of bromide ions, said emulsion having a pH of about 3.5, and having incorporated therein, -in a quantity sufficient to effectively reduce black spots, a polymer selected from the group consisting of poly(N-alkanolacrylamide); poly(N-alkanolmethacrylamide); and, polymers having the following formula:
- n is a whole number.
- a photographic element comprising a high contrast silver halide emulsion selected from the group consisting of silver halide emulsions containing 60 to 100 mole percent chloride, 0 to 40 mole perecent bromide and 0 to 5 mole percent iodide, and silver halide emulsions containing from 40 to mole percent chloride and from 10 to 60 mole percent bromide prepared by first precipitating a relatively chloride rich silver halide precipitate and converting the precipitate to a bromide enriched silver chlorobromide emulsion by the addition of bromide ions, said emulsion having incorporated therein from 10 to 30 grams per mole of silver of water soluble poly(N-B- ethanolacrylamide) and about 1 to about 1.5 cc. of concentrated sulfuric acid per mole of silver.
- a photographic element comprising a gelatin silver halide emulsion selected from the group consisting of silver halide emulsions containing 60 to mole percent chloride, 0 to 40 mole percent bromide and 0 to 5 mole percent iodide, and silver halide emulsions containing from 40 to 90 mole percent chloride and from 10 to 60 mole percent bromide prepared by first precipitating a relatively chloride rich silver halide precipitate and converting the precipitate to a bromide enriched silver chlorobromide emulsion by the addition of bromide ions, said emulsion having incorporated therein from 10 to 30 grams per mole of silver of a polymer having the following formula:
- n is a whole number.
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- Physics & Mathematics (AREA)
- Chemical & Material Sciences (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
S at Pa Y; 3,393,073 HIGH CONTRAST PHOTOGRAPHIC EMULSIONS Georges .Reutenauer, Simone Leonie Marie Elisabeth :Boyer, and Marie-Claire Andre Lucienne Prteseille, Vincennes, France, assignors'to Eastman Kodak Company, Rochester, N.Y., a corporation of New Jersey No Drawing. Filed Apr. 16, 1965, Ser. No. 448,887
This invention relates to photography, and more particularlyjto high contrast gelatin silver halide emulsions and to a" method for the preparation of halftone patterns.
In the graphic arts field, it is common to provide high contrast silver halide emulsions and to expose such'emulsiolis to a hal-ftone image. Development of the exposed emulsio'n' is carried out underspecial conditions and is believed to proceed catalytically. Such development is commonly "referred to in the graphic arts field "as infectious development. Development of high contrast emulsiohs involves a primary development stage which requires a relatively long period of induction during which the latent image is very slowly developed. The primary development depends upon the amountof light received by the film. When the amountof developed silvjer" halide reaches a well defined value, infectious development occurs causing the grains to be reduced at a very high speed until'maximumdensity is reached, regardless of the amount of light received. In practice, an area which has received a uniform exposure to radiation has, upon development, some spots which are developed more rapidly than thejwhole area. It may be that these spots are more highly sensitized than the rest of the emulsion, or the developer may reach such spots more rapidly than other areas of] the film. Whatever the cause, the results are that areas which'have not received suflicient lighting to cause infectious development show black spots having a very small diameter. This is referred to herein as 'the black spots defect. This defect, in the practice of halftone photography, causes black areas between the normal dots which connect two or more dots, thus tending to result in unfavorable blocking during photo-mechanical reproduction. It is highly desirable, therefore, to provide high contrast emulsions, and a method for obtaining halftone patterns, in which the occurrence'of the black spots defect is rediiced to a minimum. f
Oine'object of our' invention is to provide high contrast photographic silver halide emulsions which have a reduced tendency to exhibit the black spots defect upon development. Another object of our invention is to provide a method for the preparation of halftone patterns which results'in 'a substantial reduction of the black spot defect. Other object of our invention will appearherein.
Iri one embodiment of our invention, we provide a high contrast'silver halide emulsion containing a high proportion of silver chloride, and a polymer selected from the group consisting of poly(N-allcanolacrylamide); poly(N- alkanol methacrylamide); and polymershaving the following forrnula; l h
In another embodiment of our invention, we provide a method'for the preparation of halftone patterns by exposing a dried, thin photographic silver halide emulsion layer one photographic support to a halftone image and develfoping the resulting exposed silver halide image layer to a high contrast, the methodof our invention featuring the improvement which comprises employing a high contrast photographic silver halide emulsion layer which contains a high percentage'of silver chloride, and ajpoly'mer selected from the group consisting of poly(N-alkanolacrylamide); poly(N-alkanolmethacrylamide); and, polymers having the following formula:
We have further found that additional reduction of the black spot defect may be achieved when the pH of the emulsion employed in the invention is lowered from its normal pH of about 4.5 to pH of about 3.5, for example, by the addition of an acid such as sulfuric acid.
The polymers which we employ in accordance with our invention may be prepared by any suitable procedure. For example, poly(N-alkanolacrylamide) may be prepared by initially forming N-hydroxyalkylacrylamide (or methacryla-mide) in accordance with the method described in U.S. Patent 2,593,888, and these monomers may be polymerized to highly water soluble polymers using a conventional polymerization catalyst such as benzoyl peroxide. Advantageously, these polymers may be prepared by reacting poly(methacrylate) or poly(methylmethacrylate) with an alkano'lamine. This method of preparing the polymers employed in the invention is described below:
Poly (N-fi-ethanolacrylamide) 10 g. poly(methacrylate) were crushed into fine particles and refluxed with stirring in cc. ethanolamine. Heating was continued until the poly(methylacrylate) was completely dissolved (about 3 to 6 hours). The mixture was cooled, and precipitated in acetone several times to remove any remaining ethanolamine. A yield of 60% poly (N-B-ethanolacrylamide) was obtained. Calculated for N: 12.1%; found: 12.0%.
The polyamide which we employ in our invention is advantageously prepared from tartaric acid and ethylenediamine. A convenient method for the preparation of this polymer is described below.
PREPARATION OF PREPOLYMER 37.5 grams of finely crushed tartaric acid were placed in a three neck flask and dissolved with stirring in a mixture of 42 parts ethyl alcohol and 7 parts water. The temperature was raised to 70 and, upon complete dissolution of the tartaric acid, the temperature was reduced to 40 C. Ethylenediamine was then poured into the solution by means of a dropping funnel. The reaction was exothermic and the reaction vessel was cooled with ice water to maintain the temperature at about 40 C. during the reaction. The product was purified by dissolving in water followed by precipitation with methyl alcohol.
PREPARATION OF POLYMER Polymerization of the prepolymer was carried out by dissolving 60 grams of the prepolymer in 600 cc. of metacresol. The mixture was mechanically stirred and heated. Polymerization began at about C. and the temperature was maintained between 170 C. and C. until all the polymer had dissolved. The polymer was precipitated from solution by pouring in a large volume of a methanol solution. The precipitate was washed by decantation in alcohol, drained, dissolved in water and reprecipitated with methyl alcohol, drained and washed with acetone to facilitate drying. The polymer is hygroscopic and preferably is obtained in an atmosphere of low relative humidity. The degree of polymerization was about 25 and the molecular weight about 5,000.
Our invention will be more fully demonstrated by the following examples.
Example I The ethylenediamine-tartatic acid polymer obtained above was added to a spectrally sensitized high contrast silver chlorobromide gelatin emulsion at a concentration of 25 grams of the polymer per mole of silver halide. The high contrast silver chlorobromide emulsion was prepared by the method describe-d in U.S. Patent 2,756,148 and contained 65 mole percent chloride and 35 mole percent bromide. Samples of the emulsion containing the polymer as well as samples which did not contain the polymer were coated on both cellulose acetate and polyester supports. The emulsion were coated at a coverage of 478 mg. of silver per square foot and 473 mg. of gelatin per square foot. Samples of each coating were exposed on an Eastman 1B sensitometer and processed for various times in Kodak Kodalith Developer. The results obtained are shown in Table 1 below.
The polymers useful in our invention are water soluble and include the polymer of tartaric acid and ethylenediamine, poly(N-alkanolacrylamides) and poly(N-alkanolmethacrylamides). The alkanol group in such polymers preferably contains from 1-4 carbon atoms, and advantageously is an N-fi-alkanol group. These polymers are most useful in emulsions at concentrations of from 10 30 grams of polymer per mole of silver salt.
As indicated heretofore, the effectiveness of the emulsions of our invention containing the defined polymer is increased with respect to avoidance of the black spot defect by lowering the pH of the emulsion to about 3.5. Any suitable acid (inorganic or organic) may be employed which does not interfere with the photographic TABLE 1 Rel. Speed at Various Development Times Dot Quality at Various Development Times Black in Minutes in Minutes Spot Su pport Rating at 1. 75 2. 25 2. 75 3. 25 1. 75 2. 25 2. 75 3. 25 2.25 Mm.
Dev. Time Control Cellulose Acetate 100 148 186 234 8 8 5 3 4 do 71 102 138 178 7 8 8 7 1 105 155 195 240 7 8 5 3 5 +Ply1ner .do 74 112 148 182 7 8 8 7 1 In the above table, the occurrence of the black spot defect is rated on a scale of 0 to with 5 indicating the greatest occurrence of black spots and 0 indicating a substantial absence of black spots. The scale is graded evenly and assigned numbers of from 0 to 5. As may be seen in the above table, the incorporation of ethylenediaminetartaric acid polymer substantially reduces the occurrence of the black spot defect.
Example II The emulsion described in Example I was coated onto a conventional film support, and exposed to a step Wedge through a magneta contact screen. The method of using such contact screens is described in How to Use the Kodak Magenta Contact Screen, Kodak pamphlet No. Q-21, 1956. The exposed coatings were developed for 2.25 minutes in Kodalith Developer. The occurrence of the black spot defect was rated, this time on a scale from 0 to 7. Again, the gradations from 0 to 7 are equal and the most pronounced black spot defect is indicated by 7 whereas the lower the number the greater the reduction indicated in the black spot defect. The emulsion, together with the polymers of the invention and various other related polymers were tested at normal and lowered pH with the results shown in Table 2.
TABLE 2 properties of the emulsion, sulfuric and trichloroacetic acids being highly useful. Advantageously, we employ sulfuric acid in a concentration of from about 1 to 1.5 cc. concentrated sulfuric acid per mole of silver.
The polymers which we employ in the invention may be added to the emulsion in any convenient manner and at any stage of the preparation of the emulsion with the one provision that the polymers employed must be added to an emulsion which is substantially free of gelatin hardener. However, a gelatin hardener may be incorporated in the emulsion after the addition of the polymers employed in the invention.
The high contrast emulsions employed in our invention include those which contain from to 100% silver chloride. Advantageously, the emulsions employed in our invention contain from 70 to 92% silver chloride, from 8 to 30 mole percent silver bromide and up to 5 mole percent silver iodide (it being understood that these emulsions always contain at least 60 mole percent silver chloride). We may also use, in accordance with the invention, the emulsions described in U.S. Patent 2,756,148 (1956) of MacWilliam, which emulsions contain from 40 to 90 mole percent silver chloride and from 10 to 60 mole percent bromide, which emulsions are prepared by initially precipitating a relatively chloride-rich precipitate which Addenda T1280;
Sensi- Control iil e (5 g Polylgcrylamide (24 g.)
6O Polyvinylpyrrolidone (10 g.) ACAN (24 g.)
Black Spots In the above table, PEA refers to poly(N-/3-ethan0lacrylamide), PTAEDA refers to the polymer of tartaric acid and ethylenediamine, and ACAN refers to copoly- (acrylic acid-acrylonitrile) as described in US. Patent 2,968,558. As may be seen in the foregoing table, the use of the polymers of the invention substantially reduce the occurrence of the black spot defect. The black spot defect is further reduced when emulsions containing the polymers employed in the invention contain sufiicient sulfuric acid to reduce the pH thereof. The table further shows that polymers closely related to those employed in the invention such as carboxyethylcellulose, polyacrylamide, polyvinylpyrrolidone and copoly(acrylic acidacrylonitrile) fail to provide any substantial reduction in the occurrence of the black spot defect.
is subsequently converted to a bromide-enriched silver chlorobromide by the addition of bromide ions during at least the last /3 of the precipitation cycle of the emulsion making procedure. Advantageously, the silver chlorobromide is precipitated at a higher temperature (50 C. to C.) than normally is used.
Although the emulsions of our invention are preferably gelatin silver halide emulsions, any other suitable colloid binder (suitable for dispersing light-sensitive silver halide) may be employed if desired. Typical useful colloid binders include all those described in US. Patent 3,039,873, col. 13, lines 37-71.
The term half-tone as used in the foregoing description and in the following claims means not only dot patterns but also the well known line patterns. That is, line screens can also be employed according to the present invention to provide the unusual effects illustrated.
The emulsions of our invention may contain any of the sensitizers, both chemical and optical, speed increasing compounds, gelatin plasticizers, gelatin hardeners and coating aids described in US. Patent 3,039,873, cols. 9-12, and the emulsions may be coated on any suitable support, including cellulose ester, polyester, polycarbonate, polyethylene coated paper, polyolefin, and the like.
The invention has been described in detail with particular reference to preferred embodiments thereof but it will be understood that variations and modifications can be effected within the spirit and scope of the invention as described hereinabove and as defined in the appended claims.
We claim:
1. A high contrast silver halide emulsion selected from the group consisting of silver halide emulsions containing 60 to 100 mole percent chloride, to 40 mole percent bromide and 0 to mole percent iodide, and silver halide emulsions containing from 40 to 90 mole percent chloride and from 10 to 60 mole percent bromide prepared by first precipitating a relatively chloride rich silver halide precipitate and converting the precipitate to a bromide enriched silver chlorobromide emulsion by the addition of bromide ions, said emulsion having incorporated therein, in a quantity suflicient to effectively reduce black spots, a water-soluble polymer selected from the group consisting of poly(N-alkanolacrylamide); poly(N-alkanolmethacrylamide); and the polymers having the following structural formula:
0 HzN[- CHiOHiNH-ii-GHOH-OHOE-iiNH]..OHioHiNH wherein n is a whole number.
2. A photographic element comprising a high contrast photographic silver halide emulsion selected from the group consisting of silver halide emulsions containing 60 to 100 mole percent chloride, 0 to 40 mole percent bromide and 0 to 5 mole percent iodide, and silver halide emulsions containing from 40 to 90 mole percent chloride and from 10 to 60 mole percent bromide prepared by first precipitating a relatively chloride rich silver halide precipitate and converting the precipitate to a bromide enriched silver chlorobromide emulsion by the addition of bromide ions, said emulsion having incorporated therein, in a quantity suificient to effective reduce black spots, a polymer selected from the group consisting of poly (N-alkanolacrylamide) poly(N-alkanolmethacrylamide) and, polymers having the following formula:
3. A photographic element comprising a high contrast silver halide emulsion selected from the group consisting of silver halide emulsions containing 60 to 100 mole percent chloride, 0 to 40 mole percent bromide and 0 to 5 mole percent iodide, and silver halide emulsions containing from 40 to 90 mole percent chloride and from 10 to mole percent bromide prepared by first precipitating a relatively chloride rich silver halide precipitate and converting the precipitate to a bromide enriched silver chlorobromide emulsion by the addition of bromide ions, said emulsion having a pH of about 3.5, and having incorporated therein, -in a quantity sufficient to effectively reduce black spots, a polymer selected from the group consisting of poly(N-alkanolacrylamide); poly(N-alkanolmethacrylamide); and, polymers having the following formula:
wherein n is a whole number.
4. A photographic element comprising a high contrast silver halide emulsion selected from the group consisting of silver halide emulsions containing 60 to 100 mole percent chloride, 0 to 40 mole perecent bromide and 0 to 5 mole percent iodide, and silver halide emulsions containing from 40 to mole percent chloride and from 10 to 60 mole percent bromide prepared by first precipitating a relatively chloride rich silver halide precipitate and converting the precipitate to a bromide enriched silver chlorobromide emulsion by the addition of bromide ions, said emulsion having incorporated therein from 10 to 30 grams per mole of silver of water soluble poly(N-B- ethanolacrylamide) and about 1 to about 1.5 cc. of concentrated sulfuric acid per mole of silver.
5. A photographic element comprising a gelatin silver halide emulsion selected from the group consisting of silver halide emulsions containing 60 to mole percent chloride, 0 to 40 mole percent bromide and 0 to 5 mole percent iodide, and silver halide emulsions containing from 40 to 90 mole percent chloride and from 10 to 60 mole percent bromide prepared by first precipitating a relatively chloride rich silver halide precipitate and converting the precipitate to a bromide enriched silver chlorobromide emulsion by the addition of bromide ions, said emulsion having incorporated therein from 10 to 30 grams per mole of silver of a polymer having the following formula:
wherein n is a whole number.
References Cited UNITED STATES PATENTS 2,533,166 12/ 1950 Jones 260-89.7 2,593,888 4/1952 Jones 260-561 3,069,263 12/1962 Haas 96-114 XR J. TRAVIS BROWN, Acting Primary Examiner.
R. H. SMITH, Assistant Examiner.
Claims (1)
1. A HIGH CONTRAST SILVER HALIDE EMULSION SELECTED FROM THE GROUP CONSISTING OF SILVER HALIDE EMULSIONS CONTAINING 60 TO 100 MOLE PERCENT CHLORIDE, 0 TO 40 MOLE PERCENT BROMIDE AND 0 TO 5 MOLE PERCENT IODIDE, AND SILVER HALIDE EMULSIONS CONTAINING FROM 40 TO 90 MOLE PERCENT CHLORIDE AND FROM 10 TO 60 MOLE PERCENT BROMIDE PREPARED BY FIRST PRECIPITATING A RELATIVELY CHLORIDE RICH SILVER HALIDE PRECIPITATE AND CONVERTING THE PRECIPITATE TO A BROMIDE ENRICHED SILVER CHLOROBROMIDE EMULSION BY THE ADDITION OF BROMIDE IONS, SAID EMULSION HAVING INCORPORATED THEREIN, IN A QUANTITY SUFFICIENT TO EFFECTIVELY REDUCE BLACK SPOTS, A WATER-SOLUBLE POLYMER SELECTED FROM THE GROUP CONSISTING OF POLY(N-ALKANOLACRYLAMIDE);POLY(N-ALKANOLMETHACRYLAMIDE); AND THE POLYMERS HAVING THE FOLLOWING STRUCTURAL FORMULA:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US448887A US3393073A (en) | 1965-04-16 | 1965-04-16 | High contrast photographic emulsions |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US448887A US3393073A (en) | 1965-04-16 | 1965-04-16 | High contrast photographic emulsions |
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| Publication Number | Publication Date |
|---|---|
| US3393073A true US3393073A (en) | 1968-07-16 |
Family
ID=23782044
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US448887A Expired - Lifetime US3393073A (en) | 1965-04-16 | 1965-04-16 | High contrast photographic emulsions |
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