US3393073A - High contrast photographic emulsions - Google Patents

High contrast photographic emulsions Download PDF

Info

Publication number
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
Authority
US
United States
Prior art keywords
mole percent
silver halide
emulsion
bromide
poly
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US448887A
Inventor
Reutenauer Georges
Boyer Simone Leonie Elisabeth
Preteseil Marie-Clair Lucienne
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eastman Kodak Co
Original Assignee
Eastman Kodak Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Eastman Kodak Co filed Critical Eastman Kodak Co
Priority to US448887A priority Critical patent/US3393073A/en
Application granted granted Critical
Publication of US3393073A publication Critical patent/US3393073A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/005Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein
    • G03C1/04Silver 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.

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:
US448887A 1965-04-16 1965-04-16 High contrast photographic emulsions Expired - Lifetime US3393073A (en)

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

Publications (1)

Publication Number Publication Date
US3393073A true US3393073A (en) 1968-07-16

Family

ID=23782044

Family Applications (1)

Application Number Title Priority Date Filing Date
US448887A Expired - Lifetime US3393073A (en) 1965-04-16 1965-04-16 High contrast photographic emulsions

Country Status (1)

Country Link
US (1) US3393073A (en)

Cited By (45)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002062269A1 (en) 2001-02-06 2002-08-15 Goepferich Achim Spacing device for releasing active substances in the paranasal sinus
US20100198247A1 (en) * 2004-04-21 2010-08-05 Acclarent, Inc. Devices, Systems and Methods for Treating Disorders of the Ear, Nose and Throat
US20110112512A1 (en) * 2004-04-21 2011-05-12 Acclarent, Inc. Devices and methods for treating maxillary sinus disease
US8080000B2 (en) 2004-04-21 2011-12-20 Acclarent, Inc. Methods and apparatus for treating disorders of the ear nose and throat
US8100933B2 (en) 2002-09-30 2012-01-24 Acclarent, Inc. Method for treating obstructed paranasal frontal sinuses
US8114113B2 (en) 2005-09-23 2012-02-14 Acclarent, Inc. Multi-conduit balloon catheter
US8114062B2 (en) 2004-04-21 2012-02-14 Acclarent, Inc. Devices and methods for delivering therapeutic substances for the treatment of sinusitis and other disorders
US8118757B2 (en) 2007-04-30 2012-02-21 Acclarent, Inc. Methods and devices for ostium measurement
US8142422B2 (en) 2004-04-21 2012-03-27 Acclarent, Inc. Devices, systems and methods for diagnosing and treating sinusitis and other disorders of the ears, nose and/or throat
US8146400B2 (en) 2004-04-21 2012-04-03 Acclarent, Inc. Endoscopic methods and devices for transnasal procedures
US8172828B2 (en) 2004-04-21 2012-05-08 Acclarent, Inc. Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures
US8182432B2 (en) 2008-03-10 2012-05-22 Acclarent, Inc. Corewire design and construction for medical devices
US8190389B2 (en) 2006-05-17 2012-05-29 Acclarent, Inc. Adapter for attaching electromagnetic image guidance components to a medical device
US8388642B2 (en) 2005-01-18 2013-03-05 Acclarent, Inc. Implantable devices and methods for treating sinusitis and other disorders
US8414473B2 (en) 2004-04-21 2013-04-09 Acclarent, Inc. Methods and apparatus for treating disorders of the ear nose and throat
US8435290B2 (en) 2009-03-31 2013-05-07 Acclarent, Inc. System and method for treatment of non-ventilating middle ear by providing a gas pathway through the nasopharynx
US8439687B1 (en) 2006-12-29 2013-05-14 Acclarent, Inc. Apparatus and method for simulated insertion and positioning of guidewares and other interventional devices
US8485199B2 (en) 2007-05-08 2013-07-16 Acclarent, Inc. Methods and devices for protecting nasal turbinate during surgery
US8702626B1 (en) 2004-04-21 2014-04-22 Acclarent, Inc. Guidewires for performing image guided procedures
US8715169B2 (en) 2004-04-21 2014-05-06 Acclarent, Inc. Devices, systems and methods useable for treating sinusitis
US8747389B2 (en) 2004-04-21 2014-06-10 Acclarent, Inc. Systems for treating disorders of the ear, nose and throat
US8764729B2 (en) 2004-04-21 2014-07-01 Acclarent, Inc. Frontal sinus spacer
US8864787B2 (en) 2004-04-21 2014-10-21 Acclarent, Inc. Ethmoidotomy system and implantable spacer devices having therapeutic substance delivery capability for treatment of paranasal sinusitis
US8894614B2 (en) 2004-04-21 2014-11-25 Acclarent, Inc. Devices, systems and methods useable for treating frontal sinusitis
US8932276B1 (en) 2004-04-21 2015-01-13 Acclarent, Inc. Shapeable guide catheters and related methods
US8951225B2 (en) 2005-06-10 2015-02-10 Acclarent, Inc. Catheters with non-removable guide members useable for treatment of sinusitis
US8979888B2 (en) 2008-07-30 2015-03-17 Acclarent, Inc. Paranasal ostium finder devices and methods
US9039680B2 (en) 2004-08-04 2015-05-26 Acclarent, Inc. Implantable devices and methods for delivering drugs and other substances to treat sinusitis and other disorders
US9072626B2 (en) 2009-03-31 2015-07-07 Acclarent, Inc. System and method for treatment of non-ventilating middle ear by providing a gas pathway through the nasopharynx
US9089258B2 (en) 2004-04-21 2015-07-28 Acclarent, Inc. Endoscopic methods and devices for transnasal procedures
US9101384B2 (en) 2004-04-21 2015-08-11 Acclarent, Inc. Devices, systems and methods for diagnosing and treating sinusitis and other disorders of the ears, Nose and/or throat
US9107574B2 (en) 2004-04-21 2015-08-18 Acclarent, Inc. Endoscopic methods and devices for transnasal procedures
US9155492B2 (en) 2010-09-24 2015-10-13 Acclarent, Inc. Sinus illumination lightwire device
US9265407B2 (en) 2004-04-21 2016-02-23 Acclarent, Inc. Endoscopic methods and devices for transnasal procedures
US9399121B2 (en) 2004-04-21 2016-07-26 Acclarent, Inc. Systems and methods for transnasal dilation of passageways in the ear, nose or throat
US9433437B2 (en) 2013-03-15 2016-09-06 Acclarent, Inc. Apparatus and method for treatment of ethmoid sinusitis
US9468362B2 (en) 2004-04-21 2016-10-18 Acclarent, Inc. Endoscopic methods and devices for transnasal procedures
US9629684B2 (en) 2013-03-15 2017-04-25 Acclarent, Inc. Apparatus and method for treatment of ethmoid sinusitis
US9820688B2 (en) 2006-09-15 2017-11-21 Acclarent, Inc. Sinus illumination lightwire device
US10188413B1 (en) 2004-04-21 2019-01-29 Acclarent, Inc. Deflectable guide catheters and related methods
US10206821B2 (en) 2007-12-20 2019-02-19 Acclarent, Inc. Eustachian tube dilation balloon with ventilation path
US10524814B2 (en) 2009-03-20 2020-01-07 Acclarent, Inc. Guide system with suction
US11065061B2 (en) 2004-04-21 2021-07-20 Acclarent, Inc. Systems and methods for performing image guided procedures within the ear, nose, throat and paranasal sinuses
US11529502B2 (en) 2004-04-21 2022-12-20 Acclarent, Inc. Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures
US11957318B2 (en) 2021-04-29 2024-04-16 Acclarent, Inc. Methods and apparatus for treating disorders of the ear nose and throat

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2533166A (en) * 1945-10-16 1950-12-05 Gen Aniline & Film Corp Process for polymerizing watersoluble polyacrylamides and poly-alpha-substituted acrylamides
US2593889A (en) * 1946-06-20 1952-04-22 G M Mfg Company Machine for measuring and dispensing variable volumes of liquids
US3069263A (en) * 1958-12-17 1962-12-18 Polaroid Corp Photographic products and processes using alkali permeable polymeric layers

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2533166A (en) * 1945-10-16 1950-12-05 Gen Aniline & Film Corp Process for polymerizing watersoluble polyacrylamides and poly-alpha-substituted acrylamides
US2593889A (en) * 1946-06-20 1952-04-22 G M Mfg Company Machine for measuring and dispensing variable volumes of liquids
US3069263A (en) * 1958-12-17 1962-12-18 Polaroid Corp Photographic products and processes using alkali permeable polymeric layers

Cited By (121)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20080243140A1 (en) * 2001-02-06 2008-10-02 Acclarent, Inc. Spacing devices for releasing active substances in the paranasal sinus
WO2002062269A1 (en) 2001-02-06 2002-08-15 Goepferich Achim Spacing device for releasing active substances in the paranasal sinus
US8740929B2 (en) 2001-02-06 2014-06-03 Acclarent, Inc. Spacing device for releasing active substances in the paranasal sinus
US8100933B2 (en) 2002-09-30 2012-01-24 Acclarent, Inc. Method for treating obstructed paranasal frontal sinuses
US9457175B2 (en) 2002-09-30 2016-10-04 Acclarent, Inc. Balloon catheters and methods for treating paranasal sinuses
US8764786B2 (en) 2002-09-30 2014-07-01 Acclarent, Inc. Balloon catheters and methods for treating paranasal sinuses
US8317816B2 (en) 2002-09-30 2012-11-27 Acclarent, Inc. Balloon catheters and methods for treating paranasal sinuses
US8961398B2 (en) 2004-04-21 2015-02-24 Acclarent, Inc. Methods and apparatus for treating disorders of the ear, nose and throat
US11202644B2 (en) 2004-04-21 2021-12-21 Acclarent, Inc. Shapeable guide catheters and related methods
US8114062B2 (en) 2004-04-21 2012-02-14 Acclarent, Inc. Devices and methods for delivering therapeutic substances for the treatment of sinusitis and other disorders
US11864725B2 (en) 2004-04-21 2024-01-09 Acclarent, Inc. Devices, systems and methods for diagnosing and treating sinusitis and other disorders of the ears, nose and/or throat
US8123722B2 (en) 2004-04-21 2012-02-28 Acclarent, Inc. Devices, systems and methods for treating disorders of the ear, nose and throat
US8142422B2 (en) 2004-04-21 2012-03-27 Acclarent, Inc. Devices, systems and methods for diagnosing and treating sinusitis and other disorders of the ears, nose and/or throat
US8146400B2 (en) 2004-04-21 2012-04-03 Acclarent, Inc. Endoscopic methods and devices for transnasal procedures
US8172828B2 (en) 2004-04-21 2012-05-08 Acclarent, Inc. Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures
US11589742B2 (en) 2004-04-21 2023-02-28 Acclarent, Inc. Methods and apparatus for treating disorders of the ear nose and throat
US11529502B2 (en) 2004-04-21 2022-12-20 Acclarent, Inc. Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures
US8090433B2 (en) 2004-04-21 2012-01-03 Acclarent, Inc. Methods and apparatus for treating disorders of the ear nose and throat
US10098652B2 (en) 2004-04-21 2018-10-16 Acclarent, Inc. Systems and methods for transnasal dilation of passageways in the ear, nose or throat
US8414473B2 (en) 2004-04-21 2013-04-09 Acclarent, Inc. Methods and apparatus for treating disorders of the ear nose and throat
US8425457B2 (en) 2004-04-21 2013-04-23 Acclarent, Inc. Devices, systems and methods for diagnosing and treating sinusitus and other disorder of the ears, nose and/or throat
US11511090B2 (en) 2004-04-21 2022-11-29 Acclarent, Inc. Devices, systems and methods useable for treating sinusitis
US10034682B2 (en) 2004-04-21 2018-07-31 Acclarent, Inc. Devices, systems and methods useable for treating frontal sinusitis
US11065061B2 (en) 2004-04-21 2021-07-20 Acclarent, Inc. Systems and methods for performing image guided procedures within the ear, nose, throat and paranasal sinuses
US8702626B1 (en) 2004-04-21 2014-04-22 Acclarent, Inc. Guidewires for performing image guided procedures
US8715169B2 (en) 2004-04-21 2014-05-06 Acclarent, Inc. Devices, systems and methods useable for treating sinusitis
US8721591B2 (en) 2004-04-21 2014-05-13 Acclarent, Inc. Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures
US8088101B2 (en) 2004-04-21 2012-01-03 Acclarent, Inc. Devices, systems and methods for treating disorders of the ear, nose and throat
US8747389B2 (en) 2004-04-21 2014-06-10 Acclarent, Inc. Systems for treating disorders of the ear, nose and throat
US8764709B2 (en) 2004-04-21 2014-07-01 Acclarent, Inc. Devices, systems and methods for treating disorders of the ear, nose and throat
US8764729B2 (en) 2004-04-21 2014-07-01 Acclarent, Inc. Frontal sinus spacer
US8080000B2 (en) 2004-04-21 2011-12-20 Acclarent, Inc. Methods and apparatus for treating disorders of the ear nose and throat
US8764726B2 (en) 2004-04-21 2014-07-01 Acclarent, Inc. Devices, systems and methods useable for treating sinusitis
US8777926B2 (en) 2004-04-21 2014-07-15 Acclarent, Inc. Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasel or paranasal structures
US8828041B2 (en) 2004-04-21 2014-09-09 Acclarent, Inc. Devices, systems and methods useable for treating sinusitis
US8852143B2 (en) 2004-04-21 2014-10-07 Acclarent, Inc. Devices, systems and methods for treating disorders of the ear, nose and throat
US8858586B2 (en) 2004-04-21 2014-10-14 Acclarent, Inc. Methods for enlarging ostia of paranasal sinuses
US8864787B2 (en) 2004-04-21 2014-10-21 Acclarent, Inc. Ethmoidotomy system and implantable spacer devices having therapeutic substance delivery capability for treatment of paranasal sinusitis
US8870893B2 (en) 2004-04-21 2014-10-28 Acclarent, Inc. Devices, systems and methods for diagnosing and treating sinusitis and other disorders of the ears, nose and/or throat
US10188413B1 (en) 2004-04-21 2019-01-29 Acclarent, Inc. Deflectable guide catheters and related methods
US8905922B2 (en) 2004-04-21 2014-12-09 Acclarent, Inc. Devices, systems and methods for diagnosing and treating sinusitis and other disorders of the ears, nose and/or throat
US8932276B1 (en) 2004-04-21 2015-01-13 Acclarent, Inc. Shapeable guide catheters and related methods
US8945088B2 (en) 2004-04-21 2015-02-03 Acclarent, Inc. Apparatus and methods for dilating and modifying ostia of paranasal sinuses and other intranasal or paranasal structures
US9826999B2 (en) 2004-04-21 2017-11-28 Acclarent, Inc. Methods and apparatus for treating disorders of the ear nose and throat
US8961495B2 (en) 2004-04-21 2015-02-24 Acclarent, Inc. Devices, systems and methods for treating disorders of the ear, nose and throat
US11019989B2 (en) 2004-04-21 2021-06-01 Acclarent, Inc. Methods and apparatus for treating disorders of the ear nose and throat
US10441758B2 (en) 2004-04-21 2019-10-15 Acclarent, Inc. Frontal sinus spacer
US10492810B2 (en) 2004-04-21 2019-12-03 Acclarent, Inc. Devices, systems and methods for diagnosing and treating sinusitis and other disorders of the ears, nose and/or throat
US8894614B2 (en) 2004-04-21 2014-11-25 Acclarent, Inc. Devices, systems and methods useable for treating frontal sinusitis
US9649477B2 (en) 2004-04-21 2017-05-16 Acclarent, Inc. Frontal sinus spacer
US10500380B2 (en) 2004-04-21 2019-12-10 Acclarent, Inc. Devices, systems and methods useable for treating sinusitis
US9055965B2 (en) 2004-04-21 2015-06-16 Acclarent, Inc. Devices, systems and methods useable for treating sinusitis
US11020136B2 (en) 2004-04-21 2021-06-01 Acclarent, Inc. Deflectable guide catheters and related methods
US10631756B2 (en) 2004-04-21 2020-04-28 Acclarent, Inc. Guidewires for performing image guided procedures
US9089258B2 (en) 2004-04-21 2015-07-28 Acclarent, Inc. Endoscopic methods and devices for transnasal procedures
US9101384B2 (en) 2004-04-21 2015-08-11 Acclarent, Inc. Devices, systems and methods for diagnosing and treating sinusitis and other disorders of the ears, Nose and/or throat
US9107574B2 (en) 2004-04-21 2015-08-18 Acclarent, Inc. Endoscopic methods and devices for transnasal procedures
US10874838B2 (en) 2004-04-21 2020-12-29 Acclarent, Inc. Systems and methods for transnasal dilation of passageways in the ear, nose or throat
US9167961B2 (en) 2004-04-21 2015-10-27 Acclarent, Inc. Methods and apparatus for treating disorders of the ear nose and throat
US10856727B2 (en) 2004-04-21 2020-12-08 Acclarent, Inc. Endoscopic methods and devices for transnasal procedures
US20110112512A1 (en) * 2004-04-21 2011-05-12 Acclarent, Inc. Devices and methods for treating maxillary sinus disease
US9220879B2 (en) 2004-04-21 2015-12-29 Acclarent, Inc. Devices, systems and methods useable for treating sinusitis
US9241834B2 (en) 2004-04-21 2016-01-26 Acclarent, Inc. Devices, systems and methods for treating disorders of the ear, nose and throat
US9265407B2 (en) 2004-04-21 2016-02-23 Acclarent, Inc. Endoscopic methods and devices for transnasal procedures
US10695080B2 (en) 2004-04-21 2020-06-30 Acclarent, Inc. Devices, systems and methods for diagnosing and treating sinusitis and other disorders of the ears, nose and/or throat
US9351750B2 (en) 2004-04-21 2016-05-31 Acclarent, Inc. Devices and methods for treating maxillary sinus disease
US9370649B2 (en) 2004-04-21 2016-06-21 Acclarent, Inc. Devices, systems and methods useable for treating sinusitis
US9399121B2 (en) 2004-04-21 2016-07-26 Acclarent, Inc. Systems and methods for transnasal dilation of passageways in the ear, nose or throat
US9610428B2 (en) 2004-04-21 2017-04-04 Acclarent, Inc. Devices, systems and methods useable for treating frontal sinusitis
US20100198247A1 (en) * 2004-04-21 2010-08-05 Acclarent, Inc. Devices, Systems and Methods for Treating Disorders of the Ear, Nose and Throat
US10806477B2 (en) 2004-04-21 2020-10-20 Acclarent, Inc. Systems and methods for transnasal dilation of passageways in the ear, nose or throat
US9468362B2 (en) 2004-04-21 2016-10-18 Acclarent, Inc. Endoscopic methods and devices for transnasal procedures
US9554691B2 (en) 2004-04-21 2017-01-31 Acclarent, Inc. Endoscopic methods and devices for transnasal procedures
US10779752B2 (en) 2004-04-21 2020-09-22 Acclarent, Inc. Guidewires for performing image guided procedures
US10702295B2 (en) 2004-04-21 2020-07-07 Acclarent, Inc. Methods and apparatus for treating disorders of the ear nose and throat
US9084876B2 (en) 2004-08-04 2015-07-21 Acclarent, Inc. Implantable devices and methods for delivering drugs and other substances to treat sinusitis and other disorders
US9039657B2 (en) 2004-08-04 2015-05-26 Acclarent, Inc. Implantable devices and methods for delivering drugs and other substances to treat sinusitis and other disorders
US9039680B2 (en) 2004-08-04 2015-05-26 Acclarent, Inc. Implantable devices and methods for delivering drugs and other substances to treat sinusitis and other disorders
US9308361B2 (en) 2005-01-18 2016-04-12 Acclarent, Inc. Implantable devices and methods for treating sinusitis and other disorders
US8388642B2 (en) 2005-01-18 2013-03-05 Acclarent, Inc. Implantable devices and methods for treating sinusitis and other disorders
US8951225B2 (en) 2005-06-10 2015-02-10 Acclarent, Inc. Catheters with non-removable guide members useable for treatment of sinusitis
US10842978B2 (en) 2005-06-10 2020-11-24 Acclarent, Inc. Catheters with non-removable guide members useable for treatment of sinusitis
US10124154B2 (en) 2005-06-10 2018-11-13 Acclarent, Inc. Catheters with non-removable guide members useable for treatment of sinusitis
US8114113B2 (en) 2005-09-23 2012-02-14 Acclarent, Inc. Multi-conduit balloon catheter
US8968269B2 (en) 2005-09-23 2015-03-03 Acclarent, Inc. Multi-conduit balloon catheter
US9999752B2 (en) 2005-09-23 2018-06-19 Acclarent, Inc. Multi-conduit balloon catheter
US9050440B2 (en) 2005-09-23 2015-06-09 Acclarent, Inc. Multi-conduit balloon catheter
US10639457B2 (en) 2005-09-23 2020-05-05 Acclarent, Inc. Multi-conduit balloon catheter
US9198736B2 (en) 2006-05-17 2015-12-01 Acclarent, Inc. Adapter for attaching electromagnetic image guidance components to a medical device
US8190389B2 (en) 2006-05-17 2012-05-29 Acclarent, Inc. Adapter for attaching electromagnetic image guidance components to a medical device
US9629656B2 (en) 2006-05-17 2017-04-25 Acclarent, Inc. Adapter for attaching electromagnetic image guidance components to a medical device
US9179823B2 (en) 2006-09-15 2015-11-10 Acclarent, Inc. Methods and devices for facilitating visualization in a surgical environment
US9820688B2 (en) 2006-09-15 2017-11-21 Acclarent, Inc. Sinus illumination lightwire device
US9572480B2 (en) 2006-09-15 2017-02-21 Acclarent, Inc. Methods and devices for facilitating visualization in a surgical environment
US10716629B2 (en) 2006-09-15 2020-07-21 Acclarent, Inc. Methods and devices for facilitating visualization in a surgical environment
US9603506B2 (en) 2006-09-15 2017-03-28 Acclarent, Inc. Methods and devices for facilitating visualization in a surgical environment
US8439687B1 (en) 2006-12-29 2013-05-14 Acclarent, Inc. Apparatus and method for simulated insertion and positioning of guidewares and other interventional devices
US8118757B2 (en) 2007-04-30 2012-02-21 Acclarent, Inc. Methods and devices for ostium measurement
US9615775B2 (en) 2007-04-30 2017-04-11 Acclarent, Inc. Methods and devices for ostium measurements
US8485199B2 (en) 2007-05-08 2013-07-16 Acclarent, Inc. Methods and devices for protecting nasal turbinate during surgery
US9463068B2 (en) 2007-05-08 2016-10-11 Acclarent, Inc. Methods and devices for protecting nasal turbinates
US10206821B2 (en) 2007-12-20 2019-02-19 Acclarent, Inc. Eustachian tube dilation balloon with ventilation path
US11311419B2 (en) 2007-12-20 2022-04-26 Acclarent, Inc. Eustachian tube dilation balloon with ventilation path
US11850120B2 (en) 2007-12-20 2023-12-26 Acclarent, Inc. Eustachian tube dilation balloon with ventilation path
US8182432B2 (en) 2008-03-10 2012-05-22 Acclarent, Inc. Corewire design and construction for medical devices
US9861793B2 (en) 2008-03-10 2018-01-09 Acclarent, Inc. Corewire design and construction for medical devices
US10271719B2 (en) 2008-07-30 2019-04-30 Acclarent, Inc. Paranasal ostium finder devices and methods
US8979888B2 (en) 2008-07-30 2015-03-17 Acclarent, Inc. Paranasal ostium finder devices and methods
US11116392B2 (en) 2008-07-30 2021-09-14 Acclarent, Inc. Paranasal ostium finder devices and methods
US9750401B2 (en) 2008-07-30 2017-09-05 Acclarent, Inc. Paranasal ostium finder devices and methods
US11207087B2 (en) 2009-03-20 2021-12-28 Acclarent, Inc. Guide system with suction
US10524814B2 (en) 2009-03-20 2020-01-07 Acclarent, Inc. Guide system with suction
US9072626B2 (en) 2009-03-31 2015-07-07 Acclarent, Inc. System and method for treatment of non-ventilating middle ear by providing a gas pathway through the nasopharynx
US10376416B2 (en) 2009-03-31 2019-08-13 Acclarent, Inc. System and method for treatment of non-ventilating middle ear by providing a gas pathway through the nasopharynx
US9636258B2 (en) 2009-03-31 2017-05-02 Acclarent, Inc. System and method for treatment of non-ventilating middle ear by providing a gas pathway through the nasopharynx
US8435290B2 (en) 2009-03-31 2013-05-07 Acclarent, Inc. System and method for treatment of non-ventilating middle ear by providing a gas pathway through the nasopharynx
US9155492B2 (en) 2010-09-24 2015-10-13 Acclarent, Inc. Sinus illumination lightwire device
US10524869B2 (en) 2013-03-15 2020-01-07 Acclarent, Inc. Apparatus and method for treatment of ethmoid sinusitis
US9433437B2 (en) 2013-03-15 2016-09-06 Acclarent, Inc. Apparatus and method for treatment of ethmoid sinusitis
US9629684B2 (en) 2013-03-15 2017-04-25 Acclarent, Inc. Apparatus and method for treatment of ethmoid sinusitis
US11957318B2 (en) 2021-04-29 2024-04-16 Acclarent, Inc. Methods and apparatus for treating disorders of the ear nose and throat

Similar Documents

Publication Publication Date Title
US3393073A (en) High contrast photographic emulsions
US3839049A (en) Preparation of a silver salt of a fatty acid
US3150977A (en) Light-sensitive photographic materials
US2675316A (en) Photographic elements containing mordants
EP0099861B1 (en) Process for the preparation of photographic materials
US2875053A (en) Photographic elements containing polymeric esters as ultraviolet absorbing compounds
US3713833A (en) Preparation of silver salts in an organic liquid medium
US3947273A (en) Development modifiers for silver halide emulsions
US3178292A (en) Direct-print photographic silver halide emulsions
US3832181A (en) Photosensitive silver halide material containing a hydrophilic colloid hardened with a combination of formaldehyde and bis(vinylsulfonyl-methyl)ether
US3725064A (en) Photosensitive propargyl polymer composition and method of using
US3782959A (en) Polyhedral borane fogged direct-positive silver halide emulsion containing an organic sulfoxide
US3637394A (en) Photographic elements containing synthetic polymeric vehicles
US3359108A (en) Photographic emulsion having a low modulus of elasticity and process for its manufacture
US3620743A (en) Vehicles for vesicular photographic materials
US3624229A (en) Fixation of anions in hydrophilic colloid media
US3249440A (en) Radiation-sensitive elements and their preparation
US3110597A (en) Composition comprising gelatin and a potential hardener therefor
US3544327A (en) Polymeric fog stabilizers for photographic emulsions
US3576637A (en) Lith-type of emulsion containing pyrozolone
US3837861A (en) Gelatino-silver halide emulsions containing modified gelatin graft copolymers
US4186010A (en) Silver halide elements with polymers containing ketoiminoguanidinium groups
US3752674A (en) Silver halide emulsion fogged with a boron hydride and a gold compound
US3437486A (en) Monobasically sulfated vinyl copolymers as silver halide stabilizers
US3361563A (en) Cyanuric chloride sensitizer for halogen free-radical color-forming compositions