US3880665A - Hardening with a heterocyclic carbamoyl ammonium compound of a photographic material containing a silver halide layer - Google Patents

Hardening with a heterocyclic carbamoyl ammonium compound of a photographic material containing a silver halide layer Download PDF

Info

Publication number
US3880665A
US3880665A US362484A US36248473A US3880665A US 3880665 A US3880665 A US 3880665A US 362484 A US362484 A US 362484A US 36248473 A US36248473 A US 36248473A US 3880665 A US3880665 A US 3880665A
Authority
US
United States
Prior art keywords
layer
hardener
hardening
layers
compounds
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
US362484A
Inventor
Wolfgang Himmelmann
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.)
Agfa Gevaert AG
Original Assignee
Agfa Gevaert AG
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
Priority claimed from DE19722225230 external-priority patent/DE2225230C2/en
Priority claimed from DE19732317677 external-priority patent/DE2317677C2/en
Application filed by Agfa Gevaert AG filed Critical Agfa Gevaert AG
Application granted granted Critical
Publication of US3880665A publication Critical patent/US3880665A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
    • C07D213/16—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom containing only one pyridine ring
    • C07D213/20—Quaternary compounds thereof
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/28—Radicals substituted by singly-bound oxygen or sulphur atoms
    • C07D213/30—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72—Nitrogen atoms
    • C07D213/75—Amino or imino radicals, acylated by carboxylic or carbonic acids, or by sulfur or nitrogen analogues thereof, e.g. carbamates
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81—Amides; Imides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81—Amides; Imides
    • C07D213/82—Amides; Imides in position 3
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D217/00—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems
    • C07D217/02—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines
    • C07D217/10—Quaternary compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
    • C07D295/205—Radicals derived from carbonic acid
    • 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
    • G03C1/06—Silver halide emulsions; Preparation thereof; Physical treatment thereof; Incorporation of additives therein with non-macromolecular additives
    • G03C1/30—Hardeners

Definitions

  • ABSTRACT As rapidly acting hardeners for protein-containing photographic layers carbamoyl ammonium compounds are used the quaternised nitrogen atom of which being present in a 5- or 6-membered heterocyclic aromatic group.
  • metal salts such as chromium, aluminium or zirconium salts, aldehydes and halogenated aldehyde compounds, in particular formaldehyde, dialdehydes and mucochloric acid, 1,2- and 1,4-diketones such as cyclohexane-l,2-dione and quinones as well as chlorides of dibasic organic acids, the anhydrides of tetracarboxylic acids, compounds which contain several reactive vinyl groups such as vinyl sulfones, acrylamides, compounds containing at least two heterocyclic threemembered rings which can easily be split off, such as ethylene oxide and ethylene imine, polyfunctional methane sulfonic acid esters and bis-oz-chloracylamido compounds.
  • metal salts such as chromium, aluminium or zirconium salts, aldehydes and halogenated aldehyde compounds, in particular formaldehyde, dialdehydes and mucochloric
  • High molecular weight hardeners which are used particularly as hardeners of which the effect is to be confined to the layer having recently become known, for example polyacrolein and its derivatives or copolymers and alginic acid derivatives.
  • Some cross-linking agents for gelatin for example the ethylene imine compounds, also have a harmful effect on the skin and are therefore in any case unsuitable on physiological grounds.
  • Hardening of the compounds is quite satisfactory after a certain time but the compounds are only sparingly soluble in water so that hardening is liable to be irregular within the layer.
  • a process for hardening photographic layers which contain proteins and preferably gelatin has now been found which is characterised by the use of a hardener which contains in the molecule at least one carbamoyl radical with a heterocyclic, aromatic S-membered or 6-membered ring which in addition to a quaternary nitrogen atom may also contain other hetero atoms.
  • the hardeners of this invention correspond to the following general formula R R X N-CO-N Z X R/ l inwhich R represents a substituted or unsubstituted alkyl group preferably containing 1 to 3 carbon atoms, an aryl group optionally substituted with a lower alkyl radical or with halogen, e.g., phenyl, if desired substituted with methyl, ethyl or propyl, C1 or Br, or an aralkyl group, e.g., benzyl, which may be substituted in the same manner as the aryl group;
  • R has the same meaning as R or it may represent a divalent optionally substituted alkylene, arylene, aralkylene or alkyl-aryl-alkyl radical, e.g., an ethylene, propylene, phenylene or xylylene radical which is attached by its second bond to a further carbamoyl ammonium group of the formula R 4 1 --1?
  • iZ X 01" R R, and R may together represent a group required to complete a substituted or unsubstituted heterocyclic ring, such as piperidine, piperazine, or morpholine ring which may be substituted e.g., with an alkyl group containing 1 to 3 carbon atoms or with halogen such as C1 or Br;
  • R represents hydrogen or an alkyl group containing 1 to 3 carbon atoms or the group R represents an alkyl, aryl or aralkyl group but R is absent if the nitrogen to which R is attached is involved in a double bond in the heterocyclic aromatic ring formed by Z,
  • Z represents the atomic grouping required to complete a S-membered or 6-membered aromatic ring optionally substituted on the nitrogen atom, e.g., with an alkyl group containing 1 to 3 carbon atoms or it may represent the atomic grouping required to complete a condensed system such as isoquinoline, which atomic grouping may contain other hetero atoms in addition to the nitrogen atom, e.g., O or S, and
  • X represents an acid anion such as halogen Bfl
  • the preparation of the other compounds is carried out in a corresponding manner.
  • the salts can be easily prepared by addition of the suitable acids.
  • the compounds used according to the invention are preferably added to the protein layers which are to be hardened immediately before they are cast, preferably in the form of aqueous or alcoholic solutions. It is necessary to add them only shortly before the layers are cast because they react very rapidly with gelatin or other proteins normally used in photography. Once the compounds have been added, the casting solutions should be cast within a few minutes. The rate at which the hardening reaction takes place depends primarily on the concentration of proteins in the casting solution.
  • Another possiblity consists in casting solutions which have not been hardened and then coating the resulting layers with a solution of the hardening compounds.
  • photographic layers which have not been hardened or only slightly hardened may be bathed in aqueous solutions of the compounds containing sodium sulfate at some stage of processing the photographic material, for example before development.
  • photographic layers is used in this context as a general term to denote any layers used in photographic materials, for example light sensitive silver halide emulsion layers, protective layers, filter layers, antihalation layers, back coating layers or, in general, any photographic auxiliary layers.
  • the light sensitive emulsion layers for which the hardening process according to the invention is particularly suitable are, for example, those layers which are based on non-sensitized emulsions, orthochromatic, panchromatic or infra-red emulsions, X-ray emulsions and other emulsions which are spectrally sensitized.
  • the hardening process according to the invention has also proved suitable for hardening gelatin layers used for various black-and-white photographic processes and colour photographic processes.
  • the process according to the invention has proved particularly advantageous for hardening composite photographic layers used for colour photographic processes, e.g., those which contain emulsion layers with colour couplers or emulsion layers which are designed to be treated with solutions which contain colour couplers.
  • the effect of the compounds used according to the invention is not impaired by the usual photographic additives and the hardeners are also uneffected by photographically active substances such as water-soluble or emulsified water insoluble dry components, stabilizers, sensitizers and the like. Moreover, they have no influence on the light sensitive silver halide emulsions. They may be combined with any compounds from the known classes of hardeners, for example formalin, mucochloric acid, triacrylic formal, bis-vinylsulfones, bisvinylsuflonamides, dialdehydes or bischloroacetamides.
  • hardeners for example formalin, mucochloric acid, triacrylic formal, bis-vinylsulfones, bisvinylsuflonamides, dialdehydes or bischloroacetamides.
  • the layers may also contain water-soluble high polymer compounds, in particular polyvinyl alcohol, polyacrylic acid sodium and other copolymers which contain carboxyl groups, polyvinyl pyrrolidone, polyacrylamide or high molecular weight natural substances such as dextrans, dextrins, starch ether,alginic acid or alginic acid derivatives.
  • water-soluble high polymer compounds in particular polyvinyl alcohol, polyacrylic acid sodium and other copolymers which contain carboxyl groups, polyvinyl pyrrolidone, polyacrylamide or high molecular weight natural substances such as dextrans, dextrins, starch ether,alginic acid or alginic acid derivatives.
  • concentrations at which the hardeners according to the invention are used may vary within wide limits and depend mainly on the hardening compound used.
  • the hardening reaction between the compounds according to the invention and gelatin or proteins sets in immediately so that the optimum degree of hardening is reached more or less simultaneously with drying of the layers after they are cast or processed.
  • the activity of the hardening compounds is determined by means of the melting point of the layers, which can be found as follows: Half of a layer cast on a support is dipped in water which is continuously heated up to C. The temperature at which the layer runs from the support (formation of streaks) is taken as the melting point or melting off point. When measured by this method, no increase in melting point is found in any pure protein layers or gelatin layers which contain no hardener, on the contrary the layers run off at 3035C.
  • the compounds according to the invention react surprisingly quickly with proteins and therefore enable materials which contain proteins to be hardened to their optimum degree of hardness within a very short time.
  • This unexpected effect of the compounds is particularly important for the hardening of photographic materials which contain proteins as binders. Hardening can be adjusted to the required degree in a readily controlled nammer at the stage of preparation of the materials and does not require prolonged storage times with the concomitant unreliability of uncontrollable after hardening.
  • EXAMPLE 1 l by weight and 2 by weight, respectively, of compounds 2. l9 and 20 based on the dry weight of gelatin, are added in the form of an aqueous solution at pH 6.2 to 100 ml portions of a photographic silver bromide gelatin emulsion containing 10 by weight of gelatin which is ready for casting. The mixture is vigorously stirred and immediately cast on a prepared cellulose triacetate support by means of a conventional casting apparatus and dried. The usual additives are not altered. After a storage time of 24 hours at room temperature, the melting points of the layers are measured.
  • EXAMPLE 2 14 EXAMPLE 3 A 10 casein solution in water is prepared by the addition of sodium hydroxide solution. The solution is divided in 9 parts of 100 ml and 0.1 g of tartrazine is added as filter dye to each solution. 3 by weight of compounds 2, 19, 20, 21, 24, 25, 30, 31 and 37 dissolved in water are added at pH 7 before casting. The mixtures are cast on glass plates and hardened filter foils which are no longer soluble in aqueous alkali are obtained after drying.
  • EXAMPLE 4 A 20 by weight of solution of zein is prepared in a mixture of ethanol and water (8:2) and cast on the back of a cellulose acetate film. After drying, a layer which is readily soluble in a mixture of ethanol and water is obtained.
  • EXAMPLE 5 An unhardened silver halide emulsion containing 10 by weight of gelatin as binder is cast on a triacetyl cellulose support without the addition of a hardener. The layer contains all the other usual additives. Samples of the dried layer are coated with 0.5, l, 2 and 3 aqueous solutions of compounds 1. 2. 5, 24, 29 and 33 and then dried. The melting points, degree of swelling and resistance to scratching when wet are then determined on the layers. The results are summarized in the following Table.
  • the degrees of swelling are determined gravimetrically after 10 minutes treatment of the layers in distilled water at 22C and are indicated in percent.
  • a metal point of a specified size is passed over the wet layer and loaded with an increasingly heavy weight.
  • the wet scratch resistance is indicated by the weight at which the point leaves a visible scratch trace on the layer. The larger the weight the higher the scratch resisimmersion time layer melting points remarks in minutes in "C 50 tance.
  • compound comgound compound layer swelling wet scratch melting point in 7 resistance 0.5 50C 60C in p l 100C 100C soft layer 5 5 2 l00C l00C increased strength campound of layer 0.5 it 355 750 3 100C l00C very high strength 1 7, 3K) 850 of layer 2 l0 H10 280 950 untreated layer 34C 3 250 950 60 gompound 2: .5 "l 325 950 At a bath temperature of 40C, the required tmmerl o, 295 950 sion times are much shorter and layer melting points 2 3 H 52? 8 above 100C are obtained after only 45 seconds.
  • the layer is not dissolved off after l0 minutes in boiling water.
  • EXAMPLE 7 The usual additives with the exception of a hardener EXAMPLE 6 are added tp 100 ml o fa phpoqgrzgphic siLverfbrolmide e atln emu sion contalnm wei t 0 e atin. 25 by weight, based on the weight of the gelatin, g g 0 y g g f b] l f th f n f l The mixture is cast 0 a ue green coup er 0 e o owing ormu a a on baryta paper and b. on paper backed with polyethylene on both sides.
  • a 4p. green sensitive middle layer which contains 35 g of silver bromide, 80 g of gelatin and 16 g of top coating melting swelling wet scratch 'p y' p y fpy point in 7r resistance in p 5 per k f CmUISiOn, compound I: 4. a 2p. yellow filter layer of colloidal silver in gelatin, 0.5 1o'
  • a 4 blue sensitive top layer which contains 35 Z: 32 8 328 g of silver bromide, g of gelatin and 20 g 3- 3 250 950 stearylammobenzoyl acetyl-S, 3-d1carboxyanilide per kg of emulsion and compound 2: I 0 0 6 2 I f l 0.5 10 C 325 950 a u protective ayer o ge atm 22 2 is cast in known manner on a layer support of cellulose 3 235 1150 triacetate p. in thickness and dried. The film is coated with a l aqueous solution and a 2 aqueous gg a l c 350 850 65 solution of compounds 2 5, l9 and 30. l 3 8 2 The layer melting points and the temperatures at g 250 50 which the layers dissolve off are determined after drying and 12 hours storage at room temperature.
  • temperature 1 A process for providing a protein-containing with n Coalmg M layer mcltlng P f binder selected from the group consisting of gelatin, ca-
  • a photographic silver halide emulsion compound 2 1% 752C 10'100C layer coated on a support wherein the improvement comprises incorporating in a binder for the layer a compound 5 l 7? 100 C l0 100 C 2 100C g'mo c hardening amount of a hardener of the formula compound 19 l 70 l00C l0'l0OC 2 7! 100C l0'l0OC compound 30 l 71. l00C l0'l00C 2 7!
  • R is selected from the group consisting of alkyl, aryl, aralkyl groups and the methylene group substituted with a group of the formula 40 ml of a 5 70 aqueous solution of polyacrylic acid sodium salt and 10 ml of a 40 SiO suspension are added to 100 ml of a 10 gelatin solution. The solution is vigorously mixed. 0.2 g of compounds 6 and 20 are added to each 100 ml of the solution. Then the pH is adjusted to 6.2 and the mixtures are cast on cellulose triacetate supports. Layers with a melting point above N co N 100C and exellent wet strength are obtained after drying and 12 hours storage. A layer without the addition CH ONH2 of the compounds according to the invention melts in water at 40C.
  • 0.2 g of compounds 6 and 23 are added to l00 ml of R5 is Selacted f the group of one alkyl 10 aqueous solutions of acetyl gelatin which have gro ups ar ld not f when the mtmgFn to been obtained by reacting gelatin with 20 acetic anwhch attached car nes double bond f the hydride and the mixtures are cast on cellulose acetate hetemcychc aromatc rmg formed by Substltuted films. A layer containing 0.2 g of formalin instead of compounds 6 and 23 is cast for comparison.
  • the layers containing compounds 6 and 23 are re- 6'membered heterocycllc 8 whlch y sistant to boiling whereas the layer which has been Include one or more Condensed mugs and one or hardened with formalin melts at temperatures below more heleroa'loms,
  • R stands for -NR -c0-R R H, alkyl (llc) R H, alkyl (1-4 G) 9 o R", R H, alkyl (c -c 2)m lO ll R10 l2 R H, alkyl (c -c R12: H, alkyl (c -c R alkyl (c -c aryl R1 H, alkyl, aryl ..(CH -CONR R R H, alkyl (c -c aryl R H, alkyl (c -ci or R and R together represent the atomic grouping required to complete a S
  • R H alkyl, -c0-R -CO-NHR
  • R R20, R21 H alkyl
  • c -c X is the anion radical of the formula, or poly-4-vinyl- N,N-dimethyl-carbamoyl-pyridinium chloride having molecular weight of about 10,000.
  • Page 1 of 2 Column 4 lines 17 & 18 should read as follows X represents an acid anion such as halogen BF N0 S0 010;, cn oso Column 6, formula 12, the left-hand ring should read as follows Column 18, the right-hand side of the first formula should read as follows GB N Column 18, the right-hand side of the second formula should CONH UNITED STATES PATENT AND TRADEMARK OFFICE CERTIFICATE OF CORRECTION PATEN N 3,880,665 Page 2 of 2 DATED :April 29, 1975 INVENTOR(S) t Wolfgang Himmelmann It is certified that error appears in the ab0ve-identified patentand that said Letters Patent are hereby corrected as shown below:
  • the hardener is polyr-vinyl-N,N-dimethyl-carbamoylpyridinium chloride having molecular weight of about 10,000.

Abstract

As rapidly acting hardeners for protein-containing photographic layers carbamoyl ammonium compounds are used the quaternised nitrogen atom of which being present in a 5- or 6-membered heterocyclic aromatic group.

Description

United States Patent [191 Himmelmann 1 Apr. 29, 1975 I-IARDENING WITH A IIETEROCYCLIC CARBAMOYL AMMONIUM COMPOUND OF A PI-IOTOGRAPI-IIC MATERIAL CONTAINING A SILVER HALIDE LAYER Wolfgang IIimrnelmann, Opladen, Germany Assignee: Agfa-Gevaert Aktiengesellschaft,
Leverkusen, Germany Filed: May 21, 1973 Appl. No.: 362,484
Inventor:
Foreign Application Priority Data May 24, 1972 Germany 2225230 Apr. 7, 1973 Germany 2317677 US. Cl. 96/111; 106/125; 260/117;
427/338 Int. Cl G03c 1/30 [58] Field of Search 260/117; 96/111; 106/125;
Primary ExaminerNorman G. Torchin Assistant Examiner-Won H. Louie, Jr. Attorney, Agent, or FirmConno11y and Hutz [57] ABSTRACT As rapidly acting hardeners for protein-containing photographic layers carbamoyl ammonium compounds are used the quaternised nitrogen atom of which being present in a 5- or 6-membered heterocyclic aromatic group.
8 Claims, N0 Drawings HARDENING WITH A HETEROCYCLIC CARBAMOYL AMMONIUM COMPOUND OF A PHOTOGRAPHIC MATERIAL CONTAINING A SILVER HALIDE LAYER This invention relates to a process for hardening photographic layers which contain protein and in particular contain gelatin.
Numerous substances have already been described as hardeners for protein and in particular for gelatin, for example metal salts such as chromium, aluminium or zirconium salts, aldehydes and halogenated aldehyde compounds, in particular formaldehyde, dialdehydes and mucochloric acid, 1,2- and 1,4-diketones such as cyclohexane-l,2-dione and quinones as well as chlorides of dibasic organic acids, the anhydrides of tetracarboxylic acids, compounds which contain several reactive vinyl groups such as vinyl sulfones, acrylamides, compounds containing at least two heterocyclic threemembered rings which can easily be split off, such as ethylene oxide and ethylene imine, polyfunctional methane sulfonic acid esters and bis-oz-chloracylamido compounds.
High molecular weight hardeners which are used particularly as hardeners of which the effect is to be confined to the layer having recently become known, for example polyacrolein and its derivatives or copolymers and alginic acid derivatives.
Many of the above mentioned compounds, however, are unsuitable, in particular for photographic purposes. Some of them are photographically active and therefore unsuitable for hardening photographic materials whereas others cannot be used because they have such a deleterious effect on the physical properties, for example the fragility of the gelatin layers. Others again cause discoloration or alter the pH in the course of the hardening reaction. Furthermore, for hardening photographic layers it is particularly important that the hardening effect should attain its maximum as soon as possible after drying so that the material which is being hardened will not constantly change its permeability to the developer solution as, for example in the case of mucochloric acid or formaldehyde.
Some cross-linking agents for gelatin, for example the ethylene imine compounds, also have a harmful effect on the skin and are therefore in any case unsuitable on physiological grounds.
It has long been known to use trichlorotriazine and dichloroaminotriazines as hardeners. The disadvantage of these compounds is their relatively high vapour pressure and their physiological effect. Water-soluble derivatives which contain carboxylic and sulphonic acid groups and are obtained by reacting cyanuric acid chloride with 1 mol of a diaminoalkyl or diaminoarylsulfonic acid or carboxylic acid to not have these disadvantages and have therefore recently been proposed as hardeners. Their usefulness in practice is, however, limited because owing to their high solubility they decompose when left to stand in aqueous solutions and therefore rapidly lose their effectiveness. Hydroxydichlorotriazine has also been proposed as hardener. Lastly, in the case of a hardener used for photographic layers which contain gelatin, it is of major importance both for manufacturing and for processing reasons that the onset of the cross-linking reaction should be controllable within certain limits, for example by choice of the correct drying temperature of pH.
Compounds which contain two or more acrylic acid amide groups or vinylsulphone groups in the molecule are also known as hardeners for photographic gelatin layers, e.g. divinylsulfone, arylene-bis-vinylsulfones, N,N', N"-tris-acryloyl-hydrotriazine or methylene-bisvinyl-sulfonamide. I
Hardening of the compounds is quite satisfactory after a certain time but the compounds are only sparingly soluble in water so that hardening is liable to be irregular within the layer.
The consequences of the undesirable properties of known hardness indicated above are of great importance for photographic purposes because important photographic properties such as the gradation and sensitivity and in many cases also the silver covering power depend on the degree of cross-linking of the layerforming colloid and undergo changes in the course of storage. Although this disadvantage can be attenuated by a brief after-treatment of the solidified layer with ammonia or an amine, it cannot be completely eliminated. To this is added the fact that aliphatic divinylsulfones tend to damage the skin.
It is an object of this invention to develop rapidly acting hardeners for layers which contain proteins, and in particular for gelatin layers, which are used for photographic purposes.
A process for hardening photographic layers which contain proteins and preferably gelatin has now been found which is characterised by the use of a hardener which contains in the molecule at least one carbamoyl radical with a heterocyclic, aromatic S-membered or 6-membered ring which in addition to a quaternary nitrogen atom may also contain other hetero atoms.
The hardeners of this invention correspond to the following general formula R R X N-CO-N Z X R/ l inwhich R represents a substituted or unsubstituted alkyl group preferably containing 1 to 3 carbon atoms, an aryl group optionally substituted with a lower alkyl radical or with halogen, e.g., phenyl, if desired substituted with methyl, ethyl or propyl, C1 or Br, or an aralkyl group, e.g., benzyl, which may be substituted in the same manner as the aryl group;
R has the same meaning as R or it may represent a divalent optionally substituted alkylene, arylene, aralkylene or alkyl-aryl-alkyl radical, e.g., an ethylene, propylene, phenylene or xylylene radical which is attached by its second bond to a further carbamoyl ammonium group of the formula R 4 1 --1? iZ X 01" R R, and R may together represent a group required to complete a substituted or unsubstituted heterocyclic ring, such as piperidine, piperazine, or morpholine ring which may be substituted e.g., with an alkyl group containing 1 to 3 carbon atoms or with halogen such as C1 or Br;
R represents hydrogen or an alkyl group containing 1 to 3 carbon atoms or the group R represents an alkyl, aryl or aralkyl group but R is absent if the nitrogen to which R is attached is involved in a double bond in the heterocyclic aromatic ring formed by Z,
Z represents the atomic grouping required to complete a S-membered or 6-membered aromatic ring optionally substituted on the nitrogen atom, e.g., with an alkyl group containing 1 to 3 carbon atoms or it may represent the atomic grouping required to complete a condensed system such as isoquinoline, which atomic grouping may contain other hetero atoms in addition to the nitrogen atom, e.g., O or S, and
X represents an acid anion such as halogen Bfl,
ii, CHgOSOg.
The following compounds have proved to be particularly useful. The list is given only by way of example and is not intended to limit the scope of the invention.
-NR -CO-R R H,alkyl (l-u c) R H,a1kyl (1-4 0) NR R R 3 H,alkyl (c -c,
2 m lO l1 R10 l2 R H,alkyl (c -c R H,alkyl (c -c R12 lfi l l- 3 R alkyl (C -C aryl R H,alkyl,aryl
-(CH -co'nra a R H, alkyl (C -C aryl R H, alkyl (C -C or R and R together represent the atomic grouping required to complete a 5-membered or 6-membered aliphatic ring,
17 17 -(CH -CH-R R H,alkyl (C -C optlonally substltuted p l by halogen Y 18 Y -0-, -NR
R H, alkyl, -CO-R -c0-1 IHH R R ,R 'H, alkyl (c -c oil (9 NH-CO-NHCH 37.@-co-@ C19 58. ffi 9 \N- 00 l\ -NH-COCH 01 G) CH 59. G) mucocn 40 N CO C19 @v CONH A0 CHKN co 2 HZ/ C1 methyl-carbamoyl-pyridinium chloride (compound 6) which is used as an example: A. Phenyl-methyI-carbamoy] chloride 49.5 g of phosgene are carefully introduced into 400 cc of absolute toluene with cooling (22 to 25C). A so lution of 107 g of distilled N-methylaniline in 450 cc of absolute toluene is added dropwise to this solution with vigorous stirring. The mixture is then heated for l/2 hour at to 90C and cooled and the precipitated hydrochloride is suction filtered. Lastly, the solution in toluene is evaporated to dryness under vacuum with exclusion of moisture. The residue crystallises on cooling. Yield: 81 g, melting point 85C. B. 33.9 g of Compound A are stirred into 400 cc of absolute pyridine the reaction being conducted in a dark room with exclusion of moisture. The carbamoylpyridinium chloride formed precipitates after 3 hours. After the addition of an equal quantity of ether, the crystals are suction filtered, taken up with a small quantity of absolute ethanol and again precipitated with ether. The product is again suction filtered, washed thoroughly with ether and dried in a desiccator. Yield: 4] g, melting point l08l 10C.
The poly-4-vinyl-N,N-dimethyl-carbamoylpyridinium chloride corresponding to Compound 15 is prepared as follows:
l0.5 g of poly-4-vinyl-pyridinc (molecular weight) 10000) are dissolved in 150 ml of absolute ethanol. and
[0.8 g of dimethylcarbamic acid chloride are added with vigorous stirring.
Q/N co c1 49.5 g phosgene are slowly introduced into 400 ml of absolute toluene. A solution of 87 g of destilled morpholine in 450 ml of absolute toluene is added dropwise to this solution with vigorous stirring. The mixture is then heated for one-half hour at 80 to 90C and coated, and the precipitated hydrochloride is suction filtered and washed with absolute toluene. Lastly the filtrate is evaporated to dryness under vacuum with exclusion of moisture. It remains on oil which is destilled. Yield: 50 g, boiling point 72C. B. preparation of compound 30 l/20 mol of compound A were stirred into a solution of 1/20 mol of 3-acetaminopyridine in 60 ml of chlorofrom. The mixture is stirred for 2 hours at 50C with exclusion of moisture. The chloroform is then evaporated under vacuum and the highly viscous residue is mixed with a small amount of absolute ethyl ether. Then the crystalline product is suction filtered, washed with absolute ethyl ether and dried in a desiccator. Yield g, melting point ll8-123C.
The preparation of the other compounds is carried out in a corresponding manner. The salts can be easily prepared by addition of the suitable acids.
The compounds used according to the invention are preferably added to the protein layers which are to be hardened immediately before they are cast, preferably in the form of aqueous or alcoholic solutions. It is necessary to add them only shortly before the layers are cast because they react very rapidly with gelatin or other proteins normally used in photography. Once the compounds have been added, the casting solutions should be cast within a few minutes. The rate at which the hardening reaction takes place depends primarily on the concentration of proteins in the casting solution.
Another possiblity consists in casting solutions which have not been hardened and then coating the resulting layers with a solution of the hardening compounds. Alternatively, photographic layers which have not been hardened or only slightly hardened may be bathed in aqueous solutions of the compounds containing sodium sulfate at some stage of processing the photographic material, for example before development.
The term photographic layers is used in this context as a general term to denote any layers used in photographic materials, for example light sensitive silver halide emulsion layers, protective layers, filter layers, antihalation layers, back coating layers or, in general, any photographic auxiliary layers.
The light sensitive emulsion layers for which the hardening process according to the invention is particularly suitable are, for example, those layers which are based on non-sensitized emulsions, orthochromatic, panchromatic or infra-red emulsions, X-ray emulsions and other emulsions which are spectrally sensitized. The hardening process according to the invention has also proved suitable for hardening gelatin layers used for various black-and-white photographic processes and colour photographic processes.
The process according to the invention has proved particularly advantageous for hardening composite photographic layers used for colour photographic processes, e.g., those which contain emulsion layers with colour couplers or emulsion layers which are designed to be treated with solutions which contain colour couplers.
The effect of the compounds used according to the invention is not impaired by the usual photographic additives and the hardeners are also uneffected by photographically active substances such as water-soluble or emulsified water insoluble dry components, stabilizers, sensitizers and the like. Moreover, they have no influence on the light sensitive silver halide emulsions. They may be combined with any compounds from the known classes of hardeners, for example formalin, mucochloric acid, triacrylic formal, bis-vinylsulfones, bisvinylsuflonamides, dialdehydes or bischloroacetamides.
Apart from gelatins, the layers may also contain water-soluble high polymer compounds, in particular polyvinyl alcohol, polyacrylic acid sodium and other copolymers which contain carboxyl groups, polyvinyl pyrrolidone, polyacrylamide or high molecular weight natural substances such as dextrans, dextrins, starch ether,alginic acid or alginic acid derivatives.
The concentrations at which the hardeners according to the invention are used may vary within wide limits and depend mainly on the hardening compound used.
Satisfactory results are obtained with quantities of 0.1 to 10 by weight and particularly 0.2 to 6 by weight, based on the dry weight of binder.
As already mentioned above, the hardening reaction between the compounds according to the invention and gelatin or proteins sets in immediately so that the optimum degree of hardening is reached more or less simultaneously with drying of the layers after they are cast or processed.
The activity of the hardening compounds is determined by means of the melting point of the layers, which can be found as follows: Half of a layer cast on a support is dipped in water which is continuously heated up to C. The temperature at which the layer runs from the support (formation of streaks) is taken as the melting point or melting off point. When measured by this method, no increase in melting point is found in any pure protein layers or gelatin layers which contain no hardener, on the contrary the layers run off at 3035C.
The compounds according to the invention react surprisingly quickly with proteins and therefore enable materials which contain proteins to be hardened to their optimum degree of hardness within a very short time. This unexpected effect of the compounds is particularly important for the hardening of photographic materials which contain proteins as binders. Hardening can be adjusted to the required degree in a readily controlled nammer at the stage of preparation of the materials and does not require prolonged storage times with the concomitant unreliability of uncontrollable after hardening.
An additional advantage is brought by the carbamolypyridinium compounds the pyridine ring of which is substituted with hydrocarbon residues having more than 3 carbon atoms. Examples for compounds of this group are compounds 19-40.
Compounds of this shape are practically unodorous, so that the application as hardeners can be carried out without odorous annoyance. The advantage of the inodorousness of the pyridinium compounds becomes particularly clear considering the fact that the limit of perceptibility of pyridine through the sense of smell already begins at 0.0004 mg/m in air. Since the above pyridinium compounds turn out to be odorless they 13 give sufficients security that exceeding the Threshold limit value" of pyridine which is of the order of 15 mg/m is virtually impossible.
The invention will now be explained with the aid of the following examples.
EXAMPLE 1 l by weight and 2 by weight, respectively, of compounds 2. l9 and 20 based on the dry weight of gelatin, are added in the form of an aqueous solution at pH 6.2 to 100 ml portions of a photographic silver bromide gelatin emulsion containing 10 by weight of gelatin which is ready for casting. The mixture is vigorously stirred and immediately cast on a prepared cellulose triacetate support by means of a conventional casting apparatus and dried. The usual additives are not altered. After a storage time of 24 hours at room temperature, the melting points of the layers are measured.
compound quantity layer melting points added in "C 7: (without 34 hardening) 2 l 7i 100 2 7i l00 l9 1 l00 2 7i 100 20 1 9t l00 2 7r l00 The cross-linking reaction is so intensive that the layers do not dissolve even after minutes in boiling water.
EXAMPLE 2 14 EXAMPLE 3 A 10 casein solution in water is prepared by the addition of sodium hydroxide solution. The solution is divided in 9 parts of 100 ml and 0.1 g of tartrazine is added as filter dye to each solution. 3 by weight of compounds 2, 19, 20, 21, 24, 25, 30, 31 and 37 dissolved in water are added at pH 7 before casting. The mixtures are cast on glass plates and hardened filter foils which are no longer soluble in aqueous alkali are obtained after drying.
EXAMPLE 4 A 20 by weight of solution of zein is prepared in a mixture of ethanol and water (8:2) and cast on the back of a cellulose acetate film. After drying, a layer which is readily soluble in a mixture of ethanol and water is obtained.
If strips of the film are bathed in solutions of 2 g of compounds 2, 19, 2O, 21, 26, 3l, 32. 35. 37.
38 or 39 15 g of sodium sulfate and 80 ml of water for 3 minutes and then briefly washed and dried in a heating cupboard at to C, the layers are insoluble in all solvents and effectively cross-linked.
EXAMPLE 5 An unhardened silver halide emulsion containing 10 by weight of gelatin as binder is cast on a triacetyl cellulose support without the addition of a hardener. The layer contains all the other usual additives. Samples of the dried layer are coated with 0.5, l, 2 and 3 aqueous solutions of compounds 1. 2. 5, 24, 29 and 33 and then dried. The melting points, degree of swelling and resistance to scratching when wet are then determined on the layers. The results are summarized in the following Table.
The degrees of swelling are determined gravimetrically after 10 minutes treatment of the layers in distilled water at 22C and are indicated in percent.
To determine the resistance to scratching when wet, a metal point of a specified size is passed over the wet layer and loaded with an increasingly heavy weight. The wet scratch resistance is indicated by the weight at which the point leaves a visible scratch trace on the layer. The larger the weight the higher the scratch resisimmersion time layer melting points remarks in minutes in "C 50 tance.
compound comgound compound layer swelling wet scratch melting point in 7: resistance 0.5 50C 60C in p l 100C 100C soft layer 5 5 2 l00C l00C increased strength campound of layer 0.5 it 355 750 3 100C l00C very high strength 1 7, 3K) 850 of layer 2 l0 H10 280 950 untreated layer 34C 3 250 950 60 gompound 2: .5 "l 325 950 At a bath temperature of 40C, the required tmmerl o, 295 950 sion times are much shorter and layer melting points 2 3 H 52? 8 above 100C are obtained after only 45 seconds.
The stability of the hardeners according to the inven- Compfiung 5; tion in aqueous solutions depends on the additives $2 8 3-28 used. In distilled water, the hardeners are still active 3? W 2%?) ltfgg after 3 days.
-Continued -Continued compound layer swelling wct scmtch top coating melting swelling wet scratch making P I" reslsmncc point in 7: resistance in p p 5 compound 19: compound 24: 0.5 71 '|00c 410 650 0.5 70 400 650 l 7: 350 750 l 300 750 2 7r 300 800 2 7c l0'l00* 250 850 3 7: 280 900 3 200 900 d 29 10 compound 20: compoun 0.5 7 l 'l 0C 0.5 320 900 l 0 0 fig 338 l 2 280 850 2 lO'l00 250 1100 3 7! 250 200 3 250 I000 compound 25: gg g 400 650 0.5 10'1o0c 410 600 1' 7- 350 750 l 2 71 10' 100 300 950 2 300 700 3 v1 260 1100 3 270 800 110! afteronly treated 42C 800 treated 600 800 300 with water 8 36 The photographic properties were not affected.
The layer is not dissolved off after l0 minutes in boiling water.
EXAMPLE 7 The usual additives with the exception of a hardener EXAMPLE 6 are added tp 100 ml o fa phpoqgrzgphic siLverfbrolmide e atln emu sion contalnm wei t 0 e atin. 25 by weight, based on the weight of the gelatin, g g 0 y g g f b] l f th f n f l The mixture is cast 0 a ue green coup er 0 e o owing ormu a a on baryta paper and b. on paper backed with polyethylene on both sides. 0H After drying, samples of the two materials are bathed for 2 minutes in aqueous solutions contain- I 1s 37 ing 3 g of compounds 2, 5, 10, ll, 12, 13, 14, 19, 35 20, 22, 25, 28, 32, 34, 36 and 37 in 100 ml of wag H ter. The layers obtained after drying and 12 hours 5 storage are in all cases resistant to boiling (layer melting points above 100C). The hardening effect are added to an unhardened silver halide emulsion 40 obtamd Independent of the pp y which contains l0 by weight of gelatin. The usual cm which have not been treated at 37 C casting additives with the exception of a hardener are EXAMPLE 8 then added to the emulsion. The mixture is cast on a t prepared l h l terephthalate Support d d i d, An unhardened multllayered colour film consisting Samples of this layer are then coated with 0.5 to 3 of aqueous solutions of the compounds according to the l. A bottom red sensitive layer 4p. in thickness which invention. After drying and 10 hours storage, layers contains 35 g of silver bromide, 80 g of gelatin and with an exceptionally high degree of cross-linking are 24 g of l-hydroxy-4-sulfo-2-naphthoic acid hepobtained. The results are summarized in the following t d l id per k f e l i Tables. 5 2. a 2;; interlayer of gelatin,
3. a 4p. green sensitive middle layer which contains 35 g of silver bromide, 80 g of gelatin and 16 g of top coating melting swelling wet scratch 'p y' p y fpy point in 7r resistance in p 5 per k f CmUISiOn, compound I: 4. a 2p. yellow filter layer of colloidal silver in gelatin, 0.5 1o'|00c 355 750 5. a 4 blue sensitive top layer which contains 35 Z: 32 8 328 g of silver bromide, g of gelatin and 20 g 3- 3 250 950 stearylammobenzoyl acetyl-S, 3-d1carboxyanilide per kg of emulsion and compound 2: I 0 0 6 2 I f l 0.5 10 C 325 950 a u protective ayer o ge atm 22 2 is cast in known manner on a layer support of cellulose 3 235 1150 triacetate p. in thickness and dried. The film is coated with a l aqueous solution and a 2 aqueous gg a l c 350 850 65 solution of compounds 2 5, l9 and 30. l 3 8 2 The layer melting points and the temperatures at g 250 50 which the layers dissolve off are determined after drying and 12 hours storage at room temperature.
I claim: temperature 1. A process for providing a protein-containing with n Coalmg M layer mcltlng P f binder selected from the group consisting of gelatin, ca-
dissolvcs off layer sem and 2cm in a photographic silver halide emulsion compound 2 1% 752C 10'100C layer coated on a support wherein the improvement comprises incorporating in a binder for the layer a compound 5 l 7? 100 C l0 100 C 2 100C g'mo c hardening amount of a hardener of the formula compound 19 l 70 l00C l0'l0OC 2 7! 100C l0'l0OC compound 30 l 71. l00C l0'l00C 2 7! l00C 10'100C l0 R 0 I Material without top coating used C N Z X G for comparison 40C 40C H I The results show that the multi-layered colour films are effectively cross-linked by the top coating right down to the lowermost layers. in which R is selected from the group consisting of alkyl, aryl EXAMPLE 9 and aralkyl groups,
R is selected from the group consisting of alkyl, aryl, aralkyl groups and the methylene group substituted with a group of the formula 40 ml of a 5 70 aqueous solution of polyacrylic acid sodium salt and 10 ml of a 40 SiO suspension are added to 100 ml of a 10 gelatin solution. The solution is vigorously mixed. 0.2 g of compounds 6 and 20 are added to each 100 ml of the solution. Then the pH is adjusted to 6.2 and the mixtures are cast on cellulose triacetate supports. Layers with a melting point above N co N 100C and exellent wet strength are obtained after drying and 12 hours storage. A layer without the addition CH ONH2 of the compounds according to the invention melts in water at 40C.
EXAMPLE 10 or R and R combined are poly-4-vinylpyridine,
0.2 g of compounds 6 and 23 are added to l00 ml of R5 is Selacted f the group of one alkyl 10 aqueous solutions of acetyl gelatin which have gro ups ar ld not f when the mtmgFn to been obtained by reacting gelatin with 20 acetic anwhch attached car nes double bond f the hydride and the mixtures are cast on cellulose acetate hetemcychc aromatc rmg formed by Substltuted films. A layer containing 0.2 g of formalin instead of compounds 6 and 23 is cast for comparison. After dry Z 15 a group Yequlred to p p F F of ing, the layers containing compounds 6 and 23 are re- 6'membered heterocycllc 8 whlch y sistant to boiling whereas the layer which has been Include one or more Condensed mugs and one or hardened with formalin melts at temperatures below more heleroa'loms, R stands for -NR -c0-R R H, alkyl (llc) R H, alkyl (1-4 G) 9 o R", R H, alkyl (c -c 2)m lO ll R10 l2 R H, alkyl (c -c R12: H, alkyl (c -c R alkyl (c -c aryl R1 H, alkyl, aryl ..(CH -CONR R R H, alkyl (c -c aryl R H, alkyl (c -ci or R and R together represent the atomic grouping required to complete a S-membered or 6- membered aliphatic ring,
-(CH 3H-R R H, alkyl (c -c optionally substituted by halogen R Y -o-, -NR
R H, alkyl, -c0-R -CO-NHR R R20, R21 H, alkyl (c -c X is the anion radical of the formula, or poly-4-vinyl- N,N-dimethyl-carbamoyl-pyridinium chloride having molecular weight of about 10,000. 2. A process according to claim 1, characterised in that the hardener is applied from aqueous solution.
3. A process according to claim 1, characterised in that the hardener is applied from alcoholic solution.
4. A process according to claim 1, characterised in that the hardener is applied from aqueous-alcoholic solution.
5. A process according to claim 1 in which the hardener is added to the casting solution of the layer which is to be hardened and the hardener is used in quantities multilayer color materials.
UNITED STATES PATENT AND TRADEMARK OFFICE CERTIFICATE OF CORRECTION PATENT NO. 3,880,665
DATED April 29, 1975 INVENTOR(S) Wolfgang Himmelmann It is certified that error appears in the above-identified patent and that said Letters Patent are hereby corrected as shown below:
Page 1 of 2 Column 4, lines 17 & 18 should read as follows X represents an acid anion such as halogen BF N0 S0 010;, cn oso Column 6, formula 12, the left-hand ring should read as follows Column 18, the right-hand side of the first formula should read as follows GB N Column 18, the right-hand side of the second formula should CONH UNITED STATES PATENT AND TRADEMARK OFFICE CERTIFICATE OF CORRECTION PATEN N 3,880,665 Page 2 of 2 DATED :April 29, 1975 INVENTOR(S) t Wolfgang Himmelmann It is certified that error appears in the ab0ve-identified patentand that said Letters Patent are hereby corrected as shown below:
' Column 18, line 31 should read as follows or R and R may together represent a. group required to complete a substituted or unsubstituted heterocyclic ring.
Column 19, lines 22-24 should read as follows X is the anion radical,
or the hardener is polyr-vinyl-N,N-dimethyl-carbamoylpyridinium chloride having molecular weight of about 10,000.
Signed and Scaled this Twemieth D a y f January I 98] I ALI .4 nest:
RENE D. TEGTMEYER Au m' Offi Acting Commissioner of Patents and Trademarks

Claims (8)

1. A PROCESS FOR PROVIDING A PROTEIN-CONTAINING BINDER SELECTED FROM THE GROUP CONSISTING OF GELATIN, CASEIN, AND ZEIN IN A PHOTOGRAPHIC SILVER HALIDE EMULSION LAYER COATED ON A SUPPORT WHEREIN THE IMPROVEMENT COMPRISES INCORPORATING IN A BINDER FOR THE LAYER A HARDENING AMOUNT OF A HARDENER OF THE FORMULA
2. A process according to claim 1, characterised in that the hardener is applied from aqueous solution.
3. A process according to claim 1, characterised in that the hardener is applied from alcoholic solution.
4. A process according to claim 1, characterised in that the hardener is applied from aqueous-alcoholic solution.
5. A process according to claim 1 in which the hardener is added to the casting solution of the layer which is to be hardened and the hardener is used in quantities of 0.2 to 6% by weight based on the weight of the protein-containing binder in the casting solution.
6. A process as claimed in claim 1 in which the hardener is applied to the layer before processing, said hardener being in a 0.2 to 10% solution.
7. A process as claimed in claim 5 in which the hardener is coated on the layer in a 0.2 to 5% solution and the layer is then dried.
8. A process according to claim 1 characterized in that the hardener is used for hardening photographic multilayer color materials.
US362484A 1972-05-24 1973-05-21 Hardening with a heterocyclic carbamoyl ammonium compound of a photographic material containing a silver halide layer Expired - Lifetime US3880665A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19722225230 DE2225230C2 (en) 1972-05-24 1972-05-24 Process for hardening photographic layers
DE19732317677 DE2317677C2 (en) 1973-04-07 1973-04-07 Process for hardening photographic layers

Publications (1)

Publication Number Publication Date
US3880665A true US3880665A (en) 1975-04-29

Family

ID=25763308

Family Applications (1)

Application Number Title Priority Date Filing Date
US362484A Expired - Lifetime US3880665A (en) 1972-05-24 1973-05-21 Hardening with a heterocyclic carbamoyl ammonium compound of a photographic material containing a silver halide layer

Country Status (7)

Country Link
US (1) US3880665A (en)
JP (1) JPS5612853B2 (en)
CA (1) CA1019615A (en)
CH (1) CH582897A5 (en)
FR (1) FR2185807B1 (en)
GB (1) GB1383630A (en)
IT (1) IT988201B (en)

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3951940A (en) * 1974-09-30 1976-04-20 Ciba-Geigy Ag Method of producing a hardened gelatin layer using aqueous solution of a 2-halogeno pyridinium compound
US3977881A (en) * 1974-01-31 1976-08-31 Ciba-Geigy Ag Acylurea compounds
US4014862A (en) * 1972-07-12 1977-03-29 Ilford Limited Production of hardened gelatin layers by the addition of quaternary carbamoyl pyridinium compounds
US4047957A (en) * 1975-02-10 1977-09-13 Agfa-Gevaert N.V. Process of hardening protein-containing photographic layers with a mixture of a carboxyl group-activating, low molecular weight compound and a carboxyl group-activating polymer
US4055427A (en) * 1974-02-23 1977-10-25 Agfa-Gevaert Aktiengesellschaft Process of hardening a silver halide photographic material with a 1-carbamoyloxypyridinium salt
US4061499A (en) * 1975-10-11 1977-12-06 Agfa-Gevaert Aktiengesellschaft Process for hardening silver halide photographic layers with organic asymmetric monocarbodiimides
US4063952A (en) * 1974-08-17 1977-12-20 Agfa-Gevaert Aktiengesellschaft Process for hardening silver halide containing photographic layers with sulpho- or sulphoalkyl-substituted carbamoyl pyridinium compounds
US4067741A (en) * 1975-10-24 1978-01-10 Agfa-Gevaert, A.G. Hardening photographic layers containing silver halide with a 1-sulphonyl-4-amino-pyridinium salt
US4119464A (en) * 1976-06-03 1978-10-10 Agfa-Gevaert Aktiengesellschaft Process for hardening photographic layers containing gelatine
US4123281A (en) * 1975-09-06 1978-10-31 Agfa-Gevaert N.V. Photographic silver halide color material containing fast-acting hardener and 2-pyrazolin-5-one coupler precursors
US4233398A (en) * 1974-04-11 1980-11-11 Agfa-Gevaert, A.G. Process for the hardening of photographic layers utilizing fast acting hardener and polysaccharide
US4810625A (en) * 1986-04-25 1989-03-07 Agfa-Gevaert Aktiengesellschaft Photographic material with pyrazolone coupler and oil former
US5034249A (en) * 1986-08-29 1991-07-23 Agfa Gevaert Aktiengesellschaft Process for hardening layers containing proteinaceous binders
WO1993012667A1 (en) * 1991-12-26 1993-07-08 Opta Food Ingredients, Inc. Purification of zein from corn gluten meal
US5378842A (en) * 1993-12-21 1995-01-03 E. I. Du Pont De Nemours And Company Imidazolium hardeners for proteinaceous materials
US5576155A (en) * 1994-10-07 1996-11-19 Sterling Diagnostic Imaging, Inc. Fast-processing photographic recording material for medical radiography
US5601971A (en) * 1991-06-18 1997-02-11 Sterling Diagnsotic Imaging, Inc. Hardening of hydrophilic colloids with imidazolium and triazine combinations
US6028199A (en) * 1995-07-20 2000-02-22 Agfa-Gevaert Nv Hardeners for photographic materials
US6468339B1 (en) 2001-08-23 2002-10-22 Eastman Kodak Company Alumina filled gelatin

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS53113856A (en) * 1977-03-16 1978-10-04 Mitsubishi Paper Mills Ltd Gelatine curing process
JPS62291565A (en) * 1986-05-28 1987-12-18 マイルス・ラボラトリ−ズ・インコ−ポレ−テッド Curing reagent matrix film and manufacture thereof
DE3626221A1 (en) * 1986-08-02 1988-02-04 Agfa Gevaert Ag COLOR PHOTOGRAPHIC RECORDING MATERIAL FOR THE PRODUCTION OF COLORED SUPERVISORS

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2950197A (en) * 1955-04-18 1960-08-23 Eastman Kodak Co Hardening of gelatin
US3676143A (en) * 1969-08-21 1972-07-11 Agfa Gevaert Ag Treatment of exposed silver halide emulsion with acidic hardening bath following by alkaline activating bath

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1393959A (en) * 1972-07-12 1975-05-14 Ilford Ltd Hardened gelatin layers

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2950197A (en) * 1955-04-18 1960-08-23 Eastman Kodak Co Hardening of gelatin
US3676143A (en) * 1969-08-21 1972-07-11 Agfa Gevaert Ag Treatment of exposed silver halide emulsion with acidic hardening bath following by alkaline activating bath

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4014862A (en) * 1972-07-12 1977-03-29 Ilford Limited Production of hardened gelatin layers by the addition of quaternary carbamoyl pyridinium compounds
US3977881A (en) * 1974-01-31 1976-08-31 Ciba-Geigy Ag Acylurea compounds
US4055427A (en) * 1974-02-23 1977-10-25 Agfa-Gevaert Aktiengesellschaft Process of hardening a silver halide photographic material with a 1-carbamoyloxypyridinium salt
US4233398A (en) * 1974-04-11 1980-11-11 Agfa-Gevaert, A.G. Process for the hardening of photographic layers utilizing fast acting hardener and polysaccharide
US4063952A (en) * 1974-08-17 1977-12-20 Agfa-Gevaert Aktiengesellschaft Process for hardening silver halide containing photographic layers with sulpho- or sulphoalkyl-substituted carbamoyl pyridinium compounds
US3951940A (en) * 1974-09-30 1976-04-20 Ciba-Geigy Ag Method of producing a hardened gelatin layer using aqueous solution of a 2-halogeno pyridinium compound
US4047957A (en) * 1975-02-10 1977-09-13 Agfa-Gevaert N.V. Process of hardening protein-containing photographic layers with a mixture of a carboxyl group-activating, low molecular weight compound and a carboxyl group-activating polymer
US4123281A (en) * 1975-09-06 1978-10-31 Agfa-Gevaert N.V. Photographic silver halide color material containing fast-acting hardener and 2-pyrazolin-5-one coupler precursors
US4061499A (en) * 1975-10-11 1977-12-06 Agfa-Gevaert Aktiengesellschaft Process for hardening silver halide photographic layers with organic asymmetric monocarbodiimides
US4067741A (en) * 1975-10-24 1978-01-10 Agfa-Gevaert, A.G. Hardening photographic layers containing silver halide with a 1-sulphonyl-4-amino-pyridinium salt
US4119464A (en) * 1976-06-03 1978-10-10 Agfa-Gevaert Aktiengesellschaft Process for hardening photographic layers containing gelatine
US4810625A (en) * 1986-04-25 1989-03-07 Agfa-Gevaert Aktiengesellschaft Photographic material with pyrazolone coupler and oil former
US5034249A (en) * 1986-08-29 1991-07-23 Agfa Gevaert Aktiengesellschaft Process for hardening layers containing proteinaceous binders
US5601971A (en) * 1991-06-18 1997-02-11 Sterling Diagnsotic Imaging, Inc. Hardening of hydrophilic colloids with imidazolium and triazine combinations
US5580959A (en) * 1991-12-26 1996-12-03 Opta Food Ingredients, Inc. Purification of zein from corn gluten meal
US5254673A (en) * 1991-12-26 1993-10-19 Opta Food Ingredients, Inc. Purification of zein from corn gluten meal
WO1993012667A1 (en) * 1991-12-26 1993-07-08 Opta Food Ingredients, Inc. Purification of zein from corn gluten meal
US5378842A (en) * 1993-12-21 1995-01-03 E. I. Du Pont De Nemours And Company Imidazolium hardeners for proteinaceous materials
US5459029A (en) * 1993-12-21 1995-10-17 E. I. Du Pont De Nemours And Company Photographic element hardened with imidazolium hardeners
US5576155A (en) * 1994-10-07 1996-11-19 Sterling Diagnostic Imaging, Inc. Fast-processing photographic recording material for medical radiography
US6028199A (en) * 1995-07-20 2000-02-22 Agfa-Gevaert Nv Hardeners for photographic materials
US6468339B1 (en) 2001-08-23 2002-10-22 Eastman Kodak Company Alumina filled gelatin

Also Published As

Publication number Publication date
JPS5612853B2 (en) 1981-03-25
FR2185807B1 (en) 1976-09-17
CH582897A5 (en) 1976-12-15
CA1019615A (en) 1977-10-25
IT988201B (en) 1975-04-10
JPS4951945A (en) 1974-05-20
FR2185807A1 (en) 1974-01-04
GB1383630A (en) 1974-02-12

Similar Documents

Publication Publication Date Title
US3880665A (en) Hardening with a heterocyclic carbamoyl ammonium compound of a photographic material containing a silver halide layer
US4063952A (en) Process for hardening silver halide containing photographic layers with sulpho- or sulphoalkyl-substituted carbamoyl pyridinium compounds
US3689274A (en) Process of hardening photographic gelatin layers with a sulfonyl ester or a sulfonamide
US3640720A (en) Nonwandering hardening compounds and their use
US3137578A (en) Photographic emulsions containing 2-heterocyclic benzimidazole antifoggants
US3549377A (en) Method of hardening photographic gelatin-containing layers with non-ionic dichlorotriazinyl amino compounds
GB1579547A (en) Process for hardening photographic layers containing gelatine
US3645743A (en) Process for hardening protein layers
US4061499A (en) Process for hardening silver halide photographic layers with organic asymmetric monocarbodiimides
US3765901A (en) Spectral sensitization of light-sensitive silver halide emulsions
US4039520A (en) Gelatin hardening process
US3910791A (en) Silver halide photographic material containing a 2-propynylthio derivative as stabilizer
US3901708A (en) Process for hardening layers which contain gelatin within a silver halide photographic material with an aldehyde and an isonitrile
US4052373A (en) Process for hardening gelatin
US4116700A (en) Process for hardening photographic layers
US4376818A (en) Novel hardener for gelatin and method for hardening gelatin
US4043818A (en) Process for hardening photographic layers with carbodiimide compounds containing sulphobetaine groups
US3765900A (en) Spectrally sensitized silver halide emulsions
CA1057554A (en) Hardening of photographic layers
US3543292A (en) Photographic gelatin hardened with bis isoxazole compounds and their quaternary salts
US3186847A (en) Composition of gelatin and hardening agent
US3910790A (en) Color photographic materials processed in the presence of anti-color fogging agents
JPS63172267A (en) Silver halide photographic emulsion
US3761278A (en) Bonic acid ester stabilizing agent silver halide element containing a benzimidazoline 2 thione n n dicar
JPS63172265A (en) Silver halide photographic emulsion