EP0225446A1 - Water-resistant photographic paper support - Google Patents
Water-resistant photographic paper support Download PDFInfo
- Publication number
- EP0225446A1 EP0225446A1 EP86113855A EP86113855A EP0225446A1 EP 0225446 A1 EP0225446 A1 EP 0225446A1 EP 86113855 A EP86113855 A EP 86113855A EP 86113855 A EP86113855 A EP 86113855A EP 0225446 A1 EP0225446 A1 EP 0225446A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- paper support
- photographic paper
- support according
- carboxyl
- modified polyvinyl
- 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.)
- Granted
Links
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 claims abstract description 28
- 239000011248 coating agent Substances 0.000 claims abstract description 27
- 238000000576 coating method Methods 0.000 claims abstract description 27
- 239000000203 mixture Substances 0.000 claims abstract description 23
- 239000004372 Polyvinyl alcohol Substances 0.000 claims abstract description 19
- 150000001875 compounds Chemical class 0.000 claims abstract description 16
- 150000001768 cations Chemical class 0.000 claims abstract description 12
- 229920000098 polyolefin Polymers 0.000 claims abstract description 10
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims description 27
- 239000002585 base Substances 0.000 claims description 15
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 10
- 229920001577 copolymer Polymers 0.000 claims description 5
- 238000007127 saponification reaction Methods 0.000 claims description 5
- TWRXJAOTZQYOKJ-UHFFFAOYSA-L Magnesium chloride Chemical compound [Mg+2].[Cl-].[Cl-] TWRXJAOTZQYOKJ-UHFFFAOYSA-L 0.000 claims description 4
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 4
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 claims description 4
- 229910052723 transition metal Inorganic materials 0.000 claims description 4
- 150000003624 transition metals Chemical class 0.000 claims description 4
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 3
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 claims description 3
- 239000007864 aqueous solution Substances 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 229910052726 zirconium Inorganic materials 0.000 claims description 3
- WRAGBEWQGHCDDU-UHFFFAOYSA-M C([O-])([O-])=O.[NH4+].[Zr+] Chemical compound C([O-])([O-])=O.[NH4+].[Zr+] WRAGBEWQGHCDDU-UHFFFAOYSA-M 0.000 claims description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 2
- 241001448862 Croton Species 0.000 claims description 2
- AZDRQVAHHNSJOQ-UHFFFAOYSA-N alumane Chemical class [AlH3] AZDRQVAHHNSJOQ-UHFFFAOYSA-N 0.000 claims description 2
- 239000001110 calcium chloride Substances 0.000 claims description 2
- 229910001628 calcium chloride Inorganic materials 0.000 claims description 2
- 229910052804 chromium Inorganic materials 0.000 claims description 2
- 239000011651 chromium Substances 0.000 claims description 2
- LDHQCZJRKDOVOX-IHWYPQMZSA-N isocrotonic acid Chemical compound C\C=C/C(O)=O LDHQCZJRKDOVOX-IHWYPQMZSA-N 0.000 claims description 2
- 229910001629 magnesium chloride Inorganic materials 0.000 claims description 2
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 claims 1
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims 1
- 150000001342 alkaline earth metals Chemical class 0.000 claims 1
- 150000001845 chromium compounds Chemical class 0.000 claims 1
- 239000003292 glue Substances 0.000 claims 1
- 125000005395 methacrylic acid group Chemical group 0.000 claims 1
- 150000002763 monocarboxylic acids Chemical class 0.000 claims 1
- 150000003755 zirconium compounds Chemical class 0.000 claims 1
- 238000011161 development Methods 0.000 abstract description 5
- 239000000463 material Substances 0.000 abstract description 5
- 239000003795 chemical substances by application Substances 0.000 abstract description 3
- 238000004513 sizing Methods 0.000 abstract description 3
- 238000012545 processing Methods 0.000 abstract description 2
- -1 alkyl ketene dimers Chemical class 0.000 description 24
- 239000000243 solution Substances 0.000 description 19
- 238000012360 testing method Methods 0.000 description 18
- 239000004698 Polyethylene Substances 0.000 description 17
- 229920000573 polyethylene Polymers 0.000 description 17
- 230000000052 comparative effect Effects 0.000 description 9
- 238000001125 extrusion Methods 0.000 description 9
- 230000000694 effects Effects 0.000 description 8
- 238000000034 method Methods 0.000 description 8
- 230000035515 penetration Effects 0.000 description 7
- 239000010410 layer Substances 0.000 description 6
- 239000000725 suspension Substances 0.000 description 6
- 239000011247 coating layer Substances 0.000 description 5
- 235000014113 dietary fatty acids Nutrition 0.000 description 5
- 239000000194 fatty acid Substances 0.000 description 5
- 229930195729 fatty acid Natural products 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 4
- 239000012876 carrier material Substances 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 230000003287 optical effect Effects 0.000 description 4
- 239000012463 white pigment Substances 0.000 description 4
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- 229920001131 Pulp (paper) Polymers 0.000 description 3
- 239000000835 fiber Substances 0.000 description 3
- 230000006872 improvement Effects 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000003963 antioxidant agent Substances 0.000 description 2
- TZCXTZWJZNENPQ-UHFFFAOYSA-L barium sulfate Chemical compound [Ba+2].[O-]S([O-])(=O)=O TZCXTZWJZNENPQ-UHFFFAOYSA-L 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 238000005470 impregnation Methods 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 229920002401 polyacrylamide Polymers 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- 229920002126 Acrylic acid copolymer Polymers 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 108010010803 Gelatin Proteins 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- 229910010413 TiO 2 Inorganic materials 0.000 description 1
- USDJGQLNFPZEON-UHFFFAOYSA-N [[4,6-bis(hydroxymethylamino)-1,3,5-triazin-2-yl]amino]methanol Chemical compound OCNC1=NC(NCO)=NC(NCO)=N1 USDJGQLNFPZEON-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 230000003321 amplification Effects 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- QVQLCTNNEUAWMS-UHFFFAOYSA-N barium oxide Chemical compound [Ba]=O QVQLCTNNEUAWMS-UHFFFAOYSA-N 0.000 description 1
- 229910001864 baryta Inorganic materials 0.000 description 1
- 235000019445 benzyl alcohol Nutrition 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 150000001844 chromium Chemical class 0.000 description 1
- 239000011436 cob Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 229920000159 gelatin Polymers 0.000 description 1
- 239000008273 gelatin Substances 0.000 description 1
- 235000019322 gelatine Nutrition 0.000 description 1
- 235000011852 gelatine desserts Nutrition 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 1
- 229940117841 methacrylic acid copolymer Drugs 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000012764 mineral filler Substances 0.000 description 1
- 238000003199 nucleic acid amplification method Methods 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- QUBQYFYWUJJAAK-UHFFFAOYSA-N oxymethurea Chemical compound OCNC(=O)NCO QUBQYFYWUJJAAK-UHFFFAOYSA-N 0.000 description 1
- 229950005308 oxymethurea Drugs 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- GGCZERPQGJTIQP-UHFFFAOYSA-N sodium;9,10-dioxoanthracene-2-sulfonic acid Chemical compound [Na+].C1=CC=C2C(=O)C3=CC(S(=O)(=O)O)=CC=C3C(=O)C2=C1 GGCZERPQGJTIQP-UHFFFAOYSA-N 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000012209 synthetic fiber Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 238000005303 weighing Methods 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03C—PHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
- G03C1/00—Photosensitive materials
- G03C1/76—Photosensitive materials characterised by the base or auxiliary layers
- G03C1/775—Photosensitive materials characterised by the base or auxiliary layers the base being of paper
- G03C1/79—Macromolecular coatings or impregnations therefor, e.g. varnishes
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/27—Web or sheet containing structurally defined element or component, the element or component having a specified weight per unit area [e.g., gms/sq cm, lbs/sq ft, etc.]
- Y10T428/273—Web or sheet containing structurally defined element or component, the element or component having a specified weight per unit area [e.g., gms/sq cm, lbs/sq ft, etc.] of coating
- Y10T428/277—Cellulosic substrate
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
- Y10T428/3188—Next to cellulosic
- Y10T428/31895—Paper or wood
- Y10T428/31899—Addition polymer of hydrocarbon[s] only
- Y10T428/31902—Monoethylenically unsaturated
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31971—Of carbohydrate
- Y10T428/31993—Of paper
- Y10T428/31996—Next to layer of metal salt [e.g., plasterboard, etc.]
Definitions
- the invention relates to a paper support for photographic layers provided on both sides with a polyolefin coating.
- the paper core of the photographic support according to the invention is also largely protected against the action of the photographic treatment solutions at the edges which are caused by the cutting and is essentially free of dirt on the edges from the treatment solutions.
- barytened papers the surfaces of which were provided with so-called baryta layers, which consisted essentially of barium sulfate and gelatin, were previously used as carrier materials for the inclusion of photo-sensitive layers, in particular layers for black / white and color silver salt photography.
- waterproof photographic supports In order to be able to meet the requirements placed on the photographic support materials by the new automatic rapid development processes, waterproof photographic supports have been described which have been coated on both surfaces with a hydrophobic polyolefin.
- the top polyolefin coating layer of the waterproof photographic base to which a photographic emulsion layer is to be applied usually contains a white pigment to enhance the sharpness of the photographic image.
- the paper substrates coated on both sides with polyolefin are basically protected in both areas against the effects of conventional photographic treatment liquids. This protection is only interrupted at the edges of the coated papers, and the liquids have access to the paper core there. Due to the natural absorbency of paper, they penetrate the edges of the paper core and cannot be completely removed even in subsequent washing steps. Since the liquids often contain substances that change color dark when exposed to air or exposure to light, penetrated photographic treatment liquids appear as darker discolored edges after a short time, which leads to a reduction in the value of the photographic material.
- the base paper is usually provided with a strong, hydrophobic internal sizing, by adding sizing agents to the pulp suspension during the manufacture of the paper.
- the object of the invention is therefore to provide a waterproof photographic support which is free from the disadvantages described, i.e. which is also used in an automatic rapid development process. has no dirt on the edges and the paper core has the internal strength required for use in photographic supports and secure adhesion of the polyolefin coating.
- the phthalographic support according to the invention has a basic structure of a base paper and a polyolefin coating layer, which is provided on both surfaces and the light-reflecting white pigment (especially in the front coating) and optionally color pigments, optical brighteners and / or other additives such as antistatic compounds, dispersants for the white pigment and antioxidants.
- the base paper is produced in a known manner using a paper machine.
- the paper pulp suspension is sized using alkyl ketene dimers or fatty acids or fatty acid salts, epoxidized fatty acid amides or anhydrides of fatty acids and mixtures thereof.
- the paper pulp suspension can also contain synthetic fibers, mineral or organic fillers, white pigment, dye or color pigment, optical brighteners, antioxidants and / or other additives customary in the production of photographic supports, e.g. setting resins.
- Base papers of any basis weight and of any density can be used.
- the base paper is impregnated (surface-sized) with a solution of carboxyl-modified polyvinyl alcohol.
- a carboxyl-modified polyvinyl alcohol is understood to mean, for example, a vinyl alcohol croton or iso crotonic acid polymer or a vinyl alcohol acrylic or methacrylic acid copolymer.
- the vinyl alcohol-crotonic acid copolymer is preferred according to the invention.
- the carboxyl-modified polyvinyl alcohols have a viscosity of 20 to 50 mPa s in 4% solution at room temperature.
- the average molecular weight is 5,000 to 20,000, preferably 7,000 to 10,000.
- the carboxyl-modified polyvinyl alcohols used according to the invention are applied as an aqueous solution using the known and customary application methods.
- the application amount is 0.5 to 10 g / m 2, preferably 1 to 4.5 g / m 2 .
- the application quantity is less than 0.5 g / m 2 , sufficient impregnation of the paper core (base paper) is not achieved and the penetration of the photographic treatment solutions into the edges and the contamination of the edges by the photographic treatment solutions are not avoided to the desired extent.
- the improvement in properties is not linearly related to the number of carboxyl groups, so that the maxium does not occur in the carboxyl-modified polyvinyl alcohol with the largest proportion of carboxyl groups.
- carboxyl-modified polyvinyl alcohols which contain a carboxyl group content of 1.5 to 7 mol%, preferably 2.5 to 3.5 mol%.
- the effect according to the invention is enhanced, if additional polyvalent cations are introduced into the paper.
- These compounds can be selected from the group of alkaline earth compounds, for example calcium or magnesium chloride, from the group of aluminum salts, for example aluminum sulfate or aluminum chloride, and from the compounds of the transition metals. Salts of zirconium, for example zirconium ammonium carbonate or zirconium orthosulfate, and compounds of chromium, for example chromium complexes of the Werner type, are particularly preferred.
- the polyvalent cations are preferably added to the aqueous coating solution. However, they can also be added to the cellulose suspension or incorporated into the base paper before the polyvinyl alcohol solution according to the invention is used. Or they can be applied in the form of an aftertreatment (e.g. by spraying) after impregnation with the polyvinyl alcohol solution.
- the polyvalent cation compounds are in a weight ratio of 1/10 to 5/1 to the carboxylated polyvinyl alcohol. If the weight ratio falls below the value of 1/10, the amplification of the described effect is not achieved. An increase in the weight ratio to values above 5/1 brings no further improvement in the effect according to the invention.
- aqueous coating solution can also contain optical brighteners, defoamers, pigments, water repellents or crosslinking aids, such as, for example, dimethylolurea or trimethylolmelamine.
- the paper support is treated with an aqueous coating mixture of the following composition:
- the order quantity is 2 g / m 2 .
- Crotonic acid-modified polyvinyl alcohols with the following carboxyl groups are used:
- the treated paper is dried and extrusion coated with polyethylene in the usual way.
- the paper is treated with the coating mixture used in Example 1.
- the order quantity is 3 g / m 2 .
- Crotonic acid-modified polyvinyl alcohols with the following carboxyl groups are used.
- the treated paper is dried and extrusion coated in a conventional manner with polyethylene.
- An approximately 140 g / m 2 heavy paper sized with 0.3% by weight of alkyl ketene dimer, 1.6% by weight of fatty acid soap and 0.5% by weight of aluminum ions is treated with an aqueous coating mixture. which contains a crotonic acid-modified polyvinyl alcohol with a degree of saponification of 98.5% and a carboxyl group content of 3.1 mol% in the amount of 40 g / 1.
- compounds of the following polyvalent cations are added:
- the application quantity is 1.5 g / m 2 .
- the treated paper is dried and extrusion coated with polyethylene in the usual way.
- the order quantity is 4.5 g / m 2 .
- the paper is treated on both sides in a second size press with the following polyvinyl alcohol solution.
- the treated paper is dried and extrusion coated with polyethylene in the usual way.
- both sides are successively sprayed with the following saline solution via a nozzle system:
- the application quantities are 1.5 g / m 2 in the size press and 1.0 g / m 2 when spraying.
- the treated paper is dried and extrusion coated with polyethylene in the usual way.
- a paper produced according to Example 1 is treated with an aqueous coating mixture of the following composition:
- the order quantity is 3 g / m 2 .
- the treated paper is dried and extrusion coated with polyethylene in the usual way.
- a paper sheet produced according to Example 2 of DOS 32 41 599 is treated with the coating mixture described there (the application amount is 3 g / m 2 ), then dried and extrusion-coated with polyethylene in the usual way.
- a paper sheet produced according to Example 3 is treated with the coating mixture described in Comparative Example V1.
- the order quantity is 3 g / m 2 .
- the treated paper is dried and coated with polyethylene in the usual way.
- a paper of 140 g / m 2 produced according to Example 3 is treated (surface-sized) with the following coating mixture:
- the treated paper is dried and extrusion coated with polyethylene in the usual way.
- a 175 g / m 2 paper produced according to Example 1 is treated with the following coating mixture:
- the treated paper is dried and extrusion coated with polyethylene in the usual way.
- the treated papers are coated with polyethylene and then subjected to the following tests.
- Treated paper is understood here to mean paper which has undergone the treatment of the base paper by the coating mixtures in the form of applications on both sides by dipping processes (size press), spraying, application on both sides by means of roller application systems, slot casters or the like.
- the developer absorption is determined by the paper (modified Cobb test). Test pieces in the format 14 x 14 cm are cut out of the paper web, weighed exactly and clamped in a cylindrical test device. 100 ml of a commercially available photographic developer are placed in the cylinder, left to act for a period of 50 seconds and then poured off. The test specimen is erased and weighed immediately. The extent of developer uptake is given in g / m 2 .
- the test piece is subjected to a simulated photographic development process with a commercial developer containing benzyl alcohol at a temperature of about 30 ° C and for a period of 25 minutes.
- the penetration of the photographic treatment solutions is measured on both edges of the test piece with a measuring magnifier.
- the measured values are given as edge penetration (KE) in mm.
- test is carried out according to the method specified in TAPPI RC 308 with the Internal Bond Impact Tester Model B.
- Test 2.3 Determination of the adhesive force between the polyethylene coating layer and the impregnated paper core.
- the test is carried out with a tensile strength measuring device from AB Lorentzen & Wettre on 15 mm wide and 18 cm long test strips.
- the pull-off angle is 180 °
- the pull-off speed is 70 mm / min.
- the measured values are given in mN / 15 mm.
- test values on pages 18 and 19 show that the optimum in terms of edge penetration, gap resistance and adhesion to the polyethylene coating layer with a carboxyl group content is between 2.5 and 3.5 mol%.
- Comparative example V5 demonstrates that a degree of saponification of 88% for the polyvinyl alcohol used is not sufficient to achieve the desired effect.
Landscapes
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- General Physics & Mathematics (AREA)
- Paper (AREA)
- Laminated Bodies (AREA)
Abstract
Description
Die Erfindung betrifft einen beidseitig mit einem Polyolefinüberzug versehenen Papierträger für photographische Schichten.The invention relates to a paper support for photographic layers provided on both sides with a polyolefin coating.
Insbesondere betrifft sie beschichtete Papierträger für solche photographische Schichten, die einer Naßentwicklung oder Naßfixierung des photographischen Bildes mit Hilfe sogenannter photographischer Behandlungslösungen bedürfen.In particular, it relates to coated paper supports for those photographic layers which require wet development or wet fixation of the photographic image using so-called photographic processing solutions.
Der Papierkern des erfindungsgemäßen photographischen Trägers ist auch an den Kanten, die durch das Schneiden entstehen, weitestgehend gegen die Einwirkung der photographischen Behandlungslösungen geschützt und im wesentlichen von Verschmutzungen an den Kanten durch die Behandlungslösungen frei.The paper core of the photographic support according to the invention is also largely protected against the action of the photographic treatment solutions at the edges which are caused by the cutting and is essentially free of dirt on the edges from the treatment solutions.
Als Trägermaterialien für die Aufnahme phötoempfindlicher Schichten, insbesondere von Schichten für die Schwarz/Weiß-und Farbsilbersalzphotographie, wurden früher sogenannte barytierte Papiere verwendet, deren Oberflächen mit sogenannten Barytschichten, die im wesentlichen aus Bariumsulfat und Gelatine bestanden, versehen waren.So-called barytened papers, the surfaces of which were provided with so-called baryta layers, which consisted essentially of barium sulfate and gelatin, were previously used as carrier materials for the inclusion of photo-sensitive layers, in particular layers for black / white and color silver salt photography.
Um den Anforderungen, die durch die neuen automatischen Schnellentwicklungsverfahren an die photographischen Trägermaterialien gestellt werden, genügen zu können, sind in neuerer Zeit wasserfeste photographische Träger beschrieben worden, die auf beiden Oberflächen mit einem hydrophoben Polyolefin beschichtet worden sind. Die obere Polyolefinüberzugsschicht des wasserfesten photographischen Trägers, auf die eine photographische Emulsionsscbicht aufgebracht werden soll, enthält gewöhnlich ein weißes Pigment, um die Schärfe des photographischen Bildes zu erhöhen.In order to be able to meet the requirements placed on the photographic support materials by the new automatic rapid development processes, waterproof photographic supports have been described which have been coated on both surfaces with a hydrophobic polyolefin. The top polyolefin coating layer of the waterproof photographic base to which a photographic emulsion layer is to be applied usually contains a white pigment to enhance the sharpness of the photographic image.
Die beidseitig mit Polyolefin überzogenen Papierträger sind grundsätzlich in beiden Flächen gegen die Einwirkung üblicher photographischer Behandlungsflüssigkeiten geschützt. Lediglich an den Kanten der beschichteten Papiere ist dieser Schutz unterbrochen, und die Flüssigkeiten haben dort Zutritt zum Papierkern. Aufgrund einer natürlichen Saugfähigkeit von Papier dringen sie an den Kanten in den Papierkern ein und können selbst in nachfolgenden Wässerungsschritten nicht mehr vollständig entfernt werden. Da die Flüssigkeiten vielfach Substanzen enthalten, die sich bei Luftzutritt oder bei Lichteinwirkung dunkel verfärben, treten eingedrungene photographische Behandlungsflüssigkeiten nach kurzer Zeit als dunkler verfärbte Ränder in Erscheinung, was zu einer Verringerung des Wertes des photographischen Materials führt.The paper substrates coated on both sides with polyolefin are basically protected in both areas against the effects of conventional photographic treatment liquids. This protection is only interrupted at the edges of the coated papers, and the liquids have access to the paper core there. Due to the natural absorbency of paper, they penetrate the edges of the paper core and cannot be completely removed even in subsequent washing steps. Since the liquids often contain substances that change color dark when exposed to air or exposure to light, penetrated photographic treatment liquids appear as darker discolored edges after a short time, which leads to a reduction in the value of the photographic material.
Um dem Problem des Kantenverschmutzens des photographischen Trägers zu begegnen, wird das Basispapier üblicherweise mit einer starken hydrophobierenden Innenleimung versehen, indem Leimungsmittel bei der Herstellung des Papieres der Faserstoffsuspension zugesetzt werden.In order to counteract the problem of soiling the edges of the photographic support, the base paper is usually provided with a strong, hydrophobic internal sizing, by adding sizing agents to the pulp suspension during the manufacture of the paper.
Es wurde auch versucht, hydrophobierende Mittel nach dem Schneiden auf die betroffenen, neu entstandenen Kanten aufzutragen.Attempts have also been made to apply hydrophobizing agents to the affected, newly formed edges after cutting.
Jedoch genügen die Ergebnisse dieser beiden Verfahrensweisen nicht den Anforderungen, die an ein qualitativ hochwertiges photographisches Material gestellt werden.However, the results of these two procedures do not meet the requirements placed on a high quality photographic material.
In der DOS 32 41 599 wurde vorgeschlagen, das Basispapier durch Auftragen eines mit Maleinsäure oder Itaconsäure carboxylierten Polyvinylalkohols abzudichten. Jedoch konnte das dort beschriebene Verfahren in Bezug auf die Kantenverschmutzung und vor allem die innere Festigkeit des Papierkerns nicht voll befriedigen. Außerdem war die Haftung zwischen dem Polyolefinüberzug und dem Basispapier nicht gleichmäßig gut. Haftungsprüfungen lieferten stark schwankende Werte.In DOS 32 41 599 it was proposed to seal the base paper by applying a polyvinyl alcohol carboxylated with maleic acid or itaconic acid. However, the process described there was not fully satisfactory in terms of edge contamination and, above all, the internal strength of the paper core. In addition, the adhesion between the polyolefin coating and the base paper was not equally good. Liability tests delivered strongly fluctuating values.
Aufgabe der Erfindung ist es daher, einen wasserfesten photographischen Träger zur Verfügung zu stellen, der frei von den beschriebenen Nachteilen ist, d.h. der auch bei der Verwendung in einem automatischen Schnellentwicklungsprozeß. keine Verschmutzung der Kanten aufweist und dessen Papierkern die für die Verwendung in photographischen Trägern erforderliche innere Festigkeit und eine sichere Haftung des Polyolefinüberzugs besitzt.The object of the invention is therefore to provide a waterproof photographic support which is free from the disadvantages described, i.e. which is also used in an automatic rapid development process. has no dirt on the edges and the paper core has the internal strength required for use in photographic supports and secure adhesion of the polyolefin coating.
Diese Aufgabe wird durch die in den Ansprüchen beschriebenen Merkmale gelöst.This object is achieved by the features described in the claims.
Der erfindungsgemäße phtographische Träger besitzt eine Grundstruktur aus einem Basispapier und einer Polyolefinüberzugsschicht, die auf beiden Oberflächen vorgesehen ist und die lichtrefklektierendes Weißpigment (speziell in der Vorderseitenbeschichtung) sowie gegebenenfalls Farbpigmente, optische Aufheller und/oder andere Zusätze wie antistatisch wirkende Verbindungen, Dispergierhilfsmittel für das Weißpigment und Antioxidantien enthalten kann.The phthalographic support according to the invention has a basic structure of a base paper and a polyolefin coating layer, which is provided on both surfaces and the light-reflecting white pigment (especially in the front coating) and optionally color pigments, optical brighteners and / or other additives such as antistatic compounds, dispersants for the white pigment and antioxidants.
Das Basispapier wird in bekannter Weise mit Hilfe einer Papiermaschine hergestellt. Dabei wird die Papierfaserstoffsuspension unter Verwendung von Alkylketendimeren oder Fettsäuren bzw. Fettsäuresalzen, epoxidierten Fettsäureamiden oder Anhydriden von Fettsäuren sowie Mischungen hiervon geleimt. Darüber hinaus kann die Papierfaserstoffsuspension neben Zellstoffasern noch synthetische Faser, mineralische oder organische Füllstoffe, Weißpigment, Farbstoff oder Farbpigment, optische Aufheller, Antioxidantien und/oder andere bei der Herstellung photographischer Träger übliche Zusatzstoffe, z.B. verfestigende Harze, enthalten.The base paper is produced in a known manner using a paper machine. The paper pulp suspension is sized using alkyl ketene dimers or fatty acids or fatty acid salts, epoxidized fatty acid amides or anhydrides of fatty acids and mixtures thereof. In addition to pulp fibers, the paper pulp suspension can also contain synthetic fibers, mineral or organic fillers, white pigment, dye or color pigment, optical brighteners, antioxidants and / or other additives customary in the production of photographic supports, e.g. setting resins.
Es können Basispapiere beliebigen Flächengewichts und beliebiger Dichten verwendet werden.Base papers of any basis weight and of any density can be used.
Das Basispapier wird erfindungsgemäß mit einer Lösung von carboxylmodifiziertem Polyvinylalkohol imprägniert (oberflächengeleimt). Unter einem carboxylmodifizierten Polyvinylalkohol ist beispielsweise ein Vinylalkohol-Croton- oder -iso-Crotonsäurepolymer oder ein Vinylalkohol-Acryl oder -Methacrylsäurecopolymer zu verstehen. Erfindungsgemäß bevorzugt ist das Vinylalkohol-Crotonsäurecopolymer.According to the invention, the base paper is impregnated (surface-sized) with a solution of carboxyl-modified polyvinyl alcohol. A carboxyl-modified polyvinyl alcohol is understood to mean, for example, a vinyl alcohol croton or iso crotonic acid polymer or a vinyl alcohol acrylic or methacrylic acid copolymer. The vinyl alcohol-crotonic acid copolymer is preferred according to the invention.
Die carboxylmodifizierten Polyvinylalkohole zeigen in 4%iger Lösung bei Raumtemperatur eine Viskosität von 20 bis 50 mPa s. Das mittlere Molekulargewicht beträgt 5000 bis 20 000, bevorzugt 7000 bis 10 000.The carboxyl-modified polyvinyl alcohols have a viscosity of 20 to 50 mPa s in 4% solution at room temperature. The average molecular weight is 5,000 to 20,000, preferably 7,000 to 10,000.
Die erfindungsgemäß verwendeten carboxylmodifizierten Polyvinylalkohole werden als wäßrige Lösung unter Verwendung der bekannten und üblichen Auftragsverfahren aufgebracht. Die Auftragsmenge beträgt 0,5 bis 10 g/m2 vorzugsweise 1 bis 4,5 g/m2.The carboxyl-modified polyvinyl alcohols used according to the invention are applied as an aqueous solution using the known and customary application methods. The application amount is 0.5 to 10 g / m 2, preferably 1 to 4.5 g / m 2 .
Bei einer Auftragsmenge geringer als 0,5 g/m2 wird keine ausreichende Imprägnierung des Papierkerns (Basispapiers) erreicht und das Eindringen der photographischen Behandlungslösungen in die Kanten sowie das Verschmutzen der Kanten durch die photographischen Behandlungslösungen nicht im gewünschten Ausmaß vermieden.If the application quantity is less than 0.5 g / m 2 , sufficient impregnation of the paper core (base paper) is not achieved and the penetration of the photographic treatment solutions into the edges and the contamination of the edges by the photographic treatment solutions are not avoided to the desired extent.
Es wurde gefunden, daß der erfindungsgemäße Effekt nur bei Copolymeren mit einem Verseifungsgrad von wenigstens 96% erhalten wird.It has been found that the effect according to the invention is only obtained with copolymers with a degree of saponification of at least 96%.
Ist der Verseifungsgrad kleiner als 96% wird keine befriedigende Abdichtung des Papierkerns gegen das Eindringen der photographischen Behandlungslösungen erreicht.If the degree of saponification is less than 96%, a satisfactory sealing of the paper core against the penetration of the photographic treatment solutions is not achieved.
Es wurde ferner gefunden, daß die erfindungsgemäß beschriebenen Vorteile, nämlich die Verringerung des Eindringens photographischer Behandlungslösungen, Erhöhung der inneren Festigkeit des Papierkerns und der Haftung zwischen dem behandelten Basispapier und der Polyolefinüberzugsschicht, abhängig von der Anzahl der Carboxylgruppen in den verwendeten carboxylmodifizierten Polyvinylalkoholen ist.It has also been found that the advantages described according to the invention, namely the reduction in the penetration of photographic treatment solutions, the increase in the internal strength of the paper core and the adhesion between the treated base paper and the polyolefin coating layer, are dependent on the number of carboxyl groups in the carboxyl-modified polyvinyl alcohols used.
Und zwar steht die Verbesserung der Eigenschaften nicht in einem linearen Zusammenhang mit der Anzahl der Carboxylgruppen, so daß das Maxium nicht bei dem carboxylmodifizierten Polyvinylalkohol mit dem größten Carboxylgruppenanteil auftritt.In fact, the improvement in properties is not linearly related to the number of carboxyl groups, so that the maxium does not occur in the carboxyl-modified polyvinyl alcohol with the largest proportion of carboxyl groups.
Das Optimum wird vielmehr nur dann erzielt, wenn carboxylmodifizierte Polyvinylalkohole verwendet werden, die einen Carboxylgruppenanteil von 1,5 bis 7 mol-%, bevorzugt 2,5 bis 3,5 mol-%, enthalten.Rather, the optimum is only achieved if carboxyl-modified polyvinyl alcohols are used which contain a carboxyl group content of 1.5 to 7 mol%, preferably 2.5 to 3.5 mol%.
Der erfindungsgemäße Effekt wird bereits erreicht, wenn ein in bekannter Weise hergestelltes geleimtes Papier mit einer Lösung des Carboxylgruppen enthaltenden Polyvinylalkohols imprägniert wird.The effect according to the invention is already achieved when a sized paper produced in a known manner is impregnated with a solution of the polyvinyl alcohol containing carboxyl groups.
Gemäß einer bevorzugten Ausführungsform der Erfindung ist der erfindungsgemäße Effekt jedoch verstärkt, wenn zusätzlich mehrwertige Kationen in das Papier eingebracht werden. Diese Verbindungen können aus der Gruppe der Erdalkali-Verbindungen, beispielsweise Calcium- oder Magnesiumchlorid, aus der Gruppe der Aluminiumsalze, beispielsweise Aluminiumsulfat oder Aluminiumchlorid, und aus den Verbindungen der übergangsmetalle ausgewählt werden. Besonders bevorzugt werden Salze des Zirkoniums, beispielsweise Zirkoniumammoniumcarbonat oder Zirkoniumorthosulfat, und Verbindungen des Chroms, z.B. Chrom-Komplexe vom Werner-Typ.According to a preferred embodiment of the invention, however, the effect according to the invention is enhanced, if additional polyvalent cations are introduced into the paper. These compounds can be selected from the group of alkaline earth compounds, for example calcium or magnesium chloride, from the group of aluminum salts, for example aluminum sulfate or aluminum chloride, and from the compounds of the transition metals. Salts of zirconium, for example zirconium ammonium carbonate or zirconium orthosulfate, and compounds of chromium, for example chromium complexes of the Werner type, are particularly preferred.
Die mehrwertigen Kationen werden vorzugsweise der wäßrigen Beschichtungslösung zugesetzt. Sie können aber auch vor Anwendung der erfindungsgemäßen Polyvinylalkohollösung der Zellstoffsuspension zugesetzt oder dem Basispapier inkorporiert werden. Oder sie können in Form einer Nachbehandlung (z.B. durch Sprühen) nach Imprägnierung mit der Polyvinylalkohollösung aufgebracht werden.The polyvalent cations are preferably added to the aqueous coating solution. However, they can also be added to the cellulose suspension or incorporated into the base paper before the polyvinyl alcohol solution according to the invention is used. Or they can be applied in the form of an aftertreatment (e.g. by spraying) after impregnation with the polyvinyl alcohol solution.
Die mehrwertigen Kation-Verbindungen stehen zu dem carboxylierten Polyvinylalkohol in einem Gewichtsverhältnis von 1/10 bis 5/1. Unterschreitet das Gewichtsverhältnis den Wert von 1/10, wird die Verstärkung des beschriebenen Effektes nicht erlangt. Eine Erhöhung des Gewichtsverhältnisses auf Werte über 5/1 bringt keine weitere Verbesserung des erfindungsgemäßen Effektes.The polyvalent cation compounds are in a weight ratio of 1/10 to 5/1 to the carboxylated polyvinyl alcohol. If the weight ratio falls below the value of 1/10, the amplification of the described effect is not achieved. An increase in the weight ratio to values above 5/1 brings no further improvement in the effect according to the invention.
Weder durch die alleinige Verwendung der carboxylmodifizierten Polyvinylalkohole noch durch die Verwendung einer beschriebenen Kombination mit den Verbindungen mit mehrwertigen Kationen werden die photographischen Emulsionen beeinträchtigt.Neither the use of the carboxyl-modified polyvinyl alcohols alone nor the use of a combination described with the compounds with polyvalent cations impair the photographic emulsions.
Obwohl durch die Verwendung der erfindungsgemäß verwendeten Verbindungen bereits eine antistatische Ausrüstung des Papieres erreicht wird, kann der wäßrigen Beschichtungslösung, falls es gewünscht wird, zusätzlich Salz, beispielsweise Natriumchlorid oder Kaliumchlorid, zur Erhöhung der Leitfähigkeit der Papieroberfläche zugesetzt werden. Die wäßrige Beschichtungslösung kann außerdem optische Aufheller, Entschäumer, Pigmente, Hydrophobierungsmittel oder Vernetzungshilfsmittel, wie zum Beispiel Dimethylolharnstoff oder Trimethylolmelamin, enthalten.Although the use of the compounds used according to the invention already achieves an antistatic finish on the paper, if desired, additional salt, for example sodium chloride or potassium chloride, can be added to the aqueous coating solution to increase the conductivity of the paper surface. The aqueous coating solution can also contain optical brighteners, defoamers, pigments, water repellents or crosslinking aids, such as, for example, dimethylolurea or trimethylolmelamine.
Die Erfindung wird anhand der nachfolgenden Beispiele näher erläutert.The invention is illustrated by the following examples.
Ein ca. 175 g/m2 schweres Papier wird aus einer wäßrigen Faserstoffsuspension (LBKP/NBKP = 1/1), die zusätzlich 0,5 Gew.-% Polyamid-Polyamin-Epichlorhydrin, 0,5 Gew.-% kationisches Polyacrylamid, 0,5 Gew.-% anionisches Polyacrylamid und 0,4 Gew.-% Alkylketendimer mit Alkylgruppen mit 14 bis 16 Kohlenstoffatomen enthält, hergestellt. Der Papierträger wird mit einer wäßrigen Beschichtungsmischung folgender Zusammensetzung behandelt:
Die Auftragsmenge beträgt 2 g/m2.The order quantity is 2 g / m 2 .
Es werden Crotonsäure-modifizierte Polyvinylalkohole mit folgenden Carboxylgruppenanteilenverwendet:
Das behandelte Papier wird getrocknet und mit Polyethylen in üblicher Weise extrusionsbeschichtet.The treated paper is dried and extrusion coated with polyethylene in the usual way.
Ein ca. 175 g/m2 schweres Papier wird aus einer wäßrigen Faserstoffsuspension (LBKP/NBKP = 2/1), die zusätzlich 5 Gew.-% Natriumstearat und 10 Gew.-% Aluminiumsulfat enthält, hergestellt. Das Papier wird mit der in Beispiel 1 verwendeten Beschichtungsmischung behandelt. Die Auftragsmenge beträgt 3 g/m2.A paper weighing approximately 175 g / m 2 is produced from an aqueous fiber suspension (LBKP / NBKP = 2/1) which additionally contains 5% by weight of sodium stearate and 10% by weight of aluminum sulfate. The paper is treated with the coating mixture used in Example 1. The order quantity is 3 g / m 2 .
Es werden Crotonsäure-modifizierte Polyvinylalkohole mit folgenden Carboxylgruppenanteilen verwendet.
Das behandelte Papier wird getrocknet und in üblicher Weise mit Polyethylen extrusionsbeschichtet.The treated paper is dried and extrusion coated in a conventional manner with polyethylene.
Ein ca. 140 g/m2 schweres mittels 0,3 Gew.-% Alkylketendimer, 1,6 Gew.-% Fettsäureseife und 0,5 Gew.-% Aluminium-Ionen in der Papiermasse geleimtes Papier wird mit einer wäßrigen Beschichtungsmischung behandelt, die einen Crotonsäure-modifizierten Polyvinylalkohol mit einem Verseifungsgrad von 98,5 % und einem Carboxylgruppenanteil von 3,1 mol-% in der Menge von 40 g/1 enthält. Außerdem werden Verbindungen folgender mehrwertiger Kationen zugesetzt:
Die Auftragsmenge beträgt 1,5 g/m2. Das behandelte Papier wird getrocknet und mit Polyethylen in üblicher Weise extrusionsbeschichtet.The application quantity is 1.5 g / m 2 . The treated paper is dried and extrusion coated with polyethylene in the usual way.
Ein ca. 150 g/m2 schweres gemäß Beispiel 1 in der Papiermasse geleimtes Papier wird mit wäßrigen Beschichtungsmischungen folgender Zusammensetzungen behandelt:
Die Auftragsmenge beträgt 4,5 g/m2.The order quantity is 4.5 g / m 2 .
Das behandelte Papier wird getrocknet und mit einer Polyethylenüberzugsmischung folgender Zusammensetzung überzogen:
- 20 Gew.-% Hochdruckpolyethylen (Dichte 0,963, Schmelzindex 10)
- 70 Gew.-% Niederdruckpolyethylen (Dichte 0,918, Schmelzindex 7)
- 9,8 Gew.-% Ti02
- 0,1 1 Gew.% optischer Aufheller
- 0,1 Gew.-% Stabilisator
- 300 ppm Polyetherglykol (MW 600)
- 20% by weight high-pressure polyethylene (density 0.963, melt index 10)
- 70% by weight low-pressure polyethylene (density 0.918, melt index 7)
- 9.8% by weight of TiO 2
- 0.1 1% by weight of optical brighteners
- 0.1 wt% stabilizer
- 300 ppm polyether glycol (MW 600)
Ein ca. 140 g/m2 schweres Papier gemäß Beispiel 3 wird in der Papiermaschine in einer ersten Leimpresse mit der folgenden Salzlösung behandelt:
Nach einer Zwischentrocknung wird das Papier in einer zweiten Leimpresse mit folgender Polyvinylalkohollösung beidseitig behandelt.
Die Auftragsmengen betragen in beiden Fällen 1,5 g/m2.The application quantities in both cases are 1.5 g / m 2 .
Das behandelte Papier wird getrocknet und mit Polyethylen in üblicher Weise extrusionsbeschichtet.The treated paper is dried and extrusion coated with polyethylene in the usual way.
Die Prüfung des Trägermaterials wurde in diesem Fall erst nach 1wöchiger Lagerung durchgeführt.In this case, the test of the carrier material was only carried out after 1 week of storage.
Ein ca. 140 g/m2 schweres Papier gemäß Beispiel 3 wird in der Leimpresse einer Papiermaschine mit folgender Lösung behandelt:
Nach Trocknung werden nacheinander beide Seiten mit folgender Salzlösung über ein Düsensystem besprüht:
Die Auftragsmengen betragen in der Leimpresse 1,5 g/m2 und beim Besprühen 1,0 g/m2.The application quantities are 1.5 g / m 2 in the size press and 1.0 g / m 2 when spraying.
Das behandelte Papier wird getrocknet und mit Polyethylen in üblicher Weise extrusionsbeschichtet.The treated paper is dried and extrusion coated with polyethylene in the usual way.
Die Prüfung des Trägermaterials wurde in diesem Fall erst nach 1-wöchiger Lagerung durchgeführt.In this case, the test of the carrier material was only carried out after 1 week of storage.
Ein nach Beispiel 1 hergestelltes Papier wird mit einer wäßrigen Beschichtungsmischung folgender Zusammensetzung behandelt:
Die Auftragsmenge beträgt 3 g/m2. Das behandelte Papier wird getrocknet und mit Polyethylen in üblicher Weise extrusionsbeschichtet.The order quantity is 3 g / m 2 . The treated paper is dried and extrusion coated with polyethylene in the usual way.
Ein nach Beispiel 2 der DOS 32 41 599 hergestelltes Papierblatt wird mit der dort beschriebenen Beschichtungsmischung behandelt (die Auftragsmenge beträgt 3 g/m2), anschließend getrocknet und mit Polyethylen in der üblichen Weise extrusionsbeschichtet.A paper sheet produced according to Example 2 of DOS 32 41 599 is treated with the coating mixture described there (the application amount is 3 g / m 2 ), then dried and extrusion-coated with polyethylene in the usual way.
Ein nach Beispiel 3 hergestelltes Papierblatt wird mit der in Vergleichsbeispiel V1 beschriebenen Beschichtungsmischung behandelt. Die Auftragsmenge beträgt 3 g/m2. Das behandelte Papier wird getrocknet und mit Polyethylen in üblicher Weise beschichtet.A paper sheet produced according to Example 3 is treated with the coating mixture described in Comparative Example V1. The order quantity is 3 g / m 2 . The treated paper is dried and coated with polyethylene in the usual way.
Ein nach Beispiel 3 hergestelltes Papier von 140 g/m2 wird mit folgender Beschichtungsmischung behandelt (oberflächengeleimt):
Das behandelte Papier wird getrocknet und mit Polyethylen in üblicher Weise extrusionsbeschichtet.The treated paper is dried and extrusion coated with polyethylene in the usual way.
Ein nach Beispiel 1 hergestelltes Papier von 175 g/m2 wird mit folgender Beschichtungsmischung behandelt:
Das behandelte Papier wird getrocknet und mit Polyethylen in üblicher Weise extrusionsbeschichtet.The treated paper is dried and extrusion coated with polyethylene in the usual way.
Die behandelten Papiere werden mit Polyethylen beschichtet und anschließend den folgenden Prüfungen unterzogen.The treated papers are coated with polyethylene and then subjected to the following tests.
Unter behandeltem Papier wird hierbei ein Papier verstanden, das die Behandlung des Basispapieres durch die Beschichtungsmischungen in Form von beidseitigen Anträgen durch Tauchvorgänge (Leimpresse), Besprühen, beidseitigen Antragen mittels Walzenauftragssysteme, Schlitzgießern oder ähnlichem erfahren hat.Treated paper is understood here to mean paper which has undergone the treatment of the base paper by the coating mixtures in the form of applications on both sides by dipping processes (size press), spraying, application on both sides by means of roller application systems, slot casters or the like.
Bei der Prüfung wird die Entwickleraufnahme durch das Papier bestimmt (modifizierter Cobb-Test). Es werden aus der Papier bahn Prüfstücke im Format 14 x 14 cm ausgeschnitten, genau gewogen und in einer zylinderförmigen Prüfvorrichtung festgeklemmt. In den Zylinder werden 100 ml eines handelsüblichen photographischen Entwicklers gegeben, über die Zeitdauer von 50 sec. einwirken gelassen und anschließend abgeschüttet. Der Prüfling wird abgelöscht und sofort gewogen. Das Ausmaß der Entwickleraufnahme wird in g/m2 angegeben.During the test, the developer absorption is determined by the paper (modified Cobb test). Test pieces in the format 14 x 14 cm are cut out of the paper web, weighed exactly and clamped in a cylindrical test device. 100 ml of a commercially available photographic developer are placed in the cylinder, left to act for a period of 50 seconds and then poured off. The test specimen is erased and weighed immediately. The extent of developer uptake is given in g / m 2 .
Das Prüfstück wird einem simulierten photographischen Entwicklungsprozeß mit einem Benzylalkohol enthaltenden handelsüblichen Entwickler bei einer Temperatur von etwa 30°C und über eine Zeitdauer von 25 Minuten unterworfen. An beiden Kanten des Prüfstückes wird das Eindringen der photographischen Behandlungslösungen mit einer Meßlupe ausgemessen. Die Meßwerte werden als Kanteneindringen (KE) in mm angegeben.The test piece is subjected to a simulated photographic development process with a commercial developer containing benzyl alcohol at a temperature of about 30 ° C and for a period of 25 minutes. The penetration of the photographic treatment solutions is measured on both edges of the test piece with a measuring magnifier. The measured values are given as edge penetration (KE) in mm.
Die Prüfung erfolgt nach der in TAPPI RC 308 angegebenen Methode mit dem Internal Bond Impact Tester Model B.The test is carried out according to the method specified in TAPPI RC 308 with the Internal Bond Impact Tester Model B.
Die Meßwerte werden in 1/1000 Fuß x Pfund angegeben.The measurements are reported in 1/1000 feet x pounds.
Die Prüfung erfolgt mit einem Zugfestigkeitsmeßgerät der Fa. A.B. Lorentzen & Wettre an 15 mm breiten und 18 cm langen Prüfstreifen. Der Abzugswinkel beträgt 180°, die Abzugsgeschwindigkeit 70 mm/min. Die Meßwerte werden in mN/15 mm angegeben.
Die Prüfwerte auf den Seiten 18 und 19 zeigen, daß das Optimum in Bezug auf Kanteneindringen, Spaltfestigkeit und Haftung zur Polyethylenüberzugsschicht bei einem Carboxylgruppenanteil zwischen 2,5 und 3;5 mol-% liegt.The test values on pages 18 and 19 show that the optimum in terms of edge penetration, gap resistance and adhesion to the polyethylene coating layer with a carboxyl group content is between 2.5 and 3.5 mol%.
Die Gegenüberstellung zu den im Stand der Technik beschriebenen Beschichtungsmischungen (Vergleichsbeispiele V1 und V4), speziell zu der in der DOS 32 41 599 verwendeten Mischung (Vergleichsbeispiel V2), dokumentiert deutlich die Verbesserung der Werte durch die Verwendung der erfindungsgemäß beschriebenen Beschichtungslösungen. Mit dem Vergleichsbeispiel V5 wird demonstriert, daß ein Verseifungsgrad von 88% für den verwendeten Polyvinylalkohol nicht ausreicht, um den angestrebten Effekt zu erzielen.The comparison with the coating mixtures described in the prior art (comparative examples V1 and V4), specifically with the mixture used in DOS 32 41 599 (comparative example V2), clearly documents the improvement in the values by using the coating solutions described according to the invention. Comparative example V5 demonstrates that a degree of saponification of 88% for the polyvinyl alcohol used is not sufficient to achieve the desired effect.
Claims (15)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AT86113855T ATE46221T1 (en) | 1985-12-10 | 1986-10-07 | WATERPROOF PHOTOGRAPHIC PAPER CARRIER. |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19853543597 DE3543597A1 (en) | 1985-12-10 | 1985-12-10 | WATERPROOF PHOTOGRAPHIC PAPER CARRIER |
DE3543597 | 1985-12-10 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0225446A1 true EP0225446A1 (en) | 1987-06-16 |
EP0225446B1 EP0225446B1 (en) | 1989-09-06 |
Family
ID=6288090
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP86113855A Expired EP0225446B1 (en) | 1985-12-10 | 1986-10-07 | Water-resistant photographic paper support |
Country Status (7)
Country | Link |
---|---|
US (1) | US4731291A (en) |
EP (1) | EP0225446B1 (en) |
JP (1) | JPH083608B2 (en) |
AT (1) | ATE46221T1 (en) |
DE (2) | DE3543597A1 (en) |
ES (1) | ES2010652B3 (en) |
GR (1) | GR3000239T3 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5567473A (en) * | 1991-08-19 | 1996-10-22 | Eastman Kodak Company | Photographic paper with low oxygen permeability |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ATE50369T1 (en) * | 1986-07-22 | 1990-02-15 | Schoeller F Jun Gmbh Co Kg | PHOTOGRAPHIC PAPER SUPPORT AND PROCESS FOR ITS MANUFACTURE. |
DE3882368D1 (en) * | 1988-07-28 | 1993-08-19 | Schoeller F Jun Gmbh Co Kg | WATERPROOF PHOTOGRAPHIC PAPER CARRIER. |
US4988559A (en) * | 1988-11-15 | 1991-01-29 | Oji Paper Co., Ltd. | Support sheet for photographic printing sheet |
JP2659578B2 (en) * | 1989-02-06 | 1997-09-30 | 三菱製紙株式会社 | Photographic support |
US5102730A (en) * | 1990-02-20 | 1992-04-07 | Andrews Paper & Chemical Co., Inc. | Erasable reproduction material |
JP2793898B2 (en) * | 1990-09-25 | 1998-09-03 | 富士写真フイルム株式会社 | Photographic paper support |
EP0664487B1 (en) * | 1993-12-08 | 1998-07-29 | Fuji Photo Film Co., Ltd. | Silver halide light-sensitive material comprising light-sensitive polymerizable layer and an overcoating layer containing polyvinyl alcohol with acidic groups or a salt thereof |
US5464691A (en) * | 1994-07-22 | 1995-11-07 | Arizona Chemical Company | Laminated barrier film |
JP3311874B2 (en) * | 1994-10-14 | 2002-08-05 | 富士写真フイルム株式会社 | Composition for lithographic printing dampening solution |
JP3571192B2 (en) * | 1997-09-26 | 2004-09-29 | ユニ・チャーム株式会社 | Water-degradable cleaning sheet containing modified polyvinyl alcohol |
MX357920B (en) * | 2013-01-10 | 2018-07-31 | Rivera Carmona Dalila | Non-transparent art paper which prevents ink seepage. |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3241599A1 (en) * | 1981-11-10 | 1983-05-19 | Fuji Photo Film Co., Ltd., Minami-Ashigara, Kanagawa | PHOTOGRAPHIC CARRIER |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS4994275A (en) * | 1973-01-12 | 1974-09-06 | ||
DE2515823C2 (en) * | 1975-04-11 | 1984-06-07 | Felix Schoeller jr. GmbH & Co KG, 4500 Osnabrück | Process for the production of a photographic support material to be dried by microwave treatment |
JPS5684954A (en) * | 1979-12-12 | 1981-07-10 | Azona Kk | Filmmpaper laminate and its manufacture |
JPS59185690A (en) * | 1983-04-07 | 1984-10-22 | Jujo Paper Co Ltd | Ink jet recording paper |
JPS60217357A (en) * | 1984-04-12 | 1985-10-30 | Mitsubishi Paper Mills Ltd | Photographic paper coated with polyethylene |
-
1985
- 1985-12-10 DE DE19853543597 patent/DE3543597A1/en active Granted
-
1986
- 1986-10-07 DE DE8686113855T patent/DE3665505D1/en not_active Expired
- 1986-10-07 ES ES86113855T patent/ES2010652B3/en not_active Expired
- 1986-10-07 AT AT86113855T patent/ATE46221T1/en not_active IP Right Cessation
- 1986-10-07 EP EP86113855A patent/EP0225446B1/en not_active Expired
- 1986-11-21 US US06/933,488 patent/US4731291A/en not_active Expired - Fee Related
- 1986-12-10 JP JP29263986A patent/JPH083608B2/en not_active Expired - Lifetime
-
1989
- 1989-12-04 GR GR89400276T patent/GR3000239T3/en unknown
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3241599A1 (en) * | 1981-11-10 | 1983-05-19 | Fuji Photo Film Co., Ltd., Minami-Ashigara, Kanagawa | PHOTOGRAPHIC CARRIER |
Non-Patent Citations (1)
Title |
---|
PATENTS ABSTRACTS OF JAPAN, Band 5, Nr. 60 (P-58)[732], 23. April 1981; & JP-A-56 014 235 (FUJI SHASHIN FILM K.K.) 12-02-1981 * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5567473A (en) * | 1991-08-19 | 1996-10-22 | Eastman Kodak Company | Photographic paper with low oxygen permeability |
US5695862A (en) * | 1991-08-19 | 1997-12-09 | Eastman Kodak Company | Photographic paper with low oxygen permeability |
Also Published As
Publication number | Publication date |
---|---|
JPH083608B2 (en) | 1996-01-17 |
EP0225446B1 (en) | 1989-09-06 |
GR3000239T3 (en) | 1991-03-15 |
DE3543597A1 (en) | 1987-06-11 |
DE3665505D1 (en) | 1989-10-12 |
ATE46221T1 (en) | 1989-09-15 |
ES2010652B3 (en) | 1989-12-01 |
US4731291A (en) | 1988-03-15 |
JPS62138848A (en) | 1987-06-22 |
DE3543597C2 (en) | 1992-03-05 |
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