EP0268751B1 - Support photographique en papier résistant à l'eau - Google Patents

Support photographique en papier résistant à l'eau Download PDF

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Publication number
EP0268751B1
EP0268751B1 EP87112134A EP87112134A EP0268751B1 EP 0268751 B1 EP0268751 B1 EP 0268751B1 EP 87112134 A EP87112134 A EP 87112134A EP 87112134 A EP87112134 A EP 87112134A EP 0268751 B1 EP0268751 B1 EP 0268751B1
Authority
EP
European Patent Office
Prior art keywords
paper
carrier according
alkyl ketene
paper carrier
alkyl
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
EP87112134A
Other languages
German (de)
English (en)
Other versions
EP0268751A1 (fr
Inventor
Heinz-Otto Dr. Dipl.-Chem. Merz
Alois-Bernhard Dr. Dipl.-Chem. Kerkhoff
Wolfgang Chem.Ing. Storbeck
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.)
Felix Schoeller Jr Foto und Spezialpapiere GmbH
Felex Schoeller Jr and GmbH and Co KG
Original Assignee
Felix Schoeller Jr Foto und Spezialpapiere GmbH
Felex Schoeller Jr and GmbH and Co KG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Felix Schoeller Jr Foto und Spezialpapiere GmbH, Felex Schoeller Jr and GmbH and Co KG filed Critical Felix Schoeller Jr Foto und Spezialpapiere GmbH
Priority to AT87112134T priority Critical patent/ATE51966T1/de
Publication of EP0268751A1 publication Critical patent/EP0268751A1/fr
Application granted granted Critical
Publication of EP0268751B1 publication Critical patent/EP0268751B1/fr
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03Non-macromolecular organic compounds
    • D21H17/05Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/17Ketenes, e.g. ketene dimers
    • GPHYSICS
    • G03PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
    • G03CPHOTOSENSITIVE MATERIALS FOR PHOTOGRAPHIC PURPOSES; PHOTOGRAPHIC PROCESSES, e.g. CINE, X-RAY, COLOUR, STEREO-PHOTOGRAPHIC PROCESSES; AUXILIARY PROCESSES IN PHOTOGRAPHY
    • G03C1/00Photosensitive materials
    • G03C1/76Photosensitive materials characterised by the base or auxiliary layers
    • G03C1/775Photosensitive materials characterised by the base or auxiliary layers the base being of paper
    • G03C1/79Macromolecular coatings or impregnations therefor, e.g. varnishes
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/25Web or sheet containing structurally defined element or component and including a second component containing structurally defined particles
    • Y10T428/256Heavy metal or aluminum or compound thereof
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31511Of epoxy ether
    • Y10T428/31515As intermediate layer
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31725Of polyamide
    • Y10T428/31768Natural source-type polyamide [e.g., casein, gelatin, etc.]
    • Y10T428/31772Next to cellulosic
    • Y10T428/31775Paper
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/3188Next to cellulosic
    • Y10T428/31895Paper or wood
    • Y10T428/31899Addition polymer of hydrocarbon[s] only
    • Y10T428/31902Monoethylenically unsaturated

Definitions

  • the invention relates to a waterproof coated paper support for photographic layers.
  • paper coated with polyolefin on both sides as a waterproof support material for photographic layers.
  • a carrier material is known to consist of a sized base paper with synthetic resin coatings applied to both surfaces.
  • the synthetic resin coatings can consist of polyolefin and have been applied to the paper by means of extrusion coating.
  • Papers coated on both surfaces with a polyolefin resin are protected against the ingress of water and aqueous processing solutions for photographic materials: only the open edges of the laminates allow aqueous processing solutions to penetrate into the paper core, because the pulp fibers of the paper core, which are naturally hydrophilic , exposed there. For this reason, the base papers for a synthetic resin coating are usually sized to be extremely hydrophobic in order to keep the penetration of the photographic processing solutions as low as possible.
  • Known glues for photographic base papers that are highly hydrophobic for the paper are dimeric alkyl ketene. These dimerized alkyl ketenes are generally used in the neutral pH range together with cationic retention agents or strengthening resins and at least partially react with superficial OH groups of the cellulose fibers. (J.Appl.Photographic Engineering 3 (1981), Issue 7, pp.68 / 69) It is also possible to use dimeric alkylketenes together with fatty acid soaps or fatty acid anhydrides, which are precipitated with aluminum salts and fixed to the fibers to achieve an optimal glue effect will.
  • alkyl ketene dimers with alkyl chains of different lengths (“mixed" alkyl ketene dimers) are usually used.
  • the alkyl group contains between 12 and 18 carbon atoms, as in R.D. November 1978, communication 17516 is communicated.
  • Mixed alkyl ketene dimers with 16 and 18 carbon atoms are predominantly used.
  • DE-OS 33 06 768 also shows that a mixed alkyl ketene dimer with predominantly C J6 and C, 8 alkyl radicals and smaller proportions of C 2 o and more alkyl radicals is best suited, while C i4 or CJ2 alkyl radicals are less suitable are suitable to obtain a good hydrophobizing sizing of the base paper.
  • DE-OS 33 06 768 more or less precisely claims the use of alkyl ketene dimers with alkyl chain compositions by the equation are defined.
  • alkyl ketene dimers because of their good gluing effect, alone or in combination with other glue agents, are widely used for the production of photographic base papers for synthetic resin found stratification, they still have disadvantages that previously seemed insurmountable. This applies to all alkyl ketene dimers previously used for photographic papers.
  • alkyl ketene dimer does not fully react as it passes through the paper mixture. In practice, only a small part reacts with OH groups of the pulp. A larger part of the alkyl ketene dimer added to the pulp suspension for sizing is not chemically, but only physically bound in the paper fleece and therefore does not develop its full hydrophobic effect. This physically bound part consists partly of ketone, but partly of unreacted alkyl ketene dimer (Wochenblatt für Textilfabrikation 1983, p.215 f). In order to compensate for this low degree of reaction, the practice in the production of photographic base papers is carried out with additions of alkyl ketene dimer of 0.5 to 0.7% by weight, based on pulp. This amount is significantly higher than would theoretically be necessary to make the fibers hydrophobic if the reaction with OH groups described in the literature were to proceed faster and more completely.
  • Another disadvantage is that because of the large proportion of physically bound alkyl ketene dimer in the paper, the hydrogen bond between the cellulose fibers (fiber-fiber bond) is disturbed and the internal strength and rigidity of the paper are reduced as a result.
  • unreacted alkyl ketene dimer migrates to the paper surface during a short storage period of the paper, accumulates there and malfunctions in the subsequent application of synthetic resin layers, e.g. Polyolefin layers.
  • the accumulation of the unreacted alkyl ketene dimer (dust) on the surface of the paper can be so strong that deposits of alkyl ketene dimer occur on the rolls and rollers of the coating unit during extrusion coating with polyolefin.
  • rolls that come into contact with uncoated paper must be cleaned up to several times a day.
  • the base paper is sized with an alkyl ketene dimer, which is predominantly formed from behenyl ketene.
  • the paper core is preferably sized with an alkyl ketene dimer which consists of at least 60% behenyl ketene dimer with C 2 o-alkyl residues and has a maximum of 40% alkyl residues derived from shorter-chain fatty acids than C 20 .
  • Papers produced according to the invention using a behenyl ketene dimer with more than 60% C 20 alkyl radicals did not show the disadvantages set out in the description of the prior art.
  • the papers according to the invention showed neither a blooming of alkyl ketene dimer (dust) nor disproportionate disturbances in the subsequent coating with polyolefin and with photographic layers. Above all, there were no adhesion problems and no wetting problems due to the transfer of alkyl ketene dimer to the polyolefin surface.
  • Papers according to the invention showed an excellent sizing effect even with smaller additions of behenyl ketene dimer than previously customary for the pulp suspension and thus a low edge penetration of photographic treatment solutions.
  • the alkylketene dimer essentially containing behenyl chains is added to the pulp suspension in the form of an aqueous emulsion.
  • the amount of alkyl ketene dimer to be added, based on the pulp, is between 0.1 and 1.0% by weight in the product according to the invention.
  • alkyl ketene dimer with at least 60% of C2o-alkyl chains is between 0.2 and 0.7% by weight, based on the paper stock.
  • the base paper can contain the known cationic resins such as polyamide-epichlorohydrazine resin, polyacrylamide or starch derivatives. It can contain a combination of cationic and anionic resins, such as in DE-OS 33 28 463, DE-OS 32 10 621 or DE-OS 32 16 840 described, and it may contain additional other sizes such as soaps of higher fatty acids, fatty acid anhydrides or epoxidized higher fatty acid amides.
  • the additives customary in photographic base papers such as pigments, fillers, dyes and optical brighteners, can be present in the paper in the known amounts.
  • the finished, usually also surface-sized base paper is coated on both sides with synthetic resin, e.g. with polyolefin, extrusion-coated and used as a base material for photographic layers.
  • synthetic resin e.g. with polyolefin, extrusion-coated
  • a bleached short fiber pulp (hardwood sulfate pulp) was ground at a consistency of 4% to 35 ° SR.
  • the fabric was sized with the amounts of alkyl ketene dimer according to the invention (with 87% C 2 o-alkyl radicals) and 1% by weight of polyamide-polyamine-epichlorohydrin given in Table 1 under Example 1.
  • the fabric was processed in the usual way on a paper machine to photo raw paper of 175 g / m2 basis weight, the surface of the paper being sized with the following aqueous solution using a size press:
  • a portion of the base paper was then extrusion coated on both sides with polyethylene of 30 g / m 2 each, as described, for example, in Example 4 of US 38 33 380.
  • a short fiber pulp according to Example 1 was sized with the amounts of alkyl ketene dimer according to the invention mentioned in Table 1 under Example 2 (with 87% C 2o alkyl radicals), 1% by weight polyamide-polyamine-epichlorohydrin and sodium stearate and aluminum sulfate at pH 4.5.
  • the base paper was produced in a known manner in the paper machine, the impregnation solution from Example 1 being applied in the same amount as surface sizing in the size press. Part of the 175 g / m 2 paper was coated with polyethylene as in Example 1.
  • a paper was produced under the conditions described in Example 1, but the alkyl ketene dimer was a commercial product based on palmitic / stearic acid.
  • alkyl ketene dimer added are given in Table 1 under comparison 1.1 V to 1.4V.
  • a paper was produced under the conditions described in Example 2, but the alkyl ketene dimer was a commercially available product based on palmitic / stearic acid.
  • alkyl ketene dimer added are given in Table 1 under comparison 2.1 V to 2.3V.
  • a paper was produced under the conditions described in Example 1, but the alkyl ketene dimer was a product based on pure stearic acid (98% stearyl ketene content).
  • the substance was mixed with the amounts of alkyl ketene dimer according to the invention (with 87% C 2 o-alkyl radicals), 1% by weight polyamide-polyamine-epichlorohydrin and epoxidized stearic acid amide and / or cationic and / or anionic polyacrylamide given in Table 2 under Example 3 and processed on the paper machine in the usual way to form a base paper, a surface sizing with the following aqueous formulation being applied in the size press:
  • the application of the size press solution after drying was 1.7 g / m 2 .
  • the entire base paper had a weight of 110 g / m 2 .
  • Part of this base paper was extrusion-coated on both sides with 20 g / m 2 polyethylene, as is known from corresponding processes.
  • the variable amounts are listed in Table 2 under Example 4. Surface sizing, basis weight and polyethylene coating corresponded to those from Example 3.
  • a paper was produced according to the conditions described in Example 3, but the alkyl ketene dimer was a product based on palmitic / stearic acid.
  • a paper was produced according to the conditions described in Example 4, but the alkyl ketene dimer was a product based on palmitic / stearic acid.
  • a short fiber pulp (hardwood sulfate pulp) was ground at a consistency of 4% to 30 ° SR.
  • the fabric was sized with the alkyl ketene dimer according to the invention (87% C 2 o-alkyl radicals), 1% by weight polyamide-polyamine-epichlorohydrin, starch and the auxiliaries listed in Table 3 under Example 5.
  • the solution from Example 1 was applied in the size press of a paper machine in an amount of 1.5 g / m 2 and side based on dry substance (i).
  • the raw paper weight was 75 g / m 2 .
  • Part of the base paper was extrusion coated on both sides with 20 g / m 2 polyethylene.
  • a base paper was produced in accordance with Example 1.
  • the alkyl ketene dimer used differed in its C 2 o-alkyl radical content as follows:
  • a paper was produced under the conditions described in Example 5, but the alkyl ketene dimer was a product based on palmitic / stearic acid.
  • the fabric was sized with 0.7% by weight alkyl ketene dimer and 0.7% by weight polyamide-polyamine-epichlorohydrin and produced on the paper machine, the impregnating liquid from Example 1 being applied in the amount specified there using the size press.
  • Part of the 170 g / m2 heavy base paper was extrusion coated on both sides with 30 g / m 2 polyethylene.
  • the composition of the alkyl ketene dimers used was as follows:
  • the internal strength of the base papers was determined using the Scott Bond gap strength tester (Internal Bond Impact Tester Model B) according to TAPPI RC 308.
  • the stiffness values of the base papers were determined with the bending stiffness tester from Lorentzen & Wettre, Sweden, according to standard SCAN-P 29.69 and converted to specific stiffness.
  • the coated papers were scratched on the surface with a razor blade so that the polyethylene could be peeled off in 25 mm wide strips.
  • the force required for pulling was measured with an Alwetron TH 1 tensile testing machine (Lorentzen & Wettre, Sweden).
  • the base papers produced according to the invention are preferably coated on both sides with polyolefin resin layers in order to produce the waterproof backing papers for photographic layers, as described in US Pat.
  • the resin-coated paper supports are then, if appropriate after pretreatment and application of further auxiliary layers, coated in a known manner with black / white or color photographic layers.

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  • 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)

Claims (20)

1. Support en papier résistant à l'eau pour couches photographiques, contenant un papier de base qui est encollé en utilisant des alkylcétènes dimères, caractérisé en ce que le papier de base est encollé d'un dimère d'alkyl-cétène qui est formé principalement de béhényl-cétène.
2. Support en papier selon la revendication 1, caractérisé en ce que le dimère d'alkylcétène est constitué pour au moins 60% de béhénylcétène comportant des radicaux alkyle en C20, tandis que le dimère d'alkyl-cétène contient tout au plus 40% de radicaux alkyle provenant d'acides gras d'une chaîne plus courte qu'une chaîne en C20.
3. Support en papier selon la revendication 1, caractérisé en ce que le papier de base est réalisé en utilisant 0,1 à 1% en poids de dimères d'alkyl-cétènes.
4. Support en papier selon la revendication 1, caractérisé en ce que le papier de base est préparé en utilisant 0,2 à 0,7% en poids de dimères d'alkyl-cétènes.
5. Support en papier selon la revendication 1, caractérisé en ce que le papier de base est réalisé en utilisant 0,1 à 1,0% en poids de dimères d'alkyl-cétènes contenant au moins jusqu'à 80% de radicaux alkyle en C20.
6. Support en papier selon la revendication 1, caractérisé en ce que le papier de base contient, en outre, une résine cationique.
7. Support en, papier selon la revendication 1, caractérisé en ce que le papier de base contient, en outre, aussi bien une résine cationique qu'au moins une résine anionique.
8. Support en papier selon la revendication 1, caractérisé en ce que le papier de base contient d'autres agents d'encollage en plus des dimères d'alkyl-cétènes.
9. Support en papier selon la revendication 8, caractérisé en ce qu'un autre agent d'encollage est un amide d'acide gras supérieur époxydé.
10. Support en papier selon la revendication 9, caractérisé en ce que l'amide d'acide gras supérieur époxydé est un amide d'acide stéarique époxydé.
11. Support en papier selon la revendication 9, caractérisé en ce que l'amide d'acide gras époxydé est un amide d'acide béhénique époxydé.
12. Support en papier selon la revendication 8, caractérisé en ce qu'un agent suppplémentaire d'encollage est un savon d'un acide gras supérieur.
13. Support en papier selon la revendication 1, caractérisé en ce que le papier de base contient, en plus de dimères d'alkyl-cétènes, un sel d'aliminium.
14. Support en papier selon la revendication 13, caractérisé en ce que le papier de base contient au moins un autre agent d'encollage en plus des dimères d'alkyl-cétènes et du sel d'aluminium.
15. Support en papier selon les revendications 3 et 6, caractérisé en ce que le papier de base est réalisé en utilisant 0,1 à 1% en poids de dimères d'alkyl-cétènes, tandis qu'il contient au moins une résine cationique.
16. Support en papier selon la revendication 6, caractérisé en ce que la résine cationique est une résine de polyamide/polyamine/épichlorhydrine.
17. Support en papier selon la revendication 6, caractérisé en ce que la résine cationique est un poly- acrylamide cationique.
18. Support en papier selon la revendication 7, caractérisé en ce que la résine anionique est un poly- acrylamide anionique ou un amidon anionique.
19. Support en papier selon la revendication 14, caractérisé en ce que le papier de base contient, en outre, une résine cationique.
20. Support en papier selon la revendication 14, caractérisé en ce que le papier de base contient, en outre, au moins résine cationique et au moins une résine anionique.
EP87112134A 1986-10-29 1987-08-21 Support photographique en papier résistant à l'eau Expired - Lifetime EP0268751B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT87112134T ATE51966T1 (de) 1986-10-29 1987-08-21 Wasserfester fotografischer papiertraeger.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE3636790 1986-10-29
DE3636790A DE3636790C1 (de) 1986-10-29 1986-10-29 Wasserfester fotografischer Papiertraeger

Publications (2)

Publication Number Publication Date
EP0268751A1 EP0268751A1 (fr) 1988-06-01
EP0268751B1 true EP0268751B1 (fr) 1990-04-11

Family

ID=6312734

Family Applications (1)

Application Number Title Priority Date Filing Date
EP87112134A Expired - Lifetime EP0268751B1 (fr) 1986-10-29 1987-08-21 Support photographique en papier résistant à l'eau

Country Status (10)

Country Link
US (1) US4820582A (fr)
EP (1) EP0268751B1 (fr)
JP (1) JP2839495B2 (fr)
CN (1) CN1009225B (fr)
AT (1) ATE51966T1 (fr)
AU (1) AU604754B2 (fr)
DE (1) DE3636790C1 (fr)
ES (1) ES2015020B3 (fr)
GR (2) GR3000810T3 (fr)
HU (1) HU206549B (fr)

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JP2793898B2 (ja) * 1990-09-25 1998-09-03 富士写真フイルム株式会社 写真印画紙用支持体
US5264080A (en) * 1991-04-12 1993-11-23 Minnesota Mining And Manufacturing Company Archival aperture card
GB9215422D0 (en) * 1992-07-21 1992-09-02 Hercules Inc System for sizing paper and cardboard
US5362614A (en) * 1993-02-12 1994-11-08 Fuji Photo Film Co., Ltd. Photographic printing paper support
EP0776397B1 (fr) * 1994-08-16 2000-10-25 Chemisolv Limited Procede d'amelioration de la resistance de papier
EP1042555A4 (fr) * 1997-12-22 2001-08-08 Int Paper Co Articles en papier et/ou en carton avec stabilite dimensionnelle
CA2277131A1 (fr) * 1998-08-14 2000-02-14 Schweitzer-Mauduit International, Inc. Procede pour augmenter la resistance humide des enveloppes de tampon poreux a utiliser dans les articles de fumeur
DE10237913A1 (de) * 2002-08-14 2004-02-26 Basf Ag Verfahren zur Herstellung von Karton aus Cellulosefasern für die Verpackung von Flüssigkeiten
WO2005031310A2 (fr) * 2003-09-25 2005-04-07 Sagres Discovery, Inc Dimeres d'alkylcetene formant des structures fractales destines a la croissance cristalline de proteines membranaires intrinseques
JP2008501870A (ja) * 2004-06-03 2008-01-24 フジフィルム マニュファクチャリング ユーロプ ビー.ブイ. 顔料被覆紙基材
EP1770213A1 (fr) * 2005-09-28 2007-04-04 Fuji Photo Film B.V. Support d'impression
EP1770214A1 (fr) * 2005-09-28 2007-04-04 Fuji Photo Film B.V. Support d'enregistrement
US20070101853A1 (en) * 2005-11-08 2007-05-10 Consumer Electronics Corp. Method of applying a graphic design to a guitar
SE534561C2 (sv) 2009-04-03 2011-10-04 Korsnaes Ab Pigmentbestruken kartong för förpackningar, förpackning innefattande pigmentbestruken kartong, användning av sådan kartong, och ett förfarande i en process för tillverkning av kartong
CN104088192B (zh) * 2014-06-26 2016-09-07 广东葫芦堡文化科技股份有限公司 一种用于压贴在木板表面的高清喷墨介材
CN116289311B (zh) * 2023-03-29 2023-09-29 浙江百斯特化工有限公司 一种高稳定性akd施胶剂的制备方法

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JPS57185432A (en) * 1981-05-11 1982-11-15 Fuji Photo Film Co Ltd Support for use in photographic paper
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DE3434212A1 (de) * 1984-09-18 1986-03-20 Schill & Seilacher GmbH & Co, 7030 Böblingen Verfahren zur herstellung von ketendimeren und deren verwendung
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Also Published As

Publication number Publication date
US4820582A (en) 1989-04-11
GR3000810T3 (en) 1991-11-15
CN87106977A (zh) 1988-05-11
AU7920587A (en) 1988-05-05
CN1009225B (zh) 1990-08-15
JP2839495B2 (ja) 1998-12-16
AU604754B2 (en) 1991-01-03
ATE51966T1 (de) 1990-04-15
HUT51394A (en) 1990-04-28
EP0268751A1 (fr) 1988-06-01
DE3636790C1 (de) 1988-06-01
JPS63112796A (ja) 1988-05-17
GR900300098T1 (en) 1991-09-27
HU206549B (en) 1992-11-30
ES2015020B3 (es) 1990-08-01

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