WO2000041891A1 - Printable laminate - Google Patents
Printable laminate Download PDFInfo
- Publication number
- WO2000041891A1 WO2000041891A1 PCT/GB2000/000085 GB0000085W WO0041891A1 WO 2000041891 A1 WO2000041891 A1 WO 2000041891A1 GB 0000085 W GB0000085 W GB 0000085W WO 0041891 A1 WO0041891 A1 WO 0041891A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- recording layer
- layer
- printable laminate
- viscoeiastic
- tne
- Prior art date
Links
- 239000000463 material Substances 0.000 claims abstract description 107
- 230000001070 adhesive effect Effects 0.000 claims abstract description 59
- 239000000853 adhesive Substances 0.000 claims abstract description 58
- 239000006096 absorbing agent Substances 0.000 claims abstract description 45
- 229920001577 copolymer Polymers 0.000 claims description 44
- 229920006317 cationic polymer Polymers 0.000 claims description 32
- 239000000203 mixture Substances 0.000 claims description 31
- 229920000642 polymer Polymers 0.000 claims description 25
- 229920001169 thermoplastic Polymers 0.000 claims description 18
- 229920002635 polyurethane Polymers 0.000 claims description 16
- 229920002554 vinyl polymer Polymers 0.000 claims description 16
- 239000004814 polyurethane Substances 0.000 claims description 15
- 239000004416 thermosoftening plastic Substances 0.000 claims description 15
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 15
- 239000002245 particle Substances 0.000 claims description 14
- 229920001567 vinyl ester resin Polymers 0.000 claims description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 11
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical group C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 10
- 229920006397 acrylic thermoplastic Polymers 0.000 claims description 10
- 229920003086 cellulose ether Polymers 0.000 claims description 10
- 229920006287 phenoxy resin Polymers 0.000 claims description 10
- 239000013034 phenoxy resin Substances 0.000 claims description 10
- 229920003229 poly(methyl methacrylate) Polymers 0.000 claims description 10
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 claims description 10
- 229920002678 cellulose Polymers 0.000 claims description 9
- 239000001913 cellulose Substances 0.000 claims description 9
- 229920001084 poly(chloroprene) Polymers 0.000 claims description 8
- 229920000728 polyester Polymers 0.000 claims description 8
- -1 polypropylene Polymers 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
- 229920005989 resin Polymers 0.000 claims description 7
- 239000011347 resin Substances 0.000 claims description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- 239000004743 Polypropylene Substances 0.000 claims description 5
- 150000001336 alkenes Chemical class 0.000 claims description 5
- 239000004014 plasticizer Substances 0.000 claims description 5
- 229920001155 polypropylene Polymers 0.000 claims description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 4
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 4
- 229920002620 polyvinyl fluoride Polymers 0.000 claims description 4
- 229920001519 homopolymer Polymers 0.000 claims description 3
- 239000002861 polymer material Substances 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- 229920006243 acrylic copolymer Polymers 0.000 claims description 2
- 238000007789 sealing Methods 0.000 claims 3
- 150000002148 esters Chemical class 0.000 claims 2
- 239000010410 layer Substances 0.000 abstract description 159
- 230000032798 delamination Effects 0.000 abstract description 8
- 239000000758 substrate Substances 0.000 abstract description 8
- 238000000926 separation method Methods 0.000 abstract description 7
- 239000012790 adhesive layer Substances 0.000 abstract description 6
- 238000000034 method Methods 0.000 abstract description 5
- 239000005001 laminate film Substances 0.000 abstract description 2
- 239000006260 foam Substances 0.000 description 16
- 239000004094 surface-active agent Substances 0.000 description 12
- 239000000126 substance Substances 0.000 description 11
- 238000012360 testing method Methods 0.000 description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 6
- 238000000576 coating method Methods 0.000 description 6
- 238000005520 cutting process Methods 0.000 description 6
- 239000006185 dispersion Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 239000011248 coating agent Substances 0.000 description 5
- 229920006267 polyester film Polymers 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 4
- 125000000129 anionic group Chemical group 0.000 description 4
- 208000028659 discharge Diseases 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 229920002451 polyvinyl alcohol Polymers 0.000 description 4
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 239000001768 carboxy methyl cellulose Substances 0.000 description 3
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 239000003085 diluting agent Substances 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000002648 laminated material Substances 0.000 description 3
- 238000010030 laminating Methods 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 229920005789 ACRONAL® acrylic binder Polymers 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- 229920002633 Kraton (polymer) Polymers 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Natural products C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 239000008186 active pharmaceutical agent Substances 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 238000000151 deposition Methods 0.000 description 2
- FYUWIEKAVLOHSE-UHFFFAOYSA-N ethenyl acetate;1-ethenylpyrrolidin-2-one Chemical compound CC(=O)OC=C.C=CN1CCCC1=O FYUWIEKAVLOHSE-UHFFFAOYSA-N 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000011159 matrix material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- 229910017464 nitrogen compound Inorganic materials 0.000 description 2
- 150000002830 nitrogen compounds Chemical group 0.000 description 2
- 229920000191 poly(N-vinyl pyrrolidone) Polymers 0.000 description 2
- 229920000058 polyacrylate Polymers 0.000 description 2
- 230000001737 promoting effect Effects 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 238000003892 spreading Methods 0.000 description 2
- 230000007480 spreading Effects 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical class NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 241000370685 Arge Species 0.000 description 1
- 229920004394 Baypren® Polymers 0.000 description 1
- 241000212384 Bifora Species 0.000 description 1
- 241000579895 Chlorostilbon Species 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical class [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 229920002153 Hydroxypropyl cellulose Polymers 0.000 description 1
- 229920005987 OPPANOL® Polymers 0.000 description 1
- MITFXPHMIHQXPI-UHFFFAOYSA-N Oraflex Chemical compound N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 description 1
- 239000005062 Polybutadiene Substances 0.000 description 1
- 241000206607 Porphyra umbilicalis Species 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- 239000004930 VINNOL Substances 0.000 description 1
- 229920004482 WACKER® Polymers 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000006978 adaptation Effects 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 125000002877 alkyl aryl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 229920006187 aquazol Polymers 0.000 description 1
- 239000012861 aquazol Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000003851 corona treatment Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000013016 damping Methods 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 238000001548 drop coating Methods 0.000 description 1
- 229910052876 emerald Inorganic materials 0.000 description 1
- 239000010976 emerald Substances 0.000 description 1
- 239000004794 expanded polystyrene Substances 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 239000001863 hydroxypropyl cellulose Substances 0.000 description 1
- 235000010977 hydroxypropyl cellulose Nutrition 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- FJIKWRGCXUCUIG-UHFFFAOYSA-N lormetazepam Chemical compound N=1C(O)C(=O)N(C)C2=CC=C(Cl)C=C2C=1C1=CC=CC=C1Cl FJIKWRGCXUCUIG-UHFFFAOYSA-N 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 125000005395 methacrylic acid group Chemical group 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000005026 oriented polypropylene Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920000765 poly(2-oxazolines) Polymers 0.000 description 1
- 229920000768 polyamine Polymers 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 239000013047 polymeric layer Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 150000004040 pyrrolidinones Chemical class 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 239000002356 single layer Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000012815 thermoplastic material Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 229940124543 ultraviolet light absorber Drugs 0.000 description 1
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5245—Macromolecular coatings characterised by the use of polymers containing cationic or anionic groups, e.g. mordants
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5236—Macromolecular coatings characterised by the use of natural gums, of proteins, e.g. gelatins, or of macromolecular carbohydrates, e.g. cellulose
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5254—Macromolecular coatings characterised by the use of polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. vinyl polymers
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5263—Macromolecular coatings characterised by the use of polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- B41M5/5281—Polyurethanes or polyureas
Definitions
- a target substrate can be one of any number of materials including fabrics , ceramic materials , posterboard, rigid PVC, or mounting board such as, foam board or expanded PVC board which are widely used in the graphic art industry.
- the typical recording medium for receiving and transferring an image formed by an ink- jet printer has a carrier and at least two of the following layers : a release layer, a protective barrier layer, image transfer layer, and an adhesive layer.
- the International Application PCT/GB98/00481 filed February i ⁇ , 1998 for "TRANSFER FILM" describes a carrier having a transfer film which has only one layer. This single layer is a mixture of heat-activatable adhesive particles and a binder that also is ink-absorbing, thereby defining a porous matrix.
- a transfer film can be adhered to the target substrate without removing the carrier, whereby the carrier remains affixed to the layer holding the printed image, thereby providing physical protection for the image.
- Patent Application 09/107,302 filed June 20, 1998 for "PRINTABLE LAMINATE” (the disclosure of which is incorporated herein by reference), describes a printable laminate material for transferring an image produced by an ink jet printer to a target substrate.
- the printable laminate has a carrier film on one side of which is disposed an image recording layer comprising an ink absorber and a heat activatable adhesive.
- the ink absorber is a modified cellulose material, though a cellulose gum or a single cationically charged water- soluble polymer may alsc be used.
- the heat activatable adhesive is a polyurethan .
- the polyurethane of the image recording layer is in the form of small strand- like structures which are distributed throughout the i k absorber thereby forming an homogenous mixture with the ink absorber of the recording layer.
- U.S. Patent: 5,501,902 describes a multi-layer printable transfer material which can be sealed at 177 G C using a smoothing iron. However, this temperature is far too high for use with mounting boards commonly found in the graphic arts industry. Furthermore, the ⁇ 902 Patent describes the use of a powdered polymer with a particle size of up tc 2 ⁇ m. The large particle size tends to produce a printed image having a grainy appearance with a consequent loss of clarity, contrast and brilliance of the printed image.
- International Patent Application WO 98/02314 describes a printable transfer material that releases from a temporary carrier, wherein the transferred image is waterproof .
- This material uses a porous matrix of large particles of a typical size of 20 ⁇ m.
- the transfer material is subjected tc a high temperature (typically 190 "O to form a film of polymer which encapsulates the ink inside the film.
- the inventions disclosed in International Application PCT/GB98/00481 and U.S. Patent Application 09/107,302 have been further investigated, particularly regarding the ability of the printable laminate to resist the separation or delamination of the carrier film from the image recording layer. It was found that cutting or cropping of the printable laminate to obtain a proper size image for display or to obtain a mounted image having an irregular outline as found in some commercial advertising displays often causes the protective carrier layer :o separate from the recording layer .
- the present invention may provide a printable laminate material with improved resistance to delamination cf the carrier film from the image recording layer through the use of new heat activated adhesives, new ink absorbers, and combinations thereof in the recording layer.
- the printable laminate material may have improved resistance tc delamination of the carrier film provided by a layer of polymeric material having desirable viscoeiastic properties in the structure cf the printable laminate.
- a printable laminate comprising a carrier film which is substantially transparent, and an image recording layer which is disposed en the carrier film.
- the image recording layer comprises a heat activated adhesive and an ink absorber.
- the heat activatable adhesive is one or more adhesive materials such as poiyurethanes , vinyl ester copolymers, acrylics, and icnomers formed from various salts of oiefir.s and unsat rated acid copolymers.
- the adhesives are most preferable those which are available in the form of aqueous dispersions .
- the ink absorber is one cr more ink absorber materials such as blends of cationic polymers, blends of cationic polymers and cellulose either, and polyvinyl alcohol.
- the new adhesives and combinations of adhesives and ink absorbers produce an ink recording layer with a higher yield point, making the laminate less susceptible to delamination.
- a patentable laminate comprising a carrier film which is substantially transparent, a layer of viscoeiastic material disposed on the carrier film, and an image recording layer disposed on the layer of viscoeiastic material.
- the viscoeiastic material is one or more thermoplastic polymers such as polyurethanes , acrylics, vinyls, butadiene-styrene copolymers, i s opren - s tyrene copolymers, polychloroprenes , and olefinic polymers having physical properties which contribute to the "damping" of shearing forces imposed by a blade cutting the laminate.
- the image recording layer includes an ink absorber which may be one or more blends of cationic polymers, blends of cationic polymers and cellulose ether, and polyvinyi alcohol, along with a heat activatable adhesive which may include one or more materials such as polyurethanes, vinyl ester copolymers, acrylic ester copolymers, and ionomers as previously described in reference to the heat activatable adhesives such as polyurethanes, phenoxy resins, acrylics, vinyls, butadiene-styrene copolymers, i soprene - styrene copolymers, polychloroprenes, and olefinic polymers, which may be the same or different than the viscoeiastic materials as described herein above.
- a heat activatable adhesive which may include one or more materials such as polyurethanes, vinyl ester copolymers, acrylic ester copolymers, and ionomers as previously described in reference to the heat activatable adhesive
- Figure 1 shows a cross-sectional representation of an embodiment of the printable laminate of the invention which includes a carrier film, and image recording layer.
- a second embodiment cf the printable laminate of the invention which includes a carrier film, a layer of viscoeiastic material and image recording layer.
- Figure 3 shows a partial cross-sectional representation of a printable laminate of the invention in the process of being laminated to a target substrate.
- FIG 1 shows a printable laminate 10 made according to the first embodiment of the present invention.
- the printable laminate comprises a substantially transparent carrier film 12 having a first surface and a second surface, and an image recording layer 14 having an inner surface and an outer surface, the inner surface of the image recording layer being directly supported in full and intimate contact on one of the surfaces of the carrier film 12.
- the exposed outer surface cf the image recording layer is intended for receiving an ink image which typically is applied by means of an ink-jet printer (not shown) .
- the pattern of ink deposits 16 formed by the ink-jet printer diffuse through the thickness of the recording layer 14 without substantial de ⁇ radation.
- a printable laminate 20 made according to the second embodiment of the present invention is shown.
- the printable laminate 20 comprises a carrier film 12 having a first surface and a second surface, a layer of viscoeiastic material 25 likewise having a first surface and a second surface, the viscoeiastic material being directly supported on one of its surfaces in full and intimate contact on one cf surface cf the carrier film, and an image recording layer 14 having an inner surface and an outer surface, the inner surface being directly supported in full and intimate contact with the other surface of the layer of viscoeiastic material.
- the exposed outer surface of the image recording layer is intended for receiving an image applied by an ink- jet printer (not shown) , wherein the image takes the form cf a pattern of ink deposits 16 as described above in reference to Figure 1.
- the image recording layer is heated by contact of the printable laminate with the heated laminating roller
- the recording layer of this embodiment cf the invention comprising a carrier film and an image recording layer comprises a heat activated adhesive and an mk-absorper .
- the heat activated adhesive fcr use m this em odiment of tne invention is one or more adhesives selected from the group consisting cf polyurethanes, vinyl ester copolymers, acrylic ester copolymers, and cnomeric copolymers.
- Examples cf vinyl ester copolymers suitaoie for use m tne invention include materials wnich are commercially available under tne names CRODALAM 29-188 from Croda Adhesives, Newark Nottmghamsnire , UK, VINNAPAS available in tne grades EP1 , ⁇ P400, ⁇ N424, and EF424, and EF41, and VINNOL CE752, all available from Wacker-Chemie , Kunststoff, Germany.
- the acrylic ester copoivmerized with a cationic- substituted acrylic monomer is available under the name GLASCOL grades DP6-2779, and DP6-2724, from Ciba Specialty Chemicals.
- the copolymer of cationic- substituted acrylic ester and acrylamide is exemplified by the materials commercially available under the name SEDIPUR grades CL 750, and CF 604, from BASF.
- the polyoxazolines are exemplified by poly (2-ethyl-2- oxazoline) from Sigma Aldrich Company Limited of
- the heat activatable adhesive and ink absorber together comprise 90 - 100% cf the total weight of the image recording layer.
- the heat activated adhesive and ink absorber comprise from about 92 to 99% and most preferable, from 97 - 99% of the total weight of the recording layer.
- the heat activatable adhesive comprises about 33 - 77% pph (parts per hundred weight; and most preferably, about 40 - 65 pph of the total weight of the image recording layer, with at least 75% of the remaining weight of the recording layer constituted by a different, ink absorbing, preferable thermoplastic, cationic polymer material.
- the viscoeiastic material is a thermoplastic polymer witn viscoeiastic physical properties wmch exmpits good adhesion tc tne carrier film and also to the ink aosorbing layer. Desirable properties of the viscoeiastic material include a T iglass transition temperature; of less than room temperature and typically Between -55"C and *10°C. A modulus (storage modulus, or G') of between 5 x 10 and 2 x 10 dyne /cm is desirable. A viscosity (loss modulus) of between 2.2 x 10 and 4 x 10 Poise is preferable.
- acrylics useful in this embodiment of the invention include those acrylic polymers commercially available under the name DUROTAK from National Starch and Chemical Company, Slough, Berkshire, UK; ACRONAL grades from BASF.
- the vinyls suitable for use in the adhesive layer of this invention include: VINNAPAS EP1, available from Wacker Chemie of Kunststoff, Germany.
- Butadiene-styrene copolymers suitable for use in the invention are exemplified by REVINEX 80R10 from Doverstrand Ltd., Harlow, Essex, United Kingdom.
- Isoprene- styrene copolymers are exemplified by the materials available from Shell Chemicals UK Limited, Chester, UK, under the name KRATON D and KRATON G.
- Polychioroprene is commercially available from 3ayer A.G., Dormagen, Germany, under the names DISP ⁇ RCOLL C and BAYPREN .
- Suitable olefinic polymers include poiyisobutyiene commercially available from BASF, under the name OPPANOL.
- Other olefinic polymers include polybutadiene and poiyisoprene .
- the layer of viscoeiastic material may contain minor amounts of various materials to improve the performance of the printable laminate. These materials include plasticizers to further improve the desired viscoeiastic and extensible properties of the material.
- light absorbers may be added tc the viscoeiastic materials tc aid in the filtering cf various segments of the light spectrum which are transmitted through the carrier layer and eventually reach the image in the image recording layer.
- ultra-violet light absorber materials can be added to the adhesive layer to remove that part cf the UV spectrum that would tend to degrade the image held in the ink absorbing layer through the actinating effect of sunlight and artificial light.
- Suitable plasticizers such as phthalate esters, are commercially available from Alcohols Ltd., Bishop's Stortford, Hertfordshire, UK; phosphate esters are available from Ciba, Manchester, UK; and chlorinated paraffin is available from IC Chlor- Chemicals , ncorn, Cheshire, UK.
- Suitable light absorbers are known widely and include such materials sold under the trademark TINUVIN, from Ciba Chemicals, Manchester, UK.
- thermoplastic polymers for use m this embodiment in the invention may be particularly tacky when used at room temperature. Therefore it is envisioned that the carrier film may be treated with a release-coating material on the surface fcr the film opposite the adhesive layer so that the film can be easiiv unwound from a soocl or roll and unwound as needed for use m printing or mounting of tne printable laminate.
- Sucn release coatings are commonly Known ⁇ r. tne adhesives industry and include such materials as ESCOAT P ' polyvinyi octadecyl caroamate > , commercially available from Emerald Chemicals Ltd, Windsor, Berkshire, UK.
- the image recording layer cf tnis empodiment of the invention comprises a heat activatable adnesive and an ink absorper
- the heat activataple adhesive is one or more materials selected from the group consisting of polyuretnanes , vinyl ester copolymers, acrylic ester copolymers, and ionomeric copolymers, (all as previously ctescriPed m reference to the neat activatable adnesive found m tne image recording layer cf the first empodiment cf tne invention) , polyuretnanes, acrylics, vinyls, putadiene- styrene copolymers, isoprene- styrene copolymers, polychloroprenes, and olefinic polymers (all as previously described m reference to tne viscoeiastic material as described above in reference to tne present embodiment of the invention) and phenoxy resins.
- the ink absorbers for use m the present empodiment are selected from tne group consisting of blends of cationic polymers, blends of cationic polymers and cellulose ether, ana pc-yvinyl alconol, all as previously ⁇ escrioed m reference to the ⁇ n ⁇ aosorper of tne first embodiment cf tne present invention) .
- the phenoxy resin suitable for use as a heat activatable adnesive m the recording layer cf the invention s exemplified by the resin commercially available under the name PKHW-35, from Phenoxy Associates, ROCK: Hill, South Carolina.
- the image recording layer it may be necessary tc use an amphoteric surfactant m comomation witn the pnenoxy resin to act as a cr.arge reverser
- the pnenoxy resin us suppiie ⁇ _n tne form cr an anionic dispersion m water and anionic dispersions are not normally ccmpatioie with cationic polymers ' such as ink aPsorpers wnicn may be used m tne image recording layer, Therefore, the practitioner will appreciate tne need fcr re ⁇ ucmg tne negative cnarge of tne pnenoxy resin tnrougn the use of an ampnote ⁇ c surfactant.
- the ampnoteric surfactant acts as a "bri ⁇ ge” oetween tne anionic phenoxy resin and the cationic polymers m tne image recording layer. It will be appreciated tnat tne utility of ampnoteric surfactants extends oeyond the use m systems using phenoxy resins. In fact, any anionic adhesive used in connection with this invention may have its compatibility witn cationic ink apsorPers improved tnougn tne use of ampnoteric surfactants.
- An example of a suitable ampnoteric surfactant s CRODATERIC CYNA, from Cro ⁇ a Surfactants Ltd., Snaitn, Humbersi ⁇ e, UK.
- the viscoeiastic material may be deposited directly onto the carrier film m the form of an aqueous dispersion, a solution formed with an organic solvent, or -_n tne form of a hot melt.
- the viscoeiastic material layer comprises 60 - 80% by weight of tne viscoeiastic material layer and tne image recording layer ccmpined.
- tne viscoeiastic material comprises 62.5 - 80.0% and most preferaoly, 70. C - 75.0% of tne comDined amount of tne viscoeiastic material layer and tne image recording layer.
- tne UV lignt aosoroer if present, comprises about 2.0 - 5.0% py weignt cf tne tota-_ weignt cf tne viscoeiastic material laver
- the viscoeiastic material layer s typically within tne range cf 20 - 50 urn thick, w th 25 - 40 ⁇ m oemg preferable, and 30 - 35 urn being most preferable
- the recording layer m this embodiment cf the invention is applied to the carrier film m the form of an emulsion, preferable a water-based emulsion, and allowed to dry.
- the structure of tne dried film is that cf adhesive particles distributed throughout an essentially continuous layer of tne water-soluble ink abscroer .
- the size of the adhesive particles is typically m the range of 0.08 - 3.0 ⁇ m, with a O . lum particle size being preferred.
- the adhesive particles have a strand- like conformation.
- the heat activatable adhesive comprises 50 - 60 ph and most preferably, 57.8 - 59.8 pph cf the total weight cf the image recording layer, while the ink absorber comprises 34 - 50 pph, preferably 39 - 49 pph, or most preferaply, 39.2 - 41.2 ppn cf the total weight cf the image recording layer.
- the balance of the image recording layer comprises optionally comprises surfactant and/cr a thickener.
- the image recording layer may be deposited directly on to the layer of viscoeiastic material and subjected tc conditions for promoting drying.
- a test print was made with the laminate by printing an image on the laminate with a CHROMA 24 ink jet printer, commonly available from Encad Inc., San Diego, CA, USA.
- Two samples of the printed laminate cf this example were prepared in this manner.
- a first sample was laminated to a piece cf foam board of 3mm thickness and a second sample was laminated tc a piece of expanded PVC Board cf 3mm thickness using a roller iaminator set tc 100°C at a pressure of 80 psi with a feed rate speed of 2 feet per minute .
- Subsequent tc laminating, the printable laminate and mounting board were permitted to cool to room temperature. Adhesion of the laminate to the target board of each sample was tested using a sample pull test.
- a printable laminate was prepared by applying a coating cf an ink absorber layer 25g dry weight! per square meter of the laminate.
- the ink absorber layer was prepared from:
- Example 3 ⁇ is quite similar to Example 3A except that the ink absorber cf Example 3A (a blend of cationic polymers) is further blended with a relatively small amount of cellulose ether.
- the preferred dry weight coat of the image layer according to Example 3B is between 28 and 30 grams per square meter, preferably on the DEEP CRYSTAL or CRYSTAL MATT carrier film previously described. This gives luster and matt products respectively. A simple gloss effect can be obtained by coating polyester film of 50 microns tnickness.
- the dry weight percent cf the polyurethane can be in the range of 40 50 : range of tne cationic polymer blend can be 45 - 50%; and the range of the cellulose ether can be about 3 - 10%.
- the effective dry weight range can be between about 25 - 35 , preferably 28 - 30, grams per square meter.
- a corona discharge treated polyester film was used as the carrier fiim to which was applied a mixture cf the ink absorbing layer material in an amount cf ⁇ 5g per square meter ⁇ ry weignt
- the formula cf the image recording layer material as follows :
- Examples 1 - 4 support a preference that at least one of the absorber materials have thermoplastic adhesive properties (e.g., the vinyl pyrrolidone - vinyl ester copolymers LUVISKOL VA64, PVP/VA S-630 and Coilacoi VL; Klucel ⁇ ; and poiyoxazoiine .
- thermoplastic adhesive properties e.g., the vinyl pyrrolidone - vinyl ester copolymers LUVISKOL VA64, PVP/VA S-630 and Coilacoi VL; Klucel ⁇ ; and poiyoxazoiine .
- a mixture of ingredients for forming an ink absorbing layer was deposited en to a corona discharge treated polyester fiim.
- the dry weight cf the ink absorbing layer was about 35g per square meter.
- the ink absorbing layer was dried at a temperature below about 58 °C.
- the formula of the ink absorbing mixture was prepared from the following components :
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- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Laminated Bodies (AREA)
- Ink Jet (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020017008901A KR20010112242A (en) | 1999-01-15 | 2000-01-13 | Printable laminate |
AU19945/00A AU1994500A (en) | 1999-01-15 | 2000-01-13 | Printable laminate |
JP2000593482A JP2003534144A (en) | 1999-01-15 | 2000-01-13 | Printable laminate |
EP00900282A EP1144196A1 (en) | 1999-01-15 | 2000-01-13 | Printable laminate |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US23203099A | 1999-01-15 | 1999-01-15 | |
US09/232,030 | 1999-01-15 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2000041891A1 true WO2000041891A1 (en) | 2000-07-20 |
Family
ID=22871603
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/GB2000/000085 WO2000041891A1 (en) | 1999-01-15 | 2000-01-13 | Printable laminate |
Country Status (7)
Country | Link |
---|---|
EP (1) | EP1144196A1 (en) |
JP (1) | JP2003534144A (en) |
KR (1) | KR20010112242A (en) |
CN (1) | CN1139497C (en) |
AU (1) | AU1994500A (en) |
TW (1) | TW524758B (en) |
WO (1) | WO2000041891A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001025856A1 (en) * | 1999-10-01 | 2001-04-12 | Foto-Wear, Inc. | Image transfer material with image receiving layer and heat transfer process using the same |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6881458B2 (en) * | 2002-06-03 | 2005-04-19 | 3M Innovative Properties Company | Ink jet receptive coating |
KR100404335B1 (en) * | 2002-09-11 | 2003-11-05 | Shinwoo Hi Tech Co Ltd | Real picture printer board with plotter and process for production thereof |
KR100518789B1 (en) * | 2002-12-04 | 2005-10-05 | 삼성전자주식회사 | Recording medium for inkjet printer and the method thereof |
KR101158219B1 (en) * | 2010-11-10 | 2012-06-20 | 삼성전기주식회사 | Cushion sheet and method for manufacturing heat radiating printed circuit board using the same |
JP2014205246A (en) * | 2013-04-10 | 2014-10-30 | セイコーエプソン株式会社 | Paper for manufacturing recorded material, and recorded material |
CN108909230B (en) * | 2018-07-06 | 2020-04-10 | 福州艾瑞数码影像有限公司 | Weak solvent type ink jet printing medium and preparation method thereof |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4225652A (en) * | 1979-04-09 | 1980-09-30 | Minnesota Mining And Manufacturing Company | Transparent sheet material |
EP0487350A1 (en) * | 1990-11-21 | 1992-05-27 | Xerox Corporation | Coated receiver sheets |
EP0782931A1 (en) * | 1995-12-07 | 1997-07-09 | E.I. Du Pont De Nemours And Company | Receptor sheet for recording by ink-jet |
EP0858913A1 (en) * | 1997-02-17 | 1998-08-19 | Hunt Europe Limited | Transfer film |
-
2000
- 2000-01-13 JP JP2000593482A patent/JP2003534144A/en active Pending
- 2000-01-13 CN CNB008037671A patent/CN1139497C/en not_active Expired - Fee Related
- 2000-01-13 WO PCT/GB2000/000085 patent/WO2000041891A1/en not_active Application Discontinuation
- 2000-01-13 EP EP00900282A patent/EP1144196A1/en not_active Withdrawn
- 2000-01-13 KR KR1020017008901A patent/KR20010112242A/en not_active Ceased
- 2000-01-13 AU AU19945/00A patent/AU1994500A/en not_active Abandoned
- 2000-01-14 TW TW089100551A patent/TW524758B/en not_active IP Right Cessation
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4225652A (en) * | 1979-04-09 | 1980-09-30 | Minnesota Mining And Manufacturing Company | Transparent sheet material |
EP0487350A1 (en) * | 1990-11-21 | 1992-05-27 | Xerox Corporation | Coated receiver sheets |
EP0782931A1 (en) * | 1995-12-07 | 1997-07-09 | E.I. Du Pont De Nemours And Company | Receptor sheet for recording by ink-jet |
EP0858913A1 (en) * | 1997-02-17 | 1998-08-19 | Hunt Europe Limited | Transfer film |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2001025856A1 (en) * | 1999-10-01 | 2001-04-12 | Foto-Wear, Inc. | Image transfer material with image receiving layer and heat transfer process using the same |
US6869910B2 (en) | 1999-10-01 | 2005-03-22 | Foto-Wear, Inc. | Image transfer material with image receiving layer and heat transfer process using the same |
Also Published As
Publication number | Publication date |
---|---|
EP1144196A1 (en) | 2001-10-17 |
JP2003534144A (en) | 2003-11-18 |
KR20010112242A (en) | 2001-12-20 |
CN1340005A (en) | 2002-03-13 |
AU1994500A (en) | 2000-08-01 |
CN1139497C (en) | 2004-02-25 |
TW524758B (en) | 2003-03-21 |
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