EP0059276A1 - Production of decalcomanias and apparatus for the production thereof - Google Patents
Production of decalcomanias and apparatus for the production thereof Download PDFInfo
- Publication number
- EP0059276A1 EP0059276A1 EP81300821A EP81300821A EP0059276A1 EP 0059276 A1 EP0059276 A1 EP 0059276A1 EP 81300821 A EP81300821 A EP 81300821A EP 81300821 A EP81300821 A EP 81300821A EP 0059276 A1 EP0059276 A1 EP 0059276A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- ink
- decal
- layer
- design
- backing material
- 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
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 14
- 238000004144 decalcomania Methods 0.000 title claims description 7
- 238000000034 method Methods 0.000 claims abstract description 51
- 230000008569 process Effects 0.000 claims abstract description 43
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 29
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 29
- 238000007639 printing Methods 0.000 claims abstract description 16
- 238000013461 design Methods 0.000 claims description 59
- 239000000463 material Substances 0.000 claims description 57
- 239000001993 wax Substances 0.000 claims description 35
- 230000004888 barrier function Effects 0.000 claims description 20
- 238000002844 melting Methods 0.000 claims description 14
- 230000008018 melting Effects 0.000 claims description 14
- -1 polyethylene Polymers 0.000 claims description 13
- 229920005989 resin Polymers 0.000 claims description 10
- 239000011347 resin Substances 0.000 claims description 10
- 229920000642 polymer Polymers 0.000 claims description 9
- 229920001296 polysiloxane Polymers 0.000 claims description 8
- 230000004907 flux Effects 0.000 claims description 7
- 229910052751 metal Inorganic materials 0.000 claims description 6
- 239000002184 metal Substances 0.000 claims description 6
- 229920001223 polyethylene glycol Polymers 0.000 claims description 6
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 claims description 5
- 239000004698 Polyethylene Substances 0.000 claims description 5
- 239000002202 Polyethylene glycol Substances 0.000 claims description 5
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 claims description 5
- 229920000573 polyethylene Polymers 0.000 claims description 5
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 claims description 5
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 claims description 4
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 4
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 4
- 239000000853 adhesive Substances 0.000 claims description 4
- 230000001070 adhesive effect Effects 0.000 claims description 4
- 229920001577 copolymer Polymers 0.000 claims description 4
- 150000002148 esters Chemical class 0.000 claims description 4
- 150000002170 ethers Chemical class 0.000 claims description 4
- 239000012188 paraffin wax Substances 0.000 claims description 4
- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims description 3
- 239000012184 mineral wax Substances 0.000 claims description 3
- 239000003921 oil Substances 0.000 claims description 3
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 3
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 3
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 3
- 239000012178 vegetable wax Substances 0.000 claims description 3
- IMSODMZESSGVBE-UHFFFAOYSA-N 2-Oxazoline Chemical compound C1CN=CO1 IMSODMZESSGVBE-UHFFFAOYSA-N 0.000 claims description 2
- 239000004743 Polypropylene Substances 0.000 claims description 2
- 239000002253 acid Substances 0.000 claims description 2
- 150000007513 acids Chemical class 0.000 claims description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 2
- 229920006271 aliphatic hydrocarbon resin Polymers 0.000 claims description 2
- 239000012164 animal wax Substances 0.000 claims description 2
- 229920001400 block copolymer Polymers 0.000 claims description 2
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 2
- 239000000194 fatty acid Substances 0.000 claims description 2
- 229930195729 fatty acid Natural products 0.000 claims description 2
- 150000002191 fatty alcohols Chemical class 0.000 claims description 2
- 239000011888 foil Substances 0.000 claims description 2
- 125000005456 glyceride group Chemical group 0.000 claims description 2
- 125000005395 methacrylic acid group Chemical group 0.000 claims description 2
- 229920001155 polypropylene Polymers 0.000 claims description 2
- 150000003097 polyterpenes Chemical class 0.000 claims description 2
- 229920005992 thermoplastic resin Polymers 0.000 claims description 2
- 238000000151 deposition Methods 0.000 claims 5
- 230000008021 deposition Effects 0.000 claims 2
- 239000004447 silicone coating Substances 0.000 claims 2
- 238000011144 upstream manufacturing Methods 0.000 claims 2
- 230000001747 exhibiting effect Effects 0.000 claims 1
- 229910010272 inorganic material Inorganic materials 0.000 claims 1
- 239000011147 inorganic material Substances 0.000 claims 1
- 229920000620 organic polymer Polymers 0.000 claims 1
- 229920013716 polyethylene resin Polymers 0.000 claims 1
- 238000009877 rendering Methods 0.000 claims 1
- 239000000976 ink Substances 0.000 abstract description 43
- 239000000919 ceramic Substances 0.000 abstract description 10
- 238000001035 drying Methods 0.000 abstract description 10
- 238000010924 continuous production Methods 0.000 abstract 1
- 239000010410 layer Substances 0.000 description 101
- 239000012943 hotmelt Substances 0.000 description 21
- 239000000565 sealant Substances 0.000 description 20
- 239000000758 substrate Substances 0.000 description 13
- 239000003086 colorant Substances 0.000 description 10
- 238000012216 screening Methods 0.000 description 10
- 238000012546 transfer Methods 0.000 description 10
- 239000011521 glass Substances 0.000 description 7
- 239000012790 adhesive layer Substances 0.000 description 5
- 238000000576 coating method Methods 0.000 description 5
- 239000000155 melt Substances 0.000 description 5
- 239000000049 pigment Substances 0.000 description 5
- 230000035945 sensitivity Effects 0.000 description 5
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 4
- 238000005034 decoration Methods 0.000 description 4
- 238000001459 lithography Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000002966 varnish Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000011248 coating agent Substances 0.000 description 3
- 238000010276 construction Methods 0.000 description 3
- 239000004014 plasticizer Substances 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- 239000012815 thermoplastic material Substances 0.000 description 3
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
- 239000005038 ethylene vinyl acetate Substances 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 230000000149 penetrating effect Effects 0.000 description 2
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- 229910000831 Steel Inorganic materials 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 229920004482 WACKER® Polymers 0.000 description 1
- 230000002745 absorbent Effects 0.000 description 1
- 239000002250 absorbent Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 229910052910 alkali metal silicate Inorganic materials 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 229910010293 ceramic material Inorganic materials 0.000 description 1
- 235000019219 chocolate Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000000549 coloured material Substances 0.000 description 1
- 238000013005 condensation curing Methods 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000012864 cross contamination Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000010981 drying operation Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 239000000806 elastomer Substances 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000002241 glass-ceramic Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000013529 heat transfer fluid Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 238000007654 immersion Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 230000014759 maintenance of location Effects 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000007645 offset printing Methods 0.000 description 1
- 239000003605 opacifier Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 238000010023 transfer printing Methods 0.000 description 1
- UONOETXJSWQNOL-UHFFFAOYSA-N tungsten carbide Chemical compound [W+]#[C-] UONOETXJSWQNOL-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000011800 void material Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M3/00—Printing processes to produce particular kinds of printed work, e.g. patterns
- B41M3/12—Transfer pictures or the like, e.g. decalcomanias
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B44—DECORATIVE ARTS
- B44C—PRODUCING DECORATIVE EFFECTS; MOSAICS; TARSIA WORK; PAPERHANGING
- B44C1/00—Processes, not specifically provided for elsewhere, for producing decorative surface effects
- B44C1/16—Processes, not specifically provided for elsewhere, for producing decorative surface effects for applying transfer pictures or the like
- B44C1/165—Processes, not specifically provided for elsewhere, for producing decorative surface effects for applying transfer pictures or the like for decalcomanias; sheet material therefor
- B44C1/17—Dry transfer
- B44C1/1712—Decalcomanias applied under heat and pressure, e.g. provided with a heat activable adhesive
- B44C1/1716—Decalcomanias provided with a particular decorative layer, e.g. specially adapted to allow the formation of a metallic or dyestuff layer on a substrate unsuitable for direct deposition
Definitions
- This invention relates to an improved method of making decalcomania (decals) particularly of the heat release type.
- heat release decals have been primarily manufactured by screening or lithography although manufacture feasibility by rotogravure and letterpress was known.
- the use of offset rotary lithographic presses for printing the varnishes used in making heat release lithographic decals was also known as shown in U.S. Patent No. 2,640,458.
- the inks and coatings printed contain various organic solvents or oils necessarily included in the printing media to achieve printable viscosities.
- These inks and coatings are successively printed to achieve heat release decals of the basic layered structure described in U.S. Patent No. 2,970,076.
- the first three layers of a heat release decal are normally not transferable and include a backing or support material, usually paper, a barrier coat, and a wax release layer.
- a transferable portion consisting of design, sealant, overflux, and adhesive layers is deposited thereover.
- the function of the barrier coat is to prevent absorption of the wax release layer into the paper both at the time of wax application to the paper and transfer of the finish decal to a substrate surface.
- the release coat is the layer which separates the transferable portion of the decal from the non-transferable portion.
- the release coat itself is the only portion of a heat release decal which has hitherto been applied by hot melt techniques, such as roll coaters etc.
- Polyethylene glycols having molecular weights in excess of 1000 are commonly employed as the waxes for the release layer as noted in U.S. Patent Nos. 2,970,076,' 3,007,829, and 4,068,033, although both vegetable and mineral waxes can be employed as disclosed in U.S. Patent No. 2,970,076.
- the use of polyethylene glycol esters is also known, particularly, if solution coating techniques are to be employed for applying the wax (see for example U.S. Patent No. 3,533,822).
- thermoplastic as employed in relation to this adhesive layer is not synonymous to the term “thermoplastic” as applied to the thermoplastic inks discussed hereinafter.
- the materials reversibly soften with heat, hence the term "themmoplastic"
- melt processibility application
- the material used for the decal adhesive layer is applied from solution over the design.
- melt processable inks are sometimes referred to as "hot melt” inks or simply “hot colour”.
- hot melt inks or simply “hot colour”.
- the heat of the article softens the adhesive surfaces of the decal to a sufficient extent such that the design is adhered to the article being decorated.
- the heat from the article softens or melts the heat release layer of the backing, thereby causing the backing to release from the design layer. Both actions are accomplished in essentially a single operation in which the decal is pressed against the preheated article.
- the ware with the temporarily adhered vitreous design is thereafter fired in the normal manner to cause the design to become an integral part of the surface of the ware.
- the inks exhibit sufficient pressure sensitivity below their melt points so that the need for a separate adhesion layer is obviated.
- the structure and composition of the transferrable portion of the heat release decal depends somewhat on the process used to manufacture the decal. For example screening processes have previously proved to be the most economical process for manufacturing heat release decals. Screening, however, is not without its limitations and drawbacks.
- the use of solvents in the screening media necessitate drying between the decal layers so that each successive layer can be applied over or adjacent to the previous layers without distortion, smearing, or pick-back of the print.
- the solvents thus add considerable cost to the decal manufacturing process by necessitating both driers and environmental protection controls. Viscosity controls are also required to achieve viscosity stability. Low volatility solvents are often used which require more extensive drying either in terms of time or temperature.
- Time is the variable usually affected because of the desire not to melt the wax release layer during the drying operation.
- An increase in drying time means longer driers or slower process speeds. Melting of the wax during drying often results in less acceptable release when transferring the decal to the substrate.
- the backing is paper
- the dimensions of the paper are directly coupled to its moisture content. Excessive drying time shrinks the sheet by driving out moisture, conversely, increased moisture content resulting from shorter drying time expands the sheet due to absorption.
- the environmental window in which the paper can be handled is very narrow, thus affecting drying times and temperatures in conjunction with previously menti.oned wax problems.
- Thermoplastic screening requiring negligible drying, is not a viable alternative for solving these problems because the heated screens would melt the wax release layer, and thereby, prevent the backing material from accepting the screened prints. This could be prevented by screening overlayers having a melt point lower than the release layer, but this would also be impracticable because the design layer would remelt and smear upon subsequent transfer of the heat release decal to the substrate.
- silk-screened decals also have a limitation, in that, they cannot achieve the fine resolution and sharp definition obtainabl by lithographic decals; moreover, the thicker layer which results from screening is not always desirable.
- lithographic decals In a lithographic decal process, dry colour is dusted over the sheet of paper, and adheres only to the printed varnish image. The excess colour is then removed from the sheet, leaving the desired image. Due to the aforementioned shortcomings of screened decals, lithographic decals are often used in spite of process disadvantages resulting from the inability of adding colours directly to the lithographic varnish.
- the lithographic process is also not without other disadvantages, besides this obvious disadvantage of having to handle, dust, and remove the dry powders after each successive application of varnish.
- lithographic decals may have much greater resolutio than screened decals, the prints are also much thinner, a a consequence much higher levels of pigments must be used in the colours.
- overglaze decals this necessitates an overflux, i.e., a printed overglaze, which is applied over the colours to improve durability and reduce to safe levels toxic metal release.
- an overflux is sometimes used for screened decals, its use for lithographic decals in food-contact applications is mandatory.
- lithographic decals Due to the tendency of the dry colours to stick to the overflux layer, a sealant layer is required in the construction of a lithographic decal between the design layer and the overflux layer as shown in U.S. Patent No. 4,068,033.
- lithographic heat release decals have been found more difficult to manufacture than screened decals, such that, their use has been limited.
- thermoplastic colours sometimes hereinafter referred to as, hot melt colours
- hot melt colours for the design layers of the decal, and optionally all layers of the decal except the backing material
- an offset rotogravure process wherein, the melted thermoplastic materials are first transferred from a heated gravure or intaglio roll to an elastomeric offset roll, whereupon the materials cool such that they can be transferred from the offset roll at temperatures considerably below their melt points.
- the offset roll By utilizing the offset roll, it is possible to print waxes or thermoplastic hot melts of higher melt points over a wax release layer of lower melt point as long as the hot melts, thereby printed, exhibit sufficient pressure sensitivity below their melt points to adhere to a wax surface when transferring from the offset roll.
- the offset roll prevents melting of the release layer which would occur for direct gravure with heated rolls. Both the offset and backup rolls may be internally cooled, with a heat transfer fluid if necessary, to maintain a low temperature when printing onto the release layer.
- a flexographic process may be used wherein an ink applicator roll is substituted for the gravure roll and an embossed silicone roll carrying a portion of the design is substituted for the plain offset roll.
- the embossed design on the flexographic roll picks-up a uniform layer of. ink by contacting the ink applicator roll.
- the ink subsequently cools upon and is transferred from the flexographic roll in a similar manner to the offset roll described above.
- Figure 1 is a decal in cross section which may be manufactured according to the present invention illustrating the general layout which in any one particular embodiment may include less than the number of layers illustrated in the drawing.
- Figure 2 is a schematic of a multiple station printing machine for use in producing the decal illustrated in Figure 1.
- this shows a decal 10 having multiple layers of material hereinafter described.
- the decal 10 is illustrated in the general sense that certain materials may be substituted for other types. However, the arrangement of layers of materials thereon follows a functional sequence.
- Decal 10 includes a backing material 12 for supporti the remaining portions of the decal 10, a barrier layer 14 for sealing the backing material, a release layer 16 for allowing separation of the subsequent layers from the backing 12, a sealant coat 18, and a design layer on layers (multicolours) 20.
- the backing material 12 is paper
- the barrier layer 14 can be such materials as starch, casein, and alkali metal silicates with or without clay type fillers as mentioned in U.S. 2,970,076, or polyvinylacetate as mentioned in U.S. 3,445,309.
- the barrier layer can be a high melt point wax.
- the barrier layer seals the backing and prevents cross-contamination of the release layer 16 when a paper backing layer 12 is used.
- the release layer 16 is usually a wax having a melting point lower than the barrier layer 14.
- the sealant layer 18 may contain fluxes therein so that when ceramic inks or colours are used in the design layer 20 a vitreous film (overflux) is produced which reduces the release of toxic metals which may be present in the coloured materials forming the design layer 20..
- the vitreous film (overflux) also improves the overall fired decoration durability.
- the sealant layer 18 also facilitates total release of the design layer 20 from the backing 12.
- a number of layers may form the design layer 20 by sequential printing of various colour patterns one over the other to form a decorative design of high resolution.
- the barrier layer 14 may be unnecessary.
- an organic film or metal foil may be utilized which would not be absorbent to melted wax of the release layer 16, thus the barrier layer would be unnecessary because the backing material 12 would serve as its own barrier to the release layer 16.
- FIG. 2 a multiple station offset rotogravure hot melt printing machine 30 is described.
- the apparatus shown includes n stations labeled 1, 2 ...n and a pair of respective unwind and rewind reels 32 and 34.
- Each station includes one or more idler wheels 36a-c, a backup roll 38, an offset roll 40, an etched edge or gravure roll 42, and a hot melt bath 44 into which a quantity of thermoplastic ink 46 is deposited.
- Each station l-...n essentially include the same arrangement of rolls and pulleys.
- the function of the chill roll 48 is to especially reduce heat buildup in the backing material 12 and release layers 16, which may occur during high speed printing. Also the chill roll 48 helps to freeze the previously printed hot melt thermoplastic materials.
- Respective unwind and rewind idler wheels 50a and b establish the path for the backing material 12 as hereinafter described.
- a roll of backing material 12 is placed at the unwind reel 32 and passes around the unwind idler 50a, over the first idler 36a of station 1 and the subsequent downstream idler 36b between the respective backup and offset rolls 38 and 40, around the next downstream idler 36c over the chill roll 48 and thence to the second station 2 for repeat threading and so on until the backing material 12 is located about the rewind idler 50b and the rewind reel 34.
- the hot melt bath 44 carries the ink 46 which is in intimate contact with the gravure roll 42 which may be heated by an electrical or other heating device 52.
- a doctor blade 54 scrapes excess ink 46 from the gravure roll 42; and, as it rotates therafter coming in intimate contact with the offset roll 40, the ink remaining on the gravure roll 42 causes a mirror image by splitting between the two surfaces upon separation.
- the offset roll 40 rotates it comes in contact with the backing material 12 and prints its image onto the backing material 12 as supported by the backup roll 38. Each station in turn prints a different layer on the backing material 12 so that after multiple steps the decal is produced having the desired design printed thereon.
- each of the respective backup and offset rolls 38 and 40 may have heat exchange means 56 and 58 located for controlling the temperature thereof. Primarily these heat exchange means 56 and 58 would be used for cooling so that the ink which is heated on the gravure roll 42 cools to a temperature where it will have sufficient pressure sensitivity to transfer from the offset roll to the backing material 12 and yet not smear or remelt previously applied layers including respective barrier 14, release 16, and sealant 18 layers when used.
- Decals printed by the hot melt offset rotogravure process described herein exhibit significant advantages over those printed by conventional techniques.
- the resolution and definition obtainable by the process of the invention approaches that of lithographic decals and substantially exceeds that of screened decals; on the other hand, the higher pigment loadings of the colours required for lithographic decals are not needed for this process, consequently, decals printed in accordance with the present invention compare to screened decals for durability.
- Print thicknesses obtainable by this process can be adjusted from the thin prints obtained by lithographic decals up to the thicker prints obtained by screening. Unfired print thicknesses can range from .25 mil to 2.5 mil, and are a function of the depth of the design etched on the gravure roll 42.
- the decal 10 may be pressed or rolled against the heated substrate surface, or is alternatively preheated and pressed against a cold substrate surface. It may even be pressed between a heated transfer pad or roll and a cold substrate.
- the aforementioned substrate and press are not shown detailed herein as description is not necessary to the understanding of the present invention.
- the heat melts the release layer 16 (wax) thereby releasing or transferring the design 20 and sealant layers 18 to the glass or ceramic substrate (not shown).
- the release layer 16 of wax must be either the lowest melt point or the lowest melt viscosity layer in the decal 10 at the transfer temperature.
- the barrier layer 14 on the other hand should preferably not melt at the transfer temperature in order to prevent the molten wax from the release layer 16 from penetrating into the paper backing 12.
- the sealant 18 and design 20 layers must either not melt or, if molten, be of much higher viscosity than the release layer.
- Cohesive strength imparting resins are essential to the design and sealant layers to preserve their integrity during transfer and thereby prevent distortion or smearing of the decoration. It is preferable that the design and sealant layers do not melt during transfer, but both layers consequently must exhibit pressure sensitivity below the melt point of the inks 46 therein, such that, the design 20 will adhere to the substrate upon contact at the release temperature.
- Such materials and others useful in the present invention are disclosed in a copending U.K. application S.N. 80 32236 of this same date assigned to Corning Glass Works the assignee herein, the teachings of such disclosure being incorporated herein by reference.
- One embodiment of the invention herein is the use of a hot melt offset gravure process to construct a decal comprised of alternate layers of hot melt thermoplastic materials.
- the inks Preferably contain ceramic materials or pigments for the manufacture of ceramic decals for use in decorating glass or glass-ceramic tableware. It is not intended that this be strictly limited to ceramic decals but may apply to decals comprised of any other hot melt material, i.e., chocolate or similar confectionary substances for food decorations, colored waxes for labels, etc.
- the hot melt offset rotogravure process used herein consists of a heated gravure roll, also known as intaglio (etched or engraved) roll 42, preferably steel, to which the molten inks 41 are applied by inking rolls, bath immersion (shown in Fig. 2), or other suitable means.
- the temperature of the gravure roll 42 should be between 180°F. and 300°F.
- the excess ink is removed from the roll by means of the doctor blade 54.
- the gravure roll 42 then contacts offset roll 44 formed of a material having a suitable releasing surface 41. Condensation-cure silicones such as Stauffer-Wacker 04478 have been found suitable. Other releasing elastomers are also suitable.
- the silicones used herein may be the same as those used for direct transfer printing as described in U.S. Patent Nos. 3,756,165 and 3,255,695.
- the offset roll 40 picks up the printed image upon contact from the gravure roll 42, as long as the ink melt viscosity is sufficiently low (e.g. 10 to 1,000 poise) to wet the offset surface 41.
- the ink 46 subsequently cools upon the offset surface 41 to either slightly above its nelt point or below its melt point for those materials having sufficient pressure sensitivity to adhere to the surface to be printed on the backing material 12.
- the print is then transferred from the offset surface 41 to the backing material 12 by intimate mechanical contact.
- the ink 46 transfers from the offset surface 41 for which it has low affinity to a surface for which it has greater affinity. This same basic step is repeated for each layer of the decal to be printed.
- a satisfactory sealant coat is one part by weight ethylene vinyl acetate copolymer (19% vinyl acetate, ASTM D1238 melt index of 150 g/10 min.), one part glycerol ester of hydrogenated resin (R&B sofening point of 52°C.), one part paraffin wax (melt point 130°F), and six parts glass flux.
- the sealant layer be a thin layer of thermoplastic resin applied from solution over the release layer.
- a suitable resin is a n-butyl methacrylate polymer such as Elvacite 2044 (Dupont).
- Design Layer - the design layer may consist of up to 15 adjacent colours which may overlap to form 3 overlayers in limited areas.
- the inks used therein contain from 50-80% vitrifiable inorganic or ceramic colour (glass flux plus 0.5-30% pigments and opacifiers), and 20-50% organic medium.
- a suitable organic medium consists of about 20-50% cohesive strength imparting polymers, 0-50% amorphous tackifying resins, and 20-50% waxes and preferably 33 1/3% ethylene vinyl acetate copolymer, 19% acetate; 33 1/3% glycerol ester of hydrogenerated rosin; and 33 1/3% paraffin.
- the organic formulation for the design layer 20 is, in this case, the same as that used for the hot melt sealant layer 18.
- the design layer inks exhibit a R&B softening point of about between 50-95°C and a 100 RPM Brookfield Thermocel viscosity about between 50 and 1000 poise at 100°C.
- the cohesive strength imparting polymers may also be selected from the group consisting of cellulosic ethers, cellulosic esters, ethylene ester copolymers, polyethylene, polyvinylpyrrolidone, acrylic and methacrylic polymers and copolymers, and block copolymers of styrene with butadiene or isoprene.
- the amorphous tackifying resins may be selected from a group consisting of rosin and rosin derivatives, atactic polypropylene, polyterpene resins, and aliphatic hydrocarbon resins.
- the waxes may be selected from a group consisting of paraffin and microcrystalline mineral waxes, animal and vegetable waxes, fatty alcohols and acids, fatty acid esters and glycerides, low molecular weight polyethylene, polyoxyalkylene esters, polyoxyalkylene ethers, oxazoline waxes and hydrogenated oils.
- a hot melt polyethylene barrier layer may also be optionally present between the silicone release layer and the paper backing; such paper is readily commercially available and is known as polycoated release paper. The hot melt offset rotogravure process would then be used for printing the sealant and design layers onto the pressure release layer.
- This latter type of decal 10 is known for its cold release properties and can be transferred to a substrate solely upon the application of pressure.
- the wax in the ceramic colour medium formulations described in the above mentioned copending application may be replaced by a liquid low volatility plasticizer. It is important that the plasticizer be incompatible (immiscible) with the sealant layer 18, or that the design and sealant layers be of identical organic composition, in order to prevent migration of plasticizer between layers.
- Other types of hot melt inks such as described in copending U.K. application S.N. 80 32237 of this same date assigned to Corning Glass Works the assignee herein, are also applicable in the construction of pressure-release decalcomania printed by the processes described herein
- water-slide-off decals 10 wherein the wax in release layer 16 is replaced by a water soluble layer, and a high cohesive strength film is located over the design layer 20.
- the water soluble release layer 16 may also be printed by hot melt offset gravure wherein a water soluble resin such as polyvinylpyrrolidone, blended with a water soluble wax such as polyethylene glycol wax is utilized. The latter may be molecular weight of about between 1000 and 6000.
- Another embodiment of the present invention is similar to the method proposed above, in that both methods may utilize pressure-sensitive and heat sensitive thermoplastic inks; however, above, an offset rotogravure process is used for the decal manufacture, whereas in this embodiment discussed below it is proposed that a flexographic (typographic) process be used.
- a flexographic (typographic) process be used.
- the flexographic process differs from offset rotogravure process described above in that the gravure roll 42 upon which the design has been etched or engraved is replaced by plane inking roll upon which there is an ink film of uniform thickness, and the offset roll 40 is replaced by a typographic roll upon which the design is present as raised areas.
- the first roll is preferably made of metal heated to between 180 and 300°F, whereas the second roll is preferably silicone rubber.
- the flexographic processes has a limitation in print quality especially when compared to lithography and offset rotogravure since it is not capable of printing variable tones, and yields less resolution and detail.
- the flexographic process has been found to be superior to offset rotogravure for printing glass-flux filled thermoplastic inks in two respects.
- offset rotogravure it is necessary to doctor the gravure roll 42 with a blade which removes the excess ink from the roll surface leaving the ink only in the recessed design areas. Any ink left on the gravure surface in non-design areas is picked up by the offset roll and printed onto the decal backing, which results, when pigments are present in the ink, in a defect known as "haze".
- the doctor blades can be construed of very rigid wear resistant materials, such as tungsten carbide, and either not touch the roll surface at all or only touch in very limited raised wear resistant areas spaced circumferentially around the roll.
- the required flexibility of the rotogravure blades results in the second drawback of that process or the inability to doctor over large continuous recessed areas without the blade penetrating into the areas. Penetration of the blade into these areas results either in insufficient or in non-uniform ink retention by the design.
- the gravure cylinders are etched or engraved in a dot pattern such that there are always areas available for blade support.
- a gravure roll could transfer after doctoring the design or ink to an embossed flexographic surface.
Landscapes
- Printing Methods (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Meat, Egg Or Seafood Products (AREA)
- Adornments (AREA)
- Laminated Bodies (AREA)
Abstract
Description
- This invention relates to an improved method of making decalcomania (decals) particularly of the heat release type.
- Heretofore, heat release decals have been primarily manufactured by screening or lithography although manufacture feasibility by rotogravure and letterpress was known. The use of offset rotary lithographic presses for printing the varnishes used in making heat release lithographic decals was also known as shown in U.S. Patent No. 2,640,458.In all of the above mentioned processes the inks and coatings printed contain various organic solvents or oils necessarily included in the printing media to achieve printable viscosities. These inks and coatings are successively printed to achieve heat release decals of the basic layered structure described in U.S. Patent No. 2,970,076.
- The first three layers of a heat release decal are normally not transferable and include a backing or support material, usually paper, a barrier coat, and a wax release layer. A transferable portion, consisting of design, sealant, overflux, and adhesive layers is deposited thereover. The function of the barrier coat is to prevent absorption of the wax release layer into the paper both at the time of wax application to the paper and transfer of the finish decal to a substrate surface. The release coat is the layer which separates the transferable portion of the decal from the non-transferable portion. The release coat itself is the only portion of a heat release decal which has hitherto been applied by hot melt techniques, such as roll coaters etc.
- Polyethylene glycols having molecular weights in excess of 1000 are commonly employed as the waxes for the release layer as noted in U.S. Patent Nos. 2,970,076,' 3,007,829, and 4,068,033, although both vegetable and mineral waxes can be employed as disclosed in U.S. Patent No. 2,970,076. The use of polyethylene glycol esters is also known, particularly, if solution coating techniques are to be employed for applying the wax (see for example U.S. Patent No. 3,533,822).
- In a conventional heat releasable decal, it is normal to include an outermost thermoplastic or heat activatable adhesive surface at the opposite or rear side of the design. The term "thermoplastic" as employed in relation to this adhesive layer is not synonymous to the term "thermoplastic" as applied to the thermoplastic inks discussed hereinafter. In both cases the materials reversibly soften with heat, hence the term "themmoplastic" In the present invention when the term is applied to the inks it also implies melt processibility (application), by the methods and apparatus disclosed herein, whereas, the material used for the decal adhesive layer is applied from solution over the design. To avoid the ambiguity of the term thermoplastic, melt processable inks are sometimes referred to as "hot melt" inks or simply "hot colour". When, for example, the outermost thermoplastic or heat activatable surface of the decal is pressed against the surface of a preheated vitreous or ceramic article, the heat of the article softens the adhesive surfaces of the decal to a sufficient extent such that the design is adhered to the article being decorated. Concurrently, the heat from the article softens or melts the heat release layer of the backing, thereby causing the backing to release from the design layer. Both actions are accomplished in essentially a single operation in which the decal is pressed against the preheated article. The ware with the temporarily adhered vitreous design is thereafter fired in the normal manner to cause the design to become an integral part of the surface of the ware. In the present invention the inks exhibit sufficient pressure sensitivity below their melt points so that the need for a separate adhesion layer is obviated.
- The structure and composition of the transferrable portion of the heat release decal depends somewhat on the process used to manufacture the decal. For example screening processes have previously proved to be the most economical process for manufacturing heat release decals. Screening, however, is not without its limitations and drawbacks. The use of solvents in the screening media necessitate drying between the decal layers so that each successive layer can be applied over or adjacent to the previous layers without distortion, smearing, or pick-back of the print. The solvents thus add considerable cost to the decal manufacturing process by necessitating both driers and environmental protection controls. Viscosity controls are also required to achieve viscosity stability. Low volatility solvents are often used which require more extensive drying either in terms of time or temperature. Time is the variable usually affected because of the desire not to melt the wax release layer during the drying operation. An increase in drying time, however, means longer driers or slower process speeds. Melting of the wax during drying often results in less acceptable release when transferring the decal to the substrate.
- If the backing is paper, it is important to control the dimensions of the paper sheets to ensure proper registration of the subsequent design layers. The dimensions of the paper are directly coupled to its moisture content. Excessive drying time shrinks the sheet by driving out moisture, conversely, increased moisture content resulting from shorter drying time expands the sheet due to absorption. The environmental window in which the paper can be handled is very narrow, thus affecting drying times and temperatures in conjunction with previously menti.oned wax problems.
- Thermoplastic screening, requiring negligible drying, is not a viable alternative for solving these problems because the heated screens would melt the wax release layer, and thereby, prevent the backing material from accepting the screened prints. This could be prevented by screening overlayers having a melt point lower than the release layer, but this would also be impracticable because the design layer would remelt and smear upon subsequent transfer of the heat release decal to the substrate.
- In addition to process limitations, silk-screened decals also have a limitation, in that, they cannot achieve the fine resolution and sharp definition obtainabl by lithographic decals; moreover, the thicker layer which results from screening is not always desirable.
- In a lithographic decal process, dry colour is dusted over the sheet of paper, and adheres only to the printed varnish image. The excess colour is then removed from the sheet, leaving the desired image. Due to the aforementioned shortcomings of screened decals, lithographic decals are often used in spite of process disadvantages resulting from the inability of adding colours directly to the lithographic varnish.
- The lithographic process is also not without other disadvantages, besides this obvious disadvantage of having to handle, dust, and remove the dry powders after each successive application of varnish. For example, while lithographic decals may have much greater resolutio than screened decals, the prints are also much thinner, a a consequence much higher levels of pigments must be used in the colours. For overglaze decals this necessitates an overflux, i.e., a printed overglaze, which is applied over the colours to improve durability and reduce to safe levels toxic metal release. Although an overflux is sometimes used for screened decals, its use for lithographic decals in food-contact applications is mandatory. Due to the tendency of the dry colours to stick to the overflux layer, a sealant layer is required in the construction of a lithographic decal between the design layer and the overflux layer as shown in U.S. Patent No. 4,068,033. In general, lithographic heat release decals have been found more difficult to manufacture than screened decals, such that, their use has been limited.
- The present invention overcomes most of the disadvantages of screened and lithographic decals by utilizing thermoplastic colours (sometimes hereinafter referred to as, hot melt colours) for the design layers of the decal, and optionally all layers of the decal except the backing material, in conjunction with an offset rotogravure process, wherein, the melted thermoplastic materials are first transferred from a heated gravure or intaglio roll to an elastomeric offset roll, whereupon the materials cool such that they can be transferred from the offset roll at temperatures considerably below their melt points. By utilizing the offset roll, it is possible to print waxes or thermoplastic hot melts of higher melt points over a wax release layer of lower melt point as long as the hot melts, thereby printed, exhibit sufficient pressure sensitivity below their melt points to adhere to a wax surface when transferring from the offset roll. The offset roll prevents melting of the release layer which would occur for direct gravure with heated rolls. Both the offset and backup rolls may be internally cooled, with a heat transfer fluid if necessary, to maintain a low temperature when printing onto the release layer.
- In a similar manner a flexographic process may be used wherein an ink applicator roll is substituted for the gravure roll and an embossed silicone roll carrying a portion of the design is substituted for the plain offset roll. In this case the embossed design on the flexographic roll picks-up a uniform layer of. ink by contacting the ink applicator roll. The ink subsequently cools upon and is transferred from the flexographic roll in a similar manner to the offset roll described above.
- The invention will now be further described with reference to the accompanying drawings, in which Figure 1 is a decal in cross section which may be manufactured according to the present invention illustrating the general layout which in any one particular embodiment may include less than the number of layers illustrated in the drawing.
- Figure 2 is a schematic of a multiple station printing machine for use in producing the decal illustrated in Figure 1.
- Referring to Figure 1 this shows a
decal 10 having multiple layers of material hereinafter described. Thedecal 10 is illustrated in the general sense that certain materials may be substituted for other types. However, the arrangement of layers of materials thereon follows a functional sequence. -
Decal 10 includes abacking material 12 for supporti the remaining portions of thedecal 10, abarrier layer 14 for sealing the backing material, arelease layer 16 for allowing separation of the subsequent layers from thebacking 12, asealant coat 18, and a design layer on layers (multicolours) 20. - The purpose of the various layers have been previously described in the background and are basically conventional. However, the components of each of the layers, as combined in the present invention provide a
novel decal 10 with properties and advantages exceeding those presently attainable. - Traditionally for a heat release decal, the
backing material 12 is paper, and thebarrier layer 14 can be such materials as starch, casein, and alkali metal silicates with or without clay type fillers as mentioned in U.S. 2,970,076, or polyvinylacetate as mentioned in U.S. 3,445,309. Alternatively, herein, the barrier layer can be a high melt point wax. The barrier layer seals the backing and prevents cross-contamination of therelease layer 16 when apaper backing layer 12 is used. Therelease layer 16 is usually a wax having a melting point lower than thebarrier layer 14. Thus, when thedecal 10 comes in contact with a hot substrate or is heated from the opposite side of thebacking material 12, therelease layer 16 melts and allows the remaining coats to stick to the substrate and release from thebacking material 12. - The
sealant layer 18 may contain fluxes therein so that when ceramic inks or colours are used in the design layer 20 a vitreous film (overflux) is produced which reduces the release of toxic metals which may be present in the coloured materials forming thedesign layer 20.. The vitreous film (overflux) also improves the overall fired decoration durability. Thesealant layer 18 also facilitates total release of thedesign layer 20 from thebacking 12. A number of layers may form thedesign layer 20 by sequential printing of various colour patterns one over the other to form a decorative design of high resolution. - If a
nonporous backing material 12 is utilized then thebarrier layer 14 may be unnecessary. For example, an organic film or metal foil may be utilized which would not be absorbent to melted wax of therelease layer 16, thus the barrier layer would be unnecessary because thebacking material 12 would serve as its own barrier to therelease layer 16. Other variations of the present invention will be described herein but first there will be a brief description of an apparatus suitable for producing thedecals 10 of the present invention. - In Figure 2 a multiple station offset rotogravure hot melt printing machine 30 is described. The apparatus shown includes n stations labeled 1, 2 ...n and a pair of respective unwind and rewind
reels idler wheels 36a-c, abackup roll 38, an offsetroll 40, an etched edge orgravure roll 42, and ahot melt bath 44 into which a quantity of thermoplastic ink 46 is deposited. Each station l-...n essentially include the same arrangement of rolls and pulleys. Intermediate each station there may be included a so-calledchill roll 48 which may be temperature controlled by heat exchange means 49. The function of thechill roll 48 is to especially reduce heat buildup in thebacking material 12 and release layers 16, which may occur during high speed printing. Also thechill roll 48 helps to freeze the previously printed hot melt thermoplastic materials. - Respective unwind and rewind
idler wheels 50a and b establish the path for thebacking material 12 as hereinafter described. - A roll of
backing material 12 is placed at the unwindreel 32 and passes around the unwind idler 50a, over thefirst idler 36a of station 1 and the subsequentdownstream idler 36b between the respective backup and offsetrolls downstream idler 36c over thechill roll 48 and thence to thesecond station 2 for repeat threading and so on until thebacking material 12 is located about therewind idler 50b and therewind reel 34. - The
hot melt bath 44 carries the ink 46 which is in intimate contact with thegravure roll 42 which may be heated by an electrical orother heating device 52. Adoctor blade 54 scrapes excess ink 46 from thegravure roll 42; and, as it rotates therafter coming in intimate contact with the offsetroll 40, the ink remaining on thegravure roll 42 causes a mirror image by splitting between the two surfaces upon separation. As the offsetroll 40 rotates it comes in contact with thebacking material 12 and prints its image onto thebacking material 12 as supported by thebackup roll 38. Each station in turn prints a different layer on thebacking material 12 so that after multiple steps the decal is produced having the desired design printed thereon. - It should be noted that each of the respective backup and offset
rolls gravure roll 42 cools to a temperature where it will have sufficient pressure sensitivity to transfer from the offset roll to thebacking material 12 and yet not smear or remelt previously applied layers includingrespective barrier 14,release 16, andsealant 18 layers when used. - Decals printed by the hot melt offset rotogravure process described herein exhibit significant advantages over those printed by conventional techniques. The resolution and definition obtainable by the process of the invention approaches that of lithographic decals and substantially exceeds that of screened decals; on the other hand, the higher pigment loadings of the colours required for lithographic decals are not needed for this process, consequently, decals printed in accordance with the present invention compare to screened decals for durability. Print thicknesses obtainable by this process can be adjusted from the thin prints obtained by lithographic decals up to the thicker prints obtained by screening. Unfired print thicknesses can range from .25 mil to 2.5 mil, and are a function of the depth of the design etched on the
gravure roll 42. - Process advantages over both screening and lithography are substantial. Each colour and/or coating is printed in a single contact with the offset roll and is immediately ready to receive the next colour or coating. The drying procedures required for screened decals, or the dusting and removal of excess colour steps for lithographic decals are totally obviated. The
backing material 12 successively contacts a series of thermally controlled offset rolls 40. The number of offset printing stations can vary from one, for a single colour decal applied to a prewaxed andpre-sealed backing material 12, to perhaps eighteen or more for a fifteencolour decal 10 for which thebarrier 14,sealant 18, and release 16 layers may be printed if required in addition to the colours. The adhesive layer noted in the construction of heat release decals.in U.S. Patent Nos. 2,970,076 and 4,068,033 is not required for hot melt offset decals because of the adhesive nature of the hot melt materials themselves. - Application techniques for transferring the offset
decal 10 to a substrate can be identical to those used for applying heat release decals manufactured by the other processes. Thedecal 10 may be pressed or rolled against the heated substrate surface, or is alternatively preheated and pressed against a cold substrate surface. It may even be pressed between a heated transfer pad or roll and a cold substrate. The aforementioned substrate and press are not shown detailed herein as description is not necessary to the understanding of the present invention. The heat melts the release layer 16 (wax) thereby releasing or transferring thedesign 20 andsealant layers 18 to the glass or ceramic substrate (not shown). For the release to satisfactorily occur, therefore, therelease layer 16 of wax must be either the lowest melt point or the lowest melt viscosity layer in thedecal 10 at the transfer temperature. Thebarrier layer 14 on the other hand should preferably not melt at the transfer temperature in order to prevent the molten wax from therelease layer 16 from penetrating into thepaper backing 12. - The
sealant 18 and design 20 layers must either not melt or, if molten, be of much higher viscosity than the release layer. Cohesive strength imparting resins are essential to the design and sealant layers to preserve their integrity during transfer and thereby prevent distortion or smearing of the decoration. It is preferable that the design and sealant layers do not melt during transfer, but both layers consequently must exhibit pressure sensitivity below the melt point of the inks 46 therein, such that, thedesign 20 will adhere to the substrate upon contact at the release temperature. Such materials and others useful in the present invention are disclosed in a copending U.K. application S.N. 80 32236 of this same date assigned to Corning Glass Works the assignee herein, the teachings of such disclosure being incorporated herein by reference. - .One embodiment of the invention herein is the use of a hot melt offset gravure process to construct a decal comprised of alternate layers of hot melt thermoplastic materials. Preferably the inks contain ceramic materials or pigments for the manufacture of ceramic decals for use in decorating glass or glass-ceramic tableware. It is not intended that this be strictly limited to ceramic decals but may apply to decals comprised of any other hot melt material, i.e., chocolate or similar confectionary substances for food decorations, colored waxes for labels, etc.
- The hot melt offset rotogravure process used herein consists of a heated gravure roll, also known as intaglio (etched or engraved)
roll 42, preferably steel, to which themolten inks 41 are applied by inking rolls, bath immersion (shown in Fig. 2), or other suitable means. The temperature of thegravure roll 42 should be between 180°F. and 300°F. The excess ink is removed from the roll by means of thedoctor blade 54. Thegravure roll 42 then contacts offsetroll 44 formed of a material having a suitable releasingsurface 41. Condensation-cure silicones such as Stauffer-Wacker 04478 have been found suitable. Other releasing elastomers are also suitable. The silicones used herein may be the same as those used for direct transfer printing as described in U.S. Patent Nos. 3,756,165 and 3,255,695. The offsetroll 40 picks up the printed image upon contact from thegravure roll 42, as long as the ink melt viscosity is sufficiently low (e.g. 10 to 1,000 poise) to wet the offsetsurface 41. The ink 46 subsequently cools upon the offsetsurface 41 to either slightly above its nelt point or below its melt point for those materials having sufficient pressure sensitivity to adhere to the surface to be printed on thebacking material 12. The print is then transferred from the offsetsurface 41 to thebacking material 12 by intimate mechanical contact. The ink 46 transfers from the offsetsurface 41 for which it has low affinity to a surface for which it has greater affinity. This same basic step is repeated for each layer of the decal to be printed. - For heat release ceramic decals, for which the organic constituents in the transferable portion of the
decal 10 must burn off during firing without adversely affecting the glass fluxes, the following is a list of preferred materials for each layer of the decal: - 1. Barrier Layer - a relatively high melt point wax modified with an organic thickener, such as a cellulosic ether, or inorganic thickener, such as cab-o-sil, bentonite, etc. An example is one part polyethylene glycol wax (molecularr weight 6000) thickened with two parts by weight Min-U-Sil (pulverized silica from Pennsylvania Glass Sand Corp.).
- 2. Release Layer - a low melt point wax of low melt viscosity. Polyethylene glycol wax (molecular weight 1500) is suitable.
- 3. Sealant Layer - it is usually preferable that the sealant layer contains a glass flux to serve as an overflux for the decoration after firing.
- A satisfactory sealant coat is one part by weight ethylene vinyl acetate copolymer (19% vinyl acetate, ASTM D1238 melt index of 150 g/10 min.), one part glycerol ester of hydrogenated resin (R&B sofening point of 52°C.), one part paraffin wax (melt point 130°F), and six parts glass flux.
- If it is desirable that the sealant layer not contain a glass flux, then it is preferable that the sealant layer be a thin layer of thermoplastic resin applied from solution over the release layer.. A suitable resin is a n-butyl methacrylate polymer such as Elvacite 2044 (Dupont).
- 4. Design Layer - the design layer may consist of up to 15 adjacent colours which may overlap to form 3 overlayers in limited areas.
- The inks used therein contain from 50-80% vitrifiable inorganic or ceramic colour (glass flux plus 0.5-30% pigments and opacifiers), and 20-50% organic medium. A suitable organic medium consists of about 20-50% cohesive strength imparting polymers, 0-50% amorphous tackifying resins, and 20-50% waxes and preferably 33 1/3% ethylene vinyl acetate copolymer, 19% acetate; 33 1/3% glycerol ester of hydrogenerated rosin; and 33 1/3% paraffin.
- The organic formulation for the
design layer 20 is, in this case, the same as that used for the hotmelt sealant layer 18. The design layer inks exhibit a R&B softening point of about between 50-95°C and a 100 RPM Brookfield Thermocel viscosity about between 50 and 1000 poise at 100°C. - The cohesive strength imparting polymers may also be selected from the group consisting of cellulosic ethers, cellulosic esters, ethylene ester copolymers, polyethylene, polyvinylpyrrolidone, acrylic and methacrylic polymers and copolymers, and block copolymers of styrene with butadiene or isoprene.
- The amorphous tackifying resins may be selected from a group consisting of rosin and rosin derivatives, atactic polypropylene, polyterpene resins, and aliphatic hydrocarbon resins.
- The waxes may be selected from a group consisting of paraffin and microcrystalline mineral waxes, animal and vegetable waxes, fatty alcohols and acids, fatty acid esters and glycerides, low molecular weight polyethylene, polyoxyalkylene esters, polyoxyalkylene ethers, oxazoline waxes and hydrogenated oils.
- It is intended that the scope of this invention inelude
pressure release decals 10 for which a silicone, fluorosilicone or fluorocarbon material replaces wax for therelease layer 16. In the case of silicone, a hot melt polyethylene barrier layer may also be optionally present between the silicone release layer and the paper backing; such paper is readily commercially available and is known as polycoated release paper. The hot melt offset rotogravure process would then be used for printing the sealant and design layers onto the pressure release layer. - This latter type of
decal 10 is known for its cold release properties and can be transferred to a substrate solely upon the application of pressure. For acold release decal 10, the wax in the ceramic colour medium formulations described in the above mentioned copending application may be replaced by a liquid low volatility plasticizer. It is important that the plasticizer be incompatible (immiscible) with thesealant layer 18, or that the design and sealant layers be of identical organic composition, in order to prevent migration of plasticizer between layers. Other types of hot melt inks, such as described in copending U.K. application S.N. 80 32237 of this same date assigned to Corning Glass Works the assignee herein, are also applicable in the construction of pressure-release decalcomania printed by the processes described herein - It is also intended that the scope of this invention include those decals known as water-slide-off
decals 10 wherein the wax inrelease layer 16 is replaced by a water soluble layer, and a high cohesive strength film is located over thedesign layer 20. The watersoluble release layer 16 may also be printed by hot melt offset gravure wherein a water soluble resin such as polyvinylpyrrolidone, blended with a water soluble wax such as polyethylene glycol wax is utilized. The latter may be molecular weight of about between 1000 and 6000. - Another embodiment of the present invention is similar to the method proposed above, in that both methods may utilize pressure-sensitive and heat sensitive thermoplastic inks; however, above, an offset rotogravure process is used for the decal manufacture, whereas in this embodiment discussed below it is proposed that a flexographic (typographic) process be used. Each process has inherent advantages and disadvantages when compared to each other such that the preferred process will vary depending either on the design to be printed or on the layer of the decal to be printed.
- Referring to Figure 2, all items will be referred to as above except for substitutions below. The flexographic process differs from offset rotogravure process described above in that the
gravure roll 42 upon which the design has been etched or engraved is replaced by plane inking roll upon which there is an ink film of uniform thickness, and the offsetroll 40 is replaced by a typographic roll upon which the design is present as raised areas. In both cases, because of the nature of the inks herein proposed, the first roll is preferably made of metal heated to between 180 and 300°F, whereas the second roll is preferably silicone rubber. The advantages of both of these processes over screening and lithography is virtually the same since most of the advantages are inherent in the use of pressure- . sensitive thermoplastic inks. The flexographic processes, however, has a limitation in print quality especially when compared to lithography and offset rotogravure since it is not capable of printing variable tones, and yields less resolution and detail. The flexographic process, on the other hand, has been found to be superior to offset rotogravure for printing glass-flux filled thermoplastic inks in two respects. First, in offset rotogravure it is necessary to doctor thegravure roll 42 with a blade which removes the excess ink from the roll surface leaving the ink only in the recessed design areas. Any ink left on the gravure surface in non-design areas is picked up by the offset roll and printed onto the decal backing, which results, when pigments are present in the ink, in a defect known as "haze". This problem necessitates frequent blade changes during operation, and is the major drawback of the rotogravure process. In the flexographic process it is only necessary for the raised design areas to contact the metal roll surface, thereby minimizing any chance of picking up and printing unwanted ink. Although it is still necessary to doctor the inking roll (now 42) in order to control ink thickness, the doctoring is distinctly different from the doctoring required for offset rotogravure. In the latter case the blade must have sufficient flexibility or a sufficiently high wear rate to conform to thetotal gravure roll 42 surface in order to doctor effectively over rolls of the width necessary for efficient decal manufacture. For the flexographic process the doctor blades can be construed of very rigid wear resistant materials, such as tungsten carbide, and either not touch the roll surface at all or only touch in very limited raised wear resistant areas spaced circumferentially around the roll. The required flexibility of the rotogravure blades results in the second drawback of that process or the inability to doctor over large continuous recessed areas without the blade penetrating into the areas. Penetration of the blade into these areas results either in insufficient or in non-uniform ink retention by the design. To avoid this problem the gravure cylinders are etched or engraved in a dot pattern such that there are always areas available for blade support. This is satisfactory for most designs, and is preferred for many applications, but it is not satisfactory when it is necessary to print solid bold design areas or void free films. For this reason the flexographic process is preferred for printing the non-design layers of a ceramic decal, or for printing design where a continuous uniform film of colour is required. - Both processes can be used for printing heat release decalcomina, cold release decalcomania, or even the design and adhesive layers of water-slide-off decalcomania. The pressure-sensitive thermoplastic inks utilized are interchangeable between the two processes. In fact, some of the stations 1-n in Figure 2 could be of the first type described herein and others could be of the latter type.
- In yet another possible embodiment, a gravure roll could transfer after doctoring the design or ink to an embossed flexographic surface.
Claims (25)
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE8181300821T DE3174691D1 (en) | 1981-02-27 | 1981-02-27 | Production of decalcomanias and apparatus for the production thereof |
AT81300821T ATE19999T1 (en) | 1981-02-27 | 1981-02-27 | MANUFACTURING OF DECALS, AND APPARATUS FOR THE MAKING THERE. |
EP81300821A EP0059276B1 (en) | 1981-02-27 | 1981-02-27 | Production of decalcomanias and apparatus for the production thereof |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP81300821A EP0059276B1 (en) | 1981-02-27 | 1981-02-27 | Production of decalcomanias and apparatus for the production thereof |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0059276A1 true EP0059276A1 (en) | 1982-09-08 |
EP0059276B1 EP0059276B1 (en) | 1986-05-28 |
Family
ID=8188227
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP81300821A Expired EP0059276B1 (en) | 1981-02-27 | 1981-02-27 | Production of decalcomanias and apparatus for the production thereof |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP0059276B1 (en) |
AT (1) | ATE19999T1 (en) |
DE (1) | DE3174691D1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2236984A (en) * | 1990-07-13 | 1991-04-24 | Denny Damodar Kalro | Image transfer process and carrier material therefor |
EP0539924A1 (en) * | 1991-10-29 | 1993-05-05 | Manfred Neuberger | Procedure and apparatus for the production of transfer sheets for firing of images, characters, and decors on ceramic objects |
GB2317852A (en) * | 1996-10-03 | 1998-04-08 | Yu Chau Chia | Diagram attaching means for plastic products |
WO1998033663A1 (en) * | 1997-01-30 | 1998-08-06 | Leonhard Kurz Gmbh & Co. | Method for making a decorative film with hot melt adhesive layer |
US5981009A (en) * | 1997-01-30 | 1999-11-09 | Leonard Kurz Gmbh & Co. | Decorative film with hot melt adhesive layer |
Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2322445A (en) * | 1941-04-24 | 1943-06-22 | J M Huber Inc | Printing process |
US2970076A (en) * | 1957-01-14 | 1961-01-31 | Meyercord Co | Vitreous decalcomania and method of decorating ceramic articles |
US3007829A (en) * | 1959-02-09 | 1961-11-07 | Meyercord Co | Vitreous decalcomania |
US3255695A (en) * | 1963-10-16 | 1966-06-14 | Markem Machine Co | Method of printing and apparatus therefor |
US3445309A (en) * | 1966-05-04 | 1969-05-20 | Meyercord Co | Method of applying a vitreous decalcomania |
US3533822A (en) * | 1968-06-10 | 1970-10-13 | Int Paper Co | Vitreous decalcomania and coated paper base |
US3554836A (en) * | 1968-07-19 | 1971-01-12 | Minnesota Mining & Mfg | Transfer process |
GB1447068A (en) * | 1973-09-04 | 1976-08-25 | Murray Curvex Printing Ltd | Methods and means for printing or decorating articles |
US4068033A (en) * | 1976-11-17 | 1978-01-10 | Commercial Decal, Inc. | Heat-releasable decalcomanias and adhesive composition therefor |
GB2005596A (en) * | 1977-10-04 | 1979-04-25 | Letraset International Ltd | The manufacture of signs |
-
1981
- 1981-02-27 DE DE8181300821T patent/DE3174691D1/en not_active Expired
- 1981-02-27 EP EP81300821A patent/EP0059276B1/en not_active Expired
- 1981-02-27 AT AT81300821T patent/ATE19999T1/en not_active IP Right Cessation
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2322445A (en) * | 1941-04-24 | 1943-06-22 | J M Huber Inc | Printing process |
US2970076A (en) * | 1957-01-14 | 1961-01-31 | Meyercord Co | Vitreous decalcomania and method of decorating ceramic articles |
US3007829A (en) * | 1959-02-09 | 1961-11-07 | Meyercord Co | Vitreous decalcomania |
US3255695A (en) * | 1963-10-16 | 1966-06-14 | Markem Machine Co | Method of printing and apparatus therefor |
US3445309A (en) * | 1966-05-04 | 1969-05-20 | Meyercord Co | Method of applying a vitreous decalcomania |
US3533822A (en) * | 1968-06-10 | 1970-10-13 | Int Paper Co | Vitreous decalcomania and coated paper base |
US3554836A (en) * | 1968-07-19 | 1971-01-12 | Minnesota Mining & Mfg | Transfer process |
GB1447068A (en) * | 1973-09-04 | 1976-08-25 | Murray Curvex Printing Ltd | Methods and means for printing or decorating articles |
US4068033A (en) * | 1976-11-17 | 1978-01-10 | Commercial Decal, Inc. | Heat-releasable decalcomanias and adhesive composition therefor |
GB2005596A (en) * | 1977-10-04 | 1979-04-25 | Letraset International Ltd | The manufacture of signs |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2236984A (en) * | 1990-07-13 | 1991-04-24 | Denny Damodar Kalro | Image transfer process and carrier material therefor |
GB2236984B (en) * | 1990-07-13 | 1994-02-23 | Denny Damodar Kalro | Image transfer process and carrier material therefor |
EP0539924A1 (en) * | 1991-10-29 | 1993-05-05 | Manfred Neuberger | Procedure and apparatus for the production of transfer sheets for firing of images, characters, and decors on ceramic objects |
GB2317852A (en) * | 1996-10-03 | 1998-04-08 | Yu Chau Chia | Diagram attaching means for plastic products |
WO1998033663A1 (en) * | 1997-01-30 | 1998-08-06 | Leonhard Kurz Gmbh & Co. | Method for making a decorative film with hot melt adhesive layer |
US5981009A (en) * | 1997-01-30 | 1999-11-09 | Leonard Kurz Gmbh & Co. | Decorative film with hot melt adhesive layer |
US6146485A (en) * | 1997-01-30 | 2000-11-14 | Leonhard Kurz Gmbh & Co. | Method for making a decorative film with hot melt adhesive layer |
Also Published As
Publication number | Publication date |
---|---|
EP0059276B1 (en) | 1986-05-28 |
DE3174691D1 (en) | 1986-07-03 |
ATE19999T1 (en) | 1986-06-15 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4322467A (en) | Decalcomania | |
US4292104A (en) | Decalcomania manufacture | |
US4445432A (en) | Article decorating | |
US2970076A (en) | Vitreous decalcomania and method of decorating ceramic articles | |
US3255695A (en) | Method of printing and apparatus therefor | |
CA1073758A (en) | Total image transfer process | |
US4280939A (en) | Thermoplastic ink composition for decorating glass, glass-ceramic, and ceramic ware | |
EP1833680B1 (en) | Heat transfer masking sheet materials and methods of use thereof | |
US20110217088A1 (en) | Method and System for Printing Electrostatically or Electrographically Generated Images to Contoured Surfaces of Ceramic and Glass Items Such as Dishware | |
JPS5843517B2 (en) | Thermal transfer material and transfer method | |
GB2245221A (en) | Ceramic decalcomania | |
US3894167A (en) | Decalcomania for decorating ceramic ware | |
EP0059276B1 (en) | Production of decalcomanias and apparatus for the production thereof | |
EP0909662A2 (en) | Pattern printing of adhesives | |
US4261749A (en) | Thermoplastic inks suitable for pressure release-type decalcomania | |
EP0312299B1 (en) | Transfers and methods of decorating using same | |
US3967021A (en) | Decalcomanias employed in offset transfer process | |
EP0057940B1 (en) | Transfer material and method of coloring the surface of an object | |
US2476570A (en) | Decoration of ceramic ware | |
US3887420A (en) | Offset transfer of decalcomanias | |
KR0171244B1 (en) | Transfer method and transfer sheet using the same method | |
US6123794A (en) | Method for the application of an image to a porous substrate | |
US6579395B1 (en) | Transfers | |
JPH027835B2 (en) | ||
US4477510A (en) | Decalcomania |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Designated state(s): AT DE FR GB |
|
17P | Request for examination filed |
Effective date: 19830210 |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: CORNING GLASS WORKS |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT DE FR GB |
|
REF | Corresponds to: |
Ref document number: 19999 Country of ref document: AT Date of ref document: 19860615 Kind code of ref document: T |
|
REF | Corresponds to: |
Ref document number: 3174691 Country of ref document: DE Date of ref document: 19860703 |
|
ET | Fr: translation filed | ||
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed | ||
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 19940110 Year of fee payment: 14 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: AT Payment date: 19940112 Year of fee payment: 14 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 19940211 Year of fee payment: 14 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 19940222 Year of fee payment: 14 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Effective date: 19950227 Ref country code: AT Effective date: 19950227 |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 19950227 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FR Effective date: 19951031 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Effective date: 19951101 |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST |