EP4413424A1 - Elektrophotographisches verfahren zur herstellung von folienbildern - Google Patents
Elektrophotographisches verfahren zur herstellung von folienbildernInfo
- Publication number
- EP4413424A1 EP4413424A1 EP22789409.4A EP22789409A EP4413424A1 EP 4413424 A1 EP4413424 A1 EP 4413424A1 EP 22789409 A EP22789409 A EP 22789409A EP 4413424 A1 EP4413424 A1 EP 4413424A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- toner
- dry
- foiling
- color
- images
- 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.)
- Pending
Links
- 239000011888 foil Substances 0.000 title claims abstract description 235
- 238000000034 method Methods 0.000 title claims description 97
- 239000000463 material Substances 0.000 claims abstract description 163
- 238000007639 printing Methods 0.000 claims abstract description 129
- 239000002952 polymeric resin Substances 0.000 claims abstract description 106
- 229920003002 synthetic resin Polymers 0.000 claims abstract description 106
- 238000002844 melting Methods 0.000 claims abstract description 59
- 230000008018 melting Effects 0.000 claims abstract description 59
- 239000003086 colorant Substances 0.000 claims abstract description 49
- 239000000049 pigment Substances 0.000 claims abstract description 46
- 239000002245 particle Substances 0.000 claims description 140
- -1 polyethylene Polymers 0.000 claims description 38
- 239000010410 layer Substances 0.000 claims description 33
- 239000002131 composite material Substances 0.000 claims description 28
- 239000000758 substrate Substances 0.000 claims description 28
- 238000003384 imaging method Methods 0.000 claims description 24
- 229920005989 resin Polymers 0.000 claims description 21
- 239000011347 resin Substances 0.000 claims description 21
- 229920000728 polyester Polymers 0.000 claims description 16
- 229920000573 polyethylene Polymers 0.000 claims description 15
- 239000004698 Polyethylene Substances 0.000 claims description 14
- 230000009477 glass transition Effects 0.000 claims description 11
- 229920000620 organic polymer Polymers 0.000 claims description 9
- 239000012790 adhesive layer Substances 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 8
- 229920006249 styrenic copolymer Polymers 0.000 claims description 8
- 238000007641 inkjet printing Methods 0.000 claims description 5
- 229920000058 polyacrylate Polymers 0.000 claims description 4
- 229920006243 acrylic copolymer Polymers 0.000 claims description 3
- 239000001993 wax Substances 0.000 description 137
- 238000012546 transfer Methods 0.000 description 95
- 239000000203 mixture Substances 0.000 description 66
- 230000008569 process Effects 0.000 description 38
- 239000000123 paper Substances 0.000 description 27
- 238000010030 laminating Methods 0.000 description 25
- 239000003795 chemical substances by application Substances 0.000 description 17
- 230000001070 adhesive effect Effects 0.000 description 16
- 239000000853 adhesive Substances 0.000 description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 13
- 239000010408 film Substances 0.000 description 13
- 238000009472 formulation Methods 0.000 description 13
- 239000007788 liquid Substances 0.000 description 13
- 239000003921 oil Substances 0.000 description 13
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical class C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 12
- 239000000654 additive Substances 0.000 description 10
- 238000003475 lamination Methods 0.000 description 9
- 239000000178 monomer Substances 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 9
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 8
- 229920000747 poly(lactic acid) Polymers 0.000 description 8
- 239000000126 substance Substances 0.000 description 8
- 229920001577 copolymer Polymers 0.000 description 7
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 239000011230 binding agent Substances 0.000 description 6
- 229910052799 carbon Inorganic materials 0.000 description 6
- 238000000113 differential scanning calorimetry Methods 0.000 description 6
- 239000012530 fluid Substances 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 239000011148 porous material Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 5
- 239000002270 dispersing agent Substances 0.000 description 5
- 230000000694 effects Effects 0.000 description 5
- 230000003287 optical effect Effects 0.000 description 5
- 108091008695 photoreceptors Proteins 0.000 description 5
- 229920001225 polyester resin Polymers 0.000 description 5
- 239000004645 polyester resin Substances 0.000 description 5
- 239000000377 silicon dioxide Substances 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- 239000004743 Polypropylene Substances 0.000 description 4
- BQCADISMDOOEFD-UHFFFAOYSA-N Silver Chemical compound [Ag] BQCADISMDOOEFD-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 4
- 230000008901 benefit Effects 0.000 description 4
- 239000011248 coating agent Substances 0.000 description 4
- 238000000576 coating method Methods 0.000 description 4
- 238000011161 development Methods 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 238000010438 heat treatment Methods 0.000 description 4
- 239000000976 ink Substances 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 239000011159 matrix material Substances 0.000 description 4
- 239000000155 melt Substances 0.000 description 4
- YLGXILFCIXHCMC-JHGZEJCSSA-N methyl cellulose Chemical compound COC1C(OC)C(OC)C(COC)O[C@H]1O[C@H]1C(OC)C(OC)C(OC)OC1COC YLGXILFCIXHCMC-JHGZEJCSSA-N 0.000 description 4
- LYRFLYHAGKPMFH-UHFFFAOYSA-N octadecanamide Chemical compound CCCCCCCCCCCCCCCCCC(N)=O LYRFLYHAGKPMFH-UHFFFAOYSA-N 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 229920000098 polyolefin Polymers 0.000 description 4
- 229920001155 polypropylene Polymers 0.000 description 4
- 229910052709 silver Inorganic materials 0.000 description 4
- 239000004332 silver Substances 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 150000003440 styrenes Chemical class 0.000 description 4
- 239000012756 surface treatment agent Substances 0.000 description 4
- 229920002554 vinyl polymer Polymers 0.000 description 4
- 239000004925 Acrylic resin Substances 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 229910052782 aluminium Inorganic materials 0.000 description 3
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 3
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 239000006229 carbon black Substances 0.000 description 3
- 238000001311 chemical methods and process Methods 0.000 description 3
- 238000011109 contamination Methods 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000000227 grinding Methods 0.000 description 3
- 238000007726 management method Methods 0.000 description 3
- 229920000139 polyethylene terephthalate Polymers 0.000 description 3
- 239000005020 polyethylene terephthalate Substances 0.000 description 3
- 229920001296 polysiloxane Polymers 0.000 description 3
- 229920002050 silicone resin Polymers 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
- 230000000007 visual effect Effects 0.000 description 3
- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 description 2
- VSKRSEHLMRRKOS-QJWNTBNXSA-N (z,12r)-12-hydroxyoctadec-9-enamide Chemical compound CCCCCC[C@@H](O)C\C=C/CCCCCCCC(N)=O VSKRSEHLMRRKOS-QJWNTBNXSA-N 0.000 description 2
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- UAUDZVJPLUQNMU-UHFFFAOYSA-N Erucasaeureamid Natural products CCCCCCCCC=CCCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-UHFFFAOYSA-N 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- 239000005977 Ethylene Substances 0.000 description 2
- 239000004594 Masterbatch (MB) Substances 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- 239000004952 Polyamide Substances 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 2
- 239000012164 animal wax Substances 0.000 description 2
- 239000008346 aqueous phase Substances 0.000 description 2
- 235000013871 bee wax Nutrition 0.000 description 2
- 239000012166 beeswax Substances 0.000 description 2
- 229940092738 beeswax Drugs 0.000 description 2
- 239000004204 candelilla wax Substances 0.000 description 2
- 235000013868 candelilla wax Nutrition 0.000 description 2
- 229940073532 candelilla wax Drugs 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
- 235000013869 carnauba wax Nutrition 0.000 description 2
- 238000004581 coalescence Methods 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- JXTHNDFMNIQAHM-UHFFFAOYSA-N dichloroacetic acid Chemical compound OC(=O)C(Cl)Cl JXTHNDFMNIQAHM-UHFFFAOYSA-N 0.000 description 2
- 229960005215 dichloroacetic acid Drugs 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000003822 epoxy resin Substances 0.000 description 2
- UAUDZVJPLUQNMU-KTKRTIGZSA-N erucamide Chemical compound CCCCCCCC\C=C/CCCCCCCCCCCC(N)=O UAUDZVJPLUQNMU-KTKRTIGZSA-N 0.000 description 2
- FJKIXWOMBXYWOQ-UHFFFAOYSA-N ethenoxyethane Chemical compound CCOC=C FJKIXWOMBXYWOQ-UHFFFAOYSA-N 0.000 description 2
- 229940093470 ethylene Drugs 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 229910021485 fumed silica Inorganic materials 0.000 description 2
- 238000005227 gel permeation chromatography Methods 0.000 description 2
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 2
- 239000010931 gold Substances 0.000 description 2
- 229910052737 gold Inorganic materials 0.000 description 2
- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 2
- 230000002209 hydrophobic effect Effects 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 239000012182 japan wax Substances 0.000 description 2
- 229940119170 jojoba wax Drugs 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 239000000696 magnetic material Substances 0.000 description 2
- 239000006249 magnetic particle Substances 0.000 description 2
- 238000010128 melt processing Methods 0.000 description 2
- 229910044991 metal oxide Inorganic materials 0.000 description 2
- 150000004706 metal oxides Chemical class 0.000 description 2
- 150000002739 metals Chemical class 0.000 description 2
- 239000004200 microcrystalline wax Substances 0.000 description 2
- 235000019808 microcrystalline wax Nutrition 0.000 description 2
- 239000012184 mineral wax Substances 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000012170 montan wax Substances 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 239000012186 ozocerite Substances 0.000 description 2
- 239000012188 paraffin wax Substances 0.000 description 2
- 239000012169 petroleum derived wax Substances 0.000 description 2
- 235000019381 petroleum wax Nutrition 0.000 description 2
- 229920002647 polyamide Polymers 0.000 description 2
- 229920001083 polybutene Polymers 0.000 description 2
- 229920000647 polyepoxide Polymers 0.000 description 2
- 238000006116 polymerization reaction Methods 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000010298 pulverizing process Methods 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 229940037312 stearamide Drugs 0.000 description 2
- 239000012178 vegetable wax Substances 0.000 description 2
- RSWGJHLUYNHPMX-UHFFFAOYSA-N 1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylic acid Chemical compound C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 1
- OZCMOJQQLBXBKI-UHFFFAOYSA-N 1-ethenoxy-2-methylpropane Chemical compound CC(C)COC=C OZCMOJQQLBXBKI-UHFFFAOYSA-N 0.000 description 1
- RCSKFKICHQAKEZ-UHFFFAOYSA-N 1-ethenylindole Chemical compound C1=CC=C2N(C=C)C=CC2=C1 RCSKFKICHQAKEZ-UHFFFAOYSA-N 0.000 description 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 description 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- PLXMOAALOJOTIY-FPTXNFDTSA-N Aesculin Natural products OC[C@@H]1[C@@H](O)[C@H](O)[C@@H](O)[C@H](O)[C@H]1Oc2cc3C=CC(=O)Oc3cc2O PLXMOAALOJOTIY-FPTXNFDTSA-N 0.000 description 1
- 229910000906 Bronze Inorganic materials 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 239000004831 Hot glue Substances 0.000 description 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
- 229920000877 Melamine resin Polymers 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 description 1
- 238000005299 abrasion Methods 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 229920000180 alkyd Polymers 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 229920006187 aquazol Polymers 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000011449 brick Substances 0.000 description 1
- INLLPKCGLOXCIV-UHFFFAOYSA-N bromoethene Chemical compound BrC=C INLLPKCGLOXCIV-UHFFFAOYSA-N 0.000 description 1
- 239000010974 bronze Substances 0.000 description 1
- 239000011111 cardboard Substances 0.000 description 1
- 239000012876 carrier material Substances 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 238000010073 coating (rubber) Methods 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- KUNSUQLRTQLHQQ-UHFFFAOYSA-N copper tin Chemical compound [Cu].[Sn] KUNSUQLRTQLHQQ-UHFFFAOYSA-N 0.000 description 1
- XCJYREBRNVKWGJ-UHFFFAOYSA-N copper(II) phthalocyanine Chemical compound [Cu+2].C12=CC=CC=C2C(N=C2[N-]C(C3=CC=CC=C32)=N2)=NC1=NC([C]1C=CC=CC1=1)=NC=1N=C1[C]3C=CC=CC3=C2[N-]1 XCJYREBRNVKWGJ-UHFFFAOYSA-N 0.000 description 1
- 239000007771 core particle Substances 0.000 description 1
- 238000012937 correction Methods 0.000 description 1
- 229920006037 cross link polymer Polymers 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 125000004386 diacrylate group Chemical group 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000005684 electric field Effects 0.000 description 1
- 230000005670 electromagnetic radiation Effects 0.000 description 1
- 238000010894 electron beam technology Methods 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 238000005538 encapsulation Methods 0.000 description 1
- MEGHWIAOTJPCHQ-UHFFFAOYSA-N ethenyl butanoate Chemical compound CCCC(=O)OC=C MEGHWIAOTJPCHQ-UHFFFAOYSA-N 0.000 description 1
- UIWXSTHGICQLQT-UHFFFAOYSA-N ethenyl propanoate Chemical compound CCC(=O)OC=C UIWXSTHGICQLQT-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical compound FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 description 1
- SLGWESQGEUXWJQ-UHFFFAOYSA-N formaldehyde;phenol Chemical compound O=C.OC1=CC=CC=C1 SLGWESQGEUXWJQ-UHFFFAOYSA-N 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 239000012943 hotmelt Substances 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- 238000011005 laboratory method Methods 0.000 description 1
- 238000011068 loading method Methods 0.000 description 1
- 239000002932 luster Substances 0.000 description 1
- 229940002712 malachite green oxalate Drugs 0.000 description 1
- JDSHMPZPIAZGSV-UHFFFAOYSA-N melamine Chemical compound NC1=NC(N)=NC(N)=N1 JDSHMPZPIAZGSV-UHFFFAOYSA-N 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical class CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- XJRBAMWJDBPFIM-UHFFFAOYSA-N methyl vinyl ether Chemical compound COC=C XJRBAMWJDBPFIM-UHFFFAOYSA-N 0.000 description 1
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 1
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 150000005673 monoalkenes Chemical class 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 239000006174 pH buffer Substances 0.000 description 1
- 239000011087 paperboard Substances 0.000 description 1
- 229920001568 phenolic resin Polymers 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 239000011112 polyethylene naphthalate Substances 0.000 description 1
- 239000004848 polyfunctional curative Substances 0.000 description 1
- 229920001721 polyimide Polymers 0.000 description 1
- 239000009719 polyimide resin Substances 0.000 description 1
- 239000004626 polylactic acid Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 230000001698 pyrogenic effect Effects 0.000 description 1
- 239000004172 quinoline yellow Substances 0.000 description 1
- 235000012752 quinoline yellow Nutrition 0.000 description 1
- 229940051201 quinoline yellow Drugs 0.000 description 1
- IZMJMCDDWKSTTK-UHFFFAOYSA-N quinoline yellow Chemical compound C1=CC=CC2=NC(C3C(C4=CC=CC=C4C3=O)=O)=CC=C21 IZMJMCDDWKSTTK-UHFFFAOYSA-N 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 239000010939 rose gold Substances 0.000 description 1
- 229910001112 rose gold Inorganic materials 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- VEALVRVVWBQVSL-UHFFFAOYSA-N strontium titanate Chemical compound [Sr+2].[O-][Ti]([O-])=O VEALVRVVWBQVSL-UHFFFAOYSA-N 0.000 description 1
- 238000010557 suspension polymerization reaction Methods 0.000 description 1
- 238000009823 thermal lamination Methods 0.000 description 1
- 238000001757 thermogravimetry curve Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 235000013799 ultramarine blue Nutrition 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
- KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
- 229920006163 vinyl copolymer Polymers 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G13/00—Electrographic processes using a charge pattern
- G03G13/01—Electrographic processes using a charge pattern for multicoloured copies
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G13/00—Electrographic processes using a charge pattern
- G03G13/14—Transferring a pattern to a second base
- G03G13/16—Transferring a pattern to a second base of a toner pattern, e.g. a powder pattern
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G15/00—Apparatus for electrographic processes using a charge pattern
- G03G15/65—Apparatus which relate to the handling of copy material
- G03G15/6582—Special processing for irreversibly adding or changing the sheet copy material characteristics or its appearance, e.g. stamping, annotation printing, punching
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G15/00—Apparatus for electrographic processes using a charge pattern
- G03G15/65—Apparatus which relate to the handling of copy material
- G03G15/6582—Special processing for irreversibly adding or changing the sheet copy material characteristics or its appearance, e.g. stamping, annotation printing, punching
- G03G15/6585—Special processing for irreversibly adding or changing the sheet copy material characteristics or its appearance, e.g. stamping, annotation printing, punching by using non-standard toners, e.g. transparent toner, gloss adding devices
-
- G—PHYSICS
- G03—PHOTOGRAPHY; CINEMATOGRAPHY; ANALOGOUS TECHNIQUES USING WAVES OTHER THAN OPTICAL WAVES; ELECTROGRAPHY; HOLOGRAPHY
- G03G—ELECTROGRAPHY; ELECTROPHOTOGRAPHY; MAGNETOGRAPHY
- G03G15/00—Apparatus for electrographic processes using a charge pattern
- G03G15/65—Apparatus which relate to the handling of copy material
- G03G15/6588—Apparatus which relate to the handling of copy material characterised by the copy material, e.g. postcards, large copies, multi-layered materials, coloured sheet material
- G03G15/6591—Apparatus which relate to the handling of copy material characterised by the copy material, e.g. postcards, large copies, multi-layered materials, coloured sheet material characterised by the recording material, e.g. plastic material, OHP, ceramics, tiles, textiles
Definitions
- This invention relates to electrophotography in which color images are provided on substrates (receiver materials) using particulate dry color toners, and on which substrates one or more foil images are also provided in selected areas.
- this invention relates to forming foil images in selected areas of a receiver material also having one or more color toner images.
- the particulate toners used to form the color toner images and the foil images are designed with different melting temperatures to facilitate oil-free fusing and foiling operations.
- foil printing In foil printing, a colored foil that is releasably bonded to a backing material that can be known as a “foil backing” is transferred from the backing material to a substrate to form one or more foil images on a substrate.
- a colored foil and its backing material can be known in the art as a “printing foil.”
- foil printing on a substrate such as a paper
- the paper is printed with a desired image using conventional printing means (for example, a printing press or inkjet printer), and conventional printing inks or inkjet printer inks.
- U.S. Patent 6,605,174 refers to a “foiling adhesive” that is used in those areas to which it is desired to transfer foil to provide foil images.
- the demonstrated foiling adhesive is a liquid toner material that is composed of certain vinyl polymers or a polyamide.
- This foiling adhesive is printed using a xerographic (or electrophotographic) process in which the foiling adhesive is bonded to a paper or other substrate by fixing (or fusing).
- a printing foil of a desired color and luster can be pressed to the paper in the regions of the foiling adhesive and heated and the heating causes the foiling adhesive to melt and become tacky.
- the backing material is removed, the foil is detached therefrom and adhered only in the regions designed with the foiling adhesive.
- electrophotography One common method for printing color images on a receiver material is known as electrophotography, in which a latent electrostatic image of one or more colors can be formed on a dielectric photoconductive material by uniformly charging the photoconductive material, followed by discharging selected areas of the uniform charge to yield an electrostatic pattern corresponding to the desired image (“latent electrostatic image”). After the formation of such latent electrostatic image, charged toner particles are brought into the vicinity of the latent electrostatic image to develop the latent image into a visible image.
- a suitable receiver material is brought into juxtaposition with the visible image and a suitable electric field is applied to transfer the toner particles of the visible image to a “final” receiver material to form a desired “printed” image on the receiver material that can be for example a cut sheet of cellulosic paper or polymeric film.
- the receiver material is then removed from its operative association with the dielectric photoconductive material and is subjected to suitable heat and pressure to permanently fix (or fuse) the printed image in the receiver material.
- fused toner image can be monochrome or multi-colored or be in the form of a composite of multiple overlaid colors in the same or different areas of the toner image.
- the commercial SleekingTM process is a two-or multi-step procedure.
- registration of foil images and color toner images becomes a significant challenge.
- such a process results in dimensional changes of the receiver material due both to the removal of moisture and to stresses applied in the heated nip when the foiling toner is fused, as well as the same factors in the lamination step for the desired transfer of foil components.
- Liquid toners comprise organic solvents (or carrier fluids or carrier liquids) that should be removed before or during fusing onto a receiver material. Removing such solvents from color images would be necessary before foil images are formed, and this would slow down or impair the overall process to such an extent that the process would lack commercial efficiency and viability.
- the present invention provides a method for providing a foil image on a receiver material without inkjet printing, the method comprising the following A) through D):
- the present invention provides an electrophotographic imaging method for providing an article having one or more foil images using toner latent images, the method comprising the following A’) through E’):
- each corresponding dry color toner comprising dry toner particles comprising: a (a) polymeric resin, a (b) pigment colorant, and a (c) wax that has a melting temperature defined as Tcoior;
- B’ simultaneously with or subsequently to A), developing one or more foiling toner latent images in one or more foiling image areas to provide one or more foiling toner images on the intermediate receiver material, using a dry foiling toner comprising dry foiling toner particles comprising: a (a’) polymeric resin and a (c’) wax that has a melting temperature defined as Tfoiiing, wherein the one or more foiling image areas are different from the one or more color image areas, and Tfoiiing is less than Tcoior by at least 15°C;
- the method of this invention provides the following advantages compared to methods of the prior art used to provide foil images.
- An important feature of the present inventive process is that it provides the ability to fuse both a dry foiling toner and dry color toners simultaneously, in their respective image areas, thus completely avoiding the problem described above where poor registration of the foil and color images occurs.
- Another advantage of the present invention is that not requiring the receiver material already having foil images to be further printed with a color image is desirable for all dry color toner based printers because later electrostatic transfer of the dry color toners causes those dry color toners to be disrupted by the presence of the electrically conductive foil images on the receiver.
- the present invention avoids the use of liquid toners and the various technical problems in handling and use they cause.
- Specific to foil transfer it is known that residual liquid toner solvent in a liquid toner image inhibits the transfer of the printing foil, and thus the solvent level in such images should be reduced enough so that the foil transfer step can be achieved. This causes a large delay in the production process of producing foiled and color toner images.
- FIG. 1 is a graphical representation of data obtained according to Example 1 below, that is, % foil transfer versus foil transfer temperature at a particular amount of (c) wax in the several dry black toners.
- FIG. 2 is a graphical representation of data obtained according to Example 2 below, that is, % foil transfer versus foil transfer temperature using different (c) waxes in two dry magenta toners and a dry cyan toner.
- FIGS. 3 and 4 are graphical representations of the data obtained according to Example 4 below. DETAILED DESCRIPTION OF THE INVENTION Definitions
- weight % (or wt. %) is to be taken as referring to a weight-for-weight (w/w) percentage of solids in the a given composition, formulation, or wet or dry layer or image.
- electrostatic printing and “electrophotographic printing” generally refer to the process that provides a toner image that is transferred from a photoimaging substrate either directly or indirectly via an intermediate transfer member (or an intermediate receiver material) to a receiver material.
- the toner image or foiling image is not substantially absorbed into the photoimaging substrate (or receiver material) on which it is applied.
- the present invention is directed to the use of “dry” powder toners (as defined below) and does not include the use of what are known in the art as “liquid” toners comprising a carrier liquid or carrier fluid.
- fixing and “fusing” in reference to dry color toners and foiling toners are intended to refer to the same operation of melting the dry toner particles as known in the art.
- particle size as used herein in reference to either the dry color toner particles or foiling toner particles are defined in terms of the median volume diameter (D vo i) as measured using conventional diameter measuring devices such as a Coulter Multisizer (Coulter, Inc.).
- the size in a distribution of particles at which half of the total volume of particles is larger, and half of the total volume is smaller is known as the median volume diameter.
- dry toner is used to refer to a material or mixture that contains dry toner particles, typically in powder form, and that can form an image, pattern, or coating when deposited on an imaging member including a photoreceptor, photoconductor, or electrostatically-charged or magnetic surface.
- Toner can be referred to in the art as “marking particles,” “dry ink,” or “developer,” but the term developer can be used differently as described below.
- Dry toner can be a dry mixture of particles and materials. As used in the present invention, dry toner is a dry mixture of materials typically in particulate form.
- “Dry toner particles” are particles of one or more materials that can be transferred directly or indirectly using an electrophotographic printer (EP) to a receiver material to produce a desired effect, color, texture, pattern, adhesive, or coating (such as in the case of a foiling toner described below) on the receiver material.
- Dry toner particles can be ground from larger solids or chemically prepared (for example, precipitated from a solution of a pigment and a dispersant using an organic solvent), using processes and starting materials that are known in the art. Dry toner particles, both colorless and colored, generally have a range of diameters of less than or equal to 8 pm, or less than or equal to 15 pm, or even less than or equal to 30 pm.
- dry toner generally includes dry toner particles as well as other particles of various types and properties.
- dyes or pigment colorants can be present in the dry toners to provide absorption of incident electromagnetic radiation; biocides to suppress bacterial growth; desiccants to absorb moisture or gasses; binders to improve adhesion to a receiver material; and other additives that are known in the art.
- Dry toner particles themselves can be coated with even finer particles known as surface treatment agents, such as pyrogenic or colloidal silica, titania, alumina, and fine resin particles, which surface treatment agents can be coated with silanes or silicones.
- a “developer” can refer to dry toner alone as used in singlecomponent or mono-component development systems, but it can also refer to a mixture of dry toner and magnetic carrier particles in dual-component, two- component, or multi-component development systems.
- Magnetic carrier particles are generally known in the art and described for example in U.S. Patent 9,182,690 (Alexandrovich et al., Col. 9).
- pigment colorant refers to a single material or a combination of different materials that provide color, tone, or hue once applied and fused to a receiver material.
- color is meant to include any image having a tone or hue, or combination thereof, including “white” and “black” colored images.
- the identifiers “CL,” “W,” “Y,” “M,” “C,” and “K” refer to dry toners and toner images having corresponding “colorless,” “white,” “yellow,” “magenta,” “cyan,” and “black” colors or tones.
- Crystalline melting temperatures of the dry color toners and dry foiling toner ingredients such as waxes can be determined at standard atmospheric pressure using equipment and conventional methods, for example using Differential Scanning Calorimetry (DSC) and suitable known equipment designed for this purpose. Both crystalline melting temperatures and heats of melting of waxes can be determined by DSC, as the waxes themselves or as components of a complete toner composition.
- the wax melting temperature is defined as the temperature at the peak of a melting endotherm, or as the temperature at the peak of the main peak of a multiple melting endotherm material. Commonly used resins in dry toners are amorphous, and thus do not exhibit crystalline melting temperatures.
- melt flow methods for characterizing polymeric materials that are reported as “T m ” or “melting temperature”.
- a commonly used example is capillary rheometry as conducted on a device such as a commercial Shimadzu CFT-500D “Constant Test Force Extrusion Type Capillary Rheometer Flowtester”.
- a known weight of sample is subject to a constant force to induce melt flow in a capillary while the temperature is continuously increased.
- Tm can be defined as the temperature at which a certain weight of material has flowed. This is not a crystalline melting temperature but rather a melt viscosity related parameter. This method can also be calibrated such that the result is melt viscosity versus temperature.
- Glass transition temperature (T g ) is a known parameter for amorphous polymeric resins, and for dry toner particles (color or colorless, or foiling as described below), and is typically measured also using known Differential Scanning Calorimetry (DSC) equipment and processes.
- DSC Differential Scanning Calorimetry
- Number average molecular weight (M n ), typically used to characterize organic polymers, can be determined using Gel Permeation Chromatography (GPC) with polystyrene calibration and known procedures and equipment.
- GPC Gel Permeation Chromatography
- color toner refers to dry color toner particles or foiling toner particles containing one or more (b) pigment colorants described below to provide a desired color or hue having an optical density of at least 0.2 at the maximum particle coverage so as to distinguish them from “colorless” dry toner particles that have a lower optical density.
- dry color toner particles are “non-fluorescing” in that they do not emit light or “fluoresce” upon exposure to light of a different wavelength to a significant degree.
- composite when used in reference to developed color toner images or developed and fixed color toner images, refers to the one to four fundamental color toner images present in a mono- or multi-color color toner image. Black is considered a “color” for purposes of the present invention.
- a “composite color image” or “composite color toner image” can refer to one or more of the fundamental CMYK colors, wherein multiple color toner images can be formed in any desired sequence.
- White dry toner materials can be formulated with white pigments, and thus can be considered a “color” toner.
- the optical density is low when measured in reflection on a final receiver, and will not conform to the above description of color toner images having an optical density of at least 0.2 at the maximum particle coverage.
- white images are opaque, such that the optical density measured in transmission is generally greater than 0.2.
- color toner image and “color toner images” refer to the one or more areas of a print on a receiver material that are covered with the one or more dry color toner particles.
- foiling toner image and “foiling toner images” refer to the one or more areas of a print on a receiver material that are covered with dry foiling particles and ultimately printing foil.
- the one or more foiling toner images are typically different from (or exclusive thereof) the one or more color image areas on either the intermediate receiver material or the “final” receiver material. However if the order of transfer of the foiling toner image is such that it is the final layer applied to the final receiver, the foiling toner image can be on top of areas with color toner images.
- the method of the present invention is useful for providing various printed articles having foiling image areas in at least some areas of a surface of printed articles.
- the present invention is particularly useful in electrophotographic, electrostatic, or xerographic imaging or printing processes to provide both color toner images and foil images either in exclusive areas different from each other, or in processes wherein foiling toner areas are applied on top of the color image areas and designed to directly face the foil transfer material in the lamination step of transferring foil to the areas covered by the foiling toner.
- the foil images and color toner images can be formed on suitable receiver materials (substrates) that typically have first and second opposing sides or surfaces.
- the foil images and color toner images can be provided on one or both of these sides or surfaces.
- such foil images and color toner images are generally provided using digital printing processes such as electrostatic printing processes or electrophotographic printing processes that are generally known in the art and generally described by L.B. Schein in Electrophotography and Development Physics , 2 nd Edition, Laplacian Press, Morgan Hills, California, 1996 (ISBN 1-885540-02-7).
- toner images formed on a photo receptor member can be directly transferred to the “final” receiver material and then fixed.
- toner images formed on a photoreceptor are then transferred to an intermediate member, and subsequently transferred to the final receiver.
- Useful receiver materials include but are not limited to, coated or uncoated paper substrates (cellulosic or polymeric papers) in various geometric forms, polymeric films (such as transparent polymeric films), ceramics, paperboard, cardboard, metals, fibrous webs or ribbons, and other substrate materials that would be readily apparent to one skilled in the art.
- the receiver materials can be sheets of paper or polymeric films that can be fed from a supply of receiver materials.
- More particularly useful receiver materials include paper substrates that have a surface that is “coated” or in which the surface pores are generally filled with appropriate filler materials such as clays or other coating materials known in the paper forming art.
- foil toner latent images and color toner latent images can be formed on photoconductive material or photoreceptor as described above that can be in the form of charged photoconductor belts, webs, or rollers using a suitable light source such as a laser or light emitting diode.
- a suitable light source such as a laser or light emitting diode.
- Useful materials such as the photoconductor webs, belts, or rollers can be composed of various photoconductive materials known in the art.
- Forming color toner latent images according to the present invention is accomplished using dry color toners that comprise dry color toner particles comprising three essential components: a (a) polymeric resin (sometimes called a binder), or a mixture thereof, a (b) pigment colorant (or mixture thereof), and a (c) wax (or mixture thereof) that has a melting temperature that is defined as Tcoior that is generally at least 90°C or at least 100°C and up to and including 135°C or up to and including 150°C.
- Tcoior melting temperature that is generally at least 90°C or at least 100°C and up to and including 135°C or up to and including 150°C.
- the dry color toner particles can be porous or nonporous. For example, if they are porous particles, up to 60% of the volume can be occupied or unoccupied pores within the (a) polymeric resin that serves as a continuous binder phase or matrix, (b) Pigment colorants, (c) waxes, or other components can be present within the pores, within the (a) polymeric resin, or outside of both and mixed therewith. Pores in the dry toner particles can be created intentionally or unintentionally during manufacture of the dry color toners.
- the dry color toner particles are not generally perfectly spherical so it is best to define them by the median volume diameter (D vo i) that can be determined as described above. Before fixing, the dry color toner particles can have a Dvoi of at least 4 pm or of at least 5 pm and up to and including 12 pm or up to and including 20 pm, but larger or smaller particles may be useful.
- the dry color toner particles have an external particle surface and consist essentially of the (a) polymeric resin as the polymeric binder phase or matrix, and the (b) pigment colorant and the (c) wax are generally dispersed within the (a) polymeric resin.
- dry color toners generally are not intentionally rendered magnetic by incorporation of magnetic materials when they are formulated to make high color gamut images.
- dry color toners can have magnetic additives when it is desired to make “magnetic ink character recognition” or MICR images that can be used for printing magnetically readable checks of for security purposes
- Useful (a) polymeric resins of which the dry color toner particles can be composed include any organic polymer or mixture of organic polymers that are suitable for the imaging methods described herein, and particularly the thermal fixing (fusing) operations where they will melt and flow.
- Each of such organic polymeric resins is generally amorphous and has a glass transition temperature (T g ) of at least 50°C and up to and including 100°C.
- polymeric resins are known in the art to be useful for this purpose and include but are not limited to, polycarbonates, resin-modified alkyd polymers, polyamides, polyurethanes, phenol-formaldehyde polymers and various derivatives thereof, polyesters and polyester condensates, aromatic copolymers having alternative methylene and aromatic recurring units (such as styrenic recurring units), and fusible crosslinked polymers.
- Polyesters, copolymers derived at least in part from a styrenic monomer and an acrylic monomer (thus, styrenic-acrylic copolymers), and acrylic polymers derived from one or more acrylic or acrylic ester monomers can be particularly useful.
- useful (a) polymeric resins can be vinyl polymers such as styrenic homopolymers (derived from styrene or a styrene derivative) and copolymers derived from two or more ethylenically unsaturated polymerizable monomers, such as copolymers derived from one or more of styrene or a styrene derivative, vinyl naphthalene, -chlorosty rene and two or more acrylic monomers, or two or more unsaturated mono-olefins such as ethylene, propylene, butylene, and isobutylene; vinyl halides such as vinyl chloride, vinyl bromide, and vinyl fluoride; vinyl acetate, vinyl propionate, vinyl benzoate, vinyl butyrate; vinyl esters such as esters of mono carboxylic acids such as acrylates and methacrylate; nitriles such as acrylonitrile and methacrylonitrile; acrylamide and me
- some useful (a) polymeric resins can be prepared as copolymers derived from one or more ethylenically unsaturated polymerizable monomers such as styrene or a styrene derivative and one or more lower alkyl (Ci- e) acrylates or lower alkyl methacrylates.
- Some crosslinked polymeric resins are also useful such as those derived at least in part from divinyl benzene, diacrylates, or dimethacrylates. More details of useful (a) polymeric resins that are either vinyl polymers or condensation polymers are provided in U.S. Patent 9,261,808 (Tyagi et al., Col. 7, line 38 to Col. 9, line 13).
- the glass transition temperature (T g ) of the (a) polymeric resin (or mixture of polymeric resins) in each dry color toner particle is at least 55°C or at least 60°C, and up to and including 70°C or up to and including 80°C.
- the (a) polymeric resin (or mixture thereof) are present in the dry color toner in an amount of at least 50 weight % or at least 60 weight %, and up to and including 95 weight %, all based on the total dry color toner weight.
- Each useful dry color toner also contains one or more (b) pigment colorants that can be organic or inorganic in nature, to provide a suitable hue, color, or tone in the resulting fused color toner images.
- pigment colorants can be incorporated into the (a) polymeric resins in known ways, such as by including them in the dry blends described below.
- Useful (b) pigment colorants include but are not limited to, titanium dioxide, carbon black, Aniline Blue, Calcoil Blue, Chrome Yellow, Ultramarine Blue, DuPont Oil Red, Quinoline Yellow, Methylene Blue Chloride, Malachite Green Oxalate, Lamp Black, Rose Bengal, Colour Index Pigment Yellow 97, and others that are listed in Col. 10 and in the references cited therein of U.S.
- Patent 9,261,808 (noted above) as well as those described in the Colour Index, Vols. I and II, 2 nd Edition (1987) or in the Pantone® Color Formula Guide, 1 st Edition (2000-2001).
- a preferred pigment colorant set incorporated into cyan, magenta, and yellow color toner particles are Pigment Blue 15:3, Pigment Red 122, and Pigment Yellow 185, respectively.
- the (b) pigment colorants can be present in the dry color toner in an amount of at least 1 weight % or of at least 3 weight % and up to and including 25 weight % or up to and including 40 weight %, all based on the total dry color toner weight.
- the one or more dry color toners comprise at least dry cyan, yellow, magenta, and black toners that correspond to the cyan, yellow, magenta, and black toner latent images and resulting fused cyan, yellow, magenta, and black toner images
- Another essential component of the dry color toner particles is a (c) a wax having a melting temperature defined as Tcoior as described above.
- useful (c) waxes of this type include but are not limited to, low molecular weight polyolefins (polyalkenes) such as polyethylene, polypropylene, and polybutene, such as Polywax 500 and PolywaxTM 1000 waxes fromNuCera Solutions, Clariant PE130 and Licowax PEI 90 waxes from Clariant Chemicals, and Viscol 550 and Viscol 660 waxes from Sanyo.
- waxes can be obtained from Nippon Oil and Fat under the WE series; silicone resins that can be softened by heating; fatty acid amides such as oleoamide, erucamide, ricinoleamide, and stearamide; vegetable waxes such as carnauba wax, rice wax, candelilla wax, Japan wax, and jojoba wax; animal waxes such as bees wax; mineral and petroleum waxes such as montan wax, ozocerite, ceresine, paraffin wax, microcrystalline wax, and Fischer-Tropsch wax, and modified products thereof.
- Particularly useful (c) waxes include ester- based waxes and polyethylene waxes, both of which are available from various commercial sources. The melting points of such waxes are either already reported or can be determined as described above in the same manner for measuring polymer melting temperatures. It is critical that the (c) wax have a melting point (T m ) greater than or equal to Tfoiiing.
- the useful (c) wax generally can have a number average molecular weight (M n ) of at least 400 and up to and including 7,000, which value can be determined using known equipment and procedures in the industry.
- the (c) wax (or mixture thereof) is generally present in the dry color toners in an amount of at least 0.1 weight % or of at least 1 weight % and up to and including 10 weight % or up to and including 20 weight %, all based on the total weight of the dry color toner.
- dry color toners useful in the present invention can also contain a number of optional additives that are commonly useful in dry electrophotographic toners including but not limited to, charge control agents, flow additive particles (hydrophobic fumed silica particles), surface treatment agents and spacing treatment agent particles (such as titania, silica, or alumina particles).
- Dry color toners useful in the present invention can be prepared using various known processes wherein the (b) pigment colorant(s) are incorporated into the (a) polymeric resin including but not limited to, melt extrusion processes, limited coalescence processes, spray drying, and other chemical techniques. They can be prepared as “chemically prepared toners,” “polymerized toners,” or “in-situ toners.” They can be prepared using controlled growing instead of grinding. Various chemical processes include suspension polymerization, emulsion aggregation, micro-encapsulation, dispersion, and chemical milling.
- a desired (a) polymeric resin (or mixture thereof) is produced independently using a suitable polymerization process known in the art.
- the one or more (a) polymeric resins are dry blended or mixed as suitably sized polymeric resin particles with suitable (b) pigment colorant(s) and (c) wax(es) as described above) to form a uniform dry blend.
- Optional additives described above can also be incorporated into this dry blend with the three essential (a) polymeric resin, (b) pigment colorant, and (c) wax components.
- the amounts of the essential and optional components can be adjusted in the dry blend in a suitable manner that a skilled worker would readily understand to provide the desired amounts in the resulting dry color toner particles.
- the conditions for mechanical dry blending are known in the art.
- the dry blend so formed is then melt processed in a suitable apparatus such as a two-roll or hot-melt extruder, for example under low or high shear conditions to form an extruded composition.
- a suitable apparatus such as a two-roll or hot-melt extruder, for example under low or high shear conditions to form an extruded composition.
- the melt processing time can be at least 0.2 minute and up to and including 60 minutes and the time can be adjusted by a skilled worker to provide the desired melt processing temperature and uniformity in the resulting extruded composition.
- the dry blend can be melt-extruded in an extrusion device at a temperature higher than the T g of the (a) polymeric resin(s) and generally at a temperature of at least 90°C and up to and including 240°C.
- the resulting extruded composition is sometimes known as a “melt product” or a “melt slab” and is generally cooled, for example to room temperature, and then broken up (for example, pulverized) to form dry color toner particles having the desired Dvoi as described above. It is generally best to first coarse grind the extruded composition prior to a specific pulverizing operation. Grinding can be carried out using any suitable procedure, for example crushing and grinding using a fluid energy or jet mill. The particles can then be further reduced in size using high shear pulverizing devices such as a fluid energy mill, and then classified as such.
- the resulting dry color toner particles can be classified (sieved) through a 230 mesh vibratory sieve to remove non-attached metal oxide particles, agglomerates, and any other components that may not have been incorporated into the dry color toner particles.
- the dry foiling toners used in the practice of this invention comprise dry foiling toner particles having only two essential components: (a’) polymeric resin, and (c’) wax having a melting temperature defined as Tailing. It is critical as noted above that Tailing is less than Tcoior by at least 15 °C or by at least 30°C, or by at least 70°C. In addition, Tailing is generally at least 55°C and up to and including 70°C or up to and including 90°C.
- the dry foiling toners useful in this invention are similar to the dry color toners used in the practice of this invention except they have the differences as described above in wax melting temperature and in some of the properties described below.
- the dry foiling toners comprise dry foiling toner particles that can be porous or nonporous. For example, if they are porous particles, up to 60% of the volume can be occupied or unoccupied pores within the (a’) polymeric resin that serves as a continuous binder phase or matrix, (c’) Waxes or other components can be present within the pores, within the (a’) polymeric resin, or outside of both and mixed therewith.
- the dry foiling toner particles are not generally perfectly spherical so it is best to define them by the median volume diameter (Dvoi) that can be determined as described above. Before fixing, the dry foiling toner particles can have a Dvoi of at least 4 pm or of at least 5 pm and up to and including 12 pm or up to and including 20 pm, but larger or smaller particles may be useful.
- Dvoi median volume diameter
- the dry foiling toner particles can be designed to have unique a Dvoi that is more suitable for a particular use or receiver material. For example if they are to be applied to smooth receiver materials, the D voi could be in the range of at least 5 pm and up to and including 15 pm. However, when the dry foiling toner particles are to be applied to “rougher” receiver materials, they could have a larger Dvoi.
- the dry foiling toner particles have an external particle surface and consist essentially of the (a’) polymeric resin as the polymeric binder phase or matrix, and the (c’) wax is generally dispersed within the (a’) polymeric resin.
- the dry foiling toners are not intentionally rendered magnetic by incorporation of magnetic materials.
- Useful (a’) polymeric resins of which the toner particles can be composed of any organic polymer or mixture of organic polymers that are suitable for the imaging methods described herein, and particularly the thermal fixing (fusing) operations where they will melt and flow.
- Each of such organic polymeric resins is generally amorphous and has a glass transition temperature (T g ) of at least 45°C and up to and including 60°C or up to and including 70°C.
- T g glass transition temperature
- Many useful (a’) polymeric resins are known in the art to be useful for this purpose and can be the same as or different from those materials used to prepare the (a) polymeric resins and dry color toner particles as described above.
- Polyesters, styrenic copolymers derived at least in part from styrene or a styrene derivative (a styrenic copolymer) and one or more acrylic or acrylic ester monomers, and acrylic polymers can be particularly useful (a’) polymeric resins.
- the (a’) polymeric resins (or mixture thereof) can have a T g that is less than the T g of each (a) polymeric resin (or mixture thereof) forming the dry color toner particles described above.
- This difference in T g can be at least 5 °C or even at least 10°C.
- the (a’) polymeric resin (or mixture thereof) are present in the dry foiling toner in an amount of at least 60 weight % and up to and including 95 weight %, all based on the total dry foiling toner weight.
- a second essential component of the dry foiling toner particles is a (c’) a wax having a melting temperature defined as Tf O iiin g that is less than Tcoior of the (c) wax by at least 15°C, or at by at least 30°C, as described above.
- Useful (c’) waxes can be obtained from various commercial sources or prepared using known starting materials and synthetic procedures.
- the wax (c’) is chosen to serve as a “fuser release agent”, and as an “abrasion resistance agent” for the resulting fused foiling images as prepared on the receiver material, and the wax can perform these functions while also attracting the foil during the thermal lamination step where the foil is attracted to the fused foiling toner image as assisted by the wax in the foiling toner image with a crystalline melting temperature of Tf O iiin g .
- useful (c’) waxes of this type include but are not limited to, low molecular weight polyolefins (polyalkenes) such as polyethylene, polypropylene, and polybutene, such as Polywax 500 and PolywaxTM 1000 waxes fromNuCera Solutions, Clariant PE130 and Licowax PEI 90 waxes from Clariant Chemicals, and Viscol 550 and Viscol 660 waxes from Sanyo.
- polyalkenes such as polyethylene, polypropylene, and polybutene
- Polywax 500 and PolywaxTM 1000 waxes fromNuCera Solutions Clariant PE130 and Licowax PEI 90 waxes from Clariant Chemicals
- Viscol 550 and Viscol 660 waxes from Sanyo.
- waxes can be obtained from Nippon Oil and Fat under the WE series; silicone resins that can be softened by heating; fatty acid amides such as oleoamide, erucamide, ricinoleamide, and stearamide; vegetable waxes such as carnauba wax, rice wax, candelilla wax, Japan wax, and jojoba wax; animal waxes such as bees wax; mineral and petroleum waxes such as montan wax, ozocerite, ceresine, paraffin wax, microcrystalline wax, and Fischer- Tropsch wax, and modified products thereof.
- the melting points of such waxes are either already reported or can be determined as described above.
- the (c’) wax (or mixture thereof) is generally present in the dry foiling toners in an amount of at least 0.1 weight % or of at least 1 weight % and up to and including 10 weight % or up to and including 20 weight %, all based on the total weight of the dry foiling toner.
- the dry foiling toners useful in the present invention can also contain a number of optional additives that are commonly useful in electrophotographic toner materials including but not limited to, charge control agents, flow additive particles (hydrophobic fumed silica particles), surface treatment agents, and spacing treatment agent particles (such as titania, silica, or alumina particles).
- charge control agents charge control agents
- flow additive particles hydrophobic fumed silica particles
- surface treatment agents surface treatment agents
- spacing treatment agent particles such as titania, silica, or alumina particles
- the dry foiling toner particles are “colorless” as defined above, it is possible that such particles can also include one or more (b’) pigment colorants that can be organic or inorganic in nature, to provide a suitable hue, color, or tone in the resulting fused foiling toner images.
- pigment colorants can be incorporated into the (a’) polymeric resins in known ways, such as by including them in the dry blends described below.
- the (b’) pigment colorants can be the same as or different from the (b) pigment colorants described above.
- the amount of (b’) pigment colorants in the dry foiling toners can be at least 0.5 weight % or at least 3 weight % and up to and including 15 weight % or up to and including 25 weight %, all based on the total dry foiling toner weight.
- Dry foiling toners useful in the present invention can be prepared using various known processes such as those described above for preparing the dry color toners.
- a desired (a’) polymeric resin (or mixture thereof) can be produced independently using a suitable polymerization process known in the art.
- the one or more (a’) polymeric resins can be dry blended or mixed as polymeric resin particles with suitable (c’) wax(es) as described above) to form a uniform dry blend.
- Optional additives described above, including the (b’) pigment colorants, can also be incorporated into this dry blend with the two essential (a’) polymeric resin and (c’) wax components.
- the amounts of the essential and optional components can be adjusted in the dry blend in a suitable manner such that a skilled worker would readily understand to provide the desired amounts in the resulting dry foiling toner particles.
- the conditions for mechanical dry blending are known in the art.
- the dry blend so formed in then melt processed (such as melt extruded) in a suitable apparatus, cooled, for example to room temperature, and then broken up (for example pulverized) into dry foiling toner particles having the desired D voi as described above, similar to the preparation of the dry color toner particles.
- the resulting dry foiling toner particles can be classified (sieved) through a 230 mesh vibratory sieve to remove non-attached metal oxide particles, agglomerates, and any other components that may not have been incorporated into the dry color toner particles.
- the dry color toner and dry foiling toner formulations are designed such that a receiver material having thereon both color toner latent images and foiling toner latent images can pass through the fusing subsystem of the electrographic printer simultaneously without creating problems.
- the present invention provides formulations that function well in this regard while offering adequate foil transfer temperature latitude in the laminator where the fused foiling toner image should be significantly more adhesive than the fused color toner image to achieve the selective transfer of the printing foil.
- the fusing temperatures are much higher than the temperatures (FT) achieved in step D) or step E’) described below, when forming the one or more foil images.
- dry color toners and dry foiling toners used in the present invention can be used as dry mono-component developers, or each of them can be combined with carrier particles to form dry two-component developers. In all of these embodiments, a plurality (usually millions) of individual dry toner particles are used together.
- Such dry mono-component or dry two-component developers generally comprise one or more of the optional additives described above for the dry color toners and dry foiling toners, for example charge control agents or flow additive particles.
- Useful one-component developers generally comprise the dry color toner particles or dry foiling toner particles described herein as the essential component.
- Dry two-component developers generally comprise carrier particles (also known as carrier vehicles) that are known in the electrophotographic art and can be selected from a variety of materials such as uncoated carrier core particles (such as magnetic particles) and core magnetic particles that are overcoated with a thin layer of a film-forming polymer such as a silicone resin type polymer, poly(vinylidene fluoride), poly(methyl methacrylate), or mixtures thereof.
- transfer of a printing foil to a receiver material comprising one or more fused color toner images and one or more fused foiling toner images is accomplished in a device such as a thermal laminator where the roll-fed printing foil is brought into contact with receiver materials having fused color toner images in a nip formed by a heated transfer roller on the side with the printing foil and a backup pressure roller on the side of the receiver material that will not receive foil.
- Transfer of the metallized foil layer(s) of the printing foil to only the fused foiling toner images but not the fused color toner images is accomplished at appropriately selected laminating temperature, nip width, nip pressure, and operating speed, all of which operating parameters can be determined using routine experimentation in view of the teaching provided herein and in the working examples below.
- the base substrate of the printing foil can be film-like and composed of one or more transparent or nontransparent polymeric films such as a transparent film composed of polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polypropylene (PP), a poly sulfone resins, or a polyimide resin, or laminated composites thereof.
- a transparent film composed of polyethylene terephthalate (PET), polyethylene naphthalate (PEN), polypropylene (PP), a poly sulfone resins, or a polyimide resin, or laminated composites thereof.
- Cellulosic materials are also useful as the base substrate.
- a “release” layer On the base substrate can be disposed a “release” layer that can be composed of a thermo-curable resin such as a polyacrylic resin that is curable using a melamine or isocyanate hardener, or a UV or electron beam curable acrylic resin or epoxy resin, along with a suitable release agent (such as a silicone or fluoro compound) as would be known in the art.
- a suitable release agent such as a silicone or fluoro compound
- a thin metallized layer having a desired metallic or shiny finish obtained by the presence of suitable metals or metallic colorants, such as aluminum, tin, silver, chromium, nickel, and gold, or suitable alloys of metal such as bronze.
- suitable metals or metallic colorants such as aluminum, tin, silver, chromium, nickel, and gold, or suitable alloys of metal such as bronze.
- An adhesive layer typically composed of a hot melt adhesive, or thermo-sensitive adhesive can be generally disposed on the metallized layer to facilitate adhesion to the dry foiling toner.
- Such adhesive layers can compose an ethyl ene/vinyl acetate copolymer, vinyl chloride/vinyl acetate copolymer, epoxy resin, ethylene/vinyl alcohol polymer, or other polymeric resin that readily adheres to both the metallized layer as well as the dry foiling toner during transfer of the foiling film to the receiver material.
- printing foils also include a “printable layer” between the release layer and the metallized layer. This printable layer remains with the metallized layer when the base substrate is peeled away and can be printed using any number of imaging processes.
- printing foils having this or similar layer arrangements useful in the present invention can be obtained from several commercial sources, for example as Nobelus® brand sleeking films including but not limited to, their internet-advertised (www.nobelus.com) holographic metallized sleeking foil, gloss sleeking foil, cracked ice sleeking foil, gold printable sleeking foil, rainbow sleeking foil, red sleeking foil, rose gold sleeking foil, regal blue sleeking foil, silver printable sleeking foil, silver sleeking foil, and sparkle holographic metallized sleeking foil.
- Jolybar (Israel) also markets aluminum foils that can be used for this purpose.
- printing foils can be prepared using the procedures and starting materials described for example, in U.S. Patents 8,530,122 (Uchino et al.) and 8,993,208 (Matsushima et al.).
- Printing foils can be manufactured and used as having various overall thicknesses as would be known in the art, depending upon the machine being used to form the foil images and what texture may be desired in the final articles.
- the process or method of the present invention can be carried out using devices including printers, copiers, scanners, and facsimiles, and analog and digital devices, all of which can be referred to as “printers.”
- Various embodiments described herein are useful with electrostatographic devices or electrophotographic devices that employ the various dry color toners and dry foiling toners described herein that are developed on a suitable receiver material.
- the present invention is not carried out using inkjet printing in any stage or step, or in any manner.
- a digital reproduction printing system (“printer”) useful in the present invention typically includes a digital front-end processor (DFE), a print engine (also referred to in the art as a “marking engine”) for applying dry color toner and dry foiling toner to a receiver material, and one or more post-printing finishing system(s) (for example, a UV coating system, a glosser system, or a laminator system), and particularly a foil application (or SleekingTM) apparatus.
- a single device or system can be used for both providing the fused color toner images and fused foiling images as well as applying foil to the fused foiling images, as described in U.S. Patent 10,795,313B2 (Sakai et al.).
- a printer can reproduce pleasing color toner images (including black-and-white, monochrome, or polychrome images) onto a receiver material.
- This printer can also produce selected patterns of foil images on the same receiver material, which foil images do not correspond directly to a visible image, i.e. the foil images are different from the color toner images.
- the DFE receives input electronic files (such as Postscript command files) composed of images from other input devices (for example, a scanner, a digital camera, or a computer-generated image processor).
- images can include photographic renditions of nature, people, or animals or other creatures, as well as other types of visual content such as text or graphical elements, and desired foil images. Images can also include invisible content such as specifications of texture, glossiness, or protective coating patterns on the same receiver material.
- the DFE can include various function processors, such as a raster image processor (RIP), image positioning processor, image manipulation processor, color processor, or image storage processor.
- the DFE rasterizes input electronic files into image bitmaps for the print engine to print.
- the DFE permits a human operator to set up parameters such as layout, font, color, paper type, or post-finishing options.
- the print engine takes the rasterized image bitmap from the DFE and renders the bitmap into a form that can control the printing process from the exposure device to transferring the various images onto the receiver material.
- the finishing system can apply features such as protection, gloss, or binding to the prints.
- the finishing system such as for foiling, can be implemented as an integral component of a printer, or provided as a separate machine through which prints with color toner images are fed after they are printed.
- the printer can also include a color management system that accounts for characteristics of the image printing process implemented in the print engine (for example, the electrophotographic process) to provide known, consistent color reproduction characteristics.
- the color management system can also provide known color reproduction for different inputs (for example, digital camera images or film images). Color management systems are well-known in the art, and any such system can be used to provide color corrections in accordance with the present invention.
- color toner images are made in a plurality of imaging modules containing suitable dry color toner particles of different colors, all arranged in tandem, and latent color toner images are successively electrostatically transferred to a receiver material adhered to a transport web moving through the modules. Dry color toner particles are described above.
- Commercial machines of this type typically employ intermediate receiver materials (also known as “intermediate transfer members”) in the respective imaging modules for transferring visible latent color toner images from the photoreceptor to the receiver material.
- intermediate transfer members also known as “intermediate transfer members”
- Electrophotographic printers having the capability to also deposit dry colorless or clear toner using an additional imaging module are also known.
- the provision of a dry clear toner overcoat to a color toner image can be useful desirable for providing features such as protection from fingerprints, reducing certain visual artifacts, or providing desired texture or surface finish characteristics.
- the dry colorless toners described above are used similarly to the use of dry color toners.
- a dry clear toner overcoat can add cost and reduce color gamut of the color toner image and thus, it is desirable for an operator/user to determine whether or not a dry clear toner overcoat needs to be applied to the entire color toner image(s).
- a uniform layer of dry clear toner can be provided.
- a dry clear toner layer that varies inversely according to heights of the color toner images can also be used to establish level toner image stack heights.
- the respective dry color toners are generally deposited one upon the other at respective locations on the receiver material and the height of a respective color toner image stack is the sum of the toner heights of each respective dry color toner. Uniform stack height provides the color toner image(s) with a more even or uniform gloss.
- the use of printing foil (described above) to provide one or more foil images on the receiver material containing one or more color toner images can be achieved in a manner that is integral with the electrophotographic printer described above.
- the foil images can be formed using a component of the electrophotographic printer, such as by putting the dry foiling toner in one of the imaging modules in sequence with the imaging modules containing dry color toner(s), and then providing a foiling device that is integral with the electrophotographic printer that will bring the printing foil into intimate contact with the receiver material containing both the dry color toner(s) and the dry foiling toner, all after these dry toners have been fixed or fused on the receiver material.
- U.S. Patent 10,795,313B2 (noted above) describes a useful system for this purpose.
- a separate electrophotographic printer can be used to provide the color toner images and the foil images on a receiver material (for example using the Eastman Kodak NexPressSX 3900 printer described above). Foiling can then be provided on the receiver material containing color toner images and fused foiling toner using a commercial “laminator” such as the KOMFI® AMIGA 36 Custom Laminating System (available from Nobelus® Company), that is a separate machine from the electrophotographic printer.
- a commercial “laminator” such as the KOMFI® AMIGA 36 Custom Laminating System (available from Nobelus® Company), that is a separate machine from the electrophotographic printer.
- a method for providing a foil image on a receiver material is carried out using the following described steps or operations A), B), C), and D) in the same or different imaging machines.
- the present invention is carried out using only dry toners and printing foil as imaging means. No other imaging means, such as inkjet printing or use of liquid toners, is contemplated in carrying out the present invention, and these means of imaging are expressly excluded from the scope of the present invention.
- A) through D) are carried out in the noted order. However, A) and B) can be carried out simultaneously or reversed in some embodiments.
- one or more color toner latent images are provided in what are termed “color image areas” on a surface of a suitable receiver material (described above).
- the color image areas are distinguishable or different from all foiling image areas described below so that resulting foil images are generally outside all of the color toner images, but they can be adjacent in area, or have gaps in which there is no image of any type on the receiver material surface.
- the foiling image areas may be designed to overlap one or more of the color image areas when the machine configuration places the dry foiling toner on top of some of the color toner latent images such that the metallized foil of the printing foil will contact only the fused foiling toner image(s).
- a color toner latent image can also be considered a “charge-only image” prior to the application of toner particles, for example, as formed on an intermediate receiver material such as a photoconductive belt or roller.
- the one or more color toner latent images are provided either on the receiver material, or on an intermediate receiver material (such as a photoconductive belt or roller) using corresponding one or more dry color toners, each of which dry color toners is described in more detail above as being composed of dry toner particles comprising at least a (a) polymeric resin, a (b) pigment colorant, and a (c) wax having a melting temperature greater than or equal to Tcoior.
- B) is carried out simultaneously with or subsequently to this step A).
- A) can follow B) in carefully designed printing operations.
- one or more foiling toner latent images are provided in one or more foiling image areas on the receiver material surface that was “printed” in A), using a dry foiling toner that is described in more detail above as comprising dry foiling toner particles comprising at least a (a’) polymeric resin and a (c) wax having a melting temperature Tfoiiing.
- all of the one or more foiling toner latent images are different from the one or more color toner latent images described above.
- the foiling toner images are superposed on any of the color toner latent images they will be contacted with the foil and will “receive” or be adhered to the foil in the lamination step. If the foiling toner image is applied first and then a section is covered by a color image area that area of the foiling image will not result in transfer of the foil.
- the Tfoiiing should be less than Tcoior by at least 15°C or by at least 20°C, or by at least 30°C.
- This fixing operation C) is carried out using an essentially fuser oil-free environment, to provide one or more corresponding fused foiling toner images and one or more corresponding fused color toner images, all on the same receiver material.
- fuser oil-free it is meant that fuser oils are entirely absent from the fixing operation, or if present, they are used in a relatively low amount compared to conventional fuser oil fixing operations.
- the fuser oil is not used at all or it is used in such fixing operations in an amount of less than 1.5 mg of fuser oil per A-4 sheet of paper having a surface area of 621.6 cm 2 , or even less than 1 mg of fuser oil per A-4 sheet, of receiver material area.
- the fixing operation is carried out using conventional means, times, and temperatures, and typically using heated rollers and suitable pressure as are known in the electrophotographic art.
- receiver materials containing the one or more color image areas and one or more foiling image areas prepared in A) and B) and simultaneously fused (or fixed) in C), are brought into intimate contact with a printing foil (as described above) at an appropriate foiling temperature (FT) that is greater than Tfoiiing but less than Tcoior.
- FT foiling temperature
- FT can be at least 65°C or at least 70°C, and up to and including 145°C, and FT will vary with the particular foil transfer device or laminator that is used, and thus a skilled worker would know how to find an optimal FT for D) using the teaching in the art relating to foil laminating and the various instructions associated with individual commercial laminating devices.
- Some embodiments of the present invention relate to electrophotographic imaging methods for providing an article or a multiplicity of articles, each of which has one or more foil images on a surface thereof, using color toner latent images and foiling toner latent images.
- This method includes steps or operations A’), B’), C’), D’), and E’) as described below. In most of these embodiments, these five operations are earned out in the noted order. However, it is possible for A’) and B’) to be carried out simultaneously, or for B’) to precede A’).
- one or more color toner latent images are developed in one or more color image areas, to form a composite color toner image on an intermediate receiver material (as described above).
- Each corresponding dry color toner comprises dry toner particles comprising: a (a) polymeric resin, a (b) pigment colorant, and a (c) wax that has a melting temperature that is defined as Tcoior, all as described above.
- the “color toner latent images” can also be known in the art as “charge-only images” before color toner(s) is actually applied to the intermediate receiver material.
- one or more foiling toner latent images are developed in one or more foiling image areas to provide one or more foiling toner images on the intermediate receiver material, in B’), using a dry foiling toner comprising dry foiling toner particles as described above, wherein the one or more foiling image areas are different from the one or more color image areas, and Tailing is less than Tcoior by at least 15°C or by at least 30°C.
- the composite color toner image and the one or more foiling toner images can be transferred from the intermediate receiver material to a receiver material in C’) using conventional means that are provided in various electrophotographic apparatus.
- the transferred composite color toner image and the transferred one or more foiling toner images are fixed simultaneously in a fuser oil-free fusing operation, as described above, to provide a corresponding fixed composite color toner image and one or more corresponding fixed foiling toner images.
- one or more foil images are formed in the one or more foiling toner images and not in the one or more color image areas by bringing a printing foil into intimate contact with the one or more corresponding fixed foiling toner images at a foiling temperature (FT) using the conditions and equipment described above to provide an article with one or more foil images and a composite color toner image.
- FT foiling temperature
- this electrophotographic imaging method can be carried out in A’) and B’) with the application of dry black toner, dry yellow toner, dry cyan toner, dry magenta toner, and dry foiling toner to an intermediate receiver material in the listed order from corresponding individual modules of an electrophotographic printing machine.
- the dry foiling toner and the various dry color toners can be applied to an intermediate received material in any suitable different sequences.
- a method for providing a foil image on a receiver material without inkjet printing comprising the following A) through D):
- An electrophotographic imaging method for providing an article having one or more foil images using toner latent images comprising the following A’) through E’):
- each corresponding dry color toner comprising dry toner particles comprising: a (a) polymeric resin, a (b) pigment colorant, and a (c) wax that has a melting temperature defined as Tcoior;
- B’ simultaneously with or subsequently to A), developing one or more foiling toner latent images in one or more foiling image areas to provide one or more foiling toner images on the intermediate receiver material, using a dry foiling toner comprising dry foiling toner particles comprising: a (a’) polymeric resin and a (c’) wax that has a melting temperature defined as Tfoiiing, wherein the one or more foiling image areas are different from the one or more color image areas, and Tfoiiing is less than Tcoior by at least 15°C;
- D’ simultaneously fixing the transferred composite color toner image and the transferred one or more foiling toner images in a fuser oil-free fusing operation, to provide a corresponding fixed composite color toner image and one or more corresponding fixed foiling toner images; and E’) forming one or more foil images in the one or more foiling toner images and not in the one or more color image areas, by bringing a printing foil into intimate contact with the one or more corresponding fixed foiling toner images at a foiling temperature (FT) that is greater than Tfoiiing but less than Tcoior, to provide an article with one or more foil images and a composite color toner image.
- FT foiling temperature
- Tcoior is at least 90°C and up to and including 150°C.
- Tfoiiing is at least 55°C and up to and including 90°C.
- each (a) polymeric resin of each dry color toner has a glass transition temperature (T g ) of at least 55°C and up to and including 80°C.
- the receiver material is a paper substrate or a polymeric film.
- the (a) polymeric resin comprises one or more resins selected from the group consisting of polyesters, styrenic-acrylic copolymers, and acrylic polymers.
- the printing foil comprises a composite of an organic polymer substrate having disposed thereon, in order from the organic polymer substrate, a release layer, a metallized layer, and an adhesive layer.
- weight % values for components of the various dry color toners and the dry foiling toners are based on the total dry weight of the toner formulation.
- This example provides an evaluation of the efficiency of foil transfer as a function of lamination temperature from a silver-colored printing foil to various black-colored foiling toner images on the surface of a representative receiver material. These procedures simulate how best the present invention can be carried out. It was seen that a dry foiling toner comprising a suitable lower T m wax can facilitate 100% foil transfer at a selected lamination temperature at which a dry toner comprising a suitable higher T m wax will exhibit 0% foil transfer.
- the dry color toners with the suitable higher T m can be formulated to have (a) polymeric resin, and various colors such as for example, cyan, magenta, yellow and black, by incorporating various (b) pigment colorants and would be designated as dry color toners having a (c) wax having a T m defined as Tcoior, while dry toner particles having a (a’) polymeric resin and a suitable lower T m (c’) wax now designated as with Tm of this wax now defined as Tfoiiing.
- the dry foiling toner can be formulated with or without a colorant as aesthetically desired. In the final foil image, the metallized layer itself is opaque and will mask any colorant incorporated into the dry foiling toner.
- Laboratory scale dry black polyester-containing toner particles were prepared comprising 8 weight % of each of a series of (c’) waxes of varying melting temperatures.
- the mixture of (a’) polymeric resin for all samples of dry black-colored foiling toner particles comprised an equal weight blend of higher melt viscosity and lower melt viscosity amorphous polyester materials obtained from the Kao Corporation. Because the two polyesters are amorphous, they do not physically have a melting transition as do the waxes described below.
- the higher viscosity (a’) polymeric resin had a T1/2 temperature measured by the Shimadzu capillary rheometer method of 145°C, while that of the lower viscosity (a’) polymeric resin had a T1/2 value of 101°C.
- the T1/2 value is sometimes known as the softening temperature (T s ) or melting temperature (Tm).
- the glass transition temperatures (T g ) of the higher and lower viscosity (a’) polymeric resins were 61 °C and 56°C respectively, as measured by Differential Scanning Calorimetry as the second heat value at a 20°C/min scan rate.
- the (c’) waxes used in the four black-colored dry foiling toners were WE-2 having a T m of 62°C, WE-3 having a T m of 72°C, M90 having a T m of 91 °C, and Poly waxTM 1000 having a T m of 115°C.
- the WE-2 and WE-3 products are ester-based waxes that were obtained from the NOF Corporation, while the M90 and Poly waxTM 1000 products are polyethylene waxes that were obtained from the NuCera Solutions Corporation. These T m values are the peak values of the wax crystalline melting endotherms determined by Differential Scanning Calorimetry at 20°C/min.
- dry black toner compositions 2 weight % of a wax dispersant material obtained from the NuCera Solutions Corporation as DIAX L- 775; 2 weight % of a charge control agent obtained from the Orient Chemicals Corporation as Bontron® E-84; 5.6 weight % of carbon black as the (b’) pigment colorant from the Orion Carbon Corporation as NIPex® 60; and 1.3 weight % of a Pigment Blue 61 masterbatch with 40 weight % of Pigment Blue 61 and 60 weight % of the above noted lower viscosity (a’) polyester resin, prepared by the Sun Chemical Corporation.
- Patches (foiling toner latent images) of black-colored dry toner at 0.5 mg/cm 2 coverage were prepared by directly applying each to coated glossy paper of 118 g/m 2 weight used as a receiver material on a laboratory scale toning device.
- This device comprised a toning roller with a rotating magnetic core, and a transport device that translated the glossy paper over the toning roller loaded with a two-component developer comprising the sample black-colored dry foiling toner to be tested mixed with a conventional hard magnetic carrier material.
- the blackcolored dry foiling toner coverage on the glossy paper was controlled by the level of the DC bias voltage applied to the toning roller.
- the black-colored foiling toner images were fused by contacting the back of the glossy paper with a hot “shoe” set at approximately 150°C as the fusing temperature to provide black-colored fused toner images on the glossy paper surface.
- the resulting black-colored fused foiling toner images were then taped to a sheet of 20 lb. bond paper such that a strip of each could be mounted next to each other so that all samples could be passed through a laminating device at the same time.
- the silver-colored printing foil to be tested was then taped across all four black-colored fused foiling toner images to be then passed through a laminating device described below.
- the silver-colored printing foil used was obtained from the Nobelus® Corporation, version LSSF.3.1260.00984.
- This printing foil is believed to be comprised of a polyethylene terephthalate support film having in order thereon, a release layer, the silver-colored metallized layer, and an adhesive layer.
- the support film side of the silver-colored printing foil was contacted by a heated roller of the laminating device, while the adhesive layer side was brought into proximity with the black-colored fused foiling toner images on the glossy paper that contacted the non-heated pressure roller.
- the laminating device (including fuser) used in this Example 1 was built from components of a fuser assembly taken out of an Ektaprint 300 copier that was commercially available from Eastman Kodak Co.
- a printing foil transfer test was devised. This test comprised sending separate sets of the black-colored fused toner images just described through the laminating device at different heated roller temperatures at a transport speed of 1 m/min. After allowing the resulting heated and laminated structure to cool, the printing foil was pulled from each black-colored fused toner image on the glossy paper (receiver material) and the “degree of transfer” of the silver-colored removable portion of the printing foil was visually assessed on a scale of 0% to 100% transfer.
- the desired outcome is to be able to formulate dry foiling toners such that at a given temperature there will be 100% transfer to a fused foiling toner image and 0% transfer to a fused color toner image produced with dry color toners that are not designed to be “adhesive” dry foiling toners.
- the dry foiling toner can be formulated with or without a pigment colorant as desired.
- FIG. 1 describes the results of the foregoing test using the four black-colored dry toners described above. It can be seen from those results that the temperature required to provide 100% foil transfer was increased as the melting temperature of the (c’) wax component of the black-colored dry toner was increased.
- WE-2 ester-based wax with a T m of 62°C in an adhesive dry foiling toner and the Poly waxTM 1000 polyethylene wax with a T m of 115°C in a dry color toner provided an operating range where the printing foil was completely transferred as desired in foiling toner latent images but was not transferred in the color image areas.
- the speed of the laminating process has a large effect on the temperature required to transfer foil to a fused toner image.
- the nip width of the described laboratory laminating assembly was measured to be 4 mm, which is less than that present in commercial foiling laminators that typically have nip widths in the range of 2 times to 10 times this value, thus allowing the required printing foil transfer dwell times in the heated nip to be achieved at a faster speed.
- Example 2 describes the foil transfer properties of two dry magenta toners and a dry cyan toner. This example provides an evaluation of the foil transfer efficiency as a function of lamination temperature using a silver-colored printing foil to various dry toner images using either a magenta-colored toner or a cyan-colored toner formed on the surface of a representative receiver material in order to evaluate the best (c) waxes to be included in either dry foiling toners or dry color toners.
- Two dry magenta-colored toners were prepared as comprising particles having a (a) polymeric resin that was a styrenic copolymer obtained from the Image Polymers Corporation as Almacryl® XPA7379, which has a T g of 67°C and a T/ 2 (or Tm) of 133°C.
- the dry magenta-colored toners were prepared by melt compounding using a 30 mm twin screw extruder. Both dry magenta-colored toners comprised dry magenta toner particles comprising: a 50/50 mixture of PR122/PR185 magenta pigment colorants dispersed in an acrylic resin that was obtained from the Pan Technology Corporation; and the Bontron® E-84 charge control agent.
- One of the dry magenta-colored toners comprised dry magentacolored toner particles comprising 8 weight % of the ester-based wax WE-3 having a T m of 72°C as described above in Example 1, while the second dry magenta-colored toner comprised dry magenta-colored toner particles comprising 3 weight % of a polyethylene wax having a T m of 131°C that was obtained from NuCera Solutions as Poly waxTM 3000. A wax dispersant was not included in these two dry magenta-colored toner formulations.
- a dry cyan-colored toner was prepared to comprise a (a) polymeric resin that is polylactic acid (PLA), a polyester that is different from the polyester that is described in FIG. 1.
- the PLA resin was obtained as amorphous grade IngeoTM 6361D from Natureworks Corporation. It was pre-extruded at 350°C in order to reduce the polymeric molecular weight to an appropriate amount to yield good fusing properties on a commercially available Kodak NexPress printer fuser that is operated in a fuser oil-free configuration, the extrusion resulting in a decrease of the PLA T g of from 55°C to 51 °C.
- a cyan (b) pigment colorant was added as a dispersion in polyester resin of PB15:3 supplied by the Sun Chemical Corporation to provide dry cyancolored toner particles.
- the dry cyan-colored toner comprised 6 weight % of the WE-3 ester-based wax described above.
- This dry cyan-colored toner was prepared by a chemical process known in the art as evaporative limited coalescence (ELC) that is described in detail in U. S. Patent 4,833,060 (Nair et al.).
- ELC evaporative limited coalescence
- This ELC method involves preparing an organic phase with ethyl acetate solvent including solubilized or dispersed toner components, which organic phase is then dispersed in an aqueous phase containing a silica stabilizer and pH buffer to form oil-in-water droplets. After the removal of the ethyl acetate solvent, the silica stabilizer is removed with aqueous KOH and the resulting polymeric toner particles are washed and dried.
- the dry cyan-colored toner comprising the PLA polymeric resin and WE-3 ester-based wax facilitated printing foil transfer at approximately the same temperatures as the dry magenta-colored toner particles comprising the styrenic copolymer and WE-3 ester-based wax.
- the temperature range for evaluating 0% to 100% printing foil transfer was desirably less when the dry cyan-colored toner was used.
- the dry cyan-colored toner comprised of the PLA polymeric resin and the wax having a T m of 72°C can serve as a suitable dry foiling toner to facilitate 100% printing foil transfer in combination with 0% printing foil transfer to a color toner image, for example, like the dry magenta-colored toner described above comprising the PolywaxTM 3000 wax.
- the described dry cyan-colored toner can be used as a as a dry foiling toner with the (c) wax melting temperature designated as Tfoiiing, and we can define the magenta-colored toner as a dry color toner having a wax with a melting temperature defined as Tcoior.
- Dry cyan-colored toners were prepared using the laboratory technique described above in Example 1. All dry cyan-colored toner samples comprised dry cyan-colored toner particles comprising: the polyester resin blend described in Table 1; 8 weight % of Poly waxTM 1000 wax; 2 weight % of DI AX L-775 wax dispersant (NuCera Solutions Corporation); 2 weight % of E-84 charge control agent (Orient Chemicals Corporation); and 11 weight % of a 40% masterbatch of PB15:3 cyan pigment colorant dispersed in 60 weight % polyester resin from the Sun Chemical Corporation. The various polymeric resins were all obtained from the Kao Corporation, and are shown in TABLE I below.
- cyan toner latent images were prepared on a receiver material (paper sheet) from each dry cyan-colored toner and run through a fuser-based laminating assembly to evaluate printing foil transfer using the same silver colored printing foil described above.
- the raw data collected consisted of subjectively judged % of foil transfer versus foiling temperature. Two values were taken from each curve: first the highest temperature at which there was no transfer of printing foil; and a second at the lowest temperature at which there was 100% transfer of printing foil. These values are tabulated in the following TABLE I. The experiment was run with 5 °F (or 2.8°C) steps between laminating events. The temperatures reported in TABLE I are in °C.
- a dry color toner composition required a high temperature at which printing foil did not transfer to it, when fused, it was considered useful as a dry color toner for purposes of the present invention, in that it did not attract printing foil at the usual laminating conditions. If a dry color toner composition required a low temperature at which the fused color toner image (patch) exhibits 100% printing foil transfer, it was considered a good “adhesive” dry foiling toner for purposes of the present invention.
- the difference between the “highest temperature that exhibited 0% printing foil transfer” for a fused color toner image versus the “lowest temperature that exhibited 100% of the foil transferred” for a fused foiling toner image represents the working laminating temperature range for those two different toners for the present invention.
- dry cyan-colored toners should comprise high T g (a) polymeric resins for dry color toners, and low T g (a’) polymeric resins for dry foiling toners. There is some noise in the graphical plots that may be due to melt viscosity or adhesive effects due to polymeric resin acid value among the eleven dry cyan-colored toner samples that were tested.
- the dry color toners require a (c) wax as described herein to operate in a fuser oil-free fusing mode since typical silicone fuser oil (release) fluid is known to prevent sticking of the printing foil to fused foiling toner images.
- Fuser oil-free fusing of fused color toner images requires a (c) wax in the dry color toner(s) that at least partially melts at fusing temperatures so as to create a low viscosity liquid splitable layer that functions as the release fluid.
- the width of the T m range of the ester-based waxes is much narrower than that of commercially available polyethylene waxes.
- the thermogram for WE-2 wax generated by differential scanning calorimetry shows that melting starts at approximately 52°C while the melting peak is at 62°C.
- melting starts at approximately 40°C while the melting peak is at 81°C.
- NuCera also supplies a narrower melting polyethylene wax, “M80”, that has a melting peak at 81 °C as well but starts melting at approximately 45°C.
- M80 narrower melting polyethylene wax
- the ester-based waxes have a much narrower yet melting range.
- ester-based waxes are not available with as high a T m as are the commercially available polyethylene waxes.
- PolywaxTM 3000 polyethylene wax starts melting at approximately 75°C with a peak temperature at 132°C. This is a very broad melting temperature range, but its onset of melting at 75 °C will not cause image keeping issues in typical extremes for the storage of toner images.
- the polyethylene waxes described herein are best for dry color toners and color toner images but not for the dry foiling toners and foiling toner images.
- the (a’) polymeric resin T g in the range of 50°C to 60°C and the (c’) wax Tf O iiin g in the range of 60°C to 75°C are desirable. If storage or keeping conditions can be specified for shipping conditions and use conditions of the electrophotographic printer, these values for the dry foiling toner might be decreased by perhaps 5°C since the transfer of printing foil will prevent print keeping problems.
- Example 1 The data shown above in Examples 1, 2, and 3 were generated with images (patches) of all of the dry color toners and dry foiling toners being prepared on a small laboratory toning device (see for example, in Example 1).
- color toner latent images and foiling latent images were provided on a surface of a receiver material and then fused on a commercially available Kodak NexPress printer in a single pass using a fuser oil-free fuser operation. Printing foil transfer was then accomplished using the same separate laminating device used in Examples 1, 2, and 3.
- the data shown in FIG. 3 illustrate printing foil transfer versus foil transfer temperature for the same dry cyan-colored foiling toner described above in Example 2, and for the dry cyan, magenta, yellow and black dry color toners.
- All of these dry toners comprised particles comprising a styrenic copolymer resin obtained from the Image Polymers Corporation as the (a) polymeric resin and (a’) polymeric resin, each having a T g of 63°C and a T1/2 of 141°C, CPR-390.
- the cyan, magenta, and yellow (b) pigment colorants were all obtained as Hostaprint® dispersions in a vinyl copolymer resin of PB 15:3, PR122/PR185, and PY180, respectively, from Clariant Corporation.
- the dry black-color toner was prepared using NIPEX 60 carbon black as the (b) pigment colorant from Orion Engineered Carbons.
- the four dry color toners also each contained 3 weight % of Poly waxTM 3000 (Tcoior 131°C) as the (c) wax, obtained fromNuCera Solutions and 2 weight % Bontron® E-84 charge control agent obtained from Orient Corporation.
- the melt compounding was done using a 30 mm twin screw extruder.
- the four dry color toners were provided by grounding and were each then classified to approximately 6 pm volume median particle size.
- the color latent images and foiling toner latent images that were formed included 25%, 50%, 75% and 100% dry toner coverages, as well as bichrome mixtures of the dry cyan, magenta, and yellow toners (200% coverage areas).
- the receiver material used was 12 pt. coated glossy paper stock that was approximately three times thicker than that used in Inventive Examples 1, 2, and 3.
- the silver-colored printing foil used was the same as that used in Examples 1, 2, and 3 above, and the operating speed for foil transfer was again 1 m/min.
- FIG. 4 shows the results of % foil transfer versus foil transfer temperature (°C) for the 100% image areas of the five dry toners (dry color toner and dry foiling toner) used in the process. It can be seen there is approximately a range of operation of 102°C to 107°C where there was 100% foil transfer to the dry foiling toner (foiling image areas) with the lower Tfoiiing (c’) wax, and 0% foil transfer to any of the four dry color toners (color image areas). The 200% coverage color areas behaved similarly. For this target the foiling toner image coverage did not overlap the color image area coverage.
- Example 5 illustrates commercially practical toner formulations that can be simultaneously imaged and fused in one step and then foiled using a printing foil in a second step without contamination of transferred foil on the color image areas and without missing foil transfer in foiling image areas.
- the same dry cyan, magenta, yellow, and black color toners described above in Example 4 were used in this Example 5.
- the dry foiling toner was prepared using the ELC process and comprised particles composed of pre-extruded poly (lactic acid) (PLA) resin having a T g of 51 °C as the (a’) polymeric resin, and 6 weight % of WE-3 (c’) wax having Tfoiiing of 72°C, and had a 6 pm median particle size.
- PLA pre-extruded poly (lactic acid)
- WE-3 c’
- This dry foiling toner was also surface treated with the same surface formulation described above in Example 4. However, the (b’) cyan pigment colorant was left out of the composition such that the dry foiling toner was essentially “clear” or colorless and was provided as a clear fused deposit after passing through an electrophotographic hot roller oil-less fuser.
- the noted four dry color toners and the dry colorless foiling toner were printed using a commercially available Kodak NexPress electrophotographic printer on the same 12 pt. glossy coated paper as a receiver material described in Example 4.
- the various toner images were fused on an oil-less fuser installed in the NexPress printer.
- the resulting printed color toner images and foiling toner images included various types of engineering test targets as well as advertising style documents. Foiling image areas in the form of text areas were included.
- the silver-colored printing foil used in Examples 1 through 4 was not used. Instead, a “Sparkle” foil grade LSHR.3.1260.00984 printing foil obtained from the Nobelus® Corporation was utilized for the foiling operation.
- Lamination of the foiling image areas with the printing foil was carried out using a commercial laminator, that is a Komfi® Amiga 36 device manufactured by the Komfi Corporation and purchased from the Nobelus® Corporation, which was separate from the electrophotographic printer that was used to lay down various dry color toner and the dry foiling toner.
- the laminating device was operated at a speed of 2 m/min, which is twice the speed used on the laboratory fuser/laminator described for Examples 1-4.
- the laboratory laminating device was measured to have a foil transfer nip width of 4 mm, while the foil transfer nip of the Komfi® Amiga 36 laminator was measured to be 14 mm.
- the nip widths and speed settings used for the Komfi® Amiga 36 resulted in a nip residence or dwell time of 0.42 sec versus that calculated for the laboratory laminating device of 0.24 sec. This greater time for heat transfer and materials flow helps to lower the temperature required in the foil transfer process.
- the Komfi® Amiga 36 laminator has a metal heater roller while the laboratory fuser/laminator has a rubber coating formulation that conducts heat more slowly than metal, further raising the heating roller surface temperature required for foil transfer.
- Example 5 The foiling image areas provided on the receiver materials in Example 5 using the dry colorless foiling toner displayed an image quality advantage over those foiling image areas described in Inventive Example 4 where the dry cyan-colored foiling toner was used.
- Example 4 on a small scale, yet still visible to the naked eye, the printing foil did not completely transfer to all of the edges of each foiling image area, thereby leaving a slightly observable cyan ring around the silver-colored foiling image area despite the complete foil transfer to that foiling image area. There was no such ring visible when the dry foiling toner was clear and colorless. Raising the foil transfer temperature did not remove this effect. It is known in dry toner electrophotography that there are “satellite” toner particles around the edges of color image areas.
- black toner particles may not be seen as a ring around the color image area, but they can contribute to the perceived sharpness of the color image area.
- the commercial Eastman Kodak NexPress electrophotographic printer is generally acknowledged to provide color image areas that are sharp and have excellent readability even though it may exhibit satellite toner particles that are visible on the receiver material only under magnification.
- This Example illustrates the use of commercially practical dry toner formulations that were simultaneously imaged (printed) and fused in one step and then printing foil was transferred in a second step without contamination of printing foil on the color image areas and without missing areas of printing foil transfer within foiling image areas having the dry foiling toner.
- the same dry cyan, magenta, yellow, and black color toners described above in Inventive Examples 4 and 5 were used in this Example 6.
- the dry foiling toner however did not contain the WE-3 ester wax having Tfoiiing of 72°C and the PLA polymeric resin but it was composed of the WE-2 ester wax having a Tfoiiing of 62°C and a (a’) polymeric resin blend of polyesters widely used in the dry toner industry.
- the dry foiling toner that comprised a (a’) polymeric resin having particles composed of: a 55/45 polyester mixture of a first polyester having a T m of 101 °C and a T g of 56°C and a second resin having a T m of 145°C and a T g of 61 °C, both obtained from the Kao Corporation; 8 weight % WE-2 (c’) wax obtained from the NOF corporation; 2 weight % of DIAX L-775 wax dispersant obtained from the NuCera Corporation; and 2 weight % of Bontron® E-84 charge control agent obtained from the Orient Corporation.
- the components were melt-mixed using a 30 mm extruder, ground, and classified to 6 pm median particle size.
- the resulting dry foiling toner was surface treated with the same surface formulation as described in Example 4.
- the images were fused to the paper receiver material in a Kodak NexPress printer equipped with an oil-less fuser.
- Lamination of resulting foiling toner images with printing foil was carried out using a commercial laminator, a Komfi® Amiga 52 device manufactured by the Komfi® Corporation and purchased from the Nobelus® Corporation. This device had roller lengths longer than the Komfi® Amiga 36 used in Example 5 and was operated at a speed of 3 m/min instead of the 2 m/min employed with the earlier laminating device.
- the loading pressure applied to the lamination rollers was set at 6 bar (or, 6 x 10 6 dynes/cm 2 ).
- the silver-colored printing foil used in Examples 1-4 was used in this Example 6.
- the resulting foil images were produced where there was 100% printing foil transfer to the fused foiling image areas having the fused foiling toner having the lower Tf O iiin g (c’) wax and T g (a’) polymeric resin, and 0% printing foil transfer to any of the four color image areas having fused dry color toners composed of higher Tcoior for the (c) wax and higher T g for the (a) polymeric resin.
Landscapes
- Physics & Mathematics (AREA)
- General Physics & Mathematics (AREA)
- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Textile Engineering (AREA)
- Developing Agents For Electrophotography (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US202163252254P | 2021-10-05 | 2021-10-05 | |
US17/948,394 US20230107991A1 (en) | 2021-10-05 | 2022-09-20 | Electrophotographic method for providing foil images |
PCT/US2022/044315 WO2023059442A1 (en) | 2021-10-05 | 2022-09-22 | Electrophotographic method for providing foil images |
Publications (1)
Publication Number | Publication Date |
---|---|
EP4413424A1 true EP4413424A1 (de) | 2024-08-14 |
Family
ID=83690513
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP22789409.4A Pending EP4413424A1 (de) | 2021-10-05 | 2022-09-22 | Elektrophotographisches verfahren zur herstellung von folienbildern |
Country Status (2)
Country | Link |
---|---|
EP (1) | EP4413424A1 (de) |
WO (1) | WO2023059442A1 (de) |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4833060A (en) | 1988-03-21 | 1989-05-23 | Eastman Kodak Company | Polymeric powders having a predetermined and controlled size and size distribution |
WO2001051290A1 (en) | 2000-01-09 | 2001-07-19 | Indigo N.V. | Foil printing |
US8530122B2 (en) | 2010-07-30 | 2013-09-10 | Konica Minolta Business Technologies, Inc. | Foil transferring face forming toner and image forming method |
US8993208B2 (en) | 2011-04-15 | 2015-03-31 | Konica Minolta Business Technologies, Inc. | Foil transferring method and toner for forming foil transferring layer |
JP5691909B2 (ja) * | 2011-07-25 | 2015-04-01 | コニカミノルタ株式会社 | 箔画像形成方法 |
JP2013195909A (ja) * | 2012-03-22 | 2013-09-30 | Ricoh Co Ltd | 画像形成装置 |
JP5929462B2 (ja) * | 2012-04-19 | 2016-06-08 | コニカミノルタ株式会社 | 画像形成方法 |
US9261808B2 (en) | 2012-05-02 | 2016-02-16 | Eastman Kodak Company | Highlighting color toner images with fluorescing toners |
JP2014010302A (ja) * | 2012-06-29 | 2014-01-20 | Konica Minolta Inc | 画像形成方法 |
US9029431B2 (en) | 2012-11-28 | 2015-05-12 | Eastman Kodak Company | Porous particles and methods of making them |
US9182690B1 (en) | 2014-09-25 | 2015-11-10 | Eastman Kodak Company | Reducing toning spacing sensitivity |
JP2020038312A (ja) | 2018-09-05 | 2020-03-12 | コニカミノルタ株式会社 | 画像形成装置、画像印刷方法、およびコンピュータプログラム |
JP7255195B2 (ja) * | 2019-01-18 | 2023-04-11 | 富士フイルムビジネスイノベーション株式会社 | 画像形成装置及び箔画像形成装置 |
JP2020122903A (ja) * | 2019-01-31 | 2020-08-13 | 株式会社沖データ | 画像形成装置及び画像形成方法 |
-
2022
- 2022-09-22 WO PCT/US2022/044315 patent/WO2023059442A1/en active Application Filing
- 2022-09-22 EP EP22789409.4A patent/EP4413424A1/de active Pending
Also Published As
Publication number | Publication date |
---|---|
WO2023059442A1 (en) | 2023-04-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2286303B1 (de) | Tonerzusammensetzung zur verhinderung von bildblockierungen | |
US9323169B2 (en) | Preparing color toner images with metallic effect | |
US20130295502A1 (en) | Preparing toner images with metallic effect | |
US9557675B2 (en) | Receiver materials with color toner images and fluorescent highlights | |
US20150111142A1 (en) | Non-porous dry toner particles for metallic printed effect | |
US8936893B2 (en) | Fluorescing yellow toner particles and methods of use | |
US20100015421A1 (en) | Toner composition for printing on transparent and highly colored substrates | |
EP2279458A1 (de) | Entwickler für selektives drucken von erhobenen informationen mittels elektrografie | |
US20120202021A1 (en) | Printed product with raised authentication feature | |
US9259953B2 (en) | Tactile images having coefficient of friction differences | |
WO2012109045A2 (en) | Printed product with authentication bi-fluorescence feature | |
US20130295504A1 (en) | Preparing dry toner particles for metallic effect | |
EP2880852B1 (de) | Drucksystem mit rauschverminderung | |
US20230107991A1 (en) | Electrophotographic method for providing foil images | |
US9057978B2 (en) | Enhanced color toner images using fluorescing magenta toners | |
EP4413424A1 (de) | Elektrophotographisches verfahren zur herstellung von folienbildern | |
US20130295341A1 (en) | Use of fluorescing toners for imaging | |
CN118043741A (zh) | 提供箔图像的电子照相方法 | |
US9052624B2 (en) | Use of fluorescing toners for imaging | |
US20130295350A1 (en) | Highlighting color toner images with fluorescing toners | |
US9618868B2 (en) | Metallic toner particles for providing metallic effect | |
EP1367451A2 (de) | Entwickler, Entwicklerbehälter und Bilderzeugungsgerät | |
JP2013064891A (ja) | 画像形成装置 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: UNKNOWN |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE |
|
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 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE |
|
17P | Request for examination filed |
Effective date: 20240504 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR |