US20020187310A1 - Compositions and methods for printing on specialty media - Google Patents
Compositions and methods for printing on specialty media Download PDFInfo
- Publication number
- US20020187310A1 US20020187310A1 US09/859,864 US85986401A US2002187310A1 US 20020187310 A1 US20020187310 A1 US 20020187310A1 US 85986401 A US85986401 A US 85986401A US 2002187310 A1 US2002187310 A1 US 2002187310A1
- Authority
- US
- United States
- Prior art keywords
- alcohol
- acetate
- polyvinyl
- ink
- graft copolymer
- 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.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 39
- 238000000034 method Methods 0.000 title claims abstract description 30
- 238000007639 printing Methods 0.000 title claims abstract description 19
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 114
- 239000012530 fluid Substances 0.000 claims abstract description 47
- 229920000578 graft copolymer Polymers 0.000 claims abstract description 32
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 30
- 239000000758 substrate Substances 0.000 claims abstract description 30
- 229920000642 polymer Polymers 0.000 claims abstract description 26
- 229920001577 copolymer Polymers 0.000 claims abstract description 8
- 239000000049 pigment Substances 0.000 claims abstract description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 39
- 239000003906 humectant Substances 0.000 claims description 29
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 24
- 238000001879 gelation Methods 0.000 claims description 18
- 229910021538 borax Inorganic materials 0.000 claims description 16
- 229920001223 polyethylene glycol Polymers 0.000 claims description 16
- 239000004328 sodium tetraborate Substances 0.000 claims description 16
- 235000010339 sodium tetraborate Nutrition 0.000 claims description 16
- 239000002202 Polyethylene glycol Substances 0.000 claims description 15
- 238000009472 formulation Methods 0.000 claims description 12
- 239000004094 surface-active agent Substances 0.000 claims description 10
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 claims description 6
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 6
- 239000004327 boric acid Substances 0.000 claims description 6
- 125000003827 glycol group Chemical group 0.000 claims description 6
- UWHCKJMYHZGTIT-UHFFFAOYSA-N Tetraethylene glycol, Natural products OCCOCCOCCOCCO UWHCKJMYHZGTIT-UHFFFAOYSA-N 0.000 claims description 5
- 229910000365 copper sulfate Inorganic materials 0.000 claims description 5
- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 claims description 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 4
- 125000003158 alcohol group Chemical group 0.000 claims description 4
- 229960003237 betaine Drugs 0.000 claims description 4
- 239000004202 carbamide Substances 0.000 claims description 4
- 238000006266 etherification reaction Methods 0.000 claims description 4
- AVQQQNCBBIEMEU-UHFFFAOYSA-N 1,1,3,3-tetramethylurea Chemical compound CN(C)C(=O)N(C)C AVQQQNCBBIEMEU-UHFFFAOYSA-N 0.000 claims description 3
- 229960003403 betaine hydrochloride Drugs 0.000 claims description 3
- HOPSCVCBEOCPJZ-UHFFFAOYSA-N carboxymethyl(trimethyl)azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CC(O)=O HOPSCVCBEOCPJZ-UHFFFAOYSA-N 0.000 claims description 3
- 229940088638 glycereth-7 Drugs 0.000 claims description 3
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid group Chemical group C(\C=C/C(=O)O)(=O)O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- 239000000080 wetting agent Substances 0.000 claims description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 claims 2
- 239000002274 desiccant Substances 0.000 claims 1
- 239000000470 constituent Substances 0.000 abstract 1
- 239000000976 ink Substances 0.000 description 70
- 230000007062 hydrolysis Effects 0.000 description 13
- 238000006460 hydrolysis reaction Methods 0.000 description 13
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 9
- 239000000499 gel Substances 0.000 description 9
- -1 polyethylene Polymers 0.000 description 8
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 5
- 238000010304 firing Methods 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 238000007641 inkjet printing Methods 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 229920003023 plastic Polymers 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- NECRQCBKTGZNMH-UHFFFAOYSA-N 3,5-dimethylhex-1-yn-3-ol Chemical compound CC(C)CC(C)(O)C#C NECRQCBKTGZNMH-UHFFFAOYSA-N 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 239000000975 dye Substances 0.000 description 4
- 229920002689 polyvinyl acetate Polymers 0.000 description 4
- 239000011118 polyvinyl acetate Substances 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical group CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 229920000147 Styrene maleic anhydride Polymers 0.000 description 3
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 3
- SXQCTESRRZBPHJ-UHFFFAOYSA-M lissamine rhodamine Chemical compound [Na+].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=C(S([O-])(=O)=O)C=C1S([O-])(=O)=O SXQCTESRRZBPHJ-UHFFFAOYSA-M 0.000 description 3
- 229910003002 lithium salt Inorganic materials 0.000 description 3
- 159000000002 lithium salts Chemical class 0.000 description 3
- 239000002985 plastic film Substances 0.000 description 3
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 2
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 2
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000019441 ethanol Nutrition 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 230000006872 improvement Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- AGGCEDYMGLPKNS-UHFFFAOYSA-N 5,5,6-trimethylundec-3-yne-2,2-diol Chemical class CCCCCC(C)C(C)(C)C#CC(C)(O)O AGGCEDYMGLPKNS-UHFFFAOYSA-N 0.000 description 1
- MWRSABPHNREIIX-UHFFFAOYSA-N 9,9-dimethyldecan-1-ol Chemical class CC(C)(C)CCCCCCCCO MWRSABPHNREIIX-UHFFFAOYSA-N 0.000 description 1
- ALQSHHUCVQOPAS-UHFFFAOYSA-N Pentane-1,5-diol Chemical compound OCCCCCO ALQSHHUCVQOPAS-UHFFFAOYSA-N 0.000 description 1
- 239000004698 Polyethylene Substances 0.000 description 1
- 229920002565 Polyethylene Glycol 400 Polymers 0.000 description 1
- 239000004793 Polystyrene Substances 0.000 description 1
- 239000004372 Polyvinyl alcohol Substances 0.000 description 1
- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 230000005587 bubbling Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 230000008021 deposition Effects 0.000 description 1
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000007786 electrostatic charging Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229920001519 homopolymer Polymers 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000001788 irregular Effects 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical group O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920001281 polyalkylene Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229940068918 polyethylene glycol 400 Drugs 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920000056 polyoxyethylene ether Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- 230000004044 response Effects 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000009991 scouring Methods 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- 230000007480 spreading Effects 0.000 description 1
- 125000003011 styrenyl group Chemical group [H]\C(*)=C(/[H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41M—PRINTING, DUPLICATING, MARKING, OR COPYING PROCESSES; COLOUR PRINTING
- B41M5/00—Duplicating or marking methods; Sheet materials for use therein
- B41M5/0011—Pre-treatment or treatment during printing of the recording material, e.g. heating, irradiating
- B41M5/0017—Application of ink-fixing material, e.g. mordant, precipitating agent, on the substrate prior to printing, e.g. by ink-jet printing, coating or spraying
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B41—PRINTING; LINING MACHINES; TYPEWRITERS; STAMPS
- B41J—TYPEWRITERS; SELECTIVE PRINTING MECHANISMS, i.e. MECHANISMS PRINTING OTHERWISE THAN FROM A FORME; CORRECTION OF TYPOGRAPHICAL ERRORS
- B41J2/00—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed
- B41J2/005—Typewriters or selective printing mechanisms characterised by the printing or marking process for which they are designed characterised by bringing liquid or particles selectively into contact with a printing material
- B41J2/01—Ink jet
- B41J2/21—Ink jet for multi-colour printing
- B41J2/2107—Ink jet for multi-colour printing characterised by the ink properties
- B41J2/2114—Ejecting specialized liquids, e.g. transparent or processing liquids
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G81/00—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers
- C08G81/02—Macromolecular compounds obtained by interreacting polymers in the absence of monomers, e.g. block polymers at least one of the polymers being obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C08G81/021—Block or graft polymers containing only sequences of polymers of C08C or C08F
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/30—Inkjet printing inks
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/54—Inks based on two liquids, one liquid being the ink, the other liquid being a reaction solution, a fixer or a treatment solution for the ink
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S524/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S524/906—Multipackage compositions
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31855—Of addition polymer from unsaturated monomers
Definitions
- the present invention is drawn to compositions and methods for printing on specialty media.
- inks used are typically based on solvents including methyl ethyl ketone and/or ethanol.
- continuous printing systems function as a stream of ink droplets are ejected and directed by a printer nozzle.
- the ink droplets are directed additionally with the assistance of an electrostatic charging device in close proximity to the nozzle. If the ink is not used on the desired printing surface, the ink is recycled for later use.
- the ink-jet inks are typically based upon water and glycols. Essentially, with these systems, ink droplets are propelled from a nozzle by heat or by a pressure wave. Additionally, all of the ink droplets are used to form the printed image and are ejected when needed.
- ink-jet printing has become a popular way of recording images on surfaces, particularly paper. Some of these reasons include low printer noise, capability of high speed recording, multi-color recording, and potential versatility. Additionally, these advantages can be provided at a relatively low price. However, though there has been great improvement in ink-jet printing, accompanying this improvement are increased printing demands, e.g., higher speed, higher resolution, full color image formation, new applications, etc.
- Papers used for ink-jet printing have typically included high-quality and wood-free papers designed to have high ink absorptivity or papers having a coated porous surface. These papers are functionally good for ink-jet printing because the inks may be absorbed readily and dry quickly. However, such papers often do not allow for a crisp or sharp image. Additionally, there are many potential substrates that do not provide avenues for absorption, and thus, typical ink-jet inks can puddle on those surfaces. For example, non-porous plastic is such a substrate.
- Polyvinyl alcohol-acetate is a commercially available polymer produced by partial hydrolysis of polyvinyl acetate.
- different chain length and degree of hydrolysis can effect the properties of the structure.
- the solubility of polyvinyl(alcohol-acetate) in water is dependent, in part, upon the degree of hydrolysis that the polyvinyl acetate has undergone.
- a fully hydrolyzed product is typically soluble only in hot water and tends to have a high degree of crystallinity in the dry state.
- a polyvinyl(alcohol-acetate) polymer that is about 88% hydrolyzed is water-soluble at room temperature. Non-hydrolyzed polyvinyl acetate is not water-soluble.
- Polyvinyl(alcohol-acetate) has been widely used in making photo paper and special papers for ink-jet applications. However, its use as an ink-jet ink component has been very limited.
- the problems associated with the use of polyvinyl(alcohol-acetate) in ink-jet inks include poor long term and short term nozzle reliability due to increased viscosity and nozzle plugging.
- polyvinyl(alcohol-acetate) One property of polyvinyl(alcohol-acetate) is that it can be gelled in presence of some chemicals, such as borax, boric acid, or copper sulfate. However, this property has not been known to be used for ink-jet applications. Though the formation of plasticized gels can be desirable when printing on certain types of media, e.g., specialty media including non-porous plastics, the difficulties associated with jetting are problematic.
- compositions and methods for printing on specialty media such that good pen reliability could be maintained, and yet also provide good gelation properties once printed on a substrate.
- the present invention is drawn to compositions and methods for printing ink-jet inks onto various substrates, particularly on smooth non-porous substrates.
- a method of printing on specialty media comprising providing a fixing fluid containing a fixing agent, providing a dye- or pigment-based ink-jet ink containing an effective amount of a polyvinyl(alcohol-acetate) species, jetting the fixing fluid onto the specialty media forming a coated substrate, and jetting the ink-jet ink onto the coated substrate.
- the step of allowing the ink-jet ink and the fixing fluid containing the fixing agent to gel on the surface of the substrate is also a preferred step of the present invention.
- a gelled printed image on a substrate comprising (a) a fixing fluid containing an effective amount of a fixing agent, printed in contact with (b) an aqueous ink-jet ink comprising a low molecular weight humectant, an effective amount of a polyvinyl(alcohol-acetate) species, and an effective amount of a dye or pigment, such that the fixing agent and the ink-jet ink interact to form a gel on the substrate surface.
- various polyvinyl(alcohol-acetate) species can be used including known polyvinyl(alcohol-acetate) polymers as well as some new graft copolymers disclosed herein.
- a graft copolymer for ink-jet ink formulations comprising glycerol having from 2 to 3 polyvinyl(alcohol-acetate) chains attached thereto, wherein the polyvinyl(alcohol-acetate) chains have a weight average molecular weight from about 300 to 10,000.
- a graft copolymer for ink-jet ink formulations comprising a polyvinyl(alcohol-acetate) polymer having a weight average molecular weight from about 300 to 10,000, and a polyethylene glycol chain having a weight average molecular weight from about 300 to 10,000, wherein the polyethylene glycol is attached by etherification to from 5% to 30% of the alcohol groups of the polyvinyl(alcohol-acetate).
- a graft copolymer for ink-jet ink formulations comprising a low molecular weight styrene-maleic acid ester copolymer having a weight average molecular weight from about 1,000 to 10,000; a polyvinyl(alcohol-acetate) chain attached thereto, wherein the polyvinyl(alcohol-acetate) has a weight average molecular weight from about 1,000 to 10,000.
- compositions when used in connection with polyvinyl(alcohol-acetate)s, includes partially and fully hydrolyzed polyvinyl(alcohol-acetate) polymers, as well as graft copolymers containing at least one polyvinyl(alcohol-acetate).
- “Graft copolymer” includes copolymers where polyvinyl(alcohol-acetate) has been grafted into a second polymer or a second polymer has been grafted into the polyvinyl(alcohol-acetate). Additionally, more than two polymers can be present, as long as at least one is a polyvinyl(alcohol-acetate) polymer.
- “Specialty media” includes substrates that are relatively smooth, and have difficulty absorbing conventional ink-jet inks.
- plastics such as polyethylene, polyvinyl chloride and polystyrene, non-porous and low-porous coated papers, glasses, metals, and rubbers are examples of specialty media.
- “Gelling” shall be defined as a state of consistency wherein an ink-jet ink (with or without a fixing agent) exhibits substantial increase in viscosity properties such that puddling on the surface of a substrate is minimized.
- Hydrolyzed with respect to polyvinyl(alcohol-acetate), refers to the number of hydroxy groups or acetate groups that are present on the polymer.
- “Humectant” can include any substance used as a wetting or moistening agent. The use of low molecular weight humectants that do not interfere with gelation are preferred.
- Fixing agent or “fixer” shall be defined as any substance that, when combined with any polyvinyl(alcohol-acetate) species, causes some gelation to occur.
- borax sodium tetraborate
- boric acid boric acid
- copper sulfate are good fixers for use with various polyvinyl(alcohol-acetate) species.
- Fixing fluid or “fixer fluid” include any fluid(s) that contains a fixing agent in a functional concentration such that gelation will occur when in contact with an effective amount of a polyvinyl(alcohol-acetate) species.
- Image is defined as any marking on a substrate.
- a “surfactant” is a compound that contains a hydrophilic and a hydrophobic segment. Thus, when a surfactant is added to water or some other solvent, the surface tension of the system can be reduced.
- surfactants can be used for several purposes including wetting, emulsifying, dispersing, foaming, scouring, or lubricating a system.
- low molecular weight when describing humectants, includes molecular weight from about 100 to 1,000.
- Polyvinyl alcohol-acetate [PV(Al-Ac)] can be modified to form a gel by the addition of small amount of certain complexing agents, e.g., boric acid or borax. Because of these gelation properties, it is possible to use polyvinyl(alcohol-acetate)s for certain ink-jet ink applications. However, one of the main practical challenges involved in using polyvinyl(alcohol-acetate) in ink-jet inks stems from issues of reliability. To illustrate, ink-jet inks in general require humectants to be present in the formulation.
- Humectants are typically high-boiling water-miscible organic compounds, such as polyols, amides, or polyethers. Specific examples include diethylene glycol, tetraethylene glycol, trimethylolpropane, glycerol, and 2-pyrrolidinone.
- humectants will not evaporate with the water creating a soft plug at the nozzles.
- inks containing polyvinyl(alcohol-acetate) tend to crust.
- humectant added to a polyvinyl(alcohol-acetate)-containing ink-jet ink, interference with gelation properties can occur, making any gel formed less rigid.
- appropriate selection of one or more humectant that will not interfere with the polyvinyl(alcohol-acetate) gelation is preferred.
- the present invention is drawn to compositions and methods for ink-jet printing, particularly on specialty media.
- a method of printing on specialty media comprising providing a fixing fluid containing a fixing agent, providing a dye-based ink-jet ink containing an effective amount of a polyvinyl(alcohol-acetate) species, jetting the fixing fluid onto the specialty media forming a coated substrate, and jetting the ink-jet ink onto the coated substrate.
- the step of allowing the ink-jet ink and the fixing agent to gel is also a preferred step of the present invention.
- the gelling is effectuated as the fixing agent of the fixing fluid and the polyvinyl(alcohol-acetate) of the ink-jet ink contact one another and are allowed to react.
- the preferred embodiment provides that the fixing fluid be printed first, one skilled in the art would recognize that the ink-jet ink could be printed prior to the application of the fixing fluids for some applications.
- a gelled printed image on a substrate which can be prepared by the methods described above, or other equivalent methods.
- the gelled printed image comprises at least two fluids printed in layers or in series, in either order.
- one of the layers is provided as a fixing fluid containing an effective amount of a fixing agent is printed on a substrate.
- the other layer is provided as an aqueous ink-jet ink comprising a low molecular weight humectant, an effective amount of a polyvinyl(alcohol-acetate) species, and an effective amount of a dye is printed such that contact occurs with the fixing fluid.
- the image on the substrate prior to drying, can form a gel.
- the fixing fluid in order to provide appropriate gelling characteristics described above, must contain a fixing agent that interacts with a polyvinyl(alcohol-acetate) species to form a gel of appropriate consistency.
- the fixing agent can be suspended or dissolved in an appropriate fixing fluid as described.
- fixing agents include the use of borax (sodium tetraborate), boric acid, and/or copper sulfate.
- other optional ingredients can be present including certain humectants, wetting agents, surfactants, dyes, pigments, and combinations thereof, provided they do not substantially interfere with gelation.
- a humectant be present in order to prevent crusting and other known problems that occur when the humectant component is omitted.
- the humectant should be selected so that it does not interfere substantially with the gelation properties of the polyvinyl(alcohol-acetate)/fixing agent combination (once contact occurs).
- humectants include low molecular weight polymers such as polyethylene glycol, glycereth including glycereth-7 and glycereth-1 (such as those sold under the tradenames LEGTM-7 and LEGTM-1 respectively), tetraethylene glycol, urea, tetramethylurea, betaine, betaine hydrochloride, and combinations thereof.
- low molecular weight polymers such as polyethylene glycol, glycereth including glycereth-7 and glycereth-1 (such as those sold under the tradenames LEGTM-7 and LEGTM-1 respectively), tetraethylene glycol, urea, tetramethylurea, betaine, betaine hydrochloride, and combinations thereof.
- the polyvinyl(alcohol-acetate) species can be a partially hydrolyzed or fully hydrolyzed known polymer, or can be one of the new graft copolymers disclosed herein, i.e., a polyvinyl(alcohol-acetate)/second polymer graft copolymer.
- a polyvinyl(alcohol-acetate) polymer that is hydrolyzed at from 70% to 100% is preferred. More specifically, from about 75% to 90% hydrolysis is more preferred, and about 88% is most preferred.
- an effective amount of a surfactant can be added to improve drying and reliability characteristics with respect to either the ink-jet ink formulations or the fixing fluid formulations.
- Appropriate surfactants that can be added to the ink-jet ink composition in order to improve drytime and spreading include TRITONSTM (ethoxylated octylphenols), IGEPALSTM (alkyl phenoxypoly(ethleneoxy)ethanols), SILWETSTM (silicone glycol copolymers including polyalkylene oxide-modified polydimethylsiloxanes), SURFYNOLSTM (ethoxlyated tetramethyl decyndiols), TERGITOLSTM (including ethoxylated trimethylnonanols), BRIJSTM (polyoxyethylene ethers), PLURONICSTM (ethylene oxide/propylene oxide copolymers), FLUORADSTM and ZONYLSTM (fluorosurfactants), and NEODOLSTM (nonionic ethoxylated surfactants).
- a graft copolymer for ink-jet ink formulations comprising glycerol having from 2 to 3 polyvinyl(alcohol-acetate) chains attached thereto, wherein the polyvinyl(alcohol-acetate) chains have a weight average molecular weight from about 300 to 10,000.
- the polyvinyl(alcohol-acetate) can be fully or partially hydrolyzed, though it is preferred that the polymer be partially hydrolyzed with respect to the methods and images described herein.
- three polyvinyl(alcohol-acetate) chains can be etherified to a glycerol molecule.
- two polyvinyl(alcohol-acetate) chains can be etherified to a glycerol molecule.
- two polyvinyl(alcohol-acetate) chains and one polyethylene oxide chain can be etherified to a glycerol molecule.
- a graft copolymer for ink-jet ink formulations comprising a polyvinyl(alcohol-acetate) having a weight average molecular weight from about 300 to 10,000, and a polyethylene glycol chain having a weight average molecular weight from about 300 to 10,000, wherein the polyethylene glycol is attached by etherification to from 5% to 30% of the alcohol groups of the polyvinyl(alcohol-acetate).
- the polyvinyl(alcohol-acetate) polymer can be partially or fully hydrolyzed, though an 88% hydrolyzed polymer is preferred.
- a graft copolymer for ink-jet ink formulations comprising a low molecular weight styrene-maleic acid ester copolymer having a weight average molecular weight from about 1,000 to 10,000, and a polyvinyl(alcohol-acetate) chain attached thereto, wherein the polyvinyl(alcohol-acetate) has a weight average molecular weight from about 1,000 to 10,000.
- the polyvinyl(alcohol-acetate) can be fully or partially hydrolyzed, though partial hydrolysis of about 88% is preferred.
- graft copolymers that are functional with the present invention are described as follows.
- glycerol etherified with three polyvinyl alcohol-acetate 88% hydrolyzed chains is functional.
- Each side-chain can be of different or similar sizes.
- any polyvinyl(alcohol-acetate) structures at from 300 Mw to 10,000 Mw can be used.
- glycerol etherified with two 88% hydrolyzed chains of polyvinyl alcohol-acetates and one polyethylene glycol chain can be functional. Again, from 300 Mw to 10,000 Mw for either the polyvinyl(alcohol-acetate) or the polyethylene glycol provides a functional range for use.
- a partially hydrolyzed polyvinyl alcohol acetate (88% hydrolysis) randomly graft-etherified with polyethylene glycol is also functional. The degree of etherification can be varied from 5% to 30%.
- a low-molecular weight styrene-maleic acid anhydride co-polymer can be opened with polyvinyl alcohol-acetate (88% hydrolysis), and along the backbone, polyvinyl alcohol-acetate chains can be added to the opened ester.
- a fixing fluid was prepared which contained a fixing agent, i.e., borax.
- This fixing fluid comprised the ingredients described in Table 3 below. TABLE 3 Component Weight Percentage 2-pyrrolidone 7.5% 1,5-pentanediol 8.0% Trimethylolpropane 7.5% Borax (fixing agent) 7.5% Surfynol TM 465 0.2% Water balance
- the fixing fluid described above in Table 3 provides a composition that can be jetted from an ink-jet pen with good reliability. Additionally, the borax component acts as the active ingredient that is capable of forming a gel after contact with a polyvinyl(alcohol-acetate) species.
- An ink-jet ink composition was prepared which contained partially hydrolyzed polyvinyl(alcohol-acetate).
- This ink-jet ink composition comprised the ingredients described in Table 4 below.
- An ink-jet ink composition was prepared which contained partially hydrolyzed polyvinyl(alcohol-acetate).
- An inkjet ink composition was prepared which contained partially hydrolyzed polyvinyl(alcohol-acetate).
- Example 3 was deposited from an unmodified HP C4802A pen.
- the drop volume was set at around 32 pL for the HP C4800A pen (ink-jet ink) and around 8 pL for the HP C4802A pen (fixer).
- Nozzle diagnostics for each of the ink-jet inks were conducted at an increasing frequency of firing, i.e., up to 11 kHz. No firing chamber refill problems were observed up to the 11 kHz firing frequency tested.
- the substrates tested included Hammermill DP paper and HP premium transparency film plastic sheets.
- the reverse non-porous side of the sheet was used.
- the inks of Examples 4-6 a substantial immobilization of the ink to the surface of the paper was seen when the fixing agent-containing fixing fluid was present.
- the best immobilization was seen at a 75% fixing agent-containing fixing fluid to ink-jet ink ratio (by the number of drops).
- the same effect of immobilization was seen on the plastic sheet. Particularly with the plastic substrate, when no fixing fluid was applied, the inks on plastic pulled into irregular puddles.
- a poly(vinyl-acetate) polymer having a weight average molecular weight of about 12,800 Mw.
- the polyvinyl(alcohol-acetate) was dissolved in 100 ml of toluene in a 250 ml flask equipped with a condenser and a mechanical stirrer. At 40° C., 0.1 ml of aqueous 40% NaOH was added to the solution to initiate hydrolysis. After several minutes, to stop the hydrolysis, the system was extracted with water. The toluene solution of the polymer was then reacted with ethylene oxide gas at room temperature in presence of aluminum chloride.
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- Engineering & Computer Science (AREA)
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- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
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EP02253256.8A EP1258510B1 (en) | 2001-05-16 | 2002-05-09 | Printing inks for printing on various substrates |
JP2002141273A JP4152671B2 (ja) | 2001-05-16 | 2002-05-16 | 特殊媒体上に印刷するための組成物及び方法 |
US12/466,848 US8076394B2 (en) | 2001-05-16 | 2009-05-15 | Compositions and methods for printing on specialty media |
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US09/859,864 US20020187310A1 (en) | 2001-05-16 | 2001-05-16 | Compositions and methods for printing on specialty media |
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US12/466,848 Division US8076394B2 (en) | 2001-05-16 | 2009-05-15 | Compositions and methods for printing on specialty media |
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US12/466,848 Expired - Fee Related US8076394B2 (en) | 2001-05-16 | 2009-05-15 | Compositions and methods for printing on specialty media |
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US12/466,848 Expired - Fee Related US8076394B2 (en) | 2001-05-16 | 2009-05-15 | Compositions and methods for printing on specialty media |
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US (2) | US20020187310A1 (enrdf_load_stackoverflow) |
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Also Published As
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EP1258510B1 (en) | 2018-03-28 |
US8076394B2 (en) | 2011-12-13 |
EP1258510A1 (en) | 2002-11-20 |
JP2003025709A (ja) | 2003-01-29 |
US20090225127A1 (en) | 2009-09-10 |
JP4152671B2 (ja) | 2008-09-17 |
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