EP1828320A1 - Compositions d'encres flexographiques thermofusibles et leurs procedes de preparation - Google Patents
Compositions d'encres flexographiques thermofusibles et leurs procedes de preparationInfo
- Publication number
- EP1828320A1 EP1828320A1 EP04813764A EP04813764A EP1828320A1 EP 1828320 A1 EP1828320 A1 EP 1828320A1 EP 04813764 A EP04813764 A EP 04813764A EP 04813764 A EP04813764 A EP 04813764A EP 1828320 A1 EP1828320 A1 EP 1828320A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- coating composition
- cps
- wax
- ethylene
- solid
- 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.)
- Withdrawn
Links
- 238000000034 method Methods 0.000 title claims abstract description 15
- 239000000203 mixture Substances 0.000 title claims description 8
- 239000012943 hotmelt Substances 0.000 title claims description 7
- 239000008199 coating composition Substances 0.000 claims abstract description 99
- 239000007787 solid Substances 0.000 claims abstract description 45
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 27
- 239000011230 binding agent Substances 0.000 claims abstract description 23
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 22
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 22
- 238000002844 melting Methods 0.000 claims abstract description 18
- 230000008018 melting Effects 0.000 claims abstract description 18
- 238000007757 hot melt coating Methods 0.000 claims abstract description 13
- 239000001993 wax Substances 0.000 claims description 37
- 239000002904 solvent Substances 0.000 claims description 31
- 239000011248 coating agent Substances 0.000 claims description 24
- 238000000576 coating method Methods 0.000 claims description 24
- 239000004014 plasticizer Substances 0.000 claims description 11
- -1 polyethylene Polymers 0.000 claims description 11
- 229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 claims description 10
- 229920001577 copolymer Polymers 0.000 claims description 9
- 238000007639 printing Methods 0.000 claims description 9
- 239000004215 Carbon black (E152) Substances 0.000 claims description 8
- 239000005038 ethylene vinyl acetate Substances 0.000 claims description 8
- 229930195733 hydrocarbon Natural products 0.000 claims description 8
- 150000002430 hydrocarbons Chemical class 0.000 claims description 8
- 239000000049 pigment Substances 0.000 claims description 8
- 229920006242 ethylene acrylic acid copolymer Polymers 0.000 claims description 6
- 229920001038 ethylene copolymer Polymers 0.000 claims description 6
- 229920005638 polyethylene monopolymer Polymers 0.000 claims description 6
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 239000012164 animal wax Substances 0.000 claims description 5
- 238000002156 mixing Methods 0.000 claims description 5
- VOWAEIGWURALJQ-UHFFFAOYSA-N Dicyclohexyl phthalate Chemical group C=1C=CC=C(C(=O)OC2CCCCC2)C=1C(=O)OC1CCCCC1 VOWAEIGWURALJQ-UHFFFAOYSA-N 0.000 claims description 4
- 239000013032 Hydrocarbon resin Substances 0.000 claims description 4
- 239000006185 dispersion Substances 0.000 claims description 4
- 238000010438 heat treatment Methods 0.000 claims description 4
- 229920006270 hydrocarbon resin Polymers 0.000 claims description 4
- 239000004698 Polyethylene Substances 0.000 claims description 3
- 239000004163 Spermaceti wax Substances 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 235000019385 spermaceti wax Nutrition 0.000 claims description 3
- 239000000155 melt Substances 0.000 claims description 2
- 235000013873 oxidized polyethylene wax Nutrition 0.000 claims description 2
- 239000012178 vegetable wax Substances 0.000 claims description 2
- 239000002966 varnish Substances 0.000 claims 3
- 239000000758 substrate Substances 0.000 description 10
- 150000001298 alcohols Chemical class 0.000 description 6
- 239000000976 ink Substances 0.000 description 6
- 239000000123 paper Substances 0.000 description 6
- 229920006226 ethylene-acrylic acid Polymers 0.000 description 5
- 238000011161 development Methods 0.000 description 4
- 239000000178 monomer Substances 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 3
- 239000005977 Ethylene Substances 0.000 description 3
- 239000004743 Polypropylene Substances 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 229920006267 polyester film Polymers 0.000 description 3
- 229920001155 polypropylene Polymers 0.000 description 3
- 229920005989 resin Polymers 0.000 description 3
- 239000011347 resin Substances 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- 229920003345 Elvax® Polymers 0.000 description 2
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 2
- 229910052782 aluminium Inorganic materials 0.000 description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 238000003912 environmental pollution Methods 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 229920006149 polyester-amide block copolymer Polymers 0.000 description 2
- 239000005033 polyvinylidene chloride Substances 0.000 description 2
- 230000008569 process Effects 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 230000005855 radiation Effects 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000007774 anilox coating Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229940052296 esters of benzoic acid for local anesthesia Drugs 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000004880 explosion Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 229920001903 high density polyethylene Polymers 0.000 description 1
- 239000004700 high-density polyethylene Substances 0.000 description 1
- 238000003475 lamination Methods 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000003022 phthalic acids Chemical class 0.000 description 1
- 229920006122 polyamide resin Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 239000004170 rice bran wax Substances 0.000 description 1
- 235000019384 rice bran wax Nutrition 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000000214 vapour pressure osmometry Methods 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- 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
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
-
- 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
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/106—Printing inks based on artificial resins containing macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
Definitions
- This invention relates to coating compositions. More particularly, the invention relates to solvent free solid hot melt coating compositions for use in hot melt coating processes.
- Hot melt coating compositions of the present invention are a new development based on the recent successful development of hot melt printing inks.
- the disclosed inks comprise a pigment and a thermoplastic binder having a softening point between 90 0 C and 16O 0 C.
- the binder comprises a synthetic polyamide resin or synthetic polyesteramide resin, each resin being the condensation product of (1 ) an acid component comprising a dimerized fatty acid and a monocarboxylic acid and (2) an amine component comprising a diamine and, in the case of the polyesteramide resin, additionally comprising a diol and/or alkanolamine.
- thermoplastic binder (B) a thermoplastic binder
- the coating composition which is solid at room temperature, has a melting point of at least about 75°C, and when heated to a temperature between about 90 0 C and about 135°C forms a coating composition which has a coating viscosity between about 100 cps and about 1200 cps.
- the present invention also provides a method of preparing a solvent free coating composition having a linear alcohol which is a solid at room temperature, a thermoplastic binder, and a wax. When heated to between about 90 0 C and about
- the solvent free coating composition has a coating viscosity between about 100 cps and about 1200 cps.
- the present invention also provides a method for preparing a hot melt flexographic printing coating composition by preparing a pigment dispersion and mixing it with a linear alcohol which is a solid at room temperature, a thermoplastic binder, a wax and optionally, a solid plasticizer to form a homogenous solvent free coating composition having a viscosity of between about 100 cps and about 1200 cps at a temperature of between about 90 0 C and about 135°C.
- the present invention relates to a novel solvent free coating composition which is solid at room temperature and to a method of coating using this coating composition in a molten state, e.g., at coating temperatures of about 90 0 C and higher.
- solid is intended to mean that the physical state of a designated component is solid at ambient room temperature, i.e., the component has a melting point or a softening temperature substantially above ambient room temperature.
- the solvent free coating compositions of the invention are substantially free of condensation polymers or any other such component which would change the essential character of the coating composition.
- the solid linear alcohol in the invention functions as a dispersing medium to maintain a uniform suspension.
- Suitable linear alcohols include but are not limited to fully saturated, long-chain linear alcohols having a melting point of about 75°C or greater and a number-average molecular weight (M n ) of about 350 or greater.
- the linear alcohols have a M n between about 350 and about 750 and a melting point between about 75°C and about 1 1O 0 C.
- the solid linear alcohol is a Ci4 alcohol such as Unilin® alcohols which are products of the Baker Petrolite Corp.
- Unilin® alcohols are fully saturated, long-chain linear alcohols having average carbon chain lengths up to C 50 with the primary hydroxy function of the alcohol distributed among all of the carbon chain lengths.
- a particularly preferred solid linear alcohol is Unilin® 500 alcohol which has a M n of 550; a melting point of 99 0 C, a hydroxyl number of 83 mg KOH/g sample, and a viscosity at 149°C of 5.5 cps.
- Thermoplastic binders for use in the present invention should have a softening point of about 70 0 C. and therefore be solid at ambient temperature.
- Suitable thermoplastic binders include but are not limited to ethylene copolymers, hydrocarbon resins or a combination thereof.
- the thermoplastic binder is a copolymer of ethylene with either acrylic acid or vinyl acetate.
- the solid thermoplastic binder is poly(ethylene-acrylic acid) which has a Mettler Drop Pt. (ASTM D-3954) of about 90°C to about 105 0 C; a Brookfield viscosity at 140°C of about 550 cps to about 650 CPS; and an acid number between about 40 and about 120.
- a particularly preferred poly(ethylene-acrylic acid) of this type is A-C® 5120 copolymer of ethylene- acrylic acid which is marketed by Honeywell (formerly Allied Signal Inc.), Specialty Chemicals, Morristown, NJ.
- thermoplastic binder is A-C® 5120 copolymer which is a poly(ethylene-acrylic acid) having a Mettler Drop Pt. of 92°C, a Brookfield viscosity at 140 0 C of 650 cps; and an acid number of 120.
- the vinyl thermoplastic binder is poly(ethylene-vinyl acetate) in which the copolymer contains between about 15 wt.% to about 50 wt. % of vinyl acetate.
- Poly(ethylene-vinyl acetate) copolymers of this type have Melt Indexes ranging from about 8 to about 2500 and a softening point (Ring and Ball, ASTM E28 hereinafter identified as R&B") ranging from about 74°C to about 150°C.
- Polyethylene- vinyl acetate) copolymers of this type which are used in the following examples are marketed by E.I. duPont deNemours and Co. as Elvax® Ethylene/VA copolymers and by EIf Atochem as Evatane® Ethylene/VA copolymers.
- the thermoplastic binder is a hydrocarbon resin.
- Typical hydrocarbon resins which are useful in formulating the coating compositions of this invention include but are not limited to Escorez 5380 (R&B softening point 85°C), Escorez 210, (R&B softening point 94°C), Escorez 5400 (R&B softening point 100-106°C), and Escorez 5600 (R&B softening point 100-106 0 C).
- Wax Suitable waxes for use in the invention are non-volatile at coating operating temperatures and have low melt viscosities. Such waxes or mixture of waxes provide a proper degree of toughness and flexibility to the applied coating composition for the intended application.
- Typical waxes for use in the present invention include but are not limited to highly branched hydrocarbon waxes, polyethylene homopolymer waxes, oxidized polyethylene waxes (such as E-2020 from Baker Petrolite), animal waxes (such as spermaceti wax), vegetable waxes (such as rice bran wax, carnuba wax and candilla wax), and combinations thereof.
- Preferred waxes are highly branched hydrocarbon waxes which typically have a viscosity at 99°C of about 1-400 cps and preferably a viscosity at 99 0 C of about 1-20 cps.
- Waxes which have these properties include but are not limited to the animal wax spermaceti wax, which is a complex cetyl ester mixture and has a melting point of 45°C - 49 0 C, and Rosswax 3009 which is marketed by Frank B. Ross Co. Inc., Jersey City, NJ. , and has a low molecular weight polyethylene derived from high density polyethylene, has a Mn of 1000 - 1200; a molecular weight distribution in the range of about 1.0 to about 2.0; a melting point (Drop D-127) of 82°C - 104°C; and an extremely low melt viscosity.
- a particularly preferred wax of this type is VYBAR® 253 polymer marketed by Baker Petrolite.
- VYBAR® 253 polymer which is used in the following examples, is a highly branched hydrocarbon which has a number average molecular weight (Mn) of 520 (by vapor pressure osmometry); a softening point (ASTM D36) of about 67°C; and a viscosity at 99°C of about 6 cps (ASTM D3236).
- the present invention may also include one or more solid plasticizers.
- Suitable solid plasticizers include, but are not intended to be limited to, solid esters of benzoic acid, phthalic acids and aliphatic/cycloaliphatic acids with melting points above 40 0 C and which are substantially non-volatile at coating press operating temperatures, or combinations thereof.
- a preferred solid plasticizer is dicyclohexylphthalate.
- the solvent free coating composition of the present invention is prepared by first mixing a linear alcohol which is solid at room temperature, if present a solid plasticizer, a thermoplastic binders and waxes in a container at a temperature of at least 90 0 C to form a homogeneous molten coating composition which is allowed to cool to room temperature to form the solvent free coating composition of the present invention.
- the coating mixture may be heated at a temperature of at least 110 0 C, preferable at least 12O 0 C.
- the coating mixture may be heated for a period of a few hours, preferably between one to four hours, more preferably between two to three hours.
- the container for heating may be, but is not limited to, a metal can or aluminum pan.
- the solvent free coating composition may be cooled to room temperature to form a solid coating composition which can be packaged and stored for later use in hot melt coating.
- the solid coating composition comprises: an ethylene-acrylic acid copolymer, a linear alcohol which is a solid at room temperature, dicyclohexylphthalate, and a highly branched hydrocarbon wax.
- the ethylene-acrylic acid copolymer is A-C® 5120 copolymer of ethylene- acrylic acid identified above
- the solid linear alcohol is Unilin® 550 alcohol identified above
- the highly branched hydrocarbon wax is VYBAR® 253 polymer identified above.
- the solvent free coating compositions of this embodiment are particularly useful in hot melt coating on a variety of substrates giving applied coating compositions with very good adhesion and gloss.
- the solid coating composition comprises a pigment; an ethylene-vinyl acetate copolymer, a solid linear alcohol at room temperature, dicyclohexylphthalate, and a polyethylene homopolymer wax.
- the ethylene-vinyl acetate copolymer is Elvax® 4OW ethylene-vinyl acetate copolymer (containing 40 wt.% of vinyl acetate, and has a Melt Index of about 52 and a softening point of about 104°C (ring & ball ASTME28))
- the solid linear alcohol is Unilin® 550 alcohol identified above
- the polyethylene homopolymer wax is Rosswax 3009 identified above.
- the solvent free coating compositions of this embodiment are particularly useful in hot melt coating on a variety of polyester substrates and treated polyethylene substrates, providing applied coating compositions with very good adhesion and gloss.
- Each of the preferred solvent free coating compositions has a melting point of about 75°C or greater, and when heated to a temperature between about 90 0 C and about 135°C, forms a molten coating composition which has a viscosity between about 100 cps and about 1200 cps, preferably between about 100 cps and about 700 cps.
- the solvent free coating composition of the present invention is free of volatile solvents while also avoiding the problem of unreacted residual monomers which can migrate into the substrate on which the coating is applied, such as food packaging.
- the solvent free coating composition is also solid and in its clear embodiment, has a good
- the solvent free coating composition of the present invention also has good adhesion to a variety of substrates such as paper, clay, coated board, film and foil.
- the solvent free coating compositions as prepared herein are used in hot melt coatings. It is broken into small pieces and placed into a heated coating composition reservoir where it is melted and maintained slightly above its melting point, i.e., brought to a temperature between about 90 0 C and about 135°C to form a molten coating composition which has a viscosity between about 100 cps and about 1200 cps. The molten coating composition is then applied to a heated anilox roller in operational contact with the surface of a heated coating element, and printed from the surface of the flexographic plate onto a substrate such as conventional print stock, polymeric films, metal sheets, and the like.
- a substrate such as conventional print stock, polymeric films, metal sheets, and the like.
- the coating substrate may be selected from a variety of flexible films and papers including but not limited to polypropylene film with both sides corona treated, polypropylene film with both sides acrylic coated, polypropylene film with both sides PVDC coated, chemically treated polyester film, corona treated polyester film, PVDC coated polyester film, aluminum foil, and paper products such as coated paper, cardboard, corrugated paper, and the like
- the substrate may be at room temperature or may be pre-heated before coating, and optionally cooled by chill rollers after coating.
- the linear alcohol may be present in the coating composition in an amount of 5- 40 wt.%, preferably about 10-30 wt.%.
- the thermoplastic binder may be present in an amount of 35 - 65 wt. %, preferably about 45-60 wt.%.
- the wax may be present in an amount of 5-50 wt.%, preferably about 30-40 wt.%.
- the solid plasticizer may be present in an amount of 3-15 wt.%, preferably about 5-10
- the solvent free coating composition of the present invention was prepared with the following ingredients set forth in Table 1 below:
- the viscosity of the coating composition was measured at 85 cps at 120 0 C. The viscosity was determined at the designated temperature using a Carri-Med AR1000 Rheometer. A graphical representation of the viscosity of the coating at varying temperatures is set forth in Graph 1 below:
- the hot melt clear coating composition sample was tested by ASTM standard method on "Mocon” instrument model # DL 100 at various temperatures and thickness to measure Moisture-Vapor-Transmission-Rate (MVTR) value as indicated in Table 2 below.
- MVTR Moisture-Vapor-Transmission-Rate
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Paints Or Removers (AREA)
- Laminated Bodies (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
Abstract
L'invention concerne des compositions de revêtement thermofusibles, sans solvant, constituées d'un alcool linéaire solide, d'un liant thermoplastique et d'une cire, solides à température ambiante, présentant un point de fusion supérieur ou égal à environ 75 °C, qui, lorsque chauffées à une température comprise entre environ 90 °C et environ 135 °C, forment des compositions de revêtement fondues présentant une viscosité comprise entre 100 cps et 1200 cps. L'invention concerne également un procédé de préparation desdites compositions.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| PCT/US2004/041499 WO2006062523A1 (fr) | 2004-12-09 | 2004-12-09 | Compositions d'encres flexographiques thermofusibles et leurs procedes de preparation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP1828320A1 true EP1828320A1 (fr) | 2007-09-05 |
Family
ID=34959791
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP04813764A Withdrawn EP1828320A1 (fr) | 2004-12-09 | 2004-12-09 | Compositions d'encres flexographiques thermofusibles et leurs procedes de preparation |
Country Status (4)
| Country | Link |
|---|---|
| EP (1) | EP1828320A1 (fr) |
| BR (1) | BRPI0419144A (fr) |
| CA (1) | CA2590181A1 (fr) |
| WO (1) | WO2006062523A1 (fr) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7677713B2 (en) * | 2007-05-30 | 2010-03-16 | Xerox Corporation | Solid ink set incorporating naturally derived materials and processes thereof |
| MX2019012698A (es) | 2017-04-28 | 2019-12-16 | Sun Chemical Corp | Revestimiento de barrera termosellable. |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6841590B2 (en) * | 2001-12-28 | 2005-01-11 | Sun Chemical Corporation | Hot melt flexographic inks and method of preparing same |
-
2004
- 2004-12-09 EP EP04813764A patent/EP1828320A1/fr not_active Withdrawn
- 2004-12-09 CA CA002590181A patent/CA2590181A1/fr not_active Abandoned
- 2004-12-09 BR BRPI0419144-7A patent/BRPI0419144A/pt not_active IP Right Cessation
- 2004-12-09 WO PCT/US2004/041499 patent/WO2006062523A1/fr not_active Ceased
Non-Patent Citations (1)
| Title |
|---|
| See references of WO2006062523A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0419144A (pt) | 2007-11-13 |
| CA2590181A1 (fr) | 2006-06-15 |
| WO2006062523A1 (fr) | 2006-06-15 |
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Legal Events
| Date | Code | Title | Description |
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