WO2005037930A1 - Formulierungen und ihre verwendung bei der kolorierung von substraten - Google Patents
Formulierungen und ihre verwendung bei der kolorierung von substraten Download PDFInfo
- Publication number
- WO2005037930A1 WO2005037930A1 PCT/EP2004/011253 EP2004011253W WO2005037930A1 WO 2005037930 A1 WO2005037930 A1 WO 2005037930A1 EP 2004011253 W EP2004011253 W EP 2004011253W WO 2005037930 A1 WO2005037930 A1 WO 2005037930A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- pigment
- mixture
- comonomers
- formulation according
- particulate form
- Prior art date
Links
- 0 *C(C(Oc1ccc(C(c2ccccc2)=O)c(N)c1)=O)=CC=C Chemical compound *C(C(Oc1ccc(C(c2ccccc2)=O)c(N)c1)=O)=CC=C 0.000 description 2
- PWWFCNRFDRLNKZ-VRULOHATSA-N C/C=C\C=C/C(C(C(c1ccccc1)=O)(OC)OC)=C Chemical compound C/C=C\C=C/C(C(C(c1ccccc1)=O)(OC)OC)=C PWWFCNRFDRLNKZ-VRULOHATSA-N 0.000 description 1
- KTALPKYXQZGAEG-UHFFFAOYSA-N CC(C)c(cc1)cc2c1Sc(cccc1)c1C2=O Chemical compound CC(C)c(cc1)cc2c1Sc(cccc1)c1C2=O KTALPKYXQZGAEG-UHFFFAOYSA-N 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
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/10—Printing inks based on artificial resins
- C09D11/101—Inks specially adapted for printing processes involving curing by wave energy or particle radiation, e.g. with UV-curing following the printing
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0001—Post-treatment of organic pigments or dyes
- C09B67/0004—Coated particulate pigments or dyes
- C09B67/0008—Coated particulate pigments or dyes with organic coatings
- C09B67/0013—Coated particulate pigments or dyes with organic coatings with polymeric coatings
Definitions
- the present invention relates to formulations containing
- the present invention relates to a method for coloring substrates and colored substrates, produced using treated pigments in particulate form in the presence of radiation-curable molecules or molecular building blocks.
- Colored substrates should have a high brilliance of colors
- the coloring should be permanent, ie have high fastness properties, such as fastness to rubbing and fastness to perspiration. In some cases, however, the brilliance of coloration can still be lacking. This applies, for example, to the application of binder-containing colorant preparations if one wishes to generate trichromatic substances. Pigments migrate frequently after application and this can lead to color irregularities. Unwanted fat rashes are also occasionally observed, which are promoted by the migration of pigments and lead to discoloration and soiling.
- the task was therefore to provide formulations which are suitable for the coloring of substrates and avoid the above-mentioned weaknesses from the prior art.
- a further task was to provide a method for coloring substrates.
- a further object was to provide a process for the production of formulations which are suitable for the coloration of substrates.
- the task was to provide colored substrates.
- the formulations according to the invention contain pigment in particulate form.
- pigments are to be understood as meaning practically insoluble, organic or inorganic colorants as defined in DIN 55944.
- the process according to the invention preferably starts from organic pigments.
- Organic pigments selected by way of example are:
- Monoazo Pigments C.I. Pigment brown 25; C.I. Pigment Orange 5, 13, 36 and 67; C.I. Pigment Red 1, 2, 3, 5, 8, 9, 12, 17, 22, 23, 31, 48: 1, 48: 2, 48: 3, 48: 4, 49, 49: 1, 52: 1, 52: 2, 53, 53: 1, 53: 3, 57: 1, 63, 112, 146, 170, 184, 210, 245 and 251; C.I. Pigment Yellow 1, 3, 73, 74, 65, 97, 151 and 183;
- Disazo Pigments C.I. Pigment Orange 16, 34 and 44; C.I. Pigment Red 144, 166, 214 and 242; C.I. Pigment Yellow 12, 13, 14, 16, 17, 81, 83, 106, 113, 126, 127, 155, 174, 176 and 188; Anthanth ron pigments: C.I. Pigment Red 168 (C.I. Vat Orange 3);
- Anthraquinone pigments Cl Pigment Yellow 147 and 177; CI Pigment Violet 31; Anthraquinone pigments: Cl Pigment Yellow 147 and 177; CI Pigment Violet 31; Anthrapyrimidine Pigments: Cl Pigment Yellow 108 (Cl Vat Yellow 20); Quinacridone pig duck: Cl Pigment Red 122, 202 and 206; CI Pigment Violet 19;
- Indanthrone Pigments C.I. Pigment Blue 60 (C.I. Vat Blue 4) and 64 (C.I. Vat Blue 6);
- C.I. Pigment Yellow 138 C.I. Pigment Red 122, C.I. Pigment Violet 19, C.I. Pigment Blue 15: 3 and 15: 4, C.I. Pigment Black 7, C.I. Pigment Orange 5, 38 and 43 and C.I. Pigment Green 7.
- the formulations according to the invention can also contain mixtures of two or more different treated pigments.
- the formulations according to the invention contain at least one pigment which is in particulate form, i.e. in the form of particles.
- So-called raw pigments are usually used, which are untreated pigments as they occur after pigment synthesis.
- the particles can have regular or irregular shape, for example the particles can be in spherical or approximately spherical shape or in needle form.
- the quantitative ratio of pigment in particulate form to non-ionic surface-active substance can be selected in a wide range and can be, for example, in the range from 10: 1 to 2: 1.
- Step a) Water can be added while step a) is being carried out.
- Conventional non-ionic grinding aids can also be added.
- the average diameter of pigment in particulate form after step a) is usually in the range from 20 nm to 1.5 ⁇ m, preferably in the range from 50 to 200 nm, particularly preferably 100 nm.
- step b) the weight ratio of mixture of pigment particles and non-ionic surfactant to aqueous medium is generally in the range from 1: 2 to 1:15, preferably 1: 2.5 to 1: 9.
- Pressure and temperature conditions for step b) are generally not critical, for example temperatures in the range from 5 to 100 ° C. are suitable, preferably 20 to 85 ° C. and pressures in the range from normal pressure to 10 bar.
- Preferred examples of monomers or comonomers in step c) are vinylaromatic compounds and poorly water-soluble, ⁇ -unsaturated carboxylic acid derivatives.
- Redox initiators are also suitable, for example from peroxides and oxidizable sulfur compounds.
- Systems of acetone bisulfite and organic peroxide such as tert-C 4 H 9 -OOH, Na 2 S 2 O 5 (sodium disulfite) and organic peroxide such as tert-C 4 H 9 -OOH or HO-CH 2 are very particularly preferred SO 2 H and organic peroxide such as tert-CH 9 -OOH.
- Systems such as ascorbic acid / H 2 O 2 are also particularly preferred.
- the selected temperature depends on the decay characteristics of the initiator used.
- the pressure conditions are generally not critical, for example pressures in the range from normal pressure to 10 bar are suitable.
- R 6 is selected from unbranched or branched dC 10 alkyl, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, iso-pentyl, sec.-pentyl, neo-pentyl, 1, 2-dimethylpropyl, iso-amyl, n-hexyl, iso-hexyl, sec.-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n- Nonyl, n-decyl; CC 4 alkyl, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl and tert-butyl, is particularly preferred.
- styrene is used in step c) and a mixture of hard components (components which increase the hardness of a copolymer film), such as e.g. Methyl acrylate and styrene and a soft component such as e.g. Butyl acrylate.
- hard components components which increase the hardness of a copolymer film
- soft component such as e.g. Butyl acrylate.
- the second monomer or the second mixture is selected such that the glass transition temperature of the polymer or copolymer synthesized in step d) is above 0 ° C.
- the glass transition temperature of the polymer or copolymer synthesized in step d) is preferably above 10 ° C., particularly preferably above 20 ° C.
- step d At least 10% by weight of n-butyl acrylate is used in step d).
- the weight ratio of the second mixture of comonomers from step d) to pigment from step a) is in the range from 0.7 to 1 to 10: 1, preferably 1.5 to 1 to 5 to 1, particularly preferably 1.7 to 1 to 3 to 1.
- Common nonionic emulsifiers are, for example, ethoxylated mono-, di- and tri-alkylphenols (degree of ethoxylation: 3 to 50, alkyl radical: C 4 -C 12 ) and ethoxylated fatty alcohols (degree of ethoxylation: 3 to 80; alkyl radical: C 8 -C 36 ).
- Examples are the Lutensol ® brands from BASF Aktiengesellschaft and the Triton ® brands from Union Carbide.
- Typical anionic emulsifiers are, for example, alkali metal and ammonium salts of alkyl sulfates (alkyl radical: C 8 to C 12 ), of sulfuric acid semiesters of ethoxylated alkanols (degree of ethoxylation: 4 to 30, alkyl radical: C 12 -C 18 ) and ethoxylated alkyl phenols (degree of ethoxylation: 3 to 50, alkyl radical: C 4 -C 1 ), of alkyl sulfonic acids (alkyl radical: C 12 -C 18 ) and of alkylarylsulfonic acids (alkyl radical: C 9 -C 18 ).
- alkyl sulfates alkyl radical: C 8 to C 12
- sulfuric acid semiesters of ethoxylated alkanols degree of ethoxylation: 4 to 30, alkyl radical: C 12 -C 18
- Suitable cationic emulsifiers are usually a C 6 -C 18 alkyl, aralkyl or heterocyclyl-containing primary, secondary, tertiary or quaternary ammonium salts, Alkanolammoniumsaize, pyridinium salts, imidazolinium salts, oxa zoliniumsalze, morpholinium, thiazolinium, and salts of amine oxides , Quinolinium salts, isoquinolinium salts, tropylium salts, sulfonium salts and phosphonium salts.
- step d) The order of addition of the reactants from step d) is not critical per se.
- a period of time in the range from 30 minutes to 12 hours can be selected as the time for the polymerization or copolymerization in step d), 2 to 3 hours being preferred. If one or more compounds of the general formula I are selected as comonomer in step d), a time period of 40 to 60 minutes is also conceivable.
- R 10 is selected from unbranched or branched dC 10 alkyl, such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, n-pentyl, isopentyl , sec.-pentyl, neo-pentyl, 1, 2-dimethylpropyl, iso-amyl, n-hexyl, iso-hexyl, sec.-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n-decyl; particularly preferably CC 4 alkyl such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl and tert-butyl; - or hydrogen;
- R 11 selected from unbranched or branched dC 10 alkyl, such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, iso-pentyl , sec.-pentyl, neo-pentyl, 1, 2-dimethylpropyI, iso-amyl, n-hexyl, iso-hexyl, sec.-hexyl, n-heptyl, n-octyl, 2-ethylhexyl, n-nonyl, n decyl; particularly preferably dC 4 -alkyl such as methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl and tert-butyl;
- X selected from -OH, -NH 2 , -NH-CH 2 OH,
- step d 1 to 14% by weight (meth) acrylonitrile, based on the total amount of comonomers, can be used as comonomers in step d).
- comonomers in step d) are comonomers which can serve as a photoinitiator, in particular (meth) acrylic acid esters of alcohols, which can serve as a photoinitiator of radical polymerizations.
- comonomers which can serve as a photoinitiator in particular (meth) acrylic acid esters of alcohols, which can serve as a photoinitiator of radical polymerizations.
- optionally substituted (meth) acryloylbenzophenones of the general formula VII are very particularly preferred
- C 2 -C alkylene preferably C 2 -C alkylene; in particular - (CH 2 ) 2 -, -CH (C 2 H 5 ) - -CH 2 -CH (CH 3 ) -, - (CH 2 ) 3 -, - (CH 2 ) 4 - and -CH 2 -CH (C 2 H 5 ) -;
- R 18 is selected from CC 4 alkyl such as methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl and tert-butyl; and C 6 -C 14 aryl, optionally substituted, such as phenyl, p-hydroxyphenyl, p-dimethylaminophenyl, p-methylphenyl, 1-naphthyl, 2-naphthyl, 9-anthryl, 1-anthryl, 2-anthryl, in particular phenyl, and the remaining variables are defined as above.
- Comonomers of the general formulas P1 to P4 can be prepared by methods known per se.
- An esterification step or transesterification step of precursors of the formulas is customary in the production
- the effectiveness of photoinitiators can be increased by adding at least synergists, for example at least one amine, in particular tertiary amine.
- Suitable amines are, for example, triethylamine, N, N-dimethylethanolamine, N-methylethanolamine, triethanolamine, aminoacrylates such as, for example, the unmodified polyether acrylates.
- synergist can be added up to 5% by weight, based on the total weight of the formulation according to the invention.
- step d) 0.1 to 2% by weight, preferably 0.2 to 1.5% by weight, of at least one comonomer, which can serve as a photoinitiator, can be polymerized.
- step d) 0.1 to 2% by weight, preferably 0.2 to 1.5% by weight, of an isomer mixture of VII can be polymerized in.
- Formulations according to the invention are usually aqueous dispersions of pigment treated as described above in particulate form and can have a solids content of 10 to 50% by weight, preferably 30 to 40% by weight.
- Formulations according to the invention further contain at least one radiation-curable component (B).
- a formulation according to the invention contains at least one compound per Molecule carries at least two ethylenically unsaturated double bonds, which are preferably isolated from one another, ie they are not conjugated. It is preferably at least one compound which carries at least two (meth) acrylic acid groups, for example di- or polycarboxylic acids esterified at least twice with (meth) acrylic acid, or at least two di- or polyisocyanates reacted with functional (meth) acrylic acid derivatives hereinafter also referred to as urethane (meth) acrylates.
- Compounds of the general formula VI a, VI b or VI d are very particularly preferred
- R 13 , R 14 different or preferably the same and selected from hydrogen and methyl
- Y 1 , Y 2 , Y 3 , Y 4 the same or different and selected from sulfur, NH and in particular oxygen,
- b and f, c and h, Y 1 and Y 4 , Y 2 and Y 3 and R 13 and R 14 are each the same in pairs.
- R the same or different and selected from methyl and hydrogen
- n is an integer from 0 to 2, preferably 1;
- R 16 is selected from C 1 -C 4 -alkyl, such as, for example, nC 4 H 9 , nC 3 H 7 , iso-C 3 H 7 and preferably C 2 H 5 and CH 3 , or phenyl,
- a 4 , A ⁇ A 6 the same or different and selected from d-Cao-alkylene, such as -CH 2 -, -CH (CH 3 ) -, -CH (C 2 H 5 ) -, -CH (C 6 H 5 ) -, - (CH 2 ) 2 -, - (CH 2 ) 3 -, - (CH 2 ) 4 -, - (CH 2 ) 5 -, - (CH 2 ) 6 -, - (CH 2 ) 7 -, - (CH 2 ) 8 -, - (CH 2 ) 9 -, - (CH 2 ) 1 o- J -CH (CH 3 ) - (CH 2 ) 2 -CH (CH 3 ) -; ice or frans-C 4 -C 10 cycloalkylene, such as c / s-1, 3-cyclopentylidene, trans-, 3-cyclopentylidene c s
- polyester (meth) acrylates obtainable by, for example, reacting hydroxyl-terminated polyesters with a molecular weight M n, preferably in the range from 250 to 4000 g / mol, or polyethers with a molecular weight M n in the range from 400 to 4000 g / mol, with (meth) acrylic acid, as described, for example, in EP-B 0 126 341.
- branched compounds with at least two terminal double bonds are (meth) acrylate urethanes, preferably available as aqueous dispersions, which can be prepared by reacting polyester (meth) acrylates with preferably aromatic di- or triisocyanates, as described for example in WO 98/47975.
- Formulations according to the invention can contain 0.2 to 30% by weight, preferably 1 to 15% by weight, of radiation-curable component (B).
- formulations according to the invention contain at least one radiation-curable component as molecular building blocks.
- This special embodiment can be implemented, for example, by using selected comonomers in step d) in the treatment of the pigment or pigments in particulate form which carry molecular groups suitable for carrying out radiation curing.
- Suitable comonomers are in particular comonomers capable of crosslinking which carry at least two ethylenically unsaturated double bonds per molecule, which are preferably isolated from one another, i.e. they are not conjugated.
- At least one comonomer which carries at least two (meth) acrylic acid groups for example di- or polycarboxylic acids or urethane (meth) acrylates esterified at least twice with methacrylic acid.
- Compounds of the general formula VI a or VI b which are as defined above are very particularly preferred.
- film-forming aids are added to the formulations according to the invention.
- one or more non-polymerized photoinitiators can additionally be introduced into the pigment-polymer system via the radiation-curable component (s) (B) or optionally via the film-forming aid.
- Formulations according to the invention can contain polymer or copolymer which is derived from monomers or mixtures of comonomers from step d). The majority of the pigments in particulate form treated by the process described above are coated with two layers of polymers or copolymers, wherein the layers can be interpenetrating and do not have to be strictly different from one another. The particles characterized in this way are also referred to below as pigment-containing polymer particles.
- formulations according to the invention contain polymer or copolymer which is derived from monomers or mixtures of comonomers from step d).
- the polymer or copolymer derived from monomers or mixtures of comonomers from step d) is preferably obtained in the form of spherical particles.
- the particles characterized in this way are also called pigment-free polymer particles below.
- the weight ratio of pigment-containing polymer particles to pigment-free polymer particles is in the range from 10 to 0.1 to 10 to 3, preferably from 10 to 0.5 to 10 to 2.
- the average radii r are smaller than the average radii r (pigment-containing polymer particles), in each case based on the number average.
- At least one plasticizer (C) is added to formulations according to the invention following step d).
- Plasticizer (C) is preferably present in liquid form under normal conditions (1 atm, 20 ° C.).
- plasticizers (C) are ester compounds selected from the groups of aliphatic or aromatic di- or polycarboxylic acids fully esterified with alkanols and phosphoric acid esterified at least once with alkanol.
- alkanols are d-cio-alkanols.
- Preferred examples of aromatic di- or polycarboxylic acids fully esterified with alkanol are phthalic acid, isophthalic acid and mellitic acid fully esterified with alkanol; examples of his: di-n-octyl phthalate, di-n-nonyl phthalate, di-n-decyl phthalate, di-n-octyl isophthalate, di-n-nonyl isophthalate, di-n-decyl isophthalate.
- Preferred examples of aliphatic di- or polycarboxylic acids fully esterified with alkanol are, for example, dimethyl adipate, diethyl adipate, di-n-butyl adipate, diisobutyl adipate, dimethyl glutarate, dimethyl glutarate, glutarate, glutarate Butyl ester of diisobutyl succinate and mixtures of the above-mentioned compounds.
- Preferred examples of phosphoric acid esterified at least once with alkanol are dC 10 -alkyl-di-C 6 -C 14 -aryl phosphates such as isodecyl diphenyl phosphate.
- plasticizers (C) are aliphatic or aromatic di- or polyols esterified at least once with CC 10 - alkyl carboxylic acid.
- Preferred examples of aliphatic or aromatic di- or polyols esterified at least once with dC 10 -alkylcarboxylic acid is 2,2,4-trimethylpentane-1,3-diol-monoisobutyrate.
- plasticizers (C) are polyesters, obtainable by polycondensation of aliphatic dicarboxylic acid and aliphatic diol, for example adipic acid or succinic acid and 1,2-propanediol, preferably with an M w of 200 g / mol, and polypropylene glycol alkylphenyl ether, preferably with an M w of 450 g / mol.
- plasticizers (C) are polypropylene glycols etherified with two different alcohols and having a molecular weight M w in the range from 400 to 800 g / mol, preferably one of the alcohols can be an alkanol, in particular a dC 10 alkanol and the other alcohol can preferably be an aromatic alcohol, for example o-cresol, m-cresol, p-cresol and in particular phenol.
- Another object of the present invention is the use of the formulations according to the invention for coloring substrates.
- Another object of the present invention is a method for coloring substrates using the formulations according to the invention, hereinafter also referred to as the coloring method according to the invention, and a further subject of the present invention are colored substrates obtainable by a coloring method according to the invention.
- the coloration process according to the invention is carried out by contacting substrates with pigment treated according to the invention in particulate form and then exposing them to actinic radiation.
- actinic radiation For example, electromagnetic rays with a wavelength range from 200 nm to 450 nm are suitable as actinic radiation.
- Substrates contacted with the pigment treated according to the invention in particulate form can be exposed to actinic radiation with an energy in the range from 70 mJ / cm 2 to 1500 mJ / cm 2 .
- Actinic radiation can be introduced continuously or in the form of lightning, for example.
- a proportion of UV-C radiation of 250-260 nm wavelength is important so that crosslinking via the benzophenone group can occur.
- substrates are, for example, cellulose-containing materials such as paper, cardboard, cardboard, wood and wood-based materials, which can also be lacquered or otherwise coated, metallic materials such as foils, sheets or workpieces made of aluminum, iron, copper, silver, gold Zinc or alloys of these metals, which can be coated or otherwise coated, silicate materials such as glass, porcelain and ceramics, which can be coated, - polymeric materials of any kind such as polystyrene, polyamides, polyesters, polyethylene, polypropylene, melamine resins, polyacrylates, Polyacrylonitrile, polyurethanes, polycarbonates, polyvinyl chloride, polyvinyl alcohols, polyvinyl acetates, polyvinyl pyrrolidones and corresponding copolymers and block copolymers, biodegradable polymers and natural polymers such as gelatin, food and cosmetics
- leather is to be understood as pre-tanned, tanned and, if appropriate, retanned leather or correspondingly processed synthetic exchange material, which may have already been treated with at least one dye during at least one tanning step.
- leather in the context of the present invention can already be hydrophobicized or greased.
- textile or textile substrates are to be understood as meaning textile fibers, textile semifinished and finished products and finished goods produced therefrom, which, in addition to textiles for the clothing industry, also include carpets and other home textiles and textile structures serving technical purposes.
- This also includes unshaped structures such as flakes, line-shaped structures such as twine, threads, yarns, linen, cords, ropes, twists and body structures such as felts, fabrics, nonwovens and wadding.
- the textiles can be of natural origin, for example cotton, wool or flax, or synthetic, for example polyamide, polyester, modified polyester, polyester blend fabric, polyamide blend fabric, polyacrylonitrile, viscose, triacetate, acetate, polycarbonate, polypropylene, polyvinyl chloride, polyester microfibers and glass fiber fabric.
- the inventive method for coloring substrates is an inventive method for printing substrates by the ink-jet method.
- Another object of the present invention is the use of formulations according to the invention as or for the production of inks for the ink jet process.
- Another object of the present invention is a process for the production of inks for the ink jet process using formulations according to the invention.
- Another object of the present invention are inks for the ink jet process, produced using formulations according to the invention.
- the formulations according to the invention can be used as such to produce inks for the inkjet process according to the invention and also the pigments treated according to the invention separated from the dispersions according to the invention.
- Inks according to the invention for the ink jet process can be produced particularly easily by diluting formulations according to the invention with water, for example, and optionally mixing them with additives.
- an ink according to the invention for the ink jet process contains in the range from 1 to 50 g / 100 ml, preferably 1.5 to 15 g / 100 ml, of pigment treated according to the invention in particulate form.
- Colorant preparations according to the invention and in particular inks according to the invention for the ink jet process can contain organic solvents as additives.
- Organic solvents as additives.
- Low molecular weight polytetrahydrofuran is a preferred additive; it can be used alone or preferably in a mixture with one or more difficult to evaporate, water-soluble or water-miscible organic solvents.
- the preferably used low molecular weight polytetrahydrofuran usually has an average molecular weight M w of 150 to 500 g / mol, preferably 200 to 300 g / mol and particularly preferably approximately 250 g / mol (corresponding to a molecular weight distribution).
- Polytetrahydrofuran can be prepared in a known manner via cationic polymerization of tetrahydrofuran. This creates linear polytetramethylene glycols.
- Suitable solvents are polyhydric alcohols, preferably unbranched and branched polyhydric alcohols having 2 to 8, in particular 3 to 6, carbon atoms, such as ethylene glycol, 1, 2- and 1, 3-propylene glycol, glycerol, erythritol, pentaerythritol, pentites such as arabitol, adonite and xylitol and hexites such as sorbitol, mannitol and dulcitol.
- Other suitable solvents are polyethylene and polypropylene glycols, including the lower polymers (di-, tri- and tetramers), and their mono- (especially dC 6 -, especially C 1 -C 4 -) alkyl ethers.
- Examples include di-, tri- and tetraethylene glycol, diethylene glycol monomethyl, ethyl, propyl and butyl ether, triethylene glycol monomethyl, ethyl, propyl and butyl ether, di-, tri- and tetra-1,2 - and -1, 3-propylene glycol and di-, tri- and tetra-1, 2- and -1, 3-propylene glycol monomethyl, ethyl, propyl and butyl ether.
- pyrrolidone and N-alkylpyrrolidones are also suitable as solvents.
- pyrrolidone and N-alkylpyrrolidones the alkyl chain of which preferably contains 1 to 4, especially 1 to 2, carbon atoms.
- suitable alkylpyrrolidones are N-methylpyrrolidone, N-ethylpyrrolidone and N- (2-hydroxyethyl) pyrrolidone.
- solvents examples include 1,2- and 1,3-propylene glycol, glycerol, sorbitol, diethylene glycol, polyethylene glycol (M w 300 to 500 g / mol), diethylene glycol monobutyl ether, triethylene glycol monobutyl ether, pyrrolidone, N-methylpyrrolidone and N- ( 2-hydroxyethyl) pyrrolidone.
- Polytetrahydrofuran can also be mixed with one or more (e.g. two, three or four) of the solvents listed above.
- inks of the invention for the ink jet process can contain 0.1 to 80% by weight, preferably 5 to 60% by weight, particularly preferably 10 to 50% by weight, and very particularly preferably 10 to 30 wt .-%, contain non-aqueous solvents.
- Non-aqueous solvents as additives in particular also the particularly preferred solvent combinations mentioned, can advantageously be supplemented by urea (generally 0.5 to 3% by weight, based on the weight of the colorant preparation), which still has the water-retaining effect of the solvent mixture strengthened.
- urea generally 0.5 to 3% by weight, based on the weight of the colorant preparation
- Inks for the ink jet process according to the invention can contain further auxiliaries, such as are customary in particular for aqueous ink jet inks and in the printing and coating industry.
- auxiliaries such as are customary in particular for aqueous ink jet inks and in the printing and coating industry.
- preservatives such as 1, 2- Benzisothiazolin-3-one (commercially available as Proxel brands from Avecia Lim.) And its alkali metal salts, glutardialdehyde and / or tetramethylolacetylene diurea, Protectole®, antioxidants, degasifiers / defoamers such as acetylene diols and ethoxylated acetylenediols Contain 20 to 40 moles of ethylene oxide per mole of acetylenediol and can also have a dispersing effect, viscosity regulators, leveling agents, wetting agents (e.g.
- wetting surfactants based on ethoxylated or propoxylated fatty or oxo alcohols, propylene oxide / ethylene oxide block copolymers, Ethoxylates of oleic acid or alkylphenols, alkylphenol ether sulfates, alkylpolyglycosides, alkylphosphonates, alkylphenylphosphonates, alkylphosphates, alkylphenylphosphates or preferably polyether siloxane copolymers, in particular alkoxylated 2- (3-hydroxypropyl) hepta-methyltrisiloxanes, which generally contain 7 to 20 blocks , preferably have 7 to 12, ethylene oxide units and a block of 2 to 20, preferably 2 to 10 propylene oxide units and can be present in the colorant preparations in amounts of 0.05 to 1% by weight), anti-settling agents, gloss improvers, lubricants , Adhesion improvers, skin-preventing agents, matting agents, emuls
- these agents are part of colorant preparations according to the invention and in particular inks according to the invention for the ink jet process, their total amount is generally 2% by weight, in particular 1% by weight, based on the weight of the colorant preparations according to the invention and in particular that Inks according to the invention for the inkjet process.
- inks according to the invention for the ink jet process have a dynamic viscosity of 2 to 80 mPa-s, preferably 3 to 20 mPa-s, measured at 25 ° C.
- the surface tension of inks according to the invention for the ink jet process is generally 24 to 70 mN / m, in particular 25 to 60 mN / m, measured at 25 ° C.
- the pH of inks according to the invention for the ink jet process is generally 5 to 10, preferably 7 to 9.
- Another aspect of the present invention is a method for printing flat or three-dimensional substrates by the ink-jet method using Use of the inks according to the invention for the ink jet process.
- ink-jet inks according to the invention are printed on substrate and the print obtained is then fixed by radiation curing.
- the ink jet process the usually aqueous inks are sprayed directly onto the substrate in small droplets.
- pressure is exerted on the ink either by means of a piezoelectric crystal or a heated cannula (bubble or thermo-jet method) and ink drops are thus ejected.
- Such procedures are in text. Chem. Color, volume 19 (8), pages 23 to 29, 1987, and volume 21 (6), pages 27 to 32, 1989.
- the inks according to the invention are particularly suitable for the bubble jet process and for the process using a piezoelectric crystal.
- the inventive method for coloring textile substrates is an inventive method for textile printing.
- dye liquors for pigment dyeing or printing pastes for pigment printing are produced from the formulations described above.
- the present invention thus furthermore relates to a process for the production of dye liquors for pigment dyeing and for the production of printing pastes for pigment printing, and to the dyeing liquors and printing pastes according to the invention, hereinafter also referred to as production processes according to the invention.
- the production process according to the invention comprises the steps of mixing at least one dispersion according to the invention with auxiliaries required for the dyeing or printing process and adjusting the colorant content by dilution with water.
- the water used to carry out the manufacturing process according to the invention does not have to be completely desalinated.
- the rule is that partially demineralized water or very soft water is used, for example at 4 ° dH or less. If water is not sufficiently soft, complexing agents (water softeners) are usually used to reduce the water hardness. In general, compounds which mask Ca 2+ and Mg 2+ ions are suitable as water softeners in the pigment dyeing process.
- Particularly suitable water softeners are, for example, nitrilotriacetic acid, ethylenediaminetetraacetic acid, diethylenetriaminepentaacetic acid, hydroxyethylethylenediaminetriacetic acid or methylglycinediacetic acid.
- the amount of water added to produce the dye liquor depends on the color depth to be achieved on the textile on one side and the amount of dye liquor applied to the textile by means of a padding on the other side.
- Dyeing liquors according to the invention may also contain auxiliaries.
- Preferred auxiliaries are organic solvents in concentrations of 0 to 10% by weight, preferably 0.1 to 5% by weight.
- suitable solvents are polyethylene glycols and single etherified alkylene glycol or single etherified polyethylene glycols such as diethylene glycol mono-n-butyl ether.
- Dyeing liquors according to the invention can furthermore contain wetting agents, preferably low-foaming wetting agents, since, in the event of high turbulence in the dyeing process, foam formation can impair the quality of the dyeing due to the formation of irregularities.
- wetting agents used are: ethoxylation and / or propoxylation products of fatty alcohols or propylene oxide-ethylene oxide block copolymers, ethoxylated or propoxylated fatty or oxo alcohols, furthermore ethoxylates of oleic acid or alkylphenols, alkylphenol ether sulfates, alkylpolyglycosides, alkylphosphonates, alkylphenylphosphonates Alkyl phosphates, or alkylphenyl phosphates.
- Deaerators are based, for example, on polyether siloxane copolymers or on phosphoric acid esters. They can be contained in the dyeing liquors according to the invention in amounts of 0.01 to 2 g / l
- Dyeing liquors according to the invention can also be added as an aid to improve one or more handles.
- These are usually polysiloxanes or waxes based on polyethylene or polyethylene glycol. Polysiloxanes have the advantage of permanence, while some waxes can be washed out slowly during use. In one embodiment of the present invention, however, the addition of grip improvers can be dispensed with.
- the dynamic viscosity of the dyeing liquors according to the invention is in the range of less than 100 mPa-s, measured at 20 ° C.
- the surface tensions of the dyeing liquors according to the invention are to be adjusted so that wetting of the goods is possible. Surface tensions of less than 50 mN / m, measured at 20 ° C, are suitable.
- the production method according to the invention usually comprises mixing at least one formulation according to the invention with one or more auxiliaries listed above, such as solvents, defoamers, grip improvers, emulsifiers and / or biocides, and filling with water.
- the method usually comprises stirring the components in a mixing container, the size and shape of the mixing container being uncritical. Clarification is preferably followed by stirring.
- Another aspect of the present invention is a method for dyeing textile substrates using the dye liquors according to the invention described above.
- the process can be carried out in common machines.
- Foulards are preferred which contain two pressed rollers as an essential element through which the textile is guided.
- the liquid is filled in above the rollers and wets the textile.
- the textile is squeezed off by the pressure and a constant application is guaranteed.
- the textile is guided over a deflection roller through a trough with the dye liquor. Excess liquor is then pressed off via a pair of rollers, which is attached above the liquor, thus ensuring a constant application.
- the actual dyeing step is usually followed by thermal drying and fixing, preferably drying at temperatures from 50 to 90 ° C. over a period of 30 seconds to 3 minutes and then fixing by exposure to actinic radiation.
- a process for pigment coloring is preferred after the logging process.
- the printed and colored substrates are characterized by a special brilliance of the colors and at the same time an excellent grip of the printed or colored substrates.
- Another aspect of the present invention is therefore substrates, colored by the process described above using the dye liquors according to the invention.
- Another aspect of the present invention is the use of formulations according to the invention for textile printing.
- at least one formulation according to the invention is incorporated into a printing paste for this purpose.
- the printing paste according to the invention for textile printing is advantageously produced by mixing at least one formulation according to the invention by mixing with auxiliaries commonly used in the printing process and then adjusting the colorant content by diluting with water.
- Natural or synthetic thickeners can be used as thickeners. It is preferred to use synthetic thickeners, for example generally liquid solutions of synthetic polymers in, for example, white oil or as aqueous solutions.
- Printing pastes according to the invention can furthermore contain grip improvers which are usually selected from silicones, in particular polydimethylsiloxanes, and fatty acid esters.
- grip improvers which are usually selected from silicones, in particular polydimethylsiloxanes, and fatty acid esters.
- Examples of commercially available grip improvers that can be added to the printing pastes according to the invention are Acramin® Weichma- rather SI (Bayer AG), Luprimol SIG® and Luprimol CW® (BASF Aktiengesellschaft).
- Printing pastes according to the invention can be added as further additives, one or more emulsifiers, especially when the pastes contain thickeners containing white oil and are obtained as an oil-in-water emulsion.
- suitable emulsifiers are aryl- or alkyl-substituted polyglycol ethers.
- Commercially available examples of suitable emulsifiers are Emulsifier W® (Bayer), Luprintol PE New® and Luprintol MIP® (BASF Aktiengesellschaft), and Solegal W® (Hoechst AG).
- Pigment printing using at least one formulation according to the invention can be carried out by various methods which are known per se.
- the pigment printing process according to the invention using printing pastes according to the invention delivers printed substrates with particularly high brilliance and depth of color of the prints with an excellent grip of the printed substrates at the same time.
- the present invention therefore relates to substrates printed by the method according to the invention using the printing pastes according to the invention.
- the coloring process according to the invention is a process for finishing leather.
- the aim of finishing leather, also called coating leather, is to give leather the desired look, special haptic properties as well
- the coloration process according to the invention is based on pretanned, tanned and, if appropriate, retanned leather, which can be hydrophobicized and dyed in a manner known per se.
- At least one colored finishing dispersion which contains one or more pigments treated in particulate form according to the invention, is applied to the leather to be colored in an amount of 20 to 100 g of solid per m 2 of leather surface.
- the application can be carried out by methods known per se, for example plush, ie application with a sponge or a brush-like device, which can be covered with plush or velvet fabric, by brushing, roll coating, pouring, spraying or spraying.
- the leather treated in this way can then be dried, for example at a temperature in the range from 30 to 120 ° C., preferably 60 to 80 ° C.
- At least one colored dressing dispersion can be applied in one or more steps, which can be carried out identically or differently and can be interrupted in each case by intermediate drying at the above-mentioned temperatures.
- a colored dressing dispersion used according to the invention contains at least one formulation according to the invention.
- Colored dressing dispersions used according to the invention which are also referred to below as colored dressing dispersions according to the invention, are usually aqueous. They can contain other, non-aqueous solvents such as ethylene glycol, N-methylpyrrolidone, 3-methoxypropanol and propylene carbonate.
- primer dispersions according to the invention contain the following constituents:
- ⁇ l) at least one formulation according to the invention preferably 20 to 70% by weight, based on the total weight of the colored dressing dispersion according to the invention;
- MIT 2-methyl-2H-isothiazol-3
- CIT Chlor-2-methyl-2H-isothiazoI-3-one
- Colored finishing dispersions according to the invention can furthermore contain at least one filler and anti-adhesive.
- aqueous formulations of fatty acid esters, protein and inorganic fillers, which can be selected from silicates and clay minerals, are suitable.
- Colored finishing dispersions according to the invention can have a solids content of 10 to 80% by weight, 20 to 50% by weight being preferred.
- a top layer can then be applied by methods known per se.
- the cover layer can consist of conventional components.
- the top layer ⁇ 2) contains at least one formulation according to the invention, preferably 20 to 70% by weight, based on the total weight of the top layer according to the invention, ⁇ 2) at least one wax, such as, for example, oxidized polyethylene wax or montan wax or silicone wax, preferably 1 to 15% by weight, based on the total weight of the top layer according to the invention; ⁇ 2) optionally at least one biocide, for example selected from MIT, BIT and CIT, for example in the amounts mentioned for primer dispersions, 52) optionally at least one pigment in particulate form, ⁇ 2) optionally at least one thickener.
- ⁇ 2 contains at least one formulation according to the invention, preferably 20 to 70% by weight, based on the total weight of the top layer according to the invention, ⁇ 2) at least one wax, such as, for example, oxidized polyethylene wax or montan wax or silicone wax, preferably 1 to 15% by weight, based on the total weight of the top layer according to the invention; ⁇ 2) optionally at least one biocide,
- a finish also called a finish dispersion
- a finish can then be applied, with a finish of about 5 to 30 g / m 2 of leather surface being applied.
- the finish or top coat serves to protect the leather and, in addition to high flexibility, should also ensure good scratch resistance, oil and water resistance.
- finishes can include, for example: formulations of at least one binder based on acrylate or polyurethane, a crosslinking agent, protein, nitrocellulose emulsion, fillers based on organic or inorganic matting agents, silicone wax, fatty acid esters.
- Finishing dispersions according to the invention can contain polyurethane dispersions known per se, produced according to EP-A2 0 392 352.
- Top layers and finishing dispersions can contain one or more thickeners.
- Crosslinkable copolymers based on acrylic acid and acrylamide and thickeners based on polyurethane or polyvinylpyrrolidone or acrylate (co) polymers may be mentioned as examples.
- At least one formulation according to the invention is used in at least one step - priming, application of the top layer and finishing.
- Finishing dispersions can contain one or more thickeners.
- Crosslinkable copolymers based on acrylic acid and acrylamide may be mentioned as examples. Preferred examples are copolymers with 85 to 95% by weight of acrylic acid, 4 to 14% by weight of acrylamide and about 1% by weight of the (meth) acrylamide derivative of the formula VIII
- the mixture was stirred for a further 30 minutes at 85 ° C. and then, for chemical deodorization (residual monomer removal), simultaneously a solution of 5 g of tert-butyl hydroperoxide (70% by weight in water) in 11 g distilled water and a solution of 3 g HO-CH 2 -O-SO 2 Na in 12 g distilled water were metered in over a period of 90 minutes.
- the mixture was then cooled to room temperature and the pH was adjusted to 7 using 25% by weight aqueous ammonia.
- the photoinitiators FP1 to FP4 were dissolved in methyl methacrylate.
- aqueous dispersion containing pigment treated according to the invention in particulate form was obtained.
- the solids content was 35% by weight and the dynamic viscosity was 18 mPa-s.
- the determination of the particle diameter distribution gave a maximum at 156 nm.
- the ink 3.1 according to the invention showed a dynamic viscosity of 4 mPa-s, measured at 25 ° C., and was suitable for printing in common printers.
- the ink 3.1 according to the invention was printed on cotton (100% cotton, 250 g / m 2 ) in the form of samples. After drying at 100 ° C and immediate UV exposure (2 x 120 W / cm, 10 m / min, UV spectrum of 250-450 nm), the printed cotton showed excellent fastness to use.
- the ink 3.2 according to the invention was printed on cotton (100% cotton, 250 g / m 2 ) in the form of samples. After drying at 100 ° C and immediate UV exposure (2 x 120 W / cm, 10 m / min, UV spectrum of 250-450 nm), the printed cotton showed excellent fastness to use.
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Ink Jet (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Paints Or Removers (AREA)
Abstract
Description
Claims
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2006534649A JP2007508429A (ja) | 2003-10-14 | 2004-10-08 | 顔料配合物および基材の着色にこの配合物を使用する方法 |
EP04765888A EP1675914A1 (de) | 2003-10-14 | 2004-10-08 | Formulierungen und ihre verwendung bei der kolorierung von substraten |
US10/575,719 US20070054979A1 (en) | 2003-10-14 | 2004-10-08 | Formulations and their use in the coloration of substrates |
BRPI0415245-0A BRPI0415245A (pt) | 2003-10-14 | 2004-10-08 | formulação, uso da mesma, processo para coloração de substratos, substrato colorido, tinta para processo de jato de tinta, pasta de impressão para impressão têxtil, e, pigmento em forma particulada |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10348464.7 | 2003-10-14 | ||
DE10348464A DE10348464A1 (de) | 2003-10-14 | 2003-10-14 | Formulierungen und ihre Verwendungen bei der Kolorierung von Substraten |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2005037930A1 true WO2005037930A1 (de) | 2005-04-28 |
Family
ID=34442079
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2004/011253 WO2005037930A1 (de) | 2003-10-14 | 2004-10-08 | Formulierungen und ihre verwendung bei der kolorierung von substraten |
Country Status (7)
Country | Link |
---|---|
US (1) | US20070054979A1 (de) |
EP (1) | EP1675914A1 (de) |
JP (1) | JP2007508429A (de) |
CN (1) | CN1867638A (de) |
BR (1) | BRPI0415245A (de) |
DE (1) | DE10348464A1 (de) |
WO (1) | WO2005037930A1 (de) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006066808A1 (de) * | 2004-12-20 | 2006-06-29 | Basf Aktiengesellschaft | Verfahren zum kolorieren von zellulosehaltigen substraten |
WO2006066809A1 (de) * | 2004-12-20 | 2006-06-29 | Basf Aktiengesellschaft | Verfahren zum bedrucken oder kolorieren von substraten |
EP2507330A1 (de) * | 2009-12-04 | 2012-10-10 | Hewlett-Packard Development Company, L.P. | Einzelchargen-latextintenzusammensetzungen und verfahren |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102127312A (zh) * | 2010-12-07 | 2011-07-20 | 江南大学 | 一种Lyocell纤维原液着色用超细包覆颜料色浆的制备方法 |
JP2016527379A (ja) * | 2013-08-06 | 2016-09-08 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーE.I.Du Pont De Nemours And Company | セルロースと相互作用する成分を有する水性顔料分散体 |
CN104140713A (zh) * | 2014-08-05 | 2014-11-12 | 厦门格林泰新材料科技有限公司 | 一种水性油墨及其制备方法与应用 |
WO2017109786A1 (en) | 2015-12-23 | 2017-06-29 | Kornit Digital Ltd. | Rub-resistant inkjet composition |
Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63230705A (ja) * | 1987-03-19 | 1988-09-27 | Toyobo Co Ltd | 紫外線硬化型樹脂組成物 |
US4959297A (en) * | 1987-12-09 | 1990-09-25 | Minnesota Mining And Manufacturing Company | Ternary photoinitiator system for addition polymerization |
JPH04363309A (ja) * | 1991-06-11 | 1992-12-16 | Brother Ind Ltd | 光硬化型組成物 |
EP0528602A1 (de) * | 1991-08-16 | 1993-02-24 | Ciba-Geigy Ag | Verfahren zur Verbesserung der Lagerungsstabilität von Pigmenten |
JPH05140208A (ja) * | 1991-11-20 | 1993-06-08 | Dainippon Ink & Chem Inc | 活性エネルギー線硬化性組成物 |
JP2001072887A (ja) * | 1999-07-06 | 2001-03-21 | Kao Corp | カプセル化着色顔料 |
WO2002026892A1 (de) * | 2000-09-26 | 2002-04-04 | Basf Aktiengesellschaft | Verfahren zur herstellung von polymerumhüllten pigmentteilchen durch präzipitation |
WO2002048272A1 (en) * | 2000-12-15 | 2002-06-20 | Ucb S.A. | Surface functionalization of pigments and/or dyes for radiation curable ink printing and coating applications |
DE19680301C2 (de) * | 1995-03-15 | 2002-12-05 | Fujitsu Isotec Ltd | Pigmenthaltige Tinte für Tintenstrahldrucker |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4689049A (en) * | 1985-07-23 | 1987-08-25 | Spectrachem Corporation | Pigment print paste with improved adhesion characteristics |
US4981882A (en) * | 1989-03-31 | 1991-01-01 | Union Carbide Chemicals And Plastics Company Inc. | Method for enhancing encapsulation efficiency in coating particles in aqueous dispersions |
ES2121136T3 (es) * | 1993-12-14 | 1998-11-16 | Canon Kk | Tinta, metodo para la impresion por chorros de tinta e instrumento que utiliza la misma. |
DE19727767A1 (de) * | 1997-06-30 | 1999-01-07 | Basf Ag | Als Ink-Jet-Tinten geeignete Pigmentzubereitungen mit strahlungshärtbarem Bindemittel |
DE59805715D1 (de) * | 1997-06-30 | 2002-10-31 | Basf Ag | Pigmentzubereitungen für das ink-jet-verfahren |
JP3893262B2 (ja) * | 2000-09-14 | 2007-03-14 | キヤノン株式会社 | 水性光硬化型樹脂組成物、水性インク、インクカートリッジ、記録ユニット及びインクジェット記録装置 |
-
2003
- 2003-10-14 DE DE10348464A patent/DE10348464A1/de not_active Withdrawn
-
2004
- 2004-10-08 CN CNA2004800299588A patent/CN1867638A/zh active Pending
- 2004-10-08 US US10/575,719 patent/US20070054979A1/en not_active Abandoned
- 2004-10-08 JP JP2006534649A patent/JP2007508429A/ja not_active Withdrawn
- 2004-10-08 BR BRPI0415245-0A patent/BRPI0415245A/pt not_active IP Right Cessation
- 2004-10-08 WO PCT/EP2004/011253 patent/WO2005037930A1/de active Application Filing
- 2004-10-08 EP EP04765888A patent/EP1675914A1/de not_active Withdrawn
Patent Citations (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63230705A (ja) * | 1987-03-19 | 1988-09-27 | Toyobo Co Ltd | 紫外線硬化型樹脂組成物 |
US4959297A (en) * | 1987-12-09 | 1990-09-25 | Minnesota Mining And Manufacturing Company | Ternary photoinitiator system for addition polymerization |
JPH04363309A (ja) * | 1991-06-11 | 1992-12-16 | Brother Ind Ltd | 光硬化型組成物 |
EP0528602A1 (de) * | 1991-08-16 | 1993-02-24 | Ciba-Geigy Ag | Verfahren zur Verbesserung der Lagerungsstabilität von Pigmenten |
JPH05140208A (ja) * | 1991-11-20 | 1993-06-08 | Dainippon Ink & Chem Inc | 活性エネルギー線硬化性組成物 |
DE19680301C2 (de) * | 1995-03-15 | 2002-12-05 | Fujitsu Isotec Ltd | Pigmenthaltige Tinte für Tintenstrahldrucker |
JP2001072887A (ja) * | 1999-07-06 | 2001-03-21 | Kao Corp | カプセル化着色顔料 |
WO2002026892A1 (de) * | 2000-09-26 | 2002-04-04 | Basf Aktiengesellschaft | Verfahren zur herstellung von polymerumhüllten pigmentteilchen durch präzipitation |
WO2002048272A1 (en) * | 2000-12-15 | 2002-06-20 | Ucb S.A. | Surface functionalization of pigments and/or dyes for radiation curable ink printing and coating applications |
Non-Patent Citations (4)
Title |
---|
DATABASE WPI Section Ch Week 198844, Derwent World Patents Index; Class A82, AN 1988-312248, XP002315636 * |
DATABASE WPI Section Ch Week 199305, Derwent World Patents Index; Class A12, AN 1993-039377, XP002315638 * |
DATABASE WPI Section Ch Week 199327, Derwent World Patents Index; Class A18, AN 1993-216827, XP002315637 * |
DATABASE WPI Section Ch Week 200122, Derwent World Patents Index; Class A96, AN 2001-159265, XP002315639 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006066808A1 (de) * | 2004-12-20 | 2006-06-29 | Basf Aktiengesellschaft | Verfahren zum kolorieren von zellulosehaltigen substraten |
WO2006066809A1 (de) * | 2004-12-20 | 2006-06-29 | Basf Aktiengesellschaft | Verfahren zum bedrucken oder kolorieren von substraten |
EP2507330A1 (de) * | 2009-12-04 | 2012-10-10 | Hewlett-Packard Development Company, L.P. | Einzelchargen-latextintenzusammensetzungen und verfahren |
EP2507330A4 (de) * | 2009-12-04 | 2013-05-15 | Hewlett Packard Development Co | Einzelchargen-latextintenzusammensetzungen und verfahren |
Also Published As
Publication number | Publication date |
---|---|
BRPI0415245A (pt) | 2006-12-12 |
US20070054979A1 (en) | 2007-03-08 |
EP1675914A1 (de) | 2006-07-05 |
DE10348464A1 (de) | 2005-05-19 |
JP2007508429A (ja) | 2007-04-05 |
CN1867638A (zh) | 2006-11-22 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1749129B1 (de) | Verfahren zur behandlung von flexiblen substraten | |
EP2183327B1 (de) | Wässrige pigmentpräparationen mit anionischen additiven auf allyl- und vinyletherbasis | |
EP1834032A1 (de) | Verfahren zum bedrucken oder kolorieren von substraten | |
EP1697434A1 (de) | Mit polyadditionsprodukten umhüllte pigmente, verfahren zu ihrer herstellung und ihre verwendung | |
CN101880494A (zh) | 喷墨记录用墨液组合物 | |
WO2005083017A1 (de) | Aufzeichnungsflüssigkeiten | |
DE60216276T2 (de) | Disspersionszusammensetzung und diese enthaltende tintenstrahldruckertinte | |
DE60223742T2 (de) | Verfahren zur herstellung von farbmittel-verbundpartikeln | |
EP1641884B1 (de) | verfahren zur behandlung von pigmenten in partikulärer form | |
EP1692228A1 (de) | Farbmittelzubereitungen | |
EP1723205A2 (de) | Aufzeichnungsflüssigkeiten | |
DE60205709T2 (de) | Ink Jet Farbzusammensetzung und Druckverfahren | |
EP1675914A1 (de) | Formulierungen und ihre verwendung bei der kolorierung von substraten | |
EP2176308B1 (de) | Wässrige dispersionen, ihre herstellung und ihre verwendung | |
DE102004058271A1 (de) | Verwendung von wässrigen Dispersionen von wasserlöslichen (Co)polymerisaten von mindestens einem ethylenisch ungesättigten Monomer MON zur Herstellung von Textilhilfsmitteln | |
EP2162582A2 (de) | Wässrige formulierungen und ihre verwendung zum kolorieren oder beschichten von substraten | |
WO2005087880A1 (de) | Formulierungen und ihre verwendung zur behandlung von flexiblen substraten | |
DE102005038358A1 (de) | Verfahren zur Herstellung von Pigmentzubereitungen | |
DE102004054034A1 (de) | Verwendung von wässrigen Dispersionen von wasserlöslichen (Co)polymerisaten von mindestens einem ethylenisch ungesättigten Monomer MON zur Herstellung von Tex-tilhilfsmitteln | |
EP1659153A1 (de) | Verwendung von wässrigen Dispersionen von wasserlöslichen (Co)polymerisaten von mindestens einem ethylenisch ungesättigten Monomer MON zur Herstellung von Textilhilfsmitteln | |
DE10328716A1 (de) | Verfahren zur Behandlung von Pigmenten in partikulärer Form | |
WO2005028570A2 (de) | Formulierungen und ihre verwendung bei der beschichtung von substraten | |
DE10330412A1 (de) | Verfahren zur Behandlung von Pigmenten in partikulärer Form und Verwendung derselben bei der Kolorierung von Textil | |
DE10340777A1 (de) | Verfahren zur Behandlung von Pigmenten in partikulärer Form und Verwendung derselben bei der Kolorierung vo Leder |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
WWE | Wipo information: entry into national phase |
Ref document number: 200480029958.8 Country of ref document: CN |
|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2004765888 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2007054979 Country of ref document: US Ref document number: 10575719 Country of ref document: US Ref document number: 2006534649 Country of ref document: JP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 1664/CHENP/2006 Country of ref document: IN |
|
WWP | Wipo information: published in national office |
Ref document number: 2004765888 Country of ref document: EP |
|
ENP | Entry into the national phase |
Ref document number: PI0415245 Country of ref document: BR |
|
WWP | Wipo information: published in national office |
Ref document number: 10575719 Country of ref document: US |