WO1999046130A1 - Agent ameliorant l'impermeabilite a l'eau pour papier d'impression par jets d'encre et papier d'impression par jets d'encre - Google Patents
Agent ameliorant l'impermeabilite a l'eau pour papier d'impression par jets d'encre et papier d'impression par jets d'encre Download PDFInfo
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- WO1999046130A1 WO1999046130A1 PCT/JP1999/001139 JP9901139W WO9946130A1 WO 1999046130 A1 WO1999046130 A1 WO 1999046130A1 JP 9901139 W JP9901139 W JP 9901139W WO 9946130 A1 WO9946130 A1 WO 9946130A1
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- Prior art keywords
- recording paper
- water resistance
- ink jet
- jet recording
- weight
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- QQSDULDHZPMLLY-UHFFFAOYSA-N sodium 5-[[4-[4-[[2,4-diamino-5-[(4-sulfophenyl)diazenyl]phenyl]diazenyl]phenyl]phenyl]diazenyl]-2-hydroxybenzoic acid Chemical compound C1=CC(=CC=C1C2=CC=C(C=C2)N=NC3=CC(=C(C=C3N)N)N=NC4=CC=C(C=C4)S(=O)(=O)O)N=NC5=CC(=C(C=C5)O)C(=O)O.[Na+] QQSDULDHZPMLLY-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3271—Hydroxyamines
- C08G18/3278—Hydroxyamines containing at least three hydroxy groups
-
- 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
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5245—Macromolecular coatings characterised by the use of polymers containing cationic or anionic groups, e.g. mordants
-
- 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
- B41M5/50—Recording sheets characterised by the coating used to improve ink, dye or pigment receptivity, e.g. for ink-jet or thermal dye transfer recording
- B41M5/52—Macromolecular coatings
- B41M5/5263—Macromolecular coatings characterised by the use of polymers obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- B41M5/5281—Polyurethanes or polyureas
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/08—Processes
- C08G18/0804—Manufacture of polymers containing ionic or ionogenic groups
- C08G18/0809—Manufacture of polymers containing ionic or ionogenic groups containing cationic or cationogenic groups
- C08G18/0814—Manufacture of polymers containing ionic or ionogenic groups containing cationic or cationogenic groups containing ammonium groups or groups forming them
-
- 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
- C08G18/00—Polymeric products of isocyanates or isothiocyanates
- C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
- C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
- C08G18/30—Low-molecular-weight compounds
- C08G18/32—Polyhydroxy compounds; Polyamines; Hydroxyamines
- C08G18/3271—Hydroxyamines
- C08G18/3275—Hydroxyamines containing two hydroxy groups
Definitions
- the present invention relates to a water resistance improver for ink jet recording paper and an ink jet recording paper. More specifically, the present invention relates to a method of mixing a pulp fiber to form a slurry, or impregnating or coating plain paper or coated paper to obtain water-resistant images and characters recorded on recording paper. The present invention relates to a water resistance improver for an ink jet recording paper capable of improving ink repellency and reducing ink bleeding, and an ink jet recording paper coated with the water resistance improver.
- An ink jet printer is a printer that prints by jetting ink from nozzles in a jet shape.
- Ink jet recording is quiet, has no process such as development and fixing, has a simple recording device, can use plain paper or coated paper, and is easy to colorize and free. It has the feature of being able to record images and text and graphics, and has seen rapid growth today, and its future potential is attracting attention.
- the present invention provides a water-resistant ink jet recording paper capable of improving water resistance of images and characters recorded on the recording paper and reducing ink bleeding by coating the paper on plain paper or coated paper.
- Provide ink jet recording paper W was made for the purpose of Disclosure of the invention
- the first embodiment of the water resistance improver for ink jet recording paper of the present invention comprises (A) an organic isocyanate compound having two or more isocyanate groups, and (B) 2 to 10 hydroxyl groups and Z or
- the amine structure of the polyurethane molecule obtained by reacting a tertiary amine compound having an amino group with an equivalent ratio of (isocene group) Z (hydroxyl group and amino group) of 0.5 to 3.0 is obtained. It contains a cationic polyurethane resin obtained by quaternizing a sum or tertiary amine structure.
- the organic isocyanate compound having two or more isocyanate groups used as the component (A) in the present invention is not particularly limited.
- the tertiary amine compound having 2 to 10 hydroxyl groups and / or amino groups used as the component (B) in the present invention includes a compound represented by the general formula [1]. be able to.
- X and Y are 10— or —NH—
- R 1 is an alkyl group having 1 to 4 carbon atoms, a hydroxyalkyl group or an aminoalkyl group having 1 to 4 carbon atoms.
- R 2 and R 3 are an alkylene group having 1 to 4 carbon atoms, and n is 1 to 8.
- X and Y may be different even in the same, R 2 and R 3 may be different dates be the same. Further, when n is 2-8, even more R Masubete same may be a mixture is made different, even if all the plurality of R 3 are different even in the same is a mix Good.
- examples of the diol compound in which X and Y are —0— and R 1 is an alkyl group include N-methyldimethylolamine, N-ethyldimethylolamine, and N-butyldiamine.
- examples of the diamine compound in which X and ⁇ are ——— and R 1 is an alkyl group include, for example, methyliminobisethylamine, ethyliminobisethylamine, and butyliminobisethyl Amine, methyliminobispropylamine, butyliminobispropylamine and the like.
- triol compounds in which X and ⁇ are —0_, R 1 is a hydroxyalkyl group, and ⁇ is 1 include, for example, triethanolamine, tripropanolamine And the like.
- triamine compounds in which X and ⁇ are — ⁇ —, R 1 is an aminoalkyl group, and ⁇ is 1 include, for example, tri (2-aminoethyl) amine and triamine. (2-aminopropyl) amine and the like.
- the tertiary aminated substrate having 2 to 10 hydroxyl groups and ⁇ or amino groups further includes a compound having an amino group such as ethylene diamine, propylene diamine, or the like. And compounds to which propylene oxide, butylene oxide, styrene oxide, epichlorohydrin, tetrahydrofuran and the like are added.
- the tertiary amine compound having 2 to 10 hydroxyl groups and / or amino groups used as the component (B) one kind can be used alone, or two or more kinds can be used. The above can be used in combination.
- the tertiary amine compound used as the component (B) includes N-methylgenolamine, triethanolamine, propylene oxide adduct of ethylenediamine, methyliminobispropylamine, and tri (2-dimethylamine).
- (Aminoethyl) amine can be used particularly preferably.
- an organic isocyanate compound having two or more isocyanate groups and (B) 2 to 10 hydroxyl groups and Z or A tertiary amine compound having an amino group is prepared by adding an (isocynate group) / (hydroxyl group and amino group) equivalent ratio of 0.5 to 3.0, more preferably 0.8 to 1.5.
- an equivalent ratio of Z (hydroxyl group and amino group) is less than 0.5, the effect of improving water resistance may not be sufficiently exhibited.
- the equivalent ratio of Z (hydroxyl group and amino group) exceeds 3.0, the number of isocyanate groups not involved in the reaction increases, and a water-insoluble white powdery compound may be formed.
- the primary, secondary or tertiary amine structure of the obtained polyurethane molecule is neutralized with an acid, or the tertiary amine structure is quaternized with a quaternizing agent.
- the acid used for neutralization is not particularly limited.
- organic acids such as formic acid, acetic acid, propionic acid, butyric acid, lactic acid, malic acid, and citric acid
- inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, and hydrofluoric acid Acids can be mentioned.
- One of these acids can be used alone, or two or more can be used in combination.
- acetic acid can be particularly preferably used.
- the entire amine structure of the polyurethane molecule can be neutralized, or only a part thereof can be neutralized.
- the quaternizing agent used for the quaternization for example, oxylane compounds such as ethylene oxide, propylene oxide, butylene oxide, styrene oxide, and epichlorohydrin, dimethyl sulfate, Ester compounds such as getyl sulfate, methyl para-toluenesulfonate, Examples thereof include halides such as methyl chloride, ethyl chloride, benzyl chloride, methyl bromide, and ethyl promide.
- halides such as methyl chloride, ethyl chloride, benzyl chloride, methyl bromide, and ethyl promide.
- getyl sulfate can be particularly preferably used.
- the entire tertiary amine structure of the polyurethane molecule can be quaternized, or only a part thereof can be quaternized.
- the second embodiment of the water resistance improver for ink jet recording paper of the present invention comprises (A) an organic isocyanate compound having two or more isocyanate groups and (B) 2 to 10 hydroxy groups and / or An isocyanate group of a polyurethane molecule obtained by reacting a tertiary amine compound having an amino group with an equivalent ratio of (isocyanate unit) Z (hydroxyl group and amino group) of more than 1.0 and not more than 3.0. Then, (C) a neutralization of the amine structure of the polyurethane molecule obtained by reacting an amine compound having 1 to 4 hydroxyl groups and Z or an amino group or a quaternization of a tertiary amine structure. Containing a cationic polyurethane resin.
- an organic isocyanate compound having two or more isocyanate groups and (B) a tertiary amine compound having 2 to 10 hydroxyl groups and no or amino groups are Use the same (A) organic isocyanate compound having two or more isocyanate groups and (B) tertiary amine compound having 2 to 10 hydroxyl groups and Z or amino groups described in the first embodiment. be able to.
- an organic isocyanate compound having two or more isocyanate groups and (B) a tertiary amine compound having 2 to 10 hydroxyl groups and / or amino groups are represented by (isocyanate group)
- the polyurethane is synthesized by reacting at an equivalent ratio of / (hydroxyl group and amino group) of more than 1.0 to 3.0 or less, more preferably 1.1 to 1.5.
- (Isocyanate group) If the equivalent ratio of Z (hydroxyl group and amino group) is less than 1.0, the isocyanate group will be exhausted, and 1 to 4 hydroxyl groups and Z or amino or (C) component will be consumed. It may not be possible to react an amine compound having a group.
- (Isocyanate group) H If the equivalent ratio of the (doxyl group and the amino group) exceeds 3.0, the number of isopropyl groups not participating in the reaction increases, and a water-insoluble white powdery compound may be produced.
- (A) an organic isocyanate compound having two or more isocyanate groups and (B) a tertiary amine compound having 2 to 10 hydroxyl groups and Z or an amino group are reacted.
- the (C) amine compound having 1 to 4 hydroxy groups and Z or amino groups is further reacted with the isocyanate group of the obtained polyurethane molecule.
- the amine compound having 1 to 4 hydroxyl groups and / or amino groups to be used as the component (C) is not particularly limited.
- amine having two or more amino groups ethylenediamine 1,2-diaminopropane, 1,3-diaminopropane, diethylenetriamine, triethylenetetramine, tetraethylenepentenemin, iminobispropylamine, p-phenylenediamine, etc. having a hydroxyl group
- tertiary amine compounds include 2-dimethylaminoethanol, 3-dimethylaminopropanol, 2-getylaminoethanol, N-methyl-13-hydroxypiperidine, and N-ethyl-13-hydroxy.
- Amino groups such as hydroxypiperidine, N-methyl-1-hydroxypiperidine, and N-methyl-3-piberidinemethanol
- Examples of the tertiary amine compound having the following structure include 2-dimethylaminoethylamine, 2-ethylaminoethylamine, 3-ethylaminopropylamine, dimethylaminoethoxypropylamine, and N-aminoamine.
- Examples include nomethylbiperidine, N-aminoethylpiperidine, N-aminopropylpiperidine and the like.
- One of these amine compounds can be used alone, or two or more can be used in combination.
- 2-dimethylaminoethanol, N-methylethanolamine, triethanolamine, propylene oxide adduct of ethylenediamine, methyliminobispropylamine, tri (2-aminoethyl) amine and diethylenetriamine Liamine can be particularly preferably used.
- the primary, secondary or tertiary amine structure of the polyurethane molecule obtained by reacting the component (A) and the component (B) and further reacting the component (C) is changed with an acid.
- the acid used for the addition can be organic acids such as formic acid, acetic acid, propionic acid, butyric acid, lactic acid, malic acid, and citric acid, and inorganic acids such as hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, and hydrofluoric acid Acids can be mentioned.
- acetic acid can be particularly preferably used.
- the amine structure of the polyurethane molecule can be completely neutralized, or can be partially neutralized.
- the quaternizing agent used for the quaternization and examples thereof include oxylane compounds such as ethylene oxide, propylene oxide, butylene oxide, styrene oxide, and epichlorohydrin, dimethyl sulfate, and methyl sulfide.
- ester compounds such as sulfuric acid and methyl p-toluenesulfonate
- halides such as methyl chloride, ethyl chloride, benzyl chloride, methyl bromide and ethyl bromide.
- One of these quaternizing agents can be used alone, or two or more can be used in combination.
- getyl sulfate can be particularly preferably used.
- the tertiary amine structure of the polyurethane molecule can be entirely quaternized, or only a part thereof can be quaternized.
- a tin catalyst or an amine catalyst can be used as a promoter.
- a tin-based catalyst is not particularly limited, and examples thereof include dibutyltin dilaurate and stannasquatate.
- the amine catalyst examples thereof include triethylenediamine, triethylamine, tetramethylpropanediamine, tetramethylbutanediamine, and N-methylmorpholine.
- the reaction between (A) an organic isocyanate compound having two or more isocyanate groups and (B) a tertiary amine compound having 2 to 10 hydroxyl groups and Z or an amino group is zero.
- the reaction can be carried out in a solvent, or directly for the reaction of the isocyanate group for the purpose of suppressing the reaction of the reaction system and controlling the base viscosity. It can also be carried out in the presence of an organic solvent that does not participate.
- organic solvent examples include ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, and diisobutyl ketone, methyl formate, ethyl formate, propyl formate, butyl formate, methyl acetate, ethyl acetate, and acetic acid.
- ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, and diisobutyl ketone
- methyl formate ethyl formate
- propyl formate propyl formate
- butyl formate methyl acetate
- ethyl acetate methyl ethyl acetate
- acetic acid such as propyl, butyl acetate, methyl propionate, ethyl propionate, and butyl propionate
- nitrogen compound solvents such as N, N-dimethylformamide and N-methylpyrrol
- the amino group is reacted by reacting the isocyanate group with water.
- the reaction conditions for the isocyanate groups and water are not particularly limited.For example, polyurethane in which the isocyanate groups remain is dissolved or dispersed in an excessive amount of water, and the temperature is from room temperature to 60 ° C, more preferably 30 to 40 ° C. By reacting at 50 ° C for 0.5 to 5 hours, more preferably 1 to 3 hours, the isocyanate group can be decomposed and converted to an amino group. By converting the isocyanate group into an amino group, the stability of the water resistance improver for ink jet recording paper can be improved.
- the form of the water resistance improver for ink jet recording paper of the present invention is not particularly limited.
- the amine structure is neutralized or the tertiary amine structure is quaternized, and if necessary, unreacted isocyanate is used.
- the cationic polyurethane resin decomposed by reacting a single group with water may be dissolved or dispersed in an aqueous medium.
- the aqueous medium is not particularly limited, and may be, for example, a medium obtained by adding a polar organic solvent to water.
- the polar organic solvent to be added is not particularly limited.
- the water resistance improver for ink jet recording paper of the present invention may contain a known binder, inorganic pigment, organic pigment and the like, if necessary.
- the binder include oxidized starch and polyvinyl alcohol.
- Inorganic pigments include, for example, light calcium carbonate, heavy calcium carbonate, kaolin (white clay), tanolek, calcium sulfate, barium sulfate, titanium oxide, zinc oxide, zinc sulfate, zinc carbonate, satin white, aluminum silicate, and cesium oxide.
- Examples include earth, calcium silicate, synthetic silica, aluminum hydroxide, alumina, and lithopone.
- the organic pigment include styrene-based plastic pigment, acrylic-based plastic pigment, and urea resin pigment.
- the method of using the water resistance improver for the ink jet recording paper of the present invention For example, pulp that has been refined in a mixing chest at the time of preparation of the stock, together with fillers, chemicals, dyes, etc. Papermaking can be performed by adding a water resistance improver for ink jet recording paper.
- the pulp fibers to be used are mainly wood pulp usually used, but other fibrous substances such as synthetic pulp, synthetic fibers and glass fibers can also be used.
- the water resistance for the ink jet recording paper of the present invention After preparing a treatment bath containing an improver and impregnating plain paper or coated paper, excess impregnating liquid on the front and back of plain paper or coated paper can be removed by a size press and dried. .
- the water-resistance improver for ink jet recording paper of the present invention can be coated on plain paper or coated paper.
- the method of coating with a water resistance improver for ink jet recording paper is easy in process control, can cope with high-mix low-volume production, and uses a cationic polyurethane resin on the surface of paper. Since it can be effectively used by being present only in the layer portion, it can be particularly preferably implemented.
- the coating amount is 0. 1 ⁇ 1 0. 0 g Z m 2 as cationic polyurethane resin, 0.2 to 5 More preferably, it is 0 g / m 2 .
- the method of coating the water resistance improver for ink jet recording paper of the present invention includes an air knife coater, a roll coater, a blade coater, a bar coater, a brush coater, and a Champrexco. It can be coated on plain paper or coated paper by gravure, and dried.
- a dye mordant When using the water resistance improver for ink jet recording paper of the present invention, a dye mordant, a defoamer, a dispersant, a thickener, a colorant, an antistatic agent, a preservative, a water-soluble resin, an adhesive, and the like are used. Can be used together.
- the dye mordant include dicyandiamide condensate, polyamine, and polyethyleneimine.
- the water-soluble resin and the adhesive include, for example, cellulose derivatives such as oxidized starch, etherified starch, carboxymethylcellulose, and hydroxyethyl cellulose, casein, gelatin, soybean protein, polyvinyl alcohol and derivatives thereof, and maleic anhydride resin.
- Conjugated polymer latex such as styrene-butadiene copolymer, methyl methacrylate-butadiene copolymer, acrylic polymer latex such as acrylic acid ester, methacrylic acid ester polymer or copolymer, ethylene monovinyl acetate
- Aqueous adhesives such as latex of vinyl polymers such as copolymers, thermosetting resins such as melamine resin and urea resin, polymethyl methacrylate, polyurethane resin, unsaturated polyester resin, vinyl chloride-vinyl acetate
- thermoplastic resins such as copolymers, polyvinyl butyral, and alkyd resins. it can.
- Plain paper is generally used acidic paper or neutral paper, and coated paper is coated paper coated with a binder, inorganic pigment, organic pigment, or the like.
- the dye in the water based ink and the cationic polyurethane resin in the ink jet recording paper are combined, and the dye It is considered that dissolution is prevented and the water resistance is improved.
- the aqueous ink used preferably contains an anionic direct dye or an acid dye as a dye, and preferably further contains a wetting agent, a dye dissolving agent, a preservative, and the like.
- Anionic direct dyes used in aqueous inks include, for example, CI D irect B lack 2, 4, 9, 11, 14, 17, 19, 22, 27, 32, 36, 38, 41, 48, 49, 51, 56, 62, 71, 74, 75, 77, 78, 80, 105, 106, 107, 108, 112, 113, 117, 132, 146, 154, 194, CI Direct Ye 1 low 1 , twenty four,
- Acid B lack 1, 2, 7, 15, 17, 24, 26, 28, 31, 41, 48, 52, 60, 63, 94, 107, 109, 112 , 118, 119, 121, 122, 131, 155, 156, CI Acid Ye 1 low 1, 3, 4, 7, 11, 12, 13, 14, 17, 18, 19, 23, 25, 29, 34, 36, 38, 40, 41, 4
- the Inkujini' preparative recording sheet for improving water resistance agent is non-volatile content 2.6% by weight of the aqueous solution was diluted with water, the printing paper A having a basis weight of 64 gZm 2 as defined in JISP 3101, 19.2 gZm 2 using barcode one coater By coating and drying, ink jet recording paper coated with a cationic polyurethane resin 0.5 gZm 2 is obtained.
- ⁇ The printed area does not wash away or bleed.
- ⁇ The printed portion is slightly blurred.
- an ink jet printer [Epson Corp., MJ-700V2C], print a single black dot on the ink jet recording paper, observe the dots using a magnifying glass with a magnification of 50 times, and observe the dots according to the following criteria. evaluate.
- a four-necked flask purged with nitrogen was charged with 20 parts by weight of N-N-dimethylformamide and 84 parts by weight of hexamethylene diisocyanate. After cooling to 30 ° C or lower, 45 parts by weight of N-methylgenolamine was added, and the mixture was reacted at 0 ° C for 1 hour. After completion of the reaction, the mixture was cooled, 58 parts by weight of getyl sulfuric acid was added dropwise at 1 hour at 40 ° C, and the mixture was reacted at 80 ° C for 3 hours. After cooling the reaction mixture, water 707. One part by weight was added, and the unreacted isocyanate was reacted with water at 40 ° C. for 2 hours to obtain a water resistance improver for ink jet recording paper comprising a 20% by weight aqueous solution of a thionic polyurethane resin. .
- An ink jet recording paper was prepared using the water resistance improver for ink jet recording paper, and the water resistance and ink bleeding prevention were evaluated.
- the printed portion was not washed away by water or bleeding, but the bleeding was slightly observed in the cyan printed portion. No bleeding was observed in the dot portion where the black single color was printed.
- An ink jet recording paper was prepared using the water resistance improver for the ink jet recording paper, and the water resistance and the ink bleeding prevention were evaluated.
- the black and magenta print areas were not washed away or bleed, but the cyan and yellow print areas showed some bleeding. No bleeding was observed in the dot portion where the black single color was printed.
- Example 1 85.5 parts by weight of ethylenediamine propylene oxide adduct (average molecular weight: 450) was added in place of 45 parts by weight of N-methylethylenolamine, and the dropping amount of methylsulfuric acid was 28.9 parts by weight.
- a water resistance improver for ink jet recording paper was obtained in the same manner as in Example 1 except that the amount of water added was 753.6 parts by weight.
- An ink jet recording paper was prepared using the water resistance improver for ink jet recording paper, and the water resistance and the ink bleeding prevention were evaluated. Regarding any single color of black, cyan, magenta and yellow, the printed portion was not washed away by water or bleeding. Also, a slight bleeding appears in the dot area where the black single color is printed. Admitted.
- An ink jet recording paper was prepared using the water resistance improver for ink jet recording paper, and the water resistance and ink bleeding prevention were evaluated.
- the printed portion was not washed away by water or bleeding, but the bleeding was slightly observed in the cyan printed portion. No bleeding was observed in the dot portion where the black single color was printed.
- N-Methyljetanolamine 45 Instead of 5 parts by weight, 18.2 parts by weight of tri (2-aminoethyl) amine and 22.5 parts by weight of N-methylethanolamine were added. In the same manner as in Example 1 except that 8.5 parts by weight and the added amount of water were 661.4 parts by weight, an ink jet recording paper comprising a 20% by weight aqueous solution of a thionic polyurethane resin was used. A water resistance improver was obtained.
- Ink jet recording paper was prepared using this water resistance improver for ink jet recording paper, and the water resistance and ink bleeding prevention were evaluated.
- the printed portion was not washed away by water or bleeding, but the bleeding was slightly observed in the yellow printed portion. No bleeding was observed in the dot portion where the black single color was dot-printed.
- Example 2 The procedure of Example 2 was repeated except that the amount of N-methylethanolamine was 59 parts by weight, the amount of getyl sulfate added was 76 parts by weight, and the amount of water was 637 parts by weight.
- a water resistance improver for ink jet recording paper comprising a 5% by weight aqueous solution of a cationic polyurethane resin was obtained.
- An ink jet recording paper was prepared using the water resistance improver for ink jet recording paper, and the water resistance and ink bleeding prevention were evaluated. The black and magenta prints were not washed away or bleed, but the cyan and yellow prints showed some bleeding. No bleeding was observed in the dot portion where the black single color was dot-printed.
- a four-necked flask purged with nitrogen was charged with 28 parts by weight of N, N-dimethylformamide and 17.6 parts by weight of hexamethylene diiso- cyanate. After cooling to 30 ° C or lower, 63 parts by weight of N-methyljetanolamine was added, and the mixture was reacted at 0 ° C for 1 hour. After completion of the reaction, neutralization was performed by adding 31.8 parts by weight of acetic acid, and then 63.3.3 parts by weight of water was added. The unreacted isocyanate was reacted with water at 40 ° C for 2 hours. As a result, a water resistance improver for ink jet recording paper comprising a 20% by weight aqueous solution of a thionic polyurethane resin was obtained.
- An ink jet recording paper was prepared using the water resistance improver for ink jet recording paper, and the water resistance and ink bleeding prevention were evaluated.
- the black and magenta print areas were not washed away or bleed, but the cyan and yellow print areas showed some bleeding. Slight bleeding was observed in the dot portion where the black single color was dot-printed.
- Example 7 except that 131.6 parts by weight of xylylenediisocyanate was charged instead of 17.6 parts by weight of hexamethylene diisocyanate and the amount of water added was 689.3 parts by weight.
- a water resistance improver for ink jet recording paper comprising a 20% by weight aqueous solution of a thionic polyurethane resin was obtained.
- Ink jet recording paper was prepared using the water resistance improver for ink jet X recording paper, and the water resistance and ink bleeding prevention were evaluated. Regarding the single color of black, magenta and yellow, the printed portion was not washed away by water or bleeding, but the bleeding was slightly observed in the cyan printed portion. Some bleeding was observed in the dot portion where the black single color was printed. Example 9
- a four-necked flask purged with nitrogen was charged with 20 parts by weight of N, N-dimethylformamide and 84 parts by weight of hexamethylene diisocyanate. After cooling to 30 ° C or lower, 77.4 parts by weight of N-methyljetanolamine was added, and the mixture was reacted at 70 ° C for 1 hour. After completion of the reaction, the mixture was cooled, 100 parts by weight of getyl sulfuric acid was dropped at 40 ° C. over 1 hour, and the mixture was reacted at 80 ° C. for 3 hours. After the reaction mixture was cooled, 58.9.9 parts by weight of water was added thereto to obtain a water resistance improver for ink jet recording paper comprising a 30% by weight aqueous solution of a thionic polyurethane resin.
- An ink jet recording paper was prepared using the water resistance improver for ink jet recording paper, and the water resistance and the ink bleeding prevention were evaluated.
- the black and magenta prints were not washed away or bleed, but the cyan and yellow prints showed some bleeding. Slight bleeding was observed in the dot portion where the black single color was dot-printed.
- a nitrogen-substituted four-necked flask was charged with 20 parts by weight of N, N-dimethylformamide and 84 parts by weight of hexamethylene diisocyanate. After cooling to 30 ° C or lower, add 45 parts by weight of N-methylgenolamine and react at 70 ° C for 1 hour, then add 21.4 parts by weight of 2-dimethylaminoethanol. The reaction was further performed at 70 ° C for 1 hour. After completion of the reaction, the mixture was cooled, 95.2 parts by weight of getyl sulfuric acid was added dropwise at 40 ° C. over 1 hour, and the mixture was reacted at 80 ° C. for 3 hours. After cooling the reaction mixture, 71.6.8 parts by weight of water was added to obtain a water resistance improver for ink jet recording paper comprising a 25% by weight aqueous solution of a thionic polyurethane resin.
- An ink jet recording paper was prepared using the water resistance improver for ink jet recording paper, and the water resistance and ink bleeding prevention were evaluated. Regarding any single color of black, cyan, magenta and yellow, the printed portion was not washed away by water or bleeding. No bleeding was observed in the dot portion where the black single color was dot-printed.
- Example 1 Add 28.6 parts by weight of N-methylethanolamine instead of 21.4 parts by weight of 2-dimethylaminoethanol, and add 58 parts by weight of getyl sulfate and 6 26.8 parts of water.
- a water-proofing agent for an ink jet recording paper comprising a 25% by weight aqueous solution of a cationic polyurethane resin was obtained in the same manner as in Example 10 except that the amount was changed to parts by weight.
- Ink jet recording paper was prepared using the water resistance improver for ink jet recording paper, and the water resistance and the ink bleeding prevention were evaluated. Regarding any single color of black, cyan, magenta and yellow, the printed portion was not washed away by water or bleeding. No bleeding was observed in the dot portion where the black single color was dot-printed.
- a water resistance improver for ink jet recording paper was obtained in the same manner as in Example 10 except that it was made up of a 20% by weight aqueous solution of a thionic polyurethane resin. Ink jet recording paper was prepared using the improver, and the water resistance and the ink bleeding prevention were evaluated. Regarding any single color of black, cyan, magenta and yellow, the printed portion was not washed away by water or bleeding. No bleeding was observed in the dot portion where the black single color was dot-printed.
- the ink jet recording paper is made using the water resistance improver for ink jet recording paper. Were prepared and evaluated for water resistance and ink bleeding prevention. Regarding any single color of black, cyan, magenta and yellow, the printed portion was not washed away by water or bleeding. No bleeding was observed in the dot portion where the black single color was dot-printed.
- Example 1 was repeated except that the addition amount of 2-dimethylaminoethanol was 21.1 parts by weight, the drop amount of getyl sulfate was 58 parts by weight, and the addition amount of water was 604.3 parts by weight.
- a water resistance improver for ink jet recording paper comprising a 25% by weight aqueous solution of a thion polyurethane resin was obtained.
- An ink jet recording paper was prepared using the water resistance improver for ink jet recording paper, and the water resistance and ink bleeding prevention were evaluated. Regarding any single color of black, cyan, magenta and yellow, the printed portion was not washed away by water or bleeding. No bleeding was observed in the dot portion where the black single color was dot-printed.
- a nitrogen-substituted four-necked flask was charged with 20 parts by weight of N-N-dimethylformamide and 84 parts by weight of hexamethylene diisocyanate. After cooling to 30 ° C or lower, 45 parts by weight of N-methyljetanolamine was added, and the mixture was reacted at 70 ° C for 1 hour. Then, 27.1 parts by weight of methyliminobispropylamine was added to 9 parts by weight. An aqueous amine solution partially neutralized with 14.4 parts by weight of 9% by weight acetic acid was added, and the mixture was further reacted at 70 at 2 hours.
- An ink jet recording paper was prepared using the water resistance improver for the ink jet recording paper, and the water resistance and the ink bleeding prevention were evaluated. Regarding any single color of black, cyan, magenta and yellow, the printed portion was not washed away by water or bleeding. In addition, bleeding was observed in the dots printed with black dots. It did not fit.
- a water resistance improver for an ink jet recording paper comprising an aqueous solution of a 30% by weight cationic polyurethane resin was obtained.
- An ink jet recording paper was prepared using the water resistance improver for ink jet recording paper, and the water resistance and the ink bleeding prevention were evaluated. Regarding any single color of black, cyan, magenta and yellow, the printed portion was not washed away by water or bleeding. No bleeding was observed in the dot portion where the black single color was dot-printed.
- Methyliminobispropylamine 27.1 parts by weight of 9.9% by weight acetic acid 14.4 parts by weight of amine aqueous solution instead of diaminetriamine 24.7 parts by weight of 99% by weight acetic acid 28. 25% by weight of a polyurethane resin was prepared in the same manner as in Example 15 except that an aqueous amine solution partially neutralized with 8 parts by weight was added and the amount of water added was changed to 58.6.3 parts by weight. A water resistant improver for ink jet recording paper comprising a resin aqueous solution was obtained.
- An ink jet recording paper was prepared using the water resistance improver for ink jet recording paper, and the water resistance and ink bleeding prevention were evaluated. Regarding the single colors of black, cyan, magenta and yellow, the printed portion was not washed away by water or drooled. No bleeding was observed in the dot portion where the black single color was dot-printed.
- a nitrogen-substituted four-necked flask was charged with 20 parts by weight of N, N-dimethylformamide and 67.2 parts by weight of hexamethylene diisocyanate. Cool below 30 ° C Then, N-methyljetanolamine (119 parts by weight) was added, and the mixture was reacted at 70 ° C. for 1 hour. After the completion of the reaction, the mixture was cooled, and 664.8 parts by weight of water and 60 parts by weight of acetic acid were added to obtain a water resistance improver for an ink jet recording paper comprising a 20% by weight aqueous solution of a cationic polyurethane resin.
- An ink jet recording paper was prepared using the water resistance improver for ink jet recording paper, and the water resistance and the ink bleeding prevention were evaluated. Regarding any single color of black, cyan, magenta and yellow, the printed portion was clearly washed away by water and bleeding. In addition, bleeding was observed in the dot portion where the black single color was dot-printed.
- Ink jet recording paper was prepared using the water resistance improver for ink jet recording paper, and the water resistance and ink bleeding prevention were evaluated. Regarding any single color of black, cyan, magenta and yellow, the printed portion was clearly washed away by water and bleeding. In addition, bleeding was observed in the dot portion where the black single color was dot-printed.
- Inkjet recording paper was prepared using polyethyleneimine (average molecular weight 1,200) instead of the cationic polyurethane resin, and the water resistance and the prevention of ink bleeding were evaluated.
- the printed portion was slightly blurred, and for cyan and yellow single colors, the printed portion was clearly flushed with water and bleed. In addition, bleeding was observed in the dot portion where the black single color was dot-printed.
- Example 1 Example 2 Example 3 Example 4 Example 5 Example 5 Example 6 Example 7
- Example 8 Example 9 Example 10 Example 10 Example 11 Example 12 Example 13 Example 14
- MIB PA 6 MIB PA 6
- HMD I Hexamethylene diisocyanate
- EDAPO Propylene oxide adduct of ethylene diamine (average molecular weight 450).
- TAEA Tri (2-aminoethyl) amine.
- the ink jet recording paper prepared by coating the ink jet recording paper water resistance improver of Examples 1 to 17 of the present invention was excellent in all inks. It has water resistance and also has excellent bleeding prevention properties.
- the water resistance improver of Comparative Example 1 where the equivalent ratio of (A) the organic isocyanate compound and (B) the (isosinate group) Z (hydroxyl group) of the tertiary amine compound is 0.4
- the ink jet recording paper prepared using polyethyleneimine of Comparative Example 3 which is conventionally used as a water resistance improver of Comparative Example 2 with a water resistance improver of 3.3, and Also have poor water resistance and ink bleeding prevention properties.
- the water resistance improver for ink jet recording paper of the present invention By coating the water resistance improver for ink jet recording paper of the present invention, the water resistance of images and characters recorded using an ink jet printer can be improved, and an image with excellent image quality without ink bleeding can be obtained. One page can be recorded.
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Ink Jet Recording Methods And Recording Media Thereof (AREA)
- Ink Jet (AREA)
- Paper (AREA)
Description
Claims
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP99939179A EP1068959A4 (en) | 1998-03-10 | 1999-03-10 | WATERPROOFING AGENT FOR INK JET PRINTING PAPER AND INK JET PRINTING PAPER |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP10/58538 | 1998-03-10 | ||
JP10058538A JPH11254809A (ja) | 1998-03-10 | 1998-03-10 | インクジェット記録用紙用耐水性向上剤及びインクジェット記録用紙 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1999046130A1 true WO1999046130A1 (fr) | 1999-09-16 |
Family
ID=13087228
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP1999/001139 WO1999046130A1 (fr) | 1998-03-10 | 1999-03-10 | Agent ameliorant l'impermeabilite a l'eau pour papier d'impression par jets d'encre et papier d'impression par jets d'encre |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP1068959A4 (ja) |
JP (1) | JPH11254809A (ja) |
WO (1) | WO1999046130A1 (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6613866B2 (en) * | 1999-03-24 | 2003-09-02 | Alzo International Inc. | Urethane surfactants and their use in personal care formulations |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100379411B1 (ko) * | 1999-06-28 | 2003-04-10 | 엘지전자 주식회사 | 바이오칩 및 그의 생체 물질 패터닝 및 측정 방법 |
JP4919799B2 (ja) * | 2004-03-29 | 2012-04-18 | 第一工業製薬株式会社 | 金属材料表面処理用水系塗料組成物 |
US9527328B2 (en) | 2010-10-29 | 2016-12-27 | Lubrizol Advanced Materials, Inc. | Aqueous cationic polyurethane dispersions |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63280681A (ja) * | 1987-05-13 | 1988-11-17 | Mitsubishi Paper Mills Ltd | インクジェット記録媒体 |
JPH09183938A (ja) * | 1995-12-28 | 1997-07-15 | Shin Etsu Polymer Co Ltd | 表面被覆用組成物 |
JPH09216458A (ja) * | 1996-02-15 | 1997-08-19 | Meisei Kagaku Kogyo Kk | インクジェット記録用シート |
JPH09267544A (ja) * | 1996-04-01 | 1997-10-14 | Konica Corp | インクジェット記録用紙 |
JPH1086505A (ja) * | 1996-09-12 | 1998-04-07 | Nikka Chem Co Ltd | インクジェット記録紙用耐水化剤 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4110286A (en) * | 1977-02-07 | 1978-08-29 | Alcolac Inc. | Stable polyurethane latices, emulsifiable prepolymers therefor and methods of making the same |
-
1998
- 1998-03-10 JP JP10058538A patent/JPH11254809A/ja active Pending
-
1999
- 1999-03-10 EP EP99939179A patent/EP1068959A4/en not_active Withdrawn
- 1999-03-10 WO PCT/JP1999/001139 patent/WO1999046130A1/ja not_active Application Discontinuation
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS63280681A (ja) * | 1987-05-13 | 1988-11-17 | Mitsubishi Paper Mills Ltd | インクジェット記録媒体 |
JPH09183938A (ja) * | 1995-12-28 | 1997-07-15 | Shin Etsu Polymer Co Ltd | 表面被覆用組成物 |
JPH09216458A (ja) * | 1996-02-15 | 1997-08-19 | Meisei Kagaku Kogyo Kk | インクジェット記録用シート |
JPH09267544A (ja) * | 1996-04-01 | 1997-10-14 | Konica Corp | インクジェット記録用紙 |
JPH1086505A (ja) * | 1996-09-12 | 1998-04-07 | Nikka Chem Co Ltd | インクジェット記録紙用耐水化剤 |
Non-Patent Citations (1)
Title |
---|
See also references of EP1068959A4 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6613866B2 (en) * | 1999-03-24 | 2003-09-02 | Alzo International Inc. | Urethane surfactants and their use in personal care formulations |
Also Published As
Publication number | Publication date |
---|---|
EP1068959A4 (en) | 2003-06-11 |
EP1068959A1 (en) | 2001-01-17 |
JPH11254809A (ja) | 1999-09-21 |
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