CN111454609A - PP decorative film gravure printing water-based ink without pretreatment and preparation method thereof - Google Patents

PP decorative film gravure printing water-based ink without pretreatment and preparation method thereof Download PDF

Info

Publication number
CN111454609A
CN111454609A CN202010302880.3A CN202010302880A CN111454609A CN 111454609 A CN111454609 A CN 111454609A CN 202010302880 A CN202010302880 A CN 202010302880A CN 111454609 A CN111454609 A CN 111454609A
Authority
CN
China
Prior art keywords
parts
water
based ink
pretreatment
decorative film
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN202010302880.3A
Other languages
Chinese (zh)
Inventor
许华君
许少宏
罗英武
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Hangzhou Hiwetech Chemical Technology Co ltd
Original Assignee
Hangzhou Hiwetech Chemical Technology Co ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hangzhou Hiwetech Chemical Technology Co ltd filed Critical Hangzhou Hiwetech Chemical Technology Co ltd
Priority to CN202010302880.3A priority Critical patent/CN111454609A/en
Publication of CN111454609A publication Critical patent/CN111454609A/en
Pending legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D11/00Inks
    • C09D11/02Printing inks
    • C09D11/10Printing inks based on artificial resins
    • C09D11/106Printing inks based on artificial resins containing macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D11/00Inks
    • C09D11/02Printing inks
    • C09D11/03Printing inks characterised by features other than the chemical nature of the binder
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D11/00Inks
    • C09D11/02Printing inks
    • C09D11/10Printing inks based on artificial resins
    • C09D11/106Printing inks based on artificial resins containing macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C09D11/107Printing inks based on artificial resins containing macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds from unsaturated acids or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D11/00Inks
    • C09D11/02Printing inks
    • C09D11/10Printing inks based on artificial resins
    • C09D11/106Printing inks based on artificial resins containing macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C09D11/108Hydrocarbon resins

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Inks, Pencil-Leads, Or Crayons (AREA)

Abstract

The invention provides a PP decorative film gravure printing water-based ink without pretreatment and a preparation method thereof, wherein the water-based ink is prepared from the following raw materials in parts by weight: 30-50 parts of film-forming resin, 10-20 parts of pigment, 2-4 parts of dispersing agent, 0.5-1.5 parts of wetting agent, 0.3-1 part of thickening agent, 2-4 parts of cosolvent, 0.08-0.15 part of defoaming agent and 24.42-58.05 parts of deionized water; the invention adopts a water-based system, thereby being green and environment-friendly; the storage life of the ink system is more than one year; the product does not need to carry out pretreatment such as corona, flame, plasma or precoating primer liquid on the PP decorative film, can be directly printed on the PP decorative film through gravure printing, and has good transfer printing property and leveling property; after the product is printed on a PP decorative film, the water resistance is good, and the adhesive force is excellent.

Description

PP decorative film gravure printing water-based ink without pretreatment and preparation method thereof
Technical Field
The invention relates to water-based ink and a preparation method thereof, in particular to water-based ink which can be printed on a PP decorative film through gravure printing without pretreatment such as corona, flame, plasma or precoating primer liquid on the PP decorative film and a preparation method thereof.
Background
The PP decorative film is a paint-free furniture surface application decorative film made of polypropylene, has visual effect comparable to that of wood veneer, and is very suitable for flat pasting, cladding and conditional 3D plastic uptake. The PP decorative film has the advantages of scratch resistance, pollution resistance, drug resistance, weather resistance and the like, is very suitable for the application of paint-free doors, cabinets and wallboards, has good tolerance, enables the decorative surface to be as new as long as possible, and can never change color and have the same quality under the conditions of various pollution, chemical agents and direct illumination, which can not be achieved by a plurality of PVC films.
In addition, the PP decorative film does not contain 13 substances such as formaldehyde/acetaldehyde/toluene/xylene and the like, does not contain heavy metals such as chromium/cadmium/lead/arsenic and the like, does not use a plasticizer in production, can be degraded in recovery, only releases water and carbon dioxide in combustion, does not generate any toxic gas, and thus becomes a preferred decorative material for places such as homes, schools, hotels and the like. The PP decorative film is popular in the Japanese household field, but belongs to a small product in China, and is applied in a small scale only in some high-end fields.
Disclosure of Invention
The invention aims to provide water-based ink capable of being applied to a PP decorative film and a preparation method thereof, and the ink can be directly printed on the PP decorative film through gravure printing without carrying out pretreatment such as corona, flame, plasma or precoating primer liquid on the PP decorative film.
The technical scheme of the invention is as follows:
the PP decorative film gravure printing water-based ink without pretreatment is composed of the following raw materials in parts by weight:
30-50 parts of film-forming resin, 10-20 parts of pigment, 2-4 parts of dispersing agent, 0.5-1.5 parts of wetting agent, 0.3-1 part of thickening agent, 2-4 parts of cosolvent, 0.08-0.15 part of defoaming agent and 24.42-58.05 parts of deionized water.
Further:
the pigment is any one of azo condensed type organic red, benzimidazolone organic yellow, phthalocyanine organic blue, carbon black and inorganic titanium white, preferably any one of pigment red 166(P.R.166, Zhejiang lily group Co., Ltd.), pigment yellow P-HG (P.Y.180, Zhejiang lily group Co., Ltd.), BF435 (P.B.15: 3, Zhejiang lily group Co., Ltd.), SPECIA L B L ACK 4 (Germany Degussa Co., Ltd.) and R900 (DuPont).
The dispersant is one or a mixture of more than two of polycarboxylate, polyacrylic acid derivative, maleic anhydride copolymer, condensed naphthalene sulfonate, polycarboxylic acid and polyvinyl alcohol in any proportion, and particularly preferred is polycarboxylic acid KP010 (Shanghai Dedeye trade Co., Ltd.).
The wetting agent is one or a mixture of more than two of polyacrylate wetting agents (such as M3077, Shanghai De Shuichi trade company, Ltd.; Resiflow 50, BYK company), organic silicon resin wetting agents (such as Silcn 353, Shanghai De Shuichi trade company, Ltd.), (modified) polyalkyl oxide wetting agents (such as L evaslip W-461, E L EMENTIS company) and fluoro olefin wetting agents (such as 9100, Shiloda chemical technology company, Ltd.), preferably polyacrylate wetting agents, particularly preferably Resiflow 50(BYK company).
The thickener is a polyacrylic thickener (e.g., polyacrylic thickener)
Figure BDA0002454671690000011
420, tequila;
Figure BDA0002454671690000012
425, tequila;
Figure BDA0002454671690000013
450, tequila;
Figure BDA0002454671690000014
125, texite corporation), polyacrylate thickeners (e.g. L atekoll D, BASF corporation), polyurethane thickeners (e.g. kamex corporation)
Figure BDA0002454671690000015
510, tequila;
Figure BDA0002454671690000016
644, tequila;
Figure BDA0002454671690000017
655, squad) in any ratio, preferably a polyurethane thickener, particularly preferably a polyurethane thickener
Figure BDA0002454671690000018
655 (texite).
The cosolvent is one or a mixture of more than two of methanol, ethanol and isopropanol in any proportion.
The antifoaming agent may be a lower alcohol antifoaming agent (e.g., a lower alcohol antifoaming agent)
Figure BDA0002454671690000021
DF 1760, demote corporation;
Figure BDA0002454671690000022
DF3163, Demodex corporation), mineral oil type antifoaming agents (e.g., Drewplus T-4507, ASH L AND-AQUA L ON corporation), silicone type antifoaming agents (e.g., Pulca 1918, Kyoka Fine chemical industries (Shanghai) Co., Ltd.; Drewplus TS-4400, ASH L AND-AQUA L ON corporation; Drewplus TS-4481, ASH L AND-AQUA L ON corporation), preferably lower alcohol type antifoaming agents, particularly preferably lower alcohol type antifoaming agents
Figure BDA0002454671690000023
DF3163 (tequila).
The film-forming resin is a mixture of vinyl chloride-ethylene copolymer resin, chlorinated polypropylene and chlorinated modified fluorinated poly (methyl methacrylate-methyl acrylate-methylene succinic acid) resin emulsion, and particularly preferably the mixture is mixed according to the following weight ratio:
20-40 parts of vinyl chloride-ethylene copolymer resin, 10-27 parts of chlorinated polypropylene and 33-70 parts of chlorinated modified fluorinated poly (methyl methacrylate-methyl acrylate-methylene succinic acid) resin emulsion.
Wherein the vinyl chloride-ethylene copolymer resinThe fat is particularly preferably
Figure BDA0002454671690000024
Vinyl chloride CEN8752(WACKER Co.);
the chlorinated polypropylene is preferably
Figure BDA0002454671690000025
EW-5303(TOYOBO Co., Ltd.),
Figure BDA0002454671690000026
EW-5250(TOYOBO Co., Ltd.),
Figure BDA0002454671690000027
EH-801(TOYOBO corporation) in any ratio or in any mixture of two or more;
the preparation method of the chlorinated modified fluorinated poly (methyl methacrylate-methyl acrylate-methylene succinic acid) resin emulsion comprises the following steps of (fluorinated poly (methyl methacrylate-methyl acrylate-methylene succinic acid) resin emulsion is disclosed in the invention patent of PVC furniture film/PVF plastic film aqueous adhesive and a preparation method thereof of the company, the patent grant number is Z L201810479890.7; vinylidene chloride is added in the preparation process of a shell layer monomer phase for chlorination modification):
(1) preparation of core layer monomer phase
Mixing 16.3 parts of methyl methacrylate monomer, 10.2 parts of methyl acrylate monomer, 0.0014 part of isooctyl 3-mercaptopropionate (chain transfer reagent) and 1.5 parts of nonionic emulsifier at room temperature (20-30 ℃), and stirring and dissolving at the speed of 450rpm for 30min to obtain a core layer monomer phase;
(2) preparation of shell monomer phase
Mixing 4.5 parts of vinylidene chloride, 6.9 parts of methyl methacrylate monomer, 5.3 parts of methyl acrylate monomer, 0.2 part of methylene succinic acid monomer, 0.16 part of 2- (perfluorohexyl) ethyl methacrylate monomer, 0.0008 part of isooctyl 3-mercaptopropionate (chain transfer agent), 0.2 part of nonionic emulsifier and 0.1 part of fluorine surfactant at room temperature, and stirring and dissolving at the speed of 500rpm for 40min to obtain a shell layer monomer phase;
(3) preparation of priming phase
Adding 1.5 parts of anionic emulsifier, 0.8 part of nonionic emulsifier and 0.04 part of potassium persulfate (initiator) into 35 parts of deionized water, and stirring and dissolving at the speed of 400rpm to obtain a priming phase;
(4) stage of polymerization
Heating the priming phase obtained in the step (3), adjusting the stirring speed to 200rpm when the temperature is raised to 80 ℃, dropwise adding the nuclear layer monomer phase obtained in the step (1), completing dropwise adding within 2h, then dropwise adding the shell layer monomer phase obtained in the step (2), completing dropwise adding within 3h, and when the nuclear layer monomer phase begins to be dropwise added for 10-20min, enabling the system to generate blue light, beginning to dropwise add an initiator aqueous solution at the moment, keeping the initiator aqueous solution and all monomers to be dropwise added simultaneously, and then keeping the temperature and stirring for 2h to finish the polymerization reaction stage;
the initiator aqueous solution is obtained by dissolving 0.2 part of potassium persulfate in 18 parts of deionized water;
(5) post-treatment stage
After the polymerization reaction stage is finished, cooling to 75 ℃, adding tert-butyl hydrogen peroxide aqueous solution, stirring for 10min under heat preservation, then adding rongalite aqueous solution, stirring for 10min under heat preservation, then cooling to room temperature, adding preservative aqueous solution, and finally filtering (using a 200-mesh nylon filter bag) to discharge, thus obtaining the chlorinated modified fluorinated poly (methyl methacrylate-methyl acrylate-methylene succinic acid) emulsion resin;
the tert-butyl hydroperoxide aqueous solution is obtained by dissolving 0.08 part of tert-butyl hydroperoxide in 0.2 part of deionized water;
the rongalite aqueous solution is obtained by dissolving 0.08 part of rongalite in 0.2 part of deionized water;
the preservative aqueous solution is obtained by dissolving 0.02 part of preservative in 0.2 part of deionized water;
in the preparation method, the parts are all parts by weight.
The invention also provides a preparation method of the PP decorative film gravure printing water-based ink, which comprises the following steps of (by weight):
at room temperature, sequentially adding 10-20 parts of deionized water, 2-4 parts of dispersing agent, 2-4 parts of cosolvent and 0.04-0.08 part of defoaming agent into a dispersion kettle, stirring and mixing uniformly at the speed of 100 plus materials and 200rpm, then adding 10-20 parts of pigment, stirring and mixing uniformly at the speed of 200 plus materials and 300rpm, transferring to a horizontal sand mill for grinding for 4-6 times until the particle size of the particles reaches below 300nm, and then filtering (using a 200-mesh nylon filter bag) for discharging to obtain color paste; then adding 30-50 parts of film-forming resin, 14.42-38.05 parts of deionized water, the obtained color paste, 0.5-1.5 parts of wetting agent, 0.3-1 part of thickening agent and 0.04-0.07 part of defoaming agent into a dispersion cylinder in sequence, stirring at the speed of 200-250rpm for 0.5-1h, filtering (using a 200-mesh nylon filter bag) and discharging to obtain the PP decorative film gravure printing water-based ink.
Compared with the prior art, the invention has the beneficial effects that:
1. an aqueous system is adopted, so that the environment is protected;
2. the storage life of the ink system is more than one year;
3. the product does not need to carry out pretreatment such as corona, flame, plasma or precoating primer liquid on the PP decorative film, can be directly printed on the PP decorative film through gravure printing, and has good transfer printing property and leveling property;
4. after the product is printed on a PP decorative film, the water resistance is good, and the adhesive force is excellent.
Drawings
FIG. 1 is a graph showing the printing effect of red ink printed on a PP decorative film by a KPP gravure proofing machine according to example 1 of the present invention;
FIG. 2 is a graph showing the printing effect of the yellow ink printed on the PP decorative film by a KPP gravure proofing machine in example 2 of the present invention;
FIG. 3 is a printing effect diagram of the blue ink printed on the PP decorative film by the KPP gravure proofing machine according to the embodiment 3 of the present invention;
FIG. 4 is a graph showing the printing effect of the black ink printed on the PP decorative film by the KPP gravure proofing machine according to example 4 of the present invention;
fig. 5 is a printing effect diagram of white ink printed on a PP decorative film by a KPP gravure proofing machine in example 5 of the present invention.
Detailed Description
The invention will be further described with reference to specific examples, but the scope of the invention is not limited thereto.
The particle size and particle size distribution of the aqueous color paste were measured on a Malvern ZETASIZER 3000HAS particle sizer at a test temperature of 25 ℃.
The storage stability of the water-based ink means that the gloss oil is kept still for 18 days at the temperature of 60 ℃, and the storage stability of the water-based ink is more than 12 months without precipitation and delamination.
The water resistance of the water-based ink coating is determined according to GB1733-1993, and the water-based ink coating is qualified as the water-based ink coating does not fade, reduce the glossiness, foam, fall off and the like after the sample is soaked for 100 hours, and the longer the soaking time is, the better the water resistance is, and the change does not occur.
The adhesion test of the water-based ink is carried out according to GB/T13217.7-2009, and the adhesion fastness of the resin is considered to be excellent when the adhesion fastness is more than or equal to 95%.
The printing effect of the aqueous ink was evaluated as follows: and (3) printing the water-based single-color ink (red, yellow, blue, black and white) on a PP decorative film by using a KPP gravure proofing machine at a printing speed of 40m/min, drying at 50 ℃, and observing the leveling effect of the printing color block by naked eyes.
The chlorinated modified fluorinated poly (methyl methacrylate-methyl acrylate-methylenesuccinic acid) emulsion resin used in the following examples was prepared as follows:
(1) preparation of core layer monomer phase
Mixing 16.3kg of methyl methacrylate monomer (Industrial chemical Co., Ltd., Guangzhou city), 10.2kg of methyl acrylate monomer (Shanghai Miruil chemical technology Co., Ltd.), 0.0014kg of isooctyl 3-mercaptopropionate chain transfer reagent and 1.5kg of ER-40(ADEKA Co., Ltd.) nonionic emulsifier at room temperature, and stirring and dissolving at 450rpm for 30min to obtain a core layer monomer phase;
(2) preparation of shell monomer phase
At room temperature, 4.5kg of vinylidene chloride, 6.9kg of methyl methacrylate monomer, 5.3kg of methyl acrylate monomer, 0.2kg of methylene succinic acid monomer (national institute of chemical Co., Ltd.), and 0.16kg of 2- (perfluorohexyl) ethylmethacrylic acidAcid ester monomer (Bailingwei science and technology Co., Ltd.), 0.0008kg of isooctyl 3-mercaptopropionate chain transfer reagent, 0.2kg of ER-40(ADEKA Co., Ltd.) nonionic emulsifier, and 0.1kg of CapstoneTMFS-10 (DuPont) fluorine surfactant, and stirring at 500rpm for 40min to obtain shell monomer phase;
(3) preparation of priming phase
1.5kg of DowfaxTM8390(DOW corporation) anionic emulsifier, 0.8kg of ER-40(ADEKA corporation) nonionic emulsifier, and 0.04kg of potassium persulfate initiator were added to 35kg of deionized water, and stirred at 400rpm to dissolve, thereby obtaining a strike-bottom phase;
(4) stage of polymerization
Heating the priming phase obtained in the step (3), adjusting the stirring speed to 200rpm when the temperature is raised to 80 ℃, dropwise adding the core layer monomer phase obtained in the step (1), completing dropwise adding within 2h, then dropwise adding the shell layer monomer phase obtained in the step (2), completing dropwise adding within 3h, and when the dropwise adding of the core layer monomer phase is started for 10-20min, enabling the system to generate blue light, then dropwise adding an initiator aqueous solution, wherein the initiator aqueous solution is prepared by dissolving 0.2kg of potassium persulfate initiator in 18kg of deionized water, keeping the initiator aqueous solution and all monomers to be simultaneously dropwise added, keeping the temperature and stirring for 2h, and completing the polymerization reaction stage;
(5) post-treatment stage
After the polymerization reaction stage is finished, cooling to 75 ℃, adding a tert-butyl hydrogen peroxide aqueous solution, wherein the tert-butyl hydrogen peroxide aqueous solution is obtained by dissolving 0.08kg of tert-butyl hydrogen peroxide in 0.2kg of deionized water, stirring for 10min under heat preservation, then adding a rongalite aqueous solution, the rongalite aqueous solution is obtained by dissolving 0.08kg of rongalite in 0.2kg of deionized water, stirring for 10min under heat preservation, then cooling to room temperature, adding an antiseptic aqueous solution, the antiseptic aqueous solution is obtained by adding 0.02kg of DeuAdd MB-11 (Demodex) antiseptic into 0.2kg of deionized water, and finally filtering and discharging with a 200-mesh nylon filter bag to obtain the chlorinated and modified fluorinated poly (methyl methacrylate-methyl acrylate-methylenesuccinic acid) emulsion resin.
Example 1:
15kg of deionized water, 2kg of KP010 (Shanghai Ded trade Co., Ltd.), 3kg of ethanol (Suzhou Europe chemical Co., Ltd.), and 0.08kg of ethanol were mixed at room temperature
Figure BDA0002454671690000041
Adding DF3163 (Demodesty company) into a dispersion kettle in sequence, stirring and mixing uniformly at the speed of 100rpm, adding 10kg of pigment Red 166(P.R.166, Zhejiang lily group Co., Ltd.), stirring and mixing uniformly at the speed of 200rpm, transferring to a horizontal sand mill (TBM-50, Taiyao (Shanghai) industries Co., Ltd.) for grinding for 4 times until the particle size reaches below 300nm, and filtering and discharging with a 200-mesh nylon filter bag to obtain red paste; then sequentially adding 6kg of
Figure BDA0002454671690000042
Vinyl chloride CEN8752(WACKER Co.) 3kg
Figure BDA0002454671690000043
EH-801(TOYOBO Co.), 21kg of chlorinated modified fluorinated poly (methyl methacrylate-methyl acrylate-methylene succinic acid) emulsion resin, 38.05kg of deionized water, 30.08kg of the red paste, 1kg of Resiflow W50(BYK Co.), 0.8kg of
Figure BDA0002454671690000044
655 (Demodex corporation), and 0.07kg
Figure BDA0002454671690000045
DF3163 (Demodex) is added into a dispersion tank, stirred for 1h at the speed of 200rpm and then filtered out by a nylon filter bag with 200 meshes to obtain the PP decorative film gravure printing water-based red ink.
Example 2:
15kg of deionized water, 2kg of KP010 (Shanghai Ded trade Co., Ltd.), 4kg of ethanol (Suzhou Europe chemical Co., Ltd.), and 0.06kg of ethanol were mixed at room temperature
Figure BDA0002454671690000046
DF3163 (Germany modest Co.) was added sequentiallyStirring and mixing uniformly in a dispersion kettle at the speed of 150rpm, adding 10kg of pigment yellow P-HG (P.Y.180, Zhejiang lily group stock kg Co., Ltd.), stirring and mixing uniformly at the speed of 300rpm, transferring to a horizontal sand mill (TBM-50, Taiyai (Shanghai) industries Co., Ltd.) for grinding for 4 times until the particle size reaches below 300nm, and filtering and discharging by using a 200-mesh nylon filter bag to obtain yellow slurry; then sequentially adding 7.5kg of
Figure BDA0002454671690000047
Vinyl chloride CEN8752(WACKER Co.), 4.5kg
Figure BDA0002454671690000048
EH-801(TOYOBO Co.), 18kg of chlorinated modified fluorinated poly (methyl methacrylate-methyl acrylate-methylene succinic acid) emulsion resin, 36.88kg of deionized water, 31.06kg of yellow paste, 1kg of Resiflow W50(BYK Co.), 1kg of
Figure BDA0002454671690000049
655 (Demodex corporation), and 0.06kg
Figure BDA0002454671690000051
DF3163 (Demodex) is added into a dispersion tank, stirred for 1h at the speed of 200rpm and then filtered out by a nylon filter bag with 200 meshes to obtain the PP decorative film gravure printing water-based yellow ink.
Example 3:
15kg of deionized water, 3kg of KP010 (Shanghai Ded trade Co., Ltd.), 4kg of ethanol (Suzhou Eurter chemical Co., Ltd.), and 0.05kg of ethanol were mixed at room temperature
Figure BDA0002454671690000052
DF3163 (Demodex corporation) was sequentially added to a dispersion vessel, and after stirring and mixing them at 150rpm, 10kg of BF435 (P.B.15: 3, Lilium Thunbergii group GmbH) was added, and after stirring and mixing them at 300rpm, they were transferred to a horizontal sand mill (TBM-50, Taiyao (Shanghai) industries Co., Ltd.) and ground for 5 times until the particle size reached 300nm or less, and then nylon of 200 mesh was usedFiltering the filter bag and discharging to obtain blue paste; then sequentially adding 7.5kg of
Figure BDA0002454671690000053
Vinyl chloride CEN8752(WACKER Co., Ltd.), 6kg
Figure BDA0002454671690000054
EH-801(TOYOBO Co.), 16.5kg of chlorinated modified fluorinated poly (methyl methacrylate-methyl acrylate-methylene succinic acid) emulsion resin, 36.kg of deionized water, 32.05kg of the blue paste, 1.2kg of Resiflow W50(BYK Co.), 0.7kg of
Figure BDA0002454671690000055
655 (Demodex corporation), and 0.05kg
Figure BDA0002454671690000056
DF3163 (Demodex) was put into a dispersion jar, stirred at 200rpm for 1 hour, and then filtered out with a 200 mesh nylon filter bag to obtain a PP decorative film gravure water-based blue ink.
Example 4:
20kg of deionized water, 4kg of KP010 (Shanghai Ded trade Co., Ltd.), 4kg of ethanol (Suzhou Eurter chemical Co., Ltd.), and 0.05kg of ethanol were mixed at room temperature
Figure BDA0002454671690000057
DF3163 (Germany and modest company) is sequentially added into a dispersion kettle, stirred and mixed uniformly at the speed of 200rpm, 10kg of SPECIA L B L ACK 4 (Germany and Germany, stirred and mixed uniformly at the speed of 200rpm, and then transferred to a horizontal sand mill (TBM-50, Taiyao, Shanghai) industry Co., Ltd.) to be ground for 6 times until the particle size reaches below 300nm, and then filtered and discharged by a 200-mesh nylon filter bag to obtain black paste, and then 16kg of black paste is sequentially added
Figure BDA0002454671690000058
Vinyl chloride CEN8752(WACKER Co.), 10.67kg
Figure BDA0002454671690000059
EH-801(TOYOBO Co.), 13.33kg of chlorinated modified fluorinated poly (methyl methacrylate-methyl acrylate-methylene succinic acid) emulsion resin, 15.1.kg of deionized water, 43.05kg of the above black slurry, 1.5kg of Resiflow W50(BYK Co.), 0.3kg of
Figure BDA00024546716900000510
655 (Demodex corporation), and 0.05kg
Figure BDA00024546716900000511
DF3163 (Demodex) is added into a dispersion tank, stirred for 0.5h at the speed of 250rpm and then filtered out by a nylon filter bag with 200 meshes to obtain the PP decorative film gravure printing water-based black ink.
Example 5:
10kg of deionized water, 2kg of KP010 (Shanghai Ded trade Co., Ltd.), 2kg of ethanol (Suzhou Eurter chemical Co., Ltd.), and 0.04kg of ethanol were mixed at room temperature
Figure BDA00024546716900000512
Adding DF3163 (Demodex) into a dispersion kettle in sequence, stirring and mixing uniformly at the speed of 200rpm, adding 20kg of R900 (DuPont), stirring and mixing uniformly at the speed of 200rpm, transferring to a horizontal sand mill (TBM-50, Taiyai (Shanghai) industries, Co., Ltd.) for grinding for 4 times until the particle size reaches below 300nm, and filtering and discharging with a 200-mesh nylon filter bag to obtain white slurry; then sequentially adding 20kg of
Figure BDA00024546716900000513
Vinyl chloride CEN8752(WACKER Co.), 13.33kg
Figure BDA00024546716900000514
EH-801(TOYOBO Co.), 16.67kg of chlorinated modified fluorinated poly (methyl methacrylate-methyl acrylate-methylene succinic acid) emulsion resin, 14.42 kg of deionized water, 34.04kg of the above white slurry, 0.5kg of Resiflow W50(BYK Co.), 1kg of
Figure BDA00024546716900000515
655 (Demodex corporation), and 0.04kg
Figure BDA00024546716900000516
DF3163 (Demodex) is added into a dispersion tank, stirred for 0.5h at the speed of 200rpm and then filtered out by a nylon filter bag with 200 meshes to obtain the PP decorative film gravure printing water-based white ink.
TABLE 1 Experimental results of examples
Figure BDA00024546716900000517
Figure BDA0002454671690000061
The above-described embodiments are intended to illustrate rather than to limit the invention, and any modifications and variations of the present invention are within the spirit of the invention and the scope of the claims.

Claims (9)

1. The PP decorative film gravure printing water-based ink without pretreatment is characterized by comprising the following raw materials in parts by weight:
30-50 parts of film-forming resin, 10-20 parts of pigment, 2-4 parts of dispersing agent, 0.5-1.5 parts of wetting agent, 0.3-1 part of thickening agent, 2-4 parts of cosolvent, 0.08-0.15 part of defoaming agent and 24.42-58.05 parts of deionized water;
the film-forming resin is a mixture of vinyl chloride-ethylene copolymer resin, chlorinated polypropylene and chlorinated modified fluorinated poly (methyl methacrylate-methyl acrylate-methylene succinic acid) resin emulsion.
2. The pretreatment-free water-based ink for gravure printing of PP decorative films as claimed in claim 1, wherein the weight ratio of each component in the film-forming resin is as follows:
20-40 parts of vinyl chloride-ethylene copolymer resin, 10-27 parts of chlorinated polypropylene and 33-70 parts of chlorinated modified fluorinated poly (methyl methacrylate-methyl acrylate-methylene succinic acid) resin emulsion.
3. The pretreatment-free water-based ink for gravure printing of PP decorative films according to claim 1, wherein the pigment is any one of azo condensed organic red, benzimidazolone organic yellow, phthalocyanine organic blue, carbon black and inorganic titanium white.
4. The PP decorative film gravure water-based ink without pretreatment of claim 1, wherein the dispersant is one or a mixture of more than two of polycarboxylate, polyacrylic acid derivative, maleic anhydride copolymer, condensed naphthalene sulfonate, polycarboxylic acid and polyvinyl alcohol in any proportion.
5. The pretreatment-free PP decorative film gravure water-based ink as claimed in claim 1, wherein the wetting agent is one or a mixture of two or more of polyacrylate wetting agents, silicone resin wetting agents, (modified) polyalkyl oxide wetting agents and fluoro olefin wetting agents in any proportion.
6. The pretreatment-free water-based ink for gravure printing of PP decorative films as claimed in claim 1, wherein the thickener is one or a mixture of two or more of polyacrylic thickeners, polyacrylate thickeners and polyurethane thickeners in any proportion.
7. The pretreatment-free water-based ink for gravure printing of PP decorative films as claimed in claim 1, wherein the cosolvent is one or a mixture of more than two of methanol, ethanol and isopropanol in any proportion.
8. The pretreatment-free water-based ink for gravure printing of PP decorative films as claimed in claim 1, wherein the defoamer is one or a mixture of more than two of lower alcohol defoamer, mineral oil defoamer and silicone defoamer in any proportion.
9. The preparation method of the PP decorative film gravure water-based ink without pretreatment, as claimed in claim 1, is characterized in that the preparation method comprises the following steps:
at room temperature, sequentially adding 10-20 parts of deionized water, 2-4 parts of dispersing agent, 2-4 parts of cosolvent and 0.04-0.08 part of defoaming agent into a dispersion kettle, stirring and mixing uniformly at the speed of 100 plus materials and 200rpm, then adding 10-20 parts of pigment, stirring and mixing uniformly at the speed of 200 plus materials and 300rpm, transferring to a horizontal sand mill for grinding for 4-6 times until the particle size of particles reaches below 300nm, and then filtering and discharging to obtain color paste; then adding 30-50 parts of film-forming resin, 14.42-38.05 parts of deionized water, the obtained color paste, 0.5-1.5 parts of wetting agent, 0.3-1 part of thickening agent and 0.04-0.07 part of defoaming agent into a dispersion cylinder in sequence, stirring at the speed of 200-250rpm for 0.5-1h, filtering and discharging to obtain the PP decorative film gravure printing water-based ink.
CN202010302880.3A 2020-04-17 2020-04-17 PP decorative film gravure printing water-based ink without pretreatment and preparation method thereof Pending CN111454609A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202010302880.3A CN111454609A (en) 2020-04-17 2020-04-17 PP decorative film gravure printing water-based ink without pretreatment and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202010302880.3A CN111454609A (en) 2020-04-17 2020-04-17 PP decorative film gravure printing water-based ink without pretreatment and preparation method thereof

Publications (1)

Publication Number Publication Date
CN111454609A true CN111454609A (en) 2020-07-28

Family

ID=71676212

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202010302880.3A Pending CN111454609A (en) 2020-04-17 2020-04-17 PP decorative film gravure printing water-based ink without pretreatment and preparation method thereof

Country Status (1)

Country Link
CN (1) CN111454609A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115386262A (en) * 2022-09-26 2022-11-25 杭州海维特化工科技有限公司 Gravure ink with essence and negative ions slowly released and applied to automobile interior decoration plastic film and preparation method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101717596A (en) * 2009-12-08 2010-06-02 杭华油墨化学有限公司 Water-based ink for package printing of high-adhesion film and manufacturing method thereof
CN106832090A (en) * 2016-12-23 2017-06-13 湖北工程学院 Acrylic acid ester emulsion of flexible PVC water-based ink and preparation method thereof
CN107384013A (en) * 2017-09-11 2017-11-24 杭州海维特化工科技有限公司 A kind of PVC furniture film intaglio printing water-based ink and preparation method thereof
US20180134906A1 (en) * 2015-04-06 2018-05-17 Kao Corporation Aqueous ink
CN108587530A (en) * 2018-05-18 2018-09-28 杭州海维特化工科技有限公司 A kind of PVC furniture film/PVF plastic foil Aqueous Adhesives and preparation method thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101717596A (en) * 2009-12-08 2010-06-02 杭华油墨化学有限公司 Water-based ink for package printing of high-adhesion film and manufacturing method thereof
US20180134906A1 (en) * 2015-04-06 2018-05-17 Kao Corporation Aqueous ink
CN106832090A (en) * 2016-12-23 2017-06-13 湖北工程学院 Acrylic acid ester emulsion of flexible PVC water-based ink and preparation method thereof
CN107384013A (en) * 2017-09-11 2017-11-24 杭州海维特化工科技有限公司 A kind of PVC furniture film intaglio printing water-based ink and preparation method thereof
CN108587530A (en) * 2018-05-18 2018-09-28 杭州海维特化工科技有限公司 A kind of PVC furniture film/PVF plastic foil Aqueous Adhesives and preparation method thereof

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
薄遵彦等: "《新型建筑材料性能与应用》", 31 August 2005 *
藏广州: "《凹版印刷技术分册》", 30 November 2003 *
陈蕴智等: "《印刷材料学》", 30 June 2011 *
马静君等: "《柔印技术问答》", 31 October 2008 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115386262A (en) * 2022-09-26 2022-11-25 杭州海维特化工科技有限公司 Gravure ink with essence and negative ions slowly released and applied to automobile interior decoration plastic film and preparation method thereof

Similar Documents

Publication Publication Date Title
CN107384013B (en) PVC furniture film gravure printing water-based ink and preparation method thereof
CN109439124B (en) Water-based matte self-crosslinking acrylic emulsion for wood lacquer and synthetic method thereof
CN101704914B (en) Waterborne rust conversion polymer emulsion, coating thereof and method for preparing same
CN101307137B (en) Water dispersion of self-drying acrylic modified alkyd resin and industrial topcoat using the water dispersion as base
CN101429267B (en) Preparation and uses of epoxy/acrylic acid hybridisation emulsion
CN107384011B (en) PVC floor film gravure printing water-based ink and preparation method thereof
CN110078867B (en) Core-shell pure acrylic emulsion for exterior wall coating and preparation method and application thereof
CN110894394A (en) Water-based polyester amino baking varnish coating and preparation method and application thereof
CN101319113B (en) Medium-temperature baking type fluorine-carbon paint and its use method
CN102140149A (en) Aqueous emulsion composition, and emulsion resin prepared by using same and use thereof
CN103756601B (en) Metal(lic)powder tackiness agent and preparation method thereof and wallpaper, textiles
CN104559465A (en) Environment-friendly aqueous printing ink and preparation method thereof
KR20150027698A (en) A process for preparing color dispersions and the color dispersions made thereof
CN111454609A (en) PP decorative film gravure printing water-based ink without pretreatment and preparation method thereof
CN115141503B (en) Bio-based polymer cement waterproof coating
CN113621290A (en) Low-VOC high-gloss water-based steel drum outer wall coating and preparation method thereof
CN104311728A (en) Thermoplastic acrylic resin for water transfer printing, preparation method of thermoplastic acrylic resin and water transfer printing ink composition
CN1817988A (en) Nanometer composite water based paint of imitated curtain wall and production thereof
CN102702411A (en) Core-shell matte emulsion as well as preparation method and application of core-shell matte emulsion in water matte gloss oil
CN113929825B (en) Carboxyl styrene-butadiene latex for building coating and preparation method thereof
CN102286131A (en) Organic fluorine monomer modified epoxy acrylate emulsion and preparation method thereof as well as antifouling paint containing the emulsion and preparation method thereof
CN104725570A (en) Latex and preparation method thereof
CN104830192A (en) High-weatherability and high-toughness aqueous paint
CN113321442A (en) Method for preparing redispersible latex powder by taking modified silicone-acrylic emulsion as raw material
CN113583510A (en) Pre-impregnated paper gravure printing water-based ink and preparation method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20200728