CN111363411A - Rubber ink composition, preparation method and application method - Google Patents

Rubber ink composition, preparation method and application method Download PDF

Info

Publication number
CN111363411A
CN111363411A CN202010392470.2A CN202010392470A CN111363411A CN 111363411 A CN111363411 A CN 111363411A CN 202010392470 A CN202010392470 A CN 202010392470A CN 111363411 A CN111363411 A CN 111363411A
Authority
CN
China
Prior art keywords
parts
ink composition
castor oil
rubber
rubber ink
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.)
Granted
Application number
CN202010392470.2A
Other languages
Chinese (zh)
Other versions
CN111363411B (en
Inventor
赵宇晗
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.)
Dra Jet Print Technology Co ltd
Original Assignee
Dra Jet Print 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 Dra Jet Print Technology Co ltd filed Critical Dra Jet Print Technology Co ltd
Priority to CN202010392470.2A priority Critical patent/CN111363411B/en
Publication of CN111363411A publication Critical patent/CN111363411A/en
Application granted granted Critical
Publication of CN111363411B publication Critical patent/CN111363411B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

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
    • C09D11/30Inkjet printing inks
    • C09D11/38Inkjet printing inks characterised by non-macromolecular additives other than solvents, pigments or dyes
    • 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
    • C09D11/03Printing inks characterised by features other than the chemical nature of the binder
    • C09D11/037Printing inks characterised by features other than the chemical nature of the binder characterised by the pigment
    • 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
    • C09D11/102Printing inks based on artificial resins containing macromolecular compounds obtained by reactions other than those only involving unsaturated carbon-to-carbon bonds
    • C09D11/103Printing inks based on artificial resins containing macromolecular compounds obtained by reactions other than those only involving unsaturated carbon-to-carbon bonds of aldehydes, e.g. phenol-formaldehyde resins
    • 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
    • C09D11/30Inkjet printing inks
    • C09D11/32Inkjet printing inks characterised by colouring agents
    • C09D11/322Pigment inks
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2321/00Characterised by the use of unspecified rubbers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2461/00Characterised by the use of condensation polymers of aldehydes or ketones; Derivatives of such polymers
    • C08J2461/04Condensation polymers of aldehydes or ketones with phenols only
    • C08J2461/06Condensation polymers of aldehydes or ketones with phenols only of aldehydes with phenols
    • C08J2461/14Modified phenol-aldehyde condensates

Abstract

The invention belongs to the technical field of printing ink, and particularly relates to a rubber printing ink composition, a preparation method and an application method, wherein the rubber printing ink composition comprises, by weight, 5-15 parts of rosin modified castor oil phenolic resin, 1-3 parts of castor oil mercaptopropionate, 3-20 parts of a pigment, 0.5-2 parts of a dispersing agent, 0.5-1.5 parts of an anti-settling agent, 1-5 parts of an adhesion promoter and 60-80 parts of an organic solvent. The rubber ink composition can be directly sprayed on tire rubber at a temperature of 80-130 ℃, vulcanized for 20-50 minutes at a temperature of 150-180 ℃, and has the advantages of high adhesive force, good temperature resistance and difficult discoloration.

Description

Rubber ink composition, preparation method and application method
Technical Field
The invention belongs to the technical field of printing ink, and relates to a rubber printing ink composition, a preparation method and an application method.
Background
The rubber ink is an ink printed on rubber, and is required to resist high temperature in a rubber processing process, and has less yellowing or no yellowing and good adhesive force, but the existing rubber ink has defects.
Disclosure of Invention
It is an object of the present invention to overcome the disadvantages of the prior art and to provide a rubber ink composition.
Another object of the present invention is to provide a method for preparing a rubber ink composition.
It is still another object of the present invention to provide a method for using a rubber ink composition.
The technical scheme of the invention is as follows:
the rubber ink composition comprises, by weight, 5-15 parts of rosin modified castor oil phenolic resin, 1-3 parts of castor oil mercaptopropionate, 3-20 parts of pigment, 0.5-2 parts of dispersing agent, 0.5-1.5 parts of anti-settling agent, 1-5 parts of adhesion promoter and 60-80 parts of organic solvent.
In the invention, the viscosity (35 ℃) of the rosin modified castor oil phenolic resin is 2000-4000 cP.
In the invention, the castor oil mercaptopropionate is obtained by esterification reaction of castor oil and mercaptopropionic acid.
In the invention, the pigment is selected from one or more of inorganic pigments or organic pigments. The inorganic pigment may be at least one selected from titanium dioxide, cadmium yellow, iron blue, chrome red, lithopone, iron red, iron yellow, chromium oxide green, lead chrome green, iron blue, cobalt blue and ultramarine. The organic pigment may be selected from at least one of permanent orange RN, gold brilliant red C, benzidine yellow G, macromolecular orange 4R, macromolecular red R, permanent red F5R, c.i. pigment violet 1, c.i. pigment orange 17, c.i. pigment blue 17, c.i. pigment violet 3, c.i. phthalocyanine blue 15, phthalocyanine red, phthalocyanine violet, permanent violet RL, pigment yellow 2GLT and permanent orange HSL.
In the present invention, the dispersant is selected from polymeric dispersants. The polymeric dispersant may be selected from polycarboxylate dispersants.
In the invention, the anti-settling agent is selected from one or more of organic bentonite, fumed silica, castor oil derivatives, polyamide wax and modified hydrogenated castor oil.
In the invention, the adhesion promoter is selected from silane coupling agents. The silane coupling agent may be selected from the group consisting of silane coupling agents containing a carbon-carbon unsaturated double bond, including but not limited to vinyltrimethoxysilane, vinyltriethoxysilane, vinylmethyldimethoxysilane, vinylmethyldiethoxysilane, methacryloxypropyltrimethoxysilane, methacryloxypropyltriethoxysilane, methacryloxypropylmethyldimethoxysilane, and methacryloxypropylmethyldiethoxysilane.
In the invention, the organic solvent is one or more selected from butanone, cyclohexanone, butyl acetate, N-butanol, propylene glycol monomethyl ether, ethylene glycol monomethyl ether, dipropylene glycol monomethyl ether, diethylene glycol monomethyl ether, N-Dimethylformamide (DMF), N-dimethylacetamide (DMAc), 1,2, 4-trimethylbenzene and 1,3, 5-trimethylbenzene.
According to the preparation method of the rubber ink composition, the raw material components are accurately weighed according to the formula, the organic solvent is added into a stirring kettle, the rosin modified castor oil phenolic resin and the castor oil mercaptopropionate are added, stirring and dissolving are carried out, the pigment, the dispersing agent, the anti-settling agent and the adhesion promoter are added, and the rubber ink composition is obtained after full mixing and uniform dispersion.
The application method of the rubber ink composition disclosed by the invention is directly sprayed on rubber at the temperature of 80-130 ℃, and the rubber ink composition is cured for 20-50 minutes at the temperature of 150-180 ℃. Or spraying the coating on rubber at room temperature, and curing at 150-180 ℃ for 20-50 minutes. The rubber may be selected from natural rubber, tyre rubber, ethylene propylene rubber, styrene butadiene rubber, neoprene rubber, isoprene rubber or butyl rubber.
The rubber ink composition of the present invention has a viscosity (25 ℃) of 1 to 18 mPas.
The invention has the beneficial effects that:
(1) after the rubber ink composition is sprayed on rubber and heated and cured, the rubber ink composition has good adhesive force and good temperature resistance and is not easy to yellow.
(2) The rubber ink composition is convenient to apply, can be directly sprayed on rubber at normal temperature and then heated and cured, and can also be directly sprayed on rubber at 80-130 ℃ and then heated and cured.
Detailed Description
The technical solution of the present invention is further illustrated and described by the following detailed description.
Unless otherwise specified, the parts in the following embodiments are parts by weight.
Example 1
According to the formula: 5 parts of rosin modified castor oil phenolic resin, 1 part of castor oil mercaptopropionate, 3 parts of iron yellow pigment, 0.5 part of polymeric dispersant, 0.5 part of organic bentonite, 1 part of vinyl trimethoxy silane and 60 parts of diethylene glycol monomethyl ether.
Adding diethylene glycol monomethyl ether into a stirring kettle, adding rosin modified castor oil phenolic resin and castor oil mercaptopropionate, stirring for dissolving, adding iron yellow pigment, a polymer type dispersant, organic bentonite and vinyl trimethoxy silane, fully mixing, and uniformly dispersing to obtain the rubber ink composition, which is marked as C-1.
Example 2
According to the formula: 15 parts of rosin modified castor oil phenolic resin, 3 parts of castor oil mercaptopropionate, 18.5 parts of titanium dioxide, 1.5 parts of permanent violet RL pigment, 2 parts of polymeric dispersant, 1.5 parts of fumed silica, 5 parts of methacryloxypropyltriethoxysilane, 20 parts of 1,3, 5-trimethylbenzene and 60 parts of propylene glycol monomethyl ether.
Adding 1,3, 5-trimethylbenzene and propylene glycol monomethyl ether into a stirring kettle, adding rosin modified castor oil phenolic resin and castor oil mercaptopropionate, stirring for dissolving, adding titanium dioxide, permanent violet RL pigment, a polymer dispersant, fumed silica and methacryloxypropyl triethoxysilane, fully mixing, and uniformly dispersing to obtain the rubber ink composition which is marked as C-2.
Example 3
According to the formula: 10 parts of rosin modified castor oil phenolic resin, 2 parts of castor oil mercaptopropionate, 9.5 parts of titanium dioxide, 0.7 part of benzidine yellow G pigment, 1 part of polymeric dispersant, 1 part of modified hydrogenated castor oil, 3 parts of vinyl triethoxysilane, 20 parts of butanone and 50 parts of DMF.
Adding butanone and DMF into a stirring kettle, adding rosin modified castor oil phenolic resin and castor oil mercaptopropionate, stirring for dissolving, adding titanium dioxide and benzidine yellow G pigment, benzidine yellow G dispersing agent, modified hydrogenated castor oil and vinyl triethoxysilane, fully mixing, and uniformly dispersing to obtain the rubber ink composition, which is marked as C-3.
Example 4
According to the formula: 12 parts of rosin modified castor oil phenolic resin, 1.3 parts of castor oil mercaptopropionate, 14 parts of titanium dioxide, 1 part of C.I. pigment blue 17 pigment, 1.3 parts of polymeric dispersant, 1.2 parts of organic bentonite, 2.5 parts of methacryloxypropyltrimethoxysilane, 15 parts of butyl acetate and 58 parts of dipropylene glycol monomethyl ether.
Adding butyl acetate and dipropylene glycol monomethyl ether into a stirring kettle, adding rosin modified castor oil phenolic resin and castor oil mercaptopropionate, stirring for dissolving, adding titanium dioxide, a C.I. pigment blue 17 pigment, a polymer type dispersing agent, organic bentonite and methacryloxypropyl trimethoxy silane, fully mixing, and uniformly dispersing to obtain the rubber ink composition, which is marked as C-4.
Example 5
According to the formula: 8 parts of rosin modified castor oil phenolic resin, 1.6 parts of castor oil mercaptopropionate, 7 parts of titanium dioxide, 0.6 part of phthalocyanine violet pigment, 1.3 parts of polymeric dispersant, 1.2 parts of polyamide wax, 4 parts of methacryloxypropyl methyldimethoxysilane and 65 parts of ethylene glycol monomethyl ether.
Adding ethylene glycol monomethyl ether into a stirring kettle, adding rosin modified castor oil phenolic resin and castor oil mercaptopropionate, stirring for dissolving, adding titanium dioxide, phthalocyanine violet pigment, a polymer dispersant, polyamide wax and methacryloxypropyl methyldimethoxysilane, fully mixing, and uniformly dispersing to obtain the rubber ink composition, which is marked as C-5.
Example 6
According to the formula: 12 parts of rosin modified castor oil phenolic resin, 2.5 parts of castor oil mercaptopropionate, 3.2 parts of permanent orange RN pigment, 1 part of polymeric dispersant, 1.1 parts of castor oil derivative anti-settling agent, 2.5 parts of vinyl methyl dimethoxysilane and 65 parts of cyclohexanone, and mixing.
Adding cyclohexanone into a stirring kettle, adding rosin modified castor oil phenolic resin and castor oil mercaptopropionate, stirring for dissolving, adding the permanent orange RN pigment, the polymeric dispersant, the castor oil derivative anti-settling agent and the vinyl methyl dimethoxyl silane, fully mixing, and uniformly dispersing to obtain the rubber ink composition, which is marked as C-6.
Comparative example 1
According to the formula: 12 parts of rosin modified castor oil phenolic resin, 3.2 parts of permanent orange RN pigment, 1 part of polymeric dispersant, 1.1 parts of castor oil derivative anti-settling agent, 2.5 parts of vinyl methyl dimethoxy silane and 65 parts of cyclohexanone.
Adding cyclohexanone into a stirring kettle, adding rosin modified castor oil phenolic resin, stirring for dissolving, adding permanent orange RN pigment, a polymer type dispersing agent, a castor oil derivative anti-settling agent and vinyl methyl dimethoxy silane, fully mixing, and uniformly dispersing to obtain the rubber ink composition, wherein the mark is C-7.
Comparative example 2
According to the formula: 12 parts of rosin modified phenolic resin, 2.5 parts of castor oil mercaptopropionate, 3.2 parts of permanent orange RN pigment, 1 part of polymeric dispersant, 1.1 parts of castor oil derivative anti-settling agent, 2.5 parts of vinyl methyl dimethoxysilane and 65 parts of cyclohexanone, and mixing.
Adding cyclohexanone into a stirring kettle, adding rosin modified phenolic resin and castor oil mercaptopropionate, stirring for dissolving, adding the permanent orange RN pigment, the polymeric dispersant, the castor oil derivative anti-settling agent and the vinyl methyl dimethoxyl silane, fully mixing, and uniformly dispersing to obtain the rubber ink composition, wherein the mark is C-8.
Comparative example 3
According to the formula: 12 parts of castor oil modified phenolic resin, 2.5 parts of castor oil mercaptopropionate, 3.2 parts of permanent orange RN pigment, 1 part of polymeric dispersant, 1.1 parts of castor oil derivative anti-settling agent, 2.5 parts of vinyl methyl dimethoxysilane and 65 parts of cyclohexanone.
Adding cyclohexanone into a stirring kettle, adding castor oil modified phenolic resin and castor oil mercaptopropionate, stirring for dissolving, adding permanent orange RN pigment, a polymer type dispersing agent, a castor oil derivative anti-settling agent and vinyl methyl dimethoxyl silane, fully mixing, and uniformly dispersing to obtain the rubber ink composition, wherein the mark is C-9.
The properties of the rubber ink compositions C-1 to C-9 are shown in Table 1.
The rubber ink compositions C-1 to C-9 were sprayed on a tire at normal temperature and cured at 160 ℃ for 40 minutes, and the properties are shown in Table 1.
The rubber ink compositions C-1 to C-9 were sprayed on a tire at 110 ℃ and cured at 160 ℃ for 40 minutes, the properties of which are shown in Table 1.
TABLE 1
Figure BDA0002486333490000051
Therefore, the rubber ink composition has better adhesive force and temperature resistance after being sprayed on the surface of rubber and cured.
The foregoing has shown and described the fundamental principles, principal features and advantages of the invention. It should be understood by those skilled in the art that the present invention is not limited by the foregoing embodiments, which are merely preferred embodiments of the present invention, and the scope of the present invention should not be limited thereby, and that equivalent changes and modifications made within the scope of the present invention and the specification should be covered thereby. The scope of the invention is defined by the appended claims and equivalents thereof.

Claims (10)

1. The rubber ink composition is characterized by comprising, by weight, 5-15 parts of rosin modified castor oil phenolic resin, 1-3 parts of castor oil mercaptopropionate, 3-20 parts of pigment, 0.5-2 parts of a dispersing agent, 0.5-1.5 parts of an anti-settling agent, 1-5 parts of an adhesion promoter and 60-80 parts of an organic solvent.
2. The rubber ink composition according to claim 1, wherein the viscosity (35 ℃) of the rosin-modified castor oil phenol resin is 2000 to 4000 cP.
3. The rubber ink composition of claim 1, wherein the castor oil mercaptopropionate is obtained from an esterification reaction of castor oil and mercaptopropionic acid.
4. The rubber ink composition according to claim 1, wherein the pigment is one or more selected from inorganic pigments and organic pigments.
5. The rubber ink composition of claim 1, the dispersant being selected from polymeric dispersants.
6. The rubber ink composition according to claim 1, wherein the anti-settling agent is one or more selected from the group consisting of organobentonite, fumed silica, castor oil derivatives, polyamide wax, and modified hydrogenated castor oil.
7. The rubber ink composition of claim 1, the adhesion promoter being selected from silane coupling agents.
8. The rubber ink composition according to claim 1, wherein the organic solvent is one or more selected from the group consisting of methyl ethyl ketone, cyclohexanone, butyl acetate, N-butanol, propylene glycol monomethyl ether, ethylene glycol monomethyl ether, dipropylene glycol monomethyl ether, diethylene glycol monomethyl ether, N-dimethylformamide, N-dimethylacetamide, 1,2, 4-trimethylbenzene and 1,3, 5-trimethylbenzene.
9. A method for preparing the rubber ink composition as described in any one of claims 1 to 8, wherein the rubber ink composition is obtained by accurately weighing each raw material component according to a formula, adding the organic solvent into a stirring tank, adding the rosin-modified castor oil phenolic resin and the castor oil mercaptopropionate, stirring for dissolution, adding the pigment, the dispersant, the anti-settling agent, and the adhesion promoter, mixing thoroughly, and dispersing uniformly.
10. A method of using the rubber ink composition of any one of claims 1 to 8, wherein the composition is directly sprayed on the rubber at 80 to 130 ℃ and cured at 150 to 180 ℃ for 20 to 50 minutes.
CN202010392470.2A 2020-05-11 2020-05-11 Rubber ink composition, preparation method and application method Active CN111363411B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202010392470.2A CN111363411B (en) 2020-05-11 2020-05-11 Rubber ink composition, preparation method and application method

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202010392470.2A CN111363411B (en) 2020-05-11 2020-05-11 Rubber ink composition, preparation method and application method

Publications (2)

Publication Number Publication Date
CN111363411A true CN111363411A (en) 2020-07-03
CN111363411B CN111363411B (en) 2022-06-07

Family

ID=71205835

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202010392470.2A Active CN111363411B (en) 2020-05-11 2020-05-11 Rubber ink composition, preparation method and application method

Country Status (1)

Country Link
CN (1) CN111363411B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114752253A (en) * 2020-12-29 2022-07-15 苏州圣瑞赛标识科技有限公司 Complete water-based code-spraying ink for tires and preparation method and application thereof
CN116676015A (en) * 2023-07-10 2023-09-01 徐工集团工程机械股份有限公司 Printing ink composition and preparation method and application thereof
WO2024027463A1 (en) * 2023-07-10 2024-02-08 徐工集团工程机械股份有限公司 Ink composition, and preparation method and use thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102911330A (en) * 2012-10-16 2013-02-06 山西省应用化学研究所 Vegetable oil modified rosin phenolic resin and preparation method thereof
CN104086728A (en) * 2014-07-25 2014-10-08 广西众昌树脂有限公司 Preparation method of modified phenolic resin
CN107936696A (en) * 2017-12-27 2018-04-20 明光瑞泰工业有限公司 A kind of automobile tire coding ink and preparation method thereof
CN108431154A (en) * 2015-12-22 2018-08-21 株式会社普利司通 Application composition, cured film, laminated body and tire

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102911330A (en) * 2012-10-16 2013-02-06 山西省应用化学研究所 Vegetable oil modified rosin phenolic resin and preparation method thereof
CN104086728A (en) * 2014-07-25 2014-10-08 广西众昌树脂有限公司 Preparation method of modified phenolic resin
CN108431154A (en) * 2015-12-22 2018-08-21 株式会社普利司通 Application composition, cured film, laminated body and tire
CN107936696A (en) * 2017-12-27 2018-04-20 明光瑞泰工业有限公司 A kind of automobile tire coding ink and preparation method thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114752253A (en) * 2020-12-29 2022-07-15 苏州圣瑞赛标识科技有限公司 Complete water-based code-spraying ink for tires and preparation method and application thereof
CN116676015A (en) * 2023-07-10 2023-09-01 徐工集团工程机械股份有限公司 Printing ink composition and preparation method and application thereof
WO2024027463A1 (en) * 2023-07-10 2024-02-08 徐工集团工程机械股份有限公司 Ink composition, and preparation method and use thereof

Also Published As

Publication number Publication date
CN111363411B (en) 2022-06-07

Similar Documents

Publication Publication Date Title
CN111363411B (en) Rubber ink composition, preparation method and application method
CN107286740B (en) UV-LED offset printing ink and preparation method thereof
CN104151925B (en) High temperature resistant ink and preparation method thereof and OGS contact panels
CN107778979A (en) The sub- gravure ink of the general mute black appliances of insulation of PET and PI films and preparation method
CN104834183B (en) Thermosetting ink composition
CN108504171B (en) UV-LED glass substrate white ink and preparation method thereof
CN109575681B (en) Water-based free radical-cation hybrid photocuring ink and application thereof
WO2017073309A1 (en) Low-temperature baking-adapted resist ink
CN116769349B (en) Phenoxy copolymer-containing doped anti-welding ink, and preparation method and application thereof
CN114292550A (en) Formula and preparation method of ultra-high reflection UV (ultraviolet) ink
CN112341863A (en) UV ink-jet ink and preparation method thereof
JP3813750B2 (en) Color filter manufacturing method and color filter
CN109705620B (en) Alkali-resistant yellow disperse dye composition
CN111349366A (en) UV-LED inkjet ink for PVC leather printing and preparation method thereof
CN114958084B (en) Preparation method of low-viscosity high-solid-content anti-offset composite ink for flexography
CN105462306A (en) Curable resin composition, dry film, cured product and printed wiring board
JP2690855B2 (en) Ink composition for color filter
JP2690856B2 (en) Ink composition for color filter
CN111909118B (en) Oxetane compound, photocurable composition, ink and use thereof
CN111518432A (en) High-temperature-resistant UV (ultraviolet) curing printing ink
Harui et al. Novel ambient temperature curable two-component waterborne silicone-acrylic coatings
CN112552737A (en) Offset printing powder-spraying-free ink
CN111378327A (en) Ink composition and preparation method thereof
CN116376353B (en) Silk screen printing ink and preparation method thereof
CN107686677A (en) A kind of preparation method of the resistance to ink of environment-friendly type

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
GR01 Patent grant
GR01 Patent grant